NASSAWADOX REHABILITATION AND NURSING

9468 HOSPITAL ROAD, NASSAWADOX, VA 23413 (757) 442-5600
For profit - Limited Liability company 145 Beds EASTERN HEALTHCARE GROUP Data: November 2025
Trust Grade
0/100
#263 of 285 in VA
Last Inspection: May 2022

Over 2 years since last inspection. Current conditions may differ from available data.

Overview

Nassawadox Rehabilitation and Nursing has received a Trust Grade of F, indicating significant concerns about the quality of care provided. They rank #263 out of 285 nursing homes in Virginia, placing them in the bottom half of facilities in the state. However, it is noteworthy that the facility is improving, with issues decreasing from 29 in 2022 to 4 in 2023. Staffing is a moderate concern with a rating of 2 out of 5 stars and a 40% turnover rate, which is better than the state average. On the positive side, the facility has not incurred any fines, indicating compliance with regulations, and they provide average RN coverage, which is important for catching potential problems early. Despite these strengths, there are serious weaknesses to consider. For example, inspectors found that staff failed to provide necessary treatment for a resident's pressure ulcer, which had progressed to an unstageable stage with dead tissue. Additionally, another resident's deteriorating pressure ulcer was not reported to a physician in time, resulting in further complications. Families should weigh these factors carefully when considering this facility for their loved ones.

Trust Score
F
0/100
In Virginia
#263/285
Bottom 8%
Safety Record
High Risk
Review needed
Inspections
Getting Better
29 → 4 violations
Staff Stability
○ Average
40% turnover. Near Virginia's 48% average. Typical for the industry.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most Virginia facilities.
Skilled Nurses
⚠ Watch
Each resident gets only 27 minutes of Registered Nurse (RN) attention daily — below average for Virginia. Fewer RN minutes means fewer trained eyes watching for problems.
Violations
⚠ Watch
56 deficiencies on record. Higher than average. Multiple issues found across inspections.
★☆☆☆☆
1.0
Overall Rating
★★☆☆☆
2.0
Staff Levels
★★★☆☆
3.0
Care Quality
★☆☆☆☆
1.0
Inspection Score
Stable
2022: 29 issues
2023: 4 issues

The Good

  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover below average (40%)

    8 points below Virginia average of 48%

Facility shows strength in fire safety.

The Bad

1-Star Overall Rating

Below Virginia average (3.0)

Significant quality concerns identified by CMS

Staff Turnover: 40%

Near Virginia avg (46%)

Typical for the industry

Chain: EASTERN HEALTHCARE GROUP

Part of a multi-facility chain

Ask about local staffing decisions and management

The Ugly 56 deficiencies on record

5 actual harm
Sept 2023 2 deficiencies
CONCERN (E) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0567 (Tag F0567)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on information from the family interview, staff interview, and review of facility documents, the facility's staff failed t...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on information from the family interview, staff interview, and review of facility documents, the facility's staff failed to deposit monthly personal needs allowance funds in the account for 1 of 8 residents (Resident #1), in the survey sample. The findings included: Resident #1 was originally admitted to the facility on [DATE]. The resident has never been discharged from the facility. The current diagnoses included Alzheimer's Disease Unspecified and Unspecified Dementia. The annual Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 06/24/2023 coded the resident as not having the ability to complete the Brief Interview for Mental Status (BIMS). He was coded to have short and long-term memory problems. An interview was conducted with the Resident Representative/Family Member #1 on 09/06/23 at approximately 11:10 AM. She stated that the facility has been withholding monies from Resident #1's personal account because he should be getting a $40 monthly allowance. An interview was conducted with the Ombudsman (OSM/Other Staff Member #5) on 09/06/23 at approximately 9:15 AM., The Ombudsman stated that when Family Member #1 was Representative Payee/RP, she didn't pay the facility, but now that the facility is currently the RP., the resident doesn't have money in his account even though he's entitled to receive his $40 per month for personal funds. An interview was conducted with the BOM/Business Office Manager/OSM #2 on 9/06/23 at approximately 12:00 PM. She stated the accounting ledger was reviewed from August 2021 to current (9/06/23) but the account had not been set up for Resident #1 to receive his forty dollars ($40/month) a month. She said the facility had been Representative Payee/Rep. since October 2022 and that his income was coming to the facility for care costs and is being applied to the past due balance and arrears. The resident's statement of personal funds account was reviewed with the BOM. The Review dates on the ledger were 10/03/22-9/01/23. It Read: Allowance: $0. Date opened 09/08/22. Current Balance: $0. On 9/6/23 at 5:20 p.m., the BOM presented the surveyor with a Record of the Deposit of Resident #1's personal funds dated 9/6/2023 at 4:13 PM, $480.00 was deposited to his account. A review of Resident #1's Statement dated 9/07/23 showed a credit adjustment of $480, $40 monthly x 12 months (October 2022-September 2023 per BOM. Policy: Resident Personal Funds. Date: 11/01/21. Date Reviewed: 12/01/22. The Policy reads: The resident has a right to manage his or her financial affairs to include the right to know, in advance what charges a facility may impose against a resident's personal funds. Deposit of funds: Residents whose care is funded by Medicaid; the facility will deposit the resident's personal funds in excess of $50 in an interest-bearing account. On 9/07/23 at approximately 1:15 PM., a final interview was conducted with the Administrator, DON (Director of Nursing), the BOM (Business Office Manager), and Medical Records/MR staff. The MR staff stated there were no MR requests on file from the Resident's Family Member #1 nor from the Ombudsman. The BOM stated that the $40 had been credited back to the Resident's account and that moving forward he would get his $40 monthly.
CONCERN (E) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0568 (Tag F0568)

Could have caused harm · This affected multiple residents

Based on information from a family interview, staff interview, and review of facility documents, the facility's staff failed to ensure resident and other funds were not commingled with facility funds ...

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Based on information from a family interview, staff interview, and review of facility documents, the facility's staff failed to ensure resident and other funds were not commingled with facility funds for six (6) of 6 reviewed resident accounts (Resident #1, Resident #2, Resident #3, Resident #4, Resident #5, and Resident #6), in the survey sample. The findings included: All six (6) resident statements of accounts were reviewed and noted to be commingled with other accounts such as care costs and direct deposits. The $40 personal allowances were not listed in the description on the resident's ledger. 1. Resident #1- On 9/6/23 at 11:10 a.m., an interview was conducted with Family Member #1 (FM #1). She said that she was going through financial hardship because the facility was keeping all her husband's money including her spousal support and the resident's $40 allowance. She stated, I have a (name of legal service) helping me to get my money. The administration and business office staff wouldn't talk to me when I called. They became his Rep., Payee in October (2022). She also said that she had obtained a few appeals to keep her husband in the facility because they were trying to discharge him, but she was not able to care for him in the home. On 9/06/23 at approximately 3:45 p.m., the Administrator stated she was told that all monies had to remain in the resident's account to cover his arrearage. Prior to the survey exit, the Business Office Manager (BOM) showed evidence to the survey team of certified mail on 9/07/23 at approximately 9:30 AM., with several documents attached. A letter addressed to Family Member #1, in reference to Resident #1 read: Enclosed you will find a check in the amount of $13,631.47. This is the amount due to you after Spousal Support has been calculated minus the pension that you were receiving. A breakdown has been included with the check. A Certified Mail Receipt was attached to the above documents dated 9/07/23 at 08:45 AM. 2. Resident #2- Resident statement dated 10/03/22-9/01/23 included Social Security Income, care costs, beauty shop, and barber costs. Although it was determined that the resident was receiving their personal funds of 40/month, it was not listed in the description on the ledger. 3. Resident #3- Resident statement dated 10/03/22-9/01/23 included care costs and direct deposits. Although it was determined that the resident was receiving their personal funds of 40/month, it was not listed in the description on the ledger. 4. Resident #4-Resident statement dated 10/03/22-9/01/23 included direct deposits. Although it was determined that the resident was receiving their personal funds of 40/month, it was not listed in the description on the ledger. 5. Resident #5-Resident statement dated 7/03/23-9/01/23 included care costs. Although it was determined that the resident was receiving their personal funds of 40/month, it was not listed in the description on the ledger. 6. Resident #6-Resident statement dated 10/03/22-09/01/23 included care costs and direct deposits. Although it was determined that the resident was receiving their personal funds of 40/month, it was not listed in the description on the ledger. An interview was conducted on 9/07/23 at approximately 1:45 PM., with the BOM concerning the resident's statements. She said that the personal funds of $40 per month were included in the resident's statements which are subtracted from the care cost because there's no separate ledger to itemize their personal fund amounts. Policy: Accounting and Records. Date: 11/01/21. Date Reviewed: 12/01/22. The Policy reads: The resident has a right to manage his or her financial affairs to include the right to know, in advance what charges a facility may impose against a resident's personal funds. 1. The facility will establish and maintain a system that assures a full complete and separate accounting, according to generally accepted accounting principles, of each resident's personal funds entrusted to the facility on the resident's behalf. 2. The system will preclude any commingling of resident funds with facility funds or with the funds of any person other than another resident.
Jun 2023 2 deficiencies
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Report Alleged Abuse (Tag F0609)

Could have caused harm · This affected 1 resident

Based on staff interviews, record review, facility documentation and hospital record review, the facility staff failed to report an allegation of abuse for 1 of 2 residents (Resident #1) in the survey...

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Based on staff interviews, record review, facility documentation and hospital record review, the facility staff failed to report an allegation of abuse for 1 of 2 residents (Resident #1) in the survey sample. The finding included: Resident #1 was originally admitted the nursing facility on 03/29/23. The resident was discharged to an acute hospital setting on 06/08/23, returned on 06/17/23. Diagnosis for Resident #1 included but not limited to Dementia with behavioral/psychotic/mood disturbances with anxiety. The most recent Minimum Data Set (MDS - an assessment protocol) a quarterly assessment with an Assessment Reference Date (ARD) of 06/07/23 coded the resident's Brief Interview for Mental Status (BIMS) scored 00 of a possible 15 with severe impairment for daily decision-making. The MDS coded Resident #1 total dependence of one with bathing, extensive assistance of one with toilet use, personal hygiene and dressing, limited assistance of one with transfer, bed mobility, and eating for Activities of Daily Living (ADL) care. A review of Resident #1's person-centered care plan revised on 04/11/23 documented with the potential to be a physically aggressive towards staff/residents related to dementia. The goal set for the resident by the staff was not to harm self or others through the next review date 10/10/23. Some of the interventions to manage the resident's goal is to analyze times of day, places, circumstances, triggers, and what de-escalates behavior and document, administer medications as ordered and monitor/document for side effects and effectiveness, when the resident becomes agitated: intervene before agitation escalates; guide away from source of distress; engage calmly in conversation; if response is aggressive, staff to walk calmly away, and approach later. A review of Resident #1's nursing progress notes entered on 06/8/23, by Registered Nurse (RN) #1 stated she was called to the activity room by Certified Nursing Assistant (CNA) #1. The notes indicated the resident was found unresponsive, lying face down on the floor with blood under her face with both arms under her body. Resident #1 was transferred via 911 (emergent) to the local hospital and admitted . A phone call was placed to RN #1 on 06/29/23 at 8:21 a.m., and again at 9:53 a.m., but was unable to leave a message. A message was heard that stated the person you are trying to reach is not available at this time, please try again later. The RN was assigned to Resident #1 on 06/08/23 (7p-7a) the day an allegation of abuse was made against the nursing staff at (name of facility). On 06/29/23 at 12:33 p.m., an interview was conducted with License Practical Nurse (LPN) #1. LPN #1 worked on 06/08/23, the day Resident #1 was transferred and admitted to the hospital. She stated she observed the resident on the floor in the day room, face down with blood under her head. She stated a pressure dressing was applied by RN #1. The LPN stated she did not see any bruising to the resident's extremities. A review of the hospital records revealed Resident #1 presented in the emergency room (ER) on 06/08/23 from (name of nursing facility) for further evaluation due recent fall and altered mental status. The record indicated the resident was bagged 911 transport for decreased respiratory rate of four (4) and hypoxia (lack of enough oxygen in the tissues to sustain bodily function and oxygen saturations in the 80's (normal is 95 percent (%) or greater). A laceration noted to the right forehead that is consistent with the reported fall and her two (2) front teeth were chipped. A skin assessment was completed during the ER visit with gross ecchymosis (bruising) noted on both wrists and ankles. The note indicated Resident #1 showed obvious signs of abuse while residing at (name of nursing facility). The resident's advocate and local sheriff's department were notified to file a case due to possible abuse from staff at nursing home. On 06/09/23, three images of x-rays were performed on each ankle and foot with bilateral ankle swelling/evidence of injury. The x-ray showed normal alignment and normal mineralization with no osseous lesions or fractures. On 06/09/23, three images of x-rays were performed to the left and right wrist. The right wrist noted with swelling/deformity, hand, and wrist trauma with no acute fracture. The soft tissues are normal. Degenerative changes in the interphalangeal joints of both hands with no acute fracture. The soft tissues are normal. There is no acute abnormality in either wrist or hand. On 06/30/23 at 9:30 a.m., an interview was conducted with the Director of Nursing (DON). She stated the Director of Admissions informed her and the Administrator the hospital discharge summary contained an allegation of abuse against (name of nursing home). She stated the discharged summary indicated Resident #1 had been restrained while residing in the nursing facility. She stated she asked the nursing staff on the memory care unit if they witnessed Resident #1 being restrained or abused by any staff members and they all, replied No. The DON stated you have 24 hours to report an allegation of abuse. A phone interview was conducted with the Admissions Director on 06/30/23 at 10:39 a.m. She stated as soon as she read Resident #1's hospital discharge paperwork (not sure of the actual date), but it was when the resident was discharged from the initial hospital to another hospital. She stated the discharge summary alleged abuse against the nursing facility. She stated she immediately informed the Administrator and DON about the allegation of abuse. On 06/30/23 at 1:15 p.m., the Administrator, Director of Nursing informed of the above findings. The Administrator stated a Facility Reported Incident (FRI) for the above allegation of abuse was never sent to the Ombudsman or Virginia Department of Health. The facility's policy titled Abuse, Neglect, Exploitation or Misappropriate - Reporting and Investigating, revised on 09/22. It is the facility's policy all reports of resident abuse (including injuries of unknown origin), neglect, exploitation, or the theft/misappropriation of resident property are reported to local, state, and federal agencies (as required by current regulations) and thoroughly investigated by facility management. Findings of all investigations are document and reported. Reporting Allegations to the Administrator and Authorities read in part: 1. If resident abuse, neglect, exploitation, misappropriation of resident property or injury of unknown source is suspected, the suspicion must be reported immediately to the administrator and to their officials according to state law. 2. The administrator or the individual making the allegation immediately reports his other suspicion to the following persons or agencies: a. The state licensing/certification agency responsible for surveying/licensing the facility. b. The local/state ombudsman 3. Immediately is defined as within two (2) hours of an allegation involving abuse or result in serious bodily injury; or with 24 hours of an allegation that does not involve abuse or result in serious bodily injury.
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Investigate Abuse (Tag F0610)

Could have caused harm · This affected 1 resident

Based on staff interviews, record review and facility documentation and hospital record review, the facility staff failed to investigate an allegation of abuse for 1 of 2 residents (Resident #1) in th...

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Based on staff interviews, record review and facility documentation and hospital record review, the facility staff failed to investigate an allegation of abuse for 1 of 2 residents (Resident #1) in the survey sample. The finding included: Resident #1 was originally admitted the nursing facility on 03/29/23. The resident was discharged to an acute hospital setting on 06/08/23, returned on 06/17/23. Diagnosis for Resident #1 included but not limited to Dementia with behavioral/psychotic/mood disturbances with anxiety. The most recent Minimum Data Set (MDS - an assessment protocol) a quarterly assessment with an Assessment Reference Date (ARD) of 06/07/23 coded the resident's Brief Interview for Mental Status (BIMS) scored 00 of a possible 15 with severe impairment for daily decision-making. The MDS coded Resident #1 total dependence of one with bathing, extensive assistance of one with toilet use, personal hygiene and dressing, limited assistance of one with transfer, bed mobility, and eating for Activities of Daily Living (ADL) care. A review of Resident #1's person-centered care plan revised on 04/11/23 documented with the potential to be a physically aggressive towards staff/residents related to dementia. The goal set for the resident by the staff was not to harm self or others through the next review date 10/10/23. Some of the interventions to manage the resident's goal was to analyze times of day, places, circumstances, triggers, and what de-escalates behavior and document, administer medications as ordered and monitor/document for side effects and effectiveness, when the resident becomes agitated: intervene before agitation escalates; guide away from source of distress; engage calmly in conversation; if response is aggressive, staff to walk calmly away, and approach later. A review of Resident #1's nursing progress entered on 06/8/23, by Registered Nurse (RN) #1 stated she was called to the activity room by Certified Nursing Assistant (CNA) #1. The noted stated the resident was found unresponsive, lying face down on the floor with blood under her face with both arms under her body. Resident #1 was transferred via 911 (emergent) to the local hospital and admitted . A phone call was placed to RN #1 on 06/29/23 at 8:21 a.m., and again at 9:53 a.m., but was unable to leave a message. A message was heard that stated the person you are trying to reach is not available at this time, please try again later. The RN was assigned to Resident #1 on 06/08/23 (7p-7a) the day an allegation of abuse was made against the nursing staff at (name of facility). On 06/29/23 at 12:33 p.m., an interview was conducted with License Practical Nurse (LPN) #1. LPN#1 worked on 06/08/23, the day Resident #1 was transferred and admitted to the hospital. She stated she observed the resident on the floor in the day room, face down with blood under her head. She stated a pressure dressing was applied by RN #1. The LPN stated she did not see any bruising to the resident's extremities. A review of the hospital records revealed Resident #1 presented in the emergency room (ER) on 06/08/23 from (name of nursing facility) for further evaluation due recent fall and altered mental status. The record indicated the resident was bagged 911 transport for decreased respiratory rate of four (4) and hypoxia (lack of enough oxygen in the tissues to sustain bodily function and oxygen saturations in the 80's (normal is 95 percent (%) or greater). A laceration noted to the right forehead that is consistent with the reported fall and her two (2) front teeth were chipped. A skin assessment was completed during the ER visit with gross ecchymosis (bruising) noted on both wrists and ankles. The note indicated Resident #1 showed obvious signs of abuse while residing at (name of nursing facility). The residents advocate and local sheriff's department were notified to file a case due to possible abuse from staff at nursing home. On 06/09/23, three images of x-rays were performed on each ankle and foot with bilateral ankle swelling/evidence of injury. The x-ray showed normal alignment and normal mineralization with no osseous lesions or fractures. On 06/09/23, three images of x-rays were performed to the left and right wrist. The right wrist noted with swelling/deformity, hand, and wrist trauma with no acute fracture. The soft tissues are normal. Degenerative changes in the interphalangeal joints of both hands with no acute fracture. The soft tissues are normal. There is no acute abnormality in either wrist or hand. On 06/28/23 at 10:30 a.m., an interview was conducted with Certified Nursing Assistant (CNA) #1. The CNA stated she was on lunch break when a resident was yelling a resident was on the floor in the resident's day room. She stated the resident was observed face down on the floor with blood underneath her head. She stated she immediately informed RN #1. The CNA stated she did not observe any bruises to Resident #1 wrist or ankles. CNA #2 was interviewed on 06/29/23 at 1:00 p.m. She stated some forms of abuse are mental, physical (holding a resident down, grabbing them, the use of restraints) locking them in their room. She stated she never saw bruising to the Resident #1's wrist or ankles. She said the DON asked if she ever observed Resident #1 ever being restrained or abused by staff, she replied, No. She stated she was never asked to write a statement. On 06/30/23 at 9:30 a.m., an interview was conducted with the Director of Nursing (DON). She stated the Director of Admissions informed her and the Administrator the hospital discharge summary contained an allegation of abuse against (name of nursing home). She stated the discharged summary indicated Resident #1 had been restrained while residing in the nursing facility. She stated she asked the nursing staff on the memory care unit if they witnessed Resident #1 being restrained or abused by any staff members and they all, replied No. The DON stated she never completed an investigation. A phone interview was conducted with the Admissions Director on 06/30/23 at 10:39 a.m. She stated as soon as she read Resident #1's hospital discharge paperwork (not sure of the actual date), but it was when the resident was discharged from the initial hospital to another hospital. She stated the discharge summary alleged abuse against the nursing facility. She stated she immediately informed the Administrator and DON about the allegation of abuse. On 06/30/23 at 1:15 p.m., the Administrator, Director of Nursing informed of the above findings. No further information was provided prior to exit. The facility's policy titled Abuse, Neglect, Exploitation or Misappropriate - Reporting and Investigating, revised on 09/22. It is the facility's policy all reports of resident abuse (including injuries of unknown origin), neglect, exploitation, or the theft/misappropriation of resident property are reported to local, state, and federal agencies (as required by current regulations) and thoroughly investigated by facility management. Findings of all investigations are document and reported. Investigating Allegations read in part: 1. All allegations are thoroughly investigated. The administrator initiates investigations. 2. Investigations may be assigned to an individual trained in reviewing, investigating, and reporting such allegations. 11. Upon conclusion of the investigating, the investigator records the findings of the investigation on approved documentation forms and provides the completed documentation to the administrator.
May 2022 29 deficiencies 5 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Notification of Changes (Tag F0580)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** The facility staff failed to notify the physician or the wound Nurse Practitioner of a deteriorating stage II pressure ulcer pri...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** The facility staff failed to notify the physician or the wound Nurse Practitioner of a deteriorating stage II pressure ulcer prior to advancing to an unstageable pressure ulcer for 1 out of 55 residents (Resident #291) in the survey sample. The finding included: Resident #291 was originally admitted to the facility on [DATE]. Diagnosis for Resident #291 included but are not limited to Parkinson disease and muscle weakness. Resident #291's admission Assessment (14-day) with an ARD of 03/19/22 coded Resident #291 Brief Interview for Mental Status (BIMS) scored a 99 indicating short and long term memory problems and severe cognitive impairment - never/rarely made decisions. Resident #291 was coded total dependence of two with toilet use, bed mobility and bathing, total dependence of one with dressing, personal hygiene and eating and for Activities of Daily Living (ADL). Resident #291 was coded as having no mood, rejection of care or behavioral problems. Resident #291's person-centered care plan initiated on 03/21/22 identified the resident has a pressure ulcer in her sacral area, at risk for further skin breakdown related to incontinence and impaired mobility. The goal set for the resident by the staff was that the resident will remain free of new skin breakdown through next review date. Some of the interventions/approaches the staff would use to accomplish this goal is to follow facility policies/protocols for the prevention/treatment of skin breakdown, assess/record/monitor wound healing, measure length, width and depth where possible, assess and document status of wound perimeter, wound bed and healing progress and report improvements and declines to the physician. The skin/wound admission note dated 03/10/22 indicated Resident #291 had a stage II sacral ulcer measuring 2.0 cm x 1.0 cm x 0.2 cm with very dark skin, non-blachable measuring (15 cm x 9 cm) surrounding the sacral ulcer. A review of Resident #291's nurse's note revealed the resident was transferred to the hospital on [DATE] at approximately 6:50 p.m., and returned on 03/15/22 at approximately 4:00 p.m. Further review of the nurse's note revealed no new skin impairments noted since the last admission assessment on 03/10/22. The admission/readmission note on 03/15/22 under skin integrity revealed a stage II sacral pressure. During the review of Resident #291's clinical record revealed there were no weekly wound assessments made to the sacral pressure ulcer for 19 days, after her original admission to the facility. An interview was conducted with the wound NP on 05/17/22 at approximately 3:06 p.m., who said, My first time evaluating Resident #291's pressure ulcer was on 03/29/22. The wound NP said the wound was infected as evidence by the wound having a significant amount of slough with foul odor present and having significant pain over the sacral area when touched or palpated. The wound NP stated, I was never informed that Resident #291's stage II pressure ulcer had deteriorated and had advance to an unstageable. The wound NP initial progress note of the sacral pressure ulcer on 03/29/22 revealed an unstageable ulcer measuring 5 cm x 5 cm x 2 cm. The progress note stated the sacral wound had a moderate amount of serosanquinous drainage, strong odor present with 90 percent (%) slough and 10 % dermis tissue. A new medication order was given for Augmentin (antibiotic) 500 mg/125 mg every 12 hours x 10 days for a sacral wound infection. A new treatment order was given to clean the sacral wound with Dakin's, Santyl on Dakin's gauze, and cover with foam dressing daily and as needed. The wound NP progress note also stated pain is indicative of any movement, at rest she is comfortable. The wound NP also offered further recommendations to turn and reposition per facility protocol, use of a low air loss mattress and to optimize nutrition. A wound NP progress note dated 04/05/22 revealed the sacral wound pressure ulcer remained an unstageable measuring 5 cm x 5 cm x (?). The sacral wound had improved but remain with moderate amount of serosanquinous drainage, strong odor present with 90% slough and 10% dermis tissue. The wound was debrided removing thick slough tissue; pain was present with any movement. Resident #291 remains on antibiotic therapy for a sacral wound infection and will continue with the current wound treatment with Dakin's, Santyl on Dakin's gauze, and cover with foam dressing daily and as needed. A review of the wound NP progress note dated 04/11/22 indicated the following, The wound visit was performed via telehealth with the wound nurse, License Practical Nurse (LPN #3). The sacral wound is deteriorating with moderate amount of purulent drainage, strong odor present with 90% slough and 10% dermis tissue. The wound measured by onsite nurse (LPN #3) measuring 6.5 cm x 5.5 cm x 2.5 cm. The progress note recommended to continue with current sacral wound treatment with Dakin's, Santyl on Dakin's gauze, foam dressing and change daily and as needed. A new antibiotic order was given for Clindamycin 600 mg by mouth every 8 hours for 21 days for a sacral wound infection. The wound NP progress note also stated pain is indicative of any movement, at rest she is comfortable. An interview was conducted with the Medical Director (MD) on 05/18/22 at approximately 11:33 a.m., who said all pressure ulcers are followed by (name of Wound Company.) Resident #291's sacral ulcer should have been monitored, assessed and measured on a weekly basis for signs of decline or improvement. The changes in the wound should have been addressed before the wound was identified as an unstageable pressure ulcer. The MD stated, (name of Wound Company) or myself should have been notified that Resident #291's sacral ulcer was declining. An interview was conducted with the Director of Nursing (DON) and wound nurse LPN #3 on 05/12/22 at approximately 10:00 a.m. The DON said Resident #291's sacral pressure ulcer should have been evaluated by the wound NP or wound nurse, LPN #3 on a weekly basis. The weekly evaluation and monitoring is needed for early detection to determine if the wound is improving or declining. The DON said the nurses should have been assessing and documenting changes on Resident #291's sacral pressure ulcer (description of wound bed, if drainage or odor present and size of the wound) with all changes reported to LPN #3 or the wound NP for evaluation to determine if wound treatment changes were needed. A debriefing was held with the Administrator, Director of Nursing and Corporate support on 05/19/22 at approximately 2:00 p.m. Resident #291's issues was presented again. No additional information was forthcoming. The facility's policy Notification of Changes - revised on 03/10/2022. The purpose of this policy is to ensure the facility promptly informs the resident, consults the resident's physician; and notifies, consistent with his or her authority, resident's representative when there is a change requiring notification. Compliance Guidelines: The facility must inform the resident, consult with the resident's physician and /or notify the resident's family member or legal representative when there is a change requiring such notification. -Circumstances requiring notification include but not limited to a new treatment, discontinuation of current treatment due to adverse consequences, acute condition or exacerbation of a chronic condition.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Quality of Care (Tag F0684)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. The facility staff failed to ensure resident received her physician prescribed Trulicity Injection for Resident #60 Resident ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. The facility staff failed to ensure resident received her physician prescribed Trulicity Injection for Resident #60 Resident #60 was originally admitted to the facility 08/18/21 from the community. The resident has never been discharged from the facility. The current diagnoses included; Type 2 Diabetes Mellitus and Essential Hypertension. The quarterly Revision, Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 04/10/2022 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #60 cognitive abilities for daily decision making were intact. In sectionG(Physical functioning) the resident was coded as requiring total care of one person with bed mobility, transfers, locomotion, dressing, eating, toileting, personal hygiene and bathing, extensive assistance of one person/two people, limited assistance of one person, supervision after set-up. The care plan dated 4/10/2022 reads: Focus: The resident has Diabetes Mellitus. Goals: The resident will have no complications related to diabetes through the review date. Interventions: Diabetes medication as ordered by doctor. Monitor/document for side effects and effectiveness. The MAR (Medication Administration Record) Trulicity Solution Pen-injector 0.75 MG/0. 5ML (Dulaglutide) Inject 0.75 mg subcutaneously one time a day every Monday for Diabetes. -Start Date 08/23/2021 1000. Missed dosages: Monday 4/11/22. An interview was conducted with Resident #60 on 5/20/22 at 4:55 PM concerning her missed injection. She stated, I don't know what happened or why it wasn't given. Trulicity treats Diabetes Mellitus Type 2. Indicated as once-weekly SC injection adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus (T2DM). It is also indicated to reduce risk of major adverse cardiovascular (CV) events (CV death, nonfatal MI, or nonfatal stroke) in adults with T2DM who have established CV disease or multiple CV risk factors Initial: 0.75 mg SC once weekly May increase dose to 1.5 mg once weekly for additional glycemic control If additional glycemic control needed, increase to 3 mg once weekly after at least 4 weeks on the 1.5-mg dose If additional glycemic control needed, increase to maximum dose of 4.5 mg once weekly after at least 4 weeks on the 3-mg dose. https://reference.medscape.com/drug/trulicity-dulaglutide-999965. 3. The facility staff failed to follow physician orders by not administering physician prescribed medications for Resident #66. Resident #66 was originally admitted to the facility 10/16/2015 from an acute care facility and discharged on 4/11/22 to an acute care facility and returned to the Long Term Care Facility on 4/13/22. The current diagnoses included; Pneumonia and COPD (Chronic Obstructive Pulmonary Disease). The Significant change Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 04/18/2022 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #66 cognitive abilities for daily decision making were intact. In sectionG(Physical functioning) the resident was coded as requiring extensive assistance of one person with bed mobility and dressing. Requiring total dependence of one person with toilet use, personal hygiene and bathing. Requires set-up help only with eating. The care plan dated 4/17/22 reads: Focus: The resident has pain r/t (related/ to) history of pain in left arm and side secondary to CVA (Cerebral Vascular Accident) & polyneuropathy, dental pain. Goals: The resident will not have an interruption in normal activities due to pain through the review date. Interventions: Administer analgesia as per orders. Review of the MAR (Medication Administration Record) reads: Gabapentin Capsule 300 MG Give 1 capsule by mouth one time a day related to POLYNEUROPATHY, UNSPECIFIED (G62.9) -Start Date 04/13/2022 2100 (9:00 PM). Missed dosages: 4/14/22-4/18/22 4/21/22-4/24/22 and 4/27/22-4/28/22. MAR reads: Amoxicillin Tablet 875 MG Give 1 tablet by mouth two times a day for bacterial infection for 10 Days -Start Date 04/13/2022 2100 (9:00 PM). Missed dosages: 4/14/22, 4/18/22, 4/19/22, 4/21/22 and 4/22/22. Cefdinir Capsule 300 MG Give 1 capsule by mouth two times a day for UTI (Urinary Tract Infection) for 10 Days -Start Date 04/07/2022 2100. Missed dosages: 4/08/22-4/12/22, 4/14/22. An interview was conducted on 5/20/22 at 4:40 PM., with the DON (Director of Nursing) concerning the above missed medications. She stated, doing my audit I noticed night time medications on the same exact days as you, aren't being checked off. Residents confirmed they are getting medications on routine at night. Moving forward, I will do an in service on documentation. An interview was conducted with Resident #66 on 5/20/22 at 4:50 PM concerning his missed medications. He stated, As far as I know I guess I'm getting my medications. An interview was conducted with LPN (Licensed Practical Nurse) #8 at 5:00 PM., concerning Missed medication dosages for the above residents. She stated, I forgot to go back and switch the schedule to the right side (Unit). I usually work on the left side (Unit). I sign my meds. (Medications) out at the end of giving meds out. The DON talked to me two weeks ago about this. I will sign out my pills as I finish with each resident. On 05/20/2022 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. The DON stated, Medications should be administered and documented. On 05/20/2022 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided. COMPLAINT DEFICIENCY Based on information gleamed during a complaint investigation, staff interviews, and clinical record review, the facility staff failed to provide the necessary care and services for 3 of 55 residents (Resident #189) in the survey sample. For resident #189, the facility staff failed to recognize, assess and provide the necessary care and services after the resident experienced a significant change in condition presenting as shortness of breath because of low oxygen saturation 87 percent on room air. At the hospital the resident was diagnosed with acute respiratory failure, severe sepsis, a urinary tract infection and severe dehydration evidenced by a blood pressure reading of 80/50, only 30 milliliter of dark urine when catheterized and dry tongue and mucous membranes and peeling lips. Resident #189's lab values were critical upon arrival to the hospital; they included a glucose of 515 mg/dl, BUN 120 mg/dl, creatinine 6.47 mg/dl and lactic acid 2.6 mmol/L, which required hospitalization and constituted harm. For Resident #60 the facility staff failed to ensure resident received her physician prescribed Trulicity Injection. For Resident #66, the facility staff failed to ensure Gabapentin Capsules, Amoxicillin tablets and Cefdmir capsules were administered per physician orders. The findings included: 1. Resident #189 was admitted to the nursing facility on 2/23/2018 and discharged to the local hospital on [DATE]. The resident's diagnoses included; diabetes, neuropathy, depression and COVID-19 pneumonia. The quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 3/10/2020 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #189's cognitive abilities for daily (ADL) decision making were intact. In section G (Physical functioning) the resident was coded as requiring total care of one person with bathing, extensive assistance of one person with personal hygiene, extensive assistance of two with bed mobility, transfers, dressing and toileting, and independent after set-up with locomotion and eating. Interviews were attempted with multiple staff regarding Resident #189 but only one nurse stated she remembered the resident. Licensed Practical Nurse #9 stated the resident was transferred from the one Unit to the other Unit after testing COVID-19 positive. LPN #9 stated the resident began to experience breathing difficulties secondary to COVID-19 and his respiratory status deteriorated. LPN #9 stated the resident's appetite also decreased and there was a rapid change in his condition which required hospitalization. A nurse's note dated 5/1/2020 read; the resident wasn't himself. He was less talkative, stayed in bed, and had a non-productive cough without shortness of breath or a fever. The physician was notified and a chest x-ray was ordered and the results were normal. A physician's progress note dated 5/2/2020 read Resident #189 tested positive for COVID-19. He had a cough and the resident stated he felt a little short of breath. The resident's temperature was 98.4 Fahrenheit (°F), pulse 94, respirations 19 and his oxygen saturation was 92% on room air, the mucous membranes were moist and there was no labored breathing. The physician's plan was to obtain a complete blood count, basic metabolic panel, a chest x-ray and follow the resident closely. On 5/3/2020 at 8:03 a.m., nurse's note read; the resident presented with a fever of 99.5 °F, Tylenol was administered and at 3:54 p.m., the resident's temperature was still 99.5 °F , Oxygen (O2) at 2/liter (L) per minute was started and the resident continued with a good appetite. There was no documentation on 5/4/2020 or 5/5/2020, but there was a physician's order dated 5/5/2020 for Lovenox 40 mg every day for 7 days secondary to COVID-19. A nurse's dated 5/6/2020 read the resident's temperature was 99.8 °F and Tylenol was given. No documentation was available 5/7/2020, 5/8/202, 5/9/2020, or on 5/10/2020. A review of the ADL documentation revealed the resident required total care with eating or didn't eat at all from 5/7/2020 through 5/11/2020. There was not documentation of the percent eaten at each meal and there was no evidence the physician was notified of the resident's change in status to feed himself. Neither was the care plan updated to include the resident's diagnosis of COVID-19, cough, shortness of breath and the acute effects on the resident's daily status. There was also no evidence interventions were instituted to ensure the resident received necessary fluids to prevent dehydration On 5/11/2020 at 11:57 p.m., a nurse's note read the Certified Nursing Assistant informed the nurse the resident's O2 saturation was 89% and when the nurse arrived to the resident's room to ensure the O2 was on, she recognized the resident was only responsive to painful stimuli therefore; the physician and responsible party were notified and both elected to transfer the resident to the local hospital for evaluation and treatment. The hospital's Discharge summary dated [DATE] read; Upon the resident's arrival to the hospital on 5/11/2020 the hospital staff documented the resident presented to the emergency room with shortness of breath based on a low oxygen saturation, 87% on room air. The hospital diagnosed the resident with acute respiratory failure, severe sepsis, a urinary tract infection and severe dehydration evidenced by a blood pressure reading of 80/50, only 30 milliliter (ml) of dark urine returned when catheterized and a dry tongue/mucous membranes and peeling lips. Resident #189's lab values were critical upon arrival to the hospital; they included a glucose of 515 mg/dl, BUN 120 mg/dl, creatinine 6.47 mg/dl (indications of acute renal failure) and lactic acid 2.6 mmol/L, which required hospitalization. The hospital report dated 5/11/2020 read; the resident's lab results on 5/5/2020, were as follows; creatinine 1.06 mg/dl, BUN 24 mg/dl and the physician stated there was real concern the resident wasn't receiving appropriate care in the nursing home and was left without hydration resulting in his severe dehydration. The physician's note stated they would notify Adult Protective Services (APS) of the resident's condition. The hospital's documentation dated 5/11/2020, also stated they spoke with the resident's son multiple times and he assured then that his father limitation were in his mobility/walking but his cognition was good, he could communicate effectively, feed himself and participate in his ADL care, prior to this episode of illness. An interview was conducted with the APS worker on 5/18/22 at approximately 3:24 p.m. The APS worker stated Resident #189 the hospital's physician reported the resident was admitted to the hospital COVID-19 positive and it was felt proper care wasn't provided in the nursing home. The APS worker also stated she didn't investigate the concern because the resident was in the hospital. The APS worker stated the hospital reported the resident's status was critical however he wasn't mechanically ventilated because he was admitted to hospice care on 5/15/2020 and passed away on 5/16/2020. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced because they all stated they didn't know the resident.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Dental Services (Tag F0791)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interviews, clinical record review, and review of facility documents, the facility staff failed to ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interviews, clinical record review, and review of facility documents, the facility staff failed to ensure a resident received emergency dental services promptly after referrals were made adequately while experiencing the acute dental problem for 1 of 1 resident (Resident #190), with dental concerns in the survey sample. The STAT (now) dental appointment ordered 3/1/22, was scheduled on behalf of Resident #190 on 3/10/22, with a local general practice dentistry office for 3/23/22, which was 22 days after the STAT order. Prior to 3/10/22, the facility's staff was unable to provide evidence of attempting to obtain a dental appointment for Resident #190 and there was no evidence in the resident's clinical record or elsewhere of what extenuating circumstances led to the delay in obtaining the STAT ordered dental appointment. constituting harm for Resident #190. The findings included: Resident #190 was originally admitted to the facility on [DATE] and readmitted on [DATE] after an acute care hospital stay. The current diagnoses included; Alzheimer's dementia, diabetes, and a left jaw swelling/dental abscess. The significant change Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 4/7/22 coded the resident as not having the ability to complete the Brief Interview for Mental Status (BIMS). The staff interview was coded for long and short-term memory problems and severely impaired daily decision-making abilities. In section G (Physical functioning) the resident was coded as requiring total care of one person with bed mobility, transfers, dressing, eating, toileting, personal hygiene, and bathing. On 5/10/22, at approximately 2:25 p.m., Resident #190 was identified residing in a secured unit. He was lying in bed in a fetal position, utilizing oxygen by use of a nasal cannula and the resident didn't respond when spoken to. On 5/10/22, at approximately 3:30 p.m., an interview was conducted with Licensed Practical Nurse (LPN) #11. LPN #11 stated Resident #190 was very active including wandering until two months ago when he experienced a decline after developing a dental abscess. A nurse's note dated 3/1/22 revealed Resident #190 presented with a temperature of 101 degrees Fahrenheit (°F) and swelling was observed on the left side of his face. The nurse's note read that observation of his mouth revealed decayed teeth. The Nurse Practitioner (NP) ordered a STAT (immediately) dental consult and ordered antibiotic therapy; Augmentin 875 mg by mouth two times each day for 7 days. A nurse's note dated 3/2/22 at 6:40 p.m., read the resident remains on an antibiotic nevertheless his temperature was 102.4 °F, Tylenol was administered. Another nurse's note dated 3/4/22, revealed the resident's temperature was again abnormal, 101 °F, and the swelling to the left side of the resident's face had increased. The NP visited the resident on 3/4/22 to assess the left facial swelling; the assessment read that the resident was frail, in bed making mumbling sounds, while moving his head from side to side, the left face and jaw were inflamed, swollen, tender when touched and the resident was very uncomfortable. The NP assessment also read that an oral exam couldn't be performed in the facility. The NP ordered a three-view facial x-ray which was not a dental xray, but was a general xray that revealed an old non-displaced age undetermined fracture of nasal bone. Morphine Sulfate (an opioid pain medication used to treat moderate to severe pain); 0.25 milliliter by mouth every 4 hours as needed for pain, and an additional antibiotic Ceftriaxone; one dose, and a hospice consult. Resident #190 was evaluated again, on 3/7/22 by the NP. The NP documented the resident continued with facial swelling and a tooth abscess and the plan was for the resident to see the dentist as soon as possible for a tooth extraction. The NP ordered an additional one-time dose of the antibiotic Ceftriaxone. On 3/23/22, Resident #190 was seen by the general practice dentist. The dentist's progress note read, that there remained slight swelling to the left lower vestibular region but she was unable to determine if it was associated with a tooth because the resident was unable to open his mouth and/or follow directions therefore she was unable to clinically see or obtain necessary radiology to determine/diagnose the resident's dental problem. The general practice dentist provided referral information to the nursing facility to schedule an appointment with a sedation dentistry practice hence a thorough assessment could be conducted. On 3/30/22 Resident #190 was transferred to a local hospital for altered mental status. The discharge summary from the hospital dated 4/2/22 read that intravenous Unasyn was ordered for a possible dental abscess for which the resident was being treated at the nursing facility. The discharge summary also stated the resident was admitted with diagnoses of severely elevated blood glucose (417 mg/dl) and a critical blood sodium level (163 mmol/L), requiring intravenous insulin in the emergency room and three days of intravenous fluid resuscitation. During the survey on 5/13/22 at approximately 12:40 p.m., an observation was made of the resident receiving total care with the lunch meal in bed, and approximately 50% of the pureed meal was accepted. Also on 5/19/22 at approximately 5:30 p.m., an observation was made of the resident consuming the dinner meal in bed; he required total care and accepted approximately 50% of the pureed meal. A review of Resident #190's weight revealed on 3/3/22, he weighed 123.4 pounds, and on 5/18/22, 108.0 pounds, a loss of 15.4 pounds. No documentation was identified in the resident's clinical record of the facility's staff actions between 3/1/22 and 3/23/22 to ensure the resident could still eat and drink adequately while awaiting dental services. On 5/17/22 at approximately 5:45 p.m., an interview was conducted with CNA #6. CNA #6 stated she frequently worked with Resident #190 and the resident had experienced a significant decline physically and with meal consumption since the swelling was identified on the left side of his face. She stated many days the resident consumed very little (0-25%) of his meals/fluids but now his intake is better with staff assisting him slowly. On 5/13/22 at approximately 1:20 p.m., an interview was conducted with the Director of Nursing (DON). The DON stated the resident's decline was identified after he presented with a swollen left jaw on 3/1/22, which was diagnosed by the Nurse Practitioner (NP) as a dental abscess. The DON also stated the resident was seen by a local general practice dentist on 3/23/22, but the dentist couldn't examine, diagnose or treat the resident because the resident was unable to open his mouth and/or follow directions; therefore the general practice dentist provided the facility staff with information to schedule an appointment for sedation dentistry for Resident #190. The DON stated LPN #12 was responsible to schedule the sedation dentistry appointment for Resident #190 but she discontinued her employment with the facility and didn't provide the staff with the status of the appointment. As of 5/18/22, there was no evidence that the facility's staff was actively following up on the sedation dentistry appointment. The DON was unable to offer additional information on why there was such a delay in obtaining the necessary dental services or how the delay in services contributed to an additional decline in the resident's health. On 5/13/22 at approximately 4:15 p.m., a phone interview was conducted with LPN #12. LPN #12 stated she was responsible for making the sedation dentistry appointment for Resident #190. She stated she telephoned the practice, left a message with the scheduler, and was awaiting a return call with the appointment information, but she ceased employment with the nursing facility prior to obtaining the sedation dentistry appointment. LPN #12 further stated most likely the sedation dentistry practice left the appointment information on her voicemail after she separated from the facility and the administrative staff at the nursing home has access to the voicemail and can retrieve the message. On 5/19/22 at approximately 2:50 p.m., an interview was conducted with the Administrator. The Administrator stated the facility didn't have a dental contract with a practice but a local dental practice usually accommodates their residents whenever services are needed. The Administrator didn't elaborate on why it took twenty-two days for staff to obtain a dental appointment for Resident #190 but she stated because the in-house NP was monitoring and treating Resident #190's swelling to the left jaw, she felt his dental needs were met. The Administrator didn't address a documented NP progress note in which the NP stated she spoke with the DON on 3/7/22 expressing the need to have the resident evaluated by a dentist. On 5/20/22 at approximately 2:10 p.m., a phone interview was conducted with a representative from the sedation dentistry office. The representative stated a consultation is necessary prior to sedation dentistry services being provided and normally after the consultation the service is rendered within one month. The representative confirmed that an appointment for Resident #190 had not been made for the resident's name wasn't in their system. The representative further stated even in the event an appointment wasn't honored or canceled, the person's name would still be in their system. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing, and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no further concerns were voiced. The facility's policy titled Dental Services with a revision date of 01/04/22 read; It is the policy of this facility, in accordance with residents' needs, to assist residents in obtaining routine (to the extent covered under the State plan) and emergency dental care. Emergency dental services include services needed to treat an episode of acute pain in teeth, gums, or palate; broken, or otherwise damaged teeth, or any other problem of the oral cavity that required immediate attention by a dentist.
SERIOUS (H)

Actual Harm - a resident was hurt due to facility failures

Free from Abuse/Neglect (Tag F0600)

A resident was harmed · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. The facility staff failed to ensure the necessary treatment to prevent the development of a sacral pressure ulcer that was in...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. The facility staff failed to ensure the necessary treatment to prevent the development of a sacral pressure ulcer that was initially identified at an advanced stage (unstageable with 100% necrotic/dead tissue) resulting in harm for Resident #339. Resident #339 was admitted on [DATE] with diagnoses that included osteoarthritis, unspecified vascular dementia. Resident #339 clinical record review revealed a Braden Scale for Predicting Pressure Sores Risk Assessment as being completed on 11/19/21 as being at RISK. On 11/25/21 a clinical record review revealed a second Braden Scale for Predicting Pressure Sores Risk assessment was completed as being at Moderate risk. The admission, Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 11/23/2021 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 14 out of a possible 15. This indicated Resident #339 cognitive abilities for daily decision making were intact. The Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 12/14/21 reads: M0210. Unhealed Pressure Ulcers/Injuries. Does this resident have one or more unhealed pressure ulcers/injuries? Yes. Unstageable - Slough and/or eschar. Number of unstageable pressure ulcers due to coverage of wound bed by slough and/or eschar? 1. Number of these unstageable pressure injuries that were present upon admission/entry or reentry=0 (none). M1200-Skin and Ulcer Treatments: Pressure reducing device for bed: Checked off. Pressure ulcer care: Checked off. Applications of dressings to feet (with or without topical medications): In section G (Physical functioning) the resident was coded as requiring extensive of assistance of one person with bed mobility and personal hygiene, total dependence of one person with transfers, dressing, toilet use and bathing, independent set-up help with eating. The Care plan dated 12/1/21 read, Focus: The resident has an ADL (Activity of Daily Living) self-care performance deficit. Goal: The resident will maintain current level of function through the review date. Intervention: Reposition (FREQ) and as necessary to avoid injury. Monitor/document/report PRN (as needed) any changes, any potential for improvement, reasons for self-care deficit, expected course, declines in function. The Care plan dated 12/9/21 read, Focus: Resident at risk for impaired skin integrity and actual open area to sacrum r.t (relating to) incontinence, impaired mobility and dementia. Goal: The resident will maintain or develop clean and intact skin by the review date. The care plan dated 12/09/2021, read the resident will have no complications r/t area to sacrum through the review date, air mattress as per physician orders. The care plan revision dated 01/27/2022 read, avoid scratching and keep hands and body parts from excessive moisture. Keep fingernails short. Educate resident/family/caregivers of causative factors and measures to prevent skin injury. Follow facility protocols for treatment of injury. Treatment as per orders. According to the clinical record Resident #339 was admitted to the facility on [DATE] at 6:38 PM. The skin assessment noted resident to have only red areas to bilateral upper extremities from blood draws from the hospital. The clinical record dated 11/20/2021 at 12:12 PM., reads: Resident is AAOx3 (Alert and Oriented x three to person, place, and time) with no complaints voiced. Resident is incontinent of bladder, requiring assistance from staff. \ A review of the hospital Discharge summary dated [DATE] reveal no pressure ulcers were present before being transferred to the LTC (Long Term Care) facility. A review of the Long Term Care Facility's History and Physical dated 11/23/21 reveal no pressure ulcers were present on admission. Daily Nursing Skin Assessments document dated 11/18/21 read, skin is intact. A review of the ADL (Activity of Daily Living) document for December 2021 reveal that Resident #339 received bed baths from 12/01/21 through 12/08/21 with no notation of skin integrity problems, but according to the nursing notes Resident #339's wound was identified on 12/03/21 by the CNA (CNA #7). A review of the nurse's note dated on 12/03/21 (3:45 PM) read: CNA (Certified Nurse's Aide) #7 notified me (LPN #13, no longer employed at the facility) of area to sacrum. Assessed resident noted open area to sacrum with slough noted. Cleaned area and applied dressing change every 3 days/prn (as needed) until healed. RP (Responsible Party) made aware and placed in communication book. Wound nurse also made aware. The nurse's note dated on 12/5/2021 at 9:00 AM., read, Resident with pain, when asked where she pointed to her sacral area. The nurse's note dated on 12/9/2021 at 12:23 PM., read, Resident being turned every 2 hours from side to side to prevent pressure to sacral area as per order; dressing with serosanguinous drainage, dressing reapplied as needed, skin care given. The nurse's note dated 12/15/2021 at 4:29 PM read that the MDS (Minimum Data Set staff) was in with resident to obtain pain interview for scheduled quarterly for managed care stay. Resident stated that over the past 5 days she has had frequent bottom pain r/t to her wound and that at times it makes it hard to sleep and limits her day to day activity. The nurse's note dated on 12/17/2021 at 8:27 PM revealed that the Resident was medicated for comfort due to dressing change to sacrum, and that the resident was moaning. The nurse's note dated on 12/18/2021 at 10:30 AM read: Resident nonverbal, starring up at the ceiling, and displaying facial grimacing and moaning. VS: 97.3-103-20-114/52. SATS 94% RA. BS: 127. Resident being sent out to ER for further evaluation. 11:20 AM., 911 at the facility to transport resident to local Emergency Room/ER for further evaluation. The clinical record dated on 12/18/2021 7:57 PM., reads that Resident #339 was admitted to the local hospital for renal failure, sepsis, necrotizing tissue of the sacrum. During the course of investigation of the sacral pressure ulcer, it was identified when CNA (Certified Nurse's Assistant) #7 saw an area on the resident's butt on 12/03/21 at which time she alerted the nurse, LPN #3. On 5/18/22 at 3:55 pm., an interview was conducted with the WCNP (Wound Care Nurse Practitioner/OSM) #12 concerning Resident #399's sacral wound. She stated, that the wound was facility acquired on 12/03/21 and that she first assessed it on 12/07/21 as an unstageable with 100% necrosis full thickness. She stated, It's not acceptable because as a full thickness wound, I'm not able to see the extent of this wound. It could have been here for who knows how long. I rounded every Thursday. My expectation was that the wound care nurse (facility LPN #3/ADON) Licensed Practical Nurse/Assisting Director of Nursing) perform initial assessments and update me and we round on patients together. She didn't assist me. She wasn't with me consistently every single week. It got worse. Pressure and deconditioning were contributors; turn and reposition assistance, and decreased mobility. Typically residents could get an unstageable pressure ulcer over 2 or 3 days but not overnight. Prevention measures such as low air loss mattress, foam dressing on the sacrum to prevent further decomposition. It had gotten larger, still unstageable, the signs and symptoms were acute infection, malodorous and increase drainage. I cleaned it with dermal wound cleanser, calcium Ag, applied santyl and covered with foam. The Primary physician started her on Levoquin po (by mouth). I received a call from LPN #3 on January 3rd, 2022 after Resident #339 had been admitted to the hospital. Someone from corporate and LPN #3 called me about resident having necrotizing fasciitis. It's a bacterial infection, flesh eating bacteria caused when the skin is disrupted with bacteria that spreaded to her bones. Infection breaking through the skin barriers causes this. On 12/07/21, the WNP consult notes indicated the following, Unstageable sacrum pressure ulcer. Measurements: Length 2.0 x Width 2.5 cm Depth surface area 5.0 cm2. Minimal serosanguinous, 100 % necrosis. Surrounding Tissue is intact. Primary dressing: Santyl, Calcium Alginate Ag, Foam. Surgical debridement procedure was performed: Removal of subcutaneous tissue. An assessment of the sacral wound show the wound has full thickness loss, base covered with slough, consistent with an unstageable pressure injury. Due to the presence of the necrotic tissue bed, the ulcer was debrided. Plan: clean with dermal wound cleanser, pat dry, change daily and as needed. Apply santyl to the wound bed, cover with calcium alginate Ag, then foam dressing, change daily and as needed. Weekly Pressure Wound Observation consult notes dated 12/17/21 by the WNP read, 12/17/21 Pressure ulcer of Sacrum worsening. Malodorous. Wound deteriorating. A review of the medical record revealed no wound measurements until the Wound Care Nurse Practitioner (WNP) arrived on 12/17/21. On 12/17/21 the WNP consult notes read, Unstageable pressure ulcer on sacrum. Measurements: Length 5.5 cm Width 6.1 cm Depth 0.2 cm. Surface area 35.5 cm2. Exudate: moderate, purulent and malodorous. Tissue type: 100% necrosis, full thickness. Surrounding Tissue: Intact. Primary dressing: Santyl, Calcium Alginate Ag, Foam. Progress: deteriorating. Surgical debridement procedure was performed: Subcutaneous Tissue on 12/16/21. At the start of today's procedure, the ulcer is described as follows: Length 5.5 cm Width 6.1 cm Depth 0.2 cm. Surface 33.5 cm2. Exudate: moderate, purulent, malodorous. Tissue type: 100% necrosis, full thickness. The amount of surface area debrided was 100%. Assessment: The unstageable pressure injury to the sacrum is deteriorating. Due to the presence of necrotic tissue in the ulcer bed, the ulcer was debrided. Barriers to healing include infection. Signs and symptoms of acute infection include odor, purulent draining and increased pain. The primary team started the patient on Levaquin PO. A antimicrobial dressing of gentamicin cream and calcium Alginate Ag was applied for control of possible excess bioburden and to promote healing. Plan: Clean with dermal wound cleanser. Pat dry, apply Gentamicin and Santyl to the wound bed. Cover with Calcium Alginate Ag, then foam dressing. Change daily and as needed. Continue PO Levaquin for infection to sacral wound. In addition Resident #339 acquired unstageable DTI (Deep Tissue Injury) of the left heel. The clinical record reveal on 12/18/2021 Resident #339 was admitted to the local hospital for renal failure, sepsis, necrotizing tissue. According to review of the ER/emergency room medical records dated 12/18/21 at 5:14 PM, Resident #339 was presented with AMS (Altered Mental Status) and a Large Sacral Pressure Ulcer. Later tests revealed that Resident #339 was diagnosed with having a sacral decubitus ulcer with infected GAS (Bacteria called group A Streptococcus (GAS) can cause many different infections. These infections range from minor illnesses to very serious and deadly diseases-https://www.cdc.gov/groupastrep/diseases-public/index.html). According to review of the the Emergency Department (ED) report dated 12/18/21 Resident #339 was admitted to the ED in .acute distress and ill appearing. On assessment Resident had a large sacral ulcer present with foul odor. The CT (computerized tomography) scan shows: Sacral decubitus ulcer with likely infectious GAS along the lower back into the left greater than right gluteal musculature and right greater than the left perineum. There is ill defined fluid collection measuring up to 3.3 cm within the left gluteal musculature potentially developing abscess. On 12/18/21 the ED provider note list diagnoses as: Necrotizing soft tissue infection, Renal Failure, Sepsis and Sacral decubitus Ulcer Stage 4. Diagnosis management comments: Multiple conversations were made with Resident's spouse. Call in note says resident is a full code. Husband says this is not correct she is a DNR (Do Not Resuscitate). However, he would like out general surgeon (GS) to attempt to address the significant infection to her sacral region. Causing her severe sepsis and worsening mental status. We discussed comfort measures versus this intervention. Surgery was consulted and she was found to have necrotizing fasciitis and plans were made to go to the OR (Operating Room) for debridement. The OR (Operating Room) procedure note dated 12/18/21 revealed that the patient's decubitus wound was massive and necrotic. The resident had to be taken urgently to the OR to excise the necrotic tissue because the patient is in septic shock. All necrotic tissue was excised. All underlying tissue was involved all the way to the bone. Patient was intubated and critically ill. Consideration for hospice care. On 5/13/22 at 7:44 PM and at 5:00 PM a phone call was made to the Surgeon. Surveyor was not able to leave messages. An interview was conducted on 5/17/22 at 4:25 PM., with LPN (License Practical Nurse, wound care nurse/Assistant Director of Nursing) #3 concerning Resident #339. She stated, It (SACRUM) was first identified as unstageable. It progressed and we had to debride it. I did some of her wound care. It showed no signs of infection after the first surgical debridement. For preventive measures she used a specialty mattress starting 12/10/21. We medicated her before wound care. She was turned and repositioned. An interview was conducted on 5/18/22 at 10:00 AM with the complaintant concerning Resident #339. She stated, The hospital surgeon made a referral to us and he indicated that he had to perform two surgeries on patient's sacral area due to having a large infected wound. The two surgeries resulted from infection of the wound to the bone. My investigation found she had no wounds on her body until December 3rd. (2021) She was bedridden and had physical therapy from her bed. She never got out of bed. She was put on hospice. Her husband would sit with her for hours. The wound nurse (LPN #3) would only see her when the outside Wound Nurse Practitioner came in. An interview was conducted on 5/18/22 at 11:15 am with CNA (Certified Nurse's Aide) #7. Concerning Resident #399. She stated, A few days after she came she complained that her butt hurt. We would get her off her side. When I came back from being off, she had an area on her butt. I reported it to the nurse. That nurse no longer works here. The wound nurse came every week. She was not ambulatory and could not make her needs known. She had good days and bad days. I turned and reposition her every two hours. LPN #13, who was the nurse CNA #7 alerted about the area on Resident #339, was called twice throughout the survey. Voice messages were left with no return call. On 5/19/22 at 1:35 AM., an interview was conducted with RN (Registered Nurse) #1. She stated, I turned her every 2 hours due to the wound on her bottom. She was not able to make her needs known. The wound on her bottom was acquired at the facility. I didn't have to do anything with her wound because I worked the 7 pm -7 am shift. We had an investigation here earlier. I didn't find anything unusual with her vitals. I thought it was odd that she was smiling. I never got to see the wound. If it was soiled I would have changed it and seen it but I didn't have the opportunity. On 05/20/2022 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided. 2. The facility staff failed to identify a sacral wound pressure ulcer prior to advancing to an unstageable pressure ulcer measuring 5 centimeter (cm) x 5 cm x 2 cm for Resident #291. The sacral wound was infected requiring antibiotic therapy and surgical debridement (removal of dead tissue), which constituted harm. Resident #291 was originally admitted to the facility on [DATE]. Diagnosis for Resident #291 included but are not limited to Parkinson disease and muscle weakness. Resident #291's admission Assessment (14-day) with an ARD of 03/19/22 coded Resident #291 Brief Interview for Mental Status (BIMS) scored a 99 indicating short and long term memory problems and severe cognitive impairment - never/rarely made decisions. Resident #291 was coded total dependence of two with toilet use, bed mobility and bathing, total dependence of one with dressing, personal hygiene and eating and for Activities of Daily Living (ADL). Under section H - (Bladder and Bowel) was coded for always incontinent of bladder and bowel. Under section G0400 - Functional Limitation in Range of Motion (ROM) coded Resident #291 with no impairment to her upper and lower extremity. Resident #291 was coded as having no mood, rejection of care or behavioral problems. Resident #291's admission Assessment (14-day) with an ARD of 03/19/22. Under section (M0150) at risk for developing pressure ulcers was coded yes, under section (M0210) for unhealed pressure ulcers was coded yes and under section (M0300) for having current number of unhealed pressure ulcer at each stage present upon admission or reentry into the facility was coded for stage II pressure ulcer. Under section (1200) for skin, ulcer treatments were coded for having pressure reducing device for bed and pressure ulcer wound care. Resident #291's person-centered care plan initiated on 03/21/22 identified the resident has a pressure ulcer in her sacral area, at risk for further skin breakdown related to incontinence and impaired mobility. The goal set for the resident by the staff was that the resident will remain free of new skin breakdown through next review date. Some of the interventions/approaches the staff would use to accomplish this goal is to follow facility policies/protocols for the prevention/treatment of skin breakdown, assess/record/monitor wound healing, measure length, width and depth where possible, assess and document status of wound perimeter, wound bed and healing progress, specialty mattress and report improvements and declines to the physician and administer treatments as ordered and monitor for effectiveness. The person-centered care plan with a revision date of 04/01/22 identified Resident #291 on antibiotics for a sacral wound infection. The goal set for the resident by the staff was that the resident will show signs of healing and remain free of complications related to infection. One of the interventions/approaches the staff would use to accomplish this goal is to administer medications as ordered, monitor/document for side effects and effectiveness. A Braden Risk Assessment Report was completed on 3/15/22. The resident scored a 09 indicating at high risk for the development of pressure ulcers. The assessment coded under sensory perception very limited and responds only to painful stimuli; cannot communicate discomfort except by moaning or restlessness or has a sensory impairment which limits the ability to feel pain or discomfort over ½ of the body. Under moisture was coded skin is occasionally moist, requiring an extra linen change approximately once a day and coded bedfast under activity. The skin/wound admission note dated 03/10/22 indicated Resident #291 had a stage II sacral ulcer measuring 2.0 cm x 1.0 cm x 0.2 cm with very dark skin, nonblachable measuring (15 cm x 9 cm) surrounding the sacral ulcer. The note indicated that Resident #291's pressure ulcer will be evaluated by the wound Nurse Practitioner (NP) during her next visit on 03/15/22. Resident #291 had a physician order dated 03/10/22 to apply an air mattress to the bed for wound prevention and an order dated 03/11/22, for a sacral pressure ulcer treatment to apply a foam dressing every Tuesday, Thursday and Saturday (day shift). A review of Resident #291's nurse's note revealed the resident was transferred to the hospital emergency room for evaluation for an elevated temperature on 03/14/22 at approximately 6:50 p.m., and returned on 03/15/22 at approximately 4:00 p.m. Further review of the nurses note revealed no new skin impairments noted since the last admission assessment on 03/10/22. The resident was readmitted to the nursing facility on 03/15/22. The readmission note under skin integrity revealed the same sacral pressure assessed at a Stage II. A skin/wound note dated 03/22/22 at 12:08 p.m., by the wound nurse License Practical Nurse (LPN #3) revealed the wound NP (WNP) went to assess Resident #291's sacral wound but the resident had pain with body movement, thus the WNP decided to assess Resident #291's sacral wound during her next onsite visit on 03/29/22. During the review of Resident #291's clinical record revealed there were no weekly wound assessments made by the facility licensed nurses of the sacral pressure ulcer for 19 days, after her admission to the facility. An interview was conducted with the WNP on 05/17/22 at approximately 3:06 p.m., I was in the facility on 03/15/22 to assess Resident #291's sacral ulcer, but the resident was discharged to the hospital during my onsite visit. The WNP stated, My first time evaluating Resident #291's pressure ulcer was on 03/29/22. The WNP said the wound was infected as evidence by the wound having a significant amount of slough with foul odor present and having significant pain over the sacral area when touched or palpated. Resident #291 was placed on routine pain medication as well as two rounds of antibiotic therapy to help fight the sacral wound infection. The wound was not cultured due to the location of the wound (sacral area) which put the wound culture at risk for cross contamination. The WNP's initial progress note of the sacral pressure ulcer on 03/29/22 revealed an unstageable ulcer measuring 5 cm x 5 cm x 2 cm. The progress note stated the sacral wound had a moderate amount of serosanquinous drainage, strong odor present with 90 percent (%) slough and 10 % dermis tissue. A new medication order was given for Augmentin (antibiotic) 500 mg/125 mg every 12 hours x 10 days for a sacral wound infection. A new treatment order was given to clean the sacral wound with Dakin's, Santyl on Dakin's gauze, and cover with foam dressing daily and as needed. The WNP progress note also stated pain is indicative of any movement, at rest she is comfortable. The WNP also offered further recommendations to turn and reposition per facility protocol, use of a low air loss mattress and to optimize nutrition. A WNP progress note dated 04/05/22 revealed the sacral wound pressure ulcer remained an unstageable measuring 5 cm x 5 cm x (?). The sacral wound had improved but remain with moderate amount of serosanquinous drainage, strong odor present with 90% slough and 10% dermis tissue. The wound was debrided removing thick slough tissue; pain was present with any movement. Resident #291 remained on antibiotic therapy for a sacral wound infection and continued with the current wound treatment, Dakin's, Santyl on Dakin's gauze, and cover with foam dressing daily and as needed. A review of the WNP's progress note dated 04/11/22 indicated that the wound visit was performed via telehealth with the wound nurse, License Practical Nurse (LPN #3). The sacral wound was deteriorating with moderate amount of purulent drainage, strong odor present with 90% slough and 10% dermis tissue. The wound measured by onsite nurse (LPN #3) measuring 6.5 cm x 5.5 cm x 2.5 cm. The progress note recommended to continue with current sacral wound treatment with Dakin's, Santyl on Dakin's gauze, foam dressing and change daily and as needed. A new antibiotic order was given for Clindamycin 600 mg by mouth every 8 hours for 21 days for a sacral wound infection. The wound NP progress note also stated pain is indicative of any movement, at rest she was comfortable. On 05/16/22 at approximately 2:25 p.m., an interview was conducted with LPN #1. LPN #1 was assigned to performed sacral wound care to Resident #291 on 03/26/22 (7a-7p shift). The LPN stated, I have never measured Resident #291's sacral pressure ulcer. The ulcer was being measured and monitored by LPN #3 and the wound NP. An interview was conducted with the Medical Director (MD) on 05/18/22 at approximately 11:33 a.m., who said all pressure ulcers were followed by (name of Wound Company.) The MD stated, Resident #291's sacral ulcer should have been monitored, assessed and measured on a weekly basis for signs of decline or improvement. The nurses should have been monitoring the sacral pressure ulcer during every wound care dressing change for a change in condition. Apparently, the nurses were not doing a full wound assessment for change in condition because a pressure ulcer cannot go from a stage II to an unstageable requiring debridement overnight. The changes in the wound should be been addressed before the wound was identified as an unstageable pressure ulcer. The extra nutritional element recommended by the dietitian could have help with the wound healing of the sacral pressure ulcer. An interview was conducted with LPN #9 on 05/19/22 at approximately 10:44 a.m. The LPN was assigned to perform sacral wound care to Resident #291 on 03/19/22 (7a-7p shift). The nurse said an open area was noted to the sacrum with shearing/excoriation to the periwound. The LPN stated, I only do the resident's treatment not the monitoring or measuring of the wound that was being done by the wound NP or LPN #3 on a routine basis. A phone interview was conducted with LPN #12 on 05/16/22 at approximately 6:29 p.m. The LPN was assigned to perform sacral wound care to Resident on 03/22/22 (7a-7p shift). The LPN said the sacral wound appeared larger in size but I did not measure or document the change in condition of the sacral wound. The LPN stated, The wound NP and LPN #3 were assessing and monitoring Resident #291's sacral ulcer every week. A dietary/nutrition note dated 03/18/22 at 9:56 a.m., revealed Resident #291 having a suspected deep tissue injury (SDTI) to the left and right heel and a stage II pressure ulcer to the coccyx/sacral area per 03/10/22 (skin assessment). Recommendations were made for fortified foods with meals due to poor oral intake of meals, provide texture-appropriate calorie-dense snacks three times a day between meals due to poor oral intake and thickened house shake (120 mL), pudding / fortified pudding. A Dietary/Nutrition note dated 04/08/22 at 12:33 p.m., revealed the nutritional recommendations made on 03/18/22 were never addressed for fortified foods with meals due to poor oral intake of meals, provide texture-appropriate calorie-dense snacks three times a day between meals due to poor oral intake and thickened house shake (120 mL), pudding / fortified pudding. An interview was conducted with the RD on 05/17/22 at approximately 4:41 p.m., who stated, The nutrition recommendations made for Resident #291 on 03/18/22 and again on 04/08/22 were never addressed. The RD said the extra calories would have given extra protein that's needed to help with healing Resident #291's sacral pressure ulcer. The nursing note dated 04/11/22 at approximately 6:23 p.m., revealed Resident #291 with Altered Mental Status (AMS), tremors and had vomiting during dinner. A new order was given to send Resident #291 to the emergency room (ER) for evaluation and treatment. A review of the hospital records revealed that Resident #291 presented in the Emergency Department (ED) on 04/11/22 from (name of nursing facility) for further evaluation due to Altered Mental Status (AMS) and vomiting. The ED indicated Resident #291 is lethargic, disoriented and is currently on antibiotic for an infected unstageable sacral wound. The wound is observed with a strong foul odor. The sacral wound was evaluated to be a FIST size with partial wet slough, fetid (having a heavy offensive smell-https://www.merriam-webster.com/dictionary) skin and obvious deep tunneling on perimeter. The ED report indicated the resident did not meeting the criteria for Systemic inflammatory response syndrome (SIRS), but had a concerning sacral wound and was referred for evaluation and treatments by the General Surgery. The resident was started on IV Vancomycin (antibiotic) and Zosyn (antibiotic) for empiric coverage of her large sacral decubitus ulcer. After the sacral wound was evaluated by the General Surgery, he felt the wound would benefit from debridement of the wound. On 04/12/22, Resident #291 was taken into the operating room (OR), and the sacral wound was debrided. After debridment the wound was assessed as a stage III decubitus ulcer with no exposed bone at this time. The recommendation was made for a wound VAC to improve the healing process for the resident. It was noted that the resident would also benefit from significant nutritional support and should be fed by staff by the facility. An interview was conducted with the Director of Nursing (DON) and wound nurse LPN #3 on 05/12/22 at approximately 10:00 a.m. The DON said Resident #291's sacral pressure ulcer should have been evaluated by the WNP or wound nurse, LPN #3 on a weekly basis. She stated, the weekly evaluation and monitoring was needed for early detection to determine if the wound is improving or declining. The wound nurse LPN #3 stated, I was not here on 03/17/22 and 03/24/22, when Resident #291 was supposed to have her sacral wound assessed and evaluated a changes in condition. The DON said the nurses should have been assessing and documenting changes on Resident #291's sacral pressure ulcer (description of wound bed, if drainage or odor present and size of the wound) with all changes reported to LPN #3 or the wound NP for evaluation to determine if wound treatment changes were needed. According to the DON, the stage II sacral wound treatment was appropriate when admitted to the facility on [DATE]. The treatment was for a foam dressing, change every 2 days. The DON said, When the wound deteriorated to an unstageable, the treatment should have been changed but it wasn't. The DON further stated, Due to the lack of documentation, there is no way to know when Resident #291's sacral wound deteriorated to the point it had advanced to an unstageable requiring debridement and antibiotic due to infection. A debriefing was held with the Administrator, Director of Nursing and Corporate support on 05/19/22 at approximately 2:00 p.m. Resident #291's issues was presented again. No additional information was forthcoming. Definitions: -Pressure Injury: A pressure injury is localized damage to the skin and underlying soft tissue usually over a bony prominence or related to a medical or other device. The injury can present as intact skin or an open ulcer and may be painful. The injury occurs as a result of intense and/or prolonged pressure or pressure in combination with shear (http://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages/). -Pressure Injury - Stage 2 (Partial-thickness skin loss with exposed dermis_ Partial-thickness loss of skin with exposed dermis. The wound bed is viable, pink or red, moist, and may also present as an intact or ruptured serum-filled blister. Adipose (fat) is not visible and deeper tissues are not visible. Granulation tissue, slough and eschar are not present. These injuries commonly result from adverse microclimate and shear in the skin over the pelvis and shear in the heel. This stage should not be used to describe moisture associated skin damage (MASD) including incontinence associated dermatitis (IAD), intertriginous dermatitis (ITD), medical adhesive related skin injury (MARSI), or traumatic wounds (skin tears, burns, abrasions (http://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages). Pressure Injury - Stage 3 (Full-thickness skin loss) Full-thickness loss of skin,[TRUNCATED]
SERIOUS (H)

Actual Harm - a resident was hurt due to facility failures

Pressure Ulcer Prevention (Tag F0686)

A resident was harmed · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. The facility staff failed to ensure the necessary treatment to prevent the development of a sacral pressure ulcer that was i...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. The facility staff failed to ensure the necessary treatment to prevent the development of a sacral pressure ulcer that was initially identified at an advanced stage (unstageable with 100% necrotic/dead tissue) resulting in harm for Resident #339. Resident #339 was admitted on [DATE] with diagnoses that included osteoarthritis, unspecified vascular dementia. Resident #339 clinical record review revealed a Braden Scale for Predicting Pressure Sores Risk Assessment as being completed on 11/19/21 as being at RISK. On 11/25/21 a clinical record review revealed a second Braden Scale for Predicting Pressure Sores Risk assessment was completed as being at Moderate risk. The admission, Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 11/23/2021 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 14 out of a possible 15. This indicated Resident #339 cognitive abilities for daily decision making were intact. The Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 12/14/21 reads: M0210. Unhealed Pressure Ulcers/Injuries. Does this resident have one or more unhealed pressure ulcers/injuries? Yes. Unstageable - Slough and/or eschar. Number of unstageable pressure ulcers due to coverage of wound bed by slough and/or eschar? 1. Number of these unstageable pressure injuries that were present upon admission/entry or reentry=0 (none). M1200-Skin and Ulcer Treatments: Pressure reducing device for bed: Checked off. Pressure ulcer care: Checked off. Applications of dressings to feet (with or without topical medications): In section G (Physical functioning) the resident was coded as requiring extensive of assistance of one person with bed mobility and personal hygiene, total dependence of one person with transfers, dressing, toilet use and bathing, independent set-up help with eating. The Care plan dated 12/1/21 read, Focus: The resident has an ADL (Activity of Daily Living) self-care performance deficit. Goal: The resident will maintain current level of function through the review date. Intervention: Reposition (FREQ) and as necessary to avoid injury. Monitor/document/report PRN (as needed) any changes, any potential for improvement, reasons for self-care deficit, expected course, declines in function. The Care plan dated 12/9/21 read, Focus: Resident at risk for impaired skin integrity and actual open area to sacrum r.t (relating to) incontinence, impaired mobility and dementia. Goal: The resident will maintain or develop clean and intact skin by the review date. The care plan dated 12/09/2021, read the resident will have no complications r/t area to sacrum through the review date, air mattress as per physician orders. The care plan revision dated 01/27/2022 read, avoid scratching and keep hands and body parts from excessive moisture. Keep fingernails short. Educate resident/family/caregivers of causative factors and measures to prevent skin injury. Follow facility protocols for treatment of injury. Treatment as per orders. According to the clinical record Resident #339 was admitted to the facility on [DATE] at 6:38 PM. The skin assessment noted resident to have only red areas to bilateral upper extremities from blood draws from the hospital. The clinical record dated 11/20/2021 at 12:12 PM., reads: Resident is AAOx3 (Alert and Oriented x three to person, place, and time) with no complaints voiced. Resident is incontinent of bladder, requiring assistance from staff. \ A review of the hospital Discharge summary dated [DATE] reveal no pressure ulcers were present before being transferred to the LTC (Long Term Care) facility. A review of the Long Term Care Facility's History and Physical dated 11/23/21 reveal no pressure ulcers were present on admission. Daily Nursing Skin Assessments document dated 11/18/21 read, skin is intact. A review of the ADL (Activity of Daily Living) document for December 2021 reveal that Resident #339 received bed baths from 12/01/21 through 12/08/21 with no notation of skin integrity problems, but according to the nursing notes Resident #339's wound was identified on 12/03/21 by the CNA (CNA #7). A review of the nurse's note dated on 12/03/21 (3:45 PM) read: CNA (Certified Nurse's Aide) #7 notified me (LPN #13, no longer employed at the facility) of area to sacrum. Assessed resident noted open area to sacrum with slough noted. Cleaned area and applied dressing change every 3 days/prn (as needed) until healed. RP (Responsible Party) made aware and placed in communication book. Wound nurse also made aware. The nurse's note dated on 12/5/2021 at 9:00 AM., read, Resident with pain, when asked where she pointed to her sacral area. The nurse's note dated on 12/9/2021 at 12:23 PM., read, Resident being turned every 2 hours from side to side to prevent pressure to sacral area as per order; dressing with serosanguinous drainage, dressing reapplied as needed, skin care given. The nurse's note dated 12/15/2021 at 4:29 PM read that the MDS (Minimum Data Set staff) was in with resident to obtain pain interview for scheduled quarterly for managed care stay. Resident stated that over the past 5 days she has had frequent bottom pain r/t to her wound and that at times it makes it hard to sleep and limits her day to day activity. The nurse's note dated on 12/17/2021 at 8:27 PM revealed that the Resident was medicated for comfort due to dressing change to sacrum, and that the resident was moaning. The nurse's note dated on 12/18/2021 at 10:30 AM read: Resident nonverbal, starring up at the ceiling, and displaying facial grimacing and moaning. VS: 97.3-103-20-114/52. SATS 94% RA. BS: 127. Resident being sent out to ER for further evaluation. 11:20 AM., 911 at the facility to transport resident to local Emergency Room/ER for further evaluation. The clinical record dated on 12/18/2021 7:57 PM., reads that Resident #339 was admitted to the local hospital for renal failure, sepsis, necrotizing tissue of the sacrum. During the course of investigation of the sacral pressure ulcer, it was identified when CNA (Certified Nurse's Assistant) #7 saw an area on the resident's butt on 12/03/21 at which time she alerted the nurse, LPN #3. On 5/18/22 at 3:55 pm., an interview was conducted with the WCNP (Wound Care Nurse Practitioner/OSM) #12 concerning Resident #399's sacral wound. She stated, that the wound was facility acquired on 12/03/21 and that she first assessed it on 12/07/21 as an unstageable with 100% necrosis full thickness. She stated, It's not acceptable because as a full thickness wound, I'm not able to see the extent of this wound. It could have been here for who knows how long. I rounded every Thursday. My expectation was that the wound care nurse (facility LPN #3/ADON) Licensed Practical Nurse/Assisting Director of Nursing) perform initial assessments and update me and we round on patients together. She didn't assist me. She wasn't with me consistently every single week. It got worse. Pressure and deconditioning were contributors; turn and reposition assistance, and decreased mobility. Typically residents could get an unstageable pressure ulcer over 2 or 3 days but not overnight. Prevention measures such as low air loss mattress, foam dressing on the sacrum to prevent further decomposition. It had gotten larger, still unstageable, the signs and symptoms were acute infection, malodorous and increase drainage. I cleaned it with dermal wound cleanser, calcium Ag, applied santyl and covered with foam. The Primary physician started her on Levoquin po (by mouth). I received a call from LPN #3 on January 3rd, 2022 after Resident #339 had been admitted to the hospital. Someone from corporate and LPN #3 called me about resident having necrotizing fasciitis. It's a bacterial infection, flesh eating bacteria caused when the skin is disrupted with bacteria that spreaded to her bones. Infection breaking through the skin barriers causes this. On 12/07/21, the WNP consult notes indicated the following, Unstageable sacrum pressure ulcer. Measurements: Length 2.0 x Width 2.5 cm Depth surface area 5.0 cm2. Minimal serosanguinous, 100 % necrosis. Surrounding Tissue is intact. Primary dressing: Santyl, Calcium Alginate Ag, Foam. Surgical debridement procedure was performed: Removal of subcutaneous tissue. An assessment of the sacral wound show the wound has full thickness loss, base covered with slough, consistent with an unstageable pressure injury. Due to the presence of the necrotic tissue bed, the ulcer was debrided. Plan: clean with dermal wound cleanser, pat dry, change daily and as needed. Apply santyl to the wound bed, cover with calcium alginate Ag, then foam dressing, change daily and as needed. Weekly Pressure Wound Observation consult notes dated 12/17/21 by the WNP read, 12/17/21 Pressure ulcer of Sacrum worsening. Malodorous. Wound deteriorating. A review of the medical record revealed no wound measurements until the Wound Care Nurse Practitioner (WNP) arrived on 12/17/21. On 12/17/21 the WNP consult notes read, Unstageable pressure ulcer on sacrum. Measurements: Length 5.5 cm Width 6.1 cm Depth 0.2 cm. Surface area 35.5 cm2. Exudate: moderate, purulent and malodorous. Tissue type: 100% necrosis, full thickness. Surrounding Tissue: Intact. Primary dressing: Santyl, Calcium Alginate Ag, Foam. Progress: deteriorating. Surgical debridement procedure was performed: Subcutaneous Tissue on 12/16/21. At the start of today's procedure, the ulcer is described as follows: Length 5.5 cm Width 6.1 cm Depth 0.2 cm. Surface 33.5 cm2. Exudate: moderate, purulent, malodorous. Tissue type: 100% necrosis, full thickness. The amount of surface area debrided was 100%. Assessment: The unstageable pressure injury to the sacrum is deteriorating. Due to the presence of necrotic tissue in the ulcer bed, the ulcer was debrided. Barriers to healing include infection. Signs and symptoms of acute infection include odor, purulent draining and increased pain. The primary team started the patient on Levaquin PO. A antimicrobial dressing of gentamicin cream and calcium Alginate Ag was applied for control of possible excess bioburden and to promote healing. Plan: Clean with dermal wound cleanser. Pat dry, apply Gentamicin and Santyl to the wound bed. Cover with Calcium Alginate Ag, then foam dressing. Change daily and as needed. Continue PO Levaquin for infection to sacral wound. In addition Resident #339 acquired unstageable DTI (Deep Tissue Injury) of the left heel. The clinical record reveal on 12/18/2021 Resident #339 was admitted to the local hospital for renal failure, sepsis, necrotizing tissue. According to review of the ER/emergency room medical records dated 12/18/21 at 5:14 PM, Resident #339 was presented with AMS (Altered Mental Status) and a Large Sacral Pressure Ulcer. Later tests revealed that Resident #339 was diagnosed with having a sacral decubitus ulcer with infected GAS (Bacteria called group A Streptococcus (GAS) can cause many different infections. These infections range from minor illnesses to very serious and deadly diseases-https://www.cdc.gov/groupastrep/diseases-public/index.html). According to review of the the Emergency Department (ED) report dated 12/18/21 Resident #339 was admitted to the ED in .acute distress and ill appearing. On assessment Resident had a large sacral ulcer present with foul odor. The CT (computerized tomography) scan shows: Sacral decubitus ulcer with likely infectious GAS along the lower back into the left greater than right gluteal musculature and right greater than the left perineum. There is ill defined fluid collection measuring up to 3.3 cm within the left gluteal musculature potentially developing abscess. On 12/18/21 the ED provider note list diagnoses as: Necrotizing soft tissue infection, Renal Failure, Sepsis and Sacral decubitus Ulcer Stage 4. Diagnosis management comments: Multiple conversations were made with Resident's spouse. Call in note says resident is a full code. Husband says this is not correct she is a DNR (Do Not Resuscitate). However, he would like out general surgeon (GS) to attempt to address the significant infection to her sacral region. Causing her severe sepsis and worsening mental status. We discussed comfort measures versus this intervention. Surgery was consulted and she was found to have necrotizing fasciitis and plans were made to go to the OR (Operating Room) for debridement. The OR (Operating Room) procedure note dated 12/18/21 revealed that the patient's decubitus wound was massive and necrotic. The resident had to be taken urgently to the OR to excise the necrotic tissue because the patient is in septic shock. All necrotic tissue was excised. All underlying tissue was involved all the way to the bone. Patient was intubated and critically ill. Consideration for hospice care. On 5/13/22 at 7:44 PM and at 5:00 PM a phone call was made to the Surgeon. Surveyor was not able to leave messages. An interview was conducted on 5/17/22 at 4:25 PM., with LPN (License Practical Nurse, wound care nurse/Assistant Director of Nursing) #3 concerning Resident #339. She stated, It (SACRUM) was first identified as unstageable. It progressed and we had to debride it. I did some of her wound care. It showed no signs of infection after the first surgical debridement. For preventive measures she used a specialty mattress starting 12/10/21. We medicated her before wound care. She was turned and repositioned. An interview was conducted on 5/18/22 at 10:00 AM with the complaintant concerning Resident #339. She stated, The hospital surgeon made a referral to us and he indicated that he had to perform two surgeries on patient's sacral area due to having a large infected wound. The two surgeries resulted from infection of the wound to the bone. My investigation found she had no wounds on her body until December 3rd. (2021) She was bedridden and had physical therapy from her bed. She never got out of bed. She was put on hospice. Her husband would sit with her for hours. The wound nurse (LPN #3) would only see her when the outside Wound Nurse Practitioner came in. An interview was conducted on 5/18/22 at 11:15 am with CNA (Certified Nurse's Aide) #7. Concerning Resident #399. She stated, A few days after she came she complained that her butt hurt. We would get her off her side. When I came back from being off, she had an area on her butt. I reported it to the nurse. That nurse no longer works here. The wound nurse came every week. She was not ambulatory and could not make her needs known. She had good days and bad days. I turned and reposition her every two hours. LPN #13, who was the nurse CNA #7 alerted about the area on Resident #339, was called twice throughout the survey. Voice messages were left with no return call. On 5/19/22 at 1:35 AM., an interview was conducted with RN (Registered Nurse) #1. She stated, I turned her every 2 hours due to the wound on her bottom. She was not able to make her needs known. The wound on her bottom was acquired at the facility. I didn't have to do anything with her wound because I worked the 7 pm -7 am shift. We had an investigation here earlier. I didn't find anything unusual with her vitals. I thought it was odd that she was smiling. I never got to see the wound. If it was soiled I would have changed it and seen it but I didn't have the opportunity. On 05/20/2022 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided. 3. The facility staff failed to identify a sacral wound pressure ulcer prior to advancing to an unstageable pressure ulcer measuring 5 centimeter (cm) x 5 cm x 2 cm for Resident #291. The sacral wound was infected requiring antibiotic therapy and surgical debridement (removal of dead tissue), which constituted harm. Resident #291 was originally admitted to the facility on [DATE]. Diagnosis for Resident #291 included but are not limited to Parkinson disease and muscle weakness. Resident #291's admission Assessment (14-day) with an ARD of 03/19/22 coded Resident #291 Brief Interview for Mental Status (BIMS) scored a 99 indicating short and long term memory problems and severe cognitive impairment - never/rarely made decisions. Resident #291 was coded total dependence of two with toilet use, bed mobility and bathing, total dependence of one with dressing, personal hygiene and eating and for Activities of Daily Living (ADL). Under section H - (Bladder and Bowel) was coded for always incontinent of bladder and bowel. Under section G0400 - Functional Limitation in Range of Motion (ROM) coded Resident #291 with no impairment to her upper and lower extremity. Resident #291 was coded as having no mood, rejection of care or behavioral problems. Resident #291's admission Assessment (14-day) with an ARD of 03/19/22. Under section (M0150) at risk for developing pressure ulcers was coded yes, under section (M0210) for unhealed pressure ulcers was coded yes and under section (M0300) for having current number of unhealed pressure ulcer at each stage present upon admission or reentry into the facility was coded for stage II pressure ulcer. Under section (1200) for skin, ulcer treatments were coded for having pressure reducing device for bed and pressure ulcer wound care. Resident #291's person-centered care plan initiated on 03/21/22 identified the resident has a pressure ulcer in her sacral area, at risk for further skin breakdown related to incontinence and impaired mobility. The goal set for the resident by the staff was that the resident will remain free of new skin breakdown through next review date. Some of the interventions/approaches the staff would use to accomplish this goal is to follow facility policies/protocols for the prevention/treatment of skin breakdown, assess/record/monitor wound healing, measure length, width and depth where possible, assess and document status of wound perimeter, wound bed and healing progress, specialty mattress and report improvements and declines to the physician and administer treatments as ordered and monitor for effectiveness. The person-centered care plan with a revision date of 04/01/22 identified Resident #291 on antibiotics for a sacral wound infection. The goal set for the resident by the staff was that the resident will show signs of healing and remain free of complications related to infection. One of the interventions/approaches the staff would use to accomplish this goal is to administer medications as ordered, monitor/document for side effects and effectiveness. A Braden Risk Assessment Report was completed on 3/15/22. The resident scored a 09 indicating at high risk for the development of pressure ulcers. The assessment coded under sensory perception very limited and responds only to painful stimuli; cannot communicate discomfort except by moaning or restlessness or has a sensory impairment which limits the ability to feel pain or discomfort over ½ of the body. Under moisture was coded skin is occasionally moist, requiring an extra linen change approximately once a day and coded bedfast under activity. The skin/wound admission note dated 03/10/22 indicated Resident #291 had a stage II sacral ulcer measuring 2.0 cm x 1.0 cm x 0.2 cm with very dark skin, nonblachable measuring (15 cm x 9 cm) surrounding the sacral ulcer. The note indicated that Resident #291's pressure ulcer will be evaluated by the wound Nurse Practitioner (NP) during her next visit on 03/15/22. Resident #291 had a physician order dated 03/10/22 to apply an air mattress to the bed for wound prevention and an order dated 03/11/22, for a sacral pressure ulcer treatment to apply a foam dressing every Tuesday, Thursday and Saturday (day shift). A review of Resident #291's nurse's note revealed the resident was transferred to the hospital emergency room for evaluation for an elevated temperature on 03/14/22 at approximately 6:50 p.m., and returned on 03/15/22 at approximately 4:00 p.m. Further review of the nurses note revealed no new skin impairments noted since the last admission assessment on 03/10/22. The resident was readmitted to the nursing facility on 03/15/22. The readmission note under skin integrity revealed the same sacral pressure assessed at a Stage II. A skin/wound note dated 03/22/22 at 12:08 p.m., by the wound nurse License Practical Nurse (LPN #3) revealed the wound NP (WNP) went to assess Resident #291's sacral wound but the resident had pain with body movement, thus the WNP decided to assess Resident #291's sacral wound during her next onsite visit on 03/29/22. During the review of Resident #291's clinical record revealed there were no weekly wound assessments made by the facility licensed nurses of the sacral pressure ulcer for 19 days, after her admission to the facility. An interview was conducted with the WNP on 05/17/22 at approximately 3:06 p.m., I was in the facility on 03/15/22 to assess Resident #291's sacral ulcer, but the resident was discharged to the hospital during my onsite visit. The WNP stated, My first time evaluating Resident #291's pressure ulcer was on 03/29/22. The WNP said the wound was infected as evidence by the wound having a significant amount of slough with foul odor present and having significant pain over the sacral area when touched or palpated. Resident #291 was placed on routine pain medication as well as two rounds of antibiotic therapy to help fight the sacral wound infection. The wound was not cultured due to the location of the wound (sacral area) which put the wound culture at risk for cross contamination. The WNP's initial progress note of the sacral pressure ulcer on 03/29/22 revealed an unstageable ulcer measuring 5 cm x 5 cm x 2 cm. The progress note stated the sacral wound had a moderate amount of serosanquinous drainage, strong odor present with 90 percent (%) slough and 10 % dermis tissue. A new medication order was given for Augmentin (antibiotic) 500 mg/125 mg every 12 hours x 10 days for a sacral wound infection. A new treatment order was given to clean the sacral wound with Dakin's, Santyl on Dakin's gauze, and cover with foam dressing daily and as needed. The WNP progress note also stated pain is indicative of any movement, at rest she is comfortable. The WNP also offered further recommendations to turn and reposition per facility protocol, use of a low air loss mattress and to optimize nutrition. A WNP progress note dated 04/05/22 revealed the sacral wound pressure ulcer remained an unstageable measuring 5 cm x 5 cm x (?). The sacral wound had improved but remain with moderate amount of serosanquinous drainage, strong odor present with 90% slough and 10% dermis tissue. The wound was debrided removing thick slough tissue; pain was present with any movement. Resident #291 remained on antibiotic therapy for a sacral wound infection and continued with the current wound treatment, Dakin's, Santyl on Dakin's gauze, and cover with foam dressing daily and as needed. A review of the WNP's progress note dated 04/11/22 indicated that the wound visit was performed via telehealth with the wound nurse, License Practical Nurse (LPN #3). The sacral wound was deteriorating with moderate amount of purulent drainage, strong odor present with 90% slough and 10% dermis tissue. The wound measured by onsite nurse (LPN #3) measuring 6.5 cm x 5.5 cm x 2.5 cm. The progress note recommended to continue with current sacral wound treatment with Dakin's, Santyl on Dakin's gauze, foam dressing and change daily and as needed. A new antibiotic order was given for Clindamycin 600 mg by mouth every 8 hours for 21 days for a sacral wound infection. The wound NP progress note also stated pain is indicative of any movement, at rest she was comfortable. On 05/16/22 at approximately 2:25 p.m., an interview was conducted with LPN #1. LPN #1 was assigned to performed sacral wound care to Resident #291 on 03/26/22 (7a-7p shift). The LPN stated, I have never measured Resident #291's sacral pressure ulcer. The ulcer was being measured and monitored by LPN #3 and the wound NP. An interview was conducted with the Medical Director (MD) on 05/18/22 at approximately 11:33 a.m., who said all pressure ulcers were followed by (name of Wound Company.) The MD stated, Resident #291's sacral ulcer should have been monitored, assessed and measured on a weekly basis for signs of decline or improvement. The nurses should have been monitoring the sacral pressure ulcer during every wound care dressing change for a change in condition. Apparently, the nurses were not doing a full wound assessment for change in condition because a pressure ulcer cannot go from a stage II to an unstageable requiring debridement overnight. The changes in the wound should be been addressed before the wound was identified as an unstageable pressure ulcer. The extra nutritional element recommended by the dietitian could have help with the wound healing of the sacral pressure ulcer. An interview was conducted with LPN #9 on 05/19/22 at approximately 10:44 a.m. The LPN was assigned to perform sacral wound care to Resident #291 on 03/19/22 (7a-7p shift). The nurse said an open area was noted to the sacrum with shearing/excoriation to the periwound. The LPN stated, I only do the resident's treatment not the monitoring or measuring of the wound that was being done by the wound NP or LPN #3 on a routine basis. A phone interview was conducted with LPN #12 on 05/16/22 at approximately 6:29 p.m. The LPN was assigned to perform sacral wound care to Resident on 03/22/22 (7a-7p shift). The LPN said the sacral wound appeared larger in size but I did not measure or document the change in condition of the sacral wound. The LPN stated, The wound NP and LPN #3 were assessing and monitoring Resident #291's sacral ulcer every week. A dietary/nutrition note dated 03/18/22 at 9:56 a.m., revealed Resident #291 having a suspected deep tissue injury (SDTI) to the left and right heel and a stage II pressure ulcer to the coccyx/sacral area per 03/10/22 (skin assessment). Recommendations were made for fortified foods with meals due to poor oral intake of meals, provide texture-appropriate calorie-dense snacks three times a day between meals due to poor oral intake and thickened house shake (120 mL), pudding / fortified pudding. A Dietary/Nutrition note dated 04/08/22 at 12:33 p.m., revealed the nutritional recommendations made on 03/18/22 were never addressed for fortified foods with meals due to poor oral intake of meals, provide texture-appropriate calorie-dense snacks three times a day between meals due to poor oral intake and thickened house shake (120 mL), pudding / fortified pudding. An interview was conducted with the RD on 05/17/22 at approximately 4:41 p.m., who stated, The nutrition recommendations made for Resident #291 on 03/18/22 and again on 04/08/22 were never addressed. The RD said the extra calories would have given extra protein that's needed to help with healing Resident #291's sacral pressure ulcer. The nursing note dated 04/11/22 at approximately 6:23 p.m., revealed Resident #291 with Altered Mental Status (AMS), tremors and had vomiting during dinner. A new order was given to send Resident #291 to the emergency room (ER) for evaluation and treatment. A review of the hospital records revealed that Resident #291 presented in the Emergency Department (ED) on 04/11/22 from (name of nursing facility) for further evaluation due to Altered Mental Status (AMS) and vomiting. The ED indicated Resident #291 is lethargic, disoriented and is currently on antibiotic for an infected unstageable sacral wound. The wound is observed with a strong foul odor. The sacral wound was evaluated to be a FIST size with partial wet slough, fetid (having a heavy offensive smell-https://www.merriam-webster.com/dictionary) skin and obvious deep tunneling on perimeter. The ED report indicated the resident did not meeting the criteria for Systemic inflammatory response syndrome (SIRS), but had a concerning sacral wound and was referred for evaluation and treatments by the General Surgery. The resident was started on IV Vancomycin (antibiotic) and Zosyn (antibiotic) for empiric coverage of her large sacral decubitus ulcer. After the sacral wound was evaluated by the General Surgery, he felt the wound would benefit from debridement of the wound. On 04/12/22, Resident #291 was taken into the operating room (OR), and the sacral wound was debrided. After debridment the wound was assessed as a stage III decubitus ulcer with no exposed bone at this time. The recommendation was made for a wound VAC to improve the healing process for the resident. It was noted that the resident would also benefit from significant nutritional support and should be fed by staff by the facility. An interview was conducted with the Director of Nursing (DON) and wound nurse LPN #3 on 05/12/22 at approximately 10:00 a.m. The DON said Resident #291's sacral pressure ulcer should have been evaluated by the WNP or wound nurse, LPN #3 on a weekly basis. She stated, the weekly evaluation and monitoring was needed for early detection to determine if the wound is improving or declining. The wound nurse LPN #3 stated, I was not here on 03/17/22 and 03/24/22, when Resident #291 was supposed to have her sacral wound assessed and evaluated a changes in condition. The DON said the nurses should have been assessing and documenting changes on Resident #291's sacral pressure ulcer (description of wound bed, if drainage or odor present and size of the wound) with all changes reported to LPN #3 or the wound NP for evaluation to determine if wound treatment changes were needed. According to the DON, the stage II sacral wound treatment was appropriate when admitted to the facility on [DATE]. The treatment was for a foam dressing, change every 2 days. The DON said, When the wound deteriorated to an unstageable, the treatment should have been changed but it wasn't. The DON further stated, Due to the lack of documentation, there is no way to know when Resident #291's sacral wound deteriorated to the point it had advanced to an unstageable requiring debridement and antibiotic due to infection. A debriefing was held with the Administrator, Director of Nursing and Corporate support on 05/19/22 at approximately 2:00 p.m. Resident #291's issues was presented again. No additional information was forthcoming. Definitions: -Pressure Injury: A pressure injury is localized damage to the skin and underlying soft tissue usually over a bony prominence or related to a medical or other device. The injury can present as intact skin or an open ulcer and may be painful. The injury occurs as a result of intense and/or prolonged pressure or pressure in combination with shear (http://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages/). -Pressure Injury - Stage 2 (Partial-thickness skin loss with exposed dermis_ Partial-thickness loss of skin with exposed dermis. The wound bed is viable, pink or red, moist, and may also present as an intact or ruptured serum-filled blister. Adipose (fat) is not visible and deeper tissues are not visible. Granulation tissue, slough and eschar are not present. These injuries commonly result from adverse microclimate and shear in the skin over the pelvis and shear in the heel. This stage should not be used to describe moisture associated skin damage (MASD) including incontinence associated dermatitis (IAD), intertriginous dermatitis (ITD), medical adhesive related skin injury (MARSI), or traumatic wounds (skin tears, burns, abrasions (http://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages). Pressure Injury - Stage 3 (Full-thickness skin loss) Full-thickness
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0568 (Tag F0568)

Could have caused harm · This affected 1 resident

Based on observation, resident interview, staff interview, clinical record review, and review of facility documents, the facility's staff failed to provide two residents quarterly statements for 2 of ...

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Based on observation, resident interview, staff interview, clinical record review, and review of facility documents, the facility's staff failed to provide two residents quarterly statements for 2 of 55 residents (Resident #24 and Resident #60), in the survey sample. The findings include: 1. Resident #24 was originally admitted to the facility 7/18/19 from the community. The resident has never been discharged from the facility. The current diagnoses included; Type 2 Diabetes Mellitus with Diabetic Neuropathy and Unspecified Atrial Fibrillation. The Annual Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 02/19/2022 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #24s cognitive abilities for daily decision making were intact. In sectionG(Physical functioning) the resident was coded as independent set-up help only with bed mobility, transfers and toilet use. Requiring supervision set-up help with dressing, eating, personal hygiene and bathing. On 05/11/22 at approximately 1:38 PM an interview was conducted with Resident #24 concerning quarterly statements. He stated, I haven't received quarterly statements from anyone. 2. The facility staff failed to provide Resident #60 a quarterly statement. Resident # 60 was originally admitted to the facility 08/18/21 from the community. The resident has never been discharged from the facility. The current diagnoses included; Type 2 Diabetes Mellitus and Essential Hypertension. The quarterly Revision, Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 04/10/2022 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #60 cognitive abilities for daily decision making were intact. In sectionG(Physical functioning) the resident was coded as requiring total care of one person with bed mobility, transfers, locomotion, dressing, eating, toileting, personal hygiene and bathing, extensive assistance of one person/two people, limited assistance of one person, supervision after set-up. On 05/12/22 at approximately 9:36 AM during the initial tour Resident #60 was asked if she receives her quarterly statements. She stated, The social worker takes care of my business. I don't get anything with my account. I don't know off hand what I have in my account. On 05/19/22 at approximately 1:35 PM an interview was conducted with the Business Office Manager (BOM) concerning quarterly statements for the above residents. She stated, I've been working here since 12/13/21. I haven't been providing the quarterly statements to residents. I just started working on the quarterly statements but haven't sent them out yet. On 05/20/22 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0570 (Tag F0570)

Could have caused harm · This affected 1 resident

Based on staff interview, and review of facility documents, the facility staff failed to purchase a current surety bond. The findings included: On 5/12/22 at approximately 6:40 PM., received document ...

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Based on staff interview, and review of facility documents, the facility staff failed to purchase a current surety bond. The findings included: On 5/12/22 at approximately 6:40 PM., received document from Business Office Manager (BOM) concerning Surety Bond. It reads as follows: The Facility has a Surety Bond for (Amount listed) expires 11/03/23. Amount of residents with personal accounts: 57 residents with funds. 12 residents with 0 (zero) balance. Total (amount listed). Received a notarized Surety Bond Certificate from the BOM. The listing the bond number for (Operator identification and former name of the facility). As Principal in the penalty amount not to exceed (amount listed). Date 11/03/2020. Currently the facility is under a new name: (listed new name as of December 2021). On 05/20/2022 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Transfer Requirements (Tag F0622)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on clinical record review, staff interviews and facility document review the facility staff failed to ensure Comprehensive...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on clinical record review, staff interviews and facility document review the facility staff failed to ensure Comprehensive Care Plan Goals were sent upon transfer to the hospital for 2 out of 55 residents in the survey sample, Resident #47 and Resident #58. The findings included: 1. The facility staff failed to ensure Comprehensive Care Plan Goals were sent upon transfer to the hospital on 5/4/22 and 5/7/22 for Resident #47. Resident #47 was admitted to the facility on [DATE] with diagnoses to include but not limited to Anoxic Brain Damage, Bipolar Disorder and Diabetes Mellitus. Resident #47's most recent Minimum Data Set(MDS) was a Significant Change assessment with an Assessment Reference Date (ARD) of 5/15/22. The Brief Interview for Mental Status was coded as a 15 out of a possible 15 indicating the resident was cognitively intact and capable of daily decision making. Resident #47's Progress Notes were reviewed and are documented in part, as follows: .5/4/2022 08:13 a.m. Nursing Progress Note: Resident went on the side hall phone and called 911 twice and told them that he was on the LEFT Side and he was having leg pain, arm pain and chest pain. 911 and Transport were made aware of resident's medical diagnosis and stated that he still had to go to the hospital to be checked out. Vitals WNL (within normal limits). RP(Responsible Party) made aware and MD(Medical Doctor) made aware. Report called in to Transport. Facesheet, SBAR (situation, background, assessment and recommendation), and Bed hold sent with resident. RP refused to hold bed. .5/7/2022 21:17 (8:17 p.m.) Nursing Progress Note: Resident was standing and speaking on the phone in hallway as I walked by. Looking over, I witnessed him suddenly lose consciousness and fall forward face down on the floor. Resident was gingerly moved onto his back protecting cervical spine. Help was sought and arrived. Resident laid face up bleeding from Left supraorbital ridge. Pupils were reactive and resident regained consciousness. vitals were done and EMS (emergency medical services) was called. Resident was taken to Name (hospital). There was no documentation in Resident #47's clinical record to indicated that the resident's comprehensive care plan goals were sent upon transfer from the facility to the hospital on 5/4/22 or 5/7/22. On 5/17/22 at 1:15 p.m. an interview was conducted with the Director of Nursing regarding Resident #47's transfers to the hospital on 5/4/22 and 5/7/22 and if his care plan goals were sent with him. The Director of Nursing stated, I don't see where it was documented that his care plan goals were sent when he was transferred to the hospital on 5/4/22 or 5/7/22. Each time a resident is sent out to the hospital the nurses are to send a copy of the care plan goals with them and document in the progress notes that they were sent. The facility policy titled Transfer and Discharge dated 10/5/21 was reviewed and is documented in part, as follows; .Policy: It is the policy of this facility to permit each resident to remain in the facility, and not transfer or discharge the resident from the facility except in limited situations when the health and safety of the individual or other residents are endangered. 7. Emergency Transfers/Discharges- initiated by the facility for medical reasons, or for the immediate safety and welfare of a resident (nursing responsibilities unless otherwise specified). d. Complete and send with the resident (or provide as soon as practicable) a Transfer Form which documents: viii. Comprehensive care plan goals. On 5/19/22 at 9:15 a.m. the above findings were shared with the Administrator and the Director of Nursing. The Administrator stated, I expect the nurses to send a copy of the care plan goals each time a resident is transferred to the hospital and to document that it was sent. Prior to survey exit no further information was shared. 2. The facility staff failed to ensure Comprehensive Care Plan Goals were sent upon transfer to the hospital on 4/3/22 for Resident #58. Resident #58 was admitted to the facility on [DATE] with diagnoses to include but not limited to Paranoid Schizophrenia, Bipolar Disorder and Dementia. Resident #58's most recent Minimum Data Set(MDS) was a Quarterly/Medicare 5 Day assessment with an Assessment Reference Date (ARD) of 4/12/22. The Brief Interview for Mental Status was coded as a 15 out of a possible 15 indicating the resident was cognitively intact and capable of daily decision making. Resident #58's Progress Notes were reviewed and are documented in part, as follows: .4/3/2022 20:01(8:01 p.m.) Nursing Progress Note: Called to room by CNA (certified nursing assistant) . Resident found lethargic. Skin cool and clammy. Vital signs as follows T(temperature)97.4, Pulse 60, Resp. 28, BP(blood pressure) 143/113. O2 (oxygen) Sat 77 on room air. Repeat BP 80/59. O2 sat up to 96% on O2 via N/C (nasal cannula). 911 called for transport to ER (emergency room) for eval (evaluation) and treat as needed. Call placed to Name (on call company) to notify of situation. Will pass on to MD (Medical Doctor) on call. Call center called to notify of transfer and report given at this time. RP(responsible party) called and returned call and made aware of transfer to ER for eval. There was no documentation in Resident #58's clinical record to indicated that the resident's comprehensive care plan goals were sent upon transfer from the facility to the hospital on 4/3/22. On 5/17/22 at 1:15 p.m. an interview was conducted with the Director of Nursing regarding Resident #58's transfers to the hospital on 4/3/22 and if his care plan goals were sent with him. The Director of Nursing stated, I don't see where it was documented that his care plan goals were sent when he was transferred to the hospital on 4/3/22. Each time a resident is sent out to the hospital the nurses are to send a copy of the care plan goals with them and document in the progress notes that they were sent. The facility policy titled Transfer and Discharge dated 10/5/21 was reviewed and is documented in part, as follows; .Policy: It is the policy of this facility to permit each resident to remain in the facility, and not transfer or discharge the resident from the facility except in limited situations when the health and safety of the individual or other residents are endangered. 7. Emergency Transfers/Discharges- initiated by the facility for medical reasons, or for the immediate safety and welfare of a resident (nursing responsibilities unless otherwise specified). d. Complete and send with the resident (or provide as soon as practicable) a Transfer Form which documents: viii. Comprehensive care plan goals. On 5/19/22 at 9:15 a.m. the above findings were shared with the Administrator and the Director of Nursing. The Administrator stated, I expect the nurses to send a copy of the care plan goals each time a resident is transferred to the hospital and to document that it was sent. Prior to survey exit no further information was shared.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Transfer Notice (Tag F0623)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. The facility failed to notify the Office of the State Long-Term Care Ombudsman in writing of hospital discharges for resident...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. The facility failed to notify the Office of the State Long-Term Care Ombudsman in writing of hospital discharges for resident #70. Resident #70 was originally admitted to the facility on [DATE] and discharged on 3/26/22 to an acute care facility. The current diagnoses included unspecified dementia without behavioral disturbance and fracture of unspecified part of neck of right femur and closed fracture with routine healing The discharge Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 03/26/22 coded the resident as not having the ability to complete the Brief Interview for Mental Status (BIMS). The staff interview was coded for short term memory problems as well as severely impaired for daily decision making. In section G(Physical functioning) the resident was coded as requiring supervision with transfers, walking, eating and toilet use. Requiring extensive assistance with personal hygiene and dressing. Requiring total dependence with bathing. A review of nursing notes dated on 3/26/2022 at 2:12 PM reads: Family was notified of fall and need for x ray of hip and of baseball sized lump on head and wanted resident transported to ER. The Discharge MDS assessments was dated for 3/26/2022 - discharged with return anticipated. According to the facility's documentation, on 3/26/22 Resident #70 was transported to the local hospital. According to the facility's documentation on 3/31/22 Resident #70 was admitted back to the facility from the local hospital. A review of the Monthly List of Emergency Transfers for April 2022 does not include Resident #70's name on the list. An interview was conducted on 5/13/22 at 5:05 PM with OSM/Social Worker #3 concerning Resident #70. She stated, I only do ombudsman notifications when a resident is discharged home. On 05/20/2022 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided. Based on clinical record review, staff interviews and facility document review the facility staff failed to notify the Office of the State Long-Term Care Ombudsman of 3 hospital discharges and 1 hospital transfer for 3 of 55 residents in the survey sample, Resident #58, Resident #70 and Resident #36. The findings included: 1. The facility staff failed to notify the Office of the State Long-Term Care Ombudsman of Resident #58's hospital transfer on 4/3/22. Resident #58 was admitted to the facility on [DATE] with diagnoses to include but not limited to Paranoid Schizophrenia, Bipolar Disorder and Dementia. Resident #58's most recent Minimum Data Set(MDS) was a Quarterly/Medicare 5 Day assessment with an Assessment Reference Date (ARD) of 4/12/22. The Brief Interview for Mental Status was coded as a 15 out of a possible 15 indicating the resident was cognitively intact and capable of daily decision making. Resident #58's Progress Notes were reviewed and are documented in part, as follows: .4/3/2022 20:01(8:01 p.m.) Nursing Progress Note: Called to room by CNA (certified nursing assistant) . Resident found lethargic. Skin cool and clammy. Vital signs as follows T(temperature)97.4, Pulse 60, Resp. 28, BP(blood pressure) 143/113. O2(oxygen) Sat 77 on room air. Repeat BP 80/59. O2 sat up to 96% on O2 via N/C(nasal cannula). 911 called for transport to ER(emergency room) for eval(evaluation) and treat as needed. Call placed to Name (on call company) to notify of situation. Will pass on to MD(Medical Doctor) on call. Call center called to notify of transfer and report given at this time. RP(responsible party) called and returned call and made aware of transfer to ER for eval. On 5/18/22 at 1:25 p.m. an interview was conducted with the facility Social Worker regarding Resident #58's ombudsman notification of his hospital transfer on 4/3/22. The Social Worker stated, When I came back we were only faxing the ombudsman about residents who were discharged home. I don't know that I have notified the ombudsman of residents who have been transferred to the hospital. We have a new ombudsman and I called yesterday and they want notifications emailed instead of faxed. I went back to 2/7/22 and resent all hospital transfers to the ombudsman. I know now that all discharges need to be sent to the ombudsman. The facility policy titled Transfer and Discharge dated 10/5/21 was reviewed and is documented in part, as follows: 7. Emergency Transfer/Discharges: k. Social Services Director, or designee, shall provide notice of transfer to a representative of the State Long-Term Care Ombudsman via monthly list. On 5/19/22 at 9:10 a.m. the above findings were shared with the Administrator and the Director of Nursing. The Administrator stated, I expect that the Social Worker will send the ombudsman notifications via email each month for all discharges Prior to survey exit no further information was shared. 3. Resident #36 was originally admitted to the facility on [DATE] and was discharged to the hospital return anticipated on 2/3/2022. The resident's diagnosis included cirrhosis of the liver with ascites and a right inguinal hernia. The significant change Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 3/21/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #36's cognitive abilities for daily decision making were intact. A nurse's note dated 2/3/22 at 1:14 p.m., read the resident refused to go for paracentesis when it was scheduled and he began to experience extreme abdominal pain which required an assessed by the physician. The physician ordered a dose of as needed Morphine be administered for pain relief for the resident to transfer the hospital for further evaluation. A review of the clinical record revealed a discharge MDS assessment dated [DATE]. It was coded return anticipated. An interview was conducted with the Social Worker (SW) on 5/18/22 at approximately 1:25 p.m. The SW stated the Long Term Care Ombudsman was not notified of Resident #36's discharge to the hospital on 2/3/22. The SW also stated that she was only notifying the Ombudsman of discharges to the community but she learned on 5/17/22, it was her responsibility to notify the Ombudsman of discharges to the hospital. She stated all discharged [DATE] and forward she had gathered the data and sent it to the Ombudsman's office. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on a family interview, staff interview, and review of the clinical record review, the facility staff failed to develop and...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on a family interview, staff interview, and review of the clinical record review, the facility staff failed to develop and implement a person-centered comprehensive care plan to address rejection of care for 1 of 55 residents (Resident #48) in the survey sample. The findings included: Resident #48 was originally admitted to the facility 12/30/21 and readmitted [DATE] after an acute care hospital stay. The current diagnoses included; metastatic squamous cell carcinoma and encephalopathy. The significant change annual quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 4/2/2022 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 13 out of a possible 15. This indicated Resident #48's cognitive abilities for daily decision making were intact. A review of the Wound Care Nurse Practitioner's (WCNP) progress notes dated 5/3/22, 5/10/22 and 5/17/22 revealed wound care had been consulted for an ustageable pressure ulcer to the resident's sacrum and a callus to the left foot. The WCNP also documented the resident refuses care. A review of Resident #48's care plan with a revision date of 3/30/22, did not include interventions for rejection/refusal of care. On 5/20/22 at approximately 3:05 p.m., an interview was conducted with the resident's daughter. The daughter stated she has been told that her mother rejects care but that is a behavior she didn't exhibit when she home and she would have known because she resided with her. An interview was also conducted with Certified Nursing Assistant (CNA) #6 on 5/20/22 at approximately 3:15 p.m. CNA #6 stated she doesn't work with the resident routinely but she was assigned to her that day and there had been no episodes of rejection of care provided by her. An interview was also conducted with Licensed Practical Nurse (LPN) #1 on 5/20/22 at approximately 3:22 p.m. LPN #1 stated she routinely worked with the resident and she hadn't experienced problems with rejection of care but the resident did require frequent redirections. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0657 (Tag F0657)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. The facility staff failed to provide evidence that Resident #60 was invited to attend a care plan meeting and to provide evid...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. The facility staff failed to provide evidence that Resident #60 was invited to attend a care plan meeting and to provide evidence of having care plan meetings. Resident #60 was originally admitted to the facility 08/18/21 from the community. The resident has never been discharged from the facility. The current diagnoses included Type 2 Diabetes Mellitus and Essential Hypertension. The quarterly Revision, Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 04/10/2022 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #60 cognitive abilities for daily decision making were intact. In sectionG(Physical functioning) the resident was coded as requiring total care of one person with bed mobility, transfers, locomotion, dressing, eating, toileting, personal hygiene and bathing, extensive assistance of one person/two people, limited assistance of one person, supervision after set-up. A review of Resident #60's clinical record reveal that a Multidisciplinary Care Conference was held on 4/17/22. Present were Administration, Activities and the Social worker. There was no evidence that Resident #60 was invited or attended the Multidisciplinary Care Conference. A review of the clinical record show that only one Multidisciplinary Care Conference was held since Resident's admission on [DATE]. On 05/12/22 at 9:30 AM., an interview was conducted with Resident #60. She could not recall receiving a recent invitation for a care plan meeting. Resident #60 stated, They don't tell me. On 05/12/22 at 4:57 PM., an interview was conducted OSM (Other Staff Member/Social Worker) #3 concerning care plan meetings. She stated, I give them a care plan letter that's delivered by the activities department. I get a monthly sheet from the MDS (Minimum Data Set) coordinator. They get about a couple of weeks notices. (Resident #60's name) has been invited to only one meeting on 4/20/22. (Resident #60's name) was present. I can't find records of any more care plan meetings. We had an interim Social Worker. I was on LOA (Leave Of Absence) from 10/30/21-2/7/22. The care plan meetings should be every ninety days or so. We should have CP meetings. On 05/20/2022 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility staff to present additional information but no additional information was provided. Based on resident interviews, staff interviews, clinical record review and facility documentation review, the facility staff failed to invite 2 of 55 residents, (Resident #75 and #60) in the survey sample to attend their person centered care plan meeting. The findings included: 1. Resident #75 was originally admitted to the facility on [DATE]. Diagnosis for Resident #75 included but not limited to End Stage Renal Disease (ESRD). The current Minimum Data Set (MDS), a quarterly assessment with an Assessment Reference Date (ARD) of 04/24/22 coded the resident with a 15 out of a possible score of 15 on the Brief Interview for Mental Status (BIMS) indicating no cognitive impairment. An interview was conducted with Resident #75 on 05/11/22 at approximately 4:49 p.m., who stated I do not recall ever being invited to attend a care plan meeting nor did I receive a letter to attend. On 05/12/22, an interview was conducted with the Social Worker (SW) at approximately 4:52 p.m., who stated, Resident #75 should have had her first care plan meeting two weeks after being admitted to the facility, but it doesn't look like she was not given the opportunity at that time. She said, Resident #75 was invited to attend a care plan meeting on 04/19/22 but she refused but the refusal was not documented. The Administrator, Director of Nursing and Corporate were informed of the finding during a debriefing on 05/19/20 at approximately 2:00 p.m. The facility did not present any further information about the findings. The facility's policy titled Care Planning-Resident and/or Resident Representative Participation - revised 10/01/21. Policy: This facility supports the resident's and/or resident representative right to be informed of, and participate in, his or her care plan treatment (implementation of care). Policy Explanation and Compliance Guidelines: -The facility will inform the resident and/or resident representative, in a language he or she can understand, of his or her rights regarding planning and implementing care, including the right to be informed of his or her total health status. -If the participation of the resident and/or resident representative is determined not practicable for the development of the resident's care plan, an explanation will be documented in the resident's medical record.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0661 (Tag F0661)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, resident interview, staff interviews, and clinical record review, the facility staff failed to provide 1 o...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, resident interview, staff interviews, and clinical record review, the facility staff failed to provide 1 of 55 residents (Resident #84) in the survey sample with as much information as possible to encourage a smooth transition from the facility to his private home after voicing a desire to be discharged . The findings included: Resident #84 was originally admitted to the facility 4/27/22 and discharged from the facility 5/10/22. The current diagnoses included; sepsis, diabetes, chronic kidney disease, atrial flutter and heart failure, skin tear to the left lower leg/cellulitis. The admission Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 5/2/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #84's cognitive abilities for daily decision making were intact. In section G (Physical functioning) the resident was coded as requiring total care of one person with bathing, extensive assistance of two people with bed mobility and transfers, eating, and bathing, limited assistance of one person with dressing, personal hygiene, and toileting supervision after set-up with eating. The resident's care plan had a problem dated 4/29/22 which read; (name of the resident) expresses a desire to return home upon discharge. The goal read (name of the resident) will demonstrate participation in discharge planning through 5/11/22. The interventions included; Meet with the resident to outline discharge goals and revise as needed with progression. Provide discharge information including; medication recapitulation, durable medical equipment, follow-up appointments and facility contact information. Reconcile medications with the resident prior to discharge and confirm understanding. On 5/10/22 at approximately 4:50 p.m., Resident #84 was heard anxiously telling the Social Worker (SW) that he was unable to rest at the facility and he felt the lack of sleep was hindering his recovery. After the conversation with Resident #84 an observation was made of the SW leaving the resident's room, stopping at Licensed Practical Nurse (LPN) #7's medication cart and instructing LPN #7 to immediately complete a discharge AMA (against medical advice) for Resident #84. The AMA document stated the resident was leaving upon his own insistence and against the advice of his medical physician and he had been informed of the dangers of leaving the facility at that time and the facility, officers, personnel and his personal physician were released of consequences of his leaving under the current circumstances. At this time no other documents were offered to the resident. An interview was conducted with Resident #84 on 5/10/22 at approximately 5:10 p.m. The resident stated he had wrestled with staying the additional days or going home and he came to the conclusion he had to go home for he had not rested well since his admission to the facility. The resident also stated that he had slept in a recliner chair at home for many years and trying to sleep in the bed at the facility wasn't meeting his needs. The resident further stated he had physically improved with therapy services and he felt comfortable going home with his visiting nurse's help. Resident #84 stated he informed the nurse and the Social Worker early morning (approximately 9:00 a.m.) of his intent to go home on that day, 5/10/22 yet at 4:45 p.m., the Social Worker stated he couldn't leave because he didn't give the facility adequate time to arrange the services he would need in the community. He said he made it clear upon admission that he would be returning to his apartment after he regained his strength and met his goals with therapy. The resident stated that he had made contact with his visiting nurse and they were en route to transport him home. On 5/10/22 at approximately 6:00 p.m., LPN #7 provided Resident #84 with the AMA document and requested he sign it before he left the facility. A copy of the AMA was given to the resident and no further services were offered or rendered. The Resident requested assistance from LPN #7 to transfer from the bed to the wheel chair but because of her hesitancy the Resident's home visiting nurse who arrived to transport the resident home assisted the resident to transfer, pack his belongings and get into the vehicle. On 5/11/22 at approximately 11:10 a.m., an interview was conducted with the SW regarding the discharge of Resident #84. The SW stated Resident #84 notified her at the beginning of the day on 5/10/22, of his desire to discharge home for lack of the ability to sleep in the facility. The SW stated she had several meeting to attend and other duties which required her attention therefore she didn't have the opportunity to notify the physician and/or other designee to obtain orders for medications, necessary medical equipment or home health services and rehab services hadn't completed their treatment with the resident. The SW further stated the resident had previously agreed to discharge to the community on 5/13/22 which the facility's Team agreed was reasonable would allow them sufficient time to pull together his discharge plans. The SW stated she contacted the resident's emergency contact and she agreed the resident should remain in the facility until 5/13/22, and she wouldn't transport him home until then. On 5/20/22 at approximately 11:10 a.m., an interview was conducted with the primary NP who stated, during her last conversation with the resident the plan was to discharge on [DATE] instead of 5/10/22. The NP stated as she was leaving the facility on 5/9/22, she was stopped at the door and informed that Resident #84 desired to discharge from the facility that day but no one informed her of the need to speak with the resident or any write orders to ensure the resident was discharged safely. On 5/20/22 at approximately 11:10 a.m., an interview was conducted with Resident #84's treating Physical Therapist who stated the plan was for the resident to discharge on [DATE] but there was no safety risk from the therapy department positions that would make it unsafe for the resident to discharge on [DATE]. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

ADL Care (Tag F0677)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. For Resident #66 the facility staff failed to ensure a resident who was unable to carry out activities of daily living (ADL) ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. For Resident #66 the facility staff failed to ensure a resident who was unable to carry out activities of daily living (ADL) receive the necessary services to include showers. Resident #66 was originally admitted to the facility 10/16/2015 from an acute care facility and discharged on 4/11/22 to an acute care facility and returned to the Long Term Care Facility on 4/13/22. The current diagnoses included; Pneumonia and COPD (Chronic Obstructive Pulmonary Disease). The Significant change Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 04/18/2022 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #66 cognitive abilities for daily decision making were intact. In sectionG(Physical functioning) the resident was coded as requiring extensive assistance of one person with bed mobility and dressing. Requiring total dependence of one person with toilet use, personal hygiene and bathing. Requires set-up help only with eating. The care plan dated 4/17/22 reads: Focus: ADL self-care performance deficit r/t impaired mobility with right sided weakness secondary to CVA, paralytic gait, lack of coordination, muscle wasting & atrophy with history of syncope and collapse. Goal: The resident will maintain current level of function in ADLs through the review date. Interventions: BATHING/SHOWERING: The resident requires assistance by (1) staff with bathing/showering twice weekly and as necessary. A review of the shower schedule reveal that Resident #66 is scheduled for showers on Thursday and Sundays. The 7A-7P shift. A review of the ADL sheet for May 2022 show that Resident #66 has received only bed baths. An interview was conducted on 5/11/22 at 2:15 PM. with Resident #66 concerning showers. He said that he only get bed baths. He was asked if he wanted to get showers. He stated, Yes ma'am. On 05/20/2022 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided. Based on observations, clinical record review, staff interviews and facility document review the facility staff failed to ensure that 4 of 55 residents (Resident #85, #66, #13, and #69) in the survey sample who were unable to carry out grooming activities of daily living (ADL) were provided showers and nail care. The findings included: 1. The facility staff failed to ensure Resident #85 who was unable to carry out activities of daily living was offered and received a scheduled twice-weekly shower to maintain good personal hygiene during the last 4 months and failed to ensure that fingernail care was provided. Resident #85 was originally admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses to included but not limited to Contractures of both knees and lower legs, Parkinson's Disease and Alzheimer's Disease. Resident #85's most recent Minimum Data Set (MDS) was a Significant Change Assessment with an Assessment Reference (ARD) of 4/28/22. The Brief Interview for Mental Status (BIMS) was unable to be completed, however Resident #85 was coded as being severely cognitively impaired for daily decision making. Under Section G Functional Status, Resident #85 was coded as being totally dependent with one person physical assist for personal hygiene and bathing. Under Functional Limitation In Range of Motion the resident was identified with lower extremity impairment on both sides. The following observations were made of Resident #85: On 05/11/22 09:30 a.m. Resident's fingernails on both hands were noted to have dark brown debris under the nailbeds which were approximately 1 cm(centimeter) long. On 05/11/22 12:25 p.m. Resident's fingernails on both hands were noted to have dark brown debris under the nailbeds which were approximately 1 cm long. On 05/11/22 2:09 p.m. Resident's fingernails on both hands were noted to have dark brown debris under the nailbeds which were approximately 1 cm long. On 05/12/22 at 9:00 a.m. Resident's fingernails on both hands were noted to have dark brown debris under the nailbeds which were approximately 1 cm long. On 5/12/22 at 9:30 a.m. an interview was conducted with Certified Nursing Assistant (CNA)#3 who cared for Resident #85 on 5/11/22 during the 7-3 shift in regards to the above observations and the resident's shower schedule. CNA #3 stated, Yes, her nails are long and dirty. They need to be cut. The CNA's cut the residents nails. I always give her a bed bath. I'm not sure of her shower schedule. On 5/12/22 at 9:50 a.m. a wound care observation was conducted with Licensed Practical Nurse (LPN) #3, who was the facility wound nurse. After the wound care was completed LPN #3 was asked to look at Resident #85's fingernails. LPN #3 stated, Her nails need a little cleaning and cutting. Resident #85's Comprehensive Care Plan last revised 5/11/22 was reviewed. The Comprehensive Care Plan indicated the resident was at risk for ADL Self Care Deficit related to Alzheimer's, Dementia and Limited Mobility which was initiated on 11/9/20. Facility interventions put in place for Resident #85 included that the resident to be offered a shower every Monday and Thursday on the morning shift. Also in place was that during bathing the CNA was to check nail length, trim and clean the nails on bath days and as necessary, which was initiated on 11/9/20. Resident #85's Bathing Documentation Survey Reports for February, March, April and May 2022 were reviewed. The documentation indicated that the resident only received bed baths for the past 4 month. There was no documentation to show the resident was offered or given a shower in the last 4 months. The Left Side Shower Schedule Sheet was reviewed. Resident #85 was listed on the shower schedule to be given showers on Mondays and Thursdays. On 5/12/22 at 5:51 p.m. and interview was conducted with the Director of Nursing regarding Resident #85's fingernails and showers. The Director of Nursing stated, I implemented a shower schedule after I got here because I realized there was not one. (Resident #85's name) is on the shower schedule for Mondays and Thursdays. Based on her CNA bathing documentation from February to May, I only see where she has received bed baths. I don't see where she had received any showers. The CNA's should follow the shower schedule and ensure nail care in provided on shower days and as needed. The facility policy titled Activities of Daily Living (ADL) last revised 3/8/22 was reviewed and is documented in part, as follows: .Policy: The facility will ensure a resident's abilities in ADL's do not deteriorate unless deterioration is unavoidable. Policy Explanation and Compliance Guidelines: 3. A resident who is unable to carry out activities of daily living will receive the necessary services to maintain good nutrition, grooming, and personal and oral hygiene to include denture care and incontinence care. On 5/19/22 at 9:20 a.m. the above findings were shared with the Administrator and the Director of Nursing. The Director of Nursing stated, I expect the staff to follow the shower schedule and to offer showers 2 times a week and more often if requested. Also I expect fingernail care to be performed during showers or bathing or more often as needed. Prior to exit no further information was shared. 3. The facility staff failed to provide necessary fingernail care for Resident #13, a totally dependent resident for activities of daily living (ADL). Resident #13 was originally admitted to the facility 2/20/2014, was discharged to an acute care hospital 11/17/21 and returned 11/19/21. The current diagnoses; traumatic brain injury (TBI) and a seizure disorder. The quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 2/13/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 13 out of a possible 15. This indicated Resident #13's cognitive abilities for daily decision making were intact. In section G (Physical functioning) the resident was coded as requiring total care of one person with personal hygiene and bathing. On 5/18/22 at approximately 12:50 p.m., resident #13 was observed in bed. His hair was long and stringy and his finger nails were approximately 3 inches beyond the tip of his fingers and the nails were chipped and with jagged edges. Another observation was made of Resident #13 on 5/19/22 at approximately 4:10 p.m. the resident's fingernails were still long, chipped and with jagged edges. An observation was made of the resident in bed again on 5/20/22 at approximately 10:20 a.m., the fingernails were closely cut and well-manicured. Resident #13's person centered care plan dated 12/13/2020 had a problem which read; ADL self-care performance deficit related to TBI, contractures to the right upper extremity and hemiplegia on the left side, dependent on staff for all ADL's. The goal read; Resident will have all ADL needs met on an ongoing daily basis with participation as health permits through next review. One of the interventions read; Check nail length, trim and clean on bath day and as necessary. Report any changes to the nurse. On 5/20/22 at approximately 5:15 p.m., an interview was conducted with the Director of Nursing (DON). The DON stated someone performed fingernail care to all residents who required it last night and that morning. The DON was unsure why the resident's fingernails were allowed to become so long and dangerous with the chipped and jagged edges. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced. 4. The facility staff failed to ensure Resident #69 received his weekly showers. Resident #69 was admitted to the facility on [DATE] with diagnoses of inter-cranial Injury with loss of consciousness, anxiety, depression, and Traumatic Brain Injury. A Quarterly Minimum Data Set, dated [DATE] assessed this resident as having a Brief Interview Mental Status (BIMS) score of 15. A Care Plan dated 05/12/21 indicated: ADL self-care performance deficit r/t hx of TBI, anxiety, osteoarthritis, pain. - The resident will maintain current level of function through the review date. Bathing/Showering: Avoid scrubbing & pat dry sensitive skin. During an interview at 3:00 p.m. on 5/21/22 this resident stated, he was not provided his shower of Wednesday night May 20, 2022. Resident #69 stated, staff informed him they did not have time to give him a shower. He stated he was to receive showers on Wednesday's and Saturday's. During an interview on 5/21/22 at 3:30 p.m. with the Administrator and Director of Nursing (DON) they stated, Resident #69 would certainly receive his shower tonight.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0687 (Tag F0687)

Could have caused harm · This affected 1 resident

Based on clinical record review, staff interviews and facility documentation, the facility staff failed to provide necessary toenail care for 1 of 55 residents (Resident #13, a totally dependent resid...

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Based on clinical record review, staff interviews and facility documentation, the facility staff failed to provide necessary toenail care for 1 of 55 residents (Resident #13, a totally dependent resident for activities of daily living), in the survey sample. The findings include: Resident #13 was originally admitted to the facility 2/20/2014, was discharged to an acute care hospital 11/17/21 and returned 11/19/21. The current diagnoses; traumatic brain injury (TBI) and a seizure disorder. The quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 2/13/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 13 out of a possible 15. This indicated Resident #13's cognitive abilities for daily decision making were intact. In section G (Physical functioning) the resident was coded as requiring total care of one person with personal hygiene and bathing. On 5/18/22 at approximately 12:50 p.m., Resident #13 was observed in bed. His hair was long and stringy and his toe nails were approximately 2.5 inches beyond the tip of his toes and the nails were chipped and with jagged edges. The Podiatrist was observed in the facility the day before but Resident #13 didn't receive services from the podiatrist. Another observation was made of Resident #13 on 5/19/22 at approximately 4:10 p.m., the resident's toenails were still long, chipped and with jagged edges. An observation was made of the resident in bed again on 5/20/22 at approximately 10:20 a.m., the toenails were closely cut and well-manicured. Resident #13's person centered care plan dated 12/13/2020 had a problem which read; ADL self-care performance deficit related to TBI, contractures to the right upper extremity and hemiplegia on the left side, dependent on staff for all ADL's. The goal read; Resident will have all ADL needs met on an ongoing daily basis with participation as health permits through next review. One of the interventions read; Check nail length, trim and clean on bath day and as necessary. Report any changes to the nurse. On 5/20/22 at approximately 5:15 p.m., an interview was conducted with the Director of Nursing (DON). The DON stated someone performed toenail care to all residents who required it last night and that morning. The DON was unsure why the resident's toenails were allowed to become so long with the chipped and jagged edges but she stated staff should monitor during ADL care the status of the resident's toenail and have the resident's name added to the Podiatrist list for services. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0688 (Tag F0688)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interviews, and clinical record review, the facility staff failed to ensure a resident didn't experi...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interviews, and clinical record review, the facility staff failed to ensure a resident didn't experience a reduction in range of motion of bilateral knees and failed to provide necessary services to prevent further decrease in range of motion for 1 of 55 residents (Resident #190), in the survey sample. The findings included: Resident #190 was originally admitted to the facility 2/23/2017 and readmitted [DATE] after an acute care hospital stay. The current diagnoses included; Alzheimer's dementia, diabetes and a left jaw swelling. The significant change Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 4/7/22 coded the resident as not having the ability to complete the Brief Interview for Mental Status (BIMS). The staff interview was coded for long and short term memory problems and severely impaired daily decision making abilities. In section G (Physical functioning) the resident was coded as requiring total care of one person with bed mobility, transfers, dressing, eating, toileting, personal hygiene and bathing. On 5/10/22, at approximately 2:25 p.m., Resident #190 was identified residing on a secured unit. He was lying in bed in a fetal position, utilizing oxygen by use of a nasal cannula and didn't respond when spoken to. On 5/10/22 at approximately 3:30 p.m., an interview was conducted with Licensed Practical Nurse (LPN) #11. LPN #11 stated Resident #190 was very active including wandering three months ago but he experienced a the decline after several falls. On 5/11/22 at approximately 10:55 a.m., an interview was conducted with Certified Nursing Assistant (CNA) #6. CNA #6 stated she had worked the resident frequently and the resident suddenly declined from walking to no longer walk and now the ability of his knees to straighten out. CNA #6 stated the CNA staff began to place a pillow beneath his knees to help decrease further contractures of his knees. CNA #6 stated if the resident's knees are manipulated even slightly the resident cries out and attempts to push staff away. Multiple observations were made of Resident #190 throughout the survey and at each observation the resident's knees remained fixed, unable to straighten out. A nurse's note revealed Resident #190 had a fall on 2/13/22 but continued to walk unassisted the same day. The clinical record also revealed on 2/22/22, the resident presented with a change in condition and by 4/7/2022 according to the MDS assessment the resident was requiring total care with all activities of daily living. An interview was conducted on 5/13/22 at approximately 10:45 a.m., with the Physical Therapist Assistant (PTA). The PTA stated the resident had been on caseload but he developed a pressure are to the left heel which prevented further attempts at weight bearing and the resident experienced problems with a low blood pressure. On 5/13/22 at approximately 11:40 a.m., an interview was conducted with the Director of Nursing regarding Resident #190's contractures and management, she stated she would have rehabilitation services screen the resident to determine the most appropriate approaches related the the resident's bilateral knee contractures. A physical therapy progress note dated 5/15/22 was reviewed and it read; Resident #190 was reassessed by the Physical Therapist and determined not to be a candidate for PT services secondary to pain. The resident's pain level was determined based upon behaviors exhibited by the resident screaming, pulling away with attempt to touch his bilateral lower extremities, therefore not allowing PT to touch or assess his motion. Some of the recommendation included for the resident to be out of bed daily and in the vertical position, also nursing to position the patient appropriately in bed to assure joint positioning and to protect the compromise areas to bilateral heels and greater trochanters. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0692 (Tag F0692)

Could have caused harm · This affected 1 resident

The facility staff failed to assure dietary recommendations made by the Registered Dietitian (RD) were implemented for 1 out of 55 resident (Resident #291) in the survey sample. The findings included...

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The facility staff failed to assure dietary recommendations made by the Registered Dietitian (RD) were implemented for 1 out of 55 resident (Resident #291) in the survey sample. The findings included: Resident #291's admission Assessment (14-day) with an ARD of 03/19/22 coded Resident #291 Brief Interview for Mental Status (BIMS) scored a 99 indicating short and long term memory problems and with severe cognitive impairment - never/rarely made decisions. Resident #291 was coded total dependence of two with toilet use, bed mobility and bathing, total dependence of one with dressing, personal hygiene and eating and for Activities of Daily Living (ADL). Resident #291 was coded as having no mood, rejection of care or behavioral problems. Resident #291's admission Assessment (14-day) with an ARD of 03/19/22 under section (K) Swallowing/Nutritional Status coded the resident for loss of liquids from mouth when eating or drinking while holding food in mouth/cheeks or residual food in mouth after meals. Resident #291 weight at 132 pounds. The MDS was not coded for weight loss. Resident #291's person-centered care plan created on 03/26/22 identified the resident had potential for nutritional problem related to use of mechanically altered diet and poor intake. The goal set for the resident by the staff was that the resident will maintain adequate nutritional status as evidenced by maintaining weight through review date. Some of the interventions/approaches the staff would use to accomplish this goal is provide and serve supplements as ordered, Registered Dietitian (RD) to evaluate and make diet change recommendations as needed, weights as per order and monitor/document/report any signs/symptoms of dysphagia (difficulty or discomfort in swallowing), pocketing, choking, coughing, drooling, holding food in mouth, several attempts at swallowing, refusing to eat and appears to have concern during meals. A Dietary/Nutrition note dated 03/18/22 at 9:56 a.m., revealed Resident #291's current weight at 131.6 pounds. The resident's oral intake is poor (1-25 percent) of most meals and is on a regular/puree diet with honey thick liquids. Resident #291's current oral intake of meals are poor and is not adequate for meeting her nutritional needs for weight maintenance. The follow recommendations were made for fortified foods with meals due to poor oral intake of meals, provide texture-appropriate calorie-dense snacks three times a day between meals due to poor oral intake and thickened house shake (120 mL), pudding / fortified pudding and weekly weights x 1 month due to new admit. A Dietary/Nutrition note dated 04/08/22 at 12:33 p.m., revealed Resident #291's current weight now at 117.2 pounds; previous weight at 134.6 (admission weight) a significant weight loss of 17.4 % since admission. The weight loss is not intentional or desirable. The resident continues on a regular/puree diet with nectar thick liquids with oral intake varies from 26-75 percent of meals. Resident #291's clinical record does not reveal the nutritional recommendations made on 03/18/22 were ever addressed with dietary or nursing. An interview was conducted with the RD on 05/17/22 at approximately 4:41 p.m., who stated, The nutrition recommendation made for Resident #291 on 03/18/22 were never addressed with nursing or the dietary department. The extra calories would have provided Resident #291 the extra nutrition would have given the extra calories and protein needed due to her poor oral intake. Review of Resident #291's Medication Administration Record (MAR) and Treatment Administration Record (TAR) for March and April 2022 did not reveal the dietary recommendations made by the RD for fortified foods with meals, texture-appropriate calorie-dense snacks three times a day between meals and thickened house shake (120 mL), pudding / fortified pudding. An interview was conducted with Certified Nursing Assistant (CNA) #2 on 05/19/22 at approximately 11:57 a.m. The CNA said Resident #291 was never a good eater. She stated, I've never given Resident #291 any type of shakes or supplements nor did they come down on her meal tray. An interview conducted with License Practical Nurse (LPN) #9 on 05/16/22 at approximately 10:44 a.m., who said Resident #291 was a poor eater. She said the resident was fed by staff but would only take a few bits then a couple sips of water then will lock her mouth. The nurse reviewed Resident #291's orders in the computer, then stated, I did not see where the dietitian recommendations were ever put in the system as orders for supplements or snacks between meals. I have never given Resident #291 nutritional shakes but has offered extra fluids. On 05/18/22 at approximately 5:16 p.m., an interview was conducted with the Director of Nursing (DON), who stated I could not locate in Resident #291's clinical record indicating the physician was ever informed of the dietitian recommendations made on 03/18/22 and again on 04/08/22 for extra nutritional calories and protein needed due to her poor oral intake. A debriefing was held with the Administrator, Director of Nursing and Corporate support on 05/19/22 at approximately 2:00 p.m. Resident #291's issues was presented again. No additional information was forthcoming. The facility's policy titled Weight Monitoring revised on 10/01/21. Policy: Based on the resident's comprehensive assessment, the facility will ensure that all residents maintain acceptable parameters of nutritional status, such as usual body weight or desirable body weight range and electrolyte balance, unless the resident ' s clinical condition demonstrates that this is not possible or resident preferences indicate otherwise. Compliance Guidelines 4. Interventions will be identified, implemented, monitored and modified (as appropriate), consistent with the resident ' s assessed needs, choices, preferences, goals and current professional standards to maintain acceptable parameters of nutritional status. 6. Though a significant weight change may not occur, the resident may be identified as below ideal body weight by the Registered Dietitian or designee. 7. Documentation: The Registered Dietitian or Dietary Manager should be consulted to assist with interventions; actions are recorded in the nutrition progress notes.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Respiratory Care (Tag F0695)

Could have caused harm · This affected 1 resident

Based on observation, staff interviews, clinical record review and facility documentation review, the facility staff failed to provide 1 of 55 residents (Resident #288) in the survey sample with respi...

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Based on observation, staff interviews, clinical record review and facility documentation review, the facility staff failed to provide 1 of 55 residents (Resident #288) in the survey sample with respiratory care in accordance with professional standards of practice. The findings included: The facility staff failed to ensure Resident #288's had an oxygen order prior to administering oxygen. Resident #288 was originally admitted to the nursing facility on 09/19/19. Resident #288's diagnosis included but not limited to acute respiratory failure with hypoxia. Resident #288's Minimum Data Set (an assessment protocol) a quarterly assessment with an Assessment Reference Date (ARD) of 03/14/22 coded the resident's Brief Interview for Mental Status (BIMS) score 12 of a possible 15 with moderate impairment for daily decision-making. In section G (Physical functioning) the MDS coded Resident #288 requiring total dependence of two with transfer, total dependent of one with dressing, toilet use, personal hygiene and bathing, extensive assistance of one with bed mobility and supervision with eating for Activities of Daily Living (ADL) care. In section O (Special Treatment and Programs) was not coded for oxygen therapy. Resident #288's person-centered care plan with a revision date 03/28/22 identified the resident with shortness of breath related to Obstructive Sleep Apnea and need head of bed elevated to prevent shortness of breath while lying flat. The goal set for the resident by the staff was that the resident will have no complications related to SOB though the review date. Some of the interventions/approaches the staff would use to accomplish this goal is observe/document breathing patterns, report abnormalities to physician, pace and schedule activities providing adequate rest periods. During the initial on 05/10/22 at approximately 4:10 p.m., Resident #288 was observed lying in bed with oxygen on at 4 liters minute via nasal cannula. On 05/11/22 at approximately 9:30 a.m., and again at 2:43 p.m., Resident #288 was observed lying in bed with oxygen on at 4 liters minute via nasal cannula. Review of the Order Summary Report on 04/11/22 did not include an order for the use of oxygen therapy. On 05/12/22 at approximately 10:40 a.m., Resident #288 was observed lying in bed with oxygen at 4 liters via nasal cannula. On the same day at approximately 11:23 a.m., License Practical Nurse (LPN) #1 and surveyor went to Resident #288's room to check the oxygen setting. After checking Resident #288's oxygen setting, the nurse replied, That's not right, Resident #288 should be on oxygen at 2 liters, not 4 liters, let me contact his order and I'll get back with you. On the same day at approximately 1:51 p.m., Resident #288 remains on oxygen at 4 liters. On 05/13/22 at approximately 10:00 a.m., Resident #288 observed lying in bed without the use of oxygen. An interview was conducted with LPN #1 on 05/13/22 at 10:50 a.m., who stated, Resident #288 did not have an order for oxygen therapy. An interview was conducted with the Director of Nursing (DON) on 05/16/22 at approximately 2:17 p.m., who stated, The nursing staff should have never applied oxygen to Resident #288 without an order. A debriefing was held with the Administrator, Director of Nursing and Corporate support on 05/19/22 at approximately 2:00 p.m., who were informed of the above findings; no further information was provided prior to exit. The facility's policy titled Oxygen Administration - revision date 10/01/21. Policy: Oxygen is administered to residents who need it, consistent with professional standards of practice, the comprehensive person-centered care plans, and the residents' goals and preferences. Policy Explanation and Compliance Guidelines: 1. Oxygen is administered under orders of a physician, except in the case of an emergency. In such case, oxygen is administered and orders for oxygen are obtained as soon as practicable when the situation is under control. 2. Personnel authorized to initiate oxygen therapy include physicians, RNs, LPNs, and respiratory therapists. 3. Staff shall document the initial and ongoing assessment of the resident's condition warranting oxygen and the response to oxygen therapy.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Pharmacy Services (Tag F0755)

Could have caused harm · This affected 1 resident

2. The facility staff failed to ensure one license nurse had a second license nurse witness the disposal of a controlled substance (Lyrica). Resident #14 was admitted to the nursing facility on 06/27/...

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2. The facility staff failed to ensure one license nurse had a second license nurse witness the disposal of a controlled substance (Lyrica). Resident #14 was admitted to the nursing facility on 06/27/18. Diagnosis for Resident #14 included but are not limited to Polyneuropathy and pain. Resident #14's Minimum Data Set (MDS) a quarterly assessment with an Assessment Reference Date (ARD) of 02/13/22 coded the Brief Interview for Mental Status (BIMS) score a 15 out of a possible 15 indicating no cognitive impairment. Review of Resident #14's Physician Order Summary revealed the following order: Lyrica 100 mg - give 1 capsule by mouth two times a day for pain. On 05/11/22 at approximately 10:05 a.m., during the medication pass and pour observation, License Practical Nurse (LPN) #2 pulled medication for Resident #14 to include a controlled medication (Lyrica). The LPN went to administer Resident #14 his medication which he refused. The LPN returned to the medication and stated, Resident #14 refused his medication. The LPN said, I did not pull a narcotic and dumped the pulled medication in the sharp container attached to the medication cart. When asked if the medication disposed was a controlled narcotic (Lyrica), she replied, Oh, I did pull his Lyrica. The LPN stated, I guess another nurse should have wasted the Lyrica with me since it was a narcotic. An interview was conducted with the Director of Nursing (DON) on 05/16/22 at approximately 3:24 p.m. The DON stated, When Resident #14 refused his Lyrica, a controlled medication, LPN #2 should have wasted the Lyrica with another nurse. A debriefing was held with the Administrator, Director of Nursing and Corporate support on 05/19/22 at approximately 2:00 p.m., who were informed of the above findings; no further information was provided prior to exit. The facility's policy titled Controlled Substance Administration & Accountability, revised on 10/01/21. Policy: It is the policy of this facility to promote safe, high quality patient care, compliant with state and federal regulations regarding monitoring the use of controlled substances. The facility will have safeguards in place in order to prevent loss, diversion or accidental exposure. Policy Explanation and Compliance Guidelines: 5. (D) Obtaining/Removing/Destroying Medications: Two licensed staff must witness any disposal or destruction of a controlled substance and document same on the Drug Disposition Record, Controlled Drug Record, or via the automated dispensing system. Definitions: -Lyrica is used to relieve neuropathic pain (pain from damaged nerves) that can occur in your arms, hands, fingers, legs, feet, or toes (https://medlineplus.gov//druginfo/meds). Based on observations, staff interview, and clinical record reviews, the facility staff failed to have a pharmaceutical system which assured timely receiving and accurate dispensing and destruction of medications for 2 of 55 residents (Resident #13 and 14), in the survey sample. The findings included: 1. The facility staff failed to procure the anticonvulsive medication, Vimpat timely to prevent Resident #13 from missing dosages. and to ensure the medication is administered as ordered by the Practitioner. Resident #13 was originally admitted to the facility 2/20/2014, was discharged to an acute care hospital 11/17/21 and returned 11/19/21. The current diagnoses; traumatic brain injury (TBI) and a seizure disorder. The quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 2/13/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 13 out of a possible 15. This indicated Resident #13's cognitive abilities for daily decision making were intact. In section I (Active Diagnosis) the resident was coded at I5400 for a seizure disorder or epilepsy. The Physician's order summary revealed an order dated 11/19/2021 for Vimpat Tablet 200 milligrams, Give 1 tablet by two times a day for seizures. On 5/18/22 at approximately 11:15 a.m., a review of controlled medications was conducted for Resident #13. There was no Vimpat in the medication cart for Resident #13 and the Medication Administration Record revealed the last dose was administered on 5/17/22 at 8:00 p.m. Based on review of the MAR the resident didn't receive any doses of Vimpat on 5/18/22 and the medication wasn't available for the 8:00 a.m. dose on 5/19/22. An interview was conducted with Licensed Practical Nurse (LPN) #4 on 5/18/22 at 3:00 p.m. LPN #4 stated Vimpat wasn't a medication in the Cube-X system (the facility's in-house STAT medication system) and at 3:00 p.m., the Vimpat still wasn't available to be administered to Resident #13. LPN #4 stated the process for obtaining prescriptions is a little different when it is for a controlled medication because often a new prescription is necessary as it was in Resident #13 case. LPN #4 stated when the resident is down to a five day dose a refill is obtained by notifying the pharmacy and if a prescription is necessary they print the prescription and place it in the physician's book to obtain a signature. LPN #4 stated once the physician signs the prescription it is faxed to the pharmacy and a delivery is made before the on-hand stock is completed. A nurse's note dated 5/19/22 at 7:24 a.m., upon arrival it was noted that the resident's Vimpat had not arrived from pharmacy after the prescription was faxed to the pharmacy yesterday. The pharmacy was phone and the staff spoke with (name of the pharmacist) and asked when it would arrive and he stated it would be on the run tonight. The staff then asked if it could be transferred to the back-up pharmacy and the pharmacist stated that the pharmacy was experiencing a system wide error and he was unable to send to the prescription to the back-up pharmacist due to it being filled in his system and he is unable to mark it as returned. The pharmacist stated he would call the facility if the system came up prior to the truck arriving to deliver the medication. Resident #13's person centered care plan dated 12/13/2020 had a problem which read; the resident has a seizure disorder related to epilepsy. The goal read; the resident will remain free from injury related to seizure activity through review date. One of the interventions read give seizure medication as ordered by doctor. Observe/document side effects and effectiveness. On 5/20/22 at approximately 5:15 p.m., an interview was conducted with the Director of Nursing (DON). The DON stated the Nurse Practitioner stated she signed the needed prescription during her visit on 5/16/22 and put the prescription back in the physician's book for the nursing staff to fax to the pharmacy but the prescriptions weren't accounted for and the medications didn't arrive to the facility; therefore Resident #13 didn't have Vimpat on hand to be administered. The DON stated they completed an audit of controlled medications and had prescriptions written and faxed to the pharmacy and afterwards she located the prescriptions signed by the NP on 5/16/22, they were deposited in a location for destruction after they are faxed to the pharmacy, which was something she wasn't aware the staff did. The DON also stated Resident #13's Vimpat was delivered on 5/19/22 from the back-up pharmacy and he received the ordered doses. The DON stated going forward they will develop another system for obtaining controlled substances to ensure there are no further delays with obtaining the medications. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Drug Regimen Review (Tag F0756)

Could have caused harm · This affected 1 resident

Based on clinical record review, staff interviews, and review of facility documents, the facility staff failed to assure the Licensed Pharmacist recommendation were reviewed and responded to by the Ph...

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Based on clinical record review, staff interviews, and review of facility documents, the facility staff failed to assure the Licensed Pharmacist recommendation were reviewed and responded to by the Physician and/or Practitioner for 1 of 55 residents (Resident #37), in the survey sample. The findings included: The facility staff failed to assure Resident #37's gradual dose reduction recommendation offered by the licensed pharmacist were acted upon by the Physician and/or Practitioner. Resident #37 was originally admitted to the facility 5/14/2021 resident had never been discharged from the facility. The current diagnoses included; dementia and Schizophrenia. The quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 3/9/22 coded the resident as not having the ability to complete the Brief Interview for Mental Status (BIMS). The staff interview was coded for long and short term memory problems as well as severely impaired for daily decision making. A review of the Physician's Order Summary (POS) revealed an order dated 7/22/21 for Fluvoxamine Maleate ER Capsule Extended Release 24 hour, Give 150 mg by mouth one time a day for sexual disinhibition related to other sexual disorder. The resident had a care plan problem with a revision date of 7/16/21 which read; The resident has a behavior problem related a history of wandering, history of refusing medications, ADL care, vital signs, and meals related to Schizophrenia. The resident also hit a staff member, and has a history of going into male resident's room. The goal read; the resident will have fewer episodes of refusal by the next review date. The interventions included; administer medications as ordered. Monitor/document for side effects and effectiveness. Intervene as necessary to protect the rights and safety of others. Approach/Speak in a calm manner. Divert attention. Remove from situation and take to alternate location as needed. A review of the Monthly Medication Reviews (MMR) for 12 months revealed on 1/20/22 a licensed pharmacist recommended to reduce the medication Fluvoxamine Maleate from 150 mg each day to 100 mg each day and if the drug therapy needs to remain as ordered to document that in the medical record. On 5/20/22, there still was no indication the physician reviewed the recommendation, and to document in the resident's medical record if a change will be taken or why no change will take place. On 5/20/22 at approximately 5:15 p.m., an interview was conducted with the Director of Nursing (DON). The DON stated someone she was unable to show evidence the recommendation for reduction of Resident #37's medication Fluvoxamine Maleate had been addressed by the Physician and/or Practitioner but as she transition into the DON role a plan would be instituted to prevent this from occurring again. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected 1 resident

Based on the medication pass and pour observations, clinical record review, staff interviews and resident interview, the facility staff failed to ensure they were free of medication errors rates of fi...

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Based on the medication pass and pour observations, clinical record review, staff interviews and resident interview, the facility staff failed to ensure they were free of medication errors rates of five percent (%) or greater. During the medication passes totaling 25 observed opportunities for errors, two medication errors were made which resulted in a medication rate of 8%. The residents involved in the medications errors were Resident #55 and #28. The findings include: 1. Resident #55 was originally admitted to the facility 5/29/21 and had never been discharged from the facility. The current diagnoses included; dry eye syndrome. The annual Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 4/6/2022, coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #55's cognitive abilities for daily decision making were intact. On 5/10/22 at 4:48 p.m., Licensed Practical Nurse (LPN) #4 pulled one oral medication and looked through the medication cart for Resident #55's Artificial Tears Solution to administer. LPN #4 was unable to locate the medication as written on the order summary therefore the artificial tears solution wasn't administered. LPN #4 stated she would order the artificial Tears solution. Resident #55 had a physician order dated 2/7/22 for Artificial Tears Solution 0.2-0.2-1 % (Glycerin-Hypromellose-PEG 400), instill 1 drop in right eye four times a day for dry eyes. An interview was conducted with Resident #55 on 5/10/22 at 4:55 p.m., the resident stated often he doesn't receive the artificial tears and it is helpful for his dry eyes. An interview was conducted with LPN #4 on 5/11/22 at approximately 11:05 a.m. regarding Resident #55's artificial tears. LPN #4 opened the top drawer of the medication cart and stated this is the standard artificial tears medication utilized for all residents. The packaging read; Glycerin 0.2% Hypromellose 0.2% Polyethylene Glycol 400 1%. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced. 2. Resident #28 was originally admitted to the facility 8/31/2021 had never been discharged from the facility. The current diagnoses included; legal blindness and itchy eyes. The most recent Minimum Data Set (MDS) was a quarterly dated 3/3/2022 and coded the resident with a 15 out of a possible score of 15 on the Brief Interview for Mental Status (BIMS) indicating no cognitive impairment. On 5/10/22 at 6:10 p.m., Licensed Practical Nurse (LPN) #4 pulled one oral medication and looked through the medication cart for Resident #28's Refresh Liquigel Gel to administer. LPN #4 was unable to locate the medication as written on the order summary therefore the Refresh Liquigel Gel wasn't administered. LPN #4 stated she would order the Refresh Liquigel Gel. Resident #28 had a physician's orders dated 9/1/21 for Refresh Liquigel Gel 1 % (Carboxymethylcellulose Sodium), Instill 2 drop in both eyes four times a day for Itching and discharge from the eyes. An interview was conducted with Resident #28 on 5/10/22 at 6:20 p.m., the resident had no comments regarding not receiving the Refresh Liquigel drops to his eyes. An interview was conducted with LPN #4 on 5/11/22 at approximately 11:05 a.m. regarding Resident #28's artificial tears. LPN #4 opened the top drawer of the medication cart and stated this is the standard artificial tears medication utilized for all residents. The packaging read; Glycerin 0.2% Hypromellose 0.2% Polyethylene Glycol 400 1%. On 5/20/22 at approximately 5:15 p.m., an interview was conducted with the Director of Nursing (DON). The DON stated LPN #4 was correct about their standard for over the counter eye drops and the Practitioners were notified of the practice and orders were rewritten accordingly. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced. The active ingredients in over the counter eye drops are Glycerin 0.2% Hypromellose 0.2% Polyethylene Glycol 400 1%. They are lubricants for use as a protectant against further irritation or to relieve dryness of the eye - for the temporary relief of discomfort due to minor irritations of the eye, or to exposure to wind or sun. (https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4c62432b-bd6d-46ac-a5fb-8dadfda04846)
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0760 (Tag F0760)

Could have caused harm · This affected 1 resident

Based on staff interviews, and clinical record review, the facility staff failed to assure a resident was free of significant medication errors for 1 of 55 resident (Resident #13), in the survey sampl...

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Based on staff interviews, and clinical record review, the facility staff failed to assure a resident was free of significant medication errors for 1 of 55 resident (Resident #13), in the survey sample. The findings included: Resident #13 was originally admitted to the facility 2/20/14, was discharged to an acute care hospital 11/17/21 and returned 11/19/21. The current diagnoses; traumatic brain injury (TBI) and a seizure disorder. The quarterly Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 2/13/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 13 out of a possible 15. This indicated Resident #13's cognitive abilities for daily decision making were intact. In section I (Active Diagnosis) the resident was coded at I5400 for a seizure disorder or epilepsy. The Physician's Order Summary (POS) revealed an order dated 11/19/2021 for Vimpat Tablet 200 milligrams, Give 1 tablet by two times a day for seizures. On 5/18/22 at approximately 11:15 a.m., a review of controlled medications was conducted for Resident #13. There was no Vimpat in the medication cart for Resident #13 and the Medication Administration Record revealed the last dose was administered on 5/17/22 at 8:00 p.m. Based on review of the MAR the resident didn't receive any doses of Vimpat on 5/18/22 and the medication wasn't available for the 8:00 a.m. dose on 5/19/22. A review of the narcotic control count record also revealed the Vimpat wasn't signed out and administer to Resident #13 two times each day on 5/7/22, 5/8/22, 5/13/22, 5/16/22. An interview was conducted with Licensed Practical Nurse (LPN) #4 on 5/18/22 at 3:00 p.m. LPN #4 stated Vimpat wasn't a medication in the Cube-X system (the facility's in-house STAT medication system) and at 3:00 p.m., the Vimpat still wasn't available to be administered to Resident #13. LPN #4 stated the process for obtaining prescriptions is a little different when it is for a controlled medication because often a new prescription is necessary as it was in Resident #13 case. LPN #4 stated when the resident is down to a five day dose a refill is obtained by notifying the pharmacy and if a prescription is necessary they print the prescription and place it in the physician's book to obtain a signature. LPN #4 stated once the physician signs the prescription it is faxed to the pharmacy and a delivery is made before the on-hand stock is completed. A nurse's note dated 5/19/22 at 7:24 a.m., upon arrival it was noted that the resident's Vimpat had not arrived from pharmacy after the prescription was faxed to the pharmacy yesterday. The pharmacy was phone and the staff spoke with (name of the pharmacist) and asked when it would arrive and he stated it would be on the run tonight. The staff then asked if it could be transferred to the back-up pharmacy and the pharmacist stated that the pharmacy was experiencing a system wide error and he was unable to send to the prescription to the back-up pharmacist due to it being filled in his system and he is unable to mark it as returned. The pharmacist stated he would call the facility if the system came up prior to the truck arriving to deliver the medication. Resident #13's person centered care plan dated 12/13/20 had a problem which read; the resident has a seizure disorder related to epilepsy. The goal read; the resident will remain free from injury related to seizure activity through review date. One of the interventions read give seizure medication as ordered by doctor. Observe/document side effects and effectiveness. On 5/20/22 at approximately 5:15 p.m., an interview was conducted with the Director of Nursing (DON). The DON stated the Nurse Practitioner stated she signed the needed prescription during her visit on 5/16/22 and put the prescription back in the physician's book for the nursing staff to fax to the pharmacy but the prescriptions weren't accounted for and the medications didn't arrive to the facility; therefore Resident #13 didn't have Vimpat on hand to be administered. The DON stated they completed an audit of controlled medications and had prescriptions written and faxed to the pharmacy and afterwards she located the prescriptions signed by the NP on 5/16/22, they were deposited in a location for destruction after they are faxed to the pharmacy, which was something she wasn't aware the staff did. The DON also stated Resident #13's Vimpat was delivered on 5/19/22 from the back-up pharmacy and he received the ordered doses. The DON stated going forward they will develop another system for obtaining controlled substances to ensure there are no further delays with obtaining the medications. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced. VIMPAT is a prescription medicine used to treat partial-onset seizures in people 1 month of age and older with other medicines to treat primary generalized tonic-clonic seizures in people 4 years of age and older. Do not stop taking VIMPAT without first talking to your healthcare provider. Stopping VIMPAT suddenly can cause serious problems. Stopping seizure medicine suddenly in a patient who has epilepsy can cause seizures that will not stop (status epilepticus). VIMPAT is a federally controlled substance (CV) because it can be abused or lead to drug dependence. Keep your VIMPAT in a safe place, to protect it from theft. Never give your VIMPAT to anyone else, because it may harm them. Selling or giving away this medicine is against the law. (https://www.vimpat.com/)
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Medical Records (Tag F0842)

Could have caused harm · This affected 1 resident

Based on staff interview, clinical record review and a review of facility documents the facility's staff failed to ensure accurate documentation in one of 55 resident (Resident #66), clinical records....

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Based on staff interview, clinical record review and a review of facility documents the facility's staff failed to ensure accurate documentation in one of 55 resident (Resident #66), clinical records. The findings included: Resident #66 was originally admitted to the facility 10/16/15 from an acute care facility and discharged on 4/11/22 to an acute care facility and returned to the Long Term Care Facility on 4/13/22. The current diagnoses included; Pneumonia and COPD (Chronic Obstructive Pulmonary Disease). The Significant change Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 04/18/2022 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #66 cognitive abilities for daily decision making were intact. In sectionG(Physical functioning) the resident was coded as requiring extensive assistance of one person with bed mobility and dressing. Requiring total dependence of one person with toilet use, personal hygiene and bathing. Requires set-up help only with eating. The care plan dated 4/17/22 reads: Focus: The resident has pain r/t (related/ to) history of pain in left arm and side secondary to CVA (Cerebral Vascular Accident) & polyneuropathy, dental pain. Goals: The resident will not have an interruption in normal activities due to pain through the review date. Interventions: Administer analgesia as per orders. Review of the MAR (Medication Administration Record) reads: Gabapentin Capsule 300 MG Give 1 capsule by mouth one time a day related to Polyneuropathy, unspecified (G62.9) -Start Date 04/13/2022 2100 (9:00 PM). Missed dosages: 4/14/22-4/18/22 4/21/22-4/24/22 and 4/27/22-4/28/22. An interview was conducted on 5/20/22 at 4:40 PM., with the DON (Director of Nursing) concerning the above narcotic medication. She stated, During my audit I noticed night time medications on the same exact days as you, aren't being checked off. Residents confirmed they are getting medications on routine at night. Moving forward, I will do an in service on documentation. An interview was conducted with Resident #66 on 5/20/22 at 4:50 PM concerning his missed medications. He stated, As far as I know I'm getting my medications. An interview was conducted with LPN (Licensed Practical Nurse) #8 at 5:00 PM., concerning missed medication dosages for the above residents. She stated, I forgot to go back and switch the schedule to the right side (Unit). I usually work on the left side (Unit). I sign my meds (medications) out at the end of giving meds out. The DON talked to me two weeks ago about this. I will sign out my pills as I finish with each resident. On 05/20/22 at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. The DON stated, Medications should be administered and documented immediately afterward. Gabapentin is sometimes used to relieve the pain of diabetic neuropathy (numbness or tingling) due to nerve damage in people who have diabetes (https://medlineplus.gov/druginfo/meds/a694007.html).
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0849 (Tag F0849)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident interview, staff interview, clinical record review, and review of facility documents, the facility staff faile...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident interview, staff interview, clinical record review, and review of facility documents, the facility staff failed to assure the Hospice Agency provided the facility staff with the coordinated plan of care to identify which services the Hospice Agency would provide, when the services would be provided, the communication process, and when or why the nursing facility staff should notify the Hospice Agency for 1 of 1 resident receiving Hospice services (Resident #36). The findings included: Resident #36 was originally admitted to the facility on [DATE] and was discharged to the hospital return anticipated on 2/3/2022. The resident's diagnosis included cirrhosis of the liver with ascites and a right inguinal hernia. The significant change Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 3/21/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #36's cognitive abilities for daily decision making were intact. On 5/13/22 at approximately 11:30 a.m., an interview was conducted with Resident #36. The resident stated the physician's explained to him that the cirrhosis of the liver would not get better and Hospice services were recommended. The resident stated because the abdominal surgical wound was infected and with such a large amount of drainage the Hospice nurse was coming out daily to monitor and care for it and two days the hospice nurse also managed the ascites drain. Resident #36 states the hospice services doesn't have a Certified Nursing Assistant (CNA) to visit him, but the Chaplin visits approximately monthly. The Physician's order summary (POS) revealed, an order dated 3/11/22 for (name of the company) Hospice service. Another order dated 3/17/2022 read; drain abdominal ascites fluid via pleurex drain two times per week, up to 2500 cubic centimeters each attempt, to be done by the Hospice Registered Nurse and there was an order dated 4/21/22 which read; lower abdomen clean with wound cleanser, apply collagen and a dry dressing change every three days and as needed. The person centered care plan with a revision date of 3/17/22, only mentioned Hospice as an intervention under the following problem; the resident has potential for potential fluid volume overload as evidenced by ascites and/ right abdominal pain related to cirrhosis of the liver. The goal read; The resident will remain free of signs/symptoms of fluid overload through review date, as evidenced by decrease in or absence of edema, anxiety, agitation, restlessness, confusion, changes in mood or behavior, nausea/vomiting, dyspnea, congestion, orthopnea, easily fatigued, jugular vein distension. One of the interventions read; drain abdominal ascites fluid via pleurex drain two times per week, up to 2500 cc each attempt, to be done by hospice RN. An interview was conducted with Licensed Practical Nurse (LPN) #2 on 5/20/22 at approximately 12:40 p.m. LPN #2 routinely worked with Resident #36 and was stated she working most days when the hospice nurse visited the resident. LPN #2 stated they had a book in which the hospice nurse signs in letting them know she has visited the resident and what services were provided, such as abdominal wound assessment and care. LPN #2 stated she didn't have a schedule of when or if a discipline from the hospice agency would visit, she wasn't aware of what to do if the resident's drain malfunctioned, signs or symptoms to notify the hospice agency of, what to do if the abdominal wound became odorous, was with increased drainage/pain or the resident was with other signs of deterioration. LPN #2 was also unable to review the facility's hospice plan because it wasn't included with the other care plans and the hospice company's care plan wasn't available in the facility. LPN #2 stated if a concern arose she would simple telephone the agency for instructions. On 5/20/22 at approximately 5:15 p.m., an interview was conducted with the Director of Nursing (DON). The DON stated the hospice care plan and official notes were not in the facility when they were requested therefore they had to reach out to the company to have them sent to the facility. The DON stated for continuity of care the care plan and visiting notes should have been readily available to the direct care staff. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0887 (Tag F0887)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review, review of facility documents and during the course of a complaint...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review, review of facility documents and during the course of a complaint investigation, the facility's staff failed to provide and or coordinate services for 1 of 55 residents (Resident #338, a closed record resident) a requested COVID-19 vaccine. The findings included: Resident #338 was originally admitted to the facility on [DATE] after an acute care hospital stay and expired in the facility on [DATE]. The current diagnoses included; COVID19. The quarterly, Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of [DATE] coded the resident as not having the ability to complete the Brief Interview for Mental Status (BIMS). The staff interview was coded for long and short term memory problems as well as severely impaired for daily decision making. In sectionG(Physical functioning) the resident was coded as requiring limited assistance of one person with bed mobility, walking in the room and walking in the corridor. Requiring extensive assistance of one person with transfers, dressing, toilet use and personal hygiene. Requires total dependence with bathing. The Care plan dated [DATE] reads: Focus: Active diagnosis of COVID19. Goals: The resident's care and symptoms will be managed per CDC guidelines and facility protocol. Interventions: Administer meds as ordered for fever, pain, and or symptom management. The clinical record revealed that Resident #338 received her first dose COVID19 vaccine on [DATE] prior to being admitted to the facility. The clinical record revealed that facility staff spoke to RP (Responsible Party) on [DATE] at approximately 12:40 PM concerning the Johnson and Johnson Booster injection for resident. Resident's RP requesting Pfizer booster for resident. The clinical record reveal that Resident #338 tested positive for COVID 19 on [DATE] RP made aware of positive results. The clinical record reveal on [DATE] at approximately 9:16 AM. Resident's 02 saturation of 74% and O2 applied at 4 liters per on call instructions with head of bed elevated and O2 sat up to 85%. NP (Nurse Practitioner) instructed to administer prednisone 20 mg now and call family and update and give them a choice of treating her here at facility or sending to ER (Emergency Room) and after speaking with daughter was updated and she would like for resident to stay at facility until NP arrives in less than an hour for assessment and allow NP to make a decision at that time. NP made aware and will see first thing upon arriving at facility. The clinical record reads: On [DATE] at 12:25 PM., Resident noted unresponsive. The clinical record reads: On [DATE] at 9:25 AM., Resident condition unchanged. Conscious but unresponsive. RP made aware with request to send to ER for further evaluation. The clinical record reads: On [DATE] 3:30 PM. Resident returned via stretcher accompanied by transport personnel. Daughter at bedside. The clinical record reads: On [DATE] 9:27 PM., Patient (Pt.) pronounced (dead) at 8:38 PM, family is at bedside. On [DATE] at approximately 4:00 PM., an interview was conducted with LPN (Licensed Practical Nurse/wound care nurse) #3 concerning Resident #338. She stated, She received the Johnson and Johnson prior to admission on [DATE]. We have to have ten residents for the Johnson and Johnson vaccine, five residents for the Maderna vaccine and five residents for the Pfizer vaccine. I will have to check to see if I ordered the vaccine for Resident #338. On [DATE] at approximately 11:40 AM, the DON (Director of Nursing) was approached concerning Resident #338 COVID19 booster vaccine. She stated, LPN #3, said there was no order for the COVID19 booster for Resident #338. Anyone who got the Johnson & Johnson shot should take advantage of the Centers for Disease Control & Prevention's (CDC's) mix-and-match policy that allows them to choose one of the mRNA vaccines for their booster (https://www.yalemedicine.org/news/[NAME]-and-[NAME]-covid-booster#:~:text=If%20you%20got%20J%26J%20as,your%20primary%20series). 1st Booster: CDC recommends a booster of either Pfizer-BioNTech or Moderna COVID-19 vaccine for: Most people, at least 2 months after the primary dose of J&J/[NAME] COVID-19 vaccine People who are moderately or severely immunocompromised, at least 2 months after the additional dose of Pfizer-BioNTech or Moderna COVID-19 vaccine. 2nd Booster: CDC recommends a 2nd booster of either Pfizer-BioNTech or Moderna COVID-19 vaccine at least 4 months after the 1st booster for: Adults ages 50 years and older People who are moderately or severely immunocompromised (https://www.cdc.gov/coronavirus/2019-ncov/vaccines/booster-shot.html?s_cid=11706:cdc%20covid%20booster:sem.ga:p:RG:GM:gen:PTN:FY22) On [DATE] at approximately 3:45 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant and LPN #3. She was asked by the surveyor if Resident #338 received the COVID19 vaccine booster. She stated, No. An opportunity was offered to the facility's staff to present additional information but no additional information was provided. Complaint deficiency
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0558 (Tag F0558)

Could have caused harm · This affected multiple residents

Based on observation, resident interview, staff interviews, and clinical record review, the facility staff failed to make sleeping accommodations for 1 of 55 residents (Resident #84), in the survey sa...

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Based on observation, resident interview, staff interviews, and clinical record review, the facility staff failed to make sleeping accommodations for 1 of 55 residents (Resident #84), in the survey sample. The findings included: Resident #84 was originally admitted to the facility 4/27/22 and discharged from the facility 5/10/22. The current diagnoses included; sepsis, diabetes, chronic kidney disease, atrial flutter and heart failure, skin tear to the left lower leg/cellulitis. The admission Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 5/2/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 15 out of a possible 15. This indicated Resident #84's cognitive abilities for daily decision making were intact. In section G (Physical functioning) the resident was coded as requiring total care of one person with bathing, extensive assistance of two people with bed mobility and transfers, eating, and bathing, limited assistance of one person with dressing, personal hygiene, and toileting supervision after set-up with eating. The resident's care plan had a problem dated 4/30/22 which read; (name of the resident) has shortness of breath (SOB) related to heart failure and morbid obesity; he prefers the head of his bed to be elevated to prevent SOB. The goal read; the resident will have no complications related to SOB through the next review date, 5/11/22. The interventions included; Position resident with proper body alignment for optimal breathing pattern. On 5/10/22 at approximately 4:50 p.m., Resident #84 was heard anxiously telling the Social Worker (SW) that he was unable to rest at the facility and he felt the lack of sleep was hindering his recovery. After the conversation with Resident #84 an observation was made of the SW leaving the resident's room, stopping at Licensed Practical Nurse (LPN) #7's medication cart and instructing LPN #7 to immediately complete a discharge AMA (against medical advice) for Resident #84. An interview was conducted with Resident #84 on 5/10/22 at approximately 5:10 p.m. The resident stated he had wrestled with staying the additional days or going home and he came to the conclusion he had to go home for he had not rested well since his admission to the facility. The resident also stated that he had slept in a recliner chair at home for many years because of difficulty breathing and trying to sleep in the bed at the facility wasn't meeting his needs. The resident further stated he was provided with a wide bed but the positioning needed to elevate his head and feet was possible and he needed a recliner to meet his needs for sleeping. On 5/20/22 at approximately 11:10 a.m., an interview was conducted with Resident #84's treating Physical Therapist (PT) who stated on 5/15/22, Resident #84 saw a recliner in the rehabilitation gym and thought he would be able to utilize it for sleeping until he was discharged home. The PT stated she knew the chair wasn't large enough for Resident #84's body but she took it to his room as he requested. The PT said as soon as the resident saw the chair up close he realized it wasn't large enough to accommodate him and he ask the PT to take it out of the room. The PT stated as far as she knew the facility had no larger recliners in house and the option to purchase or rents one for the resident wasn't discussed. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided. The information below was obtained from the website on 5/27/22. Sleep easy. If you're having shortness of breath, especially at night, sleep with your head propped up using a pillow or a wedge. If you snore or have had other sleep problems, make sure you get tested for sleep apnea. (https://www.mayoclinic.org/diseases-conditions/heart-failure/diagnosis-treatment/drc-20373148)
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0563 (Tag F0563)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on a complaint investigation, observations and record reviews the facility staff failed to provide reasonable access to th...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on a complaint investigation, observations and record reviews the facility staff failed to provide reasonable access to the facility by an outside entity which provided services to 4 residents (Residents #31, #39, #69 and #77) and failed to have written policies and procedures regarding visitation rights of residents receiving outside services in survey sample of 55 residents. The findings included: Four residents (Resident#31, #39, #69 and #77) received Brain Injury Services from an outside entity. The facility staff failed to provide reasonable access to the facility by an outside entity which provided services for 4 residents and failed to have written policies and procedures regarding visitation rights of residents receiving outside services. Four residents (Resident#31, #39, #69 and #77) received Brain Injury Services. 1. Resident #31 was admitted to the facility on [DATE]. Diagnoses for Resident #31 included: Traumatic Hemorrhage of Cerebrum with loss of consciousness and obsessive compulsive disorder. A Quarterly Minimum Data Set, dated [DATE] assessed this resident as having a Brief Interview for Mental Status (BIMS) score of 13. A Care Plan dated 07/23/21 indicated: Encourage alternative communication with visitors Mask to be worn when out of room as tolerated as per CDC guidelines. Monitor for psychosocial changes. Resident #31 was observed in his room. He stated, he had not been out in a while to his Day Program. 2. Resident #39 was originally admitted to the facility on [DATE] and re-admitted to the facility on [DATE]. Diagnoses for Resident #39 included: Non-traumatic brain dysfunction, Alzheimer's, personality disorder, epilepsy, anemia, depression, abnormality of gait and mobility. A Quarterly Minimum Data Set, dated [DATE] assessed this resident as having a Brief Interview Mental Status (BIMS) score of 10. A Care Plan dated 05/19/21 indicated: Resident is at risk for alteration in Psychosocial well being related to restriction on visitation due to COVID-19. Resident will not experience any adverse effects throughout the review period. Encourage alternative communication with visitors Mask to be worn when out of room as tolerated as per CDC guidelines. Monitor for psychosocial changes. Resident #39 was observed eating breakfast in bed on 05/17/22 at 9:00 a.m. and later during the day at 11:45 a.m. she was noted in her wheelchair visiting the rooms of other residents. 3. Resident #69 was admitted to the facility on [DATE] with diagnoses of Interacranial Injury with loss of consciousness, anxiety, depression, and Traumatic Brain Injury. A Quarterly Minimum Data Set, dated [DATE] assessed this resident as having a Brief Interview Mental Status (BIMS) score of 15. A Care Plan dated 05/12/21 indicated: Resident is at risk for alteration in Psychosocial well being related to restriction on visitation due to COVID-19. Resident will not experience any adverse effects throughout the review period. Encourage alternative communication with visitors Mask to be worn when out of room as tolerated as per CDC guidelines. Monitor for psychosocial changes. During an interview on 05/17/22 at 10:45 a.m. with Resident #69, he stated, he goes out on Tuesdays and Thursday's for Day Program visits. Some days I do not feel like going, so I stay at the facility. 4. Resident #77 was admitted to the facility on [DATE] with diagnoses of Bipolar disorder, depression, and Traumatic Brain Injury. A 4/20/22 Significant Change MDS coded this resident in the area of BIMS as a score of (12). Care Plan dated: 05/06/21 Resident #77 is at risk for alteration in Psychosocial well being related to restriction on visitation due to COVID-19. Resident is t risk for infection r/t hx of COVID-19 co-morbidities and nursing home placement Resident will not experience any adverse effects throughout the review period. Resident will remain free from infection through next review period. Activities as per policy and CDC guidelines. Encourage alternative communication with visitors Monitor for psychosocial changes. Observe and report any changes in mental status caused by situational stressor. Provide opportunities for expression of feelings related to situational stressor. Resident #77 was observed on 5/19/22 at 3:15 p.m. in bed asleep. During an interview on 05/18/22 at 11:15 a.m. with the Infection Control Nurse she stated, The facility was only allowing a visitor to visit one person only A sign presented by the Infection Control Nurse on 05/18/22 indicated: NO one with a fever or symptoms of COVID-19, or known exposure to a COVID-19 case in the prior 14 days, is permitted in the establishment. The sign was presented in several languages. The sign did not have a date on it. A sign presented by the Infection Control Nurse on 5/18/22 indicated: No visitors in building at this time - If you would like to make an appointment to factime with your family member contact: Activities Director for appointment. Window visits are permitted. The sign did not have a date on it. During an interview on 5/18/22 at 11:45 a.m. with the Administrator she stated, the facility did not have policies and procedures for outside entity visitation. Complaint deficiency-Conclusion: Substantiated with a deficiency
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0578 (Tag F0578)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews, clinical record reviews and facility documentation review, the facility staff failed to ensure 3 out ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews, clinical record reviews and facility documentation review, the facility staff failed to ensure 3 out of 55 residents (Resident #74, 85, 30) were given the opportunity to formulate an advance directive and 1 out of 55 residents (Resident #79) in the survey sample have collaborating documentation of code status throughout the clinical record. The findings included: 1. The facility staff failed to ensure Resident #74 and or their Representative was given the opportunity to formulate an Advance Directive. Resident #74 was admitted to the nursing facility on 04/15/22. Diagnosis for Resident #74 included but not limited to cancer of the larynx (voice box). The current Minimum Data Set (MDS) an admission assessment with an Assessment Reference Date (ARD) of 04/20/22 coded the resident with a 10 of a total possible score of 15 on the Brief Interview for Mental Status (BIMS), indicating moderate cognitive impairment. Resident #74's person-centered care plan with a created date of 04/19/22 identified Resident Advance Directive is a Full Code. The goal set for the resident by the staff was that the resident's advance directive will be followed through the next review period of 10/19/22. The interventions/approaches the staff would use to accomplish this goal is to allow Resident#74 to discuss his feelings related to his advance directive. Review of the clinical record revealed that there was no advance directive for Resident #74. Review of Resident #74's Physician Order Sheet (POS) for May 2022 revealed the following order: Full Code starting on 05/12/22. An interview was conducted with the Social Worker (SW) on 05/17/22 approximately 10:14 a.m., who said an advance directive should have been completed upon admission if possible but no more than three days after being admitted to the facility. The SW stated that she was not able to provide documentation that Resident #74 and or their Representative was given the opportunity to formulate an advance directive. A debriefing was held with the Administrator, Director of Nursing and Corporate support on 05/19/22 at approximately 2:00 p.m., who were informed of the above findings; no further information was provided prior to exit. The facility's policy titled Advance Directive revised on 10/01/21. It is the policy of this facility to support and facilitate a resident's right to request, refuse and/or discontinue medical or surgical treatment and to formulate an advance directive. Policy Explanation and Compliance Guidelines: 1. On admission, the facility will determine if the resident has executed an advance directive, and if not, determine whether the resident would like to formulate an advance directive. 2. The facility will provide the resident or resident representative information, in a manner that is easy to understand, about the right to refuse medical or surgical treatment and formulate an advance directive. 3. The facility staff failed to ensure Resident #85 was given the opportunity to formulate an Advance Directive upon admission. Resident #85 was originally admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses to included but not limited to Contractures of both knees and lower legs, Stage 4 Pressure Ulcer and Alzheimer's Disease. Resident #85's most recent Minimum Data Set (MDS) was a Significant Change Assessment with an Assessment Reference (ARD) of 4/28/22. The Brief Interview for Mental Status (BIMS) was unable to be completed, however Resident #85 was coded as being severely cognitively impaired for daily decision making. Resident #85's Comprehensive Care Plan was reviewed. The Advance Directive focus indicated that the resident had DNR (Do Not Resuscitate) on file as an advance directive that was initiated on 11/12/20. Resident #85's Physician Orders were reviewed and a DO NOT RESUSCITATE order was in place with an order date of 1/27/21. Resident #85's clinical record was reviewed and there was no advance directive document located. On 5/11/22 at 2:54 p.m. the Social Worker was asked where Resident #85's Advance Directive could be located in the clinical record. The Social Worker stated, All she has is the yellow DNR(Do Not Resuscitate) that's in the chart. I just did an audit for resident code status and advance directives on 3/31/22. She had the DNR so I didn't go further with her. She doesn't have an advance directive. I thought the EMS (emergency medical services) DNR was the advance directive for her. On 5/18/22 at 1:43 p.m. an interview was conducted with the Social Worker. The Social Worker stated, I know the DNR is not an advance directive, its just a part of it. I need to do the advance directive sheet with the resident or family. She (Resident #85) does not have an advance directive in place. The facility policy titled Advance Directives last revised 10/1/21 was reviewed and is documented in part, as follows: Policy: It is the policy of this facility to support and facilitate a resident's right to request, refuse and/or discontinue medical or surgical treatment and to formulate an advance directive. Policy Explanation and Compliance Guidelines: 1. On admission, the facility will determine if the resident has executed an advance directive, and if not determine whether the resident would like to formulate an advance directive. On 5/19/22 at 9:10 a.m. the above findings were shared with the Administrator and the Director of Nursing. The Administrator stated, I expect that Advance Directives will be completed for each resident upon admission. Prior to exit no further information was shared. 2. Resident #79 was originally admitted to the facility on [DATE]. The Resident diagnoses included; dementia, high blood pressure and atrial fibrillation. The admission Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 4/25/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 13 out of a possible 15. This indicated Resident #79's cognitive abilities for daily decision making was intact. A review of the clinical record revealed a Do Not Resuscitate (DNR) form signed 4/20/22. The Physician's Order summary stated the resident was a Full Code. Review of the person-centered care plan revealed a care plan dated 4/25/22, with a problem reading; Advance Directive - DNR. The goal read; Resident will have Advanced Directives followed 10/24/22. The interventions included; allow resident to discuss his feelings regarding his advanced directive. On 5/18/22 at approximately 1:25 p.m., the Social Worker (SW) stated the resident was admitted with a signed DNR form therefore, she created a DNR care plan but she wasn't aware of how the code status was written on the Physician Order Summary (POS), but she wasn't made aware of a change in the resident's code status. On 5/18/22 at approximately 1:35 p.m., an interview was conducted with the Director of Nursing (DON) regarding Resident #79's code status. The DON stated the nurses are instructed to review the Ribbon on the POS for a quick reference of a resident's code status and if they had review the Ribbon for Resident #79, it would have stated Full Code. The DON further stated since the SW brought it to her attention the Ribbon was changed to match the signed DNR form and the resident's care plan. An interview was also conducted with Licensed Practical Nurse (LPN) #9 on 5/19/22 at approximately 10:54 a.m. LPN #9 stated in an emergency she would review the POS for a resident's code status not any other place. LPN #9 further stated if a resident has coded she wouldn't have time to look multiple places to confirm the resident's code status. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no concerns were voiced.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on a clinical record review, staff interviews and facility document review the facility staff failed to ensure accurate Mi...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on a clinical record review, staff interviews and facility document review the facility staff failed to ensure accurate Minimum Data Set (MDS) Assessments for 3 of 55 residents in the survey sample, Resident #78, Resident #79 and Resident #190. For Resident #78, the facility staff failed to ensure the Quarterly MDS dated [DATE] was accurately coded at section N0300 and section N0350. For Resident #79, the facility staff failed to ensure the admission MDS was accurately coded at section E0800. For Resident #190, the facility staff failed to ensure the Significant Change MDS dated [DATE] was accurately coded at section L0200. The findings included: 1. The facility staff failed to ensure Resident #78's Quarterly Minimum Data Set, dated [DATE] was accurately coded under section N0300 and section N0350. Resident #78 was admitted to the facility on [DATE] with diagnosis to include but not limited to Type II Diabetes Mellitus. Resident #78's most recent Minimum Data Set(MDS) was a Quarterly assessment with an Assessment Reference Date(ARD) of 4/21/22. The Brief Interview for Mental Status was a 15 out of a possible 15 indicating Resident #78 was cognitively intact and capable of daily decision making. Under Section M Medications N0300, the resident was coded as receiving 7 injections during the 7 day look back period. Also under Section M Medications N0350, Resident #78 was coded as receiving insulin 7 times during the 7 day look back period. Resident 78's Physician Orders were reviewed from admission to present. There was no physician order for Resident #78 to be administered insulin nor any other 7 day injection ordered for the resident. On 5/12/22 at 11:00 a.m. an interview was conducted with Resident #78 regarding his diabetes. Resident #78 stated, I don't take insulin for my diabetes and they haven't given me any shots here. I take a pill for my diabetes. Resident #78's Medication Administrative Record(MAR) for April 2022 was reviewed. All medications listed on the MAR were ordered to be given by mouth. On 5/12/22 at 4:01 p.m. an interview was conducted with MDS Coordinator Registered Nurse(RN) #2 regarding Resident #78's Quarterly MDS dated [DATE]. RN #2 stated, The Quarterly MDS was coded inaccurately. The error was with the insulin and injections. Name (Resident #78) wasn't on insulin. I made a mistake he wasn't on insulin during the ARD period and the MDS has been corrected. The MDS should be accurate because it is a reflection of the resident and their care. The facility policy titled MDS 3.0 Completion revised 10/1/21 was reviewed and is documented in part, as follows: .Policy: Resident's are assessed, using a comprehensive assessment process, in order to identify care needs, strengths and preference to develop an interdisciplinary care plan, and ensure appropriate reimbursement. Policy Explanation and Compliance Guideline: 1. According to federal regulations, the facility conducts initially and periodically a comprehensive, accurate and standardized assessment of each resident's clinical condition, cognitive and functional status, and use of services specified by the State . On 5/19/22 at 9:10 a.m. the above findings were shared with the Administrator and the Director of Nursing. The Administrator stated, The MDS should be coded as accurately as possibly and if an error detected it should be corrected and resubmitted. Prior to exit no further information was shared. 2. The facility staff failed to accurately code Resident #79's 4/25/22 admission Minimum Data Set (MDS) assessment to reflect rejection of care at Section E0800. Resident #79 was originally admitted to the facility on [DATE]. The Resident diagnoses included; dementia, high blood pressure and atrial fibrillation. The admission MDS assessment with an assessment reference date (ARD) of 4/25/22 coded the resident as completing the Brief Interview for Mental Status (BIMS) and scoring 13 out of a possible 15. This indicated Resident #79's cognitive abilities for daily decision making was intact. Resident #79 Physician's Order Summary included an order dated 4/21/22, for bilateral heel float boots at all times. May remove for activities of daily living (ADL) care, every shift. A nurse's note dated 4/24/22 at 6:06 p.m., read; the resident remains very confused. His vital signs are normal and he continues to take off the padded heel support boots and throw his legs off the side of the bed. He accepted his meal moderately well with prompting. There has been no complaints of pain and the scabs continue to look infection free. A review of the resident's MDS assessment date 4/25/22 revealed at Section E0800 Rejection of Care was not coded as behavior exhibited. The instructions for E0800 reads; Did the resident reject evaluation or care (e.g., bloodwork, taking medications, ADL assistance) that is necessary to achieve the resident's goals for health and well-being? The resident was observed on 5/10/22 at approximately 4:20 p.m. sitting in a recliner chair at the nurse's station. He had gray non-skid socks on his feet but not the bilateral heel float boots. Resident #79 was observed again on 5/13/22 at approximately 11:05 a.m. seat in a reclining chair with his feet on the floor. He wasn't wearing the bilateral boots to float his heels. Resident #79 was observed in bed on 5/19/22 at approximately 10:50 a.m., his bare feet were hanging over the mattress as if he was about to get up. The green pressure reducing boots could be seen in the closet just as they had been for several days. A phone interview was conducted with the Wound Care Nurse Practitioner (WCNP) on 5/17/22 at approximately 3:08 p.m. The WCNP stated the resident has the boots to float his heels as a preventative measure but she has found him to be very restless and non-compliant with the boots. The WCNP also stated it is necessary for the resident to float his heels because recently (5/10/22) he developed a deep tissue injury to the left heel, which healed on 5/17/22. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no further concerns were voiced. 3. The facility's staff failed to accurately code Resident #190's 4/7/22 significant change MDS assessment at L0200F to include mouth or facial pain, discomfort or difficulty with chewing. Resident #190 was originally admitted to the facility 2/23/2017 and readmitted [DATE] after an acute care hospital stay. The current diagnoses included; Alzheimer's dementia, diabetes and a left jaw swelling/dental abscess. The significant change Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 4/7/22 coded the resident as not having the ability to complete the Brief Interview for Mental Status (BIMS). The staff interview was coded for long and short term memory problems and severely impaired daily decision making abilities. In section G (Physical functioning) the resident was coded as requiring total care of one person with bed mobility, transfers, dressing, eating, toileting, personal hygiene and bathing. In section L0200F the resident wasn't coded for mouth or facial pain, discomfort or difficulty with chewing and the MDS was coded as none of the above for the following questions; broken or loosely fitting full or partial denture (chipped, cracked, uncleanable, or loose), no natural teeth or tooth fragment(s) (edentulous), abnormal mouth tissue (ulcers, masses, oral lesions, including under denture or partial if one is worn, obvious or likely cavity or broken natural teeth, inflamed or bleeding gums or loose natural teeth, mouth or facial pain, discomfort or difficulty with chewing, and unable to examine. A nurse's note dated 3/1/22 revealed Resident #190 presented with a temperature of 101 degrees Fahrenheit (°F) and swelling was observed to the left side of his face. The nurse's note read; an observation of his mouth revealed decayed teeth. The Nurse Practitioner (NP) ordered a STAT (immediately) dental consult and ordered antibiotic therapy; Augmentin 875 mg by mouth two times each day for 7 days. A nurse's note dated 3/2/22 at 6:40 p.m., read the resident remains on an antibiotic nevertheless his temperature was 102.4 °F, Tylenol was administered. Another nurse's note dated 3/4/22, revealed the resident's temperature was again abnormal, 101 °F and the swelling to the left side of the resident's face had increased. The NP visited the resident on 3/4/22 to assess the left facial swelling; the assessment read; the resident was frail, in bed making mumbling sounds, while moving his head from side to side, the left face and jaw were inflamed, swollen, tender when touched and the resident was very uncomfortable. The NP assessment also read; an oral exam couldn't be performed in the facility. The NP ordered a three view facial x-ray, Morphine Sulfate (an opioid pain medication used to treat moderate to severe pain); 0.25 milliliter by mouth every 4 hours as needed for pain, an additional antibiotic Ceftriaxone; one dose and a hospice consult. Resident #190 was evaluated again, on 3/7/22 by the NP. The NP documented the resident continued with facial swelling and a tooth abscess and the plan was for the resident to see the dentist as soon as possible for a tooth extraction. The NP ordered an additional one time dose of the antibiotic Ceftriaxone. On 3/23/22, Resident #190 was seen by the general practice dentist. The dentist progress note read, there remained slight swelling to the left lower vestibular region but she was unable to determine if it was associated with a tooth because the resident was unable to open his mouth and/or follow directions therefore she was unable to clinically see or obtain necessary radiology to determine/diagnose the resident's dental problem. A review of Resident #190's POS for April 2022 revealed on 4/2/22 an order for Amoxicillin Capsule 500 MG, Give one capsule by mouth three times a day for a seven days for a dental infection. The NP progress note dated 4/7/22 read the resident was started on Amoxicillin for a dental abscess and some of the resident's weight loss may be a result of the dental abscess and difficulty chewing. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no further concerns were voiced.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0868 (Tag F0868)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews, clinical record reviews, and review of facility documents, the facility staff failed to adequately id...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews, clinical record reviews, and review of facility documents, the facility staff failed to adequately identify, keep systems functioning properly and implement necessary action plans to assure the provisions of quality care for the residents using the Quality Assessment and Assurance (QA&A) committee to identify quality deficiencies in the areas of Pressure Sores F-686 and Dental Services F-791 and the facility staff failed to conduct quarterly QA&A meetings. The findings included: On 5/19/22 at approximately 2:50 p.m., the QA&A interview was conducted with the Administrator. The Administrator stated there was no evidence that QA&A meetings were conducted prior to her employment with the facility. The Administrator stated she accepted the position January 2022 and conducted the October, November and December QA&A committee meeting April 2022 and the January, February and March QA&A committee meeting May 2022. Review of the documentation for the April and May QA&A committee meetings confirmed the Medical Director, Administrator, Director of Nursing and least three other members of the facility's staff participated in the meetings. The Administrator repeated she looked and looked but was unable to locate documentation to support QA&A meetings were held at least quarterly or more often as necessary to fulfill the committee's responsibilities prior to her employment. The Administrator also stated during the interview that it was the company's protocol to identify quality deficiencies through feedback from facility employees, residents and family members as well as the regular QA&A committee members. She stated once the quality deficiencies are identified, the QA&A committee develops a performance improvement plan to address and resolve the concern. The Administrator further stated pressure ulcers had been identified by the QA&A committee and they instituted a plan January 2022, but the plan failed therefore; the performance improvement plan was re-evaluated and re-instituted in February with a facility wide skin sweep and again a concern was identified. She stated they identified lack of education about pressure ulcers weekly skin checks were deficient practices therefore they instituted a performance improvement plan for all direct care staff with a goal to institute weekly skin checks and to teach the nurses to notify the Director of Nursing or the in-house wound nurse of identified concerns. The Administrator stated 80% of nurses were reporting identified skin condition problems but they found the newly hired nurse staff weren't educated therefore the revised plan focused more attention on educating newly hired licensed nurses. The Administrator stated they were still working on the performance improvement plan for pressure ulcers and she would decide with her in-house team if the plan should be presented to the survey team. Prior to the conclusion of the survey the Administer hadn't presented the pressure ulcer performance improvement plan to the survey team. Two compliant residents were recognized with a pressure ulcer not identified by the staff until they were at an advance stage (stage 3 or more) and one complaint resident's pressure ulcer was allowed to deteriorate to an advanced stage. Other non-functioning components pertinent to having an effective pressure ulcer prevention program were that many weekly skin assessments were not conducted weekly. During the survey Resident #85 was identified with a facility acquired advanced stage pressure ulcer to the right great toe. The Stage 3 right great toe pressure area was identified during a facility skin sweep on 2/22/22. Resident #85's clinical record review revealed a Braden Scale for Predicting Pressure Sore Risk assessment completed 7/26/21 where the resident was identified as being VERY HIGH RISK with a score of 9. The clinical record review also indicated that a weekly skin review was completed on 7/22/21 and the resident did not have another weekly skin review until 3/30/22. On 5/12/22 during an interview with the Director of Nursing she stated, When I started I realized we had quite a few acquired pressure ulcers. On 2/22/22 we did a whole building skin sweep and discovered multiple residents with wounds. On Name (Resident #85) we discovered a Stage 3 to her right great toe and had the Wound NP see her that day as well. We started reviewing each resident for orders and put interventions in place. We found that Name (Resident #85) had not had a documented weekly skin assessment completed since 7/21/21. The weekly skin assessments were started back and I started a skin report for the CNA's to complete to report any new identified skin issues which are given to the charge nurse and they both have to sign it. Also I did not see where we were documenting she was being turned and repositioned every 2 hours. For Resident #291 who was admitted to the facility with a stage II sacral pressure ulcer received ongoing assessments and monitoring prior to advancing to an unstageable measuring 5 centimeter x 5 centimeter x 2 centimeter (cm). Review of Resident #291 clinical record revealed no Weekly Pressure Ulcer Observation Assessment had been conducted since admission on [DATE] until evaluated by the wound NP on 03/29/22. On 03/29/22, the sacral wound presented with serosanquinous drainage (drainage leaving a wound that is yellowish in color with small amounts of blood), strong odor and wound bed noted with 90 % slough and 10% dermis tissue (unstageable pressure ulcer). The wound was debrided on 03/29/22 by the wound NP at bedside. Resident #291 was started on Augmentin (antibiotic therapy) 500 mg/125 mg every 12 hours x 10 days for sacral wound infection. Resident #339 was identified with a facility acquired with an advanced pressure ulcer of the sacrum. The unstageable pressure ulcer with slough was first identified by the Resident's assigned CNA on 12/03/21. Resident #339 clinical record review revealed a Braden Scale for Predicting Pressure Sores Risk Assessment as being completed on 11/19/21 as being at RISK. On 11/25/21 a clinical record review revealed a second Braden Scale for Predicting Pressure Sores Risk assessment was completed as being at Moderate RISK. On 5/18/22 an interview was conducted with the Wound NP (Nurse Practitioner). She stated that the wound was facility acquired and that she first assessed it on 12/7/ 21 as an unstageable with 100% necrosis full thickness wound. It's not acceptable because as a full thickness wound, I'm not able to see the extent of this wound. It could have been here for who knows how long. According to the ER medical records dated 12/18/21 at 5:14 PM Resident #339 was presented with AMS (Altered Mental Status) and a Large Sacral Pressure Ulcer. Later tests revealed that Resident #339 was diagnosed with having a sacral decubitus ulcer with infected gas. The Administrator further stated they began reviewing Falls/Accident Hazards but they hadn't developed a plan for improvement and there was no reason to address dental services or medication procurement in the QA&A meeting. A nurse's note dated 3/1/22 revealed Resident #190 presented with a temperature of 101 degrees Fahrenheit (°F) and swelling was observed to the left side of his face. The nurse's note read; an observation of his mouth revealed decayed teeth. The Nurse Practitioner (NP) ordered a STAT (immediately) dental consult and ordered antibiotic therapy; Augmentin 875 mg by mouth two times each day for 7 days. A nurse's note dated 3/2/22 at 6:40 p.m., read the resident remains on an antibiotic nevertheless his temperature was 102.4 °F, Tylenol was administered. Another nurse's note dated 3/4/22, revealed the resident's temperature was again abnormal, 101 °F and the swelling to the left side of the resident's face had increased. The NP visited the resident on 3/4/22 to assess the left facial swelling; the assessment read; the resident was frail, in bed making mumbling sounds, while moving his head from side to side, the left face and jaw were inflamed, swollen, tender when touched and the resident was very uncomfortable. The NP assessment also read; an oral exam couldn't be performed in the facility. The NP ordered a three view facial x-ray, Morphine Sulfate (an opioid pain medication used to treat moderate to severe pain); 0.25 milliliter by mouth every 4 hours as needed for pain, an additional antibiotic Ceftriaxone; one dose and a hospice consult. Resident #190 was evaluated again, on 3/7/22 by the NP. The NP documented the resident continued with facial swelling and a tooth abscess and the plan was for the resident to see the dentist as soon as possible for a tooth extraction. The NP ordered an additional one time dose of the antibiotic Ceftriaxone. The STAT dental appointment ordered 3/1/22, was scheduled on behalf of Resident #190 on 3/10/22, with a local general practice dentistry office for 3/23/22. Prior to 3/10/22, the facility's staff was unable to provide evidence of attempting to obtain a dental appointment for Resident #190 and there was no evidence in the resident's clinical record or elsewhere of what extenuating circumstances led to the delay in obtaining the STAT ordered dental appointment. On 3/23/22, Resident #190 was seen by the general practice dentist. The dentist progress note read, there remained slight swelling to the left lower vestibular region but she was unable to determine if it was associated with a tooth because the resident was unable to open his mouth and/or follow directions therefore she was unable to clinically see or obtain necessary radiology to determine/diagnose the resident's dental problem. The general practice dentist provided referral information to the nursing facility to schedule an appointment with a sedation dentistry practice hence a thorough assessment could be conducted. On 3/30/22 Resident #190 was transferred to a local hospital for altered mental status. The Discharge summary dated [DATE] read; intravenous Unasyn was ordered for a possible dental abscess for which the resident was being treated for at the nursing facility. The Discharge summary dated [DATE], also stated the resident was admitted with diagnoses of a severely elevated blood glucose (417 mg/dl) and a critical blood sodium level (163 mmol/L), requiring intravenous insulin in the emergency room and three days of intravenous fluid resuscitation. On 5/19/22 at approximately 2:50 p.m., an interview was conducted with the Administrator. The Administrator stated the facility didn't have a dental contract with a practice but a local dental practice usually accommodates their residents whenever services are needed. The Administrator didn't elaborate on why it took twenty-two days for staff to obtain a dental appointment for Resident #190 but she stated because the in-house NP was monitoring and treating Resident #190's swelling to the left jaw, she felt his dental needs were met. The Administrator didn't address a documented NP progress note in which the NP stated she spoke with the DON on 3/7/22 expressing the need to have the resident evaluated by a dentist. On 5/20/22 at approximately 6:00 p.m., the above findings were shared with the Administrator, Director of Nursing and Corporate Consultant. An opportunity was offered to the facility's staff to present additional information but no additional information was provided and no further concerns were voiced. The facility's policy titled Dental Services with a revision date of 01/04/22 read; It is the policy of this facility, in accordance with residents' needs, to assist residents in obtaining routine (to the extent covered under the State plan) and emergency dental care. Emergency dental services includes services needed to treat an episode of acute pain in teeth, gums, or palate; broken, or otherwise damaged teeth, or any other problem of the oral cavity that required immediate attention by a dentist.
Aug 2019 17 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0557 (Tag F0557)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interviews, clinical record review and facility document review the facility staff failed to provide...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interviews, clinical record review and facility document review the facility staff failed to provide draping to prevent exposure of body parts and maintain dignity during the provision of care for 1 of 56 residents in the survey sample, Resident #124. The findings include: Resident #124 was admitted to the facility on [DATE] with diagnoses to include but not limited to, stroke and diabetes. The current MDS (Minimum Data Set) an annual with an assessment reference date of 7/1/19 assessed the resident as having long and short term memory deficits. The resident required extensive assistance of two staff for bed mobility and was dependent for transfers. Under section M. Skin Conditions the resident was coded as having a stage IV pressure injury (defined in the MDS as-full thickness tissue loss with exposed bone, tendon, or muscle. Slough, eschar may be present on some parts of the wound bed). On 8/7/19 at 12:33 p.m., an observation of the sacral dressing change was conducted. The facility wound nurse (Licensed Practical Nurse-LPN #9) preformed the dressing change with Certified Nursing Assistant (CNA #6) providing assistance with maintaining the resident on her side. Upon the surveyor entering the room, the resident was in the bed, laying on her right side and completely naked. The CNA stated she had just provided incontinent care to the resident. The curtains were not completely closed facing the B bed side, the roommate was not in the room at the time, and the door was left open. During the dressing change the resident stated, my [NAME] .the CNA stated, you got enough people seeing your [NAME] . A staff member knocked on the door and the resident stated, no men. The resident remained naked during the course of the dressing change which lasted approximately 20 minutes. After the dressing change, CNA #6 was interviewed. She was asked why the resident was not provided draping/covering to prevent exposure of body parts during the dressing change. The CNA stated, I wasn't thinking. On 8/8/19 at 9:47 a.m., the observation concern of the resident not being provided draping during the dressing change was shared with the wound nurse. The wound nurse stated She usually has a gown on .she should have had a sheet covering her, when asked why she stated, Dignity. 8/8/19 at 12:48 p.m., the resident was observed eating lunch in bed. She was asked if it would be okay if I asked her a question, her response was, I hope I can answer it. The resident was then asked how she felt being left completely naked yesterday during the dressing change, she stated, I didn't like being naked. On 8/8/19 at 3:00 p.m., during the pre-exit meeting the above findings was shared with the Administrator and the Director of Nursing (DON). The DON stated, I definitely don't think that is a common practice, she should have have taken a sheet and covered the resident. The facility policy titled Quality of Life-Dignity revised August 2016 read, in part: Policy Statement-Each resident shall be cared for in a manner that promotes and enhances quality of life, dignity, respect and individuality. Policy Interpretation and Implementation: 10. Staff shall promote, maintain and protect resident privacy, including bodily privacy during the assistance with personal care and during treatment procedures.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Safe Environment (Tag F0584)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, and clinical record review the facility staff failed to ensure medical equipment was main...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, and clinical record review the facility staff failed to ensure medical equipment was maintained in good repair for 1 of 56 residents in the survey sample, Resident #78. Resident #78's mobility chair was observed to have areas that were ripped, torn and a piece of the foam arm rest was missing. The findings include: Resident #78 was admitted to the facility on [DATE] with diagnoses to include but not limited to, seizures, traumatic brain injury, and spastic hemiplegia (Spastic hemiplegia is a neuromuscular condition of spasticity that results in the muscles on one side of the body being in a constant state of contraction) affecting the right side. The current MDS (Minimum Data Set) a quarterly with an assessment reference date of 6/11/19 coded the resident as scoring a 12 out of a 15 on the BIMS (Brief Interview for Mental Status), indicating the resident had moderately impaired cognition. The resident required extensive assistance of two staff for bed mobility and transfers. The resident was chair bound. Based on the Resident's abnormal posture and for the prevention of falls the resident was ordered a Broda chair (a seating, positional mobile chair). On the initial tour of the right side unit on 8/4/19 and at 4:29 p.m., the resident was observed sitting up in the Broda chair at the bedside. The chair was observed as follows: the left side vinyl panel was ripped and torn, the right adjustable wing for upper lateral support had multiple cracked areas in the vinyl located in proximity of where the resident face can make contact, and the right black foam arm rest was missing a piece that had been torn/ripped off measuring approximately 1.5 inches by 2 inches. The resident was observed sitting in the Broda chair each of the following days of the survey 8/5/19, 8/6/19 and 8/7/19, the Broda chair remained in the same condition. On 8/7/19 at 10:55 a.m., the right side unit manager was interviewed. She was asked about Resident #78's Broda chair in need of repair. She stated she was not made aware of it. She stated if medical equipment needs repair the request is placed into the maintenance computer system named TELS or sent to the therapy department depending on what is needed, she stated, I can't always get into that system (TELS), so then I just tell them (maintenance). She was asked to accompany this surveyor to the resident's room to look at the Broda chair. After noting the areas she stated to the resident, Looks like you'll be getting a new chair. On 8/8/19 at 3:00 p.m., during the pre-exit meeting the above findings was shared with the Administrator and the Director of Nursing. The Administrator stated, .we do have additional Broda chairs. She stated she would have expected the front line staff to have informed the unit manager. No additional information was provided to the survey team prior to exit.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Abuse Prevention Policies (Tag F0607)

Could have caused harm · This affected 1 resident

Based on staff interview and facility record review, it was determined that the facility failed to develop and implement an abuse policy to include conducting a reference screening for one (1) prospec...

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Based on staff interview and facility record review, it was determined that the facility failed to develop and implement an abuse policy to include conducting a reference screening for one (1) prospective employee out of 25 records reviewed. Review of personnel records obtained from facility revealed that no verification of reference screenings was conducted for a current employee, Certified Nursing Assistant (CNA) #9. The findings included: On 8/8/2019 at approximately 1:20 p.m., the Human Resource (HR) Director was asked to provide evidence of reference screenings for CNA #9. The HR Director stated, I don't have one for her and I was not working here then. Facility policy on Abuse Prevention Program documented in part, the following: .2. Conduct employee background checks and will not knowingly employ or otherwise engage any individual who has: a. Have been found guilty of abuse, neglect, exploitation, misappropriation of property, or mistreatment by a court of law; b. Have had a finding entered into the State nurse aide registry concerning abuse, neglect, exploitation, mistreatment of residents or misappropriation of their property; or c. Have a disciplinary action in effect against his or her professional license by a state licensure body as a result of a finding of abuse, neglect, or exploitation, mistreatment of residents or misappropriation of resident property. Facility policy did not incorporate procedures for prospective employee reference checks.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0638 (Tag F0638)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident record review, staff interviews and facility document review the facility staff failed to ensure that a Quarte...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident record review, staff interviews and facility document review the facility staff failed to ensure that a Quarterly Review Assessment was submitted no less than once every three months for 3 of 56 residents in the survey sample, (Residents #2, #3 and #4). The findings included: 1. Resident #2 was admitted on [DATE] with diagnoses to include but not limited to Type II Diabetes Mellitus and Cerebrovascular Disease. Upon completing the Resident Assessment Task is was noted that Resident #2 was triggered for a Minimum Data Set (an assessment tool) that was greater than 120 days late. Resident #2's most recent Minimum Data Set (MDS) was a Quarterly with an Assessment Reference Date (ARD) of 6/25/19. The Brief Interview for Mental Status was a 10 out of a possible 15 indicating that Resident #2 was moderately cognitively impaired but capable of some daily decision making. Under Section Z Assessment Administration: Signature of RN (Registered Nurse) Assessment Coordinator Verifying Assessment Completion was signed on 8/1/19. The CMS (Center for Medicare Services) Submission Report MDS 3.0 NH (Nursing Home) Final Validation Report for Resident #2's Quarterly MDS with the ARD of 6/11/19 was reviewed and is documented in part, as follows: Submission Date/Time: 8/1/2019 15:50:08 (3:05 P.M.) Accepted: Name: (Resident #2) Target Date: 6/25/19 Warning: Assessment Completed Late: (assessment completion date) is more than 14 days after A2300 (assessment reference date). The last Quarterly assessment submitted to CMS was on 3/18/19, which is over 4 months between quarterly assessments being completed for Resident #2. On 8/7/19 at 1:33 P.M. an interview was conducted with the MDS Coordinator regarding Resident #2's Quarterly assessments being submitted greater than 3 months apart. The MDS Coordinator stated, We just submitted his (Resident #2's) quarterly MDS on 8/1/19, it was submitted late. We have been short in the MDS department and since I got here in June we have been trying to catch up. The MDS Coordinator was also asked how often quarterly assessment should be submitted for residents. The MDS Coordinator stated, MDS's should be completed and submitted according to the RAI (Resident Assessment Instrument) Manual. On 8/8/19 at 2:13 P.M. an interview was conducted with the Administrator regarding Resident #2's late quarterly MDS. The Administrator stated, I feel our MDS's were late because we have some new MDS staff and the have difficulty with time management. I expect for the MDS's be be current and submitted on time. On 8/7/19 at 3:00 a pre-exit debriefing was held with the Administrator and the Director of Nursing where the above information was shared. Prior to exit no further information was provided. 2. Resident #3 was admitted to the facility with diagnoses to include but not limited to Dementia and Anxiety Disorder. Upon completing the Resident Assessment Task is was noted that Resident #3 was triggered for a Minimum Data Set that was greater than 120 days late. Resident #3's most recent Minimum Data Set (MDS) was a Quarterly with an Assessment Reference Date (ARD) of 6/10/19. The Brief Interview for Mental Status indicated that Resident #3 has long and short term memory deficits and was severely cognitively impaired for daily decision making. Under Section Z Assessment Administration: Signature of RN (Registered Nurse) Assessment Coordinator Verifying Assessment Completion was signed on 8/2/19. The CMS (Center for Medicare Services) Submission Report MDS 3.0 NH (Nursing Home) Final Validation Report for Resident #3's Quarterly MDS with the ARD of 6/10/19 was reviewed and is documented in part, as follows: Submission Date/Time: 8/2/2019 17:32:12 (5:32 P.M.) Accepted: Name: (Resident #3) Target Date: 6/10/19 Warning: Assessment Completed Late: (assessment completion date) is more than 14 days after A2300 (assessment reference date). The last Quarterly assessment submitted to CMS was on 3/8/19, which is over 4 months between quarterly assessments being completed for Resident #3. On 8/7/19 at 1:33 P.M. an interview was conducted with the MDS Coordinator regarding Resident #3's Quarterly assessments being submitted greater than 3 months apart. The MDS Coordinator stated, We just submitted his (Resident #3's) quarterly MDS on 8/2/19, it was submitted late. We have been short in the MDS department and since I got here in June we have been trying to catch up. The MDS Coordinator was also asked how often quarterly assessment should be submitted for residents. The MDS Coordinator stated, MDS's should be completed and submitted according to the RAI (Resident Assessment Instrument) Manual. On 8/8/19 at 2:13 P.M. an interview was conducted with the Administrator regarding Resident #3's late quarterly MDS. The Administrator stated, I feel our MDS's were late because we have some new MDS staff and the have difficulty with time management. I expect for the MDS's be be current and submitted on time. On 8/7/19 at 3:00 a pre-exit debriefing was held with the Administrator and the Director of Nursing where the above information was shared. Prior to exit no further information was provided. 3. Resident #4 was admitted to the facility on [DATE] with diagnoses to include but not limited to Type II Diabetes Mellitus and Hypertension. Upon completing the Resident Assessment Task is was noted that Resident #4 was triggered for a Minimum Data Set that was greater than 120 days late. Resident #4's most recent Minimum Data Set (MDS) was a Quarterly with an Assessment Reference Date (ARD) of 6/11/19. The Brief Interview for Mental Status indicated that Resident #4 has long and short term memory deficits and was severely cognitively impaired for daily decision making. Under Section Z Assessment Administration: Signature of RN (Registered Nurse) Assessment Coordinator Verifying Assessment Completion was signed on 8/7/19. The CMS (Center for Medicare Services) Submission Report MDS 3.0 NH (Nursing Home) Final Validation Report for Resident #4's Quarterly MDS with the ARD of 6/11/19 was reviewed and is documented in part, as follows: Submission Date/Time: 8/7/2019 14:13:05 (2:15 P.M.) Accepted: Name: (Resident #4) Target Date: 6/11/19 Warning: Assessment Completed Late: (assessment completion date) is more than 14 days after A2300 (assessment reference date). The last Quarterly assessment submitted to CMS was on 3/28/19, which is over 4 months between quarterly assessments being completed for Resident #4. On 8/7/19 at 1:33 P.M. an interview was conducted with the MDS Coordinator regarding Resident #4's Quarterly assessments being submitted greater than 3 months apart. The MDS Coordinator stated, We just submitted her (Resident #4's) quarterly MDS today, it was submitted late. We have been short in the MDS department and since I got here in June we have been trying to catch up. The MDS Coordinator was also asked how often quarterly assessment should be submitted for residents. The MDS Coordinator stated, MDS's should be completed and submitted according to the RAI (Resident Assessment Instrument) Manual. On 8/8/19 at 2:13 P.M. an interview was conducted with the Administrator regarding Resident #4's late quarterly MDS. The Administrator stated, I feel our MDS's were late because we have some new MDS staff and the have difficulty with time management. I expect for the MDS's be be current and submitted on time. The facility Policy titled :Resident Assessment Instrument last revised September 2017 was reviewed and is documented in part, as follows: Policy Interpretation and Implementation: 1. The Assessment Coordinator is responsible for ensuring that the Interdisciplinary Assessment Team conduct timely resident assessment and reviews according tot he following schedule: c. At least quarterly. On 8/7/19 at 3:00 p.m. a pre-exit debriefing was held with the Administrator and the Director of Nursing where the above information was shared. Prior to exit no further information was provided.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, clinical record review and facility document review the facility staff failed to ensure an MDS (Minimu...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, clinical record review and facility document review the facility staff failed to ensure an MDS (Minimum Data Set-an assessment tool) was accurate for 1 of 56 residents in the survey sample, Resident #121. Section E. Behaviors was not accurate for the quarterly MDS with an assessment reference date of 7/10/19. The findings include: Resident #121 was admitted to the facility on [DATE] with diagnoses to include but not limited to, unspecified dementia without behavioral disturbance, major depressive disorder, recurrent with severe psychiatric symptoms. The current MDS (Minimum Data Set) a quarterly with an assessment reference date of 7/10/19 coded the resident as having long and short term memory deficits and severely impaired daily decision making skills. Under behaviors Section E. 0200 A. the resident was coded as not exhibiting any physical behavioral symptoms directed towards others (e.g., hitting, kicking, pushing, scratching, grabbing). Resident #121 required extensive assistance of two staff for toileting needs and personal hygiene and was dependent for bathing. Review of the Medication Administration Record for July 2019 evidenced the resident was administered Ativan (an anti-anxiety drug) 1 mg PRN (as needed) for the following identified behaviors that were not coded on the 7/10/19 MDS: July 9th at 9:08 a.m.-hitting, kicking, scratching, grabbing July 10th at 9:43 a.m.-hitting, scratching, grabbing Review of the quarterly MDS Section Z. Assessment Administration evidenced the Social Worker's signature as having completed section C, D, E and Q. Section Z. reads in part: I certify that the accompanying information accurately reflects resident information for this resident . On 8/8/19 at 12:21 p.m., the above findings was shared with the MDS Coordinator. She stated, Section E.0200 A was coded incorrectly by the Social Worker and we will be completing a modification of the MDS for Section E. and submit it once it is completed. On 8/8/19 at 3:00 p.m., during the pre-exit meeting with the Administrator and the Director of Nursing the above findings was shared. The facility policy title Resident Assessment Instrument revised September 2017 reads, as follows in part: 1. The Assessment Coordinator is responsible for ensuring that the Interdisciplinary Assessment Team conduct timely resident assessments and reviews according to the following schedule: c. At least quarterly 7. All persons who have completed any portion of the MDS Resident Assessment Form must sign such document attesting to the accuracy of such information.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0658 (Tag F0658)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident interview, staff interview, facility document review and clinical record review, it was determined that facili...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident interview, staff interview, facility document review and clinical record review, it was determined that facility staff failed to implement the physician's recommendations for treatment to a non-intact blister; failed to document when the non-intact blister had healed in the clinical record; and continued to treat the non-intact blister when it was already healed for one of 56 resident in the survey sample, Resident #80. The findings included: Resident #80 was admitted to the facility on [DATE] with diagnoses that included but were not limited to Parkinson's disease, convulsions, and Schizophrenia. Resident #80's most recent MDS (minimum data set) assessment was a quarterly assessment with an ARD (assessment reference date) of 4/2/19. Resident #80 was coded as being intact in cognitive function scoring 15 out of possible 15 on the BIMS (Brief Interview of Mental Status) exam. Review of Resident #80's clinical record revealed that Resident #80 obtained a blister on 6/30/19. The following nursing notes were written: 6/30/19 at 7:20 a.m.: resident (sic) came up to nursing station stating that she spilled coffee on L (left) pinky finger. L pinky finger was red, blister noted. Resident is her own RP (responsible party). (Name of MD (Medical Doctor) made aware. resident (sic) given tylenol (1). skin blanches. area is closed and not weeping. 6/30/19 2:03 p.m., Intact blister to left hand oinky (sic) finger, silvadene (2) applied per order. 7/1/19 1:23 p.m.: Wound assessment done by nurse: Resident was seen by wound care nurse for blister noted to left pinky finger. Spoke to resident concerning origin of non-intact blister, resident stated, I think I hit it on my w/c (wheelchair) When asked again within 5 minutes resident stated I hit my hand between the door and the wheelchair When asked if she had spilled coffee on herself resident stated no (sic) I think I hit my hand on door with my w/c Area dry no bleeding no drainage noted area 2 cm (centimeters) x 0.5 cm red in color with pigmented skin layer absent at this time. Review of Resident #80's July POS (physician order summary) revealed her wound care treatment was changed to the following order: Clean L (left) pinky with dermal wound cleanser, pat dry, and apply polymem (3) every three days prn (as needed) until healed. This order was discontinued on 7/19/19. Review of the facility's investigation related to Resident #80's blister revealed that her blister was obtained from trauma rather than a burn. Further review of Resident #80's clinical record revealed that the wound care physician had evaluated Resident #80 later that day on 7/1/19. The following note was written: [AGE] year old female with non-intact blister on her left 5th finger. Patient uncertain as to cause. She described to nurse a wheelchair injury. When questioned my (sic) MD (medical doctor) , she reported catching her finger against door jam. She then said it may have been a burn. When I questioned her as to the source of the burn, she was unclear. Given patient's medical history and changing story, etiology unreliable. The wound is superficial, with a non-intact blister with mildly reddened intact skin underneath blister, which is inconsistent with a burn and inconsistent with a crush injury. Given current appearance of the wound, etiology most likely an abrasion due to unknown cause .Plan: 1. Leave wound open to air . Review of Resident #80's physician orders revealed that facility staff failed to implement the wound care physician's recommendations to leave her abrasion/non-intact blister open to air. Review of Resident #80's July 2019 TAR (treatment administration record) revealed that facility staff continued dressing her abrasion/non-intact blister with a polymen dressing until 7/19/19, when the order was discontinued. Review of Resident #80's skin assessments failed to document when her abrasion/non-intact blister had healed. On 8/8/19 at 10:39 a.m., an interview was conducted with LPN (Licensed Practical Nurse) #1, the wound care nurse. When asked the process (how an order is implemented from the physician's recommendations), LPN #1 stated that she was the nurse responsible for writing orders from the wound care physician's recommendations. LPN #1 stated that the wound care physician's recommendations should be considered an order. LPN #1 stated that she had made the nurses aware of the new order verbally but that she forgot to write the order. LPN #1 stated that she didn't recall seeing a dressing on Resident #80's finger after the wound care physician's evaluation. When asked what check marks meant on the TAR, LPN #1 stated that check marks meant a treatment was administered. LPN #1 confirmed that Resident #80's July 2019 TAR revealed that staff were dressing her wound until 7/19/19. LPN #1 stated that the nurses could have just documented that they completed the dressing but didn't really do the dressing. When asked if it was okay to document that a treatment or medication was given when it was not, LPN #1 stated that it was not okay to document care that was not provided. When asked when Resident #80's wound had healed, LPN #1 stated that she would have to check her clinical record. This writer made LPN #1 aware that a note could not be found in Resident #80's clinical record. LPN #1 stated that she would try to find a note. On 8/8/19 at 11:36 a.m., interview was conducted with RN (Registered Nurse) #2, a floor nurse. When asked what check marks meant on the MAR (medication administration record)/TARs, RN #2 stated that check marks meant a medication and/or treatment was administered. When asked if it was okay to document that a treatment was administered when it was not administered, RN #2 stated that it was not okay to falsify records. On 8/8/19 at 11:49 a.m., an attempt was made to reach the nurse who documented that she administered the polymen treatments on 7/16/19 and 7/19/19. She could not be reached for an interview. On 8/8/19 at approximately 1:30 p.m., an interview was conducted with Resident #80. Resident #80 stated that she remembered having a dressing but was not sure how long she had the dressing to her finger. On 8/8/19 at 1:32 p.m., further interview was conducted with LPN #1. LPN #1 showed this writer her personal notepad. LPN #1 stated that Resident #80's wound had healed on 7/11/19 but that she forgot to document this assessment in the clinical record. LPN #1 confirmed that Resident #80's July 2019 TAR reflected that staff were still treating her wound on 7/16/19 and 7/19/19 even though her wound had healed on 7/11/19. LPN #1 gave this writer a late entry progress note dated 8/8/19 that documented in part, the following: Late Entry for 7/11/19: Resident pinky finger was assessed by wound nurse. At this time area light pink in color no open area noted no bleeding no drainage noted. Area blanchable at this time. Area presents as healed at this time. On 8/8/19 at 3:18 p.m., ASM (administrative staff member) #1, the Administrator, and ASM #2, the ADON (Assistant Director of Nursing) were made aware of the above concerns. CSM (Corporate staff member) #1 stated that the facility used [NAME] and/or their policies as a professional standard. Facility policy titled, Medication and Treatment Orders documents in part, the following: Medications shall be administered only upon the written order .Drug and biological orders must be recorded on the Physician's Order Sheet in the resident's chart. No further information was presented prior to exit. (1) Tylenol Tablet 325 mg (Acetaminophen)- Treats minor aches and pains and also reduces fever. This information was obtained from The National Institutes of Health. https://www.ncbi.nlm.nih.gov/pubmedhealth/PMHT0008785/?report=details. (2) Silvadene- topical antimicrobial used to prevent infections from burn wounds. This information was obtained from The National Institutes of Health. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935806/. (3) Polymem-dressing that is designed to facilitate healing, relieve pain and reduce inflammation. https://polymem.com.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Pressure Ulcer Prevention (Tag F0686)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review and facility document review the facility staff failed to provide ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interview, clinical record review and facility document review the facility staff failed to provide the necessary care and treatment to prevent and promote healing of a pressure injury for 1 of 56 residents in the survey sample, Resident #124. The findings include: Resident #124 was admitted to the facility on [DATE] with diagnoses to include but not limited to, stroke and diabetes. The current MDS (Minimum Data Set) an annual with an assessment reference date of 7/1/19 assessed the resident as having long and short term memory deficits. The resident required extensive assistance of two staff for bed mobility and dependent for transfers. Under section M. Skin Conditions the resident was coded as at risk for developing pressure ulcers/injuries and having a stage IV pressure injury (defined in the MDS as a full thickness tissue loss with exposed bone, tendon, or muscle. Slough, eschar may be present on some parts of the wound bed). On 8/7/19 at 12:33 p.m., an observation of the sacral dressing change was conducted. The resident was on a low air loss mattress. The facility wound nurse (Licensed Practical Nurse-LPN #9) performed the dressing change with Certified Nursing Assistant (CNA #6) who was providing assistance with maintaining the resident on her side. During the dressing change this surveyor observed that the resident's left heel was red. After completing the dressing change the wound nurse was asked about the residents left heel. She assessed the heel and it was found to have redness, the tissue was boggy and was not blanchable in the middle. The wound nurse stated she was not aware of this pressure injury and that the resident was utilizing the specialty heel float boots, and there had been a previous order for skin prep. The wound nurse assessed the left heel and documented that during the dressing change the resident was noted to have a reddened area to the left heel. The area was boggy, measuring 3.1 cm (centimeters) in length x 2.8 cm wide with no depth. The area was blanchable closer to the outer edges and .the center of area blanches with difficulty. The wound nurse ordered skin prep to be applied to the left heel every shift until healed as there had not been a treatment initiated. Further clinical record review evidenced the last documented skin inspection report by the nursing staff was 10/11/18. There was no documentation in the clinical record of the left heel pressure injury on 8/5/19, 8/6/19, or 8/7/19. The wound care physician had assessed the resident's sacral pressure ulcer on 8/5/19, the notes indicated the left lower extremity was normal. On 8/8/19 at 9:47 a.m., an interview with the wound nurse was conducted. She was asked to clarify what she meant by on her assessment that the area blanches with difficulty, she stated, It's a stage I non-blanchable .someone should have seen it before you saw it yesterday. She stated the skin inspections should be filled out weekly. She stated the weekly skin assessment schedule should be posted at the nurses station, she further stated, .since we have had turn over it may not have been conveyed. When asked who had oversight of the weekly wound assessment schedule to ensure they are being conducted she stated, The unit managers. The wound nurse stated during the resident shower days if the certified nurse aide (CNA) finds a skin concern she is to document it on the CNA Skin Check Form and then report the area found to the charge nurse. The charge nurse will then go and do an assessment of the area. The assessment should include a description of the area in the clinical record, if it is a pressure injury this is relayed to the wound nurse so that she can assess the wound. The wound nurse stated the floor nurses do not stage pressure injuries she does. A stage I pressure ulcer/injury is defined in the MDS as: Intact skin with non-blanchable redness of a localized area usually over a bony prominence. On 8/8/19 at 10:20 a.m., a review of the CNA Skin Check Form completed on 8/5/19 evidenced CNA #7 had identified reddened areas to Resident #124 heels. The nurse (Licensed Practical Nurse #8) who was assigned to care for the resident that shift was asked if she was notified or had reviewed the CNA Skin Check Form dated 8/5/19, she stated, No, I didn't see it. The nurse was asked where the weekly skin assessment schedule was located, she stated she did not know. The right side unit manager was asked where the weekly skin assessment schedule was posted for the nurses. She stated, I am in the process of making one now, I have to create a calendar. When asked where would I find in the clinical record the weekly skin assessments conducted by a licensed nurse, she stated, Honestly, I'm going to tell you that it has probably not been done. On 8/8/19 at 3:00 p.m., during the pre-exit meeting the above findings was shared with the Administrator and the Director of Nursing. The facility policy titled Prevention of Pressure Ulcers/Injuries revised July 2017 reads in part: Purpose-The purpose of this procedure is to provide information regarding identification of pressure ulcer/injury risk factors and interventions for specific risk factors. Risk Assessment: 1. Assess the resident on admission for existing pressure ulcer/injury risk factor. Repeat the risk assessment weekly and upon any changes in condition. The National Pressure Ulcer Advisory Panel, European Pressure Ulcer Advisory Panel and Pan Pacific Pressure Injury Alliance. Prevention and Treatment of Pressure Ulcers: Quick Reference Guide. [NAME] Haesler (Ed.). Cambridge Media: [NAME] Park, Australia; 2014. Page 17 reads, in part: 4. Include a comprehensive skin assessment as part of every risk assessment to evaluate any alterations to intact skin. 5. Document all risk assessments.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interviews, clinical record review and facility document review the facility staff failed to provide...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, staff interviews, clinical record review and facility document review the facility staff failed to provide a physician ordered safety device (a lidded cup) to promote safety for 1 of 56 residents in the survey sample, Resident #8. The findings include: Resident #8 was admitted to the facility on [DATE] with diagnoses to include but not limited to, legal blindness and history of major depressive disorder, recurrent, severe with psychotic symptoms. The current MDS (Minimum Data Set) a quarterly with an assessment reference date of 7/8/19 coded the resident as scoring a 6 out of a possible 15 on the Brief Interview for Mental Status (BIMS), indicating the resident had severely impaired cognition. The resident was coded as requiring limited assistance with one person physical assist with eating, and transfers, and extensive assistance with one person physical assist with bed mobility, personal hygiene and dressing. The resident had limited range of motion to both upper and lower extremities. The Comprehensive Person Centered Plan of Care dated 4/29/16 identified the resident had risk of injury due to visual impairment diagnosis of legal blindness. One of two goals was to ensure the resident would not have injuries thru the next review. One of the interventions was listed as: Keep the resident's environment free of small objects on the floor, very hot liquids and toxic liquids. The care plan did not include a hot safety beverage device such as a lidded cup. On 8/5/19 at 1:19 p.m., the resident was observed asleep in bed, the head of the bed was elevated. The bedside table was positioned over the resident's torso. The resident's gown was visibly wet from spilled coffee on the chest area. A regular mug of coffee without a lid was observed on the lunch tray almost empty. A nurses noted dated 8/5/19 entered at 6:11 p.m., read: Late entry for 1330 (1:30 p.m.): CNA (certified nursing assistant) reported that today at lunch resident spilled her coffee on her front of her gown. Nurse went in and immediately assessed resident's skin to her chest and abdomen, no redness or discoloration was noted. Resident asked about this and she stated, oh my coffee wasn't hot, it was cool, I am fine. MD (Medical Doctor) and RP (Representative Party) notified. Hot liquids safety evaluation done and resident is at risk for injury from spills of hot liquids. New order obtained for lidded cup for all hot liquids. This nurses note was entered by the Director of Nurses (DON). On 8/6/19 at 9:30 a.m., this surveyor and surveyor #1 observed the resident was in bed, awake. The resident was asked if she had eaten breakfast or drank her coffee already. She stated, No, I couldn't get the lid off (coffee cup). The resident stated she would like another cup of coffee. The two surveyors went to the nurses station (right side) and informed the staff of the resident's request. At this time CNA #5 stated she would get the resident a cup of coffee. The CNA came back from the kitchen with a cup of coffee, she stopped at the nurses station and asked if the resident needed a special cup for the coffee, she stated the staff did not respond to her. CNA #5 continued to the resident's room. Once inside the room the CNA stated she was not sure if the resident was to have the coffee in a regular mug, she questioned it and stated to the surveyor that the resident was blind and probably needed a lidded cup. When asked why, she stated, Because she is blind .so she doesn't spill it on herself and burn herself. The CNA stated, I don't normally work with her, it should be on the Closet Care Plan which is taped inside the resident's closet. The Resident's closet was opened and the CNA Care Plan was reviewed by surveyor and CNA. There was no reference for a lidded cup for all hot liquids. The CNA then proceeded to place sugar in the coffee and then handed the coffee to the resident. Once the coffee cup reached the resident's lips, the resident stated, It's too hot! The CNA then took the cup and was going to add cold water to it. At this time, this surveyor asked the CNA to hold off until the coffee temperature was obtained. Surveyor #1 then entered the room accompanied by the Dietary Manager, the coffee temperature was obtained, the thermometer reading stopped between the 152 degree mark and the 154 degree mark, indicating the coffee was 153 degrees Fahrenheit. The CNA was asked if the kitchen staff had obtained the coffee temperature prior to handing it off to her, she stated, No. The Dietary Manager stated the kitchen staff should have obtained the resident's coffee temperature prior to it leaving the kitchen, he further stated coffee should not be higher than 150 degrees Fahrenheit when released to the floors. The Dietary Manager stated the kitchen had received a new order yesterday evening for the resident to be served all hot beverages in a lidded cup. CNA #5 stated she was not aware of this new order. At this time both surveyors went to the kitchen. Two kitchen staff were interviewed. Food Service Worker #10, who was in the process of washing dishes stated she had placed on the tray a lidded cup with coffee to be served to the resident this morning for breakfast. Food Service Worker #11, who handed the coffee in a regular mug to CNA #5 stated she was not told nor did she ask who the coffee was for. She also stated she did not temp the coffee before it left the kitchen. The Dietary Manager was asked how many lidded cups were in the facility and stated, We have 7 lidded cups and 3 residents that use them currently, including Resident #8. The facility policy titled Safety of Hot Liquids revised 10/2014 was reviewed. The policy indicated a Hot Liquid Safety Evaluation was be to completed on all residents upon admission, readmission and on change in condition. A Hot Liquid Safety Evaluation had never been done for Resident #8. The policy further reads, in part: 1. The potential for burns from hot liquids is considered an ongoing concern among residents with weakened motor skills, balance issues, impaired cognition, and nerve or musculoskeletal conditions. 4. Once risk factors for injury from hot liquids are identified, appropriate interventions will be implemented to minimize the risk from burns. Such interventions may include: a. Maintaining a hot liquids serving temperature of not more than 150 degrees Fahrenheit; b. Serving hot beverages in a cup with a lid; 5. Food service staff will monitor and maintain foods temperatures that comply with food safety requirements but do not exceed recommended temperatures to prevent scalding. Table 1. Time and Temperatures Relationship to Serious Burns-Time Required for a 3rd Degree Burn to Occur for temperatures between 148 and 155 degrees Fahrenheit is 1-2 seconds. Referenced from http://www.bt.cdc.gov/masscasualties/burns.asp The facility Incident Report dated 8/6/19 for Resident #8 read in part and was signed by the right side unit manager: Narrative of description of injuries (use additional pages, if needed): Resident received lidded cup (with) her coffee on breakfast tray-resident received another cup of coffee in a regular cup. On 8/6/19 at approximately 10:50 a.m. the Administrator and Director of Nursing were informed of the findings.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0757 (Tag F0757)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility document review and clinical record review, it was determined that facility staff failed to e...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility document review and clinical record review, it was determined that facility staff failed to ensure one of 56 residents (Resident #128) in the survey sample was free from unnecessary medication; specifically excess units of insulin. The findings included: Resident #128 was admitted to the facility on [DATE], with the most recent readmission on [DATE]. The resident was on hospice care as of 8/4/2019. The latest diagnoses included, but not limited to, type 2 diabetes mellitus with diabetic neuropathy, and pseudocyst of pancreas, and morbid obesity. Resident #128's most recent MDS (minimum data set) assessment was a 14 day scheduled assessment with an ARD (assessment reference date) of 7/9/19. Resident #128 was coded as being intact in cognitive function scoring 15 out of possible 15 on the BIMS (brief interview for mental status) exam. A review of Resident #128's comprehensive care plan dated 8/1/2019 revealed, in part, the following documentation: Problem / Need. Risk for hyper/hypoglycemia (high/low blood sugar) r/t (related to) diabetes. Resident #128 will remain free from complications associated with Diabetes through next review. Approaches include: Continue diet as ordered; Monitor intake and encourage dietary compliance; Monitor for thirst, excessive appetite, and excessive voiding; Monitor blood sugars as ordered and notify MD (medical doctor) per order; Administer medications as ordered. A review of Resident #128's physician orders, dated 7/30/2019, revealed in part, the following order related to the treatment of diabetes: Humalog (1) 10 units/ml. Generic: Insulin Lispro Kwikpen inject subq (subcutaneous) ac (with meals) & hs (at bedtime) per sliding scale: 100-125=2u (units) 126-200=4u 201-249=6u 250-299=8u 300-349=10u 350-400=12u >401=14u Review of Resident #128's August 2019 medication administration record (MAR) revealed that on 8/6/19, Resident #128's blood glucose level measured 163 at 7:30 a.m The nurse gave 10 units of sliding scale insulin which was 6 extra units of insulin. Further review of Resident #128's clinical record revealed no negative outcome from this deficient practice. Resident #128's blood sugar measured 171 at 11:30 a.m. On 8/8/19 at 11:36 a.m., a phone interview was conducted with RN (Registered Nurse) #2, the nurse who administered the 6 extra units of insulin. RN #2 was asked what the check marks indicate on the MAR. RN #2 stated, Check marks mean that it was given. When asked, what it means to administer medications on a sliding scale, RN #2 stated, Those are units given per order. When asked regarding the 10 units of Humalog administered on 8/6/2019 for a blood glucose level of 163, RN #2 stated, I don't recall that. When asked what are the negative outcomes of administering the wrong number of units of Humalog, staff #2 responded, sugar would drop, go into a coma. On 8/8/19 at approximately 2:20 p.m., a phone interview was conducted with other staff member (OSM) #5, the pharmacist. When asked if there would be any negative side effects for administering 10 units, vs the ordered 4 units of Humalog for a blood sugar of 163, OSM #5 stated, 10 units is not that high, should have checked 30 minutes after administration; could become hypoglycemic; a significant med error. There was no record of a blood sugar check 30 minutes after the administration of 10 units of Humalog on 8/6/2019. On 8/8/19 at 3:18 p.m., an interview was conducted with administrative staff member (ASM) #2, the ADON (assistant director of nursing). When asked the side effects of administering 10 units of Humalog vs. the ordered 4 units for a blood sugar reading of 163, ASM #2 stated that six extra doses was not significant but that resident could possibly become hypoglycemic. On 8/8/19 at 3:18 p.m., ASM #1, the administrator and ASM #2, the ADON (Assistant Director of Nursing) were made aware of the above concerns. Heritage Hall policy on Administering Medications (revised December 2016) states: (3). Medications must be administered in accordance with the orders, including any required time frame. (20). As required or indicated for a medication, the individual administering the medication will record in the resident's medical record: a. The date and time the medication was administered; b. The dosage; c. The route of administration; d. The injection site (if applicable); e. Any complaints or symptoms for which the drug was administered; f. Any results achieved and when those results were observed; and g. The signature and title of the person administering the drug. (1) HUMALOG is a rapid acting human insulin analog indicated to improve glycemic control in adults and children with diabetes mellitus. This information was obtained from The National Institutes of Health.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0760 (Tag F0760)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility document review and clinical record review, it was determined that facility staff failed to e...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility document review and clinical record review, it was determined that facility staff failed to ensure one of 56 residents was free from a significant medication error, Resident #128. The findings included: Resident #128 was admitted to the facility on [DATE], with the most recent readmission on [DATE]. The Resident was placed on hospice care as of 8/4/2019. The diagnoses included, but not limited to, type 2 diabetes mellitus with diabetic neuropathy, pseudocyst of pancreas, and morbid obesity. Resident #128's most recent MDS (minimum data set) assessment was a 14 day scheduled assessment with an ARD (assessment reference date) of 7/9/19. Resident #128 was coded as being intact in cognitive function scoring 15 out of possible 15 on the BIMS (brief interview for mental status) exam. A review of Resident #128's comprehensive care plan dated 8/1/2019 revealed, in part, the following documentation: Problem / Need. Risk for hyper/hypoglycemia (high/low blood sugar) r/t (related to) diabetes. (Resident #128) will remain free from complications associated with Diabetes through next review. Approaches include: Continue diet as ordered; Monitor intake and encourage dietary compliance; Monitor for thirst, excessive appetite, and excessive voiding; Monitor blood sugars as ordered and notify MD (medical doctor) per order; Administer medications as ordered. A review of Resident #128's physician orders, dated 7/30/2019, revealed, in part, the following order related to the treatment of diabetes: Humalog (1) 10 units/ml. Generic: Insulin Lispro Kwikpen inject subq (subcutaneous) ac (with meals) & hs (at bedtime) per sliding scale: 100-125=2u (units) 126-200=4u 201-249=6u 250-299=8u 300-349=10u 350-400=12u >401=14u Review of Resident #128's August 2019 medication administration record (MAR) revealed that on 8/6/19, Resident #128's blood glucose level measured 163 at 7:30 a.m The nurse gave 10 units of sliding scale insulin which resulted in 6 extra units of insulin being administered. Further review of Resident #128's clinical record revealed no negative outcome from this deficient practice. Resident #128's blood sugar measured 171 at 11:30 a.m. On 8/8/19 at 11:36 a.m., a phone interview was conducted with RN (Registered Nurse) #2, the nurse who administered the 6 extra units of insulin. RN #2 was asked what the check marks indicate on the MAR. RN #2 stated, Check marks mean that it was given. When asked, what it means to administer medications on a sliding scale, RN #2 stated, Those are units given per order. When asked regarding the 10 units of Humalog administered on 8/6/2019 for a blood glucose level of 163, RN #2 stated, I don't recall that. When asked what are the negative outcomes of administering the wrong number of units of Humalog, staff #2 responded, sugar would drop, go into a coma. On 8/8/19 at approximately 2:20 p.m., a phone interview was conducted with other staff member (OSM) #5, the pharmacist. When asked if there would be any negative side effects for administering 10 units, vs the ordered 4 units of Humalog for a blood sugar of 163, OSM #5 stated, 10 units is not that high, should have checked 30 minutes after administration, could become hypoglycemic. A significant med error. There was no record of a blood sugar check 30 minutes after the administration of 10 units of Humalog on 8/6/2019. On 8/8/19 at 3:18 p.m., an interview was conducted with administrative staff member (ASM) #2, the ADON (Assistant Director of Nursing). When asked the side effects of administering 10 units of Humalog vs. the ordered 4 units for a blood sugar reading of 163, ASM #2 stated that six extra doses was not significant but that resident could possibly become hypoglycemic. On 8/8/19 at 3:18 p.m., ASM #1, the Administrator and ASM #2, the ADON were made aware of the above concerns. Heritage Hall policy on Administering Medications (revised December 2016) states: (3). Medications must be administered in accordance with the orders, including any required time frame. (20). As required or indicated for a medication, the individual administering the medication will record in the resident's medical record: a. The date and time the medication was administered; b. The dosage; c. The route of administration; d. The injection site (if applicable); e. Any complaints or symptoms for which the drug was administered; f. Any results achieved and when those results were observed; and g. The signature and title of the person administering the drug. (1) HUMALOG is a rapid acting human insulin analog indicated to improve glycemic control in adults and children with diabetes mellitus. This information was obtained from The National Institutes of Health. https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f . Review of Davis's Drug Guide for Nurses 11th edition documents in part, the following: High Alert: Insulin -related medication errors have resulted in patient harm and death .Check type, dose, and expiration date with another licensed nurse .Toxicity and Overdose: Overdose is manifested by symptoms of hypoglycemia. Mild hypoglycemia may be treated by ingestion of oral glucose. Severe hypoglycemia is a life-threatening emergency; treatment consists of IV (intravenous) glucose, glucagon, or epinephrine .symptoms of hypoglycemia (anxiety; restlessness; tingling in hands, feet, lips or tongue; chills, cold sweats, confusion, cool, pale skin; difficulty in concentration; drowsiness .rapid heart rate, tremor, weakness, unsteady gait.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and staff interviews the facility staff failed to maintain infection prevention for 2 of 56 residents in t...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and staff interviews the facility staff failed to maintain infection prevention for 2 of 56 residents in the survey sample. For Resident #12 the facility staff failed to perform wound care in a manner to prevent infection; and for Resident #129 the facility staff failed to maintain Foley catheter tubing and bag in a manner in accordance with infection control standards and practices. The findings included: 1. Resident #12 was originally admitted to the facility 08/19/10 and readmitted on [DATE]. Resident #12's diagnoses included Diabetes Mellitus without complications and Essential Hypertension. The Quarterly Revision Minimum Data Set (MDS) assessment with an assessment reference date (ARD) of 04/16/19 coded the resident as having short term and long term memory problems. In section G (Physical functioning) the resident was coded as needing limited physical assistance bed mobility, limited assistance with transfers, supervision with locomotion, limited assistance with dressing, limited assistance with eating, one person physical assistance with toileting, personal hygiene and bathing. On 08/07/19 at approximately 9:48 AM Resident #12 was receiving wound care to his right heel by LPN (Licensed Practical Nurse) #1. As she removed the soiled kerlix dressing the resident's right heel rested on the resident's bed sheet. LPN #1 then asked Resident #12 if he was ok, he stated yes. She received assistance from CNA #7, to help raise up resident's right foot She then preceded to clean his right heel wound without difficulty. On 8/07/19 at approximately 10:10 AM with LPN #1 concerning the above issue. She stated There should have been a pad placed under him when I removed the dressing and should have placed a pad under his foot. A review of physician orders read as follows: Cleanse right heel wound with DWC pat dry, lightly pack with dakins moistened gauze wrap with rolled kerlix gauze every day and as needed. On 08/08/19 at approximately 4:22 PM an interview was conducted with LPN #10. She was asked if she was providing wound care on a resident's heel how would she proceed with it? I would have someone assist me to elevate the resident's heel. I would rest their heel on a drape. Wound Care Policy: Purpose: The purpose is to provide guidelines for the care of wounds to promote healing. Preparation: Assemble the equipment and supplies as needed. Equipment and Supplies: Disposable cloths, as indicated. Steps in the Procedure: #3 Position resident. Place disposable cloth next to resident (under the wound) to serve as a barrier to protect the bed linen and other body sites. On 08/08/19 at approximately, 3:00 PM a pre-exit interview was conducted. Present were DON and Administrator. No comments were made. 2. Resident # 129 was originally admitted to the facility for skilled services on 7/5/19 following a fall at home resulting in a left hip fracture and then readmitted on [DATE] after a hospitalization with diagnosis of Foley related sepsis Urinary Tract Infection (UTI), other diagnoses included neurogenic bladder (a dysfunction of the bladder) and dementia. The current MDS a 14 day with a assessment reference date of 7/19/19 coded the resident as having long and short term memory deficits and severely impaired cognitive skills for daily decision making. The resident was coded as having an indwelling Foley catheter (a plastic tube inserted into the bladder to drain urine). The Person Centered Plan of Care dated 8/1/19 for Resident #129 identified that the resident was at risk for injury related to the presence of an indwelling catheter related to neurogenic bladder, the resident removes his catheter securement device and pulls at catheter. The interventions did not include approaches to handle the tubing or Foley drainage bag in a manner to prevent catheter-associated urinary tract infections. 08/4/19 at 4:04 p.m., observed during the initial tour and again on 8/5/19 at 10:26 a.m., 11:43 a.m., 1:12 p.m. and 1:33 p.m. the Foley drainage bag was attached to the side of the bed, the bed was being maintained in the low position due to the resident's fall risk, the drainage bag and tubing were observed on the floor. On 8/6/19 at approximately 9:15 a.m., and 4:00 p.m., the resident was observed in bed in low position with the Foley catheter tubing and drainage bag on the floor. On 8/7/19 at 9:50 a.m., the resident was observed in a wheelchair being transported to the rehab therapy room by the private sitter. The Foley bag was observed to be in contact with the floor during the transport. At 4:06 p.m., the resident was observed sitting up in the wheelchair in front of the nurses station. The Foley drainage bag was attached under the wheelchair seat but not high enough to prevent it from making contact with the floor. On 8/8/19 at 10:13 a.m., the resident was observed asleep in bed, the Foley drainage bag and tubing were on the floor. At this time the right side unit manager was asked to come into the room. When asked if the Foley catheter bag and tubing should be making contact with the floor she stated, Absolutely not. When asked why, she stated, Because of the germs. She then stated, Thank you and I will take care of it. On 8/8/19 at 3:00 p.m., during the pre-exit meeting the above findings was shared with the Administrator and the Director of Nursing. The facility policy and procedure titled Catheter Care, Urinary revised September 2016 read as follows: Purpose-The purpose of this procedure is to prevent catheter-associated urinary tract infections. Infection Control: 2.b. Be sure the catheter tubing and drainage bag are kept off the floor. No additional information was provided prior to exit.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Transfer Requirements (Tag F0622)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Resident #128 was admitted to the facility on [DATE], with transfers to the hospital occurring on 6/1/2019, 6/16/2019 6/21/20...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Resident #128 was admitted to the facility on [DATE], with transfers to the hospital occurring on 6/1/2019, 6/16/2019 6/21/2019 and 7/21/2019. Diagnoses included, but not limited to, type 2 diabetes mellitus with diabetic neuropathy, diastolic heart failure, respiratory failure with hypoxia, stage 4--chronic kidney disease, hypokalemia, chronic ischemic heart disease, pseudocyst of pancreas, and morbid obesity. Resident #128's most recent MDS (minimum data set) assessment was a 14 day scheduled assessment with an ARD (assessment reference date) of 7/9/19. Resident #128 was coded as being intact in cognitive function scoring 15 out of possible 15 on the BIMS (brief interview for mental status) exam. There was no evidence that the required documentation; physician contact information, responsible party contact information, advanced directives, or the care plan goals were sent with the resident at the time of transfer on 6/1/2019, 6/16/2019, and 6/21/2019. On 8/8/2019 at approximately 3:20 p.m. an interview was conducted with ASM (administrative staff member) #3, the ADON (Assistant Director of Nursing), requesting evidence, upon transfer, of advanced directives, instructions for ongoing care, care plan goals physician contact information, responsible party information; yielded a transfer summary for a hospital transfer that occurred on 7/21/2019. There was no additional documentation submitted by ASM #3. Additionally, clinical record reviews conducted yielded no evidence that the referenced, required information was sent upon transfer to the hospital on 6/1/2019, 6/16/2019, and 6/21/2019. Heritage Hall policy on Transfer or Discharge Documentation (revised December 2016) includes: (4) When a resident is transferred or discharged from the facility, the following information will be documented in the medical record: a. The basis for the transfer or discharge; (1) If the resident is being transferred or discharged because his or her needs cannot be met at the facility, documentation will include: (a) the specific resident needs that cannot be met; (b) this facility's attempt to meet those needs; and (c) the receiving facility's service(s) that are available to meet those needs. b. That an appropriate notice was provided to the resident and/or legal representative; c. The date and time of the transfer or discharge; d. The new location of the resident; e. The mode of transportation; f. A summary of the resident's overall medical, physical, and mental condition; g. Disposition of personal effects; h. Disposition of medications; i. Others as appropriate or as necessary; and j. The signature of the person recording the data in the medical record. 7. Should a resident be transferred or discharged for any reason, the following information will be communicated to the receiving facility or provider: a. The basis for transfer or discharge; (1) If the resident is being transferred or discharge because his or her needs cannot be met at the facility, documentation will include: (a) the specific resident needs that cannot be met; (b) this facility's attempt to meet those needs; and (c) the receiving facility's service(s) that are available to meet those needs. b. Contact information of the practitioner responsible for the care of the resident; c. Resident representative information including contact information; d. Advance Directive information; e. All special instructions or precautions for ongoing care, as appropriate; f. Comprehensive care plan goals; and g. All other necessary information, including a copy of the residents discharge summary, and any other documentation, as applicable, to ensure a safe and effective transition of care. 2. Resident #61 was admitted to the facility on [DATE] and readmitted to the facility on [DATE]. Diagnoses for Resident #61 included but not limited to Alzheimer's disease and anxiety disorder. The current Minimum Data Set (MDS), was a discharge assessment with an Assessment Reference Date (ARD) of 02/11/19. Staff assessment of mental status coded the resident as having short term memory problems. The Discharge MDS assessments was dated for 02/11/19 - discharge return anticipated; re-admitted to the facility on [DATE]. On 02/11/19, according to the facility's documentation, EMS (Emergency Medical Services) exited the facility with (Resident #61) for transport to the hospital. On 08/08/19 the policy entitled Transfer or Discharge, Emergency was reviewed and included the following: Policy Statement: Emergency Transfers or discharges may be necessary to protect the health and/or well being of the residents. Policy Interpretation and Implementation: #4 Reads: Should it become necessary to make an emergency transfer or discharge to a hospital or other related institution, our facility will implement the following procedures: Prepare a transfer form to send with the resident. On 08/08/19 at approximately 3:00 PM a pre-exit interview was conducted with the Administrator and Director of Nursing they were informed of the above findings. They were asked what should have been done? The DON commented, We send the care plan but we were not documenting it in the nurses note. Based on medical record review, staff interviews, and facility document review, the facility staff failed to send the comprehensive care plan goals upon transfer to the hospital for 3 of 56 residents in the survey sample (Residents #101, #61, and #128). The findings included: 1. Resident #101 was originally admitted to the facility on [DATE] and was re-admitted on [DATE] with diagnoses to include but not limited to Functional Quadriplegia and End Stage Renal Disease. Resident #101's most recent Minimum Data Set (MDS) is a Quarterly with an Assessment Date (ARD) of 6/20/19. The Brief Interview for Mental Status (BIMS) was a 15 out of a possible 15 which indicated that Resident #101 is cognitively intact and capable of daily decision making. Resident #101's Detail Discharge Report was review and is documented in part, as follows: 1/18/19 Discharge to Hospital. 3/25/19 Discharge to Hospital. 5/7/19 Discharge to Hospital. 7/18/19 Discharge to Hospital. 7/21/19 Discharge to Hospital. 7/26/19 Discharge to Hospital. A medical record review indicated no documentation that comprehensive care plan goals were sent on 1/18/19, 3/25/19, 7/18/19, and 7/21/19 upon Resident #101's transfers to the hospital. On 8/8/19 at 11:30 A.M. an interview was conducted with the Director of Nursing regarding Resident #101's comprehensive care plan goals not being sent upon transfer to the hospital. The Director of Nursing stated, The care plan is a part of the Transfer Discharge Summary in the computer and I cannot find documentation for these dates. I was not aware that we had to document that the care plan goals were sent when we send a resident out. On 8/7/19 at 3:00 a pre-exit debriefing was held with the Administrator and the Director of Nursing where the above information was shared. Prior to exit no further information was provided.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0625 (Tag F0625)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Resident #128 was admitted to the facility on [DATE], with transfers to the hospital occurring on 6/1/2019, 6/16/2019 6/21/20...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Resident #128 was admitted to the facility on [DATE], with transfers to the hospital occurring on 6/1/2019, 6/16/2019 6/21/2019 and, 7/21/2019. Diagnoses included, but not limited to, type 2 diabetes mellitus with diabetic neuropathy, diastolic heart failure, respiratory failure with hypoxia, stage 4-chronic kidney disease, hypokalemia, chronic ischemic heart disease, pseudocyst of pancreas, and morbid obesity. Resident #128's most recent MDS (minimum data set) assessment was a 14 day scheduled assessment with an ARD (assessment reference date) of 7/9/19. Resident #128 was coded as being intact in cognitive function scoring 15 out of possible 15 on the BIMS (brief interview for mental status) exam. On 8/8/19 at approximately 10:40 a.m. a face-to-face interview conducted with Licensed Practical Nurse (LPN) when asked when bedholds were submitted, stated, the nurses send the bedholds. On 8/8/2019 at approximately 3:35 p.m. upon inquiry regarding documentary evidence of bedhold notification to the receiving provider, the Assistant Director of Nursing (ADON) responded, We were not aware that bedhold notification is sent with the residents upon transfer. Clinical record reviews conducted yielded no evidence that the required bedhold information was sent upon transfer to the hospital on 6/1/2019, 6/16/2019, 6/21/2019 and 7/21/2019. Facility policy on Transfer or Discharge Documentation (revised December 2016) states: 7. Should a resident be transferred or discharged for any reason, the following information will be communicated to the receiving facility or provider: a. The basis for transfer or discharge; (1) If the resident is being transferred or discharge because his or her needs cannot be met at the facility, documentation will include: (a) the specific resident needs that cannot be met; (b) this facility's attempt to meet those needs; and (c) the receiving facility's service(s) that are available to meet those needs. b. Contact information of the practitioner responsible for the care of the resident; c. Resident representative information including contact information; d. Advance Directive information; e. All special instructions or precautions for ongoing care, as appropriate; f. Comprehensive care plan goals; and g. All other necessary information, including a copy of the residents discharge summary, and any other documentation, as applicable, to ensure a safe and effective transition of care. Facility policy on Bed-Holds and Returns (revised March 2017) states: Policy Statement: Prior to transfers and therapeutic leaves, residents or resident representatives will be informed in writing of the bed-hold and return policy. 3. Prior to a transfer written information will be given to the residents and the resident representatives that explains in detail: a. The rights and limitations of the resident regarding bed-holds; b. The reserve bed payment policy as indicated by the state plan (non-Medicaid residents), or to hold a bed beyond the state bed-hold period (Medicaid residents); and d. The details of the transfer (per the Notice of Transfer). 2. Resident #61 was admitted to the facility on [DATE] and readmitted to the facility on [DATE]. Diagnoses for Resident #61 included but not limited to, Alzheimer's disease and Anxiety Disorder. The current Minimum Data Set (MDS), was a discharged assessment with an Assessment Reference Date (ARD) of 02/11/19. Staff assessment of mental status coded the resident as having short term memory problems. The Discharge MDS assessments was dated for 02/11/19 - discharge return anticipated; re-admitted to the facility on [DATE]. On 08/08/19 at approximately 3:00 PM a pre-exit interview was conducted with the Administrator and Director of Nursing they were informed of the above findings. They were asked what should have been done? The DON commented, We do issue the bed hold notice, but we were not documenting it in the nurses note. Based on medical record review, staff interviews, and facility document review the facility staff failed to send Bed Hold Notices upon transfer to the hospital for 4 of 56 residents in the survey sample, Residents #101, #61, #129 and #128. The findings included: 1. Resident #101 was originally admitted to the facility on [DATE] and was re-admitted on [DATE] with diagnoses to include but not limited to Functional Quadriplegia and End Stage Renal Disease. Resident #101's most recent Minimum Data Set (MDS) is a Quarterly with an Assessment Date (ARD) of 6/20/19. The Brief Interview for Mental Status (BIMS) was a 15 out of a possible 15 which indicated that Resident #101 is cognitively intact and capable of daily decision making. Resident #101's Detail Discharge Report was review and is documented in part, as follows: 1/18/19 Discharge to Hospital. 3/25/19 Discharge to Hospital. 5/7/19 Discharge to Hospital. 7/18/19 Discharge to Hospital. 7/21/19 Discharge to Hospital. 7/26/19 Discharge to Hospital. A medical record review indicated no documentation that Bed Hold Notices were sent on 1/18/19, 3/25/19, 5/7/19, 7/18/19, 7/21/19 and 7/26/19 upon Resident #101's transfers to the hospital. On 8/8/19 at 11:30 A.M. an interview was conducted with the Director of Nursing regarding Resident #101's Bed Hold Notices not being sent upon transfer to the hospital on 1/18/19, 3/25/19, 5/7/19 7/18/19, 7/21/19 and 7/26/19. The Director of Nursing stated, Our Bed Hold Notice is in our green transfer packet that we sent with the resident on discharge. I was not aware that we had to document that the Bed Hold Notice was sent when we send a resident out. On 8/7/19 at 3:00 a pre-exit debriefing was held with the Administrator and the Director of Nursing where the above information was shared. Prior to exit no further information was provided. 3. Resident #129 was originally admitted to the facility for skilled services on 7/5/19 following a fall at home resulting in a left hip fracture and then readmitted on [DATE] after a hospitalization with diagnosis of Foley related sepsis Urinary Tract Infection (UTI), other diagnoses included neurogenic bladder (a dysfunction of the bladder) and dementia. The current MDS (Minimum Data Set) a 14 day with an assessment reference date of 7/19/19 coded the resident as having long and short term memory deficits and severely impaired cognitive skills for daily decision making. The clinical record face sheet evidenced the resident was not his own responsible party. The resident representative was listed as a son. The resident was sent out to the emergency room and admitted to the hospital for a change in condition on 7/28/19. The resident was re-admitted to the facility on [DATE]. There was no evidence in the clinical record that the written notice which describes the bed-hold policy was provided to the resident representative at the time of transfer to the hospital on 7/28/19. On 8/6/19 at 4:15 p.m., the two nurses on the right side unit were interviewed (Licensed Practical Nurse/LPN #7 & #8). They were asked about the transfer process and bed hold policy written notification. LPN #8 stated they attempt to get the notice signed before the resident is transferred and if not the facility gets it signed as soon as possible. When asked about the policy they stated they do not document in the record that it was provided. On 8/8/19 at 3:00 p.m., during the pre-exit meeting with the Administrator and the Director of Nursing the above findings was shared. They stated that the bed hold policy and the care plan do go with the resident upon transfer, however could not provide evidence that the policy was sent. No additional information was provided prior to exit.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0657 (Tag F0657)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility document review, and clinical record review, it was determined that facility staff failed to ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, facility document review, and clinical record review, it was determined that facility staff failed to revise the care plan for three of 56 residents in the survey sample, Resident #80, #134, and #121. The findings included: 1. Facility staff failed to revise the care plan when it was determined her left pinky blister was caused from trauma rather than a burn on 7/2/19; and failed to revise the care plan when the blister had healed on 7/11/19. Resident #80 was admitted to the facility on [DATE] with diagnoses that included but were not limited to, Parkinson's disease, convulsions, and Schizophrenia. Resident #80's most recent MDS (minimum data set) assessment was a quarterly assessment with an ARD (assessment reference date) of 4/2/19. Resident #80 was coded as being intact in cognitive function scoring 15 out of possible 15 on the BIMS (Brief Interview of Mental Status) exam. Review of Resident #80's clinical record revealed that Resident #80 obtained a blister on 6/30/19. The following nursing notes were written: 6/30/19 at 7:20 a.m.: resident (sic) came up to nursing station stating that she spilled coffee on L (left) pinky finger. L pinky finger was red, blister noted. Resident is her own RP (responsible party). (Name of Medical Doctor) made aware. resident (sic) given tylenol. skin blanches. area is closed and not weeping. 6/30/19 2:03 p.m., Intact blister to left hand oinky (sic) finger, silvadene (1) applied per order. 7/1/19 1:23 p.m.: Wound assessment done by nurse: Resident was seen by wound care nurse for blister noted to left pinky finger. Spoke to resident concerning origin of non-intact blister, resident stated, I think I hit it on my w/c (wheelchair) When asked again within 5 minutes resident stated I hit my hand between the door and the wheelchair When asked if she had spilled coffee on herself resident stated no (sic) I think I hit my hand on door with my w/c Area dry no bleeding no drainage noted area 2 cm (centimeters) x 0.5 cm red in color with pigmented skin layer absent at this time. Review of Resident #80's July POS (physician order summary) revealed her wound care treatment was changed to the following order: Clean L (left) pinky with dermal wound cleanser, pat dry, and apply polymem (2) every three days prn (as needed) until healed. This order was discontinued on 7/19/19. Review of the facility's investigation related to Resident #80's blister revealed that her blister was obtained from trauma rather than a burn. Further review of Resident #80's clinical record revealed that the wound care physician had evaluated Resident #80 later that day on 7/1/19. The following note was written: [AGE] year old female with non-intact blister on her left 5th finger. Patient uncertain as to cause. She described to nurse a wheelchair injury. When questioned my (sic) MD (medical doctor) , she reported catching her finger against door jam. She then said it may have been a burn. When I questioned her as to the source of the burn, she was unclear. Given patient's medical history and changing story, etiology unreliable. The wound is superficial, with a non-intact blister with mildly reddened intact skin underneath blister, which is inconsistent with a burn and inconsistent with a crush injury. Given current appearance of the wound, etiology most likely an abrasion due to unknown cause .Plan: 1. Leave wound open to air . Review of Resident #80's skin assessments failed to document when her abrasion/non-intact blister had healed. Review of Resident #80's care plan dated 6/30/18 documented the following: At Risk for Impaired Skin integrity r/t (related to) history of burn to pinky finger .Change dressing as per orders. Ensure resident had lid on coffee. Monitor site for s/s (signs/symptoms) of infections and report any to MD (medical director). The care plan was not revised once it was determined that her blister was caused from trauma rather than a burn. The care plan was also not revised once her blister was healed. On 8/8/19 at 10:39 a.m., an interview was conducted with LPN (licensed practical nurse) #1, the wound care nurse. When asked the cause of Resident #80's blister, LPN #1 stated that it was from trauma and that the facility had conducted an investigation and interviewed staff and the resident regarding her blister. When asked the purpose of the care plan, LPN #1 stated the purpose of the care plan was to address the needs of each resident. When asked if it was important that it was accurate, LPN #1 stated that it was. When asked who was responsible for revising the care plan, LPN #1 stated that she did not revise the care plan that MDS was responsible for revising the care plan. When asked how MDS is made aware of any change with a resident's condition, LPN #1 stated that the floor nurses tell MDS. This writer showed LPN #1 Resident #80;s care plan. When asked if her care plan should have been revised to reflect that her blister was from trauma and not burns, LPN #1 stated that it should have been. When asked if Resident #80 still had a blister, LPN #1 stated that she did not. When asked when her blister had healed, LPN #1 stated that she wasn't sure but had to check Resident #80's clinical record. This writer made LPN #1 aware that a note could not be found in Resident #80's clinical record. LPN #1 stated that she would try to find a note. On 8/8/19 at 1:32 p.m., further interview was conducted with LPN #1. LPN #1 showed this writer her personal notepad. LPN #1 stated that Resident #80's wound had healed on 7/11/19, but that she forgot to document this assessment in the clinical record. When asked if Resident #80's care plan should have also been revised to reflect that her blister had healed, LPN #1 stated that the care plan should have been revised. LPN #1 gave this writer a late entry progress note dated 8/8/19 that documented in part, the following: Late Entry for 7/11/19: Resident pinky finger was assessed by wound nurse. At this time area light pink in color no open area noted no bleeding no drainage noted. Area blanchable at this time. Area presents as healed at this time. On 8/8/19 at 3:18 p.m., ASM (administrative staff member) #1, the administrator, and ASM #2, the ADON (Assistant Director of Nursing) were made aware of the above concerns. No further information was presented prior to exit. (1) Silvadene- topical antimicrobial used to prevent infections from burn wounds. This information was obtained from The National Institutes of Health. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935806/. (2) Polymem-dressing that is designed to facilitate healing, relieve pain and reduce inflammation. https://polymem.com. 2. Facility staff failed to revise the care plan after a fall with fracture on 6/30/18 for Resident #134. Resident #134 was admitted to the facility on [DATE] with diagnoses that included but were not limited to Alzheimer's disease, dementia, high blood pressure and cerebral aneurysm. Resident #134's most recent MDS (Minimum Data Set) assessment was a quarterly assessment with an ARD (assessment reference date) of 6/3/18. Resident #134 was coded as being severely impaired in cognitive function scoring 00 out of possible 15 on the BIMS (Brief Interview for Mental Status) exam. Resident #134 was coded as requiring extensive assistance with two plus persons with transfers. Resident #134 was also coded in Section G (functional status) as Not Steady, only able to stabilize with staff assistance with surface to surface transfers (transfer between bed and chair or wheelchair. Review of Resident #134's clinical record revealed that she had a fall on 6/30/18. It was revealed that Resident #134 had fallen because she got up unassisted. The following was documented in a nursing note: While CNA (certified nursing assistant) was moving chair to assist into chair. (sic) resident stood up and fell on fall mat. resident (sic) has complaints of L (left knee) pain. no (sic) swelling noted. resident does have some pain with movement. motrin (1)(sic) given. Review of Resident #134's care plan dated 5/2/16 revealed that Resident #134 had the following fall preventive interventions in place prior to her fall on 6/30/18: pressure alarm at all times, Hi/low bed with fall mat . Review of Resident #134's nursing [NAME] (care plan for nursing aides) revealed the following fall preventive interventions were in place as of 6/11/18: Pressure alarm at all times, gel pommel cushion to wheelchair, alarming seatbelt while in wheelchair, Hi/low bed with fall mat. Further review of Resident #134's clinical record revealed that Resident #134 sustained a fracture from the fall on 6/30/18. Review of Resident #134's physician orders revealed that she was ordered an ACE (2) wrap on 6/30/18. The following order was documented: N.O. Ace wrap left extremity loosely from mid thigh to ankle. Review of Resident #Resident #134's nursing notes revealed that she had went out to the hospital on 7/2/18 for an Ortho (orthopedic) evaluation. Resident #134 arrived back to the facility on 7/2/18 with the following order: Patient's splint needs to be removed twice a day and assess skin for breakdown. Patient should continue to be non weight bearing on left lower extremity. Continue use of wheelchair. Review of Resident #134's July 2018 TAR (treatment administration record) revealed that staff were implementing the order for her splint. Further review of Resident #134's care plan dated 5/2/16, failed to reflect her fractured femur and new orders for splint care. On 8/8/19 at 10:18 a.m., an interview was conducted with OSM (other staff member)#1, the MDS nurse. When asked who was responsible for updating care plans, OSM #1 stated that MDS updates the care plans now, but was not sure who updated the care plans back in 2018. When asked when the care plan was updated, OSM #1 stated that the care plan was updated for any new orders, change in condition, quarterly etc. When asked if a resident had a fall and obtained a fracture, if she would expect to see the care plan revised to reflect that fall and fracture, OSM # 1 stated that she would. When asked if she would expect to see care for the new fracture on the care plan, OSM #1 confirmed that she would. OSM #1 confirmed that Resident #134's fractured femur was not reflected on her comprehensive care plan and the care required for her fracture i.e. splint instructions etc. On 8/8/19 at 3:18 p.m., ASM (administrative staff member) #1, the Administrator, and ASM #2, the ADON (Assistant Director of Nursing) were made aware of the above concerns. No further information was presented prior to exit. (1) Motrin (ibuprofen) NSAID (non-steroidal l anti-inflammatory drugs) used to treat pain. This information was obtained from The National Institutes of Health.https://dailymed.nlm.nih.gov/dailymed/fda/fdaDrugXsl.cfm?setid=26cd56b0-edbb-74f3-e054-00144ff8d46c. (2) ACE wrap is an elastic bandage used to stabilize joints and to reduce swelling. This information was obtained from https://www.acebrand.com/3M/en_US/ace-brand/about-ace-brand/our-story/. Complaint Deficiency. 3. The facility staff failed to ensure the care plan was revised for identified behaviors and failed to include non-pharmacological approaches designed to meet the individual needs of Resident #121. Resident #121 was admitted to the facility on [DATE] with diagnoses to include but not limited to, unspecified dementia without behavioral disturbance, major depressive disorder, recurrent with severe psychiatric symptoms. The current MDS (Minimum Data Set) a quarterly with an assessment reference date of 7/10/19 coded the resident as having long and short term memory deficits and severely impaired daily decision making skills. Under behaviors the resident was assessed as not exhibiting any physical or verbal behaviors or potential indicators for psychosis and the resident was not exhibiting any rejection of care. Resident #121 required extensive assistance of two staff for toileting needs and personal hygiene and was dependent for bathing. Review of the Medication Administration Records (MAR's) for June 2019, July 2019 and August 2019 evidenced the resident was administered Ativan (an anti-anxiety drug) 1 mg PRN (as needed) as follows without implementation of non-pharmacological approaches prior to administration for these identified behaviors: June 9th at 8:09 a.m.-combative with staff, attempting to get up without assistance. June 12th at 12:50 p.m.-hitting, kicking, scratching, grabbing July 9th at 9:08 p.m.-hitting, kicking, scratching, grabbing July 10th at 9:43 a.m.-hitting, scratching, grabbing July 14th at 9:48 a.m.-combative during ADL care (activities of daily living) July 23rd at 8:29 a.m.-resident attempted to get out of bed, pacing the hallway July 24th at 10:31 a.m.-hitting, kicking, scratching, grabbing, cursing July 27th at 10:14 a.m.-hitting, kicking, scratching, cursing July 28th at 9:58 a.m.-hitting, kicking, scratching, grabbing, combative during care July 29th at 9:38 a.m.-hitting, kicking, scratching, grabbing, combative during ADL care July 30th at 10:13 a.m.-hitting, kicking, scratching, grabbing, cursing July 31st at 9:15 a.m.-hitting, kicking, scratching, grabbing, combative during ADL care August 1st at 9:13 a.m.-hitting, kicking, scratching, grabbing, combative during ADL care August 5th at 9:15 a.m.-hitting, kicking, scratching, grabbing, combative during ADL care A review of the Comprehensive Person Centered Care Plan dated 11/17/2015 for Resident #121, evidenced it was not revised to include the resident's behaviors of hitting, kicking,scratching, or grabbing during ADL care, nor did it include individualized approaches to minimize or reduce the use of the psychotropic drug Ativan. On 8/8/19 at 11:33 a.m., Licensed Practical Nurse (LPN #8) was interviewed as she was identified as the nurse who had administered each of the PRN Ativan doses for June, July and August 2019. She stated the resident does not want to be bothered stating, She would rather be in bed than get up .she gets agitated during ADL care. When asked if non-pharmacological approaches were implemented prior to administration she stated, Yes, we try to wait or offer snacks. When asked where the documentation of the non-pharmacological interventions are she stated, I didn't document them. When asked if the care plan had been revised to include a behavioral care plan with individualized non-pharmacological approaches to be attempted prior to the administration of PRN Ativan, she stated, No. When asked how long an order is good for with PRN psychotropic drugs, she stated, Fourteen days. The LPN was shown the order and stated it should have had a stop date and the care plan should have been revised. On 8/8/19 at 3:00 p.m., during the pre-exit meeting the above findings was shared with the Administrator and the Director of Nursing (DON). The DON concurred that the care plan should have been revised to include the resident's behaviors and non-pharmacological approaches. No additional information was provided prior to exit. The facility Policy titled Care Plans, Comprehensive Person-Centered revised December 2016 reads in part: 13. Assessment of residents are ongoing and care plans are revised as information about the residents and the resident's conditions change.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Medication Errors (Tag F0758)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, clinical record review and facility document review the facility staff failed to ensure 1 of 56 reside...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, clinical record review and facility document review the facility staff failed to ensure 1 of 56 residents in the survey sample was free from unnecessary psychotropic drugs, Resident #121. The facility staff failed to implement non-pharmacological approaches prior to administration of the anti-anxiety drug Ativan and failed to obtain a stop date for as needed (PRN) Ativan. The findings include: Resident #121 was admitted to the facility on [DATE] with diagnoses to include but not limited to, unspecified dementia without behavioral disturbance, major depressive disorder, recurrent with severe psychiatric symptoms. The current MDS (Minimum Data Set) a quarterly with an assessment reference date of 7/10/19 coded the resident as having long and short term memory deficits and severely impaired daily decision making skills. Under behaviors the resident was assessed as not exhibiting any physical or verbal behaviors or potential indicators for psychosis. And that the resident was not exhibiting any rejection of care. Resident #121 required extensive assistance of two staff for ADL care (activities of daily living) to include toileting needs and personal hygiene. The resident was dependent on staff for bathing. A review of the Comprehensive Person Centered Care Plan identified psychotropic drug use as a potential for injury related to the use of these medications as ordered for anxiety, and major depressive disorder. The approaches did not include any individualized behavioral interventions or non-pharmacological approaches to prevent/minimize usage of as needed Ativan prior to or during the provision of care. On the August 2019 Medication Administration Record (MAR) was an order for Ativan 1 milligram one tablet by mouth PRN (as needed) every eight hours for anxiety. There was no 14 day stop date for this psychotropic drug order. The resident received a PRN dose of Ativan on 8/1/19 at 9:13 a.m., and another dose on 8/5/19 at 9:15 a.m., without non-pharmacological interventions prior to administration. The behaviors for the Ativan were documented as hitting, kicking, scratching, and grabbing during ADL (activities of daily living) care. Further review of the MAR's for June 2019 and July 2019 evidenced the resident was administered Ativan 1 mg PRN without implementation of non-pharmacological approaches prior to administration with identified behaviors as follows: June 9th at 8:09 a.m.-combative with staff, attempting to get up without assistance June 12th at 12:50 a.m.-hitting, kicking, scratching, grabbing July 9th at 9:08 a.m.-hitting, kicking, scratching, grabbing July 10th at 9:43 a.m.-hitting, scratching, grabbing July 14th at 9:48 a.m.-combative during ADL care (activities of daily living) July 23rd at 8:29 a.m.-resident attempted to get out of bed, pacing the hallway July 24th at 10:31 a.m.-hitting, kicking, scratching, grabbing, cursing July 27th at 10:14 a.m.-hitting, kicking, scratching, cursing July 28th at 9:58 a.m.-hitting, kicking, scratching, grabbing, combative during care July 29th at 9:38 a.m.-hitting, kicking, scratching, grabbing, combative during ADL care July 30th at 10:13 a.m.-hitting, kicking, scratching, grabbing, cursing July 31st at 9:15 a.m.-hitting, kicking, scratching, grabbing, combative during ADL care On 8/8/19 at 11:33 a.m., Licensed Practical Nurse #8 was interviewed as she was identified as the nurse who had administered each of the PRN Ativan doses for June, July and August 2019. She stated the resident does not want to be bothered stating, She would rather be in bed than get up and She gets agitated during ADL care. When asked if non-pharmacological approaches were implemented prior to administration she stated, Yes, we try to wait or offer snacks. When asked where the documentation of the non-pharmacological interventions were she stated, I didn't document them. When asked if the care plan had been revised to include a behavioral care plan with individualized non-pharmacological approaches to be attempted prior to the administration of PRN Ativan, she stated, No. When asked how long an order is good for with PRN psychotropic drugs, she stated, Fourteen days. The LPN was shown the order and stated it should have had a stop date and the care plan should have been revised. The facility could not provide supporting documentation to evidence that individualized, non-pharmacological approaches were implemented or had failed prior to the administration of PRN Ativan for fourteen of fourteen doses administered from June 9, 2019 through August 5, 2019. On 8/8/19 at 3:00 p.m., during the pre-exit meeting the above findings was shared with the Administrator and the Director of Nursing (DON). The DON stated the non-pharmacological interventions should have been attached with the physician order. When asked if they were attached, she stated, No. The facility policy titled Antipsychotic Medications revised December 2016 addressed PRN psychotropic drugs however, it did not address non-pharmacological approaches prior to the administration of a PRN psychotropic. No additional information was provided prior to exit.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Food Safety (Tag F0812)

Could have caused harm · This affected multiple residents

Based on observation, staff interview, and facility document review, it was determined that facility staff failed to store and prepare food in a sanitary manner in the facility kitchen. The findings ...

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Based on observation, staff interview, and facility document review, it was determined that facility staff failed to store and prepare food in a sanitary manner in the facility kitchen. The findings included: On 8/4/19 at 12:40 p.m., observation of the facility kitchen was conducted. On 8/4/19 at 1:10 p.m., an open container of ham was found in the reach-in refrigerator. The open date labeled on the container of ham documented 7/22/19. A second date on the container of ham documented 7/26/19. On 8/4/19 at 1:10 p.m., a pitcher that was half way full of tomato juice was also observed in the reach in refrigerator. 7/27/19 was the date labeled on the pitcher. On 8/4/19 at 1:11 p.m., an interview was conducted with OSM (other staff member) #7, the cook. When asked about the second date labeled on the ham, OSM #7 stated that the 7/26/19 date was the use by date and that the ham should have been thrown away. OSM #7 then stated that the ham was either old or staff labeled the wrong dates on the container. OSM #7 then threw the container away. When asked about the tomato juice, OSM #7 stated that it was probably made that day and would be used by the end of the day. When asked why the date on the pitcher documented 7/27/19, OSM #7 stated that the wrong date must have been written on the pitcher. OSM #7 could not say for certain if the tomato juice was new or old. On 8/6/19 at 10:10 a.m., a second observation of the facility kitchen was conducted. Two vents in the ceiling were observed over the food prep station. The vents were accumulating condensation from the A/C (air conditioning) units. Water droplets were observed coming off the first vent and onto a tray full off hot dog buns. The tray was covered in plastic wrap. Water droplets were also observed dripping from the second vent onto the food rack that contained trays of sandwiches. The sandwiches were also covered in plastic wrap. Unidentified black spots were observed on the vents. There was also a puddle of water observed on the floor underneath the food tray rack. On 8/6/19 at approximately 10:15 a.m., an interview was conducted with OSM (other staff member) #8, the maintenance director. When asked where the condensation on the vents was coming from, OSM #8 stated that the condensation was coming from the air conditioner. OSM #8 stated that the staff in the kitchen like to turn up the A/C causing it to work harder. OSM #8 stated that the door between the dining room and kitchen was also kept open at times making the A/C unit work harder. OSM #8 stated it was currently 68 degrees (Fahrenheit) in the kitchen but at times he will notice the thermostat in the 50's. OSM #8 stated he had placed a sign up in the kitchen asking staff to not touch the thermostat. When asked if water from the vents should be dripping on the food trays, OSM #8 stated that it should not. When asked why water from the vents should not be dripping on the food trays, OSM #8 stated, I wouldn't want water on my food. When asked if the water from the vents was clean, OSM #8 stated that he didn't know. When asked what the black spots on the vents were, OSM #8 stated that he didn't know. When asked if it was mold, OSM #8 stated again that he didn't know. On 8/6/19 at 10:20 a.m., an interview was conducted with OSM #9, the dietary manager. When asked how long the vents were dripping water, OSM #9 stated that he never paid attention or any mind to the dripping water so he was not sure how long the water had been dripping like that. On 8/8/19 at 3:18 p.m., ASM (administrative staff member) #1, the Administrator, and ASM #2, the ADON (Assistant Director of Nursing) were made aware of the above concerns. No further information was presented prior to exit. Facility policy titled, Covering, Labeling, Dating Food, documents in part, the following: Refrigeration Storage: 1. All foods must be covered, labeled and dated with a date label. All food should be monitored each day to be assured that the foods will be used, consumed, or discarded by the use by date or expired date .All leftover food (previously prepared on site) food must be used or discarded within 3 days. The count begins the day the food was prepared. 4. All food items that are not secured in their original containers must be stored in closed containers and secured. The label must identify the common name of food, if food cannot easily be identified. The label must have the date the food was packaged, received or prepared and/or an expiration date. Expiration dates may be used or the food storage chart guideline may be used to determine the expiration date. Complaint Deficiency.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Garbage Disposal (Tag F0814)

Could have caused harm · This affected multiple residents

Based on observation, staff interview and facility document review, it was determined that facility staff failed to maintain the facility dumpster in a manner to prevent pests for one of two facility ...

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Based on observation, staff interview and facility document review, it was determined that facility staff failed to maintain the facility dumpster in a manner to prevent pests for one of two facility dumpsters. The findings included: On 8/4/19 at 1:15 p.m., observation of the facility dumpster was conducted with OSM #7, the cook. One of two facility dumpsters had the doors open to the front and back of the dumpster. The dumpster was over full with trash. When asked who was responsible for maintaining the facility dumpster; ensuring it was shut and free from surrounding debris, OSM #7 stated that everyone (all staff) should make sure the dumpsters are shut and the surrounding area was clean, but that it was ultimately dietary's responsibility. When asked why the dumpster should be shut, OSM #7 stated to prevent pests from getting into the trash especially the feral cats that have been spotted in the area. OSM #7 confirmed that the dumpster was not shut. On 8/8/19 at 3:18 p.m., ASM (administrative staff member) #1, the Administrator, and ASM #2, the ADON (Assistant Director of Nursing) were made aware of the above concerns. No further information was presented prior to exit. Facility policy titled, Disposal of Garbage and Refuse, documents in part, the following: Refuse containers and dumpster kept outside the facility should have tightly fitting lids and should be covered when not being loaded. Dumpster should be emptied according to the facility contract; garbage should not accumulate or be left outside the dumpster.
Nov 2017 6 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0157 (Tag F0157)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, clinical record review, staff and family interview and facility policy review, the facility staff failed ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, clinical record review, staff and family interview and facility policy review, the facility staff failed to inform Resident Representatives of a change in condition for 1 out of 29 residents (Resident #3) in the survey sample. The facility staff failed to inform Resident #3's Resident Representative of a change in condition. The findings include: Resident #3 was admitted to the nursing facility on 8/1/11 and readmitted on [DATE] with diagnoses that included high blood pressure, Type II diabetes mellitus, metabolic encephalopathy, dementia and dysphagia (swallowing problems). The most recent Minimum Data Set (MDS) was a quarterly dated 8/25/17 and coded the resident with short and long term memory problems and severely impaired in the skills necessary for daily decision making. Resident #3 was totally dependent on two staff for all activities of daily living (ADL). The resident was assessed with swallowing problems and on a mechanically altered diet. The person centered care plan dated 8/21/17 identified swallowing problems and the goal of the staff was to ensure the resident had not complications from the identified problem. One of the interventions to implement this goal included a pureed diet fed to the resident by nursing staff. On 11/7/17 at 12:30 p.m., during the orientation tour, Resident #3 was observed in bed and coughing with abdominal muscle movements. The Certified Nursing Assistant (#4) stated the resident vomited after breakfast and a mobile chest X-ray had been ordered by the charge nurse who was monitoring his condition. On 11/7/17 at 4:00 p.m., the resident was in the same condition as previously observed. The resident's charge nurse, Licensed Practical Nurse #6, stated she was told at shift change the resident was ordered to have a mobile chest X-ray because they as suspicious he may have aspirated after vomiting at breakfast time. She said the chest X-ray was not ordered stat, thus it may be a few hours before the resident received the X-ray, but he was being monitored for decline in physical status. On 11/7/17 at 4:45 p.m., Resident #3's Resident Representative approached the Charge Nurse, LPN #6, while she was passing medication and said, What is going on with my Dad, he is not responding to me like yesterday and he doesn't look so good. LPN #6 said, Weren ' t you called about his vomiting this morning and we ordering a chest X-ray to rule out aspiration pneumonia? The Resident Representative stated she had not been called and was shocked to see him look the way he looked. LPN #6 apologized and stated she should have been called. On 11/8/17 at 10:30 a.m., The Director of Nursing (DON) stated it was her expectation that the staff call Resident #3's Resident Representative when the resident vomited and the staff ordered the Chest X-ray to rule of aspiration. Resident #3 was transferred to the local hospital and admitted with a diagnosis of aspiration pneumonia. On 11/9/17 at 11:45 a.m., an interview was conducted the 7/3 LPN (#7) that was in charge of Resident #3 the day he vomited, 11/7/17. The DON was present during the interview. LPN #7 stated she was going to call the family member after the X-ray results were called to the facility. She stated it would have been best that she called the resident's representative when he vomited and they ordered the X-ray. On 11/9/17 at 1:45 p.m., during the debriefing, the Administrator was informed of the aforementioned issue. The Administrator stated she too expected the 7/3 nurse to have called the Resident's Representative to inform her of the vomiting episode and ordering of the chest X-ray. The facility's policy and procedure titled Change in a Resident's Condition or Status dated 12/2016 indicated it was their policy to .Notify the resident's representative of changes in the resident's medical/mental condition or status that may not normally resolve itself without intervention by staff or clinical interventions and is not self limiting .
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0280 (Tag F0280)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident interview, staff interviews, facility documentation review and clinical record review the facility staff faile...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident interview, staff interviews, facility documentation review and clinical record review the facility staff failed to update a care plan give a resident the opportunity to participate in her care plan meeting for 2 of 29 residents (Resident #2 and #14) in the survey sample. 1. The facility staff failed to revise Resident #2's comprehensive care plan to include a fall that occurred on 09/04/17 and 09/14/17. 2. The facility staff failed to give Resident #14 the opportunity to participate in her care plan meeting. The findings included: 1. Resident #2 was admitted to the nursing facility on 03/05/12. Diagnosis for Resident #2 included but not limited to dementia with behavioral disturbances (1). The current Minimum Data Set (MDS) a significant change assessment with an Assessment Reference Date (ARD) of 10/13/17 coded the resident with short and long term memory problems and with severe cognitive impairment - never/rarely made decisions. In addition, the MDS coded Resident #2 with total dependence of one with hygiene, bathing and toilet use, extensive assistance of one with transfers, dressing and bed mobility. Resident #2's clinical record indicated the following: On 09/04/17 at 4:20 a.m., resident was found in the floor; getting out of bed unassisted. Resident landed on her bottom with legs out before her, sitting in an upright position at the bedside. On 09/14/17 at 7:10 a.m., resident was sitting on the floor with her back against the bed. Resident reports she slipped down. Denies pain with active range of motion. The comprehensive care plan was reviewed on 11/08/17, the care plan did not address Resident #2's falls on 09/04/17 and 09/14/17. An interview was conducted with the MDS Coordinator on 11/08/17 at approximately 11:45 a.m., who stated the nurses was responsible for updating Resident #2's care plan after her fall on 09/04/17 and 09/14/17. The MDS Coordinator proceeded to say, the nurses should update the care plan but it's also discussed during our 24 hours meeting the following morning and if the care plan is not updated then I will update it. The MDS coordinator stated she didn't have time to care plan Resident #2's falls on 09/4/17 or 09/14/17. The facility administration was informed of the finding during a briefing on 11/09/17 at approximately 2:00 p.m. The facility did not present any further information about the findings. Definitions: 1. Dementia with behavioral disturbances is frequently the most challenging manifestations of dementia and are exhibited in almost all people with dementia. HTTPS://www/plumbed/22644311 2. Resident #14 was admitted to the facility on [DATE]. Diagnosis for Resident #14 included but not limited to Parkinson's (1) and Hypothyroidism (2). Resident #14 Quarterly Minimum Data Set (MDS), with an Assessment Reference Date (ARD) on 08/16/17 coded Resident #14 with a BIMS score 15 of a possible 15, indicating no memory impairment. An interview was conducted with Resident #14 on 11/07/17 at approximately 3:40 p.m. The surveyor asked Resident #14, Are you being invited to attend her care plan meetings (3) on a regular basis. Resident stated, I've only attended two meetings since I've been here. The resident proceeded to say, I'm a retired nurse so I really only don't understand how you can have a care plan meeting without inviting the resident to attend. On 11/08/17 at approximately 12:05 p.m., during an interview with the Social Worker (SW), this surveyor asked, What is the process for inviting residents to attend their care plan meeting she replied, I will call the families and invite the residents personally to attend their care plan meeting (3). The SW stated, Resident #14's family called and canceled the care plan meeting that was scheduled for August 30, 2017 but another care plan meeting was never rescheduled. The surveyor asked if Resident #14 was informed of the cancellation and if she given the opportunity to have her care plan meeting as scheduled. The SW stated, No, this is new for me; I walked into a lot after I got her; just trying to catch up but Resident #14 should have been given the opportunity to make her own decision if she wanted to attended her care plan meeting. An interview was conducted with the Administrator and Director of Nursing (DON) on 11/09/17 at approximately 9:15 a.m., the Administrator stated, The resident has the right to decide on whether or not she would like to attend her own care plan meeting; she should have been given the option. The facility administration was informed of the finding during a briefing on 11/09/17 at approximately 2:00 p.m. The facility did not present any further information about the findings. The facility's policy: Care Plans, Comprehensive Person-Centered (Revised: 12/2016). Policy Statement: A comprehensive, person-centered care plan that includes measurable objectives and timetable to meet the resident's physical, psychosocial and functional needs is developed and implemented for each resident. Policy Interpretation and Implementation 4. Each resident's comprehensive person-centered care plan will be consisted with the resident's rights to participate in the development and implementation of his or her plan of care, including the right to: -Participate in the planning process. -Identify individuals or roles to be included. -Request meetings. -Request revisions to the plan of care. -Participate in establishing the expected goals and outcomes of care. -Participate the determining the type, amount, frequency and duration of care. 5. The resident will be informed of his or her right to participate in his or her treatment. 15. The resident has the right to refuse to participate in the development of his/her. Definitions: 1. Parkinson's is a slowly progressive degenerative neurological disorder characterized by resting tremor, pill rolling of the fingers, manlike face's, shuffling gait, forward flexion of the trunk, loss of postural reflexes, and muscle rigidity and weakness (Mosby's Dictionary of Medicine, Nursing & Health Professions, 7th Edition). 2. Hypothyroidism is a condition characterized by decreased activity of the thyroid gland (Mosby's Dictionary of Medicine, Nursing & Health Professions, 7th Edition). 3. Care Plan Meeting: The nursing home staff will get your health information and review your health condition to prepare your care plan. You (if you're able), your family (with your permission), or someone acting on your behalf has the right to take part in planning your care with the nursing home staff (HTTPS://www/what-medicare-covers/part-a/care-plan-in-nursing-home. html).
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0309 (Tag F0309)

Could have caused harm · This affected 1 resident

Based on observation, resident interview staff interviews, facility documentation and clinical record review, the facility staff failed to follow physician orders for 1 out 29 Residents in the survey ...

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Based on observation, resident interview staff interviews, facility documentation and clinical record review, the facility staff failed to follow physician orders for 1 out 29 Residents in the survey sample, (Resident #22). The facility staff failed to follow the physician orders for the administration of Zofran and MS Contin for (Resident #22). Resident #22 was originally admitted to the facility 09/08/16. Diagnosis included but not limited to Cancer, (1) and anemia (2). The current Minimum Data Set (MDS) an admission assessment with an Assessment Reference Date (ARD) of 09/15/16 coded the resident with a 15 out of a possible score of 15 on the Brief Interview for Mental Status (BIMS), indicating no cognitive impairment. In addition, the MDS coded Resident #22 requiring total dependence of one with dressing, hygiene, bathing and toilet use, extensive assistance of one with bed mobility and limited assistance of one with eating for Activities of Daily Living care. Resident #22's comprehensive care plan documented resident with a stage IV breast cancer - Resident #22 is at risk for excessive weakness, tiredness, weight loss, pain and depression from cancer process. The goal: less than 3 on a 1-10 pain scale by next review. Some of the intervention/approaches to manage goal included: Medication as ordered - report if ineffective. Review of the current physician orders included but not limited to the following medications for October 2016: 1. MS Contin 60 mg tablet - give 1 tablet by mouth every 12 hours of pain. 2. Xeloda 500 mg tablet - give 4 tablets twice daily x 14 days for Cancer (chemo) - stop date 10/3/16. 3. Zofran 8 mg tablet - give 1 tablet by mouth 30 minutes before each dose of Xeloda - hold on days not receiving Xeloda. During the review of Resident's Medication Administration Record (MAR) for October 2016 indicated there was a missed doses MS Contin and the medication Zofran was administered when the order reads to hold when Xeloda is not administered. On 11/08/17 during the review of Resident #22's October 2016, Medication Administration Record (MAR) revealed the medication MS Contin was not administered on 10/14/16 at 9:00 a.m., (medication not available - hard script obtained). An interview was conducted with DON on 11/08/17 at approximate 4:50 p.m., who stated there's no reason for Resident #22 to run out of her MS Contin. The DON also stated, The nurse should have call the pharmacy and requested for the medication to come over stat (immediately) which takes about 2-3 hours for delivery. On 11/08/17 during the review of Resident #22's MAR for October 2106 indicated that resident refused Xeloda on the following days: 10/01/16 at 8:00 p.m., 10/02/16 at 8 a.m. and 8:00 p.m., but did receive the medication Zofran 8 mg even though the order reads to hold when not receiving Xeloda. An interview was conducted with the Director of Nursing (DON) on 11/8/17 at approximately 6:00 p.m., who stated the Zofran should not have been administered on the days Resident #22 refused the Xeloda. The DON proceeded to say she expects for the nurses to follow physician orders as prescribed. An interview was conducted with LPN #4 on 11/09/17 at approximately 12:10 p.m., the surveyor asked, What is the process for re-ordering controlled pain medications the LPN stated, The nurse will check the back of the card, by looking on the back of the narcotic card it will indicate whether or not a hard script is needed or how many refills are still available for reordering. The nurse stated, if the medication is scheduled; we need to make sure there is enough pills so we don't run out; no one should every go without their pain medication especially if they are terminally ill. The LPN also stated, the pharmacy can be called and they will stat over the medication but it a hard script is needed, the doctor will have to come in a write a script for the refill which can cause a delay in receiving the medication. The facility's Administration was informed of the findings during a briefing on 11/09/17 at approximately 2:00 p.m. The facility did not present any further information about the findings. The facilities policy: Administering Medications (Revised December 2012). Policy Statement: Medications shall be administered in a safe and timely manner, and as prescribed. Policy Interpretation and Implementation 3. Medications must be administered in accordance with the orders, including and required time frame. 7. The individual administering the medication must check the label THREE (3) times to verify the right resident, right medication, right dosage, right time and right method (route) of administration before giving the medication. Definitions: 1. Cancer is a neoplasm characterized by the uncontrolled growth of anaplastic cells that tend to invade surrounding tissue and to metastasize to distant body sites (Mosby's Dictionary of Medicine, Nursing & Health Professions, 7th Edition). 2. Anemia is condition when blood does not carry enough oxygen to the rest of your body (Source: NIH U.S. National Library of Medicine <https://www.nlm.nih.gov/?_ga=1.222831837.792012784.1475525034>: Medline Plus). 3. Xeloda is used in combination with other medications to treat breast cancer that has come back after . has not improved after treatment with other medications (https://medlineplus.gov/ency/article/007365.htm). 4. MS Contin is used to relieve moderate to severe pain (https://medlineplus.gov/ency/article/007365.htm). 5. Zofran is used to prevent nausea and vomiting caused by cancer chemotherapy, radiation therapy, and surgery (https://medlineplus.gov/ency/article/007365.htm). This is a complaint deficiency.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0314 (Tag F0314)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Resident #8 was admitted originally admitted to the facility on [DATE]. Diagnosis for Resident #8 included but are not limite...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Resident #8 was admitted originally admitted to the facility on [DATE]. Diagnosis for Resident #8 included but are not limited to Type 2 Diabetes (1), and a stage IV (2) sacral wound pressure ulcer (3). Resident #8 Minimum Data Set (MDS) with an Assessment Reference Date (ARD) of 10/27/17 coded the resident with a 09 of a total possible score of 15 on the Brief Interview for Mental Status (BIMS), indicating moderate cognitive impairment. In addition, the MDS coded Resident #8 requiring total dependence of two with toilet use, transfers, dressing, hygiene and bathing, extensive assistance of two with bed mobility and extensive assistance of one with eating. Resident #8 was coded always incontinent of bowel, has indwelling Foley (3). In section M (Skin Conditions) of MDS 10/27/17 coded Resident #8 at risk for developing pressure ulcers, having a stage 1 or higher. Resident #8 was coded as having a Stage 3 or 4 pressure ulcer with the following measurements: 8.4 cm x 4.5 cm x 1 cm depth, wound bed with granulation tissue-pink or red tissue with shiny, moist, granular appearance. Resident #8 revised comprehensive care plan documented Resident #8 with actual skin breakdown to sacrum related to impaired mobility secondary to left and right below knees amputation. The goals: the resident will not develop any new areas of skin breakdown and residents pressure ulcer will exhibit signs of healing as evidenced by decreased in size, improved appearance and be free from signs and symptoms (s/s) of infection. The current treatment as of 10/31/17 is to cleanse sacrum with Puracyn (wound cleanser), pat dry, apply Santyl (4) then calcium alginate (5) to wound, apply calcium alginate to periwound and cover with padded adhesive dressing daily and as needed. On 11/08/17 at approximately 10:30 a.m., the resident was observed lying in bed on a specialty mattress; position on his left side. The resident was repositioned remaining on his left. The LPN performed wound care with the assistance of the two CNA's, #7 and 8. The LPN donned a pair of gloves, removed the dressing from the sacral wound, placed the soiled dressing inside a red biohazard bag. The LPN proceeded to clean the wound in a circular motion using Puracyn (wound cleaner), area patted dry, Santyl applied to outer edges of wound bed (slough area) using tongue blade followed with Algicell dressing (6) then covered with Allevyn border (7). On 11/09/17 at approximately 10:35 a.m., and interview was conducted with LPN who stated, I should have removed my gloves after I removed the soiled dressing, washed my hands then put on another pair of gloves, cleaned the wound, remove my gloves then wash my hands again. An interview was conducted with the Director of Nursing (DON) on 11/08/17 at approximately 5:40 p.m., who stated, The nurse should have washed her hands and put on gloves before wound care was started, after the removal of the soiled dressing her gloves should have been removed, hands washed new gloves applied, cleanse the wound, removed her gloves, washed her hands, put on new gloves then after wound care was finished, gloves removed and hands wash. The facility administration was informed of the finding during a briefing on 11/09/17 at approximately 2:00 p.m. The facility did not present any further information about the findings. The facility's policy for Dressings, Dry/Clean (Revised 09/2015). Purpose: The purpose of this procedure is to provide guidelines for the application of dry, clean dressings. Steps in the Procedure to include but not limited to: 1. Clean beside stand. Establish a clean field. 2. Place the clean equipment on the clean field. Arrange the supplied so they can be easily reached. 3. Tape a biohazard or plastic bag on the bedside stand or use a waste basket below clean field. 4. Position resident and adjust clothing to provide access to affected area. 5. Wash and dry hands thoroughly. 6. Put on clean gloves, loose tape and remove soiled dressing. 7. Pull glove over dressing and discard into plastic or biohazard bag. 8. Wash and dry your hands thoroughly. 9. Open dry, clean dressing(s) by pulling corners of the exterior wrapping outward, touching only the exterior surface. Definitions: 1). Diabetes Mellitus Type II is a lifelong (chronic) disease in which there is a high level of sugar (glucose) in the blood (https://medlineplus.gov/ency/article/007365.htm). 2). Pressure Injury - Stage 4 (Full-thickness skin and tissue loss) Full-thickness skin and tissue loss with exposed or directly palpable fascia, muscle, tendon, ligament, cartilage or bone in the ulcer. Slough and/or eschar may be visible. Epibole (rolled edges), undermining and/or tunneling often occur. Depth varies by anatomical location. If slough or eschar obscures the extent of tissue loss this is an Unstageable Pressure Injury. (http://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages/). 3). Pressure Injury: A pressure injury is localized damage to the skin and underlying soft tissue usually over a bony prominence or related to a medical or other device. The injury can present as intact skin or an open ulcer and may be painful. The injury occurs as a result of intense and/or prolonged pressure or pressure in combination with shear. The tolerance of soft tissue for pressure and shear may also be affected by microclimate, nutrition, perfusion, co-morbidities and condition of the soft tissue (http://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages/). 4). Santyl is used to help the healing of burns and ulcers. Collagenase is an enzyme. It works by helping to break up and remove dead skin and tissue. This effect may also help to work better and speed up your body's natural healing process (antibiotics <http://www.webmd.com/cold-and-flu/rm-quiz-antibiotics-myths-facts. 5). Alginate Dressings are composed of calcium alginate, a gelatinous and water-insoluble substance. When in contact with a wound, the calcium alginate in the dressing reacts with sodium chloride from the wound. This turns the dressing into a hydrophilic gel that maintains a moist environment for the wound (www.medicaldepartmentstore.com/Alginate-Dressings-s/286.htm). 6). Algicell dressing manages moderately to heavily exudating wounds (https://www.hightidehealth.com/algicell-ag-alginate-dressing-home.html). 7). Allevyn Dressing allows for the formation and maintenance of a moist wound healing environment, preventing eschar formation and promoting rapid, trouble-free healing (http://www.hightidehealth.com/allevyn-adhesive-foam-dressings-home.html). Based on observation, resident interview, staff interview, facility documentation review, clinical record review the facility staff failed to follow wound care standard procedures to prevent the potential complications for two Residents (Resident #8 and Resident #11) in the survey sample size of 29. 1. The faciliy staff failed to ensure potential complications were avoided during wound care for Resident #8. 2. The facility staff failed to ensure potential complications were avoided during wound care for Resident #11. The findings included: 1. Resident #11 was admitted to the facility on [DATE]. Diagnoses for Resident #11 included but are not limited to Cerebrovascular Accident* (1), Non-Alzheimer's Dementia* (2), and Krauosis Vulvae* (3). Resident #11's Quarterly Minimum Data Set (an assessment protocol) with an Assessment Reference Date of 7/18/17 coded Resident #11 with short and long term memory problems with moderate memory impairment. During an observation on 11/8/17 at approximately 9:45 a.m., of Resident #11's wound care for an Unavoidable Atypical Unstageable Facility Acquired on 7/24/17, Pressure Ulcer* (4). Resident #11 was lying on an air mattress with bilateral heel pressure relief boots on. Licensed Practical Nurse (LPN) #3 began wound care by washing her hands. LPN #3 then sanitized Resident #11's over-bed table. After the table had dried, LPN #3 doffed her gloves and washed her hands. LPN #3, then placed a non-permeable barrier on the table and placed her supplies for wound care on the table. LPN #3 used sanitized pointed tip scissors to cut off the soiled dressing from Resident #11's Right ankle. After the soiled dressing was removed, LPN #3 did not remove her gloves and wash hands. LPN #3 using soiled gloves, proceeded to cleanse Resident #3's Right Heel Pressure Ulcer with Dermal Wound Cleanser (DWC). After cleansing the Pressure Ulcer, LPN #3 applied Santyl Ointment to the wound bed, and covered the dressing with calcium alginate dressing and then covered with a sterile dressing and secured with a gauze fluff wrap. The LPN secured the trash, removed her gloves and washed her hands. Resident #3's Clinical Record documented the following: 11/3/17 Physician Order: Cleanse Right ankle wound with Dermal Wound Cleanser (DWC), pat dry, apply santyl, cover with calcium alginate, cover with dry gauze, wrap with rolled gauze, change QD (daily) and PRN (as needed) if soiled or dislodges. 1/21/17 Physician Order: Multivit-minerals* (5) tablet take one capsule daily supplement 4/21/17 Physician Order: Prostat* (6) 30 milliliters by mouth twice a day 5/20/17 Physician Order: Med Pass* (7) 90 milliliters by mouth every night 6/14/17 Physician Order: Heel Float Boots at all times, Remove during ADL care 7/15/17 Physician Order: Fortified foods on all meal trays 12/12/16 Physician Order: Yogurt with every meal 11/14/16 Physician Order: patient to be fed all meals Resident #11's Care Plan with the following problem: 11/22/16 Potential for skin breakdown: (Resident #11) will have no skin breakdown through next review due to incontinence and immobility. Interventions included but were not limited to the following: Turn or reposition at least every two hours Treatment orders per physician Weekly skin assessments Provide diet as ordered. Record food intake % at each meal. Report decline in intake to physician Offer food substitutes if resident refuses to eat Dietician to evaluate resident nutritional status as ordered 12/22/16 Heel Float Boots while in bed. Remove for Activity of daily living care Specialty Mattress The 6/23/16 CNA Care Plan documented the following: Toileting: Assisted Bathing: Assisted Eating/Feeding: Independent Transfers: One Person Assist Ambulation: Wheel chair Seating: Orthotic Device: Boot Left Ankle/ Wear whenever out of bed Dietary Note of 11/22/16 documented the following: .been eating 26-100% of meals. Diet is Pureed with honey thickened liquids. Dietary continued to monitor Resident #11 as indicated by Dietary notes: 1/10/17, 1/22/17, 2/17/17, 3/28/17, 4/11/17, 4/21/17, 5/19/17, and 6/27/17. 7/24/17 3:37 p.m. Nursing Note of the Wound Care Nurse LPN #3 documented: Resident was seen by Dr. (# 5) for new area to Right ankle. Area was cleansed with DWC pat dry and surgically excised of 5.62 centimeters (cm) of devitalized tissue and necrotic subcutaneous fat to a depth of 0.3 cm revealing healthy belled tissue at this time. Santyl ointment was applied to bound bed covered with calcium alginate then covered with dry gauze wrapped with rolled gauze secured with tape at the time . 7/24/17 Note of Dr. (#5) documented the following: Date wound identified: 7/24/17 Location: Right ankle Stage: Unstageable due to slough/eschar Drainage: Serous, Small Measurements: Length: 2.5 cm Width: 2.5 cm Depth: 0.00 cm Wound Bed: Eschar 90% Nutritional Review: Average Breakfast Intake: 50% Average Lunch Intake: 50% Average Dinner intake: 75% Current Weight 181.20 pounds admission Weight: 219 pounds Lab Work: 4/20/17 Prealbumin* (8) 16.8 Low (normal Range mg/dL (milligrams per deci Liter) 18.38) 7/6/17 Hemaglobin* (9) 11.3 Low (normal Range gm/dL (grams per deci Liter) 12 to 16) 10/26/17 Albumin* (10) 2.8 Low (normal Range gm//dL: 3.4 to 4.8) 10/26/17 Hemaglobin 11.4 Low (normal Range gm/dL 12 to 16) LPN #3 was asked on 11/8/17 at approximately 10:00 a.m., if she had bandage scissors. LPN #3 stated, Somewhere. LPN #3 was asked on 11/8/17 at approximately 4:00 p.m. if she should have washed her hands again during wound care of Resident #11. LPN #3 stated that she didn't know and that she had been nervous during the observation. After the surveyor asked if she should have removed her soiled gloves and washed her hands after cleansing the Pressure Ulcer, she stated, I probably should have. When asked why, LPN #3 stated, I guess to prevent problems. LPN #3 stated that she found her bandage scissors and by using the sharp tipped scissors she could have cut Resident #3's skin under the dressing. Doctor (Dr.) #5, the Facility's Wound Care Physician, stated during a phone interview on 11/9/17 at approximately 9:49 a.m. that Resident #3's Right Ankle Pressure ulcer was unavoidable as the skin around the area was very different. She stated that Resident #11's Responsible Party, did not want a biopsy performed or any extensive procedures done due to Resident #11's risk factors. Doctor (Dr.) #4, the Facility's Palliative Care Physician, stated during an interview on 11/9/17 at approximately 11:15 a.m. that Resident #3 had an Atypical wound, complicated by limited mobility after a Brain Stem Stroke. Dr. #4 stated that Resident #3's skin over the Right ankle had no fatty tissue under the skin that would result in a Pressure Ulcer going from a Stage I to an Unstageable extremely quickly. Dr. #4 also stated that Resident #3's diagnosis of Krauosis Vulvae in addition to Resident #3's immobility contributed to her Unavoidable Pressure Ulcer. Review of the Facility Policy titled, Dressings, Dry/Clean with a revision date of 9/2015 documented the following: Steps in the Procedure: Clean bedside stand. Establish a clean field. Place the clean equipment on the clean field. Wash and dry your hands thoroughly. Put on clean gloves. Loosen tape and remove soiled dressing. Pull glove over dressing and discard into plastic or biohazard bag. Wash and dry your hands thoroughly Open dry, clean dressing(s) by pulling corners of the exterior wrapping outward, touching only the exterior surface. Label tape or dressing with date, time and initials. Place on clean field. Using clean technique, open other products prescribed. Wash and dry your hands thoroughly. Put on clean gloves. Assess the wound and surrounding skin for edema, redness, drainage, tissue healing progress and wound stage. Cleanse the wound with ordered cleanser. Use dry gauze to pat the wound dry. Apply the ordered dressing and secure .per order. Discard disposable items into the designated container. Remove disposable gloves and discard into designated container. Wash and dry your hands thoroughly. Clean the bedside stand. Wash and dry your hands thoroughly. The facility administration was informed of the findings during a briefing on 11/9/17 at approximately 2:02 p.m. The facility did not present any further information about the findings. DEFINITIONS: 1. Cerebrovascular Accident: (CVA) Stroke: Medline Plus documented: Strokes happen when blood flow to your brain stops. Within minutes, brain cells begin to die. There are two kinds of stroke. The more common kind, called ischemic stroke, is caused by a blood clot that blocks or plugs a blood vessel in the brain. The other kind, called hemorrhagic stroke, is caused by a blood vessel that breaks and bleeds into the brain. Mini-strokes or transient ischemic attacks (TIAs), occur when the blood supply to the brain is briefly interrupted. 2. Non-Alzheimer's Dementia: Denentia that is not Alzheimer's Disease: Medline Plus documented: Dementia is the name for a group of symptoms caused by disorders that affect the brain. It is not a specific disease. People with dementia may not be able to think well enough to do normal activities, such as getting dressed or eating. They may lose their ability to solve problems or control their emotions. Their personalities may change. They may become agitated or see things that are not there. 3. Krauosis Vulvae: National Institute of Health documented: a condition that causes the genitals to become raw and itchy, and then shrink. 4. Unstageable Pressure Ulcer: National Pressure Ulcer Advisory Panel documented: Unstageable Pressure Injury: Obscured full-thickness skin and tissue loss Full-thickness skin and tissue loss in which the extent of tissue damage within the ulcer cannot be confirmed because it is obscured by slough or eschar. If slough or eschar is removed, a Stage 3 or Stage 4 pressure injury will be revealed. Stable eschar (i.e. dry, adherent, intact without erythema or fluctuance) on the heel or ischemic limb should not be softened or removed 5. Multi vit with Minerals: Medline Plus documented: multi-vitamin with minerals 6. Prostat: Medline documented: a product that delivers high concentration of protein and calories in a low volume 7. Med Pass: Medline documented: Fortified Nutrition provides a convenient way to supplement calories and protein · Designed to be used as a medication pass drink 8. Pre-albumin: Medline Plus documented: used as a marker of nutritional status. 9. Hemaglobin: Medline Plus documented: A hemoglobin test measures the levels of hemoglobin in your blood. Hemoglobin is a protein in your red blood cells that carries oxygen from your lungs to the rest of your body. If your hemoglobin levels are abnormal, it may be a sign that you have a blood disorder. 10. Albumin: Medline Plus documented: An albumin blood test measures the amount of albumin in your blood. Albumin is a protein made by your liver. Albumin helps keep fluid in your bloodstream so it doesn't leak into other tissues. It is also carries various substances throughout your body, including hormones, vitamins, and enzymes. Low albumin levels can indicate a problem with your liver or kidneys.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0323 (Tag F0323)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, resident interview, staff interview, facility documentation review, clinical record review the facility st...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, resident interview, staff interview, facility documentation review, clinical record review the facility staff failed to ensure safety measures to prevent a potential accident of cutting a Resident's skin, were utilized when cutting off a soiled dressing using pointed tipped scissors and not bandage scissors for 1 Resident, (Resident #11) in the survey sample size of 29. The findings included: Resident #11 was admitted to the facility on [DATE]. Diagnoses for Resident #11 included but are not limited to Cerebrovascular Accident* (1), Non-Alzheimer's Dementia* (2), and Krauosis Vulvae* (3). Resident #11's Quarterly Minimum Data Set (an assessment protocol) with an Assessment Reference Date of 7/18/17 coded Resident #11 with short and long term memory problems with moderate memory impairment. During an observation on 11/8/17 at approximately 9:45 a.m., of Resident #11's wound care for an Unavoidable Atypical Unstageable Facility Acquired on 7/24/17, Pressure Ulcer* (4). Resident #11 was lying on an air mattress with bilateral heel pressure relief boots on. Licensed Practical Nurse (LPN) #3 began wound care by washing her hands. LPN #3 then sanitized Resident #11's over-bed table. After the table had dried, LPN #3 doffed her gloves and washed her hands. LPN #3, then placed a non-permeable barrier on the table and placed her supplies for wound care on the table. LPN #3 used sanitized pointed tip scissors to cut off the soiled dressing from Resident #11's Right ankle. After the soiled dressing was removed, LPN #3 did not remove her gloves and wash hands. LPN #3 using soiled gloves, proceeded to cleanse Resident #3's Right Heel Pressure Ulcer with Dermal Wound Cleanser (DWC). After cleansing the Pressure Ulcer, LPN #3 applied Santyl Ointment to the wound bed, and covered the dressing with calcium alginate dressing and then covered with a sterile dressing and secured with a gauze fluff wrap. The LPN secured the trash, removed her gloves and washed her hands. Resident #3's Clinical Record documented the following: 11/3/17 Physician Order: Cleanse Right ankle wound with Dermal Wound Cleanser (DWC), pat dry, apply santyl, cover with calcium alginate, cover with dry gauze, wrap with rolled gauze, change QD (daily) and PRN (as needed) if soiled or dislodges. 1/21/17 Physician Order: Multivit-minerals* (5) tablet take one capsule daily supplement 4/21/17 Physician Order: Prostat* (6) 30 milliliters by mouth twice a day 5/20/17 Physician Order: Med Pass* (7) 90 milliliters by mouth every night 6/14/17 Physician Order: Heel Float Boots at all times, Remove during ADL care 7/15/17 Physician Order: Fortified foods on all meal trays 12/12/16 Physician Order: Yogurt with every meal 11/14/16 Physician Order: patient to be fed all meals Resident #11's Care Plan with the following problem: 11/22/16 Potential for skin breakdown: Resident #11) will have no skin breakdown through next review due to incontinence and immobility. Interventions included but were not limited to the following: Turn or reposition at least every two hours Treatment orders per physician Weekly skin assessments Provide diet as ordered. Record food intake % at each meal. Report decline in intake to physician Offer food substitutes if resident refuses to eat Dietician to evaluate resident nutritional status as ordered 12/22/16 Heel Float Boots while in bed. Remove for Activity of daily living care Specialty Mattress Dietary Note of 11/22/16 documented the following: .been eating 26-100% of meals. Diet is Pureed with honey thickened liquids. Dietary continued to monitor Resident #11 as indicated by Dietary notes: 1/10/17, 1/22/17, 2/17/17, 3/28/17, 4/11/17, 4/21/17, 5/19/17, and 6/27/17. 7/24/17 3:37 p.m. Nursing Note of the Wound Care Nurse LPN #3: .Resident was seen by Dr. (# 5) for new area to Right ankle. Area was cleansed with DWC pat dry and surgically excised of 5.62 centimeters (cm) of devitalized tissue and necrotic subcutaneous fat to a depth of 0.3 cm revealing healthy belled tissue at this time. Santyl ointment was applied to bound bed covered with calcium alginate then covered with dry gauze wrapped with rolled gauze secured with tape at the time . 7/24/17 Note of Dr. (#5) documented the following: Date wound identified: 7/24/17 Location: Right ankle Stage: Unstageable due to slough/eschar Drainage: Serous, Small Measurements: Length: 2.5 cm Width: 2.5 cm Depth: 0.00 cm Wound Bed: Eschar 90% Nutritional Review: Average Breakfast Intake: 50% Average Lunch Intake: 50% Average Dinner intake: 75% Current Weight 181.20 pounds admission Weight: 219 pounds Lab Work: 4/20/17 Prealbumin* (8) 16.8 Low (normal Range mg/dL 18.38) 7/6/17 Hemaglobin* (9) 11.3 Low (normal Range gm/dL 12 to 16) 10/26/17 Albumin* (10) 2.8 Low (normal Range gm//dL: 3.4 to 4.8) 10/26/17 Hemaglobin 11.4 Low (normal Range gm/dL 12 to 16) LPN #3 was asked on 11/8/17 at approximately 10:00 a.m., if she had bandage scissors. LPN #3 stated, Somewhere. LPN #3 stated that she found her bandage scissors and by using the sharp tipped scissors she could have cut Resident #3's skin under the dressing. The Director of Nursing #2 was asked on 11/8/17 at approximately 4:10 p.m. what type of scissors should be used to cut off a soiled dressing. The Director of Nursing #2 stated that bandage scissors are the correct type of scissors to be used to not potentially cut the patient's skin. Doctor (Dr.) #5, the Facility's Wound Care Physician, stated during a phone interview on 11/9/17 at approximately 9:49 a.m. that Resident #3's Right Ankle Pressure ulcer was unavoidable as the skin around the area was very different. She stated that Resident #11's Responsible Party, did not want a biopsy performed or any extensive procedures done due to Resident #11's risk factors. Doctor (Dr.) #4, the Facility's Palliative Care Physician, stated during an interview on 11/9/17 at approximately 11:15 a.m. that Resident #3 had an Atypical wound, complicated by limited mobility after a Brain Stem Stroke. Dr. #4 stated that Resident #3's skin over the Right ankle had no fatty tissue under the skin that would result in a Pressure Ulcer going from a Stage I to an Unstageable extremely quickly. Dr. #4 also stated that Resident #3's diagnosis of Krauosis Vulvae in addition to Resident #3's immobility contributed to her Unavoidable Pressure Ulcer. The Director of Nursing was asked if the Facility had any policy related to the type of scissors to use during wound care on 11/8/17 at approximately 4:10 p.m. The Director of Nursing stated that there was no specific policy or statement in the wound care policy related to the type of scissors. The Director of Nursing stated, that her expectation for her nursing staff was to utilize bandage scissors so as not to potentially cause any accident potentials. The facility administration was informed of the findings during a briefing on 11/9/17 at approximately 2:02 p.m. The facility did not present any further information about the findings. DEFINITIONS: 1. Cerebrovascular Accident: (CVA) Stroke: Medline Plus documented: Strokes happen when blood flow to your brain stops. Within minutes, brain cells begin to die. There are two kinds of stroke. The more common kind, called ischemic stroke, is caused by a blood clot that blocks or plugs a blood vessel in the brain. The other kind, called hemorrhagic stroke, is caused by a blood vessel that breaks and bleeds into the brain. Mini-strokes or transient ischemic attacks (TIAs), occur when the blood supply to the brain is briefly interrupted. 2. Non-Alzheimer's Dementia: Denentia that is not Alzheimer's Disease: Medline Plus documented: Dementia is the name for a group of symptoms caused by disorders that affect the brain. It is not a specific disease. People with dementia may not be able to think well enough to do normal activities, such as getting dressed or eating. They may lose their ability to solve problems or control their emotions. Their personalities may change. They may become agitated or see things that are not there. 3. Krauosis Vulvae: National Institute of Health documented: a condition that causes the genitals to become raw and itchy, and then shrink. 4. Unstageable Pressure Ulcer: National Pressure Ulcer Advisory Panel documented: Unstageable Pressure Injury: Obscured full-thickness skin and tissue loss Full-thickness skin and tissue loss in which the extent of tissue damage within the ulcer cannot be confirmed because it is obscured by slough or eschar. If slough or eschar is removed, a Stage 3 or Stage 4 pressure injury will be revealed. Stable eschar (i.e. dry, adherent, intact without erythema or fluctuance) on the heel or ischemic limb should not be softened or removed 5. Multi vit with Minerals: Medline Plus documented: multi-vitamin with minerals 6. Prostat: Medline documented: a product that delivers high concentration of protein and calories in a low volume 7. Med Pass: Medline documented: Fortified Nutrition provides a convenient way to supplement calories and protein · Designed to be used as a medication pass drink 8. Pre-albumin: Medline Plus documented: used as a marker of nutritional status. 9. Hemaglobin: Medline Plus documented: A hemoglobin test measures the levels of hemoglobin in your blood. Hemoglobin is a protein in your red blood cells that carries oxygen from your lungs to the rest of your body. If your hemoglobin levels are abnormal, it may be a sign that you have a blood disorder. 10. Albumin: Medline Plus documented: An albumin blood test measures the amount of albumin in your blood. Albumin is a protein made by your liver. Albumin helps keep fluid in your bloodstream so it doesn't leak into other tissues. It is also carries various substances throughout your body, including hormones, vitamins, and enzymes. Low albumin levels can indicate a problem with your liver or kidneys.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0441 (Tag F0441)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, clinical record review, staff interviews and revised of the facility documentation the facility staff fail...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, clinical record review, staff interviews and revised of the facility documentation the facility staff failed to maintain an infection control program to provide a safe, sanitary environment to prevent the development and transmissions of disease and infection for 2 of 29 residents (Resident #8 and 11) in the survey sample. 1. The facility staff failed to implement appropriate hand hygiene during a sacral wound care dressing change for Resident #8. 2. The facility staff failed to implement appropriate hand hygiene during a right ankle care dressing change for Resident #11. The findings included: 1. Resident #8 was admitted originally admitted to the facility on [DATE]. Diagnosis for Resident #8 included but are not limited to Type 2 Diabetes (1), and a stage IV (2) sacral wound pressure ulcer (3). Resident #8 Minimum Data Set (MDS) with an Assessment Reference Date (ARD) of 10/27/17 coded the resident with a 09 of a total possible score of 15 on the Brief Interview for Mental Status (BIMS), indicating moderate cognitive impairment. In section M (Skin Conditions) of MDS 10/27/17 coded Resident #8 at risk for developing pressure ulcers, having a stage 1 or higher. Resident #8 was coded as having a Stage 3 or 4 pressure ulcer with the following measurements: 8.4 cm x 4.5 cm x 1 cm depth, wound bed with granulation tissue-pink or red tissue with shiny, moist, granular appearance. Resident #8 revised comprehensive care plan documented Resident #8 with actual skin breakdown to sacrum related to impaired mobility secondary to left and right below knees amputation. The goals: the resident will not develop any new areas of skin breakdown and residents pressure ulcer will exhibit signs of healing as evidenced by decreased in size, improved appearance and be free from signs and symptoms (s/s) of infection. The current treatment as of 10/31/17 is to cleanse sacrum with Puracyn (wound cleanser), pat dry, apply Santyl (4) then calcium alginate (5) to wound, apply calcium alginate to periwound and cover with padded adhesive dressing daily and as needed. On 11/08/17 at approximately 10:30 a.m., the resident was observed lying in bed on a specialty mattress; position on his left side. The resident was repositioned remaining on his left side. The LPN performed wound care with the assistance of the two CNA's, #7 and 8. The LPN removed the dressing from the sacral wound, placed the soiled dressing inside a red biohazard bag. The LPN proceeded to clean the wound with circular motion using Puracyn, area patted dry, Santyl applied to a tongue blade then applied the Santyl to outer edges of wound bed (slough area) followed with Algicell dressing, covered with Allevyn border, gloves removed, hands washed, red bag removed then placed inside red bag located on the side of the treatment cart. On 11/09/17 at approximately 10:35 a.m., and interview was conducted with LPN #3 who stated, I should have removed my gloves after I removed the soiled dressing, washed my hands then put on another pair of gloves, cleaned the wound, remove my gloves then wash my hands again. An interview was conducted with the Director of Nursing (DON) on 11/09/17 at approximately 5:05 p.m., who stated, The nurse should have washed her hands before wound care was started, after the removal of soiled dressing, after cleaning the wound and again after the dressing change was completed. The facility administration was informed of the finding during a briefing on 11/09/17 at approximately 2:00 p.m. The facility did not present any further information about the findings. The facility's policy for Hand/Hand Hygiene (Revised 08/2015). Purpose: This facility considers hand hygiene the primary means to prevent the spread of infections. Policy Interpretation and Implementation included but not limited to: 1. All personnel shall be trained and regularly in-serviced on the importance of hand hygiene in preventing the transmission of healthcare-associated infections. 2. All personnel shall follow the handwashing/hand hygiene procedures to help prevent the spread of infections to other personnel, residents, and visitors. 7. Use an alcohol-based hand rub containing at least 62% alcohol; or, alternatively, soap (antimicrobial or non-antimicrobal) and water for the following situations: -Before handling clean or soiled dressings, gauze pads, etc. -Before moving from a contaminated body site to a clean body site during resident care. -After contact with blood or bodily fluids. -After handling used dressings, contaminated equipment, etc. 9. The use of gloves does not replace hand washing/hand hygiene. Integration of gloves use along with routine hand hygiene is recognized as the best practice for preventing healthcare-associated infections. Definitions: 1). Diabetes Mellitus Type II is a lifelong (chronic) disease in which there is a high level of sugar (glucose) in the blood (https://medlineplus.gov/ency/article/007365.htm). 2). Pressure Injury - Stage 4 (Full-thickness skin and tissue loss) Full-thickness skin and tissue loss with exposed or directly palpable fascia, muscle, tendon, ligament, cartilage or bone in the ulcer. Slough and/or eschar may be visible. Epibole (rolled edges), undermining and/or tunneling often occur. Depth varies by anatomical location. If slough or eschar obscures the extent of tissue loss this is an Unstageable Pressure Injury. (http://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages/). 3). Pressure Injury: A pressure injury is localized damage to the skin and underlying soft tissue usually over a bony prominence or related to a medical or other device. The injury can present as intact skin or an open ulcer and may be painful. The injury occurs as a result of intense and/or prolonged pressure or pressure in combination with shear. The tolerance of soft tissue for pressure and shear may also be affected by microclimate, nutrition, perfusion, co-morbidities and condition of the soft tissue (http://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages/). 4). Santyl is used to help the healing of burns and ulcers. Collagenase is an enzyme. It works by helping to break up and remove dead skin and tissue. This effect may also help to work better and speed up your body's natural healing process (antibiotics <http://www.webmd.com/cold-and-flu/rm-quiz-antibiotics-myths-facts. 5). Alginate Dressings are composed of calcium alginate, a gelatinous and water-insoluble substance. When in contact with a wound, the calcium alginate in the dressing reacts with sodium chloride from the wound. This turns the dressing into a hydrophilic gel that maintains a moist environment for the wound (www.medicaldepartmentstore.com/Alginate-Dressings-s/286.htm). 6). Algicell dressing manages moderately to heavily exudating wounds (https://www.hightidehealth.com/algicell-ag-alginate-dressing-home.html). 7). Allevyn Dressing allows for the formation and maintenance of a moist wound healing environment, preventing eschar formation and promoting rapid, trouble-free healing (http://www.hightidehealth.com/allevyn-adhesive-foam-dressings-home.html). 2. Resident #11 was admitted to the facility on [DATE]. Diagnoses for Resident #11 included but are not limited to Cerebrovascular Accident* (1), Non-Alzheimer's Dementia* (2), and Krauosis Vulvae* (3). Resident #11's Quarterly Minimum Data Set (an assessment protocol) with an Assessment Reference Date of 7/18/17 coded Resident #11 with short and long term memory problems with moderate memory impairment. During an observation on 11/8/17 at approximately 9:45 a.m., of Resident #11's wound care for an Unavoidable Atypical Unstageable Facility Acquired on 7/24/17, Pressure Ulcer* (4). Resident #11 was lying on an air mattress with bilateral heel pressure relief boots on. Licensed Practical Nurse (LPN) #3 began wound care by washing her hands. LPN #3 then sanitized Resident #11's over-bed table. After the table had dried, LPN #3 doffed her gloves and washed her hands. LPN #3, then placed a non-permeable barrier on the table and placed her supplies for wound care on the table. LPN #3 used sanitized pointed tip scissors to cut off the soiled dressing from Resident #11's Right ankle. After the soiled dressing was removed, LPN #3 did not remove her gloves and wash hands. LPN #3 using soiled gloves, proceeded to cleanse Resident #3's Right Heel Pressure Ulcer with Dermal Wound Cleanser (DWC). After cleansing the Pressure Ulcer, LPN #3 applied Santyl Ointment to the wound bed, and covered the dressing with calcium alginate dressing and then covered with a sterile dressing and secured with a gauze fluff wrap. The LPN secured the trash, removed her gloves and washed her hands. Resident #3's Clinical Record documented the following: 11/3/17 Physician Order: Cleanse Right ankle wound with Dermal Wound Cleanser (DWC), pat dry, apply santyl, cover with calcium alginate, cover with dry gauze, wrap with rolled gauze, change QD (daily) and PRN (as needed) if soiled or dislodges. 1/21/17 Physician Order: Multivit-minerals* (5) tablet take one capsule daily supplement 4/21/17 Physician Order: Prostat* (6)* (7) 30 milliliters by mouth twice a day 5/20/17 Physician Order: Med Pass 90 milliliters by mouth every night 6/14/17 Physician Order: Heel Float Boots at all times, Remove during ADL care 7/15/17 Physician Order: Fortified foods on all meal trays 12/12/16 Physician Order: Yogurt with every meal 11/14/16 Physician Order: patient to be fed all meals Resident #11's Care Plan with the following problem: 11/22/16 Potential for skin breakdown: (Resident #11) will have no skin breakdown through next review due to incontinence and immobility. Interventions included but were not limited to the following: Turn or reposition at least every two hours Treatment orders per physician Weekly skin assessments Provide diet as ordered. Record food intake % at each meal. Report decline in intake to physician Offer food substitutes if resident refuses to eat Dietician to evaluate resident nutritional status as ordered 12/22/16 Heel Float Boots while in bed. Remove for Activity of daily living care Specialty Mattress Dietary Note of 11/22/16 documented the following: .been eating 26-100% of meals. Diet is Pureed with honey thickened liquids. Dietary continued to monitor Resident #11 as indicated by Dietary notes: 1/10/17, 1/22/17, 2/17/17, 3/28/17, 4/11/17, 4/21/17, 5/19/17, and 6/27/17. 7/24/17 3:37 p.m. Nursing Note of the Wound Care Nurse LPN #3 documented: .Resident was seen by Dr. (# 5) for new area to Right ankle. Area was cleansed with DWC pat dry and surgically excised of 5.62 centimeters (cm) of devitalized tissue and necrotic subcutaneous fat to a depth of 0.3 cm revealing healthy belled tissue at this time. Santyl ointment was applied to bound bed covered with calcium alginate then covered with dry gauze wrapped with rolled gauze secured with tape at the time . 7/24/17 Note of Dr. (#5) documented the following: Date wound identified: 7/24/17 Location: Right ankle Stage: Unstageable due to slough/eschar Drainage: Serous, Small Measurements: Length: 2.5 cm Width: 2.5 cm Depth: 0.00 cm Wound Bed: Eschar 90% Nutritional Review: Average Breakfast Intake: 50% Average Lunch Intake: 50% Average Dinner intake: 75% Current Weight 181.20 pounds admission Weight: 219 pounds Lab Work: 4/20/17 Prealbumin* (8) 16.8 Low (normal Range mg/dL 18.38) 7/6/17 Hemaglobin* (9) 11.3 Low (normal Range gm/dL 12 to 16) 10/26/17 Albumin* (10) 2.8 Low (normal Range gm//dL: 3.4 to 4.8) 10/26/17 Hemaglobin 11.4 Low (normal Range gm/dL 12 to 16) LPN #3 was asked on 11/8/17 at approximately 10:00 a.m., if she had bandage scissors. LPN #3 stated, Somewhere. LPN #3 was asked on 11/8/17 at approximately 4:00 p.m. if she should have washed her hands again during wound care of Resident #11. LPN #3 stated that she didn't know and that she had been nervous during the observation. After the surveyor asked if she should have removed her soiled gloves and washed her hands after cleansing the Pressure Ulcer, she stated, I probably should have. When asked why, LPN #3 stated, I guess to prevent problems. LPN #3 stated that she found her bandage scissors and by using the sharp tipped scissors she could have cut Resident #3's skin under the dressing. Doctor (Dr.) #5, the Facility's Wound Care Physician, stated during a phone interview on 11/9/17 at approximately 9:49 a.m. that Resident #3's Right Ankle Pressure ulcer was unavoidable as the skin around the area was very different. She stated that Resident #11's Responsible Party, did not want a biopsy performed or any extensive procedures done due to Resident #11's risk factors. Doctor (Dr.) #4, the Facility's Palliative Care Physician, stated during an interview on 11/9/17 at approximately 11:15 a.m. that Resident #3 had an Atypical wound, complicated by limited mobility after a Brain Stem Stroke. Dr. #4 stated that Resident #3's skin over the Right ankle had no fatty tissue under the skin that would result in a Pressure Ulcer going from a Stage I to an Unstageable extremely quickly. Dr. #4 also stated that Resident #3's diagnosis of Krauosis Vulvae in addition to Resident #3's immobility contributed to her Unavoidable Pressure Ulcer. Review of the Facility Policy titled, Handwashing/Hand Hygiene with a revision date of 8/2015 documented the following: Wash hands with soap (antimicrobial or non-antimicrobial) and water for the following situations: After handling used dressings, contaminated equipment, etc.: The use of gloves does not replace hand washing/hand hygiene. Integration of glove use along with routine hand hygiene is recognized as the best practice for preventing healthcare-associated infections. Review of the Facility Policy titled, Dressings, Dry/Clean with a revision date of 9/2015 documented the following: Steps in the Procedure: Clean bedside stand. Establish a clean field. Place the clean equipment on the clean field. Wash and dry your hands thoroughly. Put on clean gloves. Loosen tape and remove soiled dressing. Pull glove over dressing and discard into plastic or biohazard bag. Wash and dry your hands thoroughly Open dry, clean dressing(s) by pulling corners of the exterior wrapping outward, touching only the exterior surface. Label tape or dressing with date, time and initials. Place on clean field. Using clean technique, open other products prescribed. Wash and dry your hands thoroughly. Put on clean gloves. Assess the wound and surrounding skin for edema, redness, drainage, tissue healing progress and wound stage. Cleanse the wound with ordered cleanser. Use dry gauze to pat the wound dry. Apply the ordered dressing and secure .per order. Discard disposable items into the designated container. Remove disposable gloves and discard into designated container. Wash and dry your hands thoroughly. Clean the bedside stand. Wash and dry your hands thoroughly. The facility administration was informed of the findings during a briefing on 11/9/17 at approximately 2:02 p.m. The facility did not present any further information about the findings. DEFINITIONS: 1. Cerebrovascular Accident: (CVA) Stroke: Medline Plus documented: Strokes happen when blood flow to your brain stops. Within minutes, brain cells begin to die. There are two kinds of stroke. The more common kind, called ischemic stroke, is caused by a blood clot that blocks or plugs a blood vessel in the brain. The other kind, called hemorrhagic stroke, is caused by a blood vessel that breaks and bleeds into the brain. Mini-strokes or transient ischemic attacks (TIAs), occur when the blood supply to the brain is briefly interrupted. 2. Non-Alzheimer's Dementia: Denentia that is not Alzheimer's Disease: Medline Plus documented: Dementia is the name for a group of symptoms caused by disorders that affect the brain. It is not a specific disease. People with dementia may not be able to think well enough to do normal activities, such as getting dressed or eating. They may lose their ability to solve problems or control their emotions. Their personalities may change. They may become agitated or see things that are not there. 3. Krauosis Vulvae: National Institute of Health documented: a condition that causes the genitals to become raw and itchy, and then shrink. 4. Unstageable Pressure Ulcer: National Pressure Ulcer Advisory Panel documented: Unstageable Pressure Injury: Obscured full-thickness skin and tissue loss Full-thickness skin and tissue loss in which the extent of tissue damage within the ulcer cannot be confirmed because it is obscured by slough or eschar. If slough or eschar is removed, a Stage 3 or Stage 4 pressure injury will be revealed. Stable eschar (i.e. dry, adherent, intact without erythema or fluctuance) on the heel or ischemic limb should not be softened or removed 5. Multi vit with Minerals: Medline Plus documented: multi-vitamin with minerals 6. Prostat: Medline documented: a product that delivers high concentration of protein and calories in a low volume 7. Med Pass: Medline documented: Fortified Nutrition provides a convenient way to supplement calories and protein · Designed to be used as a medication pass drink 8. Pre-albumin: Medline Plus documented: used as a marker of nutritional status. 9. Hemaglobin: Medline Plus documented: A hemoglobin test measures the levels of hemoglobin in your blood. Hemoglobin is a protein in your red blood cells that carries oxygen from your lungs to the rest of your body. If your hemoglobin levels are abnormal, it may be a sign that you have a blood disorder. 10. Albumin: Medline Plus documented: An albumin blood test measures the amount of albumin in your blood. Albumin is a protein made by your liver. Albumin helps keep fluid in your bloodstream so it doesn't leak into other tissues. It is also carries various substances throughout your body, including hormones, vitamins, and enzymes. Low albumin levels can indicate a problem with your liver or kidneys.
Understanding Severity Codes (click to expand)
Life-Threatening (Immediate Jeopardy)
J - Isolated K - Pattern L - Widespread
Actual Harm
G - Isolated H - Pattern I - Widespread
Potential for Harm
D - Isolated E - Pattern F - Widespread
No Harm (Minor)
A - Isolated B - Pattern C - Widespread

Questions to Ask on Your Visit

  • "What safeguards are in place to prevent abuse and neglect?"
  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • No fines on record. Clean compliance history, better than most Virginia facilities.
  • • 40% turnover. Below Virginia's 48% average. Good staff retention means consistent care.
Concerns
  • • Multiple safety concerns identified: Federal abuse finding, 5 harm violation(s). Review inspection reports carefully.
  • • 56 deficiencies on record, including 5 serious (caused harm) violations. Ask about corrective actions taken.
  • • Grade F (0/100). Below average facility with significant concerns.
Bottom line: This facility has a substantiated abuse finding. Extreme caution advised. Explore alternatives.

About This Facility

What is Nassawadox Rehabilitation And Nursing's CMS Rating?

CMS assigns NASSAWADOX REHABILITATION AND NURSING an overall rating of 1 out of 5 stars, which is considered much below average nationally. Within Virginia, this rating places the facility higher than 0% of the state's 100 nursing homes. A rating at this level reflects concerns identified through health inspections, staffing assessments, or quality measures that families should carefully consider.

How is Nassawadox Rehabilitation And Nursing Staffed?

CMS rates NASSAWADOX REHABILITATION AND NURSING's staffing level at 2 out of 5 stars, which is below average compared to other nursing homes. Staff turnover is 40%, compared to the Virginia average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Nassawadox Rehabilitation And Nursing?

State health inspectors documented 56 deficiencies at NASSAWADOX REHABILITATION AND NURSING during 2017 to 2023. These included: 5 that caused actual resident harm and 51 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Nassawadox Rehabilitation And Nursing?

NASSAWADOX REHABILITATION AND NURSING is owned by a for-profit company. For-profit facilities operate as businesses with obligations to shareholders or private owners. The facility is operated by EASTERN HEALTHCARE GROUP, a chain that manages multiple nursing homes. With 145 certified beds and approximately 128 residents (about 88% occupancy), it is a mid-sized facility located in NASSAWADOX, Virginia.

How Does Nassawadox Rehabilitation And Nursing Compare to Other Virginia Nursing Homes?

Compared to the 100 nursing homes in Virginia, NASSAWADOX REHABILITATION AND NURSING's overall rating (1 stars) is below the state average of 3.0, staff turnover (40%) is near the state average of 46%, and health inspection rating (1 stars) is much below the national benchmark.

What Should Families Ask When Visiting Nassawadox Rehabilitation And Nursing?

Based on this facility's data, families visiting should ask: "What safeguards and monitoring systems are in place to protect residents from abuse or neglect?" "Can you walk me through typical staffing levels on day, evening, and night shifts?" "Can I visit during a mealtime to observe dining assistance and food quality?" "How do you handle medical emergencies, and what is your hospital transfer rate?" These questions are particularly relevant given the substantiated abuse finding on record and the below-average staffing rating.

Is Nassawadox Rehabilitation And Nursing Safe?

Based on CMS inspection data, NASSAWADOX REHABILITATION AND NURSING has documented safety concerns. The facility has 1 substantiated abuse finding (meaning confirmed case of resident harm by staff or other residents). The facility has a 1-star overall rating and ranks #100 of 100 nursing homes in Virginia. Families considering this facility should ask detailed questions about what corrective actions have been taken since these incidents.

Do Nurses at Nassawadox Rehabilitation And Nursing Stick Around?

NASSAWADOX REHABILITATION AND NURSING has a staff turnover rate of 40%, which is about average for Virginia nursing homes (state average: 46%). Moderate turnover is common in nursing homes, but families should still ask about staff tenure and how the facility maintains care continuity when employees leave.

Was Nassawadox Rehabilitation And Nursing Ever Fined?

NASSAWADOX REHABILITATION AND NURSING has no federal fines on record. CMS issues fines when nursing homes fail to meet care standards or don't correct problems found during inspections. The absence of fines suggests the facility has either maintained compliance or corrected any issues before penalties were assessed. This is a positive indicator, though families should still review recent inspection reports for the full picture.

Is Nassawadox Rehabilitation And Nursing on Any Federal Watch List?

NASSAWADOX REHABILITATION AND NURSING is not on any federal watch list. The most significant is the Special Focus Facility (SFF) program, which identifies the bottom 1% of nursing homes nationally based on persistent, serious quality problems. Not being on this list means the facility has avoided the pattern of deficiencies that triggers enhanced federal oversight. This is a positive indicator, though families should still review the facility's inspection history directly.