RESORTS OF AUGSBURG

6811 CAMPFIELD ROAD, BALTIMORE, MD 21207 (410) 486-4573
For profit - Corporation 131 Beds Independent Data: November 2025
Trust Grade
48/100
#169 of 219 in MD
Last Inspection: April 2024

Within standard 12-15 month inspection cycle. Federal law requires annual inspections.

Overview

Resorts of Augsburg has a Trust Grade of D, which indicates that the facility is below average and has some concerning issues. It ranks #169 out of 219 nursing homes in Maryland, placing it in the bottom half, and #34 out of 43 in Baltimore County, meaning there are only a few local options that are better. The facility's situation is worsening, with the number of issues increasing from 9 in 2019 to 24 in 2024. On a positive note, staffing is a strength with a rating of 4 out of 5 stars, although the turnover rate is 48%, which is average for the state. However, the facility has concerning fines of $23,896, which is higher than 75% of nursing homes in Maryland and suggests ongoing compliance problems. While there is adequate RN coverage, specific incidents of concern include a resident eloping from a locked unit and expired food items being found in the kitchen. Additionally, the facility failed to post staffing information in accessible areas, which is crucial for transparency. Overall, while there are some strengths in staffing, the increasing number of issues and specific incidents raise significant concerns.

Trust Score
D
48/100
In Maryland
#169/219
Bottom 23%
Safety Record
Low Risk
No red flags
Inspections
Getting Worse
9 → 24 violations
Staff Stability
⚠ Watch
48% turnover. Above average. Higher turnover means staff may not know residents' routines.
Penalties
✓ Good
$23,896 in fines. Lower than most Maryland facilities. Relatively clean record.
Skilled Nurses
✓ Good
Each resident gets 53 minutes of Registered Nurse (RN) attention daily — more than average for Maryland. RNs are trained to catch health problems early.
Violations
⚠ Watch
37 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★☆☆☆
2.0
Overall Rating
★★★★☆
4.0
Staff Levels
★★★★☆
4.0
Care Quality
★★☆☆☆
2.0
Inspection Score
Stable
2019: 9 issues
2024: 24 issues

The Good

  • 4-Star Staffing Rating · Above-average nurse staffing levels
  • 4-Star Quality Measures · Strong clinical quality outcomes
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record

Facility shows strength in staffing levels, quality measures, fire safety.

The Bad

2-Star Overall Rating

Below Maryland average (3.0)

Below average - review inspection findings carefully

Staff Turnover: 48%

Near Maryland avg (46%)

Higher turnover may affect care consistency

Federal Fines: $23,896

Below median ($33,413)

Minor penalties assessed

The Ugly 37 deficiencies on record

Apr 2024 24 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

Resident Rights (Tag F0550)

Could have caused harm · This affected 1 resident

Based on observations, resident and staff interviews , and record reviews, it was determined that the facility failed to treat residents with respect and dignity in an environment that promotes enhanc...

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Based on observations, resident and staff interviews , and record reviews, it was determined that the facility failed to treat residents with respect and dignity in an environment that promotes enhancement of quality of life. This was evident for 3 (Resident #55, #81, #84) out of 4 residents reviewed for dignity during the recertification survey. The findings include: 1. During observation rounds on 4/4/2024 at 8:30 am, the surveyor observed 2 urinals on the floor in resident #55's room. An empty urinal was laying on the floor against the wall closest to the entrance of the room. Another urinal with amber colored fluid was observed laying in between the bedside table and the wall. The resident was yelling for the nurse stating, I need a razor to shave my face. During an interview on 4/4/2024 at 8:32 am with Resident #55, s/he stated that the nurse came to empty the urinal and placed the urinal on the floor. During an interview on 4/4/24 at 8:40 am with Licensed Practical Nurse (LPN) staff # 10, she stated she didn't know who put the urinals on the floor. During a follow-up observation on 4/4/2024 at 8:53 am, the urinals were still observed on the floor in the same locations. Review of resident #55's medical record on 4/4/2024 at 11:32 am revealed the resident has diagnoses that include blindness and dementia. 2. During an observation of the lunch meal on the Water's Edge nursing unit on 04/15/24 at 12:04 PM, the surveyor observed Staff #49 standing over Resident #81 while assisting the resident with eating. Staff #49 was also observed with his/her cell phone in his/her hand while assisting Resident #81 with the lunch meal. 3. Continued observation revealed that after assisting Resident #81, Staff #49 proceeded to assist Resident #84 with the lunch meal. Staff #49 sat down next to Resident #84 and placed his/her cell phone on the table. Staff #49 was observed interacting with his/her cell phone while assisting Resident #84 with the lunch meal. In an interview with the 04/15/24 day shift charge nurse, Staff #28, at 12:12 PM, Staff #28 stated that Staff #49 was supposed to be going with another resident to an appointment. Staff #28 stated that he/she asked Staff #49 to assist the residents on the Waters Edge unit with the lunch meal.
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

Free from Abuse/Neglect (Tag F0600)

Could have caused harm · This affected 1 resident

Based on administrative and medical record review, and interviews with facility staff it was determined the facility failed to keep a resident safe from neglect when an employee failed assist a reside...

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Based on administrative and medical record review, and interviews with facility staff it was determined the facility failed to keep a resident safe from neglect when an employee failed assist a resident with Activities of Daily Living (ADL) as required. This was found to be evident for 1 (Resident #1) of 9 residents reviewed for abuse during the survey. Findings include: Intake MD00200445 was reviewed on 4/16/24 at 4:00 PM for allegations of resident neglect. According to the intake report, Geriatric Nurse Assistant (GNA # 85) placed resident # 1 dinner tray in his/her room on the bedside table across the room and out of the resident's reach. Further review of the facility's investigation found a notice of Corrective Action Form dated 12/14/23 indicating the following: GNA # 85 did not follow proper protocol for providing a meal to the resident and did not assist the resident with ADL's as requested by the resident. The facility spoke with the employee on 12/19/23 about termination and sent a letter. An interview was conducted with the DON on 4/16/24 at 5:00 PM and she stated the facility underwent new ownership that became effective as of January 2024. She confirmed that upon her review of the investigation, the employee (#85) was terminated for not adhering to protocols and providing a resident with a dinner meal and ADL assistance. The Administrative team was made aware of all concerns at the time of exit on 4/18/24 at 1:30 PM.
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 administrative and medical record review and interviews with facility staff, it was determined the facility failed to complete a thorough investigation into abuse allegations for a resident w...

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Based on administrative and medical record review and interviews with facility staff, it was determined the facility failed to complete a thorough investigation into abuse allegations for a resident with an injury of unknown origin. This was found to be evident for 1 (Resident # 1) of 9 residents reviewed for abuse during the survey. Findings include: Intake # MD00199866 was reviewed on 4/15/24 at 9:00 AM for allegations of abuse for an injury of unknown origin. Review of the facility's investigation revealed resident # 1 was admitted with the following but not limited diagnosis: Osteoarthritis (Degenerative Joint Disease). According to the investigation on 11/23/23 the resident's assigned GNA (Geriatric Nurse Assistant) stated that at approximately 8:00 PM while providing care, she noticed that the resident right lower leg was swollen and rotated outward. The nurse confirmed this finding after her assessment and the resident was sent to the emergency room for further evaluation. The resident returned with diagnosis of fracture of right tibia and fibula. An interview was conducted with the DON on 4/15/24 at 9:50 AM and she was asked to explain the facility's process of investigating for an injury of unknown origin and she stated the following: All injuries of unknown origin are reported from staff to DON, then an investigation is begun to include staff interviews, and the resident if possible. Review of the medical record and notification of the physician. An assessment is done by the provider/physician. Pertinent team members will meet to determine the root cause. The DON stated that an injury of unknown is looked at as abuse and the police are notified. She added that if staff can tell the administration team what happened through the investigation, then the police will not be notified if the explanation is definitive. All the information is documented within the investigation. The DON was made aware that law enforcement was not notified per the facility's investigation. She was asked to provide documentation of staff and resident interviews to the survey team. During another interview on 4/16/24 at 10:55 AM with the Interim Administrator (Staff # 9) and the DON, they stated that the current administration signed ownership of the facility in January 2024 and that the previous owner did not leave a copy of staff and/or resident statements and were unable to provide the survey team with documentation of interview statements by staff or residents. All concerns were discussed with the administration team at the time of exit on 4/18/24 at 1:30 PM.
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

Deficiency F0655 (Tag F0655)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident medical record review and interviews it was determined the facility failed to provide a resident and his/her r...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on resident medical record review and interviews it was determined the facility failed to provide a resident and his/her representative a complete summary or complete written summary of the resident's initial baseline care plan. This was evident for 1 resident (#17) out of 53 residents reviewed during the survey. The findings include the following: A facility must provide the resident and their representative with a summary of the baseline care plan that includes but is not limited to the initial goals of the resident, a summary of the resident's medications and dietary instructions, any services and treatments to be administered by the facility and personnel acting on behalf of the facility and any updated information based on the details of the comprehensive care plan, as necessary. Review of resident #17's medical record on 04/08/2024 at 01:45 PM revealed that resident (#17) was admitted to the facility on [DATE] and there was no evidence or documentation found that resident (#17) or his/her representative was provided a complete summary or a complete written summary of resident #17's initial baseline care plan that included all the requirements as stated above. During an interview on 04/09/2024 at 04:05 PM the Director of Nursing staff (#2) stated that she was not able to find documentation stating or showing that a complete summary or complete written summary of resident #17's initial baseline care plan was provided to resident (#17) or his/her representative.
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

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 administrative and medical record review, and interviews with facility staff it was determined the facility failed to d...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on administrative and medical record review, and interviews with facility staff it was determined the facility failed to develop a care plan for a resident at risk for wandering. This was found to be evident for 1 (Resident # 73) of 7 residents reviewed for accidents during the facility's survey. Findings include: A care plan is a guide that addresses the unique needs of each resident. It is used to plan, assess, and evaluate the effectiveness of the resident care. MD00172344 was reviewed on 4/10/24 at 10:30 AM for allegations that Resident # 73 was observed out of the building in the adjacent parking lot. Further review of the resident medical record on the same date at 11:15 AM revealed the resident has the following but limited diagnosis: Vascular Dementia (refers to changes to memory, thinking, and behavior resulting from conditions that affect the blood vessels in the brain). Review of a wandering assessment that was done on 5/18/21 upon admission, indicated a score of nine (9). A score of 9 indicates the resident is at risk to wander. There was no care plan in place for wandering at this time. An interview was conducted with the DON on 4/10/24 at 2:00 PM and she was asked to provide the survey team with a copy of the resident wandering care plan. She was unable to provide this documentation to the survey team. She provided a copy of resident # 73 elopement care plan that had an initiation date of 9/19/21. The DON stated that the care plan was initiated after the resident was observed outside of the building in the parking lot. The DON acknowledged that a care plan should have been developed at the time the wandering assessment was completed upon the resident's admission on [DATE] to address the specific concerns. All concerns were discussed with the administration team at the time of exit on 4/18/24 at 1:30 PM.
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

Deficiency F0658 (Tag F0658)

Could have caused harm · This affected 1 resident

Based on record review and interview with facility staff, it was determined that facility nursing staff failed to follow professional standards of nursing when documenting medications. This was eviden...

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Based on record review and interview with facility staff, it was determined that facility nursing staff failed to follow professional standards of nursing when documenting medications. This was evident for 1 of 9 residents (Resident #260) reviewed for abuse. The findings include: It is the standard of nursing practice to document administered medications immediately after administration. Failing to do this results in an inaccurate record where it cannot be determined when a medication was actually given and has the potential to result in medication errors (such as a resident receiving a dose twice, or two doses of a medication being given too close in time). On 4/8/24 at 8:39 AM, review of the facility's investigation packet for MD00199456 revealed a written statement from Geriatric Nursing Assistant (GNA #5) dated 11/11/23 that stated while they were giving out breakfast, they noticed Resident #260's right wrist was swollen, and immediately reported it to the charge nurse [LPN #48]. On 4/10/24 at 8:21 AM, review of the medical record revealed a Progress Note written by LPN #48 dated 11/11/23 at 6:22 PM that stated, Resident #260 was noted this morning with a swollen right wrist and complained of pain. The resident was unable to state what happened. The Nurse Practitioner (NP) on call was notified who ordered an x-ray to rule out a fracture. The resident is stable at this time and pain managed during the shift. On 4/11/24 at 2:00 PM, record review of the medication administration record (MAR) for the month of November 2023 revealed on 11/11/23, Resident #260 was documented with 10/10 pain during the Pain Assessment for night shift. Furthermore, the resident was ordered Tylenol Oral Tablet 325mg, Give 2 tablets by mouth every 6 hours as needed for pain. The medication was ordered on 6/1/23 at 11:56 AM and the order was active until it was discontinued on 11/12/23 at 5:27 AM. For the month being reviewed [November 2023], from 11/1/23 to 11/12/23, there was no documented administration of the medication in the patient's medical record. On 4/12/24 at 1:48 PM, in an interview with the Director of Nursing (DON), she was made aware that Resident #260 was confirmed via x-ray to have sustained a right wrist fracture and there was no documentation of pain medication being administered for almost an entire day. The surveyor requested the DON to look into this and provide any documentation. No such records were provided to the survey team by the time of survey exit. The first dose of pain medication documented for Resident #260 after their swelling was noted at breakfast on 11/11/23 and with documented complaints of pain was on 11/12/23 at 6:53 AM. The Administration Team was made aware of all concerns at the time of survey exit on 4/18/24 at 1:30 PM.
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

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 reviews of a closed medical record and staff interview, it was determined that the facility nursing staff failed to upd...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on reviews of a closed medical record and staff interview, it was determined that the facility nursing staff failed to update a resident's physician prescribed wound care treatment orders after the facility wound consultant updated the treatment orders after a weekly assessment. This was evident for 1 (Resident #257) 4 residents reviewed for pressure ulcers during the recertification survey. The findings include: Review of Resident's #257's closed medical record on 04/09/24 revealed that Resident #257 was admitted to the facility on [DATE]. Resident #257 was seen by the facility wound consultant on 09/26/23 and was identified with a left heel deep tissue injury and a bilateral sacrum wound. The wound consultant noted Resident #257's wounds to be chronic and require continued topical wound dressing therapy. The wound consultant gave orders instructing the nurses to apply a betadine dressing to the left heel and apply medihoney, calcium alginate and a foam dressing to the bilateral sacrum wounds daily. Resident #257 was seen in the facility by the facility wound consultant on 10/03/23, 10/10/23, and 10/17/23 who noted improvement in Resident #257's left heel and bilateral sacrum wounds at each visit. On 10/24/23, the facility wound consultant assessed Resident #257's wounds at the bedside. The facility wound consultant changed the dressing to Resident #257's left heel by instructing the nurses to now apply Betadine to eschar only, and apply hydrogel to the granulation zone only, and cover with a Non-adherent or ABD pad, and wrap the area with Kling. On 10/31/23, the facility wound consultant assessed Resident #257's wounds at the bedside. The facility wound consultant changed the dressing to Resident #257's bilateral sacrum wounds instructing the nurses to apply medihoney, calcium alginate apply border foam dressing to the open/granulating wound daily. The wound consultant also ordered the nursing staff to apply Nystatin mixed with dimethicone lotion to the Moisture-associated skin damage (MASD)/fungal periwound, three times a day, and with each incontinent episode. On 11/07/23, the facility wound consultant continued the same 10/31/23 daily treatment to the bilateral sacrum wounds and instructed the nursing staff to apply betadine to the left heel. The facility wound consultant indicated that there was no change to Resident #257's wounds since 10/31/23. A review of Resident #257's medication and treatment orders failed to reveal the nursing staff had updated Resident #257's wound care instructions after each wound care assessment. A review of Resident #257's medication and treatment administration records and physician orders from 09/20/23 through 11/07/23 revealed that the nursing staff were documenting that; 1) the medication Santyl External ointment was being applied to the sacrum area every day, 2) applied medihoney to the left buttock wound every day, and 3) applied skin prep to bilateral heels every shift. Further review of Resident #257's closed medical record failed to reveal the nursing staff had changed Resident 257's wound care treatment orders after the 10/24/23 and 10/31/23 wound consultant visit. The nursing staff also failed to update the physician orders following the wound consultant's 10/24/23 and 10/31/23 wound assessments. In an interview with the facility wound care consultant on 04/18/24 at 3:19 PM, the nurse surveyor informed the wound consultant that the nursing staff were documenting that they were applying Santyl and medihoney to the bilateral sacrum wound and applying skin prep to the left heel during the time Resident #257 was admitted to the facility. The wound consultant stated that this was news to him/her.
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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Intake MD00200917 was reviewed by the surveyor on 04.05.2024 at 11:30 AM. Resident # 54 was admitted to the facility with the...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Intake MD00200917 was reviewed by the surveyor on 04.05.2024 at 11:30 AM. Resident # 54 was admitted to the facility with the following but not limited diagnoses: Alzheimer's, dementia with behavioral disturbance, vascular dementia, and major depression disorder. The resident was assessed to have scored a 01 out of 15 on the BIM's assessment upon admission and throughout the current stay at the facility indicating severe cognitive impairment. On the day of the elopement incident, 12.24.23, Resident #54 was described as ambulatory with a steady gait per the record review performed by the surveyor on 04.05.24 at 12:45 PM. The former administrator, staff # 31 submitted the facility report to the Office of Healthcare Quality (OHCQ) on 12.25.23 at 7:20 PM however the elopement incident occurred on 12.24.23 at 07:39 PM. At 12:22 PM on 04.05.24, the surveyor reviewed the progress notes dated: 12.24.23 at 9:00 PM, written by LPN #16 that he/she was notified by a GNA #42, assigned to resident # 54. GNA # 42 was unable to locate the resident at 7:29 PM. LPN #16 and other staff members on the unit began searching for the resident on the unit. LPN #16 notified the nursing supervisor. LPN #16 wrote that the nursing supervisor notified the other nursing units and security. The police were not notified. GNA# 42, assigned to the resident and LPN #16 searched for the resident outside the building. Resident #54 was found sitting on a chair at the ambulance entrance. Resident #54 was described as laughing, unable to explain how she/he got outside the building. The Resident was accompanied by staff back to the unit. The nursing supervisor performed the head-to-toe assessment of resident # 54, found no skin discoloration, no scratches, or bruises, vital signs stable, routine medications administered and were tolerated by the resident. Per the progress note written by LPN # 16, upon return to the unit on 12.24.23 between 8:00 and 8:15 PM, Resident #54 was toileted and placed in bed. One to one direct supervision was initiated. The family and the provider were notified. A review of the medical record and care plan on 04.10.24 at 1:45 PM revealed: Resident #54 had an area of focus as having a behavior problem (wandering, attempting to leave the unit, elopement, entering other resident's rooms, combativeness, aggression towards staff, refusing care) related to unspecified psychosis. The care plan had a initiation date of 01.08.2019, with a revision date of 12.26.2023. The primary goal: the resident would have fewer episodes of wandering, trying to leave the unit, combativeness, and aggression towards staff by the review date. The goals were initiated on 01.08.2019, the revision date was 12.29.23, and the target date was written as 01.02.2024. The interventions listed were (1) administer antipsychotic medications as ordered. Monitor/document for side effects and effectiveness. The goal was initiated on 01.08.2019 and revised on 01.08.2019. (2) The second goal listed on the care plan was: Anticipate and meet the resident's needs and the date initiated: 01.08.2019. (3) Goal #6 stated: 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 an alternative location as needed. (Goal #9) Psych services for behavior and medication management initiated on 01.08.2019 and revision on: 08.11.2020. (4) Goal # 10, Staff and visitors to ensure they check that no resident follows them off the unit through doors or elevators without a licensed nurse knowledge. (May refer to signs posted on all exits on the unit). The date goal #10 was initiated: 12.26.23 and revised on 01.08.24. (5) Staff to do more frequent check/rounds on the resident's whereabouts each shift and re-direct as needed. The initiation was 04.27.23 and revision on 01.18.24 per the hard copy of the resident #54's care plan. At 2:07 PM on 04.10.24 the surveyor reviewed the counterpoint health services documentation by staff # 84, psychiatric nurse practitioner documented on 01.09.24. The progress note referred to the last date the resident was seen by psychiatry was on 12.12.23 and was currently being seen in January 2024 as a follow-up for dementia and depression. The psychiatric medications the resident was taking as of 01.09.24 was Seroquel 25 mg QHS. The progress note did not mention any reference to resident#54's elopement that occurred on 12.24.23. On 04.05.24 at 08:35 AM while in the conference room speaking to the survey team, the DON stated that all the facility incident reports that was requested by the team leader on 04.04.24 were not available. The folders for the facility incident reports only had the incident report inside but not the proof of staff training, staff and resident interviews, and other related documents related to Resident #54. At 3:00 PM on 04.10.24 the surveyor interviewed GNA # 12 who worked on the 7 AM-7:30 PM shift 12.24.23 on the Sudbrook clinical unit, where resident #54 was located. GNA #12 stated that he/she was not assigned to resident #54 however, was contacted by the nurse supervisor at 7:45 PM on her personal cellphone. GNA #12 stated that the supervisor asked whether the employee had seen resident # 54 at the end of his/her shift. GNA #12 stated that he/she reported to the supervisor that he/she had not seen resident #54 at the end of his/her shift. The surveyor was unable to interview, the 7:00 PM -7:30 AM agency nurse #44 assigned to resident #54 on 12.24.23 when the elopement occurred secondary to the employee not being an active employee. Also, the surveyor was unable to contact (by telephone) the GNA #37, who is currently no longer employed by the facility and who was assigned to resident # 54 on 12.24.23 on the 7 AM-7:30 PM. Additionally, LPN#38 who was Resident #54's assigned nurse on the 7 AM-7 PM shift was currently on medical leave per the current DON. The surveyor attempted to interview Resident #54 regarding the elopement on 04.05.24 at 10:40 AM without success. The resident was not able to recall the incident and was disoriented to time, place, and date. On 04.11.24 at 11:30 AM the surveyor interviewed GNA #43 who worked 7 PM-7 AM shift on 12.24.23 but was not assigned to resident #54. GNA #43 stated he/she did not observe resident #54 elope from the unit on 12.24.23. GNA #43 stated that she/he was informed that the resident was able to follow another resident's husband off the unit in order to elope which included the resident following the visitor to the elevator after exiting the unit. At 3:53 PM on 04.11.24, the surveyor interviewed RN # 47 regarding the elopement of the resident #54 on 12.24.23 at 07:29 PM. RN #47 stated that she/he was not assigned to the resident. This employee stated that the supervisor for night shift was LPN #16 and she/he (RN #47) was the charge nurse on 12.24.23, the date of resident #54's elopement and that all staff participated in the search for the resident. The facility failed to adequately supervise resident #54 who had been diagnosed with dementia with a history of wandering, and exit seeking behavior therefore the resident was able to elope from the Sudbrook unit on 12.24.23 at approximately 7:29 PM. This deficient practice was reviewed during the survey with the facility administrative team and was reviewed during the exit interview on 04.18.24. Based on administrative and record review it was determined the facility failed to provide adequate supervision for residents at risk for wandering. This was found to be evident for 2 (Resident # 73 and # 54) of 10 residents reviewed for wandering during the facility's survey. Findings include: 1. Intake MD00172344 was reviewed on 4/10/24 at 10:30 AM for allegations that resident # 73 was observed outside of the building in the adjacent parking lot. On 4/10/24 a review of resident # 73's medical record revealed the resident has the following but not limited diagnosis: Aphasia (a language disorder caused by damage in the brain that controls language expression and comprehension) following nontraumatic intracranial hemorrhage and Hemiplegia and Hemiparesis (muscle weakness or partial paralysis on one side of the body) following nontraumatic intracerebral hemorrhage affecting left non-dominant side. The Minimum Data Set (MDS) is a federally mandated assessment tool used by nursing home staff to gather information on each resident's strengths and needs. Information collected drives resident care planning decisions. The Brief Interview for Mental Status (BIMS) is an assessment that measures a person's cognitive ability using a scoring system that ranges from 0-15 points; 0-7 suggests severe impairment, 8-12 suggests moderate cognitive impairment and 13-15 suggests that cognition is intact. Review of the 5-day assessment dated [DATE] Section (C) for cognition patterns on 4/10/24 at 11:00 AM revealed a BIMS score of (99) which means the resident couldn't be assessed and was incomplete. Review of a wandering assessment that was done on 5/18/21 upon admission, indicates a score of nine (9). A score of 9-10 indicates the resident was at risk to wander. There was no care plan in place for wandering at this time. Review on 4/10/24 of the facility's investigation and several signed type statements from staff revealed the following: A signed typed statement by a Registered Nurse (RN) (#36) revealed on 9/19/21 at about 3:00 PM a GNA informed RN (# 36) that resident # 73 was observed outside by the church area and had to assist the resident back to the floor. The resident's family visited and when the family was about to leave the resident attempted to follow. The GNA no longer works for the facility and attempts to contact the GNA were unsuccessful. A written statement by the maintenance staff # 46 revealed that on 9/19/21 he was instructed to assess doors and alarms by chapel. All doors are properly secured and functioning. An interview was conducted with the Interim Administrator (#9) and current DON (# 2) and Regional DON (# 8) on 4/10/24 at 2:00 PM and the interim administrator stated that the current administration team was new. The facility signed new ownership in January of 2024. He further stated that he was unable to provide additional information regarding this incident. He was asked about the layout of the facility and explained that all units on the second floor have an access code to gain entry and to exit, with one unit designated as a locked unit. The first floor is not a locked unit. Resident # 73 resided on the first floor at the time of the incident. An interview was conducted with nurse (#36) on 4/10/24 at 2:55 PM and he stated that he has worked at the facility for approximately twenty years. He was asked to provide an account of the incident and stated the following: He is very familiar with resident # 73 and while working on 9/19/21 during the day shift a GNA reported to him that resident # 73 was confused and attempted to leave. He was unable to provide the name of the GNA. The nurse #36 stated that the resident was ambulatory and attempted to follow family when they were leaving and needed to be distracted to allow the family to leave. Nurse #36 stated that when the family left the resident was placed in an open dining area near the nurse station on close monitoring after the incident. He stated that the resident had not made attempts to leave since the incident on 9/19/21. He stated that staff had been educated regarding safety precautions for residents at risk. An interview was conducted with the maintenance staff (#46) on 4/11/24 at 9:27 AM and he stated he worked for the facility for 19 years. In September of 2021 he was instructed to assess the building exit doors because resident # 73 got out of the building. He stated that no elevators were checked by him, only the exit doors. He further stated that the doors near the chapel were checked because this was the area where the resident was found and that there was an elevator located in the same area. Further review of the resident care plan on 4/11/24 at 10:50 AM revealed an elopement care plan for resident # 73, initiated on 9/19/21 for attempting to leave the facility with family. The interventions include the following: Distract resident from wandering by offering pleasant diversions, structured activities, food, conversation, television, preferred books. Identify patterns of wandering: is wandering purposeful, aimless, or escapist? Is looking for something? Does it indicate the need for more exercise? Triggers for eloping are family visits. During another interview with the interim administrator (#9) on 4/11/24 at 11:45 AM he stated that all the security systems in the building that have key codes were installed in 2017. There were no repairs/additions to the key-scan security system after the current provider came in on 5/25/21. All concerns were discussed with the Administration team at the time of exit on 4/18/24 at 1:30 PM.
CONCERN (D)

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

Deficiency F0697 (Tag F0697)

Could have caused harm · This affected 1 resident

Based on record review and interview it was determined that facility staff failed to notify the provider when a resident reported that their pain medication was ineffective. This was evident for 1 (#2...

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Based on record review and interview it was determined that facility staff failed to notify the provider when a resident reported that their pain medication was ineffective. This was evident for 1 (#26) of 3 residents reviewed for pain management. The findings include: A medical record review for Resident #26 6/25/24 at 12:25 PM revealed the resident was recently diagnosed with a liver mass. The physician documented that the condition can be painful and ordered the resident to have hydromorphone (an opioid to treat pain). Review of the physician's orders revealed the resident had an order for hydromorphone 2mg give 1 tablet every 4 hours for pain levels of 4-6 and a second order for hydromorphone 2 mg give 2 tables every 4 hours for pain levels of 7-10. During an interview with Resident #26 on 06/26/2024 at 9:21 AM s/he reported that s/he was in constant pain. The resident went on to report that s/he had pain medication earlier this morning when the pain level was at an 8, however his/her pain level was still at a 6. When asked the resident stated that the nurse had not returned to see if the pain medication had been effective or not. (It is a standard of practice to reassess the pain level after administering pain medication in 1 hour). The surveyor offered to get the nurse for the resident to which the resident stated they would like to see the nurse. An interview with Licensed Practical Nurse (LPN) #16 at 6/26/24 at 9:34 AM revealed that she was not informed that Resident #26 had received pain medication by the off going nurse and therefore had not followed up with the resident. LPN #16 reported that she had went to the resident's room at 7:00 AM and introduced herself and stated she was making her rounds to check on residents and asked about pain. She was made aware that the resident was continuing to complain of a pain level of 6 after being medicated earlier this morning. She was unable to tell the surveyor about this resident's medical conditions and the need for pain medication. A subsequent interview with LPN #16 on 06/26/2024 10:22 AM revealed that she had went into the resident's room and determined the pain medication had not been effective. However, she failed to notify the physician that the resident's pain medication had been ineffective 1.5 hours after administration. A subsequent review of Resident #26's medication administration record with Unit Manager #8 on 6/25/24 at 9:44 AM revealed the resident was administered 2 hydromorphone 2 mg tablets at 6:55 AM. This meant the resident had to wait about a 1 ½ before the next dose was due. On 06/26/2024 at 11:18 AM in an interview the DON indicated the nurse should document the severity of the pain, location, and effectiveness of the medication and what was given. Staff who give a pain medication at the end of their shift should pass it on and the next shift follow up with effectiveness. The DON also indicated If the nurse was the resident's regular nurse she would expect them to know about his/her condition and if not when the resident complains of pain they should ask the resident about it and explore the medical record. The DON revealed that if a resident continued to have a pain then the nurse would check for a breakthrough medication and if there is none then they should call the physician. On 6/26/24 at 11:30 AM a review of Resident #26's medication administration revealed that after the resident reported his/her pain levels was at a 6 at 9:21 AM, the nurse failed to act until 11:23 AM when she administered another dose of pain medication to the resident. The medication was allowed to be given as early as 10:55 AM. An interview on 06/26/2024 at 12:18 PM with Nurse Practitioner (NP) #17 revealed that she expected staff to notify her if a resident's pain was ineffective and there was no order for a breakthrough pain medication. Cross Reference F658
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

Drug Regimen Review (Tag F0756)

Could have caused harm · This affected 1 resident

Based on medical record reviews and staff interviews, it was determined that the physician or medical director did not address the pharmacist medication regimen recommendation. This was evident for 1(...

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Based on medical record reviews and staff interviews, it was determined that the physician or medical director did not address the pharmacist medication regimen recommendation. This was evident for 1(Resident #26) of 5 residents reviewed for medication regimen reviews. The findings include: On 4/12/24 at 11:00 am, the surveyor reviewed the monthly Pharmacist Medication Regimen Review (MRR) for October of 2023 for Resident #26. On the October 2023 MRR there was a recommendation by pharmacist #81 to draw a Thyroid Stimulating Hormone (TSH) lab and Thyroxine (T4) lab that was ordered but not completed. The TSH lab test measures the level of the thyroid stimulating hormone in the blood and the T4 lab measures the amount of thyroxine, a thyroid hormone, in the blood. There was no action or note in the medical records by the physician or medical director addressing the pharmacist's recommendation. On 4/12/24 at 2:58 pm, an interview was conducted with the Director of Nursing (DON). The DON stated that they were unable to locate a response from the physician or a follow-up pharmacy review that was addressed by the physician for the MRR conducted in October 2023. On 4/15/24 at 11:00 am, the DON presented this surveyor with an outcome to the MRR dated 10/3/23 in which the pharmacist documented on 4/12/24 that a mistake was made on the October 2023 pharmacist MRR recommendation. The pharmacist documented, Disregard recommendation. Lab order noted in error. Only a CBC (Complete Blood Count) was ordered which was drawn.
CONCERN (D)

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

Deficiency F0806 (Tag F0806)

Could have caused harm · This affected 1 resident

Based on interviews and observations it was determined the facility failed to provide resident (#41) with an accurate menu of meals being served and offering resident (#41) food preference choices as ...

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Based on interviews and observations it was determined the facility failed to provide resident (#41) with an accurate menu of meals being served and offering resident (#41) food preference choices as well as other alternative food options. This was evident for 1 resident (#41) out of 53 residents reviewed during the survey. The findings include: During an interview on 04/05/24 at 11:09 AM resident (#41) stated that the facility gives him/her what they want to give him/her, there are no menus given to him/her and he/she does not have any choices when it comes to the food. Resident (#41) stated the facility just puts the tray in front of you and if you do not like it then you get nothing else offered to you. During an interview on 04/10/24 at 11:15 AM Dietary Manager staff (#7) stated that the facility is on week 2 of their menu cycle, menus are to be reviewed with the resident by the facility caregivers and each resident has a menu in their room with an alternative menu to choose from if resident does not want what is being served for that meal. Staff (#7) also stated that staff are to call down to the kitchen two hours before a meal is trayed and prepared if the resident would like something else. During an interview on 04/10/24 at 11:50 AM Registered Nurse staff (#35) stated that the residents are served the trays the kitchen sends to us and if residents do not want the tray after we serve them, then staff can call down to kitchen to order what the resident wants but it may take some time for it to be sent. Staff (#35) showed this surveyor a menu that was posted in the kitchen area on floor one Powdermill that was week 1 of the facility menu cycle and staff (#35) further stated that it was not the correct meals that the residents get served. Staff (#35) stated that there are no menus in the residents' rooms, and they do not use menus to offer residents choices before meals are sent up from the kitchen. During observation rounds on 04/10/2024 at 11:52 AM with Registered Nurse staff (#35) the facility week 2 menu cycle was found posted in the kitchen on floor one Powdermill not week 1 cycle menu. During observation rounds on 04/10/24 at 11:59 AM it was observed that that there was no weekly or alternative menus in resident #41's room for resident (#41) to use to reference his/her meals of choice. During an interview on 04/10/24 at 12:01 PM Dietary Manager staff (#7) stated that the menu cycle week 1 that was posted in the kitchen on floor one Powdermill was wrong, someone should be changing the menu every Sunday and it should be menu cycle week 2. On 04/10/24 at 12:20 PM this surveyor made Dietary Manager staff (#9) and Regional Director of Nursing staff (#8) aware of the above findings and they both stated that this would be corrected and looked into.
CONCERN (D)

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

Deficiency F0807 (Tag F0807)

Could have caused harm · This affected 1 resident

Based on interview and observation it was determined the facility failed to provide resident (#41) with drinks that are consistent with resident needs as stated on his/her meal ticket. This was eviden...

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Based on interview and observation it was determined the facility failed to provide resident (#41) with drinks that are consistent with resident needs as stated on his/her meal ticket. This was evident for 1 resident (#41) out of 53 residents reviewed during the annual survey. The findings include the following: During an interview on 04/10/2024 at 12:10 PM resident (#41) stated and pointed out they do not send what is on my paper that I am supposed to get, and this happens all the time, referring to the meal ticket that was placed on resident #41's meal tray. During a dining observation on 04/10/2024 at 12:10 PM it was observed that residents #41's meal ticket stated that he/she should receive a total of 8 oz of apple juice and resident (#41) only received one 4 oz. container of apple juice on his/her tray. On 04/10/2024 at 12:15 PM Dietary Manager staff (#7) was made aware of the above findings and resident (#41) was given another 4 oz container of apple juice on his/her tray to drink.
CONCERN (D)

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

Deficiency F0839 (Tag F0839)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on review of employee files and online sources and interviews with facility staff, it was determined that the facility fai...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on review of employee files and online sources and interviews with facility staff, it was determined that the facility failed to ensure Geriatric Nursing Assistant (GNA) staff had active, current certification. This was evident for 1 of 5 GNAs (GNA #11) reviewed for staff qualifications during the survey. The findings include: The Maryland Board of Nursing (MBON) is the agency charged with the regulatory oversight of the practice of nursing in the State. The MBON's mission is to preserve the field of nursing by advancing safe, quality care in Maryland through licensure, certification, education, and accountability for public protection. All nursing assistants must be certified in order to work. The primary source verification of certification status is found in the Look Up A License feature of the MBON website. This secure program is updated daily. On [DATE] at 1:07 PM, review of the Look Up A License feature on the MBON website showed the certification status for GNA #11 as non-renewed and with an expiration date of [DATE]. On [DATE] at 1:10 PM, in an interview with the Director of Nursing (DON), she stated she could not explain why GNA #11 was currently working with expired certification but would look into it. On [DATE] at 1:46 PM, in an interview with the DON, she stated that GNA #11's certification was expired, and that they were on the way to MBON now. The Administration Team was made aware of the concerns at the time of survey exit on [DATE] at 1:30pm.
CONCERN (D)

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

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

Based on observations and interviews it was determined that the facility staff failed to maintain infection control practices as evidenced by having uncovered linen carts, a pillow and two pads for si...

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Based on observations and interviews it was determined that the facility staff failed to maintain infection control practices as evidenced by having uncovered linen carts, a pillow and two pads for side rails on the floor in the linen closet, and the soap and hand sanitizer dispensers were empty in the Soiled Utility Room on the unit Sudbrook. This deficient practice was evident for one linen closet and one utility room observed during the survey. The findings include: On 04/17/24 at 9:38 am the surveyor and Infection Preventionist/Educator #6 opened the door to the linen closet on Waters Edge Unit and observed the linen was not covered and a pillow and a box of gloves were on the floor inside the linen closet. Infection Preventionist/Educator #6 verbalized the linen cart is not removed from the closet. The cart is brought upstairs, and the linen cart is refilled. On 04/17/24 at 9:47 am the surveyor observed two blue side rail pads on the floor in the linen closet on Sudbrook. Infection Preventionist/Educator #6 verbalized they should not have been on the floor. On 04/17/24 at 10:01 am Geriatric Nursing Assistant #53 verbalized the two blue side rail pads could have come from a resident's room and they usually don't have them lying around. On 04/17/24 10:07 AM observation of the Soiled Utility Room South side of Sudbrook unit revealed the hand sanitizer dispenser and both soap dispensers were empty. On 04/18/24 10:14 am during an interview with Facilities Maintenance Manager/Environmental Services Director #77 the staff are supposed to let him know when the hand sanitizer/soap dispensers are empty, and they are supposed to check them every other day. The environmental services staff are supposed to check and fill out the soap and hand sanitizer dispensers.
CONCERN (D)

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

Safe Environment (Tag F0921)

Could have caused harm · This affected 1 resident

Based on observation and interviews it was determined that the facility staff failed to notify maintenance personnel of maintenance problems on the unit Sudbrook. The deficient practice was evident on...

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Based on observation and interviews it was determined that the facility staff failed to notify maintenance personnel of maintenance problems on the unit Sudbrook. The deficient practice was evident on 1 unit. The findings include: On 04/17/24 at 9:38 am while the surveyor was on the unit Sudbrook with Infection Preventionist/Educator #6 the surveyor attempted to turn the light on in the linen closet and the light did not come on. On 04/17/24 at 9:49 am while on the unit Sudbrook near the nursing station, the surveyor observed the right side of the food cart open, and the trays were exposed. The surveyor attempted to close the door several times to no avail. During an interview with Licensed Practical Nurse #28 he/she verbalized the staff should have reported the issue to the kitchen immediately. The aides and nurses collected the trays and put them on the cart. When Dietary Aide #67 reached the unit to retrieve the food cart the surveyor asked if he/she was aware the right door did not close Dietary Aide #67 reported Certified Dietary Manager #7 was made aware of the problem on the previous day. On 04/17/24 at 9:55 am Geriatric Nursing Assistant (GNA) #68 verbalized trying to close the door on the right side of the food cart multiple times, and it did not close. GNA #23 verbalized the door on the food cart would not close after placing the trays on the food cart. On 04/17/24 at 10:07 am the surveyor was in the Soiled Utility Room on the South Side of Sudbrook and the light did not come on in the room where the trash chute was located. On 04/17/24 at 10:14 am the surveyor asked LPN #54 what the process was for the staff to follow when there was a maintenance issue on the unit. LPN #54 verbalized they have a red folder for staff to write maintenance problems on the unit. Maintenance comes to check the book daily. The surveyor checked the maintenance log to see if the food cart and two non-working lights on the unit were documented and they were not. On 04/18/24 10:07 am during an interview with Facilities Maintenance Manager/Environmental Services Director #77, the surveyor asked if the department had a maintenance schedule and what was the process for notifying the department of maintenance issues. Facilities Maintenance Manager/Environmental Services Director #77 verbalized the maintenance schedule consists of filter changes, checking smoke detectors, checking the generators etc. Fire drills are done once a month and disaster drills are done once a year. There is a book for water treatment. The staff have two cell phones and receive calls and emails about maintenance issues. There is one tech for long term care, but he can pull a tech from another part of the facility if needed ant they make rounds and check the red maintenance logs daily.
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

Deficiency F0943 (Tag F0943)

Could have caused harm · This affected 1 resident

Based on review of facility policy and employee files and interviews with facility staff, it was determined that the facility failed to ensure staff participation in mandatory abuse training. This was...

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Based on review of facility policy and employee files and interviews with facility staff, it was determined that the facility failed to ensure staff participation in mandatory abuse training. This was evident for 1 of 5 Geriatric Nursing Assistants (GNA #43) reviewed for abuse training during survey. The findings include: On 4/16/24 at 10:43 AM, review of the facility's policy entitled, Residents/Patient Rights- Abuse, Neglect, Mistreatment or Misappropriation of Resident/Patient's Property, revealed, All employees, including management staff and volunteers, will receive training upon orientation and annually. On 4/16/24 at 2:46 PM, review of employee files revealed GNA #43 was hired on 6/23/23 and did not reveal documentation of participation in any type of abuse training. On 4/17/24 at 1:30 PM, the facility provided a copy of GNA #43's printed Relias transcript of completed online trainings. The document entitled, Training Hours, revealed GNA #43 did not participate in any type of abuse training. Furthermore, review of the Reporting Abuse Training Attendance Sheet conducted on 2/8/24 by Staff #6 and Staff #24 did not reveal GNA #43's signature of participation. In an interview with Staff #9 on 4/17/24 at 4:07 PM, he stated the employee files provided to the survey team contained any, and all documents related to that employee. Furthermore, he stated that anything pertaining to an employee would be inside the employee's file and would not need to be requested separately. In an interview with the Director of Nursing (DON) and Staff #9 on 4/18/24 at 9:52 AM, when asked about the training clinical staff, such as nurses and GNA's, must receive before providing care to residents, the DON stated all clinical staff must participate in twelve mandatory competencies including an abuse training. The DON and Staff #9 were made aware that GNA #43, who was hired on 6/23/23, had no documentation in her employee folder demonstrating abuse training, had no abuse training on her Relias Training Hours transcript, and did not sign the attendance sheet from February 2024's abuse training provided by the facility. The Administration Team was made aware of all concerns at the time of survey exit on 4/18/24 at 1:30 PM.
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

Deficiency F0947 (Tag F0947)

Could have caused harm · This affected 1 resident

Based on the review of employee records and staff interview, it was determined that the facility failed to provide documentation that a Geriatric Nursing Assistance's (GNA) was given abuse training at...

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Based on the review of employee records and staff interview, it was determined that the facility failed to provide documentation that a Geriatric Nursing Assistance's (GNA) was given abuse training at least once every 12 months. This was evident for 1 of 4 GNA employee records (Staff #25) reviewed during the sufficient and competent nursing staffing task during the recertification survey. The findings include: A review of facility reported incident MD00198544 on 04/09/24 revealed an allegation Resident #259 was the victim of staff to resident verbal abuse on 09/30/23. The surveyor was unable to review the facility investigation due to staff being unable to locate the investigation documents. A review of Staff member #25's employee records failed to reveal that Staff member #25 was provided abuse training one year prior to the alleged 09/30/23 incident. Further review of Staff member #25's educational records revealed that Staff member #25 received Recognizing, Reporting, and Preventing Abuse training last on 08/30/2022. In an interview with the facility director of nurses (DON) on 04/11/24 at 10:22 am, the DON stated that the current facility ownership did not have access to employee educational records prior to the sale of the facility on 01/01/24. The DON was unable to provide the surveyor with documentation that staff member #25 had received abuse training that occurred in 2023.
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

Report Alleged Abuse (Tag F0609)

Could have caused harm · This affected multiple residents

3. According to record review, Resident #54 was diagnosed with major depressive disorder, adult failure to thrive, Alzheimer's disease, severe dementia with behavioral disturbance, peripheral vascular...

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3. According to record review, Resident #54 was diagnosed with major depressive disorder, adult failure to thrive, Alzheimer's disease, severe dementia with behavioral disturbance, peripheral vascular disease, abnormal weight loss. The medical record documented a brief interview for mental status (BIMS) score of 01/15 for the resident from the time of admission through the time of the incapacity evaluation on 02.26.24 indicating severe cognitive impairment. On 04.05.24 at 08:30 AM the surveyor reviewed the intake, MD00200917, a facility related incident report regarding Resident # 54 and the elopement that occurred on 12.24.23 at 19:29. The intake revealed that the resident #54 eloped unwitnessed, from a locked unit via an elevator and was able to exit to the courtyard of the facility, was discovered missing at 7:29 PM and returned to the unit by 8:15 PM by staff members. The incident report was submitted to the state agency on 12.25.23 at 19:20 PM which was more than the required 2 hour minimum for reporting. On 04.05.24 at 09:15 AM the DON stated that the facility report for Resident #54 was incomplete and that the administration team would contact the former owners of the facility to obtain the additional documentation related to the 12.24.23 elopement incident. At the time of the exit conference on 04.18.24 at 1:30 PM the facility had not provided any additional documentation related to Resident # 54's elopement. 4. According to record review, Resident # 10 was diagnosed with severe vascular dementia, cerebral vascular disease, major depressive disorder, and schizoaffective disorder upon admission on 12.27.21. The minimum data set assessment (MDS) completed on 03.05.24 reflected a brief interview for mental status (BIMS) score of 7 out of 15 for Resident #10 indicating moderate cognitive impairment. On 04.08.24 at 09:30 AM the surveyor reviewed the intake, MD00203719, related to a facility reported incident that was submitted to the OHCQ. Resident #10 alleged that a male geriatric nursing assistant (staff # 51) committed sexual abuse towards him/her on 03.11.24 in the morning by allegedly inappropriately touching of the resident. The facility initiated an investigation at 12:15 PM on 03.11.24 and notified the family representative who was present during the start of the initial investigation. The outcome of the facility investigation that was documented in the final incident report stated the allegations were unproven. On 04.10.24 at 10:30 AM during an interview with the DON the surveyor was informed that the previous owners did not provide all related documents related to the facility incident reports in the folders that are currently being distributed to surveyors for review. The initial facility report was submitted to OHCQ on 03.11.24 at 5:00 PM electronically per the copy of the document provided to the surveyor by the facility. However, Resident #10 reported the allegation on 03.11.24 at 12:15 PM to the nurse manager, staff #50. There was a delay in the facility reporting the alleged abuse to OHCQ based on the documentation reviewed by the surveyor. The facility failed to report an allegation of neglect related to the elopement of resident #54 and an allegation of abuse towards resident # 10 to OHCQ within the two-hour timeframe requirement. These areas of concern related to the timely submission of facility related incident reports were discussed with the facility administrative team during the survey process and at the time of exit on 4/18/24 at 1:30 PM. 2. Review on 04/12/24 at 11:35 AM of the facility's abuse neglect, mistreatment or misappropriation of resident's property policy revealed staff should report all allegations of abuse immediately to their supervisor. On 04/15/24 at 12:15 pm while reviewing the facility's investigation for MD00201069 involving Resident #69 the surveyor read the Administrator was notified of the incident of suspected abuse on 12/29/23 at 9:08 am. Further review of the report revealed the incident was submitted to the state agency on 12/29/23 at 10:02 pm which was outside of the 2-hour window required to report a potential abuse/neglect allegation. Based on reviews of the facility investigation and other pertinent information, reviews of a closed medical record, and staff interview, it was determined that the facility 1) failed to report allegations of possible abuse to the local police within 2 hours when a resident (# 255) was identified with an injury of unknown source (fracture). and 2) failed to notify the state agency within 2 hours of a potential abuse/neglect incident. This was evident for 4 (Resident # 69, # 54 and # 10, #255) of 9 residents reviewed for abuse during the recertification survey. The findings include: 1. A review of the facility abuse policy on 04/16/24 revealed under Section V. Reporting, any witnessed or suspected violations involving mistreatment, neglect, or abuse, including injuries of an unknown source and misappropriation of resident property, must be reported immediately to the employee's supervisor. Under Section P. indicated that: Local law enforcement agencies will be notified as appropriate. Under Section VIII. Abuse Coordinator Procedures: K. Should the investigation reveal that abuse, neglect, mistreatment, or misappropriation of resident's/patient's property occurred, the Abuse Coordinator or designee will report such findings to the local Police Department, (if applicable) the Ombudsman, and the New Jersey Department of Health & Senior Services and Risk Management within twenty-four (24) hours. It is to noted that the facility changed ownership on 01/01/24. A review of Resident #255's closed medical record on 04/16/24 revealed that Resident #255 suffered from dementia and was unable to communicate with staff as to the possible cause when Resident #255 was identified with swelling and bruising to the left lower leg on 03/16/24 at 9:30 am. Reviews of facility reported incident (FRI) MD00203805 on 04/11/24 revealed an allegation Resident #255 was observed with bruising to the left knee on 03/16/24. Review of the facility investigation revealed that Resident #255 was identified with swelling and bruising to the left knee, by Staff #12, at 9:30 am on 03/16/24. Resident #255's physician and family were made aware of the new swelling and bruising. On 03/17/24 at 8:45 am, the facility director of nurses (DON) was made aware of the x-rays results which identified a fracture of Resident #255's left tibia and fibula (lower leg). The facility investigation indicated that the DON notified the facility administrator of Resident #255's left tibia and fibula fracture at 11 am. Further review of the facility investigation indicated the facility did not notify the local law enforcement of an injury of unknown source. In an interview with Staff #12 on 04/16/24 at 2:55 PM, Staff #12 stated that he/she was the employee who observed swelling and bruising to Resident #255's left leg area on 03/16/24 at 9:30 am. Staff #12 stated that he/she observed big bruising to Resident #255's left leg. Staff #12 stated that Resident #255 was currently receiving hospice services on 03/16/24. Staff #12 also stated that Resident #255 did not complain of pain, showed signs of being in pain, or could explain how he/she received the swelling and bruising to the left leg.
CONCERN (E)

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

Staffing Information (Tag F0732)

Could have caused harm · This affected multiple residents

Based on observations and interviews with facility staff, it was determined that the facility failed to ensure staffing information was posted in a prominent place readily accessible to residents and ...

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Based on observations and interviews with facility staff, it was determined that the facility failed to ensure staffing information was posted in a prominent place readily accessible to residents and visitors. This was evident for 2 (Watersedge and Sudbrook) of 4 units in the facility reviewed for staffing information. The findings include: On 4/4/24 at 8:18 AM, the surveyor did not observe staffing information posted on the Watersedge unit. On 4/4/24 at 8:30 AM, the survey team did not observe staffing information posted on the Sudbrook unit. In an interview with Geriatric Nursing Assistant (GNA #12), they stated even though it [staffing information] was not posted, we know who our residents are for the day because we always have the same schedule. On 4/15/24 at 11:20 AM, the survey team did not observe staffing information posted on the Sudbrook unit. In an interview with Licensed Practical Nurse, (LPN #28), when asked where staffing information was posted, they stated it was in here [a binder inside the nurse's station]. LPN #54 made a copy of the staffing information and posted it on the bulletin board across from the nurse's station. On 4/16/24 at 2:31 PM, the surveyor did not observe staffing information posted on the Watersedge unit. In an interview with GNA #22, when asked where staffing information was posted on the unit, they stated it was posted on the other side [Sudbrook unit]. Furthermore, they stated, for the past couple weeks they had worked on the unit, there had not been staffing information posted. On 4/17/24 at 9:39 AM, the survey team did not observe staffing information posted on the Watersedge unit. On 4/17/24 at 10:00 AM, in an interview with LPN #28, they stated the expectation is that staffing information is posted on each unit. The surveyor made them aware that there was not a posted staffing sheet on the Watersedge unit at this time. LPN #28 stated it is the nurse's responsibility to post the staffing schedule at the beginning of the shift and that today, LPN #90, was the nurse responsible for posting the staffing information on Watersedge today. The surveyor asked LPN #90 if they posted the staffing information on Watersedge today and she said no. The Administration Team was made aware of the concerns at the time of survey exit on 4/18/2024 at 1:30pm.
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

Food Safety (Tag F0812)

Could have caused harm · This affected multiple residents

Based on observations and staff interviews it was determined the facility failed to: 1) store food in accordance with professional standards for food safety; 2) ensure that staff are preparing food un...

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Based on observations and staff interviews it was determined the facility failed to: 1) store food in accordance with professional standards for food safety; 2) ensure that staff are preparing food under sanitary conditions; and 3) ensure that appropriate testing supplies were not outdated to evaluate the safe operation of the facility kitchen dishwasher. This was evident during the kitchen observation of the recertification survey. The findings include: 1) An initial tour of the facility kitchen was completed on 04/04/2024 at 08:00 AM with Dietary Manager staff (#7) and the following was observed. Review of the following items failed to reveal an expiration date: One can of medium sliced beets One can of lightly seasoned tomato sauce Several (amount) spice containers of spices One gallon container of deluxe style mayonnaise One gallon container of ranch dressing. Additionally, the following items were found to be expired: Three containers of Thickened Orange Juice from concentrate moderately thick honey consistency had an expiration date of 09/24/2023. Two containers of Redi-Shred Hashbrown Potatoes had an expiration date of March 2024 One container of sugar Free low calorie breakfast syrup had an expiration date of 05/07/2023. During an interview on 4/4/2024 at 8:28 AM with Dietary Manager staff #7 confirmed the findings and stated the above listed items should have been labeled with an expiration date. Staff (#7) also stated that the above listed items were expired and would be discarded right away. 2) During observation rounds of the facility kitchen on 04/05/2024 at 1:16 PM Dietary Manager staff (#7) and Dietary Aide staff (#19) were observed not wearing a hair net. Staff (#7) was made aware of this observation. During observation rounds of the facility kitchen on 04/18/2024 at 11:47 AM it was observed that there were no hairnets to apply before entering the kitchen. During observation rounds of the facility kitchen on 04/18/2024 at 11:47 AM Lead [NAME] staff (#80) was observed not wearing a beard restraint and his/her beard was exposed. Dietary Manager staff (#7) was made aware of this observation. During an interview on 04/18/2024 at 11:49 AM Lead [NAME] staff (#80) was asked why there were not any hairnets near the entry of the kitchen and he/she stated that someone may have used the last one and discarded the box. Staff (#80) was also asked if staff wear beard coverings/restraints and he stated that they do not use beard coverings in the kitchen. During observation rounds and interview on 04/18/2024 at 11:51 AM Dietary Manager staff (#7) was observed not wearing a hairnet or beard restraint. Staff (#7) stated he has never worn a hairnet because he has no hair. It was observed that staff (#7) had scalp hair, facial hair, and a beard. 3) During observation rounds of the facility kitchen on 04/05/2024 at 1:50 PM it was observed that the Hydrion ph and sanitizer test strips that were being used by Dietary Manager staff (#7) to test the facility kitchen dishwasher water sanitation concentration level had expired on 06/30/2021. All concerns were discussed with the Administration team on 4/18/24 at 1:30 PM
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

Medical Records (Tag F0842)

Could have caused harm · This affected multiple residents

Based on administrative and medical record reviews and staff interview, it was determined that the facility failed to: 1) accurately maintain medical records for a resident (# 19); and 2) maintain a c...

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Based on administrative and medical record reviews and staff interview, it was determined that the facility failed to: 1) accurately maintain medical records for a resident (# 19); and 2) maintain a completed copy of an investigation into an allegation of staff to resident abuse; 3) provide complete access to closed resident electronic medical records; and 4) identify and maintain accurate electronic medical records by having nursing staff members signing off resident care that was performed by the assigned staff member. This was evident for 8 of 8 records reviewed for accuracy of medical records during an recertification survey. The findings include: 1) Review of resident (#19) medical record on 04/10/2024 at 3:30 PM revealed residents (#19) current care plan had a focus area stating that resident (#19) was at risk for wandering and elopement related to his/her medical diagnosis of Alzheimer Dementia. This focus area was initiated on 07/26/2022 and last revised on 01/18/2024. On 04/10/2024 at approximately 4:00 PM the Director of Nursing staff (#2) provided the survey team with a list of all facility residents that were at risk for wandering and elopement. On review of the resident list, resident (#19) was not listed. During an interview on 04/10/2024 at 4:20 PM the Director of Nursing staff (#2) was made aware that residents (#19) current care plan states he/she was at risk for wandering and elopement and was also not listed on the facility list of residents that were at risk for wandering and elopement as provided. Staff (#2) stated that resident (#19) was not a risk for wandering and elopement and the care plan needed to be corrected. On 04/12/2024 at approximately 10:30 AM the Director of Nursing staff (#2) provided this surveyor with a copy of residents (#19) Elopement Evaluation that was completed on 04/11/2024 at 11:30 AM. On review of the evaluation it indicated that residents (#19) score was 3 and was not at risk for elopement at time of the assessment. The Director of Nursing staff (#2) also provided this surveyor with a copy of resident (#19) revised care plan. On review of the revised care plan provided, it stated that on 04/11/2024 that focus area stating that resident (#19) was at risk for wandering/elopement related to a his/her medical diagnosis of Alzheimer Dementia was resolved. 2) A review of the facility investigation into facility reported incident (FRI) MD00198544 on 04/10/24 only revealed a police report case number. The allegation of staff to resident abuse was made by a family member on 10/02/23 for Resident #259. The facility file did not contain investigation reports, staff interviews, evidence that the alleged staff to resident physical abuse was conducted or reported to the State Survey Agency or local Ombudsman. In an interview with the facility director of nurses (DON) on 04/10/24 at 2:20 pm, the DON confirmed that the facility had changed owners on 01/01/24. The DON also stated that s/he was only able to locate the police report case number document. The DON also stated that s/he could not locate any other documents or information that the former owners and staff had conducted an investigation related to the allegation of staff to resident abuse on 10/02/23. 3) During a review of complaints MD00173689, MD00184359, MD00194492, MD00199492, and facility reported incidents MD00195163 and MD00198544 during the recertification survey, the facility was unable to grant surveyor full access to residents #252, #253, #256, #257, #258, and #259's closed electronic medical records. Specifically, the Documentation Survey Record V2 for each discharged resident prior to 01/01/24. The Documentation Survey Record V2 is the electronic document where each GNA (geriatric nursing assistant) documents the care they provided to each resident during a particular shift. The surveyor can validate or not validate the care provided to each resident during a particular shift. In an interview with the facility DON on 04/17/24 at 1:39 pm, the DON stated that the facility was unable to give the surveyor access to any resident's closed record prior to 01/01/24. The DON also stated that the facility did not have the ability to grant surveyor access to any discharged resident's closed record prior to 01/01/24 when the new company purchased the facility. 4) Reviews of facility reported incident (FRI) MD00203805 on 04/11/24 revealed an allegation Resident #255 was observed with bruising to the left knee on 03/16/24. Review of the facility investigation revealed that Resident #255 was identified with swelling and bruising to the left knee, by Staff member #12, at 9:30 am on 03/16/24. Review of Resident #255's electronic medical record revealed documentation Staff #53 had charted Resident #255's morning care on 03/16/24. In an interview with Staff #53 on 04/16/24 at 11:21 AM, Staff #53 stated that he/she was not assigned nor provided care for Resident #255 on the morning of 03/16/24. Staff #53 stated that Staff #12 was assigned to Resident #255 the morning of 03/16/24. Staff #53 stated that Staff #12 charted care provided to Resident #255 under his/her computer access login information on the morning of 03/16/24. Staff #53 stated that he/she did not sign out of the computer after he/she had completed charting and left the computer logged in and available for other staff to use. In an interview with Staff #12 on 04/16/24 at 2:55 pm, Staff #12 confirmed that he/she was assigned to and charted in the electronic medical record for Resident #255 using Staff #53's computer access on 03/16/24. Staff #12 stated that he/she was assigned to Resident #255 during the day shift on 03/16/24. Staff #12 stated that he/she was the employee who identified the swelling and bruising to Resident #255's left knee area on 03/16/24 at 9:30 am. Staff #12 stated that he/she does have his/her own computer access to the residents electronic medical records but computer access may not work at times.
CONCERN (E)

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

Deficiency F0865 (Tag F0865)

Could have caused harm · This affected multiple residents

Based on administrative record review and interviews with facility staff it was determined the facility failed to have an effective Quality Assurance Performance Improvement (QAPI) program in place to...

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Based on administrative record review and interviews with facility staff it was determined the facility failed to have an effective Quality Assurance Performance Improvement (QAPI) program in place to address identified quality deficiencies. This was found to be evident during the facility's survey. The findings Include: During the facility's current survey conducted on April 4, 2024, thru April 18, 2024, deficient practice was identified in the following areas: Quality of Care with one example of a resident (# 17) who did not receive pain medication with a suspected fracture, Supervision of residents with a history of wandering, Functioning call bell system and Neglect and Abuse allegations. An employee (# 85) was terminated in December 2023 for not following protocols for providing Activities of Daily Living (ADL's) assistance to a resident (#1). During an interview with the DON on 4/18/24 at 10:00 AM she was informed that the facility provided the survey team with attendance sheets for monthly meetings conducted by the Quality Assurance (QA) committee for December 2022, January 2023, February 2023, April 2023, June 2023, January 2024, and February 2024. The DON was asked to explain how identified concerns are brought to the QAPI team and what process was put in place to ensure that these identified concerns do not occur again, and she stated the following: She stated that all concerns are brought to the QAPI team for review. A root cause analysis is completed, and an improvement plan is then implemented. All staff are educated, specific to the identified areas of concern. The DON was asked to provide documentation of staff education and facility's improvement plan that was implemented after the occurrence in December 2023 regarding resident # 1. The DON acknowledged that neglect and abuse should have been presented to the QA team in January 2024 following the incident and it was not done and was unable to provide documentation to the survey team. In addition, the DON was unable to provide documentation of identified concerns and processes that were implemented from the period of July 2023 through November of 2023. She stated that corrective measures will be put in place. All concerns were discussed with the Administration team at the time of exit on 4/18/24 at 1:30 PM.
CONCERN (E)

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

Deficiency F0868 (Tag F0868)

Could have caused harm · This affected multiple residents

Based on administrative record review and interviews with facility staff it was determined the facility failed to ensure that the Quality Assessment and Assurance (QAA) committee met at least on a qua...

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Based on administrative record review and interviews with facility staff it was determined the facility failed to ensure that the Quality Assessment and Assurance (QAA) committee met at least on a quarterly basis to address identified concerns and evaluate the effectiveness of their action plan. This was found to be evident during a review of the facility's Quality Assurance Performance and Improvement (QAPI) meeting attendance sheets during the survey. Findings include: The survey team requested copies of the QAPI monthly attendance sheets for January 2023 thru February 2024 on 4/18/24 at 10:00 AM. The facility provided copies of QAPI attendance sheets for the following months: December 2022, January 2023, February 2023, April 2023, June 2023, January 2024, and February 2024. During an interview with the DON on the same date at 11:00 AM she was asked how often the QAPI committee members meet to address all identified concerns that are brought before the team, and she stated that stated that the standard for the internal team members is that they are to meet monthly. She went on to say that all other vendors or outside resources are invited quarterly. Some of the vendors or outside resources are the Pharmacy, Behavior Health Group, and Outside Imaging Group. The DON acknowledged that the facility did not meet the standard requirements for meeting monthly and on a quarterly bases for the months of July 2023 thru November 2023. All concerns were discussed with the Administration team at the time of exit on 4/18/24 at 1:30 PM.
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 F0919 (Tag F0919)

Could have caused harm · This affected multiple residents

Based on observations and interviews it was determined the facility failed to maintain a working call bell system. This was evident for 1 resident (#5) out of 7 residents and 2 rooms (#113 and #127) o...

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Based on observations and interviews it was determined the facility failed to maintain a working call bell system. This was evident for 1 resident (#5) out of 7 residents and 2 rooms (#113 and #127) out of 6 rooms during the survey. The findings include: During observation rounds on 04/05/2024 at 9:20 AM on the facility's first floor nursing station, Meadowood, call lights were noted to be going off. The call lights were observed for approximately 25 minutes. This surveyor observed the nurses' station on Meadowood for possible staff, no one was present at that time. The monitor for the call lights at the nursing station read system failure for Rooms #113 and #127. During an interview and observation on 04/05/2024 at 9:51 AM resident (#5) call bell was pressed by this surveyor and call bell did not work. During an interview on 04/05/2024 at 10:00 AM Regional Administrator staff (#9) was made aware of the above observations by this surveyor. Staff (#9) stated that he would check into the call bell system right away.
Jun 2019 9 deficiencies
CONCERN (D)

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

Resident Rights (Tag F0550)

Could have caused harm · This affected 1 resident

2. Resident #26 was observed sitting in the common area in his/her Geriatric chair on 6-17-19 at 9:50 AM and 6-18-19 at 8:30 AM. Resident #26 is totally dependent on the facility staff for all care du...

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2. Resident #26 was observed sitting in the common area in his/her Geriatric chair on 6-17-19 at 9:50 AM and 6-18-19 at 8:30 AM. Resident #26 is totally dependent on the facility staff for all care due to impaired cognition. The chair had a 3 in x 5 in paper with his/her name taped to the back of the chair. The name label was visible to all who walked past Resident #26. This dignity issue was discussed with the Director of Nursing(DON) and the Staff # 5 on 6-19-19 at 8:40 AM and confirmed by the DON. Based on observation and staff interview it was determined that the facility staff failed to ensure residents' dignity was maintained. This was evident for 4 out of the 34 residents reviewed as part of the survey: The findings are: 1. This surveyor observed on 6/18/19 at 8:12 AM one resident eating breakfast while the other two residents at the table were waiting for their food. Two tables over and closer to the unit entrance there are two breakfast trays. One is in front of a resident who is eating from the breakfast tray and the other is in front of an empty chair. A resident was brought over at 8:14 AM and began eating. A second tray was placed in front of one of the residents at the first table at 8:27 AM. The third resident was moved to different table and served a tray at 8:30 AM. The Director of Nursing was interviewed on 6/20/19 at 11:31 AM. She said she would address the issue with her staff.
CONCERN (D)

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

Deficiency F0578 (Tag F0578)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and interview, it was determined the facility staff failed to void an older MOLST form located in...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and interview, it was determined the facility staff failed to void an older MOLST form located in a resident's active medical record for Resident (#73) and failed to ensure an advance directive which allowed for medical decisions was in place for Resident (#129). This was evident for 2 of 5 residents selected for review of advance directives and 2 of 38 residents selected for review during the annual survey process. The findings include: An advance directive is a written statement of a person's wishes regarding medical treatment, often including a living will, made to ensure those wishes are carried out should the person be unable to communicate them to a doctor. Advance directives only apply to health care decisions and do not affect financial or money matters. The Maryland MOLST is a portable and enduring medical order form covering options for cardiopulmonary resuscitation and other life-sustaining treatments. The medical orders are based on a resident's or Power of Attorney (POA) wishes about medical treatments. The use of MOLST increases the likelihood that a resident's wishes regarding life-sustaining treatments are honored throughout the health care system. Do Not Resuscitate (DNR) is a legal order, written or oral depending on country, indicating that a person does not want to receive cardiopulmonary resuscitation (CPR) if that person's heart stops beating. 1. The facility staff failed to void an older MOLST form from the active medical record. Medical record review for Resident #73 revealed on [DATE] the resident's surrogate completed a MOLST indicating the resident was to be a DNR: transfer to hospital for severe pain, may perform any medical test, may use antibiotics (oral, intravenous, intramuscular) and no hemodialysis. Further record review revealed on [DATE] the surrogate revised and changed the MOLST to reflect: do not transfer to hospital but treat with options available outside the hospital and do not perform any medical test for diagnosis or treatment. It was noted the facility staff placed the back of the MOLST completed on [DATE] to the MOLST completed on [DATE] in a plastic sleeve in the hard copy medical record. It is the expectation that when a MOLST has been updated or changed, the outdated MOLST either be removed from the active medical record and archived or have a line drawn through it and marked as void to decrease any confusion on the validity of the active MOLST. Interview with the Director of Nursing on [DATE] at 1:00 PM confirmed the facility staff failed to remove an outdated MOLST from the active medical record for Resident #73. 2. The facility staff failed to ensure advance directives were in place for Resident #52. Medical record review for Resident #129 revealed the physician completed and revised a MOLST on [DATE]. At that time, it was indicated the completion of the MOLST, and end of life orders are based on: the patient's health care agent as named in the patient's advance directive. Further record review revealed the medical record contained a Power of Attorney (POA); however, the POA was for financial decisions: real estate transactions, baking transactions, making investments, tax matters, insurance transactions and government benefits to name a few. There is no evidence the POA had the authority to make medical decisions other than: to make arrangements for my admission to or discharge from, or transfer from any hospital, hospice, nursing home, adult home, assisted living or other similar care facility. Interview with the social worker on [DATE] 10:00 AM confirmed the medical record failed to reveal an advance directive naming a POA the authority to make end of life decisions for Resident #129. Interview with the Director of Nursing on [DATE] at 1:00 PM confirmed the facility staff failed to ensure the evidence of an advance directive for Resident #129 allowing medical decisions for end of life care was available.
CONCERN (D)

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

Deficiency F0655 (Tag F0655)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and staff interview, it was determined the facility failed to provide the resident and their repr...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and staff interview, it was determined the facility failed to provide the resident and their representative with a summary of the baseline care plan within 48 hours of admission to the facility. This was evident for 1 (Resident #97) of 3 residents reviewed during an annual recertification survey. The findings include: A care plan is a guide that addresses the unique needs of each resident. It is used to plan, assess and evaluate the effectiveness of the resident's care. Review of Resident #97's medical record on 6/17/19 revealed Resident #97 was admitted to the facility on [DATE]. Review of the medical record failed to reveal documentation that a copy of the baseline care plan was provided to Resident #97 or Resident #97's responsible party within 48 hours after admission. In an interview with the facility Social Worker on 6/20/19 at 8:30 AM the facility Social Worker confirmed the facility staff did not supply Resident #97 nor his/her responsible party with a copy of the baseline care plan after being admitted to the facility. The facility staff must take steps to supply a copy of the baseline care plan within 48 hours of a resident's admission.
CONCERN (D)

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

Quality of Care (Tag F0684)

Could have caused harm · This affected 1 resident

Based on interview, observation and medical record review the facility staff failed to provide all treatments and services as ordered by the physician for Residents (#22 and #76). This is evident for ...

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Based on interview, observation and medical record review the facility staff failed to provide all treatments and services as ordered by the physician for Residents (#22 and #76). This is evident for 2 out of 2 residents selected for review during the investigation stage of the survey process. 1. A review of Resident #76's clinical record revealed that the resident's primary physician wrote an order for the resident to receive Boost Breeze (a nutritional supplement) 8 ounces one time a day and document the percentage of the supplement consumed each time. A review of the Medication Administration Record for March, April, May and June of 2019 revealed that nursing staff has not documented the amount consumed as ordered. The Director of Nursing was interviewed on 06/19/19 at 09:47 AM. She confirmed that the nursing staff did not document the amount of Boost Breeze consumed. 2. Surveyor observation of medication pass on 6/18/19 at 8:20 AM revealed facility staff #3 failed to administer medications in accordance with the standard of practice. Medications (oral) are delivered by pharmacy and placed in a plastic bag with the resident's name and room number. Medications are then documented using an electronic medical record (EMR). The EMR is facilitated using a lap top computer which contains the residents name, room number and medications to be administered, including times to be administered. During observation of the medication pass, the facility staff indicated the battery was dead on the computer. At that time, the facility staff approached the room of Resident #22. The facility staff obtained the plastic bag containing the medications for Resident #22, opened the bag and proceeded to administer the oral medications to the resident; however, failed to check the EMR to determine the accuracy of the medications being administering. Failure of the facility staff to use the EMR denied the staff to document the administration of the medications to Resident #22. Failure to use the EMR puts the facility staff at risk for administering medications which may have been discontinued or doses changed. It was noted, the administration of medication for Resident #22 also resulted in the failure to administer 3 medications. Interview with the Director of Nursing on 6/18/19 at 9:00 AM confirmed the standard of practice is the use of the EMR to administer medications. The Director of Nursing and Nursing Home Administrator was made aware of this practice and the medication error rate immediately after medication pass observation. Interview with the Director of Nursing on 6/20/19 at 1:00 PM confirmed facility staff #3 failed to provide care to Resident #22 which represented professional standards. See F 759
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 medical record review and interview, the facility staff failed to perform and/or document weekly skin and wound assessm...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and interview, the facility staff failed to perform and/or document weekly skin and wound assessments for a Resident (#43) with a pressure ulcer. This was evident for 1 out of 6 residents selected for review during the investigation stage of the survey process. The findings included: A pressure ulcer also known as pressure sore or decubitus ulcer is any lesion caused by unrelieved pressure that results in damage to the underlying tissue. Pressure ulcers are staged according the their severity from Stage I (area of persistent redness), Stage II (superficial loss of skin such as an abrasion, blister or shallow crater), Stage III (full thickness skin loss involving damage to subcutaneous tissue presenting as a deep crater) or Stage IV (full thickness skin loss with extensive damage to muscle, bone or tendon). Resident #43 was admitted from the hospital on [DATE], without any pressure ulcers. Reviewed of Resident #43's medical record revealed a BRADEN scale assessment for predicting pressure sore risk. The Braden Scale is an evidenced-based tool, that predicts the risk for developing a hospital or facility acquired pressure ulcer/injury. The Braden Scale uses a scores from less than or equal to 9 to as high as 23. The lower the number, the higher the risk for developing an acquired ulcer/injury. Resident #43's scored 22 on the BRADEN scale a score of 19-23 is at no risk for developing a pressure sore. Review of the medical records revealed that on 3/6/19, resident #43 developed a pressure ulcer to his/her left ankle in the facility that is now currently a Stage 3 ulcer. Further review of the Resident's medical record revealed there were no weekly skin assessments and wound sheets observation documented for the resident. The standard of practice for the care of pressure ulcers is for the facility staff to conduct weekly assessments and document findings that include the location, measurement, stage and characteristics of a pressure ulcer. This information provides facility staff with information to determine whether the pressure ulcer is healing or worsening at future assessments and to evaluate which treatment plan would be most effective to heal the ulcer. Interview with the Director of Nursing on 6/20/19 at 12:30 PM confirmed the facility staff failed to thoroughly assess and document a resident's pressure ulcers according to current practice standards.
CONCERN (D)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

Based on record review, observation and staff interview, it was determined the facility staff failed to ensure that the resident's environment was free from potential accidents (#77). This was evident...

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Based on record review, observation and staff interview, it was determined the facility staff failed to ensure that the resident's environment was free from potential accidents (#77). This was evident for 1 of 38 residents selected for review during the annual survey process. The findings include: Surveyor interview with Resident #77 on 6/17/19 at 12:00 PM revealed the resident indicated there was medication at the bedside. Surveyor observation of Resident 77's room on 6/18/19 at 1:50 PM and 6/19/19 at 9:15 AM revealed the resident had a meter dose inhaler at the bedside. The ProAir inhaler multi-dose inhaler was noted at the bed side. ProAir inhaler is used to prevent and treat wheezing and shortness of breath caused by breathing problems (such as asthma, chronic obstructive pulmonary disease). Further record review revealed no evidence that the resident was assessed to determine the ability to use the inhaler or a physician's order allowing the resident the ability to administer self-medications. Interview with the Director of Nursing on 6/20/19 at 1:00 PM confirmed the facility staff failed to maintain an environment for Resident #77 free from potential accidents.
CONCERN (D)

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

Deficiency F0700 (Tag F0700)

Could have caused harm · This affected 1 resident

Based on record review, observation and interview, it was determined the facility staff failed to apply 1/4 side rails to a resident's bed (#86) as ordered. This was evident for 1 of 38 residents sele...

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Based on record review, observation and interview, it was determined the facility staff failed to apply 1/4 side rails to a resident's bed (#86) as ordered. This was evident for 1 of 38 residents selected for review during the annual survey process. The findings include: Medical record review for Resident #86 revealed on 1/29/19 the physician ordered: 1/4 side rails as enablers for turning and repositioning. A side rail is structural support attached to the frame of a bed and intended to prevent a patient from falling. Bed rails include any combination of partial or full rails (e.g., one-side half-rail, one-side full rail, two-sided half-rails or quarter-rails, rails along the side of the bed that block three-quarters to the whole length of the mattress from top to bottom, etc.). The potential for serious injury is more likely from a fall from a bed with raised side rails rather than from a fall from a bed where side rails are not used. Surveyor observation of Resident #86 on 6/17/19 at 1:00 PM, 6/18/19 at 1:45 PM and 6/19/19 at 9:15 AM revealed the resident in bed; however, the facility staff placed 2 full side rails on the bed for Resident #86. Interview with the Director of Nursing on 6/19/19 at 1:00 PM revealed the facility does not have beds with full side rails and was unaware of where that bed came from. Interview with the Nursing Home Administrator on 6/20/19 at 1:00 PM revealed the bed with the 2 full side rails was a hospice bed and was unaware of where the bed came from; however, the facility staff failed to intervene and obtain a bed that provided the resident with 1/4 side rails as ordered by the physician (until surveyor intervention).
CONCERN (D)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected 1 resident

Based on observation, it was determined the facility staff failed to properly store medications. This was observed once during an annual recertification survey. The findings include: An observation w...

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Based on observation, it was determined the facility staff failed to properly store medications. This was observed once during an annual recertification survey. The findings include: An observation was made on 06/19/19 at 12:55 PM on the second-floor rehabilitation unit. The surveyor observed an unattended and unlocked treatment cart. The treatment cart held schedule II narcotic medications for the resident's residing on the second-floor rehabilitation unit. No nursing staff members were attending the medication cart at the time of the observation. The charge nurse was immediately made aware of the observation.
CONCERN (E)

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

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected multiple residents

Based on observation of medication pass and interview, it was determined the facility staff failed to obtain a medication error rate less than 5% (Residents #22, #16 and #20). This includes 3 out of 6...

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Based on observation of medication pass and interview, it was determined the facility staff failed to obtain a medication error rate less than 5% (Residents #22, #16 and #20). This includes 3 out of 6 residents observed for medication pass, 21 errors out of 35 opportunities with a medication error rate of 62.86%. The findings include: The facility uses an Electronic Medical Record (EMR) for the administration and documentation of medications for administration to the residents. The physician's orders for the medications are entered the EMR with the times of medication administration. During medication observation, the computer will display yellow for the medication to be administered in that time frame. Any medication outside the time frame of administration will be gray. When gray, the facility staff is not able to document administration since it is not in the ordered time frame. Medications must be given within a ½ hour of the time that is listed on the medication log. This means that you have ½ hour before the medication is due, and ½ hour after it is due to administer the medication in order to be on time with medication administration. The Five Rights of Medication Administration. One of the recommendations to reduce medication errors and harm is to use the five rights: the right patient, the right drug, the right dose, the right route, and the right time. Medications (oral) are delivered by pharmacy and placed in a plastic bag with the resident's name and room number. Medications are then documented using an electronic medical record (EMR). The EMR is facilitated using a lap top computer which contains the residents name, room number and medications to be administered, including times to be administered. Observation of medication pass revealed facility staff #3 administered medications to Residents #16 and #20 outside of the ordered time frame and failed to document the administration of those medications. Error 1. The facility staff failed to administer a medication to Resident #22. Medical record review for Resident #22 revealed on 3/1/16 the physician ordered: Restasis .05%, 1 drop both eyes every day. Restasis eye drops are used to treat chronic dry eye that may be caused by inflammation. Observation of medication pass on 6/18/19 at 8:20 AM revealed facility staff #3 failed to administer the eye drop as ordered. Error 2. The facility staff failed to administer a medication to Resident #22. Medical record review for Resident #22 revealed on 11/10/16 the physician ordered: Alphagan .1%, left eye, 3 times a day. Alphagan is indicated for the reduction of elevated intraocular pressure (IOP) in patients with open-angle glaucoma. Observation of medication pass on 6/18/19 at 8:20 AM revealed facility staff #3 failed to administer the eye drop as ordered. Error 3. The facility staff failed to administer a medication to Resident #22. Medical record review for Resident #22 revealed on 4/1/17 the physician ordered: MiraLAX 17 gram by mouths every day. MiraLAX is a gentle laxative that provides relief from occasional constipation. Observation of medication pass on 6/18/19 at 8:20 AM revealed facility staff #3 failed to administer the MiraLAX as ordered. Error 4. The facility staff failed to administer medication to Resident #16 at the correct time. Medical record review revealed on 2/27/17 the physician ordered: Calcium 600 + D tablet (Calcium Carbonate-Vit D), 1 tablet a day for supplement. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:25 AM and failed to document the administration of the medication since it was out of the time frame. Error 5. The facility staff failed to administer medication to Resident #16 at the correct time. Medical record review revealed on 2/27/17 the physician ordered: Celebrex 200, 1 time a day for arthritic pain. Celebrex is a nonsteroidal anti-inflammatory drug used to treat pain or inflammation. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:25 AM and failed to document the administration of the medication since it was out of the time frame. Error 6. The facility staff failed to administer medication to Resident #16 at the correct time. Medical record review revealed on 5/16/18 the physician ordered: Lasix 40, 1 time a day for leg edema. Lasix is a diuretic which increases urinary output. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:25 AM and failed to document the administration of the medication since it was out of the time frame. Error 7. The facility staff failed to administer medication to Resident #16 at the correct time. Medical record review revealed on 12/20/18 the physician ordered: Metformin 500 mg, 1 tablet 2 times a day for Diabetes. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:25 AM and failed to document the administration of the medication since it was out of the time frame. Error 8. The facility staff failed to administer medication to Resident #16 at the correct time. Medical record review revealed on 2/27/17 the physician ordered: Omega-3 fatty acid, 1 by mouth, 1 time a day as a supplement. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:25 AM and failed to document the administration of the medication since it was out of the time frame. Error 9. The facility staff failed to administer medication to Resident #16 at the correct time. Medical record review revealed on 8/29/18 the physician ordered: -Vitamin D3-5000 IU, 1 capsule, 1 time a day as a supplement. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:25 AM and failed to document the administration of the medication since it was out of the time frame. Error 10. The facility staff failed to administer medication to Resident #16 at the correct time. Medical record review revealed on 4/23/18 the physician ordered: Advair Diskus Aerosol, 1 inhalation 2 times a day for wheezing, rinse after use. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:25 AM and failed to document the administration of the medication since it was out of the time frame. Error 11. The facility staff failed to rinse Resident #16's mouth after the use of Advair per order. Medical record review revealed on 4/23/18 the physician ordered: Advair Diskus Aerosol, 1 inhalation 2 times a day for wheezing, rinse after use. Advair Diskus (fluticasone and salmeterol oral inhaler) is a combination of a corticosteroid and a beta2-adrenergic bronchodilator used to treat asthma and chronic bronchitis, including COPD associated with chronic bronchitis. Rinse your mouth with water without swallowing after each dose of Advair Diskus. This will help lessen the chance of getting a yeast infection (thrush) in the mouth and throat. Observation of medication pass revealed the facility staff #3 administered the Advair; however, failed to rinse Resident #16's mouth. Error 12. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 6/25/18 the physician ordered: Norvasc 10 milligrams (Mgs), by mouth 1 time a day for blood pressure. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 13. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 2/8/18 the physician ordered: Aspirin 81 mgs, 1 time a day for coronary artery disease. Low dose aspirin helps the blood flow and decreases the chance of blood clots. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 14. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 6/25/18 the physician ordered: Coreg 6.25 mgs, 1 tablet 2 times a day for blood pressure. Coreg lowers the blood pressure and heart rate. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 14. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 2/4/19 the physician ordered: Folic acid, 1 mg by mouth 1 time a day as a supplement. Folic acid is a B vitamin. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 15. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 4/4/18 the physician ordered: Lasix 40 mg by mouth 1 time a day for leg edema. Lasix is a diuretic which increases urinary output and decreasing any excess fluid. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 16. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 6/13/19 the physician ordered: Lisinopril 5 mg by mouth 1 time a day for blood pressure. Lisinopril is a medication that lowers the blood pressure. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 17. The facility staff failed to obtain the blood pressure for Resident #20 as ordered. Medical record review for Resident #20 revealed on 6/13/19 the physician ordered: Lisinopril 5 mg by mouth 1 time a day for blood pressure, monitor blood pressure daily for 7 days-notify NP if SBP (top number) less < than 110. Observation of medication pass revealed the facility staff administered the medication to Resident #20; however, failed to take the blood pressure as ordered. Lisinopril is a medication that lowers the blood pressure. Error 18. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 2/8/18 the physician ordered: Mycophenolate 250 mg, 1 tablet 2 times a day for organ rejection. Mycophenolate (CellCept) is used with other medications to help prevent transplant organ rejection (attack of the transplanted organ by the immune system of the person receiving the organ) in adults who have received heart and liver transplants. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 19. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 2/8/18 the physician ordered: Omeprazole 20 mg by mouth 1 time a day for GERD. Omeprazole oral capsule is used to reduce the amount of acid in your stomach. It's used to treat gastric or duodenal ulcers, gastroesophageal reflux disease (GERD), erosive esophagitis, and hypersecretory conditions. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 20. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 5/8/19 the physician ordered: Tacrolimus .5, 1 time a day for organ rejection, give with 3 mg. Tacrolimus is an immunosuppressive drug whose main use is after organ transplant to reduce the activity of the patient's immune system and so the risk of organ rejection. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. Error 21. The facility staff failed to administer medication to Resident #20 at the correct time. Medical record review for Resident #20 revealed on 4/3/19 the physician ordered: Tacrolimus 3, 1 time a day for organ rejection, give with .5 mg to equal 3.5 mgs. Tacrolimus is an immunosuppressive drug whose main use is after organ transplant to reduce the activity of the patient's immune system and so the risk of organ rejection. Medical record review revealed the medication was to be administered at 10:00 AM; however, the facility staff administered the medication at 8:35 AM and failed to document the administration of the medication since it was out of the time frame. (Of note, the facility staff administered 3- 1 mg tablets of the medication). The Director of Nursing and Nursing Home Administrator was notified immediately after medication pass of the error rate and the practice of facility staff #3 in administering medications outside the time frame and failure to document the administration of the medications for Residents #22, #16 and #20.
Mar 2018 4 deficiencies
CONCERN (D)

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

Transfer Notice (Tag F0623)

Could have caused harm · This affected 1 resident

Based on record reviews and staff interviews, it was determined the facility failed to inform or provide notification to the Department of Aging, the Ombudsman office, of resident transfers to the hos...

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Based on record reviews and staff interviews, it was determined the facility failed to inform or provide notification to the Department of Aging, the Ombudsman office, of resident transfers to the hospital. This was evident for three residents, #116, #119, and #128 out of 30 selected for review during the annual survey process. The findings include: 1. The facility failed to provide written notification to the Ombudsman when Resident #116 was sent to the hospital 11/28/17, 911 for emergency evaluation and treatment for swelling of the abdominal cavity with hematuria and enlarged scrotum. The resident was sent to the hospital per physician order. Documentation in the record reveals physician and family notification of the transfer, but there is no documentation in the record that the Ombudsman was notified in writing of the resident transfer. The resident returned to the facility after his hospitalization. 2. The facility failed to provide written notification to the Ombudsman office (Dept. of Aging) when Resident #119 was sent to the hospital from the wound care clinic on 11/28/17 and admitted for treatment. Further review of the record reveals Resident #119 was sent to the hospital 3/1/18 and was admitted , returning 3/6/18. There is documentation that the family member was with the resident during both transfers to the acute care hospital but no documentation that the Ombudsman was notified in writing of these transfers. 3. The facility failed to provide written notification to the Dept. of Aging, the Ombudsman, when Resident #128 was sent to the hospital 12/15/17 in acute respiratory distress. There is documentation in the record that the responsible party and physician were notified of the transfer, but no documentation that the Ombudsman's office was notified in writing or email of the transfer. The resident was only in the facility less than 24 hours but no evidence of notification to the Ombudsman. The resident has not returned to the facility. The Administrator, the Director of Nursing and the Social Worker confirmed the lack of notification to the Department of Aging, Ombudsman office on 3/15/18 at 2PM.
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 medical record review and staff interview it was determined the facility staff failed to ensure that the information us...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and staff interview it was determined the facility staff failed to ensure that the information used to complete the Minimum Data Set (MDS) comprehensive assessments for functional status was accurate for Resident #67. This was evident for 1 of 20 residents reviewed during the final stage of this survey. The Minimum Data Set (MDS) is a comprehensive assessment of the resident completed by the facility staff. The MDS is a multi-disciplinarian tool that allows many facets of the resident's care [cognition, behavior, mobility, activities of daily living, accidents, activities, weight, pain and medications to name a few] to be addressed. The MDS assessment is part of a broader RAI (Resident Assessment Instrument) process. The RAI process ties the assessment and care plan to the delivery of care to meet the needs of the resident. MDS or Minimum Data Set coordinators are nurses that are tasked to ensure that patient servicing is well documented especially during the assessment phase in facilities that are accredited or offer Medicaid or Medicare services. The prospective payment system (PPS) is defined as Medicare's predetermined pricing structure to pay for medical treatment and services. A care plan is a guide that addresses the unique needs of each resident. It is used to plan, assess and evaluate the effectiveness of the resident's care. The findings include: Medical record review revealed resident #67 was admitted to the facility with diagnoses that included but were not limited to Muscle Weakness Dementia and Parkinson's disease. Review of the 5-day PPS assessment dated [DATE] and a Significant Change MDS assessment dated [DATE] revealed facility staff coded the resident in Section G Functional Status G0400 Functional Limitation in Range in Motion A- Upper Extremity as a 0 (no impairment) for both extremities. On 3/13/18 at 11:37 AM during an interview with the resident the surveyor noted the resident had a right-hand contracture and that no splint had been applied to the hand. Contractures are the chronic loss of joint motion due to structural changes in non-bony tissue. The MDS inaccuracy was confirmed with the MDS Coordinator on 3/15/18 at 10:35 AM.
CONCERN (E)

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

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected multiple residents

Based on medical record review and staff interview it was determined the facility failed to develop a care plan that addressed: 1) treatment and services for Resident #67's right upper extremity contr...

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Based on medical record review and staff interview it was determined the facility failed to develop a care plan that addressed: 1) treatment and services for Resident #67's right upper extremity contracture; 2) oral care for a resident (Resident #86) noted to have poor oral hygiene. This was evident for 1 of 30 residents reviewed during the final stage of this survey. A care plan is a guide that addresses the unique needs of each resident. It is used to plan, assess and evaluate the effectiveness of the resident ' s care. Contractures are the chronic loss of joint motion due to structural changes in non-bony tissue. The findings included: 1)Medical record review revealed resident #67 was admitted to the facility with diagnoses that included but were not limited to Muscle Weakness Dementia and Parkinson's disease. The resident was functionally impaired and required staff assistance with ADLs. During an interview with the resident on 3/13/18 at 11:37 AM the surveyor noted the resident had a right-hand contracture and that no splint had been applied to the hand. Further observation on 3/14/18 at 2:55 PM revealed that no splint was applied to the resident's right hand. Further medical record review revealed the facility failed to develop a care plan to address contracture management for this functionally impaired resident, to prevent further decline in range of motion. If the joints, muscles, ligaments, and tendons are not exercised they will contract or stiffen. The findings were discussed with the Unit Manager on 3/15/18 at 11:35 AM. 2) The facility failed to develop a care plan to address oral care for a resident (Resident #86) noted to have poor oral hygiene During an interview with the surveyor on 03/13/18 at 9:57 AM Resident #86 complained of mouth pain. The resident stated s/he had teeth pulled several weeks ago and was still having some discomfort. Medical Record Review on 3/14/18 revealed a physician's progress note, dated 1/10/18, that reported the resident was seen for redness and swelling on the right side of her/his face. The physician noted the resident had poor dental hygiene and a broken tooth in the back of his/her mouth. A dental consult note dated 1/11/18 reported the resident had 3 teeth extracted due to abscess. A Nurse Practitioner documented on 2/1/18 that the resident had gingivitis. Review of the March 2018 Medication and Treatment Administration Records failed to evidence monitoring of the resident's oral care by facility staff. Further review of the medical record on 3/14/18 revealed the facility failed to develop a plan to monitor/manage poor oral hygiene for Resident #86 and the ADL care plan did not contain interventions to address the resident's poor oral health. The findings were discussed during the exit conference on 3/15/18 at 3:45 PM.
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 medical record review and staff interview it was determined the facility failed to: 1)update the care plan that address...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and staff interview it was determined the facility failed to: 1)update the care plan that addressed falls for a functionally impaired resident (Resident #30), who sustained a fracture after a fall, based on a comprehensive assessment and included individualized interventions; 2) revise a care plan that addressed impaired skin integrity for a resident (Resident #67) who repeatedly sustained skin tears; 3) update a care plan for Resident #41 that incorporated her/his preference for bathing; and 4) review and revise a care plan that addressed activities for a functionally and cognitively impaired resident based on Resident #28's abilities, interests and treatment needs. This was evident for 4 of 4 residents reviewed for care plan updates during the final stages of this survey. The Minimum Data Set (MDS) is a comprehensive assessment of the resident completed by the facility staff. The MDS is a multi-disciplinarian tool that allows many facets of the resident's care [cognition, behavior, mobility, activities of daily living, accidents, activities, weight, pain and medications to name a few] to be addressed. The MDS assessment is part of a broader RAI (Resident Assessment Instrument) process. The RAI process ties the assessment and care plan to the delivery of care to meet the needs of the resident. A care plan is a guide that addresses the unique needs of each resident. It is used to plan, assess and evaluate the effectiveness of the resident's care. The findings include: Medical record review on 3/14/18 revealed Resident #30 was admitted to the facility with diagnoses that included but were not limited to Heart failure, Abnormalities of Gait and Mobility, Transient Ischemic Attacks and Generalized Muscle Weakness. Review of the quarterly MDS assessment dated [DATE] revealed a BIMS score of 12 out of 15 in Section C Cognitive Patterns. Brief Interview for Mental Status (BIMS) is an assessment that assists staff in determining a resident's cognitive status. A score of 13-15 indicates cognitively intact, 08-12 indicates moderately impaired, and 00-07 indicates severe impairment. Review of the Annual MDS assessment dated [DATE]- MDS revealed the resident required supervision and assistance with transfers and the resident triggered for falls. An incident note dated 12/21/17 at 4:55 PM reported facility staff answered the call light to Resident #30's room and observed the resident lying on the right side of bed on the floor, on her/his back, complaining of left hip pain. It is further noted that the left leg was shorter than the right leg. An order was obtained to send the resident via 911 to the hospital where it was determined s/he had a hip fracture. A Morse Fall assessment dated [DATE] indicated the resident was a high risk for falls. A care plan that addressed an actual fall related to unsteady gait was initiated on 5/4/17. Interventions added on 12/21/17 included maintain a clutter free environment, continue interventions on the at-risk plan, and physical therapy consult for strength and mobility. The reason for the fall that occurred on 12/21/17 was not clear. It was not noted if the resident was attempting to go to the bathroom, if s/he rolled out of bed or there were other contributing factors that could be addressed in the care plan. There was no indication that clutter contributed to the fall. The surveyor sought clarification regarding the at-risk plan but facility staff did not provide clarity. The plan did not reflect recommendations from the therapy department, the level of supervision needed to maintain safety or resident involvement. The findings were discussed with the Director of Nursing on 3/15/18 at 12:35 PM. 2)The facility failed to revise a care plan, based on a comprehensive assessment, that addressed impaired skin integrity for a resident (Resident #67) who repeatedly sustained skin tears. Medical record review revealed resident #67 was admitted to the facility with diagnoses that included but were not limited to Muscle Weakness Dementia and Parkinson's disease. Medical record review on 3/15/18 at 11:37 AM revealed documentation of skin injuries as follows: 7/7/17 -A Weekly Wound Observation Tool noted a new skin tear to the back of the hand; 7/31/17-Skin Observation Tool noted the resident had a skin tear to the left lower leg due to hitting her/his leg against the wheelchair leg; 8/22/17Skin Observation Tool noted a scab to left hand; 10/17/17- Skin Observation Tool noted a skin tear to the right arm; 12/15/17- A Nursing Communication Form noted a skin tear to the right hand; 12/29/17- A Nursing Communication Form noted a skin tear to the right hand; 1/19/18- Skin Observation Tool noted a skin tear to the left hand; 1/25/17- A Nursing Communication Form SBAR noted a skin tear to the right wrist; 1/30/18- A Skin Observation Tool noted a skin tear to the left lower leg; and 3/2/18-Skin Observation Tool noted treatment to right wrist skin tear continues. During an interview with the surveyor on 03/13/18 at 11:37 AM the surveyor noted an abrasion to the resident's right hand. The Resident stated, I keep hitting it. The medical record contained a care plan, initiated on 7/7/17 with an intervention that staff would identify potential causative factors (of skin injuries) and eliminate/resolve those factors. Review of the care plan, initiated on 12/29/17, that addressed actual skin tear related to fragile skin contained interventions that were initiated on 12/29/17. One of the interventions directed staff to apply geri-sleeves (Protects residents' arms and legs against damage caused by friction and shearing) to prevent skin tears or worsening condition of the skin. In interview with the surveyor on 3/15/18 at 11:40 AM the Unit Manager stated the resident's skin is very fragile and sometimes the resident is resistive to care which places her/him at risk for skin injuries. This is not indicated on the care plan along with interventions to address combative behavior during care. Medical record review failed to reveal a comprehensive review of factors contributing to skin tears for Resident #67 and adjustments to the care plan to maintain skin integrity. 3) The facility failed to address the Resident #41's preference for showers versus baths. During an interview with the surveyor on 03/13/18 at 11:24 AM the resident's responsible party (RP) expressed the desire for the resident to have more showers. Review of the medical record on 3/15/18 at 1:18 PM revealed an ADL care plan initiated on 12/23/15. The plan does not address the resident's preference for showers versus baths. Review of the ADL Records revealed there was no indication the resident received a shower between the periods 1/1/18-2/1/18, 2/17/18, 2/18/18- 3/5/18 and 3/2/18- 3/15/18. Activities of Daily Living, or ADLs, are the basic tasks of everyday life, such as eating, bathing, dressing, toileting, and transferring. During an interview with the surveyor on 3/15/18 at 2:35 PM the Unit Manager stated Resident #41 was to receive showers twice a week on the 11-7 shift. The Unit Manager stated the facility maintained shower books, where staff document showers, in addition to the electronic ADL records. The Unit Manager stated that when residents refuse showers the charge nurse is notified so that he/she can address the refusal. Review of the shower book on 3/15/18, for the period January 2018- March 2018, revealed staff documented that the resident refused showers or did not receive a shower. The medical record did not indicate the refusals were reported or addressed. Review of the care plan notes for January 2017- January 2018 revealed the issue of the resident's bathing preference or refusals was not addressed. The findings were discussed with the Director of Nursing during the exit conference on 3/15/18 at 3:45 PM. 4)The facility failed to review and revise a care plan that addressed activities for a functionally and cognitively impaired resident based on Resident #28 ' s abilities, interests and treatment needs. Medical record review revealed Resident #28 was admitted to the facility with diagnoses that included but were not limited to Functional Quadriplegia, Contracture of the upper and lower extremities, Seizure Disorder, Degenerative Disease of the Nervous System and Brain Injury. Review of the quarterly MDS assessment dated [DATE] revealed facility staff coded the resident as severely cognitively impaired in Section C Cognitive Patterns. A review of the activities care plan, initiated on 12/15/15 revealed the interventions had not been updated since the plan was initiated. One of the interventions directs staff to ensure that the activities the resident is attending are compatible with physical and mental capabilities and are age appropriate. The plan stated the resident needed 1:1 room visits/activities if s/he is unable to attend out of room events. It was unclear from reviewing the care plan what the resident's preferences were. During an interview with the surveyor on 3/15/18 at 1:00 PM the Director of Activities stated the resident liked music. Review of the documentation of therapeutic recreation programs provided to the resident revealed the content of the programs was not indicated or the amount of time spent with the resident. The findings were discussed with the Director of Nursing during the exit conference on 3/15/18 at 3:45 PM @ 11:53 AM.
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

  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • No major safety red flags. No abuse findings, life-threatening violations, or SFF status.
Concerns
  • • 37 deficiencies on record. Higher than average. Multiple issues found across inspections.
  • • $23,896 in fines. Higher than 94% of Maryland facilities, suggesting repeated compliance issues.
  • • Grade D (48/100). Below average facility with significant concerns.
Bottom line: Trust Score of 48/100 indicates significant concerns. Thoroughly evaluate alternatives.

About This Facility

What is Resorts Of Augsburg's CMS Rating?

CMS assigns RESORTS OF AUGSBURG an overall rating of 2 out of 5 stars, which is considered below average nationally. Within Maryland, 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 Resorts Of Augsburg Staffed?

CMS rates RESORTS OF AUGSBURG's staffing level at 4 out of 5 stars, which is above average compared to other nursing homes. Staff turnover is 48%, compared to the Maryland average of 46%.

What Have Inspectors Found at Resorts Of Augsburg?

State health inspectors documented 37 deficiencies at RESORTS OF AUGSBURG during 2018 to 2024. These included: 37 with potential for harm.

Who Owns and Operates Resorts Of Augsburg?

RESORTS OF AUGSBURG is owned by a for-profit company. For-profit facilities operate as businesses with obligations to shareholders or private owners. The facility operates independently rather than as part of a larger chain. With 131 certified beds and approximately 118 residents (about 90% occupancy), it is a mid-sized facility located in BALTIMORE, Maryland.

How Does Resorts Of Augsburg Compare to Other Maryland Nursing Homes?

Compared to the 100 nursing homes in Maryland, RESORTS OF AUGSBURG's overall rating (2 stars) is below the state average of 3.0, staff turnover (48%) is near the state average of 46%, and health inspection rating (2 stars) is below the national benchmark.

What Should Families Ask When Visiting Resorts Of Augsburg?

Based on this facility's data, families visiting should ask: "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?" "Can I speak with family members of current residents about their experience?"

Is Resorts Of Augsburg Safe?

Based on CMS inspection data, RESORTS OF AUGSBURG has a clean safety record: no substantiated abuse findings (meaning no confirmed cases of resident harm), no Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death), and is not on the Special Focus Facility watch list (a federal program monitoring the lowest-performing 1% of nursing homes). The facility has a 2-star overall rating and ranks #100 of 100 nursing homes in Maryland. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Resorts Of Augsburg Stick Around?

RESORTS OF AUGSBURG has a staff turnover rate of 48%, which is about average for Maryland 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 Resorts Of Augsburg Ever Fined?

RESORTS OF AUGSBURG has been fined $23,896 across 4 penalty actions. This is below the Maryland average of $33,318. While any fine indicates a compliance issue, fines under $50,000 are relatively common and typically reflect isolated problems that were subsequently corrected. Families should ask what specific issues led to these fines and confirm they've been resolved.

Is Resorts Of Augsburg on Any Federal Watch List?

RESORTS OF AUGSBURG 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.