Medilodge of Alpena

301 Long Rapids Road, Alpena, MI 49707 (989) 356-2194
For profit - Individual 132 Beds MEDILODGE Data: November 2025
Trust Grade
70/100
#48 of 422 in MI
Last Inspection: August 2025

Inspected within the last 6 months. Data reflects current conditions.

Overview

Medilodge of Alpena has a Trust Grade of B, which means it is considered a good choice for families looking for a nursing home. They rank #48 out of 422 facilities in Michigan, placing them in the top half, and are the best option out of two in Alpena County. However, the facility's trend is worsening, with issues increasing from 4 in 2024 to 8 in 2025. While staffing is a strength with a 4 out of 5 rating and a turnover rate of 41%, which is below the state average, there are serious concerns as well, including a failure to recognize a resident's change in condition that led to hospitalization and death. Additionally, two residents developed pressure wounds that required hospitalization, highlighting the need for improved care practices.

Trust Score
B
70/100
In Michigan
#48/422
Top 11%
Safety Record
Moderate
Needs review
Inspections
Getting Worse
4 → 8 violations
Staff Stability
○ Average
41% turnover. Near Michigan's 48% average. Typical for the industry.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most Michigan facilities.
Skilled Nurses
✓ Good
Each resident gets 48 minutes of Registered Nurse (RN) attention daily — more than average for Michigan. RNs are trained to catch health problems early.
Violations
⚠ Watch
22 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★★★★
5.0
Overall Rating
★★★★☆
4.0
Staff Levels
★★★★★
5.0
Care Quality
★★★★☆
4.0
Inspection Score
Stable
2024: 4 issues
2025: 8 issues

The Good

  • 4-Star Staffing Rating · Above-average nurse staffing levels
  • 5-Star Quality Measures · Strong clinical quality outcomes
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover below average (41%)

    7 points below Michigan average of 48%

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

The Bad

Staff Turnover: 41%

Near Michigan avg (46%)

Typical for the industry

Chain: MEDILODGE

Part of a multi-facility chain

Ask about local staffing decisions and management

The Ugly 22 deficiencies on record

2 actual harm
Aug 2025 5 deficiencies
CONCERN (D)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to supply appropriate devices to ensure resident safety w...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to supply appropriate devices to ensure resident safety while smoking for one Resident (#104) of one resident reviewed for safe smoking. Findings include:Resident #104 (R104)On 8/19/2025 at 3:08 PM, R104 was observed in the hallway on her way to the smoking area outside. The smoking times listed for the facility were every two hours on odd hours of the clock. On 8/20/2025 at 1:17 PM, three resident smokers were observed in the outdoor pavilion smoking area accompanied by Certified Nursing Aide (CNA) A and one visitor. R104 was smoking a cigarette and was not wearing a smoking apron for protection against burns. Several ashtrays were on the table with one ashtray positioned directly in front of R104. While R104 was smoking, she backed her wheelchair away from the table and was observed not using the ashtray and flicking ashes from her burning cigarette into the air. The ashes were drifting in the air and not controlled. When questioned, R104 admitted to not wearing a smoking apron and stated she usually did. CNA A stated she did not usually take the smokers out at 1:00 PM as the hall assignments had recently changed, CNA A said, I had no idea (R104 should be wearing a smoking apron.) When R104 was discussing her physical abilities, she said, My fingers are so bad I can't even snap them indicating she had trouble even holding a cigarette at times. The Electronic Medical Record (EMR) for R104 included a Minimum Data Set (MDS) assessment dated [DATE] revealing an admission date of 8/22/24 and a Brief Interview for Mental Status (BIMS) score of 6 out of 15, indicating severely impaired cognition. A review of a physician's order, initiated 9/25/24, stated, Resident to wear a smoking apron at smoke times. Nurse to ensure resident has apron to wear while smoking and that she is using it. The most recent Nursing Quarterly/Significant Change Evaluation -V9 completed on 5/26/25, included a smoking assessment. The summary of this evaluation read, Resident may smoke, at this time 2. Yes, with smoking aid(s), and Smoking aids needed included Smoking apron and Cigarette holder. Both were checked as needed for safety while smoking. The current care plan for R104 reviewed on 8/20/25 included a focus of: Resident chooses to smoke dated as initiated: 8/22/2024. The goal was written as, Resident will smoke safely at the designated area(s) at scheduled times through the next review. Date Initiated: 08/22/2024 Target Date: 08/26/2025. Interventions included, Smoking apron - Date Initiated: 09/25/2024. During an interview on 8/20/2025 at approximately 2:00 PM, the Director of Nursing (DON) stated there had been a recent evaluation of R104s capabilities and a cigarette holder was no longer needed, and this intervention had been removed from the care plan. The DON did not present the documentation for this care plan revision, and it was not found in the EMR during the time of the survey. The DON did confirm R104 should have had a smoking apron in place for her protection while smoking. The facility policy titled Smoking Policy Smoking Campus - Residents dated as reviewed/revised on 5/31/2023 read in part: It is the policy of this facility to establish and maintain safe resident smoking practices. The Attending Physician and the Director of Nursing Services (DNS) shall have the authority to make the determination as to what restrictions, if any, will need to be placed on the resident's smoking privileges. Smoking restrictions may be imposed on residents at any time if the Attending Physician and/or Director of Nursing determine that the resident is not able to smoke safely with supervision. Smoking restrictions (such as need for smoking apron, or specific scheduled smoking times), shall. (be) for the safety and well-being of the resident.
CONCERN (D)

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

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to ensure a medication error rate less than 5 percent, with 3 errors identified, out of 25 medication administration opportuniti...

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Based on observation, interview, and record review, the facility failed to ensure a medication error rate less than 5 percent, with 3 errors identified, out of 25 medication administration opportunities observed. This deficient practice resulted in a medication error rate of 11.54 percent, and the potential for the administration of non-therapeutic doses of medication, and preparation of medication not according to manufacturer's instructions. Findings include: Error 1 and 2. Resident #94 (R94) - During observation of preparation of oral medications for R94 on 8/20/25 at 7:50 AM, Licensed Practical Nurse (LPN) D dispensed cyanocobalamin 500 micrograms (mcg), one tablet into a medication cup prepared for R94. LPN D completed her preparation for morning medication pass for R94 which included 0700 (7:00 AM) and 0800 (8:00 AM) medications. LPN D was asked how much cyanocobalamin was dispensed and replied, One. That's what the order says. LPN D was asked to check her dose of cyanocobalamin that was stored in her medication cart and replied, It is only 500 mcg. I need to give her two I guess. LPN D was asked if that was the only dose supplied in the facility and replied, I think so. I guess I will need to change the order to reflect the correct amount to dispense. Review of R94's physician order, dated 8/7/25, revealed an order for cyanocobalamin 1000 mcg, give one tablet by mouth one time a day at 8:00 AM for B-12 deficiency. Review of R94's physician order, dated 7/18/25, revealed an order for metoclopramide 5 milligrams (mg), give one tablet by mouth before meals for gastroparesis, administer 30 minutes to an hour prior to meals at 7:00 AM, 11:00 AM, and 4:00 PM. Review of R94's medication administration time for metoclopramide, revealed that this medication was dispensed and given at 8:17 AM (17 minutes late). On 8/20/25 at 8:20 AM, an interview was conducted with LPN D, who was asked if R94 liked her metoclopramide prior to breakfast and replied, Yes. LPN D was asked what time breakfast trays came down from kitchen and replied, Around 9:00 AM. LPN D was asked if the metoclopramide was to be given at 7:00 AM then that would be too early to dispense then why she (LPN D) did not have the order time changed to 8:00 AM and replied, I am not sure, but that is a good question because all her (R94) other medications are given at 8:00 AM, and that makes more sense. Error 3. Resident #126 (R126) - During observation of preparation of a rapid-acting insulin pen for R126 on 8/20/25 at 9:00 a.m., LPN D primed the rapid-acting insulin pen by dialing the insulin pen to 2 units and proceeded to prime the pen holding it horizontal (sideways). LPN D administered the insulin in R126's left lower quadrant and held post injection for only six seconds. Review of R126's medication administration record (MAR), dated August 2025, revealed that the rapid-acting insulin was administered in R126's right upper quadrant of her abdomen. On 8/20/25 at 3:35 PM, an interview was conducted with the Director of Nursing (DON), who was made aware of the medication error rate and replied, The nurses are to refer to the manufacturer guidelines for insulin. Priming is done by holding the insulin pen upright (vertical) and post injection hold time is ten seconds. Review of the [rapid-acting insulin pen name] instructions, revealed the following, in part: .Wipe the pen tip (rubber seal) with an alcohol swab . Dial a test dose of 2 Units. Hold pen with the needle pointing up and lightly tap the insulin reservoir so the air bubbles rise to the top of the needle. This will help you get the most accurate dose. Press the injection button all the way in and check to see that insulin comes out of the needle. The dial will automatically go back to zero after you perform the test. If no insulin comes out, repeat the test 2 more times . Keep the pen straight, insert the needle into your skin. Press and hold the button to give the dose. Keep the button pressed and hold for ten seconds. Release the button and remove the needle from your skin . Review of the policy titled, Medication Administration, dated 1/17/23, read in part, Policy: Medications are administered by licensed nurses, or other staff who are legally authorized to do so in this state, as ordered by the physician and in accordance with professional standards of practice, in a manner to prevent contamination or infection. Policy Explanation and Compliance Guidelines.10. Review MAR to identify medication to be administered. 11. Compare medication source with MAR to verify resident name, medication name, form, dose, route, and time of administration.b. Administer within 60 minutes prior to or after scheduled time unless otherwise ordered by physician.
CONCERN (D)

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

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure current infection control practices were mainta...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure current infection control practices were maintained for two Residents (#10 & #126) of 24 residents reviewed for infection control practices related to medication administration and reusable oxygen tubing.Findings include:Resident #10 (R10) Review of the Minimum Data Set (MDS) assessment, dated 6/17/2025, revealed R10 was admitted to the facility on [DATE] with diagnoses including heart failure, chronic respiratory failure, diabetes and dementia. Further review of the MDS assessment revealed R10 had moderate cognitive impairment, required substantial/maximal assistance with personal hygiene and was dependent on staff for transfers and mobility. Review of R10's active physician's orders revealed the following: Oxygen: Run [at] 3 L/Min [liters per minute] via NC [nasal cannula] 24 hours per day continuous. Every day and night shift. Start Date: 6/09/2025. Upon entering R10's room on 8/19/2025 at 12:50 PM, a portable oxygen concentrator was observed to be positioned on the floor next to R10's room. The concentrator was running and set to deliver 3 liters per minute of supplemental oxygen. The tubing dated 8/17 [2025] attached to the concentrator was observed to be draped over a bedside table with a portion of the tubing and an unsheathed nasal cannula resting on a handbag that was positioned atop the table. It was noted there was no protective barrier between the table with the handbag and the tubing and nasal cannula. R10 was not present at the time of the observation. On 8/20/2025 at 8:32 AM the portable oxygen was again observed to be positioned next to R10's bed. The tubing, dated 8/17 [2025], attached to the concentrator was observed to be wrapped around the upper left grab bar of the resident's bed with the unsheathed nasal cannula draped over the head of the bed and resting on the bottom portion of the bed frame, approximately six inches from the ground. R10 was not present at the time of the observation. During an interview on 8/21/2025 at 12:34 PM, the Director of Nursing (DON) reported the expectation was for oxygen tubing to be housed in a clear plastic bag when not in use and if tubing was found touching the floor or a surface deemed to be dirty, the tubing and nasal cannula should be replaced with a new set to avoid resident use of contaminated oxygen tubing. Review of the facility policy titled, “Infection Prevention and Control Program,” implemented 8/20/2020, revealed the following: “The facility has established and maintains an infections preventions and control program designed to provide a safe, sanitary, and comfortable environment and to help prevent the development and transmission of communicable diseases and infections as per accepted [NAME] standards and guidelines … Non-sterile supplies are stored and maintained as clean prior to use.” Resident #126 (R126) On 8/20/25 at 7:50 AM, an observation of R126's medication pass in the main dining room was completed with Licensed Practical Nurse (LPN) “D” who approached R126 seated with three other unidentified residents and placed R126's water, medication cup, and inhaler on the dining room table without a barrier and proceeded to administer R126's medications. LPN “D” separated the water cup with an empty cup and handed R126 her inhaler and then after R126 used the inhaler placed in back on the dining room table without a barrier. After the administration of R126's medication LPN “D” returned the inhaler to her medication cart without sanitizing the inhaler before placing it back into her medication cart. On 8/20/25 at 9:00 AM, an observation was made of LPN “D” administering R126's medications in R126's room and upon entry R126 was utilizing the bathroom. LPN “D” entered R126's bathroom and placed R126's two insulins on top of the bathroom sink vanity without a barrier. LPN “D” assisted R126 in the bathroom, to her bed, and proceeded to wash her hands. During LPN “D's” hand washing LPN “D” turning the water off with her bare hands. LPN “D” then picked up the two insulins for R126 and placed them on R126's bedside table without a barrier. LPN “D” prepped R126's abdomen and proceeded with the first insulin administration while the second insulin pen fell to R126's floor. LPN “D” pick the insulin pen off the floor and placed it back onto R126's bedside table without sanitizing the pen. LPN “D” then gave the second insulin injection to R126 and returned to her medication cart without sanitizing the pen and returned it to her medication cart. On 8/20/25 at 3:35 PM, an interview was conducted with the Director of Nursing (DON), who was asked if for infection control purposes, during medication pass, if items had to be set down that were reusable, and returned to the medication cart, needed a barrier such as a tissue or paper towel and replied, “Yes, staff should be using a barrier if setting medications like this down and returning them to the medication cart and sanitizing them. The insulin pen should have been sanitized before using it if it fell to the floor.”
CONCERN (E)

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

Deficiency F0628 (Tag F0628)

Could have caused harm · This affected multiple residents

Based on interview and record review, the facility failed to provide written bed hold notifications to residents and/or responsible parties for eight Residents (#2, #7, #9, #10, #11, #27, #59, & #87) ...

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Based on interview and record review, the facility failed to provide written bed hold notifications to residents and/or responsible parties for eight Residents (#2, #7, #9, #10, #11, #27, #59, & #87) of nine residents reviewed for hospitalizations. Findings include:Resident #87 (R87) was transferred to the hospital Emergency Department (ED) on 3/13/25. There was no documentation in the Electronic Medical Record (EMR) indicating the resident/responsible party were provided a bed hold notice. Resident #10 (R10) Review of a “Transfer Notice,” dated 6/4/2025 from R10's EMR, revealed the R10 was transferred to the emergency department on 6/4/2025 due to lethargy and decreased alertness. Further review of R10's EMR revealed the Resident was hospitalized following the transfer with return to the facility on 6/9/2025. In review of the EMR, it was noted there was no documentation or signed document indicating the Resident or the Resident's representative was provided with the facility bed hold policy at the time of transfer or thereafter. Resident #11 (R11) Review of a “Transfer Notice,” dated 6/20/2025 and gleaned from R11's EMR, revealed the Resident was transferred to the emergency department on 5/19/2025 for evaluation and treatment of osteomyelitis. Further review of R11's EMR revealed the Resident was hospitalized following the transfer with return to the facility on 5/29/2025. In review of the EMR, it was noted there was no documentation or signed document indicating R11 or R11's representative was provided with the facility bed hold policy at the time of transfer or thereafter. During an interview on 8/21/2025 at 10:38 AM, the Nursing Home Administrator (NHA) reported the facility was not currently supplying information to residents or resident's representatives about bed holds when transferred out to the hospital. The NHA stated he was unsure where the communication breakdown was among staff responsible for providing the information on bed holds but he was now aware and had begun to educate staff of the need to supply the information at the time of transfer or as soon as possible following transfer. Resident #7 (R27) was sent to the ED 8/17/25. There was no documentation in the EMR indicating the resident or responsible party were provided required written bed hold information. Resident #27 (R27) was sent to the ED 5/4/25. There was no documentation in the EMR indicating the resident or responsible party were provided required written bed hold information. During an interview on 8/20/2025 at 2:15 PM, The Nursing Home Administrator (NHA) stated he did not see (in the EMR) that facility bed hold policy was explained (to the resident or responsible parties). Resident #59 (R59) was sent to the ED on 6/22/25 and 7/25/25. The EMR did not contain documentation of the resident or responsible party being provided written bed hold information. Resident #9 (R9) was transferred to the ED 4/7/25, 5/24/25, and 8/1/25. No required written information regarding bed holds to the resident or responsible party were located in the EMR for any of the transfers. Resident #2 (R2) was sent to the ED 4/16/25. There was no documentation in the EMR indicating the resident or responsible party was provided required written bed hold information. The Administrator (NHA) was interviewed on 8/20/25 at 2:00 PM. The NHA said the facility did not issue written bed hold information to residents/responsible parties when residents were transferred to the ED because it depended on their payor source. The NHA said bed hold information was not issued for residents who had Medicaid. On 8/20/25 at 2:47 PM, the NHA confirmed there was no written bed hold information for residents who were transferred to the ED regardless of payor source. The NHA said the policy for written notification of bed holds was reviewed with the business office manager and admissions person who would be responsible for completing written notification of bed holds for all future transfers. The policy “Bed Hold Prior to Transfer” dated as reviewed/revised on 4/22/25 read, in part: “… It is the policy of this facility to provide written information to the resident and/or the resident representative regarding bed hold policies prior to transferring a resident to the hospital or the resident goes on therapeutic leave…the written information given to the resident and/or resident representative will include the following: a. The duration of the state bed-hold, if any, during which the resident is permitted to return and resume residence in the nursing facility b. The reserve bed payment policy in the state plan, if any c. The facility policies regarding bed-holds periods to include permitting residents to return to the next available bed. D. Conditions upon which the resident would return to the facility…6. The facility will provide this written information to all facility residents, regardless of their payment source…”
CONCERN (E)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure safe storage of medications and labeling for t...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure safe storage of medications and labeling for three of three medication carts reviewed for medication storage. Findings include: On [DATE] at 9:30 AM, the A-hall medication cart was observed for medication storage and was found to have five insulin pens without an expiration date. One insulin pen had an opened date of [DATE] and would have been expired on [DATE] and remained in the active medication supply. On [DATE] at 9:40 AM, an interview was conducted with Licensed Practical Nurse (LPN) D, who was asked how long the insulins in her cart were good to use and replied, I don't know. I would have to ask the unit manager. LPN D was asked if she was unsure how long the insulin pens were good for how would she know when to discard them and replied, I guess I better find out. On [DATE] at 2:15 PM, the E-hall medication cart was observed for medication storage and was found to have 13 insulin pens and two insulin vials without an expiration date. On [DATE] at 2:25 PM, an interview was conducted with LPN F, who was asked why none of the insulins had an expiration date on them and replied, Well because we discard all of them when it has been 28 days. LPN F was made aware that currently a nursing staff member was unaware of how long certain insulins were good to utilize and if they were pulled to work in any of the five units they would be unaware if the insulin they were administering was still good to use and replied, I guess we need to add an expiration date to all of them then. On [DATE] at 3:35 PM, an interview was conducted with the Director of Nursing (DON) who was made aware that the medication carts lacked an expiration date on all the insulins and that there was currently a nursing staff member who was unaware of how long the insulin medication was good to utilize and replied, The insulins should have an opened date and an expiration date on all of them. On [DATE] at 4:00 PM, the D-hall medication cart was observed for medication storage and was found to have one insulin pen without an expiration date. On [DATE] at 4:02 PM, an interview was conducted with LPN B who verified that there was no expiration date on the insulin pen. On [DATE] at 4:13 PM, an observation was made of the A-hall medication cart which was unlocked and unsecured. During the six minutes the A-hall medication cart was left unlocked and unattended two unidentified residents went strolling by the A-hall medication cart. On [DATE] at 4:13 PM, an interview was conducted with Certified Nurse Aide (CNA) K, who was asked if nurses were to leave the medication cart unlocked and replied, Well no. CNA K was asked where the nurse was and replied, In helping with the other aide(CNA). On [DATE] at 4:19 PM, an interview was conducted with LPN D, who was asked when she returned to the medication cart why she left the medication cart unlocked and unattended and replied, I wasn't thinking. I just went and was helping out. Review of policy titled, Medication Storage, dated [DATE], read in part, Policy: It is the policy of this facility to ensure all medications housed on our premises will be stored according to the manufacturer's recommendations and sufficient to ensure proper sanitation, temperature, light, ventilation, moisture control, segregation, and security. Policy Explanation and Compliance Guidelines. 1. General Guidelines: a. All drugs and biologicals will be stored in locked compartments. Review of policy titled, Storage of Medications, dated 9/2018, read in part, Policy: Medications and biologicals are stored safely, securely, and properly, following manufacturer's recommendations or those of the supplier. The medication supply is accessible only to licensed nursing personnel, pharmacy personnel, or staff members lawfully authorized to administer medications.Expiration Dating (Beyond-Use Dating).3. Certain medications or package types, such as IV [intravenous] solutions, multiple dose injectable vials, ophthalmics, nitroglycerin tablets, and blood sugar testing solutions and strips require an expiration date shorter than the manufacturer's expiration date once opened to ensure medication purity and potency.
Feb 2025 3 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

Quality of Care (Tag F0684)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure quality of care was provided for two Residents...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure quality of care was provided for two Residents (R8, and R9) of nine residents reviewed for quality of care by failing to: 1. provide diabetic foot care and 2. perform proper assessments and charting for new admissions. Findings include: This citation pertains to intake: MI00149326. Resident #8 (R8) Review of R8's MDS assessment dated [DATE], revealed admission to the facility on 4/10/24, with active diagnoses that included: heart failure, depression, diabetes mellitus, and hypertension. R8 scored a 15 of 15 on the BIMS assessment reflective of intact cognition. On 2/5/25 at 9:10 AM, an observation was made of R8 in her room sitting up on the side of her bed leaning over her bedside table. R8 was not wearing any socks or shoes. R8 was asked how she was doing and why her toenails were so long and replied, I know they are long and ugly. R8 was observed to have bilateral great toenails to be an inch long, her left foot second through fifth toes were a half an inch long, and her right foot second and third toenails were a half an inch long. R8 was asked if she had diabetes mellitus and replied, Yes, I really would like them cut. I need to get them cut. Review of R8's care plan, dated 4/11/24, read in part .Resident has an impaired metabolic status related to diabetes .Diabetic foot checks every evening, monitor for impairments with skin and nails . On 2/6/25 at 11:45 AM, this Surveyor, the DON, and Nurse Manager / LPN J went to see R8 in her room to observe her toenails. Both the DON and LPN J agreed that R8's toenails were too long. R8 stated that she was never offered podiatry services when she was admitted . On 2/6/25 at 12:00 PM, the DON stated podiatry services were just at the facility on 1/29/25, but R8 was not on the list to be seen. The DON could not find any documentation that R8 was offered podiatry services upon admission to the facility. The DON was asked why R8 was not added to the podiatry list after daily diabetic foot assessments. The DON did not have an answer when asked about why podiatry services were not offered on admission. The DON also stated, I'm not sure why they [nursing] wouldn't cut R8's toenails with her being diabetic and they are very long. Review of policy Skin Integrity - Foot Care, dated 10/26/23, read in part Policy: It is the policy of this facility to ensure residents receive proper treatment and care to maintain mobility and good foot health. This policy pertains to maintaining the skin integrity of the foot. Policy Explanation and Compliance Guidelines: 1. The facility will provide foot care and treatment in accordance with professional standards of practice, including the prevention of complications from the resident's medical conditions .3. Interventions for Prevention and to Promote Healing: a. Interventions will be based on specific factors identified in the risk assessment, skin assessments, and assessments of any foot ulcers. i. As needed, licensed nurses with adequate training may perform nail care to non-diabetic residents, or diabetic residents who are low risk as determined by podiatrist or physician . Resident #9 (R9) Review of R9's MDS assessment dated [DATE], revealed admission to the facility on 2/1/25, with active diagnoses that included: hypertension, atrial fibrillation (abnormal beating of the heart), depression, diabetes mellitus, and anxiety. On 2/6/5 at 8:25 AM, a phone interview was conducted with MD E regarding R9's lab results. MD E stated he was contacted via phone on 2/6/25 by nursing staff with reports of abnormal labs for R9. MD E advised the facility to send R9 to the hospital for further evaluation. MD E stated he was upset the facility did not make him aware of R9's wishes to change providers to them. MD E stated he would have handled laboratory diagnostics sooner and indicated it may have made a difference in the outcome. On 2/6/25 at 9:00 AM, a review of R9's medical record was conducted, and the following was identified: a. R9 was originally admitted to the facility on [DATE] for rehabilitation and was receiving skilled nursing services. b. admission weights for three consecutive days were ordered but no weight was obtained for R9 on 2/2/25. c. R9 was ordered to have vital signs for each 12-hour shift as part of the new admission process, but no vital signs were recorded on 2/2/25 or 2/3/25. d. No skilled nursing assessment was documented for R9 on 2/3/25. e. R9's skilled nursing assessments completed on 2/2/25 and 2/4/25 were completed using vital signs from 2/1/25. Review of R9's progress note, dated 2/6/25 at 1:00 AM, read in part Resident's labs were reviewed with provider, received orders to ship out resident based on plenty of abnormal labs .and resident's status of being a full code .Resident stated 'I haven't felt good for the past few days' . On 2/6/25 at 9:30 AM, an interview was conducted with the DON who was asked the reason a comprehensive vital assessment was not recorded every 12 hours in R9's EMR. The DON replied, I am not sure. Let's look at the vital sign sheets to see if staff added her to get a full set of vitals each shift. Review of vital sign sheets, dated 2/2/25 and 2/3/25, revealed that R9's name was not added to the sheets to have her vital signs taken for any of the three shifts over the course of two days. Review of R9's Prehospital Care Report Summary, dated 2/6/25 at 12:39 AM, read in part .Chief Complaint: Abnormal labs. Secondary Complaint: Abdominal pain .Vital Signs .pulse: 145 . atrial fibrillation . On 2/6/25 at 9:45 AM, the DON confirmed R9 should have had vital signs taken on 2/2/25 and 2/3/25 and a weight should have been obtained on 2/3/25. The DON agreed that the expectation for nursing is to ensure there is a new set of vital signs with each skilled nursing assessment and not use vital signs from prior days. The DON stated the expectation was for staff to perform three consecutive weights as part of the new admission process, and if one was missed, then staff were expected to start the process over until there were three consecutive weights. The DON stated R9 originally had a different physician on admission, but then decided to change physicians and MD E was never notified of the change until he was notified of the abnormal labs.
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

Pharmacy Services (Tag F0755)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure medications were dispensed and destroyed per s...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure medications were dispensed and destroyed per standards of practice and per facility policy for two Residents (#1 and #4) of nine residents reviewed for pharmacy services. Findings include: This citation pertains to intake: MI00149326. Resident #1 (R1) Review of R1's Minimum Data Set (MDS) assessment dated [DATE], revealed admission to the facility on [DATE], with active diagnoses that included: heart failure, asthma, diabetes mellitus, and anxiety. R1 scored a 15 of 15 on the Brief Interview of Mental Status (BIMS) assessment reflective of intact cognition. On [DATE] at 8:45 AM, R1 was observed in her room, finishing breakfast at her bedside table. An empty disposable medication cup labeled with R1's last name was observed next to her breakfast tray. R1 stated the floor nurse had recently dropped off her morning medications. When asked if the nurse ensured R1 had taken their medication before leaving the room, R1 replied, No, she just left it, and I have not seen her since. Review of R1's nursing quarterly evaluation, dated [DATE], revealed under section O, self-administration of medications: a. select option that reflects resident's wishes for self-administration of medication: Does not wish to start self-administration. R1's care plan had no goals/interventions for self-administration of medications. On [DATE] at 2:20 PM, an interview was conducted with the Director of Nursing (DON) who was asked the purpose of labeling medication cups. The DON replied, If they (nursing) were pre popping pills or if a resident was not available at the time of administration. Resident #4 (R4) Review of R4's Minimum Data Set (MDS) assessment dated [DATE], revealed admission to the facility on [DATE], with active diagnoses that included: diabetes mellitus, seizures, arthritis, and falls. R4 scored a 11 of 15 on the BIMS assessment, reflective of moderately impaired cognition. On [DATE] at 1:30 PM, several pills were observed on the floor and were picked up. During an interview at the same time, Licensed Practical Nurse (LPN) D was given the pills upon entry to R4's room. LPN D acknowledged the pills should not have been on the floor and threw the pills away in R4's trash. On [DATE] at 2:00 PM, an interview was conducted with the DON who was asked if she was aware of the loose pills found in R4's room. The DON replied, Yes, I talked to the nurse yesterday and took the trash out of R4's room. I asked (LPN D) why she threw them in the trash, and (LPN D) was not sure why she did that. The nurses know that they either dispose of them in the drug buster or the sharps container. Review of R4's physician order, dated [DATE], revealed the following order: phenobarbital (controlled schedule IV barbiturate medication) 64.8 mg, give one tablet by mouth two times a day for history of seizures. Review of the policy Medication Administration, dated [DATE], read in part Policy: Medications are administered by licensed nurses, or other staff who are legally authorized to do so in this state, as ordered by the physician and in accordance with professional standards of practice, in a manner to prevent contamination or infection. Policy Explanation and Compliance Guidelines .15. Observe resident consumption of medication . Review of policy Medication-Destruction of Unused Drugs, dated [DATE], read in part Policy: All unused, contaminated, or expired prescription drugs shall be disposed of in accordance with state laws and regulations (refer to any state-specific requirements). Policy Explanation and Compliance Guidelines: 1. Drugs will be destroyed in a manner that renders the drugs unfit for human consumption and disposed of in compliance with all current and applicable state and federal requirements .6. Schedule II, III, and IV controlled drugs must be destroyed by the Director of Nursing Services and another licensed nurse .
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 F0776 (Tag F0776)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** This citation pertains to intake: MI00149326. Based on interview and record review, the facility failed to ensure radiology exam...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** This citation pertains to intake: MI00149326. Based on interview and record review, the facility failed to ensure radiology exams were obtained as ordered for one Resident (#7) of 9 residents reviewed for radiology services. Findings include: Resident #7 (R7) Review of R7's Minimum Data Set (MDS) assessment dated [DATE], revealed admission to the facility on 3/8/24, with active diagnoses that included: hypertension, depression, diabetes mellitus, and gout. R7 scored a 15 of 15 on the Brief Interview of Mental Status (BIMS) assessment reflective of intact cognition. On 2/5/25 at 11:20 AM, an interview was conducted with Medical Doctor (MD) E who stated he was displeased with the nursing staff at the facility because he ordered a bilateral [both side] foot x-ray for R7 on 1/20/25 and when he returned to the facility on 1/23/25 his x-ray was never ordered. On 2/26/25 at 2:45 PM, an interview was conducted with R7 in his room who was asked about his toes being run over by another female resident and replied, Yes, it was about two weeks ago. We were all lined up to go outside to smoke at the end of C-hall. This lady came by in her wheelchair and ran over my toes. She never realized that she did it and I never made a big deal out of it. We were going to smoke. R7 was asked if his toes hurt and replied, Just a little. Not as bad as they did when it first happened. Review of physician progress note, dated 1/20/25, read in part: The following is a summary of today's visit .1. Assessment: Pain in toe. Provider Plan: Will get x-ray of bilateral toes and appointment with podiatry . Review of physician progress note, dated 1/23/25, read in part: The following is a summary of today's visit .1. Assessment: Pain in toe. Provider Plan: Bilateral toe pain/cellulitis - x-rays pending, will start [name brand antibiotic] 875 mg (milligrams) po (by mouth) bid (twice daily) x ten days . Review of physician progress note, dated 1/27/25, read in part: The following is a summary of today's visit .1. Assessment: Cellulitis of unspecified toe. Provider Plan: Continue with clinda (sic) (antibiotic name brand abbreviated) po tid (three times daily) and appointment with podiatry pending . Review of R7's radiology exam dated 1/25/25, revealed there was no fracture to R7's toes with a report date of 1/26/25. Review of R7's progress note, dated 1/27/25 at 9:30 AM, read Bilateral tarsal XRs (x-rays) have resulted - negative for fracture or trauma. On 2/6/25 at 3:00 PM, an interview was conducted with Licensed Practical Nurse (LPN) F who was asked if he recalled receiving orders from the physician for R7 to obtain an x-ray for bilateral feet. LPN F replied, No, I do not recall receiving an order for x-rays. On 2/6/25 at 4:00 PM, an interview was conducted with Registered Nurse (RN) H regarding the accident report she made following the incident. RN 'H recalled, I am not sure when R7's toes got ran over, but it was prior to 1/24/25. The physician came in and asked me the results of the x-ray on 1/23/25. I said, 'What x-ray?' It was brought to my attention there should have been one [x-ray] ordered so I ordered it on that day [1/23/25]. Review of R7's incident and accident report, dated 1/24/25, read in part .Resident states that his big toes got run over by 'a lady in a wheelchair who didn't know where she was going.' .Provider aware, who orders bilateral foot x-rays to rule out abnormalities. Order placed .Order also procured for wound monitoring and skin prep to scabbed area on right hallux .Prophylactic antibiotics are in place for these areas as well. Resident states his toes were run over by a lady while waiting to go smoke . On 2/6/25 at 4:10 PM, an interview was conducted with the Director of Nursing (DON) who was asked why there was a delay in obtaining the x-ray for R7. The DON replied, I don't know. If it was ordered on the 20th then it should have been performed that day. Review of policy Laboratory and Diagnostic Guidelines, dated 10/26/23, read in part Policy: This guideline is set up to track the timely completion, reporting and monitoring of laboratory and diagnostic tests, results, and notifications which are used to monitor resident status and/or therapeutic medication levels. Policy Explanation and Compliance Guidelines: 1. The facility may consider tracking laboratory (lab) and diagnostic test through various sources. The system is based on the lab provider and facility efficiency. a. Tracking log, b. Electronic portal, c. Calendar, d. Other 2. Routine laboratory or diagnostic test may be placed on a calendar or schedule, or other mechanism. The mechanism should allow for ease of the facility staff to recognize upcoming lab and diagnostic tests .
Aug 2024 4 deficiencies 2 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Quality of Care (Tag F0684)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to recognize a change in condition for one Resident (R70) out of 23 re...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to recognize a change in condition for one Resident (R70) out of 23 residents reviewed for quality of care. This deficient practice resulted in hospitalization and death. Findings include: Resident #70 (R70) Review of the admission record for R70, revealed an original admission to the facility on 3/11/24, with medical diagnoses including congestive heart failure (heart does not pump or fill adequately), chronic obstructive pulmonary disease (chronic inflammatory lung disease that causes obstructed airflow from the lungs), morbid obesity, and muscle weakness. Review of progress note, dated 3/11/24 at 11:08 AM, read in part, .Resident admits to SNF (skilled nursing facility) for short term rehab . Review of physician progress note, dated 3/11/24 at 12:30 PM, read in part, .His goal is to rehab and discharge to home . Review of medication administration record (MAR), dated 7/1/24 through 7/10/24, revealed the following lab orders: a.) 7/3/24 - Lab to draw CBC (complete blood count) [identifies and counts the seven types of cells found in the blood], BMP (basic metabolic panel) [provides information about chemical balances and metabolism in the blood], Iron Studies [measures the iron in blood], and HgbA1C [measures the average blood sugar (glucose) level over the past two to three months]. b.) 7/10/24 - Lab to draw CBC, BMP, and Iron Studies. Review of R70's labs, drawn on 5/8/24, revealed the following: a.) CMP (comprehensive metabolic panel) [measures the bodies fluid balance, levels of electrolytes, and how well the kidneys and liver are functioning] - BUN (blood urea nitrogen) 38 mg/dL (milligrams per deciliter) high (normal range is 9 to 20) [measures how well the kidneys are functioning], Serum Creatinine 1.49 mg/dL high (normal range is 0.66 to 1.25 / measures how well kidneys are functioning), Calcium 7.3 mg/dL low (normal range is 8.4 to 10.2), and Sodium 128 mg/dL low (normal range is 137 to 145). b.) BNP, NT pro (natriuretic peptide test) [measures a protein called BNP in the blood and can be a sign and indicator of severity of heart failure] - BNP, NT pro 5,020 pg/mL (picograms per milliliter) elevated [normal range is < 300]. *Note highly elevated lab value. c.) Lab CBC with differential [measures white blood cell counts] - WBC's 0.9 K/uL (Kilo/microliter) low [normal range is 3.5 to 11.0], RBC's 3.36 M (million)/uL low [normal range is 4.10 to 5.70], Hemoglobin 9.3 G (Grams)/DL low [normal range is 13.5 to 17.0], and Hematocrit 28.3 low [normal range is 40.0% to 50.0%]. *Notation on lab work by Registered Nurse (RN) Q, revealed doctor made aware at 10:00 PM on 5/9/24 (no new orders noted in progress notes or on printed lab results). Signed off by doctor not dated. Providers (nurse practitioner into see R70 on 5/15/24 - no notes regarding labs or follow up and doctor into see R70 on 5/22/24 - no notes regarding labs or follow up). Review of R70's labs, drawn on 7/3/24, revealed the following: Lab CBC with differential - WBC's 0.9 K/uL low, RBC's 3.33 M/uL low, Hemoglobin 9.4 G/DL low, and Hematocrit 29.7 low. *Note R70 history of CHF and no follow up BNP on this date. Review of R70's labs, drawn on 7/10/24, revealed the following: Lab CBC with differential - WBC's 0.9 K/uL low, RBC's 3.31 M/uL low, Hemoglobin 9.7 G/DL low, and Hematocrit 29.5 low. *Note R70 history of CHF and no follow up BNP on this date. Review of blood pressure and pulse, dated 7/7/24 through 7/15/24, revealed the following: a.) On 7/7/24 at 2:46 PM - blood pressure 100/51 and pulse 94. b.) No blood pressure or pulse documented on 7/8/24, 7/9/24 or 7/10/24. c.) On 7/11/24 at 10:55 AM - blood pressure 88/41 and pulse 88. d.) On 7/11/24 at 2:54 PM - blood pressure 100/50 and pulse 97. e.) On 7/12/24 at 3:59 PM - blood pressure 104/68 and pulse 106. f.) No blood pressures or pulse documented for 7/13/24. g.) On 7/14/24 at 11:17 AM - blood pressure 84/44 and pulse 113. h.) On 7/15/24 at 10:00 AM - blood pressure 78/42 and pulse 128. *Note a follow up set of vital signs should have been repeated on 7/11/24 at approximately 7:00 PM and then again at 11:00 PM and none were obtained per algorithm of sepsis that was initiated on 7/11/24. The blood pressures and pulses above were not repeated on 7/14/24 or documented as communicated to the physician from nursing. On 7/14/24 no sepsis pathway screening was completed with R70's decreased blood pressure and increased pulse. Review of facility document titled, Sepsis Pathway, no dated, revealed the following: a.) Sepsis vital signs include - WBC [white blood cell count] > 12,000 or < 4,000, temperature > 100.0 or < 96.0, or increase > 2 degrees F (Fahrenheit) above baseline, heart rate > 90, respiratory rate > 20, and if a resident has an increased baseline change heart rate > 110 and respiratory rate > 25. b.) According to the sepsis pathway algorithm if R70 met one sepsis vital sign to continue through the pathway. Then to call the physician. Next screen the (urine, chest x-ray or lab [CBC], monitor for vital signs, blood pressure, pulse oximetry every four hours times four, and to notify primary physician of any changes. c.) According to the sepsis pathway algorithm if R70 met two sepsis vital signs to call physician. Then initiate treatment within four hours with intravenous fluids, obtain blood cultures times two, CBC with differentials, BMP, and Lactate [measures the amount of lactic acid in the blood], start antibiotic protocol. Continue to monitor the vital signs, blood pressure, pulse oximetry every two hours times four, and to notify primary physician of any changes Finally, transfer to hospital if systolic blood pressure is < 90, end organ dysfunction, progress to three sepsis vital signs. Review of R70's situation, background, assessment, and recommendation (SBAR), dated 7/10/24 at 3:17 PM (effective date and time), revealed in the 'situation' section, a change in condition of worsening wounds and decrease in blood pressures that started on 7/10/24, and indicated since initial discovery, these findings had gotten worse. Vital signs dated as most recent for 7/11/24 at 2:54 PM were as follows: a.) Blood pressure 100/50, pulse 97, respiratory rate 16, temperature 97.8 - date obtained 7/11/24 at 2:54 PM, and weight 410.0 pounds - date obtained 6/12/24 at 3:46 PM. b.) Sepsis pathway worksheet - marked as negative. *Note marked incorrectly and should have been marked positive with relevant information obtained on 7/10/24 with blood pressure 88/44, labs drawn 7/3/24 white blood cell counts below 400 and vitals should have continued every 4 hours x 4 unless continued to be out of range then more monitoring should have continued. c.) Documentation of SBAR under section R tilted Request, item number 6 was dated and timed 7/10/24 at 7:00 AM (indicating that was the original time the SBAR was filled out). *Note making it difficult to discern what time the actual event started to occur. Review of R70's physician progress note, dated 7/12/24, read in part, .Nursing to update with changes/concerns. Review of R70's task for amount eaten, dated 7/2/24 through 7/15/24, revealed that on 7/11/24 no food intake was consumed and marked as resident refused breakfast and dinner and lunch zero intake recorded, on 7/14/24 refused breakfast and dinner and lunch only ate half, and on 7/15/24 refused breakfast. Review of R70's SBAR, dated 7/15/24 at 10:27 AM (effective date and time), revealed in the 'situation' section a change in condition of hypotension, tachycardia, slow speech and verbal response. Inappropriate responses/using the wrong words during interaction, refusing meals. Vital signs dated as most recent for 7/15/24 at 10:00 AM were as follows: a.) Blood pressure 78/42, pulse 128, respiratory rate 16, temperature 97.5 and (weight 410.0 pounds - dated 6/12/24 at 3:46 PM). b.) Mental status changes - increased confusion. d.) Sepsis pathway worksheet - marked as negative. *Note marked incorrectly and should have been marked positive with relevant information obtained on 7/10/24, and labs drawn on 7/3/24 white blood cell counts below 400. c.) Assessment - Sepsis, several non-healing wounds. d.) Nursing notes - Spoke with (resident's name) regarding his vital signs and educated on s/s (signs and symptoms) of sepsis. (Resident's name) stated he was willing to go to the hospital. e.) Documentation of SBAR under section R tilted Request, item number 6 was dated and timed 7/15/24 at 10:45 AM (indicating that was the original time the SBAR was filled out). *Note making it difficult to discern what time the actual event started to occur. On 7/31/24 at 4:11 PM, during a telephone interview, Licensed Practical Nurse (LPN) R was asked if she recalled R70 and acknowledged; The blood pressure was low, but I didn't feel he had a change of condition, so I did not call the doctor. *Note vital signs on 7/14/24 when LPN R worked were as follows: On 7/14/24 at 11:17 AM - blood pressure 84/44 and pulse 113. On 8/1/24 at 10:45 AM, an interview with RN Q was conducted. RN Q was asked about sepsis protocol, and replied, Nurses follow the pathway and call the physician. RN Q was asked if she correctly filled out the SBAR sepsis screening dated 7/15/24. After reviewing it with this Surveyor RN Q replied, Apparently not. RN Q was then asked if R70 was diabetic and replied, No. I guess I should have checked his blood glucose too. I was just trying to get him out. Me not doing that did not make any difference. He got sent out anyway. Review of R70's local emergency medical services (EMS) transport run sheet, dated 7/15/24, revealed the following: a.) Call received 11:08 AM b.) On scene 11:16 AM c.) Pulse 120 at 11:22 AM d.) Blood pressure 70/40 at 11:25 AM e.) Intravenous site placed successful at 11:30 AM with fluid challenge initiated (20 gauge right antecubital [inner elbow/bend of arm]). f.) Blood pressure 60/40 at 11:32 AM g.) Respirations 28 at 11:36 AM h.) Narrative history: Dispatched via 911 to the above locations for the above patient for possible sepsis. The patient was admitted to the SNF (skilled nursing facility) on March 11th. The patient has multiple non healing wounds on his buttocks, as well as his legs, some are from pressure, some are venous insufficiency. i.) Unable to sign - comment: Patient is alert, and in critical condition. Review of R70's local hospital admission documentation, dated 7/15/24 through 7/16/24, revealed the following: a.) admitted to emergency department (ED) in room [ROOM NUMBER] on 7/15/24 at 11:41 AM b.) Vital signs in ED: Pulse 129, respirations 26, and blood pressure 69/37 c.) Physician exam in ED: He is ill-appearing and toxic appearing. d.) ED course note: Patient is seen and evaluated upon arrival. He does state that he would want medication to keep his blood pressure at a normal level. e.) Hospital labs drawn in ED on 7/15 that were found abnormal: 1.) pro-BNP 21,400 2.) Lactate 2.6 (normal values are below 0.5 and values >0.5 to 2.0 suggest an intermediate likelihood of sepsis and/or septic shock) 3.) A second lactate was drawn and resulted as 4.8 4.) A third lactate was drawn and resulted as 8.4 5.) Procalcitonin 5.26 (a serum biomarker that helps distinguish bacterial infection from other causes of infection) Serum concentrations are normally <0.5, and >2.00 are high risk of sever sepsis and/or septic shock. 6.) BUN 113 7.) Creatinine 3.69 8.) WBC 1.4 9.) Arterial blood gases: pH 7.16, pCO2 39, pO2 27, HCO3 13.3, and O2 Sat. 28 (measure oxygen and carbon dioxide in the blood) R70's lab values indicate metabolic acidosis (a condition where too much acid accumulates in the blood). This condition is treated with intravenous fluids, bicarbonate, and possibly hemodialysis (mechanical blood filtration). f.) admitted to intensive care unit (ICU) on 7/15/24 at approximately 4:02 PM g.) Hospital medications included but not limited to cefepime (antibiotic), sodium chloride 2.5 liters (intravenous fluids to support body fluid volume), vancomycin (antibiotic), amiodarone (antiarrhythmic to help control fast heart rate), hydrocodone (narcotic pain medication), morphine (opioid pain medication), norepinephrine (sympathomimetic/helps to increase blood pressure back to a normal range), phenylephrine (vasoconstrictor/used to treat septic and neurogenic shock and hypotension), piperacillin-tazobactam (antibiotic), and vasopressin (antidiuretic hormone/used to increase blood pressure). h.) Discharge summary: admitted to ICU for septic shock and presumed infected deep decubitus ulcers involving the sacrococcygeal region. Despite aggressive supportive care directed at his sepsis including multiple vasopressors, systemic steroids, fluids, antibiotic therapy the patient's condition declined. He passed away early the morning of July 16 (approximately 13 hours after he was admitted ). Review of hospital history and physical, dated 7/15/24, read in part, .Chief complaint: General malaise .multiple poor healing wounds .He has been on cephalexin long-term .He states his appetite has been down .Decubitus ulcers about his sacral region are deep and malodorous .Weight 7/15/24 at 11:50 AM resulted as 409 pounds and at 4:25 PM resulted at 389 pounds .eyes were sunken .edema present in bilateral lower extremities .multiple skin tears and pressure ulcerations/decubitus are noted about his sacrococcygeal area, abdominal wall and lower extremities. See pictures .Principal problem: Septic shock source felt to be decubitus ulcers .Decubital ulcer concerns related to deep infection as evidence by his clinical presentation and odor emanating from the wound .Cellulitis and abscess of buttocks concerns related to deep infection as evidence by his clinical presentation and odor emanating from the wound . Review of hospital nursing notes, dated 7/16/24, read in part, Doctor .called to bedside many times through the night, patient going in and out of SVT (supraventricular tachycardia a heart rate > 150 beats per minute), maxed on norepinephrine, vasopressin, and phenylephrine. Amiodarone drip running. Central line placed. Unable to obtain an arterial line placement. Time of death 12:32 AM . Review of a hospital progress note, dated 7/15/24, read in part Called to ICU on 7/15/24 at 11:03 PM regarding patient not doing well having runs of tachycardia (rapid heartbeat >170 beats per minute) .Patient's extremities lower are (sic) have mottled appearance (a bluish-red, laced-like pattern under the skin/deoxygenated blood pools beneath the skin's surface). Patient with ongoing hypotension (decrease blood pressure) on norepinephrine and vasopressin. Added phenylephrine to try titrate down norepinephrine. Patient with ongoing clinical decline despite max medical support. Patient passed away on 7/16/24 at 12:32 AM. On 7/31/24 at 3:30 PM, an interview was conducted with RN/Infection Control H and was asked if R70's wound had ever been swabbed for culture and replied, Never had a swab to clarify what bacteria he had from his wounds or the weeping of serious fluid. He was put on Hospice related to his wounds recommended by doctor at the wound clinic. On 8/1/24 at 10:27 AM, an interview was conducted with the DON and was asked if R70 was on the same antibiotic each time he had a skin infection and replied, He was not on the same antibiotic. He was started on a 20-day course because he was on it before, and it worked. The DON went on to explain that R70's wound was not cultured at all. On 8/1/24 at 10:50 AM, during an interview, the DON was asked about the sepsis pathway and if it was comparable to the charting that was on the electronic medical record and replied, Yes. We collaborated with the local hospital to develop the Sepsis Pathway/screening tool. The DON was asked about R70's SBAR (situation, background, assessment, and recommendation) dated 7/10/24 and replied, I don't' know what time the documentation was completed. It was locked on the 11th. The vital signs should have been from the 10th and not the 11th. The DON confirmed that the sepsis screening tool was improperly filled out and she should have checked R70's blood glucose level and reviewed most recent labs. The DON stated, The only thing I felt was a change was his heart rate. The DON was then asked if there was any reason why R70 did not have increased monitoring of vital signs if he had a change in condition and was suspected to have sepsis and replied, He was on pertinent charting for infection already. The DON was then asked about R70's lactic acid level and replied, To be septic you have to be 4.3, and lactic acid was 2.6. *Notes according to the National Library of Medicine the normal lactic acid level is < 0.5 ng/mL (nanograms per milliliters), and a value of 2.0 ng/mL suggests a significantly increased risk of sepsis and/or septic shock. The DON further explained that R70 developed wounds and thought he was dying. He had all these things going on. I think he was dying. The DON was asked if R70 ever told her he wanted to die and replied, No. He did not say he wanted to die. He was non-adherent. On 8/1/24 at 11:57AM, a telephone interview was conducted with Nurse Practitioner (NP) T and was asked about R70 and the low blood pressure and increased pulse he had on 7/10/24 and 7/14/24. NP T replied, He should have been more closely monitored after the change in condition on 7/10/24. The nurses should have been getting a set of vital signs at minimum every shift. On 8/1/24 at 2:16 PM, an interview was conducted with Physician U who stated, I don't know if they called me on 7/10/24 regarding the low vitals, but they said they repeated them on 7/11/24 and they were normal. Regarding the lab work and no follow-up labs in June, he refused and that was indicated on the lab sheet. The wound was cultured, and I stuck a swab around, but it was dry, and I would have made a note in my documentation when I saw him. Looking back, I felt the nurses could have had better documentation. *Note reviewed physician rounding notes and found no supporting documentation that the wound was ever cultured or attempted to be cultured. Wound evaluations indicated moderate amounts of drainage. Lab sheets were reviewed and no written documentation of a refusal for lab draws was found. Review of R70's death certificate, dated 7/17/24, revealed R70 died from septic shock from infected sacral wounds and congestive heart failure on 7/16/24. Review of policy titled, Notification of Changes, dated 1/1/22, read in part, Policy: The purpose of this policy is to ensure the facility promptly informs the resident, consults the resident's physician; and notifies, consistent with his or her authority resident's representative when there is a change requiring notification For changes of condition the facility may use: 1. SBAR (Situation, Background, Assessment, and Recommendation) process for assessment .3. Sepsis protocols. Circumstances requiring notification include .2. Significant change in the resident's physical, mental or psychosocial condition such as deterioration in health, mental or psychosocial status. This may include: a. Life-threatening conditions, or b. Clinical complications . *Note requested skilled nursing assessment notes from when R70 was on skilled charting to review any education that was provided to R70 regarding cares, and none was received at the time of survey exit.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Pressure Ulcer Prevention (Tag F0686)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to prevent the development of pressure wound for two Resi...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to prevent the development of pressure wound for two Residents (R33 & R70) out of three residents reviewed for pressure ulcer care. This deficient practice resulted in deterioration of pressure wound, sepsis, and hospitalization, requiring wound debridement for R70. Findings include: Resident #70 (R70) Review of the admission record for R70, revealed an original admission to the facility on 3/11/24, with medical diagnoses including congestive heart failure (heart does not pump or fill adequately), chronic obstructive pulmonary disease (chronic inflammatory lung disease that causes obstructed airflow from the lungs), morbid obesity, and muscle weakness. Review of R70's progress note, dated 3/11/24 at 11:08 AM, read in part, .Resident admits to SNF (skilled nursing facility) for short term rehab . Review of R70's physician progress note, dated 3/11/24 at 12:30 PM, read in part, .His goal is to rehab and discharge to home . Review of R70's admission skin assessment, dated 3/11/24, completed by LPN (Licensed Practical Nurse)/Unit manager L, revealed the following left lateral ribs weeping and right great toe two small, dried blood blisters. *Note no other skin impairments or open areas identified on admission. On 7/30/24 at 4:00 PM, an interview was conducted with LPN L, who was asked what kind of intervention was put into place for R70 related to the left lateral ribs weeping and replied, I wiped it off at the time of the skin assessment. I don't know if it started weeping again. I did not put any interventions in place. I did not feel he needed any. Review of R70's skin inspection shower documentation, dated 3/19/24, revealed excoriation and reddened areas on the groin and buttocks and signed off by an unidentified nurse's initials. Review of R70's interdisciplinary progress note, dated 3/20/24, read in part, .MASD (moisture associated skin damage) to rear medial left thigh. Area measures 7.7 x 1.4 x 0.1 (centimeters) .occasional incontinence . An admission MDS (Minimum Data Set) assessment, dated 3/17/24, section E0800, read in part, .Did the resident reject evaluation or care that is necessary to achieve the resident's goals for health and well-being .Behavior not exhibited .section M skin conditions, revealed R70 was at risk for developing pressure ulcers and had no unhealed pressure ulcers . An MDS assessment, dated 6/17/24, section E0800, read in part, .Did the resident reject evaluation or care that is necessary to achieve the resident's goals for health and well-being .Behavior not exhibited .section M skin conditions, revealed R70 had a stage 1 or greater pressure ulcer, was at risk for developing pressure ulcers, and had two stage 3 (full thickness tissue loss) pressure ulcers that were not present on admission . Review of R70's skin and wound evaluation, dated 4/11/24 through 5/29/24 revealed the following: Wound #3- a.) 4/11/24 - Wound #3 undiagnosed, rear left flank/lateral, minutes old, in house acquired, and measured 1.56 L (length) x 0.79 W (width) cm. b.) 4/30/24 - Wound #3 MASD, rear left flank/lateral, 1 month old, and measured 0.73 L x 2.17 W x 0.2 D (depth) cm c.) 5/7/24 - Wound #3 MASD, rear left flank/lateral, 1 month old, and measured 1.21 L x 2.77 W x 0.4 D cm d.) 5/14/24 - Wound #3 MASD, rear left flank/lateral, 1 month old, and measured 1.7 L x 3.23 W x 0.3 D cm e.) 5/21/24 - Wound #3 MASD, rear left flank/lateral, 1 month old, and measured 2.45 L x 3.14 W x 2.3 D cm f.) 5/24/24 - Wound #3 MASD, rear left flank/lateral, 1 month old, and measured 2.17 L x 3.83 W x 3.0 D cm g.) 5/29/24 - Wound #3 MASD, rear left flank/lateral, 1 month old, and measured 2.53 L x 4.11 W x 4.5 D cm, and with undermining 0.3 cm from 1 to 2 o'clock. Wound #4- a.) 4/11/24 - Wound #4 Pressure - unstageable, right ischial tuberosity (bony prominence on buttocks), 4 hours old, in house acquired, and measured 1.64 L x 1.29 W cm b.) 4/16/24 - Wound #4 Pressure - unstageable, right ischial tuberosity, 4 hours old, in house acquired, and measured 2.29 L x 1.32 W x 0.2 D cm c.) 4/23/24 - Wound #4 Pressure - unstageable, right ischial tuberosity, 4 hours old, in house acquired, and measured 1.67 L x 1.25 W cm *Note picture shows depth, but none was measured d.) 4/30/24 - Wound #4 Pressure - unstageable, right ischial tuberosity, 4 hours old, in house acquired, and measured 1.08 L x 1.74 W x 0.2 D cm e.) 4/30/24 - Wound #4 Pressure - stage 3, right ischial tuberosity, 4 hours old, in house acquired, and measured 1.44 L x 1.75 W x 0.4 D cm f.) 5/14/24 - Wound #4 Pressure - stage 3, right ischial tuberosity, 4 hours old, in house acquired, and measured 2.0 L x 2.19 W x 0.3 D cm g.) 5/21/24 - Wound #4 Pressure - stage 3, right ischial tuberosity, 4 hours old, in house acquired, and measured 2.56 L x 2.54 W x 2.0 D cm, and moderate serosanguineous drainage h.) 5/24/24 - Wound #4 Pressure - stage 3, right ischial tuberosity, 4 hours old, in house acquired, and measured 2.31 L x 2.37 W x 1.5 D cm, undermining 0.2 cm, and moderate serosanguineous drainage with a faint odor i.) 5/29/24 - Wound #4 Pressure - stage 3, right ischial tuberosity, 4 hours old, in house acquired, and measured 3.05 L x 2.4 W x 0.3 D cm, undermining 0.3 cm, and moderate serosanguineous drainage with a faint odor. Wound #6- a.) 5/21/24 - Wound #6 Pressure - stage 3, right iliac crest, age unknown, in house acquired, and measured 1.13 L x 1.1 W x 0.2 D cm b.) 5/24/24 - Wound #6 Pressure - stage 3, right iliac crest, age unknown, in house acquired, and measured 2.39 L x 1.45 W x 0.2 D cm c.) 5/29/24 - Wound #6 Pressure - stage 3, right iliac crest, age unknown, in house acquired, and measured 2.81 L x 2.1 W x 0.1 D cm. Wound #7- a.) 5/21/24 - Wound #7 Open lesion, coccyx - middle, age unknown, in house acquired, and measured 1.42 L x 0.67 W x 0.2 D cm b.) 5/24/24 - Wound #7 Open lesion, coccyx - middle, age unknown, in house acquired, and measured 0.6 L x 0.3 W cm c.) 5/29/24 - Wound #7 Open lesion, coccyx - middle, age unknown, in house acquired, and measured 3.73 L x 0.33 W x 0.1 D cm. Review of R70's skin and wound evaluation, dated 7/10/24, revealed the following: a.) Wound #11 Pressure - Stage 3, right ischial tuberosity (second open area to this locations), new - 21 hours old, in house acquired, and measured 1.5 L x 0.56 W x 0.2 D cm. A wound clinic progress note, dated 6/3/24, read in part, .patient presents to the wound care center today as a New patient for multiple wounds on multiple areas on his body .One wound is on his torso started as weeping which did created (sic) a ulcer since in SNF (skilled nursing facility) .He also has one on his right gluteal fold that was discovered by staff at SNF this had a wound vac on .Debridement done on all wounds today . Further review of the wound clinic note revealed the following - wound on right gluteus, right hip, sacrum, and left gluteus: a.) The date acquired was: 5/6/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Right Sacrum. The wound measures 0.9 cm length x 1.2 cm width x 0.4 cm depth. There is a medium amount of serosanguineous drainage noted. There is a small (1-33%) red granulation within the wound bed. There is a large (67-100%) amount of necrotic tissue within the wound bed including Adherent Slough. b.) The date acquired was: 4/8/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Right Gluteal fold. The wound measures 2.5 cm length x 1.6 cm width x 0.4 cm depth. There is a medium amount of serosanguineous drainage noted. There is a small (1-33%) red granulation within the wound bed. There is a large (67-100%) amount of necrotic tissue within the wound bed including Adherent Slough. c.) The date acquired was: 4/8/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Left Lateral Back. The wound measures 2.2 cm length x 3.5 cm width x 2.5 cm depth. There is tunneling at 12:00 with a maximum distance of 1 cm. There is a medium amount of serosanguineous drainage noted. There is a small (1-33%) red granulation within the wound bed. There is a large (67-100%) amount of necrotic tissue within the wound bed including Adherent Slough. d.) The date acquired was: 4/8/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Right Lateral Back. The wound measures 0.1 cm length x 0.2 cm width x 0.5 cm depth. There is a medium amount of serosanguineous drainage noted. There is a small (1-33%) red granulation within the wound bed. There is a large (67-100%) amount of necrotic tissue within the wound bed including Adherent Slough. A wound clinic progress note, dated 6/12/24, read in part, .Patient presents to wound center today for follow-up evaluation and management of a (sic) ulcer on his buttock as well as an ulcer on his left lateral abdomen. Upon evaluation at today's encounter the buttock ulcer is full-thickness, there is devitalized tissue and slough within the ulcer .Patient agreed and debridement was accomplished. There is undermining at this ulcer .Patient stated the debridement was very painful and he also states that simple palpation causes extreme pain in the area . Further review of the wound clinic note revealed the following wound measurements: a.) The date acquired was: 5/6/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Right Sacrum. The wound measures 0.7 cm length x 0.9 cm width x 0.507 cm depth. There is a medium amount of serosanguineous drainage noted. b.) The date acquired was: 4/8/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Right Gluteal fold. The wound measures 1.2 cm length x 1.2 cm width x 1.197 cm depth. There is a medium amount of serosanguineous drainage noted. c.) The date acquired was: 4/8/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Left Lateral Back. The wound measures 1.5 cm length x 3.5 cm width x 4.096 cm depth. There is tunneling. There is a medium amount of serosanguineous drainage noted. *Note wounds had worsened and increased in size from prior visit on 6/3/24. A wound clinic progress note, dated 6/26/24, read in part, .Patient presents to wound center today for follow-up. Wounds today are stable. Unable to evaluate sacrum wound based on limited mobility. Debridement completed on wounds today . Further review of the wound clinic note revealed the following wound measurements: a.) The date acquired was: 4/8/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Right Gluteal fold. The wound measures 2.8 cm length x 1.3 cm width x 0.4 cm depth. There is a medium amount of serosanguineous drainage noted. b.) The date acquired was: 4/8/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Left Lateral Back. The wound measures 2.6 cm length x 4.8 cm width x 3.2 cm depth. There is tunneling. There is a medium amount of serosanguineous drainage noted. c.) The date acquired was: 4/8/24. The wound is currently classified as a Category/Stage III wound with etiology of Pressure Ulcer and is located on the Right Lateral Back. The wound measures 0.5 cm length x 0.5 cm width x 0.2 cm depth. *Note: Plan follow-up appointment - return in 1 week. *Note wounds had worsened and increased in size from prior visit on 6/12/24. Review of R70's care plan, dated 3/12/24, read in part, .Focus: Resident is at risk for impaired skin integrity related to Morbid Obesity, CHF, Muscle Weakness, Braden Score 15. Goal: Resident will have intact skin .Interventions .Low air loss mattress (4/11/24) .If resident refuses interventions/treatments, encourage compliance to minimize further skin impairment (3/19/24) .Provide incontinence care as needed (3/19/24) .Assist resident with turning and repositioning as needed (3/19/24) . Review of R70's progress note, dated 4/11/24, read in part, Resident is noted to have 2 new areas of impairment. Resident has an abrasion on his left rear lateral flank that measures 1.6 cm x 0.8 cm x 0.1 cm. He has an unstageable pressure ulcer on his R (right) ischial tuberosity measuring 1.6 cm x 1.3 cm x 0.1 cm .A LALM (low air loss mattress) was ordered and resident is refusing at this time .[R70 stated] I have a call in 7 minutes that I have to be back in bed for. This writer asked if we would be able to place LALM later in the day today after his call. He sighed and asked if he had to get out of bed for this writer stated yes. He stated, This will just have to be done tomorrow then. A physician order for R70, dated 4/11/24, revealed low air loss mattress and was discontinued on 4/11/24. A physician order for R70, dated 4/25/24, revealed low air loss mattress was reordered. *Note a lack of explanation as to why the low air loss mattress was not initiated on the following Monday on 4/15/24. Review of R70's progress note, dated 4/25/24, read in part, .Maintenance was notified and placed a bari (bariatric)-LALM. Orders placed . A physician progress noted, dated 5/1/24, read in part, Patient continues participating with therapy as ordered. Staff has noted a new abrasion to sacrum today, treatment in place and appropriate .No changes to plan of care. A nurse practitioner progress note, dated 5/15/24 (late entry), read in part, Patient continues participating with therapy as ordered. Nursing monitors and treats abrasion to sacrum, treatment in place and appropriate. New R (right) iliac crest wound noted during care. Tx (treatment) ordered and appropriate .No changes to plan of care. Review of R70's interdisciplinary progress note, dated 5/16/24, read in part, .In regards to his mood, the resident stated that he was an attorney in (City Omitted) for 245 (sic) years, and that he is used to a very short and to the point manner of conversation. He also stated that even as a child he was not very social. The resident stated he is not to the social culture of the Midwest where people are very friendly and caring, and that where he is from the people just say what they want/need, without much small talk . Review of R70's interdisciplinary progress note, dated 5/22/24, read in part, During weekly assessment of residents wounds it has been noted that wounds are showing s/s (signs and symptoms) of infection. Wounds appear to have increased purulent drainage, increased redness, and are worsening . A physician progress note, dated 5/22/24, read in part, Patient is participating with therapy as ordered. Patient is on [brand name antibiotic] cephalexin regimen for wound are (sic) until 5/31 .Provider orders staff to call wound clinic .open wounds . Review of R70's progress note, dated 5/23/24, read in part, .Was upset when I brought him his 1400 (2:00 PM) medicine, I explained that he asked me to change it till (sic) this time he was fine with it . Review of R70's progress note, dated 5/28/24 at 2:51 PM, read in part, .copious drainage, tender with dressing changes . Review of R70's progress note, dated 5/28/24 at 2:53 PM, read in part, .He stated that when he is positioned on his side, he feels bed frame . *Note no explanation as to why R70 felt the bed frame or indication of poor repositioning. Review of R70's interdisciplinary progress note, dated 5/29/24, read in part, .Times of medications have been adjusted per residents' preferences and he continues to complain, once reminded he becomes more understanding . A physician progress note, dated 6/3/24 (late entry), read in part, Patient has completed [brand name antibiotic] cephalexin regimen for wound care. Has been referred to wound clinic . Review of R70's physician progress note, dated 6/14/24, read in part, Patient seen for nursing reporting left side is weeping. Left hip with edema, light drainage .Last day of OT (occupational therapy currently ordered for the 15th . Review of R70's progress note, dated 6/17/24, revealed, While I was in room with am meds, I inquired about staff offering to change bed linens and complete hygiene cares. [R70] replied that it can wait til (until) tomorrow. MASD education provided and [R70] then agreed it can be done sometime today. *Note when R70 was reapproached with educated and explanation given in this progress note he became compliant with cares at that time. A physician progress note, dated 6/28/24, read in part, Patient is seen for concern of recurrence of cellulitis to right ankle .He reports worsening of discomfort since completion of [brand name antibiotic] cephalexin earlier this month .Orders given for cephalexin .for cellulitis of Right foot and ankle .wound clinic follow up. Review of R70's progress note, dated 7/2/24, read in part, Resident refused treatments for wound change due to pain. Medication is being ordered to be given 1 hour prior to wound change for tomorrow . Review of R70's progress note, dated 7/3/24, revealed, [R70] was very pleasant and cooperative with staff today. Pain med given prior to dressing changes and very effective. Review of R70's behavior progress note, dated 7/4/24, revealed, Remained appropriate with all Interactions. He was aware a dressing change was going to be completed to his L (left) side. I noticed that the dressing to his coccyx was coming loose and removed dressing. [R70's name] responded you're not changing that one. I informed him that it needed to be changed, he was no longer resistant. Review of R70's physician order, dated 4/4/24, revealed the following order cephalexin oral capsule 500 mg (milligram), give 2 capsules by mouth two times a day for LLE (left lower extremity) cellulitis for 10 days. Review of R70's physician order, dated 5/21/24, revealed the following order cephalexin oral capsule 500 mg (milligram), give 2 capsules by mouth two times a day for wounds for 10 days. Review of R70's physician order, dated 6/30/24, revealed the following order cephalexin oral capsule 500 mg (milligram), give 2 capsules by mouth two times a day for cellulitis to R (right) lat (lateral) malleolus for 20 days. All R70's occupational therapy (OT) progress notes were reviewed, dated 4/17/24 through 5/20/24, revealed the following 25 treatment opportunities with 20 great and or good participation, 2 refusals, 2 actively participates, and 1 needs encouragement. All R70's physical therapy (PT) progress notes were reviewed, dated 4/17/24 through 5/20/24, revealed the following 25 treatment opportunities with 10 active participation, 11 compliant, 2 moderate encouragements, 1 needed extra time procession new information, and 1 refusal related to not feeling well. A PT progress note, dated 5/6/24, read in part, .Demonstrates some slurred words and potential altered mental status - reported to nursing for further evaluation. Additionally, pt (patient) brought up ideations about dying and suicidal thoughts which were also reported to nursing and social work. *Note social services notes were reviewed and no social service note found on or within a few days of R70 voicing such thoughts. Review of R70's turning and repositioning every shift documentation, dated 3/20/24 through 3/31/24, revealed the following: 4 indicating refusal of turning, 4 not filled out and blank on the 10 to 6 shift, and overall, 4 turning and repositioning refusals out of 32 opportunities. Review of R70's target behavior documentation, dated 3/20/24 through 3/31/24, revealed the following: 5 indicating behaviors, 3 not filled out and blank on the 10 to 6 shift, and overall, 5 behaviors out of 32 opportunities. Review of R70's turning and repositioning every shift documentation, dated 4/1/24 through 4/30/24, revealed the following: 1 indicating refusal of turning, 3 not filled out and blank on the 10 to 6 shift, and overall, 1 turning and repositioning refusals out of 90 opportunities. Review of R70's target behavior documentation, dated 4/1/24 through 4/30/24, revealed the following: 8 indicating behaviors, 8 not filled out and blank on the 10 to 6 shift, and overall, 5 behaviors out of 90 opportunities. Review of R70's turning and repositioning every shift documentation, dated 4/1/24 through 4/12/24 (changed to every two hours at 2:00 PM on 4/12/24), revealed the following: 2 indicating refusal of turning, 3 not filled out and blank on the 10 to 6 shift, and overall, 2 turning and repositioning refusals out of 34 opportunities. Review of R70's target behavior documentation, dated 5/1/24 through 5/31/24, revealed the following: 7 indicating behaviors, 9 not filled out and blank on the 10 to 6 shift, and overall, 7 behaviors out of 93 opportunities. Review of R70's target behavior documentation, dated 6/1/24 through 6/30/24, revealed the following: 11 indicating behaviors, 13 not filled out and blank, and overall, 11 behaviors out of 90 opportunities. Review of R70's target behavior documentation, dated 7/1/24 through 7/15/24, revealed the following: 8 indicating behaviors, 4 not filled out and blank, and overall, 8 behaviors out of 43 opportunities. *Note R70 did have some resistance to cares at times, but over all did not show indefinite non-compliance or consistent behaviors. On 7/31/24 at 4:11 PM, a telephone interview was conducted with LPN R and was asked about R70 and his wounds and replied, We had to give him pain medicine prior to wound care. We would have to go in there with multiple, multiple people. The last time I did them I did them all. The facility wound nurse did the wound care on Tuesday, staff nurses did wound care the rest of the week. One Tuesday he didn't let them get done. He didn't like people in the room. I think he was working. Left side, buttocks, and one on his right leg. We had to do it so quick there was no looking - he was screaming the whole time in pain. On 7/31/24 at 3:30 PM, an interview was conducted with RN/Infection Control H and was asked if R70's wound had ever been swabbed for culture and replied, Never had a swab to clarify what bacteria he had from his wounds or the weeping of serious fluid. He was put on Hospice related to his wounds recommended by doctor at the wound clinic. On 8/1/24 at 10:27 AM, an interview was conducted with the DON and was asked if R70 was on the same antibiotic each time he had a skin infection and replied, He was not on the same antibiotic. He was started on a 20-day course because he was on it before, and it worked. The DON went on to explain that R70's wound was not cultured at all. Not even from the wound clinic. The DON also explained that R70 was still working from his laptop in his room but was not sure what kind of work and did acknowledge he had a zoom meeting and important phone calls during his stay at the facility. On 8/1/24 at 10:50 AM, an interview with the DON and was asked about the development of R70's wounds and replied, We thought he was dying. He had all these things going on. I think he was dying. The DON was asked if R70 ever told her he wanted to die and replied, No. He did not say he wanted to die. He was non-adherent. Review of policy titled, Pressure Injury Prevention Guidelines, dated 3/20/24, read in part, Policy: To prevent the formation of avoidable pressure injuries and to promote healing of existing pressure injuries, it is the policy of this facility to implement evidence-based interventions for residents who are assessed at risk or who have a pressure injury present . Review of policy titled, Pressure Injury Prevention and Management, dated 1/1/22, read in part, Policy: This facility is committed to the prevention of avoidable pressure injuries and the promotion of healing of existing pressure injuries . Review of policy titled, Antibiotic Prescribing Practices, dated 10/26/23, read in part, Policy: Antibiotic use protocols, including prescribing practices, are implemented as part of the facility's Antibiotic Stewardship Program for the purpose of optimizing the treatment of infections and reducing adverse events associated wit antibiotic use .The facility will utilize a 5 D's approach to antibiotic prescribing: a. Diagnosis .b. Drug: The prescribed medication will be appropriate for the treatment site and identified organism. c. Dose .d. Duration .e. De-escalation: Reassessment of empiric precautions will be conducted for appropriateness and necessity, factoring in results of diagnostic tests, laboratory results, and/or changes in the clinical status of the resident. Resident #33 (R33) Review of R33's admission record, revealed an original admission to the facility on 5/2/24, with medical diagnoses including chronic obstructive pulmonary disease (COPD), Crohn's (bowel disorder) disease, heart failure, and hypertension. R33's admission MDS, dated [DATE], revealed a Brief Interview for Mental Status (BIMS) score of 03 out of 15 indicating severe cognitive impairment. On 7/29/24 at 2:30 PM, an observation was made of R33 lying in her bed covered with a sheet. On her nightstand there was a green pressure relieving boot green in color. On 7/30/24 at 10:08 AM, an observation of R33 receiving wound care by Registered Nurse (RN) S in her room. RN S was asked how R33 developed the pressure injury to her heel and replied, It was facility acquired. I don't think she had it when she first admitted . During the wound care treatment R33 replied, It does hurt when you touch it. I just wish the scab would fall off and it would go away. Review of R33's wound assessment, dated 5/24/24, revealed the development of a right heel pressure injury in house acquired and described as deep tissue injury, with wound measurements of 0.8 x 1.4 centimeters and no depth. Review of R33's progress note, dated 6/28/24, read in part, .Resident has a stage III pressure area to the right heel . Review of R33's wound assessment, dated 7/9/24, revealed a pressure injury stage three on the right heel, in house acquired, with measurements of 0.5 x 0.8 cm. Review of R33's MDS, section E0800, dated 5/13/24, read in part, .Did the resident reject evaluation or care that is necessary to achieve the resident's goals for health and well-being .Behavior not exhibited . Review of R33's care plan, dated 5/2/24, read in part, .Resident has impaired skin integrity .5/24/24 R (right) heel DTI (deep tissue injury) changed to a stage 3 on 6/24/24 .Encourage/assist as needed to elevate heels off the mattress . Review of progress note, dated 7/31/24 at 9:08 AM, read in part, .A new BIMS was completed where resident was able to score a 10 . On 7/31/24 at 12:25 PM, an interview was conducted with R33 and was asked if she ever refused to wear her boot to protect her heel or decline her heels to be off the mattress and replied, I do what I am told. I didn't have to wear the boots until after the heel was hurt. I do not refuse to use the heel thing. On 7/31/24 at 12:30 PM, an interview was conducted with Certified Nurse Aide (CNA) O and was asked about R33 and replied, She uses the heels up thing and does not refuse to use it. On 7/31/24 at 12:35 PM, an interview was conducted with Licensed Practical Nurse (LPN) P and was asked about R33 and replied, I recall her being pleasant and remember she was compliant. No refusal of cares. On 7/31/24 at 12:40 PM, an interview was conducted with CNA I and was asked about R33 and replied, She was easy to take care of. She didn't give me any problems. On 7/31/24 12:50 PM, an interview was conducted with LPN/Unit Manager K and was asked when the nurses are required to start the charting on a non-compliant resident and replied, Typically as soon as we identify it. LPN K was then asked if any charting had been made prior to the development of R33's DTI and confirmed no notes prior to developing DTI. On 7/31/24 at 1:20 PM, an interview was conducted with the Director of Nursing (DON) and was asked when interventions and refusals of care should be added to the plan of care and replied, Interventions right away and refusals of care should be documented as they occur. Confirmed that no notes of refusals prior to the development of R33's DTI and more interventions should have been put into place prior to the development of her DTI. The DON confirmed there was an incident and accident report created on 5/24/24 related to R33's DTI. A copy was requested but was not received before the exit of the survey. Review of R33's task list, revealed the following: float heels implemented on 5-2-24 the day of admission, then green pressure relieving boots orders added 5-24-24 and behavior documentation (on the day the DTI developed), and then 6-4-24 the heels up device ordered.
CONCERN (D)

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

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to ensure a medication administration error rate of less than five percent, with three errors identified out of 25 opportunities...

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Based on observation, interview, and record review, the facility failed to ensure a medication administration error rate of less than five percent, with three errors identified out of 25 opportunities, affecting one Resident (R10) of four residents observed for medication administration, resulting in a medication error rate of 8.00 percent. Findings include: On 7/30/24 at 11:55 AM, medication administration was observed with Registered Nurse (RN) J for R10. RN J was observed dispensing 2.5 milliliters (ml) of metoclopramide oral solution with a concentration of 5 milligrams (mg) / 5 ml. RN J was asked to verify the order and then the medication concentration. After order and medication concentration were verified, RN J replied, I need to give 2.5 ml more. I always give 2.5 ml. The order must have been changed. RN J then drew up another 2.5 ml of metoclopramide to be administered. Review of R10's physician order, dated 1/16/24, revealed the current order for metoclopramide was to give 5 ml via G-tube, three times a day for GERD (gastroesophageal reflux disease/acid reflux). On 7/30/24 at 12:20 PM, medication administration was observed with RN J in R10's room. RN J checked for placement of R10's G-tube, administered three medications (carbamazepine 10 ml, metoclopramide 5 ml, and diazepam 2 mg) and then administered tube feed. RN J was asked if she flushed R10's G-tube prior to medication administration with water and then again prior to tube feed administration and replied, I thought I did. I guess I did not. During medication administration for R10 a second Surveyor was also observing and verified RN J missed both water flushes. Review of R10's physician order, dated 8/6/23, revealed the current order for [name brand tube feeding formula] 1.5 cal (calorie), 360 ml bolus feed TID (three times a day) via gravity administration. On 7/30/24 at 12:45 PM, an interview was conducted with the Director of Nursing (DON) and was asked what her expectation was for medication administration via G-tube feeding and medication pass for G-tube and replied, I would expect that nurses follow physician orders and policy for medication pass via G-tubes. The DON was made aware of the errors that RN J had made and replied, She did fine last year. The DON verified the order for R10 and confirmed the errors. Review of policy titled, Medication Administration, dated 1/17/23, read in part, Policy: Medications are administered by licensed nurses .as ordered by the physician and in accordance with professional standards of practice, in a manner to prevent contamination or infection .10. Review MAR [medication administration record] to identify medication to be administered. 11. Compare medication source (bubble pack, vial .) with MAR to verify resident name, medication name, form, dose, route, and time . Review of facility document titled, Validation Checklist Medications via Feeding Tube, undated, read in part, .7. Using a clean syringe (at least 30 ml syringe) administered medications appropriately, flushing prior to and between medications using at least 15 ml water flush before each medication .
CONCERN (E)

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

Deficiency F0804 (Tag F0804)

Could have caused harm · This affected multiple residents

Based on observation, interview, and record review the facility failed to provide food in a manner that was a palatable (preferable) temperature for 19 of 23 residents interviewed. This deficient prac...

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Based on observation, interview, and record review the facility failed to provide food in a manner that was a palatable (preferable) temperature for 19 of 23 residents interviewed. This deficient practice resulted in frustration with meals and the potential for weight loss and inadequate nutrition. Findings include: During an interview on 7/30/24 at 7:08 a.m., Confidential Resident C8 stated, the food is always cold, it doesn't matter what meal it is .the food is cold. During an observation on 7/30/24 at approximately 7:15 a.m., Confidential Residents C10 and C11 were talking to each other at a table in the dining room. C10 stated the food is going to be cold . C11 stated the food is always cold. During an interview on 7/30/24 at 8:16 a.m., Confidential Resident C12 stated the food is warm for the first time ever. During an interview on 7/30/24 at 8:44 a.m., Confidential Resident C13 stated the food is ok, but not that warm. During a confidential group interview on 7/30/24 at 10:30 a.m., 5 (C7, C14, C15, C16, C17) of 12 residents agreed the food is not palatable due to cold temperatures of food. C14 stated, the food in my room is cold .the food in the dining room is cold .I would ask the staff to warm up the food, but I would be asking at every meal . the food is like rubber. C16 stated, the food is cold . everyone in here would say the food is cold but they won't say anything . C7 stated, the food is cold .we don't get toast, it is either burnt or just bread . the eggs are overcooked, cold, and rubbery. C15 stated my food is cold. C17 stated my food is cold. During an interview on 7/31/24 at 10:10 a.m., C15 stated, residents do bring up concerns in resident council . during the meeting there have been complaints about cold food. During an interview on 7/31/24 at 10:12 a.m., C14 stated I have brought up my concerns in resident council . I have definitely brought up my concerns about the temperature of the food . [Certified Dietary Manager (CDM) C] comes down to the meetings and I tell her about the cold food temperatures, eggs, and toast . I have been here about a year, and I have complained to the Nursing Home Administrator about the cold food, and nothing has changed . they wanted me to go to the dining room to eat, why would I do that . I then could sit in the dining room for two hours and wait to eat cold food . now I just eat the cold food in my room During an interview on 7/31/24 at 12:02 p.m., C7 stated, I have told [CDM C] how cold the food is .the food is cold all the time, it is so upsetting. During an interview on 7/31/24 at 12:12 p.m., Certified Dietary Manager C stated, I attend resident council meetings . the residents have complained about the cold temperatures of the food in the resident council meetings. The CDM did not offer any corrective action completed to address these complaints. Review of policy titled, Resident Council, date implemented 8/7/20, read in part . The purpose of the resident council allow residents to . discuss concerns . make recommendations for improvement of resident services provided by the facility . the Nursing Home Administrator (NHA) reviews the minutes to ensure all groups concerns and grievances are investigated. During an interview on 7/31/24 at 12:21 p.m., the NHA stated There was a resident in the past who commented about the food, but I have not heard from anyone. During an interview on 7/31/24 at 5:35 p.m., this surveyor requested a policy regarding serving palatable food and/or a policy regarding dignified dining experience from Dietician B . policies were not provided by facility. On 7/31/24 at 9:34 a.m., CNA I was asked about two confidential residents (C7 and C14) who reported their meals were sometimes received cold, especially at breakfast. CNA I stated, With 120 residents, it's hard to keep up .It would be nice if the little carts [short open plastic wheeled carts with shelves] had doors on them to keep the food warmer. CNA I reported these small open carts held up to six meal trays at the most and did not hold the food temperatures as well as the large metal closed meal tray carts. CNA I confirmed they sometimes heard the residents complaining about the food being cold on their usual hall (B hall) and heard complaints about the eggs not tasting good. CNA I stated, The eggs don't look like when I make them; they don't look good to eat. On 7/31/24 at approximately 12:00 p.m., Surveyors observed the residents in the main dining room had not received their lunch meal. There were 40 residents in the main dining room. On 7/31/24 at 12:13 p.m., this Surveyor observed approximately 40 residents in the main dining room, and only three residents had been served their lunch meal trays. On 7/31/24 at approximately 12:18 p.m., C6 was observed without a lunch tray and stated, I would rather be eating. I would like to have my food by now. On 7/31/24 at 12:19 p.m., C20 was observed without a lunch tray, and said, You can wait for hours [for the meal], and shared it made them feel frustrated. On 7/3124 at 12:23 p.m., C6 was observed without a lunch tray in front of them On 7/31/24 at approximately 12:23 p.m., at least 20 residents had not been served their lunch meal. On 7/31/24 at 12:31 p.m., C7 was observed without their lunch meal. C7 reported they had been waiting a half hour and stated, It is not unusual, and said I need to eat because I am diabetic. They have plenty [staff] to help, and I don't know why it is taking so long. On 7/31/24 at 12:33 p.m. C18 stated, I have been waiting 45 minutes [for their lunch], and explained they could not wait any longer, as they had to go to the bathroom. C18 then left the dining room. On 7/31/24 at 12:33 p.m., this Surveyor observed several staff in the dining room, with some waiting in the serving line for additional trays. The main lunch meal was observed as hamburger with lettuce and tomato, with mashed potatoes and gravy, or tater tots. On 7/31/24 at 12:34 p.m., this Surveyor observed nine residents without a lunch meal tray in the main dining room. On 7/31/24 at approximately 12:36 p.m. C8 was observed being served their lunch meal. C8 stated, I wait a half hour or more .My food is cold. C8 said it made them feel frustrated. C8 declined another entrée or tray when asked, as they said they just wanted to eat since they waited so long. . On 7/31/24 at 12:36 p.m., the Director of Nursing (DON) was observed in the dining room and was notified C8 reported their hamburger was cold. C8 was heard telling the DON their food was cold and declined another tray or reheating of their lunch meal. On 7/31/24 at approximately 12:38 p.m., C9 was observed being served their lunch meal. C9 stated, I don't think it's ok to wait . It gets me upset, as I don't want to wait a half hour [for their meal]. On 7/31/24 at 12:40 p.m., the last few residents in the dining room were observed receiving their lunch trays. A review of the Be Our Guest document, no date, provided by the facility indicated the meal service was communicated to residents, families and staff as follows: Breakfast beginning at 7:15 a.m., Lunch beginning at 11:50 a.m. and Dinner beginning at 5:00 p.m. daily. Review of the policy, Resident Meal Service, revised 01/01/2022, revealed, Each resident shall receive the correct diet, with preferences accommodated as feasible, and shall receive prompt meal service and appropriate feeding assistance . During an interview on 7/30/24 at 9:16 a.m., Confidential Resident C4 was asked about the timeliness of meals, and the palatability/temperature of the food when delivered. C4 stated, It was 9:45 a.m. when I got my breakfast last week one day. The food is cold most times because the meals are usually late. They blame a lot of this stuff on you guys, you know (State Agency]. Food is often cold. Mostly evening meal is cold food . Lunch and dinner is often cold. Every one (of the meals) is the worst. I think it is because it was so delayed in getting to us. Review of Resident Council meeting minutes on 7/30/24 at 3:30 p.m., with meeting dates from December 2023 through July 2024, found all documentation showing there were no complaints documented about any food concerns during that time period, although facility residents and staff had confirmed the food palatability related to being cold was brought up as a concern frequently in resident council. Review of the Grievance binder, received from the Nursing Home Administrator (NHA) on 7/30/24 at 3:40 p.m., revealed only one complaint, dated 5/2/24, that breakfast was served cold. No other grievances were documented for cold food between December 2023 and July 2024. During an interview on 7/31/24 at 8:47 a.m., Confidential Resident C4 said he had requested french toast but by the time it was delivered he had already eaten his meal. When asked if the food was always hot, C4 stated, No. It is not. During an interview on 7/30/24 at 9:12 a.m., Confidential Staff C19 was asked if facility residents complained about the food temperature. C19 stated, .It is often not hot. Resident do complaint about their food being cold. C19 directed this surveyor to Confidential Resident C2, as a Resident who had complained directly to C19 multiple times about cold food.
Aug 2023 8 deficiencies
CONCERN (D)

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

Deficiency F0658 (Tag F0658)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to check for peg tube residual and properly clean a glucometer according to accepted nursing standards of practice, for two Resi...

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Based on observation, interview, and record review, the facility failed to check for peg tube residual and properly clean a glucometer according to accepted nursing standards of practice, for two Residents (#9 and #39) reviewed for professional standards of practice. This deficient practice resulted in the potential for adverse effects related to tube feeding administration and the spread of blood borne pathogens. Findings include: Resident #39 (R39) On 8/9/23, at 11:39 AM, an observation was made on C-Hall. Registered Nurse (RN) H was performing a finger stick blood glucose on R39. RN H was observed not wearing any protective gloves and proceeded to prick the end of R39's fingers on her right hand. RN H then took the reading and pulled out the blood contaminated strip with an bare hand and threw it in the medication cart sharps container. RN H then placed the dirty glucometer back in her medication cart in the top drawer with the testing strips bottle, and then closed the draw without sanitizing the glucometer. RN H failed to sanitize her hands post blood glucose finger stick check on R39. Resident #9 (R9) During the medication administration observation for R9 on 8/9/23 at 12:35 PM, RN H was performing medication pass via peg tube and peg tube bolus feeding. Licensed Practical Nurse (LPN) I was in training and observing the performance of this procedure for R9 by RNH. RN H failed to check residual on R9's peg tube prior to administering medications and tube feed bolus. On 8/9/23 at 1:05 PM, an interview was conducted with LPN I. LPN I was asked if she recalled the residual amount and replied, No. LPN I confirmed that RN H had not checked residual on R9 prior to administering medications and tube feed bolus. On 8/10/23 at 11:15 AM, an interview was conducted with the Director of Nursing (DON). The DON confirmed that nurses should be checking for residual on peg tubes. The DON reviewed the policy and procedure and replied, The policy also states that they should be checking for placement as well. The DON confirmed that the nurses should be cleaning glucometers after each use. The DON further stated, We just had an education fair on this and there are two different wipes they can use, but each has a three minute dwell time and they can use either wipe to clean. On 8/10/23 at 12:40 PM, an observation was made of RN H passing medications for R39. RN H stated to R39, Let's start with your meds (medications) first. RN H failed to check for residual on R39's peg tube or check for placement and did not provide a water flush prior to administering medication in R39's peg tube. During medication pass with RN H in R39's room on 8/10/23 at 12:45 PM, there was a knock on the door. RN H summoned the knocker to proceed in R39's room. The DON stated she was there to provide education on peg tubes and proceeded to ask if RN H had checked for placement and residual and RN H replied, No. I did not check for residual or placement. I do that in the morning. The DON replied, You have to check placement and residual each time you access the peg tube to ensure placement and residual is not excessive. Review of physician orders for R39, dated 8/4/23, revealed, .check tube placement prior to administration of medications and tube feeding/flush .every shift flush tube with 50 ml (milliliters) H2O (water) before and after medication administration and feedings . Review of R39's care plan, dated 7/11/23, read in part, The resident requires tube feeding .flush tube with 50 ml H2O before and after medication administration and feedings .check residual .check tube placement prior to administration of medications and tube feeding/flush . The facility policy, Flushing a Feeding Tube, dated 6/30/22, read in part, Policy: It is the policy of this facility to ensure that staff providing care and services to the resident via a feeding tube are aware of, competent in and utilize facility protocols regarding feeding nutrition and care. Feeding tube care and services will be provided in accordance with resident needs and professional standards of practice .Policy Explanation and Compliance Guidelines: 1. Verify physician orders for tube feeding flush amount. 2. Review the resident's care plan for special needs . 9. Prior to flushing the feeding tube, the administration of medication or providing tube feedings, the nurse verifies the proper placement of the feeding tube by completing the following: a. Draw back on syringe to slowly obtain 5-10 mL of aspirate, allow aspirate to return to the stomach then flush with 30 mL of water or as ordered. 10. After tube placement has been verified, continue process of administering medications, feeding or water, as directed by the physician . The facility policy, Blood Glucose Machine Disinfection, dated 01/01/2022, read in part, Policy: The purpose of this policy is to provide guidelines for the disinfection of capillary-blood sampling devices to prevent transmission of blood borne diseases to residents and employees .Policy Explanation and Compliance Guidelines: 1. The facility will ensure blood glucose machines will be cleaned and disinfected after each use and according to manufacturer's instructions for multi-resident use. 2. The blood glucose machine should be disinfected after each use with a wipe pre-saturated with .registered healthcare disinfectant .3. Blood glucose machines should be cleaned and disinfected after each use .regardless of whether they are intended for single resident or multiple resident use. 4. Procedure: a. Obtain needed equipment and supplies: Gloves, blood glucose machine, alcohol pads, gauze pads, single-use lancet, blood glucose testing strips, disinfectant wipes .e. put on gloves .g. remove and discard gloves and clean device with disinfectant wipe .j. perform hand hygiene.
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

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure follow up was performed for a laboratory urine culture and s...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure follow up was performed for a laboratory urine culture and sensitivity for one Resident (#58) of 20 residents reviewed for quality of care. This deficient practice resulted in the delay of treatment, potential for worsening of infection and lack of monitoring for a urinary tract infection. Findings include: Resident #58 (R58) Review of R58's admission record, date printed 8/10/23, revealed, R58 was originally admitted to the facility on [DATE] with diagnoses including dementia, hypertension (elevated blood pressure), stage 4 chronic kidney disease, and history of urinary tract infections. Review of R58's progress note, dated 7/31/23 at 10:31 AM, read in part, .resident voiced that she had been having increased difficulty with urination, was experiencing nocturia (frequent nighttime urination), frequency, and burning with urination. Order procured for UCIF (urine culture if indicated) to r/o (rule out) UTI (urinary tract infection). Charge nurse aware. Review of R58's progress note, dated 8/7/23 at 10:22 PM, read in part, . The system has identified a possible drug allergy for the following order: Ciprofloxacin . tablet 250 MG (milligram) Give 1 tablet by mouth every 12 hours Infection for 5 Days until finished. Review of R58's progress note, dated 8/8/23 at 10:11 AM, read in part, . Ciprofloxacin . tablet 250 MG Give 1 tablet by mouth every 12 hours Infection for 5 Days until finished Awaiting from pharmacy, not in back up. Further review of R58's progress notes, date range 7/31/23 through 8/7/23, revealed lack of communication with the physician and other nursing staff regarding the results of the urine culture and sensitivity report. R58's progress notes, during this same time period, also revealed, the lack of facility standards of care charting for infection watch notes and antibiotic usage. Review of R58's electronic medical record (EMR), under the miscellaneous tab, revealed, R58's urine lab was collected on 7/31/23 at 12:45 PM and resulted on 7/31/23 at 5:54 PM. R58's urine lab, dated 7/31/23, results indicated microscopic examination. On 08/10/23 at 1:55 PM, an interview was conducted with B-Hall Licensed Practical Nurse (LPN) K who was asked what the policy and procedure was for lab result follow ups. LPN K replied, They are reviewed and communicated as soon as possible with the physician for further direction. LPN K was asked what kind of charting was expected for a resident with an infection who was put on antibiotics. LPN K replied, There is pertinent charting that is completed during the course of the infection and antibiotic use which every is longer then later discontinued after the infection is resolved. LPN K confirmed no pertinent charting was completed or activated and there was a delay in implementing antibiotic orders for R58. LPN K acknowledged R58's EMR lacked documentation regarding lab results being communicated to the physician. On 8/10/23 at 2:05 PM, an interview was conducted with unit manager/LPN N, who was asked to verify the process for lab results. LPN N confirmed there should de documented communication between nursing staff and the physician regarding the decision to add orders for antibiotics pending the result of a culture and sensitivity report. LPN N also confirmed pertinent charting should be started on new infections watch and newly added antibiotic medications. On 8/10/23 at 2:20 PM, an interview was conducted with the Assistant Director of Nursing (ADON)/Infection Preventionist (IP)/Registered Nurse (RN) G who confirmed R58 had a delay in treatment for her UTI. RN G also confirmed there was poor documentation and poor communication between nursing and the physician regarding the urine laboratory results. RN G stated pertinent charting should have been completed including vital signs, signs and symptoms of infection, resident presentation and tolerance of antibiotic usage. RN G confirmed there was no provider visit notes between 8/2/23 and 8/10/23. RN G acknowledged there was lack of communication in the 24-hour nursing communication reports between 08/01/23 through 08/10/23 regarding the UTI for R58. On 8/10/23 at 2:25 PM, an interview was conducted with the Director of Nursing (DON). The DON confirmed nursing staff should have contacted and alerted the physician of the pharmacy system order note indicating there was a possible drug allergy to ensure R58 was safe to continue the medication ordered to treat her UTI. The DON stated there was no policy for lab result communications, but confirmed the standard of practice was to communicate, document and consult with physicians prior to initiating antibiotic orders to treat infections. The DON confirmed there was a delay in treatment as the culture and sensitivity had resulted a couple of days after the urinalysis was obtained and sent to the local hospital laboratory.
CONCERN (D)

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

Respiratory Care (Tag F0695)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide oxygen services per standards of practice and...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide oxygen services per standards of practice and per physician orders for one Resident (#67) of one resident reviewed for oxygen services. This deficient practice resulted in the potential for the development of respiratory complications, including infections. Findings include: Resident #67 (R67) Review of the Electronic Medical Record (EMR) revealed R67 admitted to the facility on [DATE] with diagnoses including chronic obstructive pulmonary disease, chronic respiratory failure with hypoxia, venous insufficiency, anxiety disorder, hypertension, and asthma. Review of the 7/18/23 Minimum Data Set (MDS) assessment showed R67 scored a 3/15 on the Brief Interview for Mental Status (BIMS) assessment, which indicated R67 had severe cognitive impairment. R67 was marked as not receiving oxygen therapy in the MDS assessment. On 8/8/23 at 12:43 p.m., during an attempted interview, R67 could not be located in her room. R67 was having lunch in the main dining area. This Surveyor observed R67's nasal cannula laying in a garbage can near her bed with tubing dated 8/3/23. A storage bag for R67's nasal cannula was observed hanging on the side of an oxygen concentrator. On 8/9/23 at 11:34 a.m., an observation was made of R67's room as she was leaving for the main dining area. R67's nasal cannula was noted to be hanging off her left bed side rail. A storage bag for R67's nasal cannula was observed hanging on the side of an oxygen concentrator. On 8/10/23 at 9:41., R67 was observed in her room eating breakfast in bed. R67 did not have her nasal cannula on. The nasal cannula was observed placed in her recliner chair on an incontinence protective pad which had obvious stains. On 8/10/23 at 9:47 a.m., an observation was made with the Director of Nursing (DON) in R67's room. R67 had transferred to her recliner chair to eat her breakfast, and her nasal cannula was observed in her lap. The DON was informed there were three days of the nasal cannula observed in different locations of R67's bedroom, and not properly stored. The DON confirmed R67's nasal cannula should be stored properly to prevent infection. Review of the facility's Oxygen/Oxygen Administration policy revised on 12/6/22 read, in part, .The oxygen cannula will be changed every week by the Nursing Staff . Review of the facility's Oxygen Administration policy reviewed/revised on 1/1/22 read, in part, .Keep delivery devices covered in plastic bag when not in use .
CONCERN (D)

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

Deficiency F0810 (Tag F0810)

Could have caused harm · This affected 1 resident

. Based on observation, interview, and record review, the facility failed to provide dining adaptive equipment for two Residents (R4 and R46) of three residents reviewed for dining assistive devices. ...

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. Based on observation, interview, and record review, the facility failed to provide dining adaptive equipment for two Residents (R4 and R46) of three residents reviewed for dining assistive devices. This deficient practice resulted in increased difficulty with food consumption and decreased independence with eating, as well as the potential for decreased food/fluid intake and risk for weight loss. Findings include: Resident 4 (R4) On 8/9/23 at 12:23 PM, R4 was observed in the main dining room eating lunch with the assistance of Certified Nurse Aide (CNA) R. The meal card for R4 included instructions of Adap Equip (Adaptive Equipment), w/lid (with lid), plate guard, small utensils. R4 had been served: - 4 ounces of a strawberry health shake in a tumbler without a lid and - 8 ounces of milk (nectar thick) in a tumbler without a lid. CNA R was asked about the beverages and meal card and exclaimed, Oh, she (R4) should have two-handled cups with lids. CNA R then left the table to request two-handled covered mugs and after obtaining them, she poured the milk and health shake into the adaptive mugs. R4 then lifted the mug on her own and started to drink. The Electronic Medical Record (EMR) for R4 included current Physician Orders which read in part: Resident is to have plate guard and cup with handles and lid w/every meal. The order was active as of: 6/5/2023. The EMR Care Plan for R4 included a concern which read: The resident (has potential for) nutritional deficits 6/6/2022. The interventions for this concern included: OT to screen and provide adaptive equipment for feeding as needed. Plate guard and handled cup with lid to increase independence and Date Initiated: 6/5/2023. Resident 46 (R46) On 8/9/23 at 8:40 AM, R46 was observed sitting at a table in the main dining room with a large circular spill of orange juice directly in front of him. His empty 4-ounce tumbler was laying on its side atop of a soaked paper napkin. R46 was trying to propel his wheelchair without success, and he continued to bump the table. The meal card for R46 included instructions of Adap Equip, w/lid, and lip plate, and Notes: cup with lid for hot beverage. R46 had been served: - 8 ounces of coffee in a open one handled burgundy mug without a lid - 8 ounces of 2% milk in a tumbler without a lid and - 4 ounces of orange juice without a lid. All beverages were observed without lids. The EMR current Physician orders for R4 read in part: Lip plate and cup with lid to be provided at mealtimes per dietary. This order was active as of 4/24/2023. The EMR Care Plan for R4 included: Concern: The resident is at risk for nutritional declines (including unintentional weight loss, fluid volume deficits, and impaired skin integrity), and was dated 6/16/23. The interventions included: Provide lip plate, cup with lid to aid with self-feeding. And was Date Initiated: 6/16/2023. The dietary assessment completed by Certified Dietary Manager (CDM) B on 6/16/23 included: Summary: Resident continues on a NDD (National Dysphagia Diet) level III and is tolerating it well. No chewing or swallowing issues noted. Average PO (by mouth) intake x 7 days is 92%. Weight stable x 6 months. Independent eating/drinking. Adaptive equipment provided at meals. .
CONCERN (E)

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

Menu Adequacy (Tag F0803)

Could have caused harm · This affected multiple residents

Based on observation, interview and record review, the facility failed to ensure meal menus were reviewed and approved by the facility dietitian or other qualified nutrition professional to ensure the...

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Based on observation, interview and record review, the facility failed to ensure meal menus were reviewed and approved by the facility dietitian or other qualified nutrition professional to ensure the menus and production recipes were followed to ensure nutritional requirements of the residents were met. This deficient practice had the potential to result in malnutrition to nutritionally at-risk residents. Findings include: On 8/9/23 at approximately 10:20 AM, observations were made during the preparation of the noon meal. A review of the menu for the meal was conducted and revealed the following was to be served: Canned fruit plate/cottage cheese; banana muffin; margarine, cookies, sugar, salt, pepper, parsley sprig. An interview was conducted with [NAME] E at this same time. [NAME] E asked about the amount of cottage cheese to be served, as she was not clear to the amount needed to provide a nutritional meal. The vendor production recipe Canned Fruit plate/cottage cheese 3 oz (0000025569) was reviewed with [NAME] E and Kitchen Manager A. The recipe was not consistent with the amount of cottage cheese to be served. As the title suggested, there was a portion of 3 oz identified, then below that, it identified Serving utensil #8 scoop; then below that, adding to the confusion, an amount of two #10 scoops was written. [NAME] E stated, that she didn't think the fruit and cottage cheese plate was adequate for the meal. Further review of the facility menus failed to demonstrate that they had been reviewed by a registered dietitian (RD) to ensure nutritional adequacy. The facility RD was not available for interview.
CONCERN (E)

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

Deficiency F0806 (Tag F0806)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** . Resident #26 (R26) The Electronic Medical Record for R26 revealed he had been admitted on [DATE] with diagnoses which included...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** . Resident #26 (R26) The Electronic Medical Record for R26 revealed he had been admitted on [DATE] with diagnoses which included diabetes, gastro-esophageal reflux disease (GERD), chronic kidney disease, heart failure, recurring major depressive disorder, and above the knee amputation of his right leg. The most recent Minimum Data Set (MDS) assessment dated [DATE] documented R26 was cognitively intact scoring the maximum score of 15 out of 15 on the Brief Interview for Mental Status (BIMS) assessment. The MDS assessment on 6/15/23 also included a Swallowing/Nutritional Status section, which had documentation indicating R26 had a Weight Loss of 5% or more in the last month or loss of 10% or more in last 6 months and R26 was not on physician-prescribed weight-loss regimen. During an interview in his room on 8/8/23 at 11:33 AM, R26 stated the food is not so good. R26 said, They serve a lot of food I cannot eat like lots of hot dogs and hamburgers. I don't like either . During the lunch meal on 8/8/23 at 12:31 PM, R26 was observed tipping his ice cream dish up to drink every drop of his strawberry ice cream. When asked if he would like to eat his untouched spaghetti and capri vegetables, R26 replied, No, I can't eat pasta. His meal tray card read in part, Dislikes: Pasta. Notes: Send mashed potatoes in place of rice, pasta. No mashed potatoes were served to R26. During the breakfast meal on 8/9/23 at 8:35 AM, R26 received sausage. When asked about breakfast, R26 stated, I got sausage. I prefer bacon. His meal tray card read in part, Notes - bacon daily. Standing orders: bacon (2 slices). While other residents were observed to receive bacon, R26 was not served bacon. His meal tray card also indicated in the Standing Orders: 8 fl oz (fluid ounces) Orange juice. His tray contained a 4 oz tumbler of orange juice. R26 was observed to drink all 4 ounces of orange juice. The facility policy titled: Resident Food Preferences dated as reviewed/revised 1/1/22 read in part, .The resident's clinical record (orders, care plan, or other appropriate locations) will document the resident's likes and dislikes . The Dietary Manager or designee will visit residents periodically to determine if revisions are needed regarding food preferences. The nursing staff will inform the kitchen about resident requests. The Food Services Department will offer food substitutes for individuals who do not want to eat the primary meal. Based on observation, interview, and record review, the facility failed to provide food preference accommodations based on the preferences of six Residents (R26 and five confidential residents) of ten residents reviewed for food preferences. This deficient practice resulted in food dissatisfaction, decreased food consumption and potential weight loss when food preferences were not provided as requested. Findings include: A confidential group interview was conducted on 8/9/23 at 3:30 p.m. During this time, the discussion of food preferences was brought forth to the group of nine residents and the following comments were made: R800 stated, The food can be cold, and a lot of times you get things that you don't want. I told them my likes and dislikes and have been to the office several times to ask why they keep sending me these items. They said they would fix it, and I continue to get the things I don't want. R802 stated, It's always cold (the food) Sometimes I get things on my tray that I have requested not to have, and I just ask them to take it away. I find it annoying that they can't get it right. R804 stated, I always ask for extra to help keep my weight. They will send me double portions of the things I have requested not to have, and I just won't eat it. R807 stated, I am a fussy eater and I have a lot of dislikes. They continue to put it (the food) on my plate even though I have filled out my slip multiple times. One time I was told by a CNA (Certified Nurse Aide) that I needed to try the food first before I requested it to be taken away. It made me feel like a toddler sitting at the dining room table. R808 stated, I think the quality of the food has gone way down. They always send me things that I requested not to have. I continue to talk to (the Nursing Home Administrator) about the issues with the kitchen. I like what I like.
CONCERN (F)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected most or all residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to: 1.) Remove expired IV (intravenous) medications and...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to: 1.) Remove expired IV (intravenous) medications and supplies. 2.) Remove expired needles and syringes. 3.) Remove expired wound vac tubing. 4.) Remove expired respiratory suctioning and nebulizer supplies. from medication storage rooms; 5.) Remove expired healthcare disinfectant wipes. 6.) Maintain a clean medication cart free of loose pills. 7.) Properly date multi-use inhalers when opened for two of two medications, and two of three medication carts reviewed for medication storage. This deficient practice had the potential for expired IV medications/supplies to be utilized/administered, missed medication doses, medication misappropriation, reduced efficacy of healthcare disinfectant used for cleaning multi-use medical supplies, and had the potential to affect the entire resident population. Findings include: On 8/9/23 at 8:42 AM, an observation of the medication cart on B-Hall was conducted with Licensed Practical Nurse (LPN) K. There was a loose pill identified and confirmed with LPN K as a magnesium oxide 400 mg (milligram) tablet found in the second drawer of the medication cart. Observation of a bottle of Lactulose stuck to the base of the second drawer was confirmed by LPN K. The bottle had left a sticky ring on the base of the medication cart drawer when picked up. On 8/9/23 at 9:03 AM, an observation of the medication cart on D-Hall was conducted with Registered Nurse (RN) P. There were two loose pills identified and confirmed with RN P as Oxybutynin (for over active bladder)10 mg tab and Buspirone (anti-anxiety) 5 mg tab, both found in the second drawer of the medication cart. RN P also confirmed there was an opened and undated Albuterol sulfate multi-dose inhaler in the medication cart. On 8/9/23 at 9:31 AM, an observation of medication cart on E-Hall was conducted with LPN M. There were six [name brand] healthcare individual disinfectant wipes located in a drawer which were found to be expired on 03/2022 with lot #0751. LPN M confirmed these wipes were used to disinfect multi-use medical devices such as glucometers, blood pressure cuffs, and pulse oximeters. LPN M confirmed she had used one of these wipes to clean the blood glucometer that day. On 8/9/23 at 11:55 AM, an observation was made of the E-Hall medication storage room and was found to have the following: a. [name brand] suction handle with lot # L18040142S and expiration date 3/31/2023; b. [name brand] Y connector with quick connect with lot # 380244 and expiration date 5/7/2023; c. [name brand] drain adapter with lot # 360887 and expiration date 9/3/2021 and ; d. [name brand] Sterile Water for inhalation 500 ml (milliliters) with lot # [NAME]-1806180 and expiration date 6/5/2020 (prefill nebulizer kit). On 8/9/23 at 12:10 PM, an interview was conducted with Unit Manager/LPN N. LPN N confirmed the presence of expired medical supplies from the medication storage room located on E-Hall. LPN N confirmed there was a resident who was receiving wound vac care and could have potentially used some of the expired supplies. LPN N confirmed no expired medical supplies should be kept in the medication storage room and should have been discarded. On 8/10/23 at 10:36 AM, an observation was made of the C/D-Hall medication storage room and was found to have the following: a. Sodium Chloride IV solution 1000 ml with pharmacy facility yellow sticker label open date 7/6/23 and expired on 8/5/23 with lot # Y417686; b. One box of [name brand] 1 cc (cubic centimeters)/ml 25 g (gauge) x 5/8 [used for TB (tuberculosis) testing on residents and staff] 100 count with 84 left in box with lot # 18012507 and expiration date 1/25/2023; c. One IV catheter 22 g x 1 inch with lot # 18G04G8372 and expiration date 7/1/2023; d. Five [name brand] 25 g x 5/8 with lot # 18072403 and expiration date 7/24/2023; e. One needle 18 g x 1 1/2 with lot # 822709 and expiration date 7/31/2023 and; f. Five [name brand] syringe with needle 3 ml 23 g x 1 1/2 with lot # 18C25 and expiration date 2/28/2023. On 8/10/23 at 11:15 AM, an interview was conducted with the Director of Nursing (DON). The DON confirmed the presence of expired medications and medical supplies from the C/D-Hall medication room. The DON confirmed the facility does complete onsite blood draws, IV starts, intramuscular injections, intradermal injections, IV fluid resuscitation, and TB testing on residents and staff. The DON confirmed no expired medications or medical supplies should have been left in the medication storage room and should have been discarded if they were expired. Review of facility policy, Medication Storage, dated 1/1/2022, read in part, Policy: It is the policy of this facility to ensure all medications housed on our premises will be stored in the pharmacy and/or medication rooms according to the manufacturer's recommendations and sufficient to ensure proper sanitation, temperature, light, ventilation, moisture control, segregation, and security .
CONCERN (F)

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

Food Safety (Tag F0812)

Could have caused harm · This affected most or all residents

Based on observation, interview and record review, the facility failed to store, prepare, distribute, and serve food in accordance with professional standards for food service safety as evidenced by: ...

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Based on observation, interview and record review, the facility failed to store, prepare, distribute, and serve food in accordance with professional standards for food service safety as evidenced by: 1. Failing to ensure two staff persons washed their hands after being potentially contaminated. 2. Failing to ensure the ventilation system in the kitchen and dish washing rooms was properly balanced to exhaust the steam being generated by the high temperature dish machine. 3. Failing to ensure beverage containers being used by employees were stored in a manner which could not contaminate food contact surfaces. These deficient practices have the potential to result in food borne illness among any and all 109 residents of the facility. Findings include: 1. On 8/09/23 at approximately 7:45 AM observations were made with kitchen manager (KM) A, in the kitchen, during the morning meal preparation and service. At this time Dietary Aide (DA) C was observed pulling a yellow garbage can out from under a counter, removing the lid, disposing of trash, replacing the lid and pushing the container back below the counter. DA C returned to his position on the tray line and resumed duties associated with resident tray set up for the breakfast meal. DA C failed to wash his hands following the handling of the garbage can lid and returning to his tray line position. This surveyor informed DA C that he must wash his hands before resuming duties of handling residents' food trays. No intervention was directed by kitchen management. On 8/9/23 at approximately 2:22 PM, [NAME] Q was observed wiping his face with his hands, then returning to food preparation duties without washing his hands. FDA Food Code 2017 states: 2-301.14 When to Wash. FOOD EMPLOYEES shall clean their hands and exposed portions of their arms as specified under § 2-301.12 immediately before engaging in FOOD preparation including working with exposed FOOD, clean EQUIPMENT and UTENSILS, and unwrapped SINGLE-SERVICE and SINGLE-USE ARTICLES and: (A) After touching bare human body parts other than clean hands and clean, exposed portions of arms; 2. On 8/8/23 at approximately 2:30 PM, observations were made during dish washing activities in the dish room. The high temperature dish machine was generating large amounts of steam which was not being captured by the overhead exhaust hood. Condensation was observed on the wall, above the archway, separating the kitchen and dish washing areas, with the condensation dripping to the floor and onto clean dishes stored on racks below. An interview with Dietary Aide D was conducted at this time, who stated the condition of steam build up in the dish washing area was occurring every day at every meal when dish washing activities were being done. On 8/9/23 at approximately 10:20 AM, the same observations were made, with steam being discharged from the dish machine not being captured by the hood and condensation from the steam dripping onto clean food contact surfaces. At this time an interview with Maintenance Director F was conducted and confirmed the existence of the steam and failure to properly exhaust it from the work space. MD F confirmed the exhaust fans were operating, after making observations on the roof of the motor and exhaust system. Observations were made of the make up air diffusers located in the ceiling. Minimal air was observed being pushed through the units, leading to an unbalanced condition where inadequate make up air supply was not balanced with the exhaust volume of the kitchen/dish room hoods. FDA Food Code 2017 states: 4-501.11 Good Repair and Proper Adjustment. (A) EQUIPMENT shall be maintained in a state of repair and condition that meets the requirements specified under Parts 4-1 and 4-2. and: 6-202.12 Heating, Ventilating, Air Conditioning System Vents. Heating, ventilating, and air conditioning systems shall be designed and installed so that make-up air intake and exhaust vents do not cause contamination of FOOD, FOOD-CONTACT SURFACES, EQUIPMENT, or UTENSILS. 3. On 8/9/23 at approximately 10:25 AM, a disposable coffee cup was observed on a rack of clean dishes near the dish cleaning room. An interview with KM A was conducted and confirmed the cup belonged to an employee and should not have been placed on the shelf with clean food service equipment. FDA Food Code 2017 states: 2-401.11 Eating, Drinking, or Using Tobacco. (A) Except as specified in ¶ (B) of this section, an EMPLOYEE shall eat, drink, or use any form of tobacco only in designated areas where the contamination of exposed FOOD; clean EQUIPMENT, UTENSILS, and LINENS; unwrapped SINGLE-SERVICE and SINGLE-USE ARTICLES; or other items needing protection can not result. (B) A FOOD EMPLOYEE may drink from a closed BEVERAGE container if the container is handled to prevent contamination of: (1) The EMPLOYEE'S hands; (2) The container; and (3) Exposed FOOD; clean EQUIPMENT, UTENSILS, and LINENS; and unwrapped SINGLE-SERVICE and SINGLE-USE ARTICLES.
Feb 2023 2 deficiencies
CONCERN (D) 📢 Someone Reported This

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

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

Deficiency F0657 (Tag F0657)

Could have caused harm · This affected 1 resident

This citation pertains to intake MI00129940 Based on observation, interview, and record review, the facility failed to appropriately revise, update, and follow care plans to reflect resident status fo...

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This citation pertains to intake MI00129940 Based on observation, interview, and record review, the facility failed to appropriately revise, update, and follow care plans to reflect resident status for two Residents (R3 and R1) of four Residents reviewed for care plans. This deficient practice resulted in the potential for lack of implementation of appropriate interventions. Findings include: Resident #3 (R3) The medical record revealed R3 had an initial admission of 3/8/2012 and had diagnoses including congestive heart failure, chronic obstructive pulmonary disease (COPD), respiratory failure, Alzheimer's disease, anxiety disorder, and depression. On 2/21/23 at 2:39 PM, R3 was observed in his room sitting in a wheelchair with his feet on foot pedals but not elevated. The room furniture included a bed but no recliner. On 2/21/23 at 3:43 PM, R3 was observed in the main dining room taking part in a group activity. R3 was seated in his wheelchair eating refreshments and his legs were not elevated. On 2/22/23 at 8:30 AM, R3 was observed in the main dining room eating breakfast seated in his wheelchair. His feet were on foot pedals and his legs were not elevated. On 2/22/23 at 12:30 PM, , R3 was observed in the main dining room eating lunch while seated in his wheelchair. His feet were on foot pedals and his legs were not elevated. The medical record for R3 had a Care Plan with approaches of: - Resident to have padded foot support on wheelchair with elevated leg rests AAT (At All Times) while in (wheel) chair as tolerated. - The resident needs pressure relieving/reducing mattress and cushion in recliner and wheelchair. - May have an incontinence pad placed in recliner Date Initiated: 03/13/2019 - .resident sleeps in recliner at times. Date Initiated: 03/07/2018 During an interview on 2/22/23 at 2:45 PM, the Director of Nursing (DON) said R3 did previously have a recliner in his room and the care plan should have been updated to reflect the recliner had been removed from the room. The DON reviewed the medical record and noted a Physician's order to discontinue the recliner on 11/20/21. During an interview on 2/22/23 at 2:00 PM Certified Nurse Aide (CNA) B and CNA C reported R3 previously had a recliner, but no longer did. They were not aware R3 was to have his legs elevated per care plan approaches. Resident #1 (R1) The medical record revealed R1 had an initial admission of 8/15/2019 and had diagnoses including heart disease, heart failure, COPD, respiratory failure, lack of coordination, muscle weakness, unsteadiness on feet, dementia, and depression. The medical record for R1 included a Care Plan for risk of falls. The fall care plan had interventions including: The resident should wear the following footwear when in bed for safety should the resident get out of bed without assistance [gripper socks] Date Initiated: 04/22/2021. On 2/23/23 at 2:00 PM, CNA D and CNA E were in R1's room. It was observed R1 did not have gripper socks on per care plan. The facility policy titled Comprehensive Care Plans dated 1/1/21, read in part: The comprehensive care plan will be reviewed and revised by the interdisciplinary team after each comprehensive and quarterly MDS (Minimum Data Set) assessment. .
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 F0676 (Tag F0676)

Could have caused harm · This affected multiple residents

. This citation pertains to the following intakes: MI00134178, MI00130084, and MI00129940. Based on interview and record review, the facility failed to ensure residents consistently received baths and...

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. This citation pertains to the following intakes: MI00134178, MI00130084, and MI00129940. Based on interview and record review, the facility failed to ensure residents consistently received baths and/or showers for six Residents (#1, #2, #3, #4, #8, #12) of seven residents reviewed for showers/baths. This deficient practice resulted in the potential for resident embarrassment, discomfort, and body odor. Findings include: On 1/30/23, a complaint was filed with the State Agency (SA) which alleged the facility failed to give Resident #3 baths/showers. On 7/28/22, a complaint was filed with the SA which alleged the facility failed to shower Resident #8 on a regular basis. The complaint included the statement .everyday we go visit her she smells. On 7/23/22, a complaint was filed with the SA which alleged the facility residents were not receiving showers as scheduled. During an interview on 2/23/23 at 10:20 AM, Resident #10 stated she received showers on Thursdays. She stated all the residents on her hall were given showers on Thursdays. She said she had missed showers in the past due to staffing shortages and added that may have been during Covid. On 2/21/23 the Electronic Medical Records (EMR) were reviewed for the last 30 days (from 1/23/23 - 2/21/23) and revealed: - Resident #1 had one shower documented as given on 2/16/23. - Resident #2 had two showers documented as given on 2/7/23, and 2/16/23. - Resident #3 had a care plan indicating he was to receive 2 showers each week. His Activity of Daily Living (ADL) bathing task sheet also indicated .prefers to be shower by staff x 2 (two times per) week. Showers were documented on 2/3/23, 2/8/23, 2/13/23, 2/15/23. - Resident #4 had no showers documented as given. - Resident #12 had two showers documented as given on 2/10/23 and 2/17/23. During an interview on 2/24/23 at 9:35 AM, Certified Nurse Aide (CNA) F discussed staffing at the facility saying it had improved, in the past things like showers may not have gotten done, but now it is much better. During an interview on 2/24/23 at 10:00 AM, the DON reviewed the documentation for showers for Resident #8 (who had been discharge in August of 2022). She could not find documentation on the ADL task list for showers, but presented a shower sheet dated 8/23/22. This sheet revealed the skin condition for Resident #8, but did not indicate if a shower was given to her that day. During an interview on 2/23/23 at 2:45 PM, the Director of Nursing (DON) had reviewed the EMR and agreed showers were not always documented. The DON explained, We did have staffing shortages in the past and the CNAs were instructed to give bed baths instead of showers. The CNAs also were to complete Shower sheets to document skin condition and if nail care was given. While these sheets were to be completed on shower days, they did not indicate if a shower was given. The DON also stated she had been following up on Resident showers and said, I discovered in my auditing the bed baths were not charted. The EMR review revealed lack of documentation. The DON stated she could not confirm if showers were given. The facility policy titled Activities of Daily Living (ADLs) dated 10/30/20 read in part: The facility will ensure a resident's abilities in ADLs do not deteriorate unless deterioration is unavoidable. This includes the resident's ability to: bathe, dress . A resident who is unable to carry out activities of daily living will receive the necessary services to maintain good nutrition, grooming .
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 fines on record. Clean compliance history, better than most Michigan facilities.
  • • 41% turnover. Below Michigan's 48% average. Good staff retention means consistent care.
Concerns
  • • 22 deficiencies on record, including 2 serious (caused harm) violations. Ask about corrective actions taken.
Bottom line: Mixed indicators with Trust Score of 70/100. Visit in person and ask pointed questions.

About This Facility

What is Medilodge Of Alpena's CMS Rating?

CMS assigns Medilodge of Alpena an overall rating of 5 out of 5 stars, which is considered much above average nationally. Within Michigan, this rating places the facility higher than 99% of the state's 100 nursing homes. This rating reflects solid performance across the metrics CMS uses to evaluate nursing home quality.

How is Medilodge Of Alpena Staffed?

CMS rates Medilodge of Alpena's staffing level at 4 out of 5 stars, which is above average compared to other nursing homes. Staff turnover is 41%, compared to the Michigan average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Medilodge Of Alpena?

State health inspectors documented 22 deficiencies at Medilodge of Alpena during 2023 to 2025. These included: 2 that caused actual resident harm and 20 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Medilodge Of Alpena?

Medilodge of Alpena is owned by a for-profit company. For-profit facilities operate as businesses with obligations to shareholders or private owners. The facility is operated by MEDILODGE, a chain that manages multiple nursing homes. With 132 certified beds and approximately 120 residents (about 91% occupancy), it is a mid-sized facility located in Alpena, Michigan.

How Does Medilodge Of Alpena Compare to Other Michigan Nursing Homes?

Compared to the 100 nursing homes in Michigan, Medilodge of Alpena's overall rating (5 stars) is above the state average of 3.2, staff turnover (41%) is near the state average of 46%, and health inspection rating (4 stars) is above the national benchmark.

What Should Families Ask When Visiting Medilodge Of Alpena?

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 Medilodge Of Alpena Safe?

Based on CMS inspection data, Medilodge of Alpena 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 5-star overall rating and ranks #1 of 100 nursing homes in Michigan. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Medilodge Of Alpena Stick Around?

Medilodge of Alpena has a staff turnover rate of 41%, which is about average for Michigan 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 Medilodge Of Alpena Ever Fined?

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

Is Medilodge Of Alpena on Any Federal Watch List?

Medilodge of Alpena 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.