CRITICAL
(J)
Immediate Jeopardy (IJ) - the most serious Medicare violation
Notification of Changes
(Tag F0580)
Someone could have died · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interviews, Nurse Practitioner, and Medical Director interviews, the facility failed to notify the...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interviews, Nurse Practitioner, and Medical Director interviews, the facility failed to notify the physician of critical laboratory results. Resident #46's blood sugar was critically low at 37 milligrams/deciliter (mg/dl) on [DATE] and critically low at 25 mg/dl on [DATE] through laboratory work. These results were not acted on by the facility, daily insulin continued, and no further blood sugars were done. This deficient practice occurred for 1 of 2 residents reviewed for notification of changes (Resident #46).
Immediate jeopardy began on [DATE] when nursing staff failed to identify critical laboratory results resulting in the lack of physician notification and was removed on [DATE] when the facility provided an acceptable credible allegation of compliance. The facility will remain out of compliance at a scope and severity D (not actual harm with potential for more than minimal harm that is not immediate jeopardy) to ensure monitoring and all staff have been in-serviced.
The findings included:
Resident #46 was readmitted to the facility on [DATE] with diagnoses including Covid, left hip fracture and insulin-dependent diabetes mellitus. He was prescribed insulin with regular blood sugar checks during previous admission.
A hospital Discharge summary dated [DATE] included an order for long-acting basal insulin 20 units daily (long-acting means insulin enters bloodstream in 2-4 hours from administration time and can last up to 24 hours in the body) and blood sugar test strips to check blood sugars four times daily as directed. The hospital Discharge summary dated [DATE] also included an order to draw a complete blood count (CBC), basic metabolic panel (BMP), and thyroid stimulating hormone (TSH) on [DATE].
Resident #46's bloodwork dated [DATE] showed a critical low blood sugar value of 37 milligrams/deciliter (mg/dl) (normal level 70-99 mg/dl). Per laboratory report, multiple, unsuccessful attempts were made to contact the facility staff about this critical value. This result was released to the electronic medical record and faxed to the facility on [DATE] at 3:28pm.
Review of the medical record for Resident #46 revealed there was no documentation the physician was notified of the critically low blood sugar on [DATE].
Review of Resident #46's MAR showed that blood work was drawn again on [DATE] and there was no documentation that it was done on [DATE].
Resident #46's laboratory results for the BMP dated [DATE] showed a critical low blood sugar of 25 mg/dl. Per report, this critical result was called Nurse #9 on [DATE] at 5:02pm by lab technician #1. This result was released to the electronic medical record and faxed to the facility on [DATE] at 5:02 pm.
Review of the medical record for Resident #46 revealed there was no documentation the physician was notified of the critically low blood sugar on [DATE].
During an interview with lab technician #1 on [DATE] at 2:47 pm, he stated that he was never able to reach a staff member on [DATE] to relay critical sugar results but did reach Nurse #9 on [DATE] and informed him of the current critical level of 25 (mg/dl), as well as the previous result of 37 (mg/dl) at that time. He also stated that, if he was unable to reach a staff member by phone, per the laboratory policy, he would release the results to the facility's system to be flagged and would continue to try to reach the facility by phone.
During an interview with Nurse #9 on [DATE] at 9:45 am, he stated that he had no recollection of ever receiving a phone call from the lab regarding critical lab results for Resident #46. When asked about critical lab results, he stated he would contact the on-call provider, get any orders that may be needed, and then place a printed copy of the results in the doctor's folder for him/her to sign off on when they come into the facility next. He again stated that he did not recall receiving any phone calls about any critical results on [DATE].
During an interview with the Nurse Practitioner on [DATE] at 3:35 pm, the state surveyor notified her of critical lab results from [DATE] and [DATE]. She stated that she was not aware of any critical blood levels for Resident #46. She stated the phone number to contact the on call doctor was available 24 hours a day. She also stated, along with immediate verbal notification, there was a folder where the staff will put any critical lab value reports for her to review upon next visit to the facility. She also stated that she was in the facility on [DATE] and there were no critical levels in her folder for her to review.
During an interview with the Medical Director on [DATE] at 5:02 pm, the state surveyor notified him of critical lab results from [DATE] and [DATE]. He stated the phone number to contact him or whomever was on call for him is available 24 hours a day. He also stated, along with immediate verbal notification, there was a folder where the staff will put any critical lab value reports for him or his staff to review upon next visit to the facility.
The Administrator was notified of immediate jeopardy on [DATE] at 11:16am.
The facility provided a credible allegation of immediate jeopardy removal dated [DATE].
Credible Allegation of immediate jeopardy removal:
Identify those recipients who have suffered, or are likely to suffer, a serious adverse outcome as a result of the noncompliance.
Resident # 46 was deceased on [DATE] and is no longer a resident of the facility.
On [DATE], the Nurse Consultant completed an audit of 100% of all current resident's lab values to identify if there were any alert lab values that were not communicated to the Nurse Practitioner or Medical Provider for the last 60 days. The audit revealed eleven alert lab values were reviewed. Six alert lab values had provider notification upon receipt. The Director of Nurses and the Assistant Director of Nurses immediately notified the Medical Director and Individual providers on [DATE] of the five required alert lab values that were not previously communicated at the time of the lab results.
Specify the actions the entity will take to alter the process or system failure to prevent a serious adverse outcome from occurring or reoccurring and when the action will be completed.
On [DATE] the Director of Nurses and Assistant Director of Nurses began in servicing of all licensed nurses (full time, part time, and prn including agency nurses) on Critical Labs. Staff were educated on how critical labs are received, to promptly notify the physician and/or on call of all critical labs, document notification in the electronic record, and to notify the resident and RP of the critical labs.
The DON will ensure that any licensed staff who has not completed the in-service training on [DATE], will not be allowed to work until the critical lab training is completed. The critical lab in-service will be incorporated into the new employee facility orientation program for both facility and agency licensed staff. On [DATE], the DON was notified of the responsibility to ensure the critical lab in-service will be incorporated into the new employee facility orientation program for both facility and agency licensed staff by the Clinical Nurse Consultant.
Date of IJ removal [DATE]
The credible allegation of immediate jeopardy removal was verified on [DATE] as evidenced by onsite validation through record review, and staff interviews. A review of facility in-service materials titled Critical Lab Education, Changes in Condition, and Preventing Errors on Admission were reviewed for content. Staff were interviewed to validate in-service completion on signs and symptoms of hypoglycemia and physician notification regarding critical lab results. The DON, assistant DON, the floating DON, and the corporate nurse met with all floor nurses and assessed all current residents to identify any signs and symptoms of hypoglycemia. Per their assessment, no current residents were identified having any signs and symptoms of hypoglycemia. The immediate jeopardy was removed on [DATE].
CRITICAL
(J)
Immediate Jeopardy (IJ) - the most serious Medicare violation
Quality of Care
(Tag F0684)
Someone could have died · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interviews, Nurse Practitioner, and Medical Director interviews, the facility failed to monitor bl...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interviews, Nurse Practitioner, and Medical Director interviews, the facility failed to monitor blood sugar levels for a resident with insulin-dependent diabetes (Resident #46). The facility administered long acting insulin without monitoring the resident's blood sugar. On [DATE], Resident #46's blood sugar was critically low at 37 milligrams/deciliter (mg/dl) and, on [DATE], it was critically low at 25 (mg/dl) through laboratory work. These results were not acted on by the facility, daily insulin continued, and no further blood sugars were done. This deficient practice occurred for 2 of 3 sampled residents. Also, the facility failed to assess, notify the physician, and obtain orders to treat an open area on the right lower leg and left lower leg for 1 of 4 residents reviewed for pressure ulcers (Resident #15).
Immediate jeopardy began on [DATE] when staff gave Resident #46 his first insulin dose without knowing his current blood sugar level and was removed on [DATE] when the facility provided an acceptable credible allegation of immediate jeopardy removal. The facility will remain out of compliance at a scope and severity D (not actual harm with potential for more than minimal harm that is not immediate jeopardy) to ensure monitoring and all staff have been in-serviced.
The facility was also cited at a scope and severity of D for example #2 (Resident #15).
The findings included:
Resident #46 was readmitted to the facility on [DATE] with diagnoses including left hip fracture, Covid-19, and insulin-dependent diabetes mellitus. He was on insulin with regular blood sugar checks during previous admission.
A hospital Discharge summary dated [DATE] included an order for long-acting basal insulin 20 units daily (long-acting means insulin enters bloodstream in 2-4 hours from administration time and can last up to 24 hours in the body) and blood sugar test strips to check blood sugars four times daily as directed. The hospital Discharge summary dated [DATE] also included an order to draw a complete blood count, basic metabolic panel, and thyroid stimulating hormone on [DATE].
The physician's order dated [DATE] was insulin deglu[DATE] unit/milliliter-inject 20 units subcutaneously one time a day for diabetes mellitus. There were no orders for monitoring blood sugar levels.
During an interview with Nurse #8 on [DATE] at 10:05 am, she stated she completed Resident #46's admission upon arrival. She stated she faxed the hospital discharge medication orders to the pharmacy and then hand-entered the same orders into the computer system which the on-call doctor approved remotely and then the pharmacy filled the order. She stated she was aware a resident on insulin needed regular finger stick blood sugar checks but did not remember whether or not she entered that into the system as he came with a lot of orders that day. She stated she would have entered blood sugar test strips and treatment orders separate from the pharmacy order.
Resident #46's medication administration record (MAR) for [DATE] - 17, 2022 showed no current order for fingerstick blood checks. His MAR included documentation that insulin was administered on dates with staff initials.
Resident #46's bloodwork dated [DATE] showed a critical low blood sugar value of 37 milligrams/deciliter (mg/dl) (normal level 70-99 mg/dl). Per laboratory report, multiple, unsuccessful attempts were made to contact the facility staff about this critical value.
Blood work was drawn again on [DATE] because no one documented that it was done on [DATE].
Resident #46's bloodwork dated [DATE] showed a critical low blood sugar of 25 mg/dl. Per report, this critical result was called Nurse #9 on [DATE] at 5:02pm by the technician who completed the test.
During an interview with the lab technician on [DATE] at 2:47 pm, he stated that he was never able to reach a staff member on [DATE] to relay critical sugar results but did reach Nurse #9 on [DATE] and informed him of the current critical level of 25 (mg/dl), as well as the previous result of 37 (mg/dl) at that time. He also stated that, if he was unable to reach a staff member by phone, per the laboratory policy, he would release the results to the system to be flagged and would continue to try to reach the facility by phone.
During an interview with Nurse #9 on [DATE] at 9:45 am, he stated that he had no recollection of ever receiving a phone call from the lab regarding critical lab results for Resident #46. He stated that he was aware Resident #46 was on insulin. He stated that if blood sugars are done then they are put on the resident's medication administration record. He did not recall doing any fingerstick blood sugar tests on Resident #46 since he was admitted on [DATE]. He also stated Resident #46 ate pretty good while he was there. He added that he was not working on that hall when Resident #46 was admitted and wasn't responsible for entering his initial orders into the system. He was unsure who was assigned to him.
Record review showed a Nurse Aide #4 documented that Resident #46 was seen awake and sipping on water and stated he was fine on [DATE] at 3:30 am when she made rounds.
Multiple attempts to reach Nurse Aide #4 were unsuccessful.
On [DATE] at 10:15 am, a review Resident #46's meal intake report for [DATE]-[DATE] showed he consumed 76-100% of his meal one time and 51-75% one time. All other meals were either < 25% or meal was refused.
During an interview with the floating Director of Nursing on [DATE] at 3:10pm she stated you should never give insulin without knowing what the current blood sugar level is. She added that how orders are entered into the system and the lack of monitoring blood sugars was something the facility will be working on and will be included in their interdisciplinary meetings.
During an interview with the Nurse Practitioner on [DATE] at 3:35 pm, the state surveyor notified her that there were no blood sugar checks. She stated the importance of finger stick sugar checks in the presence of insulin and added that you should never administer insulin if you don't know what the current sugar level is. She stated that she was not aware of any critical blood levels for Resident #46. She stated he was newly admitted and she had not had a chance to evaluate him yet. She also stated that she was in the facility the previous day and there were no critical levels in her folder for her to review. She also stated that she expected all staff, including agency staff, to take care of the residents, for nurses to know current sugar levels prior to administering insulin, and to be able to recognize hypoglycemia signs.
During an interview with the Medical Director on [DATE] at 5:02 pm, the state surveyor notified her that there were no blood sugar checks. He stated there should be regular finger sticks with all residents who have insulin-dependent diabetes. He stated he was not aware of any critical blood sugar levels. He stated that it was vital to be aware of a resident's blood sugar levels when administering insulin.
The Administrator was notified of immediate jeopardy on [DATE] at 11:16am.
The facility provided a credible allegation of immediate jeopardy removal dated [DATE] at 7:52pm.
Credible Allegation of immediate jeopardy removal:
Identify those recipients who have suffered, or are likely to suffer, a serious adverse outcome as a result of the noncompliance.
Resident # 46 was deceased on [DATE] and is no longer a resident of the facility.
On [DATE], the Nurse Consultant completed an audit of 100% of all current insulin dependent diabetic residents to identify if they have orders for accuchecks and if they had any critical sugar labs. This audit was completed on [DATE]. The audit identified that 19 of 19 current insulin dependent diabetic residents had orders for accuchecks. No corrective actions were required. Additionally, 0 of 0 current insulin dependent diabetic residents had a critical sugar lab in the last 60 days. No corrective actions were required. All current insulin dependent diabetic residents blood sugars are being monitored as ordered.
On [DATE], the Director of Nurses and the nurse management team began an audit of residents who were potentially affected by the noncompliance by completing an audit of all new admissions/readmissions for the month of [DATE], to identify any new admissions/readmissions who are insulin dependent diabetic residents to ensure no orders for accuchecks on the discharge summary were not entered at the time of the admission. The audit was completed on [DATE]. The audit identified 18 total admissions. 2 of 18 admissions were insulin dependent diabetics with orders for accuchecks. The 2 admissions identified as insulin dependent diabetics at admission did have orders for accuchecks with blood sugars that are being monitored as ordered. No corrective actions were required.
On [DATE], the Director of Nursing and Assistant Director of Nurses met with all floor nurses and assessed all current residents to identify any signs and symptoms of hypoglycemia. No current residents were identified having any signs and symptoms of hypoglycemia. No other residents were impacted.
Specify the actions the entity will take to alter the process or system failure to prevent a serious adverse outcome from occurring or reoccurring and when the action will be completed.
On [DATE] the Director of Nurses and Assistant Director of Nurses began in servicing all licensed nurses and certified nursing assistants (full time, part time, and prn including agency nurses) on changes in condition which includes hypoglycemia and decreased meal intake. The education also included identifying signs and symptoms of hypoglycemia, assessment monitoring including blood sugar levels, following the diabetic protocol for hypoglycemia, notification of physician of signs and symptoms and documentation of assessment and actions taken in the medical record.
On [DATE] the Director of Nurses and Assistant Director of Nurses began in servicing of all licensed nurses (full time, part time, and prn including agency nurses) on Critical Labs. Staff were educated on how critical labs are received, to promptly notify the physician and/or on call of all critical labs, document notification in the electronic record, and to notify the resident and RP of the critical labs. All critical lab results are currently phoned to the nurse from a lab representative. If the lab is unable to reach the nurse at the facility, the lab representative will contact the on-call nurse to report the critical lab result. The lab manager has been provided the phone number for the nurse on-call phone number by the DON [DATE]. The lab representative facility contacts will be updated to include the nurse on-call phone number by the DON on [DATE]. The on-call nurse will then be responsible for following up to ensure the following occurs: Physician and/or on call is notified of the critical lab results, documentation of the result in the electronic record, and to notify the resident and RP of the critical labs.
On [DATE], the Director of Nursing and Assistant Director of Nurses also began in servicing of all licensed nurses (full time, part time, and prn including agency nurses) on the admissions process and review to ensure one nurse enters the orders into the EMR and a second nurse verifies the orders for accuracy. The nurses were also educated on the need to obtain blood sugar monitoring orders for all insulin dependent diabetics and those on diabetic medications. This will be reviewed for all new admissions/readmissions and those with new diagnosis or medication orders for diabetes.
The DON will ensure that all licensed nurses (full time, part time, and prn including agency nurses) who does not complete the in-service training will not be allowed to work until the training is completed.
This in-service was incorporated into the new employee facility and agency orientation for all licensed nurses (full time, part time, and prn including agency certified nursing assistants and nurses).
Date of IJ removal [DATE]
2. Resident #15 was admitted to the facility on [DATE] with diagnoses including congestive heart failure, edema and atrial fibrillation.
The quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #15 had moderately impaired cognition and required extensive assistance to total dependence with 1-2 people for his activities of daily living. He had no skin impairment.
A review of the care plan included a focus on incontinence with risk for skin breakdown initiated on [DATE] and anticoagulant therapy with an intervention to inspect skin and report abnormalities to nurse.
A Weekly Skin assessment dated [DATE] revealed no new areas.
On [DATE] at 11:43 AM, an observation was made of Resident #15 sitting in his wheelchair. A bordered gauze dressing with visible dark drainage was observed to the left lower leg. A hydrocolloid dressing was observed to the right lower leg with a date of [DATE]. Resident #15 did not know why the bandages were on his legs.
A record review revealed no documentation or orders for the areas to Resident #15 ' s right and leg lower legs.
On [DATE] at 11:49 AM, a second observation was made of Resident #15 ' s lower legs. The resident still had the bordered gauze dressing to the left lower leg and the hydrocolloid dressing dated [DATE] was still in place to the right lower leg.
On [DATE] at 8:25 AM, Nurse #7 stated she didn ' t know anything about the areas or dressings to Resident #15 ' s lower legs. Nurse #7 removed the dressing to the left lower leg and a small open area was observed with a small amount of drainage noted. The right lower leg also had a small open area present.
A nurses noted dated [DATE] at 8:25 AM by Nurse #7 read, this nurse noted open area to BLE (bilateral lower extremities). Area cleansed with normal saline and dry dressing applied. Physician notified and wound care requested to assess. Orders received.
A review of the physician ' s orders revealed an order dated [DATE] to clean right and left shin with normal saline, pat dry with gauze, apply triple antibiotic ointment, cover with dry dressing, and secure with tape twice a day until healed.
On [DATE] at 10:54 AM, an interview was conducted with the Director of Nursing who stated when a resident develops a new area on their skin, the staff member that identifies the area should document it in the medical record with the description, notify the physician and family and put a treatment order in place if needed.
CRITICAL
(J)
Immediate Jeopardy (IJ) - the most serious Medicare violation
Drug Regimen Review
(Tag F0756)
Someone could have died · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Resident #22 was admitted to the facility on [DATE] with diagnoses that included a cerebral infarction, Parkinson's disease, ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Resident #22 was admitted to the facility on [DATE] with diagnoses that included a cerebral infarction, Parkinson's disease, depression, dementia, and anxiety.
A review of the quarterly Minimum Data Set (MDS) dated [DATE] revealed Resident #22 had severe cognitive impairment with inattention, disorganized thinking and verbal behaviors directed towards others. The assessment documented she received an antipsychotic 6 days and an antidepressant 7 days of the 7-day lookback period. The antipsychotics were on a routine basis only.
A review of the electronic medical record for Resident #22 revealed an initial admission AIMS was completed on the date of [DATE].
A review of the Pharmacy medication regimen review for [DATE] written by the Pharmacy Consultant #1 for Resident #22 requested an AIMS due to the Resident receiving Olanzapine, an antipsychotic medication.
A review of the Pharmacy medication regimen review for [DATE] written by the Pharmacy Consultant #1 for Resident #22 repeated the request for an AIMS for the Resident.
A review of the Pharmacy medication regimen review for [DATE] written by the Pharmacy Consultant #1 for Resident #22 repeated the request for an AIMS for the Resident.
A review of the electronic medical record for Resident #22 revealed a second AIMS assessment was completed on [DATE].
A review of the Pharmacy medication regimen review for [DATE] written by the Pharmacy Consultant #1 for Resident #22 requested an AIMS due to the Resident continuing to receive an antipsychotic medication.
A review of the Pharmacy medication regimen review for [DATE] written by the Pharmacy Consultant #1 for Resident #22 repeated the request for an AIMS for the Resident due to her continuing to receive an antipsychotic medication.
On [DATE] at 2:04 p.m. an interview was conducted with the Unit Manager, and she revealed she received emails from the pharmacy consultant with the nursing monthly medication regimen review recommendation and request that also stated when to conduct an AIMS assessment. She revealed she was not sure if the AIMS assessment were due every three months or six months and would need to ask her Director of Nursing because she completed the AIMS assessments when she received instructions to do so in the emails from the Pharmacy consultant and Minimum Data Set (MDS) consultant. She reviewed the chart for Resident #22 and revealed she was able to see where the Pharmacy consultant documented the request for an AIMS on [DATE], [DATE], and [DATE] and then again on [DATE] and [DATE]. She stated she had been out of work due to an illness in June, 2022 and was not sure who the request had been emailed to but the AIMS was not completed in [DATE] as requested. She revealed in [DATE] and [DATE] a different Director of Nursing (DON) had been employed and the emails were going directly to the DON. The nursing recommendations requested from the Pharmacy Consultant had begun to be sent to the Unit managers in addition to the DON to improve on the follow up. She added the second AIMS was not completed until March of 2022.
An interview was conducted with the interim DON on [DATE] and he revealed the facility protocol for an AIMS assessment was to be conducted upon admission and every 6 months. He stated the facility protocol to follow up on Pharmacy consultant recommendations was for the request to be expedited as quickly as possible based on the situation and medication. He added a request for an assessment like an AIMS, the goal was for a turn around as quickly as possible, and this should be conducted before the pharmacist returns the following month.
Based on record review, consultant pharmacists, Nurse Practitioner and Medical Director interviews, the facility failed to complete an evaluation of Resident #46's medication regimen that identified the need to monitor insulin administration. Resident #46's initial medication regimen review did not identify the inadequate monitoring of insulin administration. Resident #46 received daily insulin without blood sugar testing and experienced critically low blood sugars identified through bloodwork. This was for 1 of 3 residents reviewed for pharmacy services. Also, the facility failed to retain the consultant pharmacist's findings, recommendations, and provider response in the resident's medical record or within the facility so the records were readily available for 6 of 13 residents whose medications were reviewed (Resident #24, #15, #4, #65, #168, and #218). And the facility failed to act on the Pharmacy Consultant recommendations to complete an abnormal involuntary movement (AIMS) assessment for 1 of 5 residents (Resident #22) reviewed for unnecessary medications.
Immediate jeopardy began on [DATE] when consultant pharmacist #1 reviewed Resident #46's medications and failed to recognize there were no physician orders for blood sugar testing with the administration of insulin and was removed on [DATE] when the facility provided an acceptable credible allegation of compliance. The facility will remain out of compliance at a scope and severity E (not actual harm with potential for more than minimal harm that is not immediate jeopardy) to ensure monitoring and all staff have been in-serviced.
The facility was also cited at a scope and severity of E for example #2 (Resident #24, #15, #4, #65, #168, and #218) and for example #3 (Resident #22).
The findings included:
Resident #46 was readmitted to the facility on [DATE] with diagnoses including Covid, left hip fracture and insulin-dependent diabetes mellitus. He was on insulin with regular blood sugar checks during previous admission. Resident #46 died in the facility on [DATE].
A hospital Discharge summary dated [DATE] included an order for long-acting basal insulin 20 units daily (long-acting means insulin enters bloodstream in 2-4 hours from administration time and can last up to 24 hours in the body) and blood sugar test strips to check blood sugars four times daily as directed. The hospital Discharge summary dated [DATE] also included an order to draw a complete blood count, basic metabolic panel, and thyroid stimulating hormone on [DATE].
A physician's order dated [DATE] was insulin degludec (long-acting insulin) 100 unit/milliliter-inject 20 units subcutaneously one time a day for diabetes mellitus. There were no orders for monitoring blood sugar levels.
The initial pharmacy review dated [DATE], completed by consultant pharmacist #1 showed no medication issues with Resident #46's current insulin orders. The review did not acknowledge the insulin.
Consultant pharmacist #1 was unable to be interviewed.
During an interview on [DATE] at 3:20 pm, consultant pharmacist #2 stated that consultant pharmacist #1 completed the initial medication reviews for the new admissions to the facility. She stated that they do not receive fingerstick blood sugar orders. They only receive medication orders and that is what they review and base their recommendations on. She stated that the facility was responsible for ordering and keeping up with fingerstick orders. When asked if blood sugars were something they would monitor during their pharmacy reviews, she stated no, she probably would not look at those. She stated the review was based on medication orders only.
During an interview with the Nurse Practitioner on [DATE] at 3:35 pm, she stated that she was not aware that Resident #46 was not receiving any fingerstick blood checks. She stated he was newly admitted and she had not had a chance to evaluate him yet. She also relayed the importance of finger stick sugar checks in the presence of insulin and she would expect finger stick blood sugar results to be on the resident's medication administration record for review. She added that you should not administer insulin if you don't know what the current sugar level is and that insulin is adjusted based on the daily blood sugar results.
The Administrator was notified of immediate jeopardy on [DATE] at 12:37pm.
The facility provided a credible allegation of immediate jeopardy removal dated [DATE].
Identify those recipients who have suffered, or are likely to suffer, a serious adverse outcome as a result of the noncompliance.
Resident # 46 was deceased on [DATE] and is no longer a resident of the facility.
On [DATE], the Pharmacy Director completed an audit of 18 residents who were potentially affected by the noncompliance by completing a comprehensive review of all new admissions/readmissions for the month of [DATE]. The audit consisted of a review of insulin dependent diabetics to ensure orders for diabetic monitoring are in place. The pharmacy consultant also reviewed current lab results.
Recommendations based on this review were sent to the physician by the nurse supervisor on [DATE]. These recommendations may include: additional labs, order changes, or additional diabetic monitoring. There were no other residents impacted.
Specify the actions the entity will take to alter the process or system failure to prevent a serious adverse outcome from occurring or reoccurring and when the action will be completed.
As of [DATE], the nurse consultant educated the pharmacy director on the need for all pharmacist consultants to review new admissions and readmissions to conduct comprehensive review that includes reviewing discharge summaries and comparing pre-hospital admission diabetic monitoring with readmission orders for monitoring and blood work orders and ensuring that the facility is providing comprehensive services for those residents with diabetic needs. In cases of irregularities identified, the consultant pharmacist will notify facility clinical leadership for immediate follow-up to the medical provider.
Pharmacy consultants will review all discharge summaries for new admissions and readmissions. In the event the pharmacy review identifies any insulin dependent diabetics, the consultant must review all orders to ensure orders for diabetic monitoring are in place. Additionally, the pharmacist consultant will review current labs and make recommendations to the physician if order changes, additional labs or additional diabetic monitoring is required. This will be completed at the time of the initial review to ensure residents with diabetes are receiving a comprehensive review with the necessary care and services, monitoring for their diabetes.
On [DATE], The Regional Director of Operations had a conversation with the pharmacy director detailing the process for ongoing monitoring for those residents with diabetic needs, specifically closer monitoring of chart information for new admissions and readmissions, to include reviewing the facilities practices for providing care and services. Previous pharmacy audits did not include review of blood work or orders for insulin dependent diabetics.
The Pharmacy Director will in-service all consultant staff that are assigned reviews for the facility on [DATE]. The Pharmacy Director will provide the completed in service packet the facility leadership to ensure the training has been completed and for review.
The pharmacy director will ensure that any consultant pharmacists who does not complete the in-service training will not be allowed to review charts for the facility until the training is completed. This in-service was incorporated into the new pharmacy employee orientation for the above identified staff including the agency staff orientation.
IJ Removal [DATE]
The credible allegation of immediate jeopardy removal was verified on [DATE] as evidenced by onsite validation through record review, and staff interviews. The facility nurse consultant met with the consulting pharmacist on [DATE] to complete an audit of current diabetic residents. They also met to discuss the need for reviewing discharge summaries for any monitoring orders for new and readmissions. The pharmacist will also review lab work and make recommendations depending on results. The facility immediate jeopardy removal was validated to be completed as of [DATE].
2-a) Resident #168 was admitted to the facility on [DATE] with re-entry on [DATE]. His cumulative diagnoses included diabetes, hypertension, chronic obstructive pulmonary disease, Alzheimer ' s disease, dementia with behavioral disturbance, major depressive disorder and anxiety disorder.
The resident ' s electronic medical record (EMR) included monthly MRRs completed by the consultant pharmacist. The MRRs included the following, in part:
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: repeat.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: AIMS (Abnormal Involuntary Movement Scale), GDR (gradual dose reduction).
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: f/u (follow-up), AIMS.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: AIMS, documentation.
No additional information was provided related to the consultant pharmacist ' s recommendations.
Resident #168 ' s ' s EMR revealed a consultant pharmacist conducted an initial MRR on [DATE]. The pharmacist ' s note from the MRR read: Initial pharmacist medication regimen review completed. Recommendations made, see report. No additional information was provided related to the consultant pharmacist ' s recommendations.
The resident ' s EMR included monthly MRRs completed by the consultant pharmacist. The MRRs included the following, in part:
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: AIMS, documentation.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: Repeat, AIMS.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: documentation.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: clinical doc (documentation).
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: repeat.
No additional information was provided related to the consultant pharmacist ' s recommendations.
An initial MRR was completed by a consultant pharmacist for Resident #168 on [DATE]. The pharmacist note read, Initial pharmacist medication regimen review completed. Recommendations made, see report. No additional information was provided related to the consultant pharmacist ' s recommendations.
On [DATE], a monthly MRR was conducted by the consultant pharmacist. The pharmacist recommendations read: documentation. No additional information was provided related to the consultant pharmacist ' s recommendations.
Further review of Resident #168 ' s EMR revealed there were no Pharmacy Consultation Reports included in the resident ' s medical record to provide details from the MRR recommendations dated [DATE], [DATE], [DATE], [DATE], [DATE], [DATE], [DATE], [DATE], [DATE], [DATE], [DATE], or [DATE]. Additionally, there was no documentation in Resident #168 ' s medical record to indicate the consultant pharmacist ' s findings / recommendations were reviewed or a response was received from the provider.
2-b) Resident #218 was admitted to the facility on [DATE]. Her cumulative diagnoses included Alzheimer ' s disease, osteoporosis, and depression.
The resident ' s electronic medical record (EMR) included monthly MRRs completed by the consultant pharmacist. The MRRs included the following, in part:
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: GDR (gradual dose reduction.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: f/u (follow-up).
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: APAP (acetaminophen.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: GDR.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: clinical doc (documentation).
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: prn (as needed).
No additional information was provided related to the consultant pharmacist ' s recommendations.
Resident #218 ' s most recent Minimum Data Set (MDS) was a significant change assessment dated [DATE]. The MDS assessment revealed she had severely impaired cognitive skills for daily decision making. The MDS reported the resident ' s medications included an antidepressant on 1 out of 7 days, an antibiotic on 7 out of 7 days and an opioid medication on 7 out of 7 days during the 7-day look back period.
Further review of Resident #218 ' s EMR revealed there were no Pharmacy Consultation Reports included in the resident ' s medical record to provide details from the MRR recommendations dated [DATE], [DATE], [DATE], [DATE], [DATE], or [DATE]. Additionally, there was no documentation in Resident #218 ' s medical record to indicate the consultant pharmacist ' s findings / recommendations were reviewed or a response was received from the provider.
2-c) Resident #4 was admitted to the facility on [DATE]. Her cumulative diagnoses included diabetes, renal insufficiency, and an adjustment disorder with mixed anxiety and depressed mood.
The resident ' s electronic medical record (EMR) included monthly MRRs completed by the consultant pharmacist. The MRRs included the following, in part:
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: repeat, documentation.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: documentation.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: lab.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: lab.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: GDR, repeat.
No additional information was provided related to the consultant pharmacist ' s recommendations.
Resident #4 ' s most recent Minimum Data Set (MDS) was a quarterly assessment dated [DATE]. The MDS assessment revealed she had cognitively intact skills for daily decision making. The MDS reported the resident ' s medications included insulin injection and antidepressant medication on 7 out of 7 days during the look back period.
On [DATE], a monthly MRR conducted by the pharmacist included recommendations which read: labs. No additional information was provided related to the consultant pharmacist ' s recommendations.
Further review of Resident #4 ' s EMR revealed there were no Pharmacy Consultation Reports included in the resident ' s medical record to provide details from the MRR recommendations dated [DATE], [DATE], [DATE], [DATE], [DATE] or [DATE]. Additionally, there was no documentation in Resident #4 ' s medical record to indicate the consultant pharmacist ' s findings / recommendations were reviewed or a response was received from the provider.
2-d) Resident #65 was admitted to the facility on [DATE]. Her cumulative diagnoses included anemia, hypertension, renal insufficiency, chronic obstructive pulmonary disease (COPD), anxiety disorder and depression.
The resident ' s electronic medical record (EMR) included monthly MRRs completed by the consultant pharmacist. The MRRs included the following, in part:
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: prn (as needed), lab.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: f/u (follow-up).
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: repeat.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: lab, documentation.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: repeat.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: repeat.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: documentation.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: clinical doc (documentation).
No additional information was provided related to the consultant pharmacist ' s recommendations.
Resident #65 ' s most recent Minimum Data Set (MDS) was an annual assessment dated [DATE]. The MDS assessment revealed she had moderately impaired cognitive skills for daily decision making. The MDS reported the resident ' s medications included an antidepressant, antibiotic, and opioid medication on 7 out of 7 days and a diuretic on 1 out of 7 days during the 7-day look back period.
On [DATE], a monthly MRR conducted by the consultant pharmacist included recommendations which read: Probiotic, inhalers, documentation. No additional information was provided related to the consultant pharmacist ' s recommendations.
Further review of Resident #65 ' s EMR revealed there were no Pharmacy Consultation Reports included in the resident ' s medical record to provide details from the MRR recommendations dated [DATE], [DATE], [DATE], [DATE], [DATE], [DATE], [DATE], or [DATE]. Additionally, there was no documentation in Resident #65 ' s medical record to indicate the consultant pharmacist ' s findings / recommendations were reviewed or a response was received from the provider.
2-e) Resident #15 was admitted to the facility on [DATE]. His cumulative diagnoses included a seizure disorder, hypertension, heart failure, and respiratory failure.
Resident #15 ' s most recent Minimum Data Set (MDS) was a quarterly assessment dated [DATE]. The MDS assessment revealed he had moderately impaired cognitive skills for daily decision making. The MDS reported the resident ' s medications included an antidepressant, anticoagulant, and diuretic medication on 7 out of 7 days during the look back period.
The resident ' s electronic medical record (EMR) included monthly MRRs completed by the consultant pharmacist. The MRRs included the following, in part:
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: documentation.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: lab, repeat.
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: repeat.
No additional information was provided related to the consultant pharmacist ' s recommendations.
Further review of Resident #15 ' s EMR revealed there were no Pharmacy Consultation Reports included in the resident ' s medical record to provide details from the MRR recommendations dated [DATE], [DATE] or [DATE]. Additionally, there was no documentation in Resident #15 ' s medical record to indicate the consultant pharmacist ' s findings / recommendations were reviewed or a response was received from the provider.
2-f) Resident #24 was admitted to the facility on [DATE]. His cumulative diagnoses included a history of multiple fractures, hypertension and unspecified dementia with behavioral disturbance.
The resident ' s electronic medical record (EMR) revealed a consultant pharmacist conducted an initial pharmacist medication regimen review (MRR) on [DATE]. The pharmacist ' s note from the MRR included documentation which read: Initial pharmacist medication regimen review completed. Recommendations made, see report.
Resident #24 ' s admission Minimum Data Set (MDS) dated [DATE] revealed he had moderately impaired cognitive skills for daily decision making. The resident ' s MDS assessment indicated his medications included an antipsychotic medication on 4 out of 7 days and a diuretic on 5 out of 7 days during the look back period.
The resident ' s EMR included the following monthly MRRs completed by the consultant pharmacist:
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: documentation, AIMS (Abnormal Involuntary Movement Scale).
--On [DATE], an MRR conducted by the pharmacist included recommendations which read: repeat, AIMS.
Further review of Resident #24 ' s EMR revealed there were no Pharmacy Consultation Reports included in the resident ' s medical record to provide details from the MRR recommendations dated [DATE], [DATE], or [DATE]. Additionally, there was no documentation in Resident #24 ' s medical record to indicate the consultant pharmacist ' s findings / recommendations were reviewed or a response was received from the provider.
An interview was conducted on [DATE] at 10:27 AM with the corporate floating Director of Nursing (DON) who served as the facility ' s Interim DON from [DATE] - [DATE]. During the interview, the float DON was asked if the consultant pharmacist recommendations, consultation reports and provider response for Resident #168, Resident #218, Resident #4, Resident #65, Resident #15, and Resident #24 were available for review. During a follow-up interview conducted with the floating DON, she reported only one Note to Attending Physician/Prescriber originating from a pharmacist MRR could be located. She stated no additional pharmacy recommendations were found in the residents ' medical records or elsewhere in the facility.
An interview was conducted on [DATE] at 9:56 AM with the facility ' s consultant pharmacist. During the interview, the pharmacist was asked to describe the process used at the facility for sharing the MRR monthly recommendations with the residents' provider. The pharmacist reported she would write a progress note in each resident ' s EMR to indicate whether or not she had pharmacy recommendations. She reported some recommendations were intended for nursing staff and these would go into a Nursing Note. Other pharmacy recommendations were intended for the provider. The pharmacist reported she would typically send all of her notes and recommendations via email to the DON and Regional Nurse Consultant and would flag important or urgent issues. The pharmacist stated it was up to the DON to print and distribute/delegate the Nursing Notes. The pharmacist reported she has asked the facility to upload the pharmacy recommendations with responses from the provider into each resident ' s EMR. When asked, the consultant pharmacist reiterated she would expect the pharmacy recommendations with the provider ' s response to be scanned into each resident ' s electronic medical record.
A telephone interview was conducted on [DATE] at 2:00 PM with the facility ' s Nurse Practitioner (NP). During the interview, the NP described the process employed for receiving the pharmacist's recommendations, reviewing, and responding to them. She reported she received the pharmacist ' s recommendations when the DON put them in her book. The NP stated she typically reviewed the recommendations, noted what she wanted to be done, and gave them back to the DON. The NP reported the DON would enter any order changes into the resident ' s EMR. After that, it was the NP ' s understanding that the DON would give these reports to medical records to be scanned in to the resident's EMR.
An interview was conducted on [DATE] at 3:55 PM with the facility ' s Interim DON. During the interview, the DON reported he was aware of the concern regarding the pharmacist ' s recommendations and provider responses not being available for review. The DON indicated he would expect the regulations to be followed.
SERIOUS
(G)
Actual Harm - a resident was hurt due to facility failures
Deficiency F0692
(Tag F0692)
A resident was harmed · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews with Registered Dietician (RD), and staff, the facility failed to implement ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews with Registered Dietician (RD), and staff, the facility failed to implement a high calorie nutritional supplement, as recommended by the RD for a resident with a stage 4 pressure ulcer identified as underweight on admission. The resident continued to lose weight the following month which resulted in severe weight loss that was greater than 5% for 1 of 6 residents reviewed for nutrition (Resident #35).
The findings included:
Resident #35 was admitted to the facility on [DATE] with diagnoses including pressure ulcer of sacral region and depression.
Resident #35 was ordered a regular diet on 6/3/22.
A dietary assessment dated [DATE] revealed Resident #35 was admitted on a regular diet with thin liquids. The current by mouth oral intake was noted as adequate at 50-75%. The resident had multiple wounds.
An admission Minimum Data Set assessment dated [DATE] revealed Resident #35 was cognitively intact, independent with meals, was 74 inches tall and weighed 136 pounds, did not have any swallowing disorders, and had not lost weight. The assessment did not indicate any nutritional approaches were in place. Resident #35 had a stage 4 pressure ulcer that was present on admission.
A note by the Registered Dietician (RD) dated 6/14/22 at 1:39 PM read, in part, underweight BMI (body mass index). Tolerates regular diet, fair intake. Patient declined RD recommended tube feeding in hospital to assist to improve high protein intake. Recommend provide nutrition supplement to meet nutrition needs. Start Med Pass 2.0 (a high calorie, high protein nutritional supplement) 90 milliliters by mouth three times a day to provide an additional 540 kilocalories and 23 grams of protein.
The Medication Administration Record (MAR) for June 2022 revealed the Med Pass 2.0 90 milliliters three times a day was not on the MAR.
Review of Resident #35 ' s weights documented in the electronic health record were
136.2 pounds on 6/12/22 and 127.4 pounds on 7/11/22.
A note by the RD dated 7/15/22 at 8:02 PM read, in part, 6.6 percent weight loss x 30 days. Recommend provide nutrition supplement to meet nutrition needs. Start Med Pass 2.0 90 milliliters by mouth three times a day.
A review of the July 2022 physician ' s orders revealed the order for Med Pass 2.0 90 milliliters three times a day was entered on 7/17/22.
On 7/17/22 at 11:52 AM, Resident #35 was interviewed. He stated he was a chef at a nice restaurant and the food in the facility was terrible up to a couple of days ago. He stated no one had ever asked him about food likes/dislikes.
On 7/17/22 at 11:52 AM, an interview was conducted with the Dietary Manager. She stated she came back to work at the facility on 7/3/22 and menus changed 7/6/22 due to a change in the food caterer. She stated she had not spoken to Resident #35 about food preferences, and she did not think food preferences were maintained. She added she could find no record of food preferences for Resident #35. She stated he got a daily menu that was placed on his breakfast tray, and he could choose what he wanted to eat the following day.
On 7/20/22 at 10:17 AM, the RD was interviewed. She stated she visited Resident #35 on 6/14/22 and identified him as high risk because of medical conditions and wounds. She added the Med Pass to meet increased nutritional needs. She stated when she made recommendations, she emailed them to the Administrator, the Director of Nursing and the Dietary Manager. She stated she didn ' t know why the Med Pass didn ' t get implemented in June, but she added there was some turnover in the facility including the Administrator, Director of Nursing, and the Dietary Manager, all in the last couple of months. When she saw Resident #35 again in July, she noticed the Med Pass 2.0 wasn ' t ordered and recommended it again.
On 7/20/22 at 11:16 AM, an observation was made of wound care to Resident #35 ' s sacral wound. The wound was large and covered the entire sacral area and beyond.
On 7/21/22 at 11:13 AM, the Director of Nursing was interviewed. He stated recommendations from the dietician should be put into place.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0553
(Tag F0553)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff and resident interviews, the facility failed to invite cognitively intact residents to participate...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff and resident interviews, the facility failed to invite cognitively intact residents to participate in the planning of the residents' care plan for 2 of 3 residents (Resident #60 and #4) reviewed for participation in care planning.
The findings included:
1. Resident #60 was admitted to the facility on [DATE] with diagnoses that included hemiplegia, atrial fibrillation, atherosclerotic heart disease and abnormal posture.
A review of the comprehensive annual minimum data set (MDS) dated [DATE] revealed Resident #60 was cognitively intact for decision making.
A review of a care plan meeting note dated 4/20/2022 documented a care plan meeting invitation for Resident #60's family member was mailed and invited the family member to attend on 5/4/2022.
An interview was conducted with Resident #60 on 7/18/2022 at 9:25 a.m. and she revealed she had not been invited to participate in a care plan meeting and she was not sure what a care plan meeting was at the skilled nursing facility.
On 7/19/2022 at 4:35 p.m. an interview was conducted with the MDS coordinator, and she revealed the facility process for care plan meetings was to invite the family of a resident via mail and invite a resident on the day of the care plan meeting. She added that the meeting would take place in the fine dining room and if the resident was not out of bed at the time of the care plan meeting, the meeting would take place without the resident and the individual members of the care plan meeting would be expected to meet with the Resident after the care plan meeting to tell them what had been discussed during the meeting. When asked to demonstrate the documentation of the most recent care plan meeting for Resident #60 a care plan signature form dated 5/4/2022 was provided that read: quarterly care plan meeting was conducted on 5/4/2022 and care plan invitation was sent on 4/20/2022 to the resident representative. Those in attendance were listed as: the social worker, activity director, treatment nurse, MDS nurse, and dietary manager. The Resident was not included on the list. The MDS nurse added that since COVID the care plan meetings had not taken place at the bedside, and she was not certain if the individual members had covered their portions of the care plan meeting with the Resident after the meeting because nothing was documented. She stated a change to the current care plan meeting system should occur to include invitations being sent to cognitively intact residents with a care plan meeting note that included documentation of the invitation, the subjects covered, and any updates that need to occur. She added it was her expectation that all residents that are cognitively intact understand what the care plan meeting was and that it was their right to participate.
2. Resident #4 was originally admitted to the facility on [DATE] and re-admitted on [DATE].
The quarterly minimum data set (MDS) dated [DATE] indicated Resident #4 was cognitively intact.
A review of the facility's records revealed an invitation to Resident #4's care plan meeting was mailed to the resident's responsible party on 5/25/22 for the meeting date of 6/15/22. There was no documentation available indicating Resident #4 was invited to her care plan meeting.
The care plan signature form dated 6/15/22 did not include the Resident #4's signature indicating the resident was not in attendance to her care plan meeting.
During an interview on 7/18/22 at 11:48 a.m., Resident #4 stated that she was not aware of a care plan meeting to discuss her care. She revealed she had never been invited to any care plan meetings but would like to have been invited.
On 7/19/22 at 4:35 p.m., the MDS Nurse stated that she mailed the invitations to the care plan meetings to the residents' responsible parties/families 1-2 weeks prior to the care plan meeting date. If the resident was not up and out of bed at the time of the meeting, the team would conduct the meeting and then each participant will go to the resident's room individually to meet with the resident. She added that the resident would be allowed to give input and the resident's signature obtained. She stated there was no signed medication review or care plan review to demonstrate it was covered with the resident. She added that a tweak to the system should occur to include any resident that was their own responsible party with a cognition status greater than 12 ensuring the resident understood what he/she was invited for and documentation of the meeting that includes the resident's signature, invitation documentation, and documentation of the subjects covered in the meeting with the resident.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0554
(Tag F0554)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, resident interview, staff interviews and record review, the facility's interdisciplinary team failed to as...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, resident interview, staff interviews and record review, the facility's interdisciplinary team failed to assess and document the ability of a resident to self-administer medications for 1 of 1 resident (Resident #58) who was observed to have medications at bedside.
Findings included:
Resident #58 was admitted to the facility on [DATE] with diagnoses that included, in part, end stage renal disease and diabetes.
The admission Minimum Data Set assessment dated [DATE] revealed Resident #58 was cognitively intact.
Physician (MD) orders were reviewed and included an order dated 7/11/22 for Tums Ultra (calcium carbonate antacid), 1000 milligrams; give three tablets by mouth with meals. Further review of the medical record revealed no assessments or orders were completed for the self-administration of medications.
An observation and interview were conducted with Resident #58 on 7/17/22 at 12:16 PM. A plastic medication cup that contained three Tums tablets was observed within the resident's reach on the overbed table. During an interview with Resident #58, she stated Medication Aide #1 (MA #1) gave the tablets to her late in the morning after she had already eaten her breakfast and since she was supposed to take them with meals, she told MA #1 she would take them with her lunch. Resident #58 did not think she had been assessed by the facility to self-administer medications.
On 7/18/22 at 9:59 AM an interview was completed with MA #1. She explained when she gave medications, she typically watched the resident swallow the medication before she left the room. MA #1 recalled she had administered medications to Resident #58 on 7/17/22 and said when she attempted to give the resident the Tums tablets the resident told her she wasn't going to take them at that time since she had already eaten her breakfast. MA #1 said she left the medication at the resident's bedside so she could take them later in the day when Resident #58 was ready for them. MA #1 added she knew she was not supposed to leave medications at the bedside but thought since it was just Tums and Resident #58 did not have a roommate, that it was okay to leave them for the resident to take later in the day.
During an interview with the Long Term Care Unit Manager on 7/20/22 at 9:17 AM, she explained when a nurse or medication aide gave medications to a resident, they watched the resident swallow the medications before they left the room. She stated Resident #58 had not been assessed as being able to self-administer medications and the medication aide should not have left the Tums at the bedside.
The Corporate Nurse was interviewed on 7/20/22 at 10:42 AM and stated the facility had self-administration assessments available if a resident requested permission to self-administer medications.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0558
(Tag F0558)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, resident and staff interviews and record review, the facility failed to place a resident's call light wit...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, resident and staff interviews and record review, the facility failed to place a resident's call light within reach to allow for the resident to request staff assistance if needed for 2 of 5 residents (Resident #65 and Resident #41) reviewed for accommodation of needs.
Findings included:
1. Resident #65 was admitted to the facility on [DATE] with diagnoses that included, in part, chronic obstructive pulmonary disease and hypertension.
The annual Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #65 had moderately impaired cognition. She required extensive assistance with bed mobility and was totally dependent for assistance with transfers.
The comprehensive care plan, updated 7/18/22, included a focused area of risk for falls. A care plan intervention included, ensure that call light is within reach.
On 7/17/22 at 3:08 PM, Resident #65 was observed in her bed. The call light was on the nightstand to the right of the resident's bed and the cord was draped over the side of the nightstand. During an interview with Resident #65 on 7/17/22 at 3:10 PM, she reported she was unable to reach the call light and stated when staff came into the room she told them to put the call light cord within her reach.
During an observation of Resident #65 on 7/18/22 at 4:18 PM, she was awake and in bed. The call light was observed behind the resident and underneath her pillow. Upon interview with Resident #65 on 7/18/22 at 4:19 PM, she said she could not reach the call light since it was behind her and underneath her pillow.
An interview was completed with Nurse #13 on 7/21/22 at 2:12 PM, during which she stated Resident #65 used her call light and made her needs known to staff. She explained when she provided care, before she left a resident's room, she made sure the call light was within reach of the resident or clipped to the resident's bed or clothing.
During an interview with the Interim Director of Nursing (DON) on 7/21/22 at 2:56 PM, he stated staff were educated that call lights were supposed to be in reach of the residents.
2. Resident #41 was admitted to the facility on [DATE] with diagnoses that included, in part, diabetes and hypertension.
The quarterly MDS assessment dated [DATE] revealed Resident #41 had severely impaired cognition. She required extensive assistance with bed mobility and was totally dependent for assistance with transfers.
The comprehensive care plan, updated 6/3/22, included a focused area of activities of daily living. A care plan intervention included, encourage me to use call light to call for assistance.
On 7/17/22 at 12:46 PM, Resident #41 was observed in her bed. The call light cord was in the nightstand drawer to the left of the resident's bed and the push button hung outside of the drawer. Resident #41 attempted to reach the call button from her bed but was unable to reach over far enough to push the call light button.
During an observation of Resident #41 on 7/19/22 at 9:39 AM, she was in bed and engaged in simple conversation. The call light was observed draped over the nightstand drawer and Resident #41 demonstrated she was unable to reach the call light.
An interview was completed with Nurse #7 on 7/21/22 at 11:35 AM, during which she stated Resident #41 used her call light and made her needs known to staff. She explained it was the responsibility of the nurse aides to place the call light within reach of the resident when they were finished providing care.
During an interview with the Interim DON on 7/21/22 at 2:56 PM, he stated staff were educated that call lights were supposed to be in reach of the residents.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0561
(Tag F0561)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff and resident interviews, the facility failed to honor a resident ' s choice to receive a shower...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff and resident interviews, the facility failed to honor a resident ' s choice to receive a shower twice a week for 1 of 4 residents reviewed for choices (Resident #35).
The findings included:
Resident #35 was admitted to the facility on [DATE] with diagnoses of, in part, depression, pressure ulcer to sacral region and neuromuscular dysfunction of bladder.
An admission Minimum Data Set assessment dated [DATE] revealed Resident #35 had intact cognition. He required extensive assistance of 2 people for transfers and minimum assistance for bathing. Resident #35 was non-ambulatory.
A review of the care plan dated 6/23/22 revealed a focus on activities of daily living self-care performance deficit related to deconditioning and interventions for help with activities of daily living.
A review of the shower schedule for Resident #35 revealed he was to receive a shower on Sunday and Tuesday on 7PM-7AM shift.
On 7/17/22 at 11:50 AM, an interview was conducted with Resident #35. He stated he had not had a shower since he was admitted on [DATE] and his hair was dirty and needed to be washed. He stated they tried to give hm one once, but he got very dizzy when he sat up and had to be put back into the bed. He stated he would be willing to try using a shower stretcher or a reclining chair if available. He stated he had received bed baths.
On 7/20/22 at 8:45 AM, an interview was conducted with Nursing Assistant (NA) #2. She stated she worked with Resident #35 on 7/17/22 and did not give him a shower because the resident was unable to sit up.
On 7/20/22 at 8:53 AM, an interview was conducted with NA#3. She stated every room had its own shower and the facility did not have a shower stretcher. NA#3 added there was at least one other resident that was unable to sit up and used a reclining wheelchair to receive a shower.
On 7/21/22 at 10:51 AM, the Director of Nursing (DON) was interviewed. He stated if a resident had a medical concern where they were unable to sit up to receive a shower, management should be notified so alternates could be put in place so residents can receive showers. He added that just because there was another wheelchair in the facility the reclined, did not mean it was appropriate for Resident #35. He stated physical therapy might need to get involved to determine the appropriate chair for Resident #35. The DON did not know why that had not been done yet.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Assessment Accuracy
(Tag F0641)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interviews, the facility failed to accurately code the Minimum Data Set (MDS) assessment in the...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interviews, the facility failed to accurately code the Minimum Data Set (MDS) assessment in the areas of weight loss and medications for 2 of 33 residents reviewed (Resident #15 and Resident #24).
The findings included:
1. Resident #15 was admitted to the facility on [DATE] with diagnoses of, in part, edema, congestive heart failure and dementia.
The admission Nursing assessment dated [DATE] revealed Resident #15 ' s weight on admission was 272.4 pounds.
A medical record review revealed the following weights for Resident #15:
4/9/22 271.6
4/10/22 250
5/10/22 236.8
A quarterly MDS dated [DATE] revealed Resident #15 had moderately impaired cognition, was independent with meals after set up and weighed 238 pounds. The MDS was code No for weight loss.
On 7/19/22 at 3:25 PM, the MDS Nurse was interviewed. She stated she didn ' t code the weight loss because she didn ' t think the weight was accurate.
On 7/21/22 at 3:00 PM, an interview was conducted with the Director of Nursing. He stated their intent was to ensure the MDS assessment was coded appropriately.
2. Resident #24 was admitted to the facility on [DATE]. His cumulative diagnoses included arthritis. The resident did not have a diagnosis of diabetes.
The resident ' s Electronic Medical Record (EMR) revealed his medication orders included 20 milligrams (mg) / 0.4 milliliters (ml) adalimumab (a medication which may be used to treat rheumatoid arthritis) injected subcutaneously one time a day every 14 days with a start date of 5/24/22. A review of Resident #24 ' s May 2022 Medication Administration Record (MAR) revealed the resident received one injection of adalimumab on 5/24/22 in accordance with the medication order. The May 2022 MAR did not indicate the resident received insulin.
Resident #24 ' s admission Minimum Data Set (MDS) dated [DATE] reported the resident received one injection of any type during the 7-day look back period. The MDS also indicated Resident #24 received one insulin injection during this 7-day look back period.
An interview was conducted on 7/19/22 at 3:07 PM with the facility ' s MDS Nurse. During the interview, the MDS Nurse was asked to review the Medication section of Resident #24 ' s admission MDS dated [DATE]. Upon review of both the resident ' s MDS and his EMR, the MDS nurse stated, It (the injection) was (adalimumab). He did not receive insulin. The MDS nurse confirmed Resident #24 ' s MDS should not have indicated he received an injection of insulin.
An interview was conducted on 7/21/22 at 3:00 PM with the facility's Interim Director of Nursing (DON). During the interview, the inaccuracy of the MDS for Resident #24 ' s medication was discussed. When asked, the Interim DON stated, It is our intent to ensure the MDS is coded appropriately according to the category of the medication specified.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
ADL Care
(Tag F0677)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, staff and family interviews the facility failed to provide activities of daily living (ADL)...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, staff and family interviews the facility failed to provide activities of daily living (ADL) assistance for a resident (Resident #22) that was dependent on staff to receive a shower and nail care in 1 of 5 residents reviewed for ADL care.
The findings included:
Resident #22 was admitted to the facility on [DATE] with diagnoses that included dementia, cerebral infarction, and aphasia.
A review of the quarterly Minimum Data Set (MDS) dated [DATE] revealed Resident #22 had severe cognitive impairment with no rejection of care and required total assistance of one staff member with personal hygiene and bathing.
A review of Resident #22's care plan dated 5/30/2022 revealed a focused area for ADL self care performance deficit with interventions that included Resident #22 required staff assistance with bathing and personal hygiene.
An observation was conducted of Resident #22 on 7/17/2022 at 12:11 p.m. lying in bed with long fingernails that had dark brown debris under each nail. Her hair was observed to be greasy and stuck to her head and uncombed.
An interview was conducted with Resident #22's responsible party (RP) on 7/17/2022 at 3:33 p.m. and she revealed when she visits her mother in the evening, she frequently finds her mother with hair greasy and unwashed and she does not believe her mother receives a shower on a consistent basis. She added the last shower she was aware of was greater than two weeks ago and that was the first one in over three months to her knowledge. She stated the nursing assistants would conduct a bed bath instead of a shower and could not wash her mother's hair in the bed.
An observation was conducted on 7/19/2022 at 6:10 p.m. of Resident #22 lying in bed, with her hair greasy and stuck to her head, uncombed in appearance. Her nails were observed to be long with brown debris underneath each nail.
A review of Resident #22's electronic shower task log revealed she had scheduled shower times on Tuesday and Friday, day shift with the following documented showers:
Tuesdays:
6/21/2022 no shower given.
6/28/2022 a shower was documented as given.
7/5/2022 no shower given.
7/19/2022 NA #1 documented she provided a shower at 2:48 p.m.
Fridays:
7/8/2022 no shower given.
An interview was conducted on 7/19/2022 at 6:46 p.m. with the Assistant Director of Nursing (ADON) present at Resident #22 bedside and the ADON stated the Resident's nails were too long and dirty underneath and needed to be cleaned. She stated the Resident's hair was greasy and looked like it needed to be washed.
An interview was conducted with NA #1 on 7/19/2022 at 6:54 p.m. and she revealed she did not give Resident #22 a shower on 7/19/2022 and the documentation she charted in the electronic medical chart was inaccurate and charted in error. She stated the documentation that revealed she did not give a shower to the Resident on 7/5/2022 was accurate.
An interview was conducted on 7/19/2022 at 7:16 p.m. with the Director of Nursing (DON) and he revealed it was his expectation that the highest level of care be provided to all Residents. He stated a root cause analysis would need to occur. It was his expectation that the Resident receive nail and hair care as needed, a shower when scheduled, and accurate documentation every day.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Pressure Ulcer Prevention
(Tag F0686)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff and physician interviews, the facility failed to implement orders by the wound care physician f...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff and physician interviews, the facility failed to implement orders by the wound care physician for a resident with a sacral pressure ulcer for 1 of 4 residents reviewed for pressure ulcers (Resident #218).
The findings included:
Resident #218 was admitted to the facility on [DATE] with diagnoses of, in part, spinal stenosis and dementia and expired in the facility on [DATE].
A progress note by the wound care physician dated [DATE] included treatment orders to apply santyl (a debriding agent) and calcium alginate to Resident #218 ' s sacral wound and apply skin prep to the peri-wound.
A review of the [DATE] Treatment Administration Record revealed the treatment to the wound was being done but the skin prep ordered to he peri-wound was not listed as a treatment order to be completed.
A progress note by the wound care physician dated [DATE] indicated the sacral wound deteriorated and was now unstageable due to necrosis (devitalized tissue). Treatment orders included treatment orders to apply Dakin ' s 0.5% (a broad-spectrum antimicrobial cleanser that is gentle to the skin) gauze and a dry dressing.
The treatment orders included skin prep to the peri wound (tissue surrounding wound) twice a day.
A significant change in status Minimum Data Set assessment dated [DATE] revealed Resident #218 had severely impaired cognition and required extensive to total assistance of 1-2 people with bed mobility, dressing, toileting, hygiene, bathing and eating. Resident #218 was at risk for pressure ulcers, had 1 stage 4 pressure ulcer and received pressure ulcer care.
A review of the [DATE] Treatment Administration Record revealed the treatment to the wound bed was being completed but skin prep to the peri-wound was not listed as a treatment order to be completed.
On [DATE] at 9:31 AM, an interview was conducted with the wound care physician. He stated he was very familiar with Resident #218 as she had a reopened sacral wound that continued to decline due to her condition. He stated when he made wound rounds in the facility, a staff member rounded with him. He stated he measured the wound and stages it if it is a new wound. He stated he then says out loud what the plan is going to be for treatment of the wound so the nurse that rounds with him can take down the orders and the resident knows what is going to be done as well. He stated the skin prep helps the wound dressing stick better and has alcohol in it to help keep the area clean especially with residents that have incontinence. He stated the primary dressing was the most important thing but agreed the skin prep was also important and should have been ordered and being done as well.
On [DATE] at 10:58 AM, an interview was conducted with the Director of Nursing. He stated there wasn ' t a permanent treatment nurse in the facility and they were using agency staff to complete treatments and round weekly with the wound care physician. He stated the nurse that rounds with the wound care physician should have implemented all his orders.
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 record review and interviews with staff, the facility failed to remove an air mattress from a resident ' s bed after a ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interviews with staff, the facility failed to remove an air mattress from a resident ' s bed after a fall which caused a resident to sustain another fall for 1 of 5 residents reviewed for accidents (Resident #218).
The findings included:
Resident #218 was admitted to the facility on [DATE] with diagnosis of dementia.
A quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #218 had severely impaired cognition and required extensive assistance with bed mobility and total dependence for transfers and toileting. Resident #218 was non-ambulatory and had no falls.
A review of Resident #218 ' s care plan dated [DATE] and revised on [DATE] included a focus on increased risk for falls related to confusion and a history of falls. Interventions included discontinue air mattress dated [DATE] and replace mattress dated [DATE], hi-low bed dated [DATE] and fall mats dated [DATE].
A nurse ' s note dated [DATE] at 5:46 PM read, resident observed laying on back on floor beside bed and beside dresser. No injuries noted upon initial assessment.
A Fall Repot dated [DATE] revealed Resident #218 was observed laying on back on floor by bedside dresser and bed. Alert and verbal. No apparent injuries noted. The Fall Report indicated Resident #218 ' s medical record and medications were reviewed, care plan updated, and room inspection completed. Root cause was determined to be the air mattress and intervention listed was remove air mattress.
A work order was submitted on [DATE] at 10:00 AM by Nurse #11 to remove air mattress from Resident #218 ' s bed.
A nurse ' s note dated [DATE] at 7:17 PM by Nurse #10 read, at 3:10 PM, nurse was called to the room of resident by nursing assistant. Nurse found resident lying face down on the right side of her bed. No injuries were noted to residents back, hips and lower extremities. Resident was log rolled onto a flat sheet to supine position and nurse noted a hematoma to right forehead and discoloration to right eye, skin tears to left hand and bruising to knees. On call physician gave order to send resident to emergency department. Air mattress was removed from bed and replaced with a regular mattress.
A Fall Report dated [DATE] revealed resident was found on floor beside bed, slid off air mattress. Medical record and medications reviewed; care plan updated. Root cause was determined to be displaced air. Interventions were to place mats beside bed.
A review of the Emergency Department record dated [DATE] indicated Resident #218 was brought in by emergency medical services for an unwitnessed fall at the facility. Has bruising and contusion to her right forehead. Vital signs within normal range. Computed tomography was completed of head and facial bones and spine with no acute fracture or dislocation and no acute intracranial abnormality found. X-rays to femur, tibia/fibia and pelvis showed no fracture. Resident #218 was not admitted to the hospital.
Resident #218 expired in the facility on [DATE].
On [DATE] at 2:22 PM, an interview was conducted with Nurse #12 who was the nurse that worked with Resident #218 on [DATE] when she fell out of the bed. She stated she could not recall Resident #218 at all and could not recall if the air mattress was removed from the bed on [DATE].
On [DATE] at 3:24 PM, an interview was conducted with Nurse #10. She stated when Resident #218 fell on [DATE], the air mattress was still on the bed because the resident slid off it. She stated Resident #218 was very thin and Nurse #10 didn ' t think she had enough weight for the air mattress to be effective. She was unaware of the previous intervention to remove the air mattress.
On [DATE] at 8:48 AM, an interview was conducted with the Former Maintenance worker who stated he could not recall if the air mattress was removed from Resident #218 ' s bed after the fall on [DATE]. He stated there was a box at the nurse ' s station that work orders were put in and he picked those up 1-2 times a day. He stated if it was something related to a fall, he was on top of that and there was a daily stand-up meeting and falls were discussed. He added if the work request was put in on a Friday ([DATE]), he may not have gotten to it until Monday because he did not work on the weekends.
On [DATE] at 11:03 AM, an interview was conducted with the Director of Nursing. He stated he wasn ' t at the facility in March when Resident #218 ' s falls occurred. He stated there was a daily stand-up meeting where falls have been discussed and if an intervention like removing an air mattress needed to be done, that would be discussed. He could not explain why the air mattress was still on the bed on 3/13/ 22 after the fall on [DATE] and that it should have been removed.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0760
(Tag F0760)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, staff, consultant pharmacist, and Nurse Practitioner (NP) interviews and record review, the facility fail...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, staff, consultant pharmacist, and Nurse Practitioner (NP) interviews and record review, the facility failed to hold the administration of antihypertensive medications when a resident ' s blood pressure / heart rate were outside of the parameters indicated by his physician orders. This occurred for 1 of 6 residents (Resident #24) reviewed for medications administered during the med pass observations.
The findings included:
Resident #24 was admitted to the facility on [DATE]. His cumulative diagnoses included a history of multiple fractures and hypertension.
Resident #24 ' s admission orders dated 5/21/22 included the following, in part:
--25 milligrams (mg) hydrochlorothiazide (a diuretic) to be given as one tablet by mouth once daily for hypertension;
--100 mg metoprolol succinate (an extended release formulation of an anti-hypertensive medication) to be given as one tablet by mouth once daily for hypertension.
Resident #24 ' s admission Minimum Data Set (MDS) dated [DATE] revealed he had moderately impaired cognitive skills for daily decision making. The resident required extensive assistance for bed mobility, dressing, eating, and personal hygiene. He was totally dependent on staff for transfers and toileting. Resident #24 ' s MDS reported he had a history of fall(s) 2 to 6 months prior to admission and a fracture related to a fall within 6 months prior to his admission to the facility. The resident ' s MDS assessment also indicated he sustained two or more falls without injury since his admission to the facility.
Resident #24 ' s care plan included an area of focus which read, I have had actual falls with risk for further (Date Initiated: 5/26/22; Revision on 6/3/22). The planned interventions included, in part: Med review (Date Initiated: 5/29/22; Revision on: 6/28/22); and Medication Adjustment (Date Initiated: 6/6/22).
On 6/7/22, a physician ' s order was received to add blood pressure and heart rate parameters for the administration of Resident #24 ' s antihypertensive medications. The start date for the new order was 6/8/22. The order included:
--25 mg hydrochlorothiazide to be given as one tablet by mouth once daily for hypertension; Hold for Systolic Blood Pressure (SBP is the maximum pressure the heart exerts while beating and is represented by the top number of a blood pressure reading) less than 120 and Heart Rate (HR) less than 60. Hydrochlorothiazide was scheduled to be administered to the resident at 9:00 AM each day.
--100 mg metoprolol succinate to be given as one tablet by mouth once daily for hypertension. Hold for SBP less than 120 and HR less than 60. Metoprolol succinate was also scheduled to be administered to the resident at 9:00 AM each day.
Resident #24 ' s June 2022 Medication Administration Record (MAR) was reviewed. The MAR documented the resident ' s metoprolol succinate and hydrochlorothiazide were given on each of the following dates when the SBP / HR were outside of a parameter indicated by the physician ' s orders:
--On 6/16/22, the resident ' s SBP was 118 and HR was 65; both metoprolol succinate and hydrochlorothiazide were documented as having been administered to the resident by Nurse #2.
--On 6/20/22, the resident ' s SBP was 118 and HR was 88; both metoprolol succinate and hydrochlorothiazide were documented as having been administered to the resident by Nurse #3.
--On 6/21/22, the resident ' s SBP was 104 and HR was 80; both metoprolol succinate and hydrochlorothiazide were documented as having been administered to the resident by Nurse #4.
--On 6/29/22, the resident ' s SBP was 112 and HR was 62; both metoprolol succinate and hydrochlorothiazide were documented as having been administered to the resident by Nurse #5.
A telephone interview was conducted on 7/20/22 at 2:20 PM with Nurse #2. Nurse #2 was identified as an Agency (temporary) nurse who documented on the MAR that Resident #24 ' s metoprolol succinate and hydrochlorothiazide were administered on 6/16/22 when his SBP / HR parameters indicated the medications should have been held. During the interview, the resident ' s vital signs and physician ' s order were discussed. The nurse reported she typically would have held the medications under these circumstances and coded the MAR to indicate these meds were not given. Nurse #2 stated that sometimes a resident ' s blood pressure was taken after the medications were administered. Upon further inquiry, the nurse would not elaborate on this comment.
A telephone interview was conducted on 7/20/22 at 2:35 PM with Nurse #3. Nurse #3 was identified as an Agency nurse who documented on the MAR that Resident #24 ' s metoprolol succinate and hydrochlorothiazide were administered on 6/20/22 when his SBP / HR parameters indicated the medications should have been held. When asked, the nurse reported if a medication was not given, he would check a box on the electronic MAR to indicate the med was not given per parameters. He reported a check mark with his initials would indicate the medication(s) was administered.
An interview was conducted on 7/20/22 at 2:49 PM with Nurse #4. Nurse #4 was identified as an Agency nurse who documented on Resident #24 ' s MAR that his metoprolol succinate and hydrochlorothiazide were administered on 6/21/22 when his SBP / HR parameters indicated the medications should have been held. During the interview, Resident #24 ' s June MAR was reviewed with the nurse. The MAR included the resident ' s SBP / HR and a check mark with the nurse ' s initials to indicate the medications were given on this date. When shown the information and documentation on Resident #24 ' s MAR, the nurse stated she did not know for sure whether she made an error in charting or an error in administering the medications to the resident when she should not have.
Nurse #5 could not be reached for a telephone interview. Nurse #5 was identified as an Agency nurse who documented on Resident #24 ' s MAR that his metoprolol succinate and hydrochlorothiazide were administered on 6/29/22 when his SBP / HR parameters indicated the medications should have been held.
An observation was conducted on 7/17/22 at 10:04 AM as Med Aide #1 checked Resident #24 ' s vital signs prior to administering his medications. The resident ' s vital signs included a blood pressure of 115/65 and heart rate of 69. Med Aide #1 was observed as she administered 100 mg metoprolol succinate and 25 mg hydrochlorothiazide to Resident #24 on 7/17/22 at 10:43 AM.
An interview was conducted with Med Aide #1 on 7/18/22 at 1:40 PM. At that time, the Med Aide was shown the orders on Resident #24's MAR and the vital sign results obtained at the time of the medication administration observation on 7/17/22. Upon review of the MAR, vital sign results, and parameters of the order for Resident #24 ' s metoprolol succinate and hydrochlorothiazide, Med Aide #1 stated she should not have administered these medications to the resident.
A telephone interview was conducted on 7/19/22 at 3:56 PM with the Nurse Practitioner (NP) who cared for Resident #24. During the interview, the NP stated, If there are parameters there (on the order), they should be followed. The NP reported the reason parameters were added to the anti-hypertensive medication orders was because it was thought Resident #24 may be falling due to orthostatic hypotension. She added, The parameters were implemented just to be on the safe side. When asked, the provider stated the orders given for metoprolol succinate and hydrochlorothiazide would have indicated that if only one or the other of the parameters was met, the medication needed to be held.
An interview was conducted on 7/20/22 at 10:19 AM with the facility ' s consultant pharmacist. During the interview, Resident #24 ' s orders for metoprolol succinate and hydrochlorothiazide were reviewed, along with the SBP and HR parameters given in the medication orders. The documented instances of 6/16/22, 6/20/22, 6/21/22 and 6/29/22 and the observation of these medications being administered on 7/17/22 when the resident ' s SBP / HR parameters indicated the medications should have been held were also discussed. When asked what her thoughts were regarding the metoprolol succinate and hydrochlorothiazide being given when Resident #24 ' s SBP was less than 120, the pharmacist stated, They shouldn't have been given. Upon further inquiry, the consultant pharmacist stated, It could be pretty significant with both of them (metoprolol succinate and hydrochlorothiazide).
An interview was conducted on 7/19/22 at 10:47 AM with the facility ' s Interim Director of Nursing (DON). During the interview, the vital sign parameters and instructions provided in the medication orders for Resident #24 ' s hydrochlorothiazide and metoprolol succinate were discussed. The DON stated he would expect nursing staff, To follow the guideline as it (the order) specifies. When asked if these medications should have been administered to Resident #24 given the results of his vital signs taken, the DON stated, Not according to the way the order was written.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0887
(Tag F0887)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, the facility failed to document the correct date of a Covid-19 vaccination which aff...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interview, the facility failed to document the correct date of a Covid-19 vaccination which affected the resident being offered a booster dose for 1 of 5 residents (Resident #55) reviewed for vaccination history.
The findings included:
Resident #55 was admitted to the facility on [DATE].
A review of Resident #55's discharge summary from the hospital, dated 6/3/2022, documented her immunization history to include COVID-19 Pfizer dose 1 on 5/12/2021 and COVID-19 Pfizer dose 2 on 6/1/2021.
A review of Resident #55's electronic medical record at the facility, under the immunization tab documented the second dose of COVID-19 history as 6/1/2022 rather than 6/1/2021 as indicated on the hospital discharge summary.
Resident #55's electronic medical record revealed she tested positive for COVID-19 on 7/6/2022.
An interview was conducted on 7/21/2022 at 2:17 p.m. with the Assistant Director of Nursing, the facility infection preventionist, and she reviewed Resident #55's electronic medical record and stated her vaccination date of the second dose of COVID-19 was on 6/2/2022. She reviewed the hospital discharge summary and stated the documented date was 6/1/2021 and that the date entered into the electronic medical record at the facility appeared to be a data entry error. She added that a booster dose of COVID-19 had not been offered to the Resident due to the data entry error, because a booster dose had not appeared to be due at the time.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0947
(Tag F0947)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews and record review, the facility failed to complete required dementia care training and abuse preventio...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews and record review, the facility failed to complete required dementia care training and abuse prevention training for 3 of 3 current nursing staff (Nursing Assistants #3, #4, and #5.)
Findings included:
1. Nursing Assistant (NA) #3's date of hire was [DATE]. A review of the facility's inservice records and transcript report from the facility's online training program revealed NA #3 had not completed any dementia care training or abuse prevention training in the past 12 months.
In an interview with the Corporate Floating Director of Nursing (DON) on [DATE] at 9:19 AM, she shared that dementia care training and abuse prevention training were completed through the facility's online training academy. She said the computer system auto populated for the employee to complete the training. She added the corporate office monitored the completion of courses and sent emails to staff when trainings needed to be completed. She said NA #3 had been notified by the corporate office that the trainings needed to be completed since the Center for Medicare and Medicaid Services (CMS) waiver for education that had been in effect for the public health emergency had expired.
The Interim DON was interviewed on [DATE] at 2:56 PM and stated the clinical team encouraged staff members to complete the required education and trainings and meet the deadlines.
2. NA #4's date of hire was [DATE]. A review of the facility's inservice records and transcript report from the facility's online training program revealed NA #4 had not completed any dementia care training or abuse prevention training in the past 12 months.
In an interview with the Corporate Floating Director of Nursing (DON) on [DATE] at 9:19 AM, she shared that dementia care training and abuse prevention training were completed through the facility's online training academy. She said the computer system auto populated for the employee to complete the training. She added the corporate office monitored the completion of courses and sent emails to staff when trainings needed to be completed. She said NA #4 had been notified by the corporate office that the trainings needed to be completed since the Center for Medicare and Medicaid Services (CMS) waiver for education that had been in effect for the public health emergency had expired.
The Interim DON was interviewed on [DATE] at 2:56 PM and stated the clinical team encouraged staff members to complete the required education and trainings and meet the deadlines.
3. NA #5's date of hire was [DATE]. A review of the facility's inservice records and transcript report from the facility's online training program revealed NA #5 had not completed any dementia care training or abuse prevention training in the past 12 months.
In an interview with the Corporate Floating Director of Nursing (DON) on [DATE] at 9:19 AM, she shared that dementia care training and abuse prevention training were completed through the facility's online training academy. She said the computer system auto populated for the employee to complete the training. She added the corporate office monitored the completion of courses and sent emails to staff when trainings needed to be completed. She said NA #5 had been notified by the corporate office that the trainings needed to be completed since the Center for Medicare and Medicaid Services (CMS) waiver for education that had been in effect for the public health emergency had expired.
The Interim DON was interviewed on [DATE] at 2:56 PM and stated the clinical team encouraged staff members to complete the required education and trainings and meet the deadlines.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0658
(Tag F0658)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, staff interviews, hospital and facility record reviews, the facility failed to accurately transcribe a me...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, staff interviews, hospital and facility record reviews, the facility failed to accurately transcribe a medication order identified for 1 of 6 residents (Resident #24) reviewed for medications administered during the med pass observations. The transcription error resulted in Resident #24 receiving three - 81 milligram (mg) aspirin tablets instead of one tablet daily over a period of 15 days.
The findings included:
Resident #24 was admitted to the facility on [DATE] from a hospital. His cumulative diagnoses included a recent history of multiple fractures.
A review of the resident ' s Hospital Discharge Summary included a discharge medication list. This list included the following: 81 milligram (mg) Enteric Coated (EC) aspirin to be administered as one tablet by mouth twice daily for 6 weeks per orthopedics recommendations; then resume once daily.
Resident #24 ' s admission orders for the facility were dated 5/21/22. These orders included one – 81 mg EC aspirin tablet to be administered by mouth two times a day for antiplatelet for 6 weeks with a start date of 5/22/22 and end date of 7/3/22 (scheduled for administration at 9:00 AM and 5:00 PM daily). The end date of this order was 42 days or 6 weeks after its start date. A second order was also input into the resident ' s Electronic Medical Record (EMR) on 5/21/22 for one – 81 mg EC aspirin tablet to be administered by mouth one time a day for antiplatelet with a start date of 7/3/22.
The resident ' s May 2022 and June 2022 Medication Administration Records (MARs) revealed he received one – 81 mg EC aspirin tablet administered by mouth two times a day from 5/22/22 to 6/22/22. This order was discontinued on 6/22/22 and a new medication order was input into his Electronic Medical Record (EMR) for 81 mg (EC) aspirin to be administered as one tablet by mouth every 12 hours for antiplatelet for 6 weeks with a start date of 6/22/22 and an end date of 8/3/22 (scheduled for administration at 8:00 AM and 8:00 PM daily). The medication order for one – 81 mg EC aspirin tablet to be administered by mouth one time a day for antiplatelet with a start date of 7/3/22 was re-ordered on 6/22/22.
Resident #24 ' s June 2022 and July 2022 MARs revealed the resident continued to receive one – 81 mg EC aspirin administered by mouth every 12 hours from 6/22/22 through the date of the review (7/17/22). Additionally, Resident #24 received one – 81 mg EC aspirin administered by mouth one time a day initiated on 7/3/22 and scheduled for administration at 9:00 AM daily. Both of the medication orders for the administration of aspirin were active orders and ran concurrently through the date of the review (7/17/22). Therefore, Resident #24 received a total of 3 tablets of 81 mg EC aspirin from 7/3/22 through 7/17/22.
A medication pass observation conducted on 7/17/22 at 10:43 AM revealed Resident #24 received two – 81 mg tablets of aspirin. The review of his medication orders revealed there were two current orders for 81 mg aspirin (one order initiated on 6/22/22 and a second order with a start date of 7/3/22).
An interview was conducted on 7/19/22 at 10:27 AM with a corporate floating Director of Nursing (DON) who served as the facility ' s Interim DON from 2/16/22 – 5/23/22. During the interview, the float DON confirmed Resident #24's current medication orders included two – 81 mg aspirin tablets to be given in the morning and one – 81 mg aspirin tablet to be given each evening (a total of 3 tablets daily). She reported upon review of the orders, the aspirin should have been initiated as one - 81 mg EC aspirin tablet administered twice daily for six weeks, then reduced to one tablet given once daily thereafter. The float DON also reported she reviewed the resident ' s EMR and consultation reports. She did not identify the presence of any new orders or recommendations to suggest the initial admission orders for the aspirin had been changed.
A telephone interview was conducted on 7/19/22 at 3:56 PM with the Nurse Practitioner (NP) who cared for Resident #24. During the interview, the error identified with the resident ' s aspirin was discussed. The NP reported the facility notified her of this medication error and she had requested staff review Resident #24 ' s consultations to be sure there were no new orders from orthopedics to change the original time frame for twice daily dosing of his aspirin. No change in the orders were found. She confirmed Resident #24 ' s current orders should have included only one – 81 mg aspirin tablet daily at this time.
A telephone interview was conducted on 7/20/22 at 2:20 PM with Nurse #2. Nurse #2 was identified as the nurse who input the revised orders for Resident #24 ' s 81 mg EC aspirin on 6/22/22. When asked, Nurse #2 reported she could not recall any details about inputting the orders.
An interview was conducted on 7/20/22 at 3:55 PM with the facility ' s Interim DON. During the interview, the DON reported no new aspirin orders had been identified for Resident #24. The DON stated he would concur that the duplication of aspirin orders for this resident appeared to be a transcription error.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Unnecessary Medications
(Tag F0759)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, staff interviews, and record review, the facility failed to have a medication error rate of less than 5% ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, staff interviews, and record review, the facility failed to have a medication error rate of less than 5% as evidenced by 3 medication errors out of 25 medication opportunities, resulting in a medication error rate of 12% for 1 of 6 residents (Resident #24) observed during medication pass.
The findings included:
1) Resident #24 was admitted to the facility on [DATE]. His cumulative diagnoses included a history of multiple fractures and hypertension.
On 7/17/22 at 10:04 AM, Medication Aide (Med Aide) #1 was observed as she checked Resident #24 ' s vital signs. His vital signs included a blood pressure of 115/65 and pulse of 69 beats per minute (bpm). After the resident ' s vital signs were taken, the med aide was observed as she prepared 10 oral medications for administration to Resident #24. The medications pulled for administration included one tablet of 100 milligrams (mg) metoprolol succinate (an extended release formulation of an anti-hypertensive medication). The med aide was observed as she crushed the metoprolol succinate tablet along with 8 other oral medications. The med aide stirred the crushed medications into a pudding as she prepared to administer them to Resident #24.
On 7/17/22 at 10:32 AM, Med Aide #1 was asked to stop before going into Resident #24 ' s room with the medications prepared for administration. When she was informed the metoprolol succinate tablet could not be crushed prior to administration, Nurse #1 came to the med cart to assist the med aide. At that time, Nurse #1 told the med aide to re-pull the medications for Resident #24 and instructed her not to crush the metoprolol succinate tablet. The med aide was again observed as she prepared the resident ' s medications for administration. She placed the metoprolol succinate tablet (whole) into a med cup with pudding. Med Aide #1 administered the oral medications to Resident #24 on 7/17/22 at 10:43 AM.
According to Lexi-comp, a comprehensive electronic medication database, metoprolol succinate tablets should not be crushed or chewed.
A review of Resident #24 ' s medication orders conducted on 7/18/22 revealed an order was received on 6/7/22 for 100 mg metoprolol succinate to be given as one tablet by mouth one time a day for hypertension. The order also included instructions to hold this medication for a systolic blood pressure less than 120 and a heart rate less than 60 bpm. Systolic blood pressure is the maximum pressure the heart exerts while beating and is represented by the top number of a blood pressure reading.
An interview was conducted with Med Aide #1 on 7/18/22 at 1:40 PM. At that time, the Med Aide was shown the orders on Resident #24's July 2022 Medication Administration Record (MAR) and vital signs taken at the time of the medication administration observation on 7/17/22. When she reviewed the MAR, vital sign results, and parameters of the order for Resident #24 ' s metoprolol succinate, Med Aide #1 stated she should not have administered this medication to him.
An interview was conducted on 7/19/22 at 10:47 AM with the facility ' s Interim Director of Nursing (DON). During the interview, the observations made during the medication administration pass were discussed. When asked about crushing a metoprolol succinate tablet, the DON stated, If those are listed as one medication the manufacturer and doctor specifies should not be crushed, (nursing staff) should follow those guidelines. While discussing the vital sign parameters and instructions provided in the medication order for metoprolol succinate, the DON stated he would expect nursing staff, To follow the guideline as it (the order) specifies. When asked if the medication should have been administered to Resident #24 given the results of his vital signs taken, the DON stated, Not according to the way the order was written.
When asked, the DON stated he would expect nursing staff, To follow the guideline as it (the order) specifies. When asked if these meds should have been administered to Resident #24 given the results of his vital signs taken, the DON stated, Not according to the way the order was written.
2) Resident #24 was admitted to the facility on [DATE]. His cumulative diagnoses included a history of multiple fractures and hypertension.
On 7/17/22 at 10:04 AM, Med Aide #1 was observed as she checked Resident #24 ' s vital signs. His vital signs included a blood pressure of 115/65 and pulse of 69 beats per minute (bpm). After the resident ' s vital signs were taken, the med aide was observed as she prepared 10 oral medications for administration to Resident #24. The medications pulled for administration included one tablet of 25 milligrams (mg) hydrochlorothiazide (a diuretic). Med Aide #1 administered the hydrochlorothiazide (along with the other oral medications) to Resident #24 on 7/17/22 at 10:43 AM.
A review of Resident #24 ' s medication orders conducted on 7/18/22 revealed an order was received on 6/7/22 for 25 mg hydrochlorothiazide to be given as one tablet by mouth one time a day for hypertension. The order also included instructions to hold this medication for a systolic blood pressure less than 120 and a heart rate less than 60 bpm. Systolic blood pressure is the maximum pressure the heart exerts while beating and is represented by the top number of a blood pressure reading.
An interview was conducted with Med Aide #1 on 7/18/22 at 1:40 PM. At that time, the Med Aide was shown the orders on Resident #24's July 2022 Medication Administration Record (MAR) and vital signs taken at the time of the medication administration observation on 7/17/22. When she reviewed the MAR, vital sign results, and parameters of the order for Resident #24 ' s hydrochlorothiazide, Med Aide #1 stated she should not have administered this medication to him.
An interview was conducted on 7/19/22 at 10:47 AM with the facility ' s Interim Director of Nursing (DON). During the interview, the observations made during the medication administration pass were discussed. While discussing the vital sign parameters and instructions provided in the medication order for hydrochlorothiazide, the DON stated he would expect nursing staff, To follow the guideline as it (the order) specifies. When asked if the medication should have been administered to Resident #24 given the results of his vital signs taken, the DON stated, Not according to the way the order was written.
3) Resident #24 was admitted to the facility on [DATE]. His cumulative diagnoses included a history of multiple fractures and hypertension.
On 7/17/22 at 10:11 AM, Med Aide #1 was observed as she prepared 10 oral medications for administration to Resident #24. The medications pulled for administration included two (2) tablets of 81 milligrams (mg) Enteric Coated (EC) aspirin. The med aide was observed as she crushed the EC aspirin tablets with 7 other oral medications. The med aide stirred the crushed medications into a pudding as she prepared to administer them to Resident #24.
On 7/17/22 at 10:32 AM, Med Aide #1 was asked to stop before going into Resident #24 ' s room with the medications prepared for administration. When the med aide was informed the EC aspirin tablets could not be crushed prior to administration, Nurse #1 came to the med cart to assist the med aide. At that time, Nurse #1 told the med aide to re-pull the medications for Resident #24 and she obtained a stock bottle of 81 mg chewable aspirin to be crushed in place of the EC aspirin for the resident. The med aide then crushed two chewable aspirin tablets with 6 other oral medications, stirred the crushed medications into pudding, and administered the medications to Resident #24 on 7/17/22 at 10:43 AM.
According to Lexi-comp, a comprehensive electronic medication database, enteric-coated aspirin tablets should not be crushed or chewed; these preparations should be swallowed whole.
A review of Resident #24 ' s medication orders conducted on 7/18/22 revealed an active order was received on 6/22/22 for one - 81 mg EC aspirin to be given as one tablet by mouth every 12 hours for 6 weeks with a start date of 6/22/22 and an end date of 8/3/22 (scheduled for 8:00 AM and 8:00 PM daily). Another active medication order was received on 6/22/22 for one - 81 mg EC aspirin tablet to be given by mouth one time a day with a start date of 7/3/22 (scheduled for 9:00 AM daily).
An interview was conducted on 7/19/22 at 10:47 AM with the facility ' s Interim Director of Nursing (DON). During the interview, the observations made during the medication administration pass were discussed. When asked about crushing EC aspirin tablets, the DON stated, If those are listed as one medication the manufacturer and doctor specifies should not be crushed, (nursing staff) should follow those guidelines.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0761
(Tag F0761)
Could have caused harm · This affected multiple residents
Based on observations and staff interviews, the facility failed to: 1) Label medications with the minimum information required, including the name of the resident, on 2 of 2 medication carts observed ...
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Based on observations and staff interviews, the facility failed to: 1) Label medications with the minimum information required, including the name of the resident, on 2 of 2 medication carts observed (the 300 Hall Med Cart and the 100 Hall Med Cart); 2) Discard expired medications on 2 of 2 medication carts observed (the 300 Hall Med Cart and the 100 Hall Med Cart); and 3) Label medications with the date they were opened on 1 of 2 medication carts (the 100 Hall Med Cart) and in 1 of 1 medication storage rooms (the 100/200 Med Storage Room) observed to allow its shortened expiration date to be determined.
The findings included:
1-a) An observation was conducted on 7/17/22 at 2:52 PM of the 300 Hall medication cart in the presence of Nurse #6. The observation revealed an opened Levemir FlexTouch insulin pen was stored on the med cart. There was no label on the insulin pen to indicate the resident's name, dispensed date, or date opened. Nurse #6 confirmed the insulin pen had been opened and had no identifying information on it. She stated, It shouldn't be on there and reported the pen needed to be discarded.
1-b) An observation was conducted on 7/17/22 at 2:52 PM of the 300 Hall medication cart in the presence of Nurse #6. The observation revealed an opened Insulin Lispro Kwikpen was stored on the medication cart. There was no label on the insulin pen to indicate the resident's name, dispensed date, or date opened. Nurse #6 confirmed the insulin pen had been opened and had no identifying information on it. She stated, It shouldn't be on there and reported the pen needed to be discarded.
1-c) An observation was conducted on 7/17/22 at 2:52 PM of the 300 Hall medication cart in the presence of Nurse #6. The observation revealed a medication vial containing 36 unidentified, white oval tablets was stored on the med cart. The vial was not labeled with any printed or hand-written information. Therefore, the vial of tablets did not provide any of the minimum required labeling information, including the name of the drug or the name of the resident the tablets were dispensed for.
1-d) An observation was conducted on 7/17/22 at 3:10 PM of the 100 Hall medication cart in the presence of Nurse #7. The observation revealed two metered dose inhalers (MDI) were stored in the same box (a manufacturer's box labeled for 17 micrograms (mcg) / actuation Atrovent HFA). Atrovent HFA is an inhaled medication used to treat chronic obstructive pulmonary disease (COPD). One of the inhalers stored in the box was an Atrovent HFA metered dose inhaler labeled as dispensed for Resident #40. The second MDI was an albuterol inhaler. Albuterol is an inhaled medication used to treat asthma and COPD. There was no labeling on the albuterol inhaler to indicate the name of the resident this inhaler was dispensed for. When asked, Nurse #7 stated she would need to discard the albuterol inhaler because it was not labeled with a resident's name.
A review of Resident #40's July 2022 orders and Medication Administration Record (MAR) revealed the resident had a current order for the use of a 17 mcg / actuation Atrovent HFA inhaler. However, she did not have a current order for an albuterol metered dose inhaler.
An interview was conducted on 7/19/22 at 11:07 AM with the facility's Interim Director of Nursing (DON). During the interview, the DON stated, All meds should have an identifier on it. He also reported that anything unlabeled was unsafe for both the administrator of the medication and the person receiving it. The DON stated he would want the nurse to discard these meds appropriately according to the facility guidelines.
2-a) An observation was conducted on 7/17/22 at 2:52 PM of the 300 Hall medication cart in the presence of Nurse #6. The observation revealed a medication vial containing a manufacturer ' s bottle of 0.4 milligrams (mg) nitroglycerin (a medication used to relieve angina or chest pain) sublingual (under the tongue) tablets was stored on the med cart. The pharmacy label on the medication vial indicated the nitroglycerin tablets were dispensed by an outside pharmacy for Resident #370. The manufacturer's labeling on the bottle of the nitroglycerin tablets indicated the medication ' s expiration date was October 2018. Upon review, the nurse confirmed the bottle of nitroglycerin sublingual tablets was expired.
A review of Resident #370's July 2022 orders and Medication Administration Record (MAR) revealed the resident had a current order for 0.4 nitroglycerin sublingual tablet to be given as one tablet sublingually every 5 minutes as needed for angina (chest pain). Instructions for the medication included placing the tablet under the tongue and to let it dissolve all the way; give up to 3 doses in 15 minutes; if no relief after the first dose to contact the on-call provider; do not give if the resident ' s blood pressure is less than 100/60.
2-b) An observation was conducted on 7/17/22 at 3:10 PM of the 100 Hall medication cart in the presence of Nurse #7. The observation revealed one stock bottle of 100 milligram (mg) docusate tablets (an over-the-counter stool softener) originally containing 100 tablets with approximately 50 tablets remaining was stored on the med cart. The manufacturer's expiration date printed on the bottle was June 2022. Upon review, the nurse confirmed the stock bottle of docusate tablets was expired.
An interview was conducted on 7/19/22 at 11:07 AM with the facility's Interim Director of Nursing (DON) to discuss the findings of the medication storage observations. During the interview, the DON stated, anything expired is unsafe for the administrator and the person receiving the medication. He reported all medications stored on the med cart should be within date.
3-a) An observation was conducted on 7/17/22 at 3:10 PM of the 100 Hall medication cart in the presence of Nurse #7. The observation revealed an opened 3.7 milliliter (ml) metered dose spray bottle of 200 units / actuation calcitonin (a nasal spray medication used to treat osteoporosis) dispensed on 4/23/22 for Resident #63 was stored on the med cart. The bottle was not dated as to when it had been placed on the med cart. However, the manufacturer labeling and a pharmacy auxiliary sticker indicated the medication needed to be refrigerated until opened/used. The pharmacy auxiliary sticker instructed, Discard in 35 days after date opened.
According to Lexi-comp, a comprehensive electronic medication database, an unopened bottle of calcitonin nasal spray should be stored under refrigeration at 36 degrees Fahrenheit (o F) to 46 o F. After opening, the bottle may be stored for up to 35 days at room temperature of 59 o F to 86 o F.
A review of Resident #63's medical record revealed he had a current order for 200 units / actuation calcitonin nasal spray.
3-b) An observation was conducted on 7/18/22 at 8:45 AM of the 100/200 Med Storage Room in the presence of the facility ' s Long Term Care (LTC) Unit Manager.
The observation revealed an opened multi-dose vial of Tuberculin PPD injectable medication (used for skin testing in the diagnosis of tuberculosis) was stored in the med room refrigerator. The vial was not labeled as to when it had been opened. When asked, the Unit Manager reported she would need to discard the vial of the Tuberculin PPD injectable medication due to not knowing when the vial had been opened.
The manufacturer's storage instructions for a multi-dose vial of Tuberculin PPD injectable medication indicated that once opened the product should be discarded after 30 days.
An interview was conducted on 7/19/22 at 11:07 AM with the facility's Interim Director of Nursing (DON) to discuss the findings of the medication storage observations. During the interview, the DON stated his expectations included ensuring a medication was labeled with the date it was opened so the medication ' s expiration date could be determined appropriately.
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** 3. Resident #58 was admitted to the facility on [DATE] with diagnoses that included, in part, end stage renal disease and diabet...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Resident #58 was admitted to the facility on [DATE] with diagnoses that included, in part, end stage renal disease and diabetes.
The admission Minimum Data Set assessment dated [DATE] revealed Resident #58 was cognitively intact.
The comprehensive care plan, updated 7/6/22, included a focused area of nutrition with interventions that stated, receiving therapeutic diet and RD to evaluate and make diet change recommendations as needed.
A physician (MD) order dated 7/18/22 revealed Resident #58 was to receive a liberalized renal diet.
An interview was conducted with Resident #58 on 7/17/22 at 12:16 PM and on 7/20/22 at 1:43 PM. During the interview, the resident stated she was on a renal diet and received dialysis. She reported the facility had not given her a choice in what she could eat and had not provided a menu or approved list of substitutions for her therapeutic diet to select foods from when she requested it. She said when she asked for a menu, the staff replied she was on a strict renal diet and had not given her a menu. She added in the past she had requested tomatoes, cheese, spaghetti or lasagna and it was not provided to her because of the diet restriction. Resident #58 explained she understood that if she ate foods that were not consistent with the renal diet, it increased her phosphorus and potassium levels. She said she wanted the food items occasionally, not all the time and felt her rights were not honored and she was not permitted to make choices in what she ate. She further stated the facility had not educated her about the renal diet, but she had received information from her dialysis center about foods consistent with the renal diet.
On 7/19/22 at 9:27 AM an interview was completed with the Dietary Manager. She explained all residents on regular diets, with the exception of residents on renal diets, received a lunch and dinner choice menu that they completed during breakfast. The completed menu was returned to the kitchen with the breakfast trays and choices that were selected were provided on the meal trays the following day. She said residents who were on renal diets were not permitted to have items with high potassium and therefore, had not received the choice menu. The Dietary Manager recalled she had met with Resident #58, who requested tomato products but stated she can't give them to her until the RD or MD reviewed her medical record.
During an interview with RD #1 on 7/20/22 at 10:08 AM, she explained she had filled in for the permanent RD and worked remotely when she completed nutrition assessments. She had not seen Resident #58 in person but had reviewed her medical record. She said the dialysis provider was typically inflexible with liberalizing a renal diet and when Resident #58 asked about liberalizing her diet, the dialysis center's provider denied the resident's request. The RD added if a resident was provided education about their diet and requested foods from the kitchen that were not consistent with the prescribed diet, the resident should be provided with the requested food and stated it was the resident's right to choose. RD #1 further stated she had not been consulted on changing Resident #58's diet and indicated there was not a list of approved substitutions within the prescribed liberalized diet.
The Regional [NAME] President was interviewed on 7/20/22 at 10:42 AM and stated the facility should be asking residents for dietary preferences and then provide education regarding specific diets.
Based on observations, record reviews, residents and staff interviews, the facility failed to obtain and honor residents' food preferences for 3 of 3 residents (Residents #4, #55, #58) reviewed for food choices/preferences.
Findings included:
1. Resident #4 was originally admitted to the facility on [DATE] and re-admitted on [DATE] with diagnoses which included diabetes mellitus.
The physician's order dated 2/8/22 revealed Resident #4 received a low concentrated sweet diet of soft, bite sized texture with minced and moist meats.
The quarterly minimum data set (MDS) dated [DATE] indicated Resident #4 was cognitively intact and received a therapeutic/ mechanically altered diet.
A review of the clinical records indicated there was no food preferences documentation maintained for Resident #4 prior to 7/18/22.
During an interview on 7/18/22 at 11:33 a.m. Resident #4 stated that she was tired of receiving cooked rice and mashed potatoes everyday during lunch and supper. She revealed she was not allowed to choose food items she preferred. She was unaware the facility offered a select, choice menu. She revealed someone from dietary talked with her that morning (7/18/22) about her food likes and dislikes.
On 7/19/22 a.m. at 10:00 a.m. the Dietary Manager (DM) revealed the facility changed its' food service caterer and the menus on 7/6/22. She indicated the previous food service caterer did not maintain the residents' food preference sheets. She stated she had not received any complaints from the residents concerning food choices. The DM stated that only residents receiving regular diets would receive the select choice menu allowing the resident to choose which food items he/she would like served the next day for lunch and supper.
During an observation on 7/20/22 at 1:03 p.m. Resident #4 was sitting on the side of her bed with her untouched meal tray on the overbed table next to her. The plated meal consisted of a chopped meat, zucchini, and mashed potatoes. The resident revealed she did not want the meal which included mashed potatoes again. She stated she did not request anything else, instead ate the meal leftovers from a restaurant outing with her family member, the day before.
2. Resident #55 was admitted to the facility on [DATE] with diagnosis which included hypertensive heart and chronic kidney disease with heart failure, and end-stage renal disease.
The physician's order dated 6/3/22 revealed Resident #55 received a liberalized renal diet of regular consistency.
Resident #55's Food Preference Sheet dated 6/7/22 only included the resident's renal diet of regular consistency with thin fluids. The resident's food preferences and food dislikes were not recorded.
The quarterly Minimum Data Set, dated [DATE] indicated Resident #55 was cognitively intact and received a therapeutic diet.
During an interview on 7/18/22 at 9:01a.m. Resident #55 stated that since her admission to the facility she had not been able to choose the food items she preferred on the renal diet.
On 7/19/22 a.m. at 10:00 a.m. the Dietary Manager (DM) revealed the facility changed its' food service caterer and the menus on 7/6/22. She indicated the previous food service caterer did not maintain the residents' food preference sheets. She stated she had not received any complaints from the residents concerning food choices. The DM stated that only residents receiving regular diets would receive the select choice menu allowing the resident to choose which food items he/she would like served the next day for lunch and supper.
During a second interview on 7/21/22 at 9:01 a.m., Resident #55 indicated she received a liberalized renal diet. She stated that she was aware there were different menu options within the renal diet and had been educated by the registered dietician at the dialysis center on food items she could and could not eat and on how to prepare renal diet menus. Resident #55 stated she was not given the option of the facility's select/choice menu as were the other residents. She also stated no one from the facility discussed her food preferences with her.
On 7/21/22 at 9:49 a.m., the telephone interview with the Registered Dietician (RD#1) revealed she was covering remotely for the Registered Dietician assigned to the facility. RD#1 stated the resident's food preferences should have been honored within the renal diet restrictions. She stated the resident was seen weekly by the RD at the dialysis center who educated the resident on the consequences of not following the renal diet. She indicated dialysis centers were very inflexible about residents requesting altering their diets.
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 observations and staff interviews, the facility failed to maintain sanitary conditions in the kitchen and nourishment refrigerators by not ensuring dishware were washed and rinsed at proper t...
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Based on observations and staff interviews, the facility failed to maintain sanitary conditions in the kitchen and nourishment refrigerators by not ensuring dishware were washed and rinsed at proper temperatures in the dishwashing machine; by not dating and labeling resealed food items; and by not ensuring food service equipment were clean and free from debris. The facility also failed to ensure food items not provided by the facility were dated, labeled with the resident's name and room number when stored in the snack/nourishment refrigerators in the 100/200 Hall nourishment room and in the main dining room.
Findings included:
1. During the initial tour of the kitchen with the Dietary Manager (DM) on 7/17/22 at 10:07 a.m., three wash and rinse cycles were observed during the operation of the high temperature dishwasher. The temperatures of each cycle read as followed: 1st wash reading was 168 degrees Fahrenheit and the final rinse reading was 140 degrees Fahrenheit; 2nd wash reading was 160 degrees Fahrenheit and the final rinse reading was 140 degrees Fahrenheit; and the 3rd wash reading was 169 degrees Fahrenheit and the final rinse reading was 138 degrees Fahrenheit. When questioned on the temperature requirements of the dishwasher, Dietary Staff #1 stated the wash temperature should read 165 degrees Fahrenheit and the final rinse cycle should read 180 degrees Fahrenheit. She stated the dishwasher temperatures were checked for accuracy during the second prewash cycle, before dishware were placed in the machine. Dietary staff #1 and the DM did not look at the temperature gauges on the dishwasher throughout the three observations. The temperatures of the three observations of the final rinse cycles were below the minimum requirement of 180 degrees Fahrenheit. This surveyor informed the dietary staff member and the DM the three crates of tray lid covers and food trays would have to be rewashed and rinsed due to the decreased rinse temperatures. The DM stated she would immediately notify the dishwasher vendor for repair and until repaired, all dishware would be washed in the dishwasher then rinsed and sanitized in the three-compartment sink.
2. On 7/17/22 at 10:20 a.m. observations of the food storage areas in the kitchen revealed resealed and opened food items that were not dated and labeled and/or left uncovered. There was 1-(6-inch deep) pan covered with cellophane pan of unidentifiable cooked, chopped meat that was not labeled or dated in the reach-in refrigerator. One serving scoop was placed in a 6-inch deep pan of pureed bread covered with cellophane in the serving line refrigerator. The walk-in refrigerator contained 1-open box of red grapes. The walk-in freezer contained 1-resealed bag of breadsticks not dated/labeled; 1-opened box of pulled chicken not dated; and 1-open box of omelets. In the dry storage room there was 1-resealed bag of jello mix not dated or labeled; 1-(18 pound) container of resealed apple pie filling not dated and with a brown, sticky substance around the lid's closing; 1-double sealed, resealed bag of couscous that was not dated or labeled.
3. During a tour of the kitchen on 7/17/22 at 10:22 a.m, the inside of the microwave oven revealed yellow food crumbs and stains. The Assistant Dietary Manager indicated the microwave was last utilized 1-2 days prior. There were food stains on the inside and outside of the food warmer. The lids of the large sugar bin and the table top sugar bin were covered with white grainy particles. There were 2-wire baskets containing large pieces of fried food items on top of the deep fryer. The Assistant Dietary Manager revealed the deep fryer was used the night before and the staff should have cleaned it.
4. On 7/20/22 at 1:03 p.m. the refrigerator/freezers in 1 of 2 nourishment rooms and in the main dining room was observed with resealed food items that were not dated, labeled with a resident's name and room number, and outdated, resealed items. The 100/200 hall nourishment room's refrigerator/freezer contained 2-(32 ounce) resealed containers of med plus 1.7 (nutrition drink) with a sticker date of 5/31/22, but the directions on the containers indicated the drinks were to be used within 3 days of opening. There was also 1(8 ounce) resealed container of Ensure (nutrition drink) without a resident's name or date opened. In the freezer there was 1-open box of multiple single serve icy treats without a resident's name.The dining room's refrigerator/freezer consisted of 5(16 ounce) bottles of diet sodas that were not dated or labeled with a resident's name. The freezer contained:1-box of pastries that were not dated or labeled with a resident's name and of 1-gallon of resealed ice cream not dated and labeled with a resident's name.
During an interview on 7/20/22 at 4:30 p.m. the Dietary Manager stated the dietary department was responsible for maintaining the 2-nourishment rooms on the residents' halls which were checked everyday between 1:00 p.m. and 1:30 p.m. She revealed dietary was not responsible for the refrigerator in the dining room and she was unaware of which department maintained the dining room refrigerator.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Infection Control
(Tag F0880)
Could have caused harm · This affected most or all residents
Based on record review and staff interviews, the facility failed to implement a Legionella prevention program. This had the potential to affect all 74 residents who resided in the facility.
The findi...
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Based on record review and staff interviews, the facility failed to implement a Legionella prevention program. This had the potential to affect all 74 residents who resided in the facility.
The findings included:
A review of the facility ' s Emergency Preparedness and Infection Control Programs revealed the facility had not implemented water safety management for Legionella.
On 7/21/22 at 3:01 PM, an interview was conducted with the Maintenance Director. He stated the previous administrator called him into the office one day last week and they had a training video about the water safety program. He stated the facility didn ' t know about it and had not been doing anything about it. He stated they received the policy, but no action has been taken.
MINOR
(B)
Minor Issue - procedural, no safety impact
Safe Environment
(Tag F0584)
Minor procedural issue · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and resident and staff interviews, the facility failed to provide a homelike environment for 1 of 3 rooms ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and resident and staff interviews, the facility failed to provide a homelike environment for 1 of 3 rooms reviewed on the 300 hall (room [ROOM NUMBER]) and failed to maintain a clean living environment for 2 of 8 residents (Resident #8 and Resident #58) reviewed for environment.
The findings included:
1. Resident #35 (room [ROOM NUMBER]) was admitted to the facility on [DATE].
On 7/17/21 at 12:16 PM, an observation of Resident #35 ' s room revealed two wheelchairs, 1 walker, 1 oxygen concentrator in the room. Bed linens were thrown over a chair across the room, the shelving area contained several personal items that were placed there haphazardly, and the nightstand contained multiple food items and other items that did not appear neat.
On 7/17/21 at 12:16 PM, during an interview with Resident #35, he agreed his room was messy and was like that since he moved from his other room. He added one wheelchair was his and he did not use oxygen and did not know why the oxygen concentrator was in his room.
On 7/19/22 at 10:10 AM, an interview was conducted with Housekeeper #1 who stated she did not put items away in the resident rooms, nursing assistants were responsible for that.
On 7/19/22 at 10:15 AM, an interview was conducted with NA #3 who stated the nursing assistants should put the resident ' s belongings away on admission and remove unused items and equipment.
2. Resident #8 was admitted to the facility on [DATE]. The quarterly Minimum Data Set assessment dated [DATE] indicated Resident #8 was cognitively intact.
An observation of Resident #8's room on 7/17/22 at 11:46 AM revealed dark colored stains on the bottom half of the privacy curtain.
During an interview with Resident #8 on 7/17/22 at 11:47 AM, she said she wasn't sure how long the privacy curtain had been stained and added, It's been there long enough.
Observations of Resident #8's room on 7/19/22 at 10:25 AM and 7/21/22 at 2:01 PM revealed dark colored stains on the bottom half of the privacy curtain.
During an interview with Housekeeper #2 on 7/21/22 at 2:30 PM, she shared when she cleaned residents' rooms she made observations of the privacy curtains and if they were stained or soiled, she removed the curtain and sent it to the laundry to be washed. She said there were extra privacy curtains in the laundry room that could be hung up if a resident's curtain was stained and sent to the laundry department.
On 7/21/22 at 2:01 PM, an observation of Resident #8's privacy curtain was completed with the Environmental Services Director. During an interview with the Environmental Services Director on 7/21/22 at 2:03 PM, he said housekeeping staff were responsible to make observations of the privacy curtains when they cleaned residents' rooms. If the curtain was observed to be stained or soiled, the housekeeper removed the curtain and sent it to the laundry to be washed and then hung back up in the resident's room. The Environmental Services Director confirmed dark colored stains were present on the privacy curtain in Resident #8's room and said staff should have removed the curtain and sent it to the laundry department to be cleaned.
An interview was completed with the Administrator on 7/21/22 at 3:29 PM. He said privacy curtains should be free of stains and cleaned as needed.
3. Resident #58 was admitted to the facility on [DATE]. The admission Minimum Data Set assessment dated [DATE] indicated Resident #58 was cognitively intact.
An observation of Resident #58's room on 7/17/22 at 12:16 PM revealed dark colored stains on the bottom half of the privacy curtain.
During an interview with Resident #58 on 7/17/22 at 12:17 PM, she said she had trouble seeing, but that the privacy curtain had been in her room since she was admitted to the facility.
Observations of Resident #58's room on 7/19/22 at 4:21 PM and 7/21/22 at 2:10 PM revealed dark colored stains on the bottom half of the privacy curtain.
During an interview with Housekeeper #2 on 7/21/22 at 2:30 PM, she shared when she cleaned residents' rooms she made observations of the privacy curtains and if they were stained or soiled, she removed the curtain and sent it to the laundry to be washed. She said there were extra privacy curtains in the laundry room that could be hung up if a resident's curtain was stained and sent to the laundry department.
On 7/21/22 at 2:10 PM an observation of Resident #58's privacy curtain was completed with the Environmental Services Director. During an interview with the Environmental Services Director on 7/21/22 at 2:12 PM, he said housekeeping staff were responsible to make observations of the privacy curtains when they cleaned residents' rooms. If the curtain was observed to be stained or soiled, the housekeeper removed the curtain and sent it to the laundry to be washed and then hung back up in the resident's room. The Environmental Services Director confirmed dark colored stains were present on the privacy curtain in Resident #58's room and said staff should have removed the curtain and sent it to the laundry department to be cleaned.
An interview was completed with the Administrator on 7/21/22 at 3:29 PM. He said privacy curtains should be free of stains and cleaned as needed.