SERIOUS
(G)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Actual Harm - a resident was hurt due to facility failures
Accident Prevention
(Tag F0689)
A resident was harmed · 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 provide incontinence care safely to a dependen...
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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 provide incontinence care safely to a dependent resident for 1 of 1 residents reviewed for falls. Resident #307 fell out of bed during incontinence care provided by Nursing Assistant (NA) #1 resulting in an upper lip laceration which required to 7 sutures, a laceration to the left side of the head that required 12 staples and a small laceration to the 2nd digit on the left foot.
Findings included:
Resident #307 was admitted to the facility on [DATE] with medical diagnosis which included in part: stroke with hemiparesis, vascular dementia, contractures of left wrist and hand and right hand, aphasia, and epilepsy.
Review of Resident #307's 11/23/22 annual Minimum Data Set (MDS) assessment revealed resident had severe cognitive impairment with no behaviors. Resident #307 required total assistance of 2 people with bed mobility and toileting. Resident #307 had impaired range of motion on both sides of the upper extremities and impairment on 1 side of her lower extremities. Resident #307's height was 61 inches, and her weight was 172 pounds. Resident #307 did not receive an anticoagulant during the lookback period.
Resident #307's care plan updated on 12/1/22 revealed a plan of care for activities of daily living (ADLs) personal care. The care plan interventions indicated Resident #307 was dependent for bathing and personal hygiene and required 2-person assist with bed mobility.
Resident #307's undated care guide indicated 2-person assist was required with bed mobility.
Review of Resident #307's electronic medical record revealed a nursing health status note written by Nurse # 1 on 1/22/23 at 11:21 PM. The note read in part called to room by aide, found resident on the floor face down with a large amount of blood. The note further indicated Emergency Medical Service (EMS) was alerted and Resident #307 was transported to the hospital.
Review of an incident report completed by Nurse #1 on 1/22/23 at 11:30 PM revealed she was called to the room by NA #1. The note stated that Resident #307 was observed lying face down with blood noted around the head area. The note indicated that Nurse #1 could not tell where the blood was coming from. Emergency Medical Service (EMS) was called, and Resident #307 was transferred to the hospital.
Review of a 1/23/23 statement completed by NA #1 indicated she was assigned to Resident #307 on the evening shift on 1/22/23. The statement indicated at approximately 7:15 -7:30 PM NA #1 provided incontinence care to Resident #307. NA #1 indicated Resident #307 was positioned in bed. NA #1 indicated following incontinence care she pushed the resident onto the left side with her left hand. NA #1 then placed her right hand on resident's right side and turned to reach for a clean brief when Resident #307 rolled off the bed onto the floor. NA #1 stated Resident #307 hit the nightstand with her head and landed face down on the floor. NA #1 immediately notified Nurse #1 that Resident #307 was on the floor.
Attempts were made 3 times by phone and text message to contact NA # 1 on 8/23/23 and 8/24/23 without success.
An interview was conducted on 8/22/23 at 3:55 PM with Nurse # 1. Nurse # 1 revealed she was assigned to Resident #307 on 1/22/23. Nurse # 1 stated NA #1 turned Resident #307 away from her while providing incontinence care. Nurse # 1stated Resident #307 was too close to the edge of the bed and rolled off.
An interview was conducted on 8/23/23 at 1:25 PM with Nurse #3. Nurse #3 revealed she was working the night of 1/22/23 and responded to the room following Resident #307's fall. Nurse #3 observed Resident #307 lying face down on the floor by the bed and there was a large amount of blood.
Review of the hospital records revealed an emergency department provider note dated 1/22/23 which indicated Resident #307 presented to the emergency department with profuse bleeding from a scalp and a lip laceration after a fall while staff were attending to her. Physical exam indicated Resident #307 had a 3.5 centimeter left posterior scalp laceration and a 2-centimeter upper lip laceration. Resident #307 received 7 sutures to the upper lip and 12 staples to the scalp. The note further indicated Resident #307 underwent a CT scan which revealed no cranial hemorrhage. Resident #307 returned to the facility on 1/23/23.
An interview was conducted on 8/23/23 04:35 PM with the Assistant Director of Nursing (ADON). The ADON revealed she completed the investigation of Resident #307's 1/22/23 fall. The ADON stated that as part of the investigation, NA #1 demonstrated what happened when Resident #307 fell. The ADON stated NA #1 demonstrated she turned Resident #307 away from her while providing incontinence care. The root cause analysis of the fall was improper turning and repositioning. The ADON stated if NA #1 had turned the resident toward her during care the fall could have been prevented. The ADON further stated the care guide indicated Resident #307 required 2-person assistance with mobility. The ADON stated NA # 1was trained on how to provide incontinence care to a dependent resident when she was hired. The ADON stated all nurses and NAs were retrained after this incident on how to properly turn and reposition a resident and were required to complete return demonstrations. The ADON stated NA #1 was retrained and was not allowed to provide patient care until she completed the retraining and demonstrated that she knew how to safely provide care.
An interview was conducted with the Administrator on 8/24/23 at 7:15 AM. The Administrator revealed that a full investigation of the incident was completed, and a Plan of Correction was completed after the fall. The Administrator stated that the Plan of Correction consisted of audits and in service education with all nurses, NAs and Medication Aides regarding turning and repositioning.
Interview on 8/24/23 at 2:35 PM with the Physician revealed due to Resident #307's dependent status with history of stroke with hemiparesis, the NA should not have turned the resident away from her during care.
An interview was conducted on 8/24/23 at 4:00 with the Nursing Supervisor. The Nursing Supervisor revealed Resident #307 required total care, was nonverbal and required 2 person assist with mobility. The Nursing Supervisor stated that all nurses and NAs received in service training regarding safe handling following Resident #307's fall on 1/22/23.
An interview on 8/25/23 at 9:56 AM with the Director of Nursing (DON) revealed safe handling was the root cause of the incident with Resident #307 on1/22/23. Root cause analysis was investigated and training and in services were provided to all nurses and NAs following the incident.
The facility provided the following Corrective Action Plan with a completion date of 2/15/23:
1. On 1/22/23 approximately 7:15-7:30 PM Resident #307 was in bed receiving incontinence care by one Nursing Assistant (NA). Resident #307 was positioned with the head of bed elevated with her hips in the center of the bed and legs slightly to the left. NA lowered the head of the bed, raised the bed to the height of about 2.5 to 3 feet and began to provide incontinence care. Upon interviewing the NA, she stated following incontinence care, she pushed the resident onto the left side with her left hand while raising resident's right leg up and over the left leg resulting in the resident being positioned along the edge of the bed on the left side. The NA stated when reaching for a brief, the resident continued to take a forward motion to the left side of the bed. The NA was unable to stop the forward motion of the resident and she rolled off the bed onto the floor. The assigned nurse on duty and another nurse assessed the resident, observed a large amount of blood on the floor around resident's head and determined the resident would be sent to the emergency room for evaluation. Emergency Medical Services (EMS) arrived at the facility and transported resident to the hospital for evaluation. Resident underwent a CT scan of the head which revealed no cranial hemorrhage. Resident received 7 sutures to the upper lip laceration and 12 staples to the scalp laceration. Resident remained in the emergency room overnight and returned to the facility on 1/23/23.
2. The Nurse Aide involved was not permitted to provide resident care pending investigation and education regarding safe handling and turning and repositioning. The Nursing Assistant was also asked to do a return demonstration of the incident. The Assistant Director of Nursing met with the Nursing Assistant on 1/23/23, written statement was received, and education was provided. The Nursing Assistant provided demonstration of the incident and following education completed a demonstration of proper handling and turning and repositioning.
3. Reeducation to the nursing staff to include Nursing Assistants, nurses and Medication Aides was initiated on 1/23/23 by the Assistant Director of Nursing (ADON) and nursing supervisor. Education included proper turning and positioning procedure, safe handling and following the resident care guide. All nursing staff will receive education prior to next scheduled shift. Education is congoing for new hired staff. The Director of Nursing (DON) initiated an in service with all nurses, Nursing Assistants and Medication Aides regarding positioning in bed with emphasis on the providing care in bed to the dependent resident, safe handling and utilizing the care guide.
100% audit of all resident positioning needs in bed.
100% audit utilizing a questionnaire with all cognitively intact residents regarding any concerns related to turning and positioning during care.
100% audit of all falls in the prior 30 days
100% audit of resident care plans and care guides to ensure correct information in place and updated as needed.
Staff Development Coordinator and/or Nursing Supervisor will complete 5 random weekly observations of staff providing bed mobility and proper positioning during care for 4 weeks.
4. Results of the 5 random weekly observations will be discussed at the monthly Quality Assurance and Performance Improvement (QAPI) meeting for one month to determine trends or issues that may require further interventions or monitoring to sustain substantial compliance.
5. Allegation of Compliance Date: 2/15/23.
The Corrective Action Plan was validated on 8/24/23 and concluded the facility implemented an acceptable corrective action plan on 2/15/23. Interviews with nursing staff revealed the facility had provided education and training on proper turning and repositioning and safe handling. Staff interviewed verbalized they received in service training including return demonstration of competency prior to starting their next shift. Review of the facility audit tools revealed 100% audit of resident positioning needs in bed was completed. Audit records further revealed questionnaires were completed with all cognitively intact residents regarding turning and positioning during care. 100 % of the falls in the prior 30 days were reviewed. No concerns were identified as a result of the audits.
Review of the monitoring tools of safe handling and turning and repositioning that began on 1/24/23 were completed weekly as outlined in the corrective action plan with no concerns identified.
SERIOUS
(G)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Actual Harm - a resident was hurt due to facility failures
Deficiency F0760
(Tag F0760)
A resident was harmed · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2). Resident #31 was admitted to the facility on [DATE] with medical diagnosis which included insomnia.
Resident #31's medical...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2). Resident #31 was admitted to the facility on [DATE] with medical diagnosis which included insomnia.
Resident #31's medical record revealed a physician order dated 6/14/23 for temazepam (antianxiety medication) oral capsule 15 milligrams. Give 1 capsule by mouth at bedtime for insomnia.
Resident #31's August 2023 medication administration record (MAR) revealed that on 8/15/23, 8/16/23, 8/17/23 and 8/18/23 the documentation for temazepam was charted as 10 which indicated that the medication was not administered due to not available.
Interview with Resident #31 on 8/21/23 at 12:45 PM revealed she did not receive her sleep medication for several nights due to it was not available in the facility. Resident #31 stated she was upset the nights she did not receive the medication because she could not sleep and feared she was going to have withdrawals.
Review of the Controlled Substance Count Record for Resident #31 revealed a count sheet dated 8/18/23 for temazepam 15 milligrams. The count sheet indicated 30 tablets sent by pharmacy on 8/18/23.
Interview on 8/23/23/ at 1:00 PM with Nurse #1 revealed she was assigned to Resident #31 on the evening of 8/16/23 until 11:00 PM. Nurse #1 indicated documentation of 10 on the MAR meant that the medication temazepam was unavailable. Nurse #1 stated that the medication temazepam was not in the medication cart on 8/16/23 and was not in the facility, so she did not administer it and documented 10 on the MAR. Nurse #1 revealed that she did not inform the physician that the medication was unavailable and did not attempt to obtain the medication. Nurse #1 stated she had worked at the facility for several years and knew she was supposed to obtain the medication or inform the physician it was unavailable, but she did not do so.
Interview with Nurse #2 on 8/23/23 at 1:18 PM revealed that if the supply of a medication was getting low the nurse was to call the pharmacy, order the medication on the computer or fax the refill request to the pharmacy. Nurse #2 indicated she thought temazepam was refilled without a new prescription, but she was not sure. Nurse #2 indicated the pharmacy delivered the medication that night if ordered before 4 PM. If it was requested after 4 PM, the medication was received the next night. Nurse #2 indicated the facility had an emergency kit that contained some medications, including pain medication. Nurse #2 stated temazepam was not included in the emergency kit. Nurse #3 stated that if a medication was not available, she did not give it. Nurse #2 sometimes it was recorded on the report sheet if a medication was not available for someone to follow up. Nurse #2 recalled that Resident #31 was out of the medication temazepam recently, but she did not know why or how that happened. Nurse #2 stated that documentation of 10 on the MAR indicated the medication was not administered due to it was not available.
Interview on 8/23/23 at 4:14 PM with MDS Nurse #2 revealed she was assigned to Resident #31 on the 3:00 PM -11:00 PM shift on 8/18/23. MDS Nurse #2 indicated she did not usually work the medication cart and when she did, she worked different assignments. MDS Nurse #2 stated she was not familiar with Resident #31's usual sleep patterns. MDS Nurse stated if any of the nurses noticed that a medication was running low, they could request a refill from the pharmacy. MDS Nurse #2 stated she documented a 10 on Resident #31's MAR on the evening of 8/18/23 indicating the medication was not available and she did not give it. MDS Nurse #2 stated she did not know why the medication was not available, she had not attempted to obtain it and had not notified the physician. MDS Nurse #2 revealed medication aides worked the medication carts and they don't check when refills are needed. MDS Nurse #2 stated no one was assigned to audit the medication carts for refills. MDS Nurse #2 stated she did not recall if Resident #31 was upset on 8/18/23 about not receiving her scheduled temazepam.
Interview on 8/24/23 at 5:20 AM with Nurse #3 indicated she was assigned to Resident #31 on 8/15/23 and 8/17/23 from 7:00 PM to 7:00 AM. Nurse #3 revealed some medications required a prescription for refills. Nurse #3 stated all the nurses were supposed to send requests to the provider to obtain a prescription for refills. No one was assigned to check when refills were needed or to send the requests for refill prescriptions. Nurse #3 stated when she was assigned to Resident #31 on 8/15/23 and 8/17/23, she charted 10 on the MAR for temazepam which indicated the medication was not available in the facility and she did not give it. Nurse #3 stated she should have attempted to obtain the medication and notified the physician, but she did not do so. Nurse #3 stated she did not know why she had not done these things.
Interview on 8/24/23 at 1:00 PM with Regional Pharmacy Services Manager revealed that some residents experience insomnia and nervousness or restlessness from missing a dose of temazepam.
During a follow up interview on 8/24/23 at 1:45 PM with the Regional Pharmacy Services Manager he revealed that the last prescription for temazepam was dispensed for Resident #31 on 7/14/23 for 30 tablets. On 8/18/23 a new prescription of 30 tablets of temazepam was dispensed for Resident #31. There was no refill request received from the facility prior to 8/18/23. The pharmacy received an electronic prescription on 8/18/23 for Resident #31 for temazepam 15 milligrams give one tablet at bedtime for sleep.
An interview on 8/24/23 at 2:45 PM with the Physician revealed she was not informed that Resident #31 did not receive the ordered temazepam on 8/15/23, 8/16/23, 8/17/23 and 8/18/23 due to it was not available. The physician stated that it may not have affected Resident #31 to miss the scheduled doses of temazepam, but it should have been reported and the refill should have been requested before the resident ran out of medication. The physician stated the omission of a medication for insomnia for several nights could be a significant issue.
An interview was conducted on 8/24/23 at 3:49 PM with the Nursing Supervisor. The Nursing Supervisor revealed the nurses sometimes told her and she contacted the doctor's office to request a refill for a controlled substance. The Nursing Supervisor stated that on 8/18/23 she was told the refill was needed for Resident #31's temazepam and she requested the refill from the physician. The Nursing Supervisor stated there was no one assigned to check the medications on the medication cart to be sure the residents had their ordered medications. The Nursing Supervisor further stated that she was not informed until 8/18/23 that Resident #31 required a refill of her ordered temazepam.
An interview was conducted on 8/25/23 at 10:14 AM with the Director of Nursing. The DON stated the physician was to be notified in a timely manner that a new prescription was needed for a refill of a controlled substance. The DON stated the nurses should have notified the physician when they determined the medication was unavailable to determine if there was a substitute. The DON stated the Nursing Supervisor usually handled contacting the physician when refills were needed. The DON stated she did not know why the refill request was not sent prior to the medication running out.
4. Resident #62 was admitted to the facility on [DATE] with diagnoses of dementia and anxiety.
A physician's order for Resident #62 dated 5/8/22 was for buspirone (a medication to treat anxiety) 5 milligram (mg) 1 tablet by mouth one time a day for anxiety.
A review of Resident #62's January 2023 Medication Administration Record (MAR) revealed documentation he was administered buspirone 5 mg 1 tablet by mouth one time a day for anxiety from 1/1/23 through 1/31/23.
A review of a New Prescription Summary for Resident #62 dated 1/23/23 provided by the Regional Pharmacy Services Manager on 8/24/23 revealed buspirone 10 mg take 1 tablet by mouth every morning for vascular dementia related anxiety. The effective date was 1/23/23.
A Consultant Pharmacist's Medication Regime Review for Resident #62 dated 2/16/23 revealed in part an electronic prescription had been sent to the pharmacy and Resident #62's buspirone dose was changed on 1/23/23. The pharmacy faxed this change to the facility, but this change didn't appear to have been carried out. Staff were charting the 5 mg dose as given. The follow-through documented on the form by the Director of Nursing (DON) revealed she observed staff giving one half tablet of the medication which was the correct dose of 5 mg per Resident #62's MAR. The follow through documentation by the DON was not dated.
A physician's order entered into Resident #62's medical record by the Assistant Director of Nursing (ADON) dated 2/22/23 was for buspirone 5 mg 2 tablets by mouth one time a day for anxiety (2 tablets equaled 10 mg new order dated 2/21/23).
A review of Resident #62's February 2023 MAR revealed documentation he received buspirone 5 mg 1 tablet by mouth one time a day for anxiety from 2/1/23 through 2/22/23. It further revealed documentation he received buspirone 5 mg 2 tablets by mouth one time a day for anxiety (2 tablets equaled 10 mg new order 2/21/23) from 2/23/23 through 2/28/23.
A review of Resident #62's quarterly Minimum Data Set (MDS) dated [DATE] revealed he was severely cognitively impaired. He had no hallucinations, delusions, or behaviors. He did not reject care. He received antipsychotic, antianxiety and antidepressant medication on 7 of 7 look-back period days. Antipsychotic medication was received only on a routine basis. The physician documented a gradual dose reduction as clinically contraindicated on 7/27/23.
A review of Resident #62's current comprehensive care plan revealed a focus area last revised on 5/10/23 of psychotropic drug use. The goal was for Resident #62 to have no side effects of medication through the next review. An intervention was to administer medications per the physician's order.
On 8/24/23 at 9:24 AM a telephone interview with the facility Regional Pharmacy Services Manager indicated the pharmacy received an electronic prescription for Resident #62 on 1/23/23 for buspirone 10 mg take 1 tablet by mouth every morning for vascular dementia related anxiety. He stated when an electronic prescription came directly to the pharmacy, the pharmacy faxed this information to the facility so the facility could enter it into their order system as the pharmacy did not have that capability. He went on to say the pharmacy sent 10 mg buspirone tablets to the facility for Resident #62 on 1/23/23. He further indicated buspirone was not a medication that would cause harm to Resident #62 if administered after being cut in half.
On 8/24/23 at 10:09 AM an interview with the DON indicated she conducted an observation of Resident #62's medication administration in response to the Consultant Pharmacist's Medication Regime Review for Resident #62 dated 2/16/23. She stated she did not recall the date of this observation. She further indicated Resident #62's MAR at the time of the observation reflected the most current physician's order the facility had in his record for buspirone 5 mg daily. She went on to say the buspirone dose available for Resident #62 at the time of her observation was 10 mg tablets. The DON stated she observed the staff member cut the 10 mg buspirone tablet in half and administer one half tablet equaling 5 mg to Resident #62. She went on to say she did not question why the pharmacy sent Resident #62 10 mg tablets of buspirone when the current physician's order was for one 5 mg tablet. She stated usually the form of the medication sent by the pharmacy would match the order. She further indicated she did not recall her thought process at the time. The DON stated normally if the pharmacy did not have the form of a medication ordered by the physician and needed to send a substitute there would be a label on the medication indicating this. She went on to say she did not recall this being the case for Resident #62 at that time. She further indicated the process when a physician sent an electronic prescription directly to the pharmacy was the pharmacy would then fax a copy of the prescription to the facility. The DON stated this fax usually went to the fax machine in the Nursing Supervisor's office. She went on to say the Nursing Supervisor would then put the order into the resident's medical record for display on the MAR because pharmacy did not have the capacity to do this. She stated she did not know why this had not occurred with the physician's order for Resident #62 to increase his buspirone dose to 10 mg daily dated 1/23/23. The DON went on to say the risk to Resident #62 from not receiving the ordered dose of his buspirone was experiencing increased anxiety. She stated she was not aware of any behaviors demonstrating increased anxiety by Resident #62 during that period.
On 8/24/23 at 10:55 AM an interview with the ADON indicated she would have entered the buspirone 5 mg 2 tablets by mouth one time a day for anxiety (2 tablets equaled 10 mg new order dated 2/21/23) immediately after she received it from the Nursing Supervisor. She stated the process for electronic prescriptions sent directly to the pharmacy was that the pharmacy would then fax a copy over to the facility and it would be entered in the resident's medical record. She further indicated this system was not fool proof. The ADON stated after she entered the order into Resident 62's medical record, she would have given it back to the Nursing Supervisor.
On 8/24/23 at 10:58 AM an interview with the Nursing Supervisor confirmed the facility process for electronic prescriptions sent directly to the pharmacy by a physician. She stated she did not know what happened to the New Prescription Summary for Resident #62 dated 1/23/23 for buspirone 10 mg take 1 tablet by mouth every morning for vascular dementia related anxiety. She confirmed it was not in Resident #62's medical record. She stated she did not recall ever receiving the fax from the pharmacy. The ADON went on to say there were 5 fax machines in the facility and the fax could have gone anywhere. She stated she probably got a physician's order for Resident #62 on 2/22/23 for buspirone 5 mg 2 tablets by mouth one time a day for anxiety (2 tablets equaled 10 mg new order dated 2/21/23) and gave it to the ADON to enter in Resident #62's medical record but she did not remember. She went on to say she could not find this either.
On 8/24/23 at 2:49 PM a telephone interview with Physician #1 indicated she did not really know what the facility process was for electronic prescriptions sent to the pharmacy. She stated she was familiar with Resident #62. She stated she did not think Resident #62 suffered any adverse consequences from not receiving the ordered dose of his buspirone. She stated she had not seen much change in Resident #62's behaviors in the 2 years she had been caring for him.
Based on observations, record review, staff, Regional Pharmacy Manager, and Physician interviews the facility failed to: 1) administer 25 doses of a controlled substance hypnotic medication (Ambien) as prescribed for the treatment of insomnia resulting in decreased sleep, restlessness, and anxiety (Resident #84, and Resident #6); 2) administer 4 doses of a controlled substance antianxiety medication (Temazepam) as prescribed for the treatment of insomnia resulting in decreased sleep and fear of withdrawal (Resident #31); 3) ensure the correct dose of a controlled substance medication (Dronabinol) was administered as prescribed for an appetite stimulant (Resident#256); and 4) ensure the correct dose of antianxiety medication was administered in accordance with the physician's order (Resident #62) for 5 of 5 residents reviewed for medication administration.
Findings included.
1a) Resident #84 was admitted to the facility on [DATE] with diagnoses including Chronic Obstructive Pulmonary Disease (COPD), Heart Failure, and Insomnia.
A physicians order dated 03/06/23 for Resident #84 revealed an order for Ambien 10 milligram (mg) tablets. Administer one tablet by mouth at bedtime for Insomnia.
The Minimum Data Set (MDS) admission assessment dated [DATE] revealed Resident #84 was cognitively intact. She required supervision with bed mobility, transfers, and activities of daily living (ADLs). She received scheduled hypnotics on 4 of 7 days during the assessment period.
A care plan dated 03/15/23 revealed Resident #84 received psychotropic and hypnotic medications. The interventions included in part; to administer medications per the physicians order.
Review of Resident #84's March 2023 Medication Administration Record (MAR) revealed on 3/10, 3/17, 3/18, 3/19, 3/22, 3/24, 3/26, 3/28, and 3/30, Ambien 10 mg tablets were documented on the MAR as not available for administration.
Review of Resident #84's April 2023 Medication Administration Record (MAR) revealed on 4/19, 4/20, 4/21, and 4/23, the Ambien 10 mg tablets were documented on the MAR as not available for administration.
Review of the Controlled Substance Count Record for Resident #84 for March 2023 and April 2023 revealed the entries made by staff were not legible and it could not be determined if the dose was signed out on the declining count record.
Review of the nursing progress notes dated 03/10/23 through 04/23/23 revealed no documentation as to why the Ambien 10 mg tablets were not available and were not administered to Resident #84.
During an interview on 08/23/23 03:03 PM Resident #84 was observed lying in bed in her room. She was alert and oriented. She stated she needed the Ambien each night for sleep and stated she went for a period of time a few months ago when the medication was not available, but she could not recall a specific date or time. She stated she was only told the medication was not available from the pharmacy. She stated when she didn't take the nightly dose of Ambien, she had trouble sleeping. She stated she did not get good sleep when she didn't take the medication and during that time, she would eventually fall asleep late around 2:00 -3:00 AM and then she would wake up several times during the night which caused her to be tired the following day. She stated it would also cause her to be anxious from not getting sleep, but stated she did not take medication for anxiety. She stated she didn't feel great most days and without taking Ambien and getting sleep it made her feel worse and it made her not want to get out of bed.
During a phone interview on 08/24/23 at 01:53 PM the Regional Pharmacy Services Manager stated the pharmacy was not aware of any issue with Resident #84's Ambien until they were notified by the facility on 04/21/23. He stated upon investigation their records showed that thirty Ambien 10 mg tablets were dispensed to the facility for Resident #84 on 03/13/23, and thirty tablets were dispensed to the facility on [DATE], and thirty tablets were dispensed to the facility on [DATE]. He stated the facility should have had the medication on hand and available for Resident #84 on the specified dates.
Review of the Monthly Consultant Pharmacist reports revealed no documentation regarding Resident #84's Ambien. The Pharmacy Consultant that conducted the monthly review was not available for interview during the survey period.
b.) Resident #6 was admitted to the facility on [DATE] with diagnoses including Heart Failure, Diabetes, and Insomnia.
A care plan dated 11/21/22 revealed Resident #6 received psychotropic and hypnotic medications. The interventions included in part; to administer medications per the physicians order.
A physicians order for Resident #6 dated 12/05/22 revealed Zolpidem Tartrate (Ambien) Oral Tablet 10 mgs. Give 10 mgs by mouth at bedtime for insomnia.
Review of Resident #6's March 2023 Medication Administration Record (MAR) revealed on 3/3, ¾, 3/5, 3/6, 3/8, 3/10, 3/13, and 3/16, Ambien 10 mg tablets were documented on the MAR as not available for administration.
Review of Resident #6's April 2023 Medication Administration Record (MAR) revealed on 4/2, 4/19, 4/20, 4/21, Ambien 10 mg tablets were documented on the MAR as not available for administration.
Review of the Controlled Substance Count Record for Resident #6 for March 2023 and April 2023 revealed the entries made by staff were not legible and it could not be determined if the dose was signed out on the declining count record.
A progress noted dated 04/02/23 at 8:00 PM documented by Nurse #6 revealed Ambien was not available. Resident was made aware and admitted that chronic pain kept her awake at night and will take her available Tramadol for back pain, (pain scale) 5 out of 10 which will also help her to sleep with pain relief.
During the investigation an attempt was made to contact Nurse #6 on 08/25/23 with no response.
Further review of the nursing progress notes dated 03/03/23 through 04/21/23 revealed no documentation as to why the Ambien 10 mg tablets were not available and were not administered to Resident #6.
The Minimum Data Set (MDS) most recent quarterly assessment dated [DATE] revealed Resident #6 was cognitively intact. She required extensive one-to-two-person assistance with bed mobility, transfers, and activities of daily living (ADLs). She received hypnotics during the assessment period.
During an interview on 08/23/23 at 3:00 PM Resident #6 was observed lying in bed in her room. She was alert and oriented. She stated there was a period of time a few months ago when she was not receiving her nightly dose of Ambien. She stated she was only told the medication was not available from pharmacy. She stated not getting the Ambien each night caused her to not fall asleep, or if she dozed off, she would not stay asleep. She stated she was up all hours of the night during that time and would have to watch TV during the night at 3 or 4:00 AM just to try to go to sleep. She stated she took Tramadol as needed for pain and had to take pain medication on some of those nights to relax enough to help her get to sleep. She stated she stayed in bed most of the time regardless of her medications but stated on the nights she wasn't sleeping due to not getting the Ambien, it made her feel more tired and restless during the day.
During a phone interview on 08/24/23 at 01:53 PM the Regional Pharmacy Services Manager stated the pharmacy was not aware of any issue with Resident #6's Ambien until they were notified by the facility on 04/21/23. He stated upon investigation their records showed that on 01/20/23 the pharmacy dispensed to the facility thirty tablets of Ambien 10 mgs. On 03/17/23 the pharmacy dispensed thirty tablets of Ambien 10 mgs. On 03/29/23 the pharmacy dispensed five tablets of Ambien 10 mgs, then on 04/03/23 the pharmacy dispensed thirty Ambien 10 mg tablets. He stated the facility should have had the medication on hand and available for Resident #6 on the specified dates.
Review of the Monthly Consultant Pharmacist reports revealed no documentation regarding Resident #6's Ambien. The Pharmacy Consultant that conducted the monthly review was not available for interview during the survey period.
During an interview on 08/24/23 at 07:21 AM the Administrator stated that on 04/21/23 the Nursing Supervisor was responsible for the medication cart that contained Resident #84 and Resident #6's medications due to a staff member not showing up for work that morning. She stated the Nursing Supervisor thought the narcotic count sheet didn't look right and she reported this to her. She stated they immediately started an investigation and determined the Ambien for Resident #84 and Resident #6 was missing. She stated a full investigation was completed. She contacted the pharmacy and obtained dispensing records and determined that no Ambien was returned to the pharmacy for Resident #84 or Resident #6. She stated she and the Nursing Supervisor were unaware until that time that Resident #84 or Resident #6 was not getting the nightly dose of Ambien.
During an interview on 08/24/23 at 11:42 AM the Nursing Supervisor stated on 04/21/23 a Medication Aide was assigned to Resident #84 and Resident #6's medication cart due to a staff member not showing up for work that morning. She indicated she could not recall which Medication Aide was on the cart that morning. She stated the medication aide on duty put the declining inventory sheet (Controlled Substance Count Record)in her box at the nurses station that morning. When she looked at the declining inventory sheet it was not legible and didn't look right and she immediately reported this to the Administrator. She stated she checked the medication cart at that time and there was no Ambien available on the cart for Resident #84 or Resident #6. She stated they conducted a full investigation and determined the medication was missing because it had been dispensed from pharmacy and should have been on hand. She stated that was why Resident #84 and Resident #6 did not receive the nightly dose of Ambien on the dates specified. She stated the medication ordering process included that if a medication was not available for administration the nurse could reorder through the electronic medical record if there were refills available. She stated if no refills were available the nurse would complete a handwritten order form, and give it to her, and she would call the physician to get a new order. She stated for controlled medications the physician's office would send the order directly to the pharmacy. She stated no staff had reported to her during that time from 03/10/23 through 04/23/23 that this medication was not available and that was why they didn't catch the discrepancy sooner. She stated the nurses should not continue to document on the MAR that a medication was not available without following up on the medication order with the pharmacy or by notifying her so that she could get the medication sent to the facility. She stated staff needed to get better with follow-up when medications were not available for administration. She stated she did not recall getting any reports from Resident #84 or Resident #6 or from staff regarding any adverse effects from not receiving the medications but stated she believed Resident #84 and Resident #6 would have trouble sleeping without getting the nightly dose of Ambien.
During an interview on 08/24/23 at 12:30 PM the Director of Nursing (DON) indicated the Nursing Supervisor was responsible for reordering medications. She stated an investigation was conducted regarding Resident #84 and Resident #6's Ambien. She indicated the Nursing Supervisor could provide the details regarding the Residents not receiving the Ambien.
During an interview on 08/24/23 at 4:00 PM Nurse #1 stated she typically worked the day and evening shift and was assigned to Resident #84 and Resident #6 routinely. She stated there was an issue in April 2023 that was investigated by the facility regarding missing Ambien for both Residents. She stated that if she documented on the MAR that the medication was unavailable that meant it was not on the medication cart when it was scheduled to be given. She stated typically when a medication was not available, she would either reorder through the electronic medical record or complete an order form and send it to the Nursing Supervisor who would get it ordered. She stated she could not recall if or when she notified the Nursing Supervisor that Resident #84's or Resident #6's Ambien was not available. She indicated unfortunately Resident #84, and Resident #6 did go for a while without getting the nightly dose of Ambien. She indicated she was not aware if Resident #84 or Resident #6 had any adverse effects such as not sleeping or increased anxiety on the nights that they didn't get the medication.
During a phone interview on 08/25/23 at 1:00 PM Medication Aide #1 stated she typically worked the evening shift and was routinely assigned to Resident #84 and Resident #6. She stated she recalled a period of time when both Residents did not have Ambien available. She stated an investigation was done by the facility. She stated if she documented on the MAR that the medication was unavailable that meant it was not on the medication cart at that time. She stated medications could be reordered through the electronic medical record or she would notify the Nursing Supervisor. She stated sometimes she would just notify the Nursing Supervisor verbally that a medication was out and needed to be reordered. She stated she could not recall if or when she notified the Nursing Supervisor of Resident #84 or Resident #6 not having Ambien available. She stated she did not recall if Resident #84 or Resident #6 reported any adverse effects of not receiving the medication.
During an interview on 08/25/23 at 3:30 PM Medication Aide #2 stated she typically worked the evening or night shift. She stated she was aware that Resident #84 and Resident #6 missed getting the nightly Ambien dose for a period of time. She stated she recalled an investigation being conducted regarding the medication. She stated if she documented on the MAR that the medication was unavailable that meant it was not on the medication cart and was not given. She stated she could not recall if she notified the Nursing Supervisor during that time that the medication was unavailable. She indicated she was not aware of any adverse effects it had on Resident #84 or Resident #6 when they didn't get the medication.
During an interview on 08/25/23 at 4:00 PM Nurse #4 stated he routinely worked the evening and night shift and was familiar with Resident #84 and Resident #6. He stated he could not recall the details regarding the missing Ambien. He stated if he documented the medication was not available on the MAR then it was not on the medication cart at that time and was not administered.
During a phone interview on 08/25/23 at 4:30 PM Nurse #5 stated she only worked as needed and could not recall any details regarding Resident #84 or Residents #6's Ambien. She stated if she documented on the MAR that the medication was not available that meant it was not on the medication cart at that time and it was not given.
During a phone interview on 08/25/23 at 5:00 PM Physician #1 stated she did not recall the details of Resident #84's or Resident #6's missing Ambien. She stated the facility most likely made her aware of the issue regarding the Ambien but stated she knew they had resolved the concern. She stated Resident #84 or Resident #6 not getting the nightly dose of Ambien would cause difficulty sleeping. She stated she did not recall any reported concerns made by staff of increased anxiety or restlessness regarding Resident #84 or Resident #6 but they most likely were not sleeping well during that time.
During an interview on 08/25/23 at 5:00 PM the Administrator stated during the time that staff were documenting the Ambien medication was unavailable that staff should have followed up sooner with the Nursing Supervisor. She stated Resident #84 or Resident #6 should not have gone for that length of time without follow up and without receiving the medication. She indicated Resident #84, and Resident #6 most likely did experience lack of sleep during that time since the Ambien was not administered. She stated education would be provided to all nursing staff regarding medication administration.
3). Resident #256 was admitted to the facility on [DATE] with medical diagnosis that included anorexia and moderate protein-calorie malnutrition.
Review of an admission MDS assessment for Resident #256 documented he had moderately impaired cognition. He received a mechanically altered, therapeutic diet and weighed 133 pounds. He was independent with eating and required set up help only.
The initial care plan for Resident #256 was in progress beginning on 08/11/23 and included guidance for activities of daily living and personal care.
Review of Resident #256 ' s weights revealed an admission weight on 08/11/23 of 132.6 pounds. On 08/23/23 he weighed 130.6 pounds
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0578
(Tag F0578)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and staff interviews the facility failed to ensure advanced directive information matched throughout 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 ensure advanced directive information matched throughout the medical record for 1 of 1 resident (Resident #25) reviewed for advanced directives.
Findings included:
Resident #25 was admitted to the facility on [DATE] with a diagnosis of Alzheimer's Disease.
A review of Resident #25's electronic medical record revealed an active physician's order dated [DATE] for CPR (Cardiopulmonary Resuscitation) Full Code.
A review of Resident #25's hard chart revealed a yellow DNR (Do Not Resuscitate) form signed Resident #25's attending physician on [DATE]. There was a box checked no expiration.
A review of her quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #25 was severely cognitively impaired.
On [DATE] at 10:18 AM an interview with the Director of Nursing (DON) indicated Resident #25's code status should be the same in her electronic record and her hard chart. She stated because Resident #25's code status was Full Code in the electronic record and DNR in her hard chart this could be confusing to nurses if Resident #25 needed CPR. She went on to say she would need to clarify Resident #25's wishes.
On [DATE] at 10:32 AM an interview with the Social Worker (SW) indicated Resident #25's wishes were that her code status be DNR. She stated she spoke with Resident #25's RP who expressed these wishes in May of 2022 and this had not changed. She went on to say Resident #25's code status should have been DNR beginning on [DATE] in both the electronic record and in her hard chart. The SW stated after a resident's DNR form was signed by their attending physician, she would place the form on the hard chart and enter the order into the resident's electronic record to be signed off by a nurse. She went on to say she was not sure why this had not happened with Resident #25.
On [DATE] at 2:31 PM an interview with the Administrator indicated the SW would have been responsible for entering Resident #25's DNR order into her electronic record.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0692
(Tag F0692)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff and Physician interviews the facility failed to obtain daily weights as ordered by the physician a...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff and Physician interviews the facility failed to obtain daily weights as ordered by the physician and failed to accurately document a weight or obtain a reweigh for 1 of 1 resident (Resident #4) reviewed for nutrition.
Findings included.
Resident #4 was admitted to the facility on [DATE] with diagnoses including Congestive Heart Failure (CHF), and End Stage Renal Disease with Hemodialysis.
A care plan dated 05/20/23 revealed Resident #4 had the potential for fluid volume excess related to congestive heart failure. Interventions included in part; to maintain fluid restrictions and obtain weights as ordered.
The Minimum Data Set (MDS) quarterly assessment dated [DATE] for Resident #4 revealed she was cognitively intact. She required extensive assistance with activities of daily living (ADL's). She received a therapeutic diet and had no weight loss or gain at the time of the assessment. She was compliant with care and received hemodialysis.
A physicians order dated 08/10/23 for Resident #4 revealed to obtain daily weights and notify the physician if greater than a 5 lb. (pound) weight gain.
A review of Resident #4's weights on 08/24/23 revealed the following:
08/10/23 the recorded weight was 219.6 lbs.
07/12/23 the recorded weight was 175.3 lbs.
07/07/23 the recorded weight was 179.9 lbs.
Review of Resident 4's progress notes from 08/10/23 through 08/24/23 revealed no documentation that a daily weight was recorded.
During an interview on 08/24/23 at 4:00 PM Nurse Aide #2 stated she routinely provided care for Resident #4. She stated the nurse aides typically obtained and documented the resident weights. She indicated the nurse would let them know if daily weights were needed and stated she was not aware of Resident #4 needing daily weights.
During an interview on 08/24/23 at 12:07 PM Nurse #7 stated she routinely provided care for Resident #4. She stated Resident #4 received a renal diet, was on fluid restrictions, and her weights were done monthly. She stated the nurses transcribed the orders that come in from the physician appointments. She indicated she was not aware of daily weights ordered on 08/10/23 for Resident #4 and stated she was not sure which nurse was working on 08/10/23 and missed the order. She stated it was an error. She stated the nurse aides obtained the monthly weights and the weight recorded on 08/10/23 of 219 lbs. could not be accurate and staff should have obtained a reweigh. She indicated upon review of Resident #4's electronic medical record a reweigh was not recorded.
During an interview on 08/24/23 at 1:44 PM the Nursing Supervisor stated Resident #4 was seen at Physician #2's office on 08/10/23 and returned with the physicians order for daily weights. She stated the process was for the physician orders to go to the nurse on the floor to transcribe, then the order is placed in her box. She stated she was not aware of the order on 08/10/23 for daily weights and to notify the physician if greater than a 5 lb. weight gain. She stated the weight recorded on 08/10/23 of 219 lbs. included the wheelchair weight and Resident #4 should have been reweighed at that time for accuracy. She stated a new weight was obtained this morning on 08/24/23 of 170.5 lbs. She stated the order was missed in error and would be corrected immediately.
During a phone interview on 08/25/23 at 3:15 PM Physician #2 stated Resident #4 had a diagnoses of congestive heart failure and typically CHF patients required tracking and monitoring of weights to identify fluid overload early which was why the order was written for daily weights. He stated now that Resident #4 was on hemodialysis the concern for fluid overload was less due to hemodialysis removing the excess fluid. He stated as long as Resident #4 received dialysis there would be no significant concerns with not getting daily weights done and stated she was compliant with dialysis. He stated he did expect that staff followed the physician orders and stated Resident #4 should get daily weights and weights should be recorded accurately.
During an interview on 08/25/23 at 5:00 PM the Administrator stated Resident #4 should have received daily weights since 08/10/23. She stated staff should have entered the order into the electronic medical record at that time. She stated education would be provided to nursing staff regarding entering physician orders and obtaining and accurately documenting resident weights.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Pharmacy Services
(Tag F0755)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, and interviews with staff, the resident, the Regional Pharmacy Services Manager and the Physician, the f...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, and interviews with staff, the resident, the Regional Pharmacy Services Manager and the Physician, the facility failed to acquire and administer temazepam, a controlled substance medication used for insomnia, for Resident #31 for a period of 4 days for 1 of 3 residents whose medications were reviewed.
Findings included:
Resident #31 was admitted to the facility on [DATE] with medical diagnoses which included in part: congestive heart failure, depression, and insomnia.
Review of Resident #31's medical record revealed a physician order dated 6/14/23 for temazepam oral capsule 15 milligrams. Give 1 capsule by mouth at bedtime for insomnia.
Review of Resident #31's August 2023 medication administration record (MAR) revealed that on 8/15/23, 8/16/23, 8/17/23 and 8/18/23 the documentation for temazepam was charted as 10 which indicated that the medication was not administered due to not available.
Interview with Resident #31 on 8/21/23 at 12:45 PM revealed she did not receive her sleep medication for several nights due to it was not available in the facility. Resident #31 stated she was upset the nights she did not receive the medication because she could not sleep and feared she was going to have withdrawals.
Review of the Controlled Substance Count Record for Resident #31 revealed a count sheet dated 8/18/23 for temazepam 15 milligrams. The count sheet indicated 30 tablets sent by pharmacy on 8/18/23.
Interview on 8/23/23/ at 1:00 PM with Nurse #1 revealed she was assigned to Resident #31 on the evening of 8/16/23. Nurse #1 indicated documentation of 10 on the MAR meant the medication temazepam was unavailable and she did not administer it. Nurse #1 stated that the medication temazepam was not in the medication cart on 8/16/23 and was not in the facility, so she did not administer it and documented 10 on the MAR. Nurse #1 revealed that she did not inform the physician that the medication was unavailable and did not attempt to obtain the medication.
Interview with Nurse #3 on 8/23/23 at 1:18 PM revealed that if the supply of a medication was getting low, the nurse was to call the pharmacy, order the medication on the computer or fax the refill request to the pharmacy. Nurse #3 indicated she thought temazepam was refilled without a new prescription, but she was not sure. Nurse #3 indicated the facility had an emergency kit that contained some medications, but it did not contain temazepam. Nurse #3 stated that if a medication was not available, she did not give it. Nurse #3 recalled that Resident #31 was out of the medication temazepam recently, but she did not know why or how that happened. Nurse #3 stated that documentation of 10 on the MAR indicated the medication was not administered due to it was not available.
Interview on 8/23/23 at 4:14 PM with MDS Nurse #2 revealed she was assigned to Resident #31 in the evening on 8/18/23. MDS Nurse #2 stated she documented a 10 on Resident #31's MAR on the evening of 8/18/23 indicating the medication was not available and she did not give it. MDS Nurse #2 stated she did not know why the medication was not available, she had not attempted to obtain it and had not notified the physician. MDS Nurse #2 revealed medication aides worked the medication carts and they don't check when refills were needed. MDS Nurse #2 stated no one was assigned to audit the medication carts for refills.
Interview on 8/24/23 at 5:20 AM with Nurse #3 indicated she was assigned to Resident #31 on 8/15/23 and 8/17/23. Nurse #3 revealed some medications required a prescription for refills. Nurse #3 stated all the nurses were supposed to send requests to the provider to obtain a prescription for refills. Nurse #3 further stated no one was assigned to check when the refills were needed or to send the requests to the physician to obtain prescriptions for refills of controlled substances. Nurse #3 stated she was assigned to Resident #31 on 8/15/23 and 8/17/23, she charted 10 on the MAR for temazepam which indicated the medication was not available in the facility and she did not administer it. Nurse #3 stated she did not attempt to obtain the medication or notify the physician.
An interview on 8/24/23 at 1:00 PM with the Regional Pharmacy Services Manager revealed that the physician can authorize up to 5 refills of the medication temazepam or the medication can be filled for a 6 months' supply. The Regional Pharmacy Services Manager stated that each time a supply of the medication was required, it would not necessarily require a new prescription from the physician, as long as they had not exceeded the 5 refills. The Regional Pharmacy Services Manager indicated that some residents experience insomnia and nervousness or restlessness from missing a dose of temazepam.
During a follow up interview on 8/24/23 at 1:45 PM with the Regional Pharmacy Services Manager he revealed that the refill request for Resident #31 for temazepam was received from the facility on 8/18/23. The pharmacy received an electronic prescription on 8/18/23 for Resident #31 for temazepam 15 milligrams give one tablet at bedtime for sleep. After the electronic prescription was received, the pharmacy dispensed 30 tablets of temazepam for Resident #31.
An interview was conducted on 8/24/23 at 2:45 PM with the Physician. The Physician revealed that the nurses at the facility contacted the physician's office to request refills of medications and she promptly completed the refill order. The physician stated she was not informed that Resident #31 did not receive the ordered temazepam on 8/15, 8/16, 8/17 and 8/18/23 due to it was not available. The physician stated that it may not have affected Resident #31 to miss the scheduled doses of temazepam, but it should have been reported and the refill should have been requested before the resident ran out of medication.
An interview was conducted on 8/24/23 at 3:49 PM with the Nursing Supervisor. The Nursing Supervisor revealed the nurses sometimes told her and she contacted the doctor's office to request a refill for a controlled substance. The Nursing Supervisor stated that on 8/18/23 she was told the refill was needed for Resident #31's temazepam and she requested the refill from the physician. The Nursing Supervisor stated there was no one assigned to check the medications on the medication cart to be sure the residents had their ordered medications. The Nursing Supervisor further stated that she was not informed until 8/18/23 that Resident #31 required a refill of her ordered temazepam.
An interview was conducted on 8/25/23 at 10:14 AM with the Director of Nursing. The DON stated the physician was to be notified in a timely manner that a new prescription was needed for a refill of a controlled substance. The DON stated the physician should be notified when a medication was unavailable to determine if there was a substitute. The DON stated the Nursing Supervisor usually handled contacting the physician when refills were needed. DON further stated that a medication was not to be omitted due to not available.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
QAPI Program
(Tag F0867)
Could have caused harm · This affected 1 resident
Based on record review and staff interview the facility's Quality Assessment and Assurance Committee failed to maintain implemented procedures and monitor interventions that the committee had previous...
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Based on record review and staff interview the facility's Quality Assessment and Assurance Committee failed to maintain implemented procedures and monitor interventions that the committee had previously put in place following the recertification and complaint survey of 04/13/22. This was for a recited deficiency in the area of Advance Directives (F578). The continued failure during two federal surveys of record showed a pattern of the facility's inability to sustain an effective Quality Assurance Program.
Findings included:
This tag is cross referenced to:
F578: Based on record review and staff interviews the facility failed to ensure advanced directive information matched throughout the medical record for 1 of 1 resident (Resident #25) reviewed for advanced directives.
During the recertification and complaint survey of 04/13/22, the facility was cited for failing to have an advance directive in the medical record for 1 of 1 resident reviewed for advanced directives (Resident #48).
In an interview with the Administrator on 08/25/23 at 3:22 PM she stated she was not sure why the previous plan of correction didn ' t work but she would re-evaluate the process and correct the issue. She thought that perhaps they had not monitored the issue long enough or had failed to revisit it after the audits had been completed to ensure staff were continuing to document advance directives. The previous plan of correction included an Advance Directive Audit Tool that was completed on admission and re-admission of residents by the nursing staff and reviewed weekly by the Director of Nursing for 4 weeks then monthly for 1 month. The Administrator was responsible for taking the Audits to the Quality Performance Improvement Committee monthly for 2 months.
CONCERN
(E)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0602
(Tag F0602)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review, staff, Regional Pharmacy Services Manager, and Physician interviews the facility failed to...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review, staff, Regional Pharmacy Services Manager, and Physician interviews the facility failed to protect a resident's right to be free from misappropriation of a resident's controlled hypnotic medication (Ambien) which was prescribed by the physician for insomnia. This resulted in 78 missing doses of Ambien for 2 of 2 residents (Resident #84, Resident #6) reviewed for misappropriation of medications.
Findings included.
1a.) Resident #84 was admitted to the facility on [DATE] with diagnoses including Chronic Obstructive Pulmonary Disease (COPD), Heart Failure, and Insomnia.
A physicians order dated 03/06/23 for Resident #84 revealed an order for Ambien 10 milligram (mg) tablets. Administer one tablet by mouth at bedtime for Insomnia.
The Minimum Data Set (MDS) admission assessment dated [DATE] revealed Resident #84 was cognitively intact. She required supervision with bed mobility, transfers, and activities of daily living (ADLs). She received scheduled hypnotics on 4 of 7 days during the assessment period.
A care plan dated 03/15/23 revealed Resident #84 received psychotropic and hypnotic medications. The interventions included in part; to administer medications per the physicians order.
Review of Resident #84's March 2023 Medication Administration Record (MAR) revealed multiple dates from 03/10/23 through 03/30/23, that Ambien 10 milligram (mg) tablets were documented on the MAR as not available for administration.
Review of Resident #84's April 2023 Medication Administration Record (MAR) revealed on 04/19/23 through 04/23/23, that Ambien 10 mg tablets were documented on the MAR as not available for administration.
Review of the Controlled Substance Count Record for Resident #84 for March 2023 and April 2023 revealed the entries made by staff were not legible and it could not be determined if the doses were signed out on the declining count record.
Review of the nursing progress notes dated 03/10/23 through 04/23/23 revealed no documentation as to why the Ambien 10 mg tablets were not available and were not administered to Resident #84.
During an interview on 08/23/23 03:03 PM Resident #84 was observed lying in bed in her room. She was alert and oriented. She stated she needed the Ambien each night for sleep and stated she went for a period of time a few months ago when the medication was not available, but she could not recall a specific date or time. She stated she was only told the medication was not available from the pharmacy.
b.) Resident #6 was admitted to the facility on [DATE] with diagnoses including Heart Failure, Diabetes, and Insomnia.
A care plan dated 11/21/22 revealed Resident #6 received psychotropic and hypnotic medications. The interventions included in part; to administer medications per the physicians order.
A physicians order for Resident #6 dated 12/05/22 revealed Zolpidem Tartrate (Ambien) Oral Tablet 10 mgs. Give 10 mgs by mouth at bedtime for insomnia.
Review of Resident #6's March 2023 Medication Administration Record (MAR) revealed multiple dates from 03/03/23 through 03/16/23, that Ambien 10 mg tablets were documented on the MAR as not available for administration.
Review of Resident #6's April 2023 Medication Administration Record (MAR) revealed on 4/1, 4/2, 4/19, 4/20, and 4/21, that Ambien 10 mg tablets were documented on the MAR as not available for administration.
Review of the Controlled Substance Count Record for Resident #6 for March 2023 and April 2023 revealed the entries made by staff were not legible and it could not be determined if the dose was signed out on the declining count record.
Review of the nursing progress notes dated 03/03/23 through 04/21/23 revealed no documentation as to why the Ambien 10 mg tablets were not available and were not administered to Resident #6.
The Minimum Data Set (MDS) quarterly assessment dated [DATE] revealed Resident #6 was cognitively intact. She required extensive one-to-two-person assistance with bed mobility, transfers, and activities of daily living (ADLs). She received hypnotics during the assessment period.
During an interview on 08/23/23 at 3:00 PM Resident #6 was observed lying in bed in her room. She was alert and oriented. She stated there was a period of time a few months ago when she was not receiving her nightly dose of Ambien. She stated she was only told the medication was not available from pharmacy.
Review of the facility investigation initiated on 04/21/23 revealed: On 04/21/23 the Nursing Supervisor notified the Director of Nursing (DON) and the Administrator of concerns related to the residents Ambien. Upon investigation the facility found a total of 50 missing Ambien 10 mg tablets for Resident #84 and a total of 28 missing Ambien tablets for Resident #6. The facility initiated an investigation to include review of pharmacy dispensing records for both residents. No Ambien medication was returned to the Pharmacy for either Resident. Identified residents were assessed with no difficulty sleeping. Reports were made to Adult Protective Services, the Police, the State Agency, and the Drug Enforcement Agency (DEA). No other residents received Ambien. Audits were conducted of the narcotic count sheets, packing slips, and return drug forms with no additional concerns related to narcotics. Assessments were completed for residents with difficulty sleeping, and new or worsening pain, with no negative findings. Audits were completed of the medication carts to ensure narcotic medications were present and available to administer per the physician orders. In-service training was conducted with all staff regarding misappropriation of resident property to include but not limited to medications. Witness statements were obtained. The facility investigation concluded; following staff witness statements, a review of narcotic records and pharmacy dispensing records it was substantiated that a total of 78 tablets of Ambien 10 mg tablets were unaccounted for. The facility could not determine the date that the medications became unaccounted for or how the medications became missing. The facility-initiated audits, in-services, and ongoing monitoring of the narcotic process. The allegation was substantiated due to the Ambien medication was missing.
During an interview on 08/24/23 at 07:21 AM the Administrator stated that on 04/21/23 the Nursing Supervisor was responsible for the medication cart that contained Resident #84 and Resident #6's medications due to a staff member not showing up for work that morning. She stated the Nursing Supervisor thought the narcotic count sheet didn't look right and she reported this to her. She stated they immediately started an investigation and determined the Ambien for Resident #84 and Resident #6 was missing. She stated a full investigation was completed. She contacted the pharmacy and obtained dispensing records and determined that no Ambien was returned to the pharmacy for Resident #84 or Resident #6. She stated she interviewed multiple staff members to obtain witness statements all denied changing or altering the dates and time on the Controlled Substance Count Record (narcotic declining inventory sheet). She stated the staff that were interviewed stated they were not aware that the Ambien was missing. She stated she and the Nursing Supervisor were unaware until that time that Resident #84 or Resident #6 were not getting the nightly dose of Ambien. She stated they could only speculate which staff member it was that took Resident #84 and Resident #6's Ambien. She stated that staff member called out on 04/21/23 the day the discrepancy was discovered. The staff member never returned phone calls and never showed up for work after 04/21/23. She stated they had not had any incidents of misappropriation of medications since this incident. She stated the corrective action plan completion date was 04/28/23.
During an interview on 08/24/23 at 11:42 AM the Nursing Supervisor stated on 04/21/23 a Medication Aide was assigned to Resident #84 and Resident #6's medication cart due to a staff member not showing up for work that morning. She indicated she could not recall which Medication Aide was on the cart that morning. She stated the medication aide on duty put the declining inventory sheet (Controlled Substance Count Record)in her box at the nurses station that morning. When she looked at the declining inventory sheet it was not legible and didn't look right and she immediately reported this to the Administrator. She stated she checked the medication cart at that time and there was no Ambien available on the cart for Resident #84 or Resident #6. She stated they conducted a full investigation and determined the medication was missing because it had been dispensed from pharmacy and should have been on hand. She stated that was why Resident #84 and Resident #6 did not receive the nightly dose of Ambien on the dates specified. She stated no staff had reported to her during that time from 03/10/23 through 04/23/23 that the medication was not available and that was why they didn't catch the discrepancy sooner. She stated a full investigation was conducted which included resident assessments, audits, in-service training and monitoring.
During a phone interview on 08/24/23 at 01:53 PM the Regional Pharmacy Services Manager stated the pharmacy was not aware of any issue with Resident #84's Ambien until they were notified by the facility on 04/21/23. He stated upon investigation their records showed that thirty Ambien 10 mg tablets were dispensed to the facility for Resident #84 on 03/13/23, and thirty tablets were dispensed to the facility on [DATE], and thirty tablets were dispensed to the facility on [DATE]. He stated the facility should have had the medication on hand and available for Resident #84 on the specified dates.
During a phone interview on 08/24/23 at 01:53 PM the Regional Pharmacy Services Manager stated the pharmacy was not aware of any issue with Resident #6's Ambien until they were notified by the facility on 04/21/23. He stated upon investigation their records showed that on 01/20/23 the pharmacy dispensed to the facility thirty tablets of Ambien 10 mgs. On 03/17/23 the pharmacy dispensed thirty tablets of Ambien 10 mgs. On 03/29/23 the pharmacy dispensed five tablets of Ambien 10 mgs, then on 04/03/23 the pharmacy dispensed thirty Ambien 10 mg tablets. He stated the facility should have had the medication on hand and available for Resident #6 on the specified dates.
During a phone interview on 08/25/23 at 5:00 PM Physician #1 stated she did not recall the details of Resident #84's or Resident #6's missing Ambien. She stated the facility most likely made her aware of the issue regarding the Ambien but stated she knew they had resolved the concern.
The corrective action for the noncompliance dated 04/28/23 was as follows:
On 04/21/23 the Assistant Director of Nursing (ADON) and the Nursing Supervisor initiated a 100% audit of the Medication Administration Records (MARs) and Controlled Substance Count Sheets for the last 30 days of all residents who received Controlled Substances, to include Resident #84 and Resident #6. The audit was to ensure the nurse or medication aide signed out the narcotics on the residents Control Substance Count Sheet to include quantity, date given, time given, quantity given, given by or destroyed by, quantity destroyed, method destroyed, witnessed by if destroyed, quantity left, as necessary, at the time of pulling the Controlled Substance. The audit was to ensure staff signed the electronic MAR that the narcotic was administered, and that documentation was completed for all as needed medications, to include date, hour, medication, dosage, route, reason, nurse initials, results, and response. All areas of concern were addressed by the ADON.
On 04/21/23 a 100% audit of all pharmacy packing slips for controlled substances and pharmacy Return of Control Substance Forms were initiated by the ADON and Nursing Supervisor to ensure there were no discrepancies in the Controlled Substance Count Sheets and that pharmacy received all medications per the Controlled Substance Return Form.
On 04/21/23 a 100% audit of residents receiving Zolpidem (Ambien) were assessed by the Nursing Supervisor for difficulty sleeping and/or new or worsening pain with no identified areas of concern.
On 04/21/23 the Administrator made the Medical Director, Pharmacy Consultant and Director of Pharmacy Clinical Services aware of the possible drug diversion.
On 04/21/23 the Administrator sent a 24-hour report of diversion of resident drugs to the Health Care Personnel Registry.
On 04/21/23 the Police Department was notified of the possible drug diversion by the Administrator.
On 04/21/23 The DEA was contacted by the Administrator and made aware of possible drug diversion.
On 04/21/23 an in-service was initiated with all nurses and medication aides by the Staff Development Coordinator (SDC) and Nursing Supervisor regarding Controlled Substance Diversion to include what is drug diversion, signs of diversion, following the chain of custody, declining count sheets, delivery manifest, Controlled Substance Return Forms, narcotic counts between shifts, reporting discrepancies, and documentation of narcotic administration. In-services were to be completed by 04/27/23. After 04/27/23, any staff who had not received the in-service training would receive it prior to their next scheduled work shift. All newly hired nurses and medication aides would be in-serviced during orientation by the Staff Facilitator in regard to Controlled Substance Diversion to include what is drug diversion, signs of diversion, following the chain of custody, declining count sheets, delivery manifest, Controlled Substance Return Forms, narcotic counts between shifts, reporting discrepancies, and documentation of narcotic administration.
On 04/21/23, 100% in-service training was initiated by the SDC and Nursing Supervisor with all staff regarding Misappropriation of Property. In-service to be completed by 04/27/23. After 04/27/23, any staff who had not received the in-service would receive it prior to their next scheduled work shift. All newly hired staff would be in-serviced during orientation by the Staff Facilitator regarding misappropriation.
The ADON, Nursing Supervisors, MDS nurse and Staff Development Coordinator will audit narcotic count sheets, packing slips, and return of drug sheets verified by pharmacy utilizing the Narcotic Count sheet Audit Tool 5 times per week x 4 weeks to ensure 2 nursing staff have completed the narcotic count sheet for all narcotics at the beginning and end of each shift, and to ensure nurses have completed the medication count accurately to include looking at both the count sheet and the supply on hand by both nurses and the medication aides and that Narcotics were administered per physicians order with documentation on both the MAR and the declining count sheet. The DON or ADON will address all concerns identified during the audits to include but not limited to education of the nurse.
The DON will review all audits weekly x 4 weeks to ensure all concerns were addressed.
The Director of Nursing will forward the results of the Narcotic Count sheet Audit Tool to the Quality Assurance (QA) Committee Meeting monthly x 1 month. The QA Committee will meet and review the Narcotic Return Audit Tool monthly x 1 month to identify any potential trends and determine the need for action and/or frequency of continued monitoring.
Alleged Completion Date: 04/28/23
Validation of the corrective action was completed on 08/25/23. This included staff interviews regarding the incident, and in-service training that was received to ensure understanding and knowledge of the training provided. Observations were conducted of the medication carts; controlled substance counts were conducted with nursing staff of narcotics stored on the medication carts. Controlled Substance Count Records were reviewed. Audits were verified. A QA meeting was held on 06/30/23 where audit results were discussed.
The facility's alleged completion date for the corrective action plan was validated as 04/28/23.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Drug Regimen Review
(Tag F0756)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff, physician, and Regional Pharmacy Services Manager interviews the facility failed to address drug ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff, physician, and Regional Pharmacy Services Manager interviews the facility failed to address drug irregularities noted by the Consultant Pharmacist on six consecutive monthly Medication Regimen Reviews for an antipsychotic medication prescribed by the physician for 1 of 5 residents (Resident #10) reviewed for unnecessary medications.
Findings included:
Resident #10 was admitted to the facility on [DATE] with medical diagnoses which included in part: dementia wiht behaviors and major depression with psychoses.
Review of an 8/17/22 pharmacy recommendation note to Resident #10's physician indicated a recent DISCUS (Dyskinesia Identification System condensed User Scale-an exam used to identify involuntary movements of the tongue, lips, eyes, upper and lower limbs associated with psychotropic medication, showed worsening abnormal voluntary movements. The note read in part: Please review the dose of risperidone at this time for potential discontinuation due to change in movements. The physician signed the recommendation on 8/27/22 indicating agreement with the recommendation and indicated to decrease risperidone to 0.25 milligrams once per day.
Resident #10's September Medication Administration Records (MAR) revealed resident received risperidone 0.5 mg. one time per day from 9/1/23 through 9/30/23.
Review of a 9/21/22 document titled Consultant Pharmacist's Medication Regimen Review read the MD agreed to reduce the risperidone dose due to worsening movements. I do not see that the order was carried out and I don't see an explanation as to why there was a change in plan. Please complete a medication error/incident report, make the MD aware and send pharmacy the correct order. There was no notation on the review that this was addressed or sent to the physician for review.
Resident #10's October MAR revealed resident received risperidone 0.5 mg one time per day from 10/1/23 through 10/31/23.
Review of a 10/20/22 document titled Consultant Pharmacist's Medication Regimen Review Active Recommendations Lacking a Final Response revealed a recommendation which read: This consult is being resent because either the response to last month's consult was either not found, not addressed, or not scanned into the electronic health record at the time of this review. The MD agreed to reduce the risperidone dose due to worsening movements. I do not see that the order was carried out and I don't see an explanation as to why there was a change in plan. There was no notation on the review that this was addressed.
Resident #10's November MAR revealed resident received risperidone 0.5 mg one time per day from 11/1/23 through 11/30/23.
Review of a 11/17/22 document titled Consultant Pharmacist's Medication Regimen Review Active Recommendations Lacking a Final Response revealed a recommendation which read: This consult is being resent because either the response to last month's consult was either not found, not addressed, or not scanned into the electronic health record at the time of this review. The MD agreed to reduce the risperidone dose due to worsening movements. I do not see that the order was carried out and I don't see an explanation as to why there was a change in plan. There was no notation on the review that this was addressed. There was no documentation in Resident #10's electronic health record regarding the recommendation.
Resident #10's December MAR revealed resident received risperidone 0.5 mg one time per day from 12/1/23 through 12/31/23.
Review of a 12/15/22 document titled Note to Attending Physician/Prescriber which read in part: please review the dose of risperidone at this time for potential discontinuation due to change in movements. The above was originally recommended in August 2022. Provider response was uploaded to the chart stated to reduce the risperidone to 0.25 mg once daily, but this was not carried out. Resident continues to receive risperidone 0.5 mg once daily. Please consider re-evaluation or document rational for continued use at current dosage. Handwritten documentation which stated faxed to MD was observed on the note with no signature or date. Physician/Prescriber response on the note was blank. There was no documentation in Resident #10's electronic health record regarding this.
Resident #10's January 2023 MAR indicated resident received risperidone 0.5 milligrams one time per day.
Review of a 1/18/23 document titled Consultant Pharmacist's Medication Regimen Review revealed it read in part: please review the dose of risperidone at this time for potential discontinuation due to change in movements. The above was originally recommended in August 2022. Provider response was uploaded to the chart which stated to reduce the risperidone to 0.25 mg once daily, but this was not carried out. Resident continues to receive risperidone 0.5 mg once daily. Please consider re-evaluation or document rational for continued use at current dosage. There was not documentation on the form or in the electronic health record that this was addressed.
Review of a 2/19/23 pharmacy medication regimen review for Resident #10 indicated in part Recommendation was made in August 2022 with provider response uploaded to the chart which stated to reduce risperidone to 0.25 milligrams once per day, but this was not carried out. The Resident continues to receive risperidone 0.5 milligrams once per day. Please consider reevaluation or document rationale for continued use of risperidone at current dosage. This consult was resent because either the response to last month's consult was either not found, not addressed, or not scanned into the medical record at the time of the review. The recommendation was signed as agree.
A 2/23/23 DISCUS evaluation indicated a score of 3 with oral movements which included chewing/lip smacking, puckering, sucking or thrusting the lower lip and lingual movements which included tongue thrusting or tongue in cheek observed. This was a decrease from the score of 4 on the DISCUS evaluation completed on 8/11/22.
A physician's order for Resident #10 dated 3/21/23 for risperidone tablet give 0.25 mg by mouth one time per day for major depressive disorder with psychotic symptoms was observed in resident's electronic health record.
Review of Resident #10's 5/22/23 quarterly Minimum Data Set assessment indicated resident had moderate cognitive impairment and exhibited no behaviors. Resident #10 received injections, an antipsychotic medication, and an antidepressant 7 days in the look back period.
Interview on 8/24/23 at 1:00 PM with the Regional Pharmacy Services Manager revealed the consultant pharmacist reviewed resident medications monthly. The Regional Pharmacy Services Manager indicated that the time frame to address pharmacy recommendations depends on the nature of the recommendation. The expectation was that the recommendations were addressed prior to the next monthly pharmacist visit and that the previous recommendation would be reviewed to be sure they were addressed. The Regional Pharmacy Services Manager stated that risperidone had a lower potential for abnormal movements but did have this as a risk.
Follow up interview on 8/24/23 at 1:45 PM with the Regional Pharmacy Services Manager indicated that the pharmacy had on record the pharmacy recommendation that was approved by the physician on 8/27/23. The Consultant Pharmacist sent recommendations to the facility on 9/21/22, 10/20/22, 11/17/22, 12/15/22 and 1/18/23 and 2/20/23 for follow up and clarification of the order to decrease Resident #10's risperidone per the 8/22/23 recommendation. These recommendations were not addressed.
An interview was conducted on 8/24/23 at 3:45 PM with the Nursing Supervisor. The Nursing Supervisor stated that the pharmacy recommendations were sent to the physician by the DON or ADON. The Nursing Supervisor stated that the physician made rounds in the facility and addressed the pharmacy recommendations at that time. The Nursing Supervisor stated she tried to make sure the orders were carried out when the physician addresses them. The Nursing Supervisor acknowledged she wrote the order on 8/28/22 to decrease Resident #10's risperidone per the signed pharmacy recommendation. The Nursing Supervisor further acknowledged she signed off the order which indicated she carried out the order meaning it was sent to the pharmacy and transcribed in Resident #10's electronic health record. The Nursing Supervisor revealed that nursing recommendations from the pharmacist were addressed by the DON. The Nursing Supervisor stated she addressed the physician recommendations.
An interview was conducted on 8/25/23 at 10:01 AM with the Director of Nursing (DON). The DON stated the pharmacy recommendations were sent to her or the Administrator. The DON stated when she received the recommendations, she addressed them or gave them to the physician for review. The Nursing Supervisor sent the recommendations to the physician. If the recommendations were not addressed by the physician prior to the next monthly pharmacist review, the pharmacist wrote a follow up recommendation to address. The DON revealed she had a process of keeping the pharmacist recommendations in a book and when the recommendation was addressed by the physician a folded copy was placed in the book. The DON did not indicate that there was a process to review the recommendations to ensure all of them were addressed. The DON stated she did not think Resident #10 experienced changes related to receiving the increased dose of risperidone. The DON stated she could not tell why the physician order written on 8/27/22 on the August pharmacy recommendation was not carried out other than careless oversight.
Interview on 8/25/23 at 3:00 PM with the physician revealed he was not made aware that the order to decrease risperidone for this resident was not carried out when he wrote it on 8/27/22. The physician stated he had not seen any other pharmacy recommendations regarding the medication risperidone not being carried out. The gradual dose reduction should have been completed to ensure resident received the lowest effective dose. The physician stated he expected that staff would carry out orders as written.
Follow up interview with the DON on 8/25/23 at 3:50 PM revealed she looked for the pharmacy recommendations to see what happened with the nursing recommendations that were written for this resident from August 2022 through present. The DON located copies of the Consultant Pharmacist's Medication Regimen Review Active Recommendations Lacking a Final Response dated 10/20/22 and a note to the Attending Physician/Prescriber dated 12/11/22. The DON was unable to locate other pharmacy recommendations that were sent to the facility for Resident #10. The DON was unable to state why the pharmacy recommendations for Resident #10 were not addressed other than human error.
The facility provided the following Corrective Action Plan with a completion date of 7/31/23:
1. The facility identified the following system issue regarding documentation of psychotropic medications which indicated in part:
Orders were not transcribed/initiated timely.
Pharmacist recommendations to the physician were not completed timely.
Pharmacist recommendation to nursing were not completed timely.
Concerns identified during a pharmacy review were not addressed/corrected by the facility which included medication concerns.
2. An audit was conducted by the Director of Nursing (DON) of all pharmacy recommendations for the past 90 days. All concerns identified were addressed by 7/31/23.
3. The Staff Development Coordinator and DON educated the Medical Director and all physicians regarding completion of the pharmacy recommendations timely to include rationale when declining recommendations. This education was completed by 7/31/23.
The Staff Development Coordinator educated all nurses regarding pharmacy recommendations with emphasis on ensuring the physician recommendations were reviewed by the physician timely and all new orders were transcribed accurately. This education was completed by 7/31/23.
The facility consultant educated the DON on 7/17/23 regarding pharmacy recommendations which included ensuring all recommendations were completed timely and accurately.
4.On 7/17/23 it was determined that as part of the plan of correction, a 10% audit of all Pharmacy Recommendations will be completed by the Quality Assurance nurse monthly for 3 months using an audit tool to ensure all recommendations were reviewed and completed timely and accurately.
5. On 7/17/23 it was determined that as part of the plan of correction, the pharmacy recommendation audit tool will be presented at the Quality Assurance and Performance Improvement (QAPI) meeting monthly for 3 months.
The Corrective Action Plan was validated on 8/25/23 and concluded the facility had implemented an acceptable corrective action plan on 7/31/23. Interviews with the nursing staff, revealed the facility had provided education and training regarding pharmacy recommendations.
Review of the monitoring tools that began on 7/17/23 revealed the tools were completed as outlined in the corrective action plan with no concerns identified.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Medication Errors
(Tag F0758)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff, physician, and Regional Pharmacy Services Manager interviews the facility failed to transcribe an...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff, physician, and Regional Pharmacy Services Manager interviews the facility failed to transcribe and administer an antipsychotic medication at a reduced dose per the Consultant Pharmacist recommendation due to a noted increase in abnormal movements. The failure to transcribe the reduced dose resulted in 189 doses administered at a higher dose than ordered for 1 of 5 residents (Resident #10) reviewed for psychotropic medication.
Findings included:
Resident #10 was admitted to the facility on [DATE] with medical diagnoses which included in part: dementia with behaviors and major depression with psychoses.
Review of Resident #10's care plan revealed a 5/18/21 focus, last revised on 5/24/23, of use of psychotropic drugs with potential for side effects of involuntary movements related to use of antipsychotic medication with a goal of no side effects from medication regimen. The interventions included administer medications per physician order and DISCUS (Dyskinesia Identification System Condensed User Scale- an exam used to identify involuntary movements of the tongue, lips, eyes, upper and lower limbs associated with psychotropic drug use).
Review of an 8/17/22 pharmacy recommendation note to Resident #10's physician indicated a recent DISCUS showed worsening abnormal voluntary movements with an increase in the scoring of the exam from 1 on 5/5/22 to 4 on 8/11/22 The note read in part: Please review the dose of risperidone at this time for potential discontinuation due to change in movements. The physician signed the recommendation on 8/27/22 indicating agreement with the recommendation and wrote an order on the recommendation for a dose reduction of Resident #10's risperidone dose from 0.5 milligrams once per day to 0.25 milligrams once per day. There was no documentation that this order was signed off by a nurse.
Resident #10's August and September Medication Administration Records (MAR) revealed resident received risperidone 0.5 milligram (mg.) one time per day from 8/17/22 through 9/20/22. This resulted in the resident receiving 35 doses of Risperidone at 0.5 mg when he should have received 0.25 mg of Risperidone.
Review of a 9/21/22 document titled Consultant Pharmacist's Medication Regimen Review read the MD agreed to reduce the risperidone dose due to worsening movements. I do not see that the order was carried out and I don't see an explanation as to why there was a change in plan. Please complete a medication error/incident report, make the MD aware and send pharmacy the correct order. There was no notation on the review that this was addressed or sent to the physician for review. The review contained no documentation that it was reviewed or signed off by the physician or a nurse.
Resident #10's September 2022 and October 2022 Medication Administration Records (MAR) revealed resident received risperidone 0.5 mg. one time per day from 9/21/22 through 10/20/22. This resulted in the resident receiving 30 doses of Risperidone at 0.5 mg when he should have received 0.25 mg of Risperidone.
Review of a 10/20/22 document titled Consultant Pharmacist's Medication Regimen Review Active Recommendations Lacking a Final Response revealed a recommendation which read: This consult is being resent because either the response to last month's consult was either not found, not addressed, or not scanned into the electronic health record at the time of this review. The MD agreed to reduce the risperidone dose due to worsening movements. I do not see that the order was carried out and I don't see an explanation as to why there was a change in plan. There was no notation on the review that this was addressed. The review contained no documentation that it was reviewed or signed off by the physician or a nurse.
Resident #10's October 2022 and November 2022 MAR revealed resident received risperidone 0.5 mg one time per day from 10/20/22 through 11/17/22. This resulted in the resident receiving 29 doses of Risperidone at 0.5 mg when he should have received 0.25 mg of Risperidone.
Review of a 11/17/22 document titled Consultant Pharmacist's Medication Regimen Review Active Recommendations Lacking a Final Response revealed a recommendation which read: This consult is being resent because either the response to last month's consult was either not found, not addressed, or not scanned into the electronic health record at the time of this review. The MD agreed to reduce the risperidone dose due to worsening movements. I do not see that the order was carried out and I don't see an explanation as to why there was a change in plan. There was no notation on the review that this was addressed. There was no documentation in Resident #10's electronic health record regarding the recommendation. The review contained no documentation that it was reviewed or signed off by the physician or a nurse.
Resident #10's November 2022 and December 2022 MAR revealed resident received risperidone 0.5 mg one time per day from 11/17/22 through 12/15/22. This resulted in the resident receiving 29 doses of Risperidone at 0.5 mg when he should have received 0.25 mg of Risperidone.
Review of a 12/15/22 document titled Note to Attending Physician/Prescriber which read in part: please review the dose of risperidone at this time for potential discontinuation due to change in movements. The above was originally recommended in August 2022. Provider response was uploaded to the chart stated to reduce the risperidone to 0.25 mg once daily, but this was not carried out. Resident continues to receive risperidone 0.5 mg once daily. Please consider re-evaluation or document rational for continued use at current dosage. Handwritten documentation which stated faxed to MD was observed on the note with no signature or date. Physician/Prescriber response on the note was blank. There was no documentation in Resident #10's electronic health record regarding this. The review contained no documentation that it was reviewed or signed off by the physician or a nurse.
Resident #10's December 2022 and January 2023MAR revealed resident received risperidone 0.5 mg one time per day from 12/15/22 through 1/18/22. This resulted in the resident receiving 34 doses of Risperidone at 0.5 mg when he should have received 0.25 mg of Risperidone.
Review of a 1/18/23 document titled Consultant Pharmacist's Medication Regimen Review revealed it read in part: please review the dose of risperidone at this time for potential discontinuation due to change in movements. The above was originally recommended in August 2022. Provider response was uploaded to the chart which stated to reduce the risperidone to 0.25 mg once daily, but this was not carried out. Resident continues to receive risperidone 0.5 mg once daily. Please consider re-evaluation or document rational for continued use at current dosage. There was not documentation on the form or in the electronic health record that this was addressed. The review contained no documentation that it was reviewed or signed off by the physician or a nurse.
Resident #10's January 2023 and February 2023 MAR indicated resident received risperidone 0.5 milligrams one time per day from 1/18/23 through 2/19/23. This resulted in the resident receiving 32 doses of Risperidone at 0.5 mg when he should have received 0.25 mg of Risperidone.
Review of a 2/19/23 pharmacy medication regimen review for Resident #10 indicated in part Recommendation was made in August 2022 with provider response uploaded to the chart which stated to reduce risperidone to 0.25 milligrams once per day, but this was not carried out. The Resident continues to receive risperidone 0.5 milligrams once per day. Please consider reevaluation or document rationale for continued use of risperidone at current dosage. This consult was resent because either the response to last month's consult was either not found, not addressed, or not scanned into the medical record at the time of the review. The recommendation was signed by the physician as agree. The review contained no documentation that it was reviewed or signed off by a nurse.
A 2/23/23 DISCUS evaluation indicated a score of 3 with oral movements which included chewing/lip smacking, puckering, sucking or thrusting the lower lip and lingual movements which included tongue thrusting or tongue in cheek observed. This was a decrease from the score of 4 on the DISCUS evaluation completed on 8/11/22.
A physician's order for Resident #10 dated 3/21/23 for risperidone tablet give 0.25 mg by mouth one time per day for major depressive disorder with psychotic symptoms was observed in resident's electronic health record.
A review of Resident #10's March 2023 MAR indicated risperidone 0.25 mg. one time per day was started on 3/21/23 and administered through 3/31/23.
Review of Resident #10's 4/4/23 quarterly Minimum Data Set (MDS) assessment indicated resident had moderate cognitive impairment and exhibited no behaviors. Resident #10 received an antipsychotic medication 7 days in the look back period.
Interview on 8/24/23 at 1:45 PM with the Regional Pharmacy Services Manager indicated the pharmacy had on record the pharmacy recommendation for a dose reduction of risperidone which was approved by the physician on 8/27/23. The Consultant Pharmacist sent recommendations to the facility on 9/21/22, 10/20/22, 11/17/22, 12/15/22 and 1/18/23 and 2/20/23 requesting follow up and clarification of the dose reduction to decrease Resident #10's risperidone per the 8/22/23 recommendation. These recommendations were not addressed by the physician or a nurse. The Regional Pharmacy Services Manager stated risperidone had the potential for abnormal movements which can be severe and gradual dose reduction was necessary to avoid these movements.
An interview was conducted on 8/24/23 at 3:45 PM with the Nursing Supervisor. The Nursing Supervisor stated she tried to make sure the orders were carried out when the physician addressed them. The Nursing Supervisor acknowledged she transcribed the order on 8/28/22 to decrease Resident #10's risperidone per the pharmacy recommendation which was signed by the physician. The Nursing Supervisor further acknowledged she signed off the written order indicating she carried out the order which meant she sent order to the pharmacy and transcribed it in Resident #10's electronic health record so it would transfer to the MAR. The Nursing Supervisor stated she did not know why she did not send the order for the dose reduction to the pharmacy and did not enter it in Resident #10's electronic health record. The Nursing Supervisor stated it was human error that she did not carry out the order for the dose reduction for Resident #10 as written by the physician.
An interview was conducted on 8/25/23 at 10:01 AM with the Director of Nursing (DON). The DON stated the pharmacy recommendations were sent to her or the Administrator and when she received them, she addressed them or gave them to the physician for review. The DON acknowledged the recommendations that were not addressed by the physician prior to the next monthly pharmacist review received a written follow up recommendation to address. The DON stated the follow up recommendations should have been addressed. The DON stated she did not think Resident #10 experienced changes related to the increased dose of risperidone however she indicated dose reductions were important to lessen the likelihood of permanent effects. The DON stated she could not tell why the physician order written on 8/27/22 on the August pharmacy recommendation was not carried out other than careless oversight.
Interview on 8/25/23 at 3:00 PM with the physician revealed he was not made aware that the order to decrease risperidone for this resident was not carried out when he wrote it on 8/27/22. The physician stated the gradual dose reduction should have been completed to ensure resident received the lowest effective dose and to avoid side effects associated with the higher dose. The physician stated he expected staff would carry out orders as written.
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, record review, and staff interviews the facility failed to a) ensure expired beverages were discarded and not available for use, b) ensure that frozen foods were sealed when sto...
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Based on observations, record review, and staff interviews the facility failed to a) ensure expired beverages were discarded and not available for use, b) ensure that frozen foods were sealed when stored to prevent freezer burn, c) ensure that foods were labeled, dated, stored, and left to thaw in a safe manner to prevent the potential for food borne illness. These practices had the potential to affect residents in the facility.
Findings included.
During the initial tour of the kitchen on 08/21/23 at 10:45 AM the following was observed:
a. The walk-in refrigerator was observed with a crate of approximately 50 milk cartons, each with an expiration date of 08/19/23.
b. The walk-in freezer was observed with an opened box of fried chicken patties. The plastic bag that contained the patties was left open to air, and ice had formed on the patties.
c. The following food items: a container of ground turkey sausage unlabeled and with no date, a container of turkey sausage patties unlabeled, with no date, and a container of vegetable sausage patties unlabeled, with no date were left sitting out on a cart in the kitchen at room temperature.
During an interview on 08/21/23 at 10:45 AM [NAME] #1 stated the unlabeled containers of ground turkey sausage, and turkey sausage patties were served this morning for breakfast, and he left the containers sitting out until he could cook more sausage to add to them and serve for breakfast tomorrow. He stated the vegetable sausage patties were taken out of the freezer this morning around 10:00 AM and were left sitting out at room temperature to thaw. He indicated that he thought it was okay to leave food sitting out at room temperature for a period of time or to thaw. He stated the food would be discarded. He stated he forgot to label and date the food items. He indicated he had received training on food storage.
During an interview on 08/21/23 at 10:50 AM the Dietary Manager stated the Kitchen staff had received training on food storage, as well as labeling and dating foods. He stated the sausage patties, and ground sausage should not have been left out for that length of time and the frozen vegetable sausage should not have been sitting out at room temperature to thaw and should have been placed in the refrigerator to thaw. He stated those food items would be discarded. He stated the expired milk cartons should have been either removed from service or placed in an area in the refrigerator with a Do not use label.
During a follow up interview on 08/24/23 at 1:00 PM the Dietary Manager stated he had worked at the facility for less than a year. He stated more training was needed for staff and in-services had started regarding proper food storage, labeling, and expiration dates, which were everyone's responsibility. He stated all expired foods should be removed from service and he expected foods to be stored properly and labeled and dated.
During an interview on 08/25/23 at 5:00 PM the Administrator stated she was not aware of any concerns in the Kitchen. She indicated there had been no complaints from residents regarding the food. She stated the Kitchen staff were required to follow the procedures for safe food storage.
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 staff interviews the facility failed to maintain resident rooms in good repair as evidenced by damage...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, and staff interviews the facility failed to maintain resident rooms in good repair as evidenced by damaged drywall which included visible holes in the walls, scratched walls, and peeling paint which was observed in 12 of 25 resident rooms (Rooms 2203, 2212, 2215, 2218, 2221, 2302, 2315, 3412, 3416, 3418, 3503, 3516) reviewed for the provision of a safe, clean, homelike environment.
Findings included.
During the initial tour of the facility on 08/21/23 at 11:30 AM observations of resident rooms revealed multiple rooms with holes in the drywall, large scratches in the drywall around the residents beds, and paint peeling off the walls. The following was observed:
a. room [ROOM NUMBER] revealed multiple long scratches on the walls throughout the room.
b. room [ROOM NUMBER] revealed damaged drywall at the side of the residents bed, with paint peeling off the walls.
c. room [ROOM NUMBER] revealed damaged drywall and peeling paint on walls.
d. room [ROOM NUMBER] revealed areas of drywall spackling compound on the walls that was dry and not painted, along with scratches in the drywall at the side of the residents bed.
e. room [ROOM NUMBER] revealed areas of drywall spackling compound that was dry and not painted, and scratches in the drywall at the side of the residents bed.
f. room [ROOM NUMBER] revealed scratched drywall at the head of the beds for beds A, B, and C.
g. room [ROOM NUMBER] revealed scratched drywall in room, with paint peeling off of the wall and air unit.
h. room [ROOM NUMBER] revealed drywall spackling compound at the head of the residents bed that was dry and not painted over.
i. room [ROOM NUMBER] revealed paint peeling off the walls in residents room at the head of the bed and the side of residents bed.
j. room [ROOM NUMBER] revealed damaged drywall with hole in the wall at the head of the residents bed, scratched wall at the head of the bed. Part of the towel rack was missing from the wall which was visible in the residents room.
k. room [ROOM NUMBER] revealed damaged drywall at the head of the residents bed.
l. room [ROOM NUMBER] bed B revealed multiple scratched areas in the drywall around residents bed.
During an interview on 08/25/23 at 12:00 PM the Maintenance Director stated he had worked at the facility for two years. He stated the building was over [AGE] years old, with 2 levels and a basement and there were many areas around the building that needed work. He stated that he had repaired some of the holes in the drywall in many of the resident rooms since he began working at the facility. He stated it seemed as though once the wall was repaired, over time the holes or scratches would reappear. He stated a lot of the damaged drywall around the resident beds in multiple rooms was due to the beds pushing against or hitting the wall causing damage to the walls. He stated it was on ongoing effort to try to keep all of the walls maintained and in good repair. He stated he relied on staff as well to place a work order when things needed immediate attention. He stated he would get the walls repaired as soon as possible.
During an interview on 08/25/23 at 5:00 PM the Administrator stated she was aware of areas in the building that needed to be repaired. She stated the building was over [AGE] years old and needed work. She stated there was a plan to remodel and she hoped that would occur soon due to the many areas that needed to be upgraded and repaired. She stated the Maintenance Director was responsible for keeping the walls in good repair but realized it was an ongoing effort to keep the building properly maintained due to the age of the building. She stated she would ensure that the walls in the residents rooms get repaired immediately
MINOR
(B)
Minor Issue - procedural, no safety impact
Assessment Accuracy
(Tag F0641)
Minor procedural issue · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Resident #25 was admitted to the facility on [DATE] with a diagnosis that included Alzheimer's Disease.
A review of her annua...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3. Resident #25 was admitted to the facility on [DATE] with a diagnosis that included Alzheimer's Disease.
A review of her annual Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #25 was severely cognitively impaired. It further revealed she had no obvious or likely cavity or broken natural teeth. The Care Area Assessment (CAA) for dental was not triggered.
A review of Resident #25's current comprehensive care plan last revised on 8/7/23 did not reveal a focus area for dental.
On 8/22/23 at 9:06 AM an observation of Resident #25 revealed she had multiple black teeth broken to the gumline.
On 8/24/23 at 11:32 AM an interview with MDS Nurse #1 indicated she completed the dental section of Resident #25's annual MDS dated [DATE]. She stated she normally reviewed any dental notes and observed the resident's mouth if the resident would cooperate. She stated Resident #25 did have obvious cavity and broken natural teeth. She stated she made an error when she coded this section of Resident #25's annual MDS. MDS Nurse #1 stated fixing this would trigger an additional CAA and require a significant correction.
On 8/25/23 at 2:31 PM an interview with the Administrator indicated resident's MDS assessments should accurately reflect their condition.
Based on observations, staff interviews and record review the facility failed to accurately code Minimum Data Set (MDS) assessments to reflect Hospice Services (Resident #26), application of dressings and ointments to a wound (Resident #80), and dental status (Resident #25) for 3 of 26 residents whose MDS assessments were reviewed.
Findings included:
1. Resident #26 was admitted to the facility on [DATE] with diagnoses that included Alzheimer ' s disease with late onset, adult failure to thrive and Hospice Care.
Review of a Hospice progress note dated 07/11/23 documented the Hospice Care Plan had been reviewed. Monthly progress notes were on file and reviewed.
A quarterly Minimum Data Set (MDS) assessment dated [DATE] documented Resident #26 had moderately impaired cognition. She had a life expectancy of less than six months to live. She was not receiving Hospice Services.
In an interview with the MDS Coordinator on 08/24/23 at 9:50 AM she stated Section O should have been coded to reflect Resident #26 was receiving Hospice Services. She noted Resident #26 had been admitted with Hospice Services and had no lapse in services since admission. She concluded it was a human error and she would file an assessment modification.
In an interview with the Administrator on 08/24/23 at 12:08 PM she stated that the Hospice Nurse came weekly to assess Resident #26. She stated she expected the assessment to be coded to reflect Resident #26 had received Hospice care.
2) Resident #80 was admitted to the facility on [DATE] with diagnoses that included, in part: a pressure ulcer of the sacral region Stage 4.
Review of the July 2023 Treatment Administration Record revealed dressings and ointments/medications were applied to the resident's wound during the assessment look back period on 07/05/23, 07/07/23, and 07/10/23.
Review of a quarterly MDS assessment dated [DATE] documented Resident #80 had one Stage 4 pressure ulcer that was present on admission. She had pressure relieving devices to her chair and bed. She received pressure ulcer care. She had not received dressings or ointments/medications for the wound.
In an interview with the MDS Coordinator on 08/24/23 at 9:50 AM she stated Section M of the MDS assessment for Resident #80 should have been coded to reflect that the resident had received dressings and applications of ointments/medications to the wound during the assessment period. She noted it was a human error and stated she would file an assessment modification to correct the error.
In an interview with MDS Nurse #10 on 08/24/23 at 10:00 AM she stated she had completed the assessment for Resident #80 and had no excuse for not coding the assessment to reflect the resident had received a dressing and ointments/medications to a wound during the assessment period. She commented that she simply made an entry error.
In an interview with the Administrator on 08/24/23 at 12:08 PM she stated she expected the assessments to be completed accurately.