Mcauley Residence
Inspection history, citations, penalties and survey trends for this long-term care facility in Kenmore, New York.
- Location
- 1503 Military Road, Kenmore, New York 14217
- CMS Provider Number
- 335433
- Inspections on file
- 15
- Latest survey
- January 8, 2025
- Citations (last 12 mo.)
- 0
Citation history
Health deficiencies cited at Mcauley Residence during CMS and state inspections, most recent first.
A survey revealed that a suction machine and a portable lift in the facility were not inspected and tested according to manufacturer's recommendations. The suction machine had stickers from an outside contractor, but no inspection records were found. The lift's maintenance was overdue, and facility staff believed contractor visits were automatic, leading to oversight issues.
The facility's emergency generator was not properly maintained, with missing documentation for monthly load tests, weekly checks, and a four-hour continuous run. The generator's ability to meet 30% of its nameplate rating was unknown, and the main and feeder circuit breaker inspection was delayed. The facility lacked a Director of Plant Operations for a period, and maintenance records for 2024 were missing.
The facility failed to document the monthly testing of the Firefighter's Service in its two elevators, affecting all resident-use floors. Although the maintenance staff conducted the tests, they were not recorded. The new Director of Plant Operations expected documentation, but the facility had been without a director for some time, leaving uncertainty about past testing.
A survey found that exit signs in a LTC facility did not correctly indicate egress paths, affecting both resident-use floors. Signs lacked illuminated chevrons, misleading individuals about the correct exit routes. The Director of Plant Operations and the Administrator could not locate documentation of exit sign checks, despite claims of weekly inspections.
A survey revealed that fire-rated doors in the facility were not inspected and tested annually as required by NFPA standards. The Director of Plant Operations could not find documentation of these inspections, and the Administrator confirmed that records for NFPA 80 door inspections were not maintained, leading to a citation.
Medications for several residents were found unsecured on a shelf in a nurse's station without a door or lock, accessible to residents. Staff interviews revealed a lack of awareness and adherence to the facility's medication storage policy, with medications not being placed in secure locations like medication carts or locked cabinets. The Director of Nursing and Pharmacy Consultant confirmed the shelf was not a secure storage area, posing a potential safety issue.
A resident with complaints of tooth pain was not evaluated by a dentist, despite the facility's policy requiring a comprehensive oral assessment within 14 days of admission. The resident, who had conditions including dorsalgia and hemiplegia, consented to dental services but was not included in the schedule to be seen by the dentist. Interviews revealed a lack of communication and follow-up regarding the resident's dental complaints, leading to unmet dental needs.
A survey revealed that the facility stored 54 containers of alcohol-based hand sanitizer, totaling 17.1 gallons, in the basement without a flammable liquids storage cabinet, violating NFPA 30 code. The absence of a Director of Plant Operations led to continued ordering of supplies, resulting in excess storage. The facility also lacked a policy for storing such sanitizers.
A delayed egress door on the first floor of a facility failed to release after 15 seconds as designed, despite the alarm sounding. The malfunction was observed during a test by the Director of Plant Operations from a sister facility. The facility's policy requires regular testing, and logs indicated all doors passed recent tests, yet the door did not function properly during the survey.
Deficiency in Equipment Maintenance and Inspection
Penalty
Summary
During a Life Safety Code survey, it was found that patient care-related electrical equipment was not inspected and tested according to the manufacturer's recommendations. Specifically, a Brand A suction machine located on a crash cart in Unit 1 East had stickers from an outside contractor indicating upcoming preventative maintenance, but there was no record of the device in the contractor's inventory or any inspection having been performed. The Director of Plant Operations confirmed that the outside contractor was responsible for maintaining the suction machines, and in-house staff did not perform maintenance. However, the contractor admitted that their employee might have placed the stickers on the device without conducting proper inspection procedures. Additionally, nursing staff reported they did not perform maintenance tasks such as checking or replacing internal components of the suction machine. Similarly, a Brand B portable Hoyer-type resident lift in the 1 West Unit was found to have overdue preventative maintenance. The lift had stickers from the same outside contractor, but the last recorded inspection was on 11/15/23, indicating that the required twelve-month maintenance was overdue. The Director of Plant Operations stated that the outside contractor was responsible for maintaining the lifts, and the Director of Long Term Care Facilities believed that the contractor's visits were automatic and did not require scheduling by facility staff. This lack of oversight and communication led to the deficiency in ensuring that the equipment was properly maintained and inspected as per regulatory requirements.
Plan Of Correction
Plan of Correction: Approved February 5, 2025 What corrective action will be accomplished: The suction machine on 1 East Unit and the Hoyer-type resident lift on 1 West unit have been removed from service and will not return to service until preventative maintenance is completed. All residents have the potential to be affected by the same deficient practice. Facility suction machines and Hoyer-type resident lifts will be audited by outside contractor beginning (MONTH) 3, 2025 to ensure that timely preventative maintenance has occurred. Measures to be put into place include audit of facility suction machines (monthly) and Hoyer-type resident lifts (weekly) to ensure preventative maintenance has occurred. Maintenance staff will be educated to ensure suction machine and portable resident lift are inspected, tested, and maintained per manufacturer's recommendations. Facility will maintain documentation for their inspections, testing, and maintenance. How the corrective action will be monitored: The audits will be reviewed by Administration and reported to the Quality Assurance Committee. Plant Operations Director will be responsible to ensure compliance.
Emergency Generator Maintenance Deficiencies
Penalty
Summary
The emergency generator at the facility was not properly maintained, as evidenced by several deficiencies identified during a Life Safety Code survey. The generator, which provides emergency backup power to all resident use floors and the basement, had undocumented monthly load tests and weekly checks. Additionally, there was no record of a four-hour continuous generator run within the last 36 months, and the main and feeder circuit breaker inspection was not completed annually. It was also unknown if the generator met 30 percent of its nameplate kilowatt rating during load tests, as required. Interviews revealed that the facility was without a Director of Plant Operations for a period in 2024, during which the responsibility for generator maintenance fell to the Administrator. However, the Administrator was unable to locate maintenance records for 2024, and the Director of Plant Operations from a sister facility, who assisted during this time, was not specifically assigned generator maintenance duties. The Director of Long Term Care Facilities mentioned that an outside contractor had postponed the circuit breaker inspection, and a new date had not been scheduled. The facility did not have a specific policy for generator maintenance but followed the manufacturer's instructions.
Plan Of Correction
Plan of Correction: Approved February 5, 2025 Corrective Action for Affected Area: Load test was completed (MONTH) 29, 2025, and weekly visual inspections began week of (MONTH) 20, 2025. The generator is scheduled to be run under load for four continuous hours on (MONTH) 13, 2025; at this time, the load bank test will reach its 30% as listed on the name plate. Inspection of the main and feeder circuit breakers is scheduled for (MONTH) 20, 2025. All residents have the potential to be affected by the same deficient practice. Steps to prevent recurrence include weekly visual inspection of the generator, a 30-minute load test occurred (MONTH) 29, 2025, and will occur monthly. The generator is scheduled to be run under load for four continuous hours on (MONTH) 13, 2025. Inspection of the main and feeder circuit breakers is scheduled for (MONTH) 20, 2025. Steps to Prevent Recurrence: Weekly and monthly generator audit/log forms which include weekly inspection and monthly load are being utilized. Maintenance staff will be educated to ensure monthly generator load tests are completed and documented, weekly generator checks are completed and documented, the generator is run under load for four continuous hours every 36 months and documented, an annual load bank test is completed on the generator and documented, and main and feeder circuit breaker inspection is completed annually if the generator does meet 30 percent of its nameplate kilowatt rating during load tests. How Corrective Action Will be Monitored: The audits will be completed to ensure the generator is run under load for four continuous hours every 36 months and documented, an annual load bank test is completed on the generator and documented, and main and feeder circuit breaker inspection is completed annually if the generator does meet 30 percent of its nameplate kilowatt rating during load tests. Audits will be reviewed by Administration and reported to the Quality Assurance committee. The Plant Operations Director will be responsible to ensure compliance.
Failure to Document Monthly Testing of Elevator Firefighter's Service
Penalty
Summary
During a Life Safety Code survey, it was observed that the Firefighter's Service in the facility's two elevators was not tested monthly. This deficiency affected both elevators, which serve the basement, first floor, and second floor of the facility. An interview with the Director of Plant Operations revealed that although the in-house maintenance staff was conducting monthly tests of the Firefighter's Service, they were not documenting these tests. The Director of Plant Operations had just started working at the facility and expected the testing to be documented. Additionally, the facility had been without a Director of Plant Operations for a period from 2024 to 2025, and the Administrator was unsure if the Firefighter's Service was tested during that time.
Plan Of Correction
Plan of Correction: Approved February 5, 2025 Corrective Action for Affected Area: Director of Plant operations completed Firefighters Service on both elevators. Identification of other areas potentially affected: all residents have the potential to be affected by the same deficient practice. Both elevators had firefighters service completed. Steps to prevent further recurrence: Monthly audit to occur to ensure firefighters service is completed. Maintenance staff will be educated to ensure the firefighter's service is tested and documented for all of the facility elevators. How Corrective Action Will be Monitored: Monthly audits will be reviewed by Administrator and reported to quality assurance committee. Director of Plant operations will be responsible for compliance.
Improper Exit Signage and Documentation Issues
Penalty
Summary
During a Life Safety Code survey, it was observed that required exit signs in a long-term care facility did not correctly indicate the egress path, affecting both the first and second floors used by residents. On the second floor, an illuminated exit sign in the Activities Suite was mounted perpendicular to the suite entrance, with the word 'Exit' illuminated on both sides but without chevrons to indicate the correct path of egress. This misled individuals to believe the path of egress was into rooms without exits. The Director of Plant Operations confirmed that the chevrons should have been lit to indicate the main suite entrance as the egress path. Similar issues were found on the first floor in the 1 West and 1 East Units, where exit signs at stairway entrances lacked illuminated chevrons, misleading individuals to believe the path of egress was at the end of corridors with no exits. The Director of Long Term Care Facilities noted that many exit signs had been replaced months prior. Additionally, there was a lack of documented checks of illuminated exit signs, as confirmed by the Director of Plant Operations and the Administrator, despite claims from a Maintenance Technician that checks were conducted weekly.
Plan Of Correction
Plan of Correction: Approved January 31, 2025 Corrective action for affected area: The plant operations director corrected activities in the suite, 1 West Unit north/south stairway, 1 East Unit north and south stairway, and 2 West Unit north and south stairways exit sign chevrons so they illuminated and indicate the path of egress. Steps to prevent further recurrence: A walk-through of the facility has been conducted to identify any exit signs that needed adjustment; any needed corrections were made. Steps to prevent further recurrence: Use of a monthly exit sign audit where the auditor ensures the sign reflects the correct direction. Maintenance staff will be educated on the importance of ensuring the illuminated exit signs properly identify the path of egress. How corrective action will be monitored: Audits will be reviewed by administration and reported to the quality assurance committee. The plant operations director will be responsible for correction.
Failure to Maintain Fire-Rated Doors as per NFPA Standards
Penalty
Summary
During a Life Safety Code survey, it was found that fire-rated doors in the facility were not maintained according to the National Fire Protection Association (NFPA) requirements. Specifically, the fire-rated door assemblies were not inspected and tested annually as required. This deficiency affected all resident use floors and the basement. The facility's policy, effective from November 5, 2024, stated that all fire door assemblies should be inspected and tested annually, with a written record kept for review. However, upon reviewing the facility's maintenance inspection records, there was no documentation that met the NFPA 80 requirements. Interviews conducted during the survey revealed a lack of proper record-keeping and communication regarding the inspections. The Director of Plant Operations, who had just started working at the facility, was unable to locate any documentation of the required door inspections. A Maintenance Technician mentioned that doors were checked weekly and that the Administrator had the records. However, the Administrator confirmed that while they kept logs for testing delayed egress doors, they did not maintain records for NFPA 80 door inspections. This lack of documentation and adherence to the NFPA standards led to the citation.
Plan Of Correction
Plan of Correction: Approved February 5, 2025 Corrective Action for Affected Areas: All fire rated doors were inspected and tested. Identification of other areas potentially affected: All residents have the potential to be affected by the same deficient practice. The corrective action which took place was all fire rated doors were inspected and tested. Steps to prevent further recurrence: All fire rated doors were inspected/tested and will be inspected annually. Maintenance staff will be educated to ensure the facility's fire rated door assemblies are inspected and tested annually per National Fire Protection Association requirements. How will corrective action be monitored: Results of the fire rated doors inspection and testing is to be reported to the quality assurance committee by Plant Operations Director. Plant Operations Director will be responsible for compliance.
Unsecured Medication Storage in Nurse's Station
Penalty
Summary
The facility failed to store all drugs and biologicals in locked compartments, as observed during a survey on Unit 2 East. Specifically, 16 medications for seven residents were found unattended and unsecured on a shelf in the nurse's station, which lacked a door or means to lock the area. The medications included Chlorhexidine mouth rinse, Lactulose, Sorbitol, Ipratropium Bromide and Albuterol Sulfate inhalation, Citrucel Powder, Lanta liquid, Refresh tears, and Betadine solution. These medications were accessible to residents, as the nurse's station was located near a common area where residents were present, and there was no staff within visual view to monitor the area. Interviews with various nursing staff revealed a lack of awareness and adherence to the facility's medication storage policy. Licensed Practical Nurse #2 acknowledged the medications should not have been stored on the shelf and were unsure how long they had been there. Unit Manager Licensed Practical Nurse #4 and Licensed Practical Nurse #5 were unaware that overflow medications could not be stored on the shelf, and both confirmed that the nurse's station was not a secure location. Licensed Practical Nurse #3 noticed the medications but did not take action to secure them or inform the Nursing Supervisor. The Director of Nursing and the Pharmacy Consultant both confirmed that medications should be stored in a locked, secure area, and the nurse's station shelf was not appropriate for medication storage. The Pharmacy Consultant noted that storing medications on the shelf could potentially allow resident access, posing a safety issue. The facility's process for receiving medications involved the Nursing Supervisor delivering them to the appropriate unit, expecting staff nurses to secure them in a medication cart or locked cabinet, which was not followed in this instance.
Plan Of Correction
Plan of Correction: Approved February 5, 2025 **NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** **F761- Label/store Drugs and Biologicals** 1. What corrective action will be accomplished for those residents found to have been affected by the deficient practice? a. For Resident number 94 the eye drops were removed and ordered directly through pharmacy with patient label. b. For Resident number 267 the [MEDICATION NAME] was discarded. c. For Residents 17, 22, 68, 70, 72 immediately removed the medications from the unsecure shelf and placed all their medications in their locked med cabinet and or med cart. 2. How you will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken. a. All residents who receive medication and or biologicals have the potential to be affected by this deficient practice. b. On (MONTH) 9, 2025 the DON, ADON and Manager of the unit did a complete med audit. This included all shelves in the center of the unit near common areas where residents sit and no medications were found. An audit was also completed on all medication orders as they relate to supplies on hand. (01) 3. What measures will be put in place or what systemic changes you will make to ensure that the deficient practice does not reoccur. a. Three (3) cabinets on 2 east were identified to use for stock meds and overflow meds. Maintenance installed locks and all stock and overflow medications are now in the 3 locked cabinets located in the common area above the sink off the nurse’s station. The cabinets are located high on a wall that is in the common area to residents and staff and open to the nurse’s station; the cabinets will remain locked at all times. They are against the wall above the sink. The cabinets are sufficient to hold any overflow medications which do not fit in the locked medication cart and also for stock meds. No narcotics are stored in this area. The narcotics are kept in a double locked cabinet in the nurses stations. There is no overflow area necessary for narcotics. Nursing staff will unlock and obtain overflow medication/biologicals or stock meds as needed per specific orders for patients, lock the cabinet and bring the medication/biological directly to the respective medication cart to be administered and secured and stored. All RN’s, LPN’s will be in serviced by our ADON or nurse managers on all aspects of medication administration & storage, including proper receiving of medications and biologicals from pharmacy and the immediate delivery of the medications and biologicals to the appropriate secured storage area. All RN’s and LPN’s will have the P&P reviewed regarding Medication Cart audits, Medication room audits or medication cabinet audit, medication administration & documentation, storage of medication, and ordering and receiving medications from the dispensing pharmacy. (02) 4. How the corrective action will be monitored to ensure the deficient practice will not reoccur a. Our nurse manager or designee will be completing weekly audits in the common area and nurse’s station to ensure no medications are in an unlocked area. The manager will also conduct weekly medication cart and storage cabinet audits to ensure there are no discontinued medications. Medication administration audits will also be conducted yearly with each RN and LPN’s evaluations to ensure adherence to policy & procedure. (03) b. The nurse manager and or designee is responsible for conducting medication cart audits, medication room audits, medication storage audits, and audits of any medication storage cabinet and refrigerator storage of medications weekly on all Nursing units within TMR. Any negative findings will be addressed and corrected immediately. The results of these audits are given to quality and to the DON who also reports on them at our Quarterly Quality and Resident Safety Committee for review. (04) c. Any negative findings will be addressed and corrected immediately. The results of these audits will be reported by the DON at our Quarterly Quality and Resident Safety Committee for review. d. The pharmacy consultant agreed with the decision for the new location for stock and overflow meds and the security of medications. The pharmacy consultant will audit med storage areas every 2 weeks until we achieve 100% compliance for 8 consecutive audits. Thereafter, the pharmacy consultant will conduct spot audits and a full audit of med carts and med storage yearly throughout the building. (05) e. The Audits done by the nurse manager and or designee will be done weekly until we achieve 100% compliance over 8 consecutive weeks, after which, the findings will be reviewed by the Quality Assurance Committee for compliance. The Quality Committee will provide us with a schedule to follow for future medication cart and storage cabinet audits throughout the year. Medication administration audits will continue to be conducted yearly with each RN and LPN’s evaluations. The results of these audits will be given to the Quality Department and to the DON who also reports on them at our Quarterly Quality and Resident Safety Committee for review. f. While the primary responsibility for audits will be the unit manager, weekly audits may be done by a designee. The designee may include the DON, ADON, the Quality Team, other unit manager and or supervisor. The manager of each unit will be responsible for the delegation each week depending on staff schedules. 5. The date of the correction and the title of the person responsible for the correction of the deficiency. Date of Correction: (MONTH) 5, 2025 Person Responsible: Director of Nursing
Failure to Provide Routine Dental Care for Resident
Penalty
Summary
The facility failed to provide routine dental services to meet the needs of Resident #101, who had complaints of tooth pain while chewing but was not evaluated by a dentist. The facility's policy required that within 14 days of admission, a comprehensive oral assessment should be completed by a dentist or dental hygienist unless refused by the resident. However, Resident #101, who was admitted with conditions including dorsalgia, hemiplegia, and hypertension, did not receive the necessary dental care despite documented complaints of mouth or facial pain and difficulty with chewing. The nursing admission assessment noted Resident #101's complaints of mouth or facial pain, but there was no evidence in the nursing progress notes that the resident was seen by a dentist or that a medical provider was notified of the tooth pain. Although the resident consented to dental services, they were not included in the schedule of residents to be seen by the dentist. Interviews with nursing staff revealed a lack of communication and follow-up regarding the resident's dental complaints, and the Health Information Management Clerk did not keep track of referral forms for dental issues. The facility's dental contractor stated that the dentist was not informed of Resident #101's pain, and the resident was not seen during the dentist's visits to the facility. The Director of Nursing and the Administrator both expressed expectations that the resident should have been seen by the dentist, and that communication regarding dental complaints should have been made to ensure the resident's comfort and care. The deficiency highlights a breakdown in communication and adherence to the facility's dental care policy, resulting in unmet dental needs for Resident #101.
Plan Of Correction
Plan of Correction: Approved February 4, 2025 **NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** **F790 Routine/Emergency Dental Services in SNF’s** 1. What corrective action will be accomplished for those residents found to have been affected by the deficient practice? a. For Resident 101, Dent Serv was immediately notified of need for patient to be seen for dental pain while chewing, patient was in isolation for COVID and an appointment was made for patient when out of quarantine. Patient was seen by dental service on 1/27/25. 2. How you will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken? a. All residents have the potential to be affected by the same deficient practice. b. An MDS report was run on the most recent MDS completed on all in house residents questioning L0200F Mouth or facial pain, discomfort or difficulty with chewing. A look back period went from (MONTH) 2024 to [DATE]. No other resident’s triggered for this question. 3. What measures will be put in place or what systemic changes you will make to ensure that the deficient practice does not reoccur? a. All RN’s who complete admission assessments will be in-serviced on P&P CBC-NUR-402 community based dental care and notifying the medical provider immediately of any resident complaints related to mouth or facial pain, discomfort or difficulty with chewing. They will also be in-serviced on placing a call to our dental service to schedule a visit and fill out the Dental visit form with concern for visit and fax to the Dent Serv. b. C.N.A’s and nursing staff will be in serviced to notify the patients primary nurse and or nurse manager if any resident complains of any mouth or facial pain, discomfort or difficulty with chewing. c. All RN’s will be in-serviced to ensure all new admissions sign the dental consent service form, those who wish to receive dental services will be scheduled to have a comprehensive oral assessment by the dentist or dental hygienist within 14 days of admission. d. All nursing staff will be in-serviced to add any resident complaints related to mouth or facial pain, discomfort or difficulty with chewing to 24 hour report for Nurse Manager to bring to am report. This will also include the follow up to the medical and dental provider notification. 4. How the corrective action will be monitored to ensure the deficient practice will not reoccur? a. All new admissions and readmissions will be audited within 72 hrs. of admission by nurse manager or designee to see if dental service consent form is completed, signed and also to see if any resident complains of mouth or facial pain, discomfort or difficulty chewing. b. The DON will run the MDS analyzer report each week to see if there is any resident with any complaints of mouth or facial pain, discomfort or difficulty chewing for appropriate follow up. Any deficient findings would be corrected immediately. c. The ADON will complete an audit to be filled in after am huddle with the name of each resident who is on 24 hour report with complaints of oral pain and note that medical provider and dental provider were notified and follow up visit and care is documented. Any deficient findings would be corrected immediately. d. The results of these audits will be reported by the Director of Nursing at our quarterly Quality and Resident Safety committee for review. These audits will continue until we achieve 100% compliance for 8 consecutive weeks. 5. The date of the correction and the title of the person responsible for the correction of the deficiency Date of corrections: (MONTH) 5, 2025 Person Responsible: Director of Nursing
Excessive Storage of Alcohol-Based Hand Sanitizer
Penalty
Summary
During a Life Safety Code survey, it was observed that the facility stored an excessive amount of alcohol-based hand sanitizer in the basement, exceeding the allowable limit set by the 2012 NFPA 30 code. Specifically, 54 containers, each holding 1.2 liters of sanitizer with 76 percent alcohol content, were found on open shelving in the Main Storage Room, totaling 64.8 liters or 17.1 gallons. This storage practice did not comply with the requirement to store such quantities in a flammable liquids storage cabinet. The facility lacked a Director of Plant Operations for a period, during which another individual continued ordering supplies, inadvertently leading to the accumulation of excess sanitizer. Additionally, the facility did not have a policy in place regarding the storage of alcohol-based hand sanitizers.
Plan Of Correction
Plan of Correction: Approved February 5, 2025 Corrective action for affected area: The excess alcohol-based hand sanitizer was removed from the Main Store room. Identification of other areas potentially affected: All residents have the potential to be affected by the same deficient practice; all storage areas were checked for alcohol-based hand sanitizer. Steps to prevent further recurrence: Measures to be put in place include a monthly audit of the Main Store room to monitor the amount of alcohol-based hand sanitizer in stock. An updated policy was implemented to ensure safe use and storage of alcohol-based hand sanitizer. Maintenance staff will be educated to ensure containers of alcohol-based hand sanitizer in an aggregate amount of greater than ten gallons are not stored in a single smoke compartment outside of a flammable liquids storage cabinet. How corrective action will be monitored: Monthly audit will be reviewed by administration and reported to the Quality Assurance Committee. The Director of Plant Operations will be responsible to ensure compliance.
Delayed Egress Door Malfunction
Penalty
Summary
During a Life Safety Code survey, a deficiency was identified involving a delayed egress door locking mechanism on the first floor of a facility. The mechanism, which is designed to release the door after 15 seconds when pressure is applied, failed to function as intended. This issue was observed during a test conducted by the Director of Plant Operations from a sister facility, who noted that the door did not open even after 30 seconds of pressure, despite the alarm sounding. The doors in question were located outside the Physical Therapy Gym and were equipped with signs indicating that they should open after 15 seconds of pressure. The facility's policy, titled Fire and Egress Door Inspection and Maintenance, mandates regular testing of delayed egress doors to ensure proper operation. According to the facility's log, the doors were tested weekly for alarm function and monthly for the 15-second release function, with the most recent tests conducted in December 2024 showing all doors as passing. However, during the survey, the door failed to operate as designed, and the Director of Plant Operations was unable to explain the malfunction. This deficiency affected one of the two resident use floors in the facility.
Plan Of Correction
Plan of Correction: Approved January 31, 2025 Corrective action for Affected Area: Physical Therapy gym doors were repaired on 1/6/25. Identification of other areas potentially affected: All residents have the potential to be affected by the same deficient practice. All of the facilities delayed egress door locking mechanisms were audited and are in working order. Steps to prevent further recurrence: Maintenance staff were reeducated on exit door delayed egress testing. Weekly testing of exit door alarms with delayed egress is occurring. How corrective action will be monitored: Director of Plant Operations will conduct monthly audits on each door to assure delayed egress doors are working properly. Results will be reported to the quality assurance committee. Director of Plant Operations will ensure compliance.
Latest citations in New York
A resident with spastic quadriplegic cerebral palsy, severe hypoxic ischemic encephalopathy, chronic respiratory failure, and a tracheostomy was on continuous pulse oximetry with ordered SpO2 parameters and linked Vocera alerts. When the resident’s oxygen saturation dropped significantly, the Vocera system sent sequential alarms to the primary RN, buddy RN, charge RN, and RT. The primary RN repeatedly pressed “Accept” on the alert device without assessing the resident, while the buddy RN, charge RN, and RT did not respond to the alarms, each assuming others would intervene or not recalling the alert. For approximately 25 minutes, no assigned clinician assessed the resident despite ongoing alarms, until another RN, not assigned to the resident, heard an alarm while passing the room and found the resident unresponsive and gray. A Code Blue was initiated, CPR was performed, and the resident was transferred to the hospital, where they were found to have no brain activity and later died. The facility’s investigation determined that staff failed to respond to and appropriately manage the pulse oximetry/Vocera alerts and failed to maintain and use required communication devices as expected.
A resident with Parkinson’s disease, dementia with behavioral disturbances, and known exit-seeking behaviors, care planned with a wander alarm, eloped through a 3rd floor stairwell door whose alarm had been disabled days earlier by maintenance and security while addressing a wandering system issue. A plastic barrier was placed in front of the door, but the door remained accessible and unrepaired. Video showed the resident repeatedly attempting to exit, bypassing the barrier, trying to remove the wander device, and ultimately opening the door, falling into the stairwell, and leaving the unit. Staff observed the resident at the door but did not consistently redirect them, and the resident was later found outside the building by a visitor after staff realized the resident was missing and discovered the wheelchair in the stairwell.
Two residents with psychiatric and behavioral histories were waiting by an elevator in a lobby when one, known to have prior aggressive behavior and a care plan noting risk for physical aggression, removed a wheelchair armrest and struck the other in the forehead, causing a bump and laceration that required ED evaluation. Video, staff, and security accounts confirmed that the aggressor resident was able to access and weaponize the removable armrest in a common area despite prior documented altercations and behavioral concerns, and was only on 30‑minute checks at the time, resulting in a failure to protect another resident from physical abuse.
Staff failed to respond promptly to an oxygen alert alarm for a resident with spastic quadriplegic CP, severe hypoxic ischemic encephalopathy, chronic respiratory failure, severe cognitive impairment, and total dependence for ADLs, resulting in the resident being found unresponsive with gray skin and requiring a Code Blue, CPR, and hospital transfer where no brain activity was found and life support was later withdrawn. Despite facility policy requiring alleged or suspected neglect and serious bodily injury to be reported to the State Agency within 2 hours (or within 24 hours if no serious bodily injury), the Administrator was not notified until days after the event and the NYS DOH was notified four days after the incident; the DON reported they were initially unaware of the failure to respond to alarms or of the need to report the incident, and the Administrator stated they had not been informed of the Code Blue on the day it occurred.
Surveyors found that the facility failed to implement an effective infection surveillance and reporting process during a norovirus gastroenteritis outbreak and in its routine infection tracking. During the outbreak, only a single-day tracking sheet was completed for several residents with gastrointestinal illness on two units, and daily surveillance with updated symptoms and management was not maintained as required by facility policy. Despite receiving a directive from the state health department to submit a Nosocomial Outbreak Reporting Application for the identified cluster, the DON acknowledged that the report was never submitted. Additionally, monthly infection control line lists for residents on antibiotics for various infections lacked documentation of signs and symptoms, diagnostic and lab results, precautions used, and outbreak potential, even though the IP relied on these lists for surveillance.
A resident with multiple chronic conditions and numerous scheduled medications had repeated discrepancies between scheduled morning medication times and documented administration times. On multiple days, all medications ordered for a 9:00 a.m. pass were documented as given around midday by an RN, contrary to policy requiring timely administration and immediate electronic documentation. The RN cited computer timeouts, possible late documentation, and workload pressures, while leadership acknowledged that a single nurse was responsible for passing medications to roughly 40 residents within a limited time window and that MAR review was primarily done by the passing nurse and through monthly reports, with no routine MAR review by the pharmacy consultant.
The facility did not ensure residents understood how to file grievances and failed to document and track grievances and their resolutions. Residents reported that they only voiced concerns during resident council and were unclear about the grievance process otherwise, and the designated Grievance Officer could not produce a grievance log or forms. The DON acknowledged the grievance process was informal and lacked clear documentation. In addition, a resident with significant cardiac and neurologic conditions and moderately impaired cognition had a representative who raised multiple concerns about care coordination, communication, discharge planning, call bell response, personal property, preferences, and nutrition, but these grievances were largely handled verbally, with no consistent documentation of how each concern was addressed or resolved.
Surveyors found that the facility failed to provide timely toileting assistance and call bell response for multiple residents who were dependent on staff for ADLs. A resident with Parkinson’s disease and dementia, care planned for two-hour toileting checks, was found by family with urine-saturated clothing and wheelchair cushion after a CNA admitted not changing or checking on the resident for most of a shift, and documentation showed numerous missing toileting and check entries over several months. Another resident with a history of stroke and MI, requiring maximal assist for toileting, reported long waits for morning care while the call bell rang, with staff not responding for extended periods, and the resident’s representative described multiple episodes of call bell waits exceeding an hour. Resident Council minutes, call bell audits, and observations showed repeated long call bell wait times, including bells ringing for 15–45 minutes while various staff passed the rooms without responding, and a spouse reported frequent overnight calls from a resident seeking help because call bells were unanswered.
A resident with bowel incontinence and new-onset loose, watery stools and nausea had a physician and NP order for a stool bacterial detection panel with C. difficile and a GI PCR, along with PRN Zofran. Over subsequent shifts, documentation showed the resident remained incontinent of bowel and that the ordered stool collection was repeatedly marked on the TAR as "not administered, unable to obtain" by LPNs, despite multiple incontinence episodes. There was no documentation that the NP or physician were notified that the ordered stool specimen had not been collected, even though facility policy required practitioner notification when orders were not carried out and the physician and NP later stated they expected to be informed if a lab test they ordered was not completed.
A resident with vascular dementia, behavioral disturbances, and dependence for transfers and toileting was sent to the hospital for suspected GI bleeding, with documentation indicating an unplanned hospital transfer and anticipated return. An IDT meeting held earlier did not document any discharge planning, and the resident’s care plan lacked a planned discharge. While the resident remained hospitalized, the facility issued a same-day discharge notice citing inability to meet needs and endangerment to others, based on interference from the resident’s guardians rather than documented resident behavior, and later did not accept the resident back after medical clearance. The medical record contained no IDT discharge plan and no subsequent nursing or social work notes, demonstrating a lack of documented discharge planning and coordination.
Failure to Respond to Pulse Oximetry Alarms for Tracheostomy-Dependent Resident
Penalty
Summary
The deficiency involves the facility’s failure to ensure that a resident requiring respiratory care and continuous pulse oximetry monitoring received services consistent with professional standards of practice and the resident’s care plan. The resident had spastic quadriplegic cerebral palsy, severe hypoxic ischemic encephalopathy, and chronic respiratory failure, was severely cognitively impaired, and was totally dependent on staff for all ADLs. The care plan and physician’s orders required mechanical ventilation with CPAP to tracheostomy collar overnight, humidified trach collar oxygen during the day, and maintenance of oxygen saturation above 92%, with pulse oximeter alarm parameters set to alert below 92%. The resident was equipped with a pulse oximeter linked to the Vocera alert system, which generated alarms at the bedside and on staff mobile devices when oxygen saturation fell outside ordered parameters. On the day of the incident, the resident’s oxygen saturation dropped to 84% at 8:58 AM, triggering an alert to the primary RN via the Patient Safe Solutions/Vocera system, followed by sequential escalation to the buddy RN, the charge RN, and the RT when not acknowledged. The Call Point Detailed Activity Report showed that an alert was sent to the primary RN at 8:58 AM, to the buddy RN at 8:59 AM, and to the charge RN and RT at 9:01 AM. The primary RN pressed “Accepted” on the device at 9:04 AM, and again when the system alerted at 9:17 AM and 9:18 AM, but did not go to the resident’s room to assess the resident and did not document any assessment or intervention. The buddy RN reported not recalling hearing the alert and stated they were administering medications and unaware of the resident’s distress until the rapid response was called. The charge RN acknowledged receiving the alert but did not respond timely, stating they expected the primary or buddy nurse to respond. The RT stated they received the alert but were busy with other residents and expected other staff to respond. From 8:58 AM to 9:23 AM, no assigned nurse or RT responded to the alarms or performed a clinical assessment of the resident, and the alarm cycle continued without intervention. At 9:23 AM, a second alert was triggered when the resident’s oxygen saturation dropped to 52%. An RN who was not assigned to the resident heard an alarm while passing the room, entered, and found the resident in a wheelchair, unresponsive with gray skin. This RN activated a rapid response/Code Blue, assisted in returning the resident to bed, and another RN began chest compressions. EMS was called and arrived at 9:44 AM; a pulse was briefly restored, and the resident was placed on a ventilator and transferred to the hospital, where they were determined to have no brain activity. Life support was later terminated and the resident expired. The facility’s own investigation concluded that nursing and respiratory staff failed to respond to alarms, failed to appropriately acknowledge and review alerts, failed to maintain accessibility to required communication devices, and failed to escalate when they were occupied or unable to respond, resulting in actual harm and Immediate Jeopardy to the resident and placing other monitored residents at risk.
Removal Plan
- Review camera footage, Patient Safe Solution phone verification notifications, and the pulse oximetry policy.
- Re-educate involved staff on pulse oximetry alarm response, notification handling, and escalation expectations.
- Send voice alarm presentation via email to all assistant nurse managers and assistant directors of nursing for review during evening and morning huddles.
- Ensure Vocera device functionality is reviewed and staff are instructed to keep devices accessible and operational.
- Have IT/MIS check and confirm monitoring equipment is functioning properly.
- Implement disciplinary action for staff involved.
- Discuss and initiate a root cause analysis.
- Review and revise the pulse oximetry policy.
- Provide leadership oversight.
- Implement an audit of alert response times.
Elopement of High-Risk Resident Through Disabled Stairwell Door Alarm
Penalty
Summary
The deficiency involves the facility’s failure to provide adequate supervision and maintain a safe environment for a resident with known exit-seeking behaviors and elopement risk. The resident had diagnoses of Parkinson’s disease, dementia with behavioral disturbances, and anxiety, and was assessed as having moderately impaired cognition. The resident’s MDS documented exit-seeking behaviors and daily use of a wander/elopement alarm, and the comprehensive care plan identified the resident as an elopement risk/wanderer related to disorientation to place, with an intervention for a wandering device on the ankle. A physician’s order also specified a wandering device to the right ankle with checks every shift. The 3rd floor North stairwell door alarm had been disabled by maintenance following a work order dated 07/02/2024. Maintenance and security staff attempted to address a wandering system alarm issue, and the alarm on the 3rd floor North stairwell door was turned off by removing a screw from the alarm box. A yellow plastic accordion-style barrier was placed in front of the door, and nursing staff were notified that the door was broken. However, the door itself remained accessible, and the alarm remained disabled for days prior to the elopement. Staff on the unit, including CNAs, were not all aware that the stairwell door was broken, and the door was not repaired until 07/17/2024. On the day of the incident, video footage showed the resident repeatedly exit-seeking at the 3rd floor North stairwell door over several hours. The resident moved the yellow barrier, wheeled around it, and closed it behind them. At one point, two unidentified staff observed the resident at the door, opened the barrier, and walked away without redirecting the resident. The footage documented multiple attempts by the resident to exit, including attempts to remove the wander alert bracelet and repeated efforts to push on the delayed egress bar with their leg and hands. Eventually, the resident stood from the wheelchair, pushed the crash bar, opened the door, and fell backwards into the stairwell while pulling the wheelchair through. The resident then maneuvered the wheelchair into the stairwell and exited the unit. Staff later discovered the resident missing, found the wheelchair in the stairwell, and the resident was ultimately located outside the building by a visitor and brought back inside by nursing and security. The DON’s investigation summary identified the root cause of the elopement as the 3rd floor North stairwell door alarm being disabled while the door remained broken and unsecured.
Removal Plan
- Resident #1 was placed on 15-minute safety checks and kept under line-of-sight supervision when outside of their room; continued with use of a wander alert device; and resided in a room adjacent to the nursing station for frequent observations.
- All staff were educated on the Elopement policy and what measures to take if a resident went missing, including a power point presentation and post-tests.
- All exit and stairwell doors in the facility on the 2nd and 3rd floors were repaired by an outside vendor.
Failure to Prevent Resident-to-Resident Physical Abuse in Lobby Elevator Area
Penalty
Summary
The deficiency involves the facility’s failure to protect a resident from physical abuse by another resident, despite a known history of aggressive behavior. One resident with paraplegia, mood disorder, major depressive disorder, and anxiety disorder had an established care plan noting potential for physical aggression and risk of being abused. Prior documentation showed that this resident had been involved in a physical altercation with another resident in June of the previous year, during which they reported being punched and stated they hit the other resident back. The care plan was updated at that time to reflect that the resident was abused by peers, with interventions including relocation as needed and a psychiatry referral, but later updates reflecting another resident-to-resident altercation did not include new interventions. On the day of the incident, video surveillance and witness statements documented that the aggressive resident and another resident were waiting at the elevator in the lobby, along with other residents. The second resident, who had diagnoses including schizophrenia and bipolar disorder, approached and stood next to the first resident’s wheelchair. The first resident was seen making hand gestures, then removed the left wheelchair armrest and used both hands to swing it toward the second resident. When the second resident reached toward the armrest, the first resident struck them on the forehead with the armrest, causing bleeding and resulting in a bump and small laceration. Staff arrived immediately after the assault and separated the residents, and the injured resident was later assessed and transferred to the hospital for evaluation. Interviews conducted after the event revealed differing accounts of the interaction leading up to the assault. The first resident reported that the second resident had previously used a racial epithet toward them and, on the day of the incident, again stood close, touched their shoulder, and repeated the racial epithet, prompting them to remove the armrest and strike the other resident. The second resident stated they were standing at the elevator, heard the first resident saying something, ignored it, and were then struck without warning. A security guard reported hearing the first resident tell the second resident not to stand close and to stop touching them, then observed the first resident swinging the armrest and hitting the second resident. Facility staff, including the RN Supervisor and DON, acknowledged that the incident occurred off the unit, that the aggressive resident had a history of verbal and physical abusive behavior toward staff, and that this was the first documented physical altercation between these two specific residents. Despite prior behavioral incidents and care plan documentation of aggression risk, the resident was on 30‑minute checks and was able to access and weaponize a removable wheelchair armrest in a common area, resulting in physical abuse of another resident.
Failure to Timely Respond to Oxygen Alarm and Report Suspected Neglect
Penalty
Summary
Facility staff failed to immediately report an alleged incident of neglect involving a resident who was dependent on respiratory support and continuous monitoring. The resident had spastic quadriplegic cerebral palsy, severe hypoxic ischemic encephalopathy, chronic respiratory failure, was severely cognitively impaired, and totally dependent on staff for all ADLs. On the date of the incident at 8:58 AM, the resident’s alert alarm indicated decreasing oxygen levels, but nursing and respiratory staff did not respond to the alarm or assess the resident in a timely manner, in deviation from the facility’s pulse oximetry escalation pathway and alarm response procedures. The resident was later found unresponsive with gray skin, and a Code Blue was initiated. CPR was started, and the resident was transferred to the hospital, where they were determined to have no brain activity; life support was later terminated and the resident expired. Although the facility’s policy required that alleged or suspected violations involving mistreatment, neglect, or other reportable events be reported to the State Survey Agency and other appropriate authorities no later than 2 hours after forming the suspicion if serious bodily injury occurred, or within 24 hours otherwise, the incident was not reported in accordance with these time frames. The incident occurred on one date, the Administrator was not notified until a later date, and the New York State Department of Health was not notified until four days after the event. The DON stated they were unaware that staff had failed to respond to the alerts until reviewing the alert system report and interviewing staff, and also stated they were unaware the incident should have been reported to the Department of Health, while the Administrator confirmed they had not been notified of the Code Blue on the day it occurred.
Failure to Implement Effective Infection Surveillance and Outbreak Reporting
Penalty
Summary
The deficiency involves the facility’s failure to maintain and implement an effective infection prevention and control program during a norovirus outbreak and in its ongoing surveillance activities. During a norovirus gastroenteritis outbreak, the facility identified multiple residents with gastrointestinal illness on two units, as documented on an infection control tracking sheet for a single date. The facility’s policy on routine infection control surveillance required ongoing assessment of all residents for changes in symptoms or conditions indicative of infection, but surveillance tracking was only completed for one day and was not continued or updated with symptoms or management throughout the outbreak. The DON and the Infection Preventionist (IP) both acknowledged that surveillance tracking sheets should have been completed daily during the outbreak and that they did not know why this was not done. The facility also did not comply with state reporting requirements related to the outbreak. After the cluster of gastrointestinal illness cases was identified, the NYSDOH sent an email to the DON stating that submission of a Nosocomial Outbreak Reporting Application report was required for a single case of a reportable pathogen in a nursing home resident or a cluster of cases above baseline. The DON stated they were aware of this email but confirmed that the requested outbreak report was never submitted to NYSDOH. The DON further stated that NYSDOH should have been contacted immediately when the outbreak was discovered, and that they were not the DON at the time and did not know why the previous DON failed to submit the report. In addition to the outbreak-related issues, the facility’s ongoing infection surveillance line lists for several months were incomplete. The Infection Control Line List for January, February, and March documented residents on antibiotic therapy for various infections, including wound infections, respiratory infections, urinary tract infections, bacteremia, and Clostridium difficile. However, these line lists lacked documentation of infection signs and symptoms, diagnostic tests and laboratory results, the type of precautions used, and any indication of outbreak potential. During interview, the IP confirmed that they used the line list for surveillance and monitoring of residents with infections and on antibiotics, but acknowledged that the lists did not include the required clinical details and precautions. The DON also stated that the IP was responsible for ensuring surveillance included signs and symptoms, diagnostic tests with results, and precautions to prevent outbreaks.
Incomplete and Inaccurate Medication Administration Documentation for a Resident
Penalty
Summary
The deficiency involves the facility’s failure to maintain complete and accurately documented medical records in accordance with accepted professional standards for one resident. For this cognitively intact resident with essential hypertension, adjustment disorder with mixed anxiety and depressed mood, major depressive disorder, and dementia, standing medication orders included multiple daily and twice-daily medications such as antihypertensives, antidepressants, an anticoagulant, a diuretic, an antianginal patch, an inhaler, and other agents. The facility’s medication administration policy required that medications be administered in accordance with physician orders, that documentation of administration be completed on the computer immediately after administration with the nurse’s initials at the corresponding date and time, and that at the end of each shift the medication nurse review the MAR, 24‑hour report, and nurses’ notes to ensure documentation is accurate and complete. Record review of the medication administration audit report for multiple dates in December 2024 showed discrepancies between the scheduled 9:00 a.m. administration times and the times documented as administered for this resident’s medications. On thirteen separate dates, all medications scheduled for 9:00 a.m. were documented as being administered after 12:00 p.m. but before 1:00 p.m. when a particular RN was passing medications to this resident. These documented times did not align with the scheduled administration time and were inconsistent with the policy requirement that medications be given at the right time and documented immediately after administration. The pattern of late documentation occurred on each of the identified dates when that RN was responsible for the medication pass for this resident. In interviews, the RN who administered the medications stated that the resident received most medications at 9:00 a.m. and some at 5:00 p.m., and described issues such as the computer timing out after about 10 minutes, logging the nurse out, and situations where medications might have been given earlier but not clicked off in the system. The RN reported that the documented times (for example, showing around 12:00 p.m.) might not be accurate, could reflect late documentation, and could be affected by computer glitches, but could not recall specific details from the December dates. The Assistant DON reported that one nurse on the unit was responsible for administering medications to approximately 38–40 residents, that the incoming nurse’s start of shift included a narcotic count and report that delayed the start of the medication pass to about 8:30 a.m., and that this left about two minutes per resident to complete the pass by 10:00 a.m. The Administrator stated that their expectation was that nurses review the MAR at the end of the shift and that unit managers run a monthly report, while the Pharmacy Consultant stated they did not review MARs and assumed nursing conducted internal auditing. These practices and conditions contributed to incomplete and inaccurate medication administration documentation for the resident on the identified dates.
Failure to Inform Residents of Grievance Process and Document Grievances and Resolutions
Penalty
Summary
The facility failed to ensure residents were informed about the grievance process and that grievances were documented and tracked in accordance with its grievance policy. The Social Services/Admissions Coordinator, identified as the Grievance Officer, reported that while they interviewed residents and emailed Administration about complaints they could not resolve, they were unable to provide a grievance log or grievance forms. During resident council, multiple residents stated they voiced concerns in the meeting but did not know how to file grievances outside of that setting, and there was no documented evidence listing grievances or the facility’s responses. The DON stated that grievances should be monitored by Social Services with documentation of the nature of the complaint and the resolution, but acknowledged that the process was informal, dependent on circumstances, and not completely clear, with no forms or documentation used to track grievance progress and resolution. For one resident reviewed for care planning, the facility did not consistently address and document multiple grievances raised by the resident’s representative. This resident had diagnoses including cerebral infarction, occlusion and stenosis of the left carotid artery, and myocardial infarction, with the admission MDS indicating moderately impaired cognition and involvement of the resident and family in assessment and goal setting. The representative reported numerous concerns regarding miscommunication between nursing and rehabilitation, discharge planning, appointment scheduling, call bell response time, personal property, resident preferences, nutrition, and proper diet, all of which were communicated to Administration via email and paper copies. Although a family meeting was held to discuss these concerns, the Social Services/Admissions Coordinator and the DON confirmed there was no documented evidence of how each grievance was addressed or resolved, and that most concerns were handled verbally without formal documentation or investigation of every complaint.
Failure to Provide Timely Toileting Assistance and Call Bell Response
Penalty
Summary
Surveyors identified a deficiency in the facility’s failure to provide necessary assistance with toileting and timely response to call bells for residents who were unable to perform activities of daily living independently. Facility policy on Activities of Daily Living required that residents receive appropriate treatment and services to maintain or improve their ability to carry out ADLs, including elimination and toileting, and the facility’s No Pass policy required all staff to respond to call lights and obtain help if they could not provide it themselves. Despite these policies, multiple observations, interviews, and record reviews showed that residents did not consistently receive timely toileting care or call bell responses. One resident with Parkinson’s disease, dementia, heart disease, severely impaired cognition, and total dependence on staff for toileting and hygiene was care planned to be checked for incontinence and changed as needed, and to have toileting needs anticipated every two hours with assistance to the toilet. Kardex instructions for several months reiterated two-hour toileting checks and assistance, and CNA documentation reports for January through March showed numerous missing entries for toileting and two-hour checks across multiple shifts. A nursing home investigative report documented that a family member found this resident with urine-saturated clothing and wheelchair cushion in the afternoon, and the Administrator confirmed the saturation. The CNA identified as responsible for ADLs and accountability tasks for that shift stated they did not change the resident at all during the eight-hour shift, did not perform end-of-day care, and did not inform anyone that they were unable to care for the resident, and also stated they did not check on the resident until late morning. There was conflicting documentation on the assignment sheet, and another CNA reported that the resident was checked every two hours and could indicate when cleaning was needed, while a second family member reported having observed a strong urine smell on three Sunday visits in recent months, which staff addressed when notified. Another resident with a history of stroke and myocardial infarction, and moderately impaired cognition, required maximal assistance with toileting and moderate assistance with bathing and dressing. During one observation, this resident’s call bell was ringing, and the resident reported having waited a long time for care and stated they had been waiting since early morning; staff did not respond until several minutes after the surveyor’s observation began, at which time morning care was provided. On another day, the shared room call bell was ringing while two residents in the room reported they were still in bed, unwashed, undressed, and waiting to get out of bed, stating they had been waiting about half an hour; staff arrived to assist approximately 18 minutes after the surveyor’s initial observation. The resident’s representative reported multiple episodes when call bell response times exceeded one hour and had communicated these concerns to staff. The DON stated that call bells should be responded to when heard and that 30–60 minutes was not acceptable, but also indicated that response time depended on staffing. Additional evidence of delayed call bell response and unmet toileting needs came from Resident Council minutes, call bell audits, and direct observations. Resident Council minutes over several months documented ongoing resident reports that call bell wait times were “on the longer side” and “too long,” and that more nursing staff were needed, particularly on weekends when residents reported only three CNAs were often scheduled. Facility call bell audits conducted in response to complaints documented 23 observations, including one call bell active for 45 minutes and another for 15 minutes in the same room. During one observation, a room call bell rang for at least 14 minutes while multiple staff, including a CNA, a medication nurse, a social work/admissions coordinator, and a unit clerk, passed the room without entering; when the CNA finally entered, the resident requested a bedpan and the CNA left and did not return with the bedpan for another 10 minutes. In another observation, a room call bell rang for at least 27 minutes while a medication nurse, social work/administration staff, and a unit clerk were present in the hallway or nearby but did not respond to the bell. A spouse reported receiving at least 10 overnight phone calls from a resident asking them to call the nurses’ station because no one was responding to the call bell, and also reported that it took a long time for the nurses’ station to answer the phone.
Failure to Collect Ordered Stool Specimen and Notify Practitioner of Uncompleted Lab Test
Penalty
Summary
The deficiency involves the facility’s failure to ensure that a resident received treatment and care in accordance with professional standards and practitioner orders when a stool specimen was not collected as ordered, and the ordering practitioners were not notified. The facility’s policy dated 05/2025 required that when a physician or other authorized practitioner’s order is not carried out as ordered, delayed, modified, or discontinued, the practitioner must be notified. Resident #124 had diagnoses including moderate persistent asthma, essential hypertension, and spinal stenosis, and was documented as always incontinent of bowel and dependent on staff for toileting and hygiene per the care guide, care plan, and admission MDS. On 12/11/2024, the resident developed loose, watery stools and nausea, and the physician and NP were notified, resulting in orders for a stool bacterial detection panel with C. difficile and Zofran as needed. On 12/11/2024, nursing documentation showed that the resident had an episode of loose watery stool in the morning, with the physician notified and an order given to collect stool for testing. Later that day, an RN documented that the resident had nausea and loose stool, that the NP was made aware, and that stool collection and Zofran were ordered. The NP progress note that evening documented watery stool, ordered a GI PCR to rule out gastroenteritis, and planned to monitor the resident, noting stable vitals and a mildly elevated white blood count. The functional abilities record showed the resident was incontinent of bowel on multiple shifts on 12/11/2024, 12/12/2024, and 12/13/2024. The Treatment Administration Record for December 2024 documented the stool test order on 12/11/2024 and 12/12/2024, with entries by LPN #2 and LPN #3 indicating the stool collection was “not administered, unable to obtain.” Despite repeated incontinence episodes that could have provided opportunities to obtain a specimen, there was no documented evidence that the NP or physician were notified that the ordered stool sample had not been collected. A nursing progress note on 12/12/2024 at 2:24 A.M. documented that the resident was alert, able to make needs known, had poor appetite, good fluid intake, an episode of emesis after drinking water too fast, and was feeling better afterward, but did not address the outstanding stool order. During interviews, LPN #3 acknowledged awareness of the stool collection order and documented “not administered” on two shifts but did not write a note indicating that the NP or physician had been informed that the specimen was not obtained. The LPN Unit Manager stated that whether to notify the NP or physician when a stool sample was not collected was handled on a case-by-case basis. In contrast, the Medical Director/Primary Physician and NP #1 both stated they expected to be informed if a lab test they ordered, such as a stool specimen, was not completed, and NP #1 indicated they might have added additional orders and reminded staff to collect the stool if they had known it was not obtained.
Failure to Provide Appropriate Discharge Planning and Readmission for Hospitalized Resident
Penalty
Summary
Surveyors identified that the facility failed to ensure an appropriate discharge plan for one resident who was hospitalized for a suspected gastrointestinal bleed. The resident had vascular dementia with behavioral disturbances, sequelae of cerebral infarction, constipation, and atrial fibrillation, and was dependent for toileting and transfers with documented verbal and physical behaviors toward others. After the resident vomited coffee-ground emesis, the physician ordered a transfer to the hospital emergency department to rule out a GI bleed, and the discharge MDS reflected an unplanned discharge to a short-term general hospital with return anticipated. An interdisciplinary care plan meeting held prior to the hospitalization included multiple disciplines, the resident’s companion, and two guardians, but there was no documentation that discharge planning was discussed, and the resident’s care plan contained no evidence of a planned discharge. While the resident was in the hospital, the facility issued a same-day Transfer/Discharge Notice stating that the IDT had determined the resident would be discharged that day, citing that the resident’s needs could not be met after reasonable accommodation and that the safety and health of individuals in the facility would be endangered. The notice identified interference from the resident’s two guardians as the evidence supporting these reasons, but there was no documentation that the resident personally endangered the health or safety of others. The notice included information about the right to appeal the discharge, and the discharge was appealed. When the resident was medically cleared to return, the facility did not accept the resident back. Review of the electronic medical record showed no documented IDT discharge plan and no nursing progress notes after the date of hospital transfer, and no social work progress notes after that time, indicating a lack of documented planning and coordination related to the discharge decision.
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