Eddy Heritage House Nursing And Rehabilitation Ctr
Inspection history, citations, penalties and survey trends for this long-term care facility in Troy, New York.
- Location
- 2920 Tibbits Avenue, Troy, New York 12180
- CMS Provider Number
- 335760
- Inspections on file
- 15
- Latest survey
- November 26, 2025
- Citations (last 12 mo.)
- 9 (2 serious)
Citation history
Health deficiencies cited at Eddy Heritage House Nursing And Rehabilitation Ctr during CMS and state inspections, most recent first.
A resident admitted for respite care with multiple comorbidities received four incorrect doses of morphine due to a transcription error and incomplete verification process. The resident became unresponsive with unstable vital signs, but staff did not provide interventions to reverse the opioid effects or consistently monitor the resident's condition. Communication failures led to delays in notifying the family, hospice, and facility leadership about the error, and the resident died without documented evidence of appropriate assessment or intervention.
A resident with multiple comorbidities was administered four incorrect doses of morphine sulfate due to a transcription error during order entry, resulting in a total of 80 mg over 12 hours. The error was not identified by the triple check process or by staff administering the medication, and the resident, who had not previously received morphine, became unresponsive and died. Staff did not follow medication administration and error reporting policies, and concerns raised by the family regarding the resident's condition and possible use of Narcan were not acted upon.
Surveyors found that multiple residents did not receive their medications within the prescribed time frames, and medical providers were not notified of these delays as required by facility policy. LPNs cited heavy workloads, computer issues, and resident unavailability as reasons for late administration, and staff interviews confirmed that documentation of provider notification was lacking.
A resident admitted for respite care with multiple serious diagnoses was administered morphine sulfate by nursing staff who did not question the order or dosage because the resident was on hospice, despite no prior history of morphine use. Staff failed to assess or respond to the resident's unresponsiveness after medication administration, and concerns raised by family about the use of Narcan were dismissed. This resulted in compromised dignity and access to appropriate care.
A resident received multiple incorrect doses of morphine, and despite facility policy and agreements requiring immediate notification, neither hospice nor the resident's representative was promptly informed of the medication error. The error was discovered and corrected by an RN, who notified the physician but did not escalate the issue to administration or the DON, resulting in delayed communication with the family.
A resident received multiple incorrect doses of morphine sulfate due to a transcription error, resulting in unresponsiveness and death. Despite facility policy and regulatory requirements, the serious adverse event was not reported to the NYS DOH, as the administrator, after consulting with leadership, did not believe the death was related to the medication error.
A physician failed to provide adequate supervision and signed multiple inconsistent morphine orders for a resident on hospice respite care, resulting in the administration of 80 mg of morphine over 12 hours. Pharmacy staff repeatedly sought clarification due to conflicting dosages and concentrations, but the orders remained unclear, and there was no documented physician follow-up after the medication error was discovered.
A resident with dementia, end-stage renal disease, and atrial fibrillation received routine doses of morphine sulfate despite no documented pain or shortness of breath, and with pain levels recorded as zero at each administration. Facility staff failed to ensure medication administration was clinically justified, contrary to policy and professional standards.
Facility administration failed to provide effective oversight and resource allocation, resulting in neglect, a significant medication error involving morphine sulfate, and lack of proper reporting and communication. Leadership and clinical staff were unaware of the resident's decline and did not ensure timely investigation or notification, leading to compromised resident safety and regulatory noncompliance.
A resident with dementia, squamous cell carcinoma, and anemia reported that a staff member was rough and mean, causing a bruise. The facility failed to report this suspected abuse to the New York State Department of Health within the required two-hour timeframe, as mandated by their policy. Both the Assistant Director of Nursing and the Administrator acknowledged the reporting failure.
The facility failed to thoroughly investigate alleged violations of abuse, neglect, or mistreatment for five residents. Investigations lacked interviews, witness statements, and identification of causes or preventive measures, leading to incomplete investigations and a lack of preventive actions.
The facility failed to ensure immediate and thorough assessments for two residents, one with an injury alleged to be caused by abuse and another with new onset pain leading to a delayed fracture diagnosis. Staff did not follow procedures for immediate health concerns, resulting in deficiencies in care.
Failure to Prevent Neglect and Respond to Opioid Overdose
Penalty
Summary
A facility failed to protect a resident from neglect, resulting in the administration of four incorrect doses of morphine sulfate totaling 80 milligrams over a 12-hour period. The resident, who was admitted for respite care with diagnoses including dementia, end-stage renal disease, and atrial fibrillation, had not previously received morphine at home. The error originated from a transcription mistake during the medication reconciliation process, where three out of five morphine orders were entered incorrectly and the facility's triple check system was not fully completed, lacking a third verification signature. The error was discovered only after a nurse questioned the order, at which point the incorrect order was discontinued and a corrected order was entered. Following the medication error, the resident became lethargic and unresponsive, with unstable vital signs including low blood pressure and oxygen saturation. Despite these changes, there was no documented evidence that the facility provided interventions to reverse the effects of the opioid overdose, such as administering naloxone (Narcan), even after the family inquired about it. Additionally, there was a lack of documented monitoring, assessment, or treatment for the resident's decline after the error was identified. Vital signs and nursing assessments were not consistently recorded, and there was no evidence of physician oversight or coordination with hospice regarding the medication error. Communication failures further contributed to the deficiency. The resident's representative was not notified of the medication error until after the resident's condition had significantly deteriorated. Hospice was not informed of the medication error, and attempts to contact hospice during the resident's decline were unsuccessful due to incorrect contact information. Key facility leadership, including the Director of Nursing and Administrator, were not promptly informed of the incident, and staff interviews revealed a lack of awareness and documentation regarding the resident's condition and the actions taken. The resident ultimately expired without documented evidence of appropriate monitoring or intervention following the overdose.
Removal Plan
- Post Hospice contact information in each nursing unit and include on the face sheet for residents actively on Hospice.
- Make the contact for Community Hospice visible at accessible locations such as a nursing station on each resident unit.
- Ensure that for all residents enrolled in Hospice services, the contact number for Community Hospice is visible and accessible under contacts on the residents' face sheets in both electronic and paper charts.
- Update medication error reporting policy to require the Physician/Nurse Practitioner, upon notification of medication error, to provide direction for monitoring, duration of monitoring, and expected follow up communication.
- Require documentation of the nature of the incident, individuals notified (including family and hospice as applicable), actions taken, orders received, results of continued monitoring, assessments, and communication.
- In-service all on-call Physicians and Nurse Practitioners regarding high-risk medications and review of electronic ordering for safe dosing.
- Educate all nursing staff, including agency staff, by the nursing educator/designee on the updated Medication Error Reporting policy, including directions on provider and family notification as well as resident monitoring and documentation requirements.
- Use education sign-in sheets to document that in-house and agency nurses were educated; educate remaining agency nurses if they return to the facility.
- Compare transcribed orders with original provider order for accuracy; complete and document checks in the paper chart for the next two consecutive shifts.
- Educate all nursing staff (including agency staff) by the nurse educator, supervision, or designee regarding medication reconciliation, medication transcription, triple check, and safe medication administration practices.
- In-service all in-house and agency nurses regarding the abuse/neglect and mistreatment policy, with a special focus on potential neglect related to medication errors and lack of monitoring, assessment, and documentation related to change in condition.
Significant Medication Error Resulting in Resident Death
Penalty
Summary
A significant medication error occurred when a resident admitted for respite care with diagnoses including dementia, end-stage renal disease, and atrial fibrillation, was administered four incorrect doses of morphine sulfate, totaling 80 milligrams over a 12-hour period. The original hospice order specified morphine 5 mg by mouth every four hours as needed, but during the admission process, a transcription error resulted in the order being entered as 20 mg per dose. This error was not identified during the triple check process or by subsequent staff administering the medication. Multiple staff members, including registered nurses and licensed practical nurses, were involved in the medication administration and order entry process. The error was not questioned until after the fourth dose had been given, at which point a nurse reviewed the medication and brought the issue to the attention of supervisory staff. Interviews revealed that staff assumed the order was correct, particularly because the resident was on hospice care, and did not verify the appropriateness of the dose or question the high dosage of morphine being administered. The resident, who had not previously received morphine at home, became unresponsive and died following the administration of the incorrect doses. Family members raised concerns about the resident's condition and the potential use of Narcan, but were advised by facility staff and a physician that Narcan was not appropriate or effective at that time. The facility's policies on medication administration and error reporting were not followed, and the error was only identified after significant harm had occurred.
Removal Plan
- Narcotic orders were reviewed for ongoing appropriateness and safety by Medical Director #1.
- Narcotic orders were reviewed for ongoing appropriateness and safety. Immediate education was provided to Physician #1 and Licensed Practical Nurse #1, and the order was amended by Chief Nursing Officer #1 and Medical Director #1.
- All active medication orders were reviewed by the consultant pharmacists and medical director for ongoing appropriateness and safety.
- Administrator #1 worked with electronic ordering system creators to enable a feature to run reports that reflected ordering errors for closer daily monitoring.
- All on-call physicians and nurse practitioners were in serviced by the Medical Director #1 regarding high-risk medications and review of electronic ordering for safe dosing.
- The remaining physicians and nurse practitioners were inserviced.
- ‘Transcription of Orders' policy was developed to include information regarding medication reconciliation as well as the triple check process.
- Compared transcribed orders with original provider order for accuracy. Checks were completed and documented in the paper chart for the next two consecutive shifts.
- All nursing including agency staff will be educated by nursing educator/designee prior to start of shift on the updated Medication Error Reporting policy, which includes directions on provider and family notification as well as resident monitoring and documentation requirements.
- Education Sign-In Sheets titled Transcription- Triple Check- Medication Reconsolidation, Transfer report - hand off sheet, Neglect related to Resident Monitoring - Education sign-in sheets documented in house nurses and agency nurses educated. Agency nurses left to educate if they return to the facility.
- Chief Nursing Officer #1 stated that the medication nurse was educated regarding an end date needed for the order and printing orders to place in the chart to begin the triple check process.
- Medical Director #1, and/or Administrator #1 and/or Chief Nursing Officer #1 would check orders from the previous day.
- Nurse Managers were responsible for completing audits on triple check and would bring audit results to Quality Assurance monthly meetings.
- Surveyors verified the facility conducted a daily 24-hour look back on all new medication orders by Director of Nursing #1 or designee.
- Interviews with all parties responsible for these barrier checks showed they were aware of their required responsibilities.
Failure to Administer Medications Timely and Notify Providers
Penalty
Summary
Surveyors identified that the facility failed to ensure residents received medications in accordance with provider orders and professional standards of practice. Observations, interviews, and record reviews revealed that four residents did not receive their scheduled medications within the prescribed time frames. The facility's policy required medications to be administered as ordered, and for staff to notify medical providers if medications were given late. However, medications were consistently administered late across various units, and there was no documented evidence that medical providers were notified of these delays. Specific incidents included residents with complex medical conditions such as fractures, dementia, hypertensive crises, heart failure, and anxiety disorders. For example, one resident with hypertension and dementia was scheduled to receive a Lidocaine patch and Metoprolol at specific times, but these were administered late. Another resident with heart failure and respiratory issues received Bumetanide later than ordered, and questioned the nurse about the inconsistent timing. In each case, the responsible LPNs acknowledged the delays, citing reasons such as heavy medication passes, computer system issues, and residents being unavailable due to appointments or meetings. Despite staff awareness of the need to notify medical providers about late medication administration, there was no documentation of such notifications in the electronic medical record. Interviews with nursing staff confirmed that while they sometimes verbally informed providers, they often forgot to document these communications. The facility also relied heavily on agency nurses, and staff reported that high workload and frequent interruptions contributed to the delays in medication administration.
Failure to Ensure Dignified and Equal Care Due to Unquestioned Medication Error for Hospice Resident
Penalty
Summary
The facility failed to ensure equal access to quality care and uphold the rights to dignity and self-determination for a resident receiving hospice services. Staff did not question, assess, or respond appropriately to a significant medication error involving the administration of morphine sulfate. The resident, admitted for respite care with diagnoses including dementia, end-stage renal disease, and atrial fibrillation, had not previously received morphine at home according to both hospice records and statements from health care proxies. Despite this, staff administered morphine as ordered without verifying the appropriateness of the dose or the resident's prior exposure to the medication. Licensed Practical Nurses involved in the resident's care reported that they did not question the morphine order or dosage because the resident was on hospice, even though one nurse later acknowledged the dose seemed excessive. The medication was administered multiple times, and concerns about the dosage were only raised after several doses had already been given. Registered nursing staff also deferred to the hospice status of the resident, focusing on comfort rather than reassessing the medication order or the resident's response to the drug. Family members observed that the resident was unresponsive and could not be awakened after the administration of morphine. When concerns were raised about the resident's condition and the possibility of using Narcan to reverse opioid effects, facility staff and an unnamed physician advised against it, stating it was not safe or effective at that time. The lack of timely assessment and intervention following the medication error compromised the resident's right to dignified and appropriate care, as required by facility policy and federal regulations.
Failure to Notify Hospice and Resident Representative of Significant Medication Error
Penalty
Summary
A significant medication error occurred involving a resident who was admitted for respite care and received four incorrect doses of morphine sulfate totaling 80 milligrams over a twelve-hour period. Despite facility policies and a service agreement with hospice requiring immediate notification of significant changes or medication errors to hospice and the resident's representative, there was no documented evidence that hospice was notified of the error. Additionally, the resident's representative was not informed of the medication error until nearly three weeks later, as indicated by a progress note documenting a meeting with the family to review the events surrounding the resident's passing. Interviews revealed that after the error was discovered, the responsible RN discontinued the incorrect order, notified the physician, and obtained a new order, but did not inform the Director of Nursing or administration at that time. The administrator was not present during the incident and only became aware after receiving a voicemail from the resident's representative. The family had attempted to contact the DON but did not receive a response. The medical director confirmed that the family was not immediately informed about the medication error.
Failure to Timely Report Serious Medication Error Resulting in Resident Death
Penalty
Summary
The facility failed to ensure that an alleged violation involving neglect was reported immediately, as required by state and federal regulations. Specifically, a resident admitted for respite care received four incorrect doses of morphine sulfate totaling eighty milligrams over a twelve-hour period due to a transcription error. This medication error resulted in the resident becoming lethargic, unresponsive, and experiencing unstable vital signs, ultimately leading to the resident's death. Despite the family's inquiry about administering Narcan to reverse the opioid effects, the facility did not provide this intervention. Facility policy required that all serious adverse events, including medication errors resulting in harm, be reported to the New York State Department of Health (NYS DOH). However, there was no documented evidence that the event or the medication error was reported to the NYS DOH. During interviews, the administrator stated that they did not believe the resident's death was caused by the morphine administration and, after consulting with the executive director and medical director, decided not to report the incident. This failure to report was not in accordance with facility policy or regulatory requirements.
Physician Failed to Provide Proper Supervision and Accurate Medication Orders
Penalty
Summary
A deficiency was identified when a physician failed to provide proper supervision of medical care for a resident admitted for respite care under hospice services. The physician signed multiple, inconsistent orders for morphine sulfate oral solution with varying concentrations, dosages, and administration instructions within a short period. These orders included conflicting directions such as 5 milliliters every 4 hours, 1 milliliter every 4 hours, and one-time doses, leading to unclear and inaccurate medication instructions. As a result, the resident received 80 milligrams of morphine over a 12-hour period. Pharmacy records documented repeated attempts to clarify the morphine orders with facility staff and the physician due to concerns about dosing and concentration accuracy. Despite these efforts, the orders remained inconsistent, and the pharmacy had to intervene multiple times to clarify and authorize the correct dosages. There was also a request to access Narcan for the resident, but records indicate it was never administered. Interviews revealed that the physician was not typically responsible for respite residents but was asked to handle this resident's orders. The physician admitted to not carefully reviewing the orders, particularly the concentration and dosage, and did not realize the error at the time. After the medication administration issue was discovered, there was no documented evidence that the physician provided any follow-up instructions or care to the resident.
Unnecessary Administration of Morphine Without Clinical Indication
Penalty
Summary
The facility failed to ensure that a resident’s drug regimen was free from unnecessary medications, as required by policy and regulation. Specifically, morphine sulfate, a strong opioid, was administered as a routine, standing medication to a resident admitted for respite care, despite no documented clinical evidence of pain or shortness of breath. The medication administration record showed that morphine was given every four hours, with each administration accompanied by a documented pain level of zero. There was no evidence in the clinical documentation to support the need for morphine, and the resident had not previously used morphine at home nor exhibited pain during hospice visits. The resident in question had diagnoses including dementia, end-stage renal disease, and atrial fibrillation, and was rarely understood according to a mental status assessment. The facility’s own policies required that medications be administered according to provider orders and professional standards, and that clinical documentation reflect assessments, identification of problems, and responses to care. Despite these requirements, the administration of morphine was not supported by clinical findings, and a nurse later acknowledged that the dose was excessive and should have been identified as such.
Administrative Failures Lead to Neglect and Medication Error Resulting in Resident Death
Penalty
Summary
Facility administration failed to provide effective oversight, policy enforcement, and resource allocation, resulting in multiple deficiencies that compromised resident safety and well-being. Specifically, the facility did not ensure proper use of its resources, including staff, policies, and communication systems, to protect a resident. Deficiencies cited include failure to prevent neglect, significant medication errors, lack of resident dignity, failure to report adverse events to the State Survey Agency, and failure to meet professional standards of care. The facility also failed to ensure that the medical director fulfilled their responsibilities and that resident care was properly supervised by a physician. These failures collectively contributed to a medication error involving morphine sulfate, which was transcribed as a scheduled dose instead of as needed, and this error was not promptly identified or addressed. Interviews revealed that key leadership, including two Directors of Nursing and the Administrator, were unaware of the circumstances surrounding the resident's decline and death, and did not recall being notified or involved in the incident investigation. The Administrator attributed the medication error to confusing hospice orders and staff overstimulation, and stated that errors were reviewed only after the incident. The Medical Director acknowledged the event as a significant medication error, with family communication occurring later. The Administrator also indicated that guidance was sought from the Executive Director and Medical Director regarding reporting the incident to the State Department of Health, and was advised not to report it. These actions and inactions resulted in the facility's failure to ensure resident safety and compliance with regulatory requirements.
Failure to Report Suspected Abuse in a Timely Manner
Penalty
Summary
The facility did not ensure that all alleged violations involving abuse were reported immediately, but not later than 2 hours after the allegation was made. Specifically, an allegation of physical abuse reported by a resident on 5/15/2023 was not reported to the New York State Department of Health. The resident, who had diagnoses of dementia, squamous cell carcinoma, and anemia, reported that the staff member who dressed them that morning was rough and mean, causing a bruise on their right arm. The facility's policy required that such allegations be reported immediately, but this was not done. The investigation summary form documented that the resident reported the incident to two daytime Certified Nurse Aides, stating that the overnight aide was mean and rough, causing the bruise. Despite this, the section of the form titled Department of Health Notification was left blank, and no reports were submitted to the state. Both the Assistant Director of Nursing and the Administrator acknowledged that the incident should have been reported within two hours, but it was not. This failure to report the suspected abuse in a timely manner constitutes a deficiency in the facility's compliance with state regulations.
Failure to Thoroughly Investigate Alleged Violations
Penalty
Summary
The facility did not ensure all alleged violations of abuse, neglect, or mistreatment, including injuries of unknown source, were thoroughly investigated for five residents. Specifically, for Resident #1, the facility failed to conduct a thorough investigation when the resident alleged abuse by a Certified Nurse Aide, as the investigation lacked interviews and witness statements from staff working at the time of the incident and did not identify the cause of the bruise or steps to prevent reoccurrence. For Resident #2, the facility did not determine the cause of a fracture identified and did not include steps to prevent reoccurrence of injury for the resident. For Resident #3, the facility's investigation began five days after the resident's unwitnessed fall and did not identify the cause or corrective actions to prevent reoccurrence. Additionally, for Residents #4 and #5, the facility's investigations did not identify non-adherence to the residents' care plans as contributing factors and did not include appropriate corrective actions to prevent reoccurrence. The investigations lacked thoroughness, including interviews with all potentially involved staff and residents, and did not document changes to care plans or processes. The facility's policy on Abuse Prevention and Investigation was not followed, as investigations did not include a record of interviews, an explanation of evidence reviewed, or conclusions with a discussion of their basis. The facility failed to make necessary changes to care plans, policies, procedures, and staff education as identified by the investigations. This led to incomplete investigations and a lack of preventive measures for future incidents.
Failure to Ensure Immediate Assessment and Care
Penalty
Summary
The facility did not ensure that residents received treatment and care in accordance with professional standards of practice, the comprehensive person-centered care plan, and the residents' choices. For Resident #1, the facility failed to conduct an immediate and thorough assessment of an injury alleged to be caused by abuse. The resident reported to a Certified Nurse Aide that an overnight aide was rough during care, causing a bruise on the right arm. However, the medical record and investigation summary form lacked documentation of a Registered Nurse's assessment of the injury, including details such as the bruise's size, shape, color, or characteristics. The Assistant Director of Nursing confirmed that such an assessment should have been conducted immediately following the allegation. For Resident #2, the facility did not ensure an assessment of new onset pain, resulting in a delay of treatment for a fracture. The resident, who had diagnoses including hemiplegia and mild cognitive impairment, complained of left leg pain over several days. Despite multiple progress notes documenting the pain and swelling, there was no nursing or medical provider assessment until the resident's family intervened, leading to an x-ray that confirmed a fracture. The Assistant Director of Nursing and a Registered Nurse both stated that new onset pain complaints should have been assessed immediately and not merely placed in the Doctor's Book. Interviews with facility staff, including the Assistant Director of Nursing, a Registered Nurse, and a Physician, revealed that the facility's procedures for handling immediate health concerns were not followed. The Physician indicated that emergent issues should be directly communicated rather than placed in the Doctor's Book. The failure to promptly assess and address the residents' conditions led to deficiencies in the care provided to both residents.
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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