Poudre Canyon Rehabilitation And Nursing, Llc
Inspection history, citations, penalties and survey trends for this long-term care facility in Fort Collins, Colorado.
- Location
- 1000 S Lemay Ave, Fort Collins, Colorado 80524
- CMS Provider Number
- 065166
- Inspections on file
- 20
- Latest survey
- May 15, 2025
- Citations (last 12 mo.)
- 0
Citation history
Health deficiencies cited at Poudre Canyon Rehabilitation And Nursing, Llc during CMS and state inspections, most recent first.
A nurse unfamiliar with the unit administered medications intended for another resident to a patient with dementia, epilepsy, and dysphagia, after failing to verify the patient's identity due to missing photo identification in the EMR and absent door nameplate. The patient experienced severe hypotension and required hospitalization. The error was attributed to multiple system failures, including lack of proper resident identification and non-adherence to medication administration protocols.
Multiple residents were not protected from abuse, including repeated alleged sexual abuse by a visitor and physical abuse between residents. In one case, a resident with severe cognitive impairment was subjected to inappropriate touching by a visitor on several occasions, with delayed and insufficient interventions by staff. The facility also failed to promptly investigate and report these incidents, and did not provide immediate staff education to prevent further occurrences. Additionally, two residents were involved in physical altercations without adequate preventive measures in place.
The facility did not submit final reports of abuse investigations to the State Agency within the required five-day period for multiple incidents, including physical and sexual abuse involving several residents and a visitor. Although initial reports were made and investigations completed on time, the final documentation was delayed due to the administrator's failure to submit them promptly.
The facility did not conduct thorough investigations into two abuse allegations, including one involving inappropriate sexual contact with a resident who lacked capacity to consent and another involving a physical altercation between two residents. Key interviews were not completed or documented, and there was a lack of evidence that effective interventions were implemented to ensure resident safety during the investigation process.
A facility failed to protect residents from abuse, with incidents involving inappropriate sexual behavior by a resident with a known history and physical altercations by another resident. Staff were not consistently informed or trained on monitoring requirements, leading to inadequate prevention and response to these incidents.
A facility failed to provide adequate supervision, resulting in a resident sustaining a head injury during a Hoyer lift transfer and another resident leaving the facility unsupervised twice. The first resident, with anoxic brain damage, hit her head on the lift due to erratic movements. The second resident, with dementia, left the facility without timely interventions, despite being at high risk for elopement.
The facility failed to provide palatable and attractive food, as evidenced by resident interviews and a test tray evaluation. Residents reported dissatisfaction with the taste, texture, and appearance of the food, and there was a lack of an alternative menu. A test tray evaluation found issues such as undercooked rice, salty gravy, and overcooked vegetables. The dietary manager did not effectively address these concerns.
The facility's QAPI program failed to address abuse prevention, leading to a repeat deficiency under F600. A resident with a history of sexually inappropriate behavior was not monitored, resulting in immediate jeopardy. Staff interviews revealed a lack of communication and oversight, as the resident's history was not discussed in QAPI meetings.
The facility failed to notify a physician in a timely manner when IV attempts for a resident were unsuccessful, and did not ensure timely review and follow-up of lab results for another resident. This led to deficiencies in care, as one resident's treatment plan was potentially impacted and another's condition deteriorated, requiring emergency room evaluation.
A facility failed to assess and document the use of bed rails for a resident, leading to a deficiency. The resident, with a history of epilepsy and cognitive deficits, had bed rails installed without a safety assessment, care plan, consent, or physician's order. Observations and staff interviews confirmed these oversights.
The facility had a medication administration error rate of eight percent due to an LPN failing to prime insulin pens before administering Novolog and Humalog to two residents. This oversight was observed during medication administration, where the LPN did not follow the manufacturer's instructions to prime the pens, leading to potential dosing inaccuracies. Interviews confirmed that priming is best practice to ensure correct dosing.
Two residents were administered insulin without proper priming of the insulin pens, leading to potential medication errors. An LPN failed to prime both Novolog and Humalog pens before administering doses, contrary to manufacturer recommendations. Interviews confirmed that priming is best practice to ensure correct dosing.
The facility failed to properly store and label medications, as observed in a medication cart on the secure unit. An expired bottle of nitroglycerin spray and an unlabeled container of nitroglycerin tablets were found. Staff interviews revealed that the usual practice of auditing medication carts for expired medications was not effectively implemented, leading to this deficiency.
The facility failed to ensure proper infection control practices, as a nurse did not use appropriate PPE during wound care for a resident on Enhanced Barrier Precautions, and a resident was observed using a personal cup to scoop ice directly from the ice box, contrary to sanitary guidelines.
The facility did not ensure the security of a utility room and a construction area, leaving them accessible to residents. The utility room door was repeatedly found open, exposing computer equipment, while a construction room contained tools and exposed plumbing. Staff interviews revealed a lack of awareness and oversight regarding these safety issues.
Significant Medication Error Due to Resident Misidentification
Penalty
Summary
A significant medication error occurred when a nurse administered medications intended for another resident to an 83-year-old resident with dementia, epilepsy, and dysphagia. The nurse, who was unfamiliar with the unit and the residents, failed to properly identify the resident before administering Lisinopril, Metformin, Seroquel, and Ramelteon—none of which were prescribed for the resident. The nurse did not confirm the resident’s identity using a photo in the electronic medication record (EMR) or a name on the door, as both were missing for this resident. The nurse addressed the resident by another resident’s name, and the resident’s representative did not correct her, leading to the administration of the wrong medications. Following the administration, the resident experienced severe hypotension and tachycardia, requiring transfer to the hospital for intravenous fluids and monitoring. The incident report and subsequent investigation revealed that the nurse realized the error only after returning to the medication cart. The nurse had not worked on the resident’s hall previously and relied on a report sheet that listed the wrong room number. The lack of proper resident identification systems, such as missing photos in the EMR and absent door nameplates, contributed to the error. It was also noted that 17 residents in the facility either did not have a photo in the EMR or a name on their door at the time of the incident. Interviews with staff confirmed that the nurse did not follow the facility’s medication administration policy, which requires verification of the resident’s identity using a photo and adherence to the six rights of medication administration. The nurse had previously made another medication error earlier in the month, which involved administering the wrong dose of a different medication. The facility’s investigation concluded that multiple system failures, including inadequate resident identification and failure to follow established procedures, led to the significant medication error and subsequent hospitalization of the resident.
Failure to Protect Residents from Abuse and Inadequate Investigative Response
Penalty
Summary
The facility failed to protect multiple residents from various forms of abuse, including sexual and physical abuse, as well as neglect, as evidenced by several incidents involving both visitors and other residents. In one case, a resident with anoxic brain damage and severe cognitive impairment was subjected to repeated alleged sexual abuse by a visitor, specifically her boyfriend. Despite staff witnessing inappropriate touching on multiple occasions and the resident being unable to consent due to her condition, the facility did not implement timely or effective interventions to prevent further incidents. There were delays in restricting the visitor's access, and staff were not immediately educated on measures to keep the resident safe during ongoing investigations. Additionally, the facility failed to conduct a thorough and timely investigation, including not promptly interviewing the alleged perpetrator and not submitting required reports to the State Agency within the mandated timeframe. In another set of incidents, the facility did not adequately protect two residents from physical abuse by each other. One resident, who had a history of wandering and cognitive impairment, entered another resident's room, leading to a physical altercation. The facility's response and preventive measures prior to the incident were not detailed, but the event highlights a lack of effective supervision and interventions to prevent resident-to-resident altercations, especially among those with known behavioral risks. Additionally, a separate resident was not protected from physical abuse by another resident in two separate incidents. The report details that the facility's policies required immediate investigation and protective measures when abuse was suspected or reported, but these were not consistently followed. The documentation shows that the facility's actions and inactions, including delayed or insufficient interventions, lack of timely staff education, and incomplete investigations, directly contributed to the deficiencies cited by surveyors.
Failure to Timely Submit Final Abuse Investigation Reports
Penalty
Summary
The facility failed to submit final reports of investigations into alleged abuse incidents to the State Survey and Certification Agency within the required five-day timeframe for four out of seven reported abuse allegations. The facility's policy required that all allegations of abuse, neglect, exploitation, or mistreatment be reported immediately to the administrator and appropriate agencies, with final investigation results submitted within five working days. Despite this, the facility delayed the submission of final reports for multiple incidents involving both physical and sexual abuse. Specifically, two separate physical abuse allegations involving two residents were reported initially to the State Agency, but the final reports were submitted 24 days after the deadline. Another physical abuse allegation involving two other residents had its final report submitted 11 days late. Additionally, a sexual abuse allegation involving a resident and a facility visitor was reported initially, but the final investigation report was submitted seven days after the required deadline. Interviews with the nursing home administrator (NHA) and the regional vice-president of operations confirmed that the NHA was aware of the five-day reporting requirement and acknowledged that the investigations themselves were completed on time. However, the NHA admitted to submitting the final reports late due to poor timing skills, resulting in noncompliance with state and federal regulations regarding timely reporting of abuse investigations.
Failure to Thoroughly Investigate Abuse Allegations
Penalty
Summary
The facility failed to thoroughly investigate two separate allegations of abuse, resulting in deficiencies in their response to both a sexual abuse allegation and a physical abuse incident. In the first case, a resident with severely impaired cognition and non-verbal status was allegedly inappropriately touched by her boyfriend, as witnessed by a CNA who heard the resident screaming. The CNA intervened and reported the incident, and the nurse on duty notified the nursing home administrator (NHA) and the police. However, the investigation did not include a direct interview with the witnessing CNA to clarify what was observed, nor was there documentation of an interview with the alleged assailant or evidence that the assailant was restricted from the facility during the investigation. Additionally, there was no documentation of staff education or interventions to ensure the resident's safety while the investigation was ongoing. The resident's capacity to consent to sexual activity was not assessed until after the incident, and despite a determination that the resident could not consent, effective interventions were not implemented to prevent a subsequent incident with the same individual. In the second incident, the facility failed to thoroughly investigate a physical altercation between two residents. The investigation did not specify whether any of the interviewed staff had witnessed or overheard the altercation, and there was no documentation that either resident involved was interviewed to understand the circumstances leading to the incident. The assistant director of nursing (ADON) conducted staff interviews, but these were not specific to the incident, and the NHA did not document attempts to obtain statements from the residents involved. Immediate interventions, such as placing stop signs to prevent further altercations, were mentioned, but the investigation lacked comprehensive documentation and failed to substantiate the abuse based on available statements. Both incidents demonstrate a lack of thoroughness in the facility's investigative process, including incomplete interviews, insufficient documentation, and failure to implement or document effective interventions to ensure resident safety during and after the investigation. The facility's actions did not align with its own policy, which requires immediate and comprehensive investigation of all abuse allegations, including interviews with all involved parties and thorough documentation.
Failure to Prevent Resident-to-Resident Abuse
Penalty
Summary
The facility failed to protect residents from sexual and physical abuse, specifically involving resident-to-resident interactions. Resident #50, with a known history of sexually inappropriate behaviors, was observed engaging in inappropriate touching of Resident #1. Despite being placed on 15-minute checks, staff interviews revealed a lack of awareness and inconsistent implementation of these checks. This failure to monitor and manage Resident #50's behavior put other residents at risk of sexual abuse. Additionally, Resident #43, who had a history of physical altercations, was involved in multiple incidents of physical abuse against other residents. These incidents included hitting, pushing, and grabbing residents #168, #169, and #25. The facility did not take adequate steps to prevent these altercations or protect the affected residents from harm. The facility's abuse policy, which mandates protection from all forms of abuse and immediate response to incidents, was not effectively implemented. Staff were not consistently informed or trained on the specific behaviors and monitoring requirements for residents with known aggressive or inappropriate behaviors. This lack of communication and training contributed to the facility's failure to prevent and address incidents of abuse, leaving residents vulnerable to harm.
Removal Plan
- Nursing Home Administrator (NHA) has assigned a one-to-one staff member to ensure that Resident #50 is prevented from perpetuating further sexual abuse of resident 1, 18 and other residents.
- The 1:1 staff assignment will continue until the interdisciplinary team is able to coordinate with Behavioral Health Solutions provider, speech therapist and medical director to determine a less restrictive plan of care.
- NHA or designee will inservice the one-to-one staff member regarding the responsibilities of the 1:1 staff member before the start of the shift.
- Director of Nursing (DON) or designee will complete education with all staff before their first shift back to work to ensure they receive updated training and education on Resident #50's care needs and behavioral interventions.
- DON or designee will complete a comprehensive medical record review and interviews with direct care staff to identify any residents with sexually inappropriate behaviors and update the comprehensive care plan and Kardex with effective interventions.
- DON or designee will complete interviews with all residents or resident representatives to identify any residents who have experienced unwanted touching and initiate abuse reporting and update the comprehensive care plan with effective interventions.
- DON or designee will complete education with all staff before their first shift back to work to ensure they receive updated training and education on resident-specific behavior interventions, reporting expectations including reporting any observed physical touching between residents to the abuse coordinator, accessing care plans and Kardexes and expectations for review of care plans and Kardexes at the start of each shift for any changes.
Inadequate Supervision Leads to Resident Injury and Elopement
Penalty
Summary
The facility failed to provide adequate supervision and prevent accidents for two residents, leading to significant incidents. One resident, who required a Hoyer lift and two-person assistance for transfers due to anoxic brain damage and erratic body movements, sustained a head laceration during a transfer. The incident occurred when the resident hit her head on the Hoyer lift bar, resulting in a laceration that required emergency department treatment and seven sutures. The facility's failure to monitor the resident's erratic movements closely during the transfer contributed to this injury. Another resident, diagnosed with senile degeneration of the brain and dementia, left the facility unsupervised on two occasions. Despite being identified as a high risk for wandering and elopement, the facility did not implement timely safety interventions. The resident first left the facility unsupervised to go to a gas station, and a second incident occurred without any interventions being put in place after the first elopement. The facility failed to conduct a Wander/Elopement Risk evaluation following the second incident, and a wander guard was not placed on the resident until several months later. The facility's policies and procedures for safety precautions and elopement prevention were not adequately followed, leading to these deficiencies. The lack of timely and appropriate interventions for both residents highlights the facility's failure to ensure a safe environment and adequate supervision to prevent accidents and elopements.
Facility Fails to Provide Palatable and Attractive Food
Penalty
Summary
The facility failed to provide food that was palatable and attractive, as evidenced by multiple resident interviews and a test tray evaluation. Several residents expressed dissatisfaction with the taste, texture, and appearance of the food. They reported that the food was not good, with some residents noting that the quality depended on who was cooking. Additionally, there was a lack of an alternative menu, and the kitchen often closed before residents could request different options if they were dissatisfied with their meals. The resident group interview further confirmed these issues, with comments about the food being questionable, not looking good, and being too spicy. The dietary manager was noted to not address or resolve these concerns effectively. The review of food committee meeting minutes from October 2024 to January 2025 showed that residents had previously expressed concerns about the food, such as wanting more fruit and less salty food, but there was no documentation of actions taken to address these issues. During a test tray evaluation, surveyors found the food to be unpalatable, with undercooked rice pilaf, salty gravy, hard meatballs, and overcooked brussel sprouts. The dietary manager, when interviewed, claimed that residents were satisfied with the food choices and did not acknowledge the issues with the rice pilaf.
Failure to Address Abuse Prevention in QAPI Program
Penalty
Summary
The facility failed to implement an effective Quality Assurance Performance Improvement (QAPI) program to identify and address compliance concerns, specifically related to abuse prevention. During a recertification survey, the facility was cited for failing to maintain compliance with abuse prevention standards, as evidenced by a repeat deficiency under F600. Initially cited at a G level for isolated actual harm, the deficiency escalated to a K level, indicating a pattern of immediate jeopardy to residents' health and safety. This was due to the facility's failure to monitor a resident with a known history of sexually inappropriate behavior, which was not addressed in QAPI meetings. Interviews with facility staff revealed gaps in communication and awareness regarding the resident's history of inappropriate behavior. The Nursing Home Administrator (NHA) acknowledged that the resident's history was documented but not acted upon until an incident occurred. The Medical Director was unaware of the resident's history until after the incident, indicating a lack of communication and oversight. Despite monthly QAPI meetings, the issue of sexually inappropriate behaviors was not identified as a problem, contributing to the deficiency.
Failure to Ensure Timely Physician Notification and Lab Result Follow-Up
Penalty
Summary
The facility failed to ensure timely notification of a physician when attempts to start an intravenous (IV) line for a resident were unsuccessful. Resident #167, who had severe cognitive impairment and required extensive assistance, experienced a change in condition with symptoms such as falls, shortness of breath, and decreased urine output. Despite a physician's order for immediate IV fluids, the nursing staff was unable to start the IV and did not notify the primary care physician (PCP) until the following day. This delay in communication potentially impacted the resident's treatment plan. Additionally, the facility did not ensure timely review and follow-up of laboratory results for Resident #64, who had a history of type 2 diabetes, stroke, and hypertension. The resident's physician ordered lab work due to changes in the resident's behavior, such as skipping meals and smoke breaks. Although the lab work was completed and submitted to the facility, there was no documentation indicating that the physician reviewed the results or provided feedback. The facility also failed to follow up with the physician when feedback was not received, and the resident's condition deteriorated, leading to an emergency room visit. Interviews with staff, including the Director of Nursing (DON) and the Nursing Home Administrator (NHA), revealed a lack of adherence to the facility's policy for notifying physicians of changes in a resident's condition. The DON stated that orders from physicians should be completed immediately unless there is another emergency, and if a nurse is unable to carry out an order, the physician should be notified right away. However, in both cases, there was a failure to communicate effectively with the physicians, resulting in deficiencies in the quality of care provided to the residents.
Failure to Assess and Document Bed Rail Use
Penalty
Summary
The facility failed to use a person-centered approach in determining the use of bed rails for a resident, leading to a deficiency. The facility did not assess the resident for the safe use of bed rails, including the risk of entrapment, before installing them. Additionally, the facility did not create or document a personal care plan for the safe use of bed rails, nor did they obtain consent from the resident or the resident's representative after discussing the risks and benefits. Furthermore, the facility did not obtain a physician's order for the bed rails or conduct quarterly assessments to evaluate their continued need and safety. The resident involved was a 65-year-old with a history of generalized idiopathic epilepsy, cognitive communication deficit, traumatic brain injury, sleep apnea, depression, and GERD. Despite being cognitively intact and requiring assistance with activities of daily living, the resident's comprehensive care plan and electronic medical record lacked documentation regarding the use of bed rails. Observations revealed that bed rails were installed without proper assessment or consent, and staff interviews confirmed that the necessary assessments were not completed prior to installation.
Medication Administration Errors Due to Failure to Prime Insulin Pens
Penalty
Summary
The facility failed to maintain a medication administration error rate below five percent, with an observed error rate of eight percent. This deficiency was identified during a survey where two errors were noted out of 25 opportunities for error. The errors involved the administration of insulin using Novolog and Humalog pens without priming them as per the manufacturer's instructions. Priming is essential to remove air from the needle and cartridge, ensuring the correct dose is administered. The failure to prime the insulin pens was observed during medication administration for two residents. In the first instance, an LPN administered 22 units of Novolog insulin to a resident with a blood sugar level of 352 mg/dl without priming the pen. Similarly, in the second instance, the same LPN administered eight units of Humalog insulin to another resident with a blood sugar level of 227 mg/dl, again without priming the pen. Interviews with the nurse practitioner and the director of nursing confirmed that priming the insulin pen is considered best practice to ensure the resident receives the full dose of insulin. The failure to prime the insulin pens led to the medication administration errors noted in the report.
Failure to Prime Insulin Pens Leads to Medication Errors
Penalty
Summary
The facility failed to ensure that residents were free from significant medication errors, specifically in the administration of insulin. Two residents, identified as Resident #18 and Resident #46, were administered insulin without the proper priming of the insulin pen, as observed during medication administration. The Novolog and Humalog insulin pens were not primed before administering the doses, which is against the manufacturer's recommendations. This failure to prime the insulin pens could result in the residents receiving incorrect doses of insulin. During the observations, LPN #1 was responsible for administering the insulin to both residents. For Resident #18, the LPN prepared 22 units of Novolog insulin without priming the pen, and for Resident #46, eight units of Humalog insulin were prepared and administered without priming. Interviews with the nurse practitioner and the director of nursing confirmed that priming the insulin pen is considered best practice to ensure the correct dose is administered. The facility's failure to follow these procedures led to the deficiency noted in the report.
Medication Storage and Labeling Deficiency
Penalty
Summary
The facility failed to ensure that medications and biologicals were properly stored and labeled according to professional standards. During an observation of the medication cart and treatment cart on the secure unit, it was found that there was a bottle of nitroglycerin lingual spray with an expiration date of June 2023 and a container of nitroglycerin sublingual tablets that lacked a label indicating which resident it belonged to. This indicates a failure to remove expired medications and to ensure all medications are labeled with resident information. Interviews with staff revealed that the usual practice was for the night shift nurse to audit the medication carts for expired medications. However, this process was not effectively implemented, as evidenced by the presence of expired and unlabeled medications. The Director of Nursing (DON) stated that medication carts and storage rooms were reviewed weekly, but the expired medication should have been removed and destroyed by the nurse who found it. The facility's policy requires that medications be labeled with resident information and that expired medications be returned or destroyed, which was not adhered to in this instance.
Infection Control Deficiencies in PPE Use and Ice Box Sanitation
Penalty
Summary
The facility failed to implement an effective infection prevention and control program, as evidenced by two specific deficiencies. Firstly, a registered nurse did not adhere to Enhanced Barrier Precautions (EBP) while providing wound care to a resident with a Foley catheter. Despite a sign indicating the need for EBP and the availability of personal protective equipment (PPE) such as gowns, masks, and gloves, the nurse only wore a mask and gloves, neglecting to don a gown. This oversight occurred during wound care, which involved cleaning the wound and applying medicated ointment. The nurse acknowledged the lapse, attributing it to a lack of attention to the precautionary requirements. Secondly, the facility failed to maintain sanitary conditions concerning the ice box in the dining room. An unidentified resident was observed using a personal cup to scoop ice directly from the ice box, bypassing the use of a designated ice scoop. This action was witnessed by a certified nursing assistant who did not intervene. The infection preventionist confirmed that residents were not permitted to scoop their own ice and that staff were responsible for assisting residents using a designated scoop to prevent contamination.
Facility Fails to Secure Utility and Construction Areas
Penalty
Summary
The facility failed to maintain a safe and secure environment for residents by not ensuring that certain areas were inaccessible to them. Observations revealed that the utility room door near the dining room between the 300 and 400 units was repeatedly found open on multiple occasions, exposing computer servers and cables. Staff did not close the door when placing items such as a medication cart and a two-wheel walker near the doorway, leaving the room accessible to residents. Additionally, room [ROOM NUMBER] on the 500 unit, which was under construction, was found unlocked and accessible to residents. The room contained mechanical tools, such as a drill, nails, and screws, and had exposed plumbing due to a removed drywall panel. Interviews with the maintenance director and the nursing home administrator confirmed that the utility room door was left open for ventilation purposes, and the administrator was unaware of the construction room's accessibility and contents.
Latest citations in Colorado
Two severely cognitively impaired residents in a memory care unit, both with dementia and significant behavioral risk factors, became agitated with each other and engaged in a physical altercation that resulted in a facial scratch to one resident. Facility policy required immediate intervention, separation, and monitoring to prevent abuse, and both residents’ care plans identified risks for aggression, anxiety, and resident-to-resident altercations. Staff reported that only one staff member was assigned to seven residents, that residents often invaded each other’s space, and that fights did occur, including a fist fight between these two residents during the incident in question. The facility’s investigation substantiated the event as physical abuse, demonstrating a failure to protect residents from abuse and to implement effective monitoring and behavioral interventions.
A resident with bipolar disorder, PTSD, traumatic brain injury, and moderate cognitive impairment alleged that an LPN and CNA were rough and sexually abusive during incontinence care, stating the LPN aggressively rolled him, caused his head to hit the wall, and repeatedly inserted a finger into his anus despite his protests. The facility’s investigation relied on staff statements and lack of observed rectal trauma, did not interview the roommate, and did not explore why staff continued care after the resident’s abuse allegation. The resident also reported ongoing rough transfers, inadequate repositioning in a wheelchair causing pain and bruising, and lack of assistance with proper positioning for meals, which was corroborated by observation of poor positioning, a bruise on his arm, and food spilled on his shirt. Although the care plan noted a history of false allegations and required care in pairs and investigation of voiced concerns, it lacked a specific focus on the resident’s PTSD and did not address his repeated reports that staff’s incontinence care and handling were rough and abusive.
A resident with a history of falls, fractures, and significant mobility impairment experienced an unwitnessed fall from bed, which had been left in a high position despite care-plan interventions requiring it to be kept low with a fall mat. An RN found the resident on the floor, initiated neuro checks, and documented elevated BP readings and pain but did not complete or document a thorough head-to-toe assessment before moving the resident back to bed, and did not promptly notify the MD, hospice, or the resident’s representative. Hospice was contacted several hours later due to rising BP and severe pain; a hospice RN then assessed the resident, notified the on-call MD, and obtained an order to transfer the resident to the hospital, where imaging revealed multiple fractures and a scalp contusion. Staff interviews and facility policy confirmed that standard practice required immediate RN assessment prior to moving a fallen resident, timely MD and family notification, and adherence to fall-prevention interventions, all of which were not followed in this case.
The deficiency centers on failures in transportation safety and fall management that led to serious resident injuries. A resident with dementia and bilateral lower extremity impairments was transported in a wheelchair without foot pedals, seated on a blanket and Hoyer sling, and improperly restrained when the driver misapplied the lap and shoulder belt to avoid disturbing an ostomy bag. During the trip the resident slid forward, struck both legs on a step in the vehicle, and was later found to have bilateral tibial fractures with significant bruising, swelling, and pain. The driver’s training had been informal, passed down from another staff member without documented competencies, van‑specific procedures, or clear emergency protocols, and leadership acknowledged they had not investigated the admitted misuse of the seat belt. Separately, two residents at high risk for falls experienced multiple falls, including one with a facial laceration and maxillary sinus fracture, while care‑planned fall interventions such as scheduled toileting, prompted voiding, monitoring, and assisted transfers were not consistently implemented, and IDT reviews and implementation of recommended interventions were not always timely.
A resident with severe cognitive impairment, multiple comorbidities, and a known history of alcohol use left the facility and was later found outside yelling for help and lying on the ground. Police identified the individual, determined the resident was intoxicated, and returned him to the facility, where he required wheelchair transport to his room despite normally walking without assistive devices. Officers helped the resident into bed, but nursing staff did not complete a change of condition assessment, obtain vitals, perform a head-to-toe or post-fall evaluation, or document his condition or monitoring afterward. The physician and legal guardian were not notified of the intoxication or change in condition, and there was no care plan addressing alcohol use or intoxication despite existing orders to monitor for substance use and notify the provider. A few hours later, a CNA found the resident face down on the floor, unresponsive, and he was pronounced dead, with the death certificate citing respiratory failure, aspiration event, and alcoholism; the incident was not promptly reported or thoroughly investigated at the time.
A resident with cognitive impairment and documented visual deficits requested very hot tea, which a PTA dispensed from a hot beverage machine and then further heated in a microwave, contrary to facility policy prohibiting reheating of facility-provided drinks. The PTA secured a lid on the cup and placed it at the bedside. Due to visual impairment, the resident could not locate the drinking opening, attempted to remove the lid independently, and spilled the hot liquid onto an arm and thigh, sustaining second-degree partial thickness burns over approximately 6% TBSA. Nursing and NP assessments documented bright red, blanchable burns with blistering and subsequent healing, and staff interviews confirmed that the beverage had been overheated and that the resident’s visual impairment and lack of appropriate supervision and adaptive equipment contributed to the accident.
A resident with CHF and multiple comorbidities was readmitted from the hospital with an order for metolazone 2.5 mg PRN, to be given only when weight increased by 5 lbs over baseline and 30 minutes before Lasix. Due to incorrect transcription of the hospital discharge orders into the EMR by the ADON, and the absence of a required second-nurse verification, metolazone was entered and administered as a scheduled daily medication instead of PRN. Nursing staff gave the drug daily for eight days without confirming the weight-based parameter, including on days when no weight was obtained and when the resident’s weight was stable or decreasing. During this period, the resident experienced a 12–14 lb weight loss, marked weakness, fatigue, excessive somnolence, and was later found to have hypokalemia, while continuing on other diuretics (Lasix and spironolactone). Interviews with the resident, her representative, nursing staff, the DON, PCP, and pharmacist linked these changes to the medication error, which did not follow the prescriber’s PRN order or the facility’s medication error policy.
The facility failed to maintain a full-time RN DON when the existing DON was reassigned as a temporary emergency NHA, leaving no separate RN designated to the DON role. Records showed the acting NHA held a temporary administrator permit while the staffing list indicated no full-time DON in place, despite a job description assigning the DON responsibility for 24-hour nursing oversight, staffing, and key clinical systems. Staff interviews revealed that nurses were unaware of the DON’s reassignment and continued to view this person as their direct supervisor, while the acting NHA reported performing both administrative and DON functions, including abuse coordination and state occurrence reporting, without any formal announcement or signage to inform staff, residents, or families of these role changes.
The facility’s QAPI program failed to identify and address critical quality of care issues related to resident change in condition, despite a written policy requiring comprehensive, data‑driven performance monitoring and corrective action. The facility had repeat F684 citations for quality of care and, in the current survey, was found to have not adequately assessed, monitored, documented, or communicated a resident’s change in condition, which was associated with the resident’s death and resulted in an immediate jeopardy finding. The MD reported he reviewed only those cases and policies presented to him and was unaware that the DON was also serving as the temporary emergency NHA amid leadership changes. The DON/acting NHA stated that QAPI meetings focused on standard topics and that change of condition evaluations were limited mainly to skin alterations and falls, acknowledging that staff were new to other types of change of condition assessments requiring thorough evaluation and provider/family notification.
A resident with CVA-related left-sided hemiplegia, who used a wheelchair and was cognitively intact, was moved to a different room after reporting strong chemical odors and refusing to return to the original room. Facility policy stated that staff would assist with packing and unpacking belongings for room changes, and staff reported that environmental services, nursing, or maintenance typically helped move items. In this case, however, staff repeatedly told the resident they could not move her belongings and would only escort her while she attempted to move them herself, despite her physical limitations. The NHA communicated by email that, due to prior disputes about handling of personal property, the resident was responsible for arranging family or third-party movers at her own expense, while staff would only provide access and oversight. As a result, most of the resident’s personal items remained in the original room for an extended period after she agreed to the permanent room change.
Failure to Prevent Resident-to-Resident Physical Abuse in Memory Care Unit
Penalty
Summary
The deficiency involves the facility’s failure to protect residents from abuse, specifically resident-to-resident physical abuse between two cognitively impaired residents in the memory care unit. Facility policy required that residents be free from all forms of abuse and that staff immediately intervene, ensure resident safety, and keep residents separated and monitored when an assailant is identified. Despite this policy, the facility’s own investigation of an incident on 11/26/25 documented that two residents in the memory care unit became frustrated and agitated with each other, with elevated voices and defensive body language, and moved their arms as if they were going to hit each other. One resident sustained a superficial scratch above his left eyebrow, and the investigation concluded that the other resident likely made contact, resulting in the injury, and the incident was substantiated as physical abuse. One resident involved had Alzheimer’s disease and schizophrenia, was severely cognitively impaired with a BIMS score of 1, and required maximum assistance with ADLs. His care plan identified him as being at risk for resident-to-resident altercations related to individuals invading his space and at risk for re‑traumatization, with anxiety triggered by male caregivers or those perceived to be male. Interventions in his care plan included providing opportunities for positive interaction and attention, such as stopping and talking with him while passing by. On the date of the incident, a skin assessment documented a scratch above his left eyebrow, consistent with the facility’s determination that he was the victim of physical abuse by another resident. The other resident involved had Lewy body dementia, hypertension, and depression, was also severely cognitively impaired with a BIMS score of 0, and required maximum assistance with ADLs. His behavior care plan identified a risk for verbally abusive behaviors and potential psychosocial issues due to a prior incident in which he had received unprovoked agitation with physical abuse from another resident, with interventions including monitoring for signs of aggression, fear, or psychosocial trauma and documenting behaviors and interventions. An antipsychotic medication care plan further identified him as being at risk for aggressive behaviors, including non‑redirectable agitation, with instructions to intervene immediately if agitation was observed. Staff interviews indicated that only one staff member was assigned to seven residents on the unit, that residents sometimes got into each other’s space and fights occurred, and that the two residents had been seen in a fist fight on the date of the incident, demonstrating that the facility did not effectively prevent or intervene to stop resident‑to‑resident physical abuse in accordance with its abuse prevention policy and the residents’ care plans.
Failure to Thoroughly Investigate and Address Allegations of Sexual and Rough, Abusive Care
Penalty
Summary
The deficiency involves the facility’s failure to thoroughly investigate and document allegations of sexual abuse and rough, abusive care toward a resident. The facility’s abuse policy required that all reports of resident abuse be thoroughly investigated and documented. An investigation dated 2/24/26 addressed an allegation that a resident was sexually abused during incontinence care, but the investigation did not include interviewing the resident’s roommate about what he might have seen or heard during the alleged incident. The investigation concluded the allegation was unsubstantiated based on lack of physical trauma and staff statements, and it attributed the resident’s report to cognitive decline and terminal agitation, despite the resident’s clear and consistent account during the survey interview. The resident involved was under age 65 with diagnoses including bipolar disorder, anxiety, depression, PTSD, and traumatic brain injury. A recent MDS showed moderate cognitive impairment (BIMS 12/15), aggressive behavior, and delusions, and the resident was dependent on staff for toileting, transfers, and bed mobility, using a manual wheelchair. During the facility’s investigation, the resident reported that while yelling for help after a bowel movement, a CNA entered and began care, and then an LPN took over. The resident stated he did not want the LPN to provide care, tried to swat him away, and that the LPN grabbed his hands, rolled him aggressively causing his head to hit the wall, and inserted a finger into his anus four times while wiping, despite the resident yelling for him to stop. Staff statements conflicted with the resident’s account regarding who provided care and what occurred, and the facility did not investigate why staff did not stop care and have another staff member take over when the resident alleged abuse during the episode. The resident continued to report that staff were rough and that their approach to care felt abusive, including prior rough transfers by the same LPN and improper positioning and repositioning by other staff that caused pain and bruising. On the survey date, the resident described ongoing rough care, lack of staff responsiveness to his requests, and feeling that no one listened to or believed him. He reported that staff did not assist him to sit up properly for breakfast, resulting in difficulty eating and spilled food on his shirt. Observation during the interview showed the resident slouched and slumped to the left in his wheelchair, with his left arm hanging over the side, a bruise on his upper arm where the armrest was pressing, and dried oatmeal on his shirt from the morning meal. The resident’s care plan documented a history of false allegations and required care in pairs, investigation of all concerns voiced, and a calm, slow approach, but there was no specific care plan focus addressing his PTSD or his allegations of rough or abusive incontinence care, and the facility did not pursue his ongoing reports of rough and abusive treatment during personal care.
Failure to Assess, Notify, and Respond Appropriately After Unwitnessed Fall With Major Injury
Penalty
Summary
The deficiency involves the facility’s failure to provide treatment and care in accordance with professional standards following an unwitnessed fall. A cognitively intact resident with a history of falls, prior fractures (including a right humerus fracture), osteoarthritis, muscle weakness, and difficulty walking was admitted with orders and care plan interventions that included keeping the bed in the lowest position, use of a high-impact fall mat, and a lipped mattress. The resident required maximal assistance with transfers and used a wheelchair. On the night of the incident, the resident was found on the floor on her left side in a somewhat fetal position, partially on and partially off the fall mat, with the bed raised in a high position. RN #1, who heard a loud sound and discovered the resident on the floor, documented an initial assessment that included vital signs showing elevated blood pressure and initiation of neurological monitoring. However, there was no documentation that RN #1 completed a thorough head-to-toe assessment before the resident was moved back to bed, despite facility policy requiring a nurse evaluation to determine presence of injury prior to moving a resident who has fallen. The record lacked evidence of a full assessment of injuries at the time of the fall, even though the resident later was found to have multiple fractures and a scalp contusion. Staff interviews, including from the DON and other nurses, confirmed that standard practice and policy required a complete RN assessment before moving a resident after a fall. Following the fall, RN #1 did not notify the physician, the resident’s representative, or hospice at the time of the incident, despite facility policy and staff statements that the physician and responsible party should be notified immediately after the assessment. The resident’s blood pressure continued to rise over several hours, and she complained of pain, yet the first notification was to hospice at 6:00 a.m., approximately three hours after the fall. The hospice RN arrived around 6:30 a.m., found the resident arousable to verbal stimuli with tense features, facial grimacing, and reporting severe pain, and then notified the on-call physician, who ordered transfer to the hospital. Hospital imaging revealed a left parietotemporal scalp contusion, an acute nondisplaced C7 vertebral fracture, multiple displaced fractures of at least the first six left ribs, a left scapula fracture, and a left clavicle fracture. The facility also failed to ensure the resident’s bed was maintained at a safe, low height as care-planned, and the transfer to the hospital did not occur until after hospice assessment and physician notification several hours post-fall. The resident’s representative reported that the resident lay in bed for three hours in severe pain without medical attention and that the family and physician were not notified by facility staff, but rather by hospice. Documentation showed that the facility did not contact the resident’s representative until later that afternoon, after the hospital had already identified multiple fractures and the resident was being admitted to intensive or trauma care. Staff interviews, including from CNAs, an LPN, an RN, and the DON, consistently described that facility practice required immediate RN assessment before moving a resident, prompt vital signs and neurological checks, and immediate notification of the physician and responsible party after a fall, particularly if there was pain or potential major injury. In this case, the facility failed to accurately and timely assess the resident after the fall, failed to promptly notify the physician and responsible party, did not ensure the bed was at the lowest and safest height, and did not ensure timely transfer to the hospital after an unwitnessed fall that resulted in major injury and pain. The facility’s own fall care plan and incident policy emphasized prevention of avoidable accidents, completion of a nurse evaluation prior to moving a resident who has fallen, and documentation of injury status and notifications. Despite these requirements, the EMR lacked a full head-to-toe assessment at the time of the fall, and the DON acknowledged that RN #1, an agency nurse, failed to document the fall appropriately, complete an accurate assessment, and notify the physician and the resident’s representative. The hospice RN confirmed that RN #1 did not notify the physician or the resident’s representative and that hospice was contacted due to the resident’s increased pain and rising blood pressure. These actions and omissions collectively led to the cited deficiency for failure to provide treatment and care in accordance with professional standards and the resident’s care plan following the fall.
Transportation Safety and Fall Management Failures Leading to Resident Injuries
Penalty
Summary
The deficiency involves the facility’s failure to ensure an environment free from accident hazards and to provide adequate supervision to prevent accidents, particularly in relation to transportation safety and fall prevention. One resident with vascular dementia, bilateral lower extremity impairments, and dependence on staff for transfers was transported to an outside appointment in a facility vehicle while seated in a wheelchair without foot pedals. During the trip, the resident began sliding forward in the wheelchair. The transportation driver reported he could not immediately pull over while exiting the highway, and by the time he stopped, the resident had slid further forward so that her knees and legs were resting on a step behind the driver’s seat. The resident subsequently exhibited multiple bruises, abrasions, swelling of both legs, and severe pain. Facility records and later hospital documentation identified bilateral tibial fractures associated with this transport incident. The report details that the wheelchair was secured with a four‑point tie‑down, but the resident’s body was not properly restrained. The driver later demonstrated that he had routed the shoulder portion of the seat belt around the back of the van seat instead of across the resident’s shoulders, and placed the lap portion across the resident’s chest instead of her lap. He acknowledged this was not the proper use of the seat belt and attributed his actions in part to concern about disturbing the resident’s ostomy bag. He also stated that the resident was sitting on a blanket and a Hoyer sling, which he believed contributed to sliding, and that the absence of foot pedals left nothing to stop the resident’s forward movement. The facility’s own transportation policy required that drivers and passengers wear seatbelts and shoulder harnesses any time the vehicle was in motion and that wheelchairs be made secure with straps, but there was no evidence that the seat belt system was applied as intended in this case. The report further identifies systemic issues in transportation training and oversight that contributed to the deficiency. The van driver had been in the role for a little over a month and was trained informally by the central supply coordinator, who herself had been trained years earlier by a prior driver without documented competencies, checklists, or reference to an operations manual. The central supply coordinator reported no additional training or competencies since that initial instruction and was unaware of any policy or procedure for driving emergencies or clear guidance on whom the driver should contact for clinical or mechanical emergencies during transport. The maintenance director, responsible for monthly checks of the van, used a generic medical transport checklist, had no van‑specific training or competencies, and was unsure whether an operations manual was available. The administrator acknowledged that she was not sure what competencies the trainer had when she trained the current driver, that the DON and ADON were not trained on transportation, and that no investigation was completed into the driver’s admitted misuse of the seat belt. Collectively, these actions and inactions led to the transportation‑related accident and constituted a failure to maintain an accident‑free environment and adequate supervision. In addition, the deficiency includes failures related to fall management for two other residents at high risk for falls. One resident with vascular dementia, muscle wasting, difficulty walking, and severe cognitive impairment experienced 16 falls over a defined period, including an unwitnessed fall that resulted in a facial laceration and a maxillary sinus fracture requiring emergency department evaluation. The facility had a fall management policy requiring IDT review of falls and individualized care plan interventions, and the resident’s care plan contained multiple fall interventions such as scheduled toileting, prompted voiding, use of a non‑recording video monitor, and assistance with transfers. However, the report notes that care‑planned fall interventions were not consistently implemented in a timely manner, and surveyor observations during the survey period showed that staff were not consistently following the resident’s fall interventions. The report also notes that the IDT did not consistently review falls in a timely manner or ensure that recommended interventions were implemented. For the high‑risk resident with multiple falls, IDT notes documented repeated unwitnessed and witnessed falls associated with poor safety awareness, failure to use the call light, weakness, and attempts to ambulate or transfer without assistance. New interventions such as occupational therapy evaluations, room relocation closer to staff, and pharmacy review were recommended, but one occupational therapy evaluation was recommended after a fall even though it had already been recommended after a prior fall, indicating delays or gaps in implementation. Another resident with multiple falls had no timely identification and documentation of fall interventions after several falls. These patterns demonstrate that the facility did not ensure timely IDT review of falls or consistent implementation of care‑planned fall interventions, contributing to repeated falls and at least one major injury. Overall, the cited deficiency encompasses the facility’s failure to safely transport a dependent, cognitively impaired resident in accordance with its own transportation safety policy, resulting in bilateral tibial fractures, and its failure to consistently implement and timely review fall prevention interventions for residents at high risk for falls, including residents who sustained multiple falls and a serious injury.
Removal Plan
- Temporarily suspend all facility resident transportation services and transfer transportation to an outside company pending completion of training and validation.
- Immediately remove all staff members assigned transportation responsibilities from transportation duties pending completion of retraining and competency validation.
- Transport residents requiring appointments using medical transportation services through external transportation companies.
- Implement a resident transportation risk assessment tool to identify residents who require special transportation precautions; assess all residents who utilize facility transportation using this tool.
- Implement a comprehensive transportation safety program including: updated Transportation Safety Policy; Transportation Driver Job Description with defined safety duties; Transportation Staff Competency Validation process; Pre-Transport Safety Checklist (reviewed by administrator or designee); Transportation Special Circumstances Protocol; Transportation Incident Investigation Template; Transportation Safety Training Program; and Transportation Safety QAPI Monitoring Process.
- Require wheelchairs to be secured using a four-point tie-down system.
- Require residents to be secured with lap and shoulder seatbelts.
- Verify wheelchair brakes and foot pedals prior to transport by the administrator or designee.
- Confirm resident stability before departure by the administrator or designee.
- Evaluate residents’ medical devices/special medical circumstances individually (e.g., ostomies, indwelling urinary catheters, suprapubic catheters, oxygen equipment, other devices) and implement appropriate precautions prior to transportation as necessary.
- Provide mandatory transportation safety training for all transportation staff (wheelchair securement, restraint placement, medical device accommodations, emergency response); document attendance and validate competency using a checklist, with validation by the maintenance director and clinical liaison/designee as approved by the administrator.
- Complete a Pre-Transport Safety Checklist prior to each transport verifying wheelchair brakes engaged, foot pedals attached, four-point tie-down secured, lap and shoulder restraints applied, medical devices protected, and resident stability confirmed (completed by Maintenance Director and Clinical Liaison/Designee).
- Use a transportation incident ad hoc QAPI tool to ensure structured review of any transportation-related incident (incident description, equipment review, root cause analysis, corrective action planning).
Failure to Assess and Respond to Resident Intoxication and Change in Condition Resulting in Death
Penalty
Summary
The deficiency involves the facility’s failure to ensure that a resident with multiple complex medical conditions received treatment and care in accordance with professional standards of practice following a clear change in condition related to alcohol intoxication. The resident had diagnoses including alcoholic polyneuropathy, history of traumatic brain injury, CHF, type 2 diabetes mellitus, alcoholic cirrhosis of the liver, hypertension, long-term anticoagulant use, and alcohol use with an unspecified alcohol-induced disorder. His MDS showed severe cognitive impairment and functional dependence for many ADLs, though he typically ambulated without a mobility device. Physician orders included monitoring for potential substance use each shift and documenting and notifying the physician if any substance use indicators were noted, but the January TAR documented no substance use behaviors for that month. On the day of the incident, the resident signed out of the facility in the morning and was later found outside the facility grounds by bystanders, yelling for help and lying on the ground near a hotel with a shopping cart. Police dispatch records show multiple calls reporting the resident on the ground and yelling for help, and the police ultimately identified him and returned him to the facility. The police reported to staff that the resident was intoxicated and had been wandering. Upon return, he required wheelchair transport from the front door to his room, despite normally walking without assistive devices. According to an IDT note, officers assisted him in removing his shoes and coat and helped him into bed, after which he was observed resting in his room, but no time or assessment details were documented. Record review revealed no documentation that nursing staff completed a change of condition assessment, a post-fall or post-ground-level event assessment, or any RN assessment when the resident was returned by police in an intoxicated state. There was no documentation of vital signs, head-to-toe assessment, skin evaluation, or monitoring between the time of his return and the time he was later found unresponsive. The physician and the resident’s legal guardian were not notified of his intoxication or change in condition, and there was no progress note describing his condition upon return or how he was transferred to bed. The resident’s comprehensive care plan contained no care plan addressing alcohol use, intoxication, or potential substance use, and there were no interventions related to his known history of alcohol abuse and drinking while away from the facility. Staff interviews, including with the DON/acting NHA, ADON, and RNs, confirmed that no change of condition assessment, vital signs, or physician/guardian notifications were completed despite their own descriptions of what should occur when a resident returns intoxicated. The resident was later found face down on the floor in his room, unresponsive, and was pronounced dead; his death certificate listed respiratory failure, aspiration event, and alcoholism as the causes of death. The facility also failed to promptly recognize and investigate the incident as an unexpected death associated with a significant change in condition. A frequent visitor reported that the DON/acting NHA initially did not believe an occurrence report was required for the resident’s intoxicated return and unexpected death, and the occurrence report to the state was not submitted until eight days after the death. There was no evidence of an immediate, thorough internal investigation or root cause analysis at the time of the event to determine why nurses did not complete a change in condition assessment or follow the existing physician order to monitor for substance use and notify the physician. Surveyors determined that the facility did not thoroughly assess and monitor the resident’s alcohol use and change in condition, did not document changes, and did not seek medical treatment or notify the physician and guardian when required, and that these failures contributed to serious harm and death for the resident.
Removal Plan
- NHA notified the facility medical director of the incident.
- Nursing supervisors/designees completed physical assessments/interviews on all residents to identify any changes in condition and notified the physician of any noted changes.
- Initiated a look-back audit of current and discharged residents to ensure change-of-condition policy was followed.
- Identified one current resident without a required 72-hour alert monitoring order; educated the assigned nurse regarding timely initiation of the 72-hour alert monitoring order after completing the eINTERACT change-in-condition evaluation.
- Initiated the missing 72-hour change-in-condition alert monitoring order for the identified resident, including nursing assessments and documentation on the TAR and in progress notes each shift for three days per physician-indicated frequency.
- Reviewed resident change-in-condition and notification policies/procedures for clinical accuracy.
- Educated all nursing staff on addressing changes of condition (assessment, monitoring, physician/family notification, orders, and facility policies/procedures); staff were not permitted to work a shift until education was completed.
- Educated new hires (licensed nurses and nurse aides) during orientation on change-of-condition and physician/family notification requirements and facility policies/procedures.
- DON/designee to conduct audits five times per week for three months of the 24-hour report and progress note report to ensure change-of-condition policies/procedures are followed.
- DON/designee to conduct daily nursing staff huddles Monday through Friday to monitor for changes in resident condition.
- Regional director of clinical services and regional vice president to provide clinical/administrative oversight to ensure education and audits are completed and accurate.
- DON educated by the CNO on appropriately addressing changes of condition (assessment, monitoring, physician orders, and facility policies/procedures).
- DON/designee to complete chart audits to verify detailed assessments/documentation and physician/family notification related to changes of condition.
- Regional Director of Clinical Services to visit the facility to provide general oversight and monitoring of the plan.
Burn Injury from Improperly Heated Hot Beverage and Inadequate Supervision
Penalty
Summary
The deficiency involves the facility’s failure to ensure a resident was free from accident hazards and received adequate supervision when provided a hot beverage. A resident with diagnoses including a displaced intertrochanteric fracture of the left femur with routine healing, unspecified cataract, unspecified macular degeneration, disorientation, and restlessness and agitation requested very hot tea. The resident had moderate cognitive impairment with a BIMS score of 11 and was care planned as needing set-up assistance with eating and drinking. Although an MDS assessment indicated adequate vision without corrective lenses, subsequent care planning documented vision impairment related to cataracts, macular degeneration, and diplopia, and that the resident wore an eye patch and glasses. On the day of the incident, the resident asked a physical therapy assistant (PTA) to make her tea “very hot.” The PTA dispensed hot water for tea from the kitchenette coffee machine and then heated the beverage in a microwave for an additional 30 seconds at the resident’s request. The PTA then secured a lid on the cup and placed it on the resident’s bedside table. The facility’s Hot Beverage policy, in effect at the time, stated that hot beverages were to be served at a safe, palatable temperature, that hot beverage machines were to be set and maintained at manufacturer-recommended temperatures, and that microwaves were not to be used to reheat hot beverages if the temperature was not considered palatable; instead, a fresh cup was to be poured. The policy also directed staff to report safety or decline in managing hot beverages to the IDT or therapy for review and possible care plan updates. After the PTA placed the lidded cup at the bedside, the visually impaired resident attempted to drink the tea but could not locate the opening in the lid due to her macular degeneration. The resident then attempted to remove the lid independently, during which the hot tea spilled onto her right forearm and right posterior thigh. Nursing assessment documented bright red, blanchable burns with a broken blister on the arm, and measurements of 8 cm by 5 cm on the arm and 12 cm by 22 cm on the thigh. The NP assessed the injuries as second-degree partial thickness burns involving approximately 6% total body surface area, with the resident reporting pain of 3 out of 10 and denying numbness, tingling, fevers, or chills. Subsequent documentation showed the wounds progressing with scabbing and epithelial tissue formation prior to the resident’s discharge home. Staff interviews confirmed that, following the incident, it was recognized that the tea had been heated beyond the temperature at which it was dispensed from the coffee machine and that the resident’s impaired vision contributed to her difficulty using the standard lidded cup. The DON and RN stated that the PTA had reheated the tea in the microwave without checking the temperature and then served it to the resident, contrary to the facility’s policy prohibiting reheating of facility-provided drinks in microwaves. The dietary manager and nursing staff also indicated that the facility’s practice was to avoid reheating hot beverages and to rely on the coffee machine settings, which were kept at or below 160°F, rather than using microwaves for additional heating. These actions and inactions led to the resident being provided an excessively hot beverage in a manner that did not account for her visual impairment, resulting in the burn injury. The facility’s failure centered on not adhering to its own Hot Beverage policy and not adequately supervising or accommodating the resident’s known visual impairment when providing a very hot beverage. The PTA’s use of the microwave to further heat the tea, the absence of a temperature check before serving, and the placement of a standard lid that the visually impaired resident could not safely manage independently all contributed to the incident. The care plan at the time identified the resident as needing set-up assistance and, after the incident, was updated to include interventions such as encouraging the resident to leave lids on hot beverages and to use the call light for assistance with lids, indicating that these precautions were not in place or not implemented at the time of the burn event.
Failure to Follow PRN Diuretic Order Leads to Significant Weight Loss and Hypokalemia
Penalty
Summary
The deficiency involves the facility’s failure to ensure a resident was free from significant medication errors when a diuretic, metolazone, was entered and administered as a scheduled daily medication instead of as a PRN medication with specific weight-based parameters. After an acute hospitalization for conditions including acute on chronic CHF, acute respiratory failure with hypoxia, COPD, atrial fibrillation, hypertension, morbid obesity, COVID-19, and MDRO history, the resident was readmitted to the facility. The hospital discharge order specified metolazone 2.5 mg to be taken once daily as needed for pulmonary edema due to chronic heart failure, only when the resident had a weight gain of 5 lbs over baseline, and to be given 30 minutes prior to Lasix. However, when the orders were transcribed into the facility’s EMR on readmission, metolazone was entered as a scheduled daily medication without PRN parameters, and this incorrect order did not match the hospital discharge instructions. The assistant DON, who entered the readmission orders from the hard-copy discharge packet because the phone lines were down and the usual electronic admission process was not used, input metolazone as a daily scheduled medication. The normal process of having two nurses verify and enter orders was not completed; the ADON entered the orders alone, and the second nurse verification did not occur. As a result, nursing staff administered metolazone 2.5 mg daily for eight days, in addition to the resident’s other diuretics (Lasix and spironolactone), without confirming that the resident had experienced the required 5 lb weight gain from baseline. The MAR documented daily administration of metolazone over this period, including on days when no weight was obtained, and on days when the resident’s weight was stable or decreasing rather than increasing. During this time, the resident experienced significant weight loss and symptoms consistent with a change in condition. Weight records showed a decline from approximately 190 lbs prior to hospitalization to 176.6 lbs when the error was identified, reflecting a loss of about 12–14 lbs over a short period. The resident and her representative reported that she became severely weak, excessively tired, and felt she could not regain her strength, with the representative describing the resident as very tired, exhausted, and feeling as though she could not “hang on any longer.” Clinical documentation noted significant weakness, excessive sleepiness during therapy, and that the resident was triggering for significant weight loss. Laboratory testing later showed hypokalemia, with a potassium level of 3.2 mEq/L. Interviews with nursing staff, the DON, the ADON, the PCP, the pharmacist, the resident, and the resident’s representative consistently attributed the resident’s weight loss, weakness, and low potassium at least in part to the erroneous daily administration of metolazone instead of PRN dosing based on weight gain. The facility’s own medication error policy defined a medication error as preparation or administration of medications not in accordance with the prescriber’s order, manufacturer’s specifications, or accepted professional standards, and defined a significant medication error as one that causes resident discomfort or jeopardizes health and safety. In this case, the metolazone order in the EMR did not reflect the prescriber’s PRN order with weight-based parameters, and the medication was administered without verifying the required 5 lb weight gain. The resident’s care plan for diuretic therapy called for administering diuretics as ordered, monitoring for side effects such as fatigue and increased fall risk, and reporting pertinent lab results, including potassium. Staff interviews acknowledged that the error persisted for about eight days, that medication reconciliation was not completed upon readmission, and that the lack of a second nurse verification contributed to the error. The pharmacist and PCP described the effects of metolazone, especially in combination with Lasix, as including electrolyte abnormalities, weight loss, and weakness, and characterized the error as moderate, with the potential to increase electrolyte depletion and require close monitoring.
Failure to Maintain a Full-Time RN Director of Nursing During Temporary NHA Appointment
Penalty
Summary
The deficiency involves the facility’s failure to designate a registered nurse (RN) to serve as the full-time director of nursing (DON) while the existing DON was reassigned to act as the temporary emergency licensed nursing home administrator (NHA). Record review showed that the acting NHA held an active temporary permit for emergency situations beginning on 12/30/25 and expiring on 3/30/26. A staffing list review revealed there was no full-time DON in the building during this period. The DON job description, signed by the DON, specified that the DON’s primary purpose was to plan, organize, develop, and direct nursing operations, ensure quality resident care on a 24-hour basis, oversee recruitment and hiring of licensed personnel, manage nursing schedules, monitor staffing levels, and oversee implementation of nursing service objectives, policies, and procedures, including key clinical systems such as infection prevention and control, psychotropic and controlled substance management, skin and weight systems, risk management, and hospice liaison. Staff interviews confirmed that the individual serving as the full-time temporary NHA was also functioning as the full-time DON, with no other person appointed to the DON role. The chief nursing officer stated that the temporary NHA was also acting as the full-time DON and reported not knowing there was a regulation preventing this. Nursing staff, including an LPN and an RN, reported they were unaware that the DON had been appointed as the temporary NHA and continued to view the DON as their supervisor. The acting NHA described performing both administrative and clinical leadership duties, including occurrence reporting to the state, serving as abuse coordinator and investigator, and leading stand-up meetings, while relying on two unit managers, an LPN assistant DON, and an infection preventionist to assist with clinical duties and audits. There had been no announcement to staff, residents, or families about the acting NHA appointment or her role as abuse coordinator, and there was no signage indicating this responsibility.
Failure of QAPI Program to Address Change in Condition Leading to Immediate Jeopardy
Penalty
Summary
The deficiency involves the facility’s failure to maintain an effective, comprehensive, data‑driven QAPI program that identified and addressed quality of care concerns, particularly related to changes in resident condition. The facility’s QAPI policy required ongoing tracking and measuring of performance, identification and prioritization of quality deficiencies, systematic analysis of underlying causes, and development and monitoring of corrective actions, with a focus on resident safety, health outcomes, and high‑risk or problem‑prone areas. Despite this written policy, the facility did not operate its QA program in a manner that prevented repeat deficiencies, as evidenced by prior citations at F684 (quality of care) in consecutive annual recertification surveys. Surveyors found that the QAPI committee failed to identify and address concerns related to quality of care by not ensuring that resident changes in condition were assessed, monitored, documented, and communicated when indicated. This failure rose to the level of immediate jeopardy and was associated with a serious adverse outcome resulting in a resident’s death. The cross‑referenced F684 citation states that the facility failed to provide quality care by not assessing, monitoring, documenting, and communicating a resident’s change in condition when indicated. The facility’s regulatory history showed that F684 had been cited twice previously at a D scope and severity, indicating a potential for more than minimal harm, isolated, without effective QA‑driven prevention of recurrence. Interviews further demonstrated gaps in the QAPI program’s functioning and oversight. The medical director reported he visited at least twice a month, reviewed cases and policies presented to him, and made changes based on what was brought forward in QAPI, but he was not informed that the DON was also serving as the full‑time temporary emergency licensed NHA for several months, and he described multiple leadership changes. The DON/acting NHA stated that QAPI meetings were held monthly and covered standard topics such as admissions, discharges, falls, staffing, abuse, infection control, and grievances, with use of audit tools and tracking spreadsheets. However, she acknowledged that while change of condition evaluations were being done for skin alterations and falls, staff were “new to the other types of change of condition assessments” that required thorough assessment and notification of the physician and family/guardian, and that change of condition evaluations beyond those limited areas had not been a focus of QAPI until after the incident that led to the immediate jeopardy finding.
Failure to Provide Timely Assistance With Resident Room-Change Belongings
Penalty
Summary
The deficiency involves the facility’s failure to reasonably accommodate a resident’s needs and preferences during a room change, specifically by not providing timely assistance with moving the resident’s personal belongings. The facility’s Room Change policy, revised April 2025, states that environmental services staff or a designee will assist residents to pack their belongings prior to a room change, and nursing staff will assist residents to unpack belongings and get settled into the new room. The policy does not specify who will physically move the belongings between rooms, but staff interviews indicated an expectation that environmental services, nursing, or maintenance staff would typically assist with moving items or furniture. The resident involved was under age 65 and had multiple diagnoses, including CVA with left-sided hemiparesis and spastic hemiplegia, coronary artery disease, hyperlipidemia, depression, ADHD, lower back pain, and muscle weakness. The resident was cognitively intact with a BIMS score of 15, used a wheelchair for mobility, and was independent with hygiene, toileting, bathing, and dressing, but required setup and cleanup assistance with eating. The resident had documented verbal behavioral symptoms such as yelling and cursing, and a behavior care plan that included communicating via email and following up on concerns in a timely manner. The resident reported irritation of the nose and eyes and refused to return to her original room after complaining of a strong smell of ammonia and bleach, and staff assisted her into another room that night so she could sleep. Following this move, the resident requested assistance from staff to bring toiletries, a plant, and other personal items from the original room to the new room. Progress notes documented that staff told the resident they were not allowed to move her belongings and could only accompany her while she moved them herself, despite her left-sided hemiplegia and inability to move the items independently. The resident stated she was told she needed to move the items herself or arrange for someone else to move them and that she felt she should not have to pay to move her own items because the facility had offered the room change. Email communications show that the NHA characterized the room change as an accommodation requested by the resident and informed her that, due to prior concerns about staff handling her property, her belongings should be moved by family, an authorized representative, or a third-party mover at her own expense, with staff only providing access and oversight. The resident agreed to permanently move to the new room, but most of her belongings remained in the previous room, and staff continued to only escort her to retrieve items herself. Staff interviews confirmed that, in typical room changes, families or staff would assist with moving belongings, and that in this case the facility did not expect the resident to move her own items but also did not provide direct assistance or documented resources for moving services. The permanent move of the resident’s belongings did not occur until 39 days after she agreed to the room transfer, during which time the majority of her personal items remained in the original room.
Trusted data from CMS and state health departments
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