Autumn Hills Health Care Center
Inspection history, citations, penalties and survey trends for this long-term care facility in Glendale, California.
- Location
- 430 N.glendale Ave, Glendale, California 91206
- CMS Provider Number
- 055288
- Inspections on file
- 35
- Latest survey
- February 26, 2026
- Citations (last 12 mo.)
- 7
Citation history
Health deficiencies cited at Autumn Hills Health Care Center during CMS and state inspections, most recent first.
A resident with hemiplegia and hemiparesis, who was capable of making decisions, reported that during a therapy session he touched the back of a PT’s head to get his attention, and the PT responded by turning and striking the resident’s thigh with an open hand, causing pain and leaving the resident feeling shocked, upset, and assaulted. Another PT in the room witnessed the loud slap, heard the resident protest that the PT could not do that and say he was being beaten, and noted a pattern of the PT speaking loudly and impatiently to the resident. The incident was not reported immediately, the resident was not promptly monitored, and the PT who struck the resident remained in the therapy room while therapy continued, contrary to the facility’s abuse prevention policy requiring protection of residents from physical abuse and immediate implementation of abuse protocols.
A resident with hemiplegia and hemiparesis following a cerebral infarction, who was cognitively able to make decisions, entered the rehab room during PT and lightly touched a PT on the back of the head to gain attention. The PT turned and slapped the resident’s thigh with an open hand, producing a loud sound; the resident protested verbally and later reported feeling assaulted and that the slap stung. Another PT in the room witnessed the event and noted the therapist had previously spoken loudly and impatiently to the resident, but did not report the incident that day, believing there was a 24-hour reporting window and expecting the involved PT to self-report. The involved PT also did not notify facility leadership, stating that prior reports had not led to action. Facility leadership and policy reviews confirmed this was physical abuse that should have been reported immediately to administration per the facility’s abuse reporting and prevention policies, but it was not reported until the following day, delaying investigation and protective measures.
A resident with Type 2 DM was readmitted from a GACH with discharge instructions for AC/HS fingerstick BG monitoring and parameters to notify the physician for abnormal values, but facility staff did not transcribe or obtain orders for BG checks and did not clarify the omission with the provider. The resident’s diabetes care plan referenced checking BG if low and observing for signs of hypo- and hyperglycemia but did not specify how BG would be measured, and facility policies requiring BG monitoring for diabetic residents with changes in condition or on dextrose-containing IV fluids were not followed. A stat CMP later showed a fasting BG of 351 mg/dL, which was communicated to the MD, yet no treatment for hyperglycemia was ordered; instead, the MD ordered D5W IV at a continuous rate for poor appetite, and nurses initiated and continued the infusion without reviewing the abnormal BG, without clarifying the appropriateness of D5W, and without initiating BG monitoring. Over the next days, staff failed to recognize or act on the elevated BG while D5W was infusing, and when the resident developed altered mental status, hypoxia, and other acute symptoms, EMS found D5W still running and a BG of 530 mg/dL, leading to transfer to the ED where severe hyperglycemia and uncontrolled DM were diagnosed.
A resident with Type 2 DM was readmitted from a GACH with discharge orders for AC & HS fingerstick blood sugar monitoring and parameters for notifying a physician, but the attending MD verbally chose not to renew these orders and this decision and rationale were not documented. The resident’s care plan referenced actions for low blood sugar but did not specify how BG would be measured, and facility physician orders only directed monitoring for signs and symptoms of hypoglycemia, with no AC & HS fingerstick checks or hyperglycemia monitoring. Over the stay, only three provider visits by an NP were documented, with no MD progress notes, no documented coordination between MD and NP about the decision to omit fingerstick monitoring, and no documentation of clinical reasoning for diabetes management. Despite a STAT fasting blood glucose of 351 mg/dL, the MD ordered D5W IV for nutrition, the NP’s prior NS IV order was not implemented or communicated, and the NP was not informed of the high glucose, the D5W order, or the resident’s subsequent change in condition. The resident later developed altered level of consciousness, respiratory distress, fever, and critically elevated blood glucose, leading to EMS transport and GACH admission for hyperglycemia, while facility records lacked required documentation and effective communication among the MD, NP, and nursing staff regarding diabetes management and treatment decisions.
A high fall-risk resident with cognitive impairment, unsteady gait, and a history of falls was primarily managed with bed and wheelchair pad alarms and a self-release soft belt, without individualized care plan details specifying the type and frequency of monitoring required under the facility’s Falling Star Program and Safety Supervision policies. After an initial unwitnessed fall, the care plan remained general and did not add specific monitoring interventions or document scheduled safety rounds. The resident later sustained a second unwitnessed fall discovered when a CNA responded to a sounding bed alarm, subsequently developed significant left leg pain, and was transferred to a GACH where a left femur fracture was diagnosed and ORIF surgery was performed. Staff and the DON acknowledged that the resident was high risk, that closer monitoring was expected for residents on the Falling Star Program, that no monitoring occurred during overnight hours, and that monitoring provided was only visual and not documented, demonstrating a failure to implement and document required supervision and fall-prevention measures.
A resident with cognitive impairment and total dependence for toileting did not receive timely incontinence care, resulting in prolonged exposure to moisture and the development of moisture-associated skin damage (MASD) at the coccyx. Documentation and interviews revealed a significant gap between care episodes, unaddressed requests for assistance, and lack of prompt response from staff, despite care plans and facility policy requiring frequent checks and hygiene support.
A resident with a confirmed scabies diagnosis was not promptly placed on contact precautions, and prescribed treatments were significantly delayed. The resident continued to share a room with two others who were not monitored or isolated, and there was no evidence of surveillance or assessment for exposed individuals. The resident's condition worsened, leading to hospitalization for severe skin wounds.
Three residents with significant medical and cognitive needs did not have comprehensive care plans developed or implemented as required. One resident with epilepsy did not have required side rail padding in place despite a care plan directive, and staff confirmed the intervention was not followed. Another resident with dementia and behavioral concerns lacked a care plan for cognitive impairment, and staff acknowledged this omission. A third resident using bilateral side rails also had no care plan addressing their use, with both nursing staff and the DON confirming the deficiency.
Surveyors found an open bag of hashbrowns in the kitchen freezer that was not labeled with an opened date or use-by date, contrary to facility policy and professional standards. Both the DSS and DON confirmed that proper labeling is required to ensure food safety and compliance with regulations.
A resident with severe cognitive impairment and multiple mental health diagnoses was prescribed Quetiapine and Divalproex without a valid, signed informed consent from the prescriber. Facility staff and documentation confirmed that the required consent process was incomplete, violating the resident's rights to be informed and to participate in care decisions.
Two residents with cognitive impairments were affected when one had an inaccurate wall clock and the other had no wall clock in their rooms. The absence or inaccuracy of the clocks led to disorientation and frustration, as confirmed by staff interviews and resident statements. Facility policy requires a homelike environment that supports resident orientation and comfort, which was not maintained in these cases.
A resident with chronic CHF, a history of pneumonia, and acute respiratory failure was admitted without a baseline care plan developed within 48 hours, despite physician orders for oxygen and albuterol for SOB. Nursing staff and the DON confirmed the lack of a care plan addressing the resident's respiratory and cardiac needs, contrary to facility policy, potentially delaying necessary care and services.
Two residents did not receive required safety interventions as outlined in their care plans and physician orders. One resident at high risk for falls was found without a bed pad alarm and attempting to get out of bed, while another resident with epilepsy did not have sheep skin padding on side rails as required to prevent injury during seizures. Staff and the DON confirmed that these interventions were not in place, despite facility policies mandating adherence to care plans and physician orders.
A resident with COPD, acute respiratory failure, and heart failure did not receive proper respiratory care as staff failed to assess and document baseline oxygen saturation, did not monitor oxygen levels every shift as ordered, and did not consistently document respiratory assessments before and after oxygen therapy. Additionally, oxygen tubing was found compressed in the side rail and the nasal cannula was not properly positioned, while the care plan lacked specific monitoring instructions and staff were unaware of relevant facility policies.
A LVN documented the administration of hydrocodone-acetaminophen on the MAR and Controlled Drug Record before actually giving the medication to a resident with chronic pain and mobility issues. The nurse stated this was her usual practice to ensure matching times on both records, despite facility policy requiring documentation only after administration.
A resident with a history of NSTEMI and other cardiac conditions experienced multiple episodes of chest pain, but nursing staff failed to follow physician orders for nitroglycerin administration, did not reassess or document the resident's pain, and delayed both diagnostic testing and transfer to acute care. These failures led to the resident suffering an acute myocardial infarction and subsequent death, with surveyors identifying Immediate Jeopardy due to noncompliance with care standards.
The facility failed to provide residents with reasonable access to telephones, as Station B's portable phone was missing and staff were unaware of alternative options. An LVN used her personal phone to facilitate communication, contrary to facility policy. The DON and ADM acknowledged the issue and the lack of staff training on using a facility cell phone.
A resident with diabetes and diabetic neuropathy reported feeling disrespected and embarrassed after a CNA made inappropriate comments and gestures with a hard-boiled egg. The facility failed to protect the resident from further contact with the CNA and did not monitor the resident's mood or behavior following the incident, violating their policies on dignity and abuse prevention.
A resident with type 2 diabetes mellitus had their blood sugar checked by a CNA instead of a licensed nurse, contrary to the facility's policy. The CNA performed the task at the request of an LVN, who was busy and monitored from the doorway due to the resident being in isolation. The facility's policy requires only licensed staff to conduct blood glucose tests.
A resident with major depressive disorder and paraplegia reported feeling threatened by a CNA who allegedly pointed fingers like a gun at her. The resident initially reported to the police that the CNA had a gun, but later retracted the allegation, citing a misunderstanding. Despite the facility's policy requiring prompt reporting of such incidents, the facility did not report the occurrence to the California Department of Public Health (CDPH).
A resident with major depressive disorder and paraplegia reported feeling threatened by a CNA, leading to police involvement. The facility's investigation suggested the report was false, motivated by personal feelings. Despite this, no care plan was developed to address the incident or the resident's emotional state, contrary to facility policy requiring comprehensive care plans.
The facility failed to complete POLST forms and ensure advance directive documentation for four residents, leading to incomplete records and potential conflicts with healthcare wishes. For one resident, the POLST lacked details on discussions with the responsible party, while another's POLST was undated. A third resident's POLST was unsigned by the physician, and the fourth had incomplete POLST forms. The Social Service Director found documentation in the electronic record but not in the physical chart, highlighting a process gap.
The facility was found deficient in food storage and staff hygiene practices. Observations revealed unlabeled and undated applesauce containers and an open gallon of milk without a date in the refrigerator. Additionally, a kitchen staff member entered the kitchen without a hair net, violating the facility's food handling policy. These practices could lead to food contamination and potential foodborne illnesses among residents.
A resident with dementia and hypertension was not treated with dignity during feeding, as a CNA stood while feeding instead of sitting at eye level. The facility's policy requires staff to sit at eye level to ensure respect and dignity, which was not followed in this instance.
A resident with severely impaired cognition and requiring maximum assistance was found with their call light out of reach, contrary to facility policy. Staff interviews confirmed the importance of call light accessibility for resident safety.
A resident with cognitive impairments was found restrained in bed by an overbed table left over him after breakfast, restricting his movement. Staff acknowledged the table should have been removed post-meal to allow freedom of movement. The facility's policy defines such restrictions as restraints.
The facility failed to prevent pressure ulcers for two residents by not setting an APM according to a resident's weight and not applying heel protectors as ordered. Both residents were at high risk for pressure ulcers, with one having an APM set incorrectly and the other lacking prescribed heel protectors. Staff acknowledged these oversights, which were against facility policy and professional standards.
A resident experienced significant weight loss due to the facility's failure to monitor and document nutritional intake consistently. Despite having a care plan for nutritional risk, the resident's weight dropped over 5% in a month. The lack of documentation was partly attributed to the hiring of registry CNAs. The Dietary Supervisor and DON acknowledged the oversight, and the RD admitted to not following the facility's policy on significant weight loss.
A resident with a history of respiratory issues did not receive adequate oxygen therapy as per physician's orders, with oxygen consistently administered at 2 LPM instead of the prescribed 3 LPM, and tubing obstructions were noted. This led to episodes of labored breathing and desaturation, despite the resident's severe cognitive impairment and need for complete staff assistance.
A resident with a history of traumatic brain injury and severe cognitive impairment had an incomplete POLST form, lacking signatures from both the physician and the resident's conservator. Interviews revealed confusion over who was responsible for ensuring the form's completion, with the SSD ultimately identified as responsible according to the Administrator and the SSD's job description.
The facility failed to maintain complete hospice binders for two residents under hospice care, lacking essential documentation such as nursing notes, assessments, and care plans. This deficiency hindered effective communication and collaboration between facility staff and hospice nurses, potentially impacting the delivery of appropriate hospice care.
A Hoyer lift was left unattended in a resident's room, creating a potential hazard for accidents and injury. A CNA admitted to leaving the lift while assisting a resident, acknowledging the risk of residents tripping over it. The DON confirmed that the lift should be stored properly to prevent injuries.
Failure to Protect a Resident From Physical Abuse and to Implement Abuse Protocols
Penalty
Summary
The deficiency involves the facility’s failure to protect a resident from physical abuse and to follow its Abuse Prevention Program and abuse/neglect protocols. The resident, who had hemiplegia and hemiparesis following a cerebral infarction and was documented as having capacity to understand and make decisions, reported that during a therapy session he touched the back of a physical therapist’s head to get his attention. In response, the therapist turned toward him and slapped him on the right thigh with an open hand. The resident stated the slap stung his leg, that the therapist appeared very angry and mean, and that he felt angry, shocked, upset, and assaulted. The resident reported that he had previously considered the therapist a friend and did not initially want to complain because he did not want to get anyone in trouble and considered himself a strong person. Another physical therapist in the room (PT 2) witnessed the incident and stated that the resident flicked the back of PT 1’s head, after which PT 1 rotated his chair and struck the resident once on the right thigh with an open hand. PT 2 described the slap as very loud, like someone slamming their hands on a desk, and reported that the resident yelled, “no, you can’t do that,” and “you beat me,” and appeared shocked and upset. PT 2 also reported that PT 1 often seemed annoyed with the resident and had, on multiple occasions, spoken loudly to him, telling him he talked too much and needed to be quiet. PT 1 acknowledged that the resident had touched or slapped the back of his head, that he was startled, and that he immediately turned and slapped the resident, though he claimed he slapped the resident’s hand and spoke in a low voice telling him to stop. The facility failed to identify and respond to this incident as abuse at the time it occurred. The incident was not immediately reported to the Administrator or nursing staff on the day it happened, and the resident was not immediately monitored after the slap. PT 2 allowed therapy to continue with both therapists remaining in the room and did not remove PT 1 from the resident’s presence, despite witnessing the slap and the resident’s reaction. PT 2 stated she did not report the incident immediately because she believed there was a 24‑hour reporting window, wanted to give PT 1 an opportunity to report it himself, and the resident had asked her not to report it. The incident was reported the following day after it was learned that PT 1 had not reported it. The facility’s Abuse Prevention Program stated that residents have the right to be free from abuse, including physical abuse and corporal punishment, and that administration would protect residents from abuse by anyone, but these protections were not implemented at the time of the event.
Failure to Immediately Report Witnessed Physical Abuse by Therapist
Penalty
Summary
The deficiency involves the facility’s failure to immediately report an incident of physical abuse by a physical therapist toward a resident to the Administrator within the required timeframe, as outlined in the facility’s Abuse Prevention Program and Abuse Investigation & Reporting policies. On 02/23/2026, while beginning physical therapy, Resident 1 entered the rehabilitation room and touched PT 1 on the back of the head to get his attention. In response, PT 1 rotated his chair and struck the resident once on the right thigh with an open hand, producing a loud sound described by PT 2 as similar to slamming hands on a desk. Resident 1, who had hemiplegia and hemiparesis following a cerebral infarction and had documented capacity to understand and make decisions, immediately protested, stating, "no, you can't do that" and "you beat me," and later reported feeling angry, assaulted, and that the slap stung his leg. Despite witnessing the event, neither PT 1 nor PT 2 reported the incident to the Administrator on the day it occurred. PT 2 stated that she believed there was a 24-hour reporting window and wanted to give PT 1 an opportunity to report the incident himself, and only reported it the following day to the Director of Rehabilitation after learning PT 1 had not done so. PT 1 stated he did not notify the Administrator or Director of Rehabilitation because, in his experience, when he reported concerns, no action was taken. During this time, therapy continued in the same room with both therapists present, and Resident 1 stated that no one asked him how he was or whether he was okay following the incident. Interviews with facility leadership confirmed that the incident met the definition of physical abuse and should have been reported immediately. The DON stated the incident between Resident 1 and PT 1 was considered physical abuse and should have been reported immediately to facility administration in accordance with facility policy and abuse reporting requirements. Review of the facility’s Abuse Investigation & Reporting, Abuse Prevention Program, and Abuse and Neglect Clinical Protocol policies showed that all allegations or incidents of abuse, neglect, exploitation, misappropriation, mistreatment, or injuries of unknown origin were to be promptly and immediately reported to appropriate facility management and external agencies, and that management and staff were required to address suspected or identified abuse and report it in a timely manner. The failure of PT 1 and PT 2 to immediately report the witnessed physical abuse resulted in a delay in the facility’s investigation and protection of Resident 1 from further abuse.
Failure to Monitor and Manage Blood Glucose and IV Dextrose Therapy for Diabetic Resident
Penalty
Summary
The deficiency involves the facility’s failure to provide treatment and services in accordance with professional standards of practice for a resident with Type 2 DM following readmission from a GACH. The resident’s GACH discharge recap dated 1/11/2026 included orders to renew fingerstick blood sugar monitoring AC and HS, with parameters to notify the physician for BG >250 mg/dL or <70 mg/dL and to implement a hypoglycemia protocol. Upon readmission, the facility’s admission record reflected diagnoses of Type 2 DM and sepsis, and nursing notes documented that the attending physician’s orders were “verified and carried out.” However, the physician order report from 1/11/2026–1/31/2026 did not include any orders for AC/HS fingerstick BG monitoring or monitoring for signs and symptoms of hyperglycemia, only an order to monitor for signs and symptoms of hypoglycemia three times daily. The nurse who spoke with the physician at readmission did not document that the physician declined to reorder fingerstick monitoring or the rationale, and there was no documentation in the physician or NP progress notes explaining why BG monitoring was not continued despite the diagnosis of Type 2 DM and the GACH discharge instructions. The resident’s existing care plan, titled “Risk for Unstable Blood Glucose Level,” required staff to observe for signs and symptoms of low and high BG and to check BG if it was below 70 mg/dL, with instructions to administer IM glucagon and call 911 if the resident was unconscious or without vital signs. However, the care plan did not specify how licensed nurses would measure BG levels (e.g., via fingerstick) to determine whether levels were low or high. Facility policies on blood glucose monitoring for diabetic residents experiencing a change of condition and on diabetic management required BG monitoring for residents with DM, particularly when they had changes in condition, infections, poor oral intake, or were receiving dextrose-containing IV fluids, and indicated that failure to monitor BG in such situations may place residents at risk for hyperglycemia, hypoglycemia, dehydration, and hospitalization. Despite these policies and the resident’s diagnosis of Type 2 DM, staff and the NP acknowledged that the resident was not being monitored with fingerstick BG checks and that DM management relied on oral hypoglycemic medications and periodic blood work. On 2/5/2026, a stat CMP showed a fasting BG of 351 mg/dL. Nursing documentation indicated that this abnormal lab result was communicated to the attending physician via text and voicemail, and the lab results were faxed, but the nurse did not document which value was abnormal. Another nurse later texted a screenshot of the stat lab results, including the elevated BG, to the physician. The physician did not issue new orders to address the hyperglycemia but instead ordered a 1 L NS bolus via IV (from the NP) and then, on 2/6/2026, ordered D5W IV at 60 cc/hr for a total of 3 L due to poor appetite. Nursing staff started and continued the D5W infusion without reviewing or acting on the elevated BG of 351 mg/dL, without clarifying the appropriateness of D5W in the setting of hyperglycemia, and without initiating or obtaining orders for BG monitoring. Multiple RNs later acknowledged they had not reviewed the stat lab results before starting or continuing D5W, did not clarify DM monitoring parameters with the physician, and did not monitor for signs and symptoms of hyperglycemia while the D5W was infusing. On 2/8/2026, the resident experienced a change in condition characterized by non-responsiveness, shallow respirations, tachypnea, tachycardia, fever, oxygen saturation in the 80s, and a BG of 463 mg/dL documented by facility staff. An SBAR reflected these findings and the administration of oxygen via non-rebreather at 15 L, with improved oxygen saturation. EMS was called, and paramedics found the resident with altered level of consciousness, tachycardia, labored respirations, fever, and an IV of D5W still infusing at 60 cc/hr. Paramedics reviewed prior lab results showing a fasting BG of 351 mg/dL from 2/5/2026, requested that nursing staff check a current BG (which was 530 mg/dL), and instructed the nurse to discontinue the D5W, which they observed being stopped at that time. EMS documentation and ED records indicated that the resident had been receiving D5W despite hyperglycemia, with ED notes stating that the facility had treated a BG of 350 mg/dL with dextrose. The resident was transferred to the GACH ED, where BG readings remained critically elevated, and diagnoses included uncontrolled DM and severe hyperglycemia. The facility’s DON and medical director later stated that the D5W infusion in the presence of hyperglycemia would further elevate BG and that residents with Type 1 or 2 DM should be monitored with fingerstick BG AC and HS, and the DON acknowledged that the lack of BG monitoring and failure to clarify orders contributed to the resident’s elevated glucose levels and subsequent transfer. Throughout this period, there was ineffective communication among nursing staff, the physician, and the NP regarding the resident’s change in condition, critical lab results, and ordered treatments. Nurses reported that abnormal lab results were not clearly endorsed between shifts, that they did not review the stat lab results before implementing IV fluid orders, and that they did not inform the NP about the elevated BG or the change from NS to D5W. The NP stated she was unaware of the elevated BG of 351 mg/dL, unaware that D5W was being infused instead of NS, and would not have ordered D5W in a hyperglycemic state. The attending physician stated he intentionally did not reorder fingerstick BG monitoring at readmission and ordered D5W despite knowing the resident was hyperglycemic, but did not document this plan in the record. The combination of not implementing or clarifying BG monitoring orders, not operationalizing the care plan to include specific BG measurement methods, not acting on critical lab results, and continuing D5W infusion in the presence of hyperglycemia led to the resident not receiving required monitoring and timely intervention for hyperglycemia.
Failure to Manage and Monitor Diabetes and Document Physician Oversight
Penalty
Summary
The deficiency involves a failure by the attending MD, NP, and licensed nursing staff to adequately supervise and manage the medical care of a resident with Type 2 DM, including failure to follow and/or appropriately modify GACH discharge orders, failure to document clinical reasoning and treatment decisions, and failure to communicate effectively among providers. The resident had a care plan for "Risk for Unstable Blood Glucose Level" that instructed staff to check blood glucose if it was below 70 mg/dL and to administer glucagon and call 911 if the resident was unconscious or without vital signs, and to observe for signs and symptoms of high blood glucose and report them to the physician. However, the care plan did not address how licensed nurses would measure the resident’s blood glucose levels to determine if they were below 70 mg/dL. GACH discharge orders dated 1/11/2026 directed renewal of fingerstick blood sugar checks AC & HS, with additional PRN checks and parameters to notify the physician for blood sugars greater than 250 mg/dL or less than 70 mg/dL and to implement a hypoglycemia protocol. Upon readmission on 1/11/2026 with diagnoses including Type 2 DM and sepsis, the facility’s Physician Order Reports from 1/11/2026 through 1/31/2026 did not include orders for AC & HS fingerstick blood sugar monitoring or monitoring for hyperglycemia, but only an order to monitor for signs and symptoms of hypoglycemia three times a day. A nursing progress note on 1/11/2026 documented that the attending MD was notified of the readmission and that physician orders were “verified and carried out,” but there was no documentation that the nurse clarified with the MD whether blood sugar monitoring should continue as per GACH discharge instructions. In interview, the RN stated that the MD verbally declined to renew the AC & HS fingerstick orders and said he would assess the resident the next day, but this decision and rationale were not documented in the medical record. There was no progress note by the MD on or after 1/12/2026 documenting an assessment, plan, or justification for not monitoring blood sugars, and the NP’s H&Ps and progress note did not document how blood sugar monitoring should be performed or any coordination with the MD regarding the decision not to follow the GACH blood sugar monitoring orders. From admission on 12/11/2025 through 2/8/2026, only three provider visits were documented, all authored by the NP (two H&Ps and one progress note), with no progress notes by the MD. The NP reported that she was managing the resident’s care with the MD, knew the resident had Type 2 DM, and that the DM was being monitored with random blood work (CBC, BMP), but stated the resident should have had AC & HS fingerstick monitoring and that she was unaware the GACH readmission orders for AC & HS blood sugar checks were not renewed. On 2/5/2026, the NP ordered 1 liter of NS IV for poor oral intake and hyponatremia, but she was not informed whether this was carried out, was not informed of a STAT fasting blood glucose result of 351 mg/dL, and was not informed that the MD later ordered D5W IV instead of NS. The DON confirmed that on 2/6/2026 the MD ordered 3 liters of D5W at 60 cc/hr after being notified of the high fasting blood glucose, and that licensed nurses did not clarify this order despite the elevated glucose level or question the absence of fingerstick monitoring. The MD acknowledged ordering D5W for nutrition and comfort despite knowing the resident was hyperglycemic and did not document this plan or rationale in the record. On 2/8/2026, nursing documentation and SBAR showed a significant change in condition: the resident was non-verbal, with shallow respirations, oxygen saturation of 87%, respiratory rate of 33, temperature of 100.7°F, heart rate of 133 bpm, and a blood glucose of 463 mg/dL. Oxygen at 15 L via non-rebreather was initiated, improving saturation to 95%, and 911 was called. The paramedic run report documented arrival at 4:16 PM, altered level of consciousness, non-responsiveness to name, sinus tachycardia at 130 bpm, respiratory rate of 32 with labored breathing, temperature of 101°F, and discontinuation of D5W due to a blood glucose of 530 mg/dL. GACH ED records indicated the resident was admitted for altered level of consciousness, fever, and hyperglycemia, and noted that the facility had treated a blood sugar of 350 mg/dL with dextrose. ED testing showed blood sugars of 530 mg/dL and 434 mg/dL and high urine glucose. The NP stated she was unaware of the resident’s hyperglycemic state, the administration of D5W, or the change in condition and hospitalization. The Medical Director stated that keeping a resident in a hyperglycemic state and infusing D5W in that context would not benefit the resident and that residents with Type 1 or 2 DM need AC & HS blood glucose monitoring. Facility policies on Physician Services and Physician Orders required medical evaluation, review of orders and plan of care at each required visit, appropriate progress notes, and clear physician orders, but the record lacked documentation of assessments, clinical reasoning, treatment decisions, and communication among the MD, NP, and licensed staff regarding the resident’s DM management, change in condition, critical lab results, and ordered treatments.
Failure to Implement Individualized Fall-Prevention Monitoring for High-Risk Resident
Penalty
Summary
The deficiency involves the facility’s failure to ensure adequate supervision and accident prevention for a high fall-risk resident in accordance with its own policies, including the Falling Star Program and Safety Supervision of Residents. The resident was admitted with unsteadiness on feet, a history of falls, osteoarthritis, and cognitive decline, and was later assessed as having moderately impaired cognition and requiring partial to moderate assistance with ADLs. A Fall Risk Collection record dated 12/15/2025 scored the resident at 14, indicating high fall risk and a need for increased supervision. Despite this, the resident’s care plans primarily focused on the use of a bed and wheelchair pad alarm and a self-release soft belt, with no individualized or specific interventions describing the type and frequency of monitoring or supervision required. The resident experienced an unwitnessed fall on 12/15/2025 when the bed pad alarm sounded and nursing staff found the resident on the floor next to the bed with no apparent injury. Subsequent care plan updates for falls and actual fall events continued to emphasize the use of pad alarms and a soft belt but did not add new, individualized interventions or specify additional monitoring or supervision. The facility’s Fall Management and Falling Star Program policies required staff to identify interventions related to specific risks, implement additional or different interventions if falls recurred, and determine the type and frequency of supervision based on assessed needs. However, the care plans remained general, and there was no documentation identifying specific monitoring requirements or scheduled safety rounds as outlined in the Falling Star Program policy. On 1/25/2026, the resident sustained a second unwitnessed fall when a CNA heard the bed pad alarm and found the resident lying on the floor on her back. Initial assessment documented no visible injuries, but the resident complained of left leg pain and was medicated with Tylenol. Later that day, the resident reported increased left leg pain rated 8/10, and nursing staff observed the left leg slightly externally rotated, leading to transfer to a general acute care hospital where imaging revealed a left femur fracture requiring ORIF surgery. Interviews with nursing staff and the DON confirmed that the resident was a high fall risk, that residents on the Falling Star Program were supposed to receive closer monitoring, and that there was no monitoring conducted between 11 PM and 7 AM. The DON acknowledged that the resident should have been on the Falling Star Program since admission, that care plan interventions were general and not specific to the type and frequency of monitoring, and that monitoring was only visual and not documented, demonstrating a failure to implement and document required supervision and safety measures. Additionally, although the resident was identified as high risk and on the Falling Star Program after multiple falls, there was no indication in the care plan of specific monitoring interventions such as defined observation intervals or documented safety rounds. The facility’s policies required ongoing identification of safety risks and environmental hazards and adjustment of supervision based on changes in the resident’s condition or environment, but the record did not show such individualized adjustments. After the resident’s return from the hospital with a left femur fracture and ORIF, observations showed that there was no fall mat at the bedside, and staff interviews confirmed that the resident did not have a fall mat. The DON stated that a fall mat was not used due to concern it would be an environmental hazard for the resident, but this did not change the fact that the facility had not clearly determined or documented the type and frequency of supervision required for this high-risk resident, nor had it implemented the full scope of monitoring and safety measures contemplated by its own policies.
Failure to Provide Timely Incontinence Care Resulting in Skin Breakdown
Penalty
Summary
A deficiency occurred when a resident with moderate cognitive impairment and total dependence for toileting hygiene did not receive timely assistance with incontinence care. Documentation showed that after receiving toileting assistance in the late morning, the next documented care was not provided until the evening, resulting in a gap of approximately 6.5 hours. During this period, the resident remained in a wet brief, and both the resident and a family member reported that requests for assistance were not answered. The family member observed the resident in a wet brief for several hours and reported that staff did not respond to the call light or provide care during this time. The resident had a history of heart failure, diabetes, and acute embolism, and was assessed as lacking capacity to make decisions. Care plans indicated the resident was at risk for skin breakdown and required frequent incontinence care and skin protection measures, including the use of topical ointment for moisture-associated skin damage (MASD) at the coccyx. Despite these interventions being documented, the resident developed MASD with superficial skin breakdown and bleeding, as confirmed by staff and family observations. The wound was first noted by a CNA and later reported to the wound care nurse by the family member. Interviews with staff confirmed the importance of frequent brief changes for this resident due to frequent episodes of incontinence, including loose stools. Facility policy required routine checks and assistance with hygiene and elimination for residents unable to perform activities of daily living independently. However, the lack of timely incontinence care and failure to respond to requests for assistance directly contributed to the resident's skin breakdown and discomfort.
Failure to Implement Timely Infection Control and Treatment for Scabies
Penalty
Summary
The facility failed to implement effective infection prevention and control practices for a resident diagnosed with scabies. After a dermatology evaluation confirmed scabies, the resident was not placed under contact precautions until two days after the diagnosis, despite recommendations to treat as scabies being made earlier. The resident continued to share a room with two other residents, who were not placed on isolation or monitored for symptoms, even though they were in close contact. The facility did not have an available room for isolation, and only the affected resident was placed on isolation precautions within the shared room, while the roommates were allowed to move freely within the room and the facility. The prescribed treatment for scabies, including Ivermectin and Permethrin cream, was not administered as ordered. Documentation showed that Permethrin cream was not given until twelve days after the diagnosis and eight days after the physician's order, with notes indicating delays due to waiting for the family to provide the medication. There was no evidence that the physician was notified about the missed doses on the specified dates. The resident, who had limited cognitive capacity and required maximal assistance with activities of daily living, experienced worsening skin conditions, including open, severe skin wounds, and was eventually transferred to a general acute care hospital for further evaluation and treatment. There was also a lack of monitoring and assessment for the two roommates who were exposed to the resident with scabies. Progress notes and interviews confirmed that no formal documentation, daily assessments, or diagnostic testing were conducted for these close contacts. The facility did not establish an effective surveillance system or maintain an accurate line listing of symptomatic residents and staff, as required by their own policies and CDC guidelines. This failure to follow infection control protocols and physician orders contributed to the spread and worsening of the infection.
Failure to Develop and Implement Comprehensive Care Plans for Residents
Penalty
Summary
The facility failed to develop and implement comprehensive care plans for three residents with significant medical and cognitive needs, as required by facility policy and procedure. For one resident with a history of epilepsy, severe cognitive impairment, and a care plan intervention to apply sheep skin padding to side rails to prevent injury during seizures, observations revealed that the required padding was not in place. Both the assigned LVN and the DON confirmed that the care plan was not followed, and the intervention to confirm placement of the padding every shift was not implemented. Another resident, admitted with dementia, a maxillary fracture, and concussion, was prescribed medications for dementia and was assessed as moderately cognitively impaired and dependent for multiple activities of daily living. Despite these findings and documented behavior concerns related to dementia, there was no evidence of a comprehensive care plan addressing cognitive impairment or dementia care. The baseline care plan and progress notes lacked goals or interventions for dementia, and staff interviews confirmed the absence of a dementia care plan since admission. A third resident, with dementia, difficulty walking, and muscle wasting, was assessed as severely cognitively impaired and requiring supervision for mobility. Although informed consent for the use of bilateral half side rails was documented, there was no care plan initiated to address the use of these side rails. Both the reviewing RN and the DON acknowledged the lack of a care plan for side rail use, which is necessary to guide staff in meeting the resident's needs and monitoring the effectiveness of interventions. These deficiencies were identified through record reviews, staff interviews, and direct observations.
Failure to Label Opened Food Items in Kitchen
Penalty
Summary
During a kitchen tour, surveyors observed an open plastic bag containing six hashbrowns in the facility's freezer that was not labeled with the date it was opened or a use-by date. The Dietary Service Supervisor (DSS) confirmed that, according to facility policy, all foods in the kitchen should be labeled with both an opened date and a use-by date. The DSS acknowledged that failing to label the bag could result in shortened shelf life and potential contamination. The Director of Nurses (DON) also stated that food in the kitchen should be labeled with an opened date and a use-by date, as per facility policy, to ensure staff know when to discard food and prevent serving it to residents. A review of the facility's policy and the 2022 Food Code confirmed the requirement for date marking of ready-to-eat, time/temperature control for safety foods. The deficiency was identified due to the lack of labeling on the open bag of hashbrowns, which was not in accordance with professional standards or facility policy.
Failure to Obtain Valid Informed Consent for Psychotropic Medications
Penalty
Summary
The facility failed to obtain valid informed consent for the administration of psychotropic medications, specifically Quetiapine and Divalproex, for a resident with diagnoses including dementia, psychotic disorder, and mood disorder. The resident was assessed as having severely impaired cognitive status and required varying levels of assistance with daily activities. Physician orders for these medications were present in the resident's records, but a review of the electronic health record and facility documentation revealed that informed consent forms for these drugs were either incomplete or missing the prescriber's signature, rendering them invalid. Interviews with facility staff, including a registered nurse, the medical record director, and the director of nursing, confirmed that the required informed consent process was not properly completed. Facility policy mandates that the prescriber must obtain and sign the informed consent form when psychotropic medications are ordered, ensuring that the resident or their representative is fully informed and agrees to the treatment. The lack of a valid, signed informed consent for these medications constituted a violation of the resident's rights to be informed and to participate in decisions regarding their care and treatment.
Failure to Provide Accurate and Accessible Wall Clocks for Residents
Penalty
Summary
The facility failed to provide a homelike environment for two residents by not ensuring the presence and accuracy of wall clocks in their rooms. For one resident with dementia, depression, and muscle wasting, the wall clock in the room displayed an incorrect time, as observed by both the resident and the Infection Preventionist Nurse (IPN). The IPN confirmed that the clock was not showing the correct time during the observation. For another resident with dementia, osteoarthritis, and osteoporosis, there was no wall clock present in the room. The IPN acknowledged that all rooms should have a wall clock to help residents with time orientation. During interviews, the resident without a clock expressed frustration at having to repeatedly ask staff for the time, indicating that the absence of a clock affected her comfort. The DON also stated that having an accurate wall clock in every resident's room is important for orientation and maintaining a comfortable, homelike environment. The facility's policy on quality of life and homelike environment requires staff to provide a setting that emphasizes residents' comfort, independence, and personal needs, which was not met in these instances.
Failure to Develop Baseline Care Plan Within 48 Hours of Admission
Penalty
Summary
The facility failed to develop a baseline care plan within 48 hours of admission for a resident with significant medical needs, including chronic congestive heart failure, a history of pneumonia, and acute respiratory failure with hypoxia. Upon review, it was found that the resident had physician orders for oxygen therapy and albuterol as needed for shortness of breath, and required varying levels of assistance with daily activities. Despite these needs and orders, the electronic health record did not contain a baseline care plan addressing the management of the resident's respiratory and cardiac conditions or the interventions required for shortness of breath. Interviews with nursing staff and the Director of Nursing confirmed that a baseline care plan was not created as required by facility policy, which mandates such a plan within 48 hours of admission to ensure proper care and communication among staff. The absence of this care plan was acknowledged by staff as having the potential to delay necessary care and services for the resident, as it failed to provide guidance on managing the resident's immediate medical and physical needs.
Failure to Implement Required Safety Interventions for Two Residents
Penalty
Summary
The facility failed to provide a safe and hazard-free environment for two residents by not implementing required safety interventions as outlined in their care plans and physician orders. For one resident with diagnoses including respiratory failure, chronic kidney disease, and unspecified dementia, the care plan and physician order required the use of a bed pad alarm to alert staff if the resident attempted to get out of bed unassisted. Despite being identified as high risk for falls, the resident was observed in bed without a pad alarm and attempting to get up. Interviews with nursing staff and the Director of Nursing confirmed that the bed alarm was not in place, and the physician order and care plan were not followed. Another resident, diagnosed with epilepsy, hypertension, and pneumonia, was at risk of injury during seizures. The care plan required sheep skin padding on both side rails to prevent injury during seizure activity and mandated that staff confirm placement every shift. Observations revealed that the resident's side rails were not padded, and interviews with nursing staff and the Director of Nursing confirmed that the intervention was not implemented as required by the care plan. Review of facility policies indicated that physician orders and individualized care plans are to be followed to ensure resident safety and minimize risks such as falls and injuries. In both cases, the required interventions were not in place at the time of observation, and staff acknowledged that the care plans and physician orders were not followed, resulting in an unsafe environment for the residents involved.
Failure to Provide Safe and Appropriate Respiratory Care
Penalty
Summary
Nursing staff failed to provide necessary respiratory care to a resident with chronic obstructive pulmonary disease (COPD), acute respiratory failure, and congestive heart failure, as indicated by physician orders and professional standards of practice. The staff did not properly assess or document the resident's baseline oxygen saturation (SpO2) level prior to administering oxygen therapy, nor did they consistently monitor and document oxygen saturation every shift as ordered. There was also a lack of documentation regarding respiratory assessments, including signs and symptoms of respiratory distress or shortness of breath, before and after oxygen therapy was provided. Observations revealed that the resident's oxygen tubing was compressed within the side rail, and the nasal cannula was not properly positioned in the resident's nose, which could have impeded oxygen delivery. Interviews with nursing staff indicated a lack of awareness and adherence to the physician's PRN order for oxygen therapy, with some staff keeping the resident on continuous oxygen without documented need or assessment. The care plan did not specify the frequency of monitoring, safe oxygen saturation ranges, or include detailed clinical examination or assessment instructions. Further review of facility policies and interviews with the Director of Nursing and other staff revealed that there was no specific policy for COPD or respiratory failure care, and staff were not fully aware of the standards of practice for respiratory care. The facility's policy on oxygen administration required monitoring for signs of hypoxemia and documentation of vital signs and resident response before and after therapy, but these practices were not consistently followed for this resident.
Nurse Documented Medication Administration Prior to Giving Medication
Penalty
Summary
A Licensed Vocational Nurse (LVN) failed to follow facility policy by documenting the administration of hydrocodone-acetaminophen on both the Medication Administration Record (MAR) and the Controlled Drug Record before actually giving the medication to a resident. The nurse was observed preparing the medication, signing both records, and then administering the medication several minutes later. During an interview, the LVN confirmed that it was her practice to sign the records prior to administration to ensure the times matched on both documents. The resident involved had a history of rheumatoid arthritis, an artificial hip joint, and a history of falls, and was receiving pain medication as needed. Facility policy and the Director of Nursing (DON) both specified that documentation on the MAR should only occur after the medication has been administered, as residents may still refuse the medication. The facility's policy required immediate documentation following administration, but this was not followed in this instance.
Failure to Provide Timely and Appropriate Care for Chest Pain in Resident with Cardiac History
Penalty
Summary
A resident with a history of NSTEMI, Parkinson's disease, and atherosclerotic heart disease experienced multiple episodes of chest pain while under the care of the facility. The resident had physician orders for sublingual nitroglycerin to be administered every five minutes for up to three doses for chest pain, with instructions to notify the physician if pain persisted. On several occasions, nursing staff administered only one dose of nitroglycerin, documented the effect as 'Not Effective' or 'Somewhat Effective,' and failed to administer subsequent doses as ordered. Additionally, staff did not consistently reassess the resident's pain after administration, nor did they notify the physician or document the change in condition as required by facility policy. The facility also failed to monitor and document the resident's complaints of chest pain every shift for 72 hours following episodes of unrelieved pain, as outlined in their policy for changes in condition. There were delays in carrying out physician orders for diagnostic testing, including a stat EKG, which was performed several hours after being ordered. Furthermore, there was a significant delay in transferring the resident to an acute care hospital despite ongoing severe chest pain and abnormal vital signs, with emergency services not being called until hours after the resident's condition had deteriorated. Interviews with nursing staff revealed a lack of understanding and adherence to the physician's orders and facility protocols regarding the management of chest pain and notification of changes in condition. Staff admitted to not administering additional doses of nitroglycerin, not reassessing the resident, and not promptly notifying the physician or documenting the events. The resident ultimately suffered an acute myocardial infarction, was transferred to the hospital, and died after further cardiac events. The survey identified these failures as constituting Immediate Jeopardy due to the facility's noncompliance with professional standards of practice, care planning, and physician orders for the management of chest pain.
Removal Plan
- LVN 1 and LVN 2 were provided a one-to-one re-education and training by the DON focusing on the proper evaluation of resident's change in condition (COC) particularly about residents experiencing chest pain, accurate administration of medications, timely notification of physicians, laboratory and diagnostic testing procedures (verifying that the vendor will perform the testing without delay) and appropriate documentation practices.
- The DON and the Registered Nurse Supervisor evaluated all other 9 residents who were receiving Nitroglycerin for any change in condition (COC).
- The facility would designate RN or Nursing Supervisor to evaluate residents experiencing a COC, particularly chest pain, to ensure timely and appropriate interventions.
- The DON initiated daily morning meetings for COC audits, focusing on residents with chest pain, diagnosis of NSTEMI or with prescribed nitroglycerin.
- The DON will initiate in-services for all licensed nurses (LN) for proper evaluation of residents' change in condition, with an emphasis on residents experiencing chest pain, diagnosed with NSTEMI, and prescribed nitroglycerin. The Inservice will be repeated quarterly, and incorporated into the orientation program for newly-hired LN.
Deficiency in Resident Telephone Access
Penalty
Summary
The facility failed to ensure residents had reasonable access to and privacy in their use of communication methods, specifically telephones. Station B's portable phone was missing, and there was no alternative phone readily available for residents to use. This issue was highlighted during an interview with a resident's representative, who reported ongoing problems with the facility's phone system, including long wait times and dropped calls. The representative noted that these issues had persisted for over eight years, affecting their ability to communicate with their family member residing in the facility. Licensed Vocational Nurse (LVN) 1, who was assigned to Station B, confirmed that the portable phones often had poor connections or were unavailable, leading her to use her personal cell phone to facilitate communication between residents and their families. However, LVN 1 was unaware of any additional facility cell phones available for resident use. The Director of Nursing (DON) and the Administrator (ADM) acknowledged the missing phone and the lack of in-service training for staff regarding the use of a facility cell phone as an alternative. The facility's policy and procedure on resident access to telephones emphasized the importance of providing residents with reasonable access to a private phone. However, the facility did not adhere to this policy, as evidenced by the missing phone at Station B and the lack of documentation for staff training on alternative phone use. The DON and ADM both stated that staff should not use personal phones for resident communication, yet there was no evidence of in-service training to inform staff of the available facility cell phone for such situations.
Failure to Ensure Resident Dignity and Respect
Penalty
Summary
The facility failed to ensure that a resident was treated with dignity and respect, as outlined in their policies and procedures. The resident, who was admitted with a diagnosis of diabetes and diabetic neuropathy, reported an incident involving a certified nurse assistant (CNA) who made inappropriate comments and gestures with a hard-boiled egg. The resident felt embarrassed and disrespected by the CNA's actions, which included making a loud comment about the resident's need for assistance and suggesting that no one wanted to assist the resident due to their COVID-19 positive status. The resident reported the incident to the Administrator the following day, but the facility did not take appropriate steps to protect the resident from further contact with the CNA. The Administrator brought the CNA to the resident's room to apologize, which was against the facility's policy on abuse prevention. Additionally, the facility did not conduct follow-up monitoring of the resident's mood or behavior, nor did they address the resident's feelings or preferences regarding the CNA's continued involvement in their care. The facility's policies on dignity and abuse prevention were not followed, as staff failed to promote the resident's well-being and self-esteem. The facility did not conduct an in-service for licensed nurses regarding abuse, nor did they monitor the resident for changes in mood or behavior after the incident. The lack of appropriate response and monitoring placed the resident at risk for further emotional distress and potential abuse.
Improper Blood Sugar Check by CNA
Penalty
Summary
The facility failed to ensure that a resident with type 2 diabetes mellitus received proper care and services according to the facility's policy and procedure for blood glucose testing. The resident, who required blood sugar checks, had their blood sugar level checked by a certified nurse assistant (CNA) instead of a licensed nurse (LN), as per the facility's policy. This occurred because the licensed vocational nurse (LVN) was busy and asked the CNA to perform the task, despite the facility's policy stating that only licensed staff should conduct blood glucose tests. The resident, who was admitted with a diagnosis of diabetes and diabetic neuropathy, expressed feeling uncomfortable with the CNA performing the blood sugar check, as it was not a usual practice. The CNA confirmed that it was their first time performing such a task and did so at the request of the LVN. The facility's administrator and director of staff development both acknowledged that the CNA should not have performed the blood sugar check, as it was against the facility's policy. The LVN admitted to asking the CNA to perform the check while they monitored from the doorway, as the resident was in an isolation room.
Failure to Report Alleged Abuse Incident to CDPH
Penalty
Summary
The facility failed to report an incident of unusual occurrence to the California Department of Public Health (CDPH) as per its policy and procedure. This involved a resident who was admitted with a diagnosis of major depressive disorder and paraplegia. The resident, who was cognitively intact, reported feeling threatened by a certified nurse assistant (CNA) who allegedly pointed fingers like a gun at her. The police were involved, but the facility did not report the incident to CDPH. The investigation summary revealed that the resident had gone to the police department, alleging that the CNA was carrying a gun in the facility. The resident later withdrew the allegation, stating it was a misunderstanding related to a Valentine's Day gift from the CNA. Despite the resident's retraction, the facility did not report the incident to CDPH, as required by their policy. The facility's interdisciplinary team discussed the incident, but the administrator decided not to report it, citing the resident's alertness and orientation. Interviews with the resident, family member, and staff indicated that the resident felt mistreated by the CNA and had previously been reluctant to report due to fear of retaliation. The facility's policy mandates prompt reporting of all allegations of abuse or unusual occurrences to appropriate authorities, but this was not followed. The Director of Nurses acknowledged the incident as an unusual occurrence but confirmed it was not reported to CDPH.
Failure to Develop Resident-Centered Care Plan
Penalty
Summary
The facility failed to develop a resident-centered care plan for a resident who was admitted with major depressive disorder and paraplegia. Despite the resident's capacity to understand and make decisions, as indicated in their medical records, the facility did not create a care plan addressing a specific incident where the resident reported feeling threatened by a CNA. The resident alleged that the CNA pointed fingers like a gun at them, leading to police involvement. The facility's investigation suggested that the resident made a false report due to personal feelings towards the CNA, but no care plan was developed to address this incident or the resident's emotional state. The Director of Nursing acknowledged that a care plan should have been initiated to address the false allegation incident. The facility's policy requires a comprehensive care plan to meet residents' medical, nursing, mental, and psychosocial needs, but this was not followed in this case. The resident's care plan only addressed mood disorder without specific reference to the incident involving the CNA, leaving a gap in addressing the resident's psychosocial needs and the situation's impact on their well-being.
Incomplete POLST and Advance Directive Documentation
Penalty
Summary
The facility failed to complete Physician Orders for Life-Sustaining Treatment (POLST) for four residents, which resulted in a lack of documentation regarding advance directives. For Resident 82, the POLST was signed by the physician but lacked details on discussions with the responsible party, and no advance directive notification form was present in the chart. This oversight could delay care in emergencies. Similarly, Resident 91's POLST was signed without a date, and there was no documentation indicating that the resident was informed about their rights to formulate an advance directive. Resident 59's POLST was signed by the responsible party but not by the physician, and there was no documentation showing that the responsible party was informed about the right to formulate an advance directive. The Social Service Director (SSD) indicated that such documentation should be accessible in the resident's clinical chart to ensure immediate access during emergencies. However, the SSD found the documentation in the electronic medical record, not in the physical chart, highlighting a gap in the facility's process. For Resident 79, the POLST forms were incomplete, with sections on medical interventions and advance directives left blank. Although the SSD documented the refusal of an advance directive in the electronic medical record, this information was not transferred to the physical chart. The facility's policies require that the POLST be reviewed for completeness and that any omissions be referred to the attending physician, but these steps were not consistently followed, leading to incomplete documentation and potential conflicts with residents' healthcare wishes.
Deficiencies in Food Storage and Staff Hygiene Practices
Penalty
Summary
The facility failed to ensure proper food storage and handling practices, as observed during a kitchen tour. Specifically, 26 containers of applesauce were found in the refrigerator without labels or dates, and a gallon of milk was open without a date indicating when it was opened. The Dietary Supervisor acknowledged that labeling and dating food items are crucial to prevent the consumption of expired food and to protect residents from potential foodborne illnesses. Additionally, a kitchen staff member was observed entering the kitchen without wearing a hair net, which is a violation of the facility's food handling policy. The staff member admitted to forgetting to wear the hair net due to being in a rush, acknowledging the importance of wearing it to prevent hair contamination in food and drinks. The Dietary Supervisor reiterated the significance of wearing hair nets as a protective measure to prevent contamination and ensure resident safety.
Failure to Maintain Dignity During Resident Feeding
Penalty
Summary
The facility failed to ensure respect and dignity for a resident by not maintaining eye contact during feeding. The incident involved a resident with dementia and hypertension, who was admitted to the facility initially in 2021 and readmitted in 2024. The resident required supervision or assistance with eating and other personal care activities due to severely impaired memory and cognition. During an observation, the resident was seen struggling to eat independently, and a CNA assisted by feeding the resident while standing, without sitting at eye level. The CNA acknowledged the importance of treating the resident with respect and dignity by sitting at eye level during feeding. The Director of Nursing confirmed that staff should sit at eye level to ensure dignity and respect. The facility's policy on assisting residents to eat also emphasized the need for staff to sit at eye level when feeding residents. This deficiency was identified through observation, interviews, and a review of the facility's policies.
Call Light Accessibility Deficiency
Penalty
Summary
The facility failed to ensure that a resident's call light was within reach, as observed during a survey. The resident, who was admitted with an anxiety disorder and had severely impaired cognition, required maximum assistance for daily living activities. During an observation, the call light was found hanging below the mattress, out of the resident's reach, which was against the facility's policy. Interviews with the Social Services Director and a Certified Nurse Assistant confirmed that the call light should always be within the resident's reach to enable them to call for help. The facility's policy, approved and revised earlier in the year, mandates that staff must ensure the call light is accessible to maintain resident safety. This oversight had the potential to harm the resident by preventing them from calling for assistance when needed.
Resident Restrained by Overbed Table
Penalty
Summary
The facility failed to ensure that a resident was free from involuntary physical restraints, as observed with the use of an overbed table. The resident, who had a history of metabolic encephalopathy, upper gastrointestinal bleed, and unspecified dementia, was found with an overbed table positioned over him after breakfast, restricting his freedom of movement. The resident's cognitive skills for daily decision-making were severely impaired, and he required assistance with activities of daily living. During an observation, the overbed table was placed on top of a floor mattress, which prevented the resident from moving it away. The Licensed Vocational Nurse (LVN) and Certified Nursing Assistant (CNA) both acknowledged that the overbed table should not have been left over the resident, as it restricted his movement and could be considered a form of restraint. The CNA admitted that the normal process after meal setup was to remove the table to allow the resident to move independently. The Director of Nursing (DON) confirmed that the overbed table should not be on top of the floor mattress or over the resident when not in use, as it could restrict the resident's freedom of movement. The facility's policy on physical restraints indicated that any device restricting a resident's movement, which they could not remove themselves, was considered a restraint. This oversight resulted in the resident being restrained in his bed, unable to move freely.
Failure to Implement Pressure Ulcer Prevention Measures
Penalty
Summary
The facility failed to implement appropriate interventions to prevent the development or worsening of pressure ulcers for two residents, as observed during a survey. For one resident, the Alternating Pressure Mattress (APM) was not set according to the resident's weight, as recommended by the manufacturer. The resident, who was severely impaired and required substantial assistance with daily activities, was observed with the APM set at 100 pounds, despite weighing only 79.8 pounds. This discrepancy was acknowledged by both the Licensed Vocational Nurse (LVN) and the Treatment Nurse (TN), who were responsible for ensuring the correct settings. The facility's policy and the manufacturer's guidelines both emphasized the importance of setting the APM according to the resident's weight to prevent skin breakdown and promote wound healing. Another resident, who was also at high risk for developing pressure ulcers, did not have heel protectors applied as ordered by the physician. This resident, with severe mental impairment and limited mobility, was observed without heel protectors, despite having a physician's order and care plan intervention to apply them at all times. The Treatment Nurse and Registered Nurse (RN) confirmed the absence of heel protectors and acknowledged the oversight. The facility's policy on pressure ulcer and skin care management required the implementation of appropriate treatment procedures, which was not followed in this case. The Director of Nurses (DON) confirmed the deficiencies in both cases, acknowledging that the APM should have been set according to the resident's weight and that heel protectors should have been applied as ordered. The facility's failure to adhere to its own policies and procedures, as well as professional standards of practice, resulted in the potential for the residents to develop new pressure ulcers or for existing ones to worsen.
Failure to Monitor Nutritional Status Leads to Significant Weight Loss
Penalty
Summary
The facility failed to ensure that a resident maintained acceptable nutritional status parameters, leading to a significant weight loss of more than 5% in 30 days. The resident, who had a history of diabetes, protein-calorie malnutrition, and dementia, was admitted with a care plan that included monitoring for undesirable weight changes and risk for dehydration. Despite these interventions, the resident's weight dropped from 84.4 pounds in April to 79.8 pounds in May, indicating a 4.6-pound loss. The deficiency was exacerbated by the lack of consistent documentation of the resident's food intake throughout May. Numerous entries for meals were missing, which hindered the ability to monitor the resident's nutritional intake effectively. Interviews with staff revealed that the facility had hired many registry CNAs, which may have contributed to the lack of documentation. The Dietary Supervisor and the Director of Nursing (DON) acknowledged the oversight in monitoring the resident's weight and intake. The Registered Dietician (RD) admitted to not following the facility's policy of recognizing a 5% weight loss as significant, which contributed to the lack of timely intervention. The DON also recognized the failure to initiate care plan interventions, such as weekly weight monitoring, and the importance of consistent documentation of the resident's oral intake. This oversight had the potential to lead to further weight loss and associated medical complications for the resident.
Failure to Provide Adequate Respiratory Care
Penalty
Summary
The facility failed to provide adequate respiratory care for a resident, identified as Resident 51, who required oxygen therapy. The deficiency was observed when the facility did not follow the physician's order dated 5/5/2024, which specified administering oxygen at 3 liters per minute (LPM) as needed for shortness of breath, with the option to titrate up to 5 LPM. Instead, the resident's oxygen was consistently administered at 2 LPM, as evidenced by multiple entries in the Vitals Report from 5/20/2024 to 6/10/2024, despite the updated physician's order. Additionally, the facility failed to ensure that the resident's oxygen tubing was free of obstructions, which is crucial for consistent oxygen therapy. Observations on 6/3/2024 and 6/6/2024 revealed that the nasal cannula tubing was pinched and obstructed at the connection site, which could impede the proper flow of oxygen. Licensed Vocational Nurse 1 and Treatment Nurse 1 both acknowledged the obstruction and its potential negative impact on the resident's ability to receive the necessary oxygen flow. The resident, who had a history of pneumonia, respiratory failure, and chronic congestive heart failure, was admitted with a diagnosis of pneumonia and required oxygen therapy. The resident's cognitive skills were severely impaired, necessitating complete staff assistance for daily activities. Despite these needs, the facility's staff did not adhere to the prescribed oxygen therapy protocol, leading to episodes of labored breathing and desaturation, as documented in the Nursing Progress Notes and observed during staff interviews.
Incomplete POLST Form for Resident with Severe Cognitive Impairment
Penalty
Summary
The facility failed to ensure that the Social Services Director (SSD) confirmed the completion of the Physician Orders for Life-Sustaining Treatment (POLST) form for a resident with a history of traumatic brain injury and severely impaired cognition. The POLST form, which communicates the resident's wishes regarding life-sustaining treatment, was not signed by the physician, nor was there evidence of the resident's conservator's signature. This oversight occurred despite the facility's protocol to have the POLST form filled out during admission, either by the resident or their responsible party. Interviews revealed a lack of clarity regarding the responsibility for ensuring the POLST form's completion. Registered Nurse 1 indicated that the SSD was responsible for this task, while the SSD herself was unaware of who should ensure the form's signatures and completion. The Administrator confirmed that it was indeed the SSD's responsibility. The SSD's job description also indicated that she was responsible for completing required forms in accordance with company policy and regulations.
Deficient Documentation in Hospice Binders
Penalty
Summary
The facility failed to ensure that the hospice binders for two residents, who were under hospice care, were properly completed and maintained. The hospice binders, which are essential for communication between hospice nurses and facility staff, were found to be lacking necessary documentation such as nursing notes, resident assessments, and care plans. This deficiency was identified during interviews and record reviews involving a registered nurse and the Director of Nursing. The absence of these critical documents in the hospice binders meant that facility staff were unaware of the care being provided by hospice nurses, potentially affecting the delivery of appropriate hospice care. Resident 77, admitted with diagnoses including dementia and heart failure, had a hospice binder that was missing nursing notes, assessments, and a care plan. Similarly, Resident 59, admitted with dementia and hypertension, also had a hospice binder lacking a care plan and consistent visiting notes from hospice staff. The facility's policy required that a coordinated plan of care be maintained in the hospice binders, but this was not adhered to, leading to a breakdown in communication and collaboration between the facility and hospice staff.
Unattended Hoyer Lift Poses Safety Risk
Penalty
Summary
The facility staff failed to maintain a safe environment for residents by leaving a Hoyer lift unattended in a resident's room. During an observation, the lift was found near a resident's bed, posing a risk for accidents and injury. A Certified Nursing Assistant (CNA) admitted to leaving the lift unattended while assisting a resident to a wheelchair and transporting them to the dining area. The CNA acknowledged that the lift should not be left in the room as it could cause residents to trip and get injured. The Director of Nurses (DON) confirmed that the lift should be stored outside the resident's room to prevent injuries.
Latest citations in California
Surveyors found multiple food safety deficiencies, including a cook preparing food without a beard restraint and a dietary aide with hair exposed outside a hairnet, contrary to facility policy requiring full hair coverage. The kitchen stove and oven had thick accumulations of grease, dark deposits, and sticky dust and oil residue on interior and exterior surfaces, indicating inadequate cleaning and sanitization. An opened bag of brown sugar was also found unsealed, unlabeled, and undated, despite facility policy requiring all food items to be labeled with the product name and use-by or discard date.
Surveyors found that the facility did not obtain or properly document informed consent for psychotropic medications for multiple residents. Several residents with depression, anxiety, bipolar disorder, and schizophrenia were receiving drugs such as sertraline, lorazepam, divalproex, trazodone, risperidone, escitalopram, lithium, chlorpromazine, haloperidol (including long-acting injectable), and Zyprexa without evidence that informed consent was obtained before initiation or dose changes. In some cases, consent forms were completed only after psychotropic medications had already been ordered and administered, and in others, no consent documentation existed at all, despite facility policies requiring informed consent prior to starting or increasing psychotropic therapy.
Surveyors identified a medication error rate of 17.14% during observed med passes, with multiple instances of nurses not following prescriber orders. One resident received only half the ordered dose of divalproex and in capsule form instead of the prescribed delayed-release tablet, while another was given gabapentin in capsule form instead of the ordered tablet. A G-tube resident was given ferrous sulfate instead of ordered iron glycinate, did not receive ordered docusate, and had eight medications administered via G-tube without required water flushes between each medication. Another resident did not receive a scheduled dose of quetiapine during the afternoon med pass. The report notes these failures resulted in medications not being administered according to physician orders and created potential for reduced therapeutic effect and G-tube blockage.
A resident with a history of cerebral infarction, schizophrenia, and depression was observed seated in a wheelchair during a lunch meal while a CNA stood over her and fed her with a spoon, contrary to facility policy requiring staff to sit at the resident’s eye level. The CNA later acknowledged she was expected to obtain a chair and sit beside the resident for comfort, and the DSD confirmed that staff are required to position themselves at eye level and not stand over residents when providing feeding assistance, as outlined in the facility’s dignity and meal-assistance policies.
A resident with schizophrenia had a PRN order for Zyprexa (olanzapine) 10 mg IM every 8 hours as needed for aggression renewed for an additional 14 days without a physician evaluation, contrary to facility policy and federal requirements. The DON confirmed there was no evaluation by the attending physician or prescriber before renewing the PRN antipsychotic order, despite the policy stating that PRN antipsychotic medications cannot be renewed without such an evaluation and documented appropriateness. Surveyors determined this resulted in an unnecessary psychotropic medication order.
Surveyors found that MDS assessments for two residents receiving antipsychotic medications contained incorrect dates for when prescribers had documented gradual dose reduction (GDR) as contraindicated. During interviews and record reviews, the MDSC confirmed that the GDR dates entered in Section N of the MDS did not match the dates in the residents’ plan of care notes, and acknowledged the need for correction. The MDSC and DON both stated that the MDS must accurately reflect the resident’s status to ensure services are based on current information, consistent with the facility’s policy that comprehensive MDS assessments are used to develop and revise person-centered care plans.
The facility failed to develop and implement an individualized care plan after a resident with gait and mobility abnormalities experienced an unwitnessed fall while getting out of bed. The resident reported the fall, and nursing staff, including an LVN, an RN, and the MDS coordinator, confirmed the incident and acknowledged that no short-term fall-related care plan or interventions were documented. This was inconsistent with facility policies requiring comprehensive person-centered care plans and fall risk management interventions based on assessment findings.
A resident had an order for PRN tramadol 50 mg for severe pain, and the controlled substance record showed that tablets were removed from stock on two occasions, but the MAR did not show that tramadol was administered on those dates. During interviews, an LVN acknowledged missing MAR documentation, and other nursing staff, the DSD, and the DON all stated that controlled substances were supposed to be documented on both the CSR and MAR and that the records should match. The facility’s medication administration policy required documentation immediately after administration, which was not followed in this case, resulting in inaccurate accountability of a controlled medication.
Surveyors found that a used urinal containing bloody urine was left on a resident's bedside table on multiple occasions, positioned next to a water pitcher and an empty food tray, with bloody urine visible on the outside and the lid open. A CNA confirmed the urinal should not have been stored there. The facility's infection control policy, as acknowledged by the IP, was not followed in this situation, resulting in a failure to maintain a safe and sanitary environment under the IPCP requirements.
Two residents with dementia, schizoaffective disorder, and major depressive disorder, both with moderately impaired cognition and needing moderate ADL assistance, were found unclothed together in one resident's bed. One resident later stated she did not want sexual activity and did not consent, while the other resident could not recall the encounter. An LVN reported that both residents verbally consented at the time but acknowledged no assessment had been done to determine their capacity to consent to sexual activity. The DON identified the incident as sexual abuse and confirmed that allowing sexual activity without prior capacity assessment was inconsistent with facility policy and that the resident was not protected from sexual abuse.
Unsanitary Food Handling, Equipment, and Storage Practices in Kitchen
Penalty
Summary
Surveyors identified a deficiency in food safety practices related to employee hygiene and equipment cleanliness in the facility’s kitchen. During an observation, one cook was preparing food without a beard restraint, and a dietary aide had bangs exposed outside of a hairnet while working. In an interview, the Assistant Dietary Services Supervisor (ADSS) stated that kitchen staff were required by facility policy to have their hair completely covered and to wear hair nets and beard restraints properly. Review of the facility’s policy titled “Preventing Foodborne Illness - Employee Hygiene and Sanitary Practices” confirmed that hair nets or caps and beard restraints must be worn to keep hair from contacting exposed food, clean equipment, utensils, and linens. Additional observations showed that the stovetop and oven were not maintained in a sanitary condition. The stove was covered with a thick, crusty layer of brown and black grease. The oven’s interior and exterior surfaces, including the door and handle, were coated with thick, heavy buildup of old grease and dark deposits, and the bottom of the oven had a layer of sticky dust and oil residue. The ADSS verified these conditions and acknowledged that the stove and oven required cleaning. Surveyors also found an opened, unsealed bag of brown sugar that was unlabeled and undated. The ADSS confirmed it should have been labeled and dated, and review of the facility’s “Food Storage (Dry, Refrigerated, and Frozen)” policy indicated that all food items must be labeled with the name of the food and the date by which it should be sold, consumed, or discarded.
Plan Of Correction
F812 A. How corrective action will be accomplished for those residents found to have been affected by the deficient practice. On 04/13/2026, Cook #1 immediately donned a beard restraint and ensured it was properly secured. The Dietary Aide immediately adjusted the hairnet to fully contain all hair, including bangs/fringe, prior to resuming food service duties. Both staff members were re-educated on facility grooming and infection control standards related to safe food handling. On 04/13/2026, the opened unsealed bag of brown sugar was immediately discarded. All dry storage items were reviewed for labeling, dating, sealing, and proper storage. Any items identified as unlabeled, undated, damaged, or improperly stored were immediately corrected or discarded. On 04/17/2026, the Administrator and the Registered Dietician conducted an immediate inspection of the kitchen and food service areas. No evidence of resident illness, food contamination, or foodborne outbreak related to the cited deficient practice was identified. On 04/17/2026 the Licensed Nurses conducted visual observation of all residents for any signs or symptoms of gastrointestinal distress, nausea, vomiting, diarrhea, fever, or other concerns. No adverse findings were noted. On 04/27/2026 the stove, oven interior, oven exterior surfaces, handles, and surrounding affected kitchen equipment were deep cleaned, degreased, sanitized, and returned to a clean operating condition. B. How the facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: On 04/17/2026 the Registered Dietitian and assistant dietary supervisor completed a comprehensive audit of all kitchen staff for compliance with hair restraints, beard restraints, hand hygiene, and sanitary food handling practices. On 04/17/2026 all food storage items were reviewed to ensure procedures were properly labeled, dated, sealed, rotated, and stored in accordance with facility policy and safe food handling standards. On 04/28/2026 a full kitchen sanitation audit was completed to inspect all cooking equipment, ovens, stovetops, food contact surfaces, dry storage, refrigerators, freezers, shelving, and small wares for cleanliness and sanitation. No other deficient findings identified during the audits. C. What measures will be put into place or what systemic changes the facility will make to ensure the deficient practice does not recur: On 04/16/2026 the Administrator conducted an in-service education to dietary staff and cooks regarding: Proper use of hairnets, beard restraints, and personal hygiene during food preparation. Routine cleaning and sanitizing requirements for all kitchen equipment and food contact surfaces. Dry goods storage requirements, including sealing, labeling, dating, and stock rotation. Responsibility to immediately report sanitation concerns to the Dietary Manager and Administrator. On 04/17/2026 the facility developed and implemented a Dietary Sanitation / Food Safety Daily Audit Log (Food Procurement, Storage, Preparation & Service – Sanitary Compliance). This tool is utilized daily by the Dietary Supervisor or designee to conduct routine audits and ensure ongoing compliance with food safety and sanitation standards. D. How the facility will monitor its corrective actions to ensure the deficient practice is being corrected and will not recur: Beginning 04/20/2026 the assistant Dietary Services Manager will conduct an audit weekly x 4 weeks, Monthly x 3 months or until substantial compliance is achieved using the Kitchen Sanitation & Food Safety Audit Tool to ensure compliance. Any findings will be addressed promptly. Audit results will be presented by the Administrator to the Quality Assurance and Performance Improvement (QAPI) Committee monthly for three (3) months. The QAPI Committee will review trends, ensure sustained compliance, and implement additional interventions as necessary Date of completion: 05/08/2026
Failure to Obtain and Document Informed Consent for Psychotropic Medications
Penalty
Summary
Surveyors identified a deficiency related to residents’ rights to be informed and to make treatment decisions when the facility failed to obtain and/or document informed consent for psychotropic medications for five sampled residents. The facility’s own policies required informed consent prior to initiation or dose increase of psychotropic drugs, with documentation of the discussion, understanding, and consent or refusal in the medical record. During interviews, the DON acknowledged that informed consent was supposed to be obtained before starting psychotropic medications or increasing doses, but records did not show that this occurred as required. For one resident with depression, anxiety, bipolar disorder, and multiple psychotropic prescriptions (sertraline, lorazepam, divalproex, and trazodone), review of psychotropic informed consent forms dated over several months showed no evidence of consent for the ordered doses of these medications, and the DON confirmed there were no additional consents. Another resident with schizophrenia had an order for risperidone, but the only documented psychotherapeutic drug informed consent was dated after the initial medication order, indicating consent was obtained after treatment had already begun. A third resident with depression and schizophrenia was receiving escitalopram, lithium carbonate, chlorpromazine, and haloperidol, including an additional lithium order, and the DON stated there was no documented informed consent for any of these psychotropic medications. For a fourth resident with an order for long-acting injectable haloperidol decanoate, the DON reported that the facility did not have documented informed consent for this psychotropic medication. For a fifth resident with schizophrenia, the physician ordered intramuscular Zyprexa 10 mg every eight hours as needed, and subsequent physician orders confirmed this regimen; however, the psychotherapeutic drug informed consent form was dated after the initial orders, again showing that consent was obtained only after the medication had been ordered. These findings collectively demonstrated that the facility did not ensure informed consent was obtained and documented in advance of initiating or changing psychotropic medication regimens, as required by regulation and facility policy.
Plan Of Correction
This Plan of Correction (POC) serves as our Credible Allegation of Compliance. Preparation and/or execution for this Plan of Correction does not constitute conclusions set forth in the Statement of Deficiencies. The facility will be in substantial compliance on or before 5/9/2026. The Plan of Correction is submitted as part of Federal Regulations. Title 42, Section 489.13, State Operations Manual, Section 2612 and California Health and Safety Code, Section 1280 and the facility does not waive its right to contest or pursue an appeal of the deficiency as allowed by the Federal and State Law. F552-Right to be informed/Make Treatment Decisions. How Corrective action will be accomplished for those residents found to have been affected by this practice. Resident #36-Informed consents for all the psychoactive medications were updated. For dates, please refer to the attachment of informed consents. On 4/3/26 Resident #53-Informed Consent for Risperdal was reviewed by [R] DNP. It did reflect the correct information with the exception of the date. On 4/13/26 Resident #41-Informed consents for all of the psychoactive medications were obtained and updated by [R] DNP. On 4/14/26 Resident #21-Informed consent for Haldol was obtained and updated by [R] DNP. On 3/28/26 Resident #1- Informed consent for Zyprexa was reviewed and adjusted for the increase in dosage by [R] DNP. How The facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: All the residents in the facility have the potential to be affected. Based on the QAPI that the facility had developed in early March of 2026, all the residents who are on Psychoactive meds have been audited for current informed consents and all will be completed by May 9th, 2026. What measures will be put in place or what systemic changes will you make to ensure that the deficient practice does not recur: Licensed staff have been in-serviced on 4/1/26 - 5/1/26 by Director of Nursing regarding the process of completing Informed Consents for residents with Psychoactive meds. On 4/20/2026 The DON/Designee will review any new order for Psychoactive medication on a daily basis to ensure that : Documenting the informed consents are obtained verified to protect resident rights, promote safety, and facilitate appropriate use of the medications. Document the discussion, resident/representative understanding, and consent/refusal in the medical record. Initiation or dose increase; prescriber obtains the consent before administration. In addition, Medical records designee/MRD shall review/audit for compliance on monthly basis. How the facility plans to monitor its performance to make sure the solutions are sustained and to ensure deficiency practice will not recur. The Findings from the Medical records audit will be given to DON and presented to the monthly QAA committee for review and to ensure sustained compliance monthly for 3 months, then every 6 months, then annually until compliance is met and sustained. Completion Date :5/8/2026
High Medication Error Rate and Failure to Follow Physician Orders During Med Pass
Penalty
Summary
The deficiency involves the facility failing to maintain a medication error rate below 5%, with surveyors calculating a 17.14% error rate based on six errors out of 35 observed opportunities during medication administration for four residents. For one resident, an LVN administered only 250 mg of divalproex in capsule form instead of the ordered 500 mg of divalproex delayed-release tablets prescribed twice daily for bipolar disorder. The LVN later confirmed that the resident was supposed to receive 500 mg of the delayed-release tablet formulation. Another resident with an order for gabapentin 100 mg tablets twice daily for nerve pain was given a 100 mg gabapentin capsule instead of the ordered tablet. The LVN acknowledged administering the capsule and confirmed that the order specified a tablet dosage form. A different resident with a G-tube had an order for iron glycinate oral liquid, 7.5 ml via G-tube once daily as a supplement, but was instead given ferrous sulfate liquid. The LVN confirmed that iron glycinate was ordered and that ferrous sulfate was administered in its place, meaning the ordered iron glycinate was not given. For the same G-tube resident, the LVN prepared three liquid medications (ferrous sulfate, valproic acid, and levetiracetam) but did not prepare or administer the ordered docusate liquid 10 ml via G-tube twice daily for constipation during the observed pass, and confirmed that the docusate was not given. During the G-tube medication administration, the LVN flushed the tube with 30 ml of water before starting and 30 ml after all medications were given but did not flush the tube between each of the eight medications, contrary to facility policy requiring water flushes between medications. In a separate observation, another resident with an order for quetiapine 200 mg by mouth twice daily at 8:00 AM and 4:00 PM did not receive the scheduled 4:00 PM dose during the observed medication pass; the LVN confirmed that quetiapine was not administered even though it was due at that time. The report states these failures resulted in medications not being given according to physician orders and had the potential for residents not to receive the full therapeutic effect of medications and for blockages to develop in the G-tube resident’s feeding tube.
Plan Of Correction
This Plan of Correction (POC) serves as our Credible Allegation of Compliance. Preparation and/or execution for this Plan of Correction does not constitute conclusions set forth in the Statement of Deficiencies. The facility will be in substantial compliance on or before 5/9/2026. The Plan of Correction is submitted as part of Federal Regulations. Title 42, Section 489.13, State Operations Manual, Section 2612 and California Health and Safety Code, Section 1280 and the facility does not waive its right to contest or pursue an appeal of the deficiency as allowed by the Federal and State Law. F759- Free of Medication Errors Rts 5 percent or more. How Corrective action will be accomplished for those residents found to have been affected by this practice. Resident #28-Order for Divalproex was Reviewed. On 4/14/26 Residents received 250 mg instead of 500mg. MD was notified and informed the same day. No new orders and to continue with same dosage. No adverse reaction was noted from this. Resident #7- On 4/14/26 the order for Gabapentin tablet was changed to capsule as per MD order. There was no adverse reaction noted from resident receiving the capsule format vs. the tablet format. Resident #6- On 4/14/26 Resident's MD was notified about the incorrect type of Iron supplement order. The order was clarified to Ferrous Sulfate Oral Solution 220mg/5ml give 7.5 ml via G-tube QD instead of Glycinate. In addition, the MD was notified about resident not receiving Docusate. No new orders were given. Resident did not show any adverse reaction from missing this medication. LVN #5 - On 4/15/26 LVN 5 was in-serviced by DON regarding all prescribed medication will be administered correctly and in accordance with the prescribers order. Also to ensure that the correct formulation of medication, such as capsule vs. Tablet, will be administered correctly as prescribed by the MD. In addition, she was educated on proper way of administering medication via GT and the importance of flushing with 15 ml of water in between administration of each medication. Resident #40- On 4/14/26 the MD was notified about resident not receiving Seroquel at 4pm on 4/14/26. No new orders were given. Resident did not show any adverse effects from not receiving this dose. LVN#3- was in-serviced by DON on 4/15/26 regarding not omitting any scheduled medications that have been ordered. How The facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: All residents have potential to be affected by this practice. The residents' medication administration records were reviewed by DON, and no other residents were affected by this practice. What measures will be put in place or what systemic changes will you make to ensure that the deficient practice does not recur: Licensed were in-serviced by DON on 4/15/2-26 – 5/1/26 regarding medication administration of all medications orally and via GT based on facility pharmacy Policy and Procedures. DON/Designee will conduct a GT medication administration pass/check off weekly for the first month on random shifts. Then the Pharmacy consultant will come monthly for 6 months to audit GT medication administration. All the new orders shall be reviewed daily by clinical IDT members for correct dose, root, and diagnosis. The MRD shall audit for medication administration completion on daily bases to assure that compliance is achieved. How the facility plans to monitor its performance to make sure the solutions are sustained and to ensure deficiency practice will not recur. The DON shall review the weekly audits/ monthly audits and present any issues to monthly QAA meeting for further interventions to assure compliance every 3 months Completion Date :5/8/2026
Failure to Maintain Resident Dignity During Feeding Assistance
Penalty
Summary
The facility failed to ensure a resident was treated with dignity and respect during mealtime when a CNA provided feeding assistance while standing over the resident. The resident, who had been admitted with diagnoses including cerebral infarction, schizophrenia, and depression, was seated in a wheelchair in her room during a lunch meal. At that time, the CNA remained standing and continued to feed the resident with a spoon from a standing position rather than positioning herself at the resident’s eye level. During an interview, the CNA acknowledged that she was expected to obtain a chair and sit beside the resident while assisting with meals and stated that sitting at eye level was important for resident comfort. The Director of Staff Development confirmed that staff were expected to position themselves at the resident’s eye level when providing feeding assistance and stated that the CNA should have obtained a chair and sat beside the resident to avoid the resident feeling intimidated. Review of the facility’s “Quality of Life-Dignity” policy indicated residents are to be treated with dignity and respect at all times, and the “Assistance with Meals” policy specified that staff should not stand over residents while assisting them with meals.
Plan Of Correction
This Plan of Correction (POC) serves as our Credible Allegation of Compliance. Preparation and/or execution for this Plan of Correction does not constitute conclusions set forth in the Statement of Deficiencies. The facility will be in substantial compliance on or before 5/9/2026. The Plan of Correction is submitted as part of Federal Regulations. Title 42, Section 489.13, State Operations Manual, Section 2612 and California Health and Safety Code, Section 1280 and the facility does not waive its right to contest or pursue an appeal of the deficiency as allowed by the Federal and State Law. F550-Resident Rights. How Corrective action will be accomplished for those residents found to have been affected: C.NA #1- was in-serviced 1:1 by the DON and DSD on 04/13/2026 regarding Resident's Rights to treat them with respect and dignity when feeding residents by sitting down and providing the assistance at eye level. Each resident shall be cared for in a manner that promotes and enhances his or her sense of well-being level of satisfaction with life, feeling of self-worth and self-esteem. Resident #47 – on 04/14/2026 resident was being assessed by the licensed nurse with regards to his rights as a resident that should be treated with respect and dignity when being fed. Resident has no concerns. How The facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: All the residents have the potential of being affected by this deficient practice. The consequent meal observations revealed that no other residents were being affected by the same deficient practice. What measures will be put in place or what systemic changes will you make to ensure that the deficient practice does not recur: The Nursing staff were in-serviced by the DON and DSD on 04/13/2026-05/01/2026 regarding Resident's Rights to treat them with respect and dignity when feeding residents by sitting down and providing the assistance at eye level. Each resident shall be cared for in a manner that promotes and enhances his or her sense of well-being level of satisfaction with life, feeling of self-worth and self-esteem. On 04/14/2026 the DSD and/or designee will conduct daily rounds to ensure continued compliance with the proper practice and report any deficient practice to DON. How the facility plans to monitor its performance to make sure the solutions are sustained and to ensure deficiency practice will not recur: The DON shall review compliance with the DSD rounds and report any deficient practiced to the monthly QAA committee to assure further and continued compliance monthly x 3 months then every 6 months and then annually until compliance is met and sustained. Completion Date :5/8/2026
Renewal of PRN Antipsychotic Without Required Physician Evaluation
Penalty
Summary
Surveyors identified a deficiency related to the use of psychotropic medications when a resident with a diagnosis of schizophrenia received a renewed PRN antipsychotic order without a required physician evaluation. The resident was initially admitted in January and had an admission record dated in April reflecting a diagnosis of schizophrenia. A physician’s order dated in March showed that the resident had renewed PRN orders for Zyprexa (olanzapine) 10 mg IM every 8 hours as needed for schizophrenia manifested by verbal or physical aggression, for 14 days. However, there was no documentation that the attending physician or prescribing practitioner evaluated the resident prior to renewing this PRN antipsychotic order. During an interview, the DON confirmed that there was no physician evaluation for the renewed PRN Zyprexa order and acknowledged that the physician was supposed to evaluate the resident before ordering the PRN antipsychotic. The facility’s own “Psychotropic Medication Use” policy stated that PRN orders for psychotropic medications are limited to 14 days and that PRN antipsychotic orders cannot be renewed unless the attending physician or prescriber evaluates the resident and documents the appropriateness of the medication. The prescribing information for Zyprexa injection listed somnolence as an adverse reaction, and the surveyors concluded that the resident received an unnecessary psychotropic medication order because it was renewed without the required evaluation.
Plan Of Correction
This Plan of Correction (POC) serves as our Credible Allegation of Compliance. Preparation and/or execution for this Plan of Correction does not constitute conclusions set forth in the Statement of Deficiencies. The facility will be in substantial compliance on or before 5/9/2026. The Plan of Correction is submitted as part of Federal Regulations. Title 42, Section 489.13, State Operations Manual, Section 2612 and California Health and Safety Code, Section 1280 and the facility does not waive its right to contest or pursue an appeal of the deficiency as allowed by the Federal and State Law. F 605- Rights to be Free from Chemical Restraints How Corrective action will be accomplished for those residents found to have been affected: Resident #1- was evaluated by the prescribing MD and the Order for Zyprexa was renewed on 04/16/26 for 14 days until 04/30/26. How The facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: All the residents have the potential to be affected by this deficient practice. On 04/15/2026, a review of all the residents on PRN psychoactive medications was conducted by DON. No other residents were found to be affected by this deficient practice. All the residents with Psychoactive medications had duration of therapy and were currently evaluated by the provider. What measures will be put in place or what systemic changes will you make to ensure that the deficient practice does not recur: The licensed nurses were in-serviced by DON on 4/15-5/1/26 regarding the need for having duration of therapy for all PRN psychoactive medication and the need for prescriber's evaluation at the time of renewal. All new orders for PRN psychoactive medications shall be reviewed during daily clinical meeting by IDT to assure compliance with this practice. How the facility plans to monitor its performance to make sure the solutions are sustained and to ensure deficiency practice will not recur. The DT/DON shall report any non-compliance regarding this issue to monthly QAA committee to assure further continue compliance monthly for 3 months then every 6 months, then annually until compliance is met and sustained. Completion Date :5/8/2026
Inaccurate MDS Documentation of Antipsychotic GDR Contraindications
Penalty
Summary
Surveyors identified a deficiency related to the accuracy of Minimum Data Set (MDS) assessments for two residents receiving antipsychotic medications. For one resident, review of the MDS Section N – Medications, dated 2/25/26, showed the resident was receiving an antipsychotic and that a gradual dose reduction (GDR) was documented as contraindicated. However, the clinical record indicated the prescriber had documented GDR as contraindicated on 8/14/23, and the MDS Coordinator (MDSC) acknowledged during concurrent interview and record review that the GDR date entered on the MDS was incorrect and needed to be corrected. The facility’s policy titled “Comprehensive Assessments” stated that comprehensive MDS assessments are conducted to assist in developing person-centered care plans and are used to develop, review, and revise the resident’s comprehensive care plan. For a second resident, the MDS Section N – Medications, dated 3/2/26, also indicated the resident was receiving an antipsychotic and that GDR was documented as contraindicated. The resident’s “Plan of Care Note,” dated 2/13/26, showed the prescriber had documented GDR as contraindicated on 9/14/23, but the MDSC confirmed that the GDR date recorded on the MDS was incorrect. In interviews, the MDSC stated that the MDS is a comprehensive assessment of the resident at a specific point in time and that accuracy is important to reflect correct information and to know whether services are being provided, further stating that incorrect MDS information could lead to needed services not being provided. The DON stated that the MDS was expected to be accurate and that an inaccurate MDS was not current for the resident’s care.
Plan Of Correction
This Plan of Correction (POC) serves as our Credible Allegation of Compliance. Preparation and/or execution for this Plan of Correction does not constitute conclusions set forth in the Statement of Deficiencies. The facility will be in substantial compliance on or before 5/9/2026. The Plan of Correction is submitted as part of Federal Regulations. Title 42, Section 489.13, State Operations Manual, Section 2612 and California Health and Safety Code, Section 1280 and the facility does not waive its right to contest or pursue an appeal of the deficiency as allowed by the Federal and State Law. F641-ACCURACY OF ASSESSMENTS How Corrective action will be accomplished for those residents found to have been affected: Resident #21- This resident GDR was considered on 2/13/26 by provider and stated that it was counter indicated. The MDS dated 2/25/26 was modified to reflect the consideration for GDR. Resident # 53-The MDS assessment of 3/2/26 was modified by the MDS coordinator to reflect the last GDR consideration by the MD was on 2/13/26. How The facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: All the residents who are receiving psychoactive medications have potential to be affected by this deficient practice. The DON and MDS coordinator reviewed all the residents with psychoactive medications who have had any GDRs attempted or have been evaluated for GDRs and reviewed the MDS assessment to accurately reflect these GDRs. There were no other residents identified with having the same deficient practice. What measures will be put in place or what systemic changes will you make to ensure that the deficient practice does not recur: The MDS coordinator was in-serviced by DON on 04/17/2026 regarding reflecting the correct GDR status for all the residents reviewed each month. In addition, the list of all the residents reviewed for GDRs is to be made available to MDS coordinator by DON so that the correct GDR date can be reflected on MDS. The MDS coordinator to check for accuracy and to ensure that the MDS assessments for the residents who are due each month and to report any issues to the DON. How the facility plans to monitor its performance to make sure the solutions are sustained and to ensure deficiency practice will not recur: The DON shall report issues concerning accuracy of MDS assessments in Section N to monthly QAA committee for further review and intervention to ensure continued compliance monthly x 3 months then every 6 months and annually until compliance is met and sustained. Completion Date: 05/08/2026
Failure to Develop Care Plan After Resident Fall
Penalty
Summary
The facility failed to develop and implement an individualized, person-centered care plan following an actual fall experienced by Resident 32. The resident was admitted with a diagnosis of abnormalities of gait and mobility and reported losing balance and falling while getting out of bed on 4/13/2026. Review of the resident’s Admission Record and Care Plan Report showed there was no care plan problem or interventions related to this fall incident. During interviews, the resident confirmed the fall, and nursing staff, including an LVN and an RN, acknowledged that the resident had an unwitnessed fall on 4/13/2026 and that no care plan had been developed in response. Further review with the MDS Coordinator confirmed that no care plan was created for Resident 32 after the fall, despite the expectation that a short-term care plan should have been documented and initiated by the RN. The facility’s policies on comprehensive person-centered care plans and on managing falls and fall risk state that care plans must be developed and implemented for each resident, with interventions derived from comprehensive assessments and evaluations of fall risks and causes. These policies require staff to identify and document interventions related to specific risks to prevent falls and minimize complications, which was not done for Resident 32 after the documented fall event.
Plan Of Correction
Plan of Correction – F656 Develop/Implement Comprehensive Care Plan CFR(s): 483.21(b)(1)(3) How corrective action will be accomplished for those residents found to have been affected by the deficient practice: On 4/15/26 The facility immediately corrected the deficient practice for Resident #32. Upon identification of the missing care plan following the unwitnessed fall on 4/13/2026, the Registered Nurse initiated a post-fall assessment A person-centered fall care plan, including individualized fall risk interventions, measurable goals, and monitoring parameters, was initiated and implemented in the resident's medical record. Interventions included safety precautions, fall prevention strategies, staff monitoring, and resident-specific measures based on the identified cause and circumstances of the fall. How the facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: On 4/15/26 , the Director of Nursing and MDS Coordinator, conducted a facility-wide audit of residents who experienced falls within the past 60 days to ensure that individualized short-term and/or comprehensive care plans were initiated, updated, and implemented timely following each fall incident. No other residents were affected by the deficient practice. What measures will be put into place or what systemic changes the facility will make to ensure that the deficient practice does not occur: On 4/15/26 - 5/1/26 , the Director of Nursing conducted an in-service education for licensed nurses, MDS staff, and interdisciplinary team members regarding the facility policy titled "Care Plans, Comprehensive Person-Centered" and "Falls and Fall Risk, Managing." Education included requirements for timely initiation and revision of care plans following falls, development of individualized interventions, documentation standards, implementation of interventions, and interdisciplinary communication. On 5/7/2026 The facility implemented a standardized "Post-Fall Care Plan Review Process" requiring licensed nurses to notify the MDS Coordinator/designee immediately following any actual fall event to ensure timely initiation or revision of the resident's care plan.Fall events are reviewed during daily clinical stand-up meetings to ensure care plan follow-through. How the facility will monitor its corrective actions to ensure that the deficient practice is being corrected and will not recur: The DON or designee will conduct audits of residents with falls to verify that individualized short-term and/or comprehensive care plans were initiated or revised timely and that interventions were implemented as ordered. Audits will be conducted weekly for four (4) weeks, then monthly for three (3) months or until substantial compliance is achieved. Any identified concerns will be addressed immediately through corrective action, re-education, and follow-up monitoring to ensure ongoing compliance.Audit results will be presented by the DON to the Quality Assurance and Performance Improvement (QAPI) Committee monthly for three (3) months. The QAPI Committee will review trends, ensure sustained compliance, and implement additional interventions as necessary.Completion date: 5/8/26
Failure to Reconcile Controlled Substance Records With MAR Documentation
Penalty
Summary
The deficiency involves the facility’s failure to ensure accurate accountability and documentation of controlled substances for a resident receiving tramadol for severe pain. The resident had a physician’s order dated 3/19/26 for tramadol 50 mg, one tablet by mouth every six hours as needed for severe pain. Review of the Controlled Substance Record (CSR) for this resident, dated 3/20/26, showed that nursing staff removed one tablet of tramadol on 3/24/26 at 7:48 AM and another tablet on 3/27/26 at 8:05 AM. However, the Medication Administration Record (MAR) for March 2026 did not show that tramadol was administered on those dates. During a concurrent interview and record review, an LVN acknowledged that the MAR was missing documentation and that it appeared the tramadol was not given on those dates, and stated that medication administration needed to be documented on the MAR. Additional staff interviews confirmed that facility expectations and procedures were not followed. Another LVN stated that nurses were supposed to verify controlled substance counts at each shift change to identify discrepancies and were required to document controlled substance administration in both the CSR and the MAR, and that these records should match. The Director of Staff Development stated that nurses were expected to sign out controlled medications on the CSR and document administration on the MAR, and that narcotic accountability procedures were intended to identify discrepancies. The DON similarly stated that the nurse was supposed to document the removed tramadol on the CSR and the administration on the MAR. The facility’s policy titled “Documentation of Medication Administration,” dated April 2007, indicated that administration of medication must be documented immediately after it is given, which was not reflected in the records for this resident’s tramadol doses.
Plan Of Correction
This Plan of Correction (POC) serves as our Credible Allegation of Compliance. Preparation and/or execution for this Plan of Correction does not constitute conclusions set forth in the Statement of Deficiencies. The facility will be in substantial compliance on or before 5/9/2026. The Plan of Correction is submitted as part of Federal Regulations, Title 42, Section 489.13, State Operations Manual, Section 2612 and California Health and Safety Code, Section 1280 and the facility does not waive its right to contest or pursue an appeal of the deficiency as allowed by the Federal and State Law. F755-Pharmacy services/Procedures/Pharmacist/Records How Corrective action will be accomplished for those residents found to have been affected: Resident #41-The Controlled Substance Record (CSR) for this resident was reviewed by DON on 04/14/2026. The count of Tramadol on the CSR matched the pill count in the med cart. Residents continue to use Tramadol for pain. How The facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: All the residents in the facility have the potential to be affected by this deficient practice. The DON/Designee reviewed all the Narcotic sheets/CSRs against the medication administration record for month of April 2026. There were no other residents found to be affected with the same deficient practice. C-What measures will be put in place or what systemic changes will you make to ensure the deficient practice does not recur: The licensed staff was in-serviced by DON on 04/15/2026- 05/01/2026 regarding documentation of medication administration that administration of medication must be documented after (never before) it is given. That is required for all PRN medications including Narcotics. The DON conducted a 1:1 in-service to LVN3 on 04/16/2026 regarding facility's policy on documentation of medication administration that administration of medication must be documented after (never before) it is given. The MRD shall conduct a weekly audit of Narcotic sheets in comparison to the documentation on the MARs to ensure compliance. The DON/Designee shall review these audits and intervene to ensure compliance. How the facility plans to monitor its performance to make sure the solutions are sustained and to ensure deficiency practice will not recur. The DON shall report the results of medical records audit to monthly QAA committee for review and to assure continued compliance monthly x 3 months then q 6months and then annually to ensure compliance is met and sustained. Date of Completion: 05/08/2026
Improper Storage of Used Urinal with Bloody Urine at Bedside
Penalty
Summary
Surveyors identified a deficiency in infection prevention and control when a used urinal containing bloody urine was repeatedly observed on a resident's bedside table. During a morning observation, the urinal with bloody urine was placed next to the resident's water pitcher, with visible bloody urine on the outside near the opening and the lid left open. Later the same day, the urinal with bloody urine was again observed on the same bedside table, this time next to both a water pitcher and an empty food tray, with bloody urine still visible on the outside near the opening and the lid still open. A CNA confirmed during interview that the urinal with urine was on the bedside table next to an empty food tray and acknowledged that it should not be stored there. The facility's undated infection control policy, reviewed with the Infection Preventionist, stated that the infection control policies and practices are intended to maintain a safe, sanitary, and comfortable environment and to help prevent and manage transmission of diseases and infections. The Infection Preventionist stated that this policy was not followed when the urinal with bloody urine was found on the resident's bedside table.
Plan Of Correction
This Plan of Correction (POC) serves as our Credible Allegation of Compliance. Preparation and/or execution for this Plan of Correction does not constitute conclusions set forth in the Statement of Deficiencies. The facility will be in substantial compliance on or before 5/9/2026. The Plan of Correction is submitted as part of Federal Regulations. Title 42, Section 489.13, State Operations Manual, Section 2612 and California Health and Safety Code, Section 1280 and the facility does not waive its right to contest or pursue an appeal of the deficiency as allowed by the Federal and State Law. F880-Infection Prevention and Control How Corrective action will be accomplished for those residents found to have been affected: Resident #32 prefers to keep his urinal on his bedside table and has occasional blood in the urine due to his diagnosis of Malignant Neoplasm of bladder. This issue has been addressed with the resident, and he continues to refuse to allow staff to remove his urinal or place it in a different location. On 05/04/2026 the IDT conducted an IDT meeting with the resident to make him aware of the risk involved with infection control. Resident did not want to change his preference. How The facility will identify other residents having the potential to be affected by the same deficient practice and what corrective action will be taken: All the residents have the potential to be affected by this deficient practice. On 05/04/2026 the IDT members reviewed other residents for similar issues, and no other residents were identified with the same deficient practice. What measures will be put in place or what systemic changes will you make to ensure that the deficient practice does not recur: The nursing staff have been in-serviced by DSD/DON regarding attempting/offering to remove the urinals from the bedside tables on 04/15/2026-05/01/2026. The charge nurses and/or IP nurse shall conduct daily rounds to assure compliance and report any findings to DON for further follow up. How the facility plans to monitor its performance to make sure the solutions are sustained and to ensure deficiency practice will not recur: The DON shall report any findings from the IP rounds to monthly QAA committee for further review to ensure continued compliance monthly x 3 months and then every 6 months and annually until compliance is met and sustained. Completion Date: 05/08/2026
Failure to Protect Cognitively Impaired Resident From Sexual Abuse
Penalty
Summary
The facility failed to ensure a resident was free from sexual abuse when two cognitively impaired residents were found unclothed together in one resident's bed without prior assessment of their capacity to consent to sexual activity. One resident had dementia, schizoaffective disorder, and major depressive disorder, with documentation of fluctuating capacity to understand and make decisions and a Minimum Data Set (MDS) indicating moderately impaired cognition and a need for moderate assistance with ADLs. During an interview at her bedside, this resident stated she did not want to engage in sexual activity and did not consent to sexual contact with the other resident. The second resident involved also had dementia, schizoaffective disorder, and major depressive disorder, with an MDS showing moderately impaired cognition and a need for moderate assistance with ADLs. In an interview, he stated he liked women and liked to socialize with women but could not recall whether he engaged in sexual activity with the first resident. An LVN reported observing both residents unclothed in the first resident's bed and stated that, at the time of the incident, both residents verbally consented to sexual activity, but she was not aware of any assessment having been performed to determine either resident's capacity to consent. The DON stated the incident was considered sexual abuse, that it was not the facility's practice to allow sexual activity without appropriate assessment, and that the facility failed to ensure the resident was protected from sexual abuse, contrary to the facility's abuse prevention policy.
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