VIVO HEALTHCARE WEST ORANGE

1556 MAGUIRE RD, OCOEE, FL 34761 (407) 877-2272
For profit - Corporation 120 Beds VIVO HEALTHCARE Data: November 2025
Trust Grade
63/100
#302 of 690 in FL
Last Inspection: May 2025

Inspected within the last 6 months. Data reflects current conditions.

Overview

Vivo Healthcare West Orange has a Trust Grade of C+, indicating it is decent and slightly above average among nursing homes. It ranks #302 out of 690 facilities in Florida, placing it in the top half, and #11 out of 37 in Orange County, suggesting only ten local options are better. The facility is improving, as the number of issues reported decreased from five in 2024 to two in 2025. Staffing is a concern, with a rating of 2 out of 5 stars and only 38% turnover, which is better than the state average but indicates some instability. On the downside, the facility has faced $16,801 in fines, which is average, and it has less RN coverage than 85% of Florida facilities, meaning residents might not receive adequate oversight from registered nurses. Some serious issues were noted in inspections, including a failure to ensure two residents could return from the hospital, leading to unnecessary extended stays in acute care, and a critical medication error that left another resident unresponsive. Additionally, complaints arose regarding the cleanliness of rooms, with one resident’s granddaughter highlighting that her grandmother's room had not been properly cleaned before her arrival. While there are strengths in care quality, these incidents underscore that families should carefully consider both the positive and negative aspects of this facility.

Trust Score
C+
63/100
In Florida
#302/690
Top 43%
Safety Record
Moderate
Needs review
Inspections
Getting Better
5 → 2 violations
Staff Stability
○ Average
38% turnover. Near Florida's 48% average. Typical for the industry.
Penalties
○ Average
$16,801 in fines. Higher than 56% of Florida facilities. Some compliance issues.
Skilled Nurses
⚠ Watch
Each resident gets only 26 minutes of Registered Nurse (RN) attention daily — below average for Florida. Fewer RN minutes means fewer trained eyes watching for problems.
Violations
⚠ Watch
15 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★★★☆
4.0
Overall Rating
★★☆☆☆
2.0
Staff Levels
★★★★☆
4.0
Care Quality
★★★★☆
4.0
Inspection Score
Stable
2024: 5 issues
2025: 2 issues

The Good

  • 4-Star Quality Measures · Strong clinical quality outcomes
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover below average (38%)

    10 points below Florida average of 48%

Facility shows strength in quality measures, fire safety.

The Bad

Staff Turnover: 38%

Near Florida avg (46%)

Typical for the industry

Federal Fines: $16,801

Below median ($33,413)

Minor penalties assessed

Chain: VIVO HEALTHCARE

Part of a multi-facility chain

Ask about local staffing decisions and management

The Ugly 15 deficiencies on record

2 actual harm
May 2025 2 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure Minimum Data Set (MDS) assessments were accura...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure Minimum Data Set (MDS) assessments were accurate related to special treatments, procedures and programs for 3 of 3 residents reviewed for accuracy of assessments, of a total sample of 40 residents, (#4, #8 and #46). Findings: 1. Resident #4 was admitted to the facility on [DATE] with diagnoses including epilepsy, chronic respiratory failure with hypoxia, and tracheostomy status. Review of the MDS quarterly assessment with assessment reference date (ARD) 2/21/25 revealed resident #4 had a Brief Interview for Mental Status (BIMS) score of 15/15 which indicated she was cognitively intact. The assessment indicated resident #4 received tracheostomy (a hole in the throat for breathing) care and dialysis. On 5/06/25 at 11:53 AM, resident #4 was reclined in bed with the head of the bed elevated. Resident #4 stated she did not go to dialysis. Resident #4 clarified she did not receive dialysis and had never received dialysis. 2. Resident #8 was admitted to the facility on [DATE] with diagnoses including nontraumatic brain bleed, acute respiratory failure with low oxygen and encounter for attention to tracheostomy. Review of the MDS quarterly assessment with ARD 1/25/25 revealed resident #8 had long-term and short-term memory problems and severely impaired cognitive skills for daily decision making. The assessment indicated resident #8 received tracheostomy care and had an invasive mechanical ventilator for breathing. On 5/06/25 at 10:25 AM, resident #8 was reclined in bed with the head of the bed slightly elevated. Tracheostomy tubing was in place. No ventilator tubing or equipment for a mechanical ventilator was seen in the room. On 5/07/25 at 10:28 AM, in resident #8's room, the MDS Coordinator and the A Wing Unit Manager verified resident #8 had a tracheostomy but did not use a ventilator for breathing. 3. Resident #46 was admitted to the facility on [DATE] with diagnoses that included bladder inflammation with blood in the urine. Review of the MDS admission assessment with ARD 3/28/25 revealed resident #46 had a BIMS score of 14/15 which indicated he was cognitively intact. The assessment indicated resident #46 received dialysis. On 5/05/25 at 11:29 AM, resident #46 was lying in his bed in his room. Resident #46 in response to what days he went to dialysis, stated he did not go to dialysis at all. He clarified he had never been on dialysis. On 5/07/25 at 10:32 AM, the MDS Coordinator stated she was the head of the MDS department. She reviewed the medical records for residents #4, #8 and #46. The MDS Coordinator compared each resident's diagnoses and care plans to the identified MDS assessment for each resident. She verified each MDS assessment was coded incorrectly. She was unable to explain why they were coded incorrectly. The MDS Coordinator explained the other MDS staff person completed those assessments. The MDS Coordinator stated the other MDS staff was not at the facility to explain why they MDS was coded incorrectly, and did not know when she would return. The MDS Coordinator acknowledged each resident's assessment should accurately reflect their status at the time of the assessment. The facility policy and procedure for Conducting an Accurate Resident Assessment implemented 10/01/22 indicated the purpose of the policy was to ensure all residents received an accurate assessment. The form defined accuracy of assessment meant that appropriate health care professionals correctly documented the resident's medical, functional and psychosocial problems. The form read, Each individual who completes a portion of the assessment will sign and certify the accuracy of that portion of the assessment.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Safe Environment (Tag F0921)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide a sanitary environment by failing to replace ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide a sanitary environment by failing to replace a cracked bedside floor mat for 1 of 1 residents reviewed for environmental concerns, of a total of 40 sampled residents, (#70). Findings: Resident #70 was admitted to the facility on [DATE], with a history of falling, abnormal posture, unspecified lack of coordination. Review of resident #70's care plan with revision date of 7/11/23, indicated he was at risk for falls related to deconditioning, weakness, and having a history of a fracture. Interventions included fall mats at bedside, dated 12/30/24. On 5/05/25 at 3:23 PM, resident #70 was lying in bed, a beside fall mat was on the floor. The surface was cracked and split along its entire length which revealed the layer underneath the surface. On 5/06/25 at 8:40 AM, the beside fall mat was observed on the floor at the side of resident #70's bed. The surface remained cracked and split along its entire length which revealed the layer underneath the surface. On 5/06/25 at 3:25 PM, the Director of Maintenance confirmed the cracked surface of the fall mat on the floor next to resident #70's bed. The Director of Maintenance explained nursing staff was responsible to change out any fall mats in use by residents that were in disrepair. On 5/06/25 at 3:30 PM, the B side Unit Manager agreed resident #70's bedside fall mat had a cracked surface along its length which exposed the interior of the mat. The B side Unit Manager confirmed the mat was old, and referred to it as the older version. She verified a new beside fall mat had not been obtained from central supply nor had a service request been entered into the electronic maintenance service request system for a new mat. She acknowledged because the surface of the mat was cracked and split it could not be cleaned properly.
May 2024 5 deficiencies 2 Harm
SERIOUS (G) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Actual Harm - a resident was hurt due to facility failures

Safe Transfer (Tag F0626)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to re-admit residents who were transferred to a higher level of care f...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to re-admit residents who were transferred to a higher level of care for treatment of acute conditions, for 2 of 3 residents reviewed for hospitalization, out of a total sample of 9 residents, (#2 and #3). The facility's failure to permit residents who required its care and services to return from the hospital resulted in extended stays in acute care settings after medical issues were resolved, and necessitated adjustment to unfamiliar personnel and routines in new skilled nursing facilities (SNFs), actual harm, for residents #2 and #3. Findings: 1. Review of the medical record revealed resident #3 was admitted to the facility on [DATE]. His diagnoses included weakness, need for assistance with personal care, cognitive communication deficit, history of alcohol abuse, and noncompliance with medical treatments. The resident's medical record was updated on 10/16/23 with diagnoses of major depressive disorder, adjustment disorder with anxiety, and primary insomnia. On 12/18/23, resident #3 was diagnosed with bipolar II disorder and on 1/03/24 he was diagnosed with anxiety disorder. The resident's admission Record or face sheet showed he had a court-appointed legal guardian who was his emergency contact and care conference representative. Review of the Minimum Data Set (MDS) Discharge-Return Anticipated assessment with assessment reference date (ARD) of 1/26/24 revealed resident #3 was discharged to a short-term general hospital. The document revealed during the 7-day look back period, resident #3 had physical behavioral symptoms directed towards others on one to three days, verbal behavioral symptoms directed towards others on four to six days, and other behavioral symptoms that were not directed towards others on one to three days. The document showed resident #3 rejected evaluation or care such as medications and assistance with activities of daily living on one to three days. He was totally dependent on staff for toileting hygiene, bathing, dressing, and personal hygiene. The resident required substantial to maximal assistance for bed mobility, was totally dependent on staff for transfers, and did not walk. The document indicated resident #3 had an indwelling urinary catheter. The MDS assessment revealed the resident received antipsychotic, antidepressant, hypnotic, anticoagulant, antibiotic, and opioid medication. Review of the medical record revealed resident #3 had a care plan initiated on 9/14/23 for falls related to weakness, bedbound status, and has not walked in 3 years. A care plan was initiated on 9/18/23 for behavior problems related to history of noncompliance with medications, treatment, and wound care, and verbal aggression including use of profanity, screaming, threatening, and cursing. The interventions instructed staff to administer medications as ordered and monitor or document medication effectiveness, anticipate and meet his needs, encourage him to comply with care, divert his attention, discuss his behavior, explain all procedures before starting, and intervene as necessary to protect the rights and safety of others. The resident had a care plan for the potential to be verbally aggressive due to his disease process, initiated on 9/19/23. The goal was the resident would demonstrate effective coping skills. The interventions instructed staff to administer medications as ordered, initiate a psychiatric consult as indicated, and analyze key times, places, circumstances, triggers, and what de-escalates behavior. Resident #3 had a care plan for a discharge goal of long term placement in the facility, initiated on 9/27/23. The goal was the resident would remain adjusted to long term placement. The intervention was the facility's Social Services Director (SSD) would explain the benefits of living in a long-term care facility. Review of resident #3's medical record revealed a Preadmission Screening and Resident Review (PASARR) form dated 9/13/23. The PASARR is a federal requirement to ensure individuals are not inappropriately placed in nursing homes for long term care. The Level I screen is a preliminary assessment to determine if there might be Serious Mental Illness (SMI) or Intellectual Disability (ID). If the Level I screen is positive, then referral for an in-depth Level II screen is required to determine the need for additional services and the appropriate setting, and recommend necessary services to be included in the plan of care (retrieved on 5/20/24 from www.medicaid.gov/medicaid/long-term-services-supports/institutional-long-term-care/preadmission-screening-and-resident-review/index.html). Resident #3's PASARR form indicated he was deemed appropriate for admission to a skilled nursing facility. The document revealed the Level I screen was negative as the resident had no diagnosis or suspicion of SMI or ID; therefore, he did not require a Level II screen. The medical record did not contain evidence of a revised PASARR form to reflect resident #3's new psychiatric diagnoses or a referral for a Level II screen. Review of a Psychiatric Evaluation note dated 10/16/23 revealed resident #3 was referred to psychiatry for a chief complaint of depression. The note indicated staff reported no recent issues and resident #3 was cooperative with no acute nervousness or depression. The psychiatrist noted the resident showed an adequate response to his current medications, Restoril 15 milligrams (mg) at bedtime for insomnia and Cymbalta 60 mg daily for depression. A Psychiatric Progress Note dated 11/13/23 revealed staff reported no acute changes. The psychiatrist noted resident #3 was calm, had no hallucinations or delusions, exhibited fair judgement and insight, and was aware of current events. The document read, Patient appears at baseline on current medication [regimen].no changes or recommendations at this time. Review of a Psychiatric Progress Note dated 12/18/23 revealed staff reported resident #3 had extreme mood swings with verbal outbursts. The psychiatrist observed the resident exhibiting extreme anger as he yelled profanities at staff. The progress note indicated he started Seroquel 50 mg, an antipsychotic medication, for a bipolar condition. The treatment plan was to gradually titrate the Seroquel dosage to 200 mg at bedtime. A Psychiatric Progress Note dated 1/03/24 revealed facility staff reported resident #3 had no recent issues and showed improvement on Seroquel. The psychiatrist described the resident as cooperative and wrote, Recent medication changes were beneficial for his mood and well-tolerated. Review of Progress Notes for January 2024 revealed resident #3 completed a course of antibiotic medication for a urinary tract infection (UTI) on 1/16/24. A note dated 1/16/24 indicated the interdisciplinary team (IDT) met to discuss resident #3's status and plan of care. There were no recommendations made for changes to the plan of care and no documentation of behavioral concerns. A note dated 1/16/24 revealed the resident's guardian was updated on the progress of his wounds, and there was no evidence of discussion of additional concerns. An IDT note dated 1/23/24 revealed the resident's plan of care was reviewed again with no changes required. Review of the Medication Administration Records for December 2023 and January 2024 revealed resident #3 received Seroquel 200 mg at bedtime as ordered, except for 1/23/24 and 1/24/24 when nursing documentation showed he refused the drug. Nursing notes from 1/12/24 to 1/22/24 indicated resident #3 was calm and did not exhibit behavioral symptoms. Documentation on 1/23/24 and 1/24/24 indicated nurses observed behaviors. A note dated 1/24/24 revealed he refused medication and hygiene care despite several attempts, and also cursed at staff. Progress notes dated 1/25/24 showed the resident continued to exhibit escalating behavioral symptoms, cursing/yelling at staff members and is using racial slurs. Staff were eventually able to calm him and he accepted medications and personal hygiene care. The facility notified the Advanced Practice Nurse Practitioner who ordered a urinalysis, a test of the urine to check for disorders including a UTI. Review of a Situation, Background, Appearance, Review and Notify (SBAR) form dated 1/26/24 revealed resident #3 had a change in condition related to altered mental status with symptoms of verbal aggression. The SBAR form read, Resident is screaming, cursing, lose his voice from yelling.Order to send out to [name of hospital] for evaluation and treatment. The document indicated the resident was in the facility for long term care. Review of resident #3's hospital record revealed an Emergency Department (ED) Provider Note dated 1/26/24 at 2:13 PM. The physician wrote that resident #3 presented to the hospital .for questionable altered mental status. According to [Emergency Medical Services] they were called for an altered mental status however they state the patient always acts like this.I attempted to call the facility twice both which times they hung up and I was unable to speak with any representatives. The physician's assessment showed the resident's vital signs were stable and he was in no acute distress. His admission diagnosis was cystitis, an inflammation of the bladder which is usually caused by a UTI, and he was started on intravenous antibiotic therapy. The document read, Based on the patient's presentation, it is expected that they will cross 2 midnights of care in the hospital. Review of the hospital record revealed a note dated 1/29/24, written by the hospital's Social Worker, regarding an attempt to arrange resident #3's return to the facility. The SW documented she spoke with the facility's admission staff who informed her the resident had only been there with short-term benefits, and the facility was .unable to accept [the resident] back due to being aggressive/violent towards other residents. The SW contacted the resident's guardian who informed her he was in the facility with long-term care benefits. Due to the facility's refusal to re-admit resident #3 and the absence of a home discharge location, the resident's guardian authorized the hospital SW to pursue alternate SNF placement. Review of hospital Case Management (CM) notes revealed resident #3 was medically cleared for discharge from the hospital on 1/29/24. However, over the next 10 weeks, the resident remained in the acute care hospital while the SW made continuous attempts to identify a SNF that would accept resident #3 for long-term care. A CM note dated 4/01/24 indicated the SW eventually found a SNF in another county, over 100 miles away from the facility where he resided pre-hospitalization. The note revealed there was a barrier to the discharge as the assigned court-appointed guardian was unable to follow the resident in that county, and arrangements would have to be made for a new guardian. A CM note dated 4/02/24 read, Unable to move forward with [discharge] until a new court appointed guardian. A CM note dated 4/09/24 revealed the hospital SW discussed resident #3's behaviors with his assigned nurse who stated he was cooperative and showed no signs of aggression. A CM note dated 4/12/24 revealed a local facility accepted resident #3 for long-term care on condition that the hospital arranged for a private sitter for three days to offer support during the resident's adjustment to the new facility. Review of the hospital Discharge summary dated [DATE] revealed resident #3 was discharged to the local SNF with physician orders that included Seroquel 300 mg at bedtime. Review of the hospital record revealed when resident #3 arrived at the local SNF, staff refused to admit him due to verbal behavioral symptoms. There was no evidence the requested sitter was present to assist with a smooth transition to the new location. The transport company returned the resident to the hospital and he was re-admitted for aggressive behavior. Resident #3 was restrained briefly in the ED to permit diagnostic testing, and soon calmed down. A Psychiatry Consult note dated 4/15/24 read, .the patient is calm, cooperative, not agitated, not threatening. The psychiatrist made a diagnosis of adjustment disorder with mixed disturbance emotion and indicated no medication changes were necessary. The resident was discharged to the SNF in another county on 4/19/24, once arrangements were finalized for the transfer of guardianship. On 5/08/24 at 2:35 PM, in a telephone interview, resident #3's court-appointed guardian stated the resident had a history of cardiac arrest with oxygen deprivation and alcoholism. She explained those factors contributed to his cognitive impairment and behavioral issues, and although he could be easily agitated and verbally aggressive, he never physically hurt anyone. The guardian stated on the day resident #3 was sent to the hospital, he had a UTI which probably worsened his behavioral symptoms. She explained the facility refused to take the resident back and the hospital eventually found another SNF. When asked if she knew why the facility could not re-admit resident #3, she said, That was my question. Why would another skilled nursing facility be able to provide different or better care? I really hoped they would have taken him back. The hospital and I tried to get them to take him back. I was very upset and I hoped they would take him back. The guardian confirmed she called the facility and someone told her they would not accept him. She explained she attended a care plan meeting in December 2023 or January 2024, and nobody at the facility mentioned anything out of the ordinary or that they wanted to get rid of him. She said, I am frustrated that he was being discharged for baseline behaviors that needed to be addressed. I don't think they exhausted all the available options. The guardian felt it was unfair for resident #3 to remain in the hospital for over two months, especially since his infection was resolved and his behavior was no different. She recalled while resident #3 was in the hospital, the attending physician updated her regularly, and never reported any worsening behaviors that prevented him from returning to the facility. The guardian explained the resident was currently at baseline in a regular long-term care bed in a SNF in another county. She stated the resident's court-appointed attorney said the resident liked her, but he would now have to build a relationship with a new guardian. On 5/08/24 at 10:42 AM and 5/09/24 at 11:34 AM, in telephone interviews with a hospital Case Manager, he explained resident #3 was admitted to the hospital on [DATE] and was medically cleared to return to the facility on 1/30/24. He stated on 1/29/24, the hospital SW contacted the resident's guardian and facility admissions staff to arrange his return to the facility. The Case Manager stated the facility was unwilling to re-admit resident #3 and it took approximately 10 weeks, until 4/19/24, to locate a facility that would accept him for long-term care. He stated during the resident's extended stay in the hospital, he was seen by psychiatry and had minimal changes made to his medications. The Case Manager acknowledged the hospital record revealed a physician's note dated 2/27/24 that indicated resident #3 swung at a staff member and the physician planned to order restraints if the behavior continued. He stated there were no physician orders for restraints to indicate the behavior reoccurred. On 5/08/24 at 12:06 PM, the facility's Social Services Director (SSD) recalled resident #3 had behavioral issues. She explained nursing staff often used to ask her to intervene and talk him down. The SSD stated the resident was sometimes verbally abusive to staff, but never physically abusive. The SSD stated after she calmed the resident down, he was usually apologetic as he did not mean to offend anyone. She verified resident #3 was bedbound, unable to transfer himself to a wheelchair, and refused to get out of bed. On 5/08/24 at 2:55 PM, the Director of Nursing denied knowledge of the facility's refusal to re-admit resident #3 from the hospital. She confirmed the facility was able to meet the resident's needs prior to the hospital transfer. On 5/08/24 at 3:24 PM, the SSD acknowledged a hospital case manager called her to ask if the facility would re-admit resident #3. She stated she confirmed the facility would re-admit the resident. The SSD said, We do not turn down patients who already live here. We don't dump. This is their home. The SSD stated the resident's guardian called next and informed her the facility was not an appropriate setting for the resident. She said, I don't know what transpired between the guardian and the hospital. The SSD did not respond when informed her statement was inconsistent with the details provided by the hospital CM and the resident's guardian. On 5/08/24 at 3:32 PM, in a telephone interview, the facility's Outside Marketer/Care Liaison explained her role was to work with hospital case management staff to arrange admissions and re-admissions to the facility. She stated her last note dated 3/08/24 indicated the hospital planned to send resident #3 to a brain injury clinic. The Care Liaison stated she discussed the resident's return to the facility with facility nursing staff and they were concerned about his aggressive behaviors towards other residents. She explained he was a danger to other residents as he could walk. She said, Even his guardian did not want him to return. Unfortunately, I don't think I have it documented. They were all phone conversations. The Care Liaison stated the facility could not care for residents with severe brain injuries nor those who received excessive doses of medication, so the hospital canceled the referral. She stated she checked on the resident during his hospital stay and often observed that he was sedated or chemically restrained, and on some days he was even physically restrained. The Care Liaison acknowledged the hospital was not a discharge location. She was unaware resident #3 was not a threat to residents as he had been bedbound for years prior to admission to the facility. She did not respond when informed that her statements were not corroborated by the resident's medical record and interviews with hospital case management staff and the resident's guardian. On 5/08/24 at 4:34 PM, Certified Nursing Assistant (CNA) C stated she was regularly assigned to care for resident #3. She stated he often yelled, cursed, was very disrespectful, and used racial slurs. She confirmed he was never physical with her during care, and his behavior never really changed. On 5/09/24 at 12:09 PM, CNA F described resident #3 as very loud. She stated he shouted and yelled, never got out of bed, and could not walk. CNA F recalled the resident sometimes swung at staff during care. She acknowledged there were other residents in the facility who were combative or hit out at staff and CNAs were trained to re-approach later, use two people for care, and be careful. She stated there was another resident on the same unit who used to scream and shout a lot. On 5/10/24 at 12:22 PM, the Rehab Director recalled when resident #3 refused to participate in therapy or directed profane language at staff, she would go to his room to talk to him and re-direct him. She stated he had been bedbound for about two years in another SNF before admission to this facility. The Rehab Director stated she never felt physically threatened by the resident. She verified he might swing at staff occasionally but he was not the only resident who did so. The Rehab Director said, We have difficult residents and we redirect, re-approach, reorient to give care. Review of the Facility assessment dated [DATE] revealed the facility could meet the care needs of residents who had nervous system conditions including traumatic brain injury and psychiatric and mood disorders such as psychosis, impaired cognition, mental disorders, depression, bipolar disorder, and anxiety. The document indicated staff would provide behavior and mental health care to include management of medical conditions and identification and implementation of interventions to support residents with psychiatric conditions. 2. Review of the medical record revealed resident #2 was initially admitted to the facility on [DATE] and last re-admitted on [DATE]. His diagnoses included end-stage kidney disease with hemodialysis, left leg above knee amputation, type 2 diabetes with long-term insulin use, and need for assistance with personal care. Review of the MDS Medicare 5-day assessment with ARD of 2/16/24 revealed resident #2 had no behavioral symptoms and did not reject evaluation or care that was necessary to achieve his goals for health and well-being. The MDS assessment indicated the resident had functional impairment in range of motion with an impairment of one leg, and he used a prosthetic device and a wheelchair for mobility. The resident required partial to moderate assistance for toileting hygiene, bathing, and dressing. He was always incontinent of bladder and bowel and needed a mechanically altered, therapeutic diet. The MDS assessment revealed resident #2 had medically complex conditions and he received Occupational and Physical Therapy services for two days, from 2/14/24 to 2/15/24, prior to hospitalization on 2/16/24. Review of a Notice of Denial of Medical Coverage letter dated 2/14/24 revealed resident #2's insurance company authorized SNF services until midnight on 2/23/24. Review of a nursing progress note dated 2/16/24 revealed that at approximately 3:50 AM, a CNA called the nurse to resident #2's room. The nurse indicated the resident moved his mouth but did not open his eyes. She checked his blood glucose level and obtained a critically low reading. The resident did not respond to two rounds of emergency medications administered by the nurse, and he was transferred to the hospital via ambulance. Review of the hospital record revealed a History & Physical dated 2/16/24 that indicated resident #2's chief complaint and admission diagnosis was acute metabolic encephalopathy (brain disorder) due to hypoglycemia or low blood sugar. The document read, Based on the patient's presentation, it is expected that they will cross 2 midnights of care in the hospital. Review of a Discharge summary dated [DATE] revealed the physician described resident #2 as stable and expected him to return to the facility within 24 hours. A CM note dated 2/19/24 revealed the resident had active discharge orders. The CM notified the facility's Care Liaison who told her the patient has seven skilled days and the facility was unable to accept a 3-day waiver. A CM note on 2/21/24 indicated the facility's Care Liaison informed the hospital patient request has been sent for [physician] review, please look for an alternative. CM sent referrals to additional facility, waiting for response. A CM note dated 2/25/24 indicated the resident's length of stay was now nine days although his discharge plan on admission was to return to the facility. When the hospital CM reached out to the facility's Care Liaison regarding the delay, she informed the CM the resident was a complex case. A revised Discharge summary dated [DATE] read, Case management working on placement. The hospital record showed resident #2 was eventually discharged to another SNF on the evening of 2/29/24. On 5/08/24 at 10:42 AM, in a telephone interview, a hospital Case Manager stated resident #2 was admitted to the hospital through the ED on 2/16/24 and medically cleared on 2/19/24, but the facility did not want to re-admit him due to an insurance issue. He explained the facility's Care Liaison told hospital case management staff the facility was unable to accept resident #2 as he had only seven Medicare covered days left and after that he would have to pay privately for his stay in the facility or apply for Medicaid as a payer source. The Case Manager stated resident #2's acute care needs were met and he should have left the hospital. However, he remained in the hospital for approximately two weeks, until the hospital found placement for him at another SNF. He said, We did not want him sitting in the hospital. It's not good for any patient's psychosocial well-being. The Case Manager explained any hospitalization was stressful for patients and families, even more so if there were changes with a discharge location. He stated the hospital provided hemodialysis and limited therapy services, but not the degree of therapy available in the SNF setting. The Case Manager stated there was a conference call between three hospital Case Management staff and the facility's [NAME] President (VP) of Census Development and the Care Liaison in an attempt to resolve the issue. The Case Manager stated hospital staff informed the facility representatives the Centers for Medicare & Medicaid Services (CMS) regulations indicated the SNF was obligated to re-admit resident #2 after his acute care needs were met in the hospital. He recalled the Care Liaison and the VP of Census Development informed the hospital that resident #2 could not return unless his family provided the necessary financial information to complete a Medicaid application. The Care Manager stated the hospital advised the facility representatives the financial aspect could be addressed in the facility and it should not delay discharge from hospital. He recalled the VP of Census Development stated he addressed the issue with senior leadership at the corporate level and the decision was made to deny resident #2's return to the facility. The Case Manager recalled the hospital representatives reiterated the decision was a regulatory violation, but the VP of Census Development stated they felt differently about the interpretation of that regulation. On 5/08/24 at 4:41 PM, the facility's Business Office Manager (BOM) recalled at the time resident #2 was last transferred to the hospital, he had seven paid Medicare days left. She explained prior to admission, the facility's Central Intake would request authorization from insurance companies. The BOM stated resident #2 required a new authorization each time he was re-admitted . She stated when he did not return to the facility, she assumed he was discharged home. The BOM stated she would contact Central Intake to check whether resident #2's insurance company declined to authorize re-admission. As of 5/10/24 at 4:00 PM, despite numerous requests, the BOM did not provide the requested information. On 5/09/24 at 10:59 AM, the Administrator stated she was not aware of a decision to refuse readmission for resident #2. She confirmed she was aware there were issues related to the family's compliance with requests for information needed to change his payer source. The Administrator acknowledged if the resident remained in the facility after he exhausted his Medicare paid days but refused to provide the necessary documents, the facility had the option to proceed with a 30-day discharge notice for non-payment. On 5/10/24 at 3:08 PM, in a telephone interview, the VP of Census Development confirmed he participated in a conversation with hospital case management. He recalled the hospital wanted the facility to re-admit resident #2 prior to the family and resident completing the Medicaid application process. The VP of Census Development said, His insurance would not authorize him and the family would not cooperate. [Name of the facility] did not refuse to take him back. If there was a denial we would have been notified. On 5/10/24 at 3:24 PM, after review of the medical record, the SSD validated the insurance company authorized resident #2's stay in the facility until midnight on 2/23/24. She stated she was under the impression the resident or family called 911 for the hospital transfer as they had done that in the past to avoid discharge home from the facility when the insurance decided to cut his therapy. The SSD denied knowledge that the resident was sent out for critically low blood sugar, possibly resulting from a medication error, and was not allowed to return. She stated she was told the insurance company Case Manager wanted the resident to reserve the Medicare days he had left in case he needed them after he went home. In a telephone interview on 5/14/24 at 9:46 AM, in response to an email sent on 5/10/24 at 10:36 AM, resident #2's insurance company Case Manager reviewed his chart and discovered a SNF authorization was opened on 2/21/24. She explained an authorization stayed open for at least five days. The Case Manager provided details from a Communication Note dated 2/22/24 at 9:36 AM regarding a conversation between the insurance company and a representative of the facility's offsite corporate representative. The note read, Received call from [name of facility's corporate representative], that the facility isn't accepting [the resident] back, so she requested auth[orization] be voided. On 5/14/24 at 2:06 PM, in a telephone interview, the facility's Administrator explained [name of corporate representative] did not work onsite at the facility. She said, It is someone in corporate. I'm not sure of the person's title. Review of the facility's policy and procedure for Transfer and Discharge, revised in November 2023, read, It is the policy of this facility to permit each resident to remain in the facility, and not initiate transfer of discharge from the facility, except in limited circumstances. The document defined a transfer as the movement of a resident from one certified facility to another with the expectation of return to the original site. A facility-initiated transfer or discharge was one that the resident was opposed to or did not initiate .and/or is not in alignment with the resident's stated goals for care and preferences. The policy indicated residents had the right to remain in the facility unless a transfer was necessary for the resident's welfare and his/her needs could not be met in the facility, the resident's behaviors endangered the safety and health of individuals in the facility, or if the resident refused to pay for his/her stay after appropriate notice was given. The document revealed a notice must be provided at least 30 days before a facility-initiated transfer or discharge. The policy specified that discharge would not be initiated based solely on payer source or change in payer source. The document indicated residents who were transferred to the hospital for their safety and welfare .will be permitted to return to the facility upon discharge from the acute care setting. The policy revealed residents had the right to return to the facility from the hospital pending appeal of a facility-initiated discharge and the facility would document the danger the failure to discharge the resident would pose.
SERIOUS (G) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Actual Harm - a resident was hurt due to facility failures

Quality of Care (Tag F0684)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure effective communication, collaboration, and oversight of cha...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure effective communication, collaboration, and oversight of changes to the plan of care by members of the interdisciplinary team (IDT) for 1 of 3 residents reviewed for hospitalization, out of a total sample of 9 residents, (#2). The facility's failure to thoroughly review medication orders resulted in administration of an excessive dose of insulin that rendered a resident unresponsive due to a critically low blood glucose level, and required transfer to a higher level of care for treatment, actual harm, for resident #2. Findings: Review of the medical record revealed resident #2 was admitted to the facility on [DATE] and last re-admitted on [DATE]. His diagnoses included type 2 diabetes with long-term insulin use, end-stage kidney disease with hemodialysis, left leg above knee amputation, and the need for assistance with personal care. Review of the Minimum Data Set (MDS) Medicare 5-day assessment with assessment reference date of 2/16/24 revealed resident #2 had clear speech, clear comprehension, and was able to express his ideas and wants. He had a Brief Interview for Mental Status score of 15 which indicated he was cognitively intact. The MDS assessment showed the resident had no behavioral symptoms and did not reject evaluation or care that was necessary to achieve his goals for health and well-being. The document indicated resident #2 had medically complex conditions. Resident #2 had a care plan for diabetes with use of insulin, initiated on 12/14/23. The goal was the resident would have no complications related to diabetes. The interventions instructed nurses to check his blood glucose levels as ordered, administer medication as ordered, monitor for effectiveness and side effects, and monitor for signs and symptoms of low blood glucose. Review of resident #2's medical record revealed an admission Summary that showed he was re-admitted from the hospital on 2/13/24 at approximately 8:00 PM. An Order Audit Report dated 2/13/24 at 10:08 PM revealed resident #2's attending physician ordered Detemir insulin 20 units once daily for diabetes. The order was confirmed a few minutes later at 10:12 PM by the evening shift Nursing Supervisor. Review of an Order Audit Report dated 2/14/24 at 12:50 PM revealed an Advanced Practice Registered Nurse (APRN) ordered Levemir 22 units at bedtime for type 2 diabetes. The order was confirmed on 2/15/24 at 10:55 AM by a Unit Manager (UM) who no longer worked at the facility. Detemir is the generic name for Levemir, a man-made long-acting insulin that starts to work several hours after injection and keeps working evenly over 24 hours. If prescribed once daily, Levemir is usually administered in the evening or at bedtime. The most common adverse reaction of insulin is hypoglycemia and long-standing diabetics may be less aware of symptoms (retrieved on 5/24/24 from www.drugs.com/levemir.html). Review of resident #2's Medication Administration Record (MAR) for February 2024 revealed he received a one-time dose of Detemir 22 units on 2/14/24 at 9:00 AM. The document indicated a nurse also signed for an additional dose of Detemir 20 units on 2/14/24 at 9:00 AM. The MAR was updated to reflect a new order for Levemir 22 units at bedtime on 2/14/24 at 9:00 PM, but the document was not initialed by a nurse to verify the dose was given. On 2/15/24 a 9:00 AM, resident #2 received 20 units of Detemir and the MAR showed he received an additional 22 units of Levemir 12 hours later at 9:00 PM, a total of 42 units in 24 hours. Review of a nursing progress note dated 2/16/24 revealed that at approximately 3:50 AM, a Certified Nursing Assistant called the nurse to resident #2's room. The note read, Upon arrival writer observed resident moving his mouth but not opening his eyes. Writer immediately check his blood sugar which read 25. The document indicated the nurse gave two doses of Glucagon in an attempt to increase his blood glucose level, but the resident remained unresponsive. The nurse contacted the resident's physician who instructed her to send resident #2 to the hospital via 911 for further evaluation. According to the American Diabetes Association (ADA), hypoglycemia or low blood glucose occur when the blood glucose level falls below 70 milligrams per deciliter (mg/dL). As blood glucose continues to drop, the brain is deprived of glucose and it stops functioning as it should. The ADA indicates a critical, life-threatening blood glucose value is one that is less then 54 mg/dL. Initially, hypoglycemia causes symptoms such as blurred vision, difficulty concentrating, confusion, slurred speech, numbness, and drowsiness. If untreated, low blood sugar levels can starve the brain of glucose, causing seizures, coma, and death (retrieved on 5/24/24 from www.diabetes.org/living-with-diabetes/treatment-care/hypoglycemia). Review of the Weights and Vitals Summary revealed resident #2's blood glucose level was checked on 2/16/24 at 5:30 AM and 5:35 AM, with resulting readings of 25 mg/dL. A blood sugar level below 54 mg/dL requires immediate action and severe hypoglycemia can be treated with an injection or nasal spray of Glucagon, a hormone that raises blood glucose levels (retrieved on 5/24/24 from www.medlineplus.gov). Review of the Emergency Medical Services (EMS) Run Sheet revealed a call was received from the facility on 2/16/24 at 5:15 AM, almost 90 minutes after the nurse indicated she was made aware of the resident's change in condition. The document indicated upon arrival at the facility, EMS personnel discovered resident #2 unresponsive. According to the Run Sheet, the nurse informed them she gave three doses of Glucagon and their primary impression of the resident was diabetic hypoglycemia. Resident #2 was transported to the hospital by ambulance with lights and sirens and arrived at the Emergency Department (ED) on 2/16/24 at 5:46 AM. Review of the hospital record revealed a History & Physical dated 2/16/24 that indicated resident #2 presented to the ED with altered mental status and per EMS report, he had a blood glucose level of 38 mg/dL. The document revealed his chief complaint and admission diagnosis was acute metabolic encephalopathy (brain disorder) due to hypoglycemia or low blood sugar. The ED physician documented that resident #2 was difficult to assess as he was somnolent and did not stay alert or awake long enough to respond to questions. A physician progress note dated 2/23/24 revealed resident #2's long-acting insulin was discontinued on admission to the hospital. Review of the hospital Discharge summary dated [DATE] revealed physician orders for Humalog fast-acting insulin three times daily according to a sliding scale, and Humulin N intermediate-acting insulin 5 units twice daily. On 5/09/24 at 3:02 PM, the Director of Nursing (DON) recalled resident #2 was a very brittle diabetic as his blood glucose levels varied widely. She validated she was not aware the resident's insulin order was changed two days before he was found unresponsive until informed by State Survey Agency staff. She stated she did not recall any investigation regarding the resident's transfer to the hospital for unresponsiveness with a low blood sugar as this would have been viewed as a change in condition, not an incident. Review of the Weights and Vitals Summary for the period 10/31/23 to 2/15/24 revealed during a 4-month period that covered several admissions, resident #2's blood glucose level was checked approximately three to four times daily. The 9-page document showed his readings were below 70 mg/dL on only two other occasions, 52 mg/dL on 12/20/23 and 68 mg/dL on 2/08/24, and otherwise remained between 70 mg/dL and 453 mg/dL. Resident #2's blood glucose level never dropped to 25 mg/dL as it did on the morning of 2/16/24 after he received a combined dose of Levemir 42 units in the previous 24 hours. On 5/10/24 at 9:23 AM, the DON explained the facility held a clinical team meeting, Monday through Friday at 9:00 AM, that was attended by herself, UMs, the Assistant DON, the Social Services Director, the Administrator, and the Certified Dietary Manager. She stated during these meetings, the IDT reviewed the charts of newly admitted residents, the previous day's events, nursing notes regarding high priority items or events, and any other concerns placed on the 24-hour report. The DON stated high priority items included all new orders, and laboratory and radiology results. She validated the daily IDT meeting was the opportune setting for identification of any discrepancies related to new physician orders. On 5/10/24 at 12:26 PM, in a telephone interview, the APRN stated she did not recall the exact circumstances surrounding her order for Levemir 22 units for resident #2. She explained either a nurse or the UM probably called or informed her during facility rounds that the resident's blood glucose levels were trending upward. The APRN confirmed she would have ordered an increase of two units, from Levemir 20 units once daily to 22 units once daily after review of the medical record. She stated her order would never be to add Levemir 22 units to an existing daily dose of Levemir 20 units. The APRN verified no nurse or member of nurse management contacted her regarding clarification of insulin orders. She stated the facility never informed her resident #2 was found unresponsive with a critically low blood glucose level. The APRN reiterated she would never have doubled resident #2's daily dose of insulin in that way, especially since he was a dialysis patient. She said, On those patients, we make changes slowly. On 5/10/24 at 10:26 AM, in a telephone interview, resident #2's attending physician was informed the resident received Levemir insulin 20 units in the morning on 2/15/24 according to his orders, then received an additional 22 units of Levemir insulin 12 hours later per the order of another practitioner. The attending physician stated he was not aware an additional dose of insulin was ordered to provide the resident with more than double the dosage he intended. He acknowledged the incident and outcome were concerning. 5/10/24 at 1:07 PM and 2:17 PM, the DON stated her investigation showed at the time the APRN reviewed resident #2's medical record and wrote the order for Levemir 22 units at bedtime, the attending physician's order for 20 units showed as discontinued. She explained since there was no active order for long-acting insulin, the APRN wrote the order for Levemir 22 units, an increased dosage of only two units based on resident #2's blood glucose readings. The DON explained the APRN's order was transcribed to the MAR for administration at bedtime and scheduled for 9:00 PM. When asked why the attending physician's order for Levemir 20 units daily at 9:00 AM was not visible to the APRN and then re-appeared on the MAR as a continuing order, she said, There were two orders bouncing back and forth due to the pharmacy process. She explained the facility had an automatic therapeutic interchange agreement with the physicians and as a result, the pharmacy could make adjustments to medication orders to reflect its formulary drugs. The DON stated the original order for Levemir 20 units that was entered under the attending physician's name was for a vial of Levemir. She explained the pharmacy discontinued that order and replaced it with an order for a Levemir pre-filled FlexPen. She acknowledged the APRN might have reviewed the orders at the time the pharmacy was in process of making that change. The DON stated the pharmacy's order was system-generated but still needed to be confirmed by a nurse. She validated the APRN's new order was confirmed by resident #2's UM but the order for Levemir 20 units was not discontinued at that time. The DON stated the IDT review process in the daily clinical meeting involved reviewing new physician orders, but the team did not actually pull up residents' charts during the process. She acknowledged the IDT would therefore not be able to identify if there was an associated order that needed to be discontinued or if there were any contraindications. The DON validated IDT members were ultimately responsible for the identification of concerns and discrepancies regarding medication orders. She confirmed resident #2's new order for Levemir 22 units at bedtime would not have triggered concerns as a isolated order, but if chart had been reviewed, the IDT would have noticed that the original order for Levemir 20 units in the morning remained active. The DON stated the facility never identified the IDT review process as a concern with the potential to cause medication errors. Review of the Facility assessment dated [DATE] revealed the facility could care for residents with common conditions including endocrine and metabolic diseases such as diabetes. The document indicated nursing leadership participated in daily clinical meetings to review clinical issues on each unit. The Facility Assessment revealed general care and services would include management of medical conditions by on-site physicians, nursing assessments, and early identification of changes in condition.
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0697 (Tag F0697)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure timely and effective pain management, accordin...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure timely and effective pain management, according to professional standards of practice, for 1 of 1 resident reviewed for pain management out of a total sample of 9 residents, (#6). Findings: Review of the medical record revealed resident #6 was admitted to the facility on [DATE]. Her diagnoses included type 2 diabetes, a skin infection with surgical amputation of her right great toe, peripheral vascular disease, and heart disease. Resident #6 had a care plan for risk for pain related to her right foot wound initiated on 5/08/24. The goal was the resident would not have interruptions in normal activities due to pain. The care plan interventions included administer pain management as ordered, and monitor and record pain characteristics such as quality, severity, anatomical location, onset, and duration. The document instructed nursing staff to monitor, record, and report the resident's complaints of pain or requests for pain treatment. A care plan for pain medication related to resident #6's right foot wound and acquired absence of her right great toe was initiated on 5/08/24. The goal was the resident would be free of discomfort. The approaches instructed nurses to administer pain medications as ordered. Review of the medical record revealed resident #6 had a physician order dated 5/07/24 for Tramadol 25 milligrams (mg) every eight hours as needed for severe pain, levels 7 to 10. The order was revised on 5/08/24 to administer Tramadol 50 mg every six hours as needed for moderate to severe pain. On 5/08/24 at 10:01 AM, 11:10 AM, and 1:39 PM, resident #6's granddaughter stated her grandmother was admitted to the facility at about 9:30 PM the previous night. She expressed frustration that her grandmother had not received the proper medication. The granddaughter recalled when she arrived at the facility last night, her grandmother was crying and complained of severe pain in her right foot. Resident #6's granddaughter stated she asked a nurse to administer pain medication. She said, She was to get 25 mg of Tramadol and the nurse did give a pill at about 10-ish. The granddaughter explained she left the facility and returned a few hours later, at about 4:00 AM. She stated she found her grandmother crying again, as she sat upright on the side of the bed with her legs hanging down. Resident #6 told her granddaughter the pain was much worse when her legs were elevated so she decided to remain seated instead of lying down. The granddaughter indicated when she asked the nurse for another dose of pain medication for her grandmother, the nurse informed her the pharmacy delivery had not yet arrived and .she didn't have anything to give her now. On 5/08/24 at 1:27 PM, Licensed Practical Nurse (LPN) B confirmed she was resident #6's assigned nurse yesterday, during the evening shift. LPN B explained she did not have access to the facility's medication dispensing machine, but when the resident's granddaughter requested pain medication, another nurse retrieved it from the machine. On 5/08/24 at 1:39 PM, resident #6 sat in a wheelchair in her room. Her eyes were closed, her brow was furrowed, and she explained she asked for pain medication about 15 minutes ago. The resident described her pain as severe, sharp, and intermittent, and she made a grabbing motion towards her right foot. Resident #6 explained the onset of pain was usually sudden and although it might go away for a while, it returned with the same severity if she did not receive pain medication. The resident verified when the nurse gave her a pain pill last night, her pain level was level 10, on a 0 to 10 scale. She validated at 4:00 AM this morning when her granddaughter returned to the facility, she again had level 10 pain. Resident #6 stated the nurse never brought any pain medication this morning and she eventually fell asleep sitting up. She confirmed she received pain medication only once in the 16 hours since admission. On 5/08/24 at 1:49 PM, the Director of Nursing (DON) stated an Advanced Practice Nurse Practitioner (APRN) assessed resident #6 early this morning. She acknowledged after assessing and speaking with the resident, the APRN increased the dosage and frequency of her pain medication. On 5/08/24 at 3:54 PM, in a telephone interview, Registered Nurse (RN) E stated she was assigned to resident #6 for the overnight shift which ended at 7:00 AM this morning. In a statement that conflicted with findings of interviews conducted with resident #6 and her granddaughter, RN E denied knowledge of the resident's complaints of pain during the night shift. She stated she was never asked to administer pain medication for the resident. On 5/09/24 at 9:58 AM, resident #6's son complained that despite an increase in the dosage of his mother's pain medication, they still had problems managing her pain. He said, They come in and ask if she's in pain, and if she's not in pain at that moment, they don't come back for a while. By then she is really hurting. He stated her pain was not constant, and he described it as all over the place. Resident #6's son stated neither he nor his mother was aware the pain medication was not scheduled at regular intervals, but had to be requested. Review of resident #6's Medication Administration Record (MAR) for May 2024 revealed no nursing documentation regarding administration of Tramadol 25 mg on 5/07/24 during the evening shift. The document showed resident #6 received her first dose of pain medication, Tramadol 50 mg, on 5/08/24 at 1:41 PM. The MAR indicated the resident's pain levels were 0 to 4 between 5/07/24 and 5/08/24, and not level 10 as reported by the resident and described by her granddaughter. A Nurses Note dated 5/07/24 at 10:38 PM read, Resident complain of pain at surgical site pain medication tramadol 25 mg was given will continue to monitor. The note did not include a description of the pain or its severity. The document was created by LPN B the following day, on 5/08/24 at 11:41 AM, after State Survey Agency staff identified pain management concerns for resident #6. On 5/09/24 at 1:08 PM, the DON discussed the absence of documentation regarding Tramadol 25 mg that was allegedly given to resident #6 on Tuesday, 5/07/24. The DON confirmed she investigated the situation and said, We have a little concern. She explained the pharmacy provided a report that showed removal of Tramadol 50 mg from the medication dispensing machine on 5/08/24, but there was no transaction recorded for the drug on 5/07/24. On 5/09/24 at 1:24 PM, the evening shift Nursing Supervisor validated resident #6's granddaughter came to the nurses' station soon after the resident's admission on [DATE]. She recalled the granddaughter informed the nurses of the resident's pain. The Nursing Supervisor stated after LPN B assessed resident #6, she returned to the nurses' station and explained the resident's medications were not yet available The Nursing Supervisor stated she called the pharmacy to obtain an authorization and access code to retrieve Tramadol 50 mg from the medication dispensing machine. She stated LPN B administered half a tablet and they wasted the other half. On 5/09/24 at 4:31 PM, the DON stated she followed up with the pharmacy and there was no documentation to show an authorization code was provided for the Nursing Supervisor to access the medication dispensing machine on 5/07/24. The DON acknowledged although resident #6 and her granddaughter confirmed the nurse administered a pill, there was no evidence the pill was Tramadol. On 5/10/24 at 9:16 AM, the DON stated pharmacy staff made an onsite visit within the last 24 hours and conducted a medication reconciliation that showed no discrepancies. She validated the Tramadol count in the machine matched the pharmacy's record. The facility's policy and procedure for Pharmacy Services, revised in June 2023, revealed the facility would provide pharmaceutical services to ensure accurate acquiring, dispensing, and administration of all routine and emergency drugs to meet the needs of each resident. Review of the medication dispensing machine Transactions record for the period 5/02/24 to 5/08/24 revealed no drugs were removed from the machine on 5/07/24. A Tramadol Transaction report for resident #6 was provided to the DON from the pharmacy in an email dated 5/09/24 at 11:36 AM. The document showed Tramadol 50 mg was pulled from the machine on 5/08/24 at 1:38 PM. The email read, The cabinet was not accessed for medication May 6-7. Review of the facility's policy and procedure for Pain Management, revised in August 2023, revealed the facility would provide pain management for residents that was consistent with professional standards of practice, person-centered care plans, and residents' goals. The document indicated the facility would prevent or manage a resident's pain by observation of non-verbal indicators such as restlessness, grimacing, and negative vocalizations. The policy revealed nurses would conduct pain assessments that included key characteristics and descriptors. The document showed pharmacological interventions would include consideration of around the clock administration of pain medication rather than as needed.
CONCERN (D) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Medical Records (Tag F0842)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure the medical record accurately reflected the status of and se...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure the medical record accurately reflected the status of and services provided for 1 of 3 residents reviewed for hospitalization, out of a total sample of 9 residents, (#2). Findings: Review of the medical record revealed resident #2 was admitted to the facility on [DATE] and last re-admitted on [DATE]. His diagnoses included type 2 diabetes with long-term insulin use. Resident #2 had a care plan for diabetes with use of insulin, initiated on 12/14/23. The goal was the resident would have no complications related to diabetes. The interventions instructed nurses to check his blood glucose levels and administer diabetes medication as ordered by the physician. A nursing progress note dated 2/16/24 revealed at approximately 3:50 AM, resident #2 was discovered unresponsive in bed with a critically low blood glucose level. The resident's physician gave an order to send the resident to the hospital via 911 for further evaluation. Review of a Hospital Transfer Form dated 2/16/24 at 5:40 AM revealed resident #2 was transferred to the hospital. Review of the medical record indicated resident #2 was not re-admitted from the hospital. Review of the Weights and Vitals Summary revealed a nurse documented resident #2's blood glucose level on 2/18/24 at 6:09 PM as 165 milligrams per deciliter (mgdL) and on 2/18/24 at 6:45 PM as 145 mg/dL. Review of the Medication Administration Record (MAR) for February 2024 revealed documentation of medications given to resident #2 two days after he was discharge from the facility as follows: 2/18/24 at 8:00 AM Sevelamer Carbonate 1600 mg 2/18/24 at 9:00 AM Amlodipine 5 mg 2/18/24 at 9:00 AM Finasteride 5 mg 2/18/24 at 9:00 AM Saccharomyces boulardii 250 mg 2/18/24 at 9:00 AM Dorzolamide HCl-Timolol Maleate Ophthalmic Solution 2-0.5% 2/18/24 at 9:00 AM Pregabalin 25 mg capsule 2/18/24 at 9:00 AM Cyclopentalate HCl Ophthalmic Solution 1% 2/18/24 at 9:00 AM Dicyclomine HCl 20 mg 2/18/24 at 10:00 AM Prednisone 50 mg 2/18/24 at 12:00 PM Sevelamer Carbonate 800 mg 2/18/24 at 1:00 PM Cyclopentalate HCl Ophthalmic Solution 1% 2/18/24 at 1:00 PM Dicyclomine HCl 20 mg The MAR revealed the assigned nurse checked and recorded resident #2's blood glucose levels on 2/18/24 at 7:30 AM and 11:30 AM. On 5/10/24 at 1:07 PM, the Director of Nursing (DON) was informed of nursing documentation on resident #2's MAR that indicated on 2/18/24 during the 7:00 AM to 3:00 PM shift, the assigned nurse administered all scheduled medications and checked his blood glucose levels, although the resident had been in the hospital since 2/16/24. She reviewed the medical record and validated the documentation was inaccurate. The DON stated her expectation was nurses would document the actual care provided and medications administered. Review of the facility's policy and procedure for Documentation in the Medical Record, revised in November 2023, read, Each resident's medical record shall contain an accurate representation of the actual experiences of the resident.through complete, accurate, and timely documentation. The policy indicated licensed staff would document services provided in the resident's medical record, at the time of service. The document read, False information shall not be documented.
CONCERN (E) 📢 Someone Reported This

A family member, employee, or ombudsman was alarmed enough to file a formal complaint

Potential for Harm - no one hurt, but risky conditions existed

Safe Environment (Tag F0584)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to promote the right to a clean, comfortable, and homeli...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to promote the right to a clean, comfortable, and homelike environment for 4 of 6 residents reviewed for environmental concerns out of a total sample of 9 residents, (#5, #6, #7, and #9), on 2 of 2 units, (A & B Wings). Findings: 1. Review of the medical record revealed resident #6 was admitted to the facility on [DATE]. Her diagnoses included type 2 diabetes, and a skin infection with surgical amputation of her right great toe. Review of a progress note dated 5/07/24 at 9:49 PM revealed resident #6 arrived on the A Wing and was assisted to her room. On 5/08/24 at 11:10 AM, resident #6's granddaughter expressed dissatisfaction with the condition of her grandmother's room and bathroom when she arrived from the hospital the previous night. She stated it was obvious the room had not been properly cleaned and prepared for a new resident. The granddaughter provided photographs that showed stained sheets on the bed, a significant amount of dried, brown urine stains underneath the toilet seat, and a used plastic container with brown paper towel inside was on the lid of the toilet. The plastic container was of the type used to collect and measure body fluids such as urine. The granddaughter explained after she complained, it took about two hours for someone to remove the container. She stated when no staff returned to replace the sheets as requested, she asked for clean sheets and changed them herself. On 5/08/24 at 12:22 PM, the facility's Admissions Concierge stated she was made aware of resident #6's planned admission yesterday, 5/07/24 at 8:25 AM. She stated she provided the marketing liaison at the hospital with the room number for the new resident and then updated the nurse of the pending admission. The Admissions Concierge confirmed the room was to be cleaned after removal of the previous resident's items, in preparation for the new resident. She stated she also told the Certified Nursing Assistant on the 3:00 PM to 11:00 PM shift about resident #6's expected arrival. The Admissions Concierge recalled she saw a housekeeper in the room during the day on 5/07/24. She stated she checked the room at about 4:00 PM, but did not go into the bathroom. On 5/09/24 at 11:37 AM, the Floor Technician stated on Wednesday 5/08/24, he was informed of the granddaughter's complaints and the need to clean resident #6's room. He validated the condition of the toilet was as described by the granddaughter and shown in the photograph. The Floor Technician stated Housekeeper D told him she cleaned the room on Tuesday, 5/07/24. He said, I told her she should pay more attention to cleaning. He explained all rooms were to be cleaned once daily, but prior to a new admission, rooms required a special deep clean procedure. Review of a Deep Clean Check Off List (undated) revealed the procedure included thorough cleaning of the bed frame, mattress, call bell, air conditioning unit, furniture, floors, blinds, and the toilet. On 5/09/24 at 11:57 AM, Housekeeper D stated she cleaned resident #6's room in the morning on 5/07/24, after the breakfast meal carts left the unit. She explained after lunch, she was instructed to do a deep clean for that room as there would be a new resident. Housekeeper D acknowledged a deep clean involved cleaning all areas and surfaces of the room and bathroom. She did not respond when asked to explain why the condition of the resident's room did not reflect requirements of the deep cleaning procedure. On 5/09/24 at 12:17 PM, the Rehab Director confirmed she spoke with resident #6's granddaughter on Wednesday 5/08/24. She verified the granddaughter expressed concerns about the lack of cleanliness of the room on admission and pointed out issues including dirty window blinds. The Rehab Director acknowledged she viewed the granddaughter's photographs of the dirty bathroom and said, I apologized and told her it was not acceptable. 2. Review of the medical record revealed resident #5 was admitted to the facility on [DATE]. Her diagnoses included right hip fracture, history of falling, abnormal gait and mobility, and need for assistance with personal care. Review of the Minimum Data Set (MDS) with assessment reference date of 4/29/24 revealed resident #5 had a Brief Interview for Mental Status score of 15 which indicated she was cognitively intact. On 5/08/24 at 10:26 AM, resident #5 confirmed there was a roach problem on the unit and in her room on the 500 hall. She stated she was in the A Wing common room with a visitor a few days ago, when a big roach ran across the room. The resident stated the incident occurred during the day, but she also saw big roaches in the hallway at night, headed towards her room. She explained she even used her trash can to squash a small roach on the floor. She pointed to the trash can beside her bed and said, It's under there. Resident #5 stated she asked her daughter to bring a can of roach spray for her yesterday and she stored it inside her bedside commode. She said, I wouldn't be able to sleep if I saw one near me. On 5/09/24 at 10:06 AM, Registered Nurse A lifted the lid of resident #6's bedside commode and removed a full can of ant, roach, and spider spray. Photographic evidence was obtained. Review of the A Wing Pest Sighting/Evidence Log showed documentation on 3/29/24 of roach issues on the 400, 500, and 600 hallways. On 5/03/24, the MDS Coordinator noted roaches in the MDS office and in rooms 608, 609, 610, and 611. The log indicated on 5/09/24, roaches issues were identified in room [ROOM NUMBER]. 3. Review of the medical record revealed resident #7 was admitted to the facility on [DATE]. Her diagnoses included type 2 diabetes, heart disease, and need for assistance with personal care. On 5/10/24 at 2:10 PM, resident #7 was interviewed in her room on the B Wing. She said, We have a bad roach problem, day and night. The roaches are the biggest issue. I kill the little bitty ones, but the big ones are hard to catch. The resident explained she used to be able to catch the big roaches, but she was no longer fast enough. Resident #7 confirmed she told numerous staff members, many times. During the interview, a large dark brown roach scurried from behind the oxygen concentrator near the resident's wheelchair and traveled approximately six feet to stop under the roommate's bed. The roach remained under the bed for less than one minute, then quickly crossed the room, and headed towards the area behind resident #7's bedside table. The roommate, resident #9, interjected and stated she was not surprised the roach ran around the room as it was a huge problem and everyone was aware. Resident #9 complained she had a roach in her bed as recently as last night. Review of the facility's policy and procedure for Resident Rights, revised on 9/09/22, revealed residents had rights to a dignified existence and .a safe, clean, comfortable and homelike environment, including but not limited to receiving treatment and supports for daily living safely.
Jul 2023 3 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Tube Feeding (Tag F0693)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to follow physician orders and standards of practice for...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to follow physician orders and standards of practice for residents who received their nutrition and medications through a gastrostomy tube (GT) for 1 of 2 sampled residents with a gastric tube (GT) out of a total sample of 29 residents, (#298). Findings: Review of resident #298's medical record revealed he was admitted to the facility on [DATE] from an acute care hospital. His diagnoses included diabetes mellitus type 2, dysphagia (difficulty swallowing), and gastrostomy tube. A gastrostomy tube (also called a G-tube) is a tube inserted through the belly that brings nutrition directly to the stomach (www.medlineplus.gov retrieved 08/01/23). Resident #298's Nursing Comprehensive assessment dated [DATE], revealed he was oriented to self, non-verbal, totally dependent on staff for his activities of daily living and received nutrition via tube feeding. The physician order dated 7/9/23 instructed nurse to flush tube with 30 ml (milliliters) before and after medications pass and flush with 5 ml between medications. The tube flush order did not specify what type of tube or what type of solution to flush with. The facility provided a policy dated 1/2023 for Medication Administration via Enteral Tube that read, Enteral tube placement must be verified prior to administering any fluids or medication. On 7/13/23 at approximately 6:23 PM, the facility provided an updated policy revised July 2023 which did not include checking tube placement. Review of the facility updated policy for Medication Administration via Enteral Tube read, Pharmacy will be notified that an order to give medications through an enteral tube has been received and suspensions for medications will be supplied when possible .Each medication will be administered separately, not combined or added to an enteral feeding .Flush enteral tube with at least 15 ml of water prior to administering medications unless otherwise ordered by prescriber. Dilute the solid or liquid medication and administer using a clean syringe .Flush tube again with at least 15 ml water taking into account residents volume status. Repeat with the next medication .Flush tube with a final flush . On 7/11/23 at 9:40 AM, Licensed Practical Nurse (LPN) A prepared to administer resident #289's scheduled morning medications. LPN A placed 8 different medications into 8 small plastic cups at the medications cart that included, Vitamin C 500 milligrams (mg) 1 tablet, Acetazolamide 250 mg ½ tablet, Amlodipine 10 mg 1 tablet, Carvedilol 3.125 mg 1 tablet, Carbidopa-Levodopa 25-100 mg 1 tablet, Isosorbide Mononitrate 20 mg 1 tablet, Guaifenesin extended release 600 mg 2 tablets, and Multivitamin with minerals 1 tablet. LPN A then proceeded to take the 8 small plastic cups containing medications and pill crusher into resident #289's room and placed them on the over bed table. Resident #289 was in bed with his eyes open and was nonverbal. LPN A proceeded to identify the resident and explained to him that she was going to be giving his medications via his G-tube and turned off the feeding pump which had been infusing Glucerna nutrition formula at 50 ml per hour. On 7/11/23 from approximately 10:10 AM to 10:40 AM LPN A put all 8 medications in 1 small plastic bag and proceeded to crush them with the pill crusher at the bedside. When the bedside table started to buckle due to the increased pressure, she took the pill crusher to the dresser and completed crushing them. LPN A then put all crushed tablets into a medium sized plastic cup with 30 ml of water. She mixed the medications with a spoon and poured them back and forth in another plastic cup. There were large clumps of undissolved medications in the thick mixture. LPN A did not check placement of the feeding tube prior to medication administration. LPN A initially flushed the feeding tube with 30 ml of sterile water using a 60 ml piston tip syringe. She then drew up approximately 1/3 of the thick medication mixture with the same 60 ml syringe and proceeded to administer medications via the resident's G-tube. The nurse continued intermittent flushes with 5-10 ml water and 10 to 20 ml of air in the 60 ml syringe. The medication mixture would not easily administered so she continued to add more water to the mixture and went back and forth at least 4 times putting in the water and air. She then disconnected the control valve at the end of the feeding tube attached to the resident and started milking the tubing with her fingers attempting to unplug the clumps of medication. The adapter was plugged with medication particles and could not be used any more. The nurse did a final flush of the feeding tube with 60 ml of water via piston syringe directly into resident via feeding tube without the adaptor. She then connected the formula tubing directly to the resident minus the adaptor and left the pump off with the feeding formula hanging on the IV pole. LPN A stated she was instructed to give all medications together via G-tube and was not aware if there was an order to flush the tube between each medication. On 7/11/23 at 11:34 AM, the Interim Director of Nursing (DON) said it was basic nursing to give G-tube medications separately and flush in between so the tube did not get plugged. The DON said LPN A should have put each medication in their own cup and mixed them with 5-15 ml of water and given them one at a time and flushed between them as well. On 7/11/23 at 2 PM, a follow up interview was conducted with LPN A and the DON. LPN A acknowledged the 6 medication errors and acknowledged it would have been better to give medications 1 at a time because there would be less chance of clogging up the resident's G-tube. LPN A and the DON validated that it was not appropriate to instill air into the resident's G-tube. Review of the facility policy and procedures for Care and Treatment of Feeding Tubes dated Dec. 2022 read, It is a policy of this facility to utilize feeding tubes in accordance with current clinical standard of practice, with intervention to prevent complications to the extent possible .In accordance with facility protocol, licensed nurses will monitor and check that the feeding tube is in the right locations .Tube placement will be verified before beginning a feeding and before administering medications .Medication Flush Order: Give 30 ml before and after medications pass, 5 ml between meds .
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to prevent medication administration error rate of 5% or...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to prevent medication administration error rate of 5% or greater for 1 of 3 residents sampled for medication administration, (#298). There were 6 medication errors in 29 opportunities for a medication error rate of 20.69%. Findings: Review of resident #298's medical record revealed he was admitted to the facility on [DATE] from an acute care hospital. His diagnoses included diabetes mellitus type 2 (DM), dysphagia (difficulty swallowing), hypertension, anemia, benign prostatic hyperplasia (BPH), and gastrostomy tube. A gastrostomy tube (also called a G-tube) is a tube inserted through the belly that brings nutrition directly to the stomach (www.medlineplus.gov retrieved 08/01/23). On 7/11/23 at 9:40 AM, Licensed Practical Nurse (LPN) A prepared to administer resident #289's scheduled morning medications. LPN A placed 8 different medications into 8 small plastic cups at the medications cart that included, Vitamin C 500 milligrams (mg) 1 tablet, Acetazolamide 250 mg ½ tablet, Amlodipine 10 mg 1 tablet, Carvedilol 3.125 mg 1 tablet, Carbidopa-Levodopa 25-100 mg 1 tablet, Isosorbide Mononitrate 20 mg 1 tablet, Guaifenesin extended release 600 mg 2 tablets, and Multivitamin with minerals 1 tablet. On 7/11/23 at approximately 9:50 AM, LPN A explained she did not have the resident's antibiotic or vitamin D3 available on the medication cart and that she would retrieve them from the medication storage room and from their automated medication dispenser for administration later. LPN A was informed that she would not have medication errors for vitamin D3 or antibiotic as she informed surveyor she would give them later. LPN A did not verbalize any other medications that were scheduled that she would not be giving at this time. On 7/11/23 at approximately 10 AM, LPN A proceeded to take the 8 small plastic cups containing medications and pill crusher into resident #289's room and placed them on the over bed table. Resident #289 was noted in bed with his eyes open and was nonverbal. LPN A proceeded to identify the resident and explained to him that she was going to be giving his medications via his G-tube and turned off the feeding pump which had been infusing Glucerna nutrition formula at 50 milliliters (ml) per hour. On 7/11/23 from approximately 10:10 AM to 10:40 AM LPN A put all 8 medications in 1 small plastic bag and proceeded to crush them with the pill crusher at the bedside. When the bedside table started to buckle due to the increased pressure, she took the pill crusher to the dresser and completed crushing them. LPN A then put all crushed tablets into a medium sized plastic cup with 30 ml of water. She mixed the medications with a spoon and poured them back and forth in another plastic cup. There were large clumps of undissolved medications in the thick mixture. LPN A initially flushed the feeding tube with 30 ml of sterile water using a 60 ml piston tip syringe. She then drew up approximately 1/3 of the thick medication mixture with the same 60 ml syringe and proceeded to administer medications via the resident's G-tube. The nurse continued intermittent flushes with 5-10 ml water and 10 to 20 ml of air in the 60 ml syringe. The medication mixture would not easily administered so she continued to add more water to the mixture and went back and forth at least 4 times putting in the water and air. LPN A stated she was instructed to give all medications together via G-tube and was not aware if there was an order to flush the tube between each medication. A review of the resident #298's medical record post medication administration revealed the following 6 errors for medications scheduled at 9 AM: 1.) 1000 mg of Vitamin C was ordered and only 500 mg was given 2.) Plain Multivitamin was ordered, and it was given with minerals 3.) Aspirin 81 mg oral chewable tablet for CVA (stroke) was error of omission 4.) Glipizide 10 mg tablet via G-tube for DM was error of omission 5.) Tamsulosin 0.4 mg capsule daily for BPH was error of omission 6.) Polyethylene Glycol 17-gram packet via G-tube for constipation was error of omission On 7/11/23 at 11:34 AM, the Interim Director of Nursing (DON) said it was basic nursing to give G-tube medications separately and flush in between so the tube did not get plugged. The DON was apprised of the 6 medications errors and concerns regarding LPN A not administering medications via G-tube safely and as per standards of practice. The DON said LPN A should have put each medication in their own cup and mixed them with 5-15 ml of water and given them one at a time and flushed between them as well. On 7/11/23 at 2 PM, a follow up interview was conducted with LPN A and the DON. LPN A acknowledged the 6 medication errors and said her computer mouse was not working properly and she did not see a page of the resident's medications to be given at 9:00 AM. The DON stated LPN A had not reported the computer issue to anyone. Review of the facility policy for Medication Administration revised January 2023 read, Medications are administered by licensed nurses .Review MAR [medication administration record] to identify medication to be administered. Compare medications source [bubble pack, vial, etc.] with MAR to verify resident name, medication name, form, dose, route, and time .Administer medications as ordered and in accordance with manufacturer specifications .Crush medications as ordered. Do not crush medications with [do not crush] instructions .Crushed meds are not to be combines and given all at once, if via tube feeding tube
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0865 (Tag F0865)

Could have caused harm · This affected multiple residents

Based on observation, interview, and record review, the facility failed to ensure the Quality Assurance and Performance Improvement (QAPI) committee developed and implemented timely and appropriate pl...

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Based on observation, interview, and record review, the facility failed to ensure the Quality Assurance and Performance Improvement (QAPI) committee developed and implemented timely and appropriate plans of action to prevent repeat deficient practices related to medication error rates over 5%. Findings: Review of the facility's survey history revealed repeat deficiencies concerns for medication errors over the past 5 years, and again during the current survey related to a medication error rate of 20.69%. The survey history revealed facility error rates of 6.45% on 2/10/22, 10.71% on 1/16/20 and 6.25% on 10/25/18. This will be the facility's fourth deficiency in 5 years for mediation error rate equal to or greater than 5%. On 7/13/23 at 5:18 PM, 6:23 PM, and 6:26 PM interviews were conducted with the facility's Administrator, Interim Director of Nurses (DON), and Corporate [NAME] Present (VP) of Operations regarding the facility's QAPI program. The Administrator verified they completed a plan of correction for medication errors last year but could no locate current audits for this year for medication errors except for ones done by the pharmacy nurse consultant. The DON was able to show the pharmacy consultant nurse did medication administration audits with 4 nurses in April of 2023. The VP verified that if they had ongoing PIP (Performance Improvement Plan) and audits of mediation errors that they should have documentation readily available for review but they did not. The facility could not show evidence of medication errors being discussed in QAPI meetings this year or that they had an actual PIP currently in effect for medications errors. The facility could not show evidence of current audits regarding medication errors except for routine ones that were done by the pharmacy consult nurse. The Administrator acknowledged the facility did not currently have a QAPI plan in place for Medication Errors. Review of the facility policy for Quality Assurance and Performance Improvement revised 9/1/22 read, QA is on-going, both anticipatory and retrospective in its efforts to identify how the organization is performing, including when and why facility performance is at risk or has failed to meet standards .Develop and implement appropriate plans of action to correct identified quality deficiencies .prioritizing quality deficiencies. Systematically analyzing underlying causes of systemic quality deficiencies .Monitoring and evaluations the effectiveness of corrective action/performance improvement activities and revising as needed .The facility must consider incident, prevalence, and severity of problems or potential problems identified .
Aug 2021 5 deficiencies
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0637 (Tag F0637)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to comprehensively asses a significant change for 1 of 1 resident samp...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to comprehensively asses a significant change for 1 of 1 resident sampled for decline in Activities of Daily Living (ADL) of a total sample of 41 residents, (#33). Finding. Review of resident #33's quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed the resident was independent for Bed Mobility, Transfers and Eating. The assessment showed the resident required supervision for Walking, Locomotion and Dressing. The facility assessed the resident as needing Limited Assistance of 1 staff for Toileting and Personal Hygiene. The resident was frequently incontinent of urine and bowels. Review of the quarterly MDS assessment dated [DATE] revealed the resident now required extensive assistance of 1 staff for Bed Mobility, Transfers, Toilet use and Personal Hygiene. The assessment showed the resident had declined and was now always incontinent of urine. On 8/26/21 at 4:56 PM, the resident's status was discussed with the Assistant Director of Nursing (ADON). She stated the facility did not have a MDS Coordinator. She explained the company's corporate staff had assumed the duties of completing the MDS assessments. She added the Social Service Director was completing the care plans. On 8/26/21 at 7:01 PM, the resident's MDS and ADLs were reviewed with the Director of Nursing. She stated she would have to call corporate office to find out why a significant change MDS was not completed for resident #33.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure accuracy of Minimum Data Set (MDS) assessments for 1 of 2 re...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure accuracy of Minimum Data Set (MDS) assessments for 1 of 2 residents reviewed for assessment accuracy of a total sample of 41 residents, (#67). Findings: Resident #67 was admitted to the facility on [DATE] with diagnoses of dementia without behavioral disturbances and morbid obesity. Resident #67's MDS annual assessment with assessment reference date of 7/19/21 revealed he received insulin injections on 7 of 7 days in the look-back period. Review of resident #67's medical record revealed no physician orders for insulin. Review of the Medication Administration Record (MAR) did not reflect injections administered. On 8/26/21 at 12:30 PM, the Director of Nursing (DON) stated the staff who completed the MDS assessment worked part-time and was not currently present in the facility. During review of the MDS assessment with the DON, she acknowledged the assessment was inaccurate. She stated she reached out to Registered Nurse A, the MDS coordinator, who said he made an error as the resident never received insulin injections. The DON explained the facility used the Resident Assessment Instrument (RAI) manual for instructions on coding different types of drugs. Review of the RAI version 3.0 Manual revealed section N0300: injections and N0350: insulin. These sections included directions for MDS staff to review residents' MARs for the 7-day look-back period and Count the number of days insulin injections were received The (RAI) manual revealed the results of the MDS assessment, should accurately reflect the resident's status.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0694 (Tag F0694)

Could have caused harm · This affected 1 resident

Based on observation, interview and record review, the facility failed to provide dressing changes for a Midline Catheter according to professional standards of practice for 1 of 2 residents with Intr...

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Based on observation, interview and record review, the facility failed to provide dressing changes for a Midline Catheter according to professional standards of practice for 1 of 2 residents with Intravenous (IV) catheters of a total sample of 41 residents, (#335). Finding: Resident #335 was admitted to the facility from a specialty hospital on 8/21/21 with diagnoses of respiratory failure, chronic obstructive pulmonary disease, and lung cancer. On 8/23/21 at 11:10 AM, resident #335 was observed in bed with a Midline IV Catheter to her left upper arm. The transparent dressing that covered the IV site was dated 8/14/21, and the lower end of the dressing was lifted from her skin. Resident #335 stated the IV was inserted at the hospital, and she was unsure if she was getting medications through it. A Midline Catheter is a small tube used to give treatments and to take blood samples. It is inserted into a vein in your arm . the end of the tube does not go past the top of the armpit . it can stay in place up to 30 days(retrieved on 8/27/21 from www.drugs.com). On 8/24/21 at 9:55 AM, the A wing Unit Manager (UM) stood at resident #335's bedside and noted resident #335 had a Midline IV catheter in her left arm. She acknowledged the IV dressing was loose at the lower end and was dated 8/14/21. She said, It is a problem. She explained because the dressing was lifted off the skin it was compromised and could lead to infection. She said the dressing needed to be changed or the IV discontinued if no longer needed. She stated her expectation was all assigned nurses should assess the IV site every shift. On 8/24/21 at 10:15 AM, during review of resident #335's medical record, the A Wing UM confirmed there was a physician's order dated 8/23/21 to discontinue the Midline IV. She acknowledged the physician's order had not been followed as the IV catheter was still in the resident's left arm. She said, It should have been done. She explained Midline IV dressings should be changed every 4 days and that the nurse who admitted the resident should have assessed the IV site and obtained IV care orders from the physician at that time. The A wing UM acknowledged there was no way to confirm the Midline IV was assessed because there were no related physician's orders or nursing documentation. Review of resident #335's Nursing Comprehensive Assessment dated 8/21/21 revealed no documentation of the presence of any IV catheters. Review of resident #335's Baseline Care Plan dated 8/21/21 revealed no documentation in the Special Treatments/Procedures section under IV type, location or dressing change. Review of resident #335's Order Summary Report dated 8/24/21 revealed no orders for Midline IV dressing changes or assessment. An order dated 8/23/21 read, Flush Midline/PICC every shift for patency and D/C midline/picline one time only for IV. Review of the resident's Treatment Administration Record (TAR) and Progress Notes from 8/21/21 to 8/23/21 revealed no documentation for IV dressing changes to resident #335's Midline IV. The TAR showed the Midline IV was discontinued on 8/23/21 as ordered although a progress note that read, 20 cm Midline to R upper arm was discontinued using aseptic technique per DR. order was dated 8/24/21. Facility nurses continued documenting on resident #335's Midline IV under Check Midline placement every shift and flush Midline /PICC every shift for patency through 8/25/21, even though the line was no longer in place. On 8/26/21 at 7:35 PM, the Director of Nursing stated a Midline IV should be reported to the physician on admission for their decision regarding whether the IV catheter would be utilized, discontinued, or to obtain appropriate orders for IV care. She acknowledged the nurse who received a newly admitted resident should assess and note findings including presence of an IV catheter. She acknowledged resident #335's Order Summary Report dated 8/24/21 contained no orders for the Midline IV dressing change. She confirmed the Baseline Care Plan completed at admission, dated 8/21/21 had no documentation indicating the resident had an IV. She said, It's important to assess the resident in general and what the resident needs. The facility's Policy and Procedure, Midline Dressing Changes 005-N dated October 2019 read, Midline catheter dressings will be changed at specified intervals, or when needed, to prevent catheter- related infection associated with contaminated, loosened or soiled catheter site dressings . Change midline catheter dressing 24 hours after insertion if placed with gauze, every 7 days or if it is wet, dirty, not intact or compromised in any way.
CONCERN (D)

Potential for Harm - no one hurt, but risky conditions existed

Safe Environment (Tag F0921)

Could have caused harm · This affected 1 resident

Based on observation and interview, the facility failed to provide a clean and sanitary environment to protect the health and safety of residents, staff and the public by not securing bio-medical refu...

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Based on observation and interview, the facility failed to provide a clean and sanitary environment to protect the health and safety of residents, staff and the public by not securing bio-medical refuse and debris in the waste containers. Finding: On Monday, 8/23/21 at 10:00 AM, the entrance/exit door of the facility's Corona Virus Disease 2019 (COVID 19) unit had large, red, bio-medical waste containers overflowing with bio-medical refuse. The containers were filled past capacity with bio-medical waste and the container lids could not be closed. On top of the container lids were several bags of bio-medical waste. Some of these bags were partially open with debris coming out of the bags. The Director of Nursing (DON) arrived in the area and stated she was not aware the waste bins were full. At 10:51 AM, the DON and the B Wing Unit Manger opened a storage shed that contained approximately 12 smaller empty bio-medical waste bins. At the opposite end of the rear parking area, near the maintenance building were 21 large, red, bio-medical waste bins which were full. On 8/23/21 at 11:24 AM, an interview was held with the Administrator, DON and Maintenance Director. They stated the staff that worked on the COVID 19 unit were responsible to put the red bio-medical waste trash bags into the red containers. The Maintenance Director said the Bio-waste company picked up the red containers every 2 weeks. He said his staff placed 3 empty bins outside of the COVID 19 Unit on Saturday and that no maintenance staff worked on Sunday. They said they had not been informed that the bins were getting full.
CONCERN (E)

Potential for Harm - no one hurt, but risky conditions existed

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected multiple residents

Based on observation, interview and record review, the facility failed to store medications and biologicals under proper temperature controls as indicated by manufacturer's recommendations in 1 of 2 m...

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Based on observation, interview and record review, the facility failed to store medications and biologicals under proper temperature controls as indicated by manufacturer's recommendations in 1 of 2 medications rooms, (A wing). Findings: On 8/24/21 at 4:12 PM, the A wing medication room refrigerator was opened by Registered Nurse (RN) B and the thermometer inside was immediately read at 48 degrees Fahrenheit (F). The door of the refrigerator was closed at the request of State Survey Agency staff and on 8/24/21 at 4:14 PM, the Assistant Director of Nursing (ADON) opened the door and validated the temperature on the thermometer inside the refrigerator still read 48 degrees F. The ADON explained the 11:00 PM to 7:00 AM shift nurse was supposed to check the refrigerator's temperature every night. On 8/24/21 at 4:19 PM, the Director of Nursing (DON) stated if the refrigerator temperature was out of range, the nurse was expected to initiate a maintenance request. She explained the refrigerator was frozen earlier that day and the temperature was raised to defrost it. The ADON again opened the refrigerator and immediately checked the temperature of the medications with a handheld, instant-read laser thermometer gun. The thermometer temperatures read 52 to 57 degrees F when pointed at the vials and boxes of medications. The affected medications inside the A wing refrigerator included Moderna Corona Virus Disease 2019 (COVID 19) Vaccine, Tuberculin injections, Rocephin Intravenous solution, Acidophilus, Lantus insulin, Victoza, Epoetin, Levemir insulin, Humulin insulin, Novolog insulin, Phenergan suppositories, and Ativan. Review of the medication labels found in the refrigerator revealed all medications were to be stored within 36 to 46 degrees F (retrieved on 8/27/21 from accessdata.fda.gov). The US Centers for Disease Control and Prevention Temperature Monitoring Best Practices for refrigerated vaccines listed a range of 36 to 46 degrees F, with the ideal temperature of 40 degrees F (retrieved on 8/27/21 from cdc.gov). The U.S. Pharmacopeia chapter 1079 Good Storage and Shipping Practices revealed refrigerators used to store drugs were required to maintain the product temperature between the limits as defined on the product's label. The document indicated the allowable range was 36 degrees to 46 degrees F (retrieved on 8/27/21 from usp.org). On 8/25/21 at 9:42 AM, the Maintenance Director said he had not received any service requests regarding the A wing medication room refrigerator. He explained the nurse should have submitted a work order for the refrigerator when it was identified the temperature was out of range. Review of the facility's Health Care Center Refrigerator/Freezer Temperature Log Sheet from the A wing medication room refrigerator dated August 2021 revealed temperatures logged at 48 degrees F on 8/23/21 and 8/24/21. No temperatures were recorded for 8/20/21 or 8/22/21. The Recommended Temperature Guides listed at the bottom of the log revealed refrigerated storage as 36-40 degrees F, and Although 36-45 F is acceptable, 36-40 F is the ideal refrigerated range. Review of the log for August 2021 revealed all recorded temperatures above 40 degrees F. Review of the July 2021 Medication room log sheet revealed temperatures of 50 degrees F on 7/14/21, 56 degrees F on 7/20/21, and 51 degrees F on 7/29/21. On 8/25/21 at 10:27 AM, Pharmacist D confirmed that medication refrigerators were supposed to be kept under 46 degrees F. She stated the Moderna Covid-19 vaccine, and the Tuberculin syringes should be discarded if stored at 48 degrees F as shown on the facility's temperature log. On 8/26/21 at 9:45 AM, the DON reviewed the Refrigerator/Freezer log sheet and acknowledged that if no temperature was recorded on 8/22/21 there was no way to tell if the temperature was out of range on that day. On 8/26/21 at 12:23 PM, the A wing UM stated she reviewed the refrigerator log every morning, Monday through Friday, but did not realize there was no documentation on 8/20/21 and 8/22/21. She stated she was not aware the temperature in the refrigerator had to be 36-46 degrees F. The A wing UM said, I thought that 48 degrees was ok. On 8/26/21 at 12:32 PM, in a telephone interview, RN C confirmed she recorded the temperatures of the A wing medication room on 8/23/21 and 8/24/21 when the temperature log showed 48 degrees F. RN C stated she had never received information regarding acceptable temperature ranges for the medication room refrigerator. She recalled receiving a message from the UM to simply check the temperature and write it on the log. She said, It is the only thing I received from them. RN C said she was never told to report discrepancies to maintenance or anyone else if there was a problem. On 8/26/21 at 12:58 PM, Pharmacist E stated that per the temperatures of 48 degrees F recorded on the A wing medication refrigerator log on 8/23/21 and 8/24/21, the medications were not good, and should be discarded. The facility's Medication Storage in the Facility Policy and Procedure dated April 2018, read, Medications and biologicals are stored safely, securely and properly, following manufacturer's recommendations or those of the supplier. The document revealed medication storage conditions would be monitored on a monthly basis by a pharmacy designee and any problems identified would be corrected. The policy emphasized, All medications are maintained within the temperature ranges noted in the United States Pharmacopeia (USP) and by the Centers for Disease Control (CDC). Refrigerated: 36 degrees F to 46 degrees F with a thermometer to allow temperature monitoring.
Understanding Severity Codes (click to expand)
Life-Threatening (Immediate Jeopardy)
J - Isolated K - Pattern L - Widespread
Actual Harm
G - Isolated H - Pattern I - Widespread
Potential for Harm
D - Isolated E - Pattern F - Widespread
No Harm (Minor)
A - Isolated B - Pattern C - Widespread

Questions to Ask on Your Visit

  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • 38% turnover. Below Florida's 48% average. Good staff retention means consistent care.
Concerns
  • • 15 deficiencies on record, including 2 serious (caused harm) violations. Ask about corrective actions taken.
  • • $16,801 in fines. Above average for Florida. Some compliance problems on record.
Bottom line: Mixed indicators with Trust Score of 63/100. Visit in person and ask pointed questions.

About This Facility

What is Vivo Healthcare West Orange's CMS Rating?

CMS assigns VIVO HEALTHCARE WEST ORANGE an overall rating of 4 out of 5 stars, which is considered above average nationally. Within Florida, this rating places the facility higher than 99% of the state's 100 nursing homes. This rating reflects solid performance across the metrics CMS uses to evaluate nursing home quality.

How is Vivo Healthcare West Orange Staffed?

CMS rates VIVO HEALTHCARE WEST ORANGE's staffing level at 2 out of 5 stars, which is below average compared to other nursing homes. Staff turnover is 38%, compared to the Florida average of 46%. This relatively stable workforce can support continuity of care. RN turnover specifically is 65%, which is notably high. RNs provide skilled clinical oversight, so turnover in this role can affect medical care quality.

What Have Inspectors Found at Vivo Healthcare West Orange?

State health inspectors documented 15 deficiencies at VIVO HEALTHCARE WEST ORANGE during 2021 to 2025. These included: 2 that caused actual resident harm and 13 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Vivo Healthcare West Orange?

VIVO HEALTHCARE WEST ORANGE is owned by a for-profit company. For-profit facilities operate as businesses with obligations to shareholders or private owners. The facility is operated by VIVO HEALTHCARE, a chain that manages multiple nursing homes. With 120 certified beds and approximately 106 residents (about 88% occupancy), it is a mid-sized facility located in OCOEE, Florida.

How Does Vivo Healthcare West Orange Compare to Other Florida Nursing Homes?

Compared to the 100 nursing homes in Florida, VIVO HEALTHCARE WEST ORANGE's overall rating (4 stars) is above the state average of 3.2, staff turnover (38%) is near the state average of 46%, and health inspection rating (4 stars) is above the national benchmark.

What Should Families Ask When Visiting Vivo Healthcare West Orange?

Based on this facility's data, families visiting should ask: "Can you walk me through typical staffing levels on day, evening, and night shifts?" "Can I visit during a mealtime to observe dining assistance and food quality?" "How do you handle medical emergencies, and what is your hospital transfer rate?" "Can I speak with family members of current residents about their experience?" These questions are particularly relevant given the below-average staffing rating.

Is Vivo Healthcare West Orange Safe?

Based on CMS inspection data, VIVO HEALTHCARE WEST ORANGE has a clean safety record: no substantiated abuse findings (meaning no confirmed cases of resident harm), no Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death), and is not on the Special Focus Facility watch list (a federal program monitoring the lowest-performing 1% of nursing homes). The facility has a 4-star overall rating and ranks #1 of 100 nursing homes in Florida. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Vivo Healthcare West Orange Stick Around?

VIVO HEALTHCARE WEST ORANGE has a staff turnover rate of 38%, which is about average for Florida nursing homes (state average: 46%). Moderate turnover is common in nursing homes, but families should still ask about staff tenure and how the facility maintains care continuity when employees leave.

Was Vivo Healthcare West Orange Ever Fined?

VIVO HEALTHCARE WEST ORANGE has been fined $16,801 across 2 penalty actions. This is below the Florida average of $33,247. While any fine indicates a compliance issue, fines under $50,000 are relatively common and typically reflect isolated problems that were subsequently corrected. Families should ask what specific issues led to these fines and confirm they've been resolved.

Is Vivo Healthcare West Orange on Any Federal Watch List?

VIVO HEALTHCARE WEST ORANGE is not on any federal watch list. The most significant is the Special Focus Facility (SFF) program, which identifies the bottom 1% of nursing homes nationally based on persistent, serious quality problems. Not being on this list means the facility has avoided the pattern of deficiencies that triggers enhanced federal oversight. This is a positive indicator, though families should still review the facility's inspection history directly.