ARBORS AT GALLIPOLIS

170 PINECREST DRIVE, GALLIPOLIS, OH 45631 (740) 446-7112
For profit - Limited Liability company 99 Beds ARBORS AT OHIO Data: November 2025
Trust Grade
48/100
#394 of 913 in OH
Last Inspection: April 2025

Within standard 12-15 month inspection cycle. Federal law requires annual inspections.

Overview

The Arbors at Gallipolis has a Trust Grade of D, indicating below-average performance with some concerning issues. It ranks #394 of 913 in Ohio, placing it in the top half of facilities statewide, and #2 of 3 in Gallia County, meaning only one local facility is rated higher. The facility is showing an improving trend in performance, having reduced its issues from 8 in 2023 to 7 in 2025. Staffing is a strength, with a rating of 4 out of 5 stars and a turnover rate of 25%, which is significantly better than the state average. However, the facility has incurred $57,263 in fines, which is higher than 84% of Ohio facilities, signaling potential compliance problems. There have been serious incidents reported, including a resident who fell from a shower gurney due to a broken rail and sustained a fractured femur, and another resident who was hospitalized with a fractured hip after falling from a wheelchair that lacked proper maintenance. Additionally, the facility has struggled with infection control, failing to properly track infections and maintain adequate supervision for residents at risk of falling. While there are strengths in staffing and overall performance, these serious incidents and compliance issues are concerning for families considering this nursing home.

Trust Score
D
48/100
In Ohio
#394/913
Top 43%
Safety Record
Moderate
Needs review
Inspections
Getting Better
8 → 7 violations
Staff Stability
✓ Good
25% annual turnover. Excellent stability, 23 points below Ohio's 48% average. Staff who stay learn residents' needs.
Penalties
✓ Good
$57,263 in fines. Lower than most Ohio facilities. Relatively clean record.
Skilled Nurses
○ Average
Each resident gets 37 minutes of Registered Nurse (RN) attention daily — about average for Ohio. RNs are the most trained staff who monitor for health changes.
Violations
⚠ Watch
21 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★★☆☆
3.0
Overall Rating
★★★★☆
4.0
Staff Levels
★★★★☆
4.0
Care Quality
★★★☆☆
3.0
Inspection Score
Stable
2023: 8 issues
2025: 7 issues

The Good

  • 4-Star Staffing Rating · Above-average nurse staffing levels
  • 4-Star Quality Measures · Strong clinical quality outcomes
  • Low Staff Turnover (25%) · Staff stability means consistent care
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover is low (25%)

    23 points below Ohio average of 48%

Facility shows strength in staffing levels, quality measures, staff retention, fire safety.

The Bad

3-Star Overall Rating

Near Ohio average (3.2)

Meets federal standards, typical of most facilities

Federal Fines: $57,263

Above median ($33,413)

Moderate penalties - review what triggered them

Chain: ARBORS AT OHIO

Part of a multi-facility chain

Ask about local staffing decisions and management

The Ugly 21 deficiencies on record

1 actual harm
Apr 2025 7 deficiencies
CONCERN (D)

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

Quality of Care (Tag F0684)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, facility policy review and interview, the facility failed to implement adequate and effecti...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, facility policy review and interview, the facility failed to implement adequate and effective interventions to promote healing and prevent the deterioration of a left below the knee surgical site with staples for Resident #48 at the time of the resident's admission. This affected one resident (#48) reviewed for surgical wounds and for pressure wounds.Findings include:Review of the medical record for Resident #48 revealed an admission date of 3/20/25 with diagnoses including acquired absence of left leg below knee, need for assistance with personal care, weakness, cerebral infarction, atherosclerosis of native arteries of extremities with gangrene, left leg, hemiplegia, affecting left non-dominant side, dementia, and chronic obstructive pulmonary disease. Review of Resident #48's admission skin assessment dated [DATE] revealed the resident had a left below the knee amputation with 35 surgical staples measuring 7.82 centimeters (cm) by by 2.87 cm. Review of Resident #48's nursing admission evaluation dated 03/20/25 revealed the resident required at least one person assistance with bed mobility. Review of the plan of care dated 03/20/25 for Resident #48 revealed the resident had impaired skin integrity related to recent surgery; mobility status as evidenced by: surgical wound to left leg with no intervention to elevate the left stump.Further review of the resident's plan of care revealed an activity of daily living self-care performance deficit related to acquired left below the knee amputation and hemiplegia affecting left dominant side with an intervention of bed mobility requiring a one person assist. Review of Resident #48's Braden Scale for Predicting Pressure Sore Risk dated 03/20/25 revealed a score of 17.0 on a scale of 6 (high risk) to 23 (no risk) which indicated the resident was at risk for skin breakdown.Review of the active physician orders for Resident #48 dated 03/20/25 revealed to encourage to turn and reposition frequently when in bed to prevent skin breakdown. Further review of the active physician orders for Resident #48 revealed no order to elevate the left below the knee amputation stump.Review of the medical record for Resident #48 from 03/20/25 through 03/24/25 revealed no documented evidence of elevation of the left stump, the resident being turned every two hours, the resident refusing to be turned or that the resident favored his left side. Review of an Interdisciplinary team (IDT) functional assessment for Resident #48 dated 03/24/25 revealed the resident still required substantial/maximal (staff) assistance with bed mobility.Review of the Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed a Brief Interview for Mental Status (BIMS) of 14 which suggested moderate cognitive impairment. The resident was assessed to require substantial/maximal assistance with shower/bathe self, bed mobility and total dependence on staff for toilet hygiene and transfers. This resident was also assessed to be at risk for developing pressure ulcers, had an unstageable deep tissue injury not on admission and a surgical wound. Review of Resident #48's left below the knee amputation surgical wound assessment dated [DATE] revealed the site measured at 6.64 cm by 10.20 cm and was noted to have declined. Review of the active physician's order for Resident #48 dated 03/25/25 revealed to encourage the resident to float left stump. Observation on 04/14/25 at 10:38 A.M. of Resident #48 revealed the resident was on his left side in bed with his left stump not floated/elevated. Observation on 04/14/25 at 12:41 P.M. of Resident #48 revealed the resident was on his left side in bed with his left stump not floated/elevated.Interview on 04/14/25 at 12:51 P.M. with Licensed Practical Nurse (LPN) #104 revealed Resident #48 never refused care and required (staff) assistance to be turned in bed. Observation on 04/15/25 at 10:26 A.M. revealed Resident #48 was in bed on his left side.Observation on 04/15/25 at 1:23 P.M. revealed Resident #48 was in bed on his left side.Observation on 04/15/25 at 1:28 P.M. with Certified Nurse Assistant (CNA) #205 verified Resident #48 was positioned on his left side.Interview on 04/16/25 at 9:25 A.M. with Registered Nurse (RN) #196 revealed Resident #48 never refused care and required (staff) assistance to be turned in bed. Interview on 04/16/25 at 9:27 A.M. with CNA #173 revealed Resident #48 never refused care and did favor his left side. The CNA did not recall propping (floating/elevating) the resident's left stump since he had been admitted to the facility. Interview on 04/16/25 at 9:29 A.M. with Resident #48 revealed he needed help when moving in bed because his left side was so weak. The resident stated he sometimes had a pillow under his legs but not always. The resident also revealed he did not refuse to allow staff to turn him in bed when staff ask and help him turn. At this time, the resident was observed on his left side with his left stump not floated/elevated. Observation on 04/16/25 at 9:31 A.M. with RN #196 verified Resident #48 did not have his left stump floated/elevated and the resident was on his left side with no interventions in place to assist with off-loading the pressure to his left side and/or to promote the healing of the surgical wound. Interview on 04/16/25 at 1:29 P.M. with the Director of Nursing (DON) revealed if a resident, who required (staff) assistance, refused to be turned and repositioned or was refusing to off-load/float an extremity, it was to be documented, and the physician was to be notified. Observation on 04/16/25 at 2:01 P.M. revealed Resident #48 was on his left side. Interview on 04/16/25 at 2:19 P.M. with the DON revealed Resident #48 had refused a few times to turn and reposition since being admitted to the facility. During the interview, the DON revealed the resident favored his left side and no interventions had been implemented to help off-load pressure such as pillows or a wedge. The DON also verified no orders or documentation to float/elevate the left stump were in place at the time of admission. Orders were not implemented until 03/25/25 when the resident's left below the knee amputation surgical site worsened. The DON verified orders/interventions should have been in place for the left stump to be floated at the time of admission. Interview on 04/16/25 at 2:29 P.M. with Certified Nurse Practitioner #170 revealed he was never informed of Resident #48 refusing to turn and reposition in bed or that the resident preferred his left side.Observation on 04/17/25 at 9:11 A.M. of Resident #48 revealed the resident was on his left side with no interventions to help off-load pressure/promote healing and the resident's left stump not being floated. At the time of the observation, interview with the resident revealed he does prefer to be positioned on his left side better but did not recall the staff placing pillows or a wedge so that he could lay on his left side with less pressure. Observation on 04/17/25 at 11:25 A.M. with CNA #168 verified Resident #48 was positioned on his left side with no interventions in place to off-load pressure and the resident's left stump not floated/elevated. Review of the facility policy titled Pressure Ulcer/Skin Breakdown-Clinical Protocol revised 03/20/2024 revealed the plan of care for prevention and/or treatment would include a turning schedule/off-loading.
CONCERN (D)

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

Pressure Ulcer Prevention (Tag F0686)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, observation, interview, and policy review the facility failed to implement interventions to promote skin...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, observation, interview, and policy review the facility failed to implement interventions to promote skin integrity for a resident ordered to wear a knee brace. This affected one resident (#48) of one resident reviewed for skin integrity. Findings Include: Review of the medical record for Resident #48, revealed an admission date of 3/20/25 (from the hospital). Diagnoses included but were not limited to acquired absence of left leg below knee, need for assistance with personal care, weakness, cerebral infarction, atherosclerosis of native arteries of extremities with gangrene, left leg, hemiplegia, affecting left nondominant side, dementia, and chronic obstructive pulmonary disease. Review of the hospital discharge paperwork dated 03/20/25 for Resident #48 revealed a left knee immobilizer to be on at all times. Review of the plan of care dated 03/20/25 for Resident #48 revealed the resident had impaired skin integrity related to recent surgery; mobility status as evidenced by: assist resident with turning and repositioning as needed. Further review of this resident's plan of care revealed activity of daily living self-care performance deficit related to acquired left below the knee amputation and hemiplegia affecting left dominant side with the intervention of bed mobility requiring a one person assist. Review of Resident #48's nursing admission evaluation dated 03/20/25 revealed the resident to need at least one person assistance with bed mobility. Review of Resident #48's Braden Scale for Predicting Pressure Sore Risk dated 03/20/25 revealed a score of 17.0 on a scale of 6 (high risk) to 23 (no risk) which indicated the resident was at risk for skin breakdown. Review of the physician's order dated 03/20/25 at 9:37 P.M. revealed a brace to the left below the knee amputation to be on at all times every day and night shift. Further review of this resident's physicians order dated 03/20/25 revealed to encourage to turn and reposition frequently when in bed to prevent skin breakdown. Review of Resident #48's daily skilled assessments dated 03/20/25 through 03/24/25 revealed skin assessments were completed. Review of the medical record for Resident #48 from 03/20/25 through 03/24/25 revealed no documentation of refusing to be turned every two hours and that this resident favored his left side. Review of the physical therapy notes dated 03/24/25 for Resident #48 revealed alerted nurse of skin breakdown observed from knee immobilizer, nursing assessed. Review of Resident #48's medical record revealed an assessment and treatment order for skin break down noted by physical therapy on 03/24/25. Review of Resident #48's wound assessment dated [DATE] revealed an in-house facility acquired deep tissue injury (DTI) (persistent non-blanchable deep red, maroon or purple discoloration intact skin with localized area of persistent non-blanchable deep red, maroon, purple discoloration due to damage of underlying soft tissue) to the front left thigh that measured 1.60 CM (centimeters) by 7.21 CM. Review of the active physician's orders dated 03/25/25 for Resident #48 revealed to skin prep area to front of left thigh every day and night. Review of the medical record for Resident #48 from 03/25/25 through 04/01/25 revealed minimal documentation of the resident refusing to be turned every two hours and no documentation that this resident favored his left side. Review of Resident #48's wound assessment dated [DATE] revealed an in-house facility acquired unstageable slough/eschar area to the left popliteal fossa that measured 2.68 CM by 1.91 CM by 0.1. Observation on 04/14/25 at 10:38 A.M. of Resident #48 revealed the resident to be on his left side in bed. Observation on 04/14/25 at 12:41 P.M. of Resident #48 revealed the resident to be on his left side in bed. Interview on 04/14/25 at 12:51 P.M. with Licensed Practical Nurse (LPN) #104 revealed Resident #48 never refuses care and does need assistance to be turned in bed. Observation on 04/15/25 at 10:26 A.M. revealed Resident #48 in bed on his left side. Observation on 04/15/25 at 1:23 P.M. revealed Resident #48 in bed on his left side. Observation on 04/15/25 at 1:28 P.M. with Certified Nurse Assistant (CNA) #205 verified Resident #48 to be on his left side. Interview on 04/16/25 at 9:25 A.M. with Registered Nurse (RN) #196 revealed Resident #48 never refuses care, needs assistance to be turned in bed. Interview on 04/16/25 at 9:27 A.M. with CNA #173 revealed Resident #48 never refuses care and does favor his left side. Interview on 04/16/25 at 1:29 P.M. with the Director of Nursing (DON) revealed if a resident refuses to be turned and repositioned that need assistance and if a resident is refusing to float an extremity, it is to be documented, and the physician is to be notified. Observation on 04/16/25 at 9:31 A.M. with RN #196 verified Resident #48 to be on his left side. Interview on 04/17/25 at 9:31 A.M. with Physical Therapist #171 revealed Resident #48 was in therapy on Monday which was 03/24/25 and she removed his brace and noticed the skin area to his left thigh and alerted the nursing staff to assess it. Interview on 04/17/25 at 9:33 A.M. with Licensed Practical Nurse (LPN) #104 verified Resident #48's DTI to the front left thigh was discovered on 03/24/25. Physical therapy alerted her, and she informed her Unit Manager who instructed her it would be measured the next day since Tuesdays are wound measurement day. LPN #104 verified no treatment and assessment was completed and implemented when the wound was discovered on 03/24/25. Review of the facility policy titled Pressure Ulcer/Skin Breakdown-Clinical Protocol revised 03/20/24 revealed residents with pressure ulcers receives necessary treatment and services, consistent with professional standards of practice to promote healing and prevent new ulcers from developing. The plan of care for prevention and /or treatment is to include a turning schedule/offloading care.
CONCERN (D)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, interview and facility policy and procedure review, the facility failed to ensure physician...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, interview and facility policy and procedure review, the facility failed to ensure physician ordered fall interventions were in implemented as ordered for two residents (#6 and #40) with known falls. This affected two residents of six residents reviewed for accidents. The facility census was 81. Findings Include: 1. Review of the medical record for Resident #6 revealed an initial admission date of 12/26/22 with the diagnoses including but not limited to Alzheimer's disease, atherosclerotic heart disease of native coronary artery, hypothyroidism, anxiety disorder, diverticulosis, dementia with other behavioral disturbances, psychosis, mood disorder, hyperlipidemia, insomnia, polyneuropathy, osteoarthritis, gastro-esophageal reflux disease, cardiomyopathy and dysphagia. Review of the plan of care dated 07/28/23 and last revised on 04/16/25 revealed the resident was at risk for falls/injury related to bladder incontinence, generalized weakness, history of falls, impaired cognition with decreased safety awareness, inability to use call light due to confusion, psychoactive medications use, lack of coordination, unsteadiness on feet and resident removes dycem from recliner. Interventions included encourage resident to rest whenever having periods of prolonged ambulation, non-skid strips to left side of bed, non-skid strops in front of recliner, staff education when aware of fire drill make sure she is aware of drill, therapy screen/evaluation/treat as needed, encourage resident to keep needed items within reach, encourage resident to wear glasses; assist with applying as needed, ensure the resident's room is free from accident hazards, non-skid footwear to reduce the risk of slipping as the resident allows, observe for changes in mobility, and place call light within reach. Review of the resident's comprehensive Minimum Data Set (MDS) assessment dated [DATE] revealed the resident had a severe cognitive deficit. The assessment indicated the resident had one fall with injury since the prior assessment was completed. Review of the fall risk evaluation dated 04/06/25 revealed a score of six indicating the resident was at risk for falls. Review of the resident's monthly physician orders for April 2024 identified orders dated 01/12/23 right side of bed against wall per family request, 01/14/25 non-skid strips to left side of bed every shift for fall intervention, encourage grippy socks or proper footwear when out of bed and non-skid strips in front of recliner, check placement every shift. On 04/14/25 at 3:01 P.M., observation of Resident #6' room revealed no dycem to the seat of the resident's recliner, and no nonskid strips to the left side of the bed. On 04/15/25 at 3:20 P.M., interview with Licensed Practical Nurse (LPN) #189 verified the resident's physician ordered fall interventions were not implemented as ordered. 2. Review of the medical record for Resident #40 revealed an initial admission date of 05/16/18 with the latest readmission of 02/10/23 with the diagnoses including but not limited to dementia with behavioral disturbances, chronic obstructive pulmonary disease, seizures, atrial fibrillation, schizophrenia, cardiomyopathy, secondary Parkinsonism, hypertension, dysphagia, aphasia, ataxia, anxiety disorder, gastro-esophageal reflux disease, anemia, major depressive disorder and hyperlipidemia. Review of the plan of care dated 08/10/23 and last revised on 01/24/24 revealed the resident was at risk for falls/injury related to bowel and bladder incontinence, generalized weakness, history of falls, impaired cognition with decreased safety awareness, opioid medication use, seizures, lack of coordination, difficulty walking, at risk for injury from hot liquids and will turn off pressure alarm. Interventions included dycem to wheelchair, fall mat to right side of bed, non-skid strips in front of toilet, do not leave unattended in the dining room, sensor pad alarm to bed, sensor pad alarm to wheelchair, sign in room for reminder to use call light, staff education assist resident up for meals, ensure alarms are in place and functioning, toilet frequently, toilet before and after meals, encourage resident to keep needed items within reach, encourage resident to keep wheelchair within reach, encourage resident to use call light, monitor resident's position to reduce the risk of slipping as the resident allows, observe for changes in mobility, place call light within reach, therapy screen/evaluation/treat as needed, skin breakdown, symptoms of delirium, falls, accidents, injuries, agitation, or weakness, observe for, record, and report to the nurse and/or physician any changes regarding the effectiveness of the bed modification or adverse or negative effects as a result of the bed modification, periodically evaluate the need for the resident's bed modification(s) and record continued risks and benefits of continued use of the bed modification(s), alternatives, and need for ongoing use and cool hot liquids prior to serving. Review of the resident's monthly physician orders for April 2025 identified orders dated 01/14/25 resident to have dycem present to wheelchair seat, non-skid strips in front of toilet, check placement every shift and sign in room for reminder to use call light and ask for assistance. On 04/15/25 at 3:15 P.M., observation of the resident with Certified Nursing Assistant (CNA) #126 revealed the resident had no dycem to the seat of his wheelchair. On 04/15/25 at 3:20 P.M., observation of the resident's room with LPN #189 revealed the resident had no nonskid strips in front of his toilet and the sign to remind the resident to use the call light and ask for assistance was behind the privacy curtain out of his sight. LPN #189 verified the fall interventions were not implemented as physician ordered, including the physician ordered dycem to his wheelchair seat. Review of the facility policy titled, Fall Prevention Program, dated 10/30/02 revealed each resident will be assessed for the risks of falling and will receive care and services in accordance with the level of risk to minimize the likelihood of falls.
CONCERN (D)

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

Respiratory Care (Tag F0695)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, and facility policy review, the facility failed to obtain a physician's order fo...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, and facility policy review, the facility failed to obtain a physician's order for the administration of oxygen therapy and post an oxygen warning sign. This affected one resident (#48) of one resident reviewed for respiratory care. The facility census was 81. Findings include: Review of the medical record for Resident #48, revealed an admission date of 3/20/25. Diagnoses included but were not limited to acquired absence of left leg below knee, need for assistance with personal care, weakness, cerebral infarction, atherosclerosis of native arteries of extremities with gangrene, left leg, hemiplegia, affecting left nondominant side and chronic obstructive pulmonary disease. Review of the most recent Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed a Brief Interview for Mental Status (BIMS) of 14 which suggests moderate cognitive impairment. The resident was assessed to require substantial/maximal assistance with shower/bathe self, bed mobility and total dependence on toilet hygiene and transfers. This resident was also assessed to be at risk for developing pressure ulcers and to have an unstageable deep tissue injury not on admission and a surgical wound. Review of the plan of care dated 03/23/25 for Resident #48 revealed this resident had an impaired pulmonary/respiratory status related to chronic obstructive pulmonary disease with an intervention to provide oxygen as needed when the resident exhibits signs/symptoms of difficulty breathing. Review of the active physician orders for Resident #48 revealed no order for oxygen therapy. Observation on 04/14/25 at 10:38 A.M. of Resident #48 revealed his door did not display an oxygen in use sign. Further observation revealed the resident in bed with his nasal cannula on the bed with an oxygen concentrator set to 2 liters. Observation on 04/15/25 at 10:26 A.M. of Resident #48 revealed his door did not display an oxygen in use sign and the resident to bed in bed with his nasal cannula on with the oxygen concentrator to be set to 2 liters. Observation and Interview on 04/15/25 at 9:31 A.M. with Registered Nurse #196 of Resident #48 verified no oxygen in use sign on his door and the resident to have a nasal cannula attached to an oxygen concentrator. Also verified no oxygen therapy physician order for the resident. Review of the facility policy titled Oxygen Administration revised 10/26/2023 revealed oxygen warning signs must be placed on the door of the resident's room where oxygen is in use and oxygen is administered under orders of a physician.
CONCERN (D)

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

Deficiency F0699 (Tag F0699)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interviews and facility policy and procedure review, the facility failed to comprehensively assess and d...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interviews and facility policy and procedure review, the facility failed to comprehensively assess and develop a comprehensive plan of care for one resident (#31) with post traumatic stress disorder (PTSD). This affected one of four residents reviewed for mood/behavior. The facility census was 81. Findings Include: Review of the medical record for Resident #31 revealed an initial admission date of 01/12/23 with the diagnoses including but not limited to psychosis, schizoaffective disorder, depressive type, hypertension, hypothyroidism, drug induced subacute dyskinesia, obstructive sleep apnea, tremor, anxiety disorder, severe morbid obesity, constipation, dissociative and conversion disorder, post-traumatic stress disorder, chronic kidney disease, insomnia, borderline personality disorder, major depressive disorder, bipolar disorder, osteoarthritis and overactive bladder. Review of the resident's initial social service history dated 01/19/23 revealed the resident did not have PTSD. Review of the resident's social service progress review dated 01/06/25 revealed the resident did not have PTSD. Review of the psychiatric progress note dated 03/20/25 revealed the resident's PTSD was chronic and controlled. The resident is currently on a regimen of Depakote, Latuda, Topiramate, Ingrezza, Buspar, and Wellbutrin. No new symptoms or concerns were reported during this visit. The plan was to continue with the current medication regimen. Encouraged resident to report any increase in PTSD symptoms or any side effects from the medication. Regular follow-ups will be scheduled to monitor the patient's response to the medication. Review of the resident's social service progress review dated 04/01/25 revealed the resident did not have PTSD. Review of the resident's quarterly MDS assessment dated [DATE] revealed the resident had no cognitive deficit. The assessment indicated the resident had displayed hallucinations, delusions and behaviors not directed towards others. The assessment indicated PTSD was a current diagnoses. Review of the resident's plan of care revealed no care plan addressing the resident's triggers PTSD. On 04/17/25 at 9:48 A.M., interview with Regional Registered Nurse #207 verified the resident was not assessed for PTSD and a comprehensive plan of care was not developed to assist with the care of the resident's PTSD. Review of the facility policy titled, Trauma Informed Care, dated 10/18/20 and last revised 10/24/22 revealed the policy of the facility to ensure residents who are trauma survivors receive culturally competent trauma informed care in accordance with professional standards of practice. Each resident will be screened for a history of trauma on admission. The facility social worker or designee will conduct the screening in a private setting. If the screening indicated the resident had a history of trauma and/or trauma related symptoms a physician's order will be obtained for the resident to be evaluated by a mental health professional. The facility will account for the resident's experiences, preferences, and cultural differences in order to eliminate or mitigate triggers that may cause re-traumatization of the resident. A care plan will be initiated/updated to address those residents identified. Individualized approaches will be identified and interventions put into place.
CONCERN (D)

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

Deficiency F0847 (Tag F0847)

Could have caused harm · This affected 1 resident

Based on review of facility alternative dispute resolution agreements, resident interview, staff interview, record review, and policy review, the facility failed to ensure residents understood the agr...

Read full inspector narrative →
Based on review of facility alternative dispute resolution agreements, resident interview, staff interview, record review, and policy review, the facility failed to ensure residents understood the agreement they signed. This affected two of three residents reviewed for arbitration agreements (Residents #15 and #68). The facility census was 81. Findings include: 1. Review of the record for Resident #68 revealed an admission date of 01/23/25. Review of a Minimum Data Set (MDS) assessment completed 01/27/25 revealed a Brief Interview for Mental Status (BIMS) score of 15, indicating intact cognition. Review of a facility Alternative Dispute Resolution Agreement dated 01/23/25 revealed Resident #68 signed the agreement on 02/14/25. The agreement stated it demonstrated a mutual intention to resolve disputes between them outside of court and to submit their disputes to Alternative Dispute Resolution through mediation and/or arbitration. The form also stated that the resident had been offered to, or had been able to view an audio/visual recorded video that details this agreement and what it includes. Interview with Resident #68 on 04/16/25 at 4:05 P.M. revealed it was her signature on the agreement. However, she stated she did not watch a video and did not understand what she was signing. 2. Review of the record for Resident #15 revealed an admission date of 12/04/24. Review of a MDS assessment completed 12/13/24 and 04/15/25 revealed a BIMS score of 14, indicating intact cognition. Review of a facility Alternative Dispute Resolution Agreement dated 12/07/24 revealed Resident #15 signed the agreement on 12/16/24. The agreement stated it demonstrated a mutual intention to resolve disputes between them outside of court and to submit their disputes to Alternative Dispute Resolution through mediation and/or arbitration. The form also stated that the resident had been offered to, or have been able to view an audio/visual recorded video that details this agreement and what it includes. Interview with Resident #15 on 04/16/25 at 3:15 P.M. revealed she did not remember signing the dispute resolution agreement. She stated that is was not her signature on the form. She stated anytime she signed a document, she used her middle initial between her first name and last name. The signature on the agreement did not include a middle initial. She stated she probably would not have signed the agreement anyway if she understood what it was. Review of other documents signed by Resident #15 dated 12/05/24 including consents for flu vaccine, RSV vaccine, and bed rails revealed the resident used her middle initial when signing the forms. Interview with Regional Registered Nurse #207 on 04/16/25 at 3:20 P.M. confirmed other forms signed by Resident #15 contained her middle initial and the Dispute Resolution Agreement did not. She further stated the Admissions Director who also signed the agreement no longer worked at the facility. Interview with Admissions Director #192 on 04/17/25 at 7:26 A.M. revealed the facility has a video for residents to watch that explains the arbitration agreement. Review of the facility policy titled Binding Arbitration Agreements dated 07/28/20 and revised 11/01/22 revealed this facility asks all residents to enter into an agreement for binding arbitration. The facility shall explain to the resident or his or her representative in a form and manner that he or she understands.
CONCERN (F)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected most or all residents

Based on observation and interviews, the facility failed to ensure opened multi-dose Tuberculin Purified Protein (TB) vials were dated when opened. This had the potential to affect all 81 residents re...

Read full inspector narrative →
Based on observation and interviews, the facility failed to ensure opened multi-dose Tuberculin Purified Protein (TB) vials were dated when opened. This had the potential to affect all 81 residents residing in the facility. Findings Include: On 04/17/25 10:15 A.M., observation of the third floor medication room refrigerator revealed an opened vial of Tuberculin Purified Protein one milliliter (ml) was undated to when the first dose was obtained. Registered Nurse (RN) #196 verified the vial of TB solution was not dated when opened at the time of the observation. On 04/17/25 at 10:22 A.M., observation of the second floor medication room refrigerator revealed an opened vial of Tuberculin Purified Protein one milliliter (ml) was undated to when the first dose was obtained. Licensed Practical Nurse (LPN) #157 verified the TB solution was not dated when opened at the time of the observation.
Jul 2023 8 deficiencies 1 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

Accident Prevention (Tag F0689)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, review of online manufacturer guidance, and interview the facility failed to ensure equipme...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, review of online manufacturer guidance, and interview the facility failed to ensure equipment was maintained in a safe manner to prevent falls with injury for Resident #43 and Resident #50. The facility failed to provide adequate supervision and assistance to prevent Resident #48 from falls and eloping. Actual harm occurred on 02/03/23 when Resident #50 sustained a fall when the anti-rollbacks on his wheelchair were not properly functioning. The resident complained of severe pain for three days following the incident, with a decrease in functional mobility without any type of interventions. On 02/06/23 the resident was admitted to the hospital with a fractured right hip. Actual harm also occurred on 06/01/23 when Resident #43, who required staff assistance for personal care fell from a shower gurney after the rail of the gurney broke sustaining a fractured femur. Prior to the incident, there was no evidence the facility conducted any type of preventative maintenance or inspection of the shower gurneys. This affected three residents (#43, #48, and #50) of the six residents reviewed for falls. The facility census was 80. Findings include: 1. Record review for Resident #50 revealed the resident was admitted to the facility on [DATE]. Resident #50 had diagnoses including nondisplaced fracture of greater trochanter of right femur, chronic obstructive pulmonary disease, other seizures, paroxysmal atrial fibrillation, schizophrenia, ischemic cardiomyopathy, dementia with behavioral disturbance, secondary parkinsonism, hypertension, abnormal posture, dysphagia, aphasia, ataxia, need for assistance with personal care, cognitive communication deficit, and difficulty walking. Review of a facility fall investigation, dated 02/03/23, revealed Resident #50 was observed trying to scoot himself back in his wheelchair. When attempting to stand, the wheelchair rolled partially out from under him. The anti-rollback wheels did not lock when the resident stood to shift weight back in his chair. The resident was assessed to complain of some pain to the right leg area. Record review revealed there was no nursing progress note related to this incident on 02/03/23. Review of the facility Fall - Initial assessment, dated 02/03/23, revealed the resident complained of new pain to the right middle leg at a pain level rated a four out of 10 on a scale of one to 10. Review of the facility Fall - Follow-up assessment, dated 02/04/23, revealed the resident have a pain level of three out of ten with bruising noted to the right posterior leg and knee. Review of the facility Fall - Follow-up assessment, dated 02/05/23, revealed the resident had a pain level rated a four out of ten and was refusing to stand or apply weight to the right leg. Review of the facility Fall - Follow-up assessment, dated 02/06/23, revealed the resident was assessed to have a pain level rated a seven out of ten and was at the emergency room (ER) for hip pain. Review of the Medication Administration Record for 02/2023 revealed Resident #50 was documented to have been administered as needed Tylenol for pain once on 02/05/23 and twice on 02/06/23 which staff documented to be effective. Review of Resident #50's medical record revealed there were no comprehensive assessments of the resident's hip, range of motion/mobility status, changes in medical condition and/or notification to the physician prior to 02/06/23. Review of the nurse's progress note, dated 02/06/23, revealed Registered Nurse (RN) #173 received during report information that Resident #50 had fallen on 02/03/23 and had been complaining of pain since the fall. STNAs reported to RN #173 that Resident #50 had a substantial decrease in ADL's related to standing, ambulation, and transfers. RN #172 notified the physician at this time and new orders were received to obtain an x-ray of the knee and hip area. Review of the facility Work Order #1751, created on 02/06/23, revealed anti-rollbacks on wheelchair not functioning properly. On 02/07/23 the work order was updated to set to be completed. Review of the hospital progress note dated 02/06/23 revealed Resident #50 was admitted to the hospital on [DATE] after being found to have a right intertrochanteric hip fracture which required surgical repair while the resident was in the hospital. Review of the most recent annual MDS 3.0 assessment, dated 04/06/23, revealed Resident #50 had moderately impaired cognition evidenced by a Brief Interview for Mental Status (BIMS) assessment score of 03 out of 15. This resident was assessed to require extensive assistance from two staff members for transfers, toileting, and bed mobility and to require supervision with setup assistance only for eating. Review of the care plan, revised 06/14/23, revealed Resident #50 was at risk for falls. Interventions included maintenance to repair anti-rollbacks on 12/14/22 (after sustaining a fall with no injury on 12/14/22) and maintenance to check function of anti-rollbacks and repair as needed on 02/06/23. Interview with RN #173 on 06/27/23 at 9:00 A.M. revealed upon coming back to work after being off for four days facility STNA's reported Resident #50 had a decline in ADL's since falling on 02/03/23 and was not wanting to eat or bear weight. RN #173 stated Resident #50 was ambulatory and fairly independent prior to his fall on 02/03/23. RN #23 further stated Resident #50 did not typically complain of pain and while being assessed by RN #173 the resident verbalized complaints of severe pain to his right hip and leg. RN #23 stated she notified the physician who ordered an x-ray which revealed a fracture, and the resident was sent to the hospital for evaluation and treatment. Interview with Resident #50 on 06/27/23 at 9:12 A.M. revealed the resident had fallen while attempting to stand and had to go to the hospital and have surgery. Resident #50 stated he had severe pain to the right hip and leg which he had verbalized to facility staff in the days following his fall. Interview with Director of Nursing on 06/29/23 at 9:00 A.M. verified Resident #50 had a fall on 02/03/23 and was sent out to hospital on [DATE] for evaluation and treatment for right hip fracture. 2. Record review for Resident #43 revealed the resident was admitted to the facility on [DATE] with diagnoses including chronic obstructive pulmonary disease, chronic respiratory failure with hypercapnia, anemia, dependence on supplemental oxygen, bipolar disorder, adult failure to thrive, schizoaffective disorder, contracture of left hand and elbow, muscle wasting, tremor, and muscle weakness. Review of a fall investigation, dated 06/01/23, revealed a State Tested Nursing Assistant (STNA) opened the door to the room of Resident #43 and informed the nurse the shower gurney had broken prior to the Hoyer lift transfer back into the bed and the resident had fallen on the floor. The STNA stated her, and her partner rolled resident on the gurney when the railing of the gurney snapped. Upon entering the room, the resident was observed lying on the floor and was yelling out in pain. The resident was assessed and found to have a hematoma to her right and left hands, bruising on the left side of her forehead, and was observed to yell out in pain every time her left leg was touched with a pain level of eight using the PAINAD pain scale. The physician was notified, and the resident was sent to the emergency room (ER) for evaluation. Review of the medical record for Resident #43 revealed no nurse's notes regarding the fall that occurred on 06/01/23. Review of the witness statement provided by STNA #133, dated 06/01/23, revealed she and STNA #5 showered Resident #43 on the shower gurney. When finished, the two STNAs took the resident back to her room to put her in bed. While getting the Hoyer lift ready for the transfer, the two STNAs rolled the resident toward them to get a Hoyer pad underneath her and the left side of the gurney came down and the resident fell. Review of the witness statement provided by STNA #5, dated 06/01/23, revealed Resident #43 was on the shower gurney and STNA #133 and STNA #5 were both on the side of the gurney they were rolling her towards when the gurney snapped, and the resident fell onto the floor on her left side. Review of the hospital progress note, dated 06/01/23, revealed this resident was diagnosed with a displaced intertrochanteric fracture of the left femur. Review of the care plan, revised 06/09/23, revealed the resident had a fall. An intervention (initiated 06/02/23) included staff education to inspect shower equipment prior to use. Review of the most recent significant change Minimum Data Set (MDS) assessment, dated 06/20/23, revealed Resident #43 was rarely/never understood. The assessment revealed the resident required extensive assistance from two staff members for bed mobility and toileting, required extensive assistance from one staff member for eating, and was dependent on two staff members for transfers. Interview with Maintenance Director (MD) #47 on 06/27/23 at 3:19 P.M. revealed the pipe on the shower gurney had broken during use with Resident #43. MD #47 was unsure if it was cracked before being used to shower Resident #43 as routine inspection and maintenance of the shower gurney had not been done prior to the residents fall. Maintenance Director #47 stated he was unsure of the recommendations for routine maintenance on the shower gurney but stated he would attempt to find them. Interview with Maintenance Crew employee #157 on 06/27/23 at 3:34 P.M. revealed the side rails of the shower gurney were up and the pin went through the PVC pipe on the shower gurney causing it to break and for the resident to fall. Maintenance Crew employee #157 stated prior to Resident #43's fall, there was not routine maintenance or inspection of the shower gurney, but following the incident staff were to inspect them monthly. Interview with the Director of Nursing (DON) on 06/29/23 at 8:51 A.M. verified there had not been routine maintenance or inspections of the facility shower gurneys prior to the fall experienced by Resident #43. The DON also verified the facility did not have a manual or policy for the shower gurney providing instructions on how to use, clean, or maintain the gurney in good, working condition. Review of the online guidance from Healthline Medical Products titled Recommendations from the manufacturer (https://www.healthlinemedical.com/instructions/healthline-medical-shower-gurney-maintenance/), not dated, revealed recommendations regarding gurney maintenance and use procedure revealed drop rails were not designed to hang on them and all joints of the shower gurney should be checked on a regular basis to make sure the pipes and fittings were secured. 3. Review of Resident #48's medical record revealed the resident was admitted to the facility on [DATE]. Resident #48 had diagnoses including alcohol-induced persisting dementia, seizure disorder, chronic obstructive pulmonary disease, osteoarthritis, repeated falls, difficulty walking, unsteadiness on his feet and muscle weakness. Review of Resident #48's fall risk assessment completed on 12/20/22 revealed the resident was not indicated to have had any falls occurring in the previous 90 days. He was ambulatory with the use of assistive devices. He had diagnoses and the use of certain medications that increased his risk for falls. His overall score was nine, which did not indicate the need for any fall prevention interventions at that time. A review of Resident #48's nurses' progress notes revealed the resident had an unwitnessed fall on 01/04/23 at 7:45 P.M. The note indicated the resident was previously seen sitting in his wheelchair in the dining room watching a movie. Another resident had come to the nurses' station and informed the nurse that the resident had fallen. The nurse noted the resident was already back in his wheelchair when she was made known of the fall. She asked the resident if he had fallen and he reported to the nurse that he had. He was unable to provide any further description of the fall. A review of the facility's fall investigation for the fall occurring on 01/04/23 revealed the immediate action taken to prevent further falls from occurring included the use of Dycem to his wheelchair. Review of Resident #48's quarterly/significant change evaluation dated 05/03/23 revealed the resident's risk for elopement was assessed as part of the quarterly evaluation under the cognitive/ communication assessment of that evaluation. The resident's risk factors for elopement included being cognitively impaired, having the diagnosis of dementia, being able to ambulate independently with the use of a wheelchair, and being known to wander aimlessly. He was not known to have a history of eloping when at home, leaving the facility unsupervised, or leaving the facility without informing the facility staff. As a result of that assessment, he was not deemed to be at risk for elopement at that time. A review of a nurse's note dated 05/15/23 at 5:00 P.M. revealed the resident had a witnessed fall on that date. The note indicated the resident was in the dining room when staff witnessed the resident had slid out of his wheelchair onto his buttocks on the floor. The resident reported that he had slid out of his wheelchair. The intervention added was again to use Dycem to his wheelchair that had been previously ordered with his fall occurring on 01/04/23. A review of the facility's fall investigation for the fall occurring on 05/15/23 revealed the immediate action taken following the fall included providing staff education to ensure Dycem was in place to his wheelchair as was previously ordered. A review of Resident #48's physician's orders revealed an order, dated 05/15/23 for the use of Dycem to his wheelchair at all times. Review of Resident #48's quarterly Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed the resident rarely/ never made himself understood and was rarely/ never able to understand others. He had both short- and long-term memory impairment and his cognitive skills for daily decision making was severely impaired. He was not coded on the MDS as having had any behaviors during the seven-day assessment period and was not known to reject care or display any wandering behavior. He required a limited assist of one for transfers. He required supervision with set up help for ambulation in his room. Ambulation in hall only occurred once or twice, but he only required set up help for that when it did occur. He required supervision with the assist of one for locomotion on and off the unit. Balance issues were noted but he was able to stabilize without staff assistance. A wheelchair was the only mobility device used. The resident was identified as having had falls since his prior assessment. He had two or more falls without injury, one fall with injury that was not major injury, and one fall with major injury. A review of Resident #48's active care plans revealed he had a care plan in place for being at risk for falls related to dementia, weakness, unsteadiness on feet, difficulty walking, lack of coordination, and a history of falls. The care plan originated on 12/20/17 and was last revised on 06/14/23. The goals were to reduce the risk of serious injury in the event of a fall and for the resident to be free of falls. The interventions included ensuring his call light was within reach and to encourage the resident to use it for assistance as needed. That intervention was added to the care plan on 12/20/17. The interventions also included the use of Dycem (a tacky pad that could be placed on a seat of a chair to prevent sliding) to his wheelchair. That intervention was added on 01/05/23. The care plan directed them to review information on past falls and attempt to determine the cause of falls. They were to record the possible root causes and to remove any potential causes if possible. The care plan was revised to include the intervention of educating staff to ensure proper placement of Dycem on 05/18/23. On 06/26/23 at 12:47 P.M., an observation of Resident #48 noted him to be lying in bed. His call light was on the floor under his bed and out of his reach. Further observation of Resident #48 on 06/27/23 at 10:29 A.M., noted him to be lying in bed with his call light still on the floor under his bed and out of reach. Findings were verified by LPN #135. On 06/27/23 at 10:48 A.M., an interview with LPN #135 revealed Resident #48 was at risk for falls. They typically laid him down after meals and one of the aides would have helped him to bed after breakfast. She reported his fall prevention interventions included ensuring his call light was in reach. She confirmed the resident did not have his call light in reach, as it was found under his bed on the floor. She retrieved it from the floor and secured it to the assist bar that was on the right side of his bed near his head. On 06/27/23 at 3:10 P.M., an interview with the DON confirmed Resident #48 has had multiple falls while in the facility. She confirmed the use of Dycem was added as a fall prevention intervention following the fall the resident had on 01/04/23. She also confirmed they provided education to staff to ensure the Dycem was in place in his wheelchair, after he fell again on 05/15/23. She acknowledged the fall on 05/15/23 could not be considered an unavoidable fall due to previously ordered fall prevention interventions not being in place that contributed to his fall. She also acknowledged the fall prevention intervention to ensure his call light was in reach was not implemented as per the plan of care when observations noted it to be under his bed and out of reach on 06/26/23 and again on 06/27/23. In addition, a review of Resident #48's active care plans that were reviewed/revised on 06/14/23 revealed he did not have any care plan in place for being at risk for elopement or for unsafe wandering. Further review of Resident #48's nurses' progress notes revealed a nurse's note dated 06/25/23 at 3:00 P.M. that indicated a door alarm was alarming. The alarm announced was identifying the alarm as coming from the courtyard door on the second floor. The nurse and an aide tried multiple times to silence the courtyard door but was unsuccessful in doing so. The aide informed another staff nurse working that floor who also tried multiple times to silence the alarm without success. A maintenance employee was called to report the problems they were having with an alarm sounding that could not be silenced. While awaiting a return phone call, the aide went to check other residents and found the short hall exit door to be the one alarming. She entered the code to that alarm and was able to get the alarm to stop alarming. The staff then started checking on the residents and found Resident #48 to be missing. A facility search was started, and the resident was found outside in his wheelchair by the dumpsters by one of the nurses working on the second floor and the aide assigned that unit. The resident was found alert and his skin was warm and dry. He was not found with any injuries and was not noted to be in any distress. Staff assisted him back into the facility and into bed without incident. A review of a nurse's note dated 06/25/23 at 3:30 P.M. revealed the facility's DON was notified of the door alarm situation and the resident exciting building. A new order for the use of a Wander guard alarm was given as well and placing the resident on 15-minute checks until further notice. A review of the facility's investigation for Resident #48's elopement on 06/25/23 revealed the incident description of the event was consistent with what was documented in the progress notes. The resident was not able to provide a description of the event. Predisposing physiological factors of the incident included him being confused and impaired memory. Predisposing situation factors included him being a wanderer. Two staff members (LPN #89 and STNA #25) were identified as being witnesses to the incident and provided statements. LPN #89's statement indicated the resident was found in the parking lot by the dumpster after exiting the back hallway door. STNA #25's statement indicated the resident was found outside the facility in the parking lot after exciting the facility unassisted. The facility's investigation indicated the DON was notified on 06/25/23 at 3:30 P.M. On 06/27/23 at 3:35 P.M., an interview with Maintenance Assistant #157 revealed he was the maintenance employee called by the facility staff when Resident #48 eloped from the facility on 06/25/23. He reported they informed him they had a door alarm going off that they could not get silenced. He recalled the concern was with an alarm on the second-floor courtyard door. He came into the facility to check it out. By the time he arrived, the alarm was already silenced. He was informed the alarm that was going off was from the other door at the end of the hall and not the courtyard door as was being announced overhead. He indicated the courtyard door and the short hall exit door had the same code announcement and the overhead message would refer to them both as the courtyard door, even if it was the one at the end of the hall. He was informed a resident had gotten out when he arrived and was found at the bottom of the ramp by the facility's dumpsters. He confirmed by checking his phone that he received the call at 3:12 P.M. and he was in the facility by 3:30 P.M. in which the resident was already back in the facility. On 06/27/23 at 406 P.M., an interview with the DON revealed she was called about the elopement by Resident #48 on 06/25/23 at 3:28 P.M. The staff informed her of what had happened. It was reported to her that the nurse and the aides were in other residents' rooms. They then heard an alarm go off for the courtyard door. The overhead announcement indicated it was the courtyard door. The staff told her they looked outside but did not see any residents out there. They could not get the alarm to silence and called maintenance to come in to check it out. The staff realized the courtyard door was not flashing and it was the exit door at the end of the short hall that was flashing instead. They checked the residents and found Resident #48 to be missing. They went outside and found the resident at the end of the ramp near the dumpsters. On 06/27/23 at 4:10 P.M., an observation of the courtyard door on the 2nd floor revealed it led to the facility's designated smoking area. The alarm system on the courtyard door allowed the door to be immediately opened by turning the doorknob but would sound an audible alarm if the door was opened without entering the code into a keypad. The keypad alarm box on the wall would flash red if that was the door alarming in addition to an overhead announcement that identified the courtyard door as the door alarm that had been activated. The short hall exit door was checked and noted to have a delayed egress of 15 seconds before that door could be opened. A constant audible alarm sounded when the door's bar was pushed on until the door opened and then a different sounding alarm would go off accompanied by an overhead announcement. The courtyard door and the exit door at the end of the short hall both led to the same ramp that led down to the facility's side parking lot where the dumpsters were. The ramp was made of decking material and had a long, gentle slope with handrails on both sides. The side parking lot had a black tar pavement with a raised curb that enclosed it on the back end and the side. It led to the front parking lot where a steep driveway went down into the road the facility sat on. On 06/27/23 at 4:13 P.M., further interview with the DON revealed the alarm company had told them they could not program the alarm system to differentiate between the courtyard door and the short hall exit door, due to their proximity to one another. She indicated, when she was called, Resident #48 had already been found and brought back into the facility. She suspected he was not out there very long between the time the alarm sounded and when he was found. On 06/28/23 at 8:51 A.M., an interview with LPN #89 revealed she was one of the two nurses working on the second floor on 06/25/23 when Resident #48 eloped. She was the nurse assigned the long hall and not the short hall where the resident resided. She stated the overhead message indicated the courtyard door was alarming and they could not get it to stop. She confirmed the called maintenance to come in to check the alarm out and did not realize it was another door other than the courtyard door that was going off. STNA #25 noticed the keypad at the end of the short hall exit door did not look right. She punched in the code and the door alarm silenced. They realized at that point that someone could have gone through that door and not the courtyard as was originally thought. She and the aide went out into the courtyard when the door alarm first went off and did not see any residents out there. She was not sure if they exit door at the end of the short hall was sounding for the full 15 seconds, when the door was pushed on and before it released. She was down the long hall at the time and did not hear it alarming until the announcement was made overhead for the courtyard door. She was not sure where the nurse or the aide that was working the short hall was at that time or if they heard the short hall exit door alarm before being opened. They did a head count when they realized the exit door at the end of the short hall was the one sounding and noticed Resident #48 was missing. She and the aide went outside to look for the resident and he was noted to come out from behind the dumpsters still sitting in his wheelchair. She suspected he was only out there for five to seven minutes between the time the courtyard door alarm sounded and being found in the side parking lot. This deficiency represents non-compliance investigated under Complaint Number OH00143456.
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

Free from Abuse/Neglect (Tag F0600)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on review of resident medical record, facility's self-reported incident report, facility's abuse policy and procedure, sta...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on review of resident medical record, facility's self-reported incident report, facility's abuse policy and procedure, staff personnel file, and staff interview, this facility failed to ensure residents were free from verbal and physical abuse while receiving assistance with care by a staff member. This affected one (Resident #25) of two residents reviewed for abuse. The facility census was 80. Findings include: Review of the medical record for Resident #25 revealed an admission date of 10/13/14 and a re-entry date of 07/01/20. Diagnoses included multiple sclerosis, dementia with behavioral disturbances, need for assistance with personal care, contracture of the right hand, and schizoaffective disorder bipolar type. Review of the plan of care dated 05/09/17 and revised 10/11/19 revealed Resident #25 displayed behaviors including attention-seeking related to resident has repetitive behaviors such as combing hair, wanting ice, and tying of shoes. Interventions included, cognitive/communication skill permitting, discuss behavior with resident, explain reinforce why behavior is inappropriate and unacceptable, medication as ordered. Review of the plan of care dated 01/23/19 and revised 08/29/22 revealed Resident #25 has at times physically aggressive or agitated related to poor impulse control, anger, depression, a history of harm to others, attention seeking obsessive behavior such as asking for hair to be combed, seeking medications, change of clothes, shoes, hoarding attends from other residents territorial, will rip attends to be changed when no sign of incontinence are evident, gets frustrated with staff when these request can not be attended to in residents when asked, request for lotion to be applied infrontal periarea, resident will place object in depends and in private orifices, noncompliant with pericare, will pull as tight as she can on shoes strings prior to letting staff tie them, history of altercations with other residents stacking things high up close to ceiling and heating vent. Resident will hide items in bags of chips or in depends while it is on. Interventions include to complete 15 minute checks, administer medication as ordered, provide physical and verbal cues to alleviate anxiety, redirect , refer to inpatient psych as needed, when becomes agitated, and intervene before agitation escalates. Review of Resident #25's annual Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed the resident had a Brief Interview for Mental Status (BIMS) score of 3 out of 15 indicating an severely impaired cognition for daily decision making abilities. Resident #25 was noted to display physical and verbal behaviors directed towards others 4 to 6 days a week. Resident #25 was noted to require extensive assistance from two staff members for transfers, dressing, personal hygiene, and required physical help in part of bathing from two staff members. Resident #25 was noted to display impairment to one upper and one lower extremities and required the assistance of a wheelchair for mobility. Resident #25 was receiving antipsychotic, antianxiety, and antidepressant medication seven days a week. Review of Resident #25's physician orders included a treatment order dated 06/15/23 Apply Betadine to abrasion on top of right hand and leave open to air till area is healed. Review of facility's self-reported incident report tracking #236067 dated 06/14/23 revealed an allegation of physical abuse to a resident with the suspected or alleged perpetrator being a facility staff member. Summary of incident included, State Tested Nursing Assistant (STNA) #193 was giving Resident #25 a shower along with STNA #199. STNA #193 reported that Resident #25 was agitated prior to shower due to not meeting her needs on her timeline, resident was wanting ice right then and resident was instructed she would get her more after her shower, but did have ice currently in her cup. During the shower Resident #25 became agitated due to wanting her nail care completed right then when she was getting shower, staff told her they would get her nail care after shower was completed. STNA #193 stated words were exchanged between STNA #199 and Resident #25, but couldn't remember what was said and then Resident #25 became more combative. STNA #193 then reported STNA #199 grabbed Resident #25's left wrist and was jerking it back and forth and yelled at Resident #25 I'll fuck you up. During the interview with STNA #199, she denied grabbing the residents wrist, she did report she placed her arm over Resident #25's arm to prevent this resident from hitting her and also did report she was yelling and saying curse words but didn't remember what exactly was said. Skin assessment and pain assessment completed, no pain noted. Did note bruising and abrasion noted to right hand, 3rd and 5th digits, resident was combative with care and the right arm is affected. STNA #193 reported that STNA #199 did not do anything with the right arm, and that Resident #25 was combative and swinging body around and right hand likely hit the shower chair. Resident #25 has a BIMS of 03, resident was interviewed on the night of the incident with no issues noted or any remembrance of situation, Social Services then interviewed the following day with no issues noted as well, Medical Director and Representative aware. STNA #199 was suspended pending investigation. Skin assessment completed on all residents with no issues noted, all alert and oriented residents were interviewed with no issues noted with STNA #199. A whole house education was provided for abuse, and how to address behaviors. Social Services following Resident #25 to see if any emotional or physical issues regarding the situation. Currently Resident #25 is continuing Activities of Daily Living (ADLs), going out to smoke, and coming out of personal room. Shows no signs of any distress regarding the situation. Area to 5th digit to right hand is now resolved and the area to the 3rd digit is now a scab. Reviewed STNA #199's personnel file with no findings. Facility substantiated accusation of verbal abuse, facility unable to determine if physical abuse occurred. As a result of the investigation, the facility has done the following: Reviewed STNA #199's personnel file with no findings, education provided for abuse and how to handle behaviors appropriately, Social Services monitored Resident #25. Skin assessments completed on all residents and interviews with all alert and oriented residents. Staff member STNA #199 was terminated from the facility. Review of the Statement of Witness document dated 06/14/23 created by STNA #193 revealed, STNA #199 and I were going to give Resident #25 a shower prior to going into the shower room, Resident #25 was at the ice cart, she was asking for ice before she got into the shower room. I attempted to redirect Resident #25 by explaining that she will have a fresh cup as soon as we were finished with her shower. Resident #25 became agitated with the situation and screamed, I hate you. Resident #25 then locked her wheelchair brake, STNA #199 then grabbed Resident #25's chair while the brakes was locked and yanked the chair backwards to take her to the shower room while in the shower room, I turned the water on and moved the shower chair. STNA #199 began taking resident #25's shoes and socks off, but while doing so she ripped then off of her feet and was very rushed. STNA #199 then yanked Resident #25's shirt up her back and pulled it forcefully over her head. It was time for Resident #25 to stand and STNA #199 was being aggressive with her. STNA #199 pushed Resident #25's wheelchair to the wall, where the shower bar is located aggressively and with force. STNA #199 failed to look or check to see if Resident #25's affected foot was in a safe position to transfer, STNA #199 continued to push the wheelchair close to the wall which caused Resident #25's affected foot to bend further against the wall. I told STNA #199 that her foot was against the wall, she then forcefully angled the wheelchair correctly. All while this occurred, STNA #199 seemed extremely hostile and rushed. STNA #199 instructed Resident #25 to grab onto the shower bar to pull herself to stand. STNA #199 stated she acts like she can't do anything for herself. I assisted Resident #25 to stand to transfer to the shower chair. Once in the shower chair, something happened between Resident #25 and STNA #199 that triggered and argument. Everything happened so quickly. They became physical with one another. Resident #25 swung her fist multiple times at STNA #199, while Resident #25 was swinging her fist, STNA #199 grabbed her left arm many times. STNA #199 began scramming and drew her fist back at Resident #25 and stated I'll fuck you up. Resident #25 made contact with STNA #199's upper body. STNA #199 then jerked Resident #25's arm and screamed at her. I can not remember what was said again, everything escalated so quickly. I was so overwhelmed and I intervened. I started shouting stop! stop! I help my hand up and attempted to place my arm between the two of them. I was able to hold Resident #25's hand which resulted in Resident #25 grabbing my arm and digging her nails into my arm. STNA #199 tried to get Resident #25 off of my arm, which I told her that Resident #25 was fine, that she needed to calm down. STNA #199 again grabbed Resident #25's arm and threw it down. While dressing Resident #25, I saw the open area to her right hand and a red mark that resembled the material from the shower chair on her right shoulder. After leaving the shower room, STNA #199 was telling everyone about how she was going to hit Resident #25. Shortly afterwards during nail care, STNA #199 acted as if nothing happened. Review of Statement of Witness document dated 06/14/23 created by STNA #199 revealed, We took Resident #25 to the shower. When in the shower room, she began to yell about wanting ice, we told her we could get her ice after her shower since we were taking her to bed afterward anyway. As well were undressing Resident #25, she began to insist on brushing her hair, she puts the brush back on her chair, I go to move the brush so that we can get her up into the shower chair. Resident #25 grabs the brush and attempts to hit me with it, she wanted it to stay on the chair arm. I managed to get the brush from her and then she calms down. Then as we begin to shower her again she mentions she wants nail care and we tell her we did not have the stuff to do it in the room but that we would find it after we are done in the shower room. She continues to obsess over nail care (repeatedly asking), we told her again we could not do it in that moment, she began to swing her arms and attempt to hit, she starts grabbing my clothes and hitting at the other aide in the room, at that time, she was wet and covered in soap, we were trying to calm her down. When starting peri care, resident was digging in between her legs, I asked her to mover her hand so that I can clean her. I go to use a rag to wipe her, I mention to her that her nails will cause more infections/irritation to her areas and I needed to wash it, she again asks for nail care and gets aggressive again when we tell her we could not do it in that moment. After shower was over we push the chair up to the rail for her to stand for transfer and she began to get aggressive again and swats at my face, I raise my arm to guard myself and the other aide was also trying to put her arm out to guard her from hitting. Resident #25 grabs the aids arm tightly and would not let go. I tell her we cannot help her if she is going to hit and scratch us. We finally get her calm and she is safely transferred and dressed. After leaving the shower room, I did nail care for her and she was calm. We then took her to her room and helped her to bed. Resident #25 had multiple outburst in the shower room any time she was told we couldn't do something or asked her to wait for us to do a certain task. She hit, scratched, grabbed, and yelled the entire time, but after she was out of the shower room, she calmed down. Review of the Statement of Witness document created by Licensed Practical Nurse (LPN) #145 revealed that approximately 10:00 P.M. on 06/14/23, I was seated at the nurses station charting when STNA #199 came out of the shower room with Resident #25 and approached the nursing station saying that Resident #25 was hitting her in the shower room. STNA #199 stated that she drew her fist back at her (while demonstrating what she did) and stated that she told Resident #25 If you hit me one more time, I'm going to fuck you up. I did not physically see her harming resident nor did I hear her say anything to the resident. This is what STNA #199 stated to me, LPN #77, STNA #133, and STNA #5 following Resident #25's shower. Review of the Statement of Witness document dated 06/14/23 at 10:00 P.M. created by LPN #77 revealed, I was sitting at the nurses station when STNA #199 came up yelling in a loud voice saying If Resident #25 tries to hit me one more time, I told her I would fuck her up. She also said she drew her fist back at her in the shower room. I did not visually see anything done or said to Resident #25, but this was what I witnessed from STNA #199. Review of the Statement of Witness document dated 06/14/23 created by STNA #133 revealed, STNA #199 was talking about when she was showering Resident #25 that she said If you hit me one more time, I'm going to fuck you up and stated that she pulled her fist back. Review of the Statement of Witness document dated 06/14/23 created by STNA #5 revealed, I was up at the nurses station when STNA #199 came out of the shower room with Resident #25 and stated she told resident If you hit me one more time, I'm going to fuck you up, and she said she pulled her fist back. Review of the personnel file for STNA #199 revealed a hire date of 04/15/21 and the last day worked was 06/14/23. STNA #199 was noted to have received education including Caring for Residents with Dementia on 04/26/21. All required background and abuse checks had been completed with no noted concerns. Interview on 06/29/23 at 1:30 P.M. with the Director of Nursing confirmed the noted incident between STNA #199 and Resident #25 had occurred and was investigated immediately upon being reported. STNA #199 was suspended pending investigation and was later terminated from the facility. STNA #199 was reported to the appropriate agency regarding suspected abuse. Resident #25 was assess and noted to have a scratch to the right hand on the 3rd digit and 5th digit. Review of the incident revealed STNA #199 had grabbed onto Resident #199's left hand and not the right hand so it was difficult to determine what the cause was for the injury to the right hand. Continue monitoring of Resident #25 revealed no concerns or issues regarding the incident. Review of facility policy titled Abuse, Neglect and Exploitation, dated 10/24/22 revealed Verbal Abuse means the use of oral, written, or gestured communication or sounds that willfully includes disparaging and derogatory terms to resident or their families, or within their hearing distance regardless of their age, ability to comprehend, or disability. Physical Abuse includes, but not limited to hitting, slapping, bunching, biting, and kicking. It also include controlling behavior through corporal punishment. It is the policy of this facility to provide protections for the health, welfare, and rights of each resident by developing and implementing written policies and procedures that prohibit and prevent abuse, neglect, exploitation and misappropriation of resident property. This deficiency represents non-compliance investigated under Complaint Number OH00143456.
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 record reviews and interviews the facility failed to ensure Minimum Data Set (MDS) assessments were accurately complete...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record reviews and interviews the facility failed to ensure Minimum Data Set (MDS) assessments were accurately completed to reflect physician documentation of contraindications to Gradual Dose Reductions (GDR's). This affected two residents (#31 and #42) out of the five residents reviewed for unnecessary medications during the annual survey. The facility census was 80. Findings include: 1. Record review for Resident #43 revealed this resident was admitted to the facility on [DATE] and had diagnoses including chronic obstructive pulmonary disease, chronic respiratory failure with hypercapnia, anemia, dependence on supplemental oxygen, bipolar disorder, adult failure to thrive, shizoaffective disorder, contracture of left hand and elbow, muscle wasting, tremor, and muscle weakness. Review of the significant change MDS assessment, dated 06/20/23, revealed this resident was rarely/never understood. This resident was assessed to require extensive assistance from two staff members for bed mobility and toileting, to require extensive assistance from one staff member for eating, and to be dependent upon two staff members for transfers. This resident was assessed to have received antipsychotic medications on a daily basis and to not have the physician document a GDR as being clinically contraindicated. Review of the pharmacy recommendation, dated 11/30/22 and signed by the physican on 12/02/22, revealed a GDR was contraindicated at the time. Review of the quarterly MDS assessment, dated 12/06/22, revealed this resident was assessed to have not had the physician document a GDR as being clinically contraindicated. Review of the quarterly MDS assessment, dated 01/10/23, revealed this resident was assessed to have not had the physician document a GDR as being clinically contraindicated. Review of the quarterly MDS assessment, dated 04/02/23, revealed this resident was assessed to have not had the physician document a GDR as being clinically contraindicated. Review of the quarterly MDS assessment, dated 06/05/23, revealed this resident was assessed to have not had the physician document a GDR as being clinically contraindicated. Interview with MDS Nurse #71 on 06/26/23 at 10:40 A.M. verified the physician had documented a GDR as being contraindicated on 11/30/22 and the contraindication had not been documented on any of MDS assessments following the documentation. 2. Review of the medical record for Resident #31 revealed an admission date of 12/07/16 and re-entry on 08/04/18. Diagnoses included schizoaffective disorder bipolar type, cognitive communication deficit, anxiety disorder, and recurrent major depressive disorder. Review of the pharmacy recommendation, dated 02/14/23 revealed a GDR was contraindicated at the time due to the resident with a good response, maintain the current dose. Review of Resident #31's quarterly MDS 3.0 assessment dated [DATE] revealed the resident experienced long and short term memory problems and a severely impaired cognition for daily decision making abilities. Resident #31 was noted to display verbal behaviors directors others multiple times a week. Resident #31 was noted to be receiving antipsychotic, antianxiety, and antidepressant medication 7 days a week. This resident was assessed to have not had the physician document a GDR as being clinically contraindicated. Interview with DON on 06/29/23 at 1:00 P.M. verified the physician had documented a GDR as being contraindicated on 11/30/22 and the contraindication had not been documented on any of MDS assessments following the documentation. Review of the Centers for Medicare and Medicaid Services (CMS) Long Term Care (LTC) Resident Assessment Instrument (RAI) 3.0 Users Manual Version 1.71.0, dated 10/2019, revealed the steps for assessment included: 1. Review the resident ' s medication administration records to determine if the resident received an antipsychotic medication since admission/entry or reentry or the prior OBRA assessment, whichever is more recent. 2. If the resident received an antipsychotic medication, review the medical record to determine if a gradual dose reduction has been attempted. 3. If a gradual dose reduction was not attempted, review the medical record to determine if there is physician documentation that the GDR is clinically contraindicated.
CONCERN (D)

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

ADL Care (Tag F0677)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, observation, resident interview, staff interview, and policy review, the facility failed to ensure a res...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, observation, resident interview, staff interview, and policy review, the facility failed to ensure a resident who was depended on staff for assistance with activities of daily living (ADL's) received the assistance needed with the trimming of his fingernails. This affected one (Resident #52) of two residents reviewed for ADL's. The facility census was 80. Findings include: A review of Resident #52's medical record revealed he was originally admitted to the facility on [DATE]. His diagnoses included heart failure, osteoarthritis, chronic pain, chronic fatigue, weakness, need for assistance with personal care, schizo-affective disorder, and major depressive disorder. A review of Resident #52's annual Minimum Data Set (MDS) assessment dated [DATE] revealed the resident did not have any communication issues and he was cognitively intact. He was not known to display any behaviors nor was he known to reject care during the seven days of the assessment period. He required a limited assist of one for transfers and ambulation in the hall. Supervision with the assist of one was needed for locomotion on the unit and personal hygiene. Supervision with set up help was needed for bathing. A review of Resident #52's care plans revealed the resident needed assistance with ADL's related to weakness, hypotension, bradycardia, obesity, need for assistance with personal care, lack of physical exercise, chronic fatigue, pain, unsteadiness on feet, and obesity. The care plan was originated on 04/24/19 and was last revised on 04/11/23. Interventions included during bathing/ showers they were to check nail length and trim and clean on bath days and as necessary. The care plan indicated he required supervision to limited assist of one with personal hygiene. A review of Resident #52's shower documentation under the task tab of the electronic health record for the past 30 days (05/31/23 to 06/24/23) revealed the resident was scheduled to receive showers every Wednesday and Saturday on the day shift. He was documented as last receiving a shower on 06/24/23. There was nothing under the task tab for the aides to document if nail care had been provided. On 06/26/23 at 10:04 A.M., an observation of Resident #52 noted him to be lying in bed in a supine position. His fingernails on both hands were long and in need of being trimmed. Some of the nails had a dark colored substance under the nails. An interview with the resident, at the time of the observation, revealed he would like to have his nails trimmed and needed the staff's assistance to do so. Subsequent observations on 06/27/23 at 8:45 A.M. and 06/28/23 at 8:35 A.M. noted his fingernails to remain long and in need of being trimmed. On 06/28/23 at 11:38 A.M., an interview with State Tested Nursing Assistant (STNA) #155 revealed Resident #52 required some assist with his adl's but did a lot for himself. They provided him with set up help for his showers. The resident was compliant with showers and had already been showered that day. He was asked what care was provided as part of the resident's bathing activity and indicated it included nail care. He was then asked if he had checked the resident's nails that morning and indicated he did. He did not feel they needed to be trimmed when he looked at them. He was asked to check the resident's fingernails and accompanied the surveyor back to the resident's room. The resident was walking out of his room to go to the dining room for lunch. STNA #155 checked his fingernails and confirmed they were long and in need of being trimmed. He asked the resident if he wanted them trimmed and the resident told him he did. He then stated the resident would usually tell them when he wanted them trimmed. A review of the facility's Nail Care policy revised 01/01/22 revealed the purpose of the policy was to provide guidelines for the provision of care to a resident's nails for good grooming and health. Routine cleaning and inspection of nails would be provided during ADL care on an ongoing basis. Routine nail care, to include trimming and filing, would be provided on a regular basis and as the need arises.
CONCERN (D)

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

Deficiency F0692 (Tag F0692)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review, resident and staff interview and facility's hydration review, this facility failed to ensure res...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review, resident and staff interview and facility's hydration review, this facility failed to ensure residents with a fluid restriction was monitored for appropriate fluid intake. This affected one (Resident #38) of one resident reviewed for fluid intake. Facility census was 80. Findings include: Review of the medical record for Resident #38 revealed an initial admission date of 11/24/21 and a re-entry date of 03/01/22. Diagnoses included end stage renal disease, heart failure, and difficulty in walking. Review of the plan of care created 03/26/21 and revised 04/27/23 revealed Resident #38 had a potential fluid volume overload related to kidney failure, dialysis, non complaint with fluid restrictions such as drinking pop as desired, wants cups with ice and-or water at bedside. Interventions included to administer medication as ordered and monitor, provide diet as ordered, encourage that all snacks and beverages offered at activities comply with diet and fluid restrictions, monitor vital signs, and monitor for fluid overload and report, resident is on fluid restriction. Review of Resident #38's quarterly Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed a Brief Interview for Mental Status (BIMS) score of 15 indicating an intact cognition for daily decision making abilities. No behaviors were noted with this assessment review. Resident #38 required supervision with set up assistance only for eating. Resident #38 was noted to be 61 inches tall and weighted 208 pounds with a noted weight gain. Resident #38 was noted to receive diuretics daily as well as dialysis services out side the facility. Review of the behavior charting for Resident #38 revealed no behaviors related to the resident being non-complaint with the physician ordered fluid restriction. Review of Resident #38's progress notes from 04/01/23 through 06/28/23 revealed no documentation indicating this resident was non-complaint with the physician ordered fluid restriction. Review of physician order revealed orders for Dialysis on Monday, Wednesday, and Friday with a chair time of 9:30 A.M. and pick up time varies between 8:45 A.M. and 9:15 A.M. A no added salt, renal diet, with regular textured food, and thin liquid consistency. 1500 milliliter (ml) fluid restriction, 360 ml with breakfast, 240 ml with lunch, 360 ml with dinner, 120 ml at bedtime, and nursing to provide 210 ml twice a day with medication administration. Torsemide 100 milligrams (mg) tablet, give 0.5 tablet daily for fluid overload related to end stage renal disease. Review of Resident #38's fluid intake for April 2023, May 2023, and June 2023, revealed most days of the month, Resident #38 was noted to go over her physician ordered fluid restriction of 1500 ml daily from the recorded fluid intake from meals and medication administration. Observation on 06/26/23 at 11:00 A.M. of Resident #38's room revealed two styrofoam cups sitting on the bedside table, noted to be filled with clear fluids. Observation on 06/27/23 at 12:00 P.M. and again at 3:00 P.M. of Resident #38's room revealed one styrofoam cup filled with a clear fluid and a full unopened can of soda sitting on the bed side tablet. Interview on 06/28/23 02:48 PM with the Director of Nursing (DON) revealed when the nurses complete their charting, they try to keep the behaviors charting the same as what the STNA chart on and they are limited on how many target behaviors they can put in the chart for the nurses to chart on each shift. Due to this, there is not a specific behavior to monitor related to being non-compliant with her fluid restriction. The DON claimed that Resident #38 will get her own fluids and her roommate will also give her cans of soda to drink almost daily. The DON claimed that dietary told her that even today the resident requested a extra bowl of chicken broth even though she was on a fluid restriction. The DON confirmed Resident #38's lacked documentation indicating the resident was non-complaint with the physician ordered fluid restriction and had been having a noted weigh gain. Review of provided policies and procedures revealed the facility did not have a policy and procedure related to fluid restrictions.
CONCERN (D)

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

Medication Errors (Tag F0758)

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 provide an appropriate diagnosis for the use of an antipsychotic. Th...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview the facility failed to provide an appropriate diagnosis for the use of an antipsychotic. This affected one resident (Resident #7) out of five residents reviewed for unnecessary medications. The facility census was 80. Findings include: Record Review of Resident #7 revealed this resident was admitted to the facility on [DATE] with the following medical diagnoses: dementia, atherosclerosis, hypothyroidism, spondylosis, anxiety, Alzheimer's disease, mood disorder, polyneuropathy, osteoporosis, falls, lack of coordination, cognitive communication deficit, and muscle weakness. Review of the Minimum Data Set(MDS) assessment completed on 06/16/23 revealed this resident is rarely/never understood. Review of Physician Orders revealed this resident is receiving the following medication: Seroquel 50 milligram (mg) 1 tablet by mouth three times a day for unspecified dementia. Review of current resident diagnoses revealed this resident does not have an active diagnosis of psychosis in the medical chart. Interview with the Director of Nursing on 06/27/23 at 10:15 A.M. verified unspecified dementia is an unacceptable diagnosis for the use of Seroquel.
CONCERN (E)

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

Infection Control (Tag F0880)

Could have caused harm · This affected multiple residents

Based on review of the facility's infection control logs, record review, staff interview, and policy review, the facility failed to ensure they maintained an effective infection control program that a...

Read full inspector narrative →
Based on review of the facility's infection control logs, record review, staff interview, and policy review, the facility failed to ensure they maintained an effective infection control program that adequately identified organisms causing infections within the facility and properly track those infections to identify any trends or patterns. This had the potential to affect all residents residing in the facility. The facility's census was 80. Findings include: A review of the facility's infection control logs for the past 12 months revealed the facility's infection preventionist was utilizing a floor plan to identify where infections were noted throughout the facility for each month. She had a floor plan for the second floor and a floor plan for the third floor. The floor plan was color coded to show the locations of the rooms in which different types of infections occurred. One color was used to signify each type of the following infections: urine, respiratory, skin, and other. The floor plan did not indicate what organisms were present for the different types of infections identified. There were also infection line listing reports and antibiotic usage reports for each month reviewed. The antibiotic usage report included the resident's name, infection category (soft tissue, respiratory, UTI, or other), antibiotic ordered to include dose/ route, start date, stop date, and a place to document the organism involved. The antibiotic usage report did not have any organisms identified with any of the 13 entries made to include the infection categories that should have an organism easily identifiable such as with Urinary Tract Infections (UTI's). The infection preventionist typed in null under the column for organism with all 13 entries made. The infection line listing report included similar information as the antibiotic usage report and also failed to identify any organisms identified with the infections recorded. Under the column for organism, the infection preventionist entered no response for each of the 13 entries made to record resident infections. On 06/29/23 at 1:35 P.M., an interview with Registered Nurse (RN) #91 revealed she was the facility's infection preventionist. She confirmed the facility was not obtaining microbiology testing on a routine basis to identify organisms causing infections within the facility. She stated their medical director did not like ordering laboratory testing when treating residents for infections. She stated it was rare that the physician would order a urinalysis before treating a resident for a UTI based solely on symptoms and when he did he usually did not order a culture and sensitivity along with it. She acknowledged, without obtaining cultures when able, they were not identifying the organisms present that were causing the infections they were recording on their infection control logs. Without identifying the organism, they were not able to determine if there were any trends or patterns occurring in the facility involving any specific type of infection. She reported some of the residents were ordered antibiotics for wound infections when they were sent out for an appointment with the wound clinic or surgeon. Cultures were reported as having been obtained at those appointments but they had difficulty getting those culture results, even when requested, to be able to see what organism was causing the infection. A review of the facility's Infection Surveillance policy revised 10/24/22 revealed it was the facility's policy to develop a system of infection surveillance that served as a core activity of the facility's infection prevention and control program. Its purpose was to identify infections, monitor adherence to recommended infection prevention and control practices in order to reduce infections and prevent the spread of infections. Infection surveillance was defined as an ongoing systematic collection, analysis, interpretation, and dissemination of infection-related data. The infection preventionist served as the leader in surveillance activities, maintained documentation of incidents, findings, and any corrective actions made by the facility and reported surveillance findings to the facility's Quality Assessment and Assurance Committee, and public health authorities when required. The facility would collect data to properly identify possible communicable diseases or infections before they spread by identifying data to be collected to include the infection site, pathogen (if available), signs and symptoms, resident locations, and the identification of unusual or unexpected outcomes, infection trends, and patterns. Data to be used in the surveillance activities may include, but was not limited to lab reports and antibiograms obtained from lab.
CONCERN (E)

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

Antibiotic Stewardship (Tag F0881)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on review of the facility's infection control log, infection reports, record review, review of the McGeer's criteria, staf...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on review of the facility's infection control log, infection reports, record review, review of the McGeer's criteria, staff interview, and policy review, the facility failed to maintain and implement an effective antibiotic stewardship program to ensure residents only received antibiotics when warranted and antibiotics prescribed were appropriate for the infections being treated. This affected four (Resident #33, #75, #77, and #235) of five residents reviewed for infections. The facility census was 80. Findings include: 1. A review of Resident #33's medical record revealed she was admitted to the facility on [DATE]. Her diagnoses included adult onset diabetes mellitus and peripheral vascular disease. A review of Resident #33's physician's orders revealed she had an order in place to cleanse a wound to the left sole of her foot, pat dry, apply Betadine to the wound bed, and cover with a foam dressing daily. The treatment was ordered on 05/04/23. A review of Resident #33's skin and wound assessments revealed she had what was classified as a surgical wound to her left plantar foot. The wound progress was indicated to be stable and she was followed by wound care. A review of Resident #33's progress notes revealed a nurse's note dated 06/25/23 at 9:28 A.M. that indicated documents were received from the resident's appointment she had with the podiatrist on 06/23/23. The podiatrist recommended Doxycycline 100 milligrams (mg) for 3 weeks. The recommendation was reported to her primary care physician at the facility and he ordered Doxycycline 100 mg twice a day (BID) for three weeks. A review of Resident #33's consultation reports revealed she was sent out for a podiatry appointment on 06/23/23 as indicated in her nurse's progress note dated 06/25/23. The consultation report revealed the resident had increased redness of an unspecified area and it was recommended that she take Doxycycline 100 milligrams for three weeks. No other documentation was provided on the consultation report. A review of Resident #33's infection report dated 06/26/23 revealed someone had transcribed a 3 over the 6 for the day that was originally specified in the date of that report. The infection report indicated it pertained to a wound to the left foot per the podiatrist. Under skin, there was no indication of the resident having any symptoms to include heat, swelling, pain, redness, drainage, or odor. The bottom of the infection report included a section for infection management and specified the antibiotic ordered as Doxycycline 100 mg BID for three weeks. The treatment was to be initiated on 06/26/23 and continued through 07/17/23. Additional comments indicated the physician was aware and wanted to continue the antibiotic. On 06/29/23 at 1:35 P.M., an interview with Registered Nurse (RN) #91 revealed she had been the facility's infection preventionist since August 2022. She reported the facility followed the McGeer's criteria to ensure residents met the criteria for treating infections. She indicated Resident #33 was started on Doxycycline as recommended by the podiatrist when she went out for her appointment on 06/23/23. She stated the physician agreed with the treatment and wanted the antibiotic continued despite her not meeting criteria for the treatment of cellulitis or soft tissue wounds. 2. A review of Resident #75's medical record revealed she was admitted to the facility on [DATE]. Her diagnoses included dementia, neurocognitive disorder with Lewy Bodies, and a need for assistance with personal care. A review of the facility's antibiotic usage report for May 2023 revealed she was ordered to receive Bactrim DS 800 -160 mg from 05/10/23 through 05/17/23 for the treatment of a Urinary Tract Infection (UTI). There was no organism recorded on the report to show what pathogen was causing her UTI. A review of an infection report for Resident #75 revealed the date symptoms were noticed was on 05/08/23. Symptoms included increased frequency/ urgency, dysuria, strong urine odor, and cloudy sediment in her urine. Under other comments, a urinalysis was indicated to have been obtained on 05/08/23 and results were obtained on 05/09/23. Under infection identification process, it was specified she had symptoms only. There was no indication a culture was done and organism was not identified. The section for infection management revealed Bactrim DS 800/ 160 mg was ordered BID for one week. A review of Resident #75's urinalysis report revealed nitrites were negative and 2+ Leukocyte Esterase was noted, which was abnormal. The urinalysis was not ordered to have a culture and sensitivity done with it so the organism involved was not identified and it was not clear if the antibiotic ordered was sufficient to properly treat her infection. A review of the McGeer's criteria used by the facility revealed UTI's without a catheter must have both criteria #1 and #2 met. In criteria #1, they must have at least one of the following, which included dysuria, fever or leukocytosis, and other symptoms. Criteria #2 must have at least 100,000 colonies/ milliliter of no more than two species of microorganisms in a voided urine sample or at least 100,000 colonies of any number of organisms in a specimen collected by in and out catheterization. On 06/29/23 at 1:35 P.M., an interview with RN #91 revealed their medical director did not usually order urinalysis to be completed when he suspected a resident had a UTI. He typically went by symptoms and just ordered the antibiotic he felt would be adequate to treat the infection. She stated even when a urinalysis was ordered he rarely ordered a culture and sensitivity to be done along with it. She acknowledged Resident #75 would not have met criteria for treatment of a UTI based on symptoms alone with out a urinalysis and culture being done to identify the presence of greater than 100,000 colonies of a microorganism being present in the urine sample. 3. A review of Resident #77's medical record revealed he was admitted to the facility on [DATE]. His diagnoses included a history of a stroke with hemiplegia and hemiparesis affecting his right dominant side, aphasia, difficulty walking, and need for assistance with personal care. A review of Resident #77's infection report revealed he had a symptom onset date of 06/13/23. The symptom section on the report indicated that he was having increased frequency/ urgency, pain, and hematuria. The section for the infection identification process revealed he had symptoms only. There was no indication a urine specimen had been obtained for a culture and no organisms were identified. The section for infection management revealed he was started on Bactrim DS BID for three days. Additional comments added revealed they were to continue the antibiotic per the resident's attending physician. A review of a urinalysis report for a urine specimen collected on 06/09/23 revealed his urine was positive for nitrites and Leukocyte Esterase. It was the final report and there was no indication that a culture was done to identify the organism involved or a sensitivity report to confirm whatever organism was present, it was susceptible to the antibiotic ordered. On 06/29/23 at 1:35 P.M., an interview with RN #91 confirmed there was not a culture and sensitivity (C&S) done as part of Resident #77's urinalysis. She acknowledged, without a C&S, it was not clear what organism was causing the resident's UTI or if the antibiotic ordered was effective in treating that infection. 4. A review of Resident #235's medical record revealed he was admitted to the facility on [DATE]. His diagnoses included a complete traumatic amputation of the left great toe, peripheral vascular disease, and atherosclerosis of a native artery of an unspecified extremity with gangrene. A review of the facility's infection control log for May 2023 revealed he was known to have a soft tissue skin infection with a date of onset as 05/30/23. He was started on both Levofloxacin and Doxycycline. The infection control log did not identify what organism was present that was causing the infection. A review of Resident #235's infection report revealed he had a date of onset as 05/30/23. Symptoms identified under skin included heat, swelling, and redness at the left great toe amputation incision site. Under the section for infection identification process, a specimen was indicated to have been collected for a culture on 05/30/23 at the podiatrist's office. There was no indication of what organism, if any, had been identified as a result of the culture obtained. The section for infection management indicated antibiotics were ordered by mouth that included Levofloxacin and Doxycycline. Additional comments indicated the antibiotics were to be continued per the attending physician. On 06/29/23 at 1:35 P.M., an interview with RN #91 revealed she did not receive a copy of the wound culture that had been obtained at the podiatrist's office as the infection report had indicated was collected on 05/30/23. She stated she called the podiatrist's office and requested the wound culture report, but it was never sent. She stated it was not uncommon for a wound culture to be done at another physician's office or the wound clinic that they could not get a hold of the results. She did not have access to the labs from the local hospital and was dependent on the physician's offices to send them to her. She acknowledged without those C&S reports she could not be certain the antibiotics ordered were effective in treating the organisms causing the infections. A review of the facility's Antibiotic Stewardship Program policy revised 10/24/22 revealed it was the policy of the facility to implement an antibiotic stewardship program as part of the facility's overall infection prevention and control program. The purpose of the program was to optimize the treatment of infections while reducing the adverse events associated with antibiotic use. The infection preventionist, with oversight from the DON, served as the leader of the antibiotic stewardship program and received support from the Administrator and other governing officials at the facility. The medical director and attending physicians were to support the program via active participation in developing, promoting, and implementing a facility-wide system for monitoring the use of antibiotics. The program included antibiotic use protocols and a system to monitor antibiotic usage. Antibiotic use protocols included laboratory testing being completed in accordance with current standards of practice. The facility was to use the McGeer's criteria to define infections. Antibiotics orders obtained from consulting, specialty, or emergency providers shall be reviewed for appropriateness.
Jun 2021 6 deficiencies
CONCERN (D)

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

Deficiency F0561 (Tag F0561)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and interview, the facility failed to honor one resident's bathing preference related to frequenc...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review and interview, the facility failed to honor one resident's bathing preference related to frequency and timeliness. This affected one of one resident (Resident #42) reviewed for choices. Findings Include: Review of Resident #42's medical record revealed an admission date of 03/25/21. Diagnoses included gastroparesis, end stage renal disease, congestive heart failure, anemia, diabetes mellitus, blindness, hypertension, malignant neoplasm of the left breast, insomnia osteoarthritis and major depressive disorder. Review of the resident's quarterly MDS 3.0 assessment dated [DATE] revealed the resident has clear speech, understood others, made herself understood and had no cognitive deficit as indicated by a BIMS score of 15. The resident was dependent on two staff for bathing. Review of the resident's preferences for customary routine and activities dated 03/30/21 revealed the resident prefers a shower daily on the P.M. shift. Review of the second floor shower schedule revealed the resident was scheduled for showers every Wednesday and Saturday on the 6:00 P.M. to 6:00 A.M. shift. Review of the resident's shower documentation from 03/25/21 through 06/08/21 revealed the resident was offered and/or provided a shower twice a week. On 06/07/21 at 9:45 A.M. interview with Registered Nurse (RN) verified the resident was not receiving showers as preferred on a daily basis. On 06/08/21 at 10:33 A.M. interview with the resident revealed she would prefer her shower during the 6:00 A.M. to 6:00 P.M. shift due to staff offering her a shower at 10:00 P.M. or after.
CONCERN (D)

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

Notification of Changes (Tag F0580)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interview and policy review, the facility failed to ensure the physician was notified of a residen...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interview and policy review, the facility failed to ensure the physician was notified of a resident's weight gain of two or more pounds in 24 hours in accordance to his plan of care. This affected one (Resident #63) of one residents reviewed for dialysis. Findings include: A review of Resident #63's medical record revealed he was admitted to the facility on [DATE]. His diagnoses included end stage renal disease, dependence on renal dialysis and congestive heart failure. A review of Resident #63's physician's orders revealed he was to be weighed daily. The order had been in place since 05/11/21. A review of Resident #63's care plans revealed he had a care plan in place chronic renal failure related to end stage renal disease requiring dialysis. The care plan was initiated on 05/11/21. One of the goals included the resident would not have any signs or symptoms of any complications related to fluid overload. The interventions included the need to monitor/ document/ report to the physician signs and symptoms of fluid overload to include a weight gain of over two pounds a day. A review of Resident #63's treatment administration record (TAR) for May 2021 revealed the resident's daily weights were to be recorded on the TAR. The start date for obtaining the daily weights was 05/12/21. Weights obtained on 05/13/21 and 05/14/21 reflected a weight gain of two or more pounds as the resident weighed 286.2 pounds on 05/13/21 and was 290.6 pounds on 05/14/21 (4.4 pounds). Weights obtained on 05/27/21 and 05/28/21, again showed a weight gain of greater than two pounds as the resident weighed 291.6 pounds on 05/27/21 and was 297.8 pounds on 05/28/21 reflecting a 6.2 pound weight gain. A review of Resident #63's nurse's progress notes from 05/13/21 through 05/27/21 revealed no evidence of the physician being notified of the resident's weight gains of two or more pounds between 05/13/21 to 05/14/21 and again 05/27/21 to 05/28/21. Findings were verified by Registered Nurse (RN) #100. On 06/03/21 at 10:42 A.M., an interview with RN #100 confirmed they did not have any evidence of Resident #63's physician being notified of the resident's weight gain of two or more pounds in 24 hours occurring on 05/14/21 and 05/28/21 as per his physician's orders and plan of care. A review of the facility's policy on notification of changes revised 10/20/20 revealed the purpose of the policy was to ensure the facility promptly consults the resident's physician when there was a change requiring notification. Circumstances requiring notification included a significant change in the resident's physical condition that may include clinical complications. They were also to notify the physician for circumstances that require the resident's treatment to be altered. A review of the facility's policy on care planning special needs for dialysis revised 10/30/20 revealed it was the facility's policy that they would provide the necessary care and treatment, consistent with the physician's orders and the comprehensive person centered care plan to meet special medical and nursing needs of residents receiving dialysis. Comprehensive care plans would be developed based on resident assessments, goals, and preferences in accordance with assessment and care plan procedures. Interventions would include documentation and monitoring of complications.
CONCERN (D)

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

Pressure Ulcer Prevention (Tag F0686)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, medical record review, staff interview and facility policy and procedure review, the facility failed to co...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, medical record review, staff interview and facility policy and procedure review, the facility failed to consistently and adequately assess one resident's Stage II (Partial thickness loss of dermis presenting as a shallow open ulcer with a red-pink wound bed, without slough or bruising. May also present as an intact or open/ ruptured blister.) pressure ulcer. This affected one of one resident (Resident #59) reviewed for pressure ulcers. The facility identified two residents with pressure ulcers. Findings Include: Review of Resident #59's medical record revealed an original admission date of 07/28/20 with the latest readmission of 02/21/21. Diagnoses included congestive heart failure, chronic obstructive pulmonary disease, chronic kidney disease, anemia, cardiomyopathy, atrial fibrillation, history of COVID-19, chronic pain, major depressive disorder, overactive bladder and insomnia. Review of the resident's quarterly MDS 3.0 assessment dated [DATE] revealed the resident had clear speech, sometimes understood others, sometimes made herself understood and had a severe cognitive deficit as indicated by a BIMS score of six. The resident required extensive assistance of two staff for bed mobility, transfers and toilet use. The resident was assessed as being at risk for skin breakdown and had an unhealed Stage II pressure ulcer. The facility implemented a pressure reducing device for bed, pressure ulcer care, application of non-surgical dressing and application of ointment/medications. Review of the resident's pressure ulcer scale dated 08/31/20 revealed a score of 16 indicating the resident was a low risk for skin breakdown. Review of the plan of care dated 07/28/20 revealed the resident had an actual skin impairment related to a pressure ulcer to coccyx and skin teat to left shin. Interventions included air mattress to bed, keep fingernails short, encourage geri-sleeves, encourage good nutrition and hydration. Follow facility protocols for treatment of pressure injury, keep skin clean and dry, use a draw sheet or lifting device to move resident and use caution during transfers and bed mobility to prevent striking hands against any sharp or hard surface. Review of the resident's monthly physician's orders for June 2021 identified orders dated 03/01/21 to monitor dressing to coccyx and ensure dressing is intact with the instructions to change as needed per order, cleanse area to coccyx with wound cleanser, pat dry, apply hydrogel with AG, and cover with hydrocolliod dressing every three days and as needed until resolved and 03/23/21 for an air mattress to bed with the special instructions to check placement weekly. Review of the skin and wound assessment dated [DATE] revealed the facility identified the resident had a Stage II pressure ulcer to her coccyx measuring 3.0 centimeters (cm) by 2.0 cm by 0.1 cm. The wound was described as being 100% granulation tissue. The facility implemented the treatment to cleanse the coccyx wound with wound cleanser, pat dry, apply hydrogel with alginate and cover with hydrocolloid dressing every three days and as needed until healed. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 2.0 cm by 1.5 cm by 0.1 cm and was 100% granulation tissue with serous drainage. The treatment was unchanged. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 1.2 cm by 0.8 cm by 0.1 cm and was 100% granulation tissue with serous drainage. The treatment was unchanged. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.8 cm by 0.8 cm by 0.1 cm and was 100% granulation tissue with serous drainage. The treatment was unchanged. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.8 cm by 0.8 cm by 0.1 cm and was 100% granulation tissue with serous drainage. The treatment was unchanged. Review of the medical record failed to provide a weekly skin assessment for the facility acquired Stage II pressure ulcer to the resident's coccyx. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.8 cm by 0.6 cm by 0.1 cm and was 80% granulation tissue with serous drainage. The assessment did not specify what the remaining 20% of wound bed was comprised of. There was no change to the treatment although the assessment indicated the wound had stalled in healing. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.3 cm by 0.7 cm with no depth. The assessment lacked a description of the wound, current treatment or the progress of the wound. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.2 cm by 0.5 cm with no depth measurement and was 100% granulation tissue and 10% slough. The wound was assessed as having a light amount of serous drainage. The assessment again indicated the wound had stalled in the healing process. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.6 cm by 0.4 cm with no recorded depth and was 100% granulation tissue with light serous drainage. The treatment was unchanged. The wound was assessed as being stable. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.2 cm by 0.1 cm by 0.1 cm and was 100% granulation tissue with light serous drainage. The treatment was unchanged. The wound was assessed as improving. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.5 cm by 0.4 cm by 0.1 cm and had granulation tissue with light serous drainage. The treatment was unchanged. The wound was assessed as being stalled. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.2 cm by 0.2 cm with no depth measurement and had granulation tissue with light serous drainage. The treatment was unchanged. The wound was not assessed for progress. Review of the skin and wound assessment dated [DATE] revealed the Stage II pressure ulcer measured 0.3 cm by 0.3 cm with no depth measurement and had granulation tissue with light serous drainage. The treatment was unchanged. The wound was assessed as being stable. On 06/03/21 at 2:15 P.M. observation of Registered Nurse (RN) #11 and Licensed Practical Nurses (LPN) #6 and #48 provide the physician ordered treatment to the resident's Stage II pressure ulcer to her coccyx revealed upon entry to the room the required supplies were set up on a barrier on the resident's bedside table. The staff washed their hands and donned disposable gloves. RN #11 and LPN #6 positioned the resident on her left side. LPN #48 removed the soiled dressing dated 06/02/21 and disposed of it in the trash. She washed her hands and donned a clean pair of gloves. She then cleansed the wound with wound cleanser and a 4X4, pat dry. She measured the wound with a single use paper wound measure at 0.5 cm by 0.3 cm by 0.1 cm. The wound was 100% granulation. She then washed her hands donned a clean pair of gloves applied the dermagel/AG with a sterile Q-tip and covered the wound with a hydrocolloid dressing. On 06/03/21 at 3:15 P.M. interview with RN #11 verified the lack of a weekly assessment for 04/06/21 and the lack of accuracy of the assessments. Review of the facility policy titled, Pressure Injury Prevention and Management, dated 10/30/20 revealed the facility is committed to the prevention of avoidable pressure injuries and the promotion of healing of existing pressure injuries. Assessments of pressure injuries will be performed by a licensed nurse and documented in the medical record.
CONCERN (D)

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

Deficiency F0698 (Tag F0698)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interview, and policy review, the facility failed to ensure a resident receiving dialysis, who had...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interview, and policy review, the facility failed to ensure a resident receiving dialysis, who had an order to be weighed daily, was weighed in accordance to his orders and plan of care and failed to follow the parameters included with the daily weight order by not notifying the physician when the resident had a weight gain of two or more pounds in 24 hours. They also failed to ensure the dialysis center completed the dialysis communication record to include a pre and post assessment of the resident's weights/ vital signs, medications received during his treatment and any other pertinent problems or complications that may have occurred during his dialysis treatment. This affected one (Resident #63) of one residents reviewed for dialysis. Findings include: A review of Resident #63's medical record revealed he was admitted to the facility on [DATE]. His diagnoses included end stage renal disease, dependence on renal dialysis, and congestive heart failure. A review of Resident #63's physician's orders revealed the resident had an order to be a daily weight. The order had been in place since 05/11/21. A review of Resident #63's care plans revealed he had a care plan in place for chronic renal failure related to end stage renal disease requiring dialysis. The care plan was initiated on 05/11/21. One of the goals included the resident would not have signs or symptoms of any complications related to fluid overload. The interventions included the need to monitor/ document/ report to the physician and signs or symptoms of a weight gain of over two pounds a day. The intervention was initiated on 05/11/21 as well. A review of Resident #63's treatment administration record (TAR) for May 2021 revealed the resident's daily weights were to be recorded on the TAR. The start date for the daily weights was 05/12/21. There was no evidence of a daily weight being obtained on the resident on 05/16/21, 05/18/21, 05/22/21, 05/23/21, 05/25/21 or on 05/26/21. Weights obtained on 05/13/21 and 05/14/21 reflected a weight gain of two or more pounds as the resident weighed 286.2 pounds on 05/13/21 and was 290.6 pounds on 05/14/21 (4.4 pounds). Weights again obtained on 05/27/21 and 05/28/21 showed a weight gain of greater than two pounds as the resident weighed 291.6 pounds on 05/27/21 and was 297.8 pounds on 05/28/21 reflecting a 6.2 pound weight gain. A review of Resident #63's weights recorded in his electronic health record under the vital signs tab confirmed weights were not obtained on the dates missing above. Weights reflecting a weight gain of two or more pounds was confirmed for 05/13/21 to 05/14/21 and again on 05/27/21 to 05/28/21. A review of Resident #63's nurse's progress notes from 05/13/21 through 05/27/21 revealed no evidence of the resident refusing to be weighed on the dates where his daily weights were not recorded. There was also no evidence of the physician being notified of the resident's weight gains of two or more pounds between 05/13/21 to 05/14/21 and again 05/27/21 to 05/28/21. A review of Resident #63's dialysis communication records scanned into the electronic health record revealed there were several dialysis communication records that were not completed by the dialysis center when the resident received his dialysis treatments on 05/19/21, 05/24/21, 05/28/21, and 05/31/21. The dialysis communication records for 05/19/21 and 05/24/21 did not include any documentation from the dialysis center pertaining to the resident's vital signs or weights pre and post dialysis treatments, the start and stop time of his dialysis treatments, an assessment of his shunt site, any pain or problems during his treatment or whether or not new orders were received and returned with the resident. The dialysis communication records for 05/28/21 and 05/31/21 only included pre and post vital signs and weights. Findings were verified by Registered Nurse (RN) #100. On 06/03/21 at 10:42 A.M., an interview with RN #100 confirmed they did not have any evidence of Resident #63's daily weights being obtained on the dates missing above. She also could not provide any documented evidence of the physician being notified of the resident's weight gain of two or more pounds in 24 hours occurring on 05/14/21 and 05/28/21 as per his physician's orders and plan of care. She confirmed the dialysis center did not complete and/ or include all the relevant information on the dialysis communication records that they should have when the resident received dialysis treatments. She denied anyone had reached out to the dialysis center to obtain that information when the resident returned to the facility with the incomplete dialysis communication records. A review of the facility's policy on care planning special needs for dialysis revised 10/30/20 revealed the facility would provide the necessary care and treatment, consistent with professional standards of practice, physician's orders, the comprehensive person-centered care plan, and the resident's goals and preferences, to meet the special medical and nursing needs of residents receiving dialysis. Comprehensive care plans would be developed based on resident assessments, goals, and preferences in accordance with assessment and care plan procedures. The care plan would reflect the coordination between the facility and the dialysis provider and would identify nursing home and dialysis responsibilities. Interventions would include documentation and monitoring of any complications, pre and post weights, assessing/ observing/ documenting care of access sites, lab tests, vital signs and the provisions of medications on dialysis treatment days, such as which medications were administered during dialysis, held prior to dialysis, given prior to dialysis or administered by dialysis staff. Nursing staff was to provide a report to the dialysis provider regarding the resident's condition and treatment provisions each dialysis treatment day. If no written report was received upon return from dialysis, nursing staff would call the dialysis provider to receive a report.
CONCERN (D)

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

Drug Regimen Review (Tag F0756)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Review of the medical record for Resident #57 revealed an admission date of 10/05/18. Diagnoses included dementia with behavi...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Review of the medical record for Resident #57 revealed an admission date of 10/05/18. Diagnoses included dementia with behavioral disturbances, cognitive communication deficit, and aneurysm of the carotid artery. Review of Resident #57's quarterly Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed a Brief Interview for Mental Status (BIMS) score of 08 indicating a moderately impaired cognition for decision making abilities. Resident #57 was noted to express verbal behaviors directed towards others. Resident #57 required extensive assistance from two staff members for bed mobility, transfers, dressing, and toilet use. Review of Resident #57's physician orders for May 2021 revealed: -Protonix (proton pump inhibitor to treat reflux disease) 40 milligram (mg) tablet, give daily for heartburn, -Tagament (antacid to reduce acis in the stomach) 200 mg tablet, give one tablet, twice a day for sexual behaviors. Review of the pharmacy recommendation dated 07/16/20 revealed, This resident has been taking Tagament 200 mg, three times a day for behaviors since August 2019. Please evaluate the current dose and consider a dose reduction. Continued review of this pharmacy recommendation revealed no evidence of the physician reviewing or addressing the recommendations for this medication. Review of the pharmacy recommendation dated 09/17/20 revealed, The use of acid-suppressive therapy, particularly Proton Pump Inhibitor (PPI) is associated with an increased risk of community-acquired clostridium difficile colitis (C-Difficile). There is also an association in risk with non-steroidal anti-inflammatory drug use. The incidence of C-difficile for residents on PPIs was shown to be three time normal. Please evaluate continued need for therapy and consider discontinuing Protonix. (Note-resident is also taking Tagament for increased sexual behaviors.) Continued review of this recommendation revealed no evidence of the physician reviewing or addressing the recommendation for this medication. Interview on 06/03/21 at 2:30 P.M. with Registered Nurse (RN) #11 revealed a Pharmacist will review all of the residents medication orders and if there is a concern with their current medication, then the pharmacist will make recommendation of possible changed to be make to that medication. RN #11 stated the facility will receive a print out of all the residents who were reviewed along with a list of residents who did not have any recommendations for that months. For the resident who did have recommendations, there is a sheet called, :Consultant Pharmacist's Medication Regimen Review. This paper will have the residents information on it and the exact medication that the recommendations is pertaining to. The medication order is listed followed by what the new recommended order should be or if the medication should be discontinued. The facility physician will review all of the recommendations for that current month which is normally within 10 days. The physician can either agree, disagree, or suggest other, to the medication recommendations. The physician will them either write a new order for the medications or comments why a change was not made. RN #11 confirmed Resident #57 was still currently taking the medication, Tagament, and Protonix. RN #11 also confirmed there was no evidence of the physician addressing or making any charges to Resident #57's orders in regards to the medications Tagament or Protonix. Review of the facility policy titled, Addressing Medication Regimen Review Irregularities,: dated 01/01/21 revealed , It is the policy of the facility to provide a Medication Regimen Review (MRR) for each resident in order to identify irregularities and respond to those irregularities in a timely manner to prevent the occurrence of an adverse drug event. Based on medical record review and staff interview, the facility failed to ensure pharmacy recommendations for one resident contraindicated gradual dose reduction (GDR) contained a clinical rationale and one resident's pharmacy recommendation was addressed by the physician. This affected two of five residents (Residents #28 and #57) reviewed for unnecessary medications. Findings Include: 1. Review of Resident #28's medical record revealed an admission date of 03/06/19. Diagnoses included dementia with lewy bodies, diabetes mellitus, atrophy of thyroid, early onset cerebellar ataxia, white matter disease, lupus anticoagulant syndrome, hypertension, mood disorder, major depressive disorder, anxiety disorder, dementia with behavioral disturbances and personality change due to known physiological condition. Review of the resident's comprehensive MDS 3.0 assessment dated [DATE] revealed the resident had clear speech, sometimes understood others, sometimes made herself understood and had a severe cognitive deficit. Review of the mood and behavior revealed the resident displayed physical and verbal behaviors towards others and wandered. The assessment indicated the resident received antipsychotic, antianxiety and antidepressant medications. The resident received the medications on a regular basis and the last GDR was attempted on 10/17/19. Review of the monthly physician's orders for June 2021 identified orders dated 03/06/19 for Remeron 15 milligrams (mg) by mouth one time a day for depression, Pristiq 50 mg by mouth one time a day for depression, 06/29/19 Xanax 0.5 mg by mouth two times a day for anxiety and give 1 mg two tablets by mouth at bedtime for depression, 09/30/19 Trazadone 125 mg by mouth at bedtime for insomnia and 10/02/20 Risperdal 0.5 mg by mouth two times a day for mood disorder. Review of the pharmacy recommendation dated 03/18/20 revealed the pharmacist recommended to decrease the medication Trazadone 125 mg by mouth due to receiving the medication since 09/19. The physician addressed the recommendation on 03/20/20 and disagreed documenting, the family refuses. Review of the pharmacy recommendation dated 06/25/20 revealed the pharmacist recommended a gradual dose reduction for the medication Trazadone 125 mg. The physician addressed the recommendation documented, the resident was doing well and daughter refused the reduction. Review of the pharmacy recommendation dated 09/17/20 revealed the pharmacist recommended to decrease the medication Remeron used for an appetite stimulant since 03/19. The physician addressed the recommendation on 09/22/20 and documented uses for appetite, would do more harm than good. Review of the recommendation dated 02/28/21 revealed the pharmacist recommended a GDR for the medication Pristiq 50 mg daily. The physician addressed the recommendation on 03/02/21 and declined the recommendation and documented, behaviors improved, family doesn't want this discontinued. Review of the recommendation dated 02/28/21 revealed the pharmacist recommended a GDR on the medication Risperdal 0.5 mg by mouth twice daily. The physician addressed the recommendation on 03/02/21 and documented, would do more harm then good. Review of the pharmacy recommendation dated 05/27/21 revealed the pharmacist recommended a GDR on the medication Xanax 0.5 mg by mouth twice a day. The physician addressed the recommendation on 06/03/21 and declined the recommendation documenting, patient currently stable, no changes at this time. On 06/07/21 at 3:00 P.M. interview with Registered Nurse (RN) verified the physician had not provided a rationale for the decline for the pharmacy recommended GDR for the medications antipsychotropic medications.
CONCERN (E)

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

Antibiotic Stewardship (Tag F0881)

Could have caused harm · This affected multiple residents

Based on medical record review, staff interview, review of Food and Drug Administration (FDA) information, review of a Health Day News Study, and facility policy and review, the facility failed to pro...

Read full inspector narrative →
Based on medical record review, staff interview, review of Food and Drug Administration (FDA) information, review of a Health Day News Study, and facility policy and review, the facility failed to provide adequate justification for the use of antibiotics for COVID-19 positive residents. This affected 17 residents (Residents #1, #2, #3, #4, #10, #20, #22, #24, #27, #32, #49, #50, #53, #55, #56, #60 and #61) of 56 residents who were COVID-19 positive. Findings Include: Review of medical records of Residents #1, #2, #3, #4, #10, #20, #22, #24, #27, #32, #49, #50, #53, #55, #56, #60 and #61 from 01/18/21 to 02/28/21 revealed the residents received the antibiotic Azithromycin prior to the results of a positive COVID-19 test result. There was also no documentation or evidence to support McGeer's criteria or any other assessment was utilized to determine if an antibiotic should be prescribed and administered; it was simply used for the symptoms of COVID-19. On 06/08/21 at 2:58 P.M. interview with Registered Nurse (RN) #53 verified the facility treated residents who were COVID-19 positive with the antibiotic Azithromycin. Additionally she confirmed the course of Azithromycin was completed when the positive COVID-19 results were received. Review of information on the FDA website (https://www.fda.gov) revealed the following FDA response to the question, Are antibiotics effective in preventing or treating COVID-19? No. Antibiotics do not work against viruses; they only work on bacterial infections. Antibiotics do not prevent or treat COVID-19, because COVID-19 is caused by a virus, not bacteria. Some patients with COVID-19 may also develop a bacterial infection, such as pneumonia. In that case, a health care professional may treat the bacterial infection with an antibiotic. In addition, an article from HealthDay News, dated 08/04/20 revealed the following: Early in the U.S. coronavirus pandemic, many people landing in the hospital may have been given unnecessary antibiotics, a new study suggests. The findings come from one of the hard-hit hospitals in New York City, the initial epicenter of the U.S. pandemic. Researchers there found that of COVID-19 patients admitted between March and May, just over 70% were given antibiotics. That's despite the fact that COVID-19 is caused by a virus, and very few of those patients actually had a coexisting bacterial infection. Antibiotics kill bacteria, but are useless against viral infections such as the common cold, the flu and COVID-19. Review of the facility Antibiotic Stewardship Infection Control Program, dated 11/28/17 revealed the program promotes the appropriate use of antimicrobials, including antibiotics, improves outcomes, reduces microbial resistance and decreases the spread of infections by multidrug-resistant organisms.
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
  • • 25% annual turnover. Excellent stability, 23 points below Ohio's 48% average. Staff who stay learn residents' needs.
Concerns
  • • 21 deficiencies on record, including 1 serious (caused harm) violation. Ask about corrective actions taken.
  • • $57,263 in fines. Extremely high, among the most fined facilities in Ohio. Major compliance failures.
  • • Grade D (48/100). Below average facility with significant concerns.
Bottom line: Trust Score of 48/100 indicates significant concerns. Thoroughly evaluate alternatives.

About This Facility

What is Arbors At Gallipolis's CMS Rating?

CMS assigns ARBORS AT GALLIPOLIS an overall rating of 3 out of 5 stars, which is considered average nationally. Within Ohio, this rating places the facility higher than 0% of the state's 100 nursing homes. This mid-range rating indicates the facility meets federal standards but may have areas for improvement.

How is Arbors At Gallipolis Staffed?

CMS rates ARBORS AT GALLIPOLIS's staffing level at 4 out of 5 stars, which is above average compared to other nursing homes. Staff turnover is 25%, compared to the Ohio average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Arbors At Gallipolis?

State health inspectors documented 21 deficiencies at ARBORS AT GALLIPOLIS during 2021 to 2025. These included: 1 that caused actual resident harm and 20 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Arbors At Gallipolis?

ARBORS AT GALLIPOLIS 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 ARBORS AT OHIO, a chain that manages multiple nursing homes. With 99 certified beds and approximately 84 residents (about 85% occupancy), it is a smaller facility located in GALLIPOLIS, Ohio.

How Does Arbors At Gallipolis Compare to Other Ohio Nursing Homes?

Compared to the 100 nursing homes in Ohio, ARBORS AT GALLIPOLIS's overall rating (3 stars) is below the state average of 3.2, staff turnover (25%) is significantly lower than the state average of 46%, and health inspection rating (3 stars) is at the national benchmark.

What Should Families Ask When Visiting Arbors At Gallipolis?

Based on this facility's data, families visiting should ask: "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?"

Is Arbors At Gallipolis Safe?

Based on CMS inspection data, ARBORS AT GALLIPOLIS 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 3-star overall rating and ranks #100 of 100 nursing homes in Ohio. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Arbors At Gallipolis Stick Around?

Staff at ARBORS AT GALLIPOLIS tend to stick around. With a turnover rate of 25%, the facility is 21 percentage points below the Ohio average of 46%. Low turnover is a positive sign. It means caregivers have time to learn each resident's needs, medications, and personal preferences. Consistent staff also notice subtle changes in a resident's condition more quickly. Registered Nurse turnover is also low at 15%, meaning experienced RNs are available to handle complex medical needs.

Was Arbors At Gallipolis Ever Fined?

ARBORS AT GALLIPOLIS has been fined $57,263 across 2 penalty actions. This is above the Ohio average of $33,652. Fines in this range indicate compliance issues significant enough for CMS to impose meaningful financial consequences. Common causes include delayed correction of deficiencies, repeat violations, or care failures affecting resident safety. Families should ask facility leadership what changes have been made since these penalties.

Is Arbors At Gallipolis on Any Federal Watch List?

ARBORS AT GALLIPOLIS 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.