AVENTURA AT HUMILITY HOUSE

755 OHLTOWN ROAD, AUSTINTOWN, OH 44515 (330) 505-0144
For profit - Limited Liability company 70 Beds AVENTURA HEALTH GROUP Data: November 2025
Trust Grade
45/100
#217 of 913 in OH
Last Inspection: April 2025

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

Overview

Aventura at Humility House has a Trust Grade of D, indicating below-average performance with some concerns about care and oversight. They rank #217 out of 913 nursing homes in Ohio, placing them in the top half, and #13 out of 29 in Mahoning County, meaning only a few local options are better. The facility appears to be improving, having reduced issues from 8 in 2024 to 5 in 2025, although they still have a concerning staff turnover rate of 64%, which is higher than the state average. While the facility has not incurred any fines, there have been serious incidents, including a resident who developed a Stage IV pressure ulcer due to inadequate care and another who did not receive necessary therapy interventions, leading to avoidable declines in mobility. On a positive note, the facility achieved a 5/5 rating for quality measures, indicating strong performance in overall care metrics.

Trust Score
D
45/100
In Ohio
#217/913
Top 23%
Safety Record
High Risk
Review needed
Inspections
Getting Better
8 → 5 violations
Staff Stability
⚠ Watch
64% turnover. Above average. Higher turnover means staff may not know residents' routines.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most Ohio facilities.
Skilled Nurses
○ Average
Each resident gets 33 minutes of Registered Nurse (RN) attention daily — about average for Ohio. RNs are the most trained staff who monitor for health changes.
Violations
⚠ Watch
36 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★★★☆
4.0
Overall Rating
★★★☆☆
3.0
Staff Levels
★★★★★
5.0
Care Quality
★★★☆☆
3.0
Inspection Score
Stable
2024: 8 issues
2025: 5 issues

The Good

  • 5-Star Quality Measures · Strong clinical quality outcomes
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record

Facility shows strength in quality measures, fire safety.

The Bad

Staff Turnover: 64%

18pts above Ohio avg (46%)

Frequent staff changes - ask about care continuity

Chain: AVENTURA HEALTH GROUP

Part of a multi-facility chain

Ask about local staffing decisions and management

Staff turnover is elevated (64%)

16 points above Ohio average of 48%

The Ugly 36 deficiencies on record

4 actual harm
Aug 2025 1 deficiency
CONCERN (F) 📢 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

Menu Adequacy (Tag F0803)

Could have caused harm · This affected most or all residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, interview, review of the food committee meeting minutes and review of the facility policy, ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, interview, review of the food committee meeting minutes and review of the facility policy, the facility failed to ensure dietary menus were followed. This affected one (Resident #13) of three reviewed for dietary concerns and had the potential to affect all residents receiving meals from the kitchen. The facility identified one (Resident #45) who did not consume anything by mouth. The facility census was 66. Findings include:Review of the medical record for Resident #13 revealed an admission date of 09/08/23 with diagnoses including diabetes, high cholesterol, arthritis and chronic pain. Review of the quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #13 was cognitively intact. She was independent in eating, required supervision for oral hygiene and showers, partial assistance for personal hygiene and substantial assistance for toileting. Review of the food committee meeting minutes dated 07/03/25 revealed the residents were concerned the menu did not always match the meal being served. Review of the posted menu for breakfast dated 08/15/25 revealed breakfast would consist of hot or cold cereal, breakfast quiche and milk or juice. Observation of tray line on 08/15/25 at 7:37 A.M. revealed breakfast was being served which consisted of hot or cold cereal, scrambled eggs, yogurt and donuts. Interview at the time of the observation with Dietary Manager #200 revealed he had to make some changes to the breakfast menu at the last minute. He revealed the changes had not been corrected on the master menu. Interview on 08/15/25 at 8:12 A.M. with Resident #13 revealed she did not get to choose what she wanted for breakfast, she was given whatever the kitchen served. She revealed she would prefer to know ahead of time what was being served, and she confirmed today's breakfast consisted of scrambled eggs and a doughnut. Interview 08/15/25 and 8:21 A.M. with the Administrator confirmed there were issues with the facility following menus as posted. She verified this morning's breakfast menu should have been corrected and provided to residents when changes were made. Review of the facility policy titled Displaying the Menu, dated 2023, revealed planned menus would be posted each week in an area where residents could view them and the food and nutrition services staff were responsible for posting revisions to the plan the menu in a timely manner. This deficiency represents noncompliance investigated under Master Complaint Number 1344519 (OH00167046).
Apr 2025 4 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

Pressure Ulcer Prevention (Tag F0686)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interview, review of hospital paperwork, and review of facility polices, the facility failed to implemen...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interview, review of hospital paperwork, and review of facility polices, the facility failed to implement an adequate and effective pressure ulcer prevention program for Resident #168. This affected one Resident #168 of two residents reviewed for pressure ulcers. The facility census was 68. Actual Harm occurred on 02/03/25 when Resident #168 developed an in-house acquired Stage IV pressure ulcer (Full thickness tissue loss with exposed bone, tendon or muscle. Slough may be present on some parts of the wound bed. Often include undermining and tunneling.) to the right leg from an Ace wrap and immobilizer brace. Resident #168 was admitted to the facility from the hospital on [DATE] with an Ace wrap and a knee immobilizer brace on his right leg. There were no orders on admission to manage the right knee immobilizer brace and/or the Ace wrap. The admitting nurse documented that the unit manager was to clarify the order with the orthopedic physician on 01/24/25, and no orders were obtained. There was no documented evidence that the orthopedic physician was called for orders during Resident #168's 12-day stay at the facility. The Ace wrap and leg brace were never removed from Resident #168's leg from admission on [DATE]. Resident #168 was sent to the emergency room on [DATE] with red and yellow drainage draining from his right leg under the Ace wrap and right knee immobilizer brace and was diagnosed with an infected Stage IV pressure ulcer at the hospital. Findings include: Review of the medical record for Resident #168 revealed an admission date of 01/23/25 and a discharge date of 02/03/25. Diagnoses included spontaneous rupture of extensor tendons of the right thigh, chronic kidney disease, type two diabetes mellitus, and congestive heart failure. Review of the orthopedic note from his hospital stay dated 01/22/25 revealed Resident #168 had a spontaneous rupture of his right thigh tendons. Due to Resident #168's age and comorbidities an Ace wrap and knee brace were ordered for his right leg as well as rehabilitation. Review of the after-visit summary from Resident #168's hospital discharge date d 01/23/25 revealed the resident was to be admitted to the facility for rehabilitation. No orders to maintain his right leg knee brace and Ace wrap were included. Review of the admission assessment dated [DATE] revealed Resident #168 had multiple ecchymotic (bruises) areas on his bilateral arms and legs. The nurse was unable to fully assess Resident #168 due to an Ace wrap and brace intact to his right leg. Review of the pressure ulcer risk scale completed on admission revealed Resident #168 was at risk for developing pressure ulcers. Review of the physician's order dated 01/23/25 and discontinued on 01/24/25 revealed Ace wrap and immobilizer brace to remain on right leg until orders clarified with the orthopedic doctor by the unit manager. Review of further orders revealed no clarification order and/or orders for monitoring Resident #186's skin for pressure from the Ace wrap and immobilizer brace to the right leg. Review of the baseline care plan and care plan dated 01/23/25 revealed no skin focus areas and no skin interventions and no baseline care plan related to the use of the Ace wrap and immobilizer brace to the right leg. Review of the wound physician note from 01/29/25 revealed Resident #168 had bilateral heel blisters and treatments were put into place for both heels to be cleansed with Dakin's solution (topical antiseptic), apply Skin Prep (forms a film to reduce friction) to the border, apply hydrogel (promote healing by providing moisture), and covered with bordered gauze daily and as needed. During that visit Resident #168 refused to have the wound physician remove his ace wrap and immobilizer brace. There was no follow-up after that encounter. Review of the five-day Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #168 had moderate cognitive impairment. Resident #168 had lived independently prior to his hospitalization and now required set-up to moderate assistance for all activities of daily living. Resident #168 was at risk for developing pressure ulcers but did not have one at the time of the assessment. Review of the medical record and therapy notes, revealed no documented evidence in the medical record during Resident #168's 12-day stay that staff monitored the resident's skin, checked pedal pulses, monitored for edema, and monitored for pain related to the right knee immobilizer brace and Ace wrap to the right leg. There was also no documented evidence staff attempted to call the orthopedic physician at any time to get orders for the right knee immobilizer brace and Ace wrap to the right leg that Resident #168 was admitted to the facility with. Review of the nurse's note dated 02/03/25 at 1:10 P.M. revealed therapy notified the nurse that Resident #168 was bleeding from his right leg under his surgical dressing. No orders had been given to change the dressing. The physician and family were notified, and Resident #168 was sent to the emergency room. Review of the nurse's note dated 02/03/25 at 6:01 P.M. revealed Resident #168 was still in the emergency room and being admitted with a diagnosis of wound infection. Review of the emergency room paperwork dated 02/03/25 revealed Resident #168 presented to the emergency room from a nursing home where Resident #168 was said to have pus coming from a surgical wound. Resident #168 denied ever having surgery recently and stated he realized he had a wound. He was diagnosed with chronic decubitus ulcers on bilateral heels, large ulcer on right anterior knee, and large ulcers on the posterior calf. The paperwork stated to see pictures. Review of the picture of the anterior right knee wound revealed edges dry, base had slough and eschar with visible tendon and bone. The right posterior knee wound was macerated with full skin thickness loss. Resident #168 was admitted to the hospital with a diagnosis of wound infection and had to receive intravenous antibiotics and wound care. Interview on 04/01/25 at 5:10 P.M. with the Director of Nursing (DON) confirmed when Resident #168 was admitted , the admitting nurse placed an order for the unit manager to clarify whether the right knee immobilizer brace and Ace wrap could be removed in the morning. The unit manager never clarified the order, and Resident #168's right knee immobilizer brace and Ace wrap was never removed during his 12-day stay. The DON reported when Resident #168 began bleeding from his right leg where the immobilizer brace and Ace wrap were intact, he had developed a pressure ulcer (Stage IV) from the brace that had become infected, and he was admitted to the hospital. The DON also confirmed Resident #168's family did not send him back to the facility after the hospitalization. She verified that no staff attempted to clarify the orders with the orthopedic physician, and no staff assessed Resident #168's skin, pedal pulses, pain, and/or monitored for edema at any point during the 12-day stay. Review of the facility policy titled Prevention of Pressure Injuries, revised September 2022, revealed that medical devices will be monitored regularly for comfort and signs of pressure related injuries and for prevention measures associated with specific devices, consult clinical practice guidelines. This deficiency represents noncompliance investigated under Complaint Numbers OH00162679 and OH00162590.
CONCERN (D)

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

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interview and review of the facility policies, the facility failed to maintain an accurate care plan for...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interview and review of the facility policies, the facility failed to maintain an accurate care plan for Residents #35 and #168 related to their care needs. This affected two resident (#35 and #168) reviewed for care planning. The facility census was 68. Findings include: 1. Review of the medical record for Resident #35 revealed an admission date of 01/01/25. Diagnoses included chronic respiratory failure with hypoxia, congestive heart failure, orthostatic hypertension, and chronic kidney disease stage V. Review of the quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #35 had intact cognition. Resident #35 required moderate assistance for all activities of daily living. Review of the care plan dated 03/17/25 revealed Resident #35 had peritoneal dialysis with a potential for infection. Interventions included educating the resident on diet restrictions and providing the diet as ordered. No interventions were found to assist the resident with the dialysis, how to troubleshoot if problems arise, and weight monitoring. Review of the physician's order dated 04/01/25 revealed that Resident #35 was to manage his daily peritoneal dialysis. Interview on 04/01/25 at 5:10 P.M. with Licensed Practical Nurse (LPN) MDS Coordinator #500 and the Director of Nursing (DON) confirmed Resident #35 had no interventions related to his peritoneal dialysis. They confirmed that the staff was trained and so was Resident #35. They reported that the dialysis center does have an emergency hotline for problems for the staff to use. Review of the undated facility policy peritoneal dialysis revealed staff must monitor the residents for the following problems associated with renal failure and/or dialysis. To include fluid and electrolyte imbalance, cardiovascular/hemodynamic instability, pain, infection, altered nutrition, and immobility. 2. Review of the medical record for Resident #168 revealed an admission date of 01/23/25 and a discharge date of 02/03/25. Diagnoses included spontaneous rupture of extensor tendons of the right thigh, chronic kidney disease stage three, type two diabetes mellitus, and congestive heart failure. Review of the five-day MDS assessment dated [DATE] revealed Resident #168 had moderate cognitive impairment. Resident #168 required moderate assistance for all activities of daily living. Resident #168 was identified as being at risk for developing pressure ulcers but did not have any at the time of the assessment. Review of the baseline care plan and care plan dated 01/23/25 revealed no skin interventions and no focus of skin breakdown. Review of the hospital paperwork dated 02/03/25 revealed Resident #168 was discharged to the emergency room and was diagnosed as having two stage IV pressure ulcers (Full thickness tissue loss with exposed bone, tendon or muscle. Slough may be present on some parts of the wound bed. Often include undermining and tunneling.) on his anterior and posterior knee where a leg brace was in place and bilateral unstageable heel pressure ulcers full thickness tissue loss in which the base of the ulcer is covered by slough (yellow, tan, gray, green or brown) and/or eschar (tan, brown or black) in the wound bed.) Interview on 04/01/25 at 5:10 P.M. with LPN/MDS Coordinator #500 and the DON confirmed that Resident #168 had no skin interventions in either of his care plans. Review of the facility policy titled Prevention of Pressure Injuries, revised September 2022, revealed that medical devices will be monitored regularly for comfort and signs of pressure related injuries and for prevention measures associated with specific devices, consult clinical practice guidelines.
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 record review, interview and facility policy review, the facility failed obtain daily weights as ordered by the physici...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, interview and facility policy review, the facility failed obtain daily weights as ordered by the physician for Resident #12 who had a diagnosis of congestive heart failure (CHF). This affected one resident (#12) of three residents reviewed for quality of care. The facility census was 68. Findings include: Review of Resident #12's medical record revealed an admission date of 02/21/25 with medical diagnosis including CHF, chronic embolism and thrombosis of the femoral vein, cerebral infarction, occlusion of the left carotid artery, pulmonary hypertension, Bell's Palsy, dysphasia, chronic kidney disease stage four (CKD), Alzheimer's disease, hypertension, and multiple myeloma. Review of Resident #12's plan of care start date 02/21/25 revealed nutritional risk related to CHF. Interventions included labs as ordered, recording and monitoring weights. Review of the Minimum Data Set (MDS) 3.0 admission assessment dated [DATE] revealed Resident #12's cognition was severely impaired. Resident #12 did not reject care and had no behavior symptoms. Resident #12 required minimal assistance with toilet hygiene and personal hygiene. Supervision or touching assistance was required to roll left and right in bed, sit on the side of the bed, lie back on the bed. Moderate assistance to stand from sitting, bed transfers and toilet transfers. Resident #12 was dependent on staff to walk ten feet and was always incontinent of urine. The resident was short of breath with exertion, and short of breath when lying flat. Resident #12 was on a therapeutic diet and was on an anticoagulant medication, antibiotic medication, antiplatelet medication, and anticonvulsant medication. Resident #12 received chemotherapy and oxygen therapy. Review of Resident #12's physician order dated 03/17/25 revealed an order for daily weight in the A.M. (before breakfast due to CHF and chronic kidney disease, notify the doctor of weight gain of three pounds or more in a day or five pounds in a week. Review of Certified Nurse Practitioner (CNP) #601's progress note dated 03/19/25 revealed Resident #12 was receiving skilled care after returning from the hospital. Resident #12 was in the hospital from [DATE] to 03/17/25 for dementia, weakness, and right arm swelling. Resident #12 was seen by the CHF team, infectious disease, nephrology and the vascular team in the hospital. The assessment and plan included acute on chronic CHF, follow weights and vital signs. Continue with Bumex (diuretic) and isosorbide (vasodilator to treat cardiac disease) and follow the CHF clinic recommendations. Review of Resident #12's weights in the medical record, including the medication administration record (MAR) and treatment administration record (TAR), included: • 03/18/25 at 6:18 A.M. 106.4 pounds • 03/19/25 at 6:17 A.M. 106.2 pounds • 03/20/25 at 6:00 A.M.108.2 pounds • 03/21/25 at 6:34 A.M. 104.8 pounds • 03/22/25 no documented evidence Resident #12's weight was obtained • 03/23/25 no documented evidence Resident #12's weight was obtained • 03/24/25 no documented evidence Resident #12's weight was obtained • 03/25/25 no documented evidence Resident #12's weight was obtained • 03/26/25 no documented evidence Resident #12's weight was obtained • 03/27/25 at 7:16 A.M. 104.0 pounds • 03/28/25 at 6:10 A.M. 104.6 pounds • 03/29/25 at 7:44 A.M. 104.2 pounds • 03/30/25 no documented evidence Resident #12's weight was obtained • 03/31/25 no documented evidence Resident #12's weight was obtained Interview on 04/01/25 at 9:17 A.M. with Licensed Practical Nurse (LPN) #589 revealed weekly weights and daily weights were done by the nursing assistant and documented in the electronic medical record for residents who have an order, and the weights would show in the MAR and TAR. Resident #12 needed her weight to be monitored due to CHF, fluid retention, and because Resident #12 attended the CHF clinic. Resident # 12 seldom rejected care and was very cooperative. LPN #589 verified a physician order for daily weights was on 03/18/25 and verified weights were not obtained on 03/22/25, 03/23/25, 03/24/25, 03/25/25, 03/26/25, 03/30/25 and 03/31/25. LPN #589 stated the daily weights were not obtained, and Resident # 12 was in the facility. Interview on 04/01/25 at 9:26 A.M. Resident #12 stated, I think I am supposed to get weighed, but I cannot remember the last time I was weighed. Interview on 04/01/25 at 9:29 A.M. with Certified Nursing Assistant (CNA)#600 revealed the nurse aide would know a weight needed to be obtained by reviewing the paper care plan in the morning. The nurse aide could enter the weight into the resident's electric medical record. Interview 04/02/25 at 4:25 P.M. with the Director of Nursing (DON) verified weights were not obtained on 03/22/25, 03/23/25, 03/24/25, 03/25/25, 03/26/25, 03/30/25 and 03/31/25. Review of the facility policy titled Weight Assessment and Intervention, revision date August 2022, revealed weights were recorded in each unit's weight record and individual medical record. Review of the facility policy titled Heart Failure, revision date November 2018, revealed the physician would review and make recommendations for relevant aspects of nursing care such as how often and what weights to monitor and when to report to the physician.
CONCERN (E)

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

Deficiency F0847 (Tag F0847)

Could have caused harm · This affected multiple residents

Based on review of the facility arbitration agreement and interview, the facility failed to clearly state that residents or their representatives could consult with local, state, or federal officials ...

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Based on review of the facility arbitration agreement and interview, the facility failed to clearly state that residents or their representatives could consult with local, state, or federal officials before signing or within thirty days of signing the agreement. This affected Residents #3, #12, #14, #16, #21, #24, #26, #29, #32, #35, #38, #41, #43, #45, #49, #50, #52, #53, #58, #61, #62, and #119 who signed the arbitration agreement. The facility census was 68. Findings include: Review of the arbitration agreement, undated, revealed that disputes not to be arbitrated include any communications with federal, state, or local officials, including but not limited to, federal and state surveyors, other federal or state health department employees, and representatives of the Office of the State Long-Term Care Ombudsman. The agreement also stated that the resident or authorized representative has the right to cancel this agreement by notifying the facility in writing. Such notice must be sent via certified mail to the attention of the administrator of the facility, and the notice must be post marked within sixty days of the date upon which this agreement was signed. The agreement also did not state that the residents or their representative could reach out to federal, state, or local officials before signing just that they could seek legal counsel before signing. Interview on 04/02/25 at 9:55 A.M. with Admissions #509 confirmed that she does go over every arbitration agreement when the residents are admitted . She confirmed that the arbitration agreement does state that disputes involving communication with federal, state, or local officials would not go to arbitration based on the wording. She reported she was unaware that residents or their representatives could reach out to federal, state, or local officials before signing the agreement. Admissions #509 also confirmed that residents or their representatives have sixty days to rescind the agreement after signing it by mail.
Aug 2024 3 deficiencies
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

Quality of Care (Tag F0684)

Could have caused harm · This affected 1 resident

Based on observation, interview, medical record review, and review of facility policy, the facility failed to ensure wound care was completed per physician orders for one resident (Resident #10) of th...

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Based on observation, interview, medical record review, and review of facility policy, the facility failed to ensure wound care was completed per physician orders for one resident (Resident #10) of three residents who were reviewed for appropriate wound care services. The facility census was 68. Findings include: Review of the medical record for Resident #10 revealed an admission date of 03/04/24 with diagnoses including acute and chronic respiratory failure, cardiomegaly, sleep related hypoventilation, systolic and diastolic congestive heart failure, hypertension, atrial fibrillation, stage three chronic kidney disease, glaucoma, pleural plaque with asbestos, venous insufficiency, and lymphedema. Review of the quarterly Minimum Data Set (MDS) 3.0 assessment revealed Resident #10 had intact cognition, had an impairment on one side of his upper extremities, and was dependent on a wheelchair for locomotion. Further review of the MDS revealed Resident #10 was dependent on staff for toileting, bathing, dressing his lower extremities, and personal hygiene. Review of the care plan initiated 03/18/24 revealed Resident #10 was at risk for impaired skin integrity related to respiratory failure and poor mobility. Interventions included application of appropriate wound dressings per wound doctor orders, assessments of wounds with each dressing change, elevation of legs to promote circulation and decrease fluid build-up, and appropriate wound management based on the stages of healing. Review of the physician orders revealed an order dated 08/12/24 for wound care to include a Dakin's solution cleanse to Resident #10's bilateral lower legs, ankles, and feet, then staff were to apply Neosporin ointment, cover with abdominal pads (ABDs), wrap with gauze from the toes to the knees, and then wrap with Coban (self-adhering elastic wrap) each day shift and each night shift and as needed. Review of the wound care physician's progress notes from the wound visit dated 08/07/24 revealed Resident #10 was being treated for bilateral leg lymphedema with open venous lymphatic wounds. The progress note further revealed if Coban was used, it should not be wrapped tight and Tubigrip stockings (tubular bandages) were not to be used. Observation on 08/13/24 from 3:50 P.M. to 4:30 P.M. of wound care revealed Resident #10 sat in his wheelchair with both feet placed on the floor, covered with a plastic barrier. Licensed Practical Nurse (LPN) #350 removed the old dressing from Resident #10's bilateral lower legs, starting with the Tubigrip stockings, exposing the gauze that was wrapped from his ankles up to below his knees. The removed gauze wrap from Resident #10's right leg had a moderate amount of serosanguinous drainage, and the ABD pads had scant serosanguinous drainage. The ABD pads removed from Resident #10's left leg had scant serous and serosanguinous drainage, and the ABD pad removed from the left lateral aspect of the middle of Resident #10's lower leg was noted to hold a small to moderate amount of yellowish-brown purulent drainage. Once the old dressings were removed, LPN #350 indicated she had difficulty visualizing all the open areas due to Resident #10's leg position while sitting in his wheelchair and his limited ability to lift his legs. After cleansing the open areas with Dakin's solution-soaked gauze, LPN #35 proceeded to apply Neosporin to the visible open areas, apply ABD pad, and then wrap the right leg with gauze from just above the ankle to mid-calf, and the left leg from the ankle to the top of the calf. Further observation revealed LPN #350 wrapped both lower legs from the ankle to the top of the calves, and then reapplied his Tubigrip stockings on each leg. During the observation, no wound care or dressing was noted involving Resident #10's ankles or feet, with the exception that a dry gauze pad was used to dab moisture off the top of Resident #10's reddened, edematous feet prior to putting on his socks. Interview on 08/13/24 at 4:40 P.M. with LPN #350 confirmed she wrapped Resident #10's right leg with gauze from his ankle to mid-calf and the left leg from just above his ankle to the top of his calf. During the interview, LPN #350 further confirmed both legs were then wrapped with Coban from above the ankle to the top of each calf and Tubigrip stockings were applied to both lower legs. Interview on 08/14/24 at 9:55 A.M. with wound care Physician #324 confirmed Resident #10 had chronic lymphedema and circulatory issues due to heart failure, was at risk for infection, and had a history of blisters and open sores. Physician #324 further confirmed Resident #10 should not have any compression, including application of Tubigrip stockings, until his wounds were closed and there was no evidence of infection. During the interview, Physician #324 also confirmed Resident #10 should have his dressings wrapped from his feet up to his knees due to chronic lymphedema. Interview on 08/14/24 at 3:43 P.M. with Registered Nurse (RN) Unit Manager #328 confirmed Resident #10 was to have his bilateral legs wound dressings wrapped from his feet up to his knees and Tubigrip stockings were not to be applied. Review of the policy titled Wound Care dated September 2022 revealed the physician's order was to be verified for the wound care procedure and the care plan was to be reviewed for any additional needs related to the resident's wound care. This deficiency represents non-compliance investigated under Complaint Number OH00156607 and OH00155890.
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

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected 1 resident

Based on observation, interview, medical record review and review of facility policy, the facility failed to ensure a medication error rate of less than five percent. A total of 35 medication administ...

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Based on observation, interview, medical record review and review of facility policy, the facility failed to ensure a medication error rate of less than five percent. A total of 35 medication administration opportunities revealed four medication errors, resulting in an 11.4 percent (%) error rate. This affected one resident (Resident #10) of four residents (#10, #14, #3, and #58) reviewed for medication administration. The facility census was 68. Findings included: Review of the medical record for Resident #10 revealed an admission date of 03/04/24 with diagnoses including acute and chronic respiratory failure, cardiomegaly, sleep related hypoventilation, systolic and diastolic congestive heart failure, hypertension, atrial fibrillation, stage three chronic kidney disease, glaucoma, pleural plaque with asbestos, venous insufficiency, and lymphedema. Review of the quarterly Minimum Data Set (MDS) 3.0 assessment revealed Resident #10 had intact cognition and was dependent on staff for toileting, bathing, and personal hygiene. Further review of the MDS revealed Resident #10 had a history of heart failure and received oxygen therapy. Review of the care plan initiated 03/18/24 revealed Resident #10 had an altered respiratory status and received oxygen therapy, was at risk for nutritional problems secondary to diuretic use, and had visual problems related to glaucoma. Interventions for these listed risks included administering breathing treatments as ordered, medications as prescribed, and eye medications per physician orders. Observation on 08/12/24 from 11:55 A.M. to 12:03 P.M. revealed Licensed Practical Nurse (LPN) #302 prepared 12 prescribed routine medications and one as needed medication for Resident #10's report of pain. During the observation, LPN #302 confirmed she would be administering some of the morning medication that were typically scheduled to be given between 7:00 A.M. to 10:00 A.M. with the afternoon medication pass. Observation of medication administration on 08/12/24 at 12:05 P.M. revealed Resident #10 refused his prescribed fluticasone nasal spray but took the oral medications that were placed in the medicine cup by LPN #302, including Mucinex 400 milligram (mg), 1.5 tablets (600 mg total). During medication administration observation, LPN #302 failed to administer Potassium 20 milliequivalents (mEq) oral tablet, Breztri inhalation aerosol 160-9-4.8 micrograms (mcg) per actuation, and Brimonidine 0.15% ophthalmic solution. Review of the physician orders revealed the following orders: 1. An order dated 03/06/24 for Mucinex extended release (ER) 12-hour 600 mg tablets, give two tablets by mouth two times daily for nasal congestion. 2. An order dated 08/06/24 for Potassium oral tablet, give 20 mEq once daily for seven days to start on 08/07/24. 3. An order dated 03/25/24 for Breztri Aerosphere inhalation aerosol 160-9-4.8 mcg/actuation, inhale two puffs orally two times a day related to acute and chronic respiratory failure. 4. An order dated 05/02/24 for Brimonidine Tartrate ophthalmic solution 0.15, instill one drop in both eyes three times a day for glaucoma. Interview on 08/12/24 at 3:45 P.M. with Resident #10 confirmed he did not receive any inhalation or respiratory treatments at all this date so far and he did not get all his eye drops, but could not determine which he did not get, stating I rely on the nurses to know what I am supposed to get. During the interview, Resident #10 revealed he had glaucoma and had several different types of eye drops prescribed, but he did not always get them, adding his eye drops sometimes got lost or left on the bedside table and accidentally thrown in the trash and he had to wait until the facility ordered replacement drops. Interview on 08/12/24 at 4:30 P.M. with LPN #302 confirmed Resident #10 did not get all three prescribed eye drops, potassium, or his Breztri inhaler. LPN #302 further confirmed the Mucinex administered to Resident #10 was not two tablets of the 600 mg extended-release formulation, but 1.5 tablets of the 400 mg Mucinex taken from a facility stocked medication bottle. During the interview, LPN #302 also confirmed the medication administration record (MAR) contained checkmarks for all Resident #10's morning and afternoon medications, even the medications she did not administer, including potassium, Breztri, and the Brimonidine eye drops. Review of the policy titled Medication Administration and General Guidelines from the Pharmacare USA policy & Procedure 2022 edition revealed medications were to be administered as prescribed and in accordance with the orders of the attending physician and within one hour of the scheduled time. This deficiency represents non-compliance investigated under Complaint Number OH00156293 and Complaint OH00155890.
CONCERN (E) 📢 Someone Reported This

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

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

Infection Control (Tag F0880)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and review of facility policy, the facility failed to ensure appropriate infection control proc...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and review of facility policy, the facility failed to ensure appropriate infection control procedures were followed during medication administration. This affected three residents (Residents #10, #14, and #35) of four residents observed for medication administration and had the potential to affect all 17 residents residing in the Northeast Hall. Also, the facility failed to implement an infection control program that included the use of enhanced barrier precautions. This had the potential to affect all residents. The facility census was 68. Findings include: 1. Observation on 08/12/24 from 11:55 A.M. to 12:40 P.M. of medication administration on the northeast hall by Licensed Practical Nurse (LPN) #302 revealed the following: a. LPN #302 was observed preparing medications for Resident #10 on 08/12/24 at 11:55 A.M. after exiting another resident's room without first performing hand hygiene. During this observation, LPN #302 removed two 400 milligram (mg) tablets of Mucinex from a facility-stocked medication bottle, one tablet of which dropped onto the surface of the medication cart. LPN #302 proceeded to pick up the tablet, break it in half with her bare hands, then place ½ tablet into Resident #10's medicine cup and the other half back into the original bottle. Further observation revealed Resident #10 was administered medication at 12:05 P.M. During medication administration, LPN #302 handled several items on Resident #10's bedside table, gave him his oral medications, donned a pair of gloves to administer eye drops, removed the gloves, then exited Resident #10's room. No hand hygiene was performed before or after entering or exiting Resident #10's room nor after removal of the gloves. b. LPN #302 was observed preparing medications for Resident #35 on 08/12/24 beginning approximately 12:15 P.M. During the observation, LPN #302 was observed popping clonazepam 0.5 mg, ½ tablet directly from the unit dose packet into her hand and using the other hand to place it into a medicine cup and then popping a Zofran 4 mg tablet into her left hand and then using her right hand to place the Zofran into the medicine cup. No gloves were worn and no hand hygiene was performed before or after medication preparation. At 12:20 P.M., Resident #3 was given his medication and then LPN #302 checked his blood pressure in his left wrist. During the observation, no hand hygiene was performed after direct contact with Resident #35. c. LPN #302 was observed preparing medications for Resident #14 on 08/12/24 beginning approximately 12:25 P.M. During the observation, LPN #302 was observed popping one Sinemet 25-100 mg tablet directly from the unit dose packet into her hand and using the other hand to place it into a medicine cup. Afterward, LPN #302 removed a facility-stocked bottle of docusate sodium 100 mg from the medication cart, pouring a tablet into her hand, breaking the tablet in half, then placing ½ tablet into the medicine cup and the other half back into the bottle. Further observation revealed LPN #302 popped a tramadol 50 mg tablet from the unit dose packet stored in the locked controlled substance drawer then placing it into the medicine cup. No gloves were used when handling the medication and no hand hygiene was performed at any time between touching the pills with her bare hands. Resident #14 had a blood pressure cuff placed on her left arm at 12:38 P.M., then LPN #302 donned gloves, administered eye drops, removed gloves, and removed the blood pressure cuff and exited the room. No hand hygiene was performed after exiting Resident #14's room. Interview on 08/12/24 at 12:40 P.M. with LPN #302 confirmed she did not wash her hands or use hand sanitizer between each resident and did not know what the policy was for hand hygiene during medication administration if she was just passing pills, but confirmed she was aware hand hygiene was required after direct contact with residents and after glove removal. LPN #302 confirmed at this time she had direct contact with Resident #14 and Resident #35. Further interview confirmed LPN #302 handled medications with her bare hands, including breaking some of the tablets from community-stocked medication bottles and placing the other half of those pills into the Mucinex and the Docusate sodium bottles. LPN #302 confirmed other residents used medications out of those bottles. During the interview, LPN #302 was unable to locate hand sanitizer on the medication cart and demonstrated she did not know where to find the hand sanitizer dispensers in resident rooms. Interview on 08/12/24 at 5:15 P.M. with the Director of Nursing (DON) confirmed hand hygiene should be performed between residents, after direct contact with residents, and after glove removal during medication administration. The DON also confirmed the list of other residents who were prescribed Mucinex and docusate sodium and that the medication should not have been placed back into the medication bottles so they were removed from the medication cart on this date. Review of the policy titled Medication Administration and General Guidelines from the Pharmacare USA policy & Procedure 2022 edition revealed staff administering medications were to adhere to universal precautions, using proper hand hygiene and gloves when appropriate, before beginning a medication pass, prior to handling any medication, and after coming into direct contact with a resident. The policy further specified staff should not handle pills with their bare hands and if breaking tablets was necessary, staff were to sanitize their hands, don gloves, use a tablet splitter to avoid contact with the medication, and dispose of unused portions of the medication per facility policy. 2. Observations made during the initial tour of the facility southeast, northwest, and northeast units on 08/12/24 between 10:10 A.M. and 10:25 A.M. revealed Rooms 15, 18, 25, 30, and 33 had white carts with three drawers containing personal protective equipment (PPE), but no signage indicating any type of transmission-based precautions, enhanced barrier precautions, or directions on what PPE was necessary, if any, to enter the nearby resident room. An additional white cart was observed sitting between room [ROOM NUMBER] and the emergency exit and a blanket was wadded up atop the cart and hung over the top of the top drawer. Initial observation of the secured (southwest) unit on 08/12/24 revealed no rooms had PPE carts, signage or any other indication residents residing on that unit required enhanced barrier precautions. Random intermittent observations throughout the facility during the survey from 08/12/24 through 08/14/24 revealed no staff donning PPE when entering any resident rooms near the white PPE carts. Observation of wound care on 08/13/24 from 3:50 P.M. to 4:30 P.M. for Resident #10's chronic bilateral lower leg lymphedema and venous lymphatic wounds revealed no gown was donned to render wound care. Interview on 08/14/24 at 11:10 A.M. with Registered Nurse (RN) #328 confirmed he had previously been the facility's infection preventionist and he did not believe there was an official policy, program, or list of residents on enhanced barrier precautions (EBP). During a follow-up interview on 08/14/24 at 11:20 A.M., RN #328 confirmed he verified with the Administrator and Director of Nursing (DON) that the facility had not fully implemented an EBP program yet and it was the facility's understanding that enhance barrier precautions came down as a recommendation and it was not a requirement. Observations on 08/14/24 from 11:25 A.M. to 11:40 A.M. revealed Rooms 15, 18, 25, 30, and 33 had white carts with three drawers containing personal protective equipment (PPE), but no signage indicating any type of transmission-based precautions, enhanced barrier precautions, or directions on what PPE was necessary, if any, to enter the nearby resident room. Further observation revealed one white PPE cart at the end of the northeast hall between room [ROOM NUMBER] and the exit with the same blanket wadded on top of the cart as observed on 08/12/24. Interview on 08/14/24 at 11:40 A.M. with State Tested Nurse Aide (STNA) #352 confirmed she did not know what the PPE cart between room [ROOM NUMBER] and the emergency exit was for but stated that based on her past experiences as an agency nurse working in other long-term care facilities, She assumed it held PPE that was necessary when caring for residents with feeding tubes and catheters. During the interview, STNA #352 was unable to say whether the facility had any residents who were ordered or care planned for enhanced barrier precautions. Interview on 08/14/24 at 3:25 P.M. with the DON confirmed two residents were on dialysis, four residents had urinary catheters, three residents had ostomies, and there were no residents with feeding tubes residing in the facility at the time of the survey. Interview on 08/14/24 at 3:43 P.M. with RN #328 confirmed the facility had six residents with chronic wounds, including Resident #10, and one resident with a multidrug-resistant organism (MDRO) residing in the facility. Review of the policy titled Standard Precautions last revised in November 2022 revealed no information regarding enhanced barrier precautions. Review of the policy titled Isolation - Categories of Transmission-Based Precautions last revised in August 2022 revealed no information regarding enhanced barrier precautions. Review of the Center for Clinical Standards and Quality/Quality, Safety & Oversight Group memorandum summary, reference number QSO-24-08-NH, issued 03/20/24, revealed enhanced barrier precautions (EBP) in in long-term care facilities was effective on 04/01/24 to align with nationally accepted standards. The QSO memorandum further revealed EBP was to include residents with chronic wounds and/or indwelling medical devices during high contact care regardless of their status related to multidrug-resistant organisms.
Feb 2024 4 deficiencies
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

ADL Care (Tag F0677)

Could have caused harm · This affected 1 resident

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

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review, observation, resident interview, staff interview, and policy review, the facility failed to assist a resident, who was dependent on staff for assistance with incontinence care in a timely manner. This affected one (#23) of three residents reviewed for incontinence care. The facility census was 67. Findings include: Review of Resident #23's medical record revealed an admit date of 01/03/24, with diagnoses including: fractured left femur with joint replacement, diabetes mellitus, chronic kidney disease, pulmonary disease, severe protein-calorie malnutrition, kyphosis of cervical region with cervicalgia (neck pain), anemia, thyrotoxicosis (High levels of circulating thyroid hormones.), and localized swelling, mass, and lump of both lower limbs. Review of Resident #23's Minimum Data Set (MDS) assessment dated [DATE] indicated she had intact cognition, had an indwelling urinary catheter and was occasionally incontinent of bowel. Resident #23's plan of care initiated on 01/17/24 indicated an activity of living self-care performance deficit related to displaced fractured femur. Interventions on the plan of care indicated to provide one staff member to assist with use of the toilet. Interview on 02/13/24 at 8:35 A.M., with Resident #23 revealed she had been waiting for 30 minutes for someone to assist her with incontinence care. Resident #23 stated she had asked State Tested Nursing Assistant (STNA) #74 who told her she would let her aid know of her need for incontinence care. Resident #23 stated she received stool softeners and was unable to feel the urge to have a bowel movement. Observation of Resident #23 on 02/13/24 between 8:35 A.M. and 8:50 A.M. revealed Resident #23 asked several staff members to assist her with her toileting needs. Resident #23 asked State Tested Nurse Aide (STNA) #74 to assist her with incontinence care. STNA #74 responded she had to wait until all the meal trays were picked up and proceeded to push Resident #23 in her wheelchair to her room. A few minutes later Resident #23 propelled herself out of her room stating she was informed by the staff that she would need to provide her with incontinence care because she was supposed to transfer to the assisted living facility. Resident #23 left the common area and propelled herself down the hallway and approached Licensed Practical Nurse (LPN) #82 and asked her to assist with incontinence care. LPN #82 informed Resident #23 she needed to go back to her room to ask for assistance with incontinence care. LPN #82 informed Resident #23 she would need to provide her own incontinence care if Resident #23 wanted to return to the assisted living facility. Approximately five minutes later, LPN #82 asked STNA #74 to assist Resident #23 with her incontinence care. STNA #74 proceeded to push Resident #23 back to her room to await assistance for incontinence care. At 8:50 A.M., Resident #23 propelled herself out of her room and asked the Certified Occupational Therapy Assistant (COTA) #75 to assist her with incontinence care. COTA #75 assisted Resident #23 to the therapy bathroom and provided incontinence care for Resident #23 with the assistance of Physical Therapy Assistant (PTA) #76. During the incontinence care, COTA #75 removed the feces soiled wound treatment from Resident #23's coccyx area and informed Resident #23 the nurse was busy right now and would not be able to reapply the wound treatment until later in the morning. COTA #75 assisted Resident #23 with donning an incontinence brief. Interview on 02/13/24 at 9:20 A.M., with STNA #77 revealed STNA #74 had informed her of the need to provide incontinence care for Resident #23. STNA #77 stated she had looked in Resident #23's room, but she was not there and continued to perform her other job duties. Interview on 02/13/24 at 10:28 A.M., with STNA #74 revealed LPN #73 had informed her that Resident #23 needed to go to her room and provide her own incontinence care. STNA #74 stated LPN #82 had told her to assist Resident #23 to her room to perform her own incontinence care. Interview on 02/13/24 at 2:15 P.M., with LPN #73 indicated therapy had informed the staff that Resident #23 needed to perform her own incontinence care unless she was unable to perform the incontinence care herself. Review of the policy titled Incontinence - Clinical Protocol revised 12/08/23 indicated: as appropriate, based on assessment of the category and causes of incontinence, the staff will provide scheduled toileting, prompted voiding, or other interventions to try to improve the individual's continence status. This deficiency represents non-compliance investigated under Complaint Number OH00150449.
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

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected 1 resident

Based on record review, observation, policy review, and staff interview, the facility failed to ensure a medication error rate was less than five percent. A total of 26 opportunities for error reveale...

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Based on record review, observation, policy review, and staff interview, the facility failed to ensure a medication error rate was less than five percent. A total of 26 opportunities for error revealed two medication errors resulting in a 7.69 (%) percent error rate. This affected two (#2 and #31) of two residents observed for medication administration. The facility census was 67. Findings include: 1. Review of Resident #2's medical record revealed an admission date of 10/27/22, with diagnoses including: Ogilvie syndrome (A disorder characterized by acute dilatation of the colon in the absence of an anatomic lesion that obstructs the flow of intestinal contents.), hyperemia, asthma, high blood pressure, obstructive sleep apnea, atherosclerotic heart disease, muscle strain of the left shoulder and upper arm, right/left knee pain, chronic pain, pulmonary nodule, pigmentation disorder, gastroesophageal reflux, and hyperlipidemia. Observation of Licensed Practical Nurse (LPN) #70 administer Resident #2 his medications on 02/12/24 at 8:00 A.M., revealed a failure to administer ascorbic acid (Vitamin C) 500 milligrams (mg) by mouth. LPN #70 did administer 15 other prescribed medication. Review of Resident #2's physician order dated 10/29/22 indicated to administer ascorbic acid (Vitamin C) 500 milligrams (mg) by mouth in the morning for a supplement. Resident #2's February Medication Administration Record (MAR) indicated documentation the vitamin C 500 mg medication was administered. Interview on 02/12/24 at 11:36 A.M., with LPN #70 verified the above findings. 2. Review of Resident #31's medical record revealed an admission date of 04/22/22, with diagnoses including: secondary Parkinsonism, stroke, hemiplegia/hemiparesis following a cerebral infarction (stroke) affecting the left dominant side, atherosclerotic heart disease, chronic kidney disease, seizures, mixed hyperlipidemia, bone density disorder, depression, osteoarthritis, gastroesophageal reflux, salivary gland secretion disturbance, anemia, sacrococcygeal disorder, presence of cardiac implant, breast cancer, hypertensive kidney disease, orthostatic hypotension, atrophy of thyroid, peripheral vascular disease, collagenous colitis, joint pain, and open wound of back wall of thorax without penetration into thoracic cavity. An observation on 02/12/24 at 8:20 A.M. of LPN #71 administer medications to Resident #31 revealed a failure to administer famotidine 20 mg orally. LPN #71 did administer nine other medications. Review of Resident #31's physician order dated 10/07/23 indicated to administer famotidine (pepcid) 20 mg by mouth in the morning. Review of February MAR indicated documentation LPN #71 had administered the famotidine medication. Interview on 12/12/24 at 11:30 A.M., with LPN #71 verified the above finding. Observation on 02/12/24 between 8:00 A.M. and 9:00 A.M., of LPN #70 and LPN #71 administer medications to Resident #2 and Resident #31, with 26 opportunities for error revealed two medication errors resulting in an 7.6% error rate. Review of policy titled Medication Administration and General Guidelines dated 2022, indicated medications were administered as prescribed, in accordance with State Regulations using good nursing principles and practices and only by persons legally authorized to do so. Personnel authorized to administer medications do so only after they have familiarized themselves with the medication, and otherwise authorized personnel should refer to Drug Reference material provided by facility. The procedure included medications were prepared, administered, and recorded only by licensed nursing, medical, pharmacy, or other personnel authorized by state laws and regulations to administer medications. Medications were administered in accordance with written orders of the attending physician. When administering medications, the staff adhered to the six rights of medication administration.
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

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

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

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, medical record review, policy reviews, and staff interview, the facility failed to ensure staff performed hand hygiene to prevent cross contamination during a medication administration and during a wound dressing change. This affected three (#1, #31 and #43) of six residents observed for infection control. The facility census was 67. Findings include: 1. Observation on 02/12/24 at 8:20 A.M., of Licensed Practical Nurse (LPN) #71 administer medications to Resident #31 and Resident #43 revealed LPN #71 failed to perform hand hygiene after completing Resident #31's medication administration and administered Resident #43's medications. LPN #71 obtained Resident #31's nine oral medications and administered them to Resident #31. LPN #71 handed the medications to Resident #31 and watched Resident #31 consume the medications. LPN #71 exited Resident #31's room and proceeded to dispense Resident #43's medications into a medication cup without performing hand hygiene. LPN #71 entered Resident #43's room and proceeded to administer Resident #43's medications without performing hand hygiene before or after starting the task. Interview on 02/12/24 at 8:27 A.M., with LPN #71 verified she had failed to perform hand hygiene after administering Resident #31's medications and before and after administering Resident #43's medications. 2. Review of Resident #1's medical record revealed admission date of 01/26/23 and re-admitted on [DATE], with diagnoses including: chronic kidney disease, heart attack with aortic valve stenosis and heart failure, stroke, osteoarthritis, breast cancer, hyperlipidemia, hypothyroidism, polyneuropathy, anxiety, psoriasis, morbid obesity, malaise, spinal stenosis, mood disorder, depression, and a stage 2 pressure ulcer of the buttock. Review of Resident #1's wound observation assessment dated [DATE] indicated the presence of a stage 2 pressure ulcer on the buttock measuring 3.5 centimeters (cm) long by 5.1 cm wide by 0.1 cm deep. Review of Resident #1's physician order dated 02/03/24 indicated to use Dakin's solution to cleanse the wound, apply skin preparation to the perimeter of the wound, apply Medi honey gel to the wound and cover the wound with border foam once a day. Observation on 02/13/24 at 3:00 P.M., of LPN #81 providing wound care for Resident #1 revealed a failure to perform hand hygiene. LPN #81 entered Resident #1's room with the supplies to perform the wound treatment. LPN #81 donned a pair of disposable gloves and removed the soiled wound treatment from Resident #1's right buttock. LPN #81 inspected the wound and then removed her gloves and left the room to obtain a smaller border foam dressing from the treatment cart outside the room. LPN #81 entered the room a second time and donned another pair of disposable gloves without performing hand hygiene. LPN #82 proceeded to apply the physician ordered wound treatment to Resident #1's buttock. LPN #81 then removed her gloves and exited the room and did not perform hygiene. Interview on 02/13/24 at 3:20 P.M., with LPN #81 verified she had not performed hand hygiene before and after performing Resident #1's wound treatment and between glove changes while performing the wound treatment task. Review of the policy titled Infection Prevention and Control dated July 2022, indicated the policy of this facility was to establish and maintain an infection prevention and control program designed to provide a safe, sanitary, and comfortable environment and to help prevent the development and transmission of communicable diseases and infections. The policy indicated and the hand hygiene protocol: a. All staff shall wash their hands when coming on duty, between resident contacts, after handling contaminated objects, after personal protective equipment removal, before/after eating, before/after toileting, and before going off duty. b. Staff shall wash their hands before and after performing resident care procedures. Review of the policy titled; Handwashing/Hand Hygiene revised September 2022 indicated the policy of the facility considers hand hygiene the primary means to prevent the spread of infections. Policy Interpretation and Implementation included: 1. All personnel shall be trained and regularly in-serviced on the importance of hand hygiene in preventing the transmission of healthcare-associated infections. 2. All personnel shall follow the handwashing/hand hygiene procedures to help prevent the spread of infections to other personnel, residents, and visitors. 3. Hand hygiene products and supplies (sinks, soap, towels, alcohol-based hand rub, etc.) shall be readily accessible and convenient for staff use to encourage compliance with hand hygiene policies. 4. Residents, family members and/or visitors will be encouraged to practice hand hygiene through the use of fact sheets, pamphlets and/or other written materials provided at the time of admission and/or posted throughout the facility. 5. Wash hands with soap (antimicrobial or non-antimicrobial) and water for the following situations: a. When hands are visibly soiled; and b. After contact with a resident with infectious diarrhea including, but not limited to infections caused by norovirus, salmonella, shigella and C. difficile. 6. Use an alcohol-based hand rub containing at least 62% alcohol; or, alternatively, soap (antimicrobial or non-antimicrobial) and water for the following situations: a. Before and after coming on duty. b. Before and after direct contact with residents. c. Before preparing or handling medications. d. Before performing any non-surgical invasive procedures. e. Before and after handling an invasive device (e.g., urinary catheters, IV access sites). f. Before donning sterile gloves. g. Before handling clean or soiled dressings, gauze pads, etc. h. Before moving from a contaminated body site to a clean body site during resident care.
CONCERN (E) 📢 Someone Reported This

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

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

Antibiotic Stewardship (Tag F0881)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review, infection control log review, antibiotic stewardship tool review, and staff interview, the facil...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on medical record review, infection control log review, antibiotic stewardship tool review, and staff interview, the facility failed to implement their antibiotic stewardship program that included antibiotic use protocols and a system to monitor antibiotic use. This affected nine (#1, #2, #10, #12, #31, #58, #60, #69, and #70) of nine residents identified as utilizing antibiotic for infections in the past three months. The facility census was 67. Findings include: 1. Review of Resident #12's medical record revealed an admission date of 06/09/22 and re-admitted on [DATE], with diagnoses including: dementia, head laceration, osteoarthritis of right shoulder, diabetes mellitus, high blood pressure, atherosclerotic heart disease, arthropathy, heart failure, pulmonary disease, asthma, hyperlipidemia, chronic kidney disease, gastroesophageal reflux disease, rectal cancer, anxiety, syncope, rhabdomyolysis (A rare muscle injury where muscles break down.), and depression. Review of the facility infection control log dated 02/01/24 to 02/29/24 indicated on 02/01/24 the facility identified that Resident #12 had symptoms of a urinary tract infection. Review of the facility tool for antibiotic stewardship (McGreer's Criteria for Infection Surveillance Checklist) dated 02/03/24 indicated Resident #12 did not meet the criteria for antibiotic administration. Resident #12 did not have at least one of the following microbiologic criteria: 1. Greater or equal to 100,000 colony forming units per milliliter of no more than 2 species of organisms in a voided urine sample 2. Greater or equal to 1,000 colony forming units per ml of any organism in a specimen collected by an in-and-out catheter. Review of Resident #12's physician order dated 02/03/24 indicated to administer ciprofloxacin hydrochloride (antibiotic) 500 milligrams (mg) by mouth one time of day for urinary tract infection. Interview on 02/12/24 at 1:32 P.M., with Registered Nurse (RN) #87 indicated he was the Infection Control Preventionist for the facility. RN #87 stated the Medical Director does not follow the antibiotic stewardship program protocols. RN #87 stated the Medical Director didn't obtain a urinalysis or urine cultures for Resident #12. RN #87 stated the Medical Director ordered Resident #12 the antibiotics due to his preference. 2. Review of Resident #1's medical record revealed admission date of 01/26/23 and re-admitted on [DATE], with diagnoses including: chronic kidney disease, heart disease with heart failure, stroke, edema, breast cancer, hyperlipidemia, hypothyroidism, polyneuropathy, osteoarthritis, psoriasis, morbid obesity, malaise, anxiety, chronic pain syndrome, spinal stenosis, mood disorder, depression, stage 2 pressure ulcer of the buttock, and kidney stones. Review of the infection control log dated 02/01/24 to 02/29/24, indicated Resident #1 had symptoms consistent with a urinary tract infection on 02/02/24 and 02/05/24. Review of Resident #1's physician order dated 02/04/24 and 02/06/24 indicated to administer doxycycline hyclate 100 mg orally two times a day for nine doses; and on 02/03/24 and 02/04/24, to administer one dose of ceftriaxone sodium injection reconstituted 500 mg intramuscularly one time a day for elevated temperature on each day. Review of the facility's tool for antibiotic stewardship dated 02/02/24 and 02/05/24 indicated Resident #1 did not meet the criteria for administration of antibiotics to treat a urinary tract infection. Resident #1 did not have at least one of the following microbiologic criteria: 1. Greater or equal to 100,000 colony forming units per milliliter of no more than 2 species of organisms in a voided urine sample 2. Greater or equal to 1,000 colony forming units per ml of any organism in a specimen collected by an in-and-out catheter. Interview on 02/12/24 at 1:32 P.M., with Registered Nurse (RN) #87 indicated he was the Infection Control Preventionist for the facility. RN #87 stated the Medical Director does not follow the antibiotic stewardship program protocols. RN #87 stated Resident #1 had chronic urinary tract infections and the physician automatically ordered antibiotics when Resident #1 had symptoms consistent with a urinary tract infection. Interview on 02/14/23 at 8:31 A.M., with Director of Nursing (DON) indicated during the quality assurance meetings the facility discussed the antibiotic stewardship program with the Medical Director. DON stated the Medical Director's stance was to administer antibiotics to not allow the infection to progress. Interview on 02/14/24 at 1:09 P.M., with the Medical Director indicated he didn't follow the antibiotic stewardship tool the facility used to determine if a resident with an infection met the criteria to administer antibiotics. Medical Director stated he made the decision to administer antibiotics for infections based on his knowledge and experience. The Medical Director sent a text message via phone which indicated the antibiotic stewardship program was a tool in medical decision making. The Medical Director indicated he was very aware of the antibiotic stewardship program and there were many factors that come to play in treating patients. Review of the infection control log dated 12/01/23 to 01/31/24 revealed there were eight residents (Resident #1, Resident #60, Resident #31, Resident #2, Resident #69, Resident #58, Resident #70, and Resident #10) who did not meet the antibiotic stewardship tool protocols. The eight residents were administered antibiotics. Review of the policy titled Antibiotic Stewardship revised on 10/01/22, indicated the policy was antibiotics would be prescribed and administered to residents under the guidance of the facility's antibiotic stewardship program. Policy Interpretation and Implementation 1. The purpose of our antibiotic stewardship program is to monitor the use of antibiotics in our residents. 2. Orientation, training, and education of staff will emphasize the importance of antibiotic stewardship and will include how inappropriate use of antibiotics affects individual residents and the overall community. Review of the policy titled Infection Prevention and Control Program revised on July 2022, indicated the facility would implement antibiotic stewardship including the following guidelines: a. An antibiotic stewardship program would be implemented as part of the overall infection prevention and control program. b. Antibiotic use protocols and a system to monitor antibiotic use will be implemented as part of the antibiotic stewardship program. c. The Director of Nursing or designee will serve as the leader of the antibiotic stewardship program. d. The Infection Preventionist, Medical Director, consultant pharmacist, and laboratory manager would serve as resources for the antibiotic stewardship program.
Jan 2024 1 deficiency
CONCERN (E) 📢 Someone Reported This

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

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

Employment Screening (Tag F0606)

Could have caused harm · This affected multiple residents

THE FOLLOWING DEFICIENCY REPRESENTS AN INCIDENT OF PAST NON-COMPLIANCE THAT WAS SUBSEQUENTLY CORRECTED PRIOR TO THIS SURVEY. Based on personnel record review, review of staff timecards, review of staf...

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THE FOLLOWING DEFICIENCY REPRESENTS AN INCIDENT OF PAST NON-COMPLIANCE THAT WAS SUBSEQUENTLY CORRECTED PRIOR TO THIS SURVEY. Based on personnel record review, review of staff timecards, review of staff assignments, review of court documents, policy review and staff interview, the facility failed to ensure all staff working at the facility had a completed background check and did not have a disqualifying offense. This had the potential to affect 16 (#6, #7, #8, #11, #13, #14, #17, #19, #28, #35, #36, #46, #47, #48, #67 and #72) residents identified by the facility as residing on the South Unit of the facility. The facility census was 70. Findings include: Review of State Tested Nurse Aide (STNA) #205's personnel record revealed the STNA was employed by a staffing agency, with a hire date of 05/03/22. Review of STNA #205's timecards revealed she worked in the facility 18 days in October 2023 and five days in November 2023, with the last day being 11/08/23 when the facility removed STNA #205 from the facility after being alerted to a potentially disqualifying offense. Review of staff assignment sheets from 10/01/23 through 11/08/23 confirmed STNA #205 was assigned to the South Unit on each of the scheduled work days. Interview on 01/10/24 at 8:25 A.M. with the Administrator verified STNA #205 was a former agency staff who picked up shifts through a local staffing agency the facility had a contract with. The facility was notified the STNA had a criminal record, verified this on research, and placed STNA #205 on the Do Not Return (DNR) list. The Administrator stated the contract with the staffing agency identified the agency as responsible for ensuring background checks were completed and maintenance of those records. Interview on 01/10/24 at 10:56 A.M. with Human Resources Manager (HRM) #301 revealed all facility staff received criminal background checks, abuse training, and nurse aide registry checks upon hire. On 11/07/23, HRM #301 stated the facility received a verbal tip STNA #205 had criminal charges. The facility investigated, found the claim was substantiated, removed STNA #205 from the schedule and notified the staffing agency. Interview on 01/11/24 at 11:03 A.M. with the staffing agency [NAME] President of Marketing (VPM) #701 revealed his agency could not find evidence STNA #205 had a completed criminal background check when she began employment with them. Interview on 01/11/24 at 1:37 P.M. with STNA #205 confirmed she was convicted of theft four years ago and thought it had fallen off her record. Follow-up interview via telephone on 01/19/24 at 9:03 A.M. with the Administrator confirmed STNA #205 worked on one unit, the South Unit, of the facility and had not been assigned to provide care on all units of the facility. The Administrator verified there had been no incidents of theft or concerns identified associated with STNA #205. Review of court documentation revealed STNA #205 pleaded guilty to an amended indictment of theft from a person in a protected class on 11/19/2019 and was currently on probation. Review of the staffing agency contract, dated 03/01/22, revealed the staffing agency would do background checks for all staff assigned to the facility and was to comply with all personnel requirements established by the Department of Health. During the onsite investigation, no incidents of theft or concerns were identified associated with STNA #205. Review of the facility policy titled Workforce Clearance Policy, dated 2019, revealed all facility workforce members were to be adequately reviewed during the hiring process. Review of the facility policy titled Resident Right to Freedom from Abuse, Neglect, and Exploitation Policy and Procedure, dated 2022, revealed the facility would not employ or engage individuals who have been found guilty of crimes, including misappropriation of property. The deficiency was corrected on 11/08/23 when the facility implemented the following corrective actions: • On 11/08/23 the facility discontinued the services of STNA #205 in their facility. • On 11/08/23 HRM #301 notified the staffing agency via e-mail and telephone of the findings. • On 11/08/23 HRM #301 notified the Corporate Director of Human Resources (CDHR) #505 and the Corporate Director of Staffing CDS) #500 of the findings. • On 11/08/23 HRM #301 audited all agency and facility staff to ensure background checks had been completed, with no additional concerns identified. • On 11/08/23 the Administrator educated HRM #301 on completing background checks on every agency staff prior to their first scheduled shift at the facility. • On 11/08/23 the Administrator reviewed grievance logs during the time STNA #205 worked in the facility. No concerns were identified related to STNA #205. • On 11/08/23 the facility terminated their contract with the staffing agency due to breach of contract for not completing background checks on new hires. • On 11/08/23 the Administrator began random audits of new agency staff to ensure compliance with background checks. No new concerns have been identified. This deficiency represents non-compliance investigated under Complaint Number OH00149899.
Apr 2023 1 deficiency
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

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, interview, record review, and review of the facility policy review the facility failed to ensure Resident ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, and review of the facility policy review the facility failed to ensure Resident #36's chair alarm was in place as ordered by the physician. This affected one resident (#36) of three residents reviewed for falls. The facility census was 62. Findings include: Review of the medical record for Resident #36 revealed an admission date of 05/06/21. Diagnoses included Parkinson's disease, Alzheimer's disease, generalized anxiety disorder, and schizophrenia. Review of the quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #36 was unable to complete the Brief Interview for Mental Status (BIMS) calculator to determine cognitive status. Per staff assessment, Resident #36 had short- and long-term memory problems. Resident #36 required supervision of one-person physical assist for transfers and walking in corridors, supervision with set-up for walking in room, locomotion, and toilet use. Review of the Morse Fall Scale dated 02/23/23 revealed Resident #36 was at high risk of falling. Review of the 03/21/23 progress note revealed Resident #36 had a fall on 03/21/23. Review of the physician's orders for Resident #36 revealed an order dated 03/28/23 for a [NAME] alarm while in the chair. Review of the care plan dated 05/07/21 revealed Resident #36 was at risk for falls related to unsteady gait, impaired cognition, and lack of safety awareness. Interventions included a chair sensor alarm. Review of the tasks in the electronic record for Resident #36 revealed no chair alarm was listed. Observation and interview on 04/07/23 at 12:03 P.M. with State Tested Nurse Aide (STNA) #459 revealed Resident #36 was sitting in her room in her chair. The chair alarm was observed sitting on top of the bedside table. Per STNA #459, she was not to have alarms, and if Resident #36 was to have alarms, it would be listed on her [NAME] on the inside of the door to her closet. Observation of Resident #36's [NAME] with STNA #459 revealed a chair alarm was not listed as an intervention. Interview on 04/07/23 at 12:05 P.M. with Licensed Practical Nurse (LPN) #458 confirmed Resident #36 did have an order for a bed and chair alarm and should have the alarm on while in the chair. Interview on 04/07/23 at 3:25 P.M. with STNA #492 stated she did not know Resident #36 had a bed and chair alarm ordered and confirmed the chair alarm was not listed on the [NAME] posted on the inside door of the closet and was not listed in the tasks in the electronic medical record. Interview on 04/07/23 at 2:26 P.M. with the Administrator confirmed Resident #36's chair alarm was not posted on the [NAME] located on the inside of her closet as it should have been and was having all [NAME]'s audited to ensure accuracy. Review of the facility policy Falls and Fall Risk, Managing, revised August 2022, revealed in conjunction with the attending physician, the facility would identify and implement relevant interventions. This deficiency represents non-compliance investigated under Complaint Number OH000141586.
Mar 2023 1 deficiency
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 interview, record review, and review of the facility self-reported incident (SRI) the facility failed to protect Reside...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, record review, and review of the facility self-reported incident (SRI) the facility failed to protect Resident #36 from resident-to-resident abuse. This affected one resident (#36) of three residents reviewed for abuse. The facility census was 64. Findings include: Review of the medical record for Resident #36 revealed an admission date of 05/06/22 with diagnoses including Parkinson's disease, Alzheimer's disease, generalized anxiety disorder, and schizophrenia. The resident spoke English and Italian with Italian the primary language. Review of the quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #36 had severely impaired cognition. The resident was independent for bed mobility. Supervision was needed for transfers, walking, locomotion, eating, toilet use, and personal hygiene. Review of the nursing progress note dated 02/28/23 at 12:25 P.M. revealed Resident #36 was emotional and crying. She said a man hit her face. The nurse observed the resident's right upper lip had a cut 0.5 centimeter (cm) long cut, bleeding lightly. The resident denied any further injury but was unable to explain the full incident in English. The male resident in question was removed from the area and was under one-on-one supervision. Review of the nursing progress note dated 03/01/23 revealed bruising was noted to Resident #36's right and left side of the face. An x-ray of the face was negative. Review of the SRI tracking number 232534 and investigation dated 02/28/23 revealed at approximately 12:30 P.M., staff heard Resident #36 yelling and immediately responded to her room. Resident #64 was seen leaving her room. Resident #36 stated the resident hit her. She had a small cut on her lip with some bleeding. Resident #64 was immediately put on one-to-one supervision with staff until he was sent to the hospital psychiatric unit. Resident #36 was assessed and treated by the nurse. An x-ray was obtained of her face, and it was negative. She did not require care outside of the facility. Review of the medical record for Resident #64 revealed an admission date of 09/10/22. The resident was admitted to a gero psych facility from 01/05/23 through 02/17/23. The resident was discharged to a gero psych facility on 02/28/23. Diagnoses included Alzheimer's disease, Post Traumatic Stress Disorder (PTSD), and unspecified psychosis. Review of the admission /Medicare - 5 Day MDS assessment dated [DATE] revealed Resident #64 had severely impaired cognition. Review of the progress note dated 02/28/23 at 12:25 P.M. revealed Resident #64 was observed ambulating in hall coming from room where female resident was crying and accusing him of hitting her. Resident #64 was put on one-to-one supervision due to physical aggression. Review of the progress note dated 02/28/23 at 4:32 P.M. revealed Resident #64 had been discharged to the hospital. Interview on 03/20/23 at 11:04 A.M. with State Tested Nursing Assistant (STNA) #204 revealed the STNA was on the unit at the time of the incident on 02/28/23. STNA #204 heard Resident #36 yell. The resident was holding her mouth/nose area, and there was a little blood. The resident's lip was swollen the next day. Interview on 03/20/23 at 11:34 A.M. with the Administrator revealed she was by the nursing station, heard Resident #36 scream out in Italian, and saw Resident #64 walking down the hallway. Resident #36 had an injured area on her lip. The facility sent Resident #64 out to a hospital psych unit. This deficiency represents non-compliance investigated under Complaint Number OH00140798.
Jan 2023 7 deficiencies
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

Based on interview and record review the facility failed to notify Resident #215's physician about Resident #215 being administered an intravenous (IV) medication without an order. This affected one R...

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Based on interview and record review the facility failed to notify Resident #215's physician about Resident #215 being administered an intravenous (IV) medication without an order. This affected one Resident (#215) of two residents reviewed for IV medication administration. The facility census was 61. Findings include: Review of the medical record for Resident #215 revealed an admission date of 01/17/23 with diagnoses including hemiplegia and hemiparesis following cerebral infarction affecting right dominant side, type two diabetes mellitus, and dysphagia. Review of a physician order dated 01/17/23 for Resident #215 revealed an order to administer IV dextrose with normal saline solution 5-0.45% (hydration fluid) at 100 milliliters (ml) per hour. Review of a physician order for Resident #215 dated 01/19/23 revealed an order to flush IV line with normal saline solution every shift while not in use and before and after IV medication administration. Review of a nursing progress note dated 01/19/23 at 7:03 P.M. authored by Registered Nurse (RN) #233 revealed she flushed Resident #215's IV line with heparin (a blood thinning medication) and normal saline solution. Observation of Resident #215 on 01/23/23 at 10:12 A.M. revealed an IV line in his right upper arm. Telephone interview on 01/24/23 at 12:04 P.M. with RN #233 confirmed she did administer IV heparin to Resident #215. RN #233 reported she did not have an order from the physician to administer it and did not notify the physician of the administration. RN #233 stated she entered Resident #215's room and found his IV had disconnected from the IV tubing for his hydration. She then administered one half of a 10 ml syringe of heparin into his IV line to assess patency. She then followed the heparin flush with a flush of 10 ml normal saline solution and reconnected his IV medication. Interview on 01/24/23 at 12:10 P.M. with the Director of Nursing (DON) confirmed there was no order to administer IV heparin to Resident #215 and the physician was not notified that RN #233 had administered it to him. Review of facility policy titled Change in a Resident's Condition or Status, revised September 2022, revealed the nurse will notify the resident's attending physician or physician on call when there has been an accident or incident involving the resident or the need to alter the resident's medical treatment.
CONCERN (D)

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

Deficiency F0583 (Tag F0583)

Could have caused harm · This affected 1 resident

Based on observation, record review, and interview the facility failed to maintain Resident #7's privacy during a medical treatment. This affected one Resident (#7) of three residents reviewed for pri...

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Based on observation, record review, and interview the facility failed to maintain Resident #7's privacy during a medical treatment. This affected one Resident (#7) of three residents reviewed for privacy. The facility census was 61. Findings include: Review of the medical record for Resident #7 revealed an admission date of 09/17/18 with diagnoses including Parkinson's disease, multi-system degeneration of the autonomic nervous system, and hypertension. Review of physician orders for Resident #7 dated 03/03/21 revealed an order to clean percutaneous endoscopic gastrostomy (PEG) tube with normal saline solution, pat dry, and apply Bactroban (anti-infective) two-percent ointment and apply a dry dressing every day. Observation on 01/25/23 at 11:25 A.M. with Registered Nurse (RN) #215 for Resident #7's PEG tube dressing change revealed RN #215 entered the room, cleaned the bedside table and placed his supplies on it. RN #215 left the door to the room open so the resident was visible from the hallway. RN #215 then washed his hands, applied clean gloves and raised Resident #7's gown to directly below her breasts and pulled the blankets down exposing Resident #7's PEG tube, abdomen, and incontinence brief. RN #215 exited and re-entered the room two more times during the treatment without closing the door to the room to maintain privacy for Resident #7 and without covering Resident #7 when he left the room. State Tested Nursing Assistant (STNA) #295 then came to the doorway with the open door, knocked, and entered to assess Resident #7's roommate. She then washed her hands and kicked the room door closed. RN #215 applied the anti-infective ointment and the dry dressing to Resident #7's abdomen. He then pulled Resident #7's gown down and pulled up her blankets, cleaned up, and washed his hands. Interview on 01/25/23 at 11:35 A.M. with STNA #295 confirmed the door was open to the hallway when she arrived at Resident #7's room and confirmed she did close it before assisting her roommate. Interview on 01/25/23 at 11:40 A.M. with RN #215 confirmed he did not close the door to Resident #7's room while performing the PEG tube dressing change. He reported he exited and entered the room twice during the procedure and did not recall ever opening or closing the door. Review of the facility policy titled Resident Rights, undated, revealed privacy will be maintained during medical examination or treatment and personal care.
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 interview and record review the facility failed to provide showers as scheduled to Resident #27. This affected one Resi...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to provide showers as scheduled to Resident #27. This affected one Resident (#27) of three residents reviewed for showers. The facility census was 61. Findings include: Review of the medical record for Resident #27 revealed an admission date of 12/12/18 with diagnoses including Parkinson's disease, hypertension, and chronic obstructive pulmonary disorder. Review of the care plan for Resident #27 dated 10/07/22 revealed she had an activities of daily living self-care performance deficit. Interventions included to provide bathing per schedule and encourage her to participate as able. The care plan also stated Resident #27 was to be showered every Tuesday and Saturday during the night shift. Review of the quarterly Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed Resident #27 had moderate cognitive impairment. Resident #27 required extensive one-person physical assistance for bed mobility, transfers, dressing, personal hygiene, and showers, and supervision with set up help only for eating. Resident #27 was frequently incontinent of urine and bowel. Review of shower documentation from 10/01/22 to 01/24/23 for Resident #7 revealed she only received a shower on 11/01/22, 11/08/22, 11/19/22, 12/03/22, 12/06/22, 12/10/22, 10/17/22, 12/20/22, 01/07/23, and 01/24/23. Interview on 01/23/23 at 1:05 P.M. with Resident #7's family member revealed Resident #7 was not getting two showers a week as scheduled. Interview on 01/25/23 at 1:25 P.M. with the DON confirmed Resident #27 did not receive showers twice weekly as scheduled. Review of the facility policy titled Activities of Daily Living, revised August 2022, revealed appropriate care and services will be provided for residents who are unable to carry out activities of daily living independently, with the consent of the resident and in accordance with the plan of care including appropriate support and assistance with bathing, dressing, grooming, and oral care.
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, and record review the facility failed to change Resident #2's oxygen tubing and humidification ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to change Resident #2's oxygen tubing and humidification bottle as scheduled and did not date the tubing and bottle. This affected one Resident (#2) of three residents reviewed for respiratory care. The facility census was 61. Findings include: Review of the medical record for Resident #2 revealed an admission date of 03/22/18 with diagnoses including chronic diastolic heart failure, chronic obstructive pulmonary disease, and hypertension. Review of physician orders for Resident #2 dated 03/22/18 revealed an order to apply oxygen via nasal cannula to maintain oxygen levels above 90 percent as needed. Review of the care plan for Resident #2 dated 11/14/22 revealed Resident #2 used oxygen continuously. The interventions included to keep the head of the bed at 30 degrees and apply oxygen via nasal cannula to maintain oxygen levels above 90 percent. Review of the annual Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed Resident #2 had moderate cognitive impairment. Resident #2 required extensive one-person physical assistance for bed mobility, transfers, and toilet use, limited one-person physical assistance for dressing, independent with set up help only for eating, and supervision with one-person physical assistance for personal hygiene. Observation on 01/23/23 at 10:21 A.M. of Resident #2 revealed oxygen tubing was not dated and a humidification bottle with less than one inch of fluid in it and not dated. Interview during the observation with Resident #2 confirmed the facility had not changed her tubing in a while. Observation on 01/24/23 at 10:35 A.M. of Resident #2 revealed oxygen tubing and humidification bottle not dated and the humidification bottle was empty. Interview during the observation with Resident #2 revealed the staff still had not changed her tubing or her bottle. Interview and observation on 01/24/23 at 4:14 P.M. with the Director of Nursing (DON) confirmed Resident #2's oxygen tubing and humidification bottle were not dated and the humidification bottle was empty. Resident #2 informed the DON during the observation that her tubing needed changed and needed a new humidification bottle because hers was empty. The DON reported all oxygen tubing and bottles must be changed every Sunday evening, dated, and documented. The DON could not locate any documentation as to the last time Resident #2 had her oxygen tubing changed. Review of the facility policy titled Oxygen Administration Level III, revised August 2022, revealed to periodically re-check water level in the humidifying bottle.
CONCERN (D)

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

Deficiency F0760 (Tag F0760)

Could have caused harm · This affected 1 resident

Based on interview and record review the facility administered an intravenous (IV) medication to Resident #215 without a physician's order. This affected one Resident (#215) of two residents with orde...

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Based on interview and record review the facility administered an intravenous (IV) medication to Resident #215 without a physician's order. This affected one Resident (#215) of two residents with orders for IV medications. The facility census was 61. Findings include: Review of the medical record for Resident #215 revealed an admission date of 01/17/23. Diagnoses included hemiplegia and hemiparesis following cerebral infarction affecting right dominant side, type two diabetes mellitus, and dysphagia. Review of a physician order dated 01/17/23 for Resident #215 revealed an order to administer IV dextrose with normal saline solution 5-0.45% (hydration fluid) at 100 milliliters (ml) per hour. Review of a physician order for Resident #215 dated 01/19/23 revealed an order to flush IV line with normal saline solution every shift while not in use and before and after IV medication administration. Review of a nursing progress note dated 01/19/23 at 7:03 P.M. authored by Registered Nurse (RN) #233 revealed she flushed Resident #215's IV line with heparin (a blood thinning medication) and normal saline solution. Observation of Resident #215 on 01/23/23 at 10:12 A.M. revealed an IV line in his right upper arm. Telephone interview on 01/24/23 at 12:04 P.M. with RN #233 confirmed she did administer IV heparin to Resident #215. RN #233 reported she did not have an order from the physician to administer it and did not notify the physician of the administration. RN #233 stated she entered Resident #215's room and found his IV had disconnected from the IV tubing for his hydration. She then administered one half of a 10 ml syringe of heparin into his IV line to assess patency. She then followed that heparin flush with a flush of 10 ml normal saline solution and reconnected his IV medication. Interview on 01/24/23 at 12:10 P.M. with the Director of Nursing (DON) confirmed there was no order to administer IV heparin to Resident #215 and the physician was not notified that RN #233 had administered it to him. Review of facility policy titled Flushing Central Venous and Midline Catheters effective November 2020 revealed heparin may be administered if there is a physician's order.
CONCERN (D)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review the facility failed to ensure insulin pens were properly dated in the Southeast medication cart for Resident #28, #48 and #216. This affected three R...

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Based on observation, interview, and record review the facility failed to ensure insulin pens were properly dated in the Southeast medication cart for Resident #28, #48 and #216. This affected three Residents (#28, #48, and #216) of two medication carts reviewed for storage. The facility census was 61. Findings include: Review of the medical record for Resident #28 revealed an admission date of 11/15/21 with diagnoses including chronic kidney disease stage five, type two diabetes mellitus, and anemia in chronic kidney disease. Review of physician orders dated 05/22/22 for Resident #28 revealed an order to administer 30 units of insulin glargine solution (Lantus) pen 100 units per milliliter two times a day. Review of the medical record for Resident #48 revealed an admission date of 11/01/22 and a discharge date d 01/20/23. The diagnoses included acute respiratory failure with hypoxia, acute kidney failure, and type two diabetes mellitus. Review of physician orders dated 01/13/23 revealed an order to administer insulin lispro solution subcutaneously per sliding scale before meals daily. Review of the medical record for Resident #216 revealed an admission date of 01/23/23. The diagnoses included type two diabetes mellitus, hypertension, and hyperlipidemia. Review of physician orders dated 01/24/23 revealed to administer Soliqua (insulin) 100-33 units per microgram and give 30 units subcutaneously once daily. Observation on 01/25/23 at 9:50 A.M. of the medication cart for the Southeast unit revealed Soligua insulin pen for Resident #216 was opened and not dated. Insulin lispro for Resident #48 was opened and not dated and Lantus pen for Resident #28 was opened and not dated. An interview during the observation with Licensed Practical Nurse (LPN) #297 confirmed the pens were opened and not dated as to when they were opened. LPN #297 could not confirm when the insulin pens were opened and verified all insulin pens must be dated when opened. Review of the facility policy titled Medication Storage in the Facility, undated, revealed medications and biologicals are stored safely, securely, and properly following manufacturer's recommendations or those of the supplier.
CONCERN (D)

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

Deficiency F0773 (Tag F0773)

Could have caused harm · This affected 1 resident

Based on record review and interview, the facility failed to ensure laboratory tests were obtained per physician's order. This affected one Resident (#50) of three residents reviewed for laboratory se...

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Based on record review and interview, the facility failed to ensure laboratory tests were obtained per physician's order. This affected one Resident (#50) of three residents reviewed for laboratory services. The facility census was 61. Findings include: Review of the medical record for Resident #50 revealed an admission date of 08/16/22 with diagnoses including hypertension, adult failure to thrive and dementia. Review of the physician's order dated 10/29/22 for Resident #50 revealed he was to have a Complete Blood Count (CBC), Basic Metabolic Profile (BMP) and Vitamin D labs every November, February, May and August. Further review of Resident #50's medical record revealed the last laboratory tests were obtained on 08/17/22 and there were no CBC, BMP and Vitamin D lab reports in the medical record per the 10/29/22 physician order. Interview on 01/25/23 at 11:21 A.M. with the Director of Nursing verified Resident #50's laboratory tests for a CBC, BMP and Vitamin D level were not obtained as the physician had ordered.
Dec 2022 1 deficiency
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

Pharmacy Services (Tag F0755)

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 ensure medications were obtained timely from the pharmacy and were ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure medications were obtained timely from the pharmacy and were administered as ordered. This affected one (Resident #57) of five residents reviewed for medications being administered as ordered. The facility had a census of 55 residents. Findings include: Review of the medical record revealed Resident #57 was admitted on [DATE] with diagnoses including multiple sclerosis, stage four pressure ulcer, and adjustment disorder with mixed anxiety and depressed mood. Review of the physician's order dated 11/15/22 for Resident #57 revealed an order for Morphine Sulfate 15 milligrams (mg) three times a day for pain. Review of the Medication Administration Record (MAR) for November 2022 revealed Morphine Sulfate 15 mg was not administered on 11/15/22 at 4:00 P.M., 11/16/22 at 9:00 A.M., 4:00 P.M. and 9:00 P.M., and on 11/17/22 at 9:00 A.M. and 4:00 P.M. Interview on 12/14/22 at 9:34 A.M. with the Director of Nursing (DON) verified Morphine Sulfate 15 mg was not administered on the dates listed above. She stated the pharmacy did not send the medication until the 12/17/22 because an agency nurse faxed over the order instead of sending it electronically in the computer which caused the delay because the pharmacy does the computer transmitted orders immediately and there is a delay with faxed orders. Review of the facility policy titled Administering Medications, revised August 2022, revealed medications are to be administered in accordance with the prescriber orders, including any required time frame. This deficiency represents non-compliance investigated under Master Complaint Number OH00137850 and Complaint Number OH00134551.
Dec 2019 13 deficiencies 3 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Deficiency F0688 (Tag F0688)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 14. Review of Resident #18's medical record revealed an admission date of 06/29/19. Diagnoses included dementia, protein-calorie...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 14. Review of Resident #18's medical record revealed an admission date of 06/29/19. Diagnoses included dementia, protein-calorie malnutrition, repeated falls, osteoarthritis of both hands, and Parkinson's disease. An OT evaluation dated 07/01/19 revealed ROM in the upper arms/hands and lower legs/feet were within normal limits. A QOL Program Recommendation Referral dated 08/12/19 indicated Resident #18 had recommendations for an ambulation program and recommendations for upper extremity ROM doing balloon volley and using a two pound dowel for the left upper extremity and ROM to both lower extremities using two pound dowels and three sets of repetitions in all planes. There was no recommendation as to the frequency the ROM exercises should be provided. Review of a task list report indicated LSTNAs who were to provide QOL programs were to incorporate ROM of both lower extremities and the left upper extremity into Resident #18's routine weekly. The list was silent as to the number of times the exercises were to be completed. Review of the task list documentation revealed staff documented the ROM in both lower extremities in all planes (may use 2 pound dowel) was worked into Resident #18's weekly routine, once a week. A PT evaluation dated 09/19/19 indicated Resident #18 had impaired range of motion to the right lower extremity (knee extension 20 degrees), which was a decline from the OT evaluation on 07/01/19 when no ROM deficits were identified. The left lower extremity range of motion remained within functional limits. On 12/06/19 between 8:20 A.M. and 12:00 P.M., LPTA #642 stated therapy made recommendations when residents were discharged from therapy and then it was nursing's decision whether to or how to implement the recommendations. Resident #18 had some declines in range of motion in the right knee between discharge from therapy on 08/14/19 and a therapy evaluation completed 09/19/19. LPTA #642 indicated the decline could also be related to the resident's osteoarthritis. Review of the QOL program policy, dated 10/04/18, revealed the program was to attain or maintain each resident's highest practicable physical, mental and psychosocial well-being, consistent with the resident's comprehensive assessment or MDS assessment and plan of care. The program was to be person-centered and the focus was to provide interventions the resident desired that gave the resident a sense of satisfaction with their self, the environment and control over their life. The procedure included to ensure the MDS was completed as required which would direct the specific needs of the resident. Interventions and goals were to be focused on what the resident desired and felt provided a QOL for them. The goals were to be documented on the plan of care (POC). The interventions were to be added to the point of care (the system the STNA documented tasks). Identified improvement/decline would be assessed on a subsequent MDS assessment and the POC would be adjusted as appropriate. If a decline in function was noted, new interventions would be implemented including referral to skilled therapy. Any changes would be reported to the unit manager. The LSTNA would assist residents in completing the interventions and recommendations made by skilled therapy evaluations and referrals. The LSTNA would document completion of the programs in the point of care. Review of the QOL list of programs offered revealed all programs were to be completed by the LSTNA. The programs were not specific or measurable but only said staff would walk me to the bathroom, provide range of motion (ROM) when I am getting dressed, assist me with the NuStep (a bike machine), seat me for meals at the table where I can be cued and fed and put on my splint according to my care card. Based on observation, record review and interview the facility failed to ensure range of motion (ROM) programs and/or splinting programs were provided as planned for Resident #2, #3, #9, #15, #18, #20, #22, #31, #32, #39, #40, #41, #48 and #54. This resulted in actual harm for Residents #2, #32, and #54 who experienced a decline in ROM and/or contractures (the shortening and hardening of muscles, tendons or other tissue often leading to deformity and rigidity of joints). This affected 14 of 14 residents reviewed for restorative nursing services. The facility census was 57. Findings include: 1. Resident #32 was admitted to the facility on [DATE] with diagnoses including cerebral vascular accident (CVA/stroke), with left sided hemiplegia (paralysis on one side of the body), kyphosis (curvature of the spine or hunch back), neuropathy (painful numbness and tingling usually at the extremities including the hands, feet and/or lower legs), and osteoporosis (brittle bones). Record review revealed on 07/16/18 Resident #32 developed a contracture to her left hand and developed contractures to her left knee and ankle on 10/04/18. Review of the Quality of Life (QOL) program, which was the facility's form of restorative/maintenance program, revealed a program was started on 08/02/18. The Lead State Tested Nurse Aide (LSTNA) task information revealed staff were to apply warm compresses and provide gentle hand massage to the resident's left hand then proceed to her fingers and wrist. There was no documentation the QOL program was ever provided to Resident #32. Review of the current care plan for ROM, initiated on 07/19/15, revealed Resident #32 had osteoarthritis and buckling knees due to her CVA. The resident had left foot inward rotation and required staff to reposition her foot. Resident #32 had a contracture of her left hand, ankle and knee. Interventions initiated on 10/22/18 included wear a left pressure relieving ankle and foot orthotic (PRAFO) at all times and a left knee extension splint every evening and night shift up to eight hours while in bed. In addition, staff were to provide ROM to both of the resident's lower legs/feet. Review of the current activities of daily living (ADL) care plan, initiated 10/19/18, revealed Resident #32 was to wear the left hand splint according to the physician orders. The care plan was updated on 03/11/19 and directed staff to follow the QOL tasks as assigned. Review of the current resident care card (a quick guide to each resident's individual needs which was hung in the residents room for STNA reference) revealed the resident was to have a carrot (orthotic device) placed in the palm of her hand (to position the fingers away from the palm). The orthotic had measurements for specific placement used to improve contractures in her left hand at all times. Staff were directed to slowly remove the carrot only for hygiene. The resident was to wear a left knee brace in the evening and throughout night. There was no indication for wearing the PRAFO boot. Review of the physician's orders dated 10/22/18 revealed Resident #32 was to wear the left PRAFO boot at all times to the resident's comfort with the kickstand down when in bed. The left knee extension splint was to be worn every evening and night shift up to eight hours at night in bed due to her left knee contracture. Review of the QOL STNA task information dated 11/13/18 revealed staff were to provide passive range of motion (PROM) to the left knee and ankle and to her right lower leg/foot two to three times a week. Weights may be used for strengthening. Review of the task documentation for completion revealed no documentation or evidence the QOL programs were ever provided or implemented. Review of the OT evaluation dated 01/21/19 revealed Resident #32 was seen for contracture and pain of her left hand and muscle weakness. Therapy goals included to increase wrist flexion and extension from five to 10, to increase the use of her left wrist and to prevent further contractures. The resident would tolerate a small hand roll in her left hand while wearing a palmar guard (an orthotic used as a barrier between the fingers and palm to prevent injury to the palm from severe finger flexion contractures) for one hour without complaints of pain, increase extension of the fingers/digits and thumb to five degrees in order to increase ability to put on and take off the orthotic and to increase ROM so the resident could perform hygiene and grooming. The resident was able to tolerate a massage to the hand for 10 minutes without complaints of pain to assist in increasing ROM of the hand joints. The resident wanted her fingers to be straighter and stronger for use. The resident tolerated active range of motion (AROM) to her left shoulder contracture (flexion was at 85 degrees). Review of the OT Discharge summary dated [DATE] revealed the resident met the goals including digit and thumb extensions from five to 10, wearing of the palmar guard with roll without pain, and increased her AROM to the left shoulder from 85 to 120 degrees. The wrist showed an improvement from 20 degrees flexion to 55 degrees and 20 degrees extension to 50 degrees. The resident was not able to tolerate the palmar guard as previously ordered and the orthotic was changed to a carrot. The resident was referred to the QOL program for ROM to her upper arms/hands, massages and application of the carrot orthotic. Review of the PT Discharge summary dated [DATE] revealed the resident had a reduction in pain to her left lower leg/foot, down to a four on the pain scale. The resident's knee showed an improvement from lacking knee extension from 35 degrees to 20 degrees and the ankle improved from lacking 35 degrees to 25 degrees. The resident demonstrated improvements in her ability to wear the orthotics. The resident was referred to the QOL or restorative/maintenance program for splinting/orthotic application in order to facilitate increased opportunities for functional task participation, ROM and exercises. Review of the PT evaluation dated 06/27/19 revealed Resident #32 was seen again by therapy because her therapy screen indicated she had a functional decline in standing and endurance in standing due to increased pain in the left knee and ankle. The resident had a reduction in ROM from the previous evaluation. Review of the PT Discharge summary dated [DATE] revealed the resident showed a reduction in pain to the left knee and ankle with an increase in ROM to the left ankle and knee and an increase in strength for transfers. The resident was referred to the QOL program to maintain the current level of performance and prevent decline for AROM, PROM and transfers. Review of the QOL referral dated 08/02/19 revealed staff were to provide stretches to both lower legs/feet with ROM and to ensure proper fit of the knee brace. Review of the QOL STNA task initiated 08/09/19 revealed staff were to do stretches for both lower legs/feet and ensure proper fit of the knee brace. Review of the participation documentation from 08/09/19 to the present revealed no documentation or evidence the program was ever implemented. Review of the OT evaluation dated 10/16/19 revealed the resident was seen again because she was not able to tolerate the left hand orthotic (carrot) and had a decrease in ROM from the previous evaluation. The resident not able to keep the carrot in place as planned. The resident indicated the staff had lost the carrot weeks ago and no devices were being put into her hand. Review of the OT Discharge summary dated [DATE] revealed the resident was to have a modified orthotic to the left hand and staff were educated on implementation. The resident was referred to the QOL program for ROM and monitoring/application of the modified orthotic. Review of the modification of the quarterly minimum data set (MDS) assessment dated [DATE] revealed the resident was cognitively intact and had limited ROM on one side of her body for her upper arm/hand and lower leg/foot. The assessment revealed Resident #32 was alert and oriented to all spheres and was cognitively intact for daily decision making abilities. Review of the STNA task implementation for the last 30 days revealed the following: a. resident's left knee extension splint was to be worn at night. The STNA documentation was marked as not applicable or that the splint was on during the day. On 12/02/19 at 10:14 A.M. and on 12/03/19 at 9:56 A.M. the documentation indicated the splint was in place. b. PROM to the left knee and ankle and AROM/PROM to the right leg/foot was to be done two to three times a week which may be done with two pound weights. There was no evidence this was completed. c. Incorporate stretching to both lower legs/feet and ensure proper fit of the brace in her routine. There was no evidence this was completed. d. Apply warm compresses and provide gentle hand massage to the left hand then proceed to the fingers, hand and wrist. Then apply the carrot orthotic. There was no evidence these were completed. e. The left ankle PRAFO was to be worn 24 hours a day/seven days a week. The documentation revealed staff frequently recorded it was not applicable. On 12/02/19 at 10:13 A.M. and on 12/03/19 at 9:56 A.M. the documentation indicated the PRAFO boot was in place. Review of the December 2019 treatment administration record (TAR) revealed the resident had the left knee extension splint in place during the evening and night shift on 12/02/19. Further review revealed the resident had the left ankle PRAFO in place during the afternoon shift on 12/02/19 and during the day and afternoon shifts on 12/03/19. On 12/02/19 at 10:00 A.M. and 12:34 P.M., the resident was observed in her wheelchair without any orthotics in her left hand or on her left leg or foot. On 12/02/19 at 12:35 P.M., interview with the resident revealed she was in a lot of pain. She stated the staff did not have any orthotics for her hands. She said she used to have a carrot but did not know where it was. She stated it had been a while since any one put on her PRAFO boot. She stated the staff put on her left knee extension brace sometimes during the day and did not know it was supposed to be put on at night. She stated she would wear all the orthotics because therapy said it would help with her pain. She stated staff did not always apply the devices as ordered. On 12/02/19 at 3:00 P.M. and 5:00 P.M., Resident #32 was observed in her wheelchair without any orthotics in her left hand or on her left leg. On 12/02/19 at 5:03 P.M., interview with STNA #592 verified the resident did not have any orthotics in place and she was not aware the resident was supposed to be wearing any. She stated there was a paper hanging in each resident's room as to their specific needs but said she had not reviewed it. STNA #592 proceeded to ask the resident if she wanted the orthotics on and she said she did and Licensed Practical Nurse (LPN) #585 told her she should always be wearing them. On 12/02/19 at 6:05 P.M., Resident #32 was observed without any orthotics in place. On 12/03/19 at 8:50 A.M., Resident #32 was observed without any orthotics in her hand. On 12/03/19 at 12:05 P.M., Resident #32 was observed to be holding the carrot orthotic, but it was almost out of her palm and only the tip of the carrot was in her palm. On 12/03/19 at 12:06 P.M., interview with the resident revealed someone found her carrot because it was lost and put it in her hand. She said it hurt and kept sliding out. The resident stated she was not able to put the carrot back in her palm herself and needed staff to do it. On 12/03/19 at 12:07 P.M., LPN #585 observed the carrot out of place but did not attempt to readjust the carrot to the proper position. On 12/03/19 at 2:55 P.M., 4:00 P.M., 4:55 P.M., and 6:05 P.M., Resident #32 observed without the carrot in her palm. On 12/03/19 at 6:06 P.M., interview with the resident revealed she was in a lot of pain, she said the staff removed her carrot and put it in her bag earlier but she could not reach the bag on the back of her wheelchair. On 12/04/19 at 8:45 A.M., the resident was observed without her carrot in her palm. On 12/04/19 at 8:46 A.M., interview with the resident revealed she was in too much pain to eat and her carrot was still in her bag from yesterday. On 12/04/19 at 10:15 A.M., interview with STNA #596 revealed she was not sure what orthotics the resident needed because night shift got the resident up and dressed and they were responsible for putting on all the residents interventions including orthotics. On 12/04/19 at 11:00 A.M., interview with Registered Nurse (RN) #701 verified the above concerns. On 12/04/19 at 1:15 P.M. , interview with LPN #585 revealed the orthotics help with the resident's chronic pain and he was not aware of her refusing to wear them. LPN #585 stated the carrot helps with pain but when it falls out or is removed it hurts to put it back in her hand. On 12/04/19 at 5:15 P.M., interview with RN #572, with RN #701 present, revealed she was in charge of the QOL program which replaced the restorative nursing program. RN #572 verified the QOL program did not include completing any resident assessments, did not include the development of measurable goals, monitoring progress or implementation of the programs according to skilled therapy recommendations when residents were discharged . She said the QOL program included herself and two Lead State Tested Nurse Aides (LSTNAs), LSTNA #542 and LSTNA #501. LSTNA #501 was supposed to work on the QOL programs two to three days a week and LSTNA #542 only worked weekends. RN #572 verified these LSTNAs were frequently pulled from doing the QOL programs to work the floor as STNAs as there were not enough STNAs to provide daily care for the residents. RN #572 verified there were no actual assessments completed because it was not a true restorative program. She said the facility discontinued their restorative program in October 2018 and replaced it with the QOL program. The goal of the QOL program was to improve the resident's overall QOL. RN #532 and RN #701 verified the QOL program was not implemented to maintain Resident #32's level of function when she was discharged from skilled therapy services. This resulted in the avoidable declines in ROM and function. On 12/04/19 at 6:45 P.M., interview with STNA #587 revealed she was not aware the resident was to have a hand roll in place in her contracted hand nor did she complete ROM. She said she just lifted her arms up when she was dressing her. On 12/05/19 at 9:25 A.M., interview with Physical Therapy Assistant (PTA) #642 revealed the resident's left knee extension brace was meant to be worn at night because it was an extension brace to help straighten the leg and did not help when the resident was in the wheelchair or when the resident's leg was bent. The PRAFO boot should be on during the day to stretch out the resident's foot and help with her pain. PTA #642 said she could wear it at night but she has a lot of neuropathy pain especially, at night, and she has Biofreeze cream for that. PTA #642 said Resident #32 does come to them at times, even when she is not in therapy, to ask about different things to try for her hand pain. In addition, stretching was very important to relieve the tightness in her hand before applying any orthotic. PTA #642 said they had tried different devices with her, including custom fabricated cone splints, a carrot splint and now most recently a towel roll. PTA #642 said they had picked her back up for therapy several times due to declines in ROM and worsening of her contractures. PTA #642 stated the January evaluation showed a decline in her ankle, knee and hand including her thumb ROM. The staff were not able to get her to stand up straight enough to use the sit to stand mechanical lift due to her worsening knee contracture. PTA #642 indicated the resident was also started on a hand roll with a [NAME] guard over it because she had lost all ROM in her thumb. Resident #32 was only able to open her palm 3.0 centimeters (cm). On discharge, PTA #642 said they were able to get her to wear the carrot (which needed a greater ROM) and she was able to open her palm up to 8.0 cm. They saw her again in June 2019 for a decline in AROM and PROM to the left extremities. On 08/02/19 at discharge Resident #32 was able to gain back some knee extension to be able to use the sit to stand lift but not back to her previous level. The resident has chronic pain including neuropathy in her feet and at times she can't even handle a blanket touching her toes. The resident was again referred to the QOL program. Then they picked her back up in October 2019 because the resident again had a decline in ROM of the left extremities and the carrot was not able to be maintained in position due to an increase in tightness/contracture of the palm. On discharge they were not able to open the palm enough for the carrot and had to change to a towel roll in her hand. They picked her up again just this week because the resident came to us and said she found her carrot and wanted to wear it. PTA #642 verified the declines could have been caused from not wearing the orthotics as planned. On 12/05/19 at 2:57 P.M., interview with LSTNA #501 revealed she started in this position in August 2019. Her role was to interact with the residents, do group exercises, take the residents outside when it was warm, provide them with snacks and talk to them. She said the difference in her role as a LSTNA versus working the floor as a STNA was she was to do group activities, puzzles, fold items and talk with the residents. When working as a LSTNA they did not provide personal care. LSTNA #501 verified she mostly worked in the secured dementia unit, both as a LSTNA and a floor STNA. She verified she did not get to work as a LSTNA very much, maybe one to two days in each two week period because she was usually pulled to work the floor as an STNA. She verified she rarely was able to complete ROM or ambulation programs, but if she did she documented under the LSTNA tasks in the computer. She stated the floor STNAs were responsible for applying splints. She said she works every other weekend as a floor STNA. The LSTNA said the other LSTNA, LSTNA #542, only worked weekends. She said he is also usually pulled to work the floor on the weekends she works. LSTNA #501 stated when she was asked to do the LSTNA position for the QOL programs she was told she could do what she wanted to and it was her program to do group activities mostly on the secured dementia unit. She said there were no other activity staff working in the secured dementia unit other than herself. On 12/07/19 at 12:55 P.M., phone interview with LSTNA #542 reveled he only worked weekends as an LSTNA but frequently got pulled to work the floor as they did not have enough staff to provide the care to the residents especially since October 2019. He said the facility changed the name of the restorative nursing program to the QOL program. The QOL program was less structured and there were no specific goals for residents to reach such as distance for ambulation. He said he did not do ROM programs and stated the floor staff were assigned ROM programs. He indicated he was responsible for ensuring residents had on their splints. He was also responsible for doing group exercise activities with residents. 2. Resident #54 was admitted to the facility on [DATE] with diagnosis including dementia. On 10/30/19 a diagnosis of contractures of the right knee and left elbow was added. Review of the current resident care card revealed Resident #54 was to have a right knee brace in place at all times except for hygiene, a sling to the right arm when out of bed, and a [NAME] guard was to be in his left hand at all times. Review of the PT evaluation dated 02/24/19 revealed the resident had impaired ROM of his right lower leg/foot. On discharge from PT on 04/25/19 the resident had regained his ROM. The resident was referred to the QOL program for AROM and PROM to both legs/feet. Review of the OT evaluation dated 02/25/19 revealed the resident had a contracture to the left hand and needed a resting hand splint to prevent further contractures or worsening of contractures. On discharge from OT on 05/10/19 the resident was to wear a palmar guard to the left hand at all times. The resident was referred to the QOL program for implementation of the splinting and ROM to the left arm/hand. Review of the current care plan revealed the resident had contractures to the right knee and left hand. Interventions included for him to wear the sling to the right arm when out of bed and [NAME] guards at all times for comfort according to OT recommendations. A right knee splint was to be worn according to PT recommendations. Review of the current physician order initiated 03/07/19 revealed Resident #54 was to wear the sling on the right arm when out of bed. Review of the current physician order initiated 03/22/19 revealed Resident #54 was to wear palmar guards at all times. Review of the significant change MDS 3.0 assessment dated [DATE] revealed Resident #54 was severely cognitively impaired and had limited ROM to one side for his upper arm/hand and lower leg/foot. Review of the PT evaluation dated 06/04/19 revealed Resident #54 had a decline in ROM of his right and left knees. With therapy and upon discharge on [DATE], the resident had improvement in ROM of his right and left knees with splinting to the right knee at all times. The resident was referred to the QOL program for AROM, PROM and splinting. Review of the OT evaluation dated 06/10/19 revealed Resident #54 was seen for a decrease in ROM to his left hand. The resident was not able to tolerate PROM and grimaced with three attempts. The resident was no longer able to tolerate the palmar guards. After additional therapy and upon discharge on [DATE] the resident was to have a rolled wash cloth in his palm at all times as tolerated. The resident was referred to the QOL program for ROM and splinting. Review of the current physician order, initiated 08/08/19, revealed Resident #54 was to wear the right knee splint at all times except for hygiene and bathing. Review of December 2019 TAR revealed the palmar guards, right sling and right knee splint where in place on all three shifts on 12/02/19 and 12/03/19. Review of the STNA documentation revealed the right knee splint and left hand rolled wash cloth were in place for the last 30 days, including 12/02/19 and 12/03/19. Further review revealed PROM was only performed on six of the last 30 days. On 12/02/19 at 10:05 A.M., 12:15 P.M., 3:30 P.M. and 4:22 P.M., Resident #54 was observed without any orthotics in either of his hands or to his legs. He had no sling to his right arm. His right knee was bent up and his left ankle was bent inward. On 12/02/19 at 4:25 P.M., interview with LPN #567 verified the resident did not have any of the ordered orthotics in place to either hand or leg and did not have the sling in place. LPN #567 indicated they were not aware the resident was to have these in place. On 12/02/19 at 5:40 P.M. and 6:55 P.M., Resident #54 was observed without any orthotics in place to the hands or legs and no sling was observed to the right arm. His right knee was bent up and his left ankle was bent inward. On 12/02/19 at 6:56 P.M., interview with STNA #540 verified the resident did not have on his knee brace and the STNA was not aware the resident was to wear [NAME] guards or a right arm sling. On 12/03/19 at 8:45 A.M., 12:10 P.M., 1:00 P.M., 2:53 P.M., 3:55 P.M., 4:54 P.M. and 6:10 P.M., the resident was observed without any orthotics on his hands or legs and the right arm sling was not observed on his right arm. His right knee was bent up and his left ankle was bent inward. On 12/04/19 at 8:42 A.M., Resident #54 was observed without any orthotics in either of his hands or legs and no sling was observed to his right arm. His right knee was bent up and his left ankle was bent inward. On 12/04/19 at 9:40 A.M., Resident #54 was observed with his right knee brace on but no hand orthotic or sling. On 12/04/19 at 9:51 A.M., interview with STNA #532 verified Resident #54 did not have on [NAME] guards or a sling and did not know the resident was supposed to wear them. On 12/04/19 at 9:57 A.M., interview with RN #559 verified Resident #54 did not have on the [NAME] guards or the sling. RN #559 said Resident #54 says ouch when applying the knee brace and [NAME] guards but thought it was just a behavior of his. On 12/04/19 at 11:00 A.M., interview with RN #701 verified the above concerns. On 12/04/19 at 5:15 P.M., interview with RN #572, with RN #701 present, revealed she was in charge of the QOL program which replaced the restorative nursing program. RN #572 verified the QOL program did not include completing any resident assessments, did not include the development of measurable goals, monitoring progress or implementation of the programs according to skilled therapy recommendations when residents were discharged . She said the QOL program included herself and two Lead State Tested Nurse Aides (LSTNAs), LSTNA #542 and LSTNA #501. LSTNA #501 was supposed to work on the QOL programs two to three days a week and LSTNA #542 only worked weekends. RN #572 verified these LSTNA's were frequently pulled from doing the QOL programs to work the floor as STNA's due to not having enough STNA's to provide care to the residents. RN #572 verified there were no actual assessments completed because it was not a true restorative program. She said the facility discontinued their restorative program in October 2018 and replaced it with the QOL program. The goal of the QOL program was to improve the resident's overall QOL. RN #532 and RN #701 verified the QOL program was not implemented to maintain Resident #54's current level of function when he was discharged from skilled therapy, resulting in an avoidable declines in ROM. On 12/04/19 at 6:45 P.M., interview with STNA #587 revealed she was not aware the resident was to have a hand roll in place in his contracted hand or a splint for his knee. She said she did not complete ROM with him she just lifted his arms when she was dressing him. She said she was not aware the resident was to use a sling for his right arm. On 12/05/19 at 10:05 A.M., interview with Certified Occupational Therapy Assistant (COTA) #702 and PTA #642 revealed the resident had displayed an increase in pain in his hand but he let them put on his orthotic. They said they were informed by STNA #540 she could not get a towel in the resident's hand and no one was able to find the [NAME] guard. They said Resident #54's son informed them he noticed an increase in the clenching of his hand in the last several days. PTA #642 stated she worked 11/30/19 and the resident did not have his knee brace or [NAME] guards in place. She said she was told they were soiled. COTA #702 stated she had to ask for them and did not receive them until 12/03/19. They said when they initially saw him, he had a resting hand splint over his hand and wrist and was bent for ROM in his fingers, with a small opening of his hand. They said he was not able to tolerate this and they had to change to a [NAME] guard for his left hand but it was not holding up his thumb, so on discharge he was to have a towel roll. The resident was seen again on 12/03/19 and he had some ROM in his index finger but the other fingers had minimum ROM. They said they were not able to try anything inside his palm because of the tightness. They said the therapist was able to stick her fingers into his palm and the resident's hand was so tight it took her 10 minutes to remove her fingers from his contracture. The resident's left hip was externally rotated and his left knee was flexed with internal tibia torsion, which causes his ankle to bend in, its the knee bending in so ankle does not need treatment at that time. The resident did express pain and AROM was not able to be performed to the left leg. On 12/05/19 at 10:28 A.M., interview with PT #703 revealed at d[TRUNCATED]
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Deficiency F0697 (Tag F0697)

A resident was harmed · This affected 1 resident

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

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to ensure effective management of chronic pain for one resident ( Resident #32). This resulted in actual harm when Resident #32 was unable to participate in her activities of daily living (ADLs) due to severe pain. This affected one of three residents reviewed for pain. The facility census was 57. Findings include: Resident #32 was admitted to the facility on [DATE] with diagnoses including cerebral vascular accident (CVA/stroke) with left sided hemiplegia (paralysis on one side of the body), kyphosis (curvature of the spine or hunch back), neuropathy (painful numbness and tingling usually at the extremities including the hands, feet and/or lower legs), and osteoporosis (brittle bones). On 07/16/18 Resident #32 developed a contracture (the shortening and hardening of muscles, tendons or other tissue often leading to deformity and rigidity of joints) to her left hand and on 10/04/18 she developed contractures to her left knee and ankle. Review of the modified quarterly Minimum Data Set assessment 3.0 (MDS) dated [DATE] revealed Resident #32 was alert and oriented to all spheres and was cognitively intact for daily decision making abilities. Review of the current pain care plan initiated 10/08/14 revealed Resident #32 had pain mainly in her left ankle, left leg, shoulders, and hips. The care plan indicated she also had neuropathy pain and had complaints of pain all over due to her kyphosis. The interventions included monitor for pain medication efficacy and have the resident rate her pain on a scale from zero to 10, with zero being no pain and 10 being the most pain ever. Nursing staff were to update the physician if pain persisted without effective relief. Additional interventions initiated on 07/15/18 included Resident #32 wear the left pressure relieving ankle and foot orthotic (PRAFO) according to the physician orders and on 10/19/18 wear the left knee extension splint according to physician orders. Review of Resident #32's current physician's orders revealed on 02/16/16 an order was written for Norco, an opioid pain medication containing Hydrocodone and acetaminophen (Tylenol), 5 milligrams (mg)-325 milligrams (mg) to be given every four hours only when needed for pain. It was not administered on a regular schedule. On 02/26/16, the physician ordered acetaminophen, 325 mg, two tablets every four hours only when needed for pain. On 01/08/17, a physician order was written for Norco, 5 mg-325 mg (the lowest dose), to be administered twice a day on a regular schedule for bone pain. On 04/23/18, a physician order for the topical analgesic, Biofreeze, was ordered to be rubbed on her shoulders every shift and to her left hip and foot every shift. On 10/21/18, the physician ordered Cymbalta, an antidepressant medication, 60 mg twice a day for leg pain, back pain and depression. Review of the physical therapy (PT) evaluation dated 01/18/19 revealed the resident was seen for spastic hemiplegia with affected her left side, muscle wasting and atrophy (muscle wasting) in multiple sites. The goals of therapy included to increase pain free range of motion (ROM) on Resident #32's left lower leg or extremity (LLE) to improve her ability to perform transfers. This evaluation indicated pain was limiting the resident's functional activities of daily living. The clinical impression revealed Resident #32 had increased left sided pain and weakness limiting the ability to perform sit to stand transfers and balance tasks. A physician order dated 06/20/19 revealed the Norco pain medication was increased from twice a day to three times a day at 5 mg-325 mg for pain management. Review of the physical therapy (PT) treatment session records between 06/27/19 and 08/02/19 revealed moist heat prior to manual stretching and massaging helped reduce Resident #32's pain. Review of the physical therapy daily notes from 06/26/19, 07/02/19, 07/03/19, 07/04/19, 07/05/19, 07/08/19, 07/11/19, 07/19/19, 07/25/19, 07/30/19 and 08/02/18 revealed the resident had pain that was relieved by therapy interventions including stretching and moist heat. Review of the pain evaluation dated 07/25/19 revealed the resident constantly had severe pain daily that affected her activities of daily living (ADL's). The assessment was incomplete and her pain level was not scored using there numeric scale. It only indicated the pain was severe. The plan section of this evaluation was to continue the current interventions for pain control. No new interventions were implemented for pain control. On 08/02/19 Resident #32 was discharged from PT and referred to the Quality of Life (QOL) program. Review of the QOL program referral dated 08/02/19 revealed nursing staff were to provide gentle massages prior to putting on her splints each day. Review of the task documentation records revealed the program was not implemented or provided since 08/02/19. Review of the physician's progress note dated 08/05/19 revealed Resident #32 had diffuse pain in multiples joints due to primary osteoarthritis. The resident had a lot of pain in the lower lumbar spine and neck pain with decreased range of motion to multiple joints. The resident also had a lot of pain in her cervical spine (neck area). The resident displayed abnormal reflex and muscle tone. The physician documented the resident received Norco three times a day at the lowest dose, which was 5 mg-325 mg. The resident had received Cymbalta, an antidepressant also used to relieve neuropathy pain, but it was discontinued by the psychiatrist on 07/31/19. The note indicated Resident #32 was medically stable and no changes in the plan of care were indicated. Review of the interdisciplinary team meeting notes dated 08/06/19, held with Resident #32 and her daughter, revealed the resident had chronic pain. There was no documentation or evidence they discussed options to address her ongoing, chronic pain although the pain evaluation from 07/25/19 indicated she had severe pain that limited her ability to do ADL's. Review of the physician's progress note dated 09/11/19 revealed the resident had diffuse multiple joint pain due to primary osteoarthritis. The note indicated the resident had a lot of pain in the lower lumbar spine and neck pain with decreased range of motion to multiple joints. The resident also had a lot of pain in her cervical spine. The resident displayed abnormal reflex and muscle tone. The resident received Norco three times a day. This progress note indicated Resident #32 was medically stable and no change in the plan of care was indicated. Review of the nurse's note dated 10/01/19 revealed the resident refused to take a shower because she was in so much pain. There was no evidence any addition as needed pain medication or any nonpharmacological pain relieving interventions were provided. The physician was not notified regarding pain which limited Resident #32's ADL ability. Review of the pain evaluation dated 10/07/19 revealed the resident constantly had pain daily that affected her activities of daily living. On a scale of zero to 10, with zero being no pain and 10 being the most pain, the resident scored her pain an eight. The plan section of this evaluation indicated they would continue the current interventions. There were no new interventions put into place and evidence the physician was notified in order to address her unrelieved pain. Review of the physician's progress note dated 10/09/19 revealed the same information as previous notes. Resident #32 had diffuse and multiple joint pain due to primary osteoarthritis. The resident had a lot of pain in the lower lumbar spine and neck pain with decreased range of motion to multiple joints. The resident also had a lot of pain in her cervical spine. The resident displayed abnormal reflex and muscle tone. The resident received Norco three times a day. The physician indicated they would continue with the current plan of care. Review of the occupational therapy (OT) treatment session records between 10/16/19 and 11/22/19 revealed Resident #32's pain was decreased with the provision of range of motion, gentle massage and warm moist heat. Review of the nurse's note dated 10/25/19 revealed Resident #32 complained of pain in the right anterior axilla (front shoulder area). There was no documentation of her pain level, location or that any interventions to relieve were attempted. There was no evidence any as needed pain medications were administered or that any non-pharmacological pain relieving interventions were attempted. Review of the interdisciplinary team meeting notes dated 10/29/19 with Resident #32 and her daughter revealed the resident had chronic pain. There was no documentation or evidence of discussion of any other options to address her unrelieved pain. Review of the pain evaluation dated 11/01/19 revealed Resident #32 constantly had pain, on a daily basis, that affected her activities of daily living. The resident's pain was rated as a 10 out of 10. The plan was to continue the current interventions. There were no new interventions planned or implemented to attempt to reduce her pain. Review of the physician's progress note dated 11/08/19 continued to document the same information. It indicated Resident #32 had diffuse multiple joint pain due to primary osteoarthritis. The resident had a lot of pain in the lower lumbar spine and neck pain with decreased range of motion to multiple joints. The resident also had a lot of pain in her cervical spine. The resident displayed abnormal reflex and muscle tone. The resident received Norco three times a day. The note indicated the resident was medically stable and no change in the plan of care was indicated. The resident was discharged from OT on 11/22/19 and referred to the QOL program. Review of the QOL program referral dated 11/22/19 revealed nursing staff were to provide warm compresses and gentle massage to the left hand then proceed to the fingers, hand and wrist prior to applying the orthotic. These modalities aided in pain relief during therapy. Review of the task documentation records revealed the program was not implemented or provided since 11/22/19. On 12/02/19 at 12:35 P.M., interview with Resident #32 revealed she was in terrible pain and wanted to talk to the doctor because she wanted a different or stronger medication for the pain. The resident stated she just wanted to die because she could not live with this much pain anymore. She said it had been going on for a long time and she said she tells the aides and nurses every day that she is in pain. Review of the 12/02/19 case management note (after surveyor intervention on 12/02/19) revealed RN #559 spoke to the resident who stated her pain was terrible and indicated her left leg, foot and buttock were hurting. The resident wanted the doctor to be called to see what could be done. The resident's left leg splint was not on her leg and the note indicate the resident requested it be put on because it helped with the pain. No other information was found to indicate the physician was contacted. On 12/02/19 at 5:03 P.M., interview with State Tested Nurse Aide (STNA) #592 revealed Resident #32 was always complaining of being in pain and she would inform the nurse daily. On 12/02/19 at 5:15 P.M., interview with Resident #32 revealed she was upset because she had previously asked Licensed Practical Nurse (LPN) #585 to call the doctor to get her more pain medication but he said there was nothing else they could do for her. She stated the pain was so bad in her left leg and foot. On 12/02/19 at 6:18 P.M., interview with Registered Nurse (RN) #559 revealed she was aware Resident #32 had chronic pain and said she was given her regularly ordered pain medication at 1:00 P.M. today. She also gets topical Biofreeze to her shoulder, knee, hip and foot daily. RN #559 verified she completed the pain assessments which indicated Resident #32 was always in significant pain. RN #559 verified there had not been any other pain relieving interventions implemented since 06/20/19 when the resident's Norco pain medication was increased from twice a day to three times a day. On 12/04/19 at 8:45 A.M., the resident was observed in the dining room and had not eaten any of her breakfast. Resident #32 said she was in too much pain to eat. She stated she told LPN #585 again today and he was going to see if the doctor would come in and see her. No other interventions were attempted. On 12/04/19 at 10:15 A.M., interview with STNA #596 revealed the resident was in pain daily, especially her feet, which hurt a lot at night and her left leg, foot and hand most of the time. She has been complaining of more pain more frequently and says it worse and she lets the nurse know daily. On 12/04/19 at 1:00 P.M., interview with RN #559 and Licensed Social Worker (LSW) #630 verified there was no evidence of any new pain control interventions since the increase in pain medication on 06/20/19. On 12/04/19 at 1:15 P.M., interview with LPN #585 verified the resident had chronic pain daily and she was receptive to suggestions. LPN #585 verified the resident complained of pain to him on 12/02/19 and 12/03/19 but there was no documentation in the medical record. LPN #585 verified he could not document every time the resident said she was in pain. He stated the pain medication was increased on 06/20/19 and verified there were no other interventions since then. LPN #585 said the resident did seem to be complaining of more pain and she had an increase in buttock pain. LPN #585 said she recently received a different wheelchair and thought it could be the cushion causing the increased pain but verified he had not attempted to try a different cushion. LPN #585 verified Resident #32's pain affected her everyday living including her not wanting to eat, not participating in activities and at times not wanting to get out of bed. He said the doctor was aware but he could not call the doctor every time the resident complained of pain because it was daily. On 12/04/19 at 5:15 P.M., interview with RN #532 and RN #701 verified the QOL programs recommended by PT and OT were not implemented to maintain the resident's current level of function and aid in pain relief. On 12/05/19 at 11:40 A.M., interview with Physician #704, with the Executive Director and RN #701 present, indicated they talked about Resident #32's pain monthly in the interdisciplinary team meetings (IDTs) but verified there was no documented evidence of this being discussed. He said the resident has and will always have chronic pain. He said he did not want to use opioids because they cause other problems. When asked about any non-pharmacological interventions attempted, he verified none were mentioned or attempted. He said the resident had severe kyphosis, neuropathy pain and other joint pain, neck pain, hand and leg pain. He said when the resident was in bed her feet hurt so bad and she felt better when she was up in the wheelchair. He said the psychiatrist stopped her Cymbalta which he was using to help with her neuropathy and he said it had helped. The physician had no answer when asked why he did not discuss this with the psychiatrist, restart the medication or try a different medication. He said he wouldn't put her on any stronger medications or increase the strength of her current Norco. The physician was made aware of the conversation when the resident stated she would rather be dead than to have to deal with all this pain. Physician #704 said there was nothing else they could do for the resident's chronic pain. He verified there was no documentation Resident #32 was involved in her own care and treatment related to her unrelieved pain. Review of the pain assessment and management policy, last reviewed 04/17/19, revealed the purpose was to help staff identify pain in residents and to develop interventions consistent with resident's goals and needs, including addressing the underlying causes of pain. The physician and staff would identify residents who had pain or who were at risk for having pain. Including review of the treatments the resident was currently receiving for pain both complimentary and non-pharmacologic treatments. The resident would be assessed on admission, quarterly, with a significant change and when there was an onset of new pain or worsening of existing pain. The staff would identify any situations or interventions when an increase in pain may be anticipated such as need for repositioning. The staff and physician would evaluate if the was affecting the resident's mood, activities of daily living, sleep and quality of life as well as how the pain may be contributing to social isolation, falls and range of motion issues. The physician would help identify the extent to which underlying causes of pain would be addressed or reversed. The physician would perform or order appropriate tests as needed to help clarify sources of pain. With input from the resident, the physician and staff would establish goals of pain treatment. The staff would evaluate effectiveness of the analgesic medications and document on the medication administration record. If the residents pain was complex or not responding to standard interventions, the attending physician may consider additional consultative support. If pain management was obtained, the attending physician would maintain an active role by reviewing the consults, recommendations and evaluating subsequent progress.
SERIOUS (H)

Actual Harm - a resident was hurt due to facility failures

Deficiency F0676 (Tag F0676)

A resident was harmed · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to ensure Resident's #2, #3, #5, #7, #9, #10, #15, #18, #2...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to ensure Resident's #2, #3, #5, #7, #9, #10, #15, #18, #20, #21, #24, #30, #31, #33, #39, #40, and #43 received restorative/maintenance programs to maintain function for activities of daily living (ADLs) and/or prevent decline in ADL's after being discharged from skilled therapy. This affected 17 of 17 sampled residents. Actual Harm occurred when skilled therapy recommendations were not followed/implemented by the quality of life (QOL) program resulting in an avoidable declines in ambulation for Resident's #10, #18, #21, and #33, an avoidable decline in ambulation and transfers for Resident #15, and avoidable declines in the ability to sit to stand for Resident #7 and Resident #20. Findings include: 1. Review of Resident #18's medical record revealed diagnoses including dementia, osteoarthritis of both knees and Parkinson's disease. A plan of care initiated 07/10/19 indicated Resident #18 had an activity of daily living (ADL) deficit related to dementia and needed staff assistance for ADLs. Interventions included obtaining a Physical Therapy (PT) evaluation and treating the resident as indicated per orders. Interventions also included providing QOL tasks as assigned. Resident #18 received physical therapy (PT) from 06/30/19 to 08/14/19. A QOL Program Recommendation Referral dated 08/12/19 revealed recommendations for Resident #18 to be ambulated 30 feet with a front wheeled walker with minimum assistance with a wheelchair following. A PT Discharge summary dated [DATE] indicated Resident #18 was able to ambulate up to 100 feet with a front wheeled walker needing minimum assist to contact guard assistance for safety, displaying a step to/through gait pattern needing visual cues to increase step length and cadence (voice inflection) with a wheelchair following. Resident #18's prognosis to maintain her level of function was good with consistent staff follow through. A Restorative Nursing Program/Functional Maintenance Program was completed with the Interdisciplinary team for ambulation. Review of the nursing assistant task list report, which is where specific programs were listed and where staff recorded provision of programs, revealed an entry to please ambulate Resident #18 short distances with a front wheeled walker, a gait belt and with a wheelchair to follow. Review of the documentation regarding ambulation on the task list between 08/14/19 and 09/19/19 revealed Resident #18 was ambulated three times. A PT evaluation dated 09/19/19 indicated Resident #18 was referred for PT services due to a decline in function. Resident #18 reported increased difficulty with transfers. Nursing had to downgrade the transfer device and Resident #18 declined as evidenced in increased staff assistance needed for mobility. Resident #18 needed maximum staff assistance to transfer and she was totally dependent on staff without attempts to initiate ambulation. Resident #18 did not take any steps during the PT evaluation. A QOL Program Recommendation referral form dated 10/31/19 indicated recommendations for Resident #18 to now use a sit to stand lift for transfers. A PT Discharge summary dated [DATE] indicated Resident #18 was able to ambulate 25 feet with moderate assistance. On 12/06/19 between 8:20 A.M. and 12:00 P.M., while interviewing Licensed Physical Therapy Assistant (LPTA) #642 about the quality of life program, she stated therapy made recommendations upon discharge but it was up to nursing to decide if the recommendations would be implemented. LPTA #642 verified Resident #18 had a decline after being discharged from PT on 08/14/19 resulting in PT needing to place Resident #18 back on caseload. On 12/06/19 at 2:10 P.M., State Tested Nursing Assistant (STNA) #690 stated Resident #18 transferred with a lift but she did not walk. STNA #690 stated she had never attempted to ambulate Resident #18. On 12/06/19 at 2:13 P.M., STNA #501, a QOL nursing assistant, known as a Lead State Tested Nursing Assistant (LSTNA), stated she had never ambulated Resident #18. On 12/06/19 at 3:30 P.M., Physical Therapist (PT) #643 verified when Resident #18 was discharged from PT on 08/14/19 she was able to ambulate 100 feet and a QOL program recommendation was made for nursing staff to continue to ambulate Resident #18. When Resident #18 was evaluated by therapy on 09/19/19 she was unable to ambulate. PT #643 verified inactivity and not following recommendations could result in decline in condition. Review of the QOL program policy, dated 10/04/18, revealed the program was to attain or maintain each resident's highest practicable physical, mental and psychosocial well-being, consistent with the resident's comprehensive assessment, the minimum data set (MDS), and plan of care. The program was person-centered and the focus was to provide interventions the resident desired that gave the resident a sense of satisfaction for overall well being of self, the environment and control over their life. Interventions and goals were focused on what the resident desired and felt provided a QOL. The goals were documented on the plan of care (POC). The interventions were added to the point of care (the computer system where the STNAs or LSTNA's documented task completion). Identifying improvement/decline would be assessed on a subsequent MDS assessment and the POC would be adjusted as appropriate. If a decline in function was noted a new intervention would be implemented including referral to skilled therapy. Any changes would be reported to the unit manager. The LSTNA would assist residents in completing there skilled therapy interventions and recommendations. The LSTNA would document in the point of care completion of the programs under their specific assigned tasks. Review of the QOL list of programs offered revealed all programs were to be completed by the LSTNA. The programs were not specific or measurable and only included statements such as, walk me to the bathroom, provide range of motion (ROM) when I am getting dressed, assist me with the NuStep (a bike machine), seat me for meals at the table where I am to be cued and fed and put on my splint according to my care card. 2. Review of Resident #33's medical record revealed diagnoses including myopathies, epilepsy, osteoarthritis of the hip, and repeated falls. A care plan initiated 09/12/19 revealed Resident #33 had noted declines in ADL's and required extensive assistance of one to two staff to total dependence for ADL's. Resident #33 was unable to stand and transfer unassisted. Resident #33 received PT services from 08/31/19 to 10/21/19. A Discharge summary dated [DATE] indicated Resident #33 was ambulating up to 100 feet with a front wheeled walker and minimum to moderate assistance. A QOL program recommendation referral indicated recommendations to ambulate Resident #33 50 to 75 feet with a front wheeled walker with minimal assistance of two with a wheelchair to follow. A nurse task list report revealed notations to please ambulate Resident #33 50-75 feet with a front wheeled walker with two assists. There was no indication how frequently Resident #33 was to be ambulated. Review of the nurse aide task list documentation from 10/21/19 to 11/25/19 revealed one refusal, one participation and all other entries indicated the ambulation was not applicable. A PT evaluation dated 11/25/19 revealed when PT screened Resident #33 a decline in transfers and gait were noted and he was referred for a PT evaluation and treatment. Resident #33 was totally dependent with attempts to initiate gait. On 12/06/19 between 8:30 A.M. and 12:00 P.M., Licensed Physical Therapy Assistant (LPTA) #642 was interviewed regarding the residents on the Quality of Life program. LPTA #642 verified when Resident #33 was discharged from PT on 10/21/19 he was ambulating 100 feet with minimum to moderate assistance. Resident #33 was readmitted to therapy 11/25/19 due to declines and required maximum assistance of two, was unsteady and only ambulated 25 feet. Resident #33 remained on therapy at this time. During the initial PT services, Resident #33's daughter was trained to assist with ambulation. Resident #33 was more comfortable when the daughter was present for the ambulation. However, two staff had the ability to ambulate Resident #33 without the daughter. On 12/06/19 at 3:36 P.M., Physical Therapist (PT) #643 verified therapy made recommendations for programs but it was up to nursing to determine the frequency. PT #643 verified there was no frequency set up for the ambulation. PT #643 verified Resident #33 had experienced a decline in ambulatory status between 10/21/19 and 11/25/19. On 12/06/19 at 4:05 P.M., Registered Nurse (RN) #549 verified Resident #33 was discharged from PT on 10/21/19 with recommendations for ambulation services. She said there was nobody to initiate the program and it was not started until 11/19/19. On 12/06/19 at 4:07 P.M., STNA #540 stated she had never ambulated Resident #33 or seen the LSTNAs for QOL ambulate him. STNA #540 verified she was unaware of an ambulatory program. On 12/06/19 at 4:10 P.M., Resident #33 stated he was at a rehabilitation hospital prior to his admission to the facility and was walking. He said when he was admitted to the facility he received therapy. After therapy ended, he said nobody from the nursing staff offered to ambulate him and he was back in therapy again. Resident #33 stated when he started therapy the second time he was weaker. Resident #33 stated although he would be nervous walking with nursing staff he would have participated. On 12/06/19 at 4:30 P.M., LSTNA #501 verified she had never ambulated Resident #33. Review of the QOL program policy, dated 10/04/18, revealed the program was to attain or maintain each resident's highest practicable physical, mental and psychosocial well-being, consistent with the resident's comprehensive assessment, the minimum data set (MDS), and plan of care. The program was person-centered and the focus was to provide interventions the resident desired that gave the resident a sense of satisfaction for overall well being of self, the environment and control over their life. Interventions and goals were focused on what the resident desired and felt provided a QOL. The goals were documented on POC. The interventions were added to the point of care. Identifying improvement/decline would be assessed on a subsequent MDS assessment and the POC would be adjusted as appropriate. If a decline in function was noted a new intervention would be implemented including referral to skilled therapy. Any changes would be reported to the unit manager. The LSTNA would assist residents in completing there skilled therapy interventions and recommendations. The LSTNA would document in the point of care completion of the programs under their specific assigned tasks. 3. Resident #21 was admitted to the facility on [DATE] with diagnoses which included dementia and joint disease in the right and left knees. Review of the current activities of daily living (ADL) care plan revealed staff were to follow the QOL tasks as assigned. Review of the physical therapy evaluation (PTE) dated 04/30/19 revealed Resident #21 was able to ambulate five feet with moderate assistance with the front wheeled walker (FWW). Further review of the discharge information, dated 06/03/19, indicated Resident #21 was able to ambulate 200 feet with contact guard (CG) assistance. The resident was referred to a restorative nursing program or the QOL to maintain and/or improve their current level and prevent decline in ambulation. Review of the QOL program referral form dated 06/03/19 revealed staff were to ambulate Resident #21 100 feet with a front wheeled walker and contact guard assistance. Review of the task list report revealed the ambulation program for the QOL LSTNA was not initiated until 08/07/19, over two months after the therapy referral. The task grids which is where the LSTNAs document implementation of the program revealed no documentation the ambulation program was ever provided to Resident #21. Review of the PTE dated 11/18/19 revealed Resident #21 was referred back to therapy due to increased weakness and difficulty with transfers. The resident was only able to ambulate 25 feet and needed more staff assistance. Review of the quarterly minimum data set (MDS) 3.0 assessment dated [DATE] revealed Resident #21 was severely impaired for cognition and had not walked at all during the seven day reference period. On 12/05/19 at 2:57 P.M., interview LSTNA #501 revealed she had not ambulated Resident #21 according to the QOL plan. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned to ensure Resident #21 maintained the level of function at the time of discharge from therapy and to prevent an avoidable decline in ambulation. On 12/06/19 at 10:00 A.M., interview with LPTA #642 verified Resident #21 was unable to walk 100 feet on 12/05/19. LPTA #642 verified they had wanted the resident to walk 100 feet and it was up to nursing to determine the actual program based on their needs. LPTA #642 verified when she observed the staff occasionally walking the resident it was not to the goal of 100 feet. LPTA #642 verified the resident's decline in ambulation was avoidable if the resident had been ambulated as planned. PTA #642 revealed therapy made recommendations upon discharge but it was up to nursing to decide if the recommendations would be implemented. LPTA #642 verified Resident #21 had a decline after being discharged from PT on 06/03/19 resulting in PT needing to place the resident back on caseload on 11/18/19. On 12/06/19 at 3:25 P.M., interview with the resident revealed the nursing assistants don't walk her and the only time she was walked was when she was in therapy. She said she wanted to walk more and would not refuse if staff asked her to walk because she wanted to keep up her strength. 4. Resident #15 was admitted to the facility on [DATE] with diagnoses which included cerebral vascular accident (CVA/stroke) with left (dominant side) hemiplegia (paralysis on one side of the body). Review of the current fall and ADL care plans initiated 11/11/18 revealed staff were to follow the QOL tasks as assigned. Review of the PTE dated 11/11/18 revealed the resident could ambulate 20 feet with minimum assistance with a front wheeled walker, could transfer with minimum assistance, and could ascend five steps. Review of the therapy Discharge summary dated [DATE] revealed Resident #15 could ambulate 300 feet with stand by assistance using the front wheeled walker and only needed stand by assistance with transfers. Resident #15 showed an increase in strength in range of motion (ROM) in both lower extremities (legs/feet) and was able to ascend five steps per the goal. Resident #15 was referred to the QOL program for ambulation and transfers. Review of the task list report revealed exercises for Resident #15's legs were initiated on 12/14/18 for and were to be provided by the floor STNA's, not through the QOL program. There was no evidence transfers or ambulation programs were initiated as recommended by therapy to attempt maintain Resident #15's functional abilities. Review of the PTE dated 05/06/19 revealed Resident #15 was seen again for an increase in weakness, pain/tightness in both knees with a pain score of 9/10 to the right knee and difficulty with home visits with family with a decrease in ambulation and transfers. The resident was only able to walk 75 feet with minimum assistance and a rolling walker (RW). The resident needed moderate assistance with transfers and was only able to ascend two steps. Further review of the Discharge summary dated [DATE] revealed the resident was able to ambulate 200 feet with stand by assistance and a RW, was able to ascend eight steps and was a stand by assistance with transfers. The pain to the knees was decreased to a 2/10. The resident was referred to the QOL program for ambulation and transfers. Review of the QOL referral dated 06/03/19 revealed to ambulate the resident 150 to 250 feet with the RW and provide ROM to both lower extremities. Review of the task list report revealed there was no evidence of any added programs for ambulation or transfers. Review of the PTE dated 08/20/19 revealed the resident was seen by therapy due to a family request as Resident #15 had increased pain in both knees, had a decline in functional mobility, transfers and ambulation. Therapy indicated Resident #15 was able to ambulate 75 feet with a rolled walker, had knee pain of 6/10, had to rock herself to use momentum to get going and was unsteady for transfers requiring assistance. The resident was not able to ascend any steps. Review of the therapy Discharge summary dated [DATE] revealed Resident #15 improved and was able to ambulate 125 feet with contact guard asguard assistance and was able to ascend two steps. The resident was referred to the QOL program. Review of the QOL referral dated 09/09/19 revealed Resident #15 was to ambulate 150 to 250 feet with the rolled walker and contact guard assistance. Review of the task list report revealed on 09/18/19 Resident #15 was to ambulate with the rolled walker two to three times a week. Review of the participation grids revealed there was no documentation the ambulation program for Resident #15 was implemented. Review of the annual MDS 3.0 assessment dated [DATE] revealed Resident #15 was cognitively intact, was not walked during the seven day reference period and needed extensive assistance of one staff person for transfers. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned to ensure Resident #15 maintained her level of function at the time of discharge from therapy and to prevent an avoidable decline. On 12/05/19 at 2:57 P.M., interview with LSTNA #501 revealed she was not able to ambulate the resident according the QOL plan. On 12/06/19 at 8:30 A.M., interview with LPTA #642 revealed Resident #15 had avoidable declines in ambulation and transfers due to nursing staff not implementing a restorative program or QOL program each time the resident was discharged from skilled therapy. LPTA #642 verified the resident's son called her, as he was a PT and informed her he was having increased difficulty when taking the resident to outings including ambulation, ascending steps, transfers and with ROM. LPTA #642 had an evaluation completed on 8/20/19 which again revealed the resident had a decline in ambulation, transfers, ascending steps and ROM since the last therapy discharge on [DATE]. On 12/06/19 at 3:20 P.M., interview with Resident #15 revealed the staff did not walk her. She said her son walked her wen he came to visit. She stated she would like to walk every day but staff did not have time. She said LSTNA #542 occasionally walked her down the halls but said it had been at least a month or so since that had been done. On 12/06/19 at 3:30 P.M., phone interview with Resident #15's son revealed he was a physical therapist and had concerns with the resident's declines. He said he talked to LPTA #642 about it and she was picked up in therapy due to the declines. He said his mother had improved with skilled therapy. He said he visited daily and walked his mother but said he did not see the staff performing any of the programs for her. 5. Resident #10 was admitted to the facility on [DATE] with diagnoses which included dementia and osteoarthritis. Review of the current ADL care plan revealed staff were to follow the QOL tasks as assigned. Review of the PTE dated 05/20/19 revealed Resident #10 was able to ambulate 75 feet with contact guard assistance. Review of the Discharge summary dated [DATE] revealed Resident #10 had improved and was able to ambulate 150 feet with stand by assistance. The resident was referred to the restorative or QOL program for ambulation. Review of the task list report dated 06/10/19 revealed Resident #10 was to ambulate with one person and the front wheeled walker. Review of the participation grids revealed there no documentation the ambulation program was implemented. Review of the PTE dated 09/17/19 revealed Resident #10 was referred back to skilled therapy due to a fall in the bathroom. The resident had declined from walking 100 feet with stand by assistance and could now ambulate 75 feet with contact guard assistance and the front wheeled walker. Review of the quarterly MDS 3.0 assessment dated [DATE] revealed Resident #10 was severely cognitively impaired, was unsteady with ambulation, and needed assistance of one person for ambulation. Review of the PT Discharge summary dated [DATE] revealed Resident #10 improved and was able to ambulate 150 feet with stand by assistance using the front wheeled walker. The resident was referred to the QOL program. Review of the QOL referral dated 10/29/19 revealed staff were to ambulate Resident #10 150 feet with the front wheeled walker and provide range of motion to both legs/feet. Review of the task list report revealed there was no documentation the ambulation program or the range of motion programs were implemented. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned to ensure Resident #10 maintained their current level of function and prevent an avoidable decline. They verified Resident #10 was discharged from PT on 06/07/19 and referred to the QOL program for ambulation, which was not provided, resulting in a decline in ambulation and the need for additional PT on 09/17/19. On 12/05/19 at 2:57 P.M., interview with LSTNA #501 verified she was not able to ambulate Resident #10 according the QOL plan. 6. Resident #2 was admitted to the facility on [DATE] with diagnoses which included contracted right hand and dementia. Review of the current resident care card revealed all food was to be served in separate bowls and the resident needed extensive staff assistance with eating. Review of the current nutrition care plan initiated 04/01/19 revealed the resident could feed herself with cues from staff during meals. Review of the occupational therapy (OT) evaluation dated 08/15/19 revealed on 09/09/19 the resident required increased time to complete self-feeding and displayed increased difficulty in management of the utensil with a spillage rate of 30 percent. By 09/17/19, Resident #2 was able to self-feed with regular utensils with a spillage rate of five to 10 percent. Upon discharge on [DATE], Resident #2 was able to feed herself with stand by assistance. Resident #2 was referred to the QOL program to maintain her current level of function. Review of the STNA task documentation for the last 30 days for eating revealed Resident #2 was usually fed her meals by staff and she was not feeding herself. There was no QOL task listed to indicate Resident #2 was in a program to promote independent eating as recommended by OT. On 12/02/19 at 12:20 P.M., Resident #2 was observed being fed lunch by staff and was not encouraged or cued to feed herself. On 12/03/19 at 8:41 A.M., Resident #2 was observed being fed breakfast by staff and was not encouraged or cued to feed herself. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned to ensure Resident #2 maintained her current level of function for eating meals herself. On 12/04/19 at 5:20 P.M., Resident #2 was observed being fed dinner by STNA #587. The resident was not encouraged or cued to feed herself. On 12/04/19 at 5:30 P.M., interview with STNA #587 verified she fed the resident and the resident did not make any attempts to feed herself. STNA #587 was not aware Resident #2 was able to feed herself with cueing and had not attempted to let the resident feed herself. On 12/05/19 at 9:00 A.M., interview with Certified Occupational Therapy Assistant (COTA) #702 and LPTA #642 verified Resident #2 was discharged from OT on 09/17/19 and was able to feed herself with cueing. The resident was referred to the QOL program to ensure the resident maintained her independence with eating. COTA #702 verified she was not aware the staff were feeding the resident versus encouraging her to feed herself. On 12/05/19 at 2:57 P.M., interview with LSTNA #501, the aide for the QOL program, revealed she was not involved with assisting Resident #2 with meals. 7. Resident #24 was admitted to the facility on [DATE] and diagnoses included dementia. Review of the admission MDS 3.0 assessment dated [DATE] revealed Resident #24 was severely cognitively impaired, was unsteady with walking and needed extensive assistance of one staff person for transfers. Review of the significant change MDS 3.0 assessment dated [DATE] revealed Resident #24 was severely cognitively impaired, did not walk and needed extensive assistance of two or more staff for transfers. Resident #24 was seen and treated in therapy. Review of the QOL referral form from therapy dated 11/15/19 revealed nursing staff were to ambulate Resident #24 50-75 feet with the assistance of one staff using a front wheeled walker. Review of the QOL task list report and the participation documentation revealed there was no evidence the program was ever implemented. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned to ensure Resident #24 maintained their current level of function and/or to prevent any declines in functional abilities. On 12/05/19 at 2:57 P.M., interview with the QOL aide, LSTNA #501, revealed she was not able to ambulate the resident according the QOL plan. 8. Resident #7 was admitted to the facility on [DATE] with diagnoses which included dementia. Review of the task list report revealed a QOL program initiated on 03/25/19 for staff to do sit to stand with Resident #7 two to three times a week. Review of the task documentation revealed no evidence the program was implemented. Resident #7 was referred back to therapy for skilled services and referred back to the QOL program on 09/10/19. Review of the QOL referral from therapy dated 09/10/19 revealed staff were to provide the sit to stand program at the grab bar two to three times a week. Review of the participation grids revealed this program was not implemented or provided. Review of the quarterly MDS 3.0 assessment dated [DATE] revealed Resident #7 was severely cognitively impaired and was totally dependent on two or more staff for transfers using a mechanical lift and the resident did not walk in the seven day review period. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned to ensure Resident #7 maintained their previous level of function and to prevent an avoidable decline. On 12/05/19 at 2:57 P.M., interview with LSTNA #501, the QOL aide, revealed she was not able to provide the QOL program for Resident #7 to sit to stand. 9. Resident #30 was admitted to the facility on [DATE] with diagnoses which included osteoarthritis. Review of the QOL referral from therapy dated 09/03/19 revealed LSTNAs were to provide ambulation with stand by assistance using a front wheeled walker for 150 feet. Review of the task list report for the QOL program revealed no evidence the program was ever initiated. Review of the quarterly MDS 3.0 assessment dated [DATE] revealed Resident #30 was alert, oriented and cognitively intact. This assessment indicated she needed extensive assistance with one staff person for ambulation and she was unsteady, needing staff support. Review of the QOL referral from therapy dated 11/12/19 revealed QOL staff were to provide ambulation with a front wheeled walker with contact guard assistance for 75 to 100 feet and a walk to dine program (staff are to walk the resident to eat meals in the dining room). Review of the task list report revealed there no evidence these programs were ever initiated for Resident #30. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned to ensure Resident #30 maintained her current level of function. On 12/05/19 at 2:57 P.M., interview with LSTNA #501 revealed she was not able to ambulate Resident #30 according the QOL plan. On 12/07/19 at 1:25 P.M., interview with Resident #30 revealed she was only walked in therapy. She said she wanted to be walked more so she did not need the wheelchair. She wanted to walk with her walker like she did before. 10. Resident #40 was admitted to the facility on [DATE] with diagnoses which included dementia and osteoarthritis. Review of the quarterly MDS 3.0 assessment dated [DATE] revealed Resident #40 was alert, oriented, and cognitively intact, needed extensive assistance of two or more staff for transfers and was unsteady with ambulation needing extensive assistance of one staff person. Resident #40 was seen and treated by therapy. Review of the QOL referral from therapy dated 11/04/19 revealed QOL staff were to ambulate Resident #40 50-75 feet with the assistance of one staff person using the front wheeled walker. Review of the task list report for the QOL programs revealed no evidence the program was ever initiated for Resident #40. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned for Resident #40. On 12/05/19 at 2:57 P.M., interview with LSTNA #501 revealed she was not able to ambulate Resident #40 according the QOL plan. 11. Resident #43 was admitted on [DATE] with diagnoses which included a hip fracture. Review of the PTE dated 08/31/19 revealed Resident #43 was admitted with a hip fracture and was treated by therapy. Review of the therapy Discharge summary dated [DATE] revealed Resident #43 was able to ambulate 100 feet. Review of the QOL referral form dated 10/24/19 revealed QOL staff were to ambulate Resident #43 50-100 feet with the front wheeled walker. Review of the participation grids revealed no evidence the program was ever implemented. Review of the significant change MDS 3.0 assessment dated [DATE] revealed the resident had mild cognitive impairment, was unsteady with ambulation and needed assistance of one person for ambulation. Review of the PTE dated 11/18/19 revealed Resident #43 was seen again by therapy because he began to scissor with his gait. The resident was currently receiving skilled therapy. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned for Resident #43. On 12/05/19 at 2:57 P.M., interview with LSTNA #501, the QOL aide, revealed she was not able to ambulate Resident #43 according the QOL plan. 12. Resident #20 was admitted to the facility on [DATE] with diagnoses which included Alzheimer's disease and a recent hip fracture. Review of the PTE dated 10/04/19 revealed Resident #20 was seen, treated and discharged on 11/08/19 with a referral to the QOL program. Review of the QOL referral form from therapy dated 11/08/19 revealed QOL staff were to provide the sit to stand program with maximum assistance of two staff. Review of the task list report revealed the sit to stand program was initiated on 11/19/19. Review of the participation grids revealed there no evidence the program was ever provided to Resident #20. Review of the PTE dated 12/06/19 revealed Resident #20 was picked back up by therapy and was being seen for a decrease in the ability to sit to stand and for a decline in the ability to extend the right knee. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the QOL program was not implemented as planned for Resident #20 to attempt to assist the resident to maintain their previous le[TRUNCATED]
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, medical record review and staff interview, the facility failed to provide devices to prevent skin impairme...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, medical record review and staff interview, the facility failed to provide devices to prevent skin impairment for one (Resident #18) of one resident reviewed for non-pressure related skin impairment and failed to implement the facility's bowel protocol for two (Residents #22 and #51) of five residents reviewed for medication use. Findings include: 1. Review of Resident #18's medical record revealed diagnoses including dementia, repeated falls and Parkinson's disease. A care plan initiated 07/10/19 indicated Resident #18 was admitted with skin tears. Resident #18 had thin and fragile skin and was prone to skin tears easily. Resident #18 had no safety awareness and did bump into objects when attempting to move in the wheelchair. Interventions included applying geri sleeves (protective arm coverings) and applying stockinettes on both legs at all times for skin protection. Resident #18 had a physician's order dated 08/14/19 to apply geri sleeves or long sleeves at all times except during hygiene. A quarterly Minimum Data Set (MDS) assessment dated [DATE] indicated Resident #18 was severely cognitively impaired and required extensive assistance from staff for dressing. On 11/06/19, an order was written for stockinettes on both legs at all times. On 12/02/19 at 2:05 P.M., Resident #18 was sitting in a recliner in the common area. A stockinette was only observed on the right lower leg/extremity. On 12/03/19 at 12:15 P.M., Resident #18 was sitting in the dining room feeding herself. No geri sleeves were worn. The sleeve on Resident #18's left arm was not covering the lower 2/3 of the arm between the elbow and wrist. On 12/03/19 at 2:02 P.M., Licensed Practical Nurse (LPN) #660 verified Resident #18 was not wearing geri sleeves and when her arms moved the sleeves on her shirt did not cover her arms to protect them from skin tears. 2. Review of Resident #22's medical record revealed diagnoses including dementia, anemia, and generalized osteoarthritis. Resident #22 had a physician's order to check for bowel movements every shift. If there was no bowel movement (BM) in three days, the 3:00 P.M. to 11:00 P.M. shift was to administer 30 milliliters (ml) of milk of magnesia. If there was still no BM by the following morning, a glycerin rectal suppository was to be administered. If there was no BM by 8:00 A.M. to 9:00 A.M. a fleets enema was to be administered. A plan of care revealed Resident #22 was at risk for constipation. The goal was for Resident #22 to have a normal bowel movement at least every three days. Interventions included following the facility bowel protocol and administering medications in accordance with physician orders. Review of BM records and medication administration records revealed no recorded bowel movements between 10/13/19 and 10/16/19, 10/18/19 and 10/22/19, and 11/06/19 and 11/11/19. There was evidence the nursing staff implemented the bowel protocol. Review of the facility's Bowel Protocol, last reviewed 07/05/19, revealed the charge nurse was to check residents' bowel movement records every shift in Point Click Care, the electronic medical record. If no bowel movement occurred in three days the 3:00 P.M. to 11:00 P.M. charge nurse was to administer 30 milliliters (ml) of milk of magnesia or alternative medication according to the physician's order. If there was still no BM by 6:00 A.M. the following morning, a glycerin rectal suppository or alternative medication was to be administered according to physician orders. If there were no results by 8:00 A.M., a fleets enema would be administered or an alternative medication per physician order. On 12/05/19 at 4:00 P.M., the Administrator provided paper BM records for Resident #22 indicating she had a BM 11/07/19. The Administrator indicated staff continued to look for additional information. As of 12/06/19 at 5:00 P.M. no additional information was provided regarding BMs or evidence the nursing staff implemented the bowel protocol. 3. Review of Resident #51's medical record revealed diagnoses including congestive heart failure and constipation. Resident #51 had a physician's order to check bowel movements every shift. If there was no BM in three days, the 3:00 P.M. to 11:00 P.M. shift nursing staff were to administer 30 ml of milk of magnesia. If there was no BM by 6:00 A.M. the following morning, a glycerin suppository was to be administered. If there was no BM by 8:00 A.M. and 9:00 A.M., a fleets enema was to be administered. On 12/04/19 at 2:15 P.M., Registered Nurse (RN) #582 stated the facility's bowel protocol was to administer milk of magnesia if a resident did not have a BM after three days. If there were no results, a suppository was to administered the next shift. If there were no results by the third shift, a fleets enema was to be administered. RN #582 was informed no BM was recorded between 09/20/19 and 09/24/19, 10/20/19 and 10/25/19, 10/29/19 and 11/02/19, and 11/14/19 and 11/18/19. There was no evidence of any interventions or implementation of the bowel protocol for any of these time frames. RN #582 reviewed progress notes for the recorded time frames and verified there was no documentation of staff offering to implement the bowel protocol.
CONCERN (D)

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

Deficiency F0685 (Tag F0685)

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 ensure Resident #49 received her bifocal eyeglasses as needed. This ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview the facility failed to ensure Resident #49 received her bifocal eyeglasses as needed. This affected one of one resident reviewed for visual impairment. Findings include: Resident #49 was admitted to the facility on [DATE] with diagnoses which included aphasia (not able to speak) due to multiple sclerosis. Review of the 12/13/18 vision progress note revealed the resident had moderate cataracts and visual impairment. The resident needed bifocal eyeglasses that had been ordered previously. Review of the 06/13/19 vision progress note revealed the resident had changes in the retina of both eyes. The note indicated the resident needed bifocal glasses that had been ordered previously. They were to encourage the resident to use bright light and wear her glasses. On 12/04/19 at 1:30 P.M., interview with Licensed Social Worker (LSW) #630 revealed Resident #49 did not have her bifocal glasses and there was no evidence the facility followed through to obtain glasses the resident needed. LSW #630 said she called the resident's husband today and asked him if he wanted his wife to get glasses. Resident #49's husband said to get them if she needed them. On 12/05/19 at 2:30 P.M., phone interview with Vision Technician #705 revealed when Resident #49 was seen on 06/14/18 she needed bifocals and they needed to set-up a time for a fitting. There was no evidence anyone set-up the fitting for the glasses. Vision Technician #705 said the facility should have called them to set-up the appointment.
CONCERN (D)

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

Incontinence Care (Tag F0690)

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 ensure one (Resident #2) of five residents reviewed for urinary cat...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure one (Resident #2) of five residents reviewed for urinary catheters had adequate indications for use of a urinary catheter. Findings include: Review of Resident #2's medical record revealed diagnoses including dementia, hypertension, chronic obstructive pulmonary disease, urinary tract infection (UTI) and adult failure to thrive. A quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed Resident #2 was dependent on staff for transfers and she did not walk. On 11/30/19, an order was written for a Foley catheter, a urinary catheter, every shift due to Vancomycin Resistant Enterococcus (VRE), a type of infectious organism, in the urine and for Resident #2 to be on contact isolation due to the VRE in the urine. Review of a catheter assessment dated [DATE] revealed Resident #2 had a Foley catheter due to the VRE in the urine. Review of the facility's Foley Catheter Assessment and Management policy, reviewed 08/15/19, revealed a Foley Catheter Assessment and Management form was to be completed on any resident with an indwelling urinary catheter. A plan of care was to be implemented for care of the resident, complications associated with catheter use and periodic assessment of the continued need for the catheter. On 12/05/19 at 5:55 P.M., Registered Nurse (RN) #549 verified the only reason for Resident #2's catheter use was due to the UTI. When asked about appropriate indications for use for a urinary catheter, RN #549 indicated the catheter assessment revealed diagnoses such as neurogenic bladder, urethral blockage, stage 3 or 4 pressure ulcer, or terminal illness or severe impairment making positioning and clothing changes uncomfortable or which caused intractable pain would be indications for the use of a catheter. RN #549 verified Resident #2 did not have any of those diagnoses or conditions to warrant the use of a urinary catheter.
CONCERN (D)

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

Deficiency F0692 (Tag F0692)

Could have caused harm · This affected 1 resident

Based on observation, medical record review, and interview, the facility failed to ensure a record of actual intakes was maintained for supplements for one (Resident #48) of 24 residents screened for ...

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Based on observation, medical record review, and interview, the facility failed to ensure a record of actual intakes was maintained for supplements for one (Resident #48) of 24 residents screened for nutritional status to determine effectiveness. Findings include: Review of Resident #48's medical record revealed diagnoses including adult failure to thrive, gastroesophageal reflux disease, iron deficiency anemia and Alzheimer's disease. On 02/06/19, an order was written for 240 milliliters of Ensure plus to be administered three times a day with meals. On 09/01/19, a weight of 102 pounds was recorded. On 12/02/19 a weight of 92 pounds was recorded. On 12/03/19 at 12:10 P.M., Licensed Practical Nurse (LPN) #660 was observed providing Resident #48 with 240 milliliters (ml) of liquid supplement. As of 12:58 P.M., Resident #48 had consumed approximately 1/4 of the supplement. At 1:01 P.M., Dietary Aide #579 approached Resident #48 and asked if he was finished with the supplement and proceeded to dispose of it. The December 2019 Medication Administration Record revealed a check mark indicating the supplement during lunch on 12/03/19 was administered. On 12/03/19 at 1:09 P.M., Dietary Aide #579 stated nursing staff were responsible for monitoring residents' meal intakes by 1:00 P.M. because that was when dietary staff began clearing the dishes. Dietary Aide #579 verified the Ensure plus supplement was disposed of after 1:00 P.M. because Resident #48 stated he was finished with it. On 12/03/19 at 1:59 P.M., LPN #660 verified nurses were not documenting the amount of supplement intake consumed by Resident #48. Once nurses provided the supplement they documented it was administered. LPN #660 stated she monitored Resident #48's supplement intake but did not record it anywhere. LPN #660 stated when the dietitian visited they discussed meal and supplement intakes. On 12/05/19 at 9:29 A.M., Registered Dietary Tech (DTR) #700 verified Resident #48 had weight changes in November 2019. Interventions which were implemented in the past included Speech Therapy, weekly weights, appetite stimulants, and supplements. DTR #700 stated Resident #48 liked the Ensure plus and he took it well. When asked how she knew what Resident #48's supplement intakes were DTR #700 stated they were marked on the Medication Administration Record (MAR). Registered Nurse (RN) #701 (the acting Director of Nursing), who was present, stated a checkmark on the MAR indicated the resident consumed 100% of the supplement. RN #701 was informed of the observations, record on the MAR, and the nurse interview and was not aware if the resident did not fully consume the supplement as it was still check marked on the MAR because it was offered. On 12/05/19 at 10:00 A.M., Dietitian #526 stated she relied on documentation on the MAR for information regarding supplement intake and spoke to whatever nurse was working when she visited. Licensed Practical Nurse (LPN) #585 reported intakes of the supplement were good. Dietitian #526 verified it would be more beneficial to know what the actual intake of the supplement was if Resident #48 was not consuming it in its entirety. Dietitian #526 stated she was unaware of Resident #48 not consuming the full supplement and verified she would not have any means of knowing Resident #48 was not consuming all the supplement unless she spoke to the nurse who had direct knowledge or it was recorded on the MAR. The information would be beneficial in determining the effectiveness of interventions.
CONCERN (D)

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

Infection Control (Tag F0880)

Could have caused harm · This affected 1 resident

Based on observation, policy review and interview, the facility failed to implement appropriate infection control practices during provision of incontinence care and while monitoring blood glucose lev...

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Based on observation, policy review and interview, the facility failed to implement appropriate infection control practices during provision of incontinence care and while monitoring blood glucose levels. This affected two (Residents #2 and #57) of all 57 residents observed for infection control practices. Findings include: 1. Review of Resident #2's medical record revealed diagnoses including a urinary tract infection. On 11/30/19, a physician order was written for a Foley (urinary) catheter. On 12/05/19 between 1:15 P.M. and 1:33 P.M., State Tested Nursing Assistant (STNA) #506 was observed providing catheter care to Resident #2. STNA #506 donned personal protective equipment, including gloves, prior to entering Resident #2's room. Upon entering the room, STNA #506 was observed touching multiple surfaces such as the bed controls, the bathroom door, one of the isolation barrels, the night stand drawers, and the faucet handles. STNA #506 did not change her gloves or wash her hands prior to providing the catheter care. On 12/05/19 at 1:33 P.M., STNA #506 verified she had touched multiple environmental surfaces then provided catheter care to Resident #2 with the same contaminated gloves. Review of the facility's catheter care policy, reviewed 05/15/19, indicated hands were to be washed thoroughly then gloves applied before the procedure was initiated. 2. On 12/06/19 at 4:25 P.M., Licensed Practical Nurse (LPN) #551 was observed monitoring the blood glucose level of Resident #57. Prior to going into Resident #57's room, LPN #551 stated she had cleaned the glucometer at the beginning of her shift. The glucometer was carried into the room inside a case. After the glucometer was used it was placed back into the case. After cleaning up supplies and washing her hands, LPN #551 carried the glucometer in the case to the medication cart and sat it on top of the cart. There was no indication LPN #551 was preparing to disinfect the glucometer. When asked how often the glucometer was cleaned, LPN #551 stated it was cleaned at the beginning and end of every shift and after each use. LPN #551 verified she had placed the glucometer back into the case prior to disinfecting it which had the potential to contaminate the case, thereby re-contaminating the glucometer when it was disinfected and placed back into the case. Review of the Easy Max manual (the glucometer manual) indicated the glucometer should be cleaned after every use to prevent any possibility of cross infection.
CONCERN (E)

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

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Review of Resident #18's medical record revealed diagnoses including dementia, osteoarthritis of both knees and Parkinson's d...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Review of Resident #18's medical record revealed diagnoses including dementia, osteoarthritis of both knees and Parkinson's disease. A plan of care initiated 07/10/19 indicated Resident #18 had an ADL deficit related to dementia and needed staff assistance for activities of daily living. Interventions included obtaining Physical Therapy (PT) and Occupational Therapy (OT) evaluations and treating as indicated per orders. Interventions also included providing quality of life tasks as assigned. Resident #18 received PT from 06/30/19 to 08/14/19 and OT from 07/01/19 to 08/12/19. A Quality of Life Program Recommendation Referral dated 08/12/19 revealed recommendations for Resident #18 to be ambulated 30 feet with a FWW with minimum assistance with a wheelchair following and for a range of motion (ROM) program. Review of the nursing assistant task list report revealed instructions to assist with ROM when Resident #18 was getting dressed and going to bed, as well as during activities of daily living. The task list report also indicated the Lead State Tested Nursing Assistant (LSTNA) was to incorporate ROM into Resident #18's weekly routine. The task list indicated an entry to please ambulate Resident #18 short distances with a FWW, gait belt and wheelchair to follow. On 12/06/19 between 8:20 A.M. and 12:00 P.M., while interviewing Licensed Physical Therapy Assistant (LPTA) #642 about the quality of life program, she stated therapy made recommendations upon discharge from therapy but it was up to nursing to decide if the recommendations would be implemented. On 12/06/19 at 3:30 P.M. while reviewing the therapy discharge recommendations, quality of life referral forms, and nursing assistant task list with Physical Therapist (PT) #643, she verified the therapy department made recommendations when residents were discharged from therapy services but it was nursing's decision what programs or interventions were implemented. PT #643 verified the QOL tasks and plan did not include measurable interventions or outcomes. 5. Review of Resident #33's medical record revealed diagnoses including myopathies, epilepsy, osteoarthritis of the hip, and repeated falls. A care plan initiated 09/12/19 revealed Resident #33 had noted declines in ADLs and required extensive assistance of one to two staff to total dependence from staff for ADLs. Resident #33 was unable to stand and transfer unassisted. Resident #33 received PT services from 08/31/19 to 10/21/19. A QOL program recommendation referral indicated recommendations to ambulate Resident #33 50 to 75 feet with a FWW with minimal assistance of two staff with a wheelchair to follow. A nurse task list report revealed notations to please ambulate Resident #33 50-75 feet with a FWW with two assists. There was no indication how frequently Resident #33 was to be ambulated. On 12/06/19 at 3:36 P.M., PT #643 verified therapy made recommendations for programs but it was up to nursing to determine the frequency. PT #643 verified there was no frequency set up for the ambulation in the QOL care plan to direct staff regarding the needs of Resident #33. Based on interview and record review the facility failed to ensure individualized care plans were implemented for Resident's #10, #15, #18, #21, and #33, who had quality of life (QOL) programs. This affected five of 31 residents reviewed for plans of care. Findings included: 1. Resident #21 was admitted to the facility on [DATE] with diagnoses which included dementia and arthritis of his/her right and left knees. Review of the current activities of daily living (ADL) care plan revealed staff were to follow the QOL tasks as assigned. Review of the physical therapy evaluation (PTE) dated 04/30/19 revealed the resident was able to ambulate five feet with moderate assistance with the front wheeled walker (FWW). Further review of the therapy discharge note dated 06/03/19 revealed Resident #21 was able to ambulate 200 feet with contact guard (CG). The resident was referred to the QOL program to maintain or improve his/her current level and prevent a decline in ambulation. Further review of the QOL program referral dated 06/03/19 revealed staff were to ambulate the resident 100 feet with a FWW and CG assistance. Review of the current QOL task for Resident #21 revealed staff were to walk the resident to meals. Review of the quarterly minimum data set (MDS) 3.0 dated 11/29/19 revealed the resident was severely impaired for cognition and had not walked during the seven day reference period. On 12/04/19 at 5:15 P.M., interview with Registered Nurse (RN) #572 and RN #701 verified the care plan for the QOL program simply stated staff were to follow the QOL tasks as assigned. There was no further documentation related the the QOL plan of care. 2. Resident #15 was admitted to the facility on [DATE] with diagnoses which included cerebral vascular accident (CVA/stroke) with left (dominant side) hemiplegia (paralysis on one side of the body). Review of the current fall and ADL care plans initiated 11/11/18 revealed staff were to follow the QOL tasks as assigned. Review of the PTE dated 08/20/19 revealed the resident was seen by therapy due to a family request for an increase in knee pain, a decline in functional mobility, transfers and ambulation. The resident was able to ambulate 75 feet with a rolled walker (RW). The resident had knee pain, rating it 6 out of 10 with zero being none and 10 being the worst pain ever. The resident rocked to use momentum and was unsteady for transfers requiring assistance. The resident was not able to ascend any steps. Review of the Discharge summary dated [DATE] revealed Resident #15 was able to ambulate 125 feet with CG and the RW. The knee pain had decreased to zero, the resident was able to transfer with CG assistance, and was able to ascend two steps. The resident was referred to the QOL program. Further review of the QOL referral dated 09/09/19 revealed the resident was to ambulate 150 to 250 feet with CG assistance with the RW. Review of the current QOL tasks revealed no task was implemented to ambulate the resident. Therefore there was no evidence the resident was ambulated. Review of the annual MDS 3.0 dated 11/15/19 revealed the resident was cognitively intact, was not walked during the seven day reference period and needed extensive assistance of one staff person for transfers. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the care plan for the QOL program simply stated staff were to follow the QOL tasks as assigned. There was no further documentation related the QOL plan of care and what staff were to do for Resident #15. 3. Resident #10 was admitted to the facility on [DATE] with diagnoses which included dementia and osteoarthritis. Review of the current ADL care plan revealed to follow the QOL tasks as assigned. Review of the PTE dated 05/20/19 revealed the resident was able to ambulate 75 feet with CG assistance. Review of the Discharge summary dated [DATE] revealed the resident was able to ambulate 150 feet with stand by assistance. The resident was referred to the QOL program for ambulation. Review of the QOL task dated 06/10/19 revealed the resident was to ambulate with one person and the FWW. Review of the quarterly MDS 3.0 dated 10/01/19 revealed the resident was severely cognitively impaired, was unsteady with ambulation and needed assistance of one staff person for ambulation. On 12/04/19 at 5:15 P.M., interview with RN #572 and RN #701 verified the care plan for the QOL program simply stated staff were to follow the QOL tasks as assigned. There was no further documentation related the the QOL plan of care and what staff were to do for Resident #10.
CONCERN (E)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to ensure fall interventions were in place for Resident's ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review the facility failed to ensure fall interventions were in place for Resident's #32, #49, #54 and #108 as physician ordered or planned. This affected four of five residents revealed for accidents. Findings include: 1. Resident #32 was admitted to the facility on [DATE] with diagnoses which included stroke with left sided weakness, contractures (the shortening and hardening of muscles, tendons or other tissue often leading to deformity and rigidity of joints) of the left hand, left knee and left ankle. Review of the current fall care plan revealed Resident #32 had foot drop and left sided weakness due to a stroke. The resident was to be transferred according to the orders and the resident care card (the state tested nurse aide's (STNA's) guide to each resident's individual care needs). Review of the physician's order dated 10/22/18 revealed staff were to use the sit to stand lift and a gait belt for all transfers. Review of the current resident care card revealed Resident #32 was to be transferred with one staff person using the sit to stand mechanical lift. There was no indication a gait belt was to be utilized during the transfers, as ordered by the physician on 10/22/18. On 12/04/19 at 10:30 A.M., observation of STNA #596 transferring the resident with the sit to stand lift revealed a gait belt was not used during the transfer. On 12/04/19 at 10:34 A.M., interview with STNA #596 verified she did not use the gait belt during the above transfer. On 12/04/19 at 11:00 A.M., interview with Registered Nurse (RN) #701 verified the above concerns. 2. Resident #49 was admitted to the facility on [DATE] with diagnoses which included multiple sclerosis. Review of the current resident care card revealed Resident #49 was to have a full length dycem (non-slip material) between the mattress and sheets. Review of the physician's order dated 3/15/18 revealed staff were directed to ensure a full length dycem was between the mattress and fitted sheet. Review of the quarterly MDS 3.0 dated 09/14/19 revealed the resident was moderately cognitively impaired and was dependent on staff for activities of daily living. On 12/03/19 at 2:00 P.M., the resident was observed in bed. On 12/03/19 at 4:54 P.M., the bed was observed without any dycem between the mattress and the fitted sheets. On 12/03/19 at 4:55 P.M., interview and observation with Licensed Practical Nurse (LPN) #525 confirmed there was no dycem in place on the bed for Resident #49 as ordered by the physician. 3. Resident #54 was admitted to the facility on [DATE] with diagnoses which included a stroke with left sided weakness and a history of falls. Review of the nurse's note dated 08/31/19 revealed Resident #54 was in his room and fell out of the broda chair, a specialized chair with lateral padding/support. The new intervention was to not leave the resident alone in his room when he was in the broda chair. Review of the quarterly MDS 3.0 dated 09/19/19 revealed the resident was severely cognitively impaired and was totally dependent on staff for activities of daily living. On 12/02/19 at 3:30 P.M., Resident #54 was observed in his room alone, in the broda chair. Continuous observation until 4:22 P.M., revealed the resident remained in his room alone while in the broda chair. On 12/02/19 at 4:25 P.M., interview with LPN #567 revealed he took Resident #54 to his room over an hour ago and he was returning now to give him medications. He verified the resident was in his broda chair and alone in his room. He said he was not aware the resident was not to be left alone in his room while in the broda chair. 4. Resident #108 was admitted to the facility on [DATE] after having a fall and sustaining a fracture to her right arm. Review of the cognitive assessment dated [DATE] revealed the resident was severally cognitively impaired. Review of the Morse Fall Scale dated 11/26/19 revealed Resident #108 was at high risk for falls. Review of the nurse's note dated 11/29/19 revealed the resident was making several attempt to stand up from the wheelchair. Review of the current fall care plan revealed staff were to provide and encourage use of adaptive equipment and mobility devices as planned. On 12/02/19 at 10:15 A.M., 12:00 P.M., 2:20 P.M., 3:33 P.M., 5:45 P.M. and 6:50 P.M., the resident was observed self propelling in her wheelchair. The wheelchair had anti-roll back brakes but the left brake was broken and not near the wheel and could not stop the wheelchair if needed. Anti-roll back brakes prevent the wheelchair from rolling and moving away from a person, especially if they stand and/or try to sit back down. On 12/03/19 at 9:20 A.M., the resident was observed self propelling in her wheelchair. The wheelchair had anti-roll back brakes but the left brake was broken and not near the wheel and could not stop the wheelchair if needed. On 12/03/19 at 9:42 A.M., interview with RN #549 verified the left anti-roll back brake was broke, not in place and would not be able to stop the wheelchair if needed.
CONCERN (F)

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

Deficiency F0725 (Tag F0725)

Could have caused harm · This affected most or all residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview the facility failed to maintain sufficient nursing staff to ensure the implementation of se...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview the facility failed to maintain sufficient nursing staff to ensure the implementation of services via a quality of life (QOL) program to ensure all residents identified to be in the program received the necessary range of motion, splinting, ambulation and/or activities of daily living (ADL) services following the residents discharge from skilled therapy. This affected 36 residents (#1, #2, #3, #4, #5, #7, #9, #10, #11, #12, #14, #15, #18, #19, #20, #21, #22, #24, #27, #28, #30, #31, #32, #33, #34, #39, #40, #41, #43, #44, #46, #48, #49, #53, #54 and #56) who were identified by the facility to require a QOL program and had the potential to affect all 57 residents residing in the facility. Findings include: Review of the facility QOL program revealed the following concerns: The facility failed to ensure Resident #18, #33, #21, #15, #10 and #2 received restorative/maintenance services to maintain activities of daily living (ADL) and prevent a decline in ADL's after being discharged from skilled therapy. In addition to the above six residents, 11 additional residents, Resident #24, #7, #30, #40, #43, #9, #3, #31, #22, #39 and #5 were reviewed who had referrals from skilled therapy to a restorative/maintenance program to maintain current level or function and prevent decline. (See findings under F676). The facility failed to ensure range of motion (ROM) programs and/or splinting programs were provided as planned for Resident #2, #3, #9, #15, #18, #20, #31, #32, #39, #40, #41, #48 and #54. (See findings under F688) Review of the QOL staffing schedules from 11/21/19 through 12/07/19 revealed there was no evidence the schedule reflected any dedicated staff on these dates to provide the planned programs for the residents specified to be in the programs. The following interviews were obtained during the onsite survey: a. On 12/06/19 at 10:00 A.M., interview with Physical Therapy Assistant (PTA) #642 revealed Resident #21 was unable to walk 100 feet on 12/05/19. PTA #642 verified the program wanted the resident to walk 100 feet and it was up to nursing to determine the actual program based on their needs. PTA #642 verified when she observed the staff occasionally walking the resident it was not to the goal of 100 feet. PTA #642 verified the resident's decline in ambulation was avoidable if the resident was ambulated as planned. PTA #642 revealed therapy made recommendations upon discharge but it was up to nursing to decide if the recommendations would be implemented. LPTA #642 verified Resident #21 had a decline after being discharged from PT on 06/03/19 resulting in PT needing to place the resident back on caseload on 11/18/19. On 12/06/19 at 3:25 P.M., interview with Resident #21 revealed the aids don't walk her and the only time she gets walked was when she was in therapy. She wanted to walk more and would not refuse if asked to walk because she wanted to keep up her strength. b. On 12/06/19 at 8:30 A.M., interview with PTA #642 revealed Resident #15 had avoidable declines in ambulation, transfers and ROM due to not implementing a restorative program each time the resident was discharged from skilled therapy. PTA #642 revealed the resident's son called her, he was a PT and informed her he was having increased difficulty when taking the resident to outings including ambulation ascending steps, transfers and ROM. PTA #642 had an evaluation completed on 8/20/19 which again revealed the resident had a decline in ambulation, transfers, ascending steps and ROM since the last therapy discharge on [DATE] when the resident was referred to the restorative program to ensure the resident maintained her current level of function. On 12/06/19 at 3:20 P.M., interview with Resident #15 revealed the staff did not walk her but her son did when he came to visit. The resident stated she would like to walk every day but staff did not have time. The resident stated occasionally LSTNA #542 walks me down the halls but its been at least a month or so since that's been done. During the interview, Resident #15 also revealed the facility staff did not do ROM or exercise with her and she would like them to but said they don't have time. On 12/06/19 at 3:30 P.M., phone interview with the resident's son revealed he was a physical therapist and had concerns with the resident's decline in ROM and talked to PTA #642 about it. He said his mother was picked up in therapy due to the decline and she had improvement with skilled therapy. The son visited daily and walked the resident but did not see the staff performing ROM or other programs for her. c. On 12/06/19 at 4:10 P.M. during an interview with Resident #33, the resident stated he was at a rehabilitation hospital prior to his admission to the facility and was walking. When Resident #33 was admitted to the facility he received therapy. After therapy ended, nobody from the nursing staff offered to ambulate him and he was back in therapy. Resident #33 stated when he started therapy the second time he was weaker. Resident #33 stated although he would be nervous walking with nursing staff he would have participated. The facility identified 36 residents, Resident #1, #2, #3, #4, #5, #7, #9, #10, #11, #12, #14, #15, #18, #19, #20, #21, #22, #24, #27, #28, #30, #31, #32, #33, #34, #39, #40, #41, #43, #44, #46, #48, #49, #53, #54 and #56 who were to receive a QOL program. On 12/04/19 at 5:15 P.M., interview with Registered Nurse (RN) #572, with RN #701 present, revealed she was in charge of the QOL program which replaced the restorative nursing program (RNP), in October 2018. The program was to be delivered by two part time lead State Tested Nurse Aides (LSTNA), #542 and #501. LSTNA #501 was supposed to work in the program two to three days a week and LSTNA #542 worked weekends. During the interview, it was reported that both LSTNA's were frequently pulled to work the floor as STNA staff (to provide direct resident care) as the facility did not have enough STNA staff working to provide care to the residents. This resulted in the QOL programs not being completed as planned. On 12/05/19 at 12:35 P.M., interview with the Administrator verified the QOL program was not staffed to ensure the programs were delivered as planned. On 12/05/19 at 2:57 P.M., interview with LSTNA #501 revealed she started in the QOL position in August 2019. LSTNA #501 revealed she mostly worked in the secured dementia unit as activities staff or as a floor STNA. She revealed she did not get to work as a LSTNA very much, maybe a day of two each week because she was usually pulled to work the floor as an STNA. LSTNA #501 revealed she worked on the floor every other weekend and LSTNA #542 was usually pulled to work the floor (as an STNA) on the weekends she worked. LSTNA #501 verified she had not worked in the QOL program at all this week, including from 12/01/19 through 12/05/19 because she had been pulled to the floor to work as an STNA. On 12/07/19 at 12:55 P.M., telephone interview with LSTNA #542 revealed he only worked weekends. He verified he was frequently pulled to work the floor due to the facility not having enough staff to provide care to the residents especially since October 2019. During the interview he stated he was not able to complete the QOL programs for the residents as planned. LSTNA #542 revealed he had taken time off for today and no one was scheduled to replace him to deliver the QOL programs. Review of the quality of life (QOL) program policy, dated 10/04/18, revealed the program was to attain or maintain each resident's highest practicable physical, mental and psychosocial well-being, consistent with the resident's comprehensive assessment, the minimum data set (MDS), and plan of care. The program was person-centered and the focus was to provide interventions the resident's desired that gave the resident a sense of satisfaction or over all self, the environment and control over their life. The procedure included to ensure the MDS was completed as required which would direct the specific needs of the resident. Interventions and goals were focused on what the resident desired and felt provided a QOL. The goals were documented on the plan of care (POC). The interventions were added to the point of care (the computer system the aide's documented task completion). Identifying improvement/decline would be assessed on a subsequent MDS assessment and the POC would be adjusted as appropriate. If a decline in function was noted a new intervention would be implemented including referral to skilled therapy. Any changes would be reported to the unit manager. The lead state tested nurse aide (LSTNA) would assist residents in completing there completed skilled therapy interventions and recommendations. The LSTNA would document in the point of care completion of the programs under their specific assigned tasks.
CONCERN (F)

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

Deficiency F0865 (Tag F0865)

Could have caused harm · This affected most or all residents

Based on record review, interview, and policy review, the facility failed to correct a known area of deficiency related to pain control in the facility. This affected Resident #32 and had the potentia...

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Based on record review, interview, and policy review, the facility failed to correct a known area of deficiency related to pain control in the facility. This affected Resident #32 and had the potential to affect all 57 residents residing in the facility. Findings include: During the first portion of the annual survey conducted 12/02/19 through 12/06/19, the facility was identified as not having an adequate pain control program for Resident #32, who had ongoing complaints of severe pain since 06/20/19 with no additional pain relief interventions attempted. This resulted in actual harm when Resident #32 was unable to participate in her activities of daily living (ADLs) due to severe pain. This affected one of three residents reviewed for pain. See findings at F697. Review of the Quality Assurance Performance Improvement (QAPI) meeting minutes from 07/18/19 revealed the facility identified pain control as an issue in the facility and the need for a QAPI project. They indicated this would be discussed at the next quarterly meeting. Review of the QAPI meeting minutes from 10/17/19 revealed the facility decided to not pursue the QAPI project secondary to reviewing the pain control topic and stated this was due to the elimination of the pain quality measures, and as pain control is less of a focus because the government does not want doctors over prescribing pain medications. Interview with the Administrator on 12/07/19 at 2:10 P.M. revealed the facility would need man power to implement all the needed QAPI projects and had no clear answer to further clarify why the pain control QAPI was not followed through with. Review of the facility policy titled, Quality Assurance and Performance Improvement Program, reviewed 07/19/19, stated the facility monitors care and services, drawing data from multiple sources. The policy also stated performance indicators track care processes and outcomes, including adverse events.
CONCERN (F)

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

QAPI Program (Tag F0867)

Could have caused harm · This affected most or all residents

Based on record review, interview, and policy review, the facility failed to identify and implement an appropriate plan of action for a known area of deficiency with the quality of life (QOL) program....

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Based on record review, interview, and policy review, the facility failed to identify and implement an appropriate plan of action for a known area of deficiency with the quality of life (QOL) program. This had the potential to affect all 36 residents (Residents #1, #2, #3, #4, #5, #7, #9, #10, #11, #12, #14, #15, #18, #19, #20, #21, #22, #24, #27, #28, #30, #31, #32, #33, #34, #39, #40, #41, #43, #44, #46, #48, #49, #53, #54, and #56) ordered to receive QOL programs. The facility census was 57 residents. Findings include: During the first portion of the annual survey conducted 12/02/19 through 12/06/19, concerns with the facility were identified as they were not implementing their QOL program, this program the facility implemented was to replace their previous restorative nursing program which was discontinued in October 2018. There were 36 residents identified who experienced a decrease in range of motion, ambulation and/or decline in their functional abilities. The facility failed to ensure Resident's #2, #10, #15, #18, #21, and #33 received restorative/maintenance services to maintain activities of daily living (ADL) and prevent a decline in ADL's after being discharged from skilled therapy. This affected six of six sampled residents and 11 of 11 additional residents (Resident's #24, #7, #30, #40, #43, #9, #3, #31, #22, #39 and #5) reviewed who had referrals from skilled therapy to a restorative/maintenance program to maintain current level or function and prevent declines. Harm occurred when skilled therapy recommendations were not followed through by the QOL program to maintain the resident's current level of function and prevent avoidable declines in ADL's. Resident #18 had a decline in ambulation after being discharged from physical therapy (PT) on 08/14/19 resulting in PT needing to place the resident back on caseload. Resident #33 had experienced a decline in ambulation on 10/21/19 when the resident needed to be placed back on PT caseload. Resident #21 had a decline in ambulation after being discharged from PT on 06/03/19 resulting in the resident needing to be placed back on caseload. Resident #15 had a decline in ambulation and transfers after being discharged from PT on 06/30/19 resulting in the resident needing to be placed back on caseload. Resident #10 had a decline in ambulation after being discharged from PT needing to be placed back on caseload. Resident #2 had a decline in eating after being discharged from occupational therapy (OT) on 09/17/19. OT was not aware of this decline until after surveyor intervention. See findings at F676. The facility failed to ensure range of motion (ROM) programs and/or splinting programs were provided as planned for Residents #2, #3, #9, #15, #20, #22, #31, #32, #39, #40, #41, #48 and #54. This resulted in actual harm for Residents #2, #32, and #54 who experienced declines in ROM and/or contractures (the shortening and hardening of muscles, tendons or other tissue often leading to deformity and rigidity of joints). This affected three of three residents sampled for ROM (Residents #2, #32, and #54) and 10 of 10 additional residents (Resident's #3, #9, #15, #20, #22, #31, #39, #40, #41, and #48) reviewed for ROM based on referrals from skilled PT and/or OT services. See findings at F688. Review of the facility Quality Assurance and Performance Improvement (QAPI) programs for 2019 did not reveal any QAPI projects related to the lack of an adequate QOL program. Interview with the Administrator on 12/07/19 at 2:10 P.M. revealed the facility was aware they did not have an adequate QOL program in place. The Administrator said the facility would need man power to implement all the needed QAPI projects and could not give a clear answer as to why the facility had not identified the QOL program as an area of deficiency in relation to the identified declines in range of motion, contractures, ambulation, and/or functional abilities for these residents. Review of the facility policy titled, Quality Assurance and Performance Improvement, dated 02/15/19, stated the facility's QAPI plan included tracking, investigating, and monitoring adverse events which must be investigated every time they occur.
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

  • "Why is there high staff turnover? How do you retain staff?"
  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • No fines on record. Clean compliance history, better than most Ohio facilities.
Concerns
  • • Multiple safety concerns identified: 4 harm violation(s). Review inspection reports carefully.
  • • 36 deficiencies on record, including 4 serious (caused harm) violations. Ask about corrective actions taken.
  • • Grade D (45/100). Below average facility with significant concerns.
  • • 64% turnover. Above average. Higher turnover means staff may not know residents' routines.
Bottom line: Trust Score of 45/100 indicates significant concerns. Thoroughly evaluate alternatives.

About This Facility

What is Aventura At Humility House's CMS Rating?

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

How is Aventura At Humility House Staffed?

CMS rates AVENTURA AT HUMILITY HOUSE's staffing level at 3 out of 5 stars, which is average compared to other nursing homes. Staff turnover is 64%, which is 18 percentage points above the Ohio average of 46%. High turnover can affect care consistency as new staff learn residents' individual needs.

What Have Inspectors Found at Aventura At Humility House?

State health inspectors documented 36 deficiencies at AVENTURA AT HUMILITY HOUSE during 2019 to 2025. These included: 4 that caused actual resident harm and 32 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Aventura At Humility House?

AVENTURA AT HUMILITY HOUSE 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 AVENTURA HEALTH GROUP, a chain that manages multiple nursing homes. With 70 certified beds and approximately 67 residents (about 96% occupancy), it is a smaller facility located in AUSTINTOWN, Ohio.

How Does Aventura At Humility House Compare to Other Ohio Nursing Homes?

Compared to the 100 nursing homes in Ohio, AVENTURA AT HUMILITY HOUSE's overall rating (4 stars) is above the state average of 3.2, staff turnover (64%) is significantly higher than the state average of 46%, and health inspection rating (3 stars) is at the national benchmark.

What Should Families Ask When Visiting Aventura At Humility House?

Based on this facility's data, families visiting should ask: "How do you ensure continuity of care given staff turnover, and what is your staff retention strategy?" "Can I visit during a mealtime to observe dining assistance and food quality?" "How do you handle medical emergencies, and what is your hospital transfer rate?" "Can I speak with family members of current residents about their experience?" These questions are particularly relevant given the facility's high staff turnover rate.

Is Aventura At Humility House Safe?

Based on CMS inspection data, AVENTURA AT HUMILITY HOUSE has a clean safety record: no substantiated abuse findings (meaning no confirmed cases of resident harm), no Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death), and is not on the Special Focus Facility watch list (a federal program monitoring the lowest-performing 1% of nursing homes). The facility has a 4-star overall rating and ranks #1 of 100 nursing homes in 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 Aventura At Humility House Stick Around?

Staff turnover at AVENTURA AT HUMILITY HOUSE is high. At 64%, the facility is 18 percentage points above the Ohio average of 46%. High turnover means new staff may not know residents' individual needs, medications, or preferences. It can also be disorienting for residents, especially those with dementia who rely on familiar faces. Families should ask: What is causing the turnover? What retention programs are in place? How do you ensure care continuity during staff transitions?

Was Aventura At Humility House Ever Fined?

AVENTURA AT HUMILITY HOUSE has no federal fines on record. CMS issues fines when nursing homes fail to meet care standards or don't correct problems found during inspections. The absence of fines suggests the facility has either maintained compliance or corrected any issues before penalties were assessed. This is a positive indicator, though families should still review recent inspection reports for the full picture.

Is Aventura At Humility House on Any Federal Watch List?

AVENTURA AT HUMILITY HOUSE 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.