COLORADO STATE VETERANS NURSING HOME - RIFLE

851 E 5TH ST, RIFLE, CO 81650 (970) 625-0842
Government - State 89 Beds Independent Data: November 2025 2 Immediate Jeopardy citations
Trust Grade
1/100
#140 of 208 in CO
Last Inspection: November 2024

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

Overview

The Colorado State Veterans Nursing Home in Rifle has received a Trust Grade of F, indicating significant concerns and a poor overall performance. Ranking #140 out of 208 facilities in Colorado places this nursing home in the bottom half of the state. The facility's trend is worsening, with issues increasing from 4 in 2023 to 11 in 2024. Staffing is a strength, achieving a 5/5 star rating with a turnover rate of 46%, which is below the state average. However, there were concerning incidents, such as failing to update fall care plans after resident falls and administering incorrect medication dosages without proper checks, highlighting serious deficiencies in care that families should consider carefully. Overall, while staffing appears stable, the facility struggles with critical care issues and compliance.

Trust Score
F
1/100
In Colorado
#140/208
Bottom 33%
Safety Record
High Risk
Review needed
Inspections
Getting Worse
4 → 11 violations
Staff Stability
⚠ Watch
46% turnover. Above average. Higher turnover means staff may not know residents' routines.
Penalties
⚠ Watch
$32,975 in fines. Higher than 78% of Colorado facilities, suggesting repeated compliance issues.
Skilled Nurses
✓ Good
Each resident gets 77 minutes of Registered Nurse (RN) attention daily — more than 97% of Colorado nursing homes. RNs are the most trained staff who catch health problems before they become serious.
Violations
⚠ Watch
19 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★☆☆☆
2.0
Overall Rating
★★★★★
5.0
Staff Levels
★★★★☆
4.0
Care Quality
★☆☆☆☆
1.0
Inspection Score
Stable
2023: 4 issues
2024: 11 issues

The Good

  • 5-Star Staffing Rating · Excellent nurse staffing levels
  • 4-Star Quality Measures · Strong clinical quality outcomes
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record

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

The Bad

2-Star Overall Rating

Below Colorado average (3.1)

Below average - review inspection findings carefully

Staff Turnover: 46%

Near Colorado avg (46%)

Higher turnover may affect care consistency

Federal Fines: $32,975

Below median ($33,413)

Moderate penalties - review what triggered them

The Ugly 19 deficiencies on record

2 life-threatening 2 actual harm
Nov 2024 9 deficiencies 1 IJ (1 affecting multiple)
CRITICAL (K)

Immediate Jeopardy (IJ) - the most serious Medicare violation

Accident Prevention (Tag F0689)

Someone could have died · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** D. Failure to update fall care plans and interventions to prevent falls and complete neurological assessments after a fall for R...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** D. Failure to update fall care plans and interventions to prevent falls and complete neurological assessments after a fall for Resident #18, Resident #43, and Resident #52. The Neuro (Neurological) check assessment form, dated 2024, was provided by the director of nursing (DON) on [DATE] at 12:11 p.m. It documented that when a resident experienced a fall, neurological checks are performed for 72 hours after the fall occurred. -The assessment form documented that four neurological checks must be completed every 15 minutes in the first hour after the fall event. The assessment form documented that neurological checks must be completed every 30 minutes in the second hour after the fall event. The assessment form documented that hourly neurological assessments are completed for four hours after the 30-minute checks were completed. The assessment form documented that six neurological assessments must be completed at four-hour intervals for 24 hours after the hourly neurological assessments were completed. -The assessment form documented additional neurological assessments must then be completed every shift after all previous neurological assessments were completed until 72 hours had passed since the fall occurred. 1. Resident #18 a. Resident status Resident #18, age greater than 65, was admitted on [DATE]. According to the [DATE] CPO, diagnoses included neoplasm of the prostate (prostate cancer), pulmonary embolism (blood clots in the lungs), and stroke. The [DATE] minimum data set (MDS) assessment revealed the resident was severely cognitively impaired with a brief interview for mental status (BIMS) score of six out of 15. He required substantial or maximum assistance with eating, oral hygiene, and dressing. He was dependent on direct care staff for all other care. b. Record review The fall care plan, initiated on [DATE] and revised on [DATE], documented that Resident #18 was a high fall risk. Interventions included ensuring the call light was close to the resident, frequent checks, utilizing non-slip shoes and socks, utilizing a wheelchair for mobility, and reviewing information on past falls to attempt to determine the cause of those falls. Although the resident experienced seven unwitnessed falls (see below), there were no care plan updates or evidence the interdisciplinary team (IDT) reviewed the information on the resident's falls to determine the cause for the falls and develop effective interventions as expected per facility policy and the resident's care plan. Further, the facility continued to fail to perform post-fall neurological assessments as expected (see above). Specifically: (1) The nursing falls documentation form, dated [DATE], documented Resident #18 experienced an unwitnessed fall at 9:00 a.m. The form documented Resident #18 was discovered sitting on the floor of his room in front of his recliner chair. -The Neuro check assessment form, dated [DATE], documented the facility performed two neurological assessments for Resident #18 at 9:00 a.m. and 12:20 p.m. The facility failed to perform neurological assessments for Resident #18 for 72 hours after an unwitnessed fall. (2) The nursing falls documentation form, dated [DATE], documented Resident #18 experienced an unwitnessed fall at 3:00 p.m. The form documented Resident #18 was discovered lying in a side-lying position on the floor of his room with his walker turned over in the room. The resident was discovered to have an abrasion on the right side of his face. -The Neuro check assessment form, dated [DATE], documented the facility performed three neurological assessments for Resident #18 at 3:10 p.m., 3:30 p.m., and 4:30 p.m. The facility failed to perform neurological assessments for Resident #18 for 72 hours after an unwitnessed fall. (3) The nursing falls documentation form, dated [DATE], documented Resident #18 experienced an unwitnessed fall at 3:15 a.m. The form documented Resident #18 fell out of bed and was found sitting beside his bed on the floor. -The Neuro check assessment form, dated [DATE], documented the facility performed one neurological assessment for Resident #18 at 3:15 a.m. The facility failed to perform neurological assessments for Resident #18 for 72 hours after an unwitnessed fall. (4) The nursing falls documentation form, dated [DATE], documented that Resident #18 experienced an unwitnessed fall at 9:15 a.m. The form documented Resident #18 was discovered sitting on the floor of his bathroom facing the toilet. -No documentation of neurological assessments performed on [DATE] was present in Resident #18's electronic health record (EHR). The facility failed to perform neurological assessments for Resident #18 for 72 hours after an unwitnessed fall. (5) The nursing falls documentation form, dated [DATE], documented Resident #18 experienced a fifth unwitnessed fall at 12:15 p.m. The form documented Resident #18 was discovered in his bathroom lying on his back on the floor. -The Neuro check assessment form, dated [DATE], documented the facility did not perform the 12:30 p.m. neurological assessment because the resident was using the bathroom. The form documented nursing staff did not perform the 1:00 p.m. and 1:30 p.m. neurological assessment because Resident #18 was sleeping. The form documented nursing staff did not perform the 5:00 p.m. neurological assessment because the resident was eating. The facility failed to perform neurological assessments for Resident #18 for 72 hours after an unwitnessed fall. (6) The nursing falls documentation form, dated [DATE], documented Resident #18 experienced yet another unwitnessed fall at 2:15 a.m. The form documented Resident #18 was discovered in his room on his hands and knees. The form documented the resident sustained an abrasion to his right eye. -The Neuro check assessment form, dated [DATE], documented the facility did not perform neurological assessments at 3:15 a.m., 3:45 a.m., or 4:15 a.m. because Resident #18 was sleeping. The facility failed to perform neurological assessments for Resident #18 for 72 hours after an unwitnessed fall. (7) The nursing falls documentation form, dated [DATE], documented Resident #18 experienced an unwitnessed fall at 6:30 p.m. The form documented Resident #18 was discovered sitting on the floor of his room between the bed and nightstand with his back against the wall. -No documentation of neurological assessments performed on [DATE] was present in Resident #18's electronic health record (EHR). The facility failed to document neurological assessments after the resident experienced an unwitnessed fall. 2. Resident #43 a. Resident status Resident #43, age greater than 65, was admitted on [DATE]. According to the [DATE] CPO), diagnoses included dementia, cataract, and generalized muscle weakness. The [DATE] MDS assessment revealed the resident was severely cognitively impaired and could not complete the BIMS because he was rarely or never understood. He required set-up or clean-up assistance with eating and substantial assistance with dressing and personal hygiene. He was dependent on direct care staff for all other care. b. Record Review The fall care plan, initiated on [DATE] and revised on [DATE], documented Resident #43 was a high fall risk. Interventions included ensuring his hearing aids were in place, ensuring line of sight of the resident when he was out of his room, and utilizing non-slip shoes and socks. Record review revealed the facility failed to perform post-fall neurological assessments as expected (see above) and update the resident's care plan following an unwitnessed fall on [DATE]. Specifically: The nursing falls documentation form, dated [DATE], documented that Resident #43 experienced an unwitnessed fall at 7:17 p.m. The form documented Resident #43 was discovered on the floor of his bedroom lying on his right side. -A review of the resident's care plan revealed the facility failed to update or revise the fall plan of care after Resident #43's unwitnessed fall. -The Neuro check assessment form, dated [DATE], documented the facility completed 13 neurological assessments that began at 7:20 p.m. on [DATE] and ended on [DATE] at 1:05 p.m. The facility failed to perform neurological assessments for Resident #18 for 72 hours after an unwitnessed fall. 3. Resident #52 a. Resident status Resident #52, age greater than 65, was admitted on [DATE]. According to the [DATE] CPO, diagnoses included dementia, anemia, and intervertebral disc degeneration. The [DATE] MDS assessment revealed the resident was severely cognitively impaired with a BIMS score of five out of 15. She required set-up or clean-up assistance with eating and personal hygiene. She required moderate assistance with all other care. b. Record Review The fall care plan, initiated on [DATE] and revised on [DATE], documented Resident #52 was a high fall risk because of her confusion and wandering behaviors. Interventions included ensuring her call light was within reach, encouraging Resident #52 to participate in activities, ensuring appropriate non-skid footwear, and reviewing information on past falls to attempt to determine the cause of those falls. Record review revealed the facility failed to perform post-fall neurological assessments as expected (see above) and update the resident's care plan following unwitnessed falls on [DATE] and [DATE]. Specifically: (1) The nursing falls documentation form, dated [DATE], documented that Resident #52 experienced an unwitnessed fall at 5:00 a.m. The form documented Resident #52 was discovered on the floor of the room between the armoire and the foot of the bed with her head positioned toward the wall. -A review of the resident's care plan revealed the facility failed to update or revise the fall plan of care after Resident #52's unwitnessed fall (see care plan above) -The Neuro check assessment form, dated [DATE], documented the facility completed 12 neurological assessments that began at 5:20 a.m. on [DATE] and ended on [DATE] at 8:00 p.m. The facility documented that no neurological assessment was performed on [DATE] at 11:05 p.m. because the resident was sleeping. The facility failed to perform neurological assessments for Resident #52 for 72 hours after an unwitnessed fall. (2) The nursing falls documentation form, dated [DATE], documented Resident #52 experienced an unwitnessed fall at 7:00 a.m. The form documented Resident #52 was discovered kneeling on a pillow on the floor in her room. -The facility failed to update or revise the fall plan of care after Resident #52 experienced an unwitnessed fall (see care plan above) -The Neuro check assessment form, dated [DATE], documented the facility completed six neurological assessments that began at 7:00 a.m. on [DATE] and ended on [DATE] at 9:00 p.m. The facility failed to perform neurological assessments for Resident #52 for 72 hours after an unwitnessed fall. 4. Staff interviews 1. LPN #3 was interviewed on [DATE] at 1:12 p.m. LPN #3 said if a resident had an unwitnessed fall, she would hit the emergency light immediately to get more help and check on the resident. LPN #3 said she could not recall how often neurological assessments needed to be performed after a fall, but said the neurological assessment requirements were printed on the top of each paper neurological assessment sheet. LPN #3 said that neurological assessments should always be performed to ensure the resident did not have a head injury. LPN #3 said a neurological assessment cannot be skipped because a resident is eating, sleeping, or using the bathroom. LPN #3 said if a resident fell, she would expect the plan of care to be updated or reviewed. 2. LPN #1 was interviewed on [DATE] at 1:17 p.m. LPN #1 said that if a resident had an unwitnessed fall, she would ensure the resident was okay first by assessing them. LPN #1 said she would then call for help by hitting the emergency button. LPN #1 said that she would then do neurological assessments according to facility protocol. LPN #1 said that a resident sleeping, eating, or using the bathroom is not an appropriate reason to skip a neurological assessment. LPN #1 said nurses could miss signs of injury if neurological assessments were skipped. LPN #1 said residents who fall should have their fall plans of care updated. 3. The DON was interviewed on [DATE] at 10:27 a.m. The DON said she considered a fall to be any unplanned resident descent to the floor. The DON said when a resident experiences an unwitnessed fall, she would expect nursing staff to immediately assess the resident for injuries, complete neurological assessments according to the facility protocol, and notify the DON or on-call nurse. The DON said this was important to identify if any injuries were sustained by the resident and identify what caused the fall to occur. The DON said nurses must always complete neurological assessments by the protocol schedule printed on the neurological assessment paper sheet. (see Neuro check form above). The DON said the only acceptable reason for a neurological assessment to be missed was if a resident refused a neurological assessment which would be documented on the paper neurological assessment. The DON said it was not acceptable for a resident to have a neurological assessment missed in the 72 hours after a fall because a resident was eating, sleeping, or using the bathroom. The DON said vital signs must be obtained with each neurological assessment performed by the nurse. The DON said if a resident refused to have their vital signs taken as part of the neurological assessment, the refusal should be documented on the neurological assessment form. The DON said if a resident was eating, sleeping, or using the restroom, she expected the nurse to complete the neurological assessment as soon as possible instead of skipping it. The DON said that residents who experience falls should have their plans of care updated. The DON said the interdisciplinary (IDT) team would be notified of the fall as well, and the IDT team would further review the fall to ensure appropriate interventions were placed to prevent the resident from falling the same way in the future. The DON said she would specifically want the newly identified intervention in the fall plan of care to match the cause of the fall. The DON said the new information is communicated to day shift nursing staff, and it was the responsibility of day shift nursing staff to communicate the new intervention to night shift nursing staff. The DON said it was important to update the plan of care to communicate how to prevent that fall from happening again. The DON reviewed unwitnessed fall documentation for Resident #18. The DON said that no neurological assessments were documented for falls documented on [DATE] and [DATE]. The DON said the facility did not complete neurological assessments appropriately for the other five falls identified. The DON said she was surprised that many unwitnessed falls had not been appropriately documented for Resident #18. The DON said Resident #18's plan of care was not updated or reviewed for additional interventions after unwitnessed falls he experienced on [DATE], [DATE], [DATE], and [DATE]. The DON reviewed unwitnessed fall documentation for Resident #43. The DON said the facility did not document all required neurological assessment elements including vital signs. The DON said Resident #43's fall plan of care was not updated after she fell on [DATE], [DATE], or [DATE]. The DON reviewed unwitnessed fall documentation for Resident #52. The DON said that on the unwitnessed falls documented on [DATE] and [DATE], the nursing staff started by completing neurological checks appropriately. The DON said on both dates nursing staff stopped completing neurological checks before the 72 required hours of neurological checks had been completed. The DON said Resident #52's fall plan of care was not updated after they fell on [DATE] or [DATE]. IV. SMOKING Record review and interviews revealed the facility failed to ensure Resident #29 did not smoke with his oxygen cannula on his face and hunched over his portable oxygen tank. A. Facility Policy The Smoking policy revised on [DATE] was provided by the corporate consultant (CC) on [DATE] at 9:42 a.m. It read in pertinent part: Should unsafe smoking behavior occur, the community will attempt to: educate the resident on safe smoking practices; offer smoking cessation assistance including pharmacological and behavioral support for smoking cessation; and implement a mutually agreed upon behavioral plan. Unsafe smoking behaviors include but are not limited to: -The use of oxygen while smoking. By federal requirements, smoking will not be permitted in any area where there is oxygen usage within close proximity. There must be a distance of 20 feet between smokers and oxygen. B. Resident #29 1. Resident status Resident #29, age greater than 65, was admitted on [DATE]. According to the [DATE] computerized physician order (CPO), diagnoses included chronic obstructive pulmonary disease (COPD), pulmonary embolism (blockage in an artery in the lung), tobacco use, emphysema, and dependence on supplemental oxygen. The [DATE] minimum data set (MDS) assessment revealed Resident #29 was cognitively intact with a brief interview for mental status (BIMS) score of 15 out of 15. Resident #29 was on oxygen therapy. 2. Observations and resident interview Resident #29 was observed sitting in his wheelchair in the common area near the front door on [DATE] at 9:15 a.m. Resident #29 was placing a cigarette in his mouth and self-propelled to the smoking area outside. The resident was bent forward and hunched over his knees. His oxygen nasal cannula was on his face and his portable oxygen canister was between his legs. He was smoking his cigarette and said he always kept his nasal cannula on while he smoked. Resident #29 said he always turned off the portable oxygen tank because he once caught his face on fire when he lived at home. The oxygen canister was turned to zero. 3. Staff interviews a. The NHA and CC were interviewed together on [DATE] at 9:23 a.m. The NHA said residents were assessed to figure out if the resident needed supervision while smoking or not. She said the residents left their oxygen tanks in the lobby by the front door, except for one resident. She said Resident #29 preferred to take off his oxygen outside the front door but he did not bring it to the smoking area. The CC said Resident #29 never brought his oxygen outside past the front door or kept it with him while he smoked in the smoking area. The NHA said she was unaware the resident caught himself on fire while smoking with oxygen on at home. The CC said she was going to talk with Resident #29 and have him assessed for safe smoking. b. CNA #9 was interviewed on [DATE] at 9:59 a.m. CNA #9 said residents were not supposed to wear oxygen when they went outside to smoke. She said the residents needed to take off their oxygen before they went outside and she had not seen Resident #29 smoke with his oxygen on before. c. RN #2 was interviewed on [DATE] at 10:02 a.m. RN #2 said the nursing staff removed the residents' oxygen or reminded the residents to remove it at the front door when the residents went outside to smoke. She said Resident #29 preferred to leave his oxygen outside of the front door in the shade. She said she had not seen the resident smoke with his oxygen on. d. CNA #10 was interviewed on [DATE] at 10:05 a.m. CNA #10 said she had not worked at the facility very long but knew the residents were not able to smoke with their oxygen on and had not seen Resident #29 wear his oxygen while smoking. e. RN #5 was interviewed on [DATE] at 10:20 a.m. RN #5 said oxygen tanks were not allowed in the smoking area at all because it was a huge fire and combustion risk. f. LPN #1 was interviewed on [DATE] at 11:05 a.m. LPN #1 said Resident #29 was independent enough to remove his oxygen to go smoke and he should remember that. She said she did not follow him around to ensure he took off his oxygen to smoke because it was not a required task for nursing staff. She said he should not smoke with the cannula on or the oxygen canister in between his legs because he was still at risk for combustion, even if the portable canister was turned off. She said Resident #29 was extremely independent and was able to remove and replace his oxygen before and after smoking. Based on observations, record review and interviews, the facility failed to ensure the resident environment remained as free of accident hazards as possible, and that each resident received adequate supervision and assistive devices to prevent accidents. This failure affected one discharged resident (#61) and 22 current residents (#34, #31, #22, #14, #46, #35, #2, #33, #45, #17, #21, #42, #47, #54, #4, #7, #58, #18, #43, #52, #40 and #29) out of 41 sample residents. Specifically: TRANSFER POLES On [DATE], Resident #61, severely cognitively impaired and with a history of falls, was discovered stuck between the bed and his transfer pole. The facility failed to complete a safety risk assessment for Resident #61 before placing the transfer pole and, after the incident on [DATE], failed to investigate how the resident got stuck between the transfer pole and his bed. Record review and interviews revealed the facility failed to complete safety risk assessments for all 17 current residents (#34, #31, #22, #14, #46, #35, #2, #33, #45, #17, #21, #42, #47, #54, #4, #7 and #58) who had a transfer pole, to ensure resident safety. These failures created a situation of immediate jeopardy for serious harm that required immediate corrective action. FALLS The facility failed to prevent multiple falls, complete assessments after falls, investigate falls, and timely update fall care plans for Resident #18, Resident #43, Resident #52, Resident #4, and Resident #40. SMOKING and OXYGEN The facility failed to ensure Resident #29 did not smoke with his oxygen cannula on his face and hunched over his portable oxygen tank. Findings include: I. IMMEDIATE JEOPARDY A. Situation of Immediate Jeopardy Resident #61 was admitted on [DATE] with a history of falling. The resident was identified as severely cognitively impaired. The resident was ordered a vertical transfer pole to help with self-transfers on [DATE]. The facility failed to complete a safety risk evaluation for the use of the vertical transfer pole. On [DATE], Resident #61 was discovered by a certified nurse aide (CNA) stuck between the transfer pole and his bed. The CNA triggered the resident's emergency call light because she was unable to reposition the resident without assistance. The nurse responded and found the CNA trying to remove the resident from between the transfer pole and bed. The nurse noted the resident displayed agonal breathing (gasping), his eyes were open but he was not blinking and he had no pulse. The CNA and nurse repositioned the resident on his bed and did not start cardiopulmonary resuscitation (CPR) because the resident had an order for do not resuscitate. The nurse applied oxygen and emergency medical services (EMS) was called. When EMS arrived, the resident had begun breathing on his own. The facility failed to complete a safety risk assessment for Resident #61 after the incident on [DATE]. On [DATE], the facility completed a physical restraint assessment; however, the restraint assessment did not include a safety assessment. On [DATE] at 7:20 p.m., the nursing home administrator (NHA) was notified the failure in the facility's response to the incident on [DATE] and the failure to conduct safety risk assessments for all of the 17 current residents with transfer poles created a situation of immediate jeopardy that required immediate corrective action. B. Plan to remove Immediate Jeopardy On [DATE] at 6:05 p.m., the facility submitted the following plan to remove the immediate jeopardy situation: On [DATE] physical therapy (PT) staff completed evaluations for each resident with access to a transfer pole. Evaluations included proper placement (bed height, proximity to wall and/or toilet, distance from transfer surface) as well as resident conditions that may affect transfer, any risks for entrapment for all residents with access to transfer pole i.e. shared bathrooms. Assessments included: General assessment: fall risk, cognition, transfer ability and other comorbidities that may affect ability to safely use assistive or transfer devices by PT; Bedside: to include transfer ability with multiple assistive devices to determine safest option for individual resident need. PT to establish the distance from bed to appropriate assistive device and determine safest distance based on individuality of the resident and manufacturer's recommended use to 'make sure the product has sufficient space to allow user(s) to walk between the pole or handle and any other stationary object.' Assessment will include mechanics of the bed, including possible mattress and wheel shift; Placement considered safe and appropriate by PT from beside and bathroom individual evaluation as evidenced by distance deemed safe and beneficial through multiple transfer trials with PT to determine the resident's specific body habitus. 15-minute checks performed by direct care staff on shift until evaluation or assessment is completed by therapy and further determination is made. Evaluation or assessment to be completed by the end of business day [DATE]. Education of nursing staff will be provided by director of nursing (DON), infection preventionist (IP) or lead CNA prior to staff's next scheduled shift. Lead CNA educated by DON. Education includes: 15-minute checks and resident safety for residents for increased fall risk and for the residents that still have access to a transfer pole. If a new transfer or assistive device is implemented, the above staff will continue to educate front line staff, housekeeping and maintenance. Beds will be marked and staff educated to ensure appropriate placement. Will monitor placement of device installed in relation to the mattress, if the device is at bedside, an order obtained from PT every shift by nursing, daily safety rounds by restorative and quarterly by therapy and as needed. Resident's bed and any furniture in close proximity to the device will be marked on the floor to ensure proper replacement of furniture should it need to be temporarily moved. Will continue to encourage call light use. For those residents whose transfer pole was removed, staff have been educated to provide 15-minute checks, offer transfer assistance and encourage call light use education provided to direct care staff to continue with 15-minute checks until the interdisciplinary team (IDT) determines they are no longer needed to ensure safety. Encourage residents to use call light to request assistance and staff to provide transfer assistance as indicated. Any new transfer pole request will not be ordered or initiated until therapy completes and evaluation to determine appropriateness. C. Removal of Immediate Jeopardy Based on a review of the facility's plan, observations, and record review, the NHA was informed the immediate jeopardy situation was removed on [DATE] at 6:05 p.m. However, the deficient practice remained at a G level, isolated, actual harm. II. TRANSFER POLES A. Resident #61 1. Resident status Resident #61, age greater than 65, was admitted on [DATE] and passed away on [DATE]. According to the [DATE] computerized physician orders (CPO), diagnoses included heart failure, abdominal aortic aneurysm without rupture (swelling in the artery in the stomach), chronic kidney disease, osteoarthritis of the left knee, and abnormalities of gait and mobility. The [DATE] minimum data set (MDS) assessment revealed Resident #61 had a severe cognitive impairment with a brief interview of mental status (BIMS) score of three out of 15. Resident #61 was documented to have an impairment to both lower extremities and used a wheelchair. The resident had no restraint devices documented. 2. Record review Resident #61's activities of daily living (ADLs) care plan documented a vertical transfer pole as an intervention on [DATE]. Resident #61 had a physician's order for a vertical transfer pole dated [DATE]. On [DATE], a progress note documented in Resident #61's electronic health record (EHR) revealed: -At approximately 12:45 p.m., the nurse responded to the resident's emergency call light. The nurse discovered the CNA was attempting to remove the resident from in between the transfer pole, his bed, and a chair where the resident appeared to be stuck. The resident was noted to be bent over in a crumpled-up position with his foot stuck in between the transfer pole and his bed. -The resident was unresponsive with agonal breathing and his eyes were open and not blinking. The nurse attempted to assist the CNA by keeping the resident upright while two other CNAs moved the bed to free the resident's foot. The staff moved the resident flat on his bed into a Trendelenburg position (feet placed higher than the resident's head). -Resident #61 was not responding to verbal stimuli or a sternal rub. The nurse was unable to feel the resident's pulse. The nurse sent a CNA to get the physician and another CNA to call 911 and check the resident's code status. The resident was a do not resuscitate (DNR) and CPR (cardiopulmonary resuscitation) was not provided. The physician verified there was a cessation of heartbeat during the assessment of the resident. EMS arrived and Resident #61 began breathing more at a regular rate within several minutes of being in Trendelenburg and applying oxygen. The resident was making nonsensical statements. When EMS arrived the resident was able to speak and a transfer to the hospital was not necessary. A review of the resident's record revealed no evidence the facility had completed a safety risk assessment for Resident #61 before placing the transfer pole and, after the incident on [DATE], no evidence the facility completed a safety risk assessment or investigated how the resident became stuck between the transfer pole and his bed. On [DATE], a physical restraint evaluation was completed for Resident #61 and the transfer pole. However, the evaluation did not include a safety risk assessment. In addition to the failures above for Resident #61, the facility failed to review the use of transfer poles by 17 current facility residents (see below). B. Resident #34 1. Resident status Resident #34, age greater than 65, was admitted on [DATE]. According to the [DATE] CPO, diagnoses included osteoarthritis in an unspecified hand, fibromyalgia, dementia, pain in the right hip, generalized muscle weakness, and lack of coordination. The [DATE] MDS assessment revealed Resident #34 had a severe cognitive impairment with a BIMS score of six out of 15. Resident #34 used a walker and a wheelchair. The resident had no restraint devices documented. 2. Observations On [DATE] at approximately 2:00 p.m., observations revealed Resident #34 had a vertical transfer pole next to her bed. 3. Record review Resident #34 did not have a physician's order for a vertical transfer pole. Resident #34 did not have documentation in her care plan for a vertical transfer pole. Resident #34 did not have a safety risk assessment for a vertical transfer pole. A fall risk assessment completed on [DATE] revealed Resident #34 w[TRUNCATED]
SERIOUS (G)

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 observations, record review and interviews, the facility failed to provide care and treatment to prevent the developmen...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to provide care and treatment to prevent the development and worsening of pressure injuries for one (#54) of two residents reviewed for pressure injuries out of 41 sample residents. Resident #54 was admitted to the facility on [DATE] with diagnoses of type 2 diabetes, history of toe amputation, osteomyelitis (bone infection) and neuropathy. On 9/26/24, after not wearing her podiatry ordered offloading boots due to a red area on her heel, potentially from the podiatry offloading boot and/or a screw located on her wheelchair foot pedal, Resident #54 developed a blister on her left heel which progressed into an unstageable pressure ulcer. Resident #54 had physician's orders for the offloading pressure relieving boots and the boots were care planned, however, the resident did not consistently wear the boots as ordered. The resident's refusals to wear the boots were not documented or refusals were not care planned and there were no care plan interventions directing staff what to do if the resident refused the boots. Resident #54 was able to identify why she did not consistently wear the pressure relieving boots but the facility did not ask the resident her reasoning or implement interventions to address the resident's concerns with the pressure relieving boots. Due to the facility's failures to ensure effective interventions were put in place and monitored for compliance and effectiveness, Resident #54 developed a blister to her left heel which worsened to an unstageable pressure ulcer. Additionally, Resident #54 was identified on 11/13/24 to have a potential second pressure wound developing to her right lateral foot. Findings include: I. Professional reference According to the National Pressure Injury Advisory Panel, European Pressure Injury Advisory Panel and Pan Pacific Pressure Injury Alliance Prevention and Treatment of Pressure Injuries: Clinical Practice Guideline, third edition, [NAME] Haesler (Ed.), EPUAP/NPIAP/PPPIA: 2019, retrieved from https://www.internationalguideline.com on 12/3/24, Category/Stage 1: Nonblanchable Erythema (discoloration of the skin that does not turn white when pressed, early sign of tissue damage) Intact skin with non blanchable redness of a localized area usually over a bony prominence. Darkly pigmented skin may not have visible blanching; its color may differ from the surrounding area. The area may be painful, firm, soft, warmer or cooler as compared to adjacent tissue. Category/Stage 1 may be difficult to detect in individuals with dark skin tones. May indicate 'at risk' individuals (a heralding sign of risk). Category/Stage 2: Partial Thickness Skin Loss. Partial thickness loss of dermis presenting as a shallow open ulcer with a red pink wound bed, without slough. May also present as an intact or open/ruptured serum filled blister. Presents as a shiny or dry shallow ulcer without slough or bruising. The Category/Stage should not be used to describe skin tears, tape burns, perineal dermatitis, maceration or excoriation. Category/Stage 3: Full Thickness Skin Loss. Full thickness tissue loss. Subcutaneous fat may be visible, but bone, tendon or muscle are not exposed. Slough may be present but does not obscure the depth of tissue loss. May include undermining and tunneling. The depth of a Category/Stage 3 pressure ulcer varies by anatomical location. The bridge of the nose, ear, occiput and malleolus do not have subcutaneous tissue and Category/Stage 3 ulcers can be shallow. In contrast, areas of significant adiposity can develop extremely deep Category/Stage 3 pressure ulcers. Bone/tendon is not visible or directly palpable. Category/Stage 4: Full Thickness Tissue Loss. Full thickness tissue loss with exposed bone, tendon or muscle. Slough or eschar may be present on some parts of the wound bed. Often include undermining and tunneling. The depth of a Category/Stage 4 pressure ulcer varies by anatomical location. The bridge of the nose, ear, occiput and malleolus do not have subcutaneous tissue and these ulcers can be shallow. Category/Stage 4 ulcer can extend into muscle and/or supporting structures (fascia, tendon or joint capsule) making osteomyelitis possible. Exposed bone/tendon is visible or directly palpable. Unstageable: Depth Unknown. 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) on the wound bed. Until enough slough and/or eschar is removed to expose the base of the wound, the true depth,and therefore Category/Stage, cannot be determined. Stable (dry, adherent, intact without erythema or fluctuance) eschar on the heels serves as the body's natural (biological) cover and should not be removed. Suspected Deep Tissue Injury: Depth Unknown. Purple or maroon localized area of discolored intact skin or blood-filled blister due to damage of underlying soft tissue from pressure and/or shear. The area may be preceded by tissue that is painful, firm, mushy, boggy, warmer or cooler as compared to adjacent tissue. Deep tissue injury may be difficult to detect in individuals with dark skin tones. Evolution may include a thin blister over a dark wound bed. The wound may further evolve and become covered by thin eschar. Evolution may be rapid, exposing additional layers of tissue even with optimal treatment. II. Facility policy and procedure The Wound Management policy, revised on 8/7/24, was provided by the corporate consultant (CC) on 11/22/24 at 10:02 a.m. The policy read in pertinent part, To promote wound healing and decrease the risk of developing various types of wounds, it is the policy of the facility to provide evidence-based treatments in accordance with current standards of practice and provider orders. Wound treatment should be provided in accordance with provider orders, including the cleansing method, type of dressing and frequency of dressing change. Implement appropriate interventions to decrease risk of recurrence as applicable. Treatments should be documented on the MAR (medication administration record) or TAR (treatment administration record). The effectiveness of treatments should be monitored through ongoing assessment of the wound. The resident's comprehensive care plan should be kept up to date. III. Resident #54 A. Resident status Resident #54, age greater than age [AGE], was admitted on [DATE]. According to the November 2024 computerized physician orders (CPO), diagnoses included diabetes mellitus due to underlining condition with diabetic autonomic (complication of diabetes), acute kidney failure, osteomyelitis (bone infection), unspecified open wound of unspecified toe and other abnormalities of gait and mobility. The 10/11/24 minimum data set (MDS) assessment revealed the resident was cognitively intact with a brief interview for mental status (BIMS) score of 15 out of 15. The resident did not exhibit rejection of care behaviors and used a wheelchair for mobility. According to the MDS assessment, the resident was at risk for developing pressure ulcers and had an unhealed stage one or greater pressure ulcer. The MDS assessment revealed the resident had an unstageable pressure ulcer. IV. Resident interview and observations Resident #54 was interviewed on 11/18/24 at 3:48 p.m. Resident #54 was sitting in a wheelchair in her room. She said she developed a blister on her left foot that turned into a wound. She said she did not have a lot of feeling in her foot but the boot she received (from the podiatry physician) had bothered her foot. The resident said she developed the blister shortly after being admitted to the facility. Resident #54 said she had a boot she should have been wearing but she had not put it on for the day (11/18/24). She said she was supposed to wear the boot when she was up and out of bed. She said she could put the boot on herself but staff could help her if she asked them too. Resident #54 said she should currently be wearing the soft form heel protective boot for her left foot, but the boot would get tangled up in her wheelchair and so she did not like to wear it. On 11/20/24 at 10:04 a.m. Resident #54 was laying in bed. The resident wore socks on her feet, however she was not wearing her heel protective boots. Resident #54's heels were resting directly on the bed. Resident #54 was interviewed a second time on 11/20/24 at 1:54 p.m. Resident #54 was in her wheelchair and wore a heel protective boot on her left foot. The resident's feet were both on the wheelchair foot pedals. She said she just got back from a podiatry appointment and said the wound on her left foot would be slow to heal. On 11/21/24 at 8:42 p.m. the resident was in bed. She had two soft foam heel protective boots by her walker which she was not wearing. On 11/22/24 at 9:03 a.m. Resident #54 was sitting on her bed. She did not have her heel protective boots on. The resident said she did not like wearing boots in bed because she needed a pillow between her knees for comfort, and the pillow and the boots were too much together. Resident #54 said her soft form boots were too bulky to wear in bed and with her wheelchair. She said her wheelchair foot pedals were not comfortable with the boots on. She said there was a screw that held the back strap on the foot pedal that was causing some rubbing on her foot. She said the screw was removed but the foot pedals, the size of her wheelchair and the boots together did not feel comfortable. She said no one had looked at her foot pedals or her wheelchair to determine if there could be an adjustment made to create a better fit when she wore her foam heel protective boots. V. Wound care observations and interview On 11/20/24 at 1:40 p.m. wound care was observed with the physician (PHY). Resident #54 wore a heel protective boot over a sock on her left foot. The PHY said the wound to her left foot was started by a podiatry shoe. He said the shoe caused a blister so the resident stopped using the shoe. The PHY said the podiatry shoe had a plastic insert in the heel that could not be removed and that caused the pressure to the resident's heel. The PHY said the facility had had difficulty with the local podiatry specialists and had had to watch their recommendations and devices closely over the last few months. Resident #54's left heel had eschar (dead tissue) throughout the wound. The wound measured 3.5 centimeters (cm) by 4.2 cm x 0.1 cm. The PHY said the wound was unstageable. The PHY said the wound was avoidable because of the shoe from the podiatrist, but was also unavoidable because her blood sugars were out of control when the injury occurred. The PHY placed Iodosorb (wound treatment) around the edges of eschar and a large heel dressing was placed on the resident's heel. A sock and a blue heel protective boot were placed on the resident's left foot. VI. Record review The 7/18/24 Braden Scale assessment (a tool for predicting pressure ulcer risk) identified Resident #54 was at risk for developing pressure sores The skin integrity care plan, revised 11/7/24, indicated Resident #54 had a potential/actual impairment to skin integrity to her bilateral feet related to diabetes type 2 neuropathy, fragile skin and a current chronic non healing wound. The care plan identified the resident had a recent surgical toe amputation and a history of osteomyelitis and cellulitis. The care plan interventions on 7/22/24 included directing staff to document weekly treatment to include measurement of each area of skin breakdown's width, length, depth, type of tissue and exudate and any other notable changes or observations, educating the resident/family/caregivers of causative factors and measures to prevent skin injury, encouraging good nutrition and hydration in order to promote healthier skin, following facility protocols for treatment of injury, identifying and documenting potential causative factors and eliminating/resolving where possible, monitoring/documenting location, size and treatment of skin injury and reporting abnormalities, failure to heal and signs and symptoms of an infection or maceration to the physician. The care plan interventions initiated on 10/21/24 included using caution during transfers and bed mobility to prevent striking the resident's arms, legs, and hands against any sharp or hard surface, using bilateral foot pedals on the resident's wheelchair for offloading and using offloading boots when the resident was seated and lying down. -Review of Resident #54's care plan did not identify the resident refused her offloading heel protective boots. -The care plan did not identify interventions to try if and when the resident refused to wear her heel protective boots. The skin/wound note, dated 9/26/24 at 6:17 p.m. documented Resident #54 informed the registered nurse (RN) there was an issue with her left foot. The RN assessed the resident's foot and identified the resident had a large blister covering the majority of the edge of her heel. According to the note, the blister was not present earlier during the shift when the RN changed the dressing to the resident's hallux (toe) on the same foot. The note identified the resident was not wearing her heel protective boot on 9/26/24 by choice. The RN notified the wound care nurse (WCN). A second skin/wound note, dated 9/26/24 at 9:31 p.m. documented Resident #54 had a large 3 cm by 2 cm serous (clear, liquid part of the blood) filled blister. The blister was drained and treated per the recommendations of the PHY. Resident #54 was unsure of how the blister formed but said she had noticed a red area on her left heel prior to the formation of the blister. The note identified the lack of the resident not wearing her boot could have contributed to the blister. The resident said the bottom area of the blister was sore but the pain was relieved once drained. The podiatry report dated 10/2/24 documented Resident #54 had a blister on her left heel. The resident had been using a wheelchair which had a screw on it and the resident believed the blister began due to the rubbing of the screw and the boot she was wearing had a hard area inside it. The blister had increased in size from the size of a quarter to a half dollar. The podiatry note further documented Resident #54 developed a blister on the left heel likely due to pressure from a screw on the wheelchair and from a hard boot. The blister had been drained and dressed regularly. The wound was not deep but continued wound care was necessary to prevent it from becoming deeper. The physician note dated 10/2/24 identified Resident #54 had a deep tissue pressure injury persistent and non blanchable pressure injury acquired on 10/2/24. The initial wound measured 4.5 cm width by 0.2 cm depth with a small amount of serous drainage. The physician recommended offloading and floating the resident's heels in bed and directed staff to check on the resident's feet and lower extremities every shift and ensure proper footwear. Review of the November 2024 CPO revealed the following physician's orders: Use of offloading boots (heel protective boots), ordered on 10/21/24. Wound care: change the left inner heel dressing daily. Cleanse with wound cleanser soaked gauze, remove and allow it to dry. Apply Iodosorb around the wound edges, cover with foam heel dressing and notify the provider and/or wound RN of concerns, ordered on 10/23/24. -The October 2024 medication administration record (MAR) and the treatment administration record (TAR) did not identify the active order for the use of heel protective boots. -The October 2024 MAR and TAR did not identify the tracked administration and use of the ordered heel protection. -Review of Resident #54's October 2024 electronic medical record (EMR) did not identify Resident #54 was offered and refused the physician ordered heel protective boots. The skin/wound note dated 11/6/24 documented the resident's left inner heel wound was an unstageable pressure wound measuring 3 cm by 3 cm by 0 cm. The 11/9/24 podiatry consultation report documented Resident #54 had a podiatry appointment on 11/20/24 at 11:00 a.m. The report identified Resident #54 should wear offloaders (heel protective boots) to both feet when she was not ambulating. -However, observations during the survey revealed Resident #54 was not consistently wearing her heel protective boots (see observations above). The skin/wound note, dated 11/13/24, identified the resident's right lateral foot was red but the skin was intact. The right foot would be monitored daily during wound care to the left foot and staff was to place a foam dressing if necessary and notify podiatry at the 11/20/24 appointment per the PHY. According to the wound note, the resident should be encouraged to wear foam heel protective boots for increased protection and offloading. -However, observations during the survey revealed Resident #54 was not consistently wearing her heel protective boots (see observations above). The note further documented Resident #54 left inner heel dressing was removed revealing an increased maceration (breakdown of the skin due to prolonged exposure to moisture) to 360 degrees surrounding the wound's edges due to the dressing not covering the entire site of the wound. The wound measured 3.3 cm by 4.2 cm by 0.3 cm. The podiatry report, dated 11/20/24, identified Resident #54 was seen by the podiatrist on 11/20/24. The report documented the resident reported her heel dressing was changed daily, however the dressing had not been changed before the 11/20/24 (at 11:00 a.m.) appointment. The report identified the resident's left medial heel had eschar measuring 4 cm by 3 cm with a small amount of drainage at the wound edges. According to the report, the resident did not have an offloading heel protective boot and an offloading heel boot was provided to the resident to relieve pressure. In addition, the podiatry report identified Resident #54 had a stage 0 pressure ulcer at the base of her right fifth metatarsal (a bone in the foot). The skin/wound note, dated 11/20/24, documented the resident returned from her podiatry appointment. The left heel wound measured 1.5 cm by 1 cm by 0.5 cm with 100% dry stable eschar to the wound site without drainage or odor. According to the note, the resident was to wear offloading heel protective boots to bilateral feet when she was not ambulating. -However, observations during the survey revealed Resident #54 was not consistently wearing her heel protective boots (see observations above). -The November 2024 MAR and TAR did not identify the active order for the use of heel protective boots. -The November 2024 MAR and TAR did not identify the tracked administration and use of the ordered heel protection. -Review of Resident #54's November 2024 EMR did not identify Resident #54 was offered and refused the physician ordered heel protective boots. VII. Staff interviews The WCN and the DON were interviewed together on 11/21/24 at 1:20 p.m. The WCN said Resident #54 had an unstageable pressure ulcer to her left inner heel. The WCN said on 9/26/24, Resident #54's nurse notified her that the resident had a serous filled blister on her left heel. She said the resident wore an offloading boot she received from the podiatrist as ordered on 8/1/24. The WCN said the resident told the nurse the offloading boot was giving her a red mark so she did not wear the boot on 9/26/24, potentially resulting in the blister to her heel. The WCN said the resident had been wearing the boot since shortly after her facility admission [DATE]). She said Resident #54 had not complained of the boot bothering her before 9/26/24 and a red mark was not observed on her heel. She said the offloading boot the podiatrist provided had a piece of plastic near the heel of the boot as part of its design. She said Resident #54 went to the podiatrist after the blister developed and was provided with the soft foam heel protective boots. The WCN said Resident #54 should have been wearing the heel protective boots all the time unless she was transferring from surface to surface. She said the staff should be reminding and encouraging the resident to wear the soft foam heel protective boots to both of her feet and use her wheelchair foot pedals when she was using her wheelchair. The WCN said the staff should be documenting any refusals of the heel protective boots in the MAR and TAR. The WCN said she had not care planned that Resident #54 did not consistently use and/or refused her physician ordered heel protective boots. The WCN said the resident did not feel and or understand that she should be wearing the heel protective boot of her right foot for pressure relief along with the left foot. She said she had not care planned that the resident did not want to use the right boot either. The WCN said Resident #54 felt she only needed the boot worn on her left foot to cover the wound. The WCN said she had not care planned interventions regarding what staff should do when the resident refused the heel protective boots. The DON said she had seen Resident #54 wear the left heel protective boot but not the right. She said she had not asked the resident why she did not wear the boots consistently. The WCN said the soft foam heel protective boots were bulky but she was not aware the resident felt the boot got tangled up with her wheelchair. The WCN said the resident told her the boots were uncomfortable in bed so she suggested Resident #54 try to prop a pillow under her legs, but she said she needed to evaluate if the pillow would be comfortable to her as an intervention. The WCN said Resident #54 was at risk for additional concerns because she had lost a toe (related to osteomyelitis) and did not want the same concern to happen to her foot. Certified nurse aide (CNA) #6 was interviewed on 11/22/24 at 9:15 a.m. CNA #6 said he frequently worked with Resident #54. He said he usually saw Resident #54 wearing a heel protective boot on her left foot when she was out of her room. He said she could put the boot on herself. He said the resident did not need or use a heel protective boot on her right foot. He said she only needed a heel protective boot to cover the left foot wound. CNA #6 said he was not sure if the resident should wear the heel protective boots in bed. -However, the resident had a physician's order to wear the heel protective boots and instructions from the physician to wear them except when she was ambulating (see record review above) The DON and the NHA were interviewed together on 11/22/24 at 2:12 p.m. The DON said pressure ulcers were reviewed with the IDT. She said the team reviewed the residents that currently had pressure ulcers, identified if the pressure ulcers were improving, what treatments were provided and received insight from the medical director. The DON said the staff spoke to Resident #54 on 11/21/24 (during the survey) and learned that the resident did not always wear her foot pedals as she should and the facility would be following up with her on her concerns with the foot pedals. The DON said the facility needed to work on improving documenting refusals of interventions, increasing observations of the resident and addressing concerns with the resident.
CONCERN (D)

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** III. Incident of physical abuse on 8/29/24 between Resident #52 and Resident #26 A. Facility investigation The facility's invest...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** III. Incident of physical abuse on 8/29/24 between Resident #52 and Resident #26 A. Facility investigation The facility's investigation of the incident on 8/29/24 between Resident #52 and Resident #26 was provided by the DON on 11/19/24 at 4:01 p.m. A statement written by CNA #4 on 9/3/24 documented Resident #52 and Resident #26 were observed attempting to elope from the Bookcliff hallway on 8/29/24 at approximately 5:45 p.m. CNA #4 said the door alarm went off and she responded in an attempt to redirect Resident #52 and Resident #26. CNA #4 said Resident #26 asked for keys to leave the facility and CNA #4 told Resident #26 she did not have them. CNA #4 said Resident #26 began yelling at her and Resident #52 told Resident #26 not to yell at CNA #4. CNA #4 said Resident #26 threatened to hit Resident #52. CNA #4 said Resident #52 put her hand on the back of Resident #26's neck and said she would like to see Resident #26 try. CNA #4 said Resident #26 then attempted to uppercut Resident #52 with only her index finger connecting to Resident #26's chin. CNA #4 said Resident #52 pushed Resident #26 and Resident #26 pushed Resident #52 back in response. CNA #4 said she was able to intervene and separate Resident #52 and Resident #26. A statement written by the NHA on 8/29/24 documented observations of facility camera surveillance footage between 5:30 p.m. and 6:00 p.m. on 8/29/24. The observation documented that Resident #52 and Resident #26 were observed attempting to elope through the Bookcliff stairwell exit door. The statement documented that when a staff member approached the residents, Resident #52 went into her room briefly and then returned. The statement documented that Resident #26 was observed to be tapping Resident #52 on her chin. The statement documented Resident #52 then pinched or poked Resident #26 and Resident #26 poked Resident #52 in response. The statement documented neither resident was observed to stumble or fall. The investigation documentation included new recommendations for Resident #52's medication regimen to address her anxiety and restlessness. The investigation documented the facility updated care plans for Resident #26 and Resident #52. The facility documented that the attending physician, the NHA, the DON and the social services department were notified of the incident on 8/29/24 within two hours of the event occurrence. The facility documented that the police department and adult protective services were notified at 6:45 p.m. on 8/29/24. The state health department, veteran's affairs, and the ombudsman were also notified of the event on 8/29/24. The summary of the investigation documentation, not dated, was provided by the DON on 11/19/24 at 4:01 p.m. It read in pertinent part; Abuse is unsubstantiated. Element of bodily injury or unreasonable confinement or restraint not met. Element of fear not met for verbal abuse as both residents remain at baseline prior to incident. -However, CNA #4's statement documented that Resident #26 attempted to hit Resident #52 in an uppercut motion and the statement further documented Resident #26 and Resident #52 pushed each other. -Furthermore, the NHA documented she observed via the camera footage, that Resident #26 intended to hit Resident #52 with her hand and the NHA documented Resident #52 and Resident #26 pinched and poked each other (see NHA statement above and interview below). B. Resident #52 1. Resident status Resident #52, age greater than 65, was admitted on [DATE]. According to the November 2024 CPO, diagnoses included dementia, unspecified mood disorder and unspecified depression. The 9/12/24 MDS assessment documented the resident was severely cognitively impaired with a BIMS score of five out of 15. The resident required moderate assistance with oral hygiene, dressing and toileting hygiene. The assessment documented Resident #52 was independent with all other aspects of daily mobility. The assessment documented that Resident #52 exhibited wandering behaviors on a daily basis which put her at a significant risk for her to get to a potentially dangerous place. The assessment documented that Resident #52 had exhibited physical and verbal behavioral symptoms directed towards others on one to three days during the assessment period. The assessment documented Resident #52's physical and verbal behaviors created a significant risk of causing herself physical illness or injury, significantly interfered with her care and put others at significant risk for physical injury, intruded on the safety or privacy of others and disrupted the care environment. The assessment documented that Resident #52's behaviors were getting worse. 2. Resident #52's representative interview Resident #52's representative was interviewed on 11/20/24 at 10:07 a.m. The representative said Resident #52 had severe dementia and elopement behaviors. The resident's representative said he thought Resident #52 and Resident #26 were friends. He said he had seen Resident #52 and Resident #26 arguing in the dining room, however, Resident #52 was known to argue with others around her for years even before she received her dementia diagnosis. The resident's representative said he was notified that Resident #52 and Resident #26 hit each other on 8/29/24 after trying to elope from the facility together. He said Resident #52 was not known to be physically aggressive before the event on 8/29/24. 3. Record review The elopement plan of care, initiated and revised 9/3/24, documented that Resident #52 was a high elopement risk because of her cognitive deficits. The plan of care documented the goal was for Resident #52 to be at a reduced risk of injury and elopement through the review period. The plan of care documented interventions including redirecting Resident #52 to other activities of interest when she was wandering, to keep Resident #52 within line of sight of staff members when outside of her room and to reassure Resident #52 that the animals were fed and her kids were safe. A social services quarterly note, dated 10/2/24, documented that Resident #52 was a high elopement risk and the resident needed to be within staff line of sight when outside her room. A behavior monitoring note, signed 8/30/24 by LPN #4, documented that Resident #52 and Resident #26 were observed attempting to elope on 8/29/24 after dinner. The note documented that Resident #52 punched Resident #26 in her neck. It documented that immediately thereafter, both residents were separated and placed on frequent checks. C. Resident #26 1. Resident status Resident #26, age greater than 65, was admitted on [DATE]. According to the November 2024 CPO, diagnoses included dementia, unspecified depression and anemia. The 8/22/24 significant change MDS assessment documented Resident #26 was severely cognitively impaired with a BIMS score of six out of 15. The resident required supervision with upper body dressing and oral hygiene and moderate assistance with personal hygiene. The assessment documented that Resident #26 was independent walking 50 feet, but required a helper to provide verbal cues when walking 150 feet. The assessment documented Resident #26 was independent with all other aspects of daily mobility. The assessment indicated Resident #26 experienced hallucinations and delusions but did not exhibit physical or behaviors directed towards herself or others. The assessment documented that Resident #26 exhibited wandering behaviors on one to three days during the assessment period, but the wandering behavior did not place the resident at risk of getting to a potentially dangerous place. 2. Record review The elopement plan of care, initiated 5/2/24 and revised 7/12/24, documented that Resident #26 was at a high risk of elopement because the resident would often be looking for her husband and children, and experienced increased confusion. The facility documented her elopement plan of care goal was to keep her safe through the current review period. The facility documented interventions included keeping Resident #26 within line of sight when she went upstairs to the office or visited with other residents, to offer distractions to decrease wandering behaviors, and to reassure the resident that her family was fine because Resident #26 was often confused about where she was at. A social services quarterly assessment, dated 7/17/24, documented Resident #26 did not have a history of wandering behaviors. The assessment documented Resident #26 did not have elopement precautions and Resident #26 was not at risk for elopement. -The social services quarterly assessment failed to accurately document Resident #26's wandering behaviors. An elopement assessment, dated 11/12/24, documented that Resident #26 had no history of wandering behaviors. The assessment documented Resident #26 was a moderate risk for elopement. -The elopement assessment failed to document the elopement behaviors witnessed by the facility staff on 8/29/24. D. Staff interviews Registered nurse (RN) #1 was interviewed on 11/20/21 at 9:51 a.m. RN #1 said Resident #26 and Resident #52 were both known to wander in the facility, but it was usually rare for Resident #26 to wander while it was often a daily occurrence for Resident #52 to wander. RN #1 said Resident #52 was known to help other residents and the resident would wander around to look for other residents who needed help. RN #1 said Resident #52 was easily redirected when she was observed to be wandering where she was not supposed to be. RN #1 said she had heard Resident #52 and Resident #26 hit each other a few months ago. Nursing assistant (NA) #2 was interviewed on 11/21/24 at 10:41 a.m. NA #2 said she was present in the building on 8/29/24. NA #2 said at the time, she was in the role of a student observer on the upstairs floor. NA #2 said she was not interviewed as part of the investigation between Resident #52 and Resident #26. NA #2 said she did not see anything occur that day since she was on the second floor and the event occurred on the first floor of the building. NA #2 said Resident #52 was known to wander in other resident rooms and all nursing staff knew to look out for her whenever she was moving in the building to ensure she was not going somewhere she was not supposed to. RN #2 was interviewed on 11/21/24 at 3:21 p.m. RN #2 said she heard Resident #52 and Resident #26 hit each other several months ago while trying to elope through the stairwell door. RN #2 said she was not working in the building on 8/29/24. RN #2 said when she worked downstairs she kept a close eye on both residents. RN #2 said she had not observed either Resident #52 or Resident #26 exhibit aggressive behaviors in September 2024, October 2024 or November 2024. RN #2 said care staff had to redirect Resident #52 from her wandering behaviors on a daily basis. RN #2 said she had observed Resident #26 exhibit wandering behaviors on only one occasion in the last few months. The NHA was interviewed on 11/22/24 at 11:32 a.m. The NHA said she reviewed the camera footage of the physical altercation that occurred between Resident #52 and Resident #26 on 8/29/24 but said she did not witness the original event occur. The NHA said the camera footage revealed Resident #52 approached Resident #26 from behind and placed her open hand on the back of Resident #26's neck. The NHA said she then Resident #26 brushed the chin of Resident #52. The NHA said both residents poked and pinched each other, but she could not remember when that occurred. The NHA said Resident #52 and Resident #26 were observed willfully touching each other on the camera footage. The NHA said the camera footage of the event was not available for anyone to view because the video footage had been deleted. Based on observation, record review and staff interviews, the facility failed to ensure three (#12, #26 and #52) of seven residents reviewed for abuse out of 41 sample residents was kept free from abuse. Specifically, the facility failed to: -Protect Resident #12 from physical abuse from a staff member; and, -Protect Resident #26 from verbal abuse from Resident #52. Findings include: I. Facility policy and procedure The Abuse policy, revised 9/19/24, was provided by the nursing home administrator (NHA) on 11/18/24 at 1:21 p.m. The policy read in pertinent part, It is the policy of the facility to provide protection for the health, welfare, and rights of each resident by developing and implementing written policies and procedures that prohibit and prevent mistreatment, abuse, neglect, and exploitation (MANE). The facility will take necessary precautions to prevent resident abuse by anyone including staff members, other residents, volunteers, contracted staff, family members, resident representatives, visitors, and any other individuals. The facility will provide ongoing oversight and supervision of staff in order to assure that its policies are implemented as written. The facility employees and contractors will be educated on MANE during initial orientation. Existing staff will receive annual education and as needed. Training topics should include: -Types of abuse; -Prohibiting and preventing all forms of MANE; -Identifying what constitutes MANE; -Recognizing signs of MANE, such as physical or psychosocial indicators; and, -Reporting process for MANE, including injuries of unknown sources. Understanding behavioral symptoms of residents that may increase the risk of MANE such as: -Aggressive and/or catastrophic reactions of residents; -Wandering or elopement-type behaviors; -Resistance to care; -Outbursts or yelling out; and, -Difficulty in adjusting to new routines or staff. II. Allegation of physical abuse of Resident #12 from certified nurse aide (CNA) #2 A. Allegation of physical abuse on 11/11/24 The 11/11/24 alleged abuse incident report was provided by the director of nursing (DON) on 11/20/24 at 1:49 p.m. Resident #12 alleged that a male CNA (CNA #2) held/grabbed his arms during care that the resident did not want done. The resident reported the allegation to the DON and the lead CNA on 11/11/24 at 1:38 p.m. Resident #12 reported that the male CNA (CNA #2) held/grabbed his arms so another staff member could change him when he refused wanting to be checked and changed. According to the incident report, the resident was alert and oriented and immediately assessed for injury. The assessment of the resident's right hand identified Resident #12 had a small crescent moon shaped bruise on the back side between his thumb and his first finger. He had multiple red marks on his left arm that the resident said were bruises, however, the marks were consistent with various red age spots on both his arms. According to the incident report, the facility started an investigation after the allegation of the abuse. The NHA provided the 11/11/24 alleged abuse occurrence investigation packet on 11/19/24 at 4:25 p.m. According to the alleged abuse occurrence investigation, Resident #12 reported CNA #2 entered his room on 11/11/24 at 3:00 a.m. and held him down to change his brief. The alleged abuse occurrence investigation documented the alleged assailant was placed on administrative leave pending the investigation, a skin assessment was completed for Resident #12 and other staff and residents were interviewed. The 11/11/24 interview with Resident #12 documented Resident #12 reported to the DON two staff members requested to change the resident's brief. Resident #12 declined the request which prompted CNA #2 to hold the resident's arms while the other CNA changed his brief. According to the documented interview, Resident #12 was yelling out as his arms were held and his brief was changed. The 11/11/24 interview with CNA #2 documented CNA #2 said he entered Resident #12's room and the resident was yelling at him and told him to leave his room. CNA #2 said he left the room and reported the interaction to the night shift nurse. According to the documented interview, CNA #2 said he later returned to the room with CNA #3 to change Resident #12. CNA #2 reported the resident became physically and verbally aggressive. The 11/11/24 documented interview with CNA #2 further revealed CNA #2 said he grabbed Resident #12's arm to prevent him from hitting CNA #3. CNA #2 said he did not leave the room when the resident was upset because he was told by CNA #3 that Resident #12 needed to be changed on the last rounds, no matter what. The documented interview indicated CNA #2 and CNA #3 received education from the night shift nurse to leave the situation next time and report the resident's refusal to the nurse. The 11/11/24 documented interview with CNA #3 identified CNA #3 witnessed CNA #2 grab Resident #12's arms to prevent the resident from hitting her face. The 11/11/24 alleged abuse occurrence investigation packet identified four other residents and three other staff members were interviewed as part of the initial investigation. A staff interview with CNA #4 documented another resident (Resident #37) told her CNA #2 was a bit rough in his approach and felt he could benefit from some additional training. The summary of the investigation included in the 11/11/24 alleged abuse occurrence investigation packet documented Resident #12 was combative and struck CNA #3 when she was providing cares so CNA #2 held his arm back to prevent her from being hit. According to the summary, CNA #3 felt there was no malicious intent of CNA #2 with his actions, no other residents expressed fear or experienced injury from a staff member and Resident #12 had no behavioral changes after the incident. The summary of the investigation indicated the documentation following the incident did not identify Resident #12 had new bruises or injuries consistent with the allegation noted to his arms following the incident. According to the summary, the resident had a small one centimeter (cm) bruise in between his thumb and index finger where he would normally grip his wheelchair. The summary of the investigation documented the facility did not determine physical abuse occurred because there were no injuries or bruising on the resident's arms consistent with the allegation and the resident had a noted history of prejudice. According to the summary, CNA #2 was asked to return to the facility and his contract was terminated. -However, abuse occurred because CNA #2 willfully held Resident #12's arm down while CNA #3 changed the resident. B. Resident #12 1. Resident status Resident #12, age greater than 65, was admitted on [DATE]. According to the November 2024 computerized physician orders (CPO), diagnoses included mild cognitive impairment of uncertain or unknown etiology, personal history of transient ischemic attack (TIA) and cerebral infarction without residual deficits. The 10/10/24 minimum data set (MDS) assessment documented Resident #12 had moderate cognitive impairment deficits with a brief interview for mental status (BIMS) score of 12 out of 15. He did not have inattention, disorganized thinking, hallucinations or delusions. Resident #12 used a wheelchair for mobility. According the MDS assessment, Resident #12 did not have physical or verbal behavioral symptoms directed at others or rejections of care. 2. Resident observation and interview Resident #12 was interviewed on 11/18/24 at 4:09 p.m. Resident #12 said a little over a week ago, a large male CNA (CNA #2) entered his room in the middle of the night and wanted to change Resident #12's brief and bed pad. The resident told CNA #2 he was comfortable and did not want to be changed at that time. Resident #12 said CNA #2 left the room but returned with a female CNA (CNA #3) a few minutes later. He said the CNA #3 tried to forcibly remove his underwear while CNA #2 held him down by his arms. He said both CNAs left the room after he was changed. Resident #12 said he was bruised as a result of the incident. Resident #12 pointed out small red spots on both forearms/wrists and a fading purple bruise approximately the size of a quarter, on the back side of his right hand. between his thumb and index finger. He said he had reported the incident to staff on the same day as the incident. He said he had not seen CNA #3 since the incident and had heard CNA #2 was terminated. He said he had not had any concerns with other staff. Resident #12 was interviewed a second time on 11/20/24 at 1:45 p.m. Resident #12's bruise was slightly lighter in color. He said he was not fearful of anyone. 3. Record review The cognitive impairment care plan, initiated 4/14/24, identified Resident #12 had mild cognitive impairment and needed reduced distractions during interactions. The care plan was updated on 11/11/24, after the incident, to include the following interventions: -Reminding Resident #12 he was safe in his environment; -Explaining provided tasks/care in short simple sentences; -Allowing Resident #12 time to process information and respond; -Leaving the room if Resident #12 resisted a staff provided task, making sure the resident was safe and asking a different team member to approach the resident again in a timely manner; and, -Respecting Resident #12's right to decline. The psychosocial well-being care plan, initiated 4/22/24, identified Resident #12 experienced loss of his spouse in May 2024 and loss of his home of 30 years. The care plan directed staff to allow Resident #12 time to answer questions and to verbalize his feelings, perceptions and fears and validating his concerns and feelings. The activity of daily living (ADL) care plan, initiated 10/7/24, directed staff to provide the resident with supportive care, assistance with mobility and encourage him to use the call light for assistance. According to the care plan, staff should allow Resident #12 sufficient time for dressing and undressing. -The review of progress notes and skin assessments prior to 11/11/24 did not not identify a bruise on Resident #12's hand. The 11/12/24 nurse progress note documented Resident #12's arms were assessed on 11/11/24 and 11/12/24 to ensure safety following the (11/11/24) occurrence investigation. The note identified a small crescent moon shaped bruise on his right hand between his thumb and first finger and red marks which were consistent with age spots. According to the note, there were no behavioral changes following the incident, the resident felt he was doing well and spent time with staff and family. The note documented staff would continue to monitor the red spots on his left arm. -The note did not identify the staff would continue to monitor the bruise on his hand. The 11/13/24 nurse progress note documented the nurse met with the resident on 11/13/24. According to the note, Resident #12 had no new bruising and the spots on the left arm continued to be consistent with age spots and there were no changes in shape or color. He continued to deny pain, there were no changes in his behavior and the resident felt he was doing well. -The note did not identify the staff would continue to monitor the bruise on his hand. The Personal Care: Dressing Dependent Resident training, conducted with staff on 5/14/24, was provided by the corporate consultant (CC) on 11/26/24 at 12:17 p.m. The training identified staff should never forcefully pull or tug on clothing to assist a resident while dressing because it could cause injury. -The review of the training did not identify CNA #2 or CNA #3 had attended the training. The Competency Fair staff training, conducted on 10/15/24 and 10/16/24, was provided by the CC on 11/26/24 at 12:17 p.m. The training reviewed facility policies, such as abuse training. -The review of the Competency Fair attendance sheet, identified CNA #2 and CNA #3 did not attend the training. The Emergency Response Plans staff signature sheet, dated between 1/16/24 and 11/21/24, and the facility's onboarding packet was provided by the DON on 11/22/24 at 9:34 a.m. The packet included the abuse policy and the resident rights policy. The resident rights policy identified residents had the right to be free of verbal, sexual, physical, and mental abuse, corporal punishment, and involuntary seclusion. According to the policy, the residents had the right to make choices regarding their care, including schedules, activities, healthcare providers or health care services. -The review of the Emergency Response Plans staff signature sheet revealed CNA #2 did not sign that he had received the emergency response plans and onboarding packet. C. Staff interviews The DON was interviewed on 11/20/24 at 4:10 p.m. The DON said if there was a new bruise on a resident, staff should try to determine what was the cause of the bruise. She said staff would interview the resident and notify the physician. She said the facility would make sure the resident was safe and the bruise was not caused by another person. She said the bruise would be documented in the risk management assessment. The DON said if the cause of the bruise was not known, then she would start an investigation and interview staff. The DON said the bruise on the right hand of Resident #12 was found during a skin assessment after a reported incident on 11/11/24. The DON said Resident #12 alleged, on 11/11/24, that a staff member grabbed his arms and held him. She said the resident reported the incident to her and the lead CNA. She said the CNA (CNA #2) was an agency/travel staff member. She said CNA #2 and CNA #3 were interviewed. The DON said both CNAs said Resident #12 attempted to hit CNA #3 so CNA #2 grabbed his arm to stop him. She said CNA #2 reported he grabbed the resident's left arm. The DON said the agency CNA #2 worked for was notified and CNA #2 was suspended, pending the investigation. The DON said Resident #12 did not have a bruise on his left arm. She said the bruise on the back of his right hand was in the shape of a half moon and in between his index finger and his thumb. The DON said the bruise was not identified before the 11/11/24 incident. She said she thought the bruise might have been caused by his wheelchair. She said the bruise matched up to where he would put his hand on the wheelchair. She said she was not aware of any incidents or observations which indicated that the resident injured himself from use of his wheelchair. She said it was possible the resident's bruise was caused during the 11/11/24 incident. The DON said the facility decided not to have CNA #2 return to the facility because another resident felt the CNA was rough with care. She said the term rough could be a trigger word for potential abuse. The DON said the other residents were not fearful of CNA #2 and said he was just a little rough. The social service assistant (SSA) was interviewed on 11/21/24 at 10:07 a.m. The SSA said she assisted with abuse investigations when they were reported to her. She said she was a nurse and would conduct a head to toe assessment when needed, by use of the weekly assessment form if there was a bruise that was unexplained or an allegation of abuse. The SSA said she interviewed residents anytime that there was a potential abuse allegation, including verbal and physical abuse, including a resident to resident altercation. She said if a resident was not able to answer the questions, she and the staff would make observations of their behaviors and complete an assessment for non-interviewable residents. The SSA said the social services department would report their piece of the investigation findings to the interdisciplinary team (IDT) and the NHA would make the determination if abuse was substantiated or not. The NHA was interviewed on 11/21/24 at 10:33 a.m. The NHA said she reported all allegations of abuse to the State Agency and then the social services department started the investigation with a skin assessment to check for injuries and interviews with staff. She said if a resident had a high BIMs score, they would be interviewed. She said staff should attempt to interview pertinent residents even if they had a lower BIMS score. She said if the resident was not interviewable, a non-interviewable form would be completed. The NHA said there needed to be enough information gathered to make the determination if abuse occurred. The NHA said to substantiate abuse, she needed to confirm elements of abuse occurred, such as injury and or fear, depending on what type of abuse was alleged. She said she did not determine the allegation of physical abuse towards Resident #12 was substantiated after the investigation because the resident said it was his arms that were grabbed and the bruise was found on his hand. The NHA said CNA #2 said Resident #12 kicked CNA #3 but he did not make contact with her with his hand. The NHA said Resident #12 did not indicate fear and there was no injury to his arms where he said he was grabbed. The NHA said CNA #2 was preventing the resident from striking CNA #3. She said CNA #2 was asked not to return to the facility after the incident because another resident said he was a bit rough with care. The NHA said the term rough could be a trigger word indicating potential abuse. She said the facility started an investigation when a resident alleged potential abuse. The DON was interviewed a second time on 11/21/24 at 10:54 a.m. She said CNA #2 and CNA #3 were educated by the night nurse after the incident. CNA #2 and CNA #3 were told they should have not performed ADLs after Resident #12 refused and should have informed the nurse of the refusal. The DON said both CNAs were temporary traveling staff. She said before they started working independently with the residents, they had to shadow another staff member and sign off on a packet of facility expectations and policies. She said the abuse policy was included in the packet the CNAs had to sign off on that they would have received. -However, record review revealed CNA #2 did not sign the receipt of the facility's packet that included the abuse policy. The DON was interviewed on 11/22/24 at 9:34 a.m. She confirmed CNA #2 did not sign the facility policies and expectations when he was on boarding The CC was interviewed on 11/22/24 at 12:10 p.m. The CC said the facility would make sure all temporary and current staff had reviewed and signed off on the facility policies and expectations after it was identified CNA #2 did not sign that he received the packet that included the abuse policy. The DON and the CC were interviewed together on 11/22/24 at 12:13 p.m. The CC said bruises should be monitored for 72 hours after the bruise was identified. The DON said the documentation in Resident #12's EMR did not clearly indicate the bruise to his hand was monitored. She said she recently looked at it and it was looking much better then when it was first identified on 11/11/24. The DON said Resident #12 had not made allegations towards staff before 11/11/24. The CC said restraining a resident's movement would be considered abuse. The NHA and the DON were interviewed together on 11/22/24 at 2:12 p.m. The NHA said the facility reviewed every occurrence/incident every month, including allegations of abuse and resident-to- resident altercations to identify possible trends and areas the facility needed to address. The NHA said the interdisciplinary (IDT) team tried to find the root cause of the concern, looking at what caused the incident and what could be put in place to prevent the incident from happening again. She said for resident-to-resident altercations, the team looked at interventions to help separate residents when needed and de-escalate the situation. The NHA and the DON said the facility had not looked at the lack of education provided to the temporary traveling staff. The DON said she recently requested the education the contr[TRUNCATED]
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 observations, record review and interviews, the facility failed to ensure resident choices for one (#213) of two reside...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to ensure resident choices for one (#213) of two residents reviewed for activities of daily living (ADL) out of 40 sample residents. Specifically, the facility failed to provide bathing assistance for Resident #213 per her preference. Findings include: I. Facility policy and procedure The Activities of Daily Living (ADL) policy, revised 6/6/24, was received from the corporate consultant (CC) on 11/22/24 at 1:33 p.m. It documented in pertinent part, A resident who is unable to carry out activities of daily living will receive the necessary services to maintain good nutrition, grooming, personal and oral hygiene. II. Resident #213 A. Resident status Resident #213, age less than 65, was admitted on [DATE]. According to the November 2024 computerized physician order (CPO), diagnoses included paraplegia (loss of function in the lower legs), congestive heart failure,and generalized muscle weakness. According to the 11/14/24 minimum data set (MDS) assessment Resident #213 was cognitively intact with a brief interview for mental status (BIMS) score of 15 out of 15. The MDS assessment documented Resident #213 was dependent on staff for toileting, hygiene, dressing, chair and toilet transfers. The assessment did not document the amount of assistance Resident #213 needed with bathing. B. Resident interview and observations Resident #213 was interviewed on 11/19/24 at 9:35 a.m. Resident #213 said she was admitted to the facility earlier in the month and had only received one bed bath since her admission on [DATE]. Resident #213 said she hoped to receive two baths per week. Resident #213 said she was paraplegic and had no feeling below the level of her waist. Resident #213 said that she knew her care took more time and staff, since she was unable to move or control the lower half of her body. Resident #213 said she could not sense if the lower half of her body was not clean. Resident #213 said her hair was difficult to comb because it had not been washed recently. Resident #213 said she felt sad that she required extensive assistance with bathing because she perceived her extensive ADL care needs would reduce the help other residents received on her bath days. Resident #213's hair was greasy. She was attempting to comb through it, but was struggling to do so. On 11/20/24 at 9:12 a.m., the restorative registered nurse (RRN) was discussing the daily plan to get Resident #213 out of bed and into the wheelchair with another unidentified staff member. The RRN said Resident #213 required three person assistance with a hoyer lift to get her out of bed and into the wheelchair. III. Record review The ADL/mobility plan of care, initiated on 11/15/24 and revised on 11/15/24. The plan of care documented Bathing/Showering level of assistance: Independent; set-up assistance; supervision; minimal assist; extensive assist; dependent. -A review of the resident's comprehensive care plan did not reveal documentation indicating Resident #213's bathing preferences or the level of assistance Resident #213 required with bathing. The Bathing/shower preference documentation was reviewed between 11/7/24 and 11/21/24. The facility documented Resident #213 was unavailable for bathing preference discussions on 11/18/24 and bathing preference discussions were not applicable on 11/8/24, 11/11/24 and 11/15/24 (see interviews below). The facility point of care bathing documentation was reviewed for 14 days (11/7/24 to 11/21/24). It documented Resident #213 had received two baths out of four opportunities. IV. Staff interviews Certified nurse aide (CNA) #3 was interviewed on 11/21/24 at 1:41 p.m. CNA #3 said it was normal for residents to receive two baths per week or by the resident's preference. CNA #3 said if a resident refused a bath the nurse would be told and the resident refusal would be documented in the electronic medical record (EMR). Registered nurse (RN) #2 was interviewed on 11/21/24 at 1:55 p.m. RN #2 said the residents received two baths per week on their chosen days unless the resident had a more specific preference. RN #2 said it was important to bathe residents to reduce infection risk and also because it felt nice to be clean. The director of nursing (DON) was interviewed on 11/22/24 at 10:27 a.m. The DON said she reviewed Resident #213's bathing documentation between 11/7/24 and 11/21/24. The DON said Resident #213 received two baths in the review period. The DON said Resident #213 did not receive enough baths. The DON said the residents should receive two baths per week or by their stated preference. The DON said Resident #213's bathing preference and assessment documentation did not make sense and should not have been documented as not applicable.
CONCERN (D)

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

Deficiency F0805 (Tag F0805)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to ensure two (#43 and #14) of seven residents received...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to ensure two (#43 and #14) of seven residents received food and fluids prepared in a form designed to meet their needs per speech therapy recommendation, physician's orders and the resident's care plan out of 41 sample residents. Specifically, the facility failed to ensure Resident #43 and Resident #13, who were prescribed a mechanically altered diet texture, were served food in the correct form. Findings include: I. Facility policy and procedure The Therapeutics Diets policy, revised on 6/7/24, was provided by the corporate consultant (CC) on 11/21/24 at 1:33 p.m. It read in pertinent part, Each resident has a specific food and beverage preparation detailed on a tray card so accurate diets are served. Therapeutic diets are prepared and served according to written orders from the provider and are planned and served with supervision from the dietary manager (DM) or registered dietician (RD). Specific diets and textures are referenced in the diet manual with specific content and preparation. A current diet manual is available for reference to attending physicians, nursing service and dietary staff. Residents and/or their power of attorney (POA) may refuse the recommended diet. In this case the facility must provide education, provide and ask for a signature on a dietary waiver and increase monitoring at meal times. II. Facility's diet manual The Diet Manual, revised August 2015, was provided by the nursing home administrator (NHA). It read in pertinent, Dysphagia mechanically altered: This level consists of foods that are moist, soft textured and easily formed into a bolus. Meats are ground or minced no larger than one-quarter-inch pieces: they are still moist with some cohesion. This diet is a transition from the pureed textures to more solid textures. Chewing ability is required. The textures on this level are appropriate for individuals with mild to moderate oral and/or pharyngeal dysphagia. Breads: Soft pancakes well moistened with syrup or sauce. Pureed bread mixes, pregelled or slurried breads that are gelled through entire thickness. Avoid all other breads. Vegetables:All soft, well-cooked vegetables should be smaller than half-an-inch and easily mashed with a fork. Avoid cooked corn and peas, broccoli, cabbage, brussels sprouts, asparagus or other fibrous non-tender or rubbery cooked vegetables. III. Facility recipes A. Salisbury steak Mechanical soft: Grind portions needed from regular prepared recipe into one eighth inch pieces. B. Garlic cheese biscuit It is recommended to serve pureed bread/biscuit or gelled bread for dysphagia diets, but if the speech language pathologist (SLP) at your facility signs and approves regular breads on an individual basis, chop regular portions. Make sure all particles are no more than half-an-inch by half-an-inch. -The facility served cooked biscuits with a slice of American cheese melted over the top (see observations below). IV. Resident #43 A. Resident status Resident #43, age greater than 65, was admitted on [DATE]. According to the November 2024 computerized physician order (CPO) diagnoses included dementia, acute cough and dysphagia (difficulty swallowing). The 11/4/24 minimum data set (MDS) assessment revealed Resident #43 t had long-term and short-term memory problems and was severely cognitively impaired per staff assessment. The MDS assessment indicated Resident #43 required a mechanically altered diet. B. Record review A review of the November 2024 CPO revealed the resident had a physician's order that indicated the resident was prescribed a mechanical soft diet and was to be served his food on a lipped plate, ordered on 10/14/24. A review of Resident #43's electronic medical record (EMR) did not reveal a dietary waiver indicating the resident was able to consume regular textured food cut-up (see interview below). C. Observation The following was observed on 11/21/24 at 11:44 a.m.: Resident #43 was served a Salisbury steak and a dinner roll both were cut into bite-sized pieces. -The facility failed to serve theSalisbury steak ground and puree or gel the dinner roll as indicated on the recipe (see recipe above). V. Resident #14 A. Resident status Resident #14, age greater than 65, was admitted on [DATE]. According to the November 2024 CPO diagnoses included dementia, Parkinsonism (degenerative disease that causes involuntary movements) and dysphagia. The 10/12/24 MDS assessment revealed Resident #14 t had long-term and short-term memory problems and was severely cognitively impaired per staff assessment. The MDS assessment indicated Resident #14 required a mechanically altered diet. B. Record review A review of the November 2024 CPO revealed the resident had a physician's order that indicated the resident was prescribed a mechanical soft diet and nectar thick liquids, ordered on 8/20/2020. A review of Resident #14's EMR did not indicate a dietary waiver that indicated the resident was able to consume regular textured food cut-up. The resident had a dietary waiver in place to consume thin liquids versus nectar thick (see interview below). C. Observations The following was observed on 11/21/24 at 11:44 a.m.: Resident #43 was served a regular textured Salisbury steak and a dinner roll both were cut into bite-sized pieces. -The facility failed to serve the Salisbury steak ground and puree or gel the dinner roll as indicated on the recipe (see recipe above). VI. Staff interviews Dietary aide (DA) #3 was interviewed on 11/21/24 at 11:50 a.m. DA #3 said Resident #43 and Resident #14 had waivers in place to eat regular or bite-sized textured foods. DA #3 said if a resident's plate looked like the wrong texture she would send it back to the kitchen to be fixed. DA #3 said she was unaware bread needed to be pureed or slurried on a mechanical soft diet. -However, review of the resident's EMR did not indicate dietary waivers were in place for the residents to receive regular textured food (see record review above). The cook (CK) was interviewed on 11/21/24 at 11:50 a.m. The CK said Resident #43 and Resident #14 were allowed to have bread and the Salisbury steak was the correct texture. The CK said she was unaware the bread needed to be pureed or gelled for residents who were prescribed a mechanical soft diet. The NHA, the CC and the registered dietitian (RD) were interviewed together on 11/21/24 at 12:57 p.m. The RD said the facility had not implemented the International Dysphagia Diet Standardisation Initiative (IDDSI) program yet. She said the facility modified resident's diets based on what the SLP recommended. The NHA, the CC and the RD said they were unaware the facility's diet manual indicated the mechanically soft texture required the bread to be pureed or slurried. The RD said although the Salisbury steak was made from ground beef it should not have been formed into a steak shape and cut into bite-sized pieces. The RD said the residents should have been served ground beef with the gravy.
CONCERN (D)

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

Room Equipment (Tag F0908)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to maintain all mechanical, electrical and patient care...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to maintain all mechanical, electrical and patient care equipment in safe operating condition. Specifically, the facility failed to ensure facility staff used blood pressure cuffs rated for medical use. Findings include: I. Professional reference According to the [NAME] Advantage for Basic Nursing handbook, third edition, retrieved on 11/25/24 from Treas, [NAME] S., et al. [NAME] Advantage for Basic Nursing: Thinking, Doing, and Caring. F. A. [NAME] Company, 2022., Blood Pressure - Practical Knowledge, Electronic blood pressure monitors may be less accurate than those with an aneroid monitor (a manual blood pressure measuring device). To ensure accuracy, you should auscultate (listen to) a baseline blood pressure before initiating automatic monitoring. Ensure devices are rated for medical use. The width of the blood pressure cuff bladder of a properly fitting cuff will cover approximately two-thirds of the length of the upper arm for an adult, and the entire upper arm for a child. Alternative sites you can use are the forearm, thigh, or calf. However, systolic pressure may be 20 to 30 mmHg (millimeters of mercury) higher in the lower extremities than in the arms, but diastolic pressures are similar. Abnormally high or low blood pressure readings should be rechecked by the provider. II. Facility policy The Medical Equipment policy, revised 7/1/24, was provided by the corporate consultant (CC) on 11/22/24 at 1:39 p.m. It documented that all durable medical equipment (DME) to be used for resident assessment and monitoring would be deemed medically rated for use in health care facilities. III. Observations On 11/20/24 at 8:52 a.m., licensed practical nurse (LPN) #1 was observed using a Veridian Healthcare model 01-574 model wrist type blood pressure cuff to take Resident #213's blood pressure. -LPN #5 did not use a blood pressure cuff rated for medical use to obtain Resident #213's blood pressure (see professional references above and interview below). On 11/20/24 at 10:23 a.m., registered nurse (RN) #4 was observed taking Resident #33's blood pressure using a W1101L wrist type blood pressure cuff. -RN #4 did not use a blood pressure cuff rated for medical use to obtain Resident #33's blood pressure (see professional references above and interview below). IV. Record Review On 11/20/24 at 11:57 a.m., the director of nursing (DON) said (via email) that she could not find manufacturer's instructions for the W1101L wrist type blood pressure cuff or the Veridian Healthcare model 01-574 model wrist type blood pressure cuff that documented either device was rated for medical use. The DON said both blood pressure cuffs had been removed from use in the facility on 11/20/24. V. Staff interviews LPN #1 was interviewed on 11/20/24 at 8:55 a.m. LPN #1 said she enjoyed using the Veridian Healthcare model 01-574 model wrist type blood pressure cuff to obtain blood pressures on residents. LPN #1 said she did not know if the blood pressure cuff was rated for medical use. LPN #3 was interviewed on 11/21/24 at 1:17 p.m. LPN #3 said she had used both the Veridian Healthcare model 01-574 model wrist type blood pressure cuff and the W1101L wrist type blood pressure cuff to obtain resident blood pressure readings. LPN #3 said the blood pressure cuffs were stored in a protective case on each medication cart to use whenever nurses needed to. LPN #3 said she did not know if the devices were rated for medical use. The DON was interviewed on 11/22/24 at 10:27 a.m. The DON said she had obtained the blood pressure cuffs from a medical supply company but did not verify if the blood pressure cuffs were rated for medical use. The DON said she was surprised to learn the Veridian Healthcare model 01-574 model wrist type blood pressure cuff and the W1101L wrist type blood pressure cuff were not rated for medical use. The DON said it was important for the facility to use blood pressure cuffs rated for medical use to ensure residents' vital signs were accurate. The DON said residents could receive blood pressure medications when they were not needed if the facility relied on the accuracy of a non-medically rated device to obtain resident blood pressures.
CONCERN (E)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected multiple residents

Based on record review and interviews, the facility failed to ensure all drugs and biologicals were properly stored in accordance with professional standards in two of three medication storage refrige...

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Based on record review and interviews, the facility failed to ensure all drugs and biologicals were properly stored in accordance with professional standards in two of three medication storage refrigerators. Specifically, the facility failed to maintain a medication refrigerator temperature log for the facility vaccine refrigerator and the medication refrigerator. Findings include: I. Professional reference According to the Centers for Disease Control (CDC), Handle with Care: Protect your Vaccine, Protect Your Patients, (revised on 3/19/24) was retrived on 11/26/24 from https://www.cdc.gov/vaccines/hcp/admin/storage/downloads/vaccine-storage-temperatures.pdf Keep your storage units and vaccines within the appropriate temperature ranges. Check and record storage unit min/ma (minimum/maximum) temperatures at the start of each workday. II. Facility policy and procedure The Medication Storage policy, revised on 1/25/24, was provided by the nursing home administrator (NHA) on 11/21/24 at 2:43 p.m. It documented in pertinent part, All drugs and biologicals will be stored in locked compartments (medication carts, cabinets, drawers, refrigerators, medication rooms) under proper temperature controls. II. Record review The vaccine and medication refrigerator temperature log records from 10/1/24 to 11/19/24 were provided by registered nurse (RN) #1 on 11/20/24 at 2:16 p.m. Out of 50 days of documentation opportunities, vaccine refrigerator temperatures were documented on 16 of those days. Out of 50 days of documentation opportunities, medication refrigerator temperatures were documented on 24 of those days. III. Staff interviews RN #1 was interviewed on 11/20/24 at 2:16 p.m. RN #1 said the medication and vaccine refrigerator temperatures should be logged every night by night shift nurses. RN #1 said many days had not been documented in the medication and vaccine refrigerator temperature logs. RN #1 said it was important to ensure medications were safely stored at the correct temperature so they could be safely administered to residents. The director of nursing (DON) was interviewed on 11/22/24 at 10:27 a.m. The DON said that all floor nurses were responsible for recording medication refrigerator temperatures. The DON reviewed the medication and vaccine refrigerator temperature logs between 10/1/24 and 11/19/24. The DON said many days had not been documented in the temperature logs. The DON said the vaccine and medication refrigerator temperatures should be documented daily. The DON said that if these refrigerators were not monitored by staff, then medications could expire or not work correctly for residents.
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

QAPI Program (Tag F0867)

Could have caused harm · This affected most or all residents

Based on interviews and record review, the facility failed to ensure an effective quality assurance program to identify and address facility compliance concerns was implemented, in order to facilitate...

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Based on interviews and record review, the facility failed to ensure an effective quality assurance program to identify and address facility compliance concerns was implemented, in order to facilitate improvement in the lives of nursing home residents, through continuous attention to quality of care, quality of life, and resident safety. Specifically, the quality assurance performance improvement (QAPI) program committee failed to implement an effective system to identify and address multiple concerns related to quality of care, including accidents/hazards, in which the facility failed to conduct safety risk assessments for residents with transfer poles which rose to the level of immediate jeopardy and created a situation that a serious adverse outcome was likely. Findings include: I. Facility policy The Quality Assurance Performance Improvement (QAPI) policy, updated 9/30/24, was provided by the nursing home administrator (NHA) on 11/18/24 at 1:21 p.m. The policy documented in pertinent part, It is the policy that the facility shall develop, implement, and maintain an ongoing, facility-wide, data-driven QAPI program that is focused on indicators of the outcomes of care and quality of life. Develop and implement appropriate plans of action to correct identified quality deficiencies. Regularly review and analyze data, including data collected under the QAPI program and data resulting from drug regimen reviews, and act on available data to make improvements. The QAPI plan should address the following elements: -Design and scope of the facility's QAPI program and QAA (Quality Assessment and Assurance) committee responsibilities and actions; -Policies and procedures for feedback, data collection systems, and monitoring; and, -Process addressing how the committee should conduct activities necessary to identify and correct quality deficiencies. Key components of this process include: -Tracking and measuring performance; -Establishing goals and thresholds for performance improvements; -Identifying and prioritizing quality deficiencies; -Systematically analyzing underlying causes of systemic quality deficiencies; -Developing and implementing corrective action or performance improvement activities; and, -Monitoring and evaluating the effectiveness of corrective action/performance improvement activities and revising as needed. The facility takes actions aimed at performance improvement as documented in QAA committee meeting minutes and action plans. Performance/success of the actions should be monitored and documented in subsequent QAA committee or sub-committee meetings. To ensure improvements are sustained, the effectiveness of performance improvement activities should be monitored in QAA committee meetings in accordance with the QAPI plan, but no less than annually. II. Cross-referenced citations affecting quality of care identified during the facility's recertification on 11/22/24 Cross-reference F689: The facility failed to ensure the resident environment remained as free of accident hazards as possible. The facility failed to complete a safety risk assessment before placing resident transfer poles and failed to investigate after a transfer pole accident. Additional accident/hazards failures were identified related to fall prevention and smoking while wearing a nasal cannula and a turned off oxygen tank. The deficiency was cited at a K scope and severity, immediate jeopardy, pattern. Cross-reference F686: The facility failed to prevent a resident from developing a pressure ulcer and failed to ensure interventions were consistently in place to prevent the pressure ulcer from worsening. The deficiency was cited at a G scope and severity, actual harm, isolated. Cross-reference F880: The facility failed to maintain an effective water management plan. The deficiency was cited at a F scope and severity, potential for more than minimal harm, widespread. Cross-reference F600: The facility failed to protect residents from physical abuse. The deficiency was cited at a D scope and severity, potential for more than minimal harm, isolated. Cross-reference F761: The facility failed to maintain appropriate temperatures in the medication refrigerator and the vaccine refrigerator. The deficiency was cited at an E scope and severity, potential for more than minimal harm, pattern. Cross-reference F677: The facility failed to provide bathing per resident preferences. The deficiency was cited at a D scope and severity, potential for more than minimal harm, isolated. Cross-reference F908: The facility failed to use medically rated blood pressure cuffs to obtain residents blood pressures. The deficiency was cited at a D scope and severity, potential for more than minimal harm, pattern. Cross-reference F805: The facility failed to ensure residents were served food in a form designed to meet residents' needs per physician's orders. The deficiency was cited at a D scope and severity, potential for more than minimal harm, isolated. III. Staff interviews The NHA and the director of nursing (DON) were interviewed together on 11/22/24 at 2:12 p.m. The NHA said the QAPI committee met monthly to continuously improve processes and meet standards. The NHA said all managers, the medical director, the pharmacist and the licensed social worker from a sister facility participated in the monthly QAPI meetings. The NHA said during the meetings, each manager reviewed their department reports and as a team, the committee tried to identify concerns, problem solve as a group and discuss how the facility would address the concern in attempts to resolve it. The NHA said the QAPI committee received additional insight from line staff, resident council, care conferences and morning nurse reports. The DON said each department would determine the root cause of their department concern. She said the department managers would bring their department concerns to the QAPI committee if they felt they needed to expand the discussion and analysis. The NHA said the QAPI committee created and implemented performance improvement projects/plans. She said the QAPI committee reviewed the implemented plans, made the determination if the identified concern was resolved and if the facility was able to effectively sustain system change. The NHA said if the plan did not produce a sustaining resolution to the concern, the committee would attempt to adjust the plan in efforts to resolve the concern. The DON said the QAPI committee reviewed falls monthly in the QAPI committee meeting. She said the committee looked at the number of falls in each month, whether the falls were witnessed or not, residents with multiple falls and where the falls occurred. The DON said if the facility had a resident fall several times in one month, the committee discussed the nature of the falls in an effort to gain additional insight and perspective that may not have already been identified. The DON said part of the root cause analysis was to identify if staff were properly educated and understanding why the falls happened. The DON said the process failed because the committee did not recognize what needed to be documented and not enough questions were asked to determine the full factor/cause of the falls. The NHA said the QAPI committee did not review smoking with a nasal cannula on or smoking near a turned off oxygen tank as a QAPI concern because the staff had not seen or reported to management that it was a concern. She said the resident involved in the situation was usually good about taking his oxygen off before he went outside to smoke. The DON said the QAPI committee did not review the residents' transfer poles and lack of safety assessments. The DON said the QAPI committee did not identify the assessments were not completed prior to the installation of the transfer poles. The NHA said pressure ulcers were reviewed in the QAPI committee meetings. The DON said pressure ulcers were reviewed during QAPI committee meetings. She said the team reviewed the residents who currently had pressure ulcers, identified if the pressure ulcers were improving, what treatments were being provided and received insight from the medical director on the pressure ulcers. The DON said the facility needed to work on improving documenting refusals of interventions, increasing observations of the resident and addressing concerns with the resident. The NHA said food textures were not reviewed in QAPI meetings. She said menus were reviewed but the committee had not discussed if the residents received the appropriate textured diets. The DON said diet order education with the kitchen staff had been discussed in the care concern at-risk meetings. The NHA said the registered dietitian (RD) had a weekly report of everyone with weight concerns and choking hazards. The NHA said the RD discussed any related concerns with the IDT, speech therapy and the kitchen staff and offered her recommendations. The DON said there had been a lot of confusion related to mechanical soft textures and she would like to look at new text diet texture processes and education. The DON said the use of medical grade blood pressure cuffs was not reviewed in QAPI meetings. The DON said she was not aware there was a problem with the blood pressure cuffs the facility was using. The NHA said residents' bathing preferences and choices had not been identified as a concern in QAPI meetings. She said residents did not usually address bathing preferences as a concern. She said the bathing preferences concern may have been addressed under the grievance process but the QAPI committee had not identified this as a concern. The NHA said resident-to-resident altercations were reviewed in QAPI committee meetings. She said the social services director (SSD) reviewed every occurrence identified in the previous month. The NHA said the QAPI committee discussed the occurrences to help identify trends that needed to be addressed. The NHA said the committee tried to find the root cause of the concern, looked at what caused each incident and tried to determine what could be put in place to prevent the incident from happening again. She said for resident-to-resident altercations, the team looked at interventions to help separate residents when needed and de-escalate the situations. The NHA said staff to resident physical abuse was discussed in QAPI meetings but the committee had not identified the concerns as a facility trend. The NHA and the DON said the facility had not looked at the lack of education provided to the temporary traveling staff. The DON said she recently requested the education the contract agency provided to the traveling staff. The NHA said refrigerator temperatures were reviewed in QAPI meetings, but not recently. She said in the past, audits identified concerns with consistent tracking of the temperature in the kitchen but refrigerators storing medications and vaccines had not been reviewed in QAPI committee meetings or identified as a concern. The NHA said the water management plan in relation to Legionella had not been reviewed in the QAPI meetings or identified as a concern. The NHA said the facility would look at all the identified concerns addressed and would relook at the facility's QAPI committee process, add additional audits and review how the QAPI committee analyzed facility concerns.
CONCERN (F)

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

Infection Control (Tag F0880)

Could have caused harm · This affected most or all residents

Based on record review and interviews, the facility failed to maintain an infection control program designed to provide a safe, sanitary and comfortable environment to help prevent the possible develo...

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Based on record review and interviews, the facility failed to maintain an infection control program designed to provide a safe, sanitary and comfortable environment to help prevent the possible development and transmission of infectious diseases. Specifically, the facility failed to implement an effective water management plan. Findings include: I. Professional reference According to Center for Disease Control (CDC), Controlling Legionella in Potable Water Systems, last reviewed 3/15/24, was retrieved on 11/26/24 from https://www.cdc.gov/control-legionella/php/toolkit/potable-water-systems-module.html It read in pertinent part, Operation, maintenance, and control limits guidance: Monitor temperature, disinfectant residuals, and pH frequently based on Legionella performance indicators for control. Adjust measurement frequency according to the stability of performance indicator values. For example, increase the measurement frequency if there's a high degree of measurement variability. Hot water: Store hot water at temperatures above 140°F (60°C). Ensure hot water in circulation does not fall below 120°F (49°C). Recirculate hot water continuously, if possible. Cold water: Store and circulate cold water at temperatures below the favorable range for Legionella (77-113°F, 25-45°C). Legionella may grow at temperatures as low as 68°F (20°C). Flushing: Flush low-flow piping runs and dead legs at least weekly. Flush infrequently used fixtures (eye wash stations, emergency showers) regularly as needed to maintain water quality parameters within control limits. Ensure disinfectant residual is detectable throughout the potable water system. Clean and maintain water system components, such as thermostatic mixing valves, aerators, showerheads, hoses, filters, and storage tanks, regularly. Consider testing for Legionella in accordance with the routine testing module of this toolkit. II. Facility policy and procedure The Legionella water management program policy was provided by the nursing home administrator (NHA) on 11/20/24 at 11:14 a.m. It documented in pertinent part, It is the policy of the Veterans Community Living Centers (VCLCs) to establish water management plans for reducing risk of legionella and other opportunistic pathogens in the facility's water systems. It is also the policy of the VCLCs to establish primary and secondary strategies for the prevention and control of legionella infections. C. Record Review The water management plan documentation was provided by the director of maintenance (DOM) on 11/20/24 at 12:43 p.m. The plan documented the facility had completed a legionella test on 7/18/24 which was negative. -The facility failed to document the flushing of dead legs and low-flow piping runs on all three hallways where residents resided. An email was received from the director of nursing (DON) on 10/22/24 at 9:54 a.m. The DON documented that seven rooms available for resident use had been vacant for seven contiguous days or more between 9/23/24 and 11/22/24. D. Staff interviews The DON and the NHA were interviewed together on 11/20/24 at 12:43 p.m. The DOM said all empty rooms in the facility had hot water run though all dead legs and low-flow piping runs of empty resident rooms in the facility every two weeks. The NHA said the facility flushed water in empty rooms every other week. The DOM and the NHA both said flushing the water every two weeks was sufficient to prevent the growth of legionella. The DOM said the facility tested for legionella annually. The infection preventionist (IP) and the DON were interviewed together on 11/22/24 at 9:03 a.m. The IP said she was not directly involved in the water management plan because that was the responsibility of the maintenance department in the facility. The IP said she thought water had to be flushed weekly to prevent the spread of waterborne pathogens such as legionella. The DON said she also thought water had to be flushed weekly in dead legs to prevent legionella growth. The IP and the DON both said they were not aware the facility practice was to flush water in dead legs and low-flow piping runs every two weeks.
Jun 2024 2 deficiencies 1 IJ
CRITICAL (J) 📢 Someone Reported This

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

Immediate Jeopardy (IJ) - the most serious Medicare violation

Deficiency F0760 (Tag F0760)

Someone could have died · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interviews, observations and record review, the facility failed to ensure one (#1) of five residents out of 13 sample r...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interviews, observations and record review, the facility failed to ensure one (#1) of five residents out of 13 sample residents was free from significant medication errors. On 5/16/24, when Resident #1 was no longer able to swallow oral medication prescribed for pain relief, registered nurse (RN) #1 consulted with the resident's hospice provider and primary care practitioner for alternative medication orders. Nurse practitioner (NP) #1 called in a prescription for liquid morphine sulfate 20 milligrams (mg)/5 milliliters (ml), give 3.75 ml (which equaled 15 mg) and entered the new order into the resident's electronic medical record (EMR). RN #1 obtained a bottle of liquid morphine sulfate solution from the facility's emergency stock medication supply and proceeded to administer the medication to RN #1. RN #1 failed to perform a dosage check on the bottle of morphine sulfate solution obtained from the facility's backup medication stock and compare it to the order written by NP #1. RN #1 drew up and administered 3.75 ml of the morphine sulfate solution and gave the medication to the resident. -However, the dosage of the morphine sulfate solution obtained from the facility's backup medication stock was 20 mg/1 ml, which resulted in Resident #1 receiving five times (75 mg) the amount of morphine sulfate ordered by NP #1. RN #1 failed to follow professional standards of nursing practice and perform the seven rights of medication administration to ensure safe and effective care and treatment of a resident in her care. As a result of RN #1's failure to complete a dosage check on the medication before administering the prescribed medication, Resident #1 received an excessively high dose of morphine sulfate solution (five times the prescribed dose of medication), which likely caused the acceleration of the resident's passing away. Findings include: Record review and interviews confirmed the facility corrected the deficient practice prior to the onsite investigation on 6/3/24 to 6/6/24, resulting in the deficiency being cited as past noncompliance with a correction date of 5/26/24. I. Situation of serious harm The facility failed to ensure Resident #1 was administered the correct dose of morphine sulfate solution when RN #1 failed to perform the seven rights of medication administration and check the medication label to confirm the dosage of the medication obtained from the facility's backup medication stock was the same dosage ordered by NP #1. RN #1's failure to follow NP #1's prescribed order for pain medication led to Resident #1 being given an excessively high dose of morphine sulfate on 5/15/24. Record review and interviews during the complaint investigation confirmed the deficient practice had been corrected and the facility was in substantial compliance at the time of the survey from 6/3/24 to 6/6/24. II. Facility plan On 6/3/24 the nursing home administrator (NHA) provided the facility's investigation, report of findings and records of corrective action related to the morphine sulfate solution overdose incident. The incident occurred on 5/15/24 at 7:07 p.m. On 5/16/24 an investigation was initiated upon discovery of the incident and remained ongoing pending a determination of the nurse's employment status. The facility initiated several corrective action measures including: On 5/16/24 the pharmacy consultant alerted the facility that Resident #1 was prescribed morphine sulfate solution in a concentration that was higher than the dose the facility had in its emergency backup medication stock. The pharmacy consultant recommended the facility perform a dosage check to ensure the nurses were aware of the difference in the dosage concentration of the morphine sulfate solution that was ordered by NP #1 versus the dosage concentration of the medication that was in the facility's backup medication stock. At the time of the pharmacy alert, the resident had already passed away. On 5/16/24 the facility's administration immediately interviewed RN #1, who had administered the first and only dose of the newly prescribed morphine sulfate. On 5/16/24, upon verification that RN #1 had administered an incorrect dose of morphine sulfate, RN #1 was immediately suspended, pending the outcome of the investigation. On 5/16/24, immediately upon the discovery that RN #1 had made a significant medication error, the facility administration took the following measures to place corrective actions to prevent future errors in the administration of liquid morphine sulfate. On 5/16/24 the facility conducted an audit of all residents receiving liquid morphine sulfate solution to ensure the medication orders were accurate and matched the liquid morphine sulfate medication provided by the pharmacy for each resident. On 5/16/24 the facility reported RN #1's performance was reported to the State Licensing Board for review, The licensing board opened an investigative case on 5/21/24. On 5/16/24 the facility's administration reviewed the facility's policy for Medication Administration for accuracy. No changes were required to the policy. On 5/17/24 the facility contacted hospice providers and other prescribers to educate the prescribers about the availability of the liquid morphine sulfate solution concentration that the facility had in the emergency backup medication stock. The facility requested the prescribers to prescribe effective medication dosages for morphine sulfate solution in concentrations of 20 mg/1 ml (the dosage concentration that was in the facility's backup medication stock). On 5/17/24 The facility contacted the pharmacy to ensure there was a system in place for the pharmacy to perform a medication check on all morphine sulfate solution orders to ensure accurate dosing of the initial physician's order of liquid morphine sulfate to a resident. On 5/20/24 the facility contacted Resident #1's hospice provider for guidance and other resources for the accurate administration of liquid morphine sulfate. The hospice nurse provided the facility with a resource for morphine sulfate solution conversions. The resource provided a conversion chart for various dosage concentrations of morphine sulfate solution to the dose that the facility had on hand (20 mg/1 ml) in their backup medication stock. The resource further provided instructions on how to administer and calculate dosage per medication concentration for accurate administration. By 5/26/24 all licensed nurses were educated and provided instructions on the proper administration of liquid morphine in various concentrations, including how to calculate the proper dosage of the medication if the medication on hand was not the concentration ordered by the prescriber. In addition, the nurses were instructed in methods of proper medication administration, including following the seven rights of medication administration. The facility would discuss the incident and monitor the corrective actions in the Quality Assurance and Performance Improvement meetings to determine if further corrective actions were needed. Interviews and record reviews during the complaint investigation from 6/3/24 to 6/6/24 revealed corrective actions to identify the resident and other residents who had the potential to be affected by the deficient practice, systematic changes to prevent its recurrence, and monitoring to ensure sustained corrections were in place. III. Professional reference According to the Food and Drug Administration (FDA) Highlight of Prescribing Information Morphine Sulfate Oral Solution - Scheduled II controlled substance, retrieved on 5/10/24 from https://www.accessdata.fda.gov/drugsatfda_docs/label/2010/022195s002lbl.pdf, Morphine oral solution is available in 10 mg per 5 ml, 20 mg per 5 ml and 100 mg per 5 ml (20 mg/ml) concentrations. Take care to avoid dosing errors due to confusion between different concentrations and between mg and ml. Warnings and Precautions: Risk of Medication Errors: Use caution when prescribing, dispensing, and administering to avoid dosing errors due to confusion between different concentrations and between mg and ml, which could result in accidental overdose and death. Respiratory depression: Increased risk in elderly, debilitated patients, those suffering from conditions accompanied by hypoxia, hypercapnia, or upper airway obstruction. Elderly patients (aged 65 years or older) may have increased sensitivity to morphine sulfate. Acute overdose with morphine sulfate is manifested by respiratory depression, a decrease in respiratory rate and/or tidal volume (airflow through the lungs), Cheyne-Stokes respiration (fast shallow breathing followed by slow heavier breathing and no breath), and cyanosis (shortage of oxygen in the blood and bluing of the skin), extreme somnolence progressing to stupor or coma, skeletal muscle flaccidity (condition of being soft and limp), cold and clammy skin, constricted pupils, and, in some cases, pulmonary edema, bradycardia (slowing heart rate), hypotension (low blood pressure), cardiac arrest and death. IV. Facility policies and procedures The Medication Administration policy, revised on 10/20/23, was provided by the NHA on 6/3/24 at 1:13 p.m. The policy read in pertinent part, It is the policy of (facility name) that medications are administered by licensed nurses as ordered by the licensed provider and in accordance with professional standards of practice, in a manner to prevent errors, contamination, and/or infection. The nurse is responsible for following the seven (7) rights of medication administration: -Right resident; -Right medication; -Right dose; -Right time; -Right route; -Right documentation; and, -Right to refuse. Review the medication administration record (MAR) to identify the medication to be administered. The MAR is used to reflect current orders for administration of medications and as documentation of medication administration. Compare medication source (bubble pack, vial, etc.) with MAR to verify resident name, medication name, form, dose, route, and time. Refer to drug reference material if unfamiliar with the medication such as the mechanism of action or common side effects. V. Significant medication error A. Resident status Resident #1, over the age of 65, was admitted on [DATE] and passed away on 5/15/24. According to the May 2024 computerized physician orders (CPO), diagnoses included congestive heart failure, atrial fibrillation, aortic stenosis, pulmonary hypertension and chronic pain. The 4/15/24 minimum data set (MDS) assessment revealed the resident was moderately cognitively impaired with a brief interview for mental status (BIMS) score of 12 out of 15. The assessment documented the resident was receiving opioid and antidepressant medications. The assessment documented the resident was receiving hospice care. B. Record review The facility investigation, dated 5/16/24, documented the following: On 5/16/24 at approximately 12:45 p.m., the consultant pharmacist (CP) alerted facility staff that there could have been a potential discrepancy between a medication order for morphine sulfate and the actual medication administration of the resident because the facility did not have the morphine sulfate dosage concentration that was ordered available at the facility in the emergency back up medication stock and the pharmacy had not yet delivered the ordered dosage concentration to the facility. Facility leadership initiated an immediate investigation and attempted to reach RN #1, who was the nurse who signed as having administered the resident's medication immediately after the prescriber placed the order. As a part of the investigation, RN #1 was interviewed by the director of nursing (DON) and NHA on 5/16/24 at 4:06 p.m. RN #1 was asked to explain the administration of liquid morphine sulfate prescribed to Resident #1 on 5/15/24. RN #1 said she administered a total of 3.75 ml of the liquid morphine sulfate from the 20 mg/ 1 ml dosage concentration bottle she had obtained from the facility's emergency backup medication stock. The NHA asked RN #1 to explain in detail how she measured out the dose of liquid morphine and RN #1 said she drew up the medication from the available morphine sulfate backup medication stock using a one ml syringe. RN #1 said she filled the syringe four times until she measured out 3.75 ml and poured each syringe full of liquid medication into a cup for administration. During the interview the DON read the morphine sulfate solution order from the MAR (20 mg/5 ml, give 3.75 ml), pointing out that was not the concentration the facility had in the backup medication stock. When the DON informed RN #1 that giving 3.75 ml of the facility's available dosage concentration meant that Resident #1 received 75 mg of morphine versus the prescribed dose of 15 mg that was ordered, RN #1 said she did not even notice that the order read 20 mg/5ml and assumed that the prescriber wrote the order for the standard dose that the facility had in the emergency backup medication stock. RN #1 was interviewed a second time on 5/16/24 at approximately 4:15 p.m., by the NHA, DON and a higher level of the administrative staff. RN #1 gave the same interview information and said she did not read the order or perform a dosage check and she instead assumed that the order was for morphine sulfate at a dosage concentration of 20 mg/1 ml because that was what the facility had available in the backup medication stock. Immediately following the interview, RN #1 was placed on administrative leave pending investigation. A review of Resident #1's EMR revealed the following information: A medical provider note, dated 5/15/24 at 10:59 a.m., revealed the resident was seen by NP #1 on 5/14/24, at the request of the resident's son, to evaluate and manage acute concerns when the resident reported she did not feel well. Resident #1 reported nausea after eating lunch but denied cough, congestion or breathing difficulties. The resident was using oxygen continuously at a flow rate of 3.5 liters per minute (LPM). Resident #1 was seen again by NP #1 on 5/15/24 after breakfast and continued to complain of not feeling well and not wanting to get out of bed. NP #1 recommended lab work to assess changes in condition. The resident was taking several medications for pain relief including MS Contin (morphine sulfate) oral tablet extended release15 mg two times a day for pain, duloxetine oral capsule delayed release 60 mg one time a day for chronic pain, lidocaine external patch 4 percent for pain relief of an affected area, naproxen sodium oral tablet 220 mg two times a day for arthritis pain and hydrocodone-acetaminophen oral tablet 5-325 mg every six hours as needed for pain. The physical exam revealed the resident was alert with no apparent distress and poor memory, her pupils were equal size and there was no jugular vein distention noted. The resident had normal respiration effort in the left lung but had crackling sounds in the right lung and an irregular cardiac murmur (a whooshing sound made by rapid, choppy blood flow through the heart). The resident had fluid retention in both lower extremities and both lower extremities were pale and cool to the touch. The resident's other skin areas were warm and dry. The resident's mood was euthymic (calm and tranquil). A medical provider note dated 5/15/24 at 7:01 p.m. documented RN #1 called NP #1 and informed her the patient was unable to safely take MS Contin oral tablets related to her current condition. NP #1 documented a change in morphine orders to give the resident a one-time dose of liquid morphine sulfate solution that evening and then, beginning the next day, orders for liquid morphine sulfate solution 15 mg twice a day. The May 2024 MAR documented an order for morphine sulfate solution entered on 5/15/24 at 6:59 p.m. by NP #1 and confirmed by RN #1 at 7:01 p.m. The order read, Morphine sulfate oral solution 20 mg/5 ml. Controlled drug. Give 3.75 ml by mouth one time only for chronic pain until 5/16/24. The May 2024 MAR displayed a black box warning that read in pertinent part, To reduce the risk of respiratory depression, proper dosing and titration of morphine are essential. Risk of medication errors (oral solution). Ensure accuracy when prescribing, dispensing, and administering morphine sulfate oral solution. Dosing errors due to confusion between mg and ml, and other morphine solutions of different concentrations, can result in accidental overdose and death. A nursing note, dated 5/15/24, read in pertinent part, At approximately 8:45 p.m., the certified nurse aide (CNA) alerted this nurse that there was a change in the resident's condition. The resident's skin was observed to be a waxy color and the resident took no breaths in 90 seconds. There was a faint heartbeat detected with a stethoscope. At 8:50 p.m. the resident no longer had a detectable pulse, heart sounds, breath sounds, or blood pressure. The resident's pupils were fixed and dilated. A narcotic count sheet started for Resident #1's liquid morphine sulfate solution documented that RN #1 initiated the first dose of morphine sulfate at 7:05 p.m. The form documented the morphine sulfate bottle had 30 ml of medication and the medication concentration was 20 mg/ 1 ml. RN #1 documented and signed that she drew up and gave Resident #1 3.75 ml of the morphine sulfate leaving 26.25 ml in the bottle. -However, the above amount given (3.75 ml) from the bottle of morphine sulfate was incorrect and excessive. The prescriber's order read Morphine sulfate 20 mg/5 ml give 3.75 ml. -Giving an amount of 3.75 ml at a concentration of 20 mg/1 ml meant Resident #1 received 75 mg of morphine instead of the prescribed dose of 15 mg of morphine, which was five times the prescribed dose. The May 2024 MAR revealed RN #1 gave the resident the incorrect dose of morphine sulfate at 7:07 p.m. VI. Staff interviews RN #1 was interviewed on 6/4/24 at 1:00 a.m. RN #1 said the pharmacy filled prescribed medications, however, the facility had an emergency backup medication stock for situations when a resident needed to start a medication right away and could not wait for the pharmacy to process and deliver the medication, as it could take hours or days. RN #1 said morphine sulfate solution 20 mg/1 ml was the only concentration of morphine sulfate solution available in the backup medication stock. RN #1 said when a nurse obtained morphine sulfate solution from the backup medication stock, the nurse was to verify the dosage concentration and compare it to the physician's order for accuracy. She said the verification process should occur each time the medication was administered to ensure accurate medication administration. RN #1 said she had recently received education on performing the seven rights of medication administration and was also educated on how to calculate the proper medication doses based on different concentrations of morphine sulfate solution to ensure the accuracy of the medication administered to a resident matched the prescriber's orders. The CP was interviewed on 6/4/24 at 12:36 p.m. The CP said orders were usually entered into the resident's EMR and transferred to the MAR so the nurse could administer the medication at the proper dosage, frequency, time and route. He said once a medication order was entered into the EMR, a second person, usually a nurse from the facility, was to check and verify the entered order for accuracy. The CP said after the second check was completed, the computerized system automatically sent the order electronically to the pharmacy where the pharmacist would perform a triple check to verify the order and screen for any drug interactions, warnings or inaccuracies. The CP said the third check occurred during normal business hours. The CP said if the third check revealed any concerns, the facility would be alerted of the concern. The CP said it was then up to the facility staff to contact the prescriber for further potential recommendations related to the alert and to act appropriately in coordination with the prescriber to avoid any drug interactions. The CP said the pharmacists were also available for further consultation if needed. The CP said when the physician's order for Resident #1's morphine sulfate solution at a concentration of 20 mg/5 ml was received by the pharmacy, he was concerned because he knew the nursing facility did not have the 20 mg/5 ml dosage concentration in the backup medication stock. He said the facility only had morphine sulfate solution 20 mg/1 ml in the backup medication stock and if the nurse gave the prescribed amount of 3.75 ml at the concentration of 20 mg/1 ml it would have been too much medication and would have caused an overdose of Resident #1. RN #1 was interviewed a second time on 6/4/24 at 3:02 p.m. RN #1 said she went to Resident #1's room around 6:45 p.m. to give the resident her medication. Resident #1 said she was ready to take her medications but was unable to swallow her pills so she called the resident's medical provider and requested an order for liquid morphine sulfate. RN #1 said NP #1 answered the phone call and said she would enter a new medication order for liquid morphine sulfate solution. RN #1 said the order showed up on the resident's MAR a few minutes later and she obtained the medication from the facility's backup medication stock. RN #1 said she went to the facility's backup medication stock and obtained a bottle of morphine sulfate solution in the dosage concentration of 20 mg/1 ml from the backup medication stock. RN #1 said the only morphine sulfate solution the facility had in its backup medication stock was in the dosage concentration of 20 mg/1 ml. RN #1 said at approximately 7:05 p.m., she drew up and gave Resident #1 what she thought was the prescribed dose of 3.75 ml of the morphine sulfate solution. RN #1 said when she obtained the medication from the facility's backup medication stock and went to administer the medication to Resident #1, she failed to check the order with the morphine sulfate solution on hand and did not notice that the physician's order was for a different dosage concentration than the available dosage concentration of morphine sulfate solution. She said she drew up 3.75 ml as the order indicated and administered it to the resident. RN #1 said the proper steps in medication administration were to read the physician's order to confirm that the medication on hand was the correct medication and the correct dose. She said she would also make sure to check the resident's name and make sure the resident did not have related medical allergies RN #1 said after giving Resident #1 the liquid morphine sulfate,she looked in on her a couple of times and noticed that her breathing was labored. She said a little after 8:00 p.m., the CNA informed her Resident #1 was not breathing. She said when she assessed Resident #1 she had a weak heartbeat and was not breathing. RN #1 said as the night went on she began to think more about the events of the evening and started to question the amount of morphine sulfate solution she had administered to the resident. RN #1 said following her shift, she had a discussion about the medication error with the DON. She said they discussed the incident in detail and she received education regarding medication administration. RN #1 said going forward she would perform the seven rights of medication administration and would verify all medication administrations for accuracy. RN #1 said she would also ask another nurse to double-check the physician's order with her to ensure she administered the medication correctly. NP #1 was interviewed on 6/4/24 at 3:50 p.m. NP #1 said, on 5/15/24 at approximately 7:00 p.m., she received a call from RN #1 who told her Resident #1 was unable to swallow her medication and she wanted to know if she could switch the MS Contin oral tablets over to a liquid form of morphine sulfate. NP #1 said she told RN #1 she would enter an order for liquid morphine sulfate. NP #1 said she did not discuss anything further with RN #1. The medical director (MD) was interviewed on 6/6/24 at 12:58 p.m. The MD was aware that Resident #1 was given an overdose of morphine sulfate by RN #1. The MD said, following the incident, she talked at length with the DON and the NHA about the potential causes and developed a plan of correction. The MD said the physician's order was written correctly by a provider but it was written at a strength that was not commonly used and at a dosage concentration that was not immediately available to the facility. She said the administration of the incorrect dose of morphine sulfate solution was RN #1's error as she did not check the medication strength with the physician's order before administering the medication to Resident #1. The DON was interviewed on 6/4/24 at 1:25 p.m. The DON said once she was notified by the pharmacist that there was a concern about Resident #1's morphine sulfate solution order and a potential for a medication error, she began an immediate investigation. She said the investigation revealed Resident #1 was given an incorrect dose of morphine sulfate solution. The DON said RN #1, who gave the incorrect dosage of morphine sulfate, was placed on immediate suspension. The DON said she provided immediate education to all licensed nurses on properly verifying all physician's orders for accuracy and how to calculate proper morphine doses if the provider ordered a morphine dosage concentration different from the morphine available in the facility's backup medication stock. The DON said the facility also talked to the medical providers to educate them about the facility's available dosage concentration of morphine sulfate solution. The NHA was interviewed on 6/6/24 at 3:01 p.m. The NHA said the details of the medication error incident would be presented at the next quality assurance quality improvement (QAPI) meeting. The NHA said the QAPI committee was expected to review the investigation findings and complete corrective actions to determine if further corrective actions were needed.
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

Deficiency F0712 (Tag F0712)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interviews, the facility failed to ensure timely physician visits for four (#9, #10, #12 and #13) of ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interviews, the facility failed to ensure timely physician visits for four (#9, #10, #12 and #13) of five residents reviewed for new admission physician visits out of 13 sample residents. Specifically, the facility failed to ensure the physician evaluated Resident #9, Resident #10, Resident #12 and Resident #13 within 30 days following admission to the facility. Findings include: I. Facility policy and procedure The Physician Visits and Delegation policy, revised 5/6/24, was provided by the nursing home administrator (NHA) on 6/5/24 at 1:48 p.m. It revealed in pertinent part, The physician should: -See the resident within 30 days of initial admission to the facility; -The resident must be seen at least once every 30 calendar days for the first 90 calendar days after admission and at least every 60 days thereafter by the physician or physician delegate as appropriate by state law; and, -Review the resident's total program of care including medications and treatments at each visit. II. Resident #9 A. Resident status Resident #9, age greater than 65, was admitted on [DATE]. According to the June 2024 computerized physician's order (CPO), diagnoses included heart failure, atrial fibrillation (irregular heart rhythm), edema, bladder dysfunction, pelvic pain and hypertension. The 4/30/24 minimum data set (MDS) assessment revealed the resident was cognitively intact with a brief interview for mental status (BIMS) score of 13 out of 15. The resident had an indwelling catheter and was prescribed antidepressants and diuretic medications. B. Record review -A review of Resident #9's electronic medical record (EMR) revealed the physician did not see the resident until 4/2/24, 57 days after the resident was admitted to the facility. III. Resident #12 A. Resident status Resident #12, age [AGE], was admitted on [DATE]. According to the June 2024 CPO, diagnoses included hypertension, idiopathic progressive neuropathy (weakness, numbness, and pain from nerve damage, usually in the hands and feet), sleep apnea and osteomyelitis. The 6/5/24 MDS assessment revealed the resident was cognitively intact with a BIMS score of 14 out of 15. The resident was prescribed opioid and antiplatelet medications. B. Record review -A review of Resident #12's EMR revealed the physician did not see the resident until 4/2/24, 47 days after the resident was admitted to the facility. IV. Resident #13 A. Resident status Resident #13, age [AGE], was admitted on [DATE]. According to the June 2024 CPO, diagnoses included dementia with behavioral disturbances, adjustment disorder, bipolar disorder, diabetes, hypertension and osteoarthritis. The 6/6/24 MDS assessment revealed the resident had severely impaired cognition with a BIMS score of six out of 15. The resident was prescribed antipsychotic, antidepressant, diuretic, opioid and hypoglycemic medications. B. Record review -A review of Resident #13's EMR revealed the physician did not see the resident until 4/2/24, 47 days after the resident was admitted to the facility. V. Resident #10 Resident #10, age less than 65, was admitted on [DATE]. According to the June 2024 CPO, diagnoses included heart failure, atrial fibrillation, dementia, benign prostatic hyperplasia, conjunctivitis and hypertension. The 6/5/24 MDS assessment revealed the resident had moderate cognitive impairment with a BIMS score of eight out of 15. The resident had an indwelling catheter and was prescribed antidepressants and anticoagulant medications. B. Record review -A review of Resident #10's EMR revealed the physician did not see the resident until 4/2/24, 42 days after the resident was admitted to the facility. VI. Staff interviews The director of nursing (DON) was interviewed on 6/6/24 at 9:02 p.m. The DON said residents should be seen timely by the physician following admission to the facility. The DON said the facility had talked to the residents' physician about the requirement to see the residents within 30 days of admission. The medical director (MD) was interviewed on 6/6/24 at 12:58 p.m. The MD said the facility had some issues in regards to the physician seeing residents within the first 30 days after admission and the frequency of physician's visits. The MD said she was working with the resident's physician to establish a more consistent schedule for physician visitation.
May 2023 4 deficiencies
CONCERN (D)

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 interviews and record review, the facility failed to ensure one (#42) of four out of 34 sample residents were kept free...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interviews and record review, the facility failed to ensure one (#42) of four out of 34 sample residents were kept free from physical abuse. Specifically, the facility failed to ensure effective personalized care planned behavioral interventions were in place for Resident #43, who had a history of physically abusive behaviors towards Resident #42. Findings include: I. Facility policy and procedure The Abuse policy and procedure, last reviewed on 2/21/23, was provided by the nursing home administrator (NHA) on 5/18/23 at 8:30 a.m. It read in pertinent part, Physical abuse includes, but is not limited to hitting, slapping, punching, biting, and kicking. It also includes controlling behavior through corporal punishment. Possible indicators of physical abuse include an injury that is suspicious because the source of the injury is not observed, the extent or location of the injury is unusual, or because of the number of injuries whether at a single point in time or over time. II. Incident of abuse between Resident #42 and Resident #43 Resident #42 and Resident #43 were married with Resident #43 having a history of physically abusive behaviors towards Resident #42 (see care plan below). The 5/15/23 facility's abuse investigation documented staff members observed Resident #42 sitting and visiting with Resident #43 and Resident #42 was spitting on the floor. Resident #43 told Resident #42 that was not acceptable and was observed hitting Resident #42's hand in his lap. Staff immediately separated the residents and Resident #43 was returned to the second floor, where she resided. Resident #42 remained on the first floor where he resided. Resident #42 was interviewed after the incident and did not remember the incident and did not express any fear of Resident #43. No injury was observed. The facility investigation did not indicate if the abuse was substantiated or not. -However, the abuse should be substantiated based on Resident #43 willfully hitting Resident #42. III. Resident #43 A. Resident status Resident #43, aged 84, was admitted on [DATE]. According to the May 2023 computerized physician orders (CPO) diagnoses included dementia with other behavioral disturbance, adjustment disorder and depression. The 4/13/23 minimum data set (MDS) assessment revealed the resident had moderate cognitive impairment with a brief interview for mental status score (BIMS) of 12 out of 15. She required set up assistance for eating and was independent with bed mobility, transfers, dressing, toileting and personal hygiene. It indicated she was not exhibiting verbal and physical behaviors towards others. B. Record review The behavioral care plan, initiated on 5/30/22 revised on 5/9/23, documented Resident #43 had a history of physically abusive behaviors towards Resident #42 and interfered in his care. It indicated that she was quick to act and unable to remember coping skills. The interventions included assist resident to develop more appropriate methods of coping and interacting with Resident #42 that will not interfere with care, encourage resident to express feelings appropriately, provide opportunity for positive interaction, intervene as necessary to protect rights and safety of others, approach in a calm manner, divert attention, remove from the situation. Remind the resident, when she brings Resident #42 upstairs to eat or go to activities, not to leave unattended and monitor Resident #42's location. -A review of Resident #43's comprehensive care plan did not reveal effective personalized behavioral interventions for monitoring and preventing resident's behavior during interactions with Resident #42 during mealtimes or activities. The care plan was not updated after the altercation on 5/15/23. A 5/15/23 social services progress note revealed the social worker spoke with the resident regarding the incident that Resident #42 was spitting on the floor and Resident #43 told him to stop that and then slapped his hand and arm that was on his lap to get his attention to stop the behavior. Resident #43 became teary and left the interview and verbalized that Resident #42 was unable to understand and reason anymore. The social worker followed up with the resident in her room regarding how dementia affected people and to reach out to staff before she became frustrated. A 5/16/23 nursing progress note revealed the Resident #43 was on visual checks every 15 minutes, secondary to striking Resident #42 on 5/15/23. The facility had daily behavior monitoring of the Resident #43's behavior towards other residents in the facility. The 4/19/23 to 5/18/23 behavior tracking form indicated no physical or verbal behaviors directed at others. -However, the resident had an altercation on 5/15/23 (see above). -A comprehensive review of the progress notes did not reveal any further documentation of the incident. C. Resident interview Resident #43 was interviewed on 5/16/23 at 1:30 p.m She was not able to recall the incident on 5/15/23 and asked why she could not be in the same room as her husband. IV. Resident #42 A. Resident status Resident #42, age [AGE], was admitted on [DATE]. According to the May 2023 CPO, the diagnoses included Alzheimers's disease, type II diabetes mellitus and chronic kidney disease. The 3/30/23 MDS assessment revealed the resident had severe cognitive impairment with a BIMS score of three out of 15. He required the extensive assistance of two people with bed mobility, transfers, dressing, toileting, personal hygiene and the limited assistance of one person with eating. B. Record review The behavior care plan, initiated 5/30/22 revised 4/25/23, indicated that Resident #42 had a history of being resistive to care and would swing at staff and Resident #43 when he did not want care, was agitated or angry. The interventions included allow the resident to be involved with treatment and care regime, give resident clear explanation of all care activities prior to when they occur and do not rush resident. -A comprehensive review of Resident #42's care plan did not reveal any additional person centered interventions after the altercation on 5/15/23. C. Resident interview Resident #42 was interviewed on 5/17/23 at 3:00 p.m. He was not able to answer questions when asked. V. Staff interviews Certified nursing assistant (CNA) #6 was interviewed on 5/18/23 at 11:01 a.m. She said Resident #43 was a social person and she observed that Resident #43 and Resident #42 were together frequently during activities and meals. CNA #6 said she had not been closely monitoring the two residents and had not observed any physically aggressive behaviors by Resident #43 during activities or mealtimes. Registered nurse (RN) #4 was interviewed on 5/18/23 at 1:15 p.m. She said she had not observed any aggressive behavior by Resident #43 towards Resident #42. She said that historically Resident #43 had slapped Resident #42. She was unable to recall the last instance of physical aggression towards Resident #42 by Resident #43. She said the residents were frequently together at activities and at mealtimes. The director of nursing (DON) was interviewed on 5/18/23 at 5:00 p.m. She said Resident #43 and Resident #42 lived on separate floors due to Resident #43's history of physical aggression towards Resident #42 and interference in care. Resident #43 and Resident #42 had been having supervised meals in the past. There had been no observed physically aggressive behavior by Resident #43 for a significant amount of time until the incident on 5/15/23. Resident #43 and #42 had been assessed to need to be in line of sight during activities and mealtimes but since the incident occurred they would need to be supervised with staff present and monitoring activities and mealtimes.
CONCERN (D)

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

Deficiency F0692 (Tag F0692)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to ensure effective interventions were in place to addr...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and interviews, the facility failed to ensure effective interventions were in place to address weight loss for two (#3 and #37) of seven residents reviewed for nutrition out of 34 sample residents. Specifically, the facility failed to ensure Resident #3 and #37 were provided nutritional interventions identified for their weight losss. Findings include: I. Professional reference Roigk. P. (2018) Chapter 8: Nutrition and Hydration. In K. [NAME] and J. [NAME]-[NAME] Eds. Fragility Fracture Nursing: Holistic Care and Management of the Orthogeriatric Patient (Internet). [NAME] Publishing. https://www.ncbi.nlm.nih.gov/books/NBK543833/ retrieved on 5/24/23 at 9:24 a.m. According to the North American Nursing Diagnoses Association ([NAME]) malnutrition is: 'Intake of nutrients insufficient to meet metabolic needs'. The criteria for malnutrition are: Body mass index (BMI)< (less than) 18.5 kg/m2, unintended weight loss> (greater than) 10% in the last 3-6 months, BMI < 20 kg/m2 and unintended weight loss>5% in the last 3-6 months, fasting period>7 days. II. Facility policy and procedure The Weight Monitoring policy and procedure, last revised on 5/18/23, was provided by the nursing home administrator (NHA) on 5/18/23 at 4:20 p.m. It read in pertinent part, It is the policy of the facility to establish weight baseline, to monitor weight loss and/or gain, and to monitor residents for significant changes in weight that may require intervention. Weights are to be taken and recorded at the same time each month to assure consistent monitoring. The scale(s) for evaluating weight should be calibrated routinely to assure equipment is working properly and that information is accurate. III. Resident #3 A. Resident status Resident #3, age [AGE], was admitted on [DATE]. According to the May 2023 computerized physician orders (CPO), the diagnosis included type II diabetes mellitus and vitamin B deficiency. The 2/2/23 minimum data set (MDS) assessment revealed the resident was cognitively intact with a brief interview for mental status score of 15 out 15. She required the extensive assistance of one person for dressing, toileting, personal hygiene, limited assistance of one person for bed mobility and transfers and was independent with eating. B. Observations On 5/17/23 at 9:19 a.m. snacks were not observed in the resident's room (as indicated in the care plan, see below). The resident was observed sitting in the lobby, the resident was observed not having or eating snacks. At 11:00 a.m. The resident was observed wheeling self in the hallway past a snack cart. The resident did not attempt to take snacks from the snack cart. At 11:30 a.m. the resident was observed sitting in the dining area. The resident was served lunch at 12:03 p.m. - a small green salad, small bowl of soup and a breadstick. She ate 40% of green salad, three spoonfuls of soup and 0% of breadstick. She was given a small container of ice cream and ate 20%. She was not offered an alternative to the meal or additional food prior to the ice cream. At 1:45 p.m. the resident was observed wheeling self around in the lobby area. The resident was observed not having or eating snacks. At 4:30 p.m. the resident was observed in the dining room. She ordered a half order of the special which consisted of mashed potatoes, roast beef and gravy and pudding. She ate approximately 30% of the scoop of mashed potatoes, 0% of roast beef and 80% of pudding. She was not offered an alternative meal or additional food. C. Record review The nutrition and weight management care plan, initiated on 10/8/2020 revised on 5/16/22, indicated resident was at a high nutritional risk with possibility of weight changes due to diabetes, cardiac fluid retention, desire to take in only minimal supplements and periods of poor appetite. It indicated the resident's ideal body weight (IBW) was 105 pounds (lbs) with a range of 95-115 lbs. Interventions included a regular diet with meats cut in half inch pieces, small portions and thin liquids.Ensure plus or supplement of choice every morning, shelf stable high calorie snacks for her room to consume, encourage resident to eat, monitor weight for significant weight changes, offer snack hydration cart twice a day between meals, record and monitor oral intake at meals and snacks between meals, review calories, protein and fluid needs as necessary. The resident's weights were documented as follows: -11/15/22 108 lbs (bath chair) -2/7/23 104.8 lbs (bath chair) -4/11/23 106.4 lbs (bath chair) -5/9/23 92.8 lbs (bath chair), and; -5/11/23 97.6 lbs (wheelchair) The 5/2/23 interdisciplinary weight team notes documented Resident #3 had a weight increase of 3% in one week, weight loss of 5% in one month, weight loss of 4.7% in three months and a loss of 6.8% in six months. It documented a recent weight loss but improved appetite with intake of 75-100% of meals. The resident declined any additional nutritional interventions but requested additional shelf stable snacks in her room. The 5/15/23 interdisciplinary weight team notes documented Resident #3 had weight loss of 2.9% in one week, weight loss of 8.4% in one month and 6.8% in three months. It documented variable oral intake with current intake of 95-100% of meals. It documented current interventions of Ensure plus once a day and snacks in her room. Recommendations were to try super cereal and bring in her favorite fast food. Current interventions included Ensure plus once a day and shelf stable snacks for room. -The resident's intake was indicated as 95-100% at meals, however based on observations (see above) she ordered a half order and she did not eat the full meal on both occasions. A comprehensive review of diet and supplementation orders revealed: -Ensure plus once a day, ordered 2/14/23. The medication administration record (MAR) revealed that she received the supplement once a day in the morning. -Regular diet ordered 1/3/19. D. Staff interviews Certified nurse assistant (CNA) #6 was interviewed on 5/18/23 at 11:14 a.m. She said Resident #3 was a picky eater and she did get offered Ensure and snacks. The registered dietitian (RD) was interviewed on 5/18/23 at 9:30 a.m. She said Resident #3 was hesitant to try snacks but liked M&M's with peanuts and cookies. She said she liked shelf stable snacks in her room that were kept at her bedside. The RD purchased snacks to keep at Resident #3's bedside. The RD was out of town for the last week and there was no plan for staff to supply the snacks at the resident's bedside while the RD was gone. It had only been recently discussed at the 5/15/23 IDT meeting to try super cereal and reassess food choices outside of what was being offered at the facility to bring resident food from outside of the facility. She said she did not have recent observations of Resident #3 at mealtimes. The director of nursing (DON) was interviewed on 5/18/23 at 5:30 p.m. She said monitoring and preventing significant weight loss was important for residents to prevent skin breakdown, keep them healthy and labs within normal limits. Weight loss triggered a review of the resident's weight by the RD and the interdisciplinary team and if they were trending downward they were monitored weekly. Weight loss monitoring was important to continue to discuss what did and did not work and the root causes. She said the goal was to see the weight trend back up. IV. Resident #37 A. Resident status Resident #37, age [AGE], was admitted on [DATE]. According to the March 2023 computerized physician orders (CPO), diagnoses included chronic obstructive pulmonary disease (COPD), peripheral vascular disease, abdominal aortic aneurysm (a swelling of the aorta) without rupture, alcohol dependence, and peripheral vascular angioplasty status with implants and grafts (a procedure to open narrow blocked arteries to improve blood flow. The 4/5/23 minimum data set (MDS) assessment revealed the resident's cognition was intact, with a brief interview for mental status (BIMS) score of 15 out of 15. Resident #15 required extensive physical assistance from one staff member for locomotion off unit, dressing, toileting and personal hygiene. He required limited assistance from one staff member for bed mobility, transferring and walking in his room. He did not have a known weight loss of 5% or more in the last month prior to his admission or a 10% weight loss in the last six months. B. Resident interview Resident #37 was interviewed on 5/16/23 at 3:25 p.m. The resident said he thought he had recently lost weight but it did not bother him. He said he did not have much of an appetite. He said he usually ordered from the alternate menu because he did not like the main meal. The resident said he ordered watermelon for lunch. He said the portion sizes were large. He said there was a lot of waste because he could not eat it all at one time. Resident #37 was interviewed on 5/17/23 at 3:11 p.m. He said the facility did not have a lot of items he liked. He said they have fruit and vegetables available on the snack table. He said he likes salad but he did not like their salad because they did not have the spicy Italian dressing to put on it. He said the facility had offered him a dietary supplement but he did not want it because it was too thick and it clogged him up. Resident #37 said he preferred thinner drinks like juice, compared to supplements. He said he liked seafood but it was not offered. He said would always eat seafood. He said he understands that it could be costly but he hoped it could be offered at least once a month. Resident #37 said fish was on the menu but it was usually breaded, which he did not like. He said he would eat filets of fish that were not breaded. -Interviews with Resident #37 identified the resident was able to identify food/drink preferences that he would want to eat, potentially increasing his caloric intake. C. Record review The 3/29/23 CPO identified the resident was on a regular diet with thin liquids. The 3/29/23 CPO directed staff to weigh the resident weekly. The 3/29/23 vital record under weights identified the resident's admission weight using the standing scale was 137.2 pounds (lbs). A 3/29/23 diet communication slip was provided by the dietary manager on 5/18/23. The communication slip identified Resident #37 liked seafood, wanted small portions and did not have food dislikes. The undated diet card was provided by the dietary manager on 5/18/23. The diet card read the resident did not like chicken and liked fish, coffee, cereal, eggs and toast. The 3/30/23 nutritional assessment read the resident's ideal body weight (IBW) and adjusted IBW was 134 to 162 lbs. He currently had a body mass index (BMI) of 21.5. The assessment read weight loss had been gradual over several years. According to the assessment, the resident did not like chicken and preferred fish, coffee, eggs, bacon, cereal, and other meats. The assessment indicated the resident had unintended weight loss. The nutrition plan read to monitor weight intake status and provide preferences. The 4/3/23 dietary note read Resident #37 stated he had some weight loss prior to his admission but his appetite had been rebounding. He did not want supplements at this time (4/3/23). The 4/3/23 health status note identified Resident #37 was reviewed in the weight meeting. The note read the resident was taking meals in his room and an alternate menu was provided. He was on a regular diet. The registered dietitian recommended small portions and to cut up his meat. Additional interventions included shelf stable snacks and provide preferences. The 4/15/23 weight record identified Resident #37 weighed 131.2 lbs, indicating the resident lost six lbs and 4.37% of his body weight in just over two weeks since his 3/29/23 admission. The 4/17/23 health status note identified Resident #37 was reviewed in the weight meeting. The note read the resident weighed 131.2 lbs on 4/15/23. The resident had a 2% weight loss in a week and a 4.3% weight loss since admission [DATE]). According to the note, the resident had clothes on during his 3/29/23 admission weight and lasix upon admission for diuresis could have contributed to weight loss. The resident had been skipping meals and ate very little. Interventions included to encourage food intake and to come out of his room. The assessment read staff should also encourage intake at activities and continue to provide snacks for his room. No additional interventions were identified other than encouraging the resident to eat more and provide snacks. The intervention to offer snacks was not a new intervention as identified as a 4/3/23 intervention. -However, according to the assessment, the resident's PO (by mouth) intake identified the resident ate 50-100% of his meals. The review of progress notes and nutrition concern list (weight meeting minutes) did not identify the resident was reviewed on 4/24/23 or 5/1/23 when the resident had a weight gain (see below) however, after the weight gain, the resident's weight continued to trend down. The 4/27/23 weight record identified Resident #37 gained 4.8 lbs with a weight of 136 lbs however the 5/8/23 weight record identified the resident dropped down to 129.6 lbs. The 5/8/23 weight identified the resident lost 6.4 lbs between 4/27/23 and 5/8/23. The weight identified the resident lost a total weight of 7.6 lbs at 5.54% since 3/29/23. The 5/8/23 nutrition concern list identified Resident #37 was discussed on 5/8/23 with the weight committee. According to the minutes, the resident's intake was variable and ordered very small portions. The minutes indicated the resident stated he weight fluctuates and stays low. The minutes read they were providing him his preferences and he refused nutritional interventions. The intervention read the RD was working on coming up with alternatives such as meal and snack ideas. The 5/10/23 weight record identified Resident #37 weighed 134 lbs on 4/8/23. The resident weighed 126.2 lbs on 5/10/23 indicating a 7.8 lbs weight loss. The RD 5/15/23 weight change note read the resident weighed 126.2 lbs on 5/10/23 with a 3.8% weight loss in a week and 5.9% in a month. The note confirmed the resident had significant continued weight loss. According to the note, he had variable PO intake with small portions of a minimal selection of food items and the dietary manager would continue to work with the resident to find preferences and ways to increase intake. The resident seemed to have very little interest in food and had a prior history of 12 or more beers a day and did not have a craving for sweets. The note read acute illness may have also contributed to weight loss. The resident did not have chewing or swallowing issues and had a history of declining nutritional interventions. -Review of records did not identify acute illness since admission. The 5/15/25 health status note read the resident was reviewed at the weight meeting. He had a weight of 126.2 on 5/10/23 with a 3.8% loss in one week and 5.9% in a month. According to the note, it had been very difficult to obtain preferences or to assist in coming up with nutritional strategies or even a to go to meal in which the resident could order when he did not want the special menu items. The note read the current interventions was: -Refused nutritional interventions; -Regular texture diet with thin liquids; -The dietary manager would follow up to see if they could figure out some food preferences and a way to increase intake; and, -Notify physician's assistant (PA) of significant weight loss. The nutritional management care plan, last revised on 5/15/23 read Resident #37 was at an elevated nutritional risk due to history of poor intake and weight loss prior to admission, and medical diagnosis which could contribute to increased nutritional needs. His diagnosis included COPD and alcohol dependence. According to the care plan goal, the resident would avoid significant weight loss over the next quarter. His goal weight was 155 lb. Interventions initiated on 4/3/23 included: -Weigh at the same time of day and record weekly. -Attempt to follow consistent times/type of scale/clothing/wheelchair weighed to ensure the most accurate weights. -Notify RD, and provider of weight loss greater than 5lb; -Invite the resident to activities to provide an additional avenue for intake. -Monitor meal/fluid and snack intake. -Monitor nutrition related labs prn (as needed). -Monitor/document/report PRN (as needed) any s/sx (signs and symptoms) of dehydration and dysphagia (swallowing difficulty). -Offer snack/hydration cart bid (two times a day) between meals. -Preferences: Likes coffee, does not chicken that much, likes fish and other meats, likes bananas, cookies, and will eat all breakfast foods. -Update preferences as needed. -Review calories, protein and fluid needs prn. -Stated he wished to eat half hour after taking his morning pills. -The resident did not want to be disturbed prior to 7:30 a.m. and would take his breakfast at 8:30 a.m. The review of the care plan only identified one intervention after 4/3/23 and after a 10 lb weight loss. On 5/10/23 the intervention read: (Resident #37) was not very forthcoming of his food preferences. -No other interventions were included after the resident continued to have a weight loss. In addition, the resident was able to indicate his food preferences (see resident interview above). The weekly weight record was collected on 5/18/23 after the interview with the RD (see below). The 5/18/23 weight identified the resident had a slight gain of 1.6 lbs with a weight of 127.8 lbs. D. Staff interview The RD was interviewed on 5/18/23 at 9:00 a.m. The RD confirmed Resident #37 had lost 10 lbs since his admission between 3/29/23 and 5/10/23. She said he had orders for weekly weights and had not been weighed since 5/10/23. She said she would request staff to obtain his weight today (5/18/23). The RD said she offered him high calorie dietary supplements on 4/3/23 but he refused. He said the supplements caused him too much phlegm/thick mucus. The RD said she could not get the resident to nail down a preference to help increase his calorie intake. The RD was informed the resident said he liked juice. She said there were thinner supplements that could be flavored with juice. She said she had not discussed the thin supplements with the resident and could order them and offered it to the resident. She said she asked the dietary manager this week if she could step in and help the resident identify other interests. The RD confirmed the resident had lost six lbs by 4/15/23. She said he was discussed at the weight meeting and the intervention was to offer snacks available in his room, inform him of meal options and try to find ways to increase his appetite. She said he did not like sweets. The RD said she did not look into other potential appetite stimulates. She said would speak to the PA to determine if there were additional appetite stimulating options. The RD confirmed the resident loss of almost five lbs between 5/4/23 and 5/10/23. The RD she would continue to focus on what they could offer the resident. She said she did not remember the resident liked seafood. She said she would talk to the resident about seafood options. The RD said the facility could order him shrimp. The RD said she would order the Boost Breeze clear supplement for the resident. The dietary manager (DM) was interviewed on 5/18/23 at 10:05 a.m. The DM said she attended the weekly weight meeting. She said staff had been monitoring Resident #37's weight and was trying to see what more they could do to encourage him to eat more. She said they offered an alternate menu that he would order from. The DM said the nursing home administrator (NHA) just told her to order shrimp for Resident #37. The DM said she was aware the resident liked seafood. She said she they already offered fish on the menu. The DM was informed the resident did not like most of the fish provided because it was breaded. The DM said she talked to the resident everyday and he, just like all the other residents, said he wanted a T-bone steak. She said maybe they could add more specialty items to the menu such as a special meal or ask activities if they could pick up more specialty foods for the resident. She said the resident told her that he did not like steamed vegetables. The DM said steamed vegetables were frequently on the menu. The DM said he liked salad but usually did not eat too much of it. The DM was informed the resident said he would eat more salads if he they would offer him spicy Italian dressing. She said they did not offer that dressing as an option but they could order the spicy Italian dressing for him. She said his preferences were on his diet communication card (see above). She said he did not like most of the meals provided. She said he would eat regular meals on occasion. She said he liked the chicken fried steak. She said she spoke to him a few days ago on what he might like to eat. He said he wanted more beer. The director of nursing (DON) was interviewed on 5/18/23 at 5:29 p.m. She said the facility just ordered different kinds of Boost as on 5/18/23. She said they ordered wild berry Boost for Resident #37. The DON said new residents recently admitted to the facility were followed in the weekly weight committee for the first two to three weeks and if there was a trending weight loss. The DON said the resident would be brought back to the weight meeting if the resident continued to lose weight. She said the weight committee discussed new interventions to promote weight gain and reviewed what was working and not working. She said the committee in the weight meeting would try to identify root causes of the weight loss such as pain or medications. She said the committee would continue to monitor changes if there was little to no improvement. The DON said the resident lost a lot of weight in a short period of time. She said from a nursing standpoint, increasing his calorie intake would be great for him and it would reduce his bony prominences and skin breakdown risk. She said nursing would like him to be able to eat anything he would like and eat. She said if he ate more, he could have improved strength and might feel better. The DON said the resident was not yet identified as malnourished but increased calories could reduce his risk for malnourishment. She said nursing staff would advocate for the resident's food preferences, visit with him on food options and monitor his weight.
CONCERN (E)

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

Deficiency F0658 (Tag F0658)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interviews the facility failed to ensure three (#55, #35 and #32) out of 34 sample resid...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review and interviews the facility failed to ensure three (#55, #35 and #32) out of 34 sample residents received treatment and care in accordance with professional standards of practice. Specifically, the facility failed to: -Assess a Resident #55's change of condition and notify the resident's physician in a timely manner when the resident had ongoing vomiting and when the resident's abdomen was distended and tender to touch on 3/12/23; and, -Assess Resident #35 and Resident #32 vital signs were monitored prior to the administration of a blood pressure medication. Findings include: I. Resident #55 A. Professional references [NAME], D. A., [NAME], S. [NAME], S. M. (August 2022). Bowel obstruction. National Library of Medicine. Stat Pearls (Internet) https://www.ncbi.nlm.nih.gov/books/NBK441975/ retrieved on 5/22/23. Commonly in small bowel obstruction (SBO), abdominal pain is described as intermittent and colicky but improves with vomiting. The vomiting in SBO tends to be more frequent, in larger volumes, and bilious (yellowish green vomit). [NAME], P. (April 2023). Intestinal Obstruction. Merck Manual Professional Version. https://www.merckmanuals.com/professional/gastrointestinal-disorders/acute-abdomen-and-surgical-gastroenterology/intestinal-obstruction retrieved on 5/22/23. Obstruction of the small bowel causes symptoms shortly after onset: abdominal cramps centered around the umbilicus or in the epigastrum, vomiting and, in patients with complete obstruction, obstipation (severe prolonged constipation). Patients with partial obstruction may develop diarrhea. Severe, steady pain suggests that strangulation has occurred. Sanivarapu, R. R., [NAME], G. (December 2022). Aspiration pneumonia. National Library of Medicine. Stat Pearls (Internet) https://www.ncbi.nlm.nih.gov/books/NBK470459/ retrieved on 5/22/23. The infectious pulmonary process that occurs after abnormal entry of fluids into the lower respiratory tract is termed aspiration pneumonia. The aspirated fluid can be oropharyngeal secretions or particulate matter or can also be gastric content. B. Facility policy and procedure The Change of Condition policy and procedure, reviewed on 2/1/23, was provided by the nursing home administrator (NHA) on 5/18/23 at 3:15 p.m. It revealed in pertinent part, The purpose of this policy is to ensure the (facility) promptly informs the resident, consults the resident's physician, and notifies, consistent with his or her authority, the resident's representative when there is a change requiring notification. Circumstances requiring notification include: 2. Significant change in the resident's physical, mental or psychosocial condition such as deterioration in health, mental or psychosocial status. This may include: a. Life threatening conditions, or b. Clinical complications. C. Resident status Resident #55, age [AGE], was admitted on [DATE]. According to the March 2023 computerized physician orders (CPO), the diagnoses included dementia, dysphagia (swallowing difficulty), pain and gastroesophageal reflux disease (GERD). The 3/12/23 minimum data set (MDS) assessment revealed the resident had severe cognitive impairment with deficits in short and long term memory and daily decision making. He was dependent with the assistance of two people for transfers, toileting, personal hygiene, he required extensive assistance of two or more people with bed mobility and dressing and extensive assistance of one person for eating. D. Record review The pain care plan, initiated 2/23/23, indicated that resident was unable to verbalize pain description or pain level related to dementia progression. Interventions included monitor and document side effects of pain medication. Observe for constipation, new onset or increased agitation, restlessness, confusion, hallucinations, dysphoria, nausea, vomiting, dizziness and falls and report to physician. Monitor and report any signs and symptoms of non-verbal pain changes in breathing, vocalizations, mood/behavior changes, eyes (wide open/narrow slits/shut, glazed, tearing, no focus), face (sad, crying, worried, scared, clenched teeth grimacing), body (tense, rigid, rocking, curled up, thrashing). Observe and report changes in usual routine, sleep patterns, decrease in functional abilities, decreased range of motion, withdrawal or resistance to care. The 2/26/23 physician progress notes revealed a diagnosis of GERD, dysphagia, diarrhea, constipation, colon polyps, bilious vomiting with a surgical history of appendectomy (removal of appendix), colon polyp removal and cholecystectomy (removal of gallbladder). The assessment revealed the abdomen was soft and non distended, non tender and bowel sounds active. Lung assessment revealed they were clear to auscultation (listened to lung sounds with a stethoscope) without crackles or wheezes. -A review of the physician documentation revealed no further physician assessment or follow up after 2/26/23. The 3/6/23 nursing progress notes revealed at 2:31 p.m. the resident refused to get out of bed, had refused meals and medications. He was tensed and made noises throughout the shift. The 3/6/23 nursing progress notes revealed at 5:08 p.m. the resident had a large emesis (vomiting). The 3/6/23 nursing progress notes revealed at 7:07 p.m. the resident had a large emesis and acetaminophen was held. -A review of documentation revealed no further nursing assessment, including an abdominal assessment, vital signs or communication with providers. The 3/7/23 nursing progress notes revealed at 12:20 a.m. Zofran 4 milligram (mg) was given for nausea after three emesis episodes. The 3/7/23 nursing progress notes revealed at 4:54 a.m. resident at midnight had a large emesis that was observed to be yellow with small streaks of red. The resident had a second emesis that was bile colored. The resident temperature was 100.3 degrees Fahrenheit. The resident had medium watery diarrhea. Message was sent to providers and infection control was notified. The 3/7/23 at 11:27 a.m. revealed the resident had a COVID test with negative results. -A review of documentation revealed no further nursing assessment, including an abdominal assessment or if the provider returned the message. The 3/7/23 nursing progress notes revealed at 10:27 p.m. the resident remained in bed and made continuous sounds. The resident's daughter gave resident a milkshake which he vomited. A review of documentation of 3/7/23 10:27 p.m. revealed no further nursing assessment, including an abdominal assessment, vital signs or providers being notified after resident vomited at 10:27 p.m. The 3/11/23 nursing progress notes revealed at 5:16 a.m. the resident had two episodes of emesis during the night shift and would not give a verbal response to the nurse. The 3/11/23 nursing progress notes revealed at 1:41 p.m. the resident refused oral care. -A review of documentation for 3/11/23 revealed no further nursing assessment, including an abdominal assessment, vital signs or communication with providers. The 3/12/23 nursing progress notes revealed at 12:14 a.m. the resident remained in bed with increased episodes of vomitus. Head of bed elevated and making quacking noise during care. The 3/12/23 nursing progress notes revealed at 1:53 a.m. the resident was given Zofran 4 mg for nausea. The 3/12/23 nursing notes revealed at 5:11 a.m. the resident was awake and making continuous quacking sounds. The 3/12/23 nursing progress notes revealed at 6:00 a.m. it was documented that at 5:00 a.m. the resident had a moderate amount of vomit. Resident #55's vital signs were blood pressure 150/74, heart rate 108, temperature 99.0 degrees Fahrenheit, oxygen saturation 91%. -A review of documentation revealed no further nursing assessment, including an abdominal assessment or communication with providers regarding increased heart rate, low grade temperature and vomiting. The 3/12/23 nursing progress notes revealed at 9:42 a.m. the resident vomited a large amount of food particles and Synthroid (thyroid medication) was held. The 3/12/23 nursing progress notes revealed at 9:43 a.m. the resident was left in bed at this time due to feeling sick. The 3/12/23 nursing progress notes revealed at 9:55 a.m. the resident vomited a large amount of food particles and light brownish fluid. He refused oral fluids and medications. The 3/12/23 nursing progress notes revealed the resident had vomited at 11:45 a.m. The nurse assessed the resident who appeared pale with sunken eyes and was slightly agitated. Pain medication was provided. The resident then slept and then vomited a second time. The abdomen was found to be distended and tender to the touch. The nurse was unable to assess the abdomen or lung sounds due to the resident making quacking sounds. The resident exhibited muscle rigidity and abdominal guarding. The 3/12/23 nursing progress notes revealed at 1:40 p.m. the resident's vital signs were blood pressure 100/64, temperature 99.1 degrees Fahrenheit, pulse 159, and oxygen saturation of 82%. Resident's head was raised and supplemental oxygen was administered at 2 liters via nasal cannula. Binax COVID test was done with negative results. The resident had a medium putty colored bowel movement. The 3/12/23 nursing progress notes revealed at 2:00 p.m. the on-call provider and on call nurse were notified at 2:00 p.m. A voicemail was left for the resident's power of attorney (POA). The 3/12/23 nursing progress notes revealed at 3:30 p.m. the POA requested the resident be sent to the emergency department for evaluation. The 3/12/23 nursing progress notes revealed the resident was transferred at 4:10 p.m. -A comprehensive review of the 3/12/23 documentation revealed the resident began vomiting at 5:00 a.m. with a change in vital signs, the resident did not have an abdominal assessment until 11:45 a.m. where the resident's abdomen was distended and tender to touch. The resident's vital signs were not documented at 1:40 p.m. The provider was not called until 2:00 p.m. which was over two hours later and the resident did not go to the hospital until over four hours later. The 3/12/23 nursing progress notes revealed at 10:00 p.m. report by the hospital staff to nursing home staff that the resident had a small bowel obstruction on computerized tomography (CT) with likely pneumonia on chest x-ray and potential sepsis. He was admitted to the medical surgical unit for end of life care and was treated with pain medication and intravenous fluids. The bowel elimination documentation revealed: -3/5/23 at 9:49 p.m. resident was incontinent; -3/7/23 at 5:59 a.m. resident was incontinent; -3/8/23 no bowel movement was recorded; -3/9/23 no bowel movement was recorded; -3/10/23 at 9:59 p.m. resident was incontinent; -3/11/23 at 1:50 p.m. resident was incontinent; -3/12/23 at 5:59 a.m. resident was incontinent; and, -3/12/23 at 1:59 p.m. resident was incontinent. -A review of documentation revealed no documentation of quality (formed versus diarrhea) or quantity of bowel movement. A review of the March 2023 CPO revealed: -Ondansteron (Zofran) 4 milligrams (mg) by mouth every four hours as needed for nausea, ordered 1/12/23. This medication was administered on 3/7/23 at 12:20 a.m. and on 3/12/23 at 11:53 a.m. A review of the March 2023 medication administration record (MAR) pain assessment in advanced dementia scale (PAINAD) revealed -3/6/23 day shift pain level 5, evening pain level 2, and night pain level 1. -3/7/23 day shift pain level 0, evening pain level 7 and night pain level 2. -3/8/23 day shift pain level 2, evening pain level 5 and night pain level 2. -3/9/23 day shift pain level 3, evening pain level 0 and night pain level 0. -3/10/23 day shift pain level 4, evening pain level 3 and night pain level 3. -3/11/23 day shift pain level 2, evening pain level 0 and night pain level 2. -3/12/23 day shift pain level 5. -A comprehensive review of pain assessment documented an elevated pain level on 3/6/23 day shift when resident was exhibiting tensed and vocalization behaviors, 3/7/23 evening shift when resident was experiencing emesis and making continuous sounds and 3/12/23 day shift when resident was exhibiting elevated temperature, emesis, elevated pulse and decreased oxygen saturation. C. Staff interviews Certified nurse aide (CNA) #5 was interviewed on 5/18/23 at 10:15 a.m. She said Resident #55 had been throwing up prior to being hospitalized and he had not been feeling well and was making strange quacking noises. She said physicians and nurses had talked about the quacking noises and if they were the result of the resident experiencing pain or if it was related to something else. CNA #1 was interviewed on 5/18/23 at 10:20 a.m. She said the resident had not been feeling well and had been staying in bed. He had not been eating much and had been throwing up prior to being hospitalized . Registered nurse (RN) #1 was interviewed on 5/18/23 at 10:25 a.m. She said the resident had been having an overall decline. She said she took care of the resident the day before he was hospitalized . She said he was having bowel movements but he was having instances of vomiting. She said he may have been having a pain crisis because he was making frequent quacking noises. He had been having episodes of emesis and he had normal bowel sounds. She was not aware if the providers had been notified regarding his vomiting. She said when there was a suspected change of condition, providers were notified, vital signs were monitored and for gastrointestinal symptoms an abdominal assessment should be performed. She said providers were notified for residents ' changes of condition. The director of nursing (DON) was interviewed on 5/18/23 at 5:01 p.m. She said he had been having occasional emesis the entire stay. She said that the resident made quacking noises but they had been unable to determine if it was pain related. She said providers were notified on 3/7/23 regarding the vomiting and temperature but was unable to confirm if there was an abdominal assessment, return communication or follow up with the providers. She was unable to locate documentation if the provider was notified on 3/12/23 before 2:00 p.m. She said when a resident was having symptoms of vomiting with changes in vital signs, including an elevated temperature, an abdominal assessment should be completed and the provider notified. The medical director was interviewed on 5/18/23 at 6:00 p.m. The resident exhibited during his stay at the facility was quacking vocalizations. Staff were unable to attribute the quacking noises to pain or to a tardive dyskinesia (abnormal or impaired voluntary movement) type side effect of the medications. He said when there were episodes of vomiting with a fever there should be an assessment of vital signs, abdominal assessment, monitoring for constipation and a lung assessment (to assess for aspiration). He said the provider should be notified. II. Monitoring blood pressure medication A. Professional references Khashayar.F., [NAME], J. (2022). Beta Blockers. Stat Pearls. National Library of Medicine. https://www.ncbi.nlm.nih.gov/books/NBK532906 retrieved on 5/25/23. It read in pertinent part, Beta receptors are found all over the body and induce a broad range of physiologic effects. The blockade of these receptors with beta-blocker medications can lead to many adverse effects. Bradycardia (low heart rate) and hypotension (low blood pressure) are two adverse effects that may commonly occur. The patient's heart rate and blood pressure require monitoring while using beta-blockers. Kizior, R. J., [NAME], K. J. (2023). Metoprolol. [NAME] Nursing Drug Handbook. Elsevier. p. 770. Assess B/P (blood pressure), heart rate immediately before drug administration. If pulse is 60 beats per minute or less or systolic B/P is less than 90 mmHg (millimeters of mercury) withhold medication and contact physician. B. Observations On 5/16/23 at 3:00 p.m. registered nurse (RN) #5 was observed dispensing Metoprolol 25 milligrams (mg). RN #5 checked order for parameters and was observed checking Resident #32's pulse, which was 60 beats per minute (bpm) prior to administration of medication. RN #5 was not observed checking for the resident's blood pressure prior to administration. RN #5 was observed administering Metoprolol. The physician order documented Metoprolol 25 mg twice a day. Parameters ordered to hold medication if pulse was less than 55. On 5/17/23 at 7:30 a.m. RN #4 was observed dispensing Amlodipine 5 mg. RN #4 was not observed checking for a current blood pressure or pulse prior to administration. RN #4 then administered Amlodipine medication to Resident #35. The physician order documented Amlodipine 5 mg once a day. C. Staff interviews RN #1 was interviewed on 5/18/23 at 11:45 a.m. She said before giving a blood pressure medication the residents' blood pressure and pulse should be assessed. She said if blood pressure and pulse were below baseline a reassessment should be done and physician ordered parameters should be followed. She said if there were no physician ordered parameters an assessment of the resident including a blood pressure and pulse, along with signs and symptoms of low blood pressure were done. She said a physician should be notified if the resident experienced a blood pressure less than 100-120 systolic and pulse was less than 55 bpm. The DON was interviewed on 5/18/23 at 5:22 p.m. She said blood pressure and pulse were done prior to the administration of a blood pressure medication and physician ordered parameters should be followed. If there were no physician ordered parameters, an assessment of low blood pressure which included monitoring blood pressure, pulse and monitoring for signs and symptoms should be done.
CONCERN (E)

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 observations, record review and staff interviews, the facility failed to maintain an infection prevention and control p...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record review and staff interviews, the facility failed to 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 in one of two dining rooms. Specifically, the facility failed to ensure residents had hand hygiene before meals. Findings include: I. Facility policy and procedure The Infection Prevention and Control policy, revised 1/31/23, was provided by the facility on 5/15/23. The policy read in pertinent part: The (facility's) Infection Prevention and Control (ICP) plan shall ensure the organization develops, implements and maintains an active, organization-wide program for the prevention, control and investigation of infections and communicable diseases in order to reduce the risk of epidemic and epidemic infections in residence, visitors and healthcare workers, and to optimize use of resources. According to the infection control policies the facility would implement appropriate infection prevention and control measures and communicate responsibilities about preventing and controlling infection. Responsibilities would include hand hygiene to all staff residents, families and visitors. The Hand Hygiene policy, reviewed 1/19/23, was provided by the facility on 5/18/23. The policy identified hand hygiene should be performed before and after eating. II. Observations Dinner observations were conducted 5/15/23 between 4:18 p.m. and 5:10 p.m. A free standing alcohol based hand rub (ABHR) dispenser with an orange sign requesting residents to use the ABHR was on the 2nd floor dining room near the entrance. Observations identified residents who brought themselves to the dining room did not stop to use the ABHR from the dispenser. The staff assisting residents into the dining room did stop with the residents at the dispenser and provide ABHR. Observations did not identify staff provided ABHR or hand hygiene wipes for most of the residents once they sat down and prepared for their meal, or once the residents were provided their meal. Only one resident in the dining room was provided hand hygiene before he was provided total meal assistance. In room meal delivery on 5/15/23 identified some residents were not offered hand hygiene during meal service. Between 5:14 p.m. and 5:30 p.m. the residents in room [ROOM NUMBER], #209 and #216 were not offered hand hygiene before they were served their meal tray. Observations were conducted on 5/17/23 during the lunch meal service. The meal included hand held items such as bread sticks and sandwiches. Residents were not observed to be encouraged or assisted with hand hygiene in their rooms prior to the meal. Residents assisting themselves into the dining room were not observed to use the ABHR dispenser. Staff assisting residents in their wheelchairs into the dining room, did not stop and assisted residents with ABHR. Staff did not encourage residents to use ABHR when entering the dining room. Residents were not provided or assisted with hand hygiene prior to meal service in the dining room or when offered their meal. One resident was observed touching the eating surface of his spoon with his fingers prior to eating. Another resident was observed to wipe his nose with his fingers before eating his sandwich. Observations were conducted in the dining room on 5/17/23 during dinner. Only one resident assisting herself into the dining room, used the ABHR dispenser. Residents were not provided or assisted with hand hygiene in the dining room before their meal. The 5/18/23 lunch observation did not identify residents were provided hand hygiene prior to their meal. Several residents were observed eating a hamburger with their hands. III. Resident interviews Resident #34 was interviewed on 5/17/23 at approximately 3:30 p.m. He said there was ABHR available in the dining room but he usually did not think about it or pay too much attention to it. He said staff does not remind him or encourage him to do hand hygiene in the dining room or in his room. He said he would usually wash his hands after using the restroom. Resident #7 was interviewed on 5/18/23 at 3:20 p.m. He said he was aware of an ABHR dispenser in the dining room. He said he did not usually see residents using it. Resident #7 said staff pushing residents would have to stop and assist the resident they were assisting to use the ABHR dispenser. He said he personally did not like to use the ABHR. He did not like the way it smelled or how it felt. He said he would prefer hand wipes offered in the dining room. He said his hands would feel cleaner with wipes. He said hand wipes were not offered in the dining room by staff. He said he figured if staff performed hand hygiene in the dining room, that would be enough for him. Resident #33 was interviewed on 5/18/23 at 3:26 p.m. He said he did not use the ABHR dispenser in the dining room because he used a walker. He said he would have to take his hands off the walker to use the dispenser and he was afraid if he let go of the walker he might lose his balance and fall. Resident #39 was interviewed on 5/18/23 at 3:34 p.m. He said he was not aware there was a place in the dining room that he could use ABHR before meals. IV. Staff interviews The director of nursing (DON) and the infection preventionist (IP) was interviewed on 5/18/23 at 12:30 p.m. According to the DON and the IP, the IP was new to the position and the DON was overseeing the program. The DON said the best way to prevent the spread of transmission based infections was to practice appropriate infection control such as personal protection equipment and hand hygiene. The DON said staff were trained on hand hygiene during staff in-services, online training, new hire orientation and the certified nurse aide (CNA) education class. The DON said infection control practices were included in a staff education fair last fall. She said part of the training included a return demonstration of hand hygiene. The IP said she conducted infection control rounds and audits throughout the week. She said the rounds included making sure staff performed hand hygiene. She said the audits did not include resident hand hygiene at meals. The DON said staff needed to ensure residents were offered and assisted with hand hygiene after use of the restroom, before and after eating, primarily, but not limited to anytime a resident needed and wanted hand hygiene. She said ABHR was available on the walls in the hallways but staff should be offering, reminding, encouraging, assisting the residents with hand hygiene. The DON said the residents live in a shared community environment and everyone touches everything. She said hand hygiene helped protect against the spread of transmission based infections by breaking the infection chain. The DON and the IP were informed of the above observations. The DON and the IP said they would re-educate staff on the importance of resident hand hygiene and remind residents where they could perform hand hygiene. The IP said she would do in service or activity residents with a glow light that would show them the germs on the hands and surfaces. The IP said she would include resident hand hygiene with her infection control rounds. The DON said she would look into ordering hand wipes for residents to use in the dining room and change the location and color of the sign on the ABHR dispenser stand in the dining room. V. Record review The DON provided an 11/7/22 staff inservice attendance sheet with an attached hand hygiene competency validation check list and an online course completion record on 5/19/23 via email. According to the attendance sheet, staff were in service on infection control practices, including hand hygiene. The hand hygiene competency check list requested staff to perform a return demonstration of appropriate hand hygiene practices. The course completion record identified staff completed an online training course of hand hygiene between 11/19/22 and 5/19/23. VI. Facility follow-up The DON was interviewed again on 5/18/23 at 5:17 p.m. She said the facility chose to offer hand hygiene in the dining room by way of the ABHR dispenser stand in the entry of the dining room for residents because the facility thought it would be more convenient for residents to use as opposed to the ABHR on the walls. She said they wanted a convenient system so residents could have cleaner hands just before they sat down at the dining table for meal service. She said the IP conducted staff education on 5/18/23 on the importance of resident hand hygiene. She said she changed the color of the sign to bright green which reminded residents to use. She said she would periodically change the colors of the sign to help catch staff and residents' attention. The DON said she had ordered wipe packets and hand hygiene wipes for use in the dining rooms. She said she would have a staff member assigned to each meal to assist residents with hand hygiene. The DON said the activities department scheduled an activity for residents on 6/5/23 to teach residents on the importance of infection control and hand hygiene. She said the facility may include infection control presentations as a monthly resident activity. The DON said she would continue to educate staff on infection control with a focus on resident hand hygiene before meals. She said during the 5/18/23 dinner after changing the color of the sign on the ABHR dispenser, the placement of the dispenser at the entrance of the dining room, and educating staff to remind and assist residents with hand hygiene before meals, she saw residents lining up to use the ABHR before sitting down at their meal table. The DON provided the records identifying facility follow up after the hand hygiene observations were shared with the facility on 5/19/23 via email. The records included: -An 5/18/23 dining room hand hygiene audit identified staff offered hand hygiene during the 5/18/23 dinner to all residents who ate in the dining room. The audit showed that residents in the dining room were provided hand hygiene in the dining room. According to the audit, only one resident refused hand hygiene. -An outline of hand hygiene improvements the facility would make to adhere to appropriate infection control practices, to include, one to one education with staff regarding the residents' need for hand hygiene before and after meals. According to the hand hygiene improvement outline, the staff needed increased education to remind residents to perform hand hygiene before meals. -A staff attendance sheet identified staff received resident hand hygiene before and after meals education on 5/18/23.
Feb 2022 4 deficiencies 1 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Free from Abuse/Neglect (Tag F0600)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interviews, the facility failed to ensure residents were free from abuse, neglect and exploitation fo...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interviews, the facility failed to ensure residents were free from abuse, neglect and exploitation for one (#16) of four residents reviewed for abuse out of 21 sample residents. Specifically, the facility failed to ensure Resident #16 was free from verbal abuse from a staff member. Resident #16 was told by registered nurse (RN) #6 that Resident #16 risked having to leave the facility and find another place of residence because of discussions he had with his own power of attorney (POA). The interaction with the RN left the resident feeling threatened and intimidated by the RN. He was worried about losing his home. In addition, the facility failed to thoroughly assign and complete corrective action following a substantiated allegation of verbal abuse, resulting in the continuation of Resident #16 feeling bullied and intimidated. The RN continued to approach Resident #16 after it was determined RN #6 verbally abused Resident #16. Findings include: I. Facility policy and procedure The Abuse policy, last reviewed 12/7/21, was provided by the facility on 2/9/22 at 1:29 p.m. by the nursing home administrator (NHA). The policy read in part, It is the policy of (the facility) to provide protection for the health, welfare and rights of each resident by developing and implementing written policies and procedures that prohibit and prevent mistreatment, abuse, neglect, and exploitation. (The facility) will take necessary precautions to prevent resident abuse by anyone including staff members, other residents, volunteers, contract staff, family members, resident representatives, visitors and any other individuals. Every resident has the right to be free from mistreat, abuse, neglect and exploitation. The policy defined verbal abuse as: Verbal abuse means the use of oral, written or gestured communication or sounds that willfully includes disparaging or derogatory terms to residents or their families, or within their hearing distance regardless of their age, ability to comprehend, or disability. Examples of verbal abuse include, but are not limited to: harassing a resident; mocking, insulting, ridiculing; yelling or hovering over a resident, with the intent to intimidate; threatening residents, included but not limited to, depriving a resident of care or withholding a resident from contact with family and friends; and isolating a resident from social interactions or activities. The Abuse policy under Identification of Abuse, Neglect and Exploitation read in part: Residents at risk for abusive situations are identified and appropriate care plans are developed. The Abuse policy under Reporting Abuse read in part: Assure that reporters are free from retaliation or reprisal. The Abuse policy under Protection of Abuse read in part: The facility will make efforts to ensure all residents are protected from physical and psychological harm during and after the investigation. Examples include but are not limited to: Responding immediately to protect the alleged victim and integrity of the investigation. Any employee of the facility suspected of abuse is placed on administrative leave. The employee is not permitted to enter the facility and/or around residents of the facility unless otherwise directed by the administrator, until the investigation has been completed and the final disposition has been given. Residents involved in allegations of abuse will be separated by staff .Provide Emotional support and counseling to the resident during and after the investigation, as needed. The Abuse policy under Prevention of Abuse-Training read Existing staff would receive annual education through planned in-services and as needed. Training topics would include: types of abuse prohibiting and preventing all forms of mistreatment, abuse, neglect and exploitation; identification of what constitutes mistreatment, abuse, neglect, exploitation, and misappropriation of resident property; recognizing the signs of use, neglect, exploitation and misappropriation of resident property .This facility will utilize the admission process and care conference meetings to provide residents and representatives information and how and to whom they may report concern, incidents and grievances without the fear of retribution; and provide feedback regarding the concerns that have been expressed. The Abuse policy under Follow up Reporting/Response read in part: Taking all necessary actions as a result of the investigation, which may include, but are not limited to, the following: -Analyzing the occurrence(s) to determine why abuse, neglect, misappropriation of Resident property or exploitation occurred, and what changes are needed to prevent further occurrences; -Defining how care provision would be changed and/or improved to protect residents receiving services .Training of staff on changes made and demonstration of staff competency after training was implemented . II. Resident status Resident #16, age [AGE], was admitted on [DATE] and readmitted on [DATE]. According to the February 2022 computerized physician orders (CPO), diagnoses included wedge compression fracture of T11-T12 vertebra (spine), hypertensive heart disease with heart failure, adult failure to thrive and chronic pain syndrome. The 12/7/21 minimum data set (MDS) assessment documented the resident was cognitively intact with a brief interview for mental status (BIMS) score of 14 out of 15. According to the MDS assessment, the resident was independent with eating, transfers and walking in his room. He required supervision with and without set up for bed mobility, dressing, toileting, personal hygiene and locomotion on and off the unit. The MDS identified the resident did not have behaviors or rejections of care. III. Resident interview Resident #16 was interviewed on 2/9/22 at 9:12 a.m. Resident #16 stated that he was intimidated by RN #6. The resident stated he contacted his power of attorney (POA) who was a family friend and family member of another resident, about some concerns he had regarding the facility. The resident said RN #6 was made aware of the conversation with his POA and informed him he was interfering with the other resident's cares, and the other resident and himself could be expelled from the facility. Resident #16 said he reported the incident to the director of nursing (DON). The resident said he was told the situation was under investigation. Resident #16 said a few weeks later after he reported RN #6, he entered his room and saw RN #6 looking around in the back of his room. The resident said RN #6 had a cup of medication in his hand but appeared to be looking for something, possibly to use to get back at him. The resident said he had seen a lot of bullies in his life and RN #6 was a bully. The resident said the RN still worked as his nurse or a certified nurse aide (CNA). He said sometimes nurses worked as CNAs if they needed more help on the hall. Resident #16 was interviewed again on 2/10/22 at 9:26 a.m. He said he had not had to work with RN #6 recently and thought the RN was moved to another hall, however, the RN recently approached him in the dining room. The resident said RN #6 tried to join the conversation the resident was having with his tablemates and tried to act all buddy, buddy with him. Resident #16 said it upset him. He said he did not want to see RN #6 or have to talk to him. He said he felt like the RN was a bully who was trying to control the situation. IV. Record review The care plan for Resident #16 did not reveal the resident was care planned as an at risk adult for potential or actual abuse. The nurse note on 12/20/21 at 6:20 p.m. created by RN #6 read: It was reported to this nurse that (Resident #16) made a phone call to another resident's POA to discuss current conditions at the facility. I had an extended conversation with the resident and explained it was not his responsibility nor appropriate for him to discuss another resident's care regardless of his familiarity or association with anyone's POA with (stet) expressed written consent from another resident's POA. I explained that this could be a violation of HIPPA (Health Insurance Portability and Accountability Act) regulations and that if he continued to discuss other resident's cares and conditions that it could be possible that he would be asked to leave the facility and find another place of residence. A 12/20/21 certified nurse aide (CNA) witness statement was provided on 2/14/22 at 9:41 a.m. by the NHA. The statement read Resident #16 contacted another resident's family member about his concern over the temperature in the facility. An abuse investigation report for Resident #16 was provided by the NHA on 2/9/22 at 2:37 p.m. According to the investigative report, the incident of alleged abuse occurred on 12/20/21. The facility was informed of the incident on 12/21/21 at 11:00 a.m. The investigation of alleged verbal abuse was initiated on 12/21/21. According to the initial report details, Resident #16 stated RN #6 was very unprofessional and inappropriate with his interaction concerning Resident #16 and his power of attorney (POA). The RN believed the resident was discussing the care of another resident who resided in the facility. The investigation read Resident #16 was threatened by RN #6 to be kicked out because of his behavior and the RN would not listen to his response. The resident felt the RN had no right to treat him in that manner. Statements were gathered from the alleged assailant and Resident #16. Resident #16 was interviewed on 12/21/21 at 11:00 a.m. The resident said RN #6 entered his room and sat on his bed. The resident said the nurse accused him of sharing information about another resident to his POA/family friend. According to the resident, the RN would not let him talk and said he would be kicked out if he did not stop. The resident said he refused to stop talking to his friends and the RN had no authority to tell him things like this. During the interview, the resident stated he was fearful of losing his home and being kicked out of the facility. He said he was angry and hurt that someone would speak to him in that way and not allow him to defend himself. Resident #16 said during the interview, he felt verbally threatened by RN #6. The alleged assailant interview summary, collected on 12/21/21 at 12:30 p.m., read: (RN #6) states that a CNA reported to him that (Resident #16) had been speaking with (his POA) about another resident who shares the same POA as (Resident #16). (RN # 6) reported that he informed (Resident #16) that he was not allowed to talk about things in the facility or other resident concerns with anyone as this was a HIPAA violation. He said that if (Resident #16) wanted to speak to POA about (other named resident), he would need it in writing that (Resident #16) was allowed to do that. (RN #6) stated that during the conversation, (Resident #16) tried to argue with him that (his POA) was a good friend and that he could talk to him. (RN #6) states that he 'shut him down.' In other words, (RN #6) would not allow (Resident #16) to provide an explanation as he interrupted him many times during the conversation and that 'he did not care' about what (Resident #16) was telling him. (RN #6) felt that it was not relevant to what they were discussing. When I asked (RN #6) if he thought his conversation was inappropriate or unprofessional he did not provide a clear statement. When asked if he felt that the statements could be taken as a threat, he stated he did not think so. According to the investigation, three other residents were interviewed who resided on the same hall as Resident #16 and three other staff members. The staff and residents were interviewed for any knowledge of the incident and/or having felt threatened. No additional feelings of threatening behavior or witnessing of such were reported during the interviews. The allegation was reported to police, the ombudsman, the physician, and the resident's POA. The facility implemented safety measures including the immediate request that the alleged assailant, RN #6, leave the premises. The RN was placed on administrative leave on 12/21/21, pending the conclusion of the internal investigation. The facility substantiated the allegation of verbal abuse. The investigation of abuse summary identified RN #6 did not follow HIPAA policy and his conversation with the resident was unprofessional and unwarranted. The summary read verbal abuse was substantiated, however, there was no intent. The summary identified the RN had a need for education. The summary included a second interview with Resident #16 on 12/23/21. Resident #16 stated he did not want RN #6 to enter his room and take care of him. The abuse investigation report under facility actions indicated no changes needed to the victim's treatment regime and/or care plan. The facility actions included: -The RN placed on administrative leave (see dates below). -The NHA and the DON would prepare for the external investigation meeting to gather additional information and the RN's education needs related to HIPAA and proper procedures surrounding the resident misconduct. According to the actions, the discussion would include who he was to communicate with, and what was appropriate for him to address himself versus what was not appropriate. Under facility actions, the abuse investigation report asked the facility to describe interventions that were put in place to help prevent a recurrence. The facility wrote: Education with staff regarding proper information on HIPAA. A written statement from the director of nursing (DON) was provided by the NHA on 2/14/22 (the statement was provided during the survey and not a part of the facility's investigation). The statement read: I (DON) spoke with (RN #6) on 12/21/21 in the first floor nurses station when I (DON) went to send (RN #6) home after allegations of verbal abuse were made. During this time I spoke to him on the allegations of verbal abuse and gave him a brief description of HIPAA. I then relayed to him that if he feels like a resident or staff member is violating a policy or is in the wrong, that he should take it to a manager, myself or the NHA. I informed him that he does not have the right to tell someone they may lose their home and asked if he understood how that could make someone feel. (RN #6) acknowledged my education, the allegations and voiced understanding of future ways to report to management. -According to the statement, no other education or expectations were provided to the RN at that time. An education/training attendance form was provided by the NHA on 2/10/22 at 4:31 p.m. According the form, RN #6 attended an education on investigations and abuse on 3/2/21. The online training transcript for RN #6 was provided by the NHA on 2/10/22 at 4:31 p.m. The transcript read the RN received the following education: -Understanding Abuse and Neglect training on 9/6/21. The review of the online transcript did not indicate RN #6 received additional abuse training after it was determined he verbally abused a resident; and, -Protecting Resident Rights in Nursing Facilities on 1/9/22. According to the NHA, the education was provided as part of RN #6's annual training. She said the training was not part of his corrective action interventions after the determination of verbal abuse. The course completion history for RN #6 was provided by the facility on 2/14/22. According to course history, education on effective communication was completed on 4/5/21. According to the course completion history, the RN was not assigned additional training on communication after the determination of verbal abuse. The archived training for RN #6 was provided by the facility on 2/14/22. According to the archived training, he received an overview of HIPAA privacy and security on 10/8/16. The archived training indicated the RN received HIPAA awareness in 2015. A date for the completion of the HIPAA awareness was not provided. The HIPAA policy and HIPPA notice of privacy practices was provided by the NHA via email on 2/14/22 at 11:33 a.m. According to the NHA, the HIPAA policies and practices were provided to RN #6 after the determination of verbal abuse. The policy and practices informed the RN, medical information was protected and staff must comply with those protections. The policy and practices did not state residents in a nursing facility must comply or were subject to actions such as discharge from the facility. According to the DON, RN #6 also received recent HIPAA training through their online training program. A timeline of RN #6's leave and presence in the facility was provided by the NHA on 2/14/22. The timeline read: Administrative leave start:12/21/21 Administrative leave end:12/25/21 Return to work:12/26/21 December 2021 scheduled days: 12/26/21, 12/27/21, 12/28/21 January 2022 schedule days: 1/8/22-1/11/22, 1/17/22-1/20/22, 1/22/22-1/25/22 February 2022 scheduled days: 2/1/22-2/3/22, 2/5/22-2/6/22 According the NHA, RN #6 was on vacation during the survey observation period. The staff schedule was provided by the NHA via email on 2/14/22 at 11:33 a.m. The review of the December 2021, January 2022, and February 2022 revealed RN #6 was scheduled as either a nurse or a certified nurse aide (CNA) on the same hall Resident #16 resided after verbal abuse was substantiated. The following dates indicated RN #6's strong potential of interactions with Resident #16: -On 1/17/22, the RN was scheduled as a CNA in the resident's hall. -On 1/20/22, the RN was scheduled as a day nurse in the resident's hall. -On 1/22/22, the RN was scheduled as a day CNA in the resident's hall. IV. Staff interviews The nursing home administrator (NHA) was interviewed on 2/10/22 at 2:54 p.m. with the deputy division director (DDD). The NHA said staff report all allegations of abuse, neglect, and mistreatment. She said anything deemed as reportable that meets the criteria would be reported and investigated. The NHA said RN #6 was placed on administrative leave during the investigation. After abuse was substantiated, the RN was allowed to return to the facility because the facility did not feel he was a threat to the residents because there was no willful intent. The NHA said RN #6 received immediate education on HIPAA policies and procedures. The NHA said RN #6 was informed that it was not appropriate in policy or approach when he addressed the resident on 12/20/21. She said the RN was not with (worked/around) the resident after he returned to work. She said the facility wanted to make sure the RN had understood the policies and received thorough education. The NHA said the education focused on HIPAA because RN #6 did not know residents were not bound to HIPAA regulations. The DDD said the internal investigation was complete but the corporate's external investigation was still in process. The NHA said final decision factors/actions would be determined after the employee had an opportunity to provide any new information he would like to share regarding the incident. The NHA said the employee received immediate education on HIPAA policies and procedures. She said RN #6 was already aware the other resident's family member was Resident #16's POA. The NHA said the DON spoke with Resident #16 and informed him of the investigation process. The NHA was interviewed a second time on 2/14/22 at 9:46 a.m. with the DON. The NHA said the facility substantiated the allegation of abuse because the incident was determined to be verbally abusive based on how RN #6's conversation made the resident feel. The DON said Resident #16 was interviewed regarding the 12/20/21 incident. The DON said when Resident #16 was interviewed on 12/21/21, he said was upset by the way RN #6 spoke to him. The resident said she felt intimidated by the RN. He said RN #6 threatened he would lose his home. The DON said he felt verbally abused and was worried about his potential loss in his securement in the facility. The DON said RN #6 was interviewed regarding the 12/20/21 incident. The DON said the RN was informed that the resident did not violate HIPPA and the incident was under investigation. The RN was made aware of the allegations. She said she told the RN it was not his place to tell the resident he may have to leave the facility after talking to his POA. RN #6 was sent home on leave pending the outcome of the investigation. The NHA said the facility provided a verbal education and had RN #6 review the HIPAA policies and procedures. She said the RN did not have a history of this behavior. He did not want to instill fear in the resident but said he wanted to give him a heads up of potential actions. The NHA said RN #6 felt bad that the resident was upset. His intention was not to cause verbal abuse. The RN was allowed to return to work after the completion of the internal investigation. The RN verbalized he understood how he made Resident #16 feel. The DON said she told RN #6 to stay away from Resident #16. She said she thought it was made clear to him. The DON said Resident #16 told her he found the RN in his room after the RN was asked to stay away from the resident. She said the RN should have had the other nurse pass his medications. Resident #16 told the DON that he did not want anything to do with RN #6 and he did not like him. The DON said she reminded the RN not to be the one to pass Resident #16's medications. The RN offered to apologize to the resident but Resident #16 has not been receptive to his apology yet. The DON said no additional corrective actions have been taken at this time. The NHA said RN #6 had not received additional education on abuse or effective communication since he was allowed to return to work. The DON confirmed the RN has been scheduled for the past two months since he returned from administration leave. The DON said they could have improved his education to ensure full understanding of expectations. The DON said she did not ask him why he went into Resident #16's room and after asking him to not work with him. She said she told him not to do it again. The DON said she was not aware the RN approached the resident in the dining room. She said RN #6 should not have approached Resident #16 in the dining room. The DON said the RN was primarily scheduled to work on a different floor or a different hall than where Resident #16 resided, but between staffing shortages and call ins there were times he was scheduled to work on the resident's hall. She said she would need to improve communication with the scheduler to help limit RN #6 on Resident #16's hall. The DON said no additional supervision over RN #6 was implemented after it was determined he verbally abused the resident, or after the RN was found in the resident's room or after the resident expressed the continued feelings of intimidation. The DON said she just did routine floor checks daily. The DON said she was waiting for the completion of the external investigation that was still in process before proceeding with additional corrective action such as training. She said she provided verbal education with the RN but should have provided him more intensive written education on abuse and communication. The DON said residents identified as at-risk adults should have a care plan directing staff what to look for, changes in behaviors, signs of potential abuse, and care plans should indicate to staff why the resident was at risk and how to address the risk. The DON confirmed the resident was identified at risk for abuse, as stated in the abuse investigation. The DON said Resident #16 should be care planned for risk and was not sure why a care plan was generated. The DON said moving forward, the facility would ensure more focused education and competency of the education would be implemented immediately after, or before the staff member was allowed to return to work. The DON said to help prevent potential future abuse on Resident #16 and other facility residents, the facility would improve their education, attempting to make it more user friendly and comprehensive. She said she would work with the staff scheduler to limit the times a resident had to be around a staff member who they felt uncomfortable with and review the daily schedule. The DON said she would continue to spend time with the residents and remind them they can report anything to her. The DON and the NHA said they would work on being even more involved in resident care. The social service director (SSD) was interviewed on 2/14/22 at 10:57 a.m. The SSD said when residents express concerns or feel abused by staff, she would make sure the DON and the NHA were made aware. The SSD said she would listen to the resident and validate his feelings. She said the facility needed to know when residents were upset and did not feel safe, so we could do something about it. The SSD said a plan would be put in place to include meeting with the resident regularly, reassuring them that they were safe, heard, and understood. She said her visits were not always documented, but she would continue to check in the resident. The SSD said Resident #16 was readmitted to the facility a few months ago because he felt lonely and people did not have time for him when he was at home. He was happy to return to the facility and was not someone who would normally complain about staff. The SSD said she approached Resident #16 and asked him what was bothering him. The resident said a nurse (RN #6) was invading his conversation with his POA. Resident #16 said the RN said the resident was wrong and could be kicked out of the facility. The resident said the RN would not allow him to speak and felt he was talked down to. He expressed he did not feel supported by the RN. She said no one should feel like that. The SSD reassured the resident his home was not in jeopardy and he would not have to have contact with the RN anymore. The SSD was informed Resident #16 has had to have additional contact with RN #6. The SSD said the resident should not have to have contact with the RN until he felt safe and the situation was resolved. The SSD said the RN should not have approached the resident regarding speaking to his POA. She said the resident had every right to talk to his POA. She said resident rights were reviewed with staff at least once or twice a year. She said all staff should have a good understanding of resident rights. The SSD said at risk care plans were to identify when someone has had an incident of abuse or potential abuse. She said interventions included having direct staff to listen to the residents and help with any situations that may arise. She said each at risk care plan would be individualized based on what each identified resident would need support with. The SSD reviewed Resident #16's care plan and confirmed he did not have an at risk care plan but should have. She said she would meet with her team and find out what the plan was for Resident #16, including checking the schedule of where RN #6 worked. The SSD said she would update his care plan and visit with Resident #16 to ensure he felt comfortable with the interventions and knew that he could speak to his POA at any time. The SSD she would check in with Resident #16 daily to ensure the resident felt safe, supported, and his concerns were validated. V. Facility follow-up An at risk care plan was initiated on 2/14/22. The care plan read Resident #16 was at risk for feelings of possible displacement in living arrangements as evidenced by feeling insecure and not feeling validated. Interventions included: -Staff would address any concerns/feelings of discomfort in his environment. -Staff would allow Resident #16 to express feelings, concerns and fears while offering support and validation. -Staff would monitor him for changes in mood, behavior, and/or isolation. -Staff would offer mental health as needed or allowed. -No documentation was provided before survey exit on 2/14/22 or 24 hours after regarding any further education or corrective action for RN #6 (he was on vacation during the survey).
CONCERN (D)

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

Resident Rights (Tag F0550)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews and record review, the facility failed to ensure each resident was treated with dignity and re...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews and record review, the facility failed to ensure each resident was treated with dignity and respect and cared for in a manner and in an environment that promoted maintenance or enhancement of quality of life for one (#10) of one resident reviewed for dignity out of 21 sample residents. Specifically, the facility failed to ensure Resident #10 was positioned correctly at the dining room table and while she received care from staff during meals. Findings include: I. Facility policy and procedure The Promoting/Maintaining Resident Dignity During Mealtimes policy, dated 2/10/22, was provided by the nursing home administrator (NHA) on 2/10/21 at 5:20 p.m. The date on the policy was the same date the policy was requested from the NHA. It documented the practice of this facility was to treat each resident with respect and dignity and care for each resident in a manner and in an environment that maintained or enhanced his or her quality of life, recognizing each resident's individuality and protecting the rights of each resident. It documented that all staff members involved in providing feeding assistance to residents should promote and maintain resident dignity during mealtimes. It documented staff should assist the resident with opening condiment packages, cutting necessary food items, such as ensuring each resident could see and reach their food and beverages. II. Resident #10 A. Resident status Resident #10, age [AGE], was admitted on [DATE]. According to the February 2022 computerized physician orders (CPO), diagnoses included hemiplegia and hemiparesis following cerebral infarction, dementia with behavioral disturbance, anxiety disorder, depressive episodes and dependence on her wheelchair. The 11/18/21 minimum data set (MDS) assessment revealed the resident had no cognitive impairment with a brief interview for mental status (BIMS) score of 15 out of 15. It documented the resident required supervision with set-up for her meals. B. Resident observations Resident #10 was initially observed on 2/8/22 at 12:14 p.m. She was petite, measuring 5 ' 3 who was seated in her wheelchair at a table in the first floor dining room. She was positioned at the table with her head below the level of the table's top. She was struggling to reach her food and drinks at this time. No staff was observed assisting the resident at this time. -At 12:20 p.m., the resident was seated at the dining room table with her head at table top level. She was having difficulty spooning her ice cream out of her dessert bowl. No staff were observed assisting the resident at this time. -At 12:33 p.m., the resident was observed rolling her wheelchair back and forth at the table in order to reach her food and drinks. She was observed hitting the top of her head on the side of the table. Certified nurse aide (CNA) #2 told the resident she was smacking her head on the table and telling the resident to be more careful. She did not ask the resident if her head was okay or assist the resident in any manner. She then walked away from the resident. Resident #10 was observed on 2/9/22 at 9:12 a.m. She was positioned at the dining room table with her forehead level with the table top. She was having difficulty reaching up to get her glass of juice. No staff was observed assisting the resident at this time. Resident #10 was observed on 2/10/22 at 8:20 a.m. She was seated at the dining room table, leaning slightly towards the left. Her forehead was at the level of the table top and the resident was having difficulty reaching her hot cocoa. She was observed from 12:20 p.m. through approximately 12:30 p.m., occasionally rolling her wheelchair back and forth at the dining room table. She was observed pulling herself forward in her wheelchair in order to reach her dinner roll. She dropped her spoon on the floor and called for CNA #3 to get her another spoon. The resident then propelled her wheelchair backwards out of the dining room. She returned to the dining room at approximately 12:23 p.m. At 12:25 p.m., CNA #3 was observed standing over the resident and was watching her eat a bite of blueberry cobbler off the table top after the resident had dropped it on the table. The CNA did not assist the resident with her dessert or try to prevent her from eating off the dirty top of the table where two other residents were also seated. Resident #10 was observed on 2/14/22 at 10:00 a.m. She was seated at her table in the dining room. Her eyes were level with the table top. She was observed struggling to reach her hot chocolate cup and to eat the oatmeal in her bowl. -At 11:10 a.m., staff was observed positioning the resident at an activity table in the common area. Her head was below the top of the table. -At 12:30 p.m., the resident was observed at the dining room table with her head below the level of the table top. C. Resident interview Resident #10 was interviewed on 2/10/22 at 8:20 a.m. She said she was seated so low at the dining room table that she sometimes hit her head on the tabletop reaching for her food. She said the facility had provided her a lower table in the past, but it had been sometime since they used it. She said she would like the lower table again for easier access to the food when eating. Resident #10 was again interviewed on 2/14/22 at 10:00 a.m. She said her positioning at the table was pretty uncomfortable. When asked if, besides the comfort level, she felt the positioning was undignified for an adult, she said, It's not really dignified, but I'm used to it. D. Record review Resident #10's care plan related to positioning, dated 2/9/22, documented the resident had limited physical mobility. The limitations were due to contractures and having sustained a previous stroke. The goal of this care plan was for the resident to remain free of complications related to immobility. The positioning schedule documented that the resident was to be up in her wheelchair for meals. III. Staff interviews The occupational therapist (OT) was interviewed on 2/10/22 at 10:35 a.m. He said the therapy department had previously attempted to use a lap tray for Resident #10 when she was dining, but the resident refused the tray. He said the table the resident always sat at had already been lowered as far as it could go. He said he did not want to give her a lower table because the more they compensate for her poor positioning, the less she would attempt to sit tall, which he felt she had the ability to do. He said the interdisciplinary team said Resident #10 had decompensated with her ability to position herself in the last week or so for some reason and he had a new screening request in to re-evaluate the resident for needing more assistance with her meals. -As of the survey's exit on 2/14/22 at 5:15 p.m., the OT had not completed his re-evaluation of the resident's assistance needs during meals. Registered nurse (RN) #6 was interviewed on 2/14/22 at 10:10 a.m. She said the dining room table was too high for Resident #10. She said the facility had another smaller-sized resident in the past and restorative therapy gave her a lap tray for her wheelchair that she could eat off of. She said Resident #10 refused to sit in a regular dining room chair and wanted to eat in her wheelchair. She said she did not know if restorative therapy had tried a lap tray for this resident, but felt she needed a smaller table because the resident had a lot of difficulty positioning herself at the table. She said she did not feel the resident was currently being positioned at the table in a dignified manner. She said the interaction with CNA #2 was poor because the staff should have stopped to ask the resident if she was okay when she hit her head on the table top and should have assessed for the resident's lethargy, having felt the resident must have fallen asleep at the table if she hit her head on the table top. The registered dietitian (RD) was interviewed on 2/14/22 at 12:30 p.m. She said she had brought Resident #10's poor positioning at the dining room table to the therapy department about a month ago. She said therapy tried a bedside table at the main table shortly before lunch was served this date and the resident did not want anything to do with that table. She said the resident's power of attorney (POA) was present and tried to encourage the resident to try the table, but the resident did not like something about the table. She said the dining table was at the lowest position already, but the resident looked like her positioning was even more slumped than she was a week and a half ago. She said she sent a message to the therapy department with her concerns, but felt the facility had to get creative with positioning for this resident. She said she and the restorative nurse brought up the possibility of using a computer table, which could be attached underneath the table and could adjust up or down for the resident. The RD said she did not feel this resident was appropriately positioned at the table because she could not even see her food and drinks at times and acknowledged this was a dignity issue for the resident. She said the resident's weight was stable despite the positioning issue. The NHA was interviewed on 2/14/22 at 3:21 p.m. She said she would have a conversation with the OT about Resident #10's physical ability to sit up straighter. She said she thought the facility needed to figure out something to make the resident more comfortable at meals. She said if the resident was uncomfortable and felt her positioning at the table was undignified, it was not okay. She said it was hard to find adaptive equipment that Resident #10 would accept because the resident did not want to be different. She said, we need to figure something out for her.
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 observations, interviews and record review, the facility failed to provide the highest practicable quality of care for ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews and record review, the facility failed to provide the highest practicable quality of care for one (#40) out of two residents reviewed for skin conditions or injuries out of 21 sample residents. Specifically, the facility failed to for Resident #40 ensure the resident had proper protection of her right heel wound to promote healing. Findings include: I. Professional Reference The NPUAP Pressure Injury Stages | The National Pressure Ulcer Advisory Panel - NPUAP. The National Pressure Ulcer Advisory Panel NPUAP. Web. (2/4/2018), retrieved on 2/18/22, rehttp://www.npuap.org/resources/educational-and-clinical-resources/npuap-pressure-injury-stages reads: A pressure injury is localized damage to the skin and/or underlying soft tissue, usually over a bony prominence as a result of pressure, or pressure in combination with shear. The updated staging system includes the following definitions: -Stage 1 Pressure Injury: Intact skin with a localized area of non-blanchable erythema. -Stage 2 Pressure Injury: Partial-thickness skin loss with exposed dermis. The wound bed is viable, pink or red, moist, and may also present as an intact or ruptured serum-filled blister. Adipose (fat) is not visible and deeper tissues are not visible. Granulation tissue, slough and eschar are not present. These injuries commonly result from adverse microclimate and shear in the skin over the pelvis and shear in the heel. -Stage 3 Pressure Injury: Full-thickness skin loss. Full-thickness loss of skin, in which adipose (fat) is visible in the ulcer and granulation tissue and epibole (rolled wound edges) are often present. Slough and/or eschar may be visible. If slough or eschar obscures the extent of tissue loss, this is an Unstageable Pressure Injury. -Stage 4 Pressure Injury: Full-thickness skin and tissue loss. Full-thickness skin and tissue loss with exposed or directly palpable fascia, muscle, tendon, ligament, cartilage or bone in the ulcer. Slough and/or eschar may be visible. If slough or eschar obscures the extent of tissue loss this is an Unstageable Pressure Injury. -Unstageable Pressure Injury: Obscured full-thickness skin and tissue loss. Full-thickness skin and tissue loss in which the extent of tissue damage within the ulcer cannot be confirmed because it is obscured by slough or eschar. If slough or eschar was removed, a Stage 3 or Stage 4 pressure injury will be revealed. II. Facility standards The Wound Treatment Management policy, dated 1/5/22, was provided by the nursing home administrator (NHA) on 2/10/22 at 2:19 p.m. It read in pertinent part, To promote wound healing of various types of wounds, it is the policy of the facility to provide evidence-based treatments in accordance with the current standards of practices and physician orders .Wound Treatment will be provided with physician orders, including the cleansing method, the type of dressing, and frequency of the dressing change. III. Resident status Resident #40, age [AGE], was admitted [DATE]. According to the February 2022 computerized physician orders (CPO), diagnoses included chronic obstructive pulmonary disease, pressure ulcer to right buttock (on admission), type two diabetes mellitus with diabetic peripheral angiopathy without gangrene, hereditary and idiopathy (neuropathy), unspecified. According to the 1/27/22 minimum data set (MDS) assessment, the resident was cognitively intact with a brief interview for mental status (BIMS) score of 15 out of 15. She required extensive assistance of two or more persons for bed mobility, transfers, dressing, and toileting. Resident #40 required extensive assistance of one person for personal hygiene and locomotion. The MDS coded a pressure ulcer to her buttocks present on admission, her heel was not indicated. IV. Resident interview and representative interview Resident #40 was interviewed on 2/9/22 at 10:35 a.m. She said she spent a good portion of everyday in her wheelchair and out of bed. Resident #40 said she had a wound on her right foot. She said the last couple of days, her foot was feeling better since the staff provided her with a new boot to take the pressure off. The husband of Resident #40 was interviewed on 2/14/22 at 9:36 a.m. He said Resident #40 wore a foam boot at night to take off the pressure of foot when she was in bed. He said last week (2/8/22), she started wearing a different boot during the day to protect her heel. He said the new boot has seemed to help her with the pain from her heel. V. Observation and interview Resident #40's wound care was observed on 2/10/22 between 9:33 a.m. and 9:45 a.m. The wound care was conducted by the registered nurse (RN) #2. RN #2 applied Vashe cleanser on new gauze and removed the old dressing from the right heel of Resident #40. Dried yellow old skin was on the surface of the dressing. Observations of the heel identified two distinct wounds. The first wound/injury was on the posterior (back) part of her heel. The second wound/injury was located on her lower ankle. The lower ankle wound revealed black eschar in the bed. The lower heel wound was pink with granulation and did not have measurable depth. RN #2 said she did not know how the wounds developed but she confirmed they developed at the facility as originally a large wound. RN #2 said she could not identify the stages of the injury without looking at the stage chart. During the wound care with RN #2, potential contamination of the wounds were identified. RN #2 placed the new clean dressing and two tubes of Iodophor ointment directly on the seat of the resident's wheelchair before applying the treatments. The RN did not initiate hand hygiene after she removed the old dressing of the heel, doffed her old gloves and donned new gloves to cleanse and apply new dressing over the wounds (cross-reference F880 for infection control). VI. Record review The skin injury risk care plan, initiated 1/27/22 and revised on 2/10/22, read Resident #40 was at risk for potential/actual impairment to her skin integrity including MASD (moisture associated skin damage), skin tears and /or pressure injuries related to edema, fragile skin, balance issues and incontinence. The care plan identified the resident had a large fluid filled intact blister on her right heel. The care plan also identified the blister ruptured without changes in wound care. Care planned interventions implemented on 1/27/22 read: -Heel elevating boot to be worn while in bed to promote skin integrity related to edema and right heal blister. -Monitor/reposition bilateral extremities (BLE) as needed and at least every two hours while in bed to ensure heels were elevated on a pillow or cushion. -Pressure relieving/reducing mattress to protect the skin while in bed. The care plan intervention on 2/1/22, directed staff to refer to orders for the current wound treatment plan. -The care plan did not include the use of a protection boot to her right foot when the resident was not in bed. The 1/20/22 admission assessment for Resident #40 did not identify concerns with her right heel. The 1/21/22 weekly skin assessment identified Resident #40's heels were red but blanchable indicating no development of injuries/wounds to her right heel. The 1/25/22 skin/wound note read Resident #40 had a blister to her right heel. According to the note the wound nurse notified. The note did not identify the changes to the resident's care. The 1/26/22 OT treatment note read the resident was provided an updated wheelchair to allow for better bilateral lower extremity contact with the ground for self-propelling with bilateral lower extremities. Education completed on using bilateral lower extremities and bilateral upper extremities to self-propel manual wheelchair. The resident was able to use the manual wheelchair for approximately 15 feet in the room. -The OT note did not include precautions related to the 1/25/22 identification of the resident's right heel blister. The 1/26/22 at 2:13 p.m. skin/wound note read the wound nurse assessed the resident's heel and what appeared to look consistent with a blister. According to the note, the wound nurse instructed the registered nurse on dressing the site on the right heel. The note identified an application of Betadine was placed on the site. A foam heel covering was placed over and secured with hypafix. The note indicated the heel was tender to touch. The 1/26/22 skin/wound note created by the wound nurse read she was assessed to Resident #40's right foot/heel. The wound described the area of concern as a large blister measuring 4x6 centimeters (cm). The blister was fluid filled and intact. According to the note, the resident reported pain in the area with pressure and palpation. The note indicated that wound care orders were written and the registered nurse and therapy was notified. Heel elevator boots were requested to alleviate pressure while in bed. According to the note, the resident prefered to spend most of her time lying down and/or sleeping. An air mattress was put in place while lying down for pressure prevention and offloading. The 1/27/22 skin/wound note read betadine and a heel protector in place. The note described the blister as intact. According to the note, the resident helped by elevating her legs. The resident was educated to keep her legs off the floor. The 1/27/22 OT treatment note read the resident participated in the function transfer training to wheelchair from recliner. The 1/30/22 and the 1/31/22 skin/wound note read Resident #40's right heel bandage was removed, the blister was swabbed with Betadine and a new bandage was applied. According to the notes, the resident tolerated the wound care well with no pain or discomfort. The 1/31/22 OT treatment note read the resident continued to rest by lateral lower extremities off of the foot pedals and on the back of heels where she had a blister on her right lower extremity. According to the note, she had improved with self-propelling with a manual wheelchair with no foot pedals. She requires foot pedals for transport with caregivers. The note read education was provided to staff to cue the resident to rest her bilateral lower extremities on the foot pedals and not off of the pedals. The 2/1/22 skin/wound note created by the wound nurse, read the right posterior heel blister continued to be intact and fluid filled. According to the note, the blister measured 6x6 cm. Interventions continued to include a heel flotation cushion in place when the resident was lying in bed to avoid pressure to the area and continued use of an air mattress for pressure prevention and offloading. The note indicated the resident was educated by the wound nurse as well as therapy on the importance of not placing pressure on the blistered area. According to the note, the resident verbalized understanding. The note identified the resident did not receive compression to the right lateral extremity as an effort to keep the blister intact. The note indicated that therapy and the registered dietitian were aware of the wounds and were implementing necessary interventions. The wound physician was consulted for additional treatment options for the heel. The note read the physician did not recommend new interventions at that time. The review of the 2/1/22 wound measurement, according to the skin wound note, identified the blister increased in size between 1/26/22 and 2/1/22. The 2/2/22 OT treatment note read the resident was measured for the right lower extremity podus boot for heel protection during transfers for skin integrity. Education was completed with staff regarding recommendations for functional transfers. The positioning in the wheelchair interventions was completed to include foot rest adjustments. The OT note read Resident #40's blister on the right lower extremity, per wound care, was not improving. The care plan and the orders were updated to include no ambulation and weight bearing for transfers at the time of the OT note on 2/2/22. The 2/2/22 skin/wound nurse note read an Allevyn heel protector dressing was placed on the right heel and secured with tape. The note identified the heel as a blood blister. According to the note, the fluid filled area covered the entire heel. The 2/3/22 skin/wound note read the resident's right heel dressing was removed with no drainage noted on the dressing. The heel was covered with a large blister encompassing all of the heel. The heel was swabbed with Betadine and allowed to air dry. An Allevyn heel protector was applied on her heel with a sock over her foot and the heel protector. According to the note, the resident denied pain at the site. The note identified the blister bed appeared to be dry and was still intact. The 2/5/22 skin/wound note read the wound was on the bottom and up the back side of the heel. It was covered in white thick peeling skin, with a slight odor and the surrounding skin was pink in color. According to the note, the resident complained of tenderness when removing and applying the new dressing. The 2/6/22 at 2:13p.m. skin/wound note read the resident had a dressing change and treatment per orders to the right heel. The skin is whitish in color and peeled back slightly. The 2/6/22 at 9:53 p.m. read Resident #40's right heel was missing the Allevyn heel dressing and tape. According to the note, the blister appeared to have ruptured and the resident had dried blood and peeling skin above the blister. The wound bed was described as dark red with dried skin peeling around it. The review of the note identified the blister ruptured during the same time period of the missing dressing. The 2/7/22 OT treatment note read adjustments were made to the resident's wheelchair pedals to decrease pressure on the right foot and heel. The 2/7/22 skin/wound note created by the wound nurse described the right heel blister as denuded and no longer fluid-filled. The wound bed was pink with two darker areas within. The proximal darkened area measured 1.5 x 2 cm with no measurable depth. The distal darkened area measured 2.5 x 2.5 cm with no measurable depth. According to the note, the total denuded area measures 6 x 5.5 cm with partial thickness and a scant amount of blood. The note indicated the resident reported tenderness to the entire area. The 2/8/22 OT treatment note read the resident was fitted with a shield protection boot on the right low extremity to protect the blister while sitting in the wheelchair and during functional transfers. The 2/8/22 skin and wound note read changes to the right heel blister treatment were made on 2/8/22 with new orders placed. The January 2022 CPO was reviewed for Resident #40. The order summary read as follows: The 1/27/22 order read the resident was to wear a heel elevating boot while in bed to promote skin integrity related edema and right heel blister. According to the order, staff were to monitor/reposition her bilateral extremities as needed and at least every two hours while lying in bed to ensure heels are elevated on a pillow or cushion on every shift for pressure prevention and wound healing. The 1/31/22 order read to change position every two hours during the day and elevate bilateral lower extremities when available and every two hours. The order on 2/2/22 read the resident was not to be weight-bearing on her right lower extremity except for transfers and a sit to stand mechanical light. The 2/8/22 order read to apply Iodosorb Gel 0.9 % (Cadexomer Iodine) to the right heel topically one time a day for the denuded blister. The 2/8/22 order instructed staff to monitor placement of Allevyn heel dressing q (every) shift and replace and/or secure as needed on every shift. The 2/9/22 new order for wound care for the right heel denuded blister read to apply Vashe wash and allow the site to dry. Cover with Allevyn gentle border heel dressing and daily and report changes or concerns to physician and wound nurse once a day. The 2/9/22 order read the resident was to wear a heel protection boot on the right lower extremity when out of bed. The order was placed after the blister had ruptured and after two wounds under the blister were identified. VII. Interviews RN #7 was interviewed on 2/9/22 at 12:20 p.m. Resident #40 often would drag her foot when she was in her wheelchair. She said the dragging created a blister. RN #7 said the blister had opened and now caused her pain. The RN said a new boot has been placed on the right foot for protection. She said 2/9/22 was the first day she was aware of the new boot. RN #5, who was the certified wound nurse, was interviewed on 2/10/22 at 1:12 p.m. The RN said therapy witnessed one of the areas on the heel was caused by her foot pressing against the foot pedal. She said the observation prompted therapy to fit Resident #40 with the podus boot. RN #5 was interviewed again on 2/14/22 at 1:45 p.m. RN #5 said she first observed the blister on 1/26/22. She said pressure relieving interventions were put in place. She said she felt the interventions and care provided to Resident #40 was appropriate. She said she did not consider the wound to the heel as two separated wounds even though she was recording measurements to the two separate areas because both areas were on the resident's heel and were both treated the same. She said she weekly assessed the wound. The RN said the heel would have only been staged if the wound/injury was from pressure. RN #5 said the wound was caused by friction and rubbing from her foot sliding in her sock and on the ground, creating a fluid filled blister. She determined the wound was caused by friction therefore the wound was not a pressure injury; however, as identified in the above progress notes, opportunities for pressure on the right heel were present. RN #5 said the only protection over the heel when the resident was up and out of her wheelchair was a protective cup/covering over her heel until she was fitted with a new podus boot from therapy. The wound nurse identified that no additional protective measures to the heel were put in place between the time the blister was identified on 1/25/22 and 2/8/22, when the podus boot was implemented other than a thin protective cup. The occupational therapist (OT) was interviewed on 2/14/22 at 2:22 p.m. The OT said a protective boot was implemented when Resident #40 so she could bear some weight and to reduce friction on her foot. He said the resident was frequently up and was observed to take her foot on and off her foot pedal. He said she tried to adjust the pedals to be more conducive to her not having her heel resting directly on the top of the pedal. He said he placed an order for the podis boot but she had to wait for it to arrive. The boot was fitted the following week on 2/8/22. He said the resident wears the boot (since 2/8/22), when she was out of bed, in her wheelchair and during therapy. The OT said prior to the podus boot, there was no weight bearing activities till the boot arrived to protect Resident #22's heel. The director of nursing (DON) was interviewed on 2/14/22 at 4:28 p.m. The DON said the physician assistant (PA) saw the heel on 2/10/22 via telehealth. The DON said the PA did not indicate the wound was a pressure injury at that time. The DON said a wound could start out from friction and exacerbate into a pressure injury. She said a darkened area on a wound could represent a pressure injury.
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 observations, interviews and record review, the facility failed to maintain an infection control program designed to prevent the spread of infection during wound care for one (#40) of one res...

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Based on observations, interviews and record review, the facility failed to maintain an infection control program designed to prevent the spread of infection during wound care for one (#40) of one resident with wounds, of 21 sample residents, and during the medication administration observation for one of four nurses. Specifically, the facility: -Failed to implement appropriate hand hygiene practices, glove use and sanitary conditions while providing wound care for Residents #40; and, -Failed to implement appropriate hand hygiene practices and glove use during medication administration. Findings include: I. Unsanitary wound care A. Professional standard According to the Centers for Disease and Prevention (CDC) Hand Hygiene in Healthcare Settings, last up updated 1/8/21, retrieved from https://www.cdc.gov/handhygiene/providers/index.html, on 2/17/22, included the following recommendations: Multiple opportunities for hand hygiene may occur during a single care episode. Following are the clinical indications for hand hygiene: Use an alcohol-based hand sanitizer immediately before touching a patient, before performing an aseptic task (e.g., placing an indwelling device) or handling invasive medical devices, before moving from work on a soiled body site to a clean body site on the same patient, after touching a patient or the patient's immediate environment, after contact with blood, body fluids or contaminated surfaces, and immediately after glove removal. Wash with soap and water when hands are visibly soiled, after caring for a person with known or suspected infectious diarrhea, and after known or suspected exposure to spores. When using alcohol-based hand sanitizer, put the product on hands and rub hands together. Cover all surfaces until hands feel dry. This should take around 20 seconds. B. Facility policy and procedure The Handwashing Procedure policy, dated September 2019, was provided by the infection control nurse (ICN) on 2/10/22 at 5:28 p.m., and included the following guidance: For effective hand hygiene in order to prevent the transmission of bacteria, germs, and infections, all staff shall use the hand-hygiene techniques in the following procedure. Clinical contact requires hand hygiene and will be completed before and after every clinical contact (e.g., medication pass, vital signs, transfer assistance, incontinence care). Employees should also perform hand hygiene before applying gloves to perform a procedure, after removing gloves, after working on a contaminated body site and then moving to a clean body site on the same resident, and after coming in contact with bodily fluids and dressings. C. Wound care observations for Resident #40 1. Right heel The right heel wound dressing change was observed on 2/10/22 at 9:32 a.m. with registered nurse (RN) #2 while the resident was in the tub room after being bathed. The following was observed: At 9:33 a.m., RN #2 performed hand hygiene with alcohol-based hand rub (ABHR) and donned a clean pair of gloves. She removed the right heel dressing that contained dead skin and serous drainage and discarded it. At 9:34 a.m., RN #2 doffed her gloves and donned a clean pair without performing hand hygiene. At 9:35 a.m., RN #2 cleansed the two wounds on the resident's heel, then doffed her gloves and performed hand hygiene with ABHR. At 9:38 a.m., RN #2 donned a clean pair of gloves and placed the clean dressing that would be applied to the wound and two tubes of ointment directly on the seat cushion of the resident's wheelchair. She did not place a clean surface down first to provide a sanitary place to set the dressing supplies. The RN applied the ointment and clean dressing to the wound and doffed her gloves. 2. Right gluteal fold/coccyx The right gluteal fold/coccyx wound dressing change was observed on 2/10/22 at 9:48 a.m. with RN #2 and the following was observed: At 9:48 a.m., RN #2 washed her hands at the sink and donned a clean pair of gloves. She assisted the bath aide to prepare the resident to stand up using the sit-to-stand lift, and touched the lift, the resident's shoulders, and sling with her gloved hands. At 9:53 a.m., RN #2 cleansed the open wound with the same-gloved hands, without changing her gloves or performing hand hygiene. At 9:57 a.m., RN #2 picked up the ointment from the wheelchair seat and applied it to the wound, then placed a clean dressing over it. She placed the two tubes of ointment back inside of the resident's personal wound care supply box with the other clean dressing supplies, without cleaning or sanitizing them. She doffed her gloves and performed hand hygiene with ABHR. 3. RN #2 interview RN #2 was interviewed on 2/10/22 at 12:30 p.m., and she said she routinely worked with Resident #40. She explained that during the dressing change for the resident's heel, she removed the old soiled dressing, doffed the gloves she was wearing, and did not perform hand hygiene prior to donning a clean pair of gloves, and she said she should have. She said when she placed the tubes of ointment directly on the seat of the wheelchair; she cross-contaminated the tubes and should have put down a clean surface to lay them on, or at least wiped them off before she put them away. She said she did not normally change the wound dressings in the tub room, but instead in the resident's room where she had a table with a surface to put her dressing change supplies on. RN #2 said she remembered she used the same gloves to assist the resident to stand up using the lift because she was nervous about the resident's strength, so she was helping her. She said she should have doffed the dirty gloves and performed hand hygiene prior to donning a clean pair of gloves and cleansing the wound. II. Hand hygiene and glove use during medication administration A. Facility policy and procedure The Medication Administration policy and procedure, dated 1/5/22, was provided by the ICN on 2/10/22 at 5:28 p.m., and included the following guidance: Medications were to be administered in a manner to prevent contamination or infection, which included perform hand hygiene prior to and following administering medications. B. Medication administration observation RN #4 was observed preparing and administering medications on 2/8/22 at 3:46 p.m. for Resident #22. RN #4 donned a pair of clean gloves without performing hand hygiene, then touched the medication cart drawer and pulled it open. She touched multiple medication blister pack cards, two boxes of dairy aide, and a container of Tiger Balm ointment, then poured Lactaid tablets, Tylenol and Tamsulosin into a soufflé cup without doffing the gloves or performing hand hygiene. With the same gloves, the RN touched the mouse for the computer, removed a drinking cup from a stack and poured water from a pitcher into the cup. She took the medications and water to the resident and administered them to him without doffing the gloves or performing hand hygiene. The RN doffed her gloves at 3:57 p.m. and did not perform hand hygiene. C. RN #4 interview RN #4 was interviewed on 2/8/22 at 4:00 p.m., and she said she had worked at the facility for approximately one and a half months. She said any time she was passing medications; she wanted to make sure she wore gloves so that she did not touch the pills. She said she did not routinely change gloves after touch drawer pulls, medication cards or other items in the medication cart, or sanitize her hands in between, and said she probably should. She said she normally wiped down her medication cart with alcohol pads prior to beginning any medication administration during her shift. III. Director of nurses (DON) interview The interim director of nurses (IDON) was interviewed on 2/10/22 at 2:51 p.m., and she said during wound care, gloves should be changed and hand hygiene should be performed before the start of the procedure, after dirty dressings were removed, after the nurse completed the dressing change, and before they touched anything else. She said a designated clean surface or bedside tray should be used to place the dressing supplies on during the wound care process in order to prevent the spread of infection. She said a wheelchair seat was not a suitable surface to place wound care supplies because it was not an easily cleanable surface and was not an acceptable practice. She said the tubes of ointment should have been sanitized prior to returning them to the storage box to prevent cross contamination. The IDON said hand hygiene should be performed routinely during medication administration including before the nurse started the process, in between each resident, and when they were finished. She added that if the nurse touched something in between those opportunities, they should perform hand hygiene at that time as well, so they did not spread germs from resident to resident. She said nurses did not typically wear gloves during medication administration.
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

  • "What changes have you made since the serious inspection findings?"
  • "What safeguards are in place to prevent abuse and neglect?"
  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • Licensed and certified facility. Meets minimum state requirements.
Concerns
  • • Multiple safety concerns identified: Federal abuse finding, 2 life-threatening violation(s), 2 harm violation(s), $32,975 in fines. Review inspection reports carefully.
  • • 19 deficiencies on record, including 2 critical (life-threatening) violations. These warrant careful review before choosing this facility.
  • • $32,975 in fines. Higher than 94% of Colorado facilities, suggesting repeated compliance issues.
  • • Grade F (1/100). Below average facility with significant concerns.
Bottom line: This facility has a substantiated abuse finding. Extreme caution advised. Explore alternatives.

About This Facility

What is Colorado State Veterans - Rifle's CMS Rating?

CMS assigns COLORADO STATE VETERANS NURSING HOME - RIFLE an overall rating of 2 out of 5 stars, which is considered below average nationally. Within Colorado, this rating places the facility higher than 0% of the state's 100 nursing homes. A rating at this level reflects concerns identified through health inspections, staffing assessments, or quality measures that families should carefully consider.

How is Colorado State Veterans - Rifle Staffed?

CMS rates COLORADO STATE VETERANS NURSING HOME - RIFLE's staffing level at 5 out of 5 stars, which is much above average compared to other nursing homes. Staff turnover is 46%, compared to the Colorado average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Colorado State Veterans - Rifle?

State health inspectors documented 19 deficiencies at COLORADO STATE VETERANS NURSING HOME - RIFLE during 2022 to 2024. These included: 2 Immediate Jeopardy (the most serious level, indicating potential for serious harm or death), 2 that caused actual resident harm, and 15 with potential for harm. Immediate Jeopardy findings are rare and represent the most serious regulatory concerns. They require immediate corrective action.

Who Owns and Operates Colorado State Veterans - Rifle?

COLORADO STATE VETERANS NURSING HOME - RIFLE is owned by a government entity. Government-operated facilities are typically run by state, county, or municipal agencies. The facility operates independently rather than as part of a larger chain. With 89 certified beds and approximately 61 residents (about 69% occupancy), it is a smaller facility located in RIFLE, Colorado.

How Does Colorado State Veterans - Rifle Compare to Other Colorado Nursing Homes?

Compared to the 100 nursing homes in Colorado, COLORADO STATE VETERANS NURSING HOME - RIFLE's overall rating (2 stars) is below the state average of 3.1, staff turnover (46%) is near the state average of 46%, and health inspection rating (1 stars) is much below the national benchmark.

What Should Families Ask When Visiting Colorado State Veterans - Rifle?

Based on this facility's data, families visiting should ask: "What changes have been made since the serious inspection findings, and how are you preventing similar issues?" "What safeguards and monitoring systems are in place to protect residents from abuse or neglect?" "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?" These questions are particularly relevant given the facility's Immediate Jeopardy citations and the substantiated abuse finding on record.

Is Colorado State Veterans - Rifle Safe?

Based on CMS inspection data, COLORADO STATE VETERANS NURSING HOME - RIFLE has documented safety concerns. The facility has 1 substantiated abuse finding (meaning confirmed case of resident harm by staff or other residents). Inspectors have issued 2 Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death). The facility has a 2-star overall rating and ranks #100 of 100 nursing homes in Colorado. Families considering this facility should ask detailed questions about what corrective actions have been taken since these incidents.

Do Nurses at Colorado State Veterans - Rifle Stick Around?

COLORADO STATE VETERANS NURSING HOME - RIFLE has a staff turnover rate of 46%, which is about average for Colorado nursing homes (state average: 46%). Moderate turnover is common in nursing homes, but families should still ask about staff tenure and how the facility maintains care continuity when employees leave.

Was Colorado State Veterans - Rifle Ever Fined?

COLORADO STATE VETERANS NURSING HOME - RIFLE has been fined $32,975 across 1 penalty action. This is below the Colorado average of $33,409. While any fine indicates a compliance issue, fines under $50,000 are relatively common and typically reflect isolated problems that were subsequently corrected. Families should ask what specific issues led to these fines and confirm they've been resolved.

Is Colorado State Veterans - Rifle on Any Federal Watch List?

COLORADO STATE VETERANS NURSING HOME - RIFLE 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.