DUPAGE CARE CENTER

400 N COUNTY FARM RD, WHEATON, IL 60187 (630) 665-6400
Government - County 366 Beds Independent Data: November 2025
Trust Grade
85/100
#27 of 665 in IL
Last Inspection: August 2024

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

Overview

DuPage Care Center in Wheaton, Illinois, has a Trust Grade of B+, which indicates it is above average and recommended for care. It ranks #27 out of 665 facilities in Illinois, placing it in the top half, and #3 out of 38 in Du Page County, meaning only two local options are better. However, the facility's trend is worsening, as the number of reported issues rose from 6 in 2023 to 11 in 2024. Staffing is a strong point, with a 5/5 star rating and a low turnover rate of 22%, significantly better than the state average. While there are no fines on record, two concerning incidents were reported: a resident fell from a mechanical lift during a transfer that required two staff members, leading to serious injuries, and there were multiple failures in proper food handling and medication storage that could pose risks to residents. Overall, while the nursing home has notable strengths, families should be aware of the recent increase in issues and specific incidents of concern.

Trust Score
B+
85/100
In Illinois
#27/665
Top 4%
Safety Record
Moderate
Needs review
Inspections
Getting Worse
6 → 11 violations
Staff Stability
✓ Good
22% annual turnover. Excellent stability, 26 points below Illinois's 48% average. Staff who stay learn residents' needs.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most Illinois facilities.
Skilled Nurses
✓ Good
Each resident gets 73 minutes of Registered Nurse (RN) attention daily — more than 97% of Illinois nursing homes. RNs are the most trained staff who catch health problems before they become serious.
Violations
⚠ Watch
20 deficiencies on record. Higher than average. Multiple issues found across inspections.
★★★★★
5.0
Overall Rating
★★★★★
5.0
Staff Levels
★★★★★
5.0
Care Quality
★★★★☆
4.0
Inspection Score
Stable
2023: 6 issues
2024: 11 issues

The Good

  • 5-Star Staffing Rating · Excellent nurse staffing levels
  • 5-Star Quality Measures · Strong clinical quality outcomes
  • Low Staff Turnover (22%) · Staff stability means consistent care
  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record
  • Staff turnover is low (22%)

    26 points below Illinois average of 48%

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

The Bad

No Significant Concerns Identified

This facility shows no red flags. Among Illinois's 100 nursing homes, only 1% achieve this.

The Ugly 20 deficiencies on record

1 actual harm
Aug 2024 10 deficiencies
CONCERN (D)

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

Deficiency F0558 (Tag F0558)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to place call lights within reach of residents. This ap...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to place call lights within reach of residents. This applies to 3 of 3 residents (R145, R168, R155) reviewed for accommodation of needs in a sample of 37. The findings include: 1. On August 20, 2024 at 12:46 PM, R145 was brought back to her room with the assistance of V24 (CNA/Certified Nurse Assistant). V24 wheeled R145 towards the foot of the bed and left the resident in her wheelchair at the foot of the bed. R145's call light was lying across the center of the bed, out of reach of the resident. When asked, R145 said she needed to press the call light to ask for help. R145 tried to propel herself to reach the call light but was not able to reach her call light. R145 asked R168 to reach for her call light, and R168 was not able to reach the call light. At 12:54 PM, R145 was still attempting to reach for her call light but was unable to. R145's face sheet showed R145 was admitted with diagnoses including repeated falls, wedge compression fracture, cerebral ischemia, generalized anxiety disorder, age-related osteoporosis, and weakness. R145's POS (Physician Order Set) showed R145 was on Fall Precaution. R145's MDS (Minimum Data Set) dated July 5, 2024 showed R145 had moderate cognitive impairment. R145 needed substantial assistance from staff for toileting hygiene, showering/bathing, upper and lower body dressing, putting on/taking off footwear, and personal hygiene. R145's July 9, 2024 care plan showed she had an ADL (Activities of Daily Living) self-care performance deficit [related to] limited physical mobility, gait and balance impairments from dementia .with an intervention to Encourage the resident to use call button to call for assistance. R145's care plan also showed R145 was at high risk for falls [related to] cognitive impairment, musculoskeletal impairment from recent multiple fracture [status post] orthopedic surgery; psychotropic drug use; [history] of repeated falls, with an intervention to Be sure the resident's call light is within reach and encourage the resident to use it for assistance as needed. The resident needs prompt response to all requests for assistance. 2. On August 20, 2024 at 12:42 PM, R168 was sitting in her wheelchair with the tray table in front of her. R168's call light was on the bed but out of reach of the resident. At 12:46 PM, R145 asked R168 to reach for her call light, and neither resident was able to access their call lights. R168's face sheet showed she was admitted to the facility with diagnoses including hypertension, osteoarthritis, depression, and dementia. R168's MDS dated [DATE] showed R168 had severe cognitive impairment. R168 required moderate assistance from staff for personal hygiene, substantial assistance for toileting hygiene, shower/bathing, upper and lower body dressing, and was dependent on staff for putting on/taking off footwear. R168's care plan dated May 18, 2023 showed Be sure the resident's call light is within reach and encourage the resident to use it for assistance as needed. The resident needs prompt response to all requests for assistance. On August 22, 2024 at 1:01 PM, V33 (CNA) said the call light should be within reach to the resident. V33 said he clips it to their clothes or blankets, and it be in a place where they can press it. On August 22, 2024 at 1:04 PM, V34 (CNA) said the call lights should be within reach as well as within sight to the resident, and he usually clips the call light onto them. On August 22, 2024 at 1:09 PM, V25 (CNA) said the call light needs to go near the resident so they could reach it. On August 22, 2024 at 1:11 PM, V26 (RN/Registered Nurse) said the call lights should be in a place the resident could reach. On August 22, 2024 at 1:16 PM, V35 (RN) said the call light should be where the resident could reach, and some of the residents even tell the staff where to place the call light. V35 said the staff should clip it on top of the sheets within reach of the resident. On August 22, 2024 at 9:39 AM, V2 (DON/Director of Nursing) said the call light should be within the resident's reach for those who can move their hands. V2 said the call light should be clipped on their clothes or the sheets in a place that is accessible to the resident. V2 said the staff do call light assessments as needed and if there is a change in condition. V2 said the call light should still be within reach if the resident is alert but not oriented. The facility's Call Light Protocol reviewed February 2021 showed A working call light is to remain within reach of the resident at all times when they are in their room; if they are in bed, a wheelchair, a geri chair, the toilet or a commode. 3. On 8/20/24 at 1:42 PM, R155 was observed in her wheelchair leaning to her right side with her right arm hanging over the right armrest and she was crying. R155 said that her right arm was caught and when she tried to move it, it would cause her pain. The surveyor asked her if she could use her call light to call for help and she said no. R155's call light was observed at the head of the right side of the bed tied around the top bedrails and R155 was in her wheelchair on the left side of the bed behind the foot of the bed. The surveyor put the call light on so staff could come and assist R155. V14 (nurse) came in and had to remove the adapted device on R155's armrest to release R155's trapped arm. On 8/21/24 V14 (Nurse) said that on 8/20/24 at 1:42 PM, when she came to assist R155, R155's arm was trapped in her wheelchair and her call light was out of reach. On 8/21/24 at 10:46 AM, V21 (R155's husband) said that on 8/20/24, he had visited his wife from 10:45 am - 12:50pm and her call light was out of reach the whole time as it is every day. V21 said that R155's call light was tied to the bedrail at the top of the bed as it is every day and he did not move it.
CONCERN (D)

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

Report Alleged Abuse (Tag F0609)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to report allegations of verbal abuse within 24 hours. This applies to...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to report allegations of verbal abuse within 24 hours. This applies to 1 of 2 residents (R141) reviewed for abuse in a sample of 37. Findings include: R141 admitted to the facility on [DATE] with diagnoses that includes paraplegia, neuralgia, cramp / spasm, diverticulosis, hypertension, depression, anxiety, and insomnia. R141's MDS (Minimum Data Set) dated 7/17/24 shows he is cognitively intact with a BIMS (Brief Interview for Mental Status Score) of 15. On 8/20/24 at 11:48 AM, R141 stated V40, CNA (Certified Nurse Aide) verbally abused him by saying he was a bother and no other CNAs wanted to work with him. R141 stated, V2 DON (Director of Nursing) and V5 Social Services Manager were aware of his allegations from the previous week. On 8/20/24 at 12:10 PM, V5 stated she spoke to R141 on 8/17/24 regarding removing V40 CNA from his care team. V5 stated R141 did not like the way V40 positioned him in the wheelchair. V5 stated she did not ask R141 details as to why he no longer wanted to receive care from V40. V5 stated she informed R141 she was aware a service recovery (attempt by the facility to find a resolution for a dissatisfied resident) had been initiated by V6 Social Worker in the previous week. On 8/20/24 at 12:20 PM, V6 Social Worker stated she had spoken with R141 the previous week regarding V40 being mouthy and not placing him in his wheelchair correctly. V6 stated she did not ask R141 what he meant by V40 was mouthy. V6 stated she could not recall specific details of her conversation with R141. V6 stated on 8/19/24 V5 Social Services Manager informed her R141 claimed V40 was being abusive. On 8/20/24 at 3:48 PM, V2 DON (Director of Nursing) stated R141 left her a voice mail over the weekend accusing V40 of verbal abuse. V2 stated she reviewed the message on Monday 8/19/24. V2 stated V5 followed up with R141 regarding his allegation of abuse. V2 stated R141 had a service recovery regarding the care he received from V40 CNA the prior week. V2 did not know details regarding the service recovery. V2 stated staff doing a service recovery will ask the resident what their specific concerns are and attempt to address them. On 8/21/24 at 2:45 PM, R141 stated he had spoken to V6 Social Worker regarding his allegations against V40 the prior week. On 8/21/24 at 10:17 AM, V5 Social Services Manager stated she spoke to R141 on Saturday 8/17/24 while manager on duty. V5 stated R141 told her he no longer wanted V40 to provide his care. V5 stated R141 informed her V40 places him in his wheelchair in an uncomfortable position and told him he was a bother. On 8/22/24 at 9:34 AM, V40 CNA stated he was informed on Monday 8/12/24 that R141 complained and no longer wanted him to provide his care. V40 stated on Monday 8/19/24, V39 ADON (Assistant Director of Nursing) informed him of R141's allegations of abuse and suspended him. On 08/22/24 11:37 AM, V4 Assistant Administrator / Abuse Coordinator stated anyone in leadership can file a report for an abuse allegation including on the weekend as there is a manager on duty. V4 stated abuse allegations are to be submitted to the department of health within two hours. V4 stated verbal and mental abuse is a gray area. We file a report based on the allegations. We try to get details of a concern and if we can't get to the bottom of the concern within 2 hours, we file the report with the state. It is better for us to over report allegations rather than under report. R141 makes a lot of false allegations, and it has been a challenge for us. V4 stated the word bother isn't a word that is necessarily a trigger, but it is the perception of the individual. If someone says they are being abused, it should be reported. The voicemail V2 DON received on 8/19/24 is what triggered us to file the report of abuse. The facility service recovery report submitted by V6 Social Services states R141 expressed frustration with his CNA on the morning of Sunday 8/11/24. Immediate follow up / action take was to provide active listening and apologize to R141. Nursing to follow up as appropriate. A facility provided document dated 8/13/24 from V6 Social Services interview with R141 states V40 told him you're starting to bother me. An email dated 8/16/24 from V8 Head Nurse to V6 Social Services stated CNA was reeducated on customer service and removed from resident's care list. The initial report was submitted to IDPH (Illinois Department of Health) on 8/19/24. The facility policy Resident Abuse & Theft Prevention dated 10/2023 states the Administrator, abuse prevention coordinator or designee will be notified immediately of any reports of alleged mistreatment, neglect or abuse. The Administrator, Abuse Prevention Coordinator, Nursing Administration or designee will immediately send an initial report to IDPH.
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 reviews, the facility failed to properly monitor, assess and treat a resident who ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, and record reviews, the facility failed to properly monitor, assess and treat a resident who is at risk for potential pressure ulcers. The facility also failed to properly monitor, and assess 1 resident who is unable to reposition themselves. This applies to 2 of 2 residents (R104 and R155) reviewed for quality of care. Findings include: 1. R104 is a [AGE] year old female admitted to the facility on [DATE] with diagnosis including chronic kidney disease stage 3, type 2 diabetes, unspecified mental disorder, schizoaffective disorder, urinary tract infection, E coli, altered mental status, ataxic gait, difficult in walking, history of falls, pressure ulcer of sacral region stage 3, pressure ulcers of left buttock unstageable, metabolic encephalopathy, depression, cognitive communication deficit, hyperlipidemia, muscle spasms, acquired absence of digestive tract, artificial right hip and anxiety. On 8/20/24 at 11:31 AM, R104 was observed in her bed on her back and again at 12:10 PM she was observed on her back when V17 (Wound Nurse) and V18 (Wound Doctor) came into the room to provide wound care to R104's stage 3 pressure ulcer to her coccyx wound. R104's dressing to her coccyx wound was found with brown substance on it, and an area on R104's left buttock was found with redness and the skin was blistered in some areas. The doctor assessed the area and said that it was a new open wound 3cm X 3cm caused by incontinence of urine and stool. V17 then cleaned both wounds and applied the medicated ointment as prescribed by the doctor. On 08/22/24 at 11:30 AM, V2 DON (Director of Nursing) said that her expectation is that staff provide incontinent care every 2 hours and as needed to prevent skin breakdown. V17 said that R104's wound to her left buttocks is a MASD (moisture associated skin damage) from incontinences of urine and feces. V17 said that he expects the nursing staff to change the residents and keep them dry. V17 said that he provided wound care to R104 coccyx wound on 8/19/24 and the wound to R104's left buttock was present and look the same as it did on 8/20/24. R104's electronic record did not show any record of a wound to R104's left buttock on 8/19/24. R104's 8/20/24 skin/wound note showed wound assessed and measured. Treatment done on sites. No complaints of pain made. New treatment order made and carried out. R104's 6/4/24 order showed coccyx - cleanse with normal saline, pat dry period apply calcium alginate and cover with gauze island dressing daily and PRN everyday shift for wound care. R104's 5/2/2024 order showed nurse to evaluate residence wounds for treatments. R104's 8/6/24 MDS (Minimum Data Set) shows that R104 is dependent for toileting hygiene, and she is totally dependent on staff to roll from left to right. R104's 8/6/24 care plan showed that R104 has an ADL self-care performance deficit related to activity intolerance, limited mobility, limited range of motion, and poor endurance secondary to multiple medical chronic diagnosis such as kidney disease, diabetes mellitus, lipidemia, tachycardia, ataxia, and behaviors related to schizoaffective disorder and anxiety. R104's interventions included toileting hygiene physically dependent check and change large brief. R104's 5/24/24 care plan showed she has a potential for pressure ulcer development related to impaired mobility, activity intolerance, secondary to diagnoses of diabetes mellitus 2, anxiety, schizoaffective disorder, depressive type, muscle spasms, and incontinence. The goal is that the resident will have intact skin free of redness, blisters, or discolorations. The interventions or tasks include apply skin protectant after incontinent episodes, follow facility policy protocols for prevention or treatment of skin breakdowns, monitor nutritional status, provide assistance to turn or reposition at least every two hours more often as needed or requested, monitor bed pressure relieving air mattress, and monitor-skin observation. R104's 7/26/24 care plan also showed a returned status post hospitalization for hydronephrosis, UTI (urinary tract infection), with pressure ulcer to the coccyx stage 3 (5/7/24). The goals included the resident's pressure ulcer will show signs of healing and remain free of infection. the interventions and tasks include administer treatments as ordered and monitor for effectiveness, assess, record, and monitor wound healing, daily measure length width and depth where possible. Assess and document status of wound perimeter wound bed and healing progress. Report improvements and declines to medical doctor. Avoid positioning the resident on her back, monitor nutritional status, and monitor - skin observations. R104's 8/20/2024 wound evaluation & management summary showed Site 7 etiology (Quality) moisture associated skin damage. Duration - greater than 1 days, wound size 3 x 3 x 0.1 centimeters, surface area 9.0 centimeters. cluster wound open ulceration area of 4.50 centimeters, & skin 50%. Additional wound detail - patient has new irritation to left inferior buttock with overlapping area from previous pressure site. patient is at high risk for skin breakdown due to previous wound site and this skin integrity is weakened from scar tissue as well as urinary and fecal incontinence. Dressing treatment plan - zinc ointment apply once daily as needed for 30 days. Recommendations reposition per facility protocol, & offload wound. R104's 8/20/24 skin & Wound Evaluation MASD (moisture associated skin damage) acquired in-house, left gluteus 9.0cm X 3.0cm x 3.0cm Erythema: Redness of skin - may be intense bright red to dark red or purple, additional care: incontinence management, moisture barrier, moisture control, turning repositioning program, education of off-loading and repositioning. 2. R155 is an [AGE] year old female admitted to the facility on [DATE] with diagnoses including cerebral ischemia, vascular dementia, depression, panic disorder, essential hypertension, difficulty walking, arteriosclerotic heart disease, lower back pain, and a history of falling. On 8/20/24 at 1:42 PM, R155 was observed in her wheelchair leaning to her right side with her right arm hanging over the right armrest and she was crying. R155 said that her right arm was caught and when she tried to move it, it would cause her pain. R155's wheelchair had a large bolster on her right arm rest and a lateral support to the right upper back of the wheelchair. There was an open area on the right side of the wheelchair where the 2 adaptive pieces did not meet. This opening is where R155's right arm had fallen through, and she was unable to get her arm back out. The surveyor asked her if she could use her call light to call for help and she said no. R155's call light was observed at the head of the right side of her bed tied around the top bedrails and R155 was in her wheelchair on the left side of the bed behind the foot of the bed. The call light was out of reach. The surveyor turned R155's call light on and V14 (Nurse) came to assist R155 to get her arm out. V14 attempted to bring R155's arm back over the armrest but was unable to. R155 continued to cry out in pain when she would move her arm. V14 then was observed removing the right bolster/adaptive device from R155's wheelchair so that she could get R155's arm released. On 8/21/24, V14 said that R155's arm was trapped because of the bolster on her wheelchair. V14 said that she saw that R155 could not call for help because her call light was out of reach. On 8/21/24 at 10:46 AM V21 (R155's husband) said that on 8/20/24 he visited his wife from 10:45 am until 12:50 pm. V21 said that during that time R155's call light was tied to the bedrails at the top of the bed as it is every day, and he did not move it. V21 said that the call light is never in R155's reach and he visits her every day. V21 said that his wife's arm is trapped in her wheelchair every day and it causes her pain when she tries to move it out. V21 said that the staff are aware of this because they move her arm out of being trapped every day to put the sling for the mechanical lift on her so that they can toilet her. V21 said that this has been like this for a year ever since they put the bolster on her armrest. V21 said that it causes her pain, and it is every day. On 08/22/24 at 09:15 AM, V44 (Manager of Rehabilitation Services) said that R155's has diagnoses of dementia, history of falls, and weakness and that is what causes R155 to lean. V44 said that on 7/10/2023 R155 was given a high back wheelchair with a bolster on the right armrest, and on 5/2024, R155 had increase weakness and leaning, and the facility added the right lateral support to her wheelchair. V44 said that since R155 has had the increased leaning she has been unable to reposition herself. V44 said that when R155 comes down for services at physical rehab she is leaning, and they have to reposition her. V44 said that she had not received any reports that R155's arm was being caught between the cushion on the armrest and the lateral support on her wheelchair. On 08/22/24 at 11:51 AM, V2 (DON) said that her expectations are that call lights are within reach, resident are being closely observed and frequent rounding if needed. V2 said that she expects the staff to report if a patient is falling through the adaptive devises. V2 said that this should be done so the patient can be comfortable, without pain, and free to move. R155's electronic health record showed on 1/25/24 R155's cognition is severely impaired, and she needs substantial to maximal assistance for eating, toileting, sitting to standing, and personal hygiene. R155's 4/24/21 physician order showed she is on fall precaution every shift. R155's 5/13/24 care plan showed ADL self-care deficit related to impaired mobility, cognitive deficit, generalize weakness related to a diagnosis of dementia, and a history of falls. Interventions include monitor document and report as needed any changes, any self-care deficit declines in function, encourage to use bell to call for assistance. R155's 1/23/2024 care plan showed a risk for falls related to impaired mobility, cognitive deficit, generalized weakness related to dementia and history of falls. The interventions included anticipate and meet the residents needs, be sure that the resident's call light is within reach and encourage the resident to use it for assistance as needed, the resident needs to be in a safe environment. R155's Wheel Chair System - Patient Evaluation information showed that on 7/10/2023 a high back chair with foam and a bolster to the right side was given to R155, and on 5/2/2024 a lateral support was added to the right side of the wheelchair due to increased lean.
CONCERN (D)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to safely transfer residents using a gait belt. This app...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to safely transfer residents using a gait belt. This applies to 2 of 2 residents (R68, R191) reviewed for mobility in a sample of 37. The findings include: 1. On August 21, 2024 at 2:11 PM, V25 (CNA/Certified Nurse Assistant) and V41 (Restorative Aide) assisted R68 from a lying to a sitting position. V25 applies a gait belt around R68's waist and then V25 and V41 assists R68 into a standing position, with V25 pulling R68 up by her pants. At 2:11 PM, V25 pulled R68 further back into her wheelchair using her pants instead of the gait belt. R68's face sheet showed she was admitted to the facility with diagnoses including dysphagia, gastrostomy status, failure to thrive, cognitive communication deficit, osteoporosis, and a history of falling. R68's MDS (Minimum Data Set) dated August 14, 2024 showed R68 had severe cognitive impairments and was dependent on staff to transfer from lying to sitting on side of bed, sit to stand, and bed to chair transfers. R68's care plan revised on August 7, 2024 showed Resident will require 2 [Gait Belt] total dependent assist from staff. 2. On August 21, 2024 at 11:47 AM, R191 was being assisted into the wheelchair by V31 (CNA). R191 was sitting at the edge of her bed and V31 applied the gait belt around her and brought the wheelchair close to R191. V31 then pulled and pivoted R191 using her pants into the wheelchair. At 11:51 AM, R191 was taken to the bathroom, and V31 used R191's pants to pull her up instead of the gait belt and placed her on the toilet. At 11:55 AM, V31 pivoted R191 with one hand on the gait belt and the other hand on her pants. R191 face sheet showed she was admitted with diagnoses including abnormalities of gait and mobility and repeated falls. R191's MDS dated [DATE] showed R191 had moderate cognitive impairment. R191 required substantial assistance for sitting to stand, bed to chair transfers, and toilet transfers. R191's care plan dated April 1, 2024 showed The resident has an ADL (Activities of Daily Living self-care performance deficit [related to] cognitive deficit and mobility impairment .with an intervention including bed to chair 1 person assist to Give her time to participate in holding the side rails and let her pull herself to stand and pivot to the chair. On August 21, 2024 at 2:40 PM, V25 (CNA) said the staff should use a gait belt to transfer residents for safety. V25 said staff need to make sure it was placed tightly and then the resident should be pulled up by the gait belt, not by their pants. On August 22, 2024 at 1:04 PM, V34 (CNA) said the residents should be transferred using a gait belt and they should not be pulled by their pants. On August 22, 2024 at 1:16 PM, V35 (RN/Registered Nurse) said the staff should be transferring the resident using a gait belt and should not be pulling them by their pants. V35 said the gait belt was in place to use and pulling them by their pants could hurt them. On August 22, 2024 at 12:56 PM, V32 (Physical Therapy Program Manager) said ideally, the staff should only be holding the resident by the gait belt and should not be pulling them by their pants. On August 22, 2024 at 9:39 AM, V2 (DON/Director of Nursing) said the staff should use the gait belt to lift and transfer the residents. The facility's Transfer-Gait Belt Policy reviewed August 2023 showed Place your hands toward the back of the resident and grasp the belt by inserting your thumbs downward. Fingers are to be curled under belt and next to thumbs. The belt is to be snug enough to allow your hands only enough space to grasp the belt.
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 observation, interview, and record review, the facility failed to offer hydration fluids for a resident at risk for deh...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to offer hydration fluids for a resident at risk for dehydration. This applies to 1 of 2 residents (R30) reviewed for hydration in the sample of 37. Findings include: R30's EMR (Electronic Medical Record) showed R30 had multiple diagnoses including recurrent urinary tract infections, a disorder of the kidney and ureter, neuromuscular dysfunction bladder, urinary retention, constipation, and parkinsonism. R30's MDS (Minimum Data Set) dated 5/09/2024 showed she was cognitively intact. R30's MDS continued to show she was dependent on facility staff for assistance with feeding including drinking liquids. On 8/20/2024 at 10:57 AM, R30 was in bed and said she was not getting enough water. R30 said she was having urinary discomfort and was waiting for her urine results. R30 had no water at the bedside but had a tub of thickener mixing powder. On 8/21/2024 at 11:30 AM, R30 was in bed with no water at the bedside. At 12:30 PM, R30 said she wanted to have water to drink. R30 said she was fed lunch and drank one cup of milk but did not have water. R30 did not have water at the bedside. On 8/22/2024 at 9:50 AM, R30 said she was still not receiving enough drinking water and wanted more. R30 said she only receives a small cup of lemon-thickened water with her medications. R30 said she would like to be given more lemon-thickened water throughout the day. R30 did not have water at the bedside. On 8/22/2024 at 9:53 AM, V13 (Head Unit Nurse) said staff should be offering fluids to residents between meals. V13 said residents who are in their rooms should have a water pitcher at the bedside. V13 said for those with thickened liquids they have available premade thickened liquid drinks. V13 said R30 had frequent recurrent urinary tract infections and needed more fluids. V13 said they would place lemon-thickened water at R30's bedside and offer her more fluids. On 8/22/2024 at 11:12 AM, V12 (Assistive Director of Nursing/ADON) said all residents who can drink oral fluids should be offered fluids because they are all at risk for dehydration. V12 said R30 should have been offered fluids and staff should assist her because of her swallowing precautions. R30's Care Plan dated 8/22/2024 showed multiple focus problems including a potential nutritional problem and an actual impaired urinary elimination problem. R30's care plan showed multiple interventions including Offer preferred foods/fluids within diet recommendation when possible and Encourage fluids during the day to promote prompted voiding response. R30's Annual Nutritional assessment dated [DATE] said R30's diet included moderately honey thick liquids. R30's assessment showed R30's estimated fluid needs were 2050-2100 milliliters and should be encouraged to consume moderately honey-thick liquids. R30's urinalysis lab result dated 8/20/2024 showed an abnormal urine result. The facility's policy titled Hydration Plan with a revised date of 3/2024 said Purpose: To provide residents with adequate water and fluids throughout the day to maintain proper hydration. Policy: It is the policy of DPCC to maintain resident's health at the highest level. The procedure contained in the policy will ensure that all residents will have access to ample water and liquids to maintain the proper levels of hydration required .Procedure: A. 1. The Nurses will: Offer residents/patients a full glass of water with the medication pass .Monitor residents that are acutely ill that require increased hydration due to possible elevated temperatures or infections that demand more fluids to improve their conditions .
CONCERN (D)

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

Tube Feeding (Tag F0693)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to change, date, and label a feed tubing for an enteral feed for a resident with a gastrostomy tube (G-tube). This applies to 1 ...

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Based on observation, interview, and record review, the facility failed to change, date, and label a feed tubing for an enteral feed for a resident with a gastrostomy tube (G-tube). This applies to 1 of 1 (R68) resident reviewed for gastrostomy tubes in a sample of 37. The findings include: On August 20, 2024 at 11:23 am, R68 was connected to her feeding via the gastrostomy tube and was receiving it at a rate of 50 milliliters per hour. R68's bottle of formula was dated August 19, 2024 at 4 PM and the tubing was dated August 15, 2024 at 9:53 PM. On August 21, 2024 at 11:32 AM, R68's feed tubing was not labeled or dated. On August 22, 2024 at 11:34 AM, V26 (RN/Registered Nurse) said the G-tube pump tubing was changed whenever a bottle was opened. V26 said the tubing should not be used for more than 24 hours. V26 also said the tubing needed to be dated and labeled. On August 22, 2024 at 1:16 PM, V35 (RN) said when the staff start a feeding, all the equipment needs to be brand new. V35 said the tubing and bottle need to be changed every 24 hours, or more frequently, depending on when the bag is changed. V35 said the tubing should also be dated. On August 22, 2024 at 9:39 AM, V2 (DON/Director of Nursing) said the gastrostomy feed tubing should be dated, but said for changing the tubing, she would need to double check the policy for when the tubing should be changed. As of August 23, 2024 at 3:30 PM, V2 was unable to provide a policy regarding when the tube feeding tubing should be changed. R68's face sheet showed she was admitted to the facility with diagnoses including gastrostomy status. R68's MDS (Minimum Data Set) dated August 14, 2024 showed R68 had severe cognitive impairment and was dependent on staff for eating. R68's POS (Physician Order Sheet) showed Enteral Feed Order Check tube placement before initiation of formula, medication administration, and flushing tube. The Manufacturer Guidelines for Ready-To-Hang Prefilled Enteral Feeding Containers provided by the facility, dated 2010, showed Proper identification and dating are essential for patient safety. Use formula, container, and tubing for 24 hours, or up to 48 hours after initial spike, when clean technique and only one new feeding set are used.
CONCERN (D)

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

Drug Regimen Review (Tag F0756)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to provide documentation of monthly medication reviews and obtain a doc...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review the facility failed to provide documentation of monthly medication reviews and obtain a documented physician response to pharmacy recommendations. This applies to 1 of 5 residents (R141) reviewed for unnecessary mediations in a sample of 37. Findings include: R141 admitted to the facility on [DATE] with diagnoses that includes paraplegia, neuralgia, cramp / spasm, diverticulosis, hypertension, depression, anxiety, and insomnia. R141's MDS (Minimum Data Set) dated 7/17/24 shows he is cognitively intact with a BIMS (Brief Interview for Mental Status Score) of 15. On 8/21/24 at 3:47 PM, V7 Pharmacy Manager stated he did not have documentation of the medication review done on 3/16/24 or 6/24/24. Pharmacy recommendations made on 11/27/23 did not have a physician response. On 8/22/24 at 9:53 AM, V7 Pharmacy Manager stated pharmacy recommendations are sent to the units for the physician to address when they round. Nursing is responsible for following up with the physician to address our recommendation. We do not have a policy to address the time frame in which the physician should respond to our recommendations. Pharmacy will send a follow up by the next review if we have not had a physician response. The pharmacy recommendation on 11/27/23 for Citalopram Hydrobromide continue at a reduced dose: maximum dose in the elderly (those over 60 years) is 20mg per product labeling due to the risk of QT prolongation. Please consider a dose reduction to 20mg if possible. V7 Pharmacy Manager stated a prolonged QT can cause arrhythmias in the heart if R141 has risk factors. The physician response provided by V43 Psychiatrist on 12/4/23 states not followed by me. Please refer to V42 PCP (Primary Care Physician). V7 Pharmacy Manager did not provide documentation of V42 PCP response to recommendations from 11/27/23 or documentation of pharmacy follow up with V42 PCP regarding recommendations. On 8/22/24 at 1:14 PM, V2 DON (Director of Nursing) stated the pharmacy delivers the monthly medication review to the head nurse or the charge nurse who should present it to the physician for review. V2 DON stated policy directing the time frame in which a physician should address pharmacy recommendations. V2 DON stated the physician or nurse practitioner make their rounds in the facility daily. V2 stated her expectation is that if the physician has not made rounds or addressed the pharmacy recommendations the nurse should contact him within a week. R141's current physician's orders show an increase of Citalopram Hydrobromide from 30MG (Milligrams) daily to Citalopram Hydrobromide 20MG twice daily. The facility provided policy Prescribing of Medications dated 8/2022 states if there is a question regarding an order, the pharmacist may contact the physician directly for clarification and, if necessary, may write a clarification on the patient's medical record. All current residents will undergo a monthly drug regimen review. Completion of review will be documented by the pharmacy manager or designee.
CONCERN (E)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected multiple residents

Based on observation, interview, and record review, the facility failed to date and discard as indicated insulin vials when opened. The facility failed to store medications in their original packaging...

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Based on observation, interview, and record review, the facility failed to date and discard as indicated insulin vials when opened. The facility failed to store medications in their original packaging until they were administered. This applies to 8 of 8 residents reviewed (R104, R96, R160, R197, R75, R121, R146, R73) for medication storage in the sample of 37. Findings include: 1. On 8/20/2024 at 3:40 PM, V9 (RN/Registered Nurse) was asked to check the fourth floor's medication room for medication storage. V9 said R73's opened and filled Levemir insulin vial was not dated with the open date. V9 said R146's opened and filled Fiasp insulin vial was not dated with the open date. V9 said R121's opened and filled Lantus insulin vial was not dated with the open date. V9 said R75's opened and filled Fiasp and Glargine insulin vials were not dated with the open dates. V9 said insulin vials should be dated when they are opened for proper medication storage. On 8/20/2024 at 4:40 PM, V11's (Licensed Practical Nurse/LPN) medication cart was checked for medication storage. V11 said R197's opened and filled Lantus insulin vial package said do not use after 8/12/2024. V11 said R160's opened and filled Humalog insulin vial package said do not use after 8/12/2024 and opened and filled Lantus insulin vial package said do not use after 8/18/2024. V11 said insulin vials should be discarded after the indicated do not use after date and new insulin vials should be obtained. 2. On 8/20/2024 at 4:07 PM, V10's (RN) medication cart was checked for medication storage. V10's cart had 9 pills that were loose in a clear medication cup. V10 said she removed R104's scheduled 5 PM and 9 PM medications from their packages and poured them into a medication cup. V10's cart had another 5 pills that were loose in a clear medication cup and another medication cup with a loose white powdery substance. V10 said she removed R96's scheduled 9 PM medications and Miralax powder dose. V10 said she should have not removed R104 and R96's medications from their packages before their scheduled administration times and should have not stored them in the medication cart. On 8/20/2024 at 5:00 PM, V12 (Assistive Director of Nursing/ADON) said nurses are expected to label insulin vials once opened and discard them accordingly to ensure safe medication storage and administration. V12 continued to say medications should be prepared when scheduled, administered once prepared, and not be stored in the medication carts once removed from their packages to ensure safe medication storage and administration. The facility's policy titled Medication Administration with a revised date 10/2023 said Purpose: The purpose of this policy is to assure that all medications are administered safely .Standard of Practice 8. Medications will be destroyed or disposed of in accordance with facility policy and regulatory guidelines .Procedure 6. a. Check multi-dose vials for dates: When it was first opened, and what is the last date it may be used. b. If label does not contain these 2 dates, return medication to pharmacy .Storage of Medications 1. Medications are stored in manufacturer's containers until repackaged by pharmacy .
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 observation, interview, and record review, the facility failed to use appropriate PPE (Personal Protective Equipment) f...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to use appropriate PPE (Personal Protective Equipment) for a resident on EBP (Enhanced Barrier Precautions) and failed to do proper hand hygiene to prevent the spread of infection. This applies to 5 of 5 residents (R68, R41, R155, R364, R365) reviewed for infection control in a sample of 37. The findings include: 1. On 8/20/24 at 11:23 AM, V27 (CNA/Certified Nurse Assistant) was providing personal hygiene and incontinence care for R68. R68 was on EBP due to having a G-Tube (Gastrostomy Tube). V27 applied a gown and gloves and provided incontinence care to R68, who had stool and urine in her disposable brief. V27 wiped the urine and stool off R68, then took a new incontinence brief and applied it under R68. V27 did not change her gloves or perform hand hygiene when going from the dirty brief to the clean brief. At 11:48 AM, V27 left R68's room without removing the PPE to throw the dirty linen bag in a container in the hallway. At 11:49 AM, V27 returned to the room and applied new PPE and entered R68's room, and then left the room again with all the PPE on. V27 returned with the same PPE on, washed her hands, and assisted V28 (CNA) with personal care for R68. On 8/21/24 at 1:48 PM, V25 (CNA) was providing personal hygiene and incontinence care to R68. V25 was not wearing a gown during personal care for R68. R68 had a soiled incontinence brief, and V25 provided incontinence care, and when going from dirty to clean, did not change her gloves or perform hand hygiene. On 8/21/24 at 2:40 PM, V25 said R68 was on EBP, and she should have worn the gown, gloves, and a mask when providing care. On 8/21/24 at 2:19 PM, V29 (RN/Registered Nurse) said R68 was on EBP due to having a G-Tube and so the staff needed to wear a gown and gloves for high contact activities. On 8/22/24 at 1:01 PM, V33 (CNA) said the staff should wear a mask, gown and gloves when giving care to a resident in EBP. V33 said the used PPE needed to be removed when you are about to leave the room. On 8/22/24 at 1:16 PM, V35 (RN) said when providing care for residents under EBP, staff need to wear a gown and gloves before entering the room, and before leaving the room, all the PPE needed to be removed, and hands needed to be washed. On 8/22/24 at 9:39 AM, V2 (DON/Director of Nursing) said if a resident is on EBP and the staff are providing care, the staff needed to wear a gown and gloves. V2 said the PPE should not be worn outside the rooms, and should be taken off while in the room, and handwashing needed to be performed. R68's face sheet showed she was admitted to the facility with diagnoses including gastrostomy status. R68's MDS (Minimum Data Set) dated August 14, 2024 showed R68 had severe cognitive impairment and was dependent on staff for all activities of daily living. The facility's Enhanced Barrier Precautions policy dated August 2023 showed EBP as a routine approach to infection control is based on the recognition that Standard Precautions, which requires the use of gown and glove in situations of expected exposure to blood, body fluids, skin breakdown, or mucous membranes, often have not been successfully implemented in nursing home settings. Enhanced Barrier Precautions expand the use of PPE and refer to the use of gown and gloves during high-contact resident care activities that provide opportunities for transfer of MDROs (Multi-Drug Resistant Organisms) to staff hands and clothing. MDROs may be indirectly transferred from resident-to-resident during these high-contact care activities. Nursing home residents with wounds and indwelling medical devices are at especially high risk of both acquisition of and colonization with MDROs. The use of gown and gloves for high-contact resident care activities is indicated, when Contact Precautions do not otherwise apply, for nursing home residents with wounds and/or indwelling medical devices regardless of MDRO colonization as well as for residents with MDRO infection or colonization. EBP should be maintained for the entire resident's stay or until 1) Wound(s) have healed; 2) Indwelling medical devices are no longer present. In addition to following Standard Precautions gowns and gloves should be worn during the following: Dressing, Bathing/showering, Transferring, Providing hygiene, Changing linens, Changing briefs, or assisting with toileting, Device care or use, and Wound care. 3. On 8/20/2024 at 10:41 AM, V36 (CNA-Certified Nurse Assistant) was providing bladder and bowel incontinence care to R41. After V36 cleaned R41's feces, V36 did not change her gloves and continued to apply a fresh incontinent brief. With the same soiled glove, V36 continued to assist R41 with putting on clothes. Using the same soiled gloves, she combed and flatten R41's hair. When V36 was done assisting R41 with grooming, V36 took off her gloves and did not perform hand hygiene. R41's MDS (Minimum Data Sheet) documents a BIMS (Brief Interview for Mental Status) of 6 which means R41 had severe cognitive impairment. R41 is also dependent on staff for toileting, personal hygiene, and upper and lower body dressing. R41 is always incontinent of bowel and bladder. R41's care plan dated 3/28/2024 documents that she is at risk for infection with intervention to educate resident/representative on techniques to prevent infection, such as handwashing, adequate rest, nutrition, and avoidance of crowds. 4. On 8/21/2024 at 9:13 AM, with bare hands, V37 (CNA) was observed inside R364's room tying a garbage bag with soiled incontinent pad . V37 took the garbage out of R364's room. In the hallway, V37 proceeded to double bag the garbage and put the garbage in a bin. Without performing hand hygiene, V37 proceeded to go inside R364's room and took out her meal tray, opened the meal cart which was in front of the nurse's station and put the meal tray inside the cart. R364's face sheet documents diagnosis of ESBL (Extended Spectrum Beta Lactamase) resistance in urine. R364 was on contact isolation. MDS dated [DATE] documents R364 is frequently incontinent of bowel and bladder and is dependent on staff for personal hygiene. R364's care plan did not address what staff should do to prevent infection. 5. On 8/21/2024 at 9:40 AM, R365 was observed being wheeled into the therapy room. On 8/22/2024 at 10:33 AM, R365 said she goes out to therapy early in the morning every day. She said she does not wash her hands before heading out with therapist. She said staff does not help her wash her hands before she goes to therapy. She said maybe staff thinks her hands are clean. R365's face sheet documents diagnosis of enterocolitis due to CDIFF (Clostridium Difficile) and is currently on contact isolation. R365's MDS dated [DATE] documents her BIMS score is 15 which means that she has intact cognitive functions. She is occasionally incontinent of bowel and bladder and needs partial or moderate assistance with toileting hygiene and personal hygiene. On 8/22/2024 at 10:58 AM, V32 (Therapy Program Manager) said R365 goes to the gym for therapy daily. On 8/22/2024 at 11:10 AM, V12 (ADON-Assistant Director of Nursing) said residents on contact isolation are permitted to go out of their rooms as long as incontinent care is rendered before going out of the room and residents wash their hands before going out of the room. R365's care plan did not address what staff should do to prevent infection. On 8/22/2024 at 1:14 PM, V38 (IP-Infection Preventionist) said she expects staff to perform hand hygiene before going inside a resident's room and before coming out of the room and in between providing care for patients. She said there are five steps staff needs to follow for hand hygiene. Steps are hand hygiene, put on gloves, do task, remove gloves, hand hygiene. She said hand hygiene can either be washing hands with soap and water or applying hand sanitizer. She said during peri care, staff should change gloves from dirty to clean and clean to dirty because it puts resident on higher risk for infection. She said when proper hand washing is not done on a resident with CDIFF before going out of room, there is a good chance of the CDIFF spore to spread. She said if proper handwashing is not done when needed during care, bacteria might spread to other residents. Facility's Contact Isolation Policy dated 7/2002 and reviewed 9/2023 states the following: .Policy: .Contact Isolation is an isolation category designed to prevent transmission of highly contagious or virulent infections that may be spread by direct contact. These precautions are designed for patients documented or suspected to be infected with highly transmissible or epidemiologically important pathogens for which additional precautions are needed to interrupt transmission in the facility. Procedure .3. Hand washing is indicated before and after resident contact. Hand hygiene should be performed after glove removal before leaving the resident's environment. Use an antimicrobial agent or waterless antiseptic. Facility's Hand Hygiene Policy dated 5/11/2010 and reviewed on 3/2024 states the following: . Hand hygiene is the single most effective procedure for reducing the spread of infectious organisms and cross contamination. Following is a list of some situations that require hand hygiene.Upon and after coming in contact with resident's intact skin . before moving from work on a soiled body site to a clean body site of the same resident . after handling soiled or used linens, dressings, bedpans, catheters, and urinals.After emptying garbage cans, waste baskets. 2. On 8/20/24 at 1:53 PM, V15 and V16 CNAs (Certified Nurses' Assistants) were providing incontinence care for R155. V15 and V16 with gloved hands, used a mechanical lift to assist R155 to a standing position and transport her to the toilet. They then lowered R155's pants and removed her soiled brief. R155's brief was soiled with stool and urine. V15 with gloved hands wiped R155's buttocks 5 times with the same wet towel and did not turn or fold the towel as he attempted to clean her buttocks of stool. After V15 was done cleaning R155's buttocks, he left the bathroom with his dirty gloved hands and opened R155's bedroom door, left the room, returned back to the room with plastic bags. V15 then put the soiled brief and towels in the bags, attached a clean brief and pulled R155's pants back up and then used the mechanical lift control to bring R155 back to her wheelchair. After getting R155 in her wheelchair V15 then untied R155's call light from her bedrails, moved R155's wheelchair closer to her call light and then took the plastic bags out of the room, all while still wearing his dirty gloves. V15 then put the plastic bags in 2 different containers in the hall and then removed his gloves and threw the dirty gloves in one of the containers in the hall and then cleaned his hands using the hands sanitizer on the wall next to the container. On 8/22/24 at 11:19 AM, V2 (DON) said that it is her expectation that during incontinent care staff will change their gloves and clean their hands when going from a dirty area to a clean area. It is her expectations that staff will wipe from front to back and after wiping fold the towel before wiping again. V2 said that this is to be done to prevent infections, UTIs (urinary tract infections), and cross contamination for infection control.
CONCERN (F)

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

Food Safety (Tag F0812)

Could have caused harm · This affected most or all residents

Based on observation, interview, and record review, the facility failed to properly label/date/seal/store items, remove expired items, and perform hand hygiene while in the facility kitchen. This appl...

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Based on observation, interview, and record review, the facility failed to properly label/date/seal/store items, remove expired items, and perform hand hygiene while in the facility kitchen. This applies to all residents that receive oral nutrition and foods prepared in the facility kitchen. Findings include: The facility's Long-Term Care Facility Application for Medicare and Medicaid (Form CMS-Centers for Medicare and Medicaid Services-671) dated 8/20/24 documents that the total census was 211 residents. On 8/22/24 at 1:16 PM, V39 (ADON/Assistant Director of Nursing) said there are 6 NPO (Nothing by Mouth) residents; all other residents eat from the facility kitchen. On 8/21/24 starting at 10:19 AM, V23 (Chef) was observed pureeing lunch items. After V23 pureed the chicken, she removed her gloves, pulled the garbage can out from under the counter with her bare left hand (while touching the rim of the garbage can) and threw away her gloves with her right hand. V23 then put on a new pair of gloves and did not wash her hands after touching the garbage can. V23 then put some of the roast beef and gravy into the blender to puree it. After V23 pureed the first batch of roast beef, she scooped out the rest of the not yet pureed roast beef with her gloved left hand and moved it into another silver container. V23 then grabbed a spoon, and with her gloved left hand she pulled down her face mask to taste test the consistency of the roast beef from the spoon in her right hand. After taste testing the roast beef consistency, V23 then pulled her mask back up over her nose and mouth with her gloved left hand and proceeded to puree the rest of the roast beef. V23 then poured the rest of the pureed roast beef into the silver container and covered it in plastic wrap while using her same gloved hands to touch the blender, the plastic wrap, and the steamer door handle. V23 did not wash her hands throughout the process of pureeing the chicken and roast beef after touching the garbage can and her face mask. On 8/20/24 starting at 10:40 AM, the facility kitchen was toured in the presence of V22 (Dietary Manager). The following was found: In the dry storage: 1. A large undated and unsealed bag labeled crispy onions. 2. A large undated and unsealed bag labeled croutons. In Cooler #2: 3. A 4 ounce package of sliced roast beef deli meat with a use by date of 8/10/24 and a handwritten date of 8/18/24. V22 (Dietary Manager) said he was not sure why the kitchen staff wrote 8/18/24 on the package and he would find out when the roast beef was served. On 8/21/24 at 10:16AM, V22 said the roast beef was served to residents on 7/31/24. V22 said the roast beef was labeled with the wrong date. On 8/22/24 at 12:43 PM, V22 said all food items in the kitchen should be labeled, dated, and sealed to keep the food fresh and safe to feed the residents. V22 said unsealed items are a concern because they can become contaminated by environmental contaminants. V22 said deli meat is safe in the refrigerator for 7 days, and if the package is unopened, the deli meat should be thrown away on the use by date. V22 said the unopened roast beef deli meat should have been discarded on 8/10/24. V22 said it is a concern to have deli meat improperly dated because of the risk of serving it to the resident past the use by date with the potential to make the residents ill. V22 said the kitchen staff should wash their hands with soap and water after touching the garbage can to prevent food contamination. V22 said the kitchen staff should wash their hands with soap and water after touching their face mask to prevent cross contamination. V22 said staff should never touch the food with their gloved hands and should always use a utensil to prevent food contamination. The facility's policy titled Hand Hygiene last reviewed on 3/2024 states, Purpose: To provide guidelines for hand hygiene and prevention of infections. To promote compliance with regulatory guidelines for hand hygiene. Policy: All healthcare workers and visitors will follow facility guidelines for hand hygiene .Procedure: Traditional soap and water method. Hand hygiene is the single most effective procedure for reducing the spread of infectious organisms and cross-contamination .Following is a list of some situations that require hand hygiene: Before & After: .Eating/handling food (hand wash with soap & water) . After: .Handling soiled equipment or utensils . Removing gloves or aprons The above lists do not include all opportunities to wash your hands, Remember to follow the hand hygiene guidelines anytime you question if contact with a source of contamination did occur. The facility's policy titled Labeling, Dating, and Storage of Food Items last reviewed 5/2024 states, Purpose: To ensure food is labeled, dated, and stored properly. Policy: Dining staff will label, date, and store food items properly per standard sanitation procedures. Procedure: .2. All food items will be labeled with a receiving date that correlated with the month and day received. 3 .a. Any package opened for food production will be labeled with an open date and sealed airtight prior to it being placed back into food storage locations .5. All food storage areas will be monitored regularly to discard any outdated food items from inventory stock.
Jun 2024 1 deficiency 1 Harm
SERIOUS (G) 📢 Someone Reported This

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

Actual Harm - a resident was hurt due to facility failures

Accident Prevention (Tag F0689)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure two staff assisted in transferring a resident safely while u...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure two staff assisted in transferring a resident safely while using a mechanical lift. This failure resulted in R2 falling from the mechanical lift to the floor, sustaining a right tibia fracture and an occipital contusion and transfer to the emergency department. This Applies to 1 of 5 residents (R2) reviewed for falls and accidents in a sample of 9. A care plan initiated on 10/30/2023 showed that R2 needs two staff members to assist with ADLs (Activities of Daily Living), including transfers from bed to wheelchair and vice versa. The MDS (Minimum Data Set), dated 11/22/2023, showed that R2 is cognitively intact and dependent on ADLs, requiring two or more staff members to complete activities such as transfers, dressing, personal hygiene, and bathing. A review of R2's face sheet and physician's progress notes dated 01/24/2024 showed R2 was an [AGE] year-old admitted to the facility initially on 05/01/2023 with diagnoses including muscular dystrophy, osteoarthritis, history of falls, disease of the spinal cord, history of multiple traumatic fractures, lack of coordination, vitamin D deficiency, progressive weakness, wheelchair-bound, and chronic obstructive pulmonary disease. On 06/13/2024 at 01:04 PM, R2 was in bed, alert, oriented to person, place, and time, and was interviewable. R2 said, V12 (Certified Nursing Assistant) put him in a mechanical lift by herself, and the sling was smaller to him. R2 said when she lifted him from the bed, his groin hurt, and he told V12 to take the sling off. R2 said V12 played around with the sling and took the mechanical lift near the door where his power wheelchair was, and he fell from the mechanical lift and broke his right leg and blood was coming from the back of his head. R2 said V12 ran outside the room and told other staff that she had dropped him and staff had come to assist him. Nursing progress notes dated 01/21/2024 showed that at 8:40 AM, R2 had a witnessed fall during transfer, causing injury to the head (occipital region) and right knee pain. The nursing progress notes further showed that R2 was sent to the emergency department for evaluation. R2's hospital emergency department Physician history and physical dated 01/21/2024 showed [AGE] year-old R2 presented to the hospital on 1/21/2024 with a complaint of a fall from the mechanical lift with an injury to the right leg below the knee with pain and side of the head lacerations. X-ray of the right tibia fibula lateral view on the same day showed medial tibial plateau fracture and treated with knee immobilizer 24/7 for three weeks and Neosporin antibiotic cream dressing for scalp after cleaning. On 06/13/2024 at 2:00 PM, V2 (Director of Nursing) said R2 uses a mechanical lift with two staff members assisting, and he fell from the mechanical lift while V12 (Certified Nursing Assistant-Agency) was transferring R2 from bed to his wheelchair. V2 said V12 should have waited for another staff member to help R2 transfer. V2 said the facility is not using V12 anymore, investigated, educated staff on the mechanical lift transfer, and reported to IDPH. On 06/13/2024 at 2:10 PM, V6 (Certified Nursing Assistant) said he is a regular staff member in that unit and that they should always use two or more staff to transfer residents from the mechanical lift. V6 said R2 is a dependent resident for ADLs, and V12 should have called for help to transfer R2 using the mechanical lift. A facility's policy titled Transfers-EZ Lift/EZ Stand stated, in part, that each resident will be assessed to determine the mode of transfer and the level of staff involved.
Oct 2023 5 deficiencies
CONCERN (D)

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

Deficiency F0558 (Tag F0558)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure the call light system was in reach for 1 of 1 r...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure the call light system was in reach for 1 of 1 resident (R42) reviewed for call lights not in reach in the sample of 36. The findings include: R42's admission Record, printed by the facility on 10/26/23, showed she had diagnoses including hemiplegia and hemiparesis following a cerebral infarction affecting her left side (left-sided paralysis and weakness following a stroke), vascular dementia, visual loss in her left eye, glaucoma, osteoarthritis. The facility assessment dated [DATE], showed R42 had severe cognitive impairment and was dependent on staff for eating, toileting, bathing, personal hygiene, and transfers. The assessment showed R42 was always incontinent of bowel and bladder. R42's care plan dated 12/1/21, showed she has an ADL (activities of daily living) self-care deficit related to activity intolerance, hemiplegia, impaired balance and stroke. One of the interventions in place was Encourage the resident to use bell to call for assistance. R42's care plan with a revision date of 10/25/23, showed she has impaired cognitive function/dementia or impaired though processes related to difficulty making decisions. One goal of the care plan was R42 would be able to communicate basic needs on a daily basis. R42's fall risk care plan, with a revision date of 10/25/23, showed she is at risk for falls related to poor communication/comprehension, unaware of safety needs, stroke, left hemiplegia, cognitive deficit, impaired vision, incontinence, and lack of standing tolerance. One intervention for the care plan is Be sure the resident's call light is within reach and orient her to location due to blindness. Encourage the resident to use it for assistance as needed. The resident needs prompt responses to all requests for assistance. On 10/24/23 at 12:55 PM, R42 was sitting in a reclining geriatric chair by the end of her bed. R42 said sometimes she has to wait about an hour for staff to help her. R42's call light was on the bed, not in reach of resident. R42 said that happens often and it is aggravating. R42 said she sits there, yelling for help over and over, and no one comes. R42 said staff say they cannot hear her. R42 said she cannot reach over and get the call light. On 10/26/23 at 8:36 AM, V5 (Manager of Rehab) said R42 is in a (reclining geriatric chair) because she does not have enough support, or upper trunk control to use a high-back chair due to her hemiplegia . V5 said R42 had a stroke, and it affected her left side. V5 said R42 is weak on her right side as well. V5 said R42 had therapy to try to increase her strength on her right side. She has no movement on her left side and minimal movement on her right side. V5 said it would be important to make sure the call light is within reach. She is pretty dependent on staff for everything. On 10/26/23 at 12:32 PM, V2 (Director of Nursing) said staff should absolutely make sure that the call light is within R42's reach because that is the only thing she can press for assistance. That is her means of communicating to us what she needs. The facility's Wheel Chair System-Patient Evaluation Information form, provided by the facility on 10/26/23, showed R42 was assigned a Broda chair on 1/19/23 due to sliding from a high-back recliner. The facility's Call Light Protocol, with a revision date of 6/19/2009, showed Policy .3. It is the policy of (the facility) to provide all residents with the proper equipment to notify staff that assistance is needed .Procedure: 1. A working call light is to remain within reach of the resident at all times when they are in their room; if they are in bed, a wheelchair, a Geri chair, the toilet or a commode.
CONCERN (D)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure a resident was transferred in a safe manner fo...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure a resident was transferred in a safe manner for 2 of 5 residents (R69, R87) reviewed for falls in the sample of 36. The findings include: 1. R69's face sheet showed a [AGE] year old male with diagnosis of diabetes, osteoarthritis of the knee, chronic kidney disease, bilateral artificial hip joints, muscle weakness, and malignant neoplasm of the prostate. R69's 8/30/23 facility assessment showed he was cognitively intact and required extensive assistance of one person to physically assist with transfer, bed mobility, and toilet use. R69's care plan showed he was at risk for falls. On 10/24/23 at 1:15 PM, V6 Certified Nursing Assistant (CNA) applied the mechanical stand lift transfer harness to R69's upper body and attached it to the lift. Once R69 was off the toilet and upright (with knees bent), the safety belt was noted to be very loose. This surveyor reached to the belt to show the excess slack in the belt in relation to R69's body. R69's heels extended beyond the posterior edge of the foot plate (were not on the foot plate all the way). V6 did not tighten the belt, did not ensure his feet were on the foot plate, and continued to move R69 in the lift out of the bathroom and transferred R69 to a wheelchair. R69 did not request a preference for how loose fitting the safety belt was secured. On 10/26/23, R69 said he did not believe the lift strap was secured tight enough during the transfer observed by this surveyor on 10/25/23. The strap was too loose and I did not request that it be that loose. On 10/26/23 at 12:03 PM, V5 Manager of Rehabilitation Services said her department does all the assessments to determine what transfer technique is recommended for each resident. V5 said R69's assessment done on 8/23/23 showed to use a mechanical stand lift for transfers. Not all residents can stand upright. They need to be able to bear weight, hold on with their hands and maintain that position during the transfer. Both feet should be on the foot plate during a transfer. The belt should be secure enough to the resident's body to allow for one hand to fit between the strap and the resident. It's important to use the lift correctly for resident safety. This includes ensuring both feet are on the foot plate and the strap is close to the resident's body without slack. The facility's 4/2023 Transfers-EZ Lift/EZ Stand Policy showed Safety measure: Securely fasten the safety strap around the resident's chest. Secure the buckle and pull the loose strap to tighten. The EZ Way Stand Operator's Instructions showed patients should be able to follow simple commands, bear some weight, and have upper body strength. For the safety of the patient, securely fasten the the safety strap around the patient's torso. Secure the buckle and pull the strap to tighten. As the patient is being raised, simultaneously tighten the safety strap buckled around their torso. 2. R87's face sheet, printed on 10/26/23, showed diagnoses including but not limited to cerebrovascular disease, osteoporosis, chronic pain, difficulty walking, muscle weakness, and right artificial knee joint. R87's facility assessment dated [DATE] showed staff assistance required for toilet transfer. The same assessment showed no cognitive impairment. R87's care plan showed an intervention revision dated 2/9/23 for: Restorative-transfer program-Transfer with one person gait belt. On 10/24/23 at 10:34 AM, R87 was seated on the toilet and V9 (CNA-Certified Nurse Aide) was present. V9 was wearing a gait belt around her own waist. V9 held onto both of R87's hands and instructed her to stand. R87 slowly stood up then suddenly grabbed the side bars by the toilet. V9 performed personal hygiene care while R87 was standing. R87 said, Don't wipe me too hard or I will go over and fall. V9 completed care and held R87's hands while pivoting her into the wheelchair. R87 was weak, shaky, and bent forward throughout care and the transfer. V9 did not apply the gait belt to R87 and continued to wear it around her own waist during care. On 10/24/23 at 10:44 AM, V15 (Unit Nurse) stated R87 has a history of falls and recently became a hospice resident. She has been evaluated by therapy and is a one assist with a gait belt. She needs the gait belt to transfer safely. On 10/25/23 at 9:21 AM, R87 was seated on her bed eating. R87 was alert and oriented. R87 said staff never use any gait belt to transfer her. They just hold her hands or arm while she walks. On 10/26/23 at 10:35 AM, V2 (Director of Nurses) stated gait belts are needed while transferring. Anyone who needs help stabilizing is required to always have one on. Gait belts provide support in case a resident begins to fall. (R87) absolutely needs one. She is a stand pivot and staff need to hold onto the gait belt at her back. It is unsafe to hold her by the hands or arms. The facility Gait Belt policy reviewed dated 8/2023 states: Staff must always follow the transfer method set forth in the resident assessment and care plan.
CONCERN (D)

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

Incontinence Care (Tag F0690)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to ensure incontinence care was performed in a manner to ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review the facility failed to ensure incontinence care was performed in a manner to prevent cross contamination and failed to ensure urinary drainage bags were off the floor for 3 of 3 residents (R28, R200, R22) reviewed for incontinence care in the sample of 36. The findings include: 1. R28's face sheet printed on 10/26/23 showed diagnoses including, but not limited to, depression, atrial fibrillation, hydronephrosis, and obstructive uropathy (urine accumulation in kidney). R28's facility assessment dated [DATE] showed staff assistance required for toilet use, and always incontinent of urine and bowel. R28's care plan showed a focus area related to at risk for complications from removal of right ureteral stone on 10/18/23 with recent complicated urinary tract infection and hydronephrosis, cystoscopy, right ureteral stent placement on 9/27/23. R28's physician orders showed an order start dated on 10/18/23 for: Cedfinir capsule (antibiotic) 300 milligram two times daily for infection (s/p surgical procedure stent placement) for 7 days. On 10/24/23 at 11:12 AM, R28 was lying in bed while V8 and V9 (CNAs-Certified Nurse Aides) changed her incontinence brief. Both V8 and V9 wore gloves while R28 was rolled to her side. V9 removed the urine-soaked brief from under her and used a wet towel to wipe her buttocks. V9 used the same towel area to dry her buttocks. V9 rolled R28 onto her back, while V8 exited the room to get barrier cream. V9 continued wearing the same contaminated gloves to put a fresh brief under R28, touch the bed side rails, adjusted the pillow under R28's head, and searched through the bedside table drawer. V8 returned with barrier cream and V9 applied it to R28 still wearing the dirty gloves. R28's brief was closed without any vaginal pericare performed. V8 and V9 transferred R28 using a mechanical lift into her wheelchair. V9 continued wearing the same contaminated gloves to touch the lift controls and sling. V9 exited the room and placed the mechanical lift in the hallway. V9 wore the same gloves to comb R28's hair and adjust her clothing. On 10/24/23 at 11:27 AM, V9 said R28 wets a lot so we check her every two hours. Her brief was a medium level of saturation today. V9 said incontinent residents should be cleaned with a wet cloth and dried with a fresh one. V9 said gloves should be tossed if they are dirty with bowel movement or urine. It stops germs from transferring to other residents or other items. V9 was asked why she did not cleanse R28's vaginal area after the wet brief was removed or change her gloves. V9 replied, I thought I did. I just forgot. On 10/26/23 at 10:26 AM, V2 (Director of Nurses) stated CNAs are expected to cleanse incontinent residents and change gloves appropriately. Fresh gloves should be worn before touching anything else. It stops the spread of infection. Germs on the dirty gloves can go to other areas. Pericare involves going in the correct order and thorough cleaning. It is not appropriate to use the same side towel to clean and dry. It should be folded over or get a new one. Incontinent residents need to be cleaned whenever they are wet. Urine is harsh to skin. It can cause skin irritation, odors, and skin breakdown if it remains on the body. The facility's Perineal Care policy review dated 8/2023 states: All residents will receive proper hygiene as part of our daily care procedures and infection control program. The facility's Hand Hygiene policy review dated 8/2020 states under the aftercare section: Performing your personal hygiene, removing gloves or aprons. The facility was unable to provide a glove use policy. 2. R200's admission Record, printed by the facility on 10/26/23, showed he had diagnoses including hemiplegia and hemiparesis following a cerebral infarction affecting left side (left-sided paralysis and weakness following a stroke), neuromuscular dysfunction of bladder, and urine retention. R200's Order Summary Report, printed by the facility on 10/26/23, showed an order for an indwelling (urinary drainage) catheter. R200's care plan initiated on 6/29/23 showed he had an indwelling catheter due to neurogenic bladder after a stroke. The care plan showed R200 had a personal history of UTI (urinary tract infection). On 10/24/23 at 3:52 PM, R200 was in his room, lying in bed. R200's urinary drainage bag was lying directly on the floor. The side of the urinary drainage bag with the tubing was touching the floor. On 10/26/23 at 12:44 PM, V2 (Director of Nursing) said catheter bags should be kept off of the floor to prevent infection, and for the resident's dignity. The facility's policy and procedure titled Catheter Management: Urinary Indwelling, with a revision date of 8/2023, showed 5. Secure bedside drainage bag to bed frame. Make sure the bag (is) covered and is kept off the floor. 3. R22's admission Record (Face Sheet) showed his diagnoses to include Cerebral Palsy, hemiplegia affecting his left dominate side, retention of urine, personal history of UTI's (urinary tract infections), and ESBL (Extended Spectrum Beta Lactamase) resistance. On 10/25/23 at 10:08 AM, R22 was sitting up in bed watching TV. R22 has an indwelling catheter due to urinary retention. During an inspection of the tubing and catheter bag, the bag was found to be on the floor on the right side of the bed. On 10/25/23 at 10:10 AM, R22 said, the CNA's (Certified Nursing Assistants) were just in his room giving him care. On 10/25/23 at 10:25 AM, V3 ADON (Assistant Director of Nursing) said, the catheter bag should not be touching the floor because the floor is dirty and it could increase his chance of infection. R22's 7/19/23 Progress notes showed his urine was positive for E-Coli (Escherichia coli) and proteus. R22 received IV (Intravenous) antibiotics for this infection. R22's 7/19/23 MDS (Minimum Data Set) showed he requires extensive assistance with his ADL's (Activities of Daily Living). The Catheter Management Policy and Procedure (revised 8/2023) shows it's purpose is to reduce nosocomial-associated infections (in house infections) and complications. The same document shows the urinary catheter bag should be hung on the frame of the bed and should not touch the floor.
CONCERN (E)

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

Resident Rights (Tag F0550)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide dignity for 5 of 5 residents (R19, R61, R72, ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide dignity for 5 of 5 residents (R19, R61, R72, R79, R128) reviewed for dignity in the sample of 36. The findings include: On 10/26/23 at 10:00 AM, V16 (unit secretary) was observed paging call light assistance over an intercom. She announced the room and bed number. At 10:22 AM she announced bathroom assistance with the room number. The admission record for R128 shows he was admitted to the facility 6/29/16. His 8/24/23 quarterly assessment shows him to be cognitively intact. On 10/26/23 at 11:21 AM, R128 said the overhead paging has been brought up before, and he was told it was going to be phased out. It is embarrassing when someone says toileting assist and their room number or their name. All of the shifts use the paging system. He said the secretary will announce who needs bathroom assistance and it is embarrassing for those that are incontinent or in the bathroom, everyone does not need to know that information. The admission record for R19 shows she was admitted to the facility on [DATE]. Her 10/9/23 quarterly assessment shows she is cognitively intact. On 10/26/23 at 11:41 AM, R19 said the intercom has always been used by the staff, they announce the room and what you need. When you put on the call light, they will use the phone to ask what you need. If you ask to use the bathroom, they will announce it overhead with the room number, and sometimes they will use the resident's name. She said it makes me think now everyone knows you went to the bathroom or pooped, it is embarrassing. On 10/25/23 at 1:26 PM, during the resident council meeting, R128, R19, R79, R72, and R61 said it is about 20-30 minutes waiting for call lights to be answered. The light is on so long that the nurse will get on the intercom and page 1137 needs bathroom help. R19 said they can just say that we need assistance, but they call it over the intercom what kind of help is needed, and it is embarrassing. Each said it was a dignity issue. R79 said sometimes the staff will answer the call light using the phone system and will ask the person what they want, then will announce it over the intercom. He said some of that should be private. R72 said she does not like the overhead paging. They should just say someone needs help and not what kind of help. They should not say someone has to go to the bathroom. On 10/26/23 at 12:07 PM, V2 DON (Director of Nursing) said the units have always had paging, it is not used after night time but during the day. The staff should only be announcing needing assistance. V2 said she could possibly see the bathroom announcement as a dignity issue. The facility's 8/2023 Resident Rights policy documents it is dedicated to promoting the highest quality of life for their resident's. The Center strives to ensure that these rights are protected and respected by the resident, staff, volunteers and visitors at the Center.
CONCERN (E)

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

Deficiency F0804 (Tag F0804)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on Observation, Interview and Record Review the facility failed to serve residents trays at an appetizing temperature for ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on Observation, Interview and Record Review the facility failed to serve residents trays at an appetizing temperature for eight residents (R5, R12, R128, R119, R19, R79, R72, & R61) outside of the sample. The findings include: On 10/24/23 at 11:17 AM, the first tray cart containing lunch trays was delivered to the third floor. Residents were sitting in the common area at tables. Staff were not passing any of the lunch trays. At 11:37 AM, the second tray cart containing lunch trays was delivered to the third floor. V7 CNA (Certified Nursing Assistant) took a rolling cart over to the first tray cart, opened the doors to look for certain trays and placed them on her rolling cart. V7 went to the second tray cart, opened the doors to look for certain trays and placed them on her rolling cart. V7 took 4 resident trays and walked down the hall. At 11:42 AM, V8 CNA started serving lunch trays. V9 CNA opened the first tray cart, removed a couple of trays, left the doors open and went to the second cart to look for additional trays. At 11:48 AM, there were 5 trays left sitting on the racks of the first cart that had the door left open. V7 CNA, V10 CNA, and V11 CNA removed lunch trays from the side of the first cart that had the door left open. At 11:50 AM, the last tray was removed from the first cart on the side with the door open. The tray was for R5. V13 (Dietary Manager) took temperatures of the food on R5's tray. The salmon was 116 degrees Fahrenheit and the potatoes were 119 degrees Fahrenheit. V13 stated when they temperature test for test trays the food temperatures should be 120 - 125 degrees Fahrenheit. V13 stated the reason they do two tray carts to the floor is so the first cart will come up and trays will served before the second cart comes up. V13 stated this was done so staff can serve food at the temperature it needs to be. V13 stated it was important to serve food at the appropriate temperature because it tastes better for the residents. V13 observed the staff leaving the doors open on the tray carts while searching for residents lunch trays. V13 stated that leaving the doors open on the tray carts contributes to cold food. At 12:10 PM, forty-three minutes after the first tray cart was delivered to the floor, the last meal tray on that cart was ready to be served to R12; she had a mechanical soft diet. V13 took the following temperatures in degrees Fahrenheit of R12's lunch tray: pork - 108 degrees, rice 105 degrees, and carrots 106 degrees. V13 stated the food was too cold. V13 stated he noticed staff spend a lot of time searching for trays in the carts while other staff go up and down different halls delivering lunch trays. At 12:12 PM, V12 (Registered Dietician) stated the tray carts don't go up at the same time so nursing staff can pass trays from one cart before the other cart comes so the food doesn't get cold. On 10/25/23 at 1:26 PM, during the group meeting R128, R119, R19, R79, R72 and R61 stated the food is served cold. R128 and R72 stated when the tray carts are brought up the staff is busy and they can't get the food trays out fast enough so the food is served cold. R72 stated two carts will come up to the floor and staff will sometimes wait for both of the food carts to come up before they start serving the food. R61 stated staff leave the doors open on the food carts and the food gets cold. On 10/26/23 at 10:40 AM, R5 stated the food is always cold and tastes awful. R5 stated, I don't know why it's cold all of the time; but it doesn't taste good like that. I can have it warmed up if I ask them to do that and if I can get someone to do it. The Face Sheet dated 10/26/23 for R5 showed medical diagnoses including spina bifida, paraplegia, disorder of adrenal gland, gastroesophageal reflux disease, absence of other parts of digestive tract, deficiency of other vitamins, obstructive and reflux uropathy, hypertension, and kidney stones. The Dietary Note dated 10/25/23 for R5 showed she has had an 8 percent weight loss in three months with variable appetite. R5 is provided select menus for lunch and dinner to choose her meals. R5's food preferences were updated. The Care Plan dated 8/10/23 for R5 showed she has a potential nutritional problem. Regular diet; provide and serve diet as ordered. The Minimum Data Set (MDS) dated [DATE] for R5 showed no cognitive impairment; set up only needed for eating; extensive assistance needed for bed mobility, dressing, and toilet use; total dependence on staff for transfers. The facility's Dining Services policy (no date) showed, Meals shall be prepared using quality ingredients and standardized recipes, and served in a palatable, attractive and at a safe and appetizing temperature.
Oct 2023 1 deficiency
CONCERN (D) 📢 Someone Reported This

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

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

Deficiency F0760 (Tag F0760)

Could have caused harm · This affected 1 resident

Based on interview and record review, the facility failed to ensure a resident was properly identified prior to medication administration to prevent medication errors as per facility policy. This app...

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Based on interview and record review, the facility failed to ensure a resident was properly identified prior to medication administration to prevent medication errors as per facility policy. This applies to 1 of 3 residents (R1) reviewed for medication errors in a sample of 7. The findings include: MDS (Minimum Data Set), data 8/30/23, shows R1 was cognitively intact. R1's MAR (Medication Administration Sheet), dated 9/1/23 to 9/30/23, shows R1 had physician orders for the following medications during the month of 9/2023: Oyster Shell Calcium, Ergocalciferol, Flomax, Gabapentin, Glipizide, Levothyroxine, Loratadine, Melatonin, Metoprolol Extended Release, Pravastatin Sodium, Diclofenac gel, albuterol, docusate, guaifenesisn, and acetaminophen. On 10/18/23 at 12:47 PM, R1 was sitting in a wheelchair in a small dining room and was alert, oriented, communicative, and well groomed. R1 stated, I feel OK now! R1 stated on 9/26/23, R1 was approached by V3 (Registered Nurse) who stated she was going to provide R1 his due medications. R1 stated he usually received medications at that time but when V3 provided medications to R1, R1 did not recognize the medications he was given and told V3 that the medications were not his. R1 stated he took the same medications for years and knew his medications by sight. V3 told R1 that the medications were R1's medications, but never asked R1 his name, checked for any identification, or checked is identification bracelet. R1 stated V3 left R1, walked to her medication cart, and returned to R1 telling R1 that his physician changed his medications and that the medications she provided were his. R1 stated he swallowed the medications and V3 returned to her medication cart. R1 stated V3 then returned to R1 with a paper in her hand, looked at the paper, and stated the paper had a different name written on it. R1 stated he told V3 the name on the paper was not R1's name. R1 stated V3 walked away and R1 went to his room. R1 stated he started to feel strange, told a different staff member he did not feel well, and the facility staff placed him on the toilet and encouraged him to drink water. R1 stated after telling the staff twice he was feeling dizzy while sitting on the toilet, the staff transferred him to his wheelchair. R1 stated he told staff he wanted to go to the hospital but the staff did not send him at that time. R1 stated eventually paramedics came in and took him to the hospital. R1 stated he was very upset, very scared, and did not know what to think. R1 stated he was scared because he was allergic to sulfa drugs and was afraid for hours that he might die due to the medications given in error. R1 stated he felt safe in the hospital and then better when he returned to the facility. On 10/18/23 at 11:24 AM, V3 (Registered Nurse) stated the day she floated to work on R1's unit, there were four new residents on the unit. V3 stated R1 was not new and thought she recognized R1, but V3 had not worked with R1 for some time. V3 stated she retrieved medications from her medication cart after checking the computer. V3 stated when she pulled up a resident to retrieve his medications and she thought R1 was the resident for which she was gathering medications. V3 stated she later realized the medications were prescribed for R7. V3 stated she forgot to check R1's patient identification band, check the back of R1's chair for his name, or check the computer for R1 name or picture. V3 stated R1 did question if the medications were his and also questioned why V3 checked R1's blood sugar because staff had already checked it earlier. V3 stated she then gave R7's oral medications to R1, including Coreg, Valsartan, and Eliquis, which R1 swallowed. V3 stated she also gave R1 eye drop medications and R1 told V3 he was not supposed to be receiving eyedrops. V3 stated she returned to her computer and reviewed R1's medication. V3 stated she noticed she had not yet provided insulin as was ordered for R7, drew up the insulin, and returned to R1 to provide the insulin. V3 stated R1 told V3 he did not take insulin as one of his medications. V3 stated that was when she realized she gave the wrong medications to the wrong resident and informed her supervisor immediately. V3 stated R1's physician and emergency contact were informed of the error immediately. V3 stated R1's blood pressure was initially normal but later dropped at approximately 8:00 PM and R1's physician was notified. R1's physician sent R1 to the hospital and V3 was suspended from her position at the facility. On 10/18/23 at 10:15 AM, V7 (Pharmacist) stated a resident who was regularly takes Metoprolol and who is given one dose of both Coreg and Losartan by mistake can experience dizziness and lightheadedness due to low blood pressure and low pulse rate. V7 stated R1 was given Coreg and Metoprolol, two beta blockers, which can cause a significant decrease in a resident's blood pressure and heart rate. R1 was also given Losartan which could further lower his blood pressure in addition to the two beta blockers. V7 stated in a resident sensitive to the medications, the three could provoke a resident to have a high risk of falling and injury. V7 stated if a resident's blood pressure were low enough for a sustained period of time, organ failure may result, but that those results would not likely occur due to the one-time, low doses that were administered. V7 stated that one dose of Eliquis would not be concerning with R1's diagnosis. On 10/18/23 at 10:27 AM V2 (Director of Nursing) stated V3 floated as a nurse at the facility for many years. V2 stated as soon as V3 made the medication error, V3 notified her supervisors. R1's physician was notified and gave orders to closely monitor R1. V2 stated R1's blood pressure began to drop within a few hours of close monitoring, and R1's physician was called again who ordered R1 to be given additional fluids. V2 stated the facility staff lowered R1's head of bead when R1 began to complain of dizziness and R1's blood pressure still dropped further. V2 stated R1's physician was called and ordered R1 to be sent to the hospital for closer monitoring. V2 stated R1 was admitted back to the facility within several hours and all facility nurses were provided re-training on medication administration. V2 stated it was her expectation that nurses utilize three identifiers, resident pictures, asking residents their names, and checking resident identification bands, prior to providing medications. On 10/18/23 at 1:06 PM, V8 (Physician) stated when he was told R1 mistakenly received another resident's medications including two beta blockers, V8 told the staff to monitor R1's pulse and blood pressure for changes. V8 stated the mistaken doses of Coreg and Losartan provided to R1 were not very high, but R1's pulse and his blood pressure was V8's main concern. V8 stated when R1's blood pressure dropped lower, V8 stated he considered providing intravenous fluids at the facility but instead decided to send R1 to the hospital for closer monitoring. V8 stated he was concerned R1's pulse and blood pressure could drop which could cause dizziness/fainting and R1 to fall if he were standing. V8 stated R1 was with staff and either sitting or in bed, so his risk of falling was mitigated by staff supervision. V8 stated there could be a concern with death with higher/sustained doses of the additional medications given, but it would be very unusual with the one time, lose doses of the medications that were provided. V8 stated he never saw a resident die of a one time dose of the medications R1 was provided and death for R1 would have been very, very unlikely. Progress note, dated 9/26/23, shows R1 reported a nurse gave him the wrong medication. R1 was monitored for any adverse reactions and side effects. The progress note shows during the monitoring of R1's blood pressure after being given the wrong medications, R1's blood pressure dropped from 116/77 mmHg (millimeters of mercury) at 6:00 PM to 75/63 mmHg at 10:15 PM. The progress shows R1's physician was called and R1 was ordered to be sent to the hospital via 911. Hospital records, dated 9/26/23, show R1 was reported to have systolic blood pressures in the 80's mmHg and R1 received the wrong resident's medications. The physical exam shows R1's blood pressure was initially 88/50 mmHg and R1's heart rate was normal and regular at the hospital. The records show R1 was provided fluids during observation at the hospital, was asymptomatic, and his blood pressure improved to 120/66 mmHg as of 9/27/22 at 6:09 AM. Physician Note, dated 9/27/23, shows R1 returned from the emergency room after being given the wrong medications, his blood pressure becoming low, and becoming tired. MAR, dated 9/2023, shows R7 had physician medication orders which included Coreg, Losartan, Eliquis, Artificial tears, and insulin Aspart solution at 5:00 PM on 9/26/23. Medication Administration Policy, revised 10/2023, shows the purpose of the policy was to assure that all medications are administered safely and appropriately to aid residents to overcome illness, relieve and prevent symptoms, and help in diagnosis. The policy shows, Medications prescribed for one resident cannot be administered to another resident Identify the resident in the following 3 ways: a. Ask the resident to state his/her name. b. Identify resident by reading wristband and checking the picture on the MAR (Medication Administration Record.)
Nov 2022 3 deficiencies
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 observation, interview, and record review, the facility failed to provide assistance to eat for one of thirty-five resi...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to provide assistance to eat for one of thirty-five residents (R70) reviewed for activities of daily living in the sample of 35. The findings include: On 11/28/22 at 10:32 AM, R70 was laying on her back alone in her room. The head of the bed was at a twenty-degree angle. R70's puree breakfast tray was on the over bed table. There were covers on the two full bowls of food on the tray and a lid covered R70's hot chocolate. R70 had a picture of a spoon on the wall over the head of the bed. V7 (CNA-Certified Nursing Assistant) entered the room and asked R70 if she was finished. On 11/28/22 at 10:34 AM, V7 CNA said, [R70] feeds herself but she does not eat. The staff place her tray on the overbed table, she only drinks the liquids. We leave the tray until she finishes the liquids. On 11/28/22 at 12:35 PM, V7 CNA said that the spoon above the bed shows the resident needs the staff to help them eat. On 11/30/22 at 9:22 AM, V8 RN (Registered Nurse) said, [R70] needs to be assisted to eat using the recommended swallowing strategies. On 11/30/22 at 10:21 AM, V10 (Speech Therapist) said, [R70] is an aspiration risk. [R70] is highly impulsive with rate and size and talks between bites. [R70] has delayed clearing of the food and liquids when swallowing. When drinking, [R70] will take a drink then start to talk, this opens her airway and increases risk for aspiration. She needs to take small sips, swallow and wait for the liquid to clear. With [R70's] cognition, she is unable to implement swallowing strategies independently. When it comes to swallowing, [R70] requires moderate cues for appropriate pacing, size of presentation and to decrease talking between bites. R70's Minimum Data Set, dated [DATE] showed, Brief Interview for Mental Status: Severely Impaired. Eating: Limited Assistance one-person physical assist. R70's Care Plan, revised 07/29/22, showed, Yellow Spoon protocol- see Activities of Daily Living-Swallowing Instructions- Yellow Spoon for details. The facility's undated Yellow Spoon (Resident Information Sheet) showed, R70-FEED.
CONCERN (D)

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

Accident Prevention (Tag F0689)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to ensure a fall precaution intervention was in place for 1 of 35 residents (R472) reviewed for safety in the sample of 35. The ...

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Based on observation, interview, and record review, the facility failed to ensure a fall precaution intervention was in place for 1 of 35 residents (R472) reviewed for safety in the sample of 35. The findings include: R472's Order Summary Report showed R472 had the following diagnoses: hemiplegia, hemiparesis following a cerebral infarction affecting the left side, history of a fall, and muscle weakness. The same document showed orders for fall precautions and for a bed and chair alarm. On 11/28/22 at 12:23 PM, R472 was sitting on a wheelchair in his room. On the back of R472's wheelchair was a cord. The cord was not plugged into anything. On 11/28/22 at 12:43 PM, V5 (Registered Nurse) said the cord was to the chair alarm sensor that R472 was sitting on. V5 said the cord should be plugged into the chair alarm box. R472's care plan showed R472 was at risk for falls because of mobility impairments from a stroke and a recent fall.
CONCERN (E)

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

Medication Errors (Tag F0758)

Could have caused harm · This affected multiple residents

4. R160's Order Summary Report listed active orders as of 11/1/22 that showed an order for lorazepam 0.25mg (milligrams) by mouth every 6 hours as needed with an order date of 9/17/22 and no stop date...

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4. R160's Order Summary Report listed active orders as of 11/1/22 that showed an order for lorazepam 0.25mg (milligrams) by mouth every 6 hours as needed with an order date of 9/17/22 and no stop date listed. On 11/30/22 at 9:22 AM, V4 Pharmacy Manager said psychotropic medications should have a 14-day stop date and are to be reviewed after that period to see if the medication is still necessary. The facility's Psychoactive Medication Program, with a review date of 10/13/22, showed when and why psychotropic medication is to be used and length of therapy. Based on interview and record review, the facility failed to ensure as needed (PRN) psychotropic medications had a duration/stop date for 4 of 5 residents (R472, R160, R155 and R107) reviewed for pharmacy services in the sample of 35. The findings include: 1. R472's Order Summary Report, printed on 11/29/22, showed an order for PRN lorazepam (anti-anxiety psychotropic medication). The order had a start date of 11/9/22. There was no duration/end date associated with the order. 2. R107's Order Summary Report, printed 11/29/22, showed an order for PRN Ativan (anti-anxiety psychotropic medication). The order had a start date of 1/17/22. There was no duration/end date associated with the order. 3. R155's Order Summary Report, printed 11/29/22, showed an order for PRN lorazepam. The order had a start date of 3/24/22. There was no duration/end date associated with the order.
Understanding Severity Codes (click to expand)
Life-Threatening (Immediate Jeopardy)
J - Isolated K - Pattern L - Widespread
Actual Harm
G - Isolated H - Pattern I - Widespread
Potential for Harm
D - Isolated E - Pattern F - Widespread
No Harm (Minor)
A - Isolated B - Pattern C - Widespread

Questions to Ask on Your Visit

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

Our Honest Assessment

Strengths
  • • Grade B+ (85/100). Above average facility, better than most options in Illinois.
  • • No fines on record. Clean compliance history, better than most Illinois facilities.
  • • 22% annual turnover. Excellent stability, 26 points below Illinois's 48% average. Staff who stay learn residents' needs.
Concerns
  • • 20 deficiencies on record, including 1 serious (caused harm) violation. Ask about corrective actions taken.
Bottom line: Generally positive indicators. Standard due diligence and a personal visit recommended.

About This Facility

What is Dupage's CMS Rating?

CMS assigns DUPAGE CARE CENTER an overall rating of 5 out of 5 stars, which is considered much above average nationally. Within Illinois, this rating places the facility higher than 99% of the state's 100 nursing homes. This rating reflects solid performance across the metrics CMS uses to evaluate nursing home quality.

How is Dupage Staffed?

CMS rates DUPAGE CARE CENTER's staffing level at 5 out of 5 stars, which is much above average compared to other nursing homes. Staff turnover is 22%, compared to the Illinois average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Dupage?

State health inspectors documented 20 deficiencies at DUPAGE CARE CENTER during 2022 to 2024. These included: 1 that caused actual resident harm and 19 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Dupage?

DUPAGE CARE CENTER 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 366 certified beds and approximately 192 residents (about 52% occupancy), it is a large facility located in WHEATON, Illinois.

How Does Dupage Compare to Other Illinois Nursing Homes?

Compared to the 100 nursing homes in Illinois, DUPAGE CARE CENTER's overall rating (5 stars) is above the state average of 2.5, staff turnover (22%) is significantly lower than the state average of 46%, and health inspection rating (4 stars) is above the national benchmark.

What Should Families Ask When Visiting Dupage?

Based on this facility's data, families visiting should ask: "Can I visit during a mealtime to observe dining assistance and food quality?" "How do you handle medical emergencies, and what is your hospital transfer rate?" "Can I speak with family members of current residents about their experience?"

Is Dupage Safe?

Based on CMS inspection data, DUPAGE CARE CENTER has a clean safety record: no substantiated abuse findings (meaning no confirmed cases of resident harm), no Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death), and is not on the Special Focus Facility watch list (a federal program monitoring the lowest-performing 1% of nursing homes). The facility has a 5-star overall rating and ranks #1 of 100 nursing homes in Illinois. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Dupage Stick Around?

Staff at DUPAGE CARE CENTER tend to stick around. With a turnover rate of 22%, the facility is 24 percentage points below the Illinois average of 46%. Low turnover is a positive sign. It means caregivers have time to learn each resident's needs, medications, and personal preferences. Consistent staff also notice subtle changes in a resident's condition more quickly. Registered Nurse turnover is also low at 20%, meaning experienced RNs are available to handle complex medical needs.

Was Dupage Ever Fined?

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

Is Dupage on Any Federal Watch List?

DUPAGE CARE CENTER 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.