Marquette County Medical Care Facility

200 West Saginaw Street, Ishpeming, MI 49849 (906) 485-1061
Government - City/county 140 Beds Independent Data: November 2025
Trust Grade
80/100
#42 of 422 in MI
Last Inspection: May 2025

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

Overview

Marquette County Medical Care Facility has a Trust Grade of B+, which means it is recommended and performs above average compared to similar facilities. It ranks #42 out of 422 nursing homes in Michigan, placing it in the top half of state facilities, and #3 out of 4 in Marquette County, indicating only one local option is better. The facility is improving, having reduced its serious issues from 4 in 2024 to 0 in 2025. Staffing is a strong point here, with a perfect rating of 5/5 stars and only a 25% turnover rate, which is well below the state average. Notably, the facility has not incurred any fines, suggesting good compliance with regulations. However, there are some concerns. The facility has faced serious issues, including a failure to develop a care plan for a resident with prolonged nausea, which led to significant weight loss and multiple pressure injuries. Another incident involved a resident with severe cognitive impairment who had pressure ulcers upon admission, and there were lapses in care planning for a resident who fell and sustained a skin tear. While there are strengths, these weaknesses highlight the need for careful monitoring of care plans and resident conditions.

Trust Score
B+
80/100
In Michigan
#42/422
Top 9%
Safety Record
High Risk
Review needed
Inspections
Getting Better
4 → 0 violations
Staff Stability
✓ Good
25% annual turnover. Excellent stability, 23 points below Michigan's 48% average. Staff who stay learn residents' needs.
Penalties
✓ Good
No fines on record. Clean compliance history, better than most Michigan facilities.
Skilled Nurses
✓ Good
Each resident gets 53 minutes of Registered Nurse (RN) attention daily — more than average for Michigan. RNs are trained to catch health problems early.
Violations
○ Average
9 deficiencies on record. Average for a facility this size. Mostly minor or procedural issues.
★★★★★
5.0
Overall Rating
★★★★★
5.0
Staff Levels
★★★★☆
4.0
Care Quality
★★★★★
5.0
Inspection Score
Stable
2024: 4 issues
2025: 0 issues

The Good

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

    23 points below Michigan 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 Michigan's 100 nursing homes, only 1% achieve this.

The Ugly 9 deficiencies on record

3 actual harm
Jun 2024 4 deficiencies 3 Harm
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Quality of Care (Tag F0684)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to develop a care plan and offer/recommend diagnostic te...

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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 develop a care plan and offer/recommend diagnostic testing or consultation with a Gastroenterologist or Physician Specialist to determine the source of prolonged nausea and vomiting for one Resident (R16) of one Resident reviewed for change of condition. This deficient practice resulted in R16 sustaining a 27.3% weight loss in 6 months, a decline in activities of daily living (ADL), a significant change of condition, and the development of multiple pressure injuries. Findings include: Resident #16 (R16) R16 was admitted to the facility on [DATE]. A quarterly Minimum Data Set (MDS) Assessment, dated 9/26/23, coded R16 as requiring staff assistance for activities of daily living (ADL), including partial staff assistance with ambulating, toileting, standing, and transfers. The MDS documented a Brief Interview for Mental Status (BIMS) Score of 15, indicating R16 was cognitively intact. The quarterly MDS did not code R16 with weight loss. A Significant Change MDS, dated [DATE], coded R16 as being fully dependent on staff for all ADL except eating. The MDS coded R16 as being dependent on staff for ambulating, toileting, standing, and transfers. The MDS documented a BIMS score of 13, indicated R16 remained cognitively intact. The Significant Change MDS coded R16 with weight loss. On 6/4/24 at 8:27 a.m., R16 was observed lying in bed holding an emesis basin with an untouched plate of breakfast on her bedside table. R16 said she was nauseated and was unable to move because of nausea and vomiting. R16 said she had experienced nausea and vomiting for so long that she lost weight due to inability to eat. A review of the medical record for R16 revealed a weight loss of 69.9 pounds from 12/6/23 until 6/2/24, a 27.3% loss of body weight. The care plan for R16 did not indicate the weight loss as desirable by R16. The nutritional care plan documented R16 was diagnosed with protein calorie malnutrition (a nutritional status in which reduced availability of nutrients leads to changes in body composition and function) starting 3/1/24 due to prolonged low appetite/intakes/weight loss. Progress notes for R16 revealed numerous documentation entries of nausea and vomiting. R16 was documented as experiencing intermittent nausea in August, September, and October 2023. From 11/17/23 through 11/27/23, there were 13 progress note entries detailing R16 experiencing nausea and vomiting with limited ability to eat. The medical record documented a 16.6-pound weight loss from 11/15/23 through 11/30/23, a 9.4% loss of body weight. In December 2023, R16 was transferred and subsequently admitted to the hospital with venous stasis ulcers (wounds that result from blood flow problems in the veins) and cellulitis (a skin infection that can spread rapidly and cause serious complications). R16 returned to the facility from the hospital on [DATE]. There were seven progress notes in January 2024 regarding R16 enduring nausea and vomiting. A progress note by the Registered Dietician (RD) on 1/12/24 described R16's intake as very poor. The note documented R16 was declining most meals and reporting lack of appetite despite the use of an appetite stimulant. The progress note documented, Noted MD is aware of continued poor appetite despite initiation of (a medication used to stimulate appetite) . Nausea and/or vomiting were documented fifteen times for R16 in February 2024, ten times in March 2024, nine times in April 2024, and twenty-eight times in May 2024. A progress note on 5/6/24 documented, in part: .very shaky, increased RR (respiratory rate) and heavy breathing .promethazine given at 10:00 a.m. which provided little to no relief. Stating 'I'm sick of being nauseous, I'm dry heaving, I'm so tired. Why can't I have something else for this nausea?' . Physician visit documentation for September 2023, October 2023, November 2023, December 2023, and January 2024 did not contain documentation of R16 experiencing nausea and vomiting. A physician visit note dated 2/7/24 read, in part: .she has occasional nausea .Reviewing the notes over the last month she has had really a fair amount of GI (gastrointestinal) upset .She is having a lot of nausea, is vomiting, unclear why .The weight loss at this rate is not good and she is getting a lot of (a medication used to treat nausea and vomiting) and having a lot of problems so we will get the labs and then decide . The documentation did not include any discussion with R16 regarding diagnostic testing or consultation with a physician specializing in disorders of the gastrointestinal (GI) system. A physician visit note dated 3/6/24 read, in part: .she has been having ongoing nausea . The documentation did not include a plan to address the nausea by offering to conduct diagnostic testing or referring R16 to a physician specializing in disorders of the GI system. On 4/5/24 the physician documented R16 had an episode of nausea, vomiting and diarrhea but that resolved . The documentation did not include a plan to address the nausea or offering R16 the opportunity for diagnostic testing or referral to a Gastroenterologist. The most recent physician's visit note in R16's record was dated 5/1/24 and read, in part: .reading the notes there is intermittent nausea although it seems, today anyway, being related to being moved in her bed and turned .Will treat her vertigo, which hopefully will help the nausea . The documentation did not document any discussion with R16 regarding consultation with a Gastroenterologist or obtaining diagnostic testing. R16's care plans did not contain a care plan for nausea and vomiting to provide staff with interventions to implement when R16 experienced nausea and vomiting. The medical record did not reveal a discussion with R16 regarding consultation with a specialist to determine and potentially treat the source of the nausea and vomiting, nor was R16 provided with an offer for diagnostic testing to potentially determine the source of the nausea and vomiting. The Director of Nursing (DON) and the Registered Nurse (RN) Supervisor L were interviewed on 6/5/24 at 8:05 a.m. The DON confirmed she was aware of R16 experiencing recurrent nausea and vomiting. The DON said R16's physician had ordered antiemetic medications, but admitted she was unaware if diagnostic testing or consultation with a specialist had been discussed with R16. RN L confirmed she was aware of R16 enduring persistent, intermittent nausea and vomiting and weight loss. When asked if consultation options or diagnostic testing was offered to R16, RN L said, I don't know. I'll have to look in the record. R16 was interviewed on 6/5/24 at 8:29 a.m. R16 was lying in bed with an emesis basin next to her. R16 said she was nauseated and said, I've been nauseated for so long. I just wish this was all over. R16 said her physician was in the facility today and had offered to conduct some testing. When asked if she was considering the testing, R16 said, It probably won't do any good because they'd have to move me and that would cause even more nausea. On 6/5/24 at 10:22 a.m., RN M and RN N were observed completing treatments to pressure injuries and moisture-associated skin damage (MASD) on R16's bilateral buttocks. R16 was rolled onto her left side to reveal two Stage 2 pressure injuries (partial-thickness loss of skin with exposed dermis, presenting as a shallow open ulcer) on the right gluteal cleft and one Stage 2 pressure injury on the left gluteal cleft. R16's bilateral buttocks were reddened and inflamed with skin erosion due to MASD. RN L was interviewed on 6/5/24 at 10:46 a.m. When asked if she had the opportunity to review R16's medical record to determine if R16 was offered consultation with a specialist or diagnostic testing to determine the root-cause of the nausea and vomiting, RN L said they had obtained labs and adjusted the medications for R16. RN L said they obtained lab results last week. A progress note of 5/25/24 at 2:06 p.m. was reviewed and read, in part: .Labs recently done WNL (within normal limits). When asked if the labs or medication adjustments had determined the source of the recurrent nausea and vomiting, RN L replied, The doctor is monitoring. RN L said R16's physician had spoken with R16 this morning and the physician said further diagnostic testing was not indicated. RN L said R16 declined any further actions to determine the source of the nausea and vomiting when the offer for diagnostic testing was offered to R16 on 6/5/24. When asked why diagnostic testing was not offered to R16 prior to 6/5/24, RN L said an overall decline had been experienced by R16. RN L said the decline included a change in appetite. She wasn't eating or thriving. When asked if R16 wasn't eating because of nausea and vomiting, RN L said, We were trying to deal with that with medications. When asked if the Medical Director had been made aware of the prolonged amount of time R16 had endured nausea and vomiting of an unknown cause, RN L replied, No, I don't think so. The Registered Dietician (RD) was interviewed on 6/5/24 at 11:08 a.m. The RD confirmed R16 had lost a significant amount of weight due to not eating. The RD said R16 had nausea and vomiting so she would refuse food, or eating would result in R16 vomiting. The RD said the interdisciplinary team had been discussing R16 going on comfort care measures or hospice. The RD said R16 started experiencing significant weight loss from nausea and vomiting in January 2024. R16's physician was interviewed on 6/5/24 at 11:22 a.m. The physician was asked what had been done to address R16's prolonged nausea and vomiting. The physician said she had made medication adjustments and said R16 had been on most of the available antiemetic medications. When the physician was asked what was causing the nausea and vomiting, she replied, I'll be honest with you - I don't know. She might have gastroparesis or a tumor or it could be anything. When asked if R16 had been afforded the opportunity for consultation with a Gastroenterologist or other specialist, or if diagnostic testing was offered, the physician said she offered R16 those options today, 6/5/24, and R16 had declined the offer. When asked why R16 was not provided with those options prior to 6/5/24 despite many months of nausea and vomiting with subsequent weight loss and wound development, the physician said, I think I did - I actually know I did - I don't know why I didn't document it. The physician reiterated R16's declination on 6/5/24 of further testing or consultations. The facility policy Significant Change Notification dated 1/4/23 read, in part: .Purpose: To assure that residents and/or their legal representative has the right to make choices about aspects of his/her care that will affect the quality of life of each resident .If the RN Supervisor or Charge Nurse is not satisfied that the physician's response will meet the resident's needs, then he/she may move up the chain of command to: .Medical Director . The DON was interviewed on 6/5/24 at 1:05 p.m. The DON was asked if the Medical Director had been made aware of the concerns with R16 and the prolonged duration of nausea and vomiting without being afforded the opportunity to find out the cause of the nausea and vomiting, the DON replied, No, not to my knowledge.
SERIOUS (G)

Actual Harm - a resident was hurt due to facility failures

Pressure Ulcer Prevention (Tag F0686)

A resident was harmed · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Resident #113 (R113) Review of R113's electronic medical record (EMR) revealed admission to the facility on 3/28/24 with diagnos...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Resident #113 (R113) Review of R113's electronic medical record (EMR) revealed admission to the facility on 3/28/24 with diagnoses including a left femur fracture, history of transient ischemic attack (a temporary blockage of blood flow to the brain), and encephalopathy (a type of brain injury contributing to an altered mental status). Review of R113's Brief Interview for Mental Status (BIMS) assessment, dated 4/3/24, revealed a score of 3, indicative of severe cognitive impairment. Review of Minimum Data Set (MDS) Section M, Skin Conditions, revealed R113 admitted to the facility with 2 stage II (tissue damage that affects the first two layers of skin) pressure ulcers and 1 unstageable deep pressure injury. Review of a Skin Assessment, dated 3/29/24, indicated R113 had two open stage II ulcers on the anterior left leg which measured 1.5 cm (centimeters) x 1.7 cm and 1 cm x 1.2 cm, respectively, and a deep tissue to the left heel measuring 2.6 cm x 3.5 cm. On 6/3/24 at 2:17 PM, an interview was conducted with R113 who was asked about the status of his wounds. R113 stated, It hurts. Review of a Wound Treatment Note dated 5/14/24 read, in part: .Location of Wound: Lt [left] heel . Signs of Symptoms of Infection: Odor, Increased Drainage . Any Change in Wound:? Worsened larger, blister popped, small drainage . .Lt shin with mild odor today, foul smelling . Lt heel-now opened d/t [due to] drainage noted on dressing . Review of a Wound Treatment Note dated 5/24/24 read, in part: .At this time, left shin now Stage 4 [pressure ulcer] down to what is perceived to be exposed tendon, shiny and white . Review of R113's EMR revealed no indication of physician follow-up after identification of R113's worsening wounds as indicated by Wound Treatment Notes on 5/14/24 and 5/24/24. On 6/5/24 at 11:30 AM, an interview was conducted with Wound Care Treatment Coordinator, Registered Nurse (RN) M who verified the worsening of R113's wounds since admission. RN M indicated a foul-smelling odor and/or increased drainage from a wound could be a sign of infection. When asked the reasoning behind the lack of physician follow-up in reference to the worsening of R113's wounds, RN M stated, I asked for an order for a wound care consultation referral from [Physician R] on 5/14/24 but never got a response. I asked again [for a wound care consultation referral] on 5/23/24 with no response . He [Physician R] is notorious for not coming in [to the facility] to sign orders and he doesn't like them faxed . I eventually had my supervisor contact him [Physician R] to forward it [wound care consult referral request] on . Review of email correspondence sent by RN M to Physician R revealed the following: 1. 5/14/24: PLEASE DICTATE ON THE FOLLOWING SKIN ISSUE: .Location of wound: lt heel . Type of Wound: Pressure . Pinpoint area to center of heel DTI [deep tissue injury] opened and drained scant serosanguinous drainage . Would you agree with a Wound Care Consult? 2. 5/23/24: PLEASE DICTATE ON THE FOLLOWING SKIN ISSUE: .Location of wound: left heel . Type of Wound: Pressure . Would you agree with a Wound Care Consult? Review of physician documentation did not address a wound care consult following the email communications from RN M on 5/14/24 and 5/23/24. Review of Nursing Progress Note dated 5/24/28, read: Skin: In to assess resident at this time. D/T not hearing a reply from multiple attempts to MD regarding Wound Care Consult, reached out to supervisor who will be contacting MD directly to discuss referral which family and treatment team is in favor of. Review of R113's Wound Care Consultation, dated 5/28/24, 14 days after initial identification of R113's wound progression, read, in part: .Wound #1 is located on left lower leg (distal shin). The aide with the patient is not sure how long the wound has been present for, just states that per [facility] nurses, that since developing the wound it has worsened . Wound #2 is located on left heel. The aide with the patient again is not sure how long this wound has been present for. This wound was not even listed on the paperwork brought in by the CNA [certified nursing assistant] from the facility . The aide wasn't sure with that (sic) the wound has been treated with; there is no mention in the accompanying documentation of what it's been being treated with .Wound #1/left distal shin .I suspect this is an arterial ulcer .non-pressure chronic ulcer .with unspecified severity . On 6/5/24 at 12:15 PM, an interview was conducted with the Director of Nursing (DON) regarding expectations for interdisciplinary communication regarding wound care/management. The DON stated the physician should be notified and should respond to progression of a wound in terms of size and signs and symptoms of infection including odor. The DON stated she was unsure why Physician R did not respond to the Wound Care Consult request despite rounding on R113 on 5/14/24. The DON was questioned regarding the facility protocol if the interdisciplinary team was unsatisfied with the physician's response. The DON stated, the medical director would be responsible for assisting but indicated the medical director was not notified in this case. The DON confirmed the 14-day lapse from the initial wound care consultation request on 5/14/24 to the wound care consult visit on 5/28/24 was considered a delay in treatment. Review of facility policy titled, Significant Change Notification, dated 1/4/23, read, in part: STANDARD: To ensure that a system exists for immediate notification for the resident's physician and legal representative when there is a change in psychosocial status, life threatening conditions, clinical complications, or a need to alter treatment significantly . The RN Supervisor/Charge Nurse may at any time prompt a clarification of orders. If the RN Supervisor or Charge Nurse is not satisfied that the physician's response will meet the resident's needs, then he/she may move up the chain of command: a. On-call RN b. DON/ADON [assistant director of nursing] or designee c. Medical Director d. Administrator . Review of facility policy titled, Skin Integrity Program, dated 7/18/23, read, in part: .This facility is committed to reducing the risk of pressure injuries and the promotion of healing of existing pressure injuries . The MD [medical doctor] will be updated, following a nursing assessment, for changes in preexisting or new onset of co-morbid conditions affecting skin integrity . The attending physician will be notified of the presence or lack of healing of any pressure injuries . On 6/5/24 at 9:30 AM, an observation was made of R62 during wound dressing changes completed by Registered Nurse Q. Wound measurements were as follows: a.) Right buttocks one open area (stage II) measuring 1.0-centimeter (cm) x 1.0 cm with surrounding redness 3.0 cm x 3.0 cm, b.) Left buttocks two open areas (stage II) measuring upper 1.0 cm x 0.5 cm and lower 1.0 cm x 0.4 cm with surrounding redness measuring 7.5 cm x 4.0 cm, c.) Intergluteal cleft from the coccyx to the anus open area (stage II) measuring 3.0 cm x 0.2 cm, d.) Right malleolus (unstageable) with eschar in the center measuring 1.6 cm x 0.6 cm and with surrounding redness measuring 4.9 cm x 4.2, e.) Left heel (deep tissue injury) measuring 2.7 cm x 0.6 cm with mild redness surrounding the area with a scab in the center and light purple in color. On 6/5/24 at 9:45 AM, R62 was asked if any of the wounds hurt or were tender to touch and replied, The one on my right ankle is sore to touch and my butt is really sore. I need to rest now and stabilize. On 6/5/24 at 10:00 AM, an interview was conducted with RN M in charge of wound care and was asked if R62 was admitted to the facility with all of his current open wounds and replied, No. He originally just had the one on his left heel and acquired the others after he was admitted to the facility. Based on observation, interview, and record review, the facility failed to implement and maintain interventions to prevent the development and progression of pressure ulcers (a wound affecting skin, fat, and muscle tissues) for two Residents (#62, #113) of three residents reviewed for pressure injuries. This deficient practice resulted in the development of three stage II pressure ulcers and worsening of pressure ulcers. Findings include: Resident #62 (R62): Review of R62's Electronic Medical Record (EMR) revealed admission to the facility on 5/2/24 with diagnoses including a collapsed vertebra, muscle weakness, peripheral vascular disease, and diabetes. Review of R62's most recent Minimum Data Set (MDS) assessment dated [DATE] revealed a Brief Interview for Mental Status (BIMS) score of 15, indicative of being cognitively intact. Further review of the MDS, section M, revealed R62 did not have pressure ulcers present upon admission. Review of R62's Braden Scale admission assessment (a standardized assessment which calculates risk of pressure injury) on 5/2/24, revealed a score of 13.0, indicating R62 was at risk [for pressure ulcer]. An interview was conducted with R62 on 6/4/24 at 4:30 p.m. R62 stated that he has two pressure ulcers on his buttock that he did not have when he was admitted just over a month ago. R62 expressed frustration that he needs staff assistance to turn and reposition, his wheelchair is uncomfortable, and his feet cannot reach the floor causing pressure on his lower back and buttocks. R62 was currently lying on his back in his bed. On 6/5/24 at 10:40 a.m., R62 was observed sitting in his wheelchair requesting to use the restroom. R62's legs were noted to not be able to touch the ground with his right lower leg rubbing and pushing against the metal of his wheelchair. R62 stated that this causes him immense pain. R62 was transferred to the toilet and an observation of his wheelchair showed that his Roho cushion (device used on wheelchair seats to promote skin integrity) was noted to be deflated. An interview was conducted with Occupational Therapist (OT) S on 6/5/24 at 11:00 a.m., concerning R62's wheelchair. OT S stated that Roho cushions are checked every day but that R62's wheelchair was not the best fit for him. An interview was conducted with Physical Therapist (PT) T on 6/5/24 at 11:05 a.m. PT T stated that R62's wheelchair is lowered as far as it will go, but that his legs will still not touch the ground. PT T stated that R62 did have a smaller wheelchair at the time of admission, but it was too tight and causing pain and discomfort. R62 did have a power wheelchair and was assessed for safety from OT, but since R62 is requiring supplemental oxygen, this power wheelchair is not best suited for him. PT T explained that there are no custom wheelchair companies in the region and that R62 would either need to purchase a wheelchair for himself or that the therapy department could possibly ask the facility to purchase one. PT T observed the Roho cushion and stated that it was not inflated to the correct pressure. Review of R62's plan of care revealed the following problem: At risk for skin breakdown R/t (related to): Nicotine dependence, Pacemaker, Type 2 DM (diabetes), Pain, Constipation, Sleep Apnea, Atherosclerotic heart disease, HTN (hypertension) A Fib (Atrial fibrillation), collapsed vertebra of lumbar region. Interventions were listed as: 1. BED: oversized width [NAME] air, keep linen clean, dry, and wrinkle free. Date Initiated: 5/2/24 2. .Calmoseptine to scrotum, buttocks (slit), and glutes with cares and episodes of incontinence for protection, [medication name] pump lotion to dry areas w/ (with) cares. Date Initiated: 5/2/24 3. .Elevate heels with dermasaver over foam pillow, derma boots to feet when in bed, oversized ROHO to recliner, blue heel protections to be on when in recliner, bedder foot pad to end of bed between mattress and sheet. Date Initiated: 5/2/24 4. .Repositioning: Reposition every 2-3 hours when in bed or chair, avoid shearing residents' skin during positioning, transferring, and turning, elevate heels w/ derma over pillow. Date Initiated: 5/2/24 5. Weekly skin assessment to be completed for 4 weeks to observe skin for changes to the skin's integrity. Date Initiated: 5/2/24 Review of R62's Progress Notes revealed the following data: 1. 5/2/24: a) Mid buttock 8.5 cm(centimeter) scar with slight indentation noted. b) Buttock into rectum region: 6.5x3.5 cm blanching redness. 2. 5/6/24: a) No new skin issues or concerns b) Sacral slit area measuring .8 cm with red/blanching area. 3. 5/7/24: a) No new reported skin issues or concerns 4. 5/8/24: a) No new skin issues or concerns 5. 5/9/24: a) Location of Wound - L (left) gluteal cleft. b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 1 cm, Width 1 cm e) Any Changes to Care Plan Interventions? No 6. 5/13/24: a) Location of Wound - L gluteal cleft b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 1.5 cm, Width 0.5 cm e) Any Changes to Care Plan Interventions? No 7. 5/20/24: a) Location of Wound - L gluteal cleft b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 1.1 cm, Width 1 cm e) Any Changes to Care Plan Interventions? No 8. 5/27/24: a) Location of Wound- L gluteal cleft b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 1.1 cm, Width 1 cm and superficial area .9 cm x .6 cm e) Any Changes to Care Plan Interventions? No 9. 5/29/24: a) Location of Wound - Rt (right) gluteal cleft, medial #1 b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 2 cm x 1 cm, Depth .1 cm e) Any Changes to Care Plan Interventions? No 10. 5/29/24: a) Location of Wound - Rt Gluteal Cleft, lateral #1 b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 2 cm, Depth .1 cm, Width 1 cm e) Any Changes to Care Plan Interventions? No 11. 5/29/24: a) Location of Wound - L Gluteal Cleft b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 2 cm, Depth .1 cm, Width 1 cm e) Any Changes to Care Plan Interventions? No 12. 6/3/24: a) Location of Wound - Rt Gluteal Cleft Lateral #1 b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 1 cm, Depth .1 cm, Width .9 cm e) Any Changes to Care Plan Interventions? No 13. 6/3/24 a) Location of Wound - Rt Gluteal Cleft medial #1 b) Type of Wound - Pressure c) Wound Stage: Stage II d) Wound Measurement - Length 1.5 cm, Depth .1 cm, Width 1.2 cm e) Any Changes to Care Plan Interventions? No
SERIOUS (G)

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** Resident 9 (R9) Review of R9's Minimum Data Set (MDS) assessment, dated 5/9/24, revealed an admission to the facility on 3/21/22...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Resident 9 (R9) Review of R9's Minimum Data Set (MDS) assessment, dated 5/9/24, revealed an admission to the facility on 3/21/22, with active diagnoses that included: urinary tract infection, dementia, anxiety, chronic obstructive pulmonary disease (COPD), and chronic kidney disease. R9 scored 11 of 15 on the Brief Interview for Mental Status (BIMS) reflective of moderate cognitive impairment. Review of Resident Incident Report, dated 4/29/24, reflected R9 was found sitting on the bathroom toilet at 1:15 a.m. The staff were alerted by roommate that R9 had fallen and assisted self to a standing position and ambulated to the bathroom. R9 sustained a skin tear to left arm. A review of R9's care plan, revealed no interventions to reduce accidents/falls were added to R9's care plan. During an interview on 6/5/24 at 8:45 a.m., RN (Registered Nurse)/Rehab Coordinator K stated, The care plan was not updated as it was a Urinary Tract Infection (UTI) that caused the fall ., We don't update with each fall. During an interview on 6/5/24 at 11:25 a.m., the Director of Nursing (DON) acknowledged the care plan was not revised after R9's fall to prevent further accidents. Resident 29 (R29) Review of R29's MDS assessment, dated 3/14/24, revealed an admission to the facility on 8/11/22, with active diagnoses that included: diabetes mellitus, hypertension, heart failure, chronic kidney disease, and depression. R29 scored a 13 of 15 on the BIMS reflective of intact cognition. Review of R29's Incident Report, dated 2/12/24, revealed R29 was found on the floor in her room, and she fell trying to get out of bed. A review of R29's care plan, revealed no intervention to reduce accidents was added to R29's care plan. During an interview on 6/5/24 at 8:03 a.m., RN/Rehab coordinator K confirmed no interventions were added to R29's care plan . Review of R29's Incident Report, dated 4/16/24, revealed R29 rang call light and stated that R29 slid out of bed and fell to the floor. During an interview on 6/5/24 at 8:03 a.m., RN/Rehab Coordinator K stated, a treatment was added . and should have been added to her care plan, but it was not done. Review of Resident Incident Report, dated 4/23/24, revealed R29 fell in the doorway of another resident's room. R29 reported a head injury and a bump was noted to the back of R29's head. A review of R29's care plan, revealed no intervention to reduce accidents was added to R29's care plan. During an interview on 6/5/24 at 8:03 a.m., RN/Rehab coordinator K said, Changes are in the notes but not in the care plan. During an interview on 6/5/24 at 11:25 a.m., the DON acknowledged the care plan was not revised after R29's multiple falls to prevent further accidents. Review of policy titled, Fall/Fall Risk Program, read in part, .The facility will identify residents at risk for falls and develop interventions along with a plan of care to prevent falls. The facility will respond to resident's experiencing a fall by analysis/assessment, establishment of a plan of care, and monitoring of the effectiveness of the care plan. The Rehab Coordinator/designee will identify and initiate fall interventions with staff, resident, and or family input which will be reflected in the plan of care. Interventions will be monitored for effectiveness and adjusted as necessary . Based on observation, interview, and record review the facility failed to implement, update and revise comprehensive care plans to prevent falls for three Residents (#9, #26, #29) of three residents reviewed for falls. This deficient practice resulted in falls with major injury. Findings include: Resident #26 (R26) Review of R26's Electronic Medical Record (EMR) revealed admission to the facility on 9/15/23 with diagnoses including dementia, left femur fracture, and history of falling. Review of R26's 9/21/23 Minimum Data Set (MDS) assessment revealed a Brief Interview for Mental Status (BIMS) score of 11/15, indicative of mild cognitive impairment. Further review of R26's MDS revealed she had a fall with fracture prior to admission to the facility. Review of R26's Fall Risk Assessment, dated 9/15/23 and completed on 9/20/23 revealed R26 scored a 19 presenting as a high risk for falls. Plan of Care for R26 read, in part, Resident has a fall risk score of 19. She has a history of 1 fall within the past month resulting in current fracture. No falls since admission, she has not shown any impulsive behaviors. She is working with skilled therapy and remains capable of making her own independent decisions. She will be changed from a risk closely monitor, to a potential monitor for falls. Care plan updated. Review of R26's Plan of Care in October 2023 revealed the following problems: Alteration in cognition secondary to some underlying memory loss that is present - start date: 9/18/23. Potential Alteration in performing activities of daily living resulting in risk of self-care deficit and potential falls .start date: 9/15/23. Approaches for R26 included the following interventions: I am known to self-transfer despite reminders and encouragement to call for assistance - start date 10/5/23. Potential for falls, monitor - start date 9/20/23. Review of R26's Incident and Accident Reports revealed the following entry: 10/14/23 .Floor staff heard resident yelling for help while they were assisting another resident. Upon entering the room res (resident) was laying on the floor on her left side with her head towards the door and her legs toward her bed. WC (wheelchair) was next to armoire and walker was next to the foot of her bed. Res had been noted to be ambulating without walker this shift .Res ROM (Range of Motion) WNL (within normal limits) with all extremities with the exception of her LLE (Left Lower Extremity), LLE rotated outward and shortened. Res unable to move without pain and was guarding the lateral side of her left thigh about her knee where a mass was felt by writer upon assessment .Res agreed to be sent out to hospital for further evaluation . Review of R26's Hospital Discharge Summary dated 10/19/23 read, in part, Discharge Diagnosis: Oblique left periprosthetic distal femur fracture, s/p (status post) ORIF (open reduction internal fixation [surgical repair method]) on 10/15/23 . R26 returned to the facility on [DATE]. Review of R26's Current Plan of Care revealed the following problems: Alteration in cognition secondary to diagnosis of dementia with a recent progression of disease progress. Worsening insight, judgment and recall ability's .start date: 9/18/23. Alteration in performing activities of daily living resulting in risk of self-care deficit and potential falls .start date: 9/15/23. Approaches for R26 included the following interventions: Transfers and ambulates independently with a walker. Please encourage walker usage if seen walking without her assistive devices .start date: 4/19/24. Potential for falls, monitors, signs to encourage resident to use her walker by TV and bed in room .start date: 4/19/24. An interview was conducted with R26 and her daughter on 6/3/24 at 3:29 p.m. R26 stated that she has attempted most recently to not use her walker when getting out of bed to see if she, still can do it. An interview was conducted with the Director of Nursing (DON) on 6/5/24 at 11:17 a.m. The DON confirmed that when R26 had returned to the facility after her fall in October 2023, the facility's fall watch program was either not initiated or not documented correctly. The DON stated that the facility would normally do more interventions for residents who are at high risk for falls which would include 15-minute checks stating, They could have done more. The DON agreed that the pre and post fall interventions for R26 were not appropriate or adequate.
CONCERN (D)

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

Deficiency F0557 (Tag F0557)

Could have caused harm · This affected 1 resident

Based on observation, interview, and record review, the facility failed to provide activities of daily living (ADL) care in a dignified manner to one Resident (R17) of twenty-five residents reviewed f...

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Based on observation, interview, and record review, the facility failed to provide activities of daily living (ADL) care in a dignified manner to one Resident (R17) of twenty-five residents reviewed for dignity. Finding include: On 6/3/24 at 3:10 PM, an observation was made of CNA (certified nurse aide) D assisting R17 in his room to his bathroom on the toilet. On 6/3/24 at 3:15 PM an observation was made of R17 in his bathroom with the door open to the bathroom and the room door open. R17 was using the bathroom toilet. R17 was left unattended with both the bathroom door and room door open. On 6/3/24 at 3:17 PM, an observation was made of R57 entering R17's room in her wheelchair. Approximately one minute later CNA G redirected R57 out the room door of R17. On 6/3/24 at 3:20 PM, an interview was conducted with CNA G, and was asked if R17's door should be closed and replied, The other CNA could have, yeah. The other CNA should have closed it part way because R17 is a fall risk and if it was partially closed then she [R57] would not have gone in. On 6/3/24 at 3:25 PM, an interview was conducted with CNA D, and was asked why he left R17 in his bathroom with both the bathroom door and room door open and replied, I had to go get a brief. CNA D was asked why he did not ask for assistance and replied, I don't know. CNA D was asked why he left the door open to R17's bathroom and room entry door and replied, I guess I should have closed it and left it open a little. He is a fall risk. CNA D was asked if R17 had privacy while using the bathroom and replied, No. I should have done that differently. On 6/5/24 at 10:30 AM, an interview was conducted with the Nursing Home Administrator (NHA) and was asked about closing doors to provide privacy when residents were using the bathroom and to prevent wandering residents from entering other resident's rooms and replied, I would expect for bathroom doors to be closed by staff to allow for privacy and wandering residents should not be entering rooms when others are using the bathroom. The CNA should have closed the door and not allowed the wandering resident to enter the room. Wandering residents should be redirected.
Jun 2023 4 deficiencies
CONCERN (D)

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

Comprehensive Care Plan (Tag F0656)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to implement the comprehensive, resident-centered risk 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 implement the comprehensive, resident-centered risk for skin breakdown for two Residents (R32 and R93) of twenty-three residents reviewed for care plans. This deficient practice resulted in the development of two pressure injuries for R32 and the potential for R93 to develop a pressure injury. Findings include: Resident #32 (R32) R32 was admitted to the facility on [DATE] and had diagnoses including generalized weakness, fracture of lower end of the left humerus (upper arm bone), fracture of left pubis (front pelvic area), dementia, diabetes mellitus, peripheral vascular disease (PVD), and need for assistance with personal care. Review of R32's admission Minimum Data Set (MDS) assessment, dated 6/7/23, revealed the following: R32 required extensive, two-person physical assistance with bed mobility and was totally dependent on staff for transfers. Section M- Skin Conditions, revealed R32 was at risk for developing pressure ulcers and had three unstageable pressure ulcers (wound bed covered by slough [dead tissue] and /or eschar [dried brown slough] ), and one unstageable pressure ulcer, not present upon admission. Further review of Section M, revealed a fourth pressure ulcer, deep tissue injury (DTI), not present on admission. R32's admission MDS assessment also revealed a Brief Interview for Mental Status (BIMS) assessment of 4 out of 15, indicating severe cognitive impairment. On 6/27/23 at 3:40 PM, an observation was made of R32 in his room. R32 was lying in his bed with his heels resting on the mattress, not elevated on a pillow, and was wearing gripper socks. R32 was wearing a left arm sling, with his left arm resting on his left side, and his elbow and upper arm were resting on his mattress. On 6/28/23 at 12:05 PM, an interview was conducted with Licensed Practical Nurse (LPN) F. LPN F was asked how R32 developed two pressure ulcers after admission to the facility. LPN F replied, [R32's] left arm is heavy in his sling, and we have not been able to find extra pillows but did order some more. LPN F was asked about what care plan interventions should be in place. LPN F replied, All interventions should be in place, and he should have derma saver pad, boots and heels elevated. On 6/29/23 at 8:05 AM, an observation was made of R32. R32 was lying in his bed in his room and talking with an unidentified staff member. R32's heels were observed resting directly on the bed. R32 did not have derma saver boots on and was wearing gripper socks. R32 was also not wearing a left arm sling located in the room. On 6/29/23 at 8:15 AM, an interview was conducted with LPN A. LPN A was asked why R32 did not have feet elevated, derma saver boots on or the left arm sling. LPN A replied, I have to look at his care plan. LPN A reviewed R32's care plan and then stated, [R32] should be . and immediately went to see R32. An observation of R32's wound care, provided by LPN F on 6/29/23 at 12:25 PM, revealed an intact dressing located on his left posterior heel and left elbow. Upon entry to the room, R32 was up in his wheelchair wearing socks and shoes and his left arm sling was not in place. The left arm sling was observed located on top of a dresser in his room. Upon removal of R32's wound dressings, the following was observed: One round pressure ulcer, approximately 2 centimeter (cm) in diameter, over R32's left elbow. The wound was approximately 20 % covered with yellow colored slough (dead tissue) and the remaining wound bed was pink with scant (very small amount) serosanguinous (clear liquid mixed with blood) drainage. R32's left heel DTI was light purple/pink, blanchable and without drainage. A light skin colored small scab was noted forming over the center of the left heel area, measuring approximately 0.5 cm. A review of R32's electronic medical record (EMR) revealed wound care documentation of R32's left heel DTI and left elbow began on 6/7/23. Further review revealed the following: 06/07/2023, 09:50 AM, Treatment Note: . Left Elbow . Pressure . Unstageable, Wound Measurement . Length 2.7 cm (centimeters), Width 1.4 cm, Wound bed: Slough 90 % (percent), Appearance Red/Blanchable outward 1.5 cm, . Any Change in Wound?: Worsened new unstageable wound to elbow . 06/07/2023, 02:36 PM, Treatment Note: . Left Posterior Heel . Pressure . DTI, Wound Measurement . Length 0.8 cm, Width 1.1 cm, Wound bed: Appearance Red/Blanchable outward to the lateral 4 cm, outward to the medial, distal and proximal 1 cm each area, . Any Change in Wound?: Worsened new, Description of Change: new wound . A review of R32's care plan for the problem area, Resident is at risk for developing pressure injuries or other skin breakdown R/T [related to]: Diabetes, PVD, other displaced fracture of lower end left humerous (sic) . revealed the approach for the care plan, initiated on 6/2/23, was Derma Saver boots to be in place to BLE [bilateral lower extremities] at all times while resident is in bed . ; Elevate heels off mattress at all time while in bed using a pillow with a Derma Saver footpad over it, placing both under bilateral calves so heels are not in contact with mattress r/t aiding in pressure redistribution; Observations, monitors and treatment applications as per Physician's or nursing orders; Please refer to the standards of care. Resident #93 (R93) R93 was admitted to the facility on [DATE] and had diagnoses including Alzheimer's, dementia, and contracture of muscle. Review of R93's quarterly MDS assessment, dated 5/26/23, revealed R93 required extensive, two-person physical assistance with bed mobility and was totally dependent on staff for transfers. Section C - Cognitive Patterns, revealed R93 was marked no as not being conducted related to resident being rarely/never understood under Brief Interview for Mental Status (BIMS). On 6/27/23 at 1:30 PM, an interview was attempted with R93 who did not respond to this Surveyor. R93 just stared with his mouth open. R93 was observed in his room lying in his bed wearing a hospital gown and a brief with a white bed sheet coving him, but his feet were visible. R93 had his legs crossed and was wearing gripper socks with his heels on his mattress. Upon exit a hand brace was observed hanging on a hook to the upper left of his sink a hand brace protector. On 6/27/23 at 2:30 PM, an observation was made of R93 in his room. R93 was lying in his bed, wearing a hospital gown, and had a white bed sheet over top of his torso. R93 was wearing a pair of gripper socks on his feet with his heels resting on his mattress. R93's hand brace remained on the hook near his sink in his room. On 6/28/23 at 7:40 AM, an observation was made of R93 in his room. R93 was lying in bed, with legs crossed, wearing gripper socks. R93's feet were not elevated on a pillow and he was not wearing derma saver boots. R93 was also observed rubbing his heels on the mattress. On 6/28/23 at 9:10 AM, an observation was made of R93 in his room. R93 was lying in bed with legs crossed, no pillow between them, feet not elevated with only gripper socks on, no derma saver boots on feet, and no hand brace on the left hand. On 6/29/23 at 7:45 AM, an observation was made of R93 in his room. R93 was lying in bed with bare feet, heels not elevated, legs crossed without a pillow in between them and no hand brace on the left hand. R93 was also observed rubbing his heels on the mattress. On 6/29/23 at 7:50 AM, an interview was conducted with Certified Nurse Aide (CNA) C. CNA C was asked if R93 should have protector boots on, his hand brace on and his heels elevated off his mattress. CNA C replied, He should have them on. CNA C immediately went into R93's room. CNA C then exited the room and called for CNA B to assist her with R93. CNA B was asked where R93's derma saver boots were and replied, They were in his closet. CNA B was asked if he was aware that R93 was to have his heels floated and replied, Yes, they are to be floated so they are not on his mattress. CNA B and CNA C both confirmed that care plan interventions for R93 were not being implemented. Review of R93's progress notes, dated 6/7/23 at 9:50 AM, revealed in part: Skin: MDS quarterly assessment completed for . end date of 5/26/23. [R93's] Braden scale score is 13, which is an indication that he is at a moderate risk for developing pressure injuries . is incontinent of bowel and bladder. He is an assist of 2 with transfers via a Hoyer lift, he is non-ambulatory and an assist of 1-2 for bed mobility . There are orders in place for Heel elevations . There is also a Dermasaver [sic] . The care plan has been reviewed. Review of R93's care plan for problem area, [R93] is at risk for developing pressure injuries or other skin breakdown R/T: Alzheimer's, dementia, pain, depression, functional urinary incontinence . Revealed the approach for the care plan, initiated on 4/18/2022, was Derma Saver boots to BIL [bilateral] feet at all times while in bed for pressure redistribution r/t [related to] blanching redness to heels; initiated date 1/10/2022 Elevate heels off mattress at all times while in bed using a pillow with a Derma Saver foot pad over it, placing both under bilateral calves so heels are not in contact with mattress r/t aiding in pressure redistribution. Review of R93's physician orders, dated 9/27/2022, revealed, Palm protector to left hand . During an interview on 6/29/23 at 11:00 AM, with the Director of Nursing (DON). The DON confirmed, per facility policy, a Braden scale skin assessment should have been completed on admission to the facility for R32. The DON also acknowledged a second Braden skin assessment should have been completed prior to the seventh day of R32's stay at the facility. The DON stated care plan interventions should have been followed for both R32 & R93. The DON stated the expectation was care plan interventions were to be in place. The DON confirmed anyone admitted to the facility with pressure ulcers would be considered a high risk for developing further pressure ulcers. The DON confirmed nursing should have been charting in the EMR daily on skin color, movement, and sensation with a medical device. Review of facility policy titled, Baseline Care Plan, last revised date 11/27/17, revealed the following in part: The facility will develop and implement a baseline care plan for each resident that included the instructions needed to provide effective and person-centered care of the resident that meet professional standards of quality care .
CONCERN (D)

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

Pressure Ulcer Prevention (Tag F0686)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to prevent the development of avoidable pressure ulcers ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to prevent the development of avoidable pressure ulcers for one Resident (R32) of three residents reviewed for pressure ulcers. This deficient practice resulted in the development of two pressure ulcers for R32, and the potential for complications such as infection and rehospitalization, related to pressure injuries. Findings include: Resident #32 (R32) R32 was admitted to the facility on [DATE] and had diagnoses including generalized weakness, fracture of lower end of the left humerus (upper arm bone), fracture of left pubis (front pelvis area), dementia, diabetes mellitus, peripheral vascular disease (PVD), and need for assistance with personal care. Review of R32's admission Minimum Data Set (MDS) assessment, dated 6/7/23, revealed the following: R32 required extensive, two-person physical assistance with bed mobility and was totally dependent on staff for transfers. Section M- Skin Conditions, revealed R32 was at risk for developing pressure ulcers and had three unstageable pressure ulcers (wound bed covered by slough [dead tissue]and /or eschar [dried brown slough]), and one unstageable pressure ulcer, not present upon admission. Further review of Section M, revealed a fourth pressure ulcer, deep tissue injury (DTI), not present on admission. R32's admission MDS assessment also revealed, a Brief Interview for Mental Status (BIMS) assessment of 4 out of 15, indicating severe cognitive impairment. On 6/27/23 at 3:40 PM, an observation was made of R32 in his room. R32 was lying in his bed with his heels on his mattress, not elevated on a pillow, and was wearing gripper socks. R32 was wearing a left arm sling, with his left arm resting on his left side, and his elbow and upper arm resting on his mattress. On 6/28/23 at 12:05 PM, an interview was conducted with Licensed Practical Nurse (LPN) F. LPN F was asked how R32 developed two pressure ulcers after admission to the facility. LPN F replied, [R32's] left arm is heavy in his sling, and we have not been able to find extra pillows but did order some more. LPN F was asked about what care plan interventions should be in place. LPN F replied, All interventions should be in place, and he should have derma saver pad, boots and heels elevated. On 6/29/23 at 8:05 AM, an observation was made of R32. R32 was lying in his bed in his room and talking with an unidentified staff member. R32's heels were observed resting directly on the bed. R32 did not have derma saver boots on and was wearing gripper socks. R32 was also not wearing a left arm sling located in the room. On 6/29/23 at 8:15 AM, an interview was conducted with LPN A. LPN A was asked why R32 did not have feet elevated, derma saver boots on or the left arm sling. LPN A replied, I have to look at his care plan. LPN A reviewed R32's care plan and then stated, [R32] should be . and immediately went to see R32. An observation of R32's wound care, provided by LPN F on 6/29/23 at 12:25 PM, revealed an intact dressing located on his left posterior heel and his left elbow. Upon entry to the room, R32 was up in his wheelchair wearing socks and shoes and his left arm sling was not in place. The left arm sling was observed located on top of a dresser in his room. Upon removal of R32's wound dressings, the following was observed: One round pressure ulcer, approximately 2 centimeters (cm) in diameter, over R32's left elbow. The wound was 20 % covered with yellow colored slough (dead tissue) and pink remaining wound bed with scant serosanguinous (clear liquid mixed with blood) drainage. R32's left heel DTI was light purple/pink, blanchable and without drainage. A light skin colored small scab was noted forming over the center of the left heel area, measuring approximately 0.5 cm. A review of R32's electronic medical record (EMR) revealed wound care documentation of R32's left heel DTI and left elbow began on 6/07/23. Further review revealed the following: 06/07/2023, 09:50 AM, Treatment Note: . Left Elbow . Pressure . Unstageable, Wound Measurement . Length 2.7 cm (centimeters), Width 1.4 cm, Wound bed: Slough 90 % (percent), Appearance Red/Blanchable outward 1.5 cm, . Any Change in Wound?: Worsened new unstageable wound to elbow . 06/07/2023, 02:36 PM, Treatment Note: . Left Posterior Heel . Pressure . DTI, Wound Measurement . Length 0.8 cm, Width 1.1 cm, Wound bed: Appearance Red/Blanchable outward to the lateral 4 cm, outward to the medial, distal and proximal 1 cm each area, . Any Change in Wound?: Worsened new, Description of Change: new wound . 06/11/2023, 03:26 PM, Treatment Note: SKIN: writer and additional nurse . in to reassess R [right] fourth digit, L [left] heel, Sacral region dressing, and LUE [left upper extremity] . No need for further intervention/monitor of areas. Sacral region and L heel dressing dry and intact at this time. LUE continues with dark purple/yellow bruising. Writer noting L elbow dressing with 50% drainage. Area cleansed, rinsed, pat dried with . dressing placed. No additional breakdown to LUE noted at this time . will monitor. 06/13/2023, 03:42 PM, Treatment Note: Skin: MDS admission assessment completed for . end date of 6/8/23 . Braden scale score is 13, which is an indication that he is at a moderate risk for developing pressure injuries . There is also a DTI to the left posterior heel. And an unstageable PrI [prior to admission] to the left elbow as slough is covering wound bed and it is r/t [related to] a medical device. Please refer to the treatment notes and measurements on 6/8/23 . He is an assist of 2 for transfers via a hoyer lift and non-ambulatory and an assist of 1-2 prn for bed mobility . There are orders in place for repositioning and heel elevation and daily observation of the skin to the left arm and right side of the neck r/t to the medical device in place to support the left arm. The care plan has been initiated. *Note: EMR Progress notes and/or treatment notes lacked any measurements to wounds on 6/8/2023. 06/14/2023, 03:31 PM, Treatment Note: . Left Elbow . Pressure . Unstageable (medical device), Wound Measurement . Length 2.2 cm (centimeters), Width 1.4 cm, Wound bed: Slough 100 % (percent), Appearance Red/Blanchable 75 %, Pink/Normal 25 %, . Drainage: Serosanguinous . 06/14/2023, 03:37 PM, Treatment Note: . Left Posterior Heel . Pressure . DTI, Wound Measurement . Length 0.7 cm (centimeters), Width 1.0 cm, Wound bed: Appearance dark/red/purple, Red/Blanchable 100 %, . Any Change in Wound?: Stable appearance remains unchanged . 06/15/2023, 03:12 PM, Treatment Note: SKIN: writer in to assess dressings to sacrum, L heel, and L elbow. Writer noting sling removed to LUE. Writer noting L elbow dressing dry and intact at this time . [R32] with moderate discomfort with LUE movement that seized with rest. Sacral and L heel dressings dry and intact . 06/16/2023, 03:18 PM, Treatment Note: SKIN: writer in to assess L heel, L elbow, and buttock dressing. Writer noting dressing dry and intact at this time . 06/20/2023, 04:03 PM, Treatment Note: Skin: Sacral dressing and left elbow dressing dry and intact . *Note: Wound measurements lacked documentation in the EMR after 6/14/23. Review of R32's care plan for the problem area, Resident is at risk for developing pressure injuries or other skin breakdown R/T [related to]: Diabetes, PVD, other displaced fracture of lower end left humerous (sic) . Revealed the approach for the care plan, initiated on 6/02/23, was Derma Saver boots to be in place to BLE [bilateral lower extremities] at all times while resident is in bed . ; Elevate heels off mattress at all time while in bed using a pillow with a Derma Saver footpad over it, placing both under bilateral calves so heels are not in contact with mattress r/t aiding in pressure redistribution; Observations, monitors and treatment applications as per Physician's or nursing orders; Please refer to the standards of care. A review of R32's Physician Orders revealed, Monitor left arm and neck area for any skin concerns daily r/t sling placement. (Dated 6/3/23) A review of R32's Treatment Administration Record (TAR), revealed, Chart daily: For Medicare Part A residents: if resident has any skin issues (skin tear, bruise, pressure injury, surgical wound, etc.): What is skin ., Frequency: Once A Day, start date 6/03/23. A review of R32's progress notes dated 6/3/23 through 6/28/23, revealed lack of skin condition being addressed on dates as follows: 6/03/23, 6/05/23, 6/10/23, 6/18/23, 6/19/23, 6/25/23, 6/26/23, 6/27/23, and 6/28/23. A review of R32's Observation History in the EMR, revealed a nursing admission assessment completed on 6/1/23 and a skin risk assessment with Braden scale completed on 6/13/23. R32's EMR lacked any other type of skin assessment or skin risk assessments. During an interview on 6/29/23 at 11:00 AM, with the Director of Nursing (DON). The DON confirmed, per facility policy, a Braden scale skin assessment should have been completed on admission to the facility for R32. The DON also acknowledged a second Braden skin assessment should have been completed prior to the seventh day of R32's stay at the facility. The DON stated care plan interventions should have been followed for R32. The DON stated the expectation was care plan interventions were to be in place. The DON confirmed anyone admitted to the facility with pressure ulcers would be considered a high risk for developing further pressure ulcers. The DON confirmed nursing should have been charting in the EMR daily on skin color, movement, and sensation with a medical device. During an interview on 6/29/23 at 1:30 PM, LPN F reported being responsible for wound care. LPN F confirmed R32's pressure ulcers on his left heel and left elbow were acquired after he was admitted to the facility. LPN F also confirmed that an off-loading intervention for R32's left arm should have been an intervention to assist with the prevention of the left elbow pressure ulcer. A review of the facility policy titled, Pressure Injury Prevention and Management, last reviewed 3/27/19, revealed the following in part: This facility is committed to reducing the risk of pressure injuries and the promotion of healing of existing pressure injuries .3. Assessment of Pressure Injury Risk .b. Licensed nurses will conduct a pressure injury risk assessment, using the Braden Scale on all residents upon admission/re-admission, with a change of condition, and quarterly. A review of facility policy titled, Skin Integrity Program, last reviewed 1/31/23, revealed the following in part: .Facility will initiate a program to reduce the risk of skin breakdown/skin injuries in all at risk residents. Residents experiencing skin breakdown will be assessed and evaluated with appropriate interventions initiated and monitored for effectiveness. This facility is committed to reducing the risk of pressure injuries and the promotion of healing of exiting pressure injuries .4. Risk factors and co-morbid conditions contributing to skin breakdown will be identified and modified or eliminated if current condition warrants. A. The Braden Risk Assessment Scale will be used. The risk assessment will be completed within 7 days of admission or readmission, quarterly, and with a significant change in condition. At risk residents will be assessed for skin breakdown at least weekly for four weeks following admission. Appropriate interventions will be initiated .
CONCERN (D)

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

Unnecessary Medications (Tag F0759)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure a medication error rate less that 5 percent wi...

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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 medication error rate less that 5 percent with seven medication errors observed out of 26 opportunities during medication pass. This deficient practice resulted in a medication error rate of 26.92 percent and the potential for undesirable effects related to omission of medications for Resident #45 [R45]. Findings include: During an interview and observation on 6/28/23 at 7:36 a.m., Registered Nurse (RN) K, prepared the following medications for R45: Risperdal (liquid), 1 mg (milligram), once daily Valproic Acid (liquid) 2.5 MLs (milliliters), Miralax [Polyethylene glycol (bulk laxative)], 17 grams, mixed in (120 MLs) approximately four ounces of cranberry juice. All three medications were mixed together. RN K walked the cup of juice, mixed with medications, into R45's room and placed it on the Residents' overbed table. RN K walked out of the room and left the cup of all liquid medications at the bedside. When RN K was asked if R45 had an assessment completed for self-administration of medications, RN K stated, No. She won't drink them if I try to get her to take them (while in the room). RN K said her morning medications were left on R45's overbed table until she had breakfast. When RN K was asked if she was able to leave medications at the bedside of R45, RN K stated No. RN K contacted the Director of Nursing (DON) via telephone and asked for guidance regarding the medications left in the cranberry juice at R45's bedside. On 06/28/23 at 7:48 a.m., RN K entered R45's room and encouraged R45 to continue to drink the cranberry juice with added medications. R45 refused and RN K removed the plastic cup of cranberry juice from R45's room. On 6/28/23 at 7:50 a.m., RN K entered R45's room and removed an insulated, foam cup and a small can (approximately eight ounces) of diet root beer; both with straws inserted and placed them on top of the medication cart. When asked why she had removed additional beverages from R45's room, RN K stated, These are the rest of her morning liquid medications. The diet root beer (with liquid medications) was poured into another insulated foam cup. They (beverages with liquid medications) were prepared by RN K and were sitting in R45's room waiting for breakfast. At 06/28/23 at 7:53 a.m., the DON arrived at the 100 Hall medication cart with a medication storage policy. RN K disposed of the medications that she had previously prepared and started over and began to prepare the following additional morning medications for R45: Acetaminophen (cherry flavored), 640 ML - 20 ML. Lasix 10 mg/per ML, 40 mg dose. Potassium Chloride (liquid,) 20 [NAME] (milliequivalents)/15 ML, dose 15 ML Vitamin D (liquid), 10 mcg/1mL - dose 2 ML (20 mcg). On 6/28/23 at 8:01 am., RN K entered R45's room. R45 refused the acetaminophen liquid, and all the other medications prepared. RN K stated, I know she isn't going to drink it (beverages with medication mixed in). On 6/28/23 at 8:06 a.m., RN K went to the clean utility room and retrieved two, small, insulated, foam cups. RN K emptied the medication cup contents into the two cups, applied cup covers, labeled the cups, and stored the cups in the medication cart. RN K said she would try to have R45 take the valproic acid, Risperdal, and polyethylene glycol in the cranberry juice with her breakfast tray. During an interview on 6/28/23 at 8:12 a.m., RN K acknowledged the liquid medications should not have been left in R45's room when there was not an assessment completed for R45 that authorized self-administration of medication. RN K stated she understood the concern of leaving medications in the room. On 6/28/23 at 8:13 a.m., R45's meal tray arrived in the Residents' room. RN K placed the cranberry juice with liquid medications on the over-bed table near the meal tray. RN K questioned, If I drop (cup with medications and juice) off and stand here and watch her eat, is that ok? On 6/28/23 at 8:17 a.m., R45 was observed eating breakfast and repeatedly picked up the coffee, not the juice (with liquid medications) during her meal. No observation of consumption of the medications was observed by this Surveyor. Review of the facility Administration of Medication, policy, dated 1/31/23, provided on 6/28/23 at 9:02 a.m., revealed the following, in part: .The Licensed Nurse will safeguard all medications by always locking medication carts and medication rooms when not in direct vision of nurse . The Licensed Nurse will label the medication cup with resident's name and date of medication administration if resident is not readily available or refuses the medication. The medication will be properly disposed if the medication is not administered . Dispense the medications to appropriate resident. Remain with resident until medication is swallowed with sufficient fluids . During an interview on 6/28/23 at approximately 9:05 a.m., The DON acknowledged R45 did not have an authorization for self-administration of medications. The DON said the facility would immediately begin development of an individualized plan for safe, observed administration of R45's medications.
CONCERN (E)

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

Deficiency F0700 (Tag F0700)

Could have caused harm · This affected multiple residents

Based on observation, interview, and record review, the facility failed to ensure appropriate and safe use of bedrails for nine Residents (R25, R31, R78, R84, R313, R314, R315, R501, and R502) beds, o...

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Based on observation, interview, and record review, the facility failed to ensure appropriate and safe use of bedrails for nine Residents (R25, R31, R78, R84, R313, R314, R315, R501, and R502) beds, out of nine Residents reviewed for bed safety. This deficient practice resulted in the potential for inappropriate bedrail usage and bedrail entrapment. Findings include: During an observation on 6/27/23 at approximately 1:50 p.m., the following Resident beds were observed with bedrails: R25 - bilateral mobility bars. R31 - bilateral mobility bars. R78 - bilateral mobility bars. R84 - bilateral mobility bars. During an interview on 6/28/23 at 3:05 p.m., Physical Plant Manager (Staff) G was asked about bed entrapment zone measurements for residents with bedrails. Staff G said the facility did not perform entrapment zone gap measurements on resident beds if they did not have half bedrails on their beds. Residents with mobility bedrails did not have entrapment zone gap measurements performed as required per the facility policy. On 6/28/23 at 3:05 p.m., Staff G provided a form used for bed safety inspections entitled, Bedrail/Mattress Safety Assessment, for an unidentified resident, which included a one-time Pass/Fail with no documented measurements for the following areas: ZONE: Right side of bed between mattress and lowermost portion of bedrail. Right side of bed between inside surface of the bedrail and mattress. Left side of bed between mattress and lowermost portion of bedrail. Left side of bed between inside surface of the bedrail and mattress. Staff G said that was the only form completed related to entrapment zone gap measurements for facility beds. Review of the EMR on 6/28/23 found no individualized resident assessments related to the need, safety, and use of bedrails prior to installation of the bedrails on R25, R31, R78 and R84's beds. On 6/28/23 at 3:00 p.m., the DON, Nursing Home Administrator (NHA), Assistant Director of Nursing (ADON) L, Staff G, and Rehab Coordinator H were interviewed regarding the use of bedrails in the facility. The DON confirmed no documentation was present in resident medical records for any alternative approaches to bedrails prior to installation/initiation of bedrails on facility resident beds. When asked if the DON was aware of the reason for concern related to the use of bedrails within the facility, including mobility bedrails, the DON stated, We are not doing a bedrail assessment (to determine individual need and safety of bedrail use). Rehab Coordinator (Staff) H also acknowledged no individualized resident bedrail assessments were completed to ensure bedrails were appropriate and safe for each resident. Because the facility had transitioned to mobility bars (bedrails) the NHA stated, We thought we did not have to do bedrail assessments. We didn't need to do the measurements. We didn't need to do anything because they were not bedrails. ADON L expressed understanding of the facets of a bedrail assessment that must be performed to determine the resident is safe with the use of bedrails. On 6/28/23 at 3:26 p.m., Certified Nurse Aide (CNA) J and CNA I confirmed with this Surveyor, bilateral mobility bars were in use on beds for R25, R31, R78, and R84. Review of the Assessment of Bed Rails policy, dated 1/31/23, revealed the following, in part: .To ensure resident's safety, all bed frames, mattresses and rails will be assessed according to safety guidelines, findings documented, and corrective action documented and implemented as needed. The facility will measure and monitor potential gaps on bed rails, mattresses, headboards, and footboards to maintain resident safety and prevent entrapment and injury . On each of the first 5 days following initial use, the resident bedframe, bed rails, and mattress will be monitored by the maintenance department to document proper fit of and to ensure that the maximum distance between components for that resident as recorded on assessment form . Review of the Bed Device Safety policy, dated 1/31/23, revealed the following, in part: .Education and training for maintenance and housekeeping staff will be provided related to installation, maintenance, functional safety checks and measurement of gaps for bed rails, beds, BMADs (bed mobility assistive devices) and mattresses. Review of the Guidance for Industry and FDA (Food and Drug Administration) Staff: Hospital Bed System Dimensional and Assessment Guidance to Reduce Entrapment, dated March 10, 2006, revealed the following, in part: The seven areas in the bed system where there is a potential for entrapment are identified in the drawing below. Zone 1: Within the Rail Zone 2: Under the Rail, Between the Rail supports or Next to a Single Rail Support Zone 3: Between the Rail and the Mattress Zone 4: Under the Rail, at the Ends of the Rail Zone 5: Between Split Bed Rails Zone 6: Between the End of the Rail and the side Edge of the Head or Foot Board Zone 7: Between the Head or Foot Board and the Mattress End. During an interview on 6/29/23 at 7:01 a.m., the NHA acknowledged maintenance staff should have been completing the entrapment zone measurements for five days following initial installation of bedrails, per the facility policy, for new admission beds. The NHA agreed that bedrail alternatives were not implemented, nor was an individualized assessment of resident physical and mental status being performed prior to the initiation of bedrails on facility resident beds. During an interview on 6/29/23 at 8:50 a.m., the DON and ADON both confirmed no bedrails alternatives were being attempted, and no individualized bedrail assessments were being completed prior to installation of bedrails for facility residents. On 6/29/23 at approximately 9:00 a.m., five completed Bedrail/Mattress Safety Assessment forms were provided by Staff G for review for R313, R314, R315, R501, and R502. Staff G said the forms were all completed that day (6/29/23) by Maintenance Staff M. Review of the forms revealed the following, in part: R313, Date of Assessment: 6/26/23 (date of admission, not date of assessment) . Staff signature and title: signed by Staff M, Date: 6/26/23 (date of admission, not assessment). R314, Date of Assessment: 6/27/23 (date of admission, not date of assessment) . Staff signature and title: signed by Staff M, Date: 6/27/23 (date of admission, not assessment). R315, Date of Assessment: 6/15/23 (date of admission, not date of assessment) . Staff signature and title: signed by Staff M, Date: 6/15/23 (date of admission, not assessment). R501, Date of Assessment: 6/28/23 (date of admission, not date of assessment) . Staff signature and title: signed by Staff M, Date: 6/28/23 (date of admission, not assessment). R502, Date of Assessment: 5/23/23 (date of admission, not date of assessment) . Staff signature and title: signed by Staff M, Date: 5/23/23 (date of admission, not assessment). During an interview on 6/29/23 at 10:15 a.m., Staff M confirmed he had completed all the above Bedrail/Mattress Safety Assessment forms that day (6/29/23). Staff M stated, I was given a piece of paper from Staff G that had their arrival (admission) date and I just put that date on there (the forms) . There is (sic) a few that were missing. I am not sure why they didn't get done.
Dec 2022 1 deficiency
CONCERN (D) 📢 Someone Reported This

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

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

Abuse Prevention Policies (Tag F0607)

Could have caused harm · This affected 1 resident

Based on interview and record review, the facility failed to ensure implementation of the written abuse policy including prohibition, prevention, and training to ensure appropriate abuse reporting and...

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Based on interview and record review, the facility failed to ensure implementation of the written abuse policy including prohibition, prevention, and training to ensure appropriate abuse reporting and action for one Resident (#2) of three residents reviewed for abuse. This deficiency resulted in abuse policy implementation failure when staff and the facility failed to report, prevent, and protect Resident #2 from abuse according to their policies following an allegation of abuse. Findings include: This deficient practice was related to Facility Reported Intake #MI00132916. Review of the Investigative Summary revealed Certified Nurse Aide (CNA) A reported an allegation of abuse on 11/14/22, that occurred on 11/12/22, to Registered Nurse C. The allegation was immediately reported to the Director of Nursing (DON) on 11/14/22 at 2:03 a.m. Allegation details included the following, in part: [CNA A] and [CNA B] were performing incontinence checks and [Resident #2] had a bowel movement. [CNA A] stated that she was holding [Resident #2] over on her side facing the window when CNA B held a wipe with stool in front of [Resident #2's] face and said, 'Here [Resident #2]'. [CNA A] then said that after [CNA B] finished wiping her, he punched [Resident #2] in the butt cheek 3, 4, or 5 times with a closed fist and medium force . The local police authorities were called on 11/14/22 at 3:09 a.m., and CNA B was telephoned and told not to report for work until further notice and was suspended pending investigation. During an interview on 12/21/22 at 11:03 a.m., the Nursing Home Administrator (NHA), DON, and Assistant Director of Nursing (ADON) D were interviewed regarding actions taken by the facility following 11/12/22, the day of the alleged abuse. The NHA and DON agreed CNA A should have reported the allegation of abuse immediately to the NHA and DON, and confirmed it was approximately 48 hours before she reported the allegation. When asked if CNA B had worked following 11/12/22, ADON D, who had worked on the event investigation confirmed CNA B had worked on 11/13/22, prior to knowledge of the abuse allegation. CNA B worked 12-hour shifts in the facility. Review of the Abuse Prohibition/Abuse Investigation Policy, reviewed 11/14/22, revealed the following, in part: .D. Identification: 1. Any person (defined as staff, families, visitors, or other residents) who suspects or has reasonable cause to believe that a resident has been subject to abuse must immediately report the issue to: a. The Administrator [Telephone Number and Location] And b. The Director of Nursing [Telephone Numbers and Locations]. If the allegation of abuse is reported to the Nurse, Resident Care Coordinator, Nursing supervisor, or Staff Nurse, he/she must immediately report the issue to the Administrator and Director of Nursing so that appropriate action is assured . Assure that the resident has had an immediate and thorough nursing physical examination if applicable or medical attention as necessary . In a case involving an employee, at a minimum, the employee should be separated from further contact with the resident, which may include suspension with or without pay during the investigation . In response to allegations of abuse, neglect, exploitation or mistreatment, the facility will ensure that all alleged violations involving abuse, neglect exploitation or mistreatment, including injuries of unknown source and misappropriation of resident property, are reported immediately, but not later than 2 hours after the allegation is made . The facility immediately identified the deficiency in failure to implement their abuse policy related to CNA's failure to report in the specified timeframe to the facility, and failure to ensure the protection of residents related to allegations of abuse. The following Action Plan to address the deficiency was immediately implemented and included the following steps: 1. Resident was assessed multiple times with no noted injuries or psychosocial change. Employee (CNA A) was re-educated on abuse, abuse reporting, abuse policies, and the Elder Justice Act by the DON immediately. 2. All residents have the potential to be affected. Abuse audits were performed without any additional issues. (Audits conducted 11/14/22 through 11/22/22) 3. All staff were re-educated on abuse reporting. Facility Abuse policy and procedure reviewed (11/14/22 through 11/22/22) 4. Audits will be completed three times a week x 4 weeks, once a week x's 4 weeks with results to QAPI until determined substantial compliance. The Administrator is responsible for sustained compliance. While this deficiency did occur, the facility self-identified the issues involved, educated all staff, completed a thorough investigation, and performed resident and staff audits to ensure continued compliance, therefore Past Non-Compliance has been determined.
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+ (80/100). Above average facility, better than most options in Michigan.
  • • No fines on record. Clean compliance history, better than most Michigan facilities.
  • • 25% annual turnover. Excellent stability, 23 points below Michigan's 48% average. Staff who stay learn residents' needs.
Concerns
  • • Multiple safety concerns identified: 3 harm violation(s). Review inspection reports carefully.
  • • 9 deficiencies on record, including 3 serious (caused harm) violations. Ask about corrective actions taken.
Bottom line: Generally positive indicators. Standard due diligence and a personal visit recommended.

About This Facility

What is Marquette County Medical Care Facility's CMS Rating?

CMS assigns Marquette County Medical Care Facility an overall rating of 5 out of 5 stars, which is considered much above average nationally. Within Michigan, 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 Marquette County Medical Care Facility Staffed?

CMS rates Marquette County Medical Care Facility's staffing level at 5 out of 5 stars, which is much above average compared to other nursing homes. Staff turnover is 25%, compared to the Michigan average of 46%. This relatively stable workforce can support continuity of care.

What Have Inspectors Found at Marquette County Medical Care Facility?

State health inspectors documented 9 deficiencies at Marquette County Medical Care Facility during 2022 to 2024. These included: 3 that caused actual resident harm and 6 with potential for harm. Deficiencies causing actual harm indicate documented cases where residents experienced negative health consequences.

Who Owns and Operates Marquette County Medical Care Facility?

Marquette County Medical Care Facility 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 140 certified beds and approximately 121 residents (about 86% occupancy), it is a mid-sized facility located in Ishpeming, Michigan.

How Does Marquette County Medical Care Facility Compare to Other Michigan Nursing Homes?

Compared to the 100 nursing homes in Michigan, Marquette County Medical Care Facility's overall rating (5 stars) is above the state average of 3.2, staff turnover (25%) is significantly lower than the state average of 46%, and health inspection rating (5 stars) is much above the national benchmark.

What Should Families Ask When Visiting Marquette County Medical Care Facility?

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 Marquette County Medical Care Facility Safe?

Based on CMS inspection data, Marquette County Medical Care Facility 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 Michigan. While no facility is perfect, families should still ask about staff-to-resident ratios and recent inspection results during their visit.

Do Nurses at Marquette County Medical Care Facility Stick Around?

Staff at Marquette County Medical Care Facility tend to stick around. With a turnover rate of 25%, the facility is 21 percentage points below the Michigan 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 8%, meaning experienced RNs are available to handle complex medical needs.

Was Marquette County Medical Care Facility Ever Fined?

Marquette County Medical Care Facility 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 Marquette County Medical Care Facility on Any Federal Watch List?

Marquette County Medical Care Facility 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.