GARDEN VIEW HEALTH AND REHABILITATION CENTER

2180 10TH AVENUE, VERO BEACH, FL 32960 (772) 567-5166
For profit - Corporation 72 Beds SIMCHA HYMAN & NAFTALI ZANZIPER Data: November 2025 2 Immediate Jeopardy citations
Trust Grade
11/100
#634 of 690 in FL
Last Inspection: July 2025

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

Overview

Garden View Health and Rehabilitation Center has a Trust Grade of F, which indicates significant concerns regarding the quality of care provided. With a state ranking of #634 out of 690, they are in the bottom half of Florida facilities, and they rank #5 out of 6 in Indian River County, meaning only one local option is better. The facility is worsening, with issues increasing from 6 in 2024 to 14 in 2025. Staffing is rated at 2 out of 5 stars, which is below average, and the turnover rate of 53% is concerning, as it is higher than the state average. Families should be aware that there have been serious incidents, including a resident being allowed to eat without supervision, which posed a risk of choking. Additionally, the facility failed to prepare food according to residents' dietary needs, leading to the potential for choking or aspiration. With $35,265 in fines, which is higher than 83% of Florida facilities, and less RN coverage than 87% of state facilities, these factors suggest ongoing compliance issues and a lack of sufficient nursing oversight. Overall, while there are some strengths, such as average quality measures, the significant issues highlighted in inspections raise serious concerns for families considering this facility.

Trust Score
F
11/100
In Florida
#634/690
Bottom 9%
Safety Record
High Risk
Review needed
Inspections
Getting Worse
6 → 14 violations
Staff Stability
⚠ Watch
53% turnover. Above average. Higher turnover means staff may not know residents' routines.
Penalties
⚠ Watch
$35,265 in fines. Higher than 89% of Florida facilities, suggesting repeated compliance issues.
Skilled Nurses
⚠ Watch
Each resident gets only 28 minutes of Registered Nurse (RN) attention daily — below average for Florida. Fewer RN minutes means fewer trained eyes watching for problems.
Violations
⚠ Watch
30 deficiencies on record. Higher than average. Multiple issues found across inspections.
★☆☆☆☆
1.0
Overall Rating
★★☆☆☆
2.0
Staff Levels
★★★☆☆
3.0
Care Quality
★☆☆☆☆
1.0
Inspection Score
Stable
2024: 6 issues
2025: 14 issues

The Good

  • Full Sprinkler Coverage · Fire safety systems throughout facility
  • No fines on record

Facility shows strength in fire safety.

The Bad

1-Star Overall Rating

Below Florida average (3.2)

Significant quality concerns identified by CMS

Staff Turnover: 53%

Near Florida avg (46%)

Higher turnover may affect care consistency

Federal Fines: $35,265

Above median ($33,413)

Moderate penalties - review what triggered them

Chain: SIMCHA HYMAN & NAFTALI ZANZIPER

Part of a multi-facility chain

Ask about local staffing decisions and management

The Ugly 30 deficiencies on record

2 life-threatening
Jul 2025 13 deficiencies 2 IJ
CRITICAL (J)

Immediate Jeopardy (IJ) - the most serious Medicare violation

Accident Prevention (Tag F0689)

Someone could have died · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, record reviews, and a policy review, the facility failed to ensure care and services to preve...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, record reviews, and a policy review, the facility failed to ensure care and services to prevent accidents for 3 of 9 sampled residents reviewed for nutrition and falls, as evidenced by the failure to provide supervision while eating for Resident #37; failure to implement preventative measures to prevent a fall related injury for Resident #14; and failure to complete a post fall investigation to determine the cause of the fall for Resident #20.On 06/24/25 it was determined the facility failed to ensure adequate supervision for Resident #37, a resident with diagnoses of Cerebral Infarction (Stroke) and Dysphagia (difficulty swallowing), to prevent the likelihood of choking, aspiration (the accidental ingestion of food particles or fluids into the lungs), and/or death. Resident #37, who was ordered to have a mechanically altered diet, was not supervised during meals as per her current care plan and was subsequently provided with a whole hot dog that she consumed. The resident had a history of being served potato chips, Goldfish crackers by facility staff members. The likelihood of Resident #37 choking on the hot dog with the potential of aspiration or death was determined and the Administrator was informed of the Immediate Jeopardy on 06/27/25 at 10:50 AM. The Immediate Jeopardy was identified on 06/24/25 and was removed on 06/27/25. The scope and severity were decreased to a D, no actual harm with the potential for more than minimal harm that is not Immediate Jeopardy. The scope and severity were lowered as a result of the facility's corrective actions implemented as of 06/27/25 and verified by interview, observation and record review on 06/27/25. Although, the facility submitted an acceptable removal plan, the potential for more than minimal harm remains without the implementation of a plan of correction and monitoring of the corrective actions.Cross Reference - F805. The findings included:A Review of the policy titled, Meal Supervision and Assistance revised on 11/29/22 documented that the resident will be prepared for a well-balanced meal in a calm environment, with adequate supervision and assistance to prevent accidents, provide adequate nutrition, and assure an enjoyable event. This included identifying hazards and risks. The listed guidelines for compliance included checking the meal tray before serving it to the resident to make sure that it was the correct diet ordered and that the food texture was appropriate for the resident's ability to chew and swallow. Photographic Evidence Obtained.A record review revealed that Resident #37 was admitted to the facility on [DATE]. Her diagnoses included Cerebral Infarction (Stroke) due to Embolism of the Left Carotid Artery (lack of blood flow to the brain caused by a blood clot), Hemiplegia (paralysis on one side of the body) and Hemiparesis (weakness on one side of the body) Following Cerebral Infarction Affecting the Right Dominant Side, Aphasia (impaired ability to speak) Following Cerebral Infarction, Dysphagia (swallowing difficulty) Following Cerebral Infarction, and Muscle Weakness. Review of the Minimum Data Set (MDS) assessment dated [DATE] documented this resident's Brief Interview of Mental Status (BIMS) score equaled 5, which indicated that Resident #37 had severe cognitive impairment.A record review of Resident #37's care plan, last revised on 02/13/25, revealed that Resident #37 was at risk for malnutrition due to her medical history which included Dysphagia, Aphasia, Anxiety, and Cerebrovascular Accident (stroke). Since 12/02/22, the interventions listed in the care plan included providing the diet as ordered, and monitoring for signs and symptoms of aspiration such as coughing, choking, pocketing of foods, spitting out food, wet vocal quality, and wet lungs. If symptoms of aspiration or choking were found, the physician and the Speech Language Pathologist were to be notified. An intervention since 12/02/22 specified to set-up the trays, supervise, cue, and assist the resident as needed with meals. It specified to allow adequate time to consume food/fluids provided. Record review of the medical record Listing of Tasks for Eating showed no checkmarks under the column that denoted the provision of supervision from 06/13/25 through 06/26/25. The eating task in the electronic medical record was used by Certified Nursing Assistants (CNAs) to document how much a resident ate or drank, and how much assistance was provided by the CNA.Record review revealed the physician ordered diet for Resident #37, dated 06/01/25, documented a Regular Diet, with mechanical soft texture foods, and thin consistency fluids. The diet listed in the Meal Tracker (meal ticket software program) was Regular - Mechanical Altered/Ground. The diets in the electronic medical record documented (mechanical soft), and the meal ticket software program documented (ground). Both were mechanically altered diets that were used for residents with swallowing difficulties. Photographic evidence of the meal ticket was obtained.During an observation of Resident #37's dinner meal, on 06/24/25 at 5:26 PM, Resident #37 refused her meal. The meal ticket on her tray specified that she was on a Regular-Mechanical Altered/Ground diet. Staff A, Certified Nursing Assistant (CNA), offered the resident several food options including grilled cheese, a peanut butter and jelly sandwich, and an egg salad sandwich. Resident #37 communicated that she didn't want any of those alternatives. Staff A mentioned she would look at the menu to see what other alternatives were available. Staff A saw that a hot dog was listed on the menu as an available option, and asked Resident #37 if she wanted a hot dog. Resident #37 said, yes. During an interview on 06/24/25 at 5:38 PM, while in the hallway in front of the dining room, Staff A, CNA, stated she had given Resident #37 a hot dog and she ate it. Upon receiving this information, the surveyor returned to the resident's room, Resident #37 held a quarter of the hot dog bun while still sitting on her bed. The hot dog was not visible and it appeared the resident had consumed the hotdog.During an interview on 06/24/25 at 5:42 PM with Staff A, when asked if the hot dog was whole or cut-up into small pieces, the CNA stated she served Resident #37 a whole hot dog that was not cut-up. When asked if the kitchen staff knew it was for Resident #37, Staff A said that she told the kitchen it was for Resident #37. Staff A confirmed that Resident #37 ate 100% of the hot dog.During an interview on 06/24/25 at 5:52 PM, the Certified Dietary Manager (CDM) stated that she didn't know who the hot dog was for. She reported, Resident #37 wouldn't be given a whole (intact) hot dog because of her diet; it would be mechanically ground. The CDM stated that the kitchen staff would have been able to grind it for her. The surveyor asked to see the food processor that was used for grinding up foods, and the CDM showed the surveyor a clean food processor. The surveyor asked the CDM if the kitchen staff prepared any ground hot dogs on 06/24/25, and the CDM said that they did not. She explained that no one on a ground diet ordered a hot dog that day.During an observation of the dinner meal on 06/26/25 at 5:50 PM, Resident #37 was in bed and a tray of food was on her tray table. The food on the tray included, ground beef, mashed potatoes, and vegetables were on the main dinner plate. There appeared to be warm ground chicken salad was on a separate small plate covered with plastic wrap. The resident moved the plate onto her lap and peeled back the plastic wrap. She used her fingers to pick up and taste the chicken salad. She shook her head from left to right and waved her hands back and forth. She said no ., no ., and she placed the plate back on the meal tray. She did not eat any more chicken salad. There was no staff from the facility present in Resident #37's room when she tasted the chicken salad. The surveyor continued to observe Resident #37 in her room. No staff members provided supervision for Resident #37 during the dinner meal from 5:50 PM through 6:05 PM. 2) Review of the record revealed Resident #14 was admitted to the facility on [DATE] and was sent out to the emergency room (ER) on 02/26/25 and 03/01/25, with a return to the facility those same days. Review of the current Minimum Data Set (MDS) assessment dated [DATE] documented the resident had a Brief Interview for Mental Status (BIMS) score of 1, on a 0 to 15 scale, indicating severe cognitive impairment. This MDS documented Resident #14 had a fall with injury since the prior assessment of 12/24/24.Review of the current care plan initiated on 01/21/22 documented Resident #14 was at risk for falls and fall related injury related to cognitive loss, stroke, non-ambulatory status, impaired mobility, weakness, medication use, fall history, osteopenia (small bones), and bilateral knee contractures. An intervention included providing a mat on the floor to the left side of the bed as of 11/07/23. A second intervention initiated on 12/04/23 documented the use of bilateral wedges to sides of bed for safety and fall risk prevention.Review of the current physician orders documented the need for a floor mat to the left side of the bed for safety since 11/07/23. A current order dated 06/23/25 documented the use of bed bolsters to bilateral sides of bed.Review of a change in condition form dated 02/26/25 documented Resident #14 had a fall with no apparent injury and was sent out to the hospital.Review of progress notes documented, in part, the following:a) On 02/26/25 at 4:25 PM, Resident #14 suffered an unwitnessed fall at about 3:45 PM, and was sent to the ER.b) On 02/26/25 at 10:22 PM the nursing staff received information from the ER (Emergency Room) that the resident was being returned back to the facility. A CT (Computed Tomography) of the brain and cervical spine (upper part) indicated no fractures or injuries.c) On 03/01/25 at 10:18 AM and 10:52 AM the resident's brother insisted Resident #14 return to the ER due to increased back pain and to get additional studies. The resident was sent back to the ER.d) On 03/01/25 at 8:06 PM the resident returned to the facility with diagnoses to include a closed wedge compression fracture of T10 (thoracic or mid back) vertebra and a closed compression fracture of L3 lumbar (lower back) vertebra. The resident was medicated with Dilaudid (an opioid/narcotic pain medication), Toradol (an anti-inflammatory medication), and Zofran (a medication for nausea) at 1:53 PM. He returned to the facility with orders for Percocet (an opioid/narcotic pain medication) as needed.Review of the radiology studies from the ER visit on 03/01/25 documented both compression fractures as acute/subacute, indicating they could not tell if the fracture was recent or anytime within the past few months.Review of the facility provided fall investigation documented there were interventions/strategies in place from the care plan but lacked documentation of whether the fall mat and wedges/bolsters were in place. The Assigned CNA Statement Form and Registered Nurse (RN) Statement Form both lacked documentation as to whether the fall mat and wedges/bolsters were in place. Review of the Fall Root Cause Analysis documented, in part, there were no floor mats in place.During an interview on 06/27/25 at 8:44 AM, when asked about the investigation related to the care plan interventions at the time of the fall, the Administrator, who was also the Risk Manager, did not comment, while the Director of Nursing (DON) explained the resident would play with the bed remote and had raised the bed up and rolled out of bed. The DON further stated the fall mat was in place. When asked to locate evidence of this on the fall investigation and was also notified the root cause analysis documented a lack of the fall mat, the DON stated, I'm sure I saw it but agreed to the conflicted information in the investigation.During an interview on 06/27/25 at 11:23 AM, when asked about the radiological report documentation of acute/subacute fracture, the Medical Director stated that more than likely, because of the minimal 10% height loss, the fractures were chronic. When asked about the resident's increased yelling/pain with movement, the Medical Director reviewed the full radiological report and stated the bulging disk may have been affected with the fall and caused the pain.3) Review of the record revealed Resident #20 was admitted to the facility on [DATE]. Review of the current MDS assessment dated [DATE] documented the resident had a BIMS score of 15, indicating the resident was cognitively intact.Review of a change in condition form dated 11/02/24 documented Resident #20 slipped out of the shower chair with no open injuries.During an interview on 06/23/25 at 4:08 PM, when asked about his fall in the bathroom, Resident #20 stated he was being assisted with a shower in his bathroom, was seated in the rolling shower chair, and further stated, Apparently the wheels were not locked as it went out from under me. The resident denied any fracture, but stated it happened about three months ago, that he had fallen on his bottom and had twisted his shoulder, and it took him a couple of months to recover.On 06/25/25 at 11:21 AM, the DON was asked to locate and provide evidence of the fall investigation for Resident #20 from 11/02/24. At 12:47 PM the DON provided a folder labeled with the name of Resident #20, stated, I wasn't here when it (the fall for Resident #20 in November 2024) happened and I couldn't find any investigation, so I printed out the information that I could find in PCC (Point Click Care, the facility's electronic medical record (EMR)) and filled out the Fall Investigation Form. I wanted you to have something. There aren't any statements or anything else.Review of the folder revealed the Fall Investigation Form with only page one filled out with information the DON had obtained from the EMR. The possibility of an equipment issue was not addressed in any of the documents. The Fall Investigation Form documented the fall was unwitnessed whereas the nursing post fall evaluation documented the fall as being witnessed.During a phone interview on 06/27/25 at 11:36 AM, when asked if she recalled the fall in the shower for Resident #20, Staff M, CNA, stated she did as she was present during the fall. When asked what happened, the CNA stated she really wasn't sure, but I always lock the wheels (of the shower chair). The CNA further explained the resident fell as he was trying to pull himself up with the grab bar when the chair slipped back.During an interview on 06/27/25 at 8:40 AM, the DON confirmed she had not found an investigation for the fall of Resident #20 on 11/02/24 but had found a statement. At 9:59 AM the DON returned with a statement and Fall Hand Off form. Review of the statement revealed Staff M, CNA, documented the resident was trying to stand up to dry off and the shower chair slid back, and he fell on his bottom. The Fall Hand Off form lacked any information regarding the actual fall but was an instruction sheet for the nursing staff. The DON confirmed there was no root cause analysis or evidence the event was investigated. The DON also agreed to the lack of any information related to the shower chair. The facility's Immediate Jeopardy removal plan dated 06/27/25 included the following, which was also verified:On 06/24/25 Resident #37 was immediately assessed. A speech referral was submitted to assess diet appropriateness. A chest x-ray was ordered to rule out aspiration. Respiratory assessments were initiated every shift for 72 hours for signs and symptoms of aspiration. The resident's diet order, care plan, and Kardex were reviewed and updated as indicated for accuracy. The physician and responsible party were notified. On 06/25/25 a speech evaluation was ordered for Resident #37.On 06/26/25 a FEES (Fiberoptic Endoscopic Evaluation of Swallowing) bedside study was ordered.On 06/24/25 the CNA and dietary employee involved were removed from the floor and received one-on-one education by the Staff Development Coordinator and Dietary Manager on verifying diet slips with current orders, appropriate food textures for mechanical soft diets, how to address concerns regarding tray accuracy, possible consequences of serving inappropriate diets, and ensuring proper supervision of residents who require it during meals.On 06/25/25 the facility reviewed residents with mechanically altered diets to ensure current orders matched tray ticket diets. There were 18 current residents who were on mechanically altered diets at the time of the survey.On 06/24/25 through 06/26/25 current staff were educated on supervision of residents related to accidents and incidents specifically to proper supervision of residents who require it during meals, including alternate food options and snacks as requested. Newly hired staff will receive education on supervision of residents during meal consumption in their orientation. Any contracted nurses or CNAs who are placed at the facility on assignment will receive the above education prior to starting their shift through an agency orientation packet.On 06/27/25 current staff were educated on how to respond to a choking resident. Education was done via the facility on-line portal, in person, and via telephone.On 06/27/25 the information in the facility's removal plan was verified. Observations of the lunch and dinner meals on 06/27/25 demonstrated a process to ensure physician ordered diets were being delivered to residents. A new diet communication manual was placed in the main dining room and on each tray cart. On 06/27/25 six staff, including Staff B, the CNA who provided Resident #37 with potato chips and permitted the resident to choose Gold Fish crackers were interviewed. Each staff member was able to verbalize the education provided during the week. They verbalized what needs to be done before providing an alternate food item or snack to a resident, the new process for meal tray delivery, and how residents are identified who need supervision. On 06/24/25 Resident #37 was immediately assessed by her assigned nurse. A speech referral was submitted to assess diet appropriateness. A chest x-ray was ordered to rule out aspiration and was refused by the resident. Respiratory assessments were initiated and documented every shift for 72 hours for signs and symptoms of aspiration. The resident's diet order, care plan, and Kardex were reviewed and updated as indicated for accuracy. The physician and responsible party were notified. On 06/24/25 Staff L, dietary cook and Staff A, CNA, were provided the one-on-one education.On 06/24/25 a total of 109 current staff, including all disciplines, received the education related to supervision.On 06/25/25 the speech evaluation was completed for Resident #37.On 06/25/25 an audit was completed confirming the meal textures in Meal Tracker (the dietary software used to print meal tickets) matched the physician's order for all current residents.On 06/26/25 a FEES (Fiberoptic Endoscopic Evaluation of Swallowing) bedside study was conducted. The recommendations from this study were to advance the resident diet to a mechanically soft chopped diet.On 06/27/25 it was verified that all 27 licensed nurses had CPR (cardiopulmonary resuscitation)/Heimlich maneuver (procedure recommended for a choking resident) certifications in good standing.As of 06/27/25, 100% of staff received education on responding to a choking resident via their on-line portal. In addition, 30% of current staff were educated in person and 23% via telephone on how to respond to a choking resident. Staff who received this education via telephone will receive the in-person education upon their next working shift at the facility.An Ad Hoc/Quality Assurance Performance Improvement (QAPI) meeting was held on 06/25/25 with the Medical Director, the Administrator, the Director of Nursing, the Staff Development Coordinator, and the Dietary Manager. Supervision during meal consumption was discussed. A plan for continued monitoring and sustained compliance was reviewed. An additional Ad Hoc/QAPI meeting was held on 06/26/25 to evaluate the effectiveness of the education.The facility's Immediate Jeopardy was removed on 06/27/25 at 6:50 PM.
CRITICAL (J)

Immediate Jeopardy (IJ) - the most serious Medicare violation

Deficiency F0805 (Tag F0805)

Someone could have died · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, record reviews, policy review, and review of professional standards of practice, the facility...

Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, interviews, record reviews, policy review, and review of professional standards of practice, the facility failed to prepare foods in a form to meet the individual needs for 4 of 5 sampled residents, Resident #37, Resident #10, Resident #15, and Resident #21, reviewed for nutritional concerns. This had the potential to affect 18 current residents who were on mechanically altered diets at the time of the survey.On 06/24/25 it was determined the facility failed to follow a physician ordered diet, that was mechanically altered, for Resident #37, a resident with diagnoses of dysphagia (difficulty swallowing), to prevent the likelihood of choking, aspiration (the accidental sucking in of food particles or fluids into the lungs), and or death. Resident #37, who was ordered to have a mechanically altered diet, was provided with a whole hot dog that she consumed.The likelihood of Resident #37 choking on the hot dog with the potential of aspiration or death was determined. The Administrator was informed of the Immediate Jeopardy on 06/27/25 at 10:22 AM.The Immediate Jeopardy was identified on 06/24/25, and was removed on 06/27/25. The scope and severity were decreased to a D, no actual harm with the potential for more than minimal harm that is not Immediate Jeopardy for F689 and F805. The scope and severity were lowered as a result of the facility's corrective actions implemented as of 06/27/25 and verified by interview, observation and record review on 06/27/25. Although, the facility implemented corrective actions to remove the immediacy of the deficient practice, the potential for harm remains without the implementation of a plan of correction and monitoring of the corrective actions.Cross Reference - F689.The findings included:A review of the facility's Policy titled, Nutritional Management last revised 04/27/22, documented examples of interventions for nutrition that were to be individualized to address the specific needs of each resident. One example that was listed was the mechanically altered-consistency diet that may be prescribed for a resident diagnosed with dysphagia or with chewing difficulties.The National Dysphagia Diet Task Force (2002) created the National Dysphagia Diet: Standardization for Optimal Care. It described the Level 2: Dysphagia Mechanically Altered (Dysphagia Ground) diet as foods that are moist, soft-textured, and easily formed into a bolus. Meats are ground or are minced no larger than one-quarter-inch pieces. They are still moist, with some cohesion. Hot dogs, peanut butter, potato chips, dry, coarse cakes and cookies, and bread that has not been pureed, gelled, or slurried to a moist texture, were listed as foods to avoid on the Dysphagia Ground diet.The Level 1: Dysphagia Pureed diet was described as pureed, homogenous, and cohesive foods. Foods should have a pudding-like texture.A review of information on the Mechanical Soft Diet (used by the University of Wisconsin-[NAME] integrated health system) and provided as a reference by the Corporate Certified Dietary Manager documented the Mechanical Soft diet was designed for people who had trouble chewing and swallowing. It included chopped, ground, and pureed foods, as well as foods that broke apart without a knife, (like fish). It specified that sausage, [NAME] (hot dogs), peanut butter, and chips were foods to avoid on the mechanical soft diet. 1) Record review revealed Resident #37 was admitted to the facility on [DATE]. Her diagnoses included Cerebral Infarction due to Embolism of the Left Carotid Artery (lack of blood flow to the brain caused by a blood clot), Hemiplegia (paralysis on one side of the body) and Hemiparesis (weakness on one side of the body) Following Cerebral Infarction Affecting the Right Dominant Side, Aphasia (impaired ability to speak) Following Cerebral Infarction, Dysphagia (swallowing difficulty) Following Cerebral Infarction, and Muscle Weakness. Per the Minimum Data Set (MDS) assessment dated [DATE], this resident's BIMS score equaled 5, which indicated that Resident #37 had severe cognitive impairment. At the time of admission, Resident #37 received no foods or liquids by mouth. She was dependent on tube feeding for total nutrition. She started eating by mouth and was served meals from the kitchen as of 02/01/22.A record review of Resident #37's care plan, last revised on 02/13/25, revealed that Resident #37 was at risk for malnutrition because of her medical history which included Dysphagia, Aphasia, Anxiety, and a Cerebrovascular Accident (stroke). Since 12/02/22, the interventions listed in the care plan included providing the diet as ordered, and monitoring for signs and symptoms of aspiration such as coughing, choking, pocketing of foods, spitting out food, wet vocal quality, and wet lungs. If symptoms of aspiration or choking were found, the physician and the Speech Language Pathologist were to be notified.Record review revealed the physician ordered diet for Resident #37, dated 06/01/25, was for a regular diet, with mechanical soft texture foods, and thin consistency fluids. The diet listed in the Meal Tracker (meal ticket software program) was Regular - Mechanical Altered/Ground. The diets in the electronic medical record (mechanical soft), and the meal ticket software program (ground), were both mechanically altered diets that were used for residents with swallowing difficulties. The two diets were not identical. Photographic evidence of the meal ticket was obtained.During an observation of Resident #37's dinner meal, on 06/24/25 at 5:26 PM, Resident #37 refused her meal. The meal ticket on her tray specified that she was on a Regular-Mechanical Altered/Ground diet. Staff A, Certified Nursing Assistant (CNA), offered the resident several food options including grilled cheese, a peanut butter and jelly sandwich, and an egg salad sandwich. Resident #37 communicated that she didn't want any of those alternatives. Staff A mentioned she would look at the menu to see what other alternatives were available. Staff A saw that a hot dog was listed on the menu as an available option, and asked Resident #37 if she wanted a hot dog. Resident #37 said yes. During an interview on 06/24/25 at 5:38 PM, while in the hallway in front of the dining room, Staff A, CNA, stated she had given Resident #37 a hot dog and she ate it. Upon immediate return to the resident's room, Resident #37 held a quarter of the hot dog bun while still seated in her bed. The hot dog was not visible.During an interview on 06/24/25 at 5:42 PM, when asked if the hot dog she provided was whole or cut-up into small pieces, Staff A stated she served Resident #37 a whole hot dog that was not cut-up. When asked if the kitchen staff knew it was for Resident #37, Staff A said that she told the kitchen it was for Resident #37. Staff A confirmed that Resident #37 ate 100% of the hot dog. During an interview on 06/24/25 at 5:52 PM, the Certified Dietary Manager (CDM) stated that she didn't know who the hot dog was for. She said Resident #37 wouldn't be given a whole (intact) hot dog because of her diet; it would be mechanically ground. The CDM stated that the kitchen staff would have been able to grind it for her. The surveyor asked to see the food processor that was used for grinding up foods, and the CDM showed the surveyor a clean food processor. The surveyor asked the CDM if the kitchen staff prepared any ground hot dogs on 06/24/25, and the CDM said that they did not. She explained that no one on a ground diet ordered a hot dog that day. The menu for the dinner meal on 06/24/25 was reviewed. It included a Ground Hot Dog (no bun) as an alternate entrée for residents on the mechanical altered/ground diet.During an observation on 06/24/25 at 4:45 PM, Resident #37 pointed to the picture of the place setting (plate with fork, spoon, and knife), with the word Hungry above the picture on her communication board. Photographic Evidence Obtained. During an interview with a Staff B, CNA, on 06/24/25 at 4:45 PM, when asked what she thought Resident #37 meant when she pointed to that picture, Staff B said that either she was hungry, or she didn't like her food. Staff B said Resident #37 wanted to know when dinner was ready. She said she offered Resident #37 a peanut butter and jelly sandwich that she didn't want it. When asked if snacks were available, Staff B identified a snack basket that was kept at the nurse's station. It contained graham crackers, Goldfish crackers, and soft/pliable chocolate cookies. Staff B said that she normally took the snack basket to Resident #37 and let her choose a snack from the basket. She also said that normally she gave Resident #37 potato chips. When asked how frequently she gave the resident potato chips, Staff B said that in the past 3 weeks she provided Resident #37 with potato chips two times. The CNA brought the basket of snacks to the resident. The Resident picked a bag of Goldfish crackers from the basket. The surveyor asked Staff B why Resident #37 was on a soft foods diet, and Staff B responded, I don't know, her meal ticket says regular. Then she said that Resident #37 had no problem swallowing foods and that she ate Goldfish crackers with ease. She also reported that in the past Resident #37 was also served hamburgers and fries.An observation on 06/25/25 at 8:49 AM revealed that Resident #37's meal tray had been removed from her room and placed into the meal cart. Staff C, CNA was asked to identify Resident #37's meal tray. The CNA located the tray and the resident's breakfast meal ticket. The tray was placed back onto the resident's tray table. Resident #37's tray was observed to have, a large plate with a crumpled up light-yellow biscuit that appeared to be dry. The plate and the muffin were garnished with parsley flakes. There was no sausage gravy as listed on the menu; there was no moisture providing sauce or syrup on it. During an interview on 06/25/25 at 9:52 AM, the CDM explained that sandwiches were not allowed on Resident #37's diet.An interview was conducted with the Speech Language Pathologist (SLP, expert on swallowing disorders) on 06/25/25 at 5:34 PM. When asked if the diets in the electronic medical record and the diets on the meal tickets were supposed to be identical, the SLP answered, yes. She said they should be the same. When the SLP was told that Resident #37's diet on the meal ticket documented she was on a Regular - Mechanical Altered/Ground diet, the SLP confirmed that was the diet she wanted for Resident #37. The physician's diet order in the electronic medical record was documented as Regular diet, Mechanical Soft texture, Thin consistency.During the continued interview on 06/25/25 at 5:34 PM with the SLP about the possible consequences of non-compliance with the diet texture, the SLP said that the big concerns were aspiration and choking. She explained that both Aspiration Pneumonia and choking could be fatal. When asked about Resident #37's request for a hot dog, the SLP said that it should have been ground. The SLP said that on her diet she can have soft sandwiches. When the SLP was asked about the potato chip and Goldfish crackers items, she said that hard and crunchy foods can be problematic. She said that potato chips and Goldfish crackers can be difficult to swallow because they are dry.During an interview with the SLP on 06/26/25 at 2:21 PM, when asked what the difference was between a mechanical soft and a mechanically altered ground diet, the SLP said that it depends on the specific facility and their dietary policy. She added that in her experience the mechanical soft diet also warranted ground meats. The SLP stated that having the word Regular in the diet can be confusing and easy to misinterpret. She explained that the term Regular diet meant that he was not on a therapeutic diet like a Renal diet, or a diet for hypertension or diabetes.During the continued interview with the SLP on 06/26/25 at 2:21 PM, the SLP revealed a Speech Therapy treatment encounter note dated 03/01/2022 that listed the resident's response to treatment. She stated Resident #37 was on Speech Therapy from 01/04/22 through 03/02/22. The treatment encounter note documented the SLP's recommendation was for Current Foods/Solids to be Minced + Moist Foods MM5. This terminology was documented under a note that clarified the diet as per The International Dysphagia Diet Standardization Initiative 2016. The SLP said that Resident #37 had been on a mechanical soft diet for a long time. She equated the Mechanical Soft Ground diet with the Minced and Moist diet.2) Record review revealed Resident #10 was admitted to the facility on [DATE]. Her diagnoses included Barrett's esophagus without dysplasia (changes to the lining of the esophagus without precancerous changes to the cells), Encounter for Attention to Gastrostomy (feeding tube), Moderate Protein Calorie Malnutrition, Muscle Wasting and Atrophy, and Muscle Weakness. Her diet orders since 06/10/25 included provision of 4 cartons (237 milliliters each) of Osmolite 1.5 Cal (calorie) tube feeding daily, and a regular diet, with puree texture foods, and thin consistency fluids.A record review revealed Resident #10's Brief Interview for Mental Status (BIMS) score, per the Minimum Data Set (MDS) admissions assessment dated [DATE], was 15. This indicated that she was cognitively intact. The assessment also documented that she had swallowing problems within the 7-day lookback period prior to this assessment. The care area for nutrition noted that the doctor's order for the mechanically altered diet was related to swallowing problems.A record review of Resident #10's care plan dated 06/12/25 focused on the resident's risk for malnutrition. One of the interventions listed by the Registered Dietitian was to provide the diet as ordered.During an observation on 06/23/25 at 11:55 AM, Resident #10 was provided and ate her soup, while sitting at a table in the dining room. The soup had whole grains of white rice, and whole intact yellow kernels of corn in a light-yellow broth. This was the same soup that was served to residents who were on regular diets with no dietary restrictions. There were no meal tickets on the tables for any of the residents seated in the dining room at that time. During an observation of breakfast served to the residents in the Dining Room, on 06/25/25 at 8:29 AM, it was noted that the resident received portions of pureed sausage with gravy and a pureed biscuit on a plate. It was noted that there was a garnish on the plate that appeared to be chopped parsley. 3) A record review revealed that Resident #15 was admitted to the facility on [DATE]. His medical history included Moderate Protein-Calorie Malnutrition, Gastro-Esophageal Reflux Disease with Esophagitis (Inflammation of the Esophagus), Acute Respiratory Failure with Hypoxia (a lack or lowered amount of oxygen), and Metabolic Encephalopathy (metabolic derangements that affect brain function). Per the Minimum Data Set assessment dated [DATE], this resident's BIMS score equaled 3, which indicated he had severe cognitive impairment. The care plan initiated by the Registered Dietitian on 05/08/25 focused on Resident #15's risk for altered nutrition. A listed intervention was to provide the diet as ordered.A record review of Resident #15's diet order revealed that since 05/22/25, he was on a regular diet, with puree texture foods, and thin consistency fluids. The term Regular diet meant that he was not on a therapeutic diet like a Renal diet, or a diet for hypertension or diabetes.During an observation of lunch on 06/23/25, Resident #15 was served pureed breaded shrimp, pureed cabbage, pureed carrots, and mashed potatoes. The pureed shrimp and the pureed carrots were lumpy. There were distinct pieces of breaded shrimp and carrots visible. The scoops of food were not homogenous, pudding like textures. Photographic Evidence Obtained.During an observation in the kitchen on 06/25/25 at approximately 11:55 PM, the pureed baked ham with glazed honey was lumpy. An interview was conducted on 06/25/25 at 12:00 PM with Staff D, a cook. When asked how she knew how long to puree the foods, she answered that foods were pureed until they were smooth, and until they had no chunks and no separate particles at all. Concern for the lumpy appearance of the pureed foods was voiced to the CDM, and a trial plate of the lunch meal was requested. The CDM lifted a spoonful of the pureed baked ham with glazed honey, and it had small lumps of meat surrounded by a thinner substance. Two different textures were observed. Photographic Evidence Obtained. The CDM tasted the pureed ham and said it could have been smoother. A taste of the pureed ham revealed it contained small separate particles of ham.During an interview with the Staff D, cook, on 06/25/25 at 12:15 PM, she said that this morning the pureed ham was really smooth, and most likely when it was warmed up it got lumpy. 4). Resident #21 was admitted to the facility on [DATE]. According to the resident's most recent full assessment, an Annual MDS, with a reference date of 06/15/25, Resident #21 had a BIMS score of 12, indicating the resident was cognitively intact. Resident #21's diagnoses at the time of the assessment included: Anemia, Malnutrition, COPD, Dysphagia. Resident #21's diet orders included: Regular diet, Pureed texture, Nectar consistency - 06/13/25During an observation of breakfast served to the residents in the Dining Room, on 06/24/25 at 8:24 AM, Resident #21 was served pureed French toast and pureed sausage. It was noted that there was a garnish sprinkled about the plate and on the foods that appeared to be chopped parsley. The facility's Immediate Jeopardy removal plan dated 06/27/25 included the following, which was also verified:On 06/24/25 Resident #37 was immediately assessed. A speech referral was submitted to assess diet appropriateness. A chest x-ray was ordered to rule out aspiration. Respiratory assessments were initiated every shift for 72 hours for signs and symptoms of aspiration. The resident's diet order, care plan, and Kardex were reviewed and updated as indicated for accuracy. The physician and responsible party were notified. On 06/25/25 the speech evaluation was ordered for Resident #37.On 06/26/25 a FEES (Fiberoptic Endoscopic Evaluation of Swallowing) bedside study was ordered.On 06/24/25 the CNA and dietary employee involved were removed from the floor and received one-on-one education by the Staff Development Coordinator and Dietary Manager on verifying diet slips with current orders, appropriate food textures for mechanical soft diets, how to address concerns regarding tray accuracy, possible consequences of serving inappropriate diets, and ensuring proper supervision of residents who require it during meals.On 06/25/25 the facility reviewed residents with mechanically altered diets to ensure current orders matched tray ticket diets. There were 18 current residents who were on mechanically altered diets at the time of the survey.On 06/24/25 through 06/26/25 current nursing and dietary staff were educated on verifying diet orders with current physician orders and consequences of serving inappropriate diets, to include regular meals, alternate options and snacks. Newly hired staff will receive education on these matters. Any contracted nurses or CNAs who are placed at the facility on assignment will receive the above education prior to starting their shift through an agency orientation packet.On 06/27/25 the information in the facility's removal plan was verified. Observations of the lunch and dinner meals on 06/27/25 demonstrated a process to ensure physician ordered diets were being delivered to residents. A new diet communication manual was placed in the main dining room and on each tray cart. On 06/27/25 six staff, including Staff B, the CNA, who provided Resident #37 with potato chips and permitted the resident to choose Goldfish crackers, were interviewed. Each staff member was able to verbalize the training provided during the week. They verbalized what needed to be done before providing an alternate food item or snack to a resident, and the new process for meal tray delivery.On 06/24/25 Resident #37 was immediately assessed by her assigned nurse. A speech referral was submitted to assess diet appropriateness. A chest x-ray was ordered to rule out aspiration and was refused by the resident. Respiratory assessments were initiated and documented every shift for 72 hours for signs and symptoms of aspiration. The resident's diet order, care plan, and Kardex were reviewed and updated as indicated for accuracy. The physician and responsible party were notified. On 06/24/25 Staff L, dietary cook and Staff A, CNA, were provided the one-on-one education.On 06/25/25 the speech evaluation was completed for Resident #37.On 06/25/25 an audit was completed confirming the meal textures in Meal Tracker (the dietary software used to print meal tickets) matched the physician's order for all current residents.By 06/26/25 a total of 79 nursing and dietary staff, to encompass 100%, received the above-mentioned education.On 06/26/25 a FEES (Fiberoptic Endoscopic Evaluation of Swallowing) bedside study was conducted. The recommendations from this study were to advance the resident diet to a mechanically soft chopped diet.An Ad Hoc/Quality Assurance Performance Improvement (QAPI) meeting was held on 06/25/25 with the Medical Director, the Administrator, the Director of Nursing, the Staff Development Coordinator, and the Dietary Manager. Supervision during meal consumption was discussed. A plan for continued monitoring and sustained compliance was reviewed. An additional Ad Hoc/QAPI meeting was held on 06/26/25 to evaluate the effectiveness of the education.The facility's Immediate Jeopardy was removed on 06/27/25 at 6:50 PM.
CONCERN (D)

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

Resident Rights (Tag F0550)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to provide care and services in a manner to maintain residents' dignit...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to provide care and services in a manner to maintain residents' dignity for 2 of 20 sampled residents, reviewed for dignity (Resident #118 and #218).The findings included:1. Record review revealed Resident #118 was admitted to the facility on [DATE]. An assessment completed on 06/19/25 documented a Brief Interview for Mental Status (BIMS) score of 15, on a 0 to 15 scale, indicating the resident was cognitively intact.During an interview on 06/23/25 at 1:58 PM, when asked if staff treat her with respect and dignity, Resident #118 stated, When I use the call light to be changed or if I need something, at times it takes over 30 minutes to have it answered, and then sometimes they say I'll have to wait, as they are busy. They are on their own pace, and they'll get to you when they get to you. Some of the staff have a chip on their shoulders. When asked how it makes her feel, Resident #118 stated, Not good. Some of them complain a lot. Most seem stressed out.During an interview on 06/27/25 at 3:04 PM, when told what was said by Resident #118, the Director of Nursing (DON) agreed the resident was not being treated with dignity. 2. Record review revealed Resident #218 was admitted to the facility on [DATE] with diagnoses that included Right Artificial Hip Joint, Left Artificial Hip Joint, Muscle Weakness, Muscle Atrophy, Fracture of Part of Neck of Right Femur, Subsequent Encounter for Closed Fracture with Routine Healing, Anxiety Disorder, and Major Depressive Disorder. According to an assessment of cognition performed on 06/19/25, Resident #218 had a Brief Interview for Mental Status (BIMS) score of 15. This indicated that he was cognitively intact.A review of Resident #218's care plan dated 06/17/25, documented the resident had the potential for pain related to the surgical procedure, a Total Hip Arthroplasty (THA, damaged hip joint was replaced), which was performed in the hospital prior to admission. Interventions included encouraging the resident to inform staff if experiencing pain. Another care plan dated 06/17/25, focused on Resident #218's ability for activities of daily living (ADLs). It documented that Resident #218 had an ADL self-care performance deficit related to the Right THA, weakness, impaired balance and mobility, and fall risk. The resident had a fall history that resulted in a fracture. An intervention was to keep frequently used items within reach.During an interview on 06/24/25 at 9:18 AM, Resident #218, shared two descriptions of events that occurred when he felt disrespected. First, he explained that when CNA's (Certified Nursing Assistants) entered his room, they failed to offer the resident assistance with tasks. He said that while a CNA leaned against the wall near the vanity area across from his bed, she watched him as he leaned over the edge of the bed and reached to pick something up from the floor that he dropped. The CNA didn't offer to help him. Another time Resident #218 felt disrespected was when he felt manhandled during the provision of care to receive ADL care. He explained that he told the CNA's that he could roll over slowly if he was given the time. He added that if he wasn't fast enough the CNA's grabbed onto his right hip area where he had the surgery and that hurt. When asked if he told the CNA's that he was in pain, Resident #218 said that he told them, and they still kept pushing. He said that the CNA's facial expressions didn't change. It was as if they weren't listening. Resident #218 said that this occurred two times.During an interview with the DON on 06/27/25 at 2:53 PM, the DON said that she knew Resident #218 wanted to be discharged . The DON said she was not aware about Resident #218's complaints about not being treated with dignity. When asked how CNAs were made aware that a resident recently had surgery, the DON explained that one function of the Resident's primary nurse was to tell the CNAs about special instructions for the resident. The DON also said that the CNAs should be handling the residents gently if they had surgery or not. The DON added that it was one thing to teach nurses and to provide them with education, but she couldn't give them compassion. She said that nursing 101 was to go into the room, to introduce yourself, and to be polite and to offer your services.
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 observations, record reviews, and interviews, the facility failed to maintain the call bell within the reach of 2 of 20...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record reviews, and interviews, the facility failed to maintain the call bell within the reach of 2 of 20 sampled residents, reviewed for accommodation of needs (Resident #2 and Resident #40).The findings included:1.Record review revealed Resident #2 was admitted to the facility on [DATE]. Her diagnoses included Non-Alzheimer's Dementia, Anxiety disorder, Depression, Muscle weakness, and Overactive Bladder. This resident's Brief Interview for Mental Status (BIMS) score, per the Minimum Data Set (MDS) assessment dated [DATE] was 08, indicating she was cognitively impaired. The assessment indicated Resident #2 was dependent on assistance for most activities of daily living (ADL), which included toileting, hygiene, bed mobility, and transfers. Review of Resident #2's care plan for ADL self-care performance deficit, dated 08/13/20, was related to impaired balance and mobility, weakness, limited range of movement, cognitive loss, and history of Polio Disease. The care plan listed an intervention, initiated 08/13/20, to encourage the resident to use the bell to call for assistance.Record review of Resident #2's care plan for falls, dated 05/08/24 listed an intervention to maintain the resident's call light within reach, and to respond promptly to all requests for assistance. The interventions included that Resident #2 needed a safe environment with a reachable call light.During an interview with Resident #2 on 06/23/25 at 4:39 PM, when asked if she knew where her call bell was, she was unable to find it. Observation revealed it was located on the upper area of the bed, approximately ten inches above her right shoulder. The cord that the call bell was attached to was neatly wrapped into circles. The circular coiled cord and the call bell were located on the bed, approximately ten inches above the resident's right shoulder. It was not within reach of Resident #2. When the resident was asked if she knew what the call bell was used for, she answered yes, it's to call someone if I need help. Resident #2 said thank you and added that she really needed to have the call bell within reach, and that she has needed help the past couple of days. Resident #2 placed the call bell on the blanket in her lap and said she would leave it right there.During an observation on 06/25/25 at approximately 7:05 PM, Staff M entered Resident #2's room. Staff M looked around and then exited the room. Further observation on 06/25/25 at 7:11 PM revealed Resident #2's call bell was located on the floor. (Photographic Evidence Obtained).During an interview with Staff M on 06/25/25 at approximately 7:20 PM, Staff M was asked what she did when she entered Resident #2's room at 7:05 PM. Staff M said that she wanted to make sure the resident was comfortable, had water, and that the garbage can was clean. When asked if she thought it was important for the call bell to be within reach of the resident, she said it was important for the call bell to be close to the resident in case she needed to go to the bathroom, or if she needed care, or for anything at all. Staff M then saw that the call bell was on the floor, she picked it up and placed it in the resident's lap.2. Record review revealed Resident #40 was admitted to the facility on [DATE]. Her diagnoses included Renal Insufficiency, Diabetes Mellitus, Hemiplegia following Cerebral Infarction (paralysis on one side of the body following stroke), Muscle Weakness, and Insomnia. Per the Minimum Data Set (MDS) quarterly assessment dated [DATE], Resident #40's Brief Interview for Mental Status (BIMS) score equaled 8, which indicated she was cognitively impaired. The assessment documented that she required substantial, maximal assistance for transfers, and that she was always incontinent.Record review of Resident #40's care plan for falls, last revised on 02/12/25, included an intervention to ensure the call light was within reach. The staff was to encourage the resident to use the call light when she needed assistance with standing, transferring and ambulating. Another intervention documented the need for Resident #40 to have a working and reachable call light.During an interview on 06/23/25 at 5:50 PM, Resident #40 requested assistance with adjusting the bedding for her comfort. When asked if she could press her call bell for assistance, she said she didn't know where her call bell was. The call bell was observed dangling between the mattress and the floor. Resident #40 was handed the call bell, and she pressed the button. (Photographic Evidence Obtained)During an interview with Resident #40, while she was in bed on 06/25/25 at 11:37 AM, when asked if she knew where her call bell was, she said no. She added that it would be a good idea if she knew where it was. The call bell was located on the floor behind the bed, and close to the wall (Photographic Evidence Obtained).
CONCERN (D)

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

Deficiency F0565 (Tag F0565)

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 promptly address grievances voiced for 2 of 20 samp...

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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 promptly address grievances voiced for 2 of 20 sampled residents (Resident #10 and Resident #7). The findings included: An interview was conducted on 06/23/25 at 12:47 PM, with Resident #7, who was admitted to the facility on [DATE], and with a Brief Interview for Mental Status (BIMS) of 15, according to a Quarterly Minimum Data Set (MDS) with a reference date of 05/17/25, indicating that the resident was cognitively intact. When asked of any concerns voiced by the Resident Council, Resident #7 replied, I made recommendations during the meetings when I wasn't president, I suggested that they do something with the patio and the grass, and they still haven't done anything about that. Resident #7 stated that the concern was voiced about 5 months ago, they wrote it down and that was it. I go out on the patio once in a blue moon. They just need a few more plants and some more mulch, like they do the rest of the grounds. During the Resident Council meeting on 06/24/25 at 4:15 PM, with active members of the Resident Council, when asked about the outside patio, Resident #7 reiterated concerns regarding the patio. After reiterating the concern, Resident #10, with a BIMS score of 15, according to an Admission/Medicare 5-day MDS, with a reference date of 06/13/25, agreed with the statements echoed by Resident #7. During a follow up interview, on 06/26/25 at 3:30 PM, Resident #7 repeated that the Resident Council mentioned that the back patio needs some mulch and some plants or something, when I look out my room window, the landscaping is really nice (referring to the front of the facility facing the street), when we use the patio, it is just not as appealing and is mostly rocks and dirt. Resident #7 further stated that the concern was mentioned during Resident Council in April. (There was no documentation of the concern being voiced during the Resident Council meeting from the 04/30/25 in the meeting minutes). During an interview on 06/26/25 at approximately 3:45 PM, Resident #10, who was admitted to the facility on admitted [DATE], stated, The plants are too old, and they don't take care of the outside like they used to. They don't do anything with the fallen debris on the walkways and sometimes I am afraid to fall when I get up when I am out there. Resident #10 stated that she uses the patio, Three times a week when I am in therapy. During an observation on 06/25/25, at approximately 4:00 PM, while it was raining, the roof over the screened patio was noted to have several leaks. During an interview, on 06/26/25 at 4:07 PM, with the Activities Director, when asked about the concerns regarding the patio and courtyard area that was voiced during the Resident Council meeting, the Activities Director replied, they have not mentioned it since the March 2025 meeting, because it would have been documented in the minutes and a follow up sheet would have been provided to Administration and the Administrator would have to follow through with it. We have landscaping company come in at least weekly. During a tour of the actual patio and the area around the patio, the Activities Director acknowledged that the patio was not maintained as the rest of the grounds, as described by the Resident Council. During an interview, on 06/27/25 at 8:02 AM, with Staff M, Occupational Therapist (OTA), when asked about residents voicing concerns with the patio and courtyard area, the OTA stated that residents had stated that the patio and courtyard needs some work and could use some color. During a tour of the outside patio and courtyard area, on 06/27/25 at 1:09 PM, entering from the therapy gym, it was noted that there were areas of dirt and rocks with minimal vegetation and litter, including milk cartons, used masks in the corner of the patio by the dumpster area. Trees and shrubbery were growing out of the overhanging awning of the screened in patio. There was also a planter that was more than half full of garbage that was not being used as a planter. During a tour of the outside patio and courtyard area, on 06/27/25 at 1:18 PM, accompanied by the Maintenance Director, the Maintenance Director acknowledged the container that was more than half full of garbage and stated that it was not supposed to be used for trash and that it was a planter for small trees or shrubbery.
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 F0573 (Tag F0573)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interviews and record reviews, the facility failed to respond to requests for resident's records in a timely manner for...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interviews and record reviews, the facility failed to respond to requests for resident's records in a timely manner for 1 of 2 sampled residents reviewed for records requests (Resident #69). The findings included: Resident #69 was admitted to the facility on [DATE] and discharged [DATE]. According to the resident's most recent full assessment, an Admission/Medicare 5-Day Minimum Data Set, with a reference date of 01/30/25, Resident #69 had a Brief Interview for Mental Status (BIMS) score of 03, indicating a severe cognitive impairment. Resident #69's diagnoses at the time of the assessment included: Non-Alzheimer's Dementia, Anxiety Disorder and Depression. During an interview, on 06/24/25 at 12:31 PM, with Resident 69's family member, it was reported that there had been no response from the facility to the family's request for Resident #69's medical records. The family member stated, My [.] tried to contact them several times to talk to the Business Office Manager (BOM), to get a copy of the contract. We don't believe that none of the [family members] have a copy of the admission contract and there has been no effort by the facility to provide one. At the time that he was transferred to the facility from the hospital, he was delirious and should not have signed on his own behalf. We would like to get a copy of the contract for the resident's stay. This would tell us whether there is any language about their responsibility for a resident's belongings. None of the [family members] nor the resident recall signing a contract, none have a copy, and Garden View refuses to provide it to us. We'd really like to get a copy of that contract if it exists. Review of the resident's record revealed that one of Resident #69's [family member] were designated as Power of Attorney and two of Resident #69's [family members] were designated as Health Care Surrogates. During an interview, on 06/27/25 at 12:05 PM, with Medical Records Clerk, when asked about requests for a resident's medical records, the Medical Records Clerk replied, I have them fill out a medical records release form and then I scan it into my computer and then depending on what it is for, I send it to Corporate for approval. At the conclusion of the interview, the Medical Records provided documentation of [a family member] signing admission paperwork for initial admission on [DATE] and another of the resident's daughter signing admissions documentation for readmission [DATE]. There was no documentation of any requests for copies of resident's health records and/or admission packet. During an interview, on 06/27/25 at 2:58 PM, with the BOM, when asked about Resident #69's [family member's] request for the resident's medical records, the BOM replied, I emailed it to the Social Services Director (SSD), the Assistant Director of Nursing (ADON), Staff H, LPN/Unit Manager, the Director of Nursing (DON), and the Administrator). Anytime that I receive a request for records, I send it to the Medical Records Clerk, this was a contract. I don't know what happened to the request after that. I met the [family members] when they came in. The resident's [family member] was here and one of the sisters brought me his insurance cards (one designated as Health Care Surrogate and POA), she handled most of the decision making and financials. They tag teamed very well. During an interview, on 06/27/25 at 4:14 PM, with the Administrator, the DON and the ADON, the Administrator stated that there were no requests by Resident #69's family for records. The Administrator stated, if they are not POA or HCS, we can't send them anything. During a follow up interview, on 06/27/25 at 5:02 PM, The BOM stated that she realized she forwarded the request to the wrong staff. The Surveyor reviewed the chain of emails with the BOM. The chain was as follows: 06/02/25 at 9:46 AM, the BOM received a request from Resident #69's POA/HCS requesting a copy of a contract for Resident #69. On 06/13/25 at 2:33 PM, The BOM received a follow up request from Resident #69's POA/HCS. On 06/16/25 at 8:15 AM, The BOM received a follow up request from Resident #69's POA/HCS. The BOM stated, I realized today (06/27/25) that I forwarded the request to the wrong people. when asked about responding to Resident #69's emails, the BOM did not provide a rationale for not responding to the emails.
CONCERN (D)

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

Deficiency F0605 (Tag F0605)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure behavior monitoring for 1 of 4 sampled residents, Resident #...

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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 behavior monitoring for 1 of 4 sampled residents, Resident #119, reviewed for unnecessary psychotropic medications. The findings included: Review of the record revealed Resident #119 was admitted to the facility on [DATE]. Review of the current physician orders included the administration of Seroquel and Oxcarbazepine, both twice daily for mood. The medication Seroquel had a classification of an antipsychotic drug. Psychiatric progress notes dated 06/16/25 and 06/23/25 documented, in part, monitoring for agitation, aggression, combativeness, refusal of care, refusal of medications, along with numerous symptoms of Depression. Review of the record lacked any type of behavior monitoring by staff for Resident #119. During an interview on 06/25/25 at 7:43 PM, when asked the process for staff to monitor and document resident behaviors, the Director of Nursing (DON) stated the nurses should document any behaviors on the behavior monitoring forms in the electronic medical record. During a side-by-side review of the record, the DON confirmed the lack of behavior monitoring.
CONCERN (D)

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

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record reviews, interviews, and a review of the Centers for Medicare and Medicaid Services (CMS) Resident Assessment In...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record reviews, interviews, and a review of the Centers for Medicare and Medicaid Services (CMS) Resident Assessment Instrument (RAI), the facility failed to accurately complete Minimum Data Set (MDS) assessments for 3 of 5 sampled residents, reviewed for nutrition (Resident #15, Resident #23 and Resident #37).The findings included:The CMS RAI was reviewed, which provides guidelines for assessing the needs of residents in long-term care facilities. It helps staff gather information about residents' needs in order to create individualized care plans. The RAI manual specifies that weight entries should be based on the most recent weight within the past 30 days of the Assessment Reference Date (ARD) date of the assessment. If the resident's last recorded weight was taken more than 30 days prior to the ARD date of the assessment, then the facility should weigh the resident again. If a resident cannot be weighed, the directions specify to use the standard no information code (-), and to document the rationale on the resident's medical record. The ARD date specifies the endpoint of observations to be entered into the assessment.1. Record review revealed Resident #15 was admitted to the facility on [DATE]. His diagnoses included Depressive Disorder, Malnutrition, Dementia, Gastro-Esophageal Reflux Disease with Esophagitis (stomach acid flows back into the esophagus causing inflammation to the esophageal lining), and Metabolic Encephalopathy (metabolic derangements that affect brain function). The MDS assessment with an ARD date of 05/08/25 documented that his weight was 153 pounds. According to the electronic medical record, the weight of 153 pounds was taken on 05/01/25. The most recent weight within the 30 days of the ARD date that should have been entered was 149 pounds, as documented as Resident #15's recorded weight on 05/08/25 of 149 pounds.During an interview on 06/27/25 at 7:32 PM, Staff F, the MDS Coordinator, agreed with the findings. She confirmed that the weight of 153 pounds was taken on 05/01/25, and the weight of 149 pounds reflected the correct weight that should have been entered.2. Record review revealed Resident #23 was admitted to the facility on [DATE]. His diagnoses included Cerebral Infarction, Hemiplegia and Hemiparesis affecting Left Dominant Hand Contracture, Dementia, and Depressive Disorder. The MDS assessment with an ARD date of 12/17/24 documented Resident #23's weight was 157 pounds. According to the electronic medical record (EMR), Resident #23's weight on 11/7/24 was 157 pounds. The weight that was entered reflected this resident's weight 41 days prior to the ARD date. There were no weights documented in the EMR between the dates 11/07/24 and 03/11/25. The documentation that should have been entered was (-), the standard code for no information.During an interview on 06/27/25 at 5:04 PM with Staff F, MDS Coordinator, the weight entry for Resident #23 on the assessment dated [DATE] was confirmed. Staff F confirmed the finding that the entered weight was not taken within the past 30 days.3. Record review revealed Resident #37 was admitted to the facility on [DATE]. The Minimum Data Set assessment with an ARD date 12/11/25 documented Resident #37's weight was 169 lbs. According to the EMR, the weight of 169 lbs. was taken on 02/13/25. This weight was not obtained within 30 days prior to the ARD date.During an interview on 06/27/25 at 6:20 PM with Staff F, MDS coordinator, the weight entry was confirmed. Staff F confirmed that this weight did not represent a weight taken within the past 30 days.
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 policy review, observation, interview, and record review, the nursing staff failed to follow physician orders for wound...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, observation, interview, and record review, the nursing staff failed to follow physician orders for wound care for 1 of 2 sampled residents, observed with pressure ulcers (Resident #119). The findings included: Review of the policy titled, Wound Treatment Management revised on 11/23/22 documented, in part, Policy Explanation and Compliance Guidelines: 1. Wound treatments will be provided in accordance with physician orders, including the cleansing method, type of dressing, and frequency of dressing change. Review of the record revealed Resident #119 was admitted to the facility on [DATE] with diagnoses to include osteomyelitis (infection of the bone) and stage 4 pressure ulcer (a deep wound with full-thickness tissue loss with exposed bone, tendon, or muscle). The wound care physician progress note dated 06/19/25 documented Resident #119 had two stage 4 pressure ulcers, one to the right buttock and one to the left hip. Review of the wound care progress note dated 06/19/25 documented, in part, to cleanse both wounds with wound cleanser, add a fluffed gauze moistened with Dakin's solution (a diluted bleach solution), and cover with a bordered gauze. Two physician orders dated 06/19/25 documented to cleanse both pressure ulcers with normal saline or wound cleanser, pat dry, apply wet to dry gauze with Dakin's solution 1/4 strength, and secure with bordered gauze, daily. A wound care observation for Resident #119 was made on 06/23/25 at 2:44 PM with Staff J, Licensed Practical Nurse (LPN). During the care, large pressure ulcers were noted to the right buttock and left hip. The LPN provided wound care to the right buttock first by cleansing the wound bed with Dakin's-soaked gauze. The LPN cleansed the left hip wound with the Dakin's-soaked gauze as well. During an interview on 06/25/25 at 6:59 PM, the Assistant Director of Nursing (ADON) was made aware of the wound care observation of Resident #119 by Staff J, LPN, and she agreed the wound care order had not been followed.
CONCERN (D)

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

Deficiency F0688 (Tag F0688)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record reviews, and interviews, the facility failed to provide a resident with restorative therapy per ph...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, record reviews, and interviews, the facility failed to provide a resident with restorative therapy per physician's orders for 1 of 2 sampled residents reviewed for Range of Motion (ROM), (Resident #24).The findings included:Record review revealed Resident #24 was admitted to the facility on [DATE]. His medical history included Polyosteoarthritis, Contracture of Muscle Left Lower Leg, Contracture of Muscle Right Lower Leg, Foot Drop Right Foot, Presence of Right Artificial Hip Joint, Short Achilles Tendon (Acquired) Left Ankle, Obesity, Chronic Pain Syndrome, Peripheral Vascular Disease, and Muscle Weakness. The Minimum Data Set (MDS) quarterly assessment dated [DATE] revealed that Resident #24 had a Brief Interview for Mental Status of 15, which indicated that he was cognitively intact. A review of the treatments provided in the MDS assessment dated [DATE] revealed that Resident #24 did not receive any restorative therapy during the 7-day lookback period prior to 04/24/25.Record review of Resident #24's care plan last revised on 12/11/23, documented that he required a restorative nursing program for active range of motion. The goal was to maintain the current level of function, and the interventions included to complete the restorative nursing program as written. A physician's order dated 06/10/24 was for the restorative nursing program for active and passive range of motion of the bilateral lower extremities, recumbent bike, and bilateral lower extremities splint application during daytime as tolerated three to five times per week.During an interview on 06/23/25 at 1:56 PM, Resident #24 said that the therapeutic exercises for his feet wasn't provided consistently. He stated that the restorative nursing program didn't follow the orders given by his doctor. Resident #24 said he should have been provided with the TENS (transcutaneous electrical nerve stimulation) massager daily as his doctor recommended. Resident #24 said that sometimes he received range of motion (ROM) therapy once in ten days, and sometimes he received it four days in a row; and sometimes they missed a week.During an observation on 06/23/25 at 3:58 PM, the box with the TENS massager inside of it was observed on the windowsill in Resident #24's room. Photographic Evidence Obtained. Resident #24 explained that the therapy department ordered the machine after his doctor ordered therapy with the TENS massager. Photographic evidence Obtained.During an interview on 06/25/25 at 9:10 AM, Resident #24 said that no one had used the TENS this week. He stated that the only way to get it done was if he moaned and groaned. He added that he got tired of yelling after a while. Resident #24 complained that half of the time, when the facility didn't have enough help, the restorative person (a certified nursing assistant), was reassigned to the duties of the floor Certified Nursing Assistants (CNAs).During the continued interview on 06/25/25 at 9:10 AM, when asked how not receiving consistent restorative therapy as ordered had affected him, he explained that his feet started to stiffen up when the TENS massager wasn't used. When asked if his feet were stiff at that moment, Resident #24 stated that his feet felt stiff.During an interview with Staff E, a physical therapist, on 06/25/25 at 9:21 AM, he explained that after Resident #24 was discontinued from physical therapy, he trained a few of the nursing staff on how to apply and use the TENS massager correctly.A record review of a treatment encounter signed by Staff E, on 11/15/24, documented that Staff E provided training on the electronic stimulator to the restorative staff. The treatment encounter was titled Therapy Referral to Restorative Nursing Program Form.During an interview on 06/26/25 01:48 PM, the Director of Rehab (DOR) revealed that Resident #24 was on Physical Therapy Services from 08/14/24 through 11/15/24. When asked what the process was for therapy services to be transferred from the therapy department to the restorative program, he said that a set of papers describing the indications for the therapy and the specific directions for the exercises was given to the DON (Director of Nursing) . When asked if there was a specific order in PCC (Point Click Care) that addressed the use of the TENS, or E-Stim, the DOR answered, one got missed.Record review of the Restorative Nursing Services Daily Documentation (RNSDD) Forms for the month of June was conducted. The indication for the restorative services was for Resident #24's increased risk of progression of contractures to right lower extremity. The listed goals on the RNSDD were to maintain the current range of motion, and to protect the resident's skin integrity. Documentation revealed during the second week, from June 8, 2025 through June 14, 2025 , restorative nursing for 15 minutes was provided one time. The restorative program should have been provided three to five times per week according to the doctor's order. During the fourth week, from June 22, 2025 through June 26, 2025, there was no restorative nursing program provided. Photographic Evidence Obtained.During an interview on 06/27/25 at 12:07 PM, the DON was asked to review the (RNSDD) Forms for Resident #24. When asked if she could provide any documentation about the provision of restorative therapy for Resident #24 during the week of June 22, 2025 through June 26, 2025, the DON said she couldn't show any documentation about it because there was no documentation of this activity.
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, record review, and professional standards, the facility failed to ensure appropriate care and s...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, and professional standards, the facility failed to ensure appropriate care and services to prevent an Urinary Tract Infection (UTI) for 2 of 2 sampled residents reviewed with indwelling urinary catheters, as evidenced by the failure to change the urinary drainage device collection bags using appropriate infection control techniques for Resident #36, and failure to ensure proper anchoring for the tubing of the indwelling urinary catheters for Residents #36 and #120.The findings included:Review of the Agency for Healthcare Research and Quality (AHRQ) document titled Catheter Care and Maintenance AHRQ Safety Program for Long-Term Care dated March 2017 documented, in part, Gloves play a key role in preventing hand contamination - but do NOT replace hand hygiene. Perform hand hygiene and wear gloves immediately before accessing the drainage system, emptying the drainage bag . Drainage Bag Care: . stabilize the catheter tubing and drainage bag. Leg Bags: Leg bag care and changing should be done per your facility's policy.On 06/25/25 at 11:21 AM the Director of Nursing (DON) was asked to locate and provide their policy on indwelling urinary catheter care and maintenance. The policy provided lacked any information related to changing the urinary drainage device collection bags. When asked to provide documentation for that procedure the Administrator stated they did not have that specific policy or procedure.1) Review of the record revealed Resident #36 was admitted to the facility on [DATE] with an indwelling urinary catheter and UTI. Review of the current care plan initiated on 05/27/25 documented the resident was at risk for further infections related to his urinary catheter. Interventions initiated on 06/16/25 included to change out the leg bag to straight drainage bag at bedtime or when lying in a flat/supine (facing upward) position and to utilize regular hand hygiene before and after handling of the catheter.Review of the current physician orders included to Ensure securement device in place as of 06/16/25.During an observation on 06/25/25 at 6:09 PM, Resident #36 was sitting up in his wheelchair. A leg bag was noted to the resident's leg with an anchor noted at his thigh. The catheter tubing had been placed through the anchoring device but was not secured at the Y junction of the tubing, allowing the tubing to move freely and pull tightly from the insertion point. Staff K, Certified Nursing Assistant (CNA) stated she was going to get him dressed for bed and change out the leg bag to the straight drainage bag.During the continued observation, Resident #36 was assisted to the toilet. After Resident #36 used the toilet, expelling gas, the CNA cleaned the resident's buttock with a washcloth while wearing gloves. The CNA changed her gloves without hand hygiene and cleaned the resident's back side again. Resident #36 stood up and the leg bag was noted unstrapped from the resident's leg, dangling loosely with the tubing noted to be tight from the insertion site. Staff K assisted Resident #36 into bed and proceeded to change out the leg bag to the straight drainage bag, which had a larger urine collection bag. The CNA failed to change her gloves and provide hand hygiene prior to working with the indwelling catheter. The CNA changed the leg bag to the larger drainage back without cleaning the ends of the tubing. The CNA covered the resident and stated she was done and failed to properly secure the indwelling catheter tubing into the anchor.After the observation, when asked the purpose of the anchor, Staff K, CNA, described how the straps of the leg bag held it in place. When shown the anchor on the resident's thigh and asked the purpose of that, the CNA stated, I'm not sure, but if I had to guess I would say it's to keep it from yanking up or out. When asked if the tube was secured in the anchor the CNA was able to move the tubing in the anchor as it was not secured.During an observation and interview on 06/25/25 at 6:39 PM, the Assistant DON (ADON)/Infection Preventionist (IP) was asked to observe the indwelling catheter anchoring device for Resident #36. The ADON noted the loose tubing and immediately secured the tubing into the anchor at the tubing Y junction. The ADON explained and demonstrated how to properly secure the urinary catheter tubing at the Y junction, to the CNA, who was still in the resident's room.During an interview on 06/27/25 at approximately 9:00 AM, when asked the process for changing the indwelling catheter leg bag to the large collection bag, the DON stated she would expect the CNA to clean the ends of the catheter tube with alcohol prior to hooking up the new bag. When told the CNA also failed to ensure glove change with hand hygiene after assisting Resident #36 clean himself after toilet use and prior to disconnecting the leg bag and applying the large bag, the DON had no response.2) Review of the record revealed Resident #120 was admitted to the facility on [DATE]. Review of the current Minimum Data Set (MDS) assessment dated [DATE] documented the resident had a Brief Interview for Mental Status (BIMS) score of 13, on a 0 to 15 scale, indicating the resident was cognitively intact. This MDS documented the resident had an indwelling urinary catheter.A physician's order dated 06/12/25 documented the use of the indwelling urinary device with instructions to ensure securement device was in place. A progress note dated 06/21/25 documented Resident #120 complained of urine retention, the urinary catheter was flushed, the collection bag was changed, and a urine sample was obtained for a urinalysis to rule out a UTI.Review of the current care plan dated 06/26/25 documented Resident #120 developed a UTI with the initiation of an antibiotic.An observation on 06/25/25 at 9:35 AM revealed Resident #120 in bed with the indwelling urinary large collection bag to bedside drainage. When asked if his catheter tubing was anchored, the resident was not sure but pulled his blanket to the side. Resident #120 was wearing shorts, and an anchor was noted to his thigh, but the tubing was not secured properly with the tubing Y junction in the anchor. Photographic evidence obtained.An additional observation on 06/25/25 at 5:35 PM revealed the tubing to the urinary catheter remained not secured.During an observation and interview on 06/25/25 at 6:44 PM, the ADON/IP confirmed the incorrect placement of the urinary catheter tubing for Resident #120.
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 observations and interviews, the facility failed to store, prepare, distribute, and serve food in accordance with professional standards for food service safety, sanitary conditions, and the ...

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Based on observations and interviews, the facility failed to store, prepare, distribute, and serve food in accordance with professional standards for food service safety, sanitary conditions, and the prevention of foodborne illnesses. This had the potential to affect 63 out of 66 residents who consume foods PO (by mouth).The findings included:During the initial tour of the Main Kitchen on 06/23/25 at 9:15 AM, accompanied by the CDM (Certified Dietary Manager) and the RD (Registered Dietician), the following was observed:1. The gaskets on the door of the reach in cooler had dark brown/black streaks and spots on the rubber pleats. The bottom of the gasket attached to the door was torn. Pieces of the rubberized material that were still attached to the door hung downward. The CDM agreed with this finding. Photographic Evidence Obtained.2. A bag of pasta was observed on the floor behind the lowest shelf in the dry food storage area. A large dark brown/black colored insect was dead and lying on floor in the same area. Another large dark brown/black colored insect was dead and lying on the floor under the area where the cookies were stored. There was a yellow packet of a condiment (mayonnaise or mustard) on the floor next to it. The CDM agreed with these findings and proceeded to sweep the floor. Photographic Evidence Obtained.3. The muffin pans were ladened with brown residue. The CDM agreed with this finding. Photographic Evidence Obtained.4. The storage rack for clean serving scoops and baking sheets had yellow/brown, and brown/black residue on the individual shelves. The baking sheets had dark black and yellow/brown residue on them. The CDM agreed with this finding. Photographic Evidence Obtained.5. The wash cycle temperature of the low-temp dishwasher reached 100' F. It did not reach the required temperature of 120' F. The CDM agreed with this finding. TheCDM immediately told the Maintenance Director. During an interview with the Maintenance Director at approximately 10:00 AM, he said that he raised the temperature on the hot water heater to fix the problem.6. The Vulcan fryer contained residue from food. It was not clean. When asked if it was used during breakfast, the CDM said no. When asked how often it was used, she said once per week. When asked how often it was cleaned, the CDM said that it would be cleaned that day after it was used for frying food. Photographic Evidence Obtained.
CONCERN (F)

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

Infection Control (Tag F0880)

Could have caused harm · This affected most or all residents

Based on observation, and interview, the facility failed to ensure the proper storage of linens in 3 of 3 linen carts.The findings included:On 06/25/2025, it was revealed the facility had four residen...

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Based on observation, and interview, the facility failed to ensure the proper storage of linens in 3 of 3 linen carts.The findings included:On 06/25/2025, it was revealed the facility had four residents under transmission-based precautions due to various health concerns, including positive COVID-19 status, Methicillin-resistant Staphylococcus aureus (MRSA), which is a type of staph bacteria resistant to many commonly used antibiotics, Extended-spectrum beta-lactamase (ESBL) production, which refers to enzymes that make certain bacteria resistant to many beta-lactam antibiotics, and Shingles.On 06/25/2025 at 11:09 AM, an observation revealed that the linen cart in the [NAME] Wing was torn and opened, exposing the linens inside. Additionally, a glove was found on the floor next to the linen cart. At 11:28 AM, the surveyor noted that the linen cart in the East Wing was not fully uncovered, exposing the linens to potential contamination. Similarly, at 11:33 AM, it was observed that the linen cart in the North Unit was also not fully covered, making the linens vulnerable to contaminants. Later, at 4:41 PM, the surveyor conducted another tour of the areas of concern, accompanied by the Infection Preventionist (IP). The IP acknowledged that the linen carts were torn and uncovered, which posed a risk of exposing the linens to contaminants.
Feb 2025 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

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 policy review, interview, and record review, the facility failed to ensure timely provision of medications for 2 of 3 s...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on policy review, interview, and record review, the facility failed to ensure timely provision of medications for 2 of 3 sampled residents, as evidenced by the failure to provide insulin and an antibiotic timely upon Resident #1's admission to the facility, and failure to provide insulin timely upon Resident #2's admission to the facility. The findings included: 1) Review of the record revealed Resident #1 was admitted to the facility from the hospital on [DATE] at 6:00 PM, with diagnoses to include Type 1 Diabetes. Review of the current Minimum Data Set (MDS) assessment dated [DATE] documented the resident had a Brief Interview for Mental Status (BIMS) score of 15, on a 0 to 15 scale, indicating he was cognitively intact. This MDS also documented the resident received both insulin and an antibiotic during the look-back period of 01/28/25 through 02/01/25. Review of the hospital discharge paperwork documented Resident #1 was to receive insulin, one short-acting and one long-acting, but the paperwork lacked any specific dose or frequency. Further review of the discharge paperwork revealed documentation the resident was to receive Zosyn (an antibiotic), intravenously, every 8 hours. During an interview on 02/21/25 at 11:21 AM, Resident #1 stated it took a long time to get his insulin, upon admission to the facility. The resident stated he thought it was because he was admitted to the facility late in the evening, and they had to get the insulin from an outside pharmacy. Review of the January 2025 Medication Administration Record (MAR) for Resident #1 revealed the following: a) Lantus insulin (long-acting) was ordered to start on 01/29/25 at 6 AM, but was discontinued and not provided. b) A sliding scale insulin regimen with Novolog (short-acting) was ordered to start on 01/29/25 at 7:30 AM with blood sugar checks ordered before each meal and at bedtime but was discontinued and not provided. This order was then initiated on 01/29/25 at 4:30 PM, missing three opportunities for coverage on 01/28/25 at bedtime, 01/29/25 before breakfast, and on 01/29/25 before lunch. This order was initiated nearly 24 hours after admission to the facility. The resident's blood sugar was high at 335 at that time, with a desired blood sugar of less than 200. c) Glargine insulin (long-acting) was not started or provided until 01/29/25 at 4:30 PM, nearly 24 hours after admission to the facility. The resident's blood sugar was high at 335 at that time, with a desired blood sugar of less than 200. d) The antibiotic Zosyn was ordered to start on 01/29/25 at 6:00 AM. The Zosyn was not administered at this time, as evidenced by a blank area on the MAR, but started on 01/29/25 at 2 PM, nearly 24 hours after admission to the facility. Review of the progress notes lacked any reason for the lack of medication administration. During a side-by-side record review on 02/21/25, the Assistant Director of Nursing (ADON) confirmed the lack of insulin dosing from the hospital record. The ADON stated the nurse would have had to call the physician to get clarification. The ADON stated that sometimes the issue was with which insulin the insurance would cover, and the pharmacy would then contact the facility for an order to substitute. Upon further review of the orders, the ADON noted the pharmacy had entered an order for the Novolog FlexPen to be administered as per the sliding scale on 01/28/25 at 11:35 PM, and the order was not confirmed by the nursing staff until 01/29/25 at 12:10 PM, fourteen hours later. When asked about the delivery of the FlexPens, the ADON explained the admission or night nurse should have called the physician to get an order to use their stock insulin until the pharmacy delivered the FlexPen. Upon further review of the January 2025 MAR, the ADON agreed Resident #1 did not receive any insulin until 01/29/25 at 4:30 PM, nearly 24 hours after the resident was admitted . During this continued interview, the ADON agreed with the lack of antibiotic administration on 01/29/25 at 6:00 AM. The ADON provided evidence that the Zosyn was available in the facility's stock medications at the time of the survey, although she was unsure if it was available on 01/29/25. During the exit conference on 02/21/25 at approximately 4:45 PM, the Director of Nursing (DON) stated she had reached out to the nurse who should have provided the antibiotic on 01/29/25 at 6 AM, and the nurse would not confirm if she had provided the medication or not. 2) Review of the record revealed Resident #2 was admitted to the facility on [DATE] at approximately 9:00 PM, with diagnoses to include Diabetes. Review of the February 2025 MAR for Resident #2 revealed the following: a) Insulin Asparte (short-acting) was ordered to start on 02/25/25 at 8 AM and not provided. b) Novolog (short-acting) FlexPen was ordered by the pharmacy (as an insurance approved substitute) on 02/14/25 at 11:35 PM. The order was confirmed by nursing staff on 02/15/25 at 12:14 PM, with the first dose administered at that time, 15 hours after admission. c) Insulin Glargine (long-acting) was ordered to start on 02/15/25 at 9 AM and not provided. The pharmacy placed an order for an insurance approved substitute on 02/14/25 at 11:35 PM. The nursing staff confirmed the order on 02/15/25 at 12:16 PM, with the first dose administered at 6 PM, 21 hours after admission. During an interview on 02/21/25 at approximately 4:30 PM, the ADON confirmed the medication delay.
Dec 2024 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

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 interview, policy review and record review, the facility failed to assess a resident's skin under a knee immobilizer to...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview, policy review and record review, the facility failed to assess a resident's skin under a knee immobilizer to prevent a pressure injury for 1 of 5 sampled residents (Resident #1). The findings included: The facility policy Titled Skin Assessment and revised on 10/01/22 documented in part: 1. A full body or head to toe skin assessment will be conducted by a Registered Nurse upon admission/readmission and weekly thereafter. The assessment may also be performed after a change in condition or after a newly identified pressure injury. The facility policy titled, Pressure Injury Prevention and Management, revised on 10/03/24, documented in part: The facility is committed to the prevention of avoidable pressure injuries. Avoidable means the resident developed a pressure ulcer/injury and that the facility did not do one or more of the following: evaluate the resident clinical condition and risk factors, define and implement interventions that are consistent with resident needs, resident goals and professional standards of practice. Record review revealed on 10/19/24, Resident #1 was transferred from a hospital to the facility. She had diagnosis to include unspecified Fracture of Lower end of Left Femur with encounter for closed fracture with routine healing, Pleural Effusion, Chronic Obstructive Pulmonary Disease, Hypertensive Heart Disease, Muscle Weakness, Difficulty in Walking, Muscle Wasting and Atrophy, Malnutrition, Hypothyroidism, Non-rheumatic Aortic Valve, Periprosthetic Fracture around internal prosthetic left knee joint, Hyperlipidemia, and pain in right hip. Resident #1's admission MDS (Minimum Data Set) assessment dated [DATE] documented the resident had a BIMS (Brief Interview for Mental Status) score of 5, indicating severe cognitive impairment. Further record review revealed Resident #1 arrived at the facility with a left knee immobilizer to secure her knee movements following a fracture of the lower end of her left femur. On 11/18/24 a pressure injury was found under Resident #1 left knee immobilizer after drainage was discovered from the site. Review of the record for Resident #1 indicates the last weekly skin check before the discovery of the left calf pressure injury was dated 11/04/24 and did not contain any documentation of skin injury on the resident's left calf. The next documented skin assessment was done on 11/18/24. The skin assessment was not documented as completed for 14 days. In reviewing the chart, the DON (Director of Nursing) agreed there was no documentation of a skin assessment for 2 weeks. An interview was conducted on 12/10/24 at 10:21 AM with Staff A, the Director of Rehabilitation. He was asked what the protocol was for removing an immobilizer for skin care and observation. He stated the rehabilitation department never tells nursing services they cannot remove an immobilizer for skin care or skin assessment. He stated it is standard to remove it for care unless there are orders to not remove it. On 12/10/24 at 11:05 AM Staff B, a CNA (Certified Nursing Assistant) was interviewed. She stated she has taken care of Resident #1 many times. She stated she was told by the Physical Therapy (PT) personnel not to remove Resident #1's immobilizer from her leg. She stated she wasn't sure who told her not to remove it. She didn't remove it for care. On 12/10/24 at 11:10 AM Staff C, a CNA was interviewed. She was asked about immobilizers. She stated they always look at the orders to see if the immobilizer is allowed to be removed for showers and peri care. She will follow the orders. On 12/10/24 at 11:12 AM Staff D, a CNA, was interviewed. She was asked about Resident #1's immobilizer; she stated she heard they were not supposed to take it off. She stated she was the one who discovered the drainage on Resident #1 linen, which led to the immobilizer being removed and the discovery of the pressure injury. On 12/10/24 at 11:14 AM, an interview was conducted with Staff E, a RN (Registered Nurse). She was asked about immobilizers and how she performed a skin check when a resident had an immobilizer. She stated she would remove it. She was asked about Resident #1 and her immobilizer. She stated she had removed it when she took care of Resident #1 to check her skin under the immobilizer. Further interview revealed Staff E could not recall the last time she took care of Resident #1. On 12/10/24 at 2:10 PM, Resident #1's Physician was interviewed. He was asked about Resident #1, and he stated the pressure injury under her immobilizer was preventable. He was asked about orders for checking skin integrity. He stated, I wrote protocols for the facility to follow. He stated nursing knows to check skin and circulation under an immobilizer. He stated he now has started writing orders to check skin integrity and circulation for patients with any type of immobilizer.
Mar 2024 5 deficiencies
CONCERN (D)

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

Deficiency F0561 (Tag F0561)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure showers were provided per resident preference and as schedul...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure showers were provided per resident preference and as scheduled for 1 of 3 sampled residents reviewed for choices (Resident #13). The findings included: During an interview on 03/18/24 at 10:07 AM, Resident #13 explained that staff keep her clean and dry as far as her incontinence, but they don't give her a full bed bath daily as she would like. The resident also stated she would like a shower. When asked how many showers she would like each week, the resident stated two. Resident #13 confirmed she does not get two showers weekly. Review of the record revealed Resident #13 was admitted to the facility on [DATE]. Review of the current Quarterly Minimum Data Set (MDS) assessment dated [DATE] revealed the resident was cognitively intact with a Brief Interview for Mental Status (BIMS) score of 14, on a 0 to 15 scale, indicating intact cognition. This MDS also documented the resident needed substantial assistance from staff for bathing. Review of the Significant Change MDS dated [DATE] documented it was very important for the resident to choose between a bath and a shower. Review of the current care plan initiated on 11/25/20, and revised on 03/18/24, documented the resident was at risk for decreased ability to perform ADLs (activities of daily living) in bathing, related to activity intolerance, and related to comorbidities that included quadriplegia, contractures, and traumatic brain injury. This care plan documented Resident #13 preferred showers and was dependent upon staff for showers and baths. Review of the shower schedule revealed Resident #13 was scheduled for a shower on Mondays and Thursdays during the 3 PM to 11 PM shift. Review of the tasks section of the electronic medical record for 02/19/24 through 03/19/24 documented the provision of 3 showers in 30 days, instead of the scheduled 9 showers for that same time period. The most recent shower was documented on Monday 03/18/24 by Staff A, Certified Nursing Assistant (CNA). A bed bath was also documented by the same CNA for the same day. During an interview on 03/21/24 at 9:22 AM, when asked if she provided a shower to Resident #13 on Monday, Staff A stated she had not given her a shower, but did a full bed bath instead. When shown that both a shower and bed bath were documented by her for Monday, the CNA stated it was a mistake. During a supplemental interview on 03/21/24 at 9:27 AM, when asked if she received a shower yesterday or any day this week, Resident #13 stated No. When asked if she still wanted a shower, the resident stated she did. When told she would have to get up out of bed, as the surveyor had only seen the resident up out of bed on one day that week, Resident #13 stated, I know!
CONCERN (D)

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

Assessment Accuracy (Tag F0641)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review and interview, the facility failed to ensure of an accurate Minimum Data Set (MDS) assessment related to ...

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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 of an accurate Minimum Data Set (MDS) assessment related to medications for 1 of 5 sampled residents reviewed for unnecessary medications, (Resident #62). The findings included: Review of Resident #62's electronic records revealed the resident was admitted to the facility on [DATE] with diagnoses to include Sequelae of Cerebral Infarction, Depression, Left Femur Fracture, Anxiety Disorder, Atrial Fibrillation, Muscle Weakness, and Acute Respiratory Failure. Review of the Minimum Data Set (MDS) Medicare 5-day assessment dated [DATE] documented the resident has a BIMS (Brief Interview for Mental Status) score of 12, indicating the resident's cognition is moderately intact. Review of the MDS section N, (Medications) documented the resident had 4 days of insulin injection and high-risk drugs antidepressant and anticoagulant. Review of Resident #62's diagnoses and physician orders revealed the resident did not have a diagnosis of Diabetes and did not have or had a physician's order for insulin while a resident in the facility. Further record review revealed a physician's order for Enoxaparin Sodium Injection Solution Prefilled Syringe 40 MG/0.4ML, inject 40 mg subcutaneously in the afternoon for DVT (Deep Vein Thrombosis) prevention; Start date 02/27/24 through 03/11/24 and 03/11/24-04/01/24 Enoxaparin Sodium is an anticoagulant medication (blood thinner). During an interview on 03/20/24 at 2:05 PM with Resident #62 and her daughter, she was asked about being on Insulin. She stated that she is not a Diabetic and has never been on Insulin. Her daughter confirmed this. She stated she is taking a medication that the staff injects in her stomach, which is a blood thinner. During an interview on 03/20/24 at 2:34 PM with the MDS Director, she was asked to review Resident #62's MDS record. She reviewed Section N (Medications) and was asked if the resident was a diabetic and taking Insulin, and stated, she is not a diabetic and coded it looking at the Enoxaparin as a diabetic medication. She stated, I know it is not a diabetes medication and acknowledged it was an error on her part.
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 interview and record review, the facility failed to assess for a voiced change in condition for 1 of 23 sampled residen...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to assess for a voiced change in condition for 1 of 23 sampled residents (Resident #118), and the nursing staff held blood pressure medications without ordered parameters and failed to notify the physician of the low blood pressure readings for 1 of 5 sampled residents (Resident #21). The findings included: During an interview on 03/20/24 at 1:11 PM, Resident #118 was asked if she still had her indwelling urinary catheter. Resident #118 stated she did not as it was taken out a few days ago, but volunteered she had a difficult time with a night nurse before the catheter was placed. Resident #118 explained she had a history of urinary tract infections, had had issues with voiding (urinating), and could tell when she was having difficulties. The resident stated the night before the catheter was placed, at about 3 AM, she was having horrible abdominal pain and she thought she needed a catheter because of the pressure she was feeling. Resident #118 stated the night nurse told her, Do you expect me to call the physician at this time of night. The resident explained she had told the nurse she hadn't urinated and had asked for a catheter. Resident #118 stated the night nurse told her she could not place a catheter because she was having spasms and she would continue to spasm. Resident #118 explained she then asked for some pain medication hoping for relief, but it did not help. During this description, Resident #118 demonstrated how she was having abdominal pain, grimacing, and rolling back and forth holding her abdomen. Resident #118 explained Staff D, Licensed Practical Nurse (LPN) and her day nurse, arrived and was her angel. Resident #118 stated she explained to the day nurse that she had been in horrible pain since 3 AM, and the day nurse told her that was unacceptable. The resident explained that Staff D returned, placed a catheter, and she immediately drained over 700 milliliters of urine, followed by 200 more. Resident #118 stated when that urine drained out, I felt such relief, I felt like I was just floating. During an interview on 03/20/24 at 1:14 PM, Staff D, day LPN, confirmed she had placed the urinary catheter for Resident #118 one morning, and had obtained a large amount of urine upon placement. During a supplemental interview on 03/20/24 at 3:02 PM, Resident #118 stated, Maybe that night nurse was having a bad night or something, but it wasn't like I had a headache and asking her to call the doctor for that. It could have been solved so quickly if she would have just called the physician and got an ok to cath me. I've had this before. Review of the record revealed Resident #118 was admitted to the facility on [DATE]. Review of the admission Minimum Data Set (MDS) assessment dated [DATE] documented Resident #118 was cognitively intact with a Brief Interview for Mental Status (BIMS) score of 14, on a 0 to 15 scale. This MDS documented the resident had an indwelling urinary catheter. The physician orders revealed the indwelling urinary catheter was placed on 03/07/24. During a phone interview on 03/20/24 at 4:26 PM, when asked about Resident #118 and the night prior to the placement of the indwelling urinary catheter, Staff B, night LPN, explained she was told the resident wanted to see the nurse. Staff B stated the resident was in pain and pointed to her abdomen. Staff B stated she assessed the resident's abdomen and it was soft. Staff B stated Resident #118 asked about a catheter, but when she asked if she was voiding or needed to go to the bathroom, the resident stated she was voiding and had just been to the bathroom. Staff B stated she gave Resident #118 pain medication, the resident went back to sleep, and she did not complain of pain through the rest of the night. Staff B stated she obtained her blood sugar level about 5 AM and still didn't voice any further complaints. Staff B stated Resident #118 had often complained of pain and took pain medication. Review of the March 2024 Medication Administration Record (MAR) documented Resident #118 had taken pain medication three times prior to the 3 AM pain medication for her abdominal pain. This MAR and associated progress notes revealed the following: On 03/02/24 at 1:33 AM the resident took Tylenol for complaint of bone pain in her legs rated at a 6, on a 0 to 10 scale. Follow-up rating at 2:29 AM was a 2. On 03/05/24 at 8:05 AM the resident took Oxycodone for documented chronic pain. The follow-up documented the intervention was ineffective, although the pain rating for the shift was documented as 0. On 03/06/24 at 10:03 AM the resident took Oxycodone for complaint of left hip pain rated at a 7, with a follow-up rating of 0. Staff B, the night LPN, documented she provided Oxycodone on 03/07/24 at 3:19 AM for severe pain in back rated at an 8. A follow-up note at 4:44 AM documented the resident then rated her pain at a 3. The progress notes lacked any documented assessment for the abdominal pain as voiced by Resident #118. 2) Review of the record revealed Resident #21 was admitted to the facility on [DATE]. Review of the current care plan initiated on 11/10/23 and revised on 02/16/24 documented Resident #21 had altered cardiovascular status related to hypertension. This care plan documented for staff to administer medication as per order, and to monitor for effectiveness and possible side effects. This care plan also documented for staff to monitor vital signs and to notify the physician of significant abnormalities. Review of the current orders revealed Resident #21 was taking Exforge (a medication to lower blood pressure) once daily. Review of the March 2024 Medication Administration Record (MAR) revealed the Exforge was not provided on 03/07/24 with a blood pressure of 117/57, on 03/12/24 with a blood pressure of 96/66, and on 03/13/24 with a blood pressure of 129/57. All three days the direct care nurse was Staff C, LPN. The documented reason for not administering the medication was that the blood pressure was outside of parameters for administration. Further review of the orders lacked any parameters for holding the medication. During an interview on 03/21/24 at 10:47 AM, when asked about the holding of the Exforge blood pressure medication for Resident #21 on the above three dates, Staff C stated she held it because the blood pressure was low. When asked if she asked or notified the physician, the LPN stated she did not.
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** 3) Record review revealed that Resident #16 was admitted to the facility on [DATE] with a diagnosis to include: Urinary Tract In...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 3) Record review revealed that Resident #16 was admitted to the facility on [DATE] with a diagnosis to include: Urinary Tract Infection (UTI). Review of the admission Minimum Data Set (MDS) assessment, reference date 01/12/24, documented a Brief Interview for Mental Status (BIMS) score of 08, indicating Resident #16 was moderately cognitively impaired. Laboratory test dated 03/10/24 for urinalysis, culture, and sensitivity (UA/ C&S) were reviewed. It indicated to straight catheterize the resident for a urine sample for symptom of urinary frequency, relating to strong smelling urine. It was revealed the lab was completed 03/10/24. The lab result was reported to the facility on [DATE]. The result was >100,000 CFU/ML [greater than 100,000 colony forming units per milliliter] Klebsiella pneumoniae, ESBL [Extended Spectrum Beta-Lactamase]. ESBL is an enzyme found in some strains of bacteria. ESBL bacteria can be spread from person to person on contaminated hands of both patients and healthcare workers. The risk of transmission is increased if the person has diarrhea or has a urinary catheter in place as these bacteria are often carried harmlessly in the bowel. Review of physician orders dated 03/13/24 revealed an order for Ciprofloxacin HCl [antibiotic] oral tablet, give 500 mg by mouth two times a day for UTI for 7 Days. Review of a care plan dated 03/14/24, documented, Resident #16 had a Urinary Tract Infection related to ESBL. Review of interdisciplinary progress note dated 03/14/24 recorded (Resident #16) 'was being skilled for right pelvic fracture, she was positive for ESBL as of 03/13/24, she was on an antibiotic by mouth until 03/21/24 with contact precautions.' On 03/21/24 at 9:23 AM, the surveyor met Staff G, Certified Nursing Assistant (CNA), in the hallway in front of the resident's room, to observe peri-care. The surveyor and Staff G donned gowns and gloves and entered the room. Once inside the room, Staff G and the surveyor introduced themselves to Resident #16. The resident was observed sitting in the wheelchair. Staff G removed Resident #16's shoes and assisted her to get into the bed. Staff G obtained the bed remote control and placed the bed in a high position. Staff G opened the resident's drawers, removed a basin, and went to the bathroom to collect water into the basin and left it in the bathroom. Staff G obtained a plastic bag which had towels and washcloths in it. She removed a large towel from the plastic bag, removed Resident #16's pants and adult brief and covered her private area with the large towel. At 9:27 AM, Staff G went to the bathroom and obtained the basin of water, placed the basin on the bedside table, put soap in the basin, and then placed a small washcloth in the water. At 9:29 AM, without changing her gloves, she began the peri care. She washed the peri area using one wash cloth at a time. After she completed the care, she removed her gloves, collected new gloves from her pocket and put them on without preforming hand hygiene in between glove changes. Staff G looked for cream in the drawers and applied the cream to Resident #16's groin and bottom area. After the peri care was completed, an interview was held with Staff G, who was asked why she didn't change her gloves before she began the peri care. She then acknowledged that she did not change her gloves. On 03/21/24 at approximately 9:50 AM, an interview was conducted with the Director of Nursing (DON) and the Regional Nurse Consultant. They were made aware of the concern, as the surveyor explained the whole procedure, and the matter of which the peri care was rendered. They acknowledged the findings. Based on observation, interview, record review, and policy review, the facility failed to ensure proper catheter care and services for 2 of 5 sampled residents with indwelling urinary catheters (Residents #32 and #4), and failed to ensure proper peri-care (personal care provided after an incontinent episode of urination) for 1 of 1 sampled resident observed (Resident #16). The findings included: 1) Review of the policy Catheter Care revised 01/06/23 documented after having cleaned the peri-area, 12. With a new moistened cloth, starting at the urinary meatus moving out, wipe the catheter making sure to hold the catheter in place so as to not pull on the catheter. Review of the record revealed Resident #32 was admitted to the facility on [DATE]. Review of the orders revealed an indwelling urinary catheter was placed on 02/20/24. Review of the current care plan initiated on 02/21/24, and revised on 03/11/24 documented, Resident #32 had an indwelling urinary catheter. Care plan interventions included catheter care with soap and water each shift and as needed. During an observation on 03/20/24 at 11:00 AM, Staff E, Certified Nursing Assistant (CNA) provided appropriate peri-care to the resident's front and back sides, but failed to wipe the urinary catheter tubing in any way. The CNA then placed an adult pull-up (adult incontinence brief) on Resident #32. Upon completion of care, when asked about cleaning the catheter tubing, the CNA stated, I thought I did. When asked if she had worked this week with Resident #32, the CNA stated she had. When asked if the resident had had any type of anchor or thigh strap to secure the catheter tubing that week, the CNA stated she had not. When asked if they use them at the facility, the CNA stated they do. When asked why the anchor or thigh strap would be used with the urinary catheter tubing, the CNA stated, So it won't come out. The CNA was unaware the anchor or thigh strap helped secure the urinary catheter tubing, to assist with the prevention of infection. 2) Review of the record revealed Resident #4 was admitted to the facility on [DATE]. Review of the Quarterly Minimum Data Set (MDS) assessment documented the resident was severely cognitively impaired with a Brief Interview for Mental Status (BIMS) score of 0, on a 0 to 15 scale. This MDS also indicated the resident was dependent upon staff for all activities of daily living (ADLs) and had an indwelling urinary catheter. Review of the current care plan initiated on 02/24/22 and revised on 06/29/22 documented the resident required the indwelling catheter due to urinary retention. One of the interventions was to maintain the catheter off of the floor. Observations on 02/19/24 at 8:23 AM and on 03/21/24 at 8:59 AM revealed the indwelling urinary catheter bag lying directly on the floor. On 03/21/24 the catheter bag was not hooked or secured to the bed frame in any way (Photographic Evidence Obtained). During the observation on 03/21/24, the Unit Manager was passing by the room. The Unit Manager agreed the catheter bag should not be on the floor and noted it was not hooked to the bed frame. The Unit Manager properly secured the catheter bag to the bed frame and off of the floor.
CONCERN (E)

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

Pharmacy Services (Tag F0755)

Could have caused harm · This affected multiple residents

Based on record review, interview, and policy review, the facility failed to ensure reconciliation of controlled medications for 4 of 4 sampled residents reviewed (Resident #22, #68, #37 and #6). The ...

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Based on record review, interview, and policy review, the facility failed to ensure reconciliation of controlled medications for 4 of 4 sampled residents reviewed (Resident #22, #68, #37 and #6). The findings included: Review of the policy Controlled Substance Administration & Accountability revised 10/2023 documented, 1. General Protocols: . i. The Controlled Drug Record is a permanent medical record document and in conjunction with the MAR is the source for documenting any patient-specific narcotic dispensed form the pharmacy. Review of the current Medication Monitoring/Control Records and the corresponding March 2024 Medication Administration Records (MARs) revealed the following discrepancies: 1). Resident #22, a 5 milligram (mg) tablet of oxycodone was signed out of the medication cart, as per the control record, on 03/12/24 at 12:30 PM, but not signed out on the corresponding MAR. 2). Resident #68, a 5 mg tablet of oxycodone was signed out as per the control record on 03/18/24 at 10:33 PM, but not signed out on the corresponding MAR. During this review on 03/21/24 at 12:22 PM, Staff D, Licensed Practical Nurse (LPN) agreed with the findings and confirmed the nurses were to sign out a controlled medication on both the control record and the MAR. Additional observations of the medication carts and controlled records revealed the following discrepancies: 3). Resident #37, one 50 mg tablet of Tramadol was signed out as per the control record on both 03/17/24 at 4:43 AM and on 03/19/24 at 4:36 AM, but not signed out on the corresponding MAR for either date. 4). Resident #6, one 50 mg tablet of Tramadol was signed out as per the control record on 03/14/24 at 3:13 AM, but not signed out on the corresponding MAR. During this review on 03/21/24 at 12:29 PM, Staff F, Registered Nurse (RN) agreed with the findings.
Dec 2022 10 deficiencies
CONCERN (D)

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

Deficiency F0561 (Tag F0561)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure showers were provided as per facility schedule and family re...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure showers were provided as per facility schedule and family request for 1 of 1 sampled resident (Resident #3). The findings included: Review of the record revealed Resident #3 was admitted to the facility on [DATE]. Review of the current Minimum Data Set (MDS) assessment dated [DATE] documented Resident #3 needed the total assistance of two persons for bathing. During an interview on 12/19/22 at 1:25 PM, an adult family member of Resident #3 explained the facility had a shower schedule, and Resident #3 was to get showers twice weekly on Tuesdays and Fridays, during the 3 PM to 11 PM shift. The family member further volunteered the resident had missed some showers possibly due to a lack of staff, especially on Fridays. When asked if she requested a different schedule or day, the adult family member stated, Oh, I can do that? Review of the current care plan initiated on 09/03/20 and revised on 05/20/21 documented Resident #3 had limited physical mobility and ADL (Activities of Daily Living) deficits related to comorbidities to include traumatic brain injury and impaired mobility. This care plan further documented the resident was totally dependent upon staff to meet her needs. During an interview on 12/21/22 at 3:53 PM, Staff I, Certified Nursing Assistant (CNA), explained the provision of residents' showers were documented in both the electronic medical record (EMR) and in a shower book. Review of the Tasks section of the EMR, used for documentation by the CNAs, documented as per the family, Resident #3 prefers showers on Tuesday and Friday during the 3 PM to 11 PM shift. Further review of documented showers for November and December 2022 revealed Resident #3 did not receive her scheduled shower on 11/11/22, 11/15/22, 11/25/22, 11/29/22, 12/06/22, and 12/13/22.
CONCERN (D)

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

Deficiency F0687 (Tag F0687)

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 continued podiatry services for 1 of 1 sampled...

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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 continued podiatry services for 1 of 1 sampled resident (Resident #34). The findings included: During an interview and observation on 12/19/22 at 10:40 AM, the toenails of Resident #34 were noted to be elongated, extending approximately half a centimeter past the end of his toes, and thickened. When asked if he was a diabetic, Resident #34 stated he was not. When asked if the staff cut his toenails, Resident #34 stated they did not and that a podiatrist cut them in the past. Review of the record revealed Resident #34 was admitted to the facility on [DATE]. Review of the current Minimum Data Set (MDS) assessment dated [DATE] documented Resident #34 had a Brief Interview for Mental Status (BIMS) score of 15, on a 0 to 15 scale, indicating the resident was cognitively intact. This MDS lacked any documented instances of the rejection of care, and revealed the resident needed the limited assistance of one person for personal hygiene. Further review of the record revealed a podiatry visit dated 04/19/22. This progress note documented the resident's toenails at that time were thickened, yellowed, and causing pain. This note also documented, Care of this patient by a non-skilled professional may be hazardous to the patient's health. Patient meets systemic diagnostic requirements, confirmed by the attending PCP (personal care physician), for routine foot care to prevent risks when performed by a nonprofessional. I have recommended foot care on a periodic 10-12 week basis ongoing. This would indicate Resident #34 would have needed additional podiatry services by 07/12/22. Review of the current and discontinued orders and social service notes from April 2022 lacked any mention of podiatry services. During an interview on 12/22/22 at 9:00 AM, the Social Services Director (SSD) explained she started at the facility on 10/31/22. The SSD was made aware of the 04/19/22 podiatry progress note and stated she would add Resident #34 to the podiatry list.
CONCERN (D)

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

Deficiency F0688 (Tag F0688)

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 ensure continued range of motion (ROM) services for 1 of 1 sample r...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure continued range of motion (ROM) services for 1 of 1 sample resident (Resident #3). The findings included: During an interview on 12/19/22 at 1:49 PM, the adult family member of Resident #3 voiced concern that the facility was no longer providing range of motion services to the resident. When asked if she knows why the services were not being provided, the family member stated she was unsure. Review of the record revealed Resident #3 was admitted to the facility on [DATE]. Review of the current Minimum Data Set (MDS) assessment dated [DATE] documented Resident #3 had functional limited range of motion to all four extremities. This MDS also documented the resident was not receiving therapy, restorative, or range of motion services. Review of the current orders lacked any orders for range of motion or restorative services. Review of the discontinued order dated 07/08/21 documented, Resident graduated from program will reevaluate in 1 month under the discontinued note in the order as of 11/02/21. Further review of the orders revealed Resident #3 had been receiving range of motion services via their restorative program since at least 12/16/20. Review of the current care plan initiated 09/03/20 and revised on 05/20/21 documented Resident #3 had limited physical mobility and ADL (activities of daily living) deficits related to multiple comorbidities including traumatic brain injury and contractures. One of the interventions was for staff to place rolled washcloths in both hands. During an interview on 12/21/22 at 2:24 PM, Staff H, Restorative Certified Nursing Assistant (CNA) confirmed she provides range of motion services to residents for maintenance. When asked about Resident #3, Staff H confirmed she had seen her in the past for ROM services, but was unsure why she was not currently seeing the resident. During an interview on 12/21/22 at 3:06 PM, the Director of Rehab (DOR) services confirmed they do quarterly therapy screens for the long-term residents. When asked about Resident #3 in regard to range of motion, the DOR stated he thought the resident was still on restorative services for ROM. During an interview on 12/21/22 at 3:07 PM, the Restorative Nurse stated she was not here in November 2021 when the restorative services were discontinued for Resident #3. The Restorative Nurse was unsure if Resident #3 was reevaluated in one month as per the discontinued order, or the reason why the resident was no longer on restorative services. During a subsequent interview and observation on 12/21/22 at 4:27 PM, the Restorative Nurse stated they were unable to locate the one-month reevaluations. The DOR joined the interview, again confirming he thought Resident #3 was on the restorative services, and confirmed the documented intervention for the towel palm rolls. Upon observation of Resident #3 at that time, the hand rolls were not in place. The DOR suggested reestablishing ROM services for Resident #3 to maintain her current level of mobility.
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 record review and interview, the facility failed to ensure a safe transfer for 1 of 1 sampled resident, Resident #215, ...

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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 a safe transfer for 1 of 1 sampled resident, Resident #215, reviewed for falls, as evidenced by the facility's process/policy requiring 2-person assistance for all Hoyer transfers not being followed by Certified Nursing Assistants (CNA). The findings included: Review of Policy, titled, Safe Resident Handling/Transfers, dated 11/20 with a revised review date of 01/22, documented all residents require safe handling when transferred to prevent or minimize the risk for injury to themselves and the employees that assist them. Under compliance guidelines #10, it documented two staff members must be utilized when transferring residents with a mechanical lift. Review of Resident #215's medical records documented the resident was admitted to the facility on [DATE] with diagnoses to include Pathological Fracture Left Femur, Displaced Fracture of Base of Neck of Left Femur, History of Falling, Type II Diabetes with Diabetic Neuropathy, Heart Failure, Hypertension, Anxiety, Seizures, Dementia, and Major Depressive Disorder. Review of the resident's MDS (Minimum Data Set) Admission/Medicare 5 day, dated 05/12/22, documented the resident has a BIMS (Brief Interview for Mental Status) of 8, indicating his cognition is mildly impaired. For transfers, it was documented he is totally dependent on 2-person, extensive assistance of 2-person for Bed Mobility, Dressing, Toileting, and Personal Hygiene. Review of the resident's Care Plans documented he is at risk for falls. Further review of Progress Notes, dated 12/14/22 at 3:24 PM by Staff K, LPN (Licensed Practical Nurse), documented: the aide [CNA] notified me [LPN] that a patient was on the floor. Resident assessed for injuries. Resident denied hitting his head. Gash found on left lower extremity. Physician notified and orders given to send patient to ER [Emergency Room]. Resident's injury cleaned and covered before ER transfer. Review of the fall investigation documented on 12/14/22 11:00 AM, the resident fell out of Hoyer lift machine during transfer while being assisted in transfer; 1:1 education completed with CNA regarding Hoyer safety. Staff A, CNA, received a written warning on using a mechanical lift alone without assistance. The policy of the company is that mechanical lifts require 2-person assistance for safety. During an interview on 12/19/22 at 12:51 PM, Resident #215's spouse and private aide stated they dropped him [the resident] using the Hoyer lift and he had a gash on his leg, which required 14 external stitches and some on inside. During an interview on 12/21/22 at 10:15 AM with Staff K, LPN, she stated: 'I was called in the room by an aide who told me that she heard the resident fall; (Staff B), I went into room he was lying on floor, he had gash on left side of shin. There was an aide in there, the Hoyer lift was in the room. She said she was transferring him, it started to tip over and he was on the ground on top of Hoyer Pad. I called 911.' She was asked how he is supposed to be transferred and stated, he is a Hoyer lift for transfers. During an interview on 12/21/22 at 1:05 PM with Staff L, CNA, revealed, 'I was assisting another resident and when I came out of the room I heard a loud boom and then heard a CNA call for help, she was in room [XX]. The Hoyer lift and the resident were by the door, she was trying to lift him and I told her to take the hooks out of the Hoyer so we can lift the Hoyer up. I went and got the nurse. There was blood on the floor. When we do a Hoyer we use 2 people she only used herself no one else.' During an interview on 12/21/22 at 1:10 PM with Staff A, CNA, stated I was supposed to use two-person for the Hoyer but there was no one else to help me. I got him dressed and put the Hoyer pad under him, he was lifted up and the chair underneath him, one of the wheels was stuck under the bed and it tilted over. She said the bed moved because it does not lock. I now know not to do it by myself. I have been here since [DATE]. They did retraining with me, they were pretty strict with me about using two people but I now know why. I had him the other day and did a two person transfer but really need three. During an interview on 12/21/22 at 1:17 PM with the Rehabilitation (Rehab) Director, he was asked how Resident#215 was supposed to be transferred. He stated, by a Hoyer lift, we have determined he is a Hoyer lift but for therapy purposes he is transferred by two persons standing up. He is toe-touch for weight bearing on left lower extremity, that is the side he had the fracture. During an interview on 12/22/22 at 2:46 PM with Staff B, CNA, Staff B stated, [Resident #215] 'will try his hardest to help but he is a 2-person assist to get him up in chair, 2-people for pivot, and the family is uncomfortable with Hoyer so we try not to use it. I did notice his bed moving, even when it is locked it moved. The first time was this past weekend. I think I told the nurse or CNA on hallway. I did not put it in Tells [communication system for maintenance], I should have but didn't. He is a 2-person for everything.'
CONCERN (D)

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

Deficiency F0757 (Tag F0757)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, policy review and interview, the facility failed to ensure monitoring of medications related to followin...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, policy review and interview, the facility failed to ensure monitoring of medications related to following physician ordered parameters and medication administration for 3 of 5 sampled residents (Residents #47, #215 and #25). The findings included: The facility policy, titled, Medication Administration and revised 02/09/22, documented in part: Administer medication as ordered in accordance with manufacturers specifications Observe residents' consumption of medication Sign medication administration record after administration For medications requiring vital signs, record vital signs onto the MAR (Medication Administration Record). 1. Resident #25's orders were reviewed. The resident's medication, Eszopiclone 2mg, was ordered on 11/16/22 and was to be given as 1 tablet at bedtime for insomnia. Review of the resident's MAR revealed no documentation for administration of the medication on 12/01/22, 12/03/22, 12/06/22, 12/07/22 and 12/08/22. No documentation was found to indicate why medication was not administered. The orders were reviewed for Resident #25's medication, Zosyn Solution Reconstituted 3.375 (3-0.375) GM. The medication was to be given intravenously (IV) every 6 hours for wound infection. The order was started on 11/17/22 and was to continue until 12/27/22. The times for the medication to be administered were at 12:00 AM, 6:00 AM, 12:00 PM and 6:00 PM. On 12/12/22, the 6:00 AM dose was not documented on the MAR to indicate it was given. Review of the record revealed no explanation for the missing administrated dose of the antibiotic. The medication, Omeprazole 20mg, was ordered on 11/18/22., and two capsules were to be given in the morning for Resident #25's reflux. Review of the MAR revealed no documentation the medication was given at 6:30 AM on 12/12/22. The medication, Ipratropium Albuterol Solution 0.5-2.5 MG/3ML (3 ml inhale orally via nebulizer every 4 hours), for COPD) (Chronic Obstructive Pulmonary Disease). The medication was ordered to start on 11/16/22. The medication was scheduled to be given at 12:00 AM, 4:00 AM, 8:00 AM, 12:00 PM, 4:00 PM and 8:00 PM. Review of the MAR revealed the medication was not documented as given on 12/12/22 at 4:00 AM. No documentation was found for why the medication not being administered for Resident #25. 3. Review of Resident #47's medical records revealed Resident#47 was admitted to the facility on [DATE] with diagnoses to include Unspecified Dementia with Behavioral Disturbances, Major Depressive Disorder, and Anxiety Disorder. Review of the Physician's Orders documented the resident is on Levothyroxine Sodium Tablet 50 MCG Give 1 tablet by mouth in the morning for hypothyroidism; and Pantoprazole Sodium Tablet Delayed Release 40 MG Give 1 tablet by mouth in the morning for GERD (Gastroesophagel Reflux Disease). Review of Resident #47's MAR for November 2022 and December 2022 revealed on the following days, the MAR was left blank with no documentation that the medication was given / administered: a. Levothyroxine Sodium tab 50 MCG 1 tab PO in am for Hypothyroidism 11/08/22, 11/11/22, 11/12/22, 11/16/22 and 11/27/22. b. Pantoprazole Sodium tab 11/08/22, 11/11/22, 11/12/22, 11/16/22 and 11/27/22 and 11/30/22 and 12/03/22. 4. Review of Resident #215's medical records documented the resident was admitted to the facility on [DATE] with diagnoses to include Pathological Fracture Left Femur, Displaced Fracture of Base of Neck of Left Femur, History of Falling, Type II Diabetes with Diabetic Neuropathy, Heart Failure, Hypertension, Anxiety, Seizures, Unspecified Dementia with other Behavioral Disturbances, and Major Depressive Disorder. Review of the resident's MDS (Minimum Data Set) admission / Medicare 5-day, dated 05/12/22, documented a BIMS score of 8, indicating cognition was mildly impaired. Review of Resident #215's physician orders documented the resident is on the following medications: a. Insulin Lispro (1 Unit Dial) 100 UNIT ML Solution pen-injector Inject as per sliding scale, subcutaneously before meals and at bedtime for Diabetes Mellitus. Blood sugar greater than 400 or less than 65, contact MD (medical doctor) for new orders start date 12/13/22: if 151 - 200 = 3; 201 - 250 = 5; 251 - 300 = 7; 301 - 350 = 9; 351 - 400 = 14. b. Insulin Lispro (1 Unit Dial) 100 UNIT ML Solution pen-injector Inject 18 unit subcutaneously in the morning for Diabetes Mellitus 09:00 AM, Start Date 12/12/22. c. Insulin Lispro (1 Unit Dial) 100 UNIT\/ML Solution pen-injector Inject 25 unit subcutaneously in the afternoon for Diabetes Mellitus 1:00 PM start date 12/12/22. d. Insulin Lispro (1 Unit Dial) 100 UNIT ML Solution pen-injector Inject 20 unit subcutaneously in the evening for Diabetes Mellitus 5:00 PM Start date 12/11/22. e. Insulin Glargine 100 UNIT/ML Solution pen-injector Inject 35 unit subcutaneously at bedtime for Diabetes Mellitus 10:00 PM Start Date 12/16/2022. f. Midodrine HCl Tablet 10 MG Give 1 tablet by mouth two times a day for hypotension do not administer if SBP > 140: DBP > 90. Start Date 12/12/22. Review of Resident #215's MAR revealed, on the following days, the physician orders were not followed by contacting the physician when the blood sugar was greater than 400 or less than 60. There was no evidence in the progress notes the physician was notified as well as the insulin not given as ordered: aa. On 12/15/22 at 11:30 AM, the blood sugar (BS) was 464 (progress note documented BS 504 at 10:08); Documented in progress note that 18 unit was injected subcutaneously in the morning for Diabetes Mellitus, that the blood sugar was 504, does not document that the physician was notified for blood sugar being out of parameters. bb. On 12/16/22 at 4:30 PM, documented 'N/A 5', which meant hold/see progress notes. There was not a blood sugar documented for this time and why it was not given. cc. On 12/17/22 at 6:30 AM, Blood Sugar 444; was documented '10' indicating vitals / blood sugar out of parameter. Does not document that the physician was notified. dd. On 12/17/22 at 5:00 PM, documented in progress note that the blood sugar was 134 and was out of parameters and therefore the order for Insulin Lispro (1 Unit Dial) 100 UNIT ML Solution pen-injector Inject 20 unit subcutaneously in the evening for Diabetes Mellitus was not given. No sliding scale should be given but the evening dose did not have a hold for blood sugar amount. The dose was not given and therefore did not follow physician's order. ee. On 12/18/22 at the 5:00 PM dose, documented code #10, which indicated the blood sugar was out of the parameters at 121. No sliding scale should be given but the evening dose did not have a hold for blood sugar amount. The dose was not given and therefore did not follow physician's order. ff. On 12/20/22 at the 5:00 PM dose, documented code #10, which indicated the blood sugar was out of the parameters. No sliding scale should be given but the evening dose did not have a hold for blood sugar amount. The dose was not given and therefore did not follow physician's order. gg. On 12/20/22 at 10:00 PM, Insulin Glargine 100 UNIT/ML Solution pen-injector Inject 35 unit subcutaneously at bedtime for Diabetes Mellitus; Documented code#10, which indicated the blood sugar was out of the parameters. No sliding scale should be given but the evening dose did not have a hold for blood sugar amount. The dose was not given and therefore did not follow physician's order. g. On 12/12/22, an order for Entresto tab 24-26 mg give 1 tab by mouth in AM for Hypertension, hold if systolic blood pressure is under 100 or diastolic blood pressure is under 60, start date 12/12/22. Review of the MAR documented a code of #9 indicating 'other/see progress note'. There is no note, or a B/P (blood pressure) documented. h. On 12/12/22, an order for Midodrine HCL tab 10mg give 1 tab twice a day for hypotension, do not administer if Systolic blood pressure is over 140 or diastolic blood pressure is over 90: aaa. Documented on 12/12/22 at the 9:00 AM dose the code #10, vitals outside parameters, but does not document what the blood pressure was. At 5:00 PM, the B/P was 148/82 and documented that it was given even though the physician order documented to hold if systolic blood pressure is over 140. bbb. On 12/14/22 at 5:00 PM, the B/P was 148/86 and documented that it was given even though the physician order documented to hold if systolic blood pressure is over 140. ccc. On 12/18/22 at 5:00 PM, the B/P was 144/54 and documented that it was given even though the physician order documented to hold if systolic blood pressure is over 140. ddd. On 12/19/22 at 5:00 PM, the B/P was 142/72 and documented that it was given even though the physician order documented to hold if systolic blood pressure is over 140. On 12/21/22, the B/P was 145/76 and documented it was given. During an interview on 12/21/22 at 10:24 AM with the DON (Director of Nursing), the MARS were reviewed. The DON acknowledged the MARS are not filled out completely with holes, medication given when not supposed to be when out of parameters, and could not find documentation under progress notes that the physician was ever notified when Insulin was out of the parameters. During a telephone interview with Resident #215's physician, with the DON sitting in on conversation, on 12/21/22 at 10:58 AM, he stated that the resident is a super brittle diabetic with regiment of his BS's spiking above 200-400. He is supposed to get coverage if he spikes. He is on basal insulin as well. He stated that he is supposed to get the ordered dose 4 times a day and then on top of the order dose, he is supposed to get the sliding scale insulin if he falls within the parameters. He stated he cannot recall if he ever was contacted for when his insulin was outside the parameters. 2. Resident #36 was admitted to the facility with diagnoses which included a history of Venous Thrombosis, Embolism and Hypertension. The following psychotropic medications were prescribed by the Primary Care Physician (PCP): a) Xarelto 10 MG Tablet Give 1 tablet by mouth in the evening for clot prevention. An annual Minimum Data Set (MDS), dated [DATE], documented Resident #36 has a Brief Interview For Mental Status (BIMS) score of 15, indicating cognitively was intact. A Care Plan was initiated on 12/05/20, and last revised on 12/01/22, for history of deep vein thrombosis. Interventions included providing medication as ordered and monitoring / documenting side effects and effectiveness. Review of Resident #36's November 2022 electronic Medication Administration Record (eMAR) showed orders related to observation on each shift for side effects monitoring related to anticoagulant use: discolored urine, black tarry stools, sudden severe headache, nausea and vomiting, diarrhea, muscle joint pain, lethargy, bruising, sudden changes in mental status and/or vital signs, shortness of breath, or nose bleeds. For the month of November 2022, there was no documentation of any observations being done for the evening shifts on 11/01/22 - 11/06/22, 11/08/22 - 11/09/22, 11/12/22-11/13/22, 11/15/22 - 11/16/22, 11/18/22, and 11/20/22. Staff were not utilizing Y [Yes] or N [No] for results of observations on Day shift, instead they are placing an X or na for 11/01/22 -11/02/22, 11/05/22 - 11/09/22, and 11/12/22 - 11/20/22. Staff were not utilizing Y or N for results of observations on the Night shifts, instead they are placing an X or na, for 11/01/22 -11/06/22, 11/08/22 - 11/10/22, 11/12/22 - 11/13/22, and 11/15/22 - 11/19/22.
CONCERN (D)

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

Medication Errors (Tag F0758)

Could have caused harm · This affected 1 resident

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Review of Resident #47 medical records revealed Resident #47 was admitted to the facility on [DATE] with a diagnoses to inclu...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Review of Resident #47 medical records revealed Resident #47 was admitted to the facility on [DATE] with a diagnoses to include Unspecified Dementia with Behavioral Disturbances, Major Depressive Disorder, and Anxiety Disorder. Review of the resident's Medicare 5-day MDS (Minimum Data Set), dated 09/26/22, documented the resident had behaviors 4-6 days having physical behavioral symptoms directed towards others; verbal behavioral symptoms directed towards others. Review of the resident's care plan documented the resident had the following behavior problem(s) of being physically aggressive, and verbally aggressive. Review of the Physician's Orders documented the resident is on Quetiapine Fumarate Tablet 50 MG to give 100 mg by mouth at bedtime for bipolar, Quetiapine Fumarate Tablet 25 MG to give 25 mg by mouth two times a day for bipolar, Ativan Gel 0.5 mg to apply to skin topically three times a day for anxiety, to observe for behaviors of antipsychotic Medication; Observe for behavior: screaming, fighting, and hallucinations. Document: Y if resident is having behaviors and N if the resident does not have behaviors. If Y document in the Progress Notes. every shift. Observe for behaviors of antianxiety medication; withdrawn, crying, and agitation. Document Y if resident has behaviors and N if the resident does not have behaviors. If Y document in the Progress Notes. every shift. Document side effects of Antipsychotic Medication: Indicate letter if observed: A= Sedation; B= Drowsiness; C= Dry Mouth; D= Constipation; E= Blurred Vision; F= EPS; G= Wt. Gain; H= Edema; I= Postural Hypotension; J= Sweating; K= Loss of Appetite; L= Urinary Retention; NA= None. If side effects present, document in Progress Notes and notify MD. every shift. Document side effects of Antianxiety medication: Indicate letter if observed: A= Sedation; B= Drowsiness; C= Ataxia (Drunk Walk); D= Dizziness; E= Nausea; F=Vomiting; G= Confusion; H= Headache; I= Blurred Vision; J= Skin Rash; NA= None. If side effects present, document in PNs and notify MD. every shift. Review of the Resident #47's MAR (Medication Administration Record) for Behaviors and side effects revealed on the following days, the MAR was left blank with no documentation: Side effects of Antipsychotics: day shift 12/10/22. Evening shift: 11/15/22, 12/01/22, 12/03/22, 12/05/22, 12/06/22, 12/07/22, 12/08/22 12/12/2212/16/22, 12/19/22. Night shift 12/04/22. Side Effects for Antianxiety: evening shift:12/16/22, 12/19/22. Observation of behaviors for Antipsychotic Medication: Evening 11/15, 12/16/22 and 12/19/22. Observation of behaviors for Antianxiety Medications: Evening 12/16/22 and 12/19/22. 3. Review of Resident #215's medical records documented the resident was admitted to the facility on [DATE] with diagnoses to include Pathological Fracture Left Femur, Displaced Fracture of Base of Neck of Left Femur, History of Falling, Type II Diabetes with Diabetic Neuropathy, Heart Failure, Hypertension, Anxiety, Seizures, Unspecified Dementia with other Behavioral Disturbances, and Major Depressive Disorder. Review of the resident's MDS (Minimum Data Set) admission / Medicare 5-day, dated 05/12/22, documented a BIMS score of 8, indicating cognition was mildly impaired. Review of the resident's care plan documented the resident had impaired cognitive function/impaired thought processes related to Dementia with behaviors. Review of Resident #215's physician orders documented the resident is prescribed Wellbutrin XL Tablet Extended Release 24 Hour 300 MG to give 1 tablet by mouth in the morning for depression; Quetiapine Fumarate Tablet 50 MG to give 1 tablet by mouth at bedtime for mood disorder; Observe side effects of Antidepressant Medication; sadness, tearfulness, and or self-isolation. Document Y if resident has behaviors and N if the resident does not have behaviors. If Y document every shift. Observe for side effects of the Akathisia: restlessness, pacing, inability to sit still, anxiousness, sleep disturbances. Observe for side effects of Tardive dyskinesia: lip smacking, chewing, abnormal tongue movement, spasmodic movement of arms, legs-rocking, swaying; sore throat, Seizures, Photosensitivity, Suicidal ideations, Hepatic or renal abnormalities, Ataxia, Nausea and Vomiting, Diarrhea, Abdominal Discomfort, discolored urine, black tarry stools, bruising, nose bleeds every shift for medication side effect monitoring. Observe for medication side Effect: Dystonia, torticollis (stiffness of neck), Anticholinergic symptoms: dry mouth, blurred vision, constipation, urinary retention, Hypotension, Sedation, drowsiness, Increased falls, dizziness, Cardiac abnormalities (tachycardia, bradycardia, irregular, H.R, Anxiety, agitation, Blurred Vision, Sweating, rashes, Headache, Urinary retention, hesitancy, Weakness, Hangover effect, Pseudo parkinsonism, Insomnia, New Onset Confusion every shift for medication side effect monitoring. Observe for Antipsychotic Medication; Observe for delusions, hallucinations and\/or paranoia. Document 'Y if resident is having behaviors and N if the resident does not have behaviors. If Y document every shift. Review of Resident #215's MAR for Behaviors and side effects revealed on the following days, the MAR was left blank with no documentation, as follows: Observe for side Effects for Akathisia: Day shift 12/13/22, 12/16/22. Observations of side effects for Dystonia: Days shift 12/13/22, 12/16/22, Observe for antidepressant medication side effects: Day shift 12/16/22 day. During an interview on 12/22/22 at 2:50 PM with Staff B, CNA she was asked if Resident#47 had behaviors. The CNA stated, 'when I would change her and put her in the chair, she cries but once in chair she is fine. When she cries, she says momma, momma. She is confused, and I think she thinks I am her momma. Her cognition is very low. She can follow commands but will protest.' Based on record review and interview, the facility failed to ensure documentation of behavior monitoring and monitoring of side effects for psychotropic medications 3 of 5 sampled residents (Residents #47, #215, and #36). The findings included: 1. Resident #36 was admitted to the facility with diagnoses which include Anxiety, Depressive Disorder, and Bipolar Disorder. The following psychotropic medications were prescribed by Primary Care Physician: a) Venlafaxine HCl ER Tablet Extended Release 24 Hour 150 MG Give 2 tablet by mouth one time a day related to Major Depressive Disorder. b) Trazodone HCl Tablet 100 MG Give 2.5 tablet by mouth at bedtime related to Major Depressive Disorder c) Lamictal Tablet 200 MG Give 1 tablet by mouth in the morning for mood disorder The Annual MDS, dated [DATE], documented Resident #36 had a BIMS of 15, indicating intact cognition. A Care Plan was initiated on 12/18/20, and last revised on 12/02/22, for psychotropic drug use related to diagnosis of Depression and Bipolar Disorder. Interventions included monitoring for side effects and consulting with physician and pharmacist as needed. A Care Plan was initiated on 09/20/21, and last revised on 12/01/22, for behaviors related to toileting issues, refusing to wear TED hose, having monthly weight, refusing care, getting out of bed without assistance, refusing medications and incontinence care. Review of Resident #36's electronic Medication Administration Record (eMAR) showed orders related to Antidepressant medication to observe for behaviors of sadness and crying. Instructions stated to document Y if resident has behaviors and N if the resident does not have behaviors. If Y, document in the PNs [Progress Notes] every shift. For the month of November 2022, there was no documentation of any observations being done for the evening shift on 11/01/22 - 11/06/22, 11/08/22 - 11/09/22, 11/12/22-11/13/22, 11/15/22 - 11/16/22, 11/18/22, and 11/20/22. Staff are not utilizing Y [Yes] or N [No] for results of observations on Day shift, instead they are placing an X or na [non-applicable] for 11/01/22 -11/02/22, and 11/05/22 - 11/20/22. Staff are not utilizing Y or N for results of observations on Night shift, instead they are placing an X or na, for 11/01/22 -11/06/22, 11/08/22 - 11/10/22, 11/12/22 - 11/13/22, and 11/15/22 - 11/19/22. Review of Resident #36's electronic Medication Administration Record (eMAR) showed orders related to Mood Stabilization medication to observe for behaviors of frequent mood swings, refusals of care, anger outbursts, tearfulness. Instructions stated to document Y if resident has behaviors and N if the resident does not have behaviors. If Y, document in the PNs [Progress Notes] every shift. For the month of November 2022, there is no documentation of any observation being done for the evening shift on 11/01/22 - 11/06/22, 11/08/22 - 11/09/22, 11/12/22-11/13/22, 11/15/22 - 11/16/22, 11/18/22, and 11/20/22. Staff were not utilizing Y or N for results of observations on Day shift, instead they are placing an X or na for 11/01/22 -11/02/22, and 11/05/22 - 11/09/22, 11/12/22 - 11/20/22. Staff are not utilizing Y or N for results of observations on Night shift, instead they are placing an X or na, for 11/01/22 -11/06/22, 11/08/22 - 11/10/22, 11/12/22 - 11/13/22, and 11/15/22 - 11/19/22. Review of Resident #36's electronic Medication Administration Record (eMAR) showed orders related to observation each shift for side effects monitoring related to Akathisia-restlessness/pacing/inability to sit still/anxiousness/sleep disturbances; Tardive Dyskinesia-lip smacking/chewing/abnormal tongue movement/spasmodic movement of arms/legsrocking/swaying; Sore throat; Seizures; Photosensitivity; Suicidal ideations; Hepatic or renal abnormalities; Ataxia; Nausea /Vomiting; Diarrhea; Abdominal Discomfort; discolored urine; black tarry stools; bruising; and nose bleeds. For the month of November 2022, there is no documentation of any observation being done for the evening shift on 11/01/22 - 11/06/22, 11/08/22 - 11/09/22, 11/12/22-11/13/22, 11/15/22 - 11/16/22, 11/18/22, and 11/20/22. Staff are not utilizing Y or N for results of observations on Day shift, instead they are placing an X or na for 11/01/22 -11/02/22, and 11/05/22 - 11/09/22, 11/12/22 - 11/20/22. Staff are not utilizing Y or N for results of observations on Night shift, instead they are placing an X or na, for 11/01/22 -11/06/22, 11/08/22 - 11/10/22, 11/12/22 - 11/13/22, and 11/15/22 - 11/19/22. Review of Resident #36's electronic Medication Administration Record (eMAR) showed orders related to observation each shift for side effects monitoring related to Dystonia, torticollis (stiffness of neck); Anticholinergic symptoms: dry mouth/blurred vision, constipation/urinary retention; Hypotension; Sedation/drowsiness; Increased falls/dizziness; Cardiac abnormalities (tachycardia, bradycardia, irregular, H.R., NMS); Anxiety/agitation; Blurred Vision; Sweating/rashes; Headache; Urinary retention/hesitancy; Weakness; Hangover effect; Pseudo parkinsonism; Insomnia; and New Onset Confusion. For the month of November 2022, there is no documentation of any observation being done for the evening shift on 11/01/22 - 11/06/22, 11/08/22 - 11/09/22, 11/12/22-11/13/22, 11/15/22 - 11/16/22, 11/18/22, and 11/20/22. Staff are not utilizing Y or N for results of observations on Day shift, instead they are placing an X or na for 11/01/22 -11/02/22, and 11/05/22 - 11/09/22, 11/12/22 - 11/20/22. Staff are not utilizing Y or N for results of observations on Night shift, instead they are placing an X or na, for 11/01/22 -11/06/22, 11/08/22 - 11/10/22, 11/12/22 - 11/13/22, and 11/15/22 - 11/19/22. Review of Resident #36's electronic Medication Administration Record (eMAR) showed orders related to observation each shift for side effects monitoring related to Antidepressant use. If observed, the following letters were to be used: A=Sedation; B= Drowsiness; C= Dry Mouth; D= Blurred Vision; E= Urinary Retention; F= Tachycardia; G= Muscle Tremor; H= Agitation; I= Headache; J= Skin Rash; K=Photosensitivity; L= Weight Gain; NA= None. If side effects present, document in PNs and notify MD. For the month of November 2022, there is no documentation of any observation being done for the evening shift on 11/01/22 - 11/06/22, 11/08/22 - 11/09/22, 11/12/22-11/13/22, 11/15/22 - 11/16/22, 11/18/22, and 11/20/22. Staff are not utilizing NA for none on Day shift, instead they are placing an X for 11/01/22 -11/02/22, and 11/05/22 - 11/09/22, 11/12/22 - 11/20/22. Staff were not utilizing NA for none on Night shift, instead they are placing an X for 11/01/22 -11/06/22, 11/08/22 - 11/10/22, 11/12/22 - 11/13/22, and 11/15/22 - 11/19/22. Review of Resident #36's electronic Medication Administration Record (eMAR) showed orders related to observation each shift for side effects monitoring related to Mood Stabilizer use. If observed, the following letters were to be used: A=Tremors; B= Drowsiness; C=Diarrhea; D= Constipation; E=Nausea; F= Vomiting; G=Decreased Appetite; H= Dizziness; NA= None. If side effects present, document in PNs and notify MD. For the month of November 2022, there is no documentation of any observation being done for the evening shift on 11/01/22 - 11/06/22, 11/08/22 - 11/09/22, 11/12/22-11/13/22, 11/15/22 - 11/16/22, 11/18/22, and 11/20/22. Staff are not utilizing NA for none on Day shift, instead they are placing an X for 11/01/22 -11/02/22, and 11/05/22 - 11/09/22, 11/12/22 - 11/20/22. Staff were not utilizing NA for none on Night shift, instead they are placing an X for 11/01/22 -11/06/22, 11/08/22 - 11/10/22, 11/12/22 - 11/13/22, and 11/15/22 - 11/19/22.
CONCERN (D)

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

Deficiency F0761 (Tag F0761)

Could have caused harm · This affected 1 resident

Based on observation, interview, and policy review, the facility failed to properly secure medications for 1 of 3 medication carts (West Unit), and for 1 of 3 treatment carts (East Unit). The census a...

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Based on observation, interview, and policy review, the facility failed to properly secure medications for 1 of 3 medication carts (West Unit), and for 1 of 3 treatment carts (East Unit). The census at the time of the survey was 59, and the number of independently ambulatory residents was 4. The findings included: Review of the policy, titled, Medication Storage revised 05/04/22, documented, 1. General Guidelines: a. All drugs and biologicals will be stored in locked compartments (i.e., medications carts, .) . c. During a medication pass, medications must be under the direct observation of the person administering medications or locked in the medication storage area/cart. 1. A medication pass observation was made on 12/19/22 beginning at 4:04 PM, with Staff G, Licensed Practical Nurse (LPN), on the [NAME] Unit. While the LPN was gathering the medications for Resident #25, she realized one was missing. The LPN left the medication cart at the far end of the [NAME] Unit, leaving it unlocked, and went into the medication room near the nurses' station with the evening supervisor, to get the medication out of the automated medication distribution system. Staff G returned to the medication cart and obtained the rest of the medications for Resident #25. At 4:15 PM, Staff G went into the room of Resident #25, again out of sight of the medication cart, leaving the cart against the wall between two rooms, with the unlocked drawers facing out into the hallway. A visitor, Certified Nursing Assistant (CNA), and another nurse were noted in the hallway at the time. Upon return to the medication cart, Staff G did not notice the cart was unlocked. The LPN obtained a requested pain medication for Resident #25, and returned to the resident's room, again leaving the cart unlocked. Upon return to the medication cart, the LPN did not notice the cart had been left unlocked. During the continued medication pass observation on 12/19/22 at 4:19 PM, Staff G obtained medications for Resident #12. At 4:23 PM, the LPN left the medication in the same location, went into the room of Resident #12, leaving the medication cart unlocked a third time. Upon return to the medication cart on 12/19/22 at 4:26 PM, Staff G asked the surveyor how she did with the medication pass. When asked about locking the medication cart, the LPN looked at the medication cart lock, looked surprised and stated, I didn't lock my cart? And when you were coming my way, I was telling myself, I need to lock the cart. 2. On 12/21/22 at 3:08 PM, the East Unit treatment cart was noted near the front of the East Unit hallway, against the wall and unlocked. Upon opening the drawers, multiple wound care medications / ointments and dressing supplies were noted. While standing at the treatment cart, the Director of Nursing (DON) arrived and agreed with the unlocked and unattended treatment cart. The DON summoned Staff K, direct care LPN for the East Unit, who confirmed she had left it opened.
CONCERN (E)

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

Safe Environment (Tag F0584)

Could have caused harm · This affected multiple residents

**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and interview, the facility failed to maintain a safe, clean and homelike environment for 3 of 3 hallways ...

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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations and interview, the facility failed to maintain a safe, clean and homelike environment for 3 of 3 hallways observed. The findings included: During initial observations of the facility that included resident rooms on 12/19/22-12/20/22, the surveyors observed the following: room [ROOM NUMBER]-W: the back wall to the left of the bed had a stain running down the wall. room [ROOM NUMBER] walls/bathroom doors: has rust stains on them, bathroom floor missing tile, shower drain has green residue caked on drain. room [ROOM NUMBER]-D: the resident's over-the-bed table was missing laminate on the corner of the table, the drain in bathroom was not secure, and air conditioner was caked with dirt in the vent. room [ROOM NUMBER]-W: the bathroom had multiple rust spots on the walls and door, the metal wall frame in bathroom was rusted. The walls and ceilings had a darker paint color with dark spots coming through the paint (ark mold-like), the bathroom door had scuffed marks, and doorknob did not function properly. room [ROOM NUMBER]: the molding on floor of the doorway was lifting up. room [ROOM NUMBER]-D: the back wall by the air conditioner had paint peeling along the base of wall and the walls were scuffed up. room [ROOM NUMBER]-W: large block of concrete were missing from the back wall by the air conditioner. room [ROOM NUMBER]-W: the wall was damaged along the baseboard under the TV, as well as the bottom of entry door, the bathroom was discolored in a dark gray color (dark mold-like), and the metal frame in bathroom was all rusted. room [ROOM NUMBER]: the rubber lining at doorway was lifting up. room [ROOM NUMBER]-W: the wheelchair was torn on the left arm padding and cracked on right arm padding. room [ROOM NUMBER]-P: there is a bed pan with dried urine in it and the floor of the shower was wet along the caulking of the shower. A private aide for this resident stated that there wass urine on the floor in the shower that had been there since he was admitted , he does not use the shower or the bathroom, he has a catheter. She then stated there was a bed pan in bathroom as well with what looks like urine in it, that she stated is not his. She stated that the resident's bed moves everytime they work on him (give care). The resident's bed rolls, and has only one lock on the left bottom of bed. room [ROOM NUMBER]-D: the resident's chair rail behind the bed was missing; there was a sugar packet with debris behind the bed; and the resident stated that it had been there a while. room [ROOM NUMBER]: initially no resident in room until 12/21/22; the sink was dripping, clothes were located in closet that belonged to another resident in another room, the drain in shower was not secure and had missing screws, the shower head was hanging down against wall, the rubber piece at doorway was lifting up, and the table tray was all rusty. The bathroom frame had caulking peeling away from the frame. room [ROOM NUMBER]: the room had no residents but had 'used' urinals observed in bathroom, there was no mattress on bed and the bed controls were lying on floor. The laminate was pulling away from door and the side table. The hallway ceiling lights were blinking on all three hallways. There were four lights blinking on the East Wing, one blinking on the [NAME] Wing and three blinking on the North Wing. East hallway: the metal plate was lifting up. On 12/19/22 at 9:30 AM, the Housekeeping / Environmental Service person was asked if rooms [ROOM NUMBERS] were clean and ready for a new admit, he stated they were clean. A tour was completed on 12/21/22 at 2:50 PM with Maintenance Director who acknowledged the findings. He said 'the lights blinking, I am aware of the lights but when I change one out then another light will start to blink.' He then stated that they called an electrician. A secondary tour was completed on 12/22/22 at 9:40 AM with the Housekeeping / Environmental Services person, Maintenance, the Administrator and Regional Director of Environmental Services, who acknowledged the findings. During an interview on 12/22/22 at 1:15 PM with Staff A, Certified Nursing Assistant (CNA), she was asked who she told that the bed moved and did not lock? She stated, I told a nurse and a CNA I think'. She stated that the wheel got stuck under the bed. She did not put it in the Tells System. An interview with the Administrator and the Director Of Nursing on 12/22/22 at 2:00 PM, when asked to provide a policy on the process of notifying maintenance for work to be completed, they both stated that there is not a policy on this, that all staff are responsible for putting requests in the Tells system, even the aides, and they are aware of this because we discuss it at staff meetings. During an interview on 12/22/22 at 2:46 PM with Staff B, CNA, Staff B said she 'did notice the resident's bed moved, even when it is locked. The first time was this past weekend. I think I told the nurse or CNA on the hall. I did not put it in Tells System, I should have but didn't.'
CONCERN (E)

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

Infection Control (Tag F0880)

Could have caused harm · This affected multiple residents

Based on observation, interview, and policy review, the facility failed to maintain an infection control program to ensure a safe and sanitary environment to help prevent the development and transmiss...

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Based on observation, interview, and policy review, the facility failed to maintain an infection control program to ensure a safe and sanitary environment to help prevent the development and transmission of communicable diseases and infections for 5 of 8 sampled residents. Staff nurses C, D, and F, failed to properly clean and or disinfect the glucometer (device used to obtain a resident's blood sugar level) for Residents #15, #7, and #215. Staff G and E failed to clean nebulizer equipment as per facility policy, after use by Resident #25. Staff E touched pills with her bare hands while preparing the medications for Resident #25. Staff D utilized a syringe and water container that had fallen to the floor during tube feeding administration for Resident #43. Additionally, Staff C greeted all residents on the North Unit at the beginning of two different shifts, touching or assisting several of them, without any hand hygiene between the resident contact. The findings included: Review of the policy, titled, Blood glucose Monitoring revised 01/2022, documented, Policy Explanation: 3. The nurse will abide by the infection control practices of cleaning and disinfection of the glucometer as per the manufacturer's instructions and in accordance with the facility's glucometer disinfection policy. Procedure: 3. Perform hand hygiene and don gloves. 14. Discard the lancet in a puncture resistant sharps container. 18. Clean and disinfect the glucometer as per manufacturer's instructions. Review of the policy, titled, Nebulizer Therapy revised 11/2021, documented, Care of the Equipment 1. Clean after each use. 2. Wash hands before handling equipment. 3. Disassemble parts after every treatment. 4. Rinse the nebulizer cup and mouthpiece with sterile or distilled water. 5. Shake off excess water. 6. Air dry on an absorbent towel. 7. Once completely dry, store the nebulizer cup and the mouthpiece in a zip lock bag. Review of the policy, titled, Medication Administration revised 02/09/22, documented, 13. Remove medication from source, taking care not to touch medication with bare hand. 1a. On 12/19/22 at 3:17 PM, Staff C, Registered Nurse (RN), was standing in front of her medication cart, preparing to start evening blood sugar checks. The RN was holding her clipboard that had two zip lock bags, each containing a glucometer for a different resident (Resident #15 and #7). Taking both glucometers with her, the RN went into the room of Resident #15, placing a paper towel on the resident's over the bed table. The RN placed her clipboard directly on the resident's over-the-bed table, pulled the glucometer for Resident #15 out of the plastic bag and placed it on the paper towel, obtained the blood sugar level for the resident, scooped up the used lancet, strip and alcohol pad into her gloved hand, and removed the glove to dispose of in the trash. The RN then placed the used glucometer back into the plastic bag without any type of cleaning or disinfecting. During the process, the plastic bag with the glucometer for Resident #7 slid off the RN's clipboard and onto the paper towel, and the plastic bag for the glucometer for Resident #15 slipped directly on the resident's over-the-bed table. During the continued observation on 12/19/22 at 3:22 PM, Staff C went into the main dining room to locate Resident #7. The RN placed the container of glucometer strips directly on the table and went to find a paper towel. Upon return, the RN placed the plastic bag containing the glucometer for Resident #7 directly on the dining room table. The RN pulled out the equipment from the plastic bag and placed it on the paper towel. The RN took the resident's finger and started the procedure, looking up at the surveyor and asked if it was okay to do it without gloves. The surveyor simply stated it was up to her. The RN left the dining room, went out to obtain gloves, and returned to the dining room with gloves donned. The RN completed the blood sugar level, placing the used glucometer back into the plastic bag. While walking back to the cart, the RN dropped the container of glucometer strips on the floor. Upon return to the medication cart, the RN placed the two plastic bags with the resident's glucometers, and the dropped container of strips back into the top drawer of the medication cart. The RN then placed the trash to include the lancet, used strip, and alcohol pad into the garbage. During a subsequent interview on 12/21/22 at 4:00 PM, Staff C, who had just finished using a glucometer, summoned the surveyor and stated, I know I have to clean it and grabbed an alcohol pad and wiped off the glucometer, took a second alcohol pad and while trying to place it on the end of the glucometer at the strip insertion site, stated, I don't know why I am doing this but they told me to. When asked why she did not clean or disinfect the glucometer during the observation on 12/19/22, the RN stated, Because they did not tell me to do so. I was in home care for 20 plus years. I was just told to clean them. The surveyor asked the evening supervisor to show Staff C the facility's process for cleaning and disinfecting glucometers. The supervisor explained the process using the disinfectant wipes. 1b. On 12/19/22 at 3:47 PM, Staff F, LPN, stated she was ready to do a blood sugar level for Resident #215. The LPN obtained a zip lock bag from the medication cart that contained the glucometer, along with other needed supplies to include the canister of glucometer strips. The LPN entered the resident's room, placed the clear plastic bag with all the supplies directly on the resident's over-the-bed table. The LPN took a paper towel and placed the items from the bag onto the towel. The LPN obtained the blood sugar level, and placed the used glucometer and container of strips into the plastic bag. After hand washing, the LPN returned to the medication cart, placed the container of strips back into the top drawer of the medication cart, along with the plastic bag with the used glucometer. The LPN did not disinfect the glucometer. During a subsequent interview on 12/21/22 at 4:15 PM, Staff F was reminded of the observations with the glucometer, plastic bag, and container of strips from 12/19/22 and agreed with the infection control issues. 1c. On 12/21/22 at 11:40 AM, Staff D, LPN, obtained a blood sugar level from Resident #15. After the procedure, the LPN appropriately threw away all disposable items and then placed the glucometer directly on the resident's over-the-bed table to wash her hands. The LPN then took the glucometer and placed it directly on top of the medication cart. After proper disinfection of the glucometer, the LPN stated she was done and asked how she did. When informed of the observation of the used glucometer directly from resident's table to the top of the medication cart, the LPN understood the infection control concern and proceeded to wipe off the top of the medications cart with a disinfectant wipe. 2. On 12/19/22 at 4:01 PM, the surveyor arrived at the medication cart located near the room of Resident #25, who was holding her nebulizer treatment while it was running. Staff G, LPN, returned to her medication cart from a different room and informed the surveyor she had set up the resident's nebulizer and did an assessment. The LPN was prepping to do another resident's medications. At 4:03 PM, Resident #25 stopped the nebulizer and put the equipment back into the drawer. Staff G was followed until 4:26 PM, and she failed to return to Resident #25's room to clean the nebulizer equipment. On 12/19/22 at 5:04 PM, the Director of Nursing (DON) informed the surveyor she had educated Staff G on the nebulizer policy. The DON was informed the LPN failed to clean the nebulizer equipment. 3. A medication observation was made on 12/21/22 at 8:24 AM with Staff E, RN, for Resident #25. During this medication pass, the RN removed 10 pills from the pill packets. The RN touched the pills with her bare hands on several occasions, while popping the pill out of the pill pack. After administering all of the pills, the RN set up the resident's nebulizer, did a respiratory assessment, then provided the medication. The RN stated she would stay with the resident, reassess her at the end of the treatment, and wash out the equipment with tap water and place back into the plastic bag. The RN was made aware the policy documented to clean with sterile or distilled water and allow to air dry, and the RN stated she had never done that. The RN was also made aware of the touching of the pills with her bare fingers and agreed to the infection control concerns. 4. During an observation on 12/19/22 at 12:18 PM, Staff D, LPN, went into the room of Resident #43 to start the resident's tube feeding. While opening the new tubing set and setting up supplies, the LPN knocked over the large syringe and container used during tube feeding or medication administration, and both fell onto the floor. The LPN picked up the syringe and container from the floor and rinsed them off in the resident's sink. The LPN proceeded to fill up the canister and put the tap water into the new set. The LPN used the syringe to flush the resident's feeding tube with tap water. During a subsequent interview on 12/21/22 at 11:40 AM, Staff D, LPN was asked about using the syringe and container for Resident #43, after having dropped them on the floor. The LPN stated, Yes, but I washed them off. 5. On 12/19/22 at 2:59 PM, Staff C, LPN, arrived to the North Unit and introduced herself to the day nurse and the surveyor. Staff C proceeded to go to every room on the North Unit, to introduce herself to the residents and do a quick observation. Although not all rooms were observed, the LPN was seen patting two of the residents, moving an over-the-bed table in one room, and assisting one resident by handing them the call bell. The LPN failed to perform any hand hygiene between each resident. On 12/21/22 at 3:05 PM, Staff C was observed doing the same routine, going in and out of every resident room without any type of hand hygiene. During an interview at this time, the LPN was made aware of the observation of failing to perform hand hygiene between resident contact, and stated she hadn't thought of that.
MINOR (C)

Minor Issue - procedural, no safety impact

Deficiency F0730 (Tag F0730)

Minor procedural issue · This affected most or all residents

Based on personnel file review, interview, and policy review, the facility failed to complete a performance review of nurse aides at least once every 12 months for 3 of 3 sampled nurse aides (Staff H,...

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Based on personnel file review, interview, and policy review, the facility failed to complete a performance review of nurse aides at least once every 12 months for 3 of 3 sampled nurse aides (Staff H, I, and J). The findings included: Review of the policy, titled, Required Training, Certification and continuing Education for Nurse Aides, revised 07/25/22, documented, 6. In-service training will be provided by qualified personnel and will be based on the needs of the residents in the facility and any areas of weakness as determined in the nurse aide's performance reviews and facility assessment. During a side-by-side review of personnel files on 12/22/22 at 3:23 PM, the Business of Manager / Human Resources Director was asked the facility's practice regarding performance evaluations. The Human Resources Director explained that each department head should be doing annual evaluations around their anniversary date of hire. The Human Resources Director was asked to locate and provide the most current performance evaluation for Staff H, Restorative Certified Nursing Assistant (CNA) who was hired on 09/07/20; Staff I, CNA, who was hired on 04/25/12; and Staff J, CNA, who was hired on 05/21/12. The Human Resources Director looked through the three personnel files and could not locate any current performance evaluations. The most recent performance evaluation located was from 2020. During an interview on 12/22/22 at 3:42 PM, the Director of Nursing (DON), who had been at the facility as DON for at least two years, confirmed she was responsible for the annual performance evaluations for the nursing staff, including the nurse aides, on or about their anniversary date. The DON volunteered they had recently initiated a new form, but she had not used it yet. The DON agreed the evaluations had not been completed for the three sampled staff, and that she had not done any of the nurse aide annual evaluations.
Understanding Severity Codes (click to expand)
Life-Threatening (Immediate Jeopardy)
J - Isolated K - Pattern L - Widespread
Actual Harm
G - Isolated H - Pattern I - Widespread
Potential for Harm
D - Isolated E - Pattern F - Widespread
No Harm (Minor)
A - Isolated B - Pattern C - Widespread

Questions to Ask on Your Visit

  • "What changes have you made since the serious inspection findings?"
  • "Can I speak with families of current residents?"
  • "What's your RN coverage like on weekends and overnight?"

Our Honest Assessment

Strengths
  • • Licensed and certified facility. Meets minimum state requirements.
Concerns
  • • Multiple safety concerns identified: 2 life-threatening violation(s), $35,265 in fines. Review inspection reports carefully.
  • • 30 deficiencies on record, including 2 critical (life-threatening) violations. These warrant careful review before choosing this facility.
  • • $35,265 in fines. Higher than 94% of Florida facilities, suggesting repeated compliance issues.
  • • Grade F (11/100). Below average facility with significant concerns.
Bottom line: Trust Score of 11/100 indicates significant concerns. Thoroughly evaluate alternatives.

About This Facility

What is Garden View Center's CMS Rating?

CMS assigns GARDEN VIEW HEALTH AND REHABILITATION CENTER an overall rating of 1 out of 5 stars, which is considered much below average nationally. Within Florida, this rating places the facility higher than 0% of the state's 100 nursing homes. A rating at this level reflects concerns identified through health inspections, staffing assessments, or quality measures that families should carefully consider.

How is Garden View Center Staffed?

CMS rates GARDEN VIEW HEALTH AND REHABILITATION CENTER's staffing level at 2 out of 5 stars, which is below average compared to other nursing homes. Staff turnover is 53%, compared to the Florida average of 46%. RN turnover specifically is 64%, which is notably high. RNs provide skilled clinical oversight, so turnover in this role can affect medical care quality.

What Have Inspectors Found at Garden View Center?

State health inspectors documented 30 deficiencies at GARDEN VIEW HEALTH AND REHABILITATION CENTER during 2022 to 2025. These included: 2 Immediate Jeopardy (the most serious level, indicating potential for serious harm or death), 27 with potential for harm, and 1 minor or isolated issues. Immediate Jeopardy findings are rare and represent the most serious regulatory concerns. They require immediate corrective action.

Who Owns and Operates Garden View Center?

GARDEN VIEW HEALTH AND REHABILITATION CENTER is owned by a for-profit company. For-profit facilities operate as businesses with obligations to shareholders or private owners. The facility is operated by SIMCHA HYMAN & NAFTALI ZANZIPER, a chain that manages multiple nursing homes. With 72 certified beds and approximately 69 residents (about 96% occupancy), it is a smaller facility located in VERO BEACH, Florida.

How Does Garden View Center Compare to Other Florida Nursing Homes?

Compared to the 100 nursing homes in Florida, GARDEN VIEW HEALTH AND REHABILITATION CENTER's overall rating (1 stars) is below the state average of 3.2, staff turnover (53%) is near the state average of 46%, and health inspection rating (1 stars) is much below the national benchmark.

What Should Families Ask When Visiting Garden View Center?

Based on this facility's data, families visiting should ask: "What changes have been made since the serious inspection findings, and how are you preventing similar issues?" "Can you walk me through typical staffing levels on day, evening, and night shifts?" "Can I visit during a mealtime to observe dining assistance and food quality?" "How do you handle medical emergencies, and what is your hospital transfer rate?" These questions are particularly relevant given the facility's Immediate Jeopardy citations and the below-average staffing rating.

Is Garden View Center Safe?

Based on CMS inspection data, GARDEN VIEW HEALTH AND REHABILITATION CENTER has documented safety concerns. Inspectors have issued 2 Immediate Jeopardy citations (the most serious violation level indicating risk of serious injury or death). The facility has a 1-star overall rating and ranks #100 of 100 nursing homes in Florida. Families considering this facility should ask detailed questions about what corrective actions have been taken since these incidents.

Do Nurses at Garden View Center Stick Around?

GARDEN VIEW HEALTH AND REHABILITATION CENTER has a staff turnover rate of 53%, which is 7 percentage points above the Florida average of 46%. Moderate turnover is common in nursing homes, but families should still ask about staff tenure and how the facility maintains care continuity when employees leave.

Was Garden View Center Ever Fined?

GARDEN VIEW HEALTH AND REHABILITATION CENTER has been fined $35,265 across 1 penalty action. The Florida average is $33,432. While any fine indicates a compliance issue, fines under $50,000 are relatively common and typically reflect isolated problems that were subsequently corrected. Families should ask what specific issues led to these fines and confirm they've been resolved.

Is Garden View Center on Any Federal Watch List?

GARDEN VIEW HEALTH AND REHABILITATION 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.