CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0554
(Tag F0554)
Could have caused harm · This affected 1 resident
Based on observation, record review, and interview during the recertification survey conducted 4/19/23 -4/27/23 the facility failed to determine if medication self-administration was clinically approp...
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Based on observation, record review, and interview during the recertification survey conducted 4/19/23 -4/27/23 the facility failed to determine if medication self-administration was clinically appropriate for 1 of 1 resident (Resident #98) reviewed. Specifically, Resident #98 was observed on 5 days with Odomzo (generic name sonidegib, a chemotherapeutic medication) in a cup at their bedside and there was no assessment to determine the resident's ability to safely self-administer medications or a physician order for self-administration of medications.
The facility policy Self Administration of Medication dated 5/2018 documented residents who desired to self-administer medications required review and approval of the interdisciplinary care planning team members and an order from the attending physician. The medications would be stored in a locked drawer in the resident's room, and the self-administered medications would be monitored by licensed nursing staff.
Resident #98 was admitted to the facility with diagnoses including basal cell carcinoma of the skin. The 2/17/23 Minimum Data Set (MDS) assessment documented the resident was cognitively intact and was independent with activities of daily living (ADL).
The 10/16/18 comprehensive care plan (CCP) documented the resident had deficits in ADL function. Interventions included the resident was independent with most ADLs. The resident had basal cell carcinoma and interventions included administer medications per medical orders.
The 6/30/22 physician orders documented Odomzo capsule 200 milligrams (mg) once every 24 hours for basal cell carcinoma. There was no order for the resident to self-administer medications.
A 3/17/23 progress note by physician #40 documented the resident was seen for a mandated 30/60 day visit. The resident had basal cell cancer, was stable, and was followed by oncology. The resident had two cancerous lesions removed and they had healed, and the resident continued to receive Odomzo. There was no documentation of the resident's ability to safely self-administer medications.
During an observation and interview on 4/19/23 at 10:33 AM the resident stated they took a pill for their cancer. The resident entered their room and returned to the hallway with a reddish colored pill and swallowed it. They stated they took the pill approximately 2 hours after eating their breakfast every day. The resident showed the pamphlet titled sonidegib (Odomzo) that came with the medication.
The April 2023 medication administration record (MAR) documented Odomzo 200 mg capsule was administered on 4/19/23 at 7:11 AM by licensed practical nurse (LPN) #10.
On 4/20/23 at 10:39 AM, Resident #98 was observed in their room. The resident stated they were getting ready to take their Odomzo. The resident walked to their over the bed tray table and retrieved a reddish colored pill from a clear plastic medication cup and swallowed the pill. They stated one day they had forgotten to take the medication until 3:00 PM. The resident stated they did not set any alarms to remind them to take their pill, and they were usually pretty sharp.
The April 2023 MAR documented Odomzo 200 mg capsule was administered on 4/20/23 at 8:32 AM by LPN #10.
On 4/21/23 at 9:30 AM, the resident was observed seated in a straight back chair in the hallway, the resident gave permission to the surveyor to enter their room, and a reddish colored capsule with sonidegib 200 mg printed on the capsule was observed in a plastic medication cup on the resident's over the bed tray table.
The April 2023 MAR documented Odomzo 200 mg capsule was administered on 4/21/23 at 6:53 AM by LPN #10.
On 4/24/23 at 9:23 AM, the resident was not in their room and a reddish colored capsule with sonidegib 200 mg printed on the capsule was observed in a plastic medication cup on their over the bed tray table.
The April 2023 MAR documented Odomzo 200 mg capsule was administered on 4/24/23 at 8:09 AM by registered nurse (RN) Unit Manager #22.
On 4/25/23 at 9:38 AM, Resident #98 was observed in the dining room conversing with another resident and at 10:05 AM, a reddish colored capsule with sonidegib 200 mg printed on the capsule was observed in a plastic medication cup on the resident's over the bed tray table in their room.
The April 2023 MAR documented Odomzo 200 mg capsule was administered on 4/25/23 at 7:00 AM by LPN #10.
There was no documented evidence that Resident #98 had been assessed for the ability to safely self-administer medications or had a physician's order to self-administer medications.
During an interview on 4/25/23 at 11:02 AM LPN #10 stated if a resident was able to self-administer their own medications it would be listed on the MAR and the resident would need a physician order to do so. They stated when they administered the medication to a resident, they were supposed to ensure the resident took the medication prior to leaving the resident and the time stamp on the MAR was when the medication was given to the resident. They stated they did not watch Resident #98 take their medication, as the resident usually came to them and asked for their medication in the morning. They were unaware the resident was keeping medication in their room to take later. They stated they should have watched the resident take their medication for safety reasons and to ensure they were taking their ordered medications. If they were aware the resident wanted to take their medications at a different time or wanted to keep their medications in their room, they would have notified the Nurse Manager or a medical provider.
During an interview on 4/25/23 at 11:16 AM RN Unit Manager #22 stated a resident needed a self-medication administration assessment completed before they were able to take their own medications or to keep medications in their room. The resident would also need a physician order and it would be listed on the MAR. The nurse who administered medications should ensure that the resident had taken all their medications per physician orders. Resident #98 did not have a self-medication administration assessment, did not have a physician order to administer their own medication, and they were unaware the resident was keeping medication in their room to take later. Resident #98 never mentioned they kept medication in their room to take later or they wanted to self-administer their own medications. If they were aware the resident wanted to take their medications at a different time, they would have notified the physician to get an order for the resident's preferred time. If the resident wanted to self-administer their own medications, they would have assessed the resident's ability, discussed the resident's wish with the interdisciplinary team, and obtained a physician order. The RN stated they had provided Resident #98 with their medications on 4/24/23 and thought the resident had taken all their medications at that time. They stated it was important for residents to take their medications as ordered and if a resident was keeping medication in their room, it was a potential safety concern.
During an interview on 4/26/23 at 4:33 PM nurse practitioner (NP) #39 stated a resident needed a medical order to self-administer their medications. They stated Resident #98 received a chemotherapy medication for their active basal cell cancer. It was important for the nurse to ensure the resident was taking their prescribed medications as ordered. If they were aware the resident wanted to take their medication at a different time, they would have changed the order time.
During an interview on 4/26/23 at 4:33 PM the Director of Nursing (DON) stated residents needed an order to administer their own medications and they should have a self-medication administration assessment completed annually and as needed. The nurse who gave the resident their medication should ensure that the resident took all their medications per physician orders. If they did not it was a potential accident hazard.
10 NYCRR 415.3(e)(1)(vi)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0582
(Tag F0582)
Could have caused harm · This affected 1 resident
Based on record review and interview during the recertification survey conducted 4/19/23-4/27/23 the facility failed to provide the appropriate liability and appeal notices to Medicare beneficiaries f...
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Based on record review and interview during the recertification survey conducted 4/19/23-4/27/23 the facility failed to provide the appropriate liability and appeal notices to Medicare beneficiaries for 1 of 3 residents (Resident #438) reviewed. Specifically, Residents #438 remained in the facility after discontinuation of Medicare Part A services and the facility did not provide the resident with a Skilled Nursing Facility Advanced Beneficiary Notice of Non-coverage (SNF ABN) CMS-10055 (Centers for Medicare and Medicaid Services) for Medicare Part A as required.
Findings include:
The CMS form instructions for the Skilled Nursing Facility Advanced Beneficiary Notice of Non-coverage (SNF ABN) CMS-10055 (expiration date 1/31/26) documents that a Skilled Nursing Facility Advanced Beneficiary Notice of Non-coverage (SNF ABN) CMS-10055 must be issued by providers (including independent laboratories, home health agencies, and hospices), physicians, practitioners, and suppliers to Original Medicare (fee for service - FFS) beneficiaries in situations where Medicare payment is expected to be denied. The SNF ABN must be delivered far enough in advance that the beneficiary or representative has time to consider the options and make an informed choice prior to services ending.
Resident #438 was admitted to the facility with diagnoses including Alzheimer's Disease, hypothyroidism, and chronic kidney disease. The 10/14/22 Minimum Data Set (MDS) assessment documented it was a SNF PPS (Prospective Payment System) Part A discharge (end of stay) assessment.
The SNF Beneficiary Protection Notification Review documented the resident's Medicare Part A skilled services start date was 9/19/22 and the last covered day of Part A service was 10/14/22. The facility initiated the discharge from Medicare Part A services when benefit days were not exhausted. An SNF ABN form CMS-10055 was not provided to the resident. The explanation why the form was not provided was checked as other: Private Pay.
During an interview on 4/27/23 at 8:48 AM the MDS Coordinator stated they issued SNF ABN CMS-10055 frequently at the same time they issued the Notice of Medicare Non-Coverage (NOMNC) CMS-10123. They stated that the only time they would not issue a SNF ABN CMS-10055 was if a resident was discharged to the community the day after their covered Medicare Part A services ended. The MDS Coordinator stated if a resident remained in the facility past their covered Medicare Part A services, issuing a SNF ABN CMS-10055 was required. They stated MDS registered nurse (RN) #33 issued the NOMNC CMS-10123 to the resident. The resident went to long-term care in the facility and should have been issued a SNF ABN CMS-10055.
During an interview on 4/27/23 at 9:11 AM MDS RN #33 stated they issued SNF ABN CMS-10055 when they were instructed to by the MDS Coordinator. They stated that the SNF ABN CMS-1005 was supposed to be issued in almost all circumstances unless the resident was discharging home the day after Medicare Part A services were done. They stated they did not know why the SNF ABN CMS-10055 was not issued for Resident #438. Any resident staying in the facility for long term care after being discharged from Medicare Part A services should have been issued a SNF ABN CMS-10055.
10 NYCRR 415.3(g)(2)(iii)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
ADL Care
(Tag F0677)
Could have caused harm · This affected 1 resident
Based on observation, record review, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure residents who were unable to carry out activities of daily...
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Based on observation, record review, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure residents who were unable to carry out activities of daily living (ADLs) received the necessary services to maintain good nutrition, grooming, and personal and oral hygiene for 2 of 10 residents (Residents #108 and 109) reviewed. Specifically, Resident #108 was not assisted with shaving, nail care, or eating; and Resident #109 was not assisted with eating.
Findings include:
The facility policy, ADL Assistance and Supervision revised 1/8/18 documented the nursing assistant would provide assistance with daily activity (ADL) assistance/supervision to assigned residents and assist other nursing assistants in providing (ADL) care as needed. The Team Leader would monitor the (ADL) assistance/supervision provided for residents throughout the shift and give appropriate guidance to the nursing assistants. The Unit Manager would record the ADL assistance on the EMR (electronic medical record), monitor assistance/supervision provided for residents, and provide appropriate guidance to the nursing staff.
The facility policy, Shaving a Male Resident revised 5/8/18 documented a nursing assistant would shave the face of a male resident if the resident was unable to do the procedure safely by themself. This procedure would be carried out daily, or as needed.
The facility policy, Hygiene/Grooming revised 7/24/18 documented designated nursing staff would ensure that residents were clean and appropriately groomed at all times. The individual preferences of residents for personal care and grooming would be established and documented. Residents would be provided with care to maintain or improve abilities to perform hygiene and grooming tasks, as needed. AM care included oral hygiene; a partial bath; perineal care (as necessary/ordered) and any specific hygiene care (such as catheter or colostomy care) on days when no shower/bath was scheduled. Hygiene care was repeated before and after meals and throughout the day as needed.
1) Resident #108 was admitted to the facility with diagnoses including Alzheimer's disease and hypertension. The 2/23/23 Minimum Data Set (MDS) assessment documented the resident had severely impaired cognition, had no behaviors, required limited assistance of 1 for eating, and extensive assistance of 2 for bathing, dressing and personal hygiene.
The comprehensive care plan (CCP) initiated 10/2/22 and revised 1/2/23 documented Resident #108 required limited assistance of 1 for eating and was a messy eater, and extensive assistance of 2 for bathing and personal hygiene. Interventions included to provide finger foods if the resident wandered, set up their meal without the tray, provide cues to help facilitate bringing food and drinks up to their mouth to minimize mess, approach in a calm, gentle manner, and re-approach if the resident refused care.
The 4/26/23 resident care instructions documented the resident could safely be assisted with meals from a feeding assistant, required limited assistance of 1 for eating, required cues for eating, could not understand what was required of them, required guidance from staff, and required extensive assistance of one for personal hygiene and bathing.
The following observations of Resident #108 were made:
- on 4/19/23 at 12:34 PM sitting in the dining room approximately 3-4 feet away from the table feeding themself lunch and spilling food on themself and the floor. The resident had ¼ inch- ½ inch long facial hair. The resident was not assisted with eating or positioning. At 12:43 PM, licensed practical nurse (LPN) # 34 called for a staff member to get them a towel and cleaned up the spilled food under the resident's chair. The LPN did not position the resident closer to the table or assist them with eating.
- on 4/20/23 at 12:43 PM, sitting at a dining room table with facial hair approximately ½ inch long.
- on 4/21/23 at 11:21 AM, sitting in the dining room approximately 1-1/2 feet away from the table while waiting for lunch. The resident had facial hair on their chin and face approximately ½ inch long. At 11:34 AM the resident was eating lunch and spilling their food. Certified nursing assistant (CNA) # 36 walked by the resident and did not offer to push the resident closer to the table or assist them with eating. At 11:40 AM, the resident continued to attempt to feed themself and was spilling food on their lap. The resident was sitting approximately 1-1/2 feet away from the table and was sitting at an angle. Several staff members walked by the resident and did not assist them with positioning or eating. At 11:46 AM support aide # 37 asked the resident how they were doing and did not help with eating or positioning. At 11:53 AM the resident dropped their peaches on the floor and bent over to pick them up. Their chair remained at an angle away from the table. The resident continued to spill food on their pants and was not helped by staff. At 12:15 PM the resident completed their meal and there was food on their pants, on the floor, and on the table in front of their plate. CNA # 36 handed the resident chocolate milk, and the resident spilled the milk on their pants and on the floor and CNA #36 did not attempt to assist the resident.
- on 4/24/23 at 12:39 PM, sitting at the dining room table eating lunch and spilling food on the table and their lap. Staff did not cue or assist the resident with eating. At 12:40 PM, LPN #34 removed the resident's plate while they were still eating and placed their dessert in front of them. LPN #34 did not ask the resident if they were finished eating their meal.
- on 4/25/23 at 9:43 AM, walking down the hall with facial hair approximately a ½ inch long with a brown substance under their fingernails.
- on 4/26/23 at 10:03 AM, sitting in the dining room with food particles and stains on their pants, long facial hair, and a brown substance under their fingernails.
During an interview on 4/26/23 at 10:05 AM, CNA # 36 stated Resident #108 should sit at a 90-degree angle for eating. Resident #108 required limited assistance of one for eating, extensive assistance of 2 for ADL care, and the CNAs were responsible for ADL care. The resident should have been cued and assisted with eating. The CNA stated Resident #108 had not been shaved in 3 weeks. They stated they should re-approach the resident with care if they became agitated and did not know why the resident had not been shaved.
During an interview on 4/26/23 at 10:30 AM, LPN # 34 stated Resident #108 required set up with limited assistance for eating. They stated they asked for towels and cleaned up food under the resident's chair and did not assist the resident with eating. They stated Resident #108 required extensive assistance of 1-2 for their ADLs and did not refuse care. LPN #34 stated they would assist the CNAs with shaving and nail care but had not assisted with Resident #108's shaving or nail care.
During an interview on 4/26/23 at 10:45 AM RN #35 stated Resident #108 required extensive assistance of 1-2 for ADL care and should be reapproached if agitated. They stated shaving and nail care was completed by CNAs and should be done with morning care. Resident #108 required limited assistance of 1 for eating and should be pushed up to the table for positioning.
2) Resident #109 was admitted to the facility with diagnoses including vascular dementia and unspecified occlusion (blockage) of the coronary artery. The Minimum Data Set (MDS) assessment documented the resident had severely impaired cognition, had no behaviors, and required supervision with assistance of 1 for eating.
The comprehensive care plan (CCP) initiated 8/17/20 and revised 1/5/23 documented the resident had ADL deficits related to muscular weakness. Interventions included limited assistance of 1 for eating, divided plate, and assist with appropriate use of silverware, cut all items into bite-sized pieces to be easily scooped with spoon or stabbed with a fork, and place any items from bowls onto divided plate. The resident may require intermittent verbal and/or tactile cues for appropriate use of silverware, assistance to be fed with non-finger food items (varied daily based on mood and behaviors), and one item at a time was recommended.
The 4/26/23 resident care instructions documented Resident #109 was on aspiration (inhaling food/fluid into lungs) precautions, could be safely assisted with meals by a feeding assistant, and required limited assistance of 1-person physical assistance for eating and intermittent cueing to use their silverware.
The following observations were made of Resident #109:
- on 4/19/23 at 12:25 PM, sitting in the dining room eating lunch with their drinks and dessert on a tray on the windowsill behind them. The resident was not eating the main meal. At 12:49 PM LPN #34 handed the resident a glass of orange juice and did not cue or assist the resident with eating. At 12:57 PM LPN #34 handed the resident their strawberries after the main meal was completed and all other residents were removed from the dining room. The resident remained in the dining room unattended and was not assisted or cued with eating.
- on 4/21/23 at 11:38 PM, registered nurse (RN) #35 handed the resident their lunch on a divided plate and told the resident to use their spoon. The resident picked the spoon up and smashed their food around the plate, did not eat, and set their spoon down. No cueing or assistance with eating was provided by staff. At 12:04 PM, the resident finished a cup of coffee while the rest of their drinks and dessert were on a tray behind them. At 12:12 PM the resident was trying to drink out of an empty coffee cup while their drinks were behind them. No staff assistance with drinks was offered. At 12:16 PM, the resident had a plate of baked ziti and continued to attempt to eat. CNA # 26 handed the resident their milk and did not offer to feed or assist the resident during the meal. At 12:25 PM, the resident had consumed less than 25% of their meal, drank 240 milliliters (ml) of coffee, and 60 ml of their milk. At 12:27 PM, CNA #36 handed the resident their orange, took away the resident's untouched main meal and did not offer an alternative meal, cueing, or assistance.
- on 4/24/23 at 12:27 PM, sitting in a recliner chair across from nursing station with milk and only a dessert in front of them. Their plate of food remained in the dining room untouched. The resident was not helped or cued by staff.
During an interview on 4/26/23 at 10:13 AM CNA #36 stated Resident #109 required assistance of 1 for eating. The resident often mixed drinks in their food. Staff were supposed to offer alternative items such as sandwiches to the resident, but they often just took their plate away. Resident #109 often expressed hunger. CNA #36 stated they did not know why staff did not think about giving additional alternatives to the resident if they did not eat.
During an interview on 4/26/23 at 10:45 AM LPN #34 stated Resident #109 required supervision, cueing, and set up with their meals but would require feeding assistance at times. The resident would mix their drinks in their food. They stated staff should offer the resident a sandwich if they did not eat.
During an interview on 4/26/23 at 10:55 AM RN #35 stated Resident #109 had declining vision, required limited assistance of 1 for eating, would often require cues to remind them of food still on their plate, and would require a staff member to pull up a chair and assist them with eating when they were not eating well. They stated staff needed to be re-educated if Resident #109 did not eat and staff did not offer any alternative meal items.
10NYCRR 415.12 (a)(3)
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 observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility fai...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure a resident with limited range of motion (ROM) received appropriate treatment and services to increase ROM and/or prevent further decrease in ROM for 2 of 4 residents (Residents #66 and #93) reviewed. Specifically, Resident #93 was not wearing their bilateral palm devices (helps prevent hand contractures) as care planned during multiple observations; and Resident #66 did not have their neck brace applied appropriately and was not wearing positioning and palm devices as care planned for multiple observations.
The facility policy Splint, Brace Care updated 5/23/2018 documented that appropriately trained nursing staff would provide assistance as needed through a scheduled program of applying and removing a splint or brace, monitor the resident's skin and circulation under the device, and reposition the limb as needed. The program for use of splints and/or braces was documented by therapy on the interdisciplinary care plan and the nursing assistant documented the splint/brace program in the electronic medical record (EMR) along with any refusals which must also be verbally reported to the Unit Manager.
1) Resident #66 was admitted to the facility with diagnoses including dementia and contractures (tightening of the muscles, tendons, skin, and surrounding tissues that causes the joints to shorten and stiffen) of the right and left hand. The 2/13/23 Minimum Data Set (MDS) assessment documented the resident had severely impaired cognition, did not reject care, required extensive assistance of one for bed mobility, dressing, toileting, was totally dependent on one for hygiene, totally dependent on two for transfers, and had limited range of motion (ROM) in bilateral (both sides) arms and legs.
The comprehensive care plan (CCP), revised 06/15/2021, documented that resident was at risk for limited ROM due to muscle weakness and contractures. Interventions included a neck support brace during meals only, to be applied while supine (lying flat on the back) in bed or reclined in the wheelchair while in a supine position prior to meals. If the resident refused the neck brace, they were to be assisted by the nurse for the meal. The resident was to have a carrot hand contracture device placed in their right hand and a rolled washcloth was to be place in their left hand during AM care. If the resident refused the carrot hand contracture device, a rolled washcloth was to be used in place of the carrot. Ensure hips were aligned while in their wheelchair with the head rest applied, foot buddy, wedge on left side with arm on top of wedge, like an arm rest, and bean pillow under right elbow and brought up between forearm and bicep, so their elbow was slightly extended.
The 2/8/23 occupational therapist (OT) evaluation documented the resident had bilateral upper extremity contractures. Resident #66 was totally dependent for all meals, attempted to initiate self feeding, and required their neck support device on for all meals. The resident was on a nursing rehabilitation program for splint assistance that included a blue neck support applied prior to all meals. Instructions for application included to apply neck support while the resident was supine in bed or reclined while in their wheelchair to achieve a supine position. Staff were to remove the pillow and allow the resident's head to relax back onto the bed or wheelchair, align the resident's head and neck to midline, and apply the neck support with the small side slightly below the chin. The neck support strap was to be loosely applied behind the neck, the strap was marked on the back to indicate application location, and red stitches indicated where the stopping location was. If the resident refused to wear the neck brace they were be assisted with eating by a nurse. A second nursing rehabilitation program for splint assistance included a carrot in the resident's right hand and a rolled washcloth in the resident's left hand after AM care. Instructions included to utilize a rolled washcloth in the resident's right hand if the carrot was refused. A third nursing rehabilitation program instructed to ensure the resident's hips were aligned while in their wheelchair with an applied head rest, foot buddy on wheelchair legs, wedge on left side with their arm on top of the wedge, like an arm rest, and a bean pillow under the right elbow and brought up between the forearm and bicep so the elbow was slightly extended.
The 3/22/23 nurse practitioner (NP) progress note documented the resident had contractures to bilateral upper extremities with very limited range of motion (ROM) in both the upper and lower extremities and bilateral hand splints were in place.
The care instructions ([NAME]) documented that a rehab carrot was to be placed in the resident's right hand and a rolled washcloth in their left hand after AM care. If the resident declined the carrot, staff were to use a rolled washcloth. The [NAME] also included instructions for the application of the neck support for meals and placement of body positioning devices.
Resident #66 was observed without a right or left hand contracture device in place:
- on 4/19/23 at 1:40 PM while sitting in their wheelchair in the dining room.
- on 4/21/23 at 10:27 AM while sitting in their wheelchair in their room, and at 12:06 PM while sitting in their wheelchair in the dining room.
- on 4/24/23 at 9:01 AM while sitting in their wheelchair in the dining room, at 9:24 AM while lying in bed, at 12:23 PM while sitting up in their wheelchair in the dining room, and at 2:17 PM while lying in bed.
The 4/2023 activities of daily living (ADL) record, completed by certified nursing assistants (CNAs), documented following for the right and left hand contracture devices:
- on 4/19/23 applied on the day and evening shift.
- on 4/21/23 not applicable on the day shift and not applied on the evening shift.
- on 4/24/23 applied on the day shift and not applied on the evening shift.
Resident #66 was observed:
- on 4/21/23 at 1:03 PM in the dining room being assisted with their meal by an LPN. The resident's neck was tilted down against their chest, and they did not have on the neck brace on while eating.
- on 4/24/23 at 12:54 PM registered nurse (RN) Clinical Educator #42 applied the neck brace while the resident was sitting up in their wheelchair. The resident's neck was tilted down and slightly to the right. The neck brace was not applied according to the care planned directions.
- on 4/25/23 at 12:52 PM CNA #43 tilted the resident's head back by the top of the resident's head/forehead while the resident was in an upright seated position and slid on the neck brace. The neck brace was not applied according to the care planned directions.
The 4/2023 ADL record, completed by CNAs, documented the functional maintenance plan that included the application of the resident's neck support device for swallowing per plan of care was:
- followed for all three meals on 4/21/23.
- followed for all three meals on 4/24/23.
- followed for breakfast and lunch on 4/25/23.
Resident #66 was observed without positioning devices implemented per their CCP:
- on 4/21/23 at 10:27 AM and at 12:06 PM sitting in their wheelchair without a supportive pillow device for their right arm/wrist.
- on 4/24/23 at 12:23 PM with no black wedge for their left arm shelf support.
The 4/2023 activities of daily living (ADL) record, completed by certified nurse aides (CNAs), documented the functional maintenance plan that included the application of positioning devices in the wheelchair per plan of care were:
- followed for both day and evening shifts on 4/21/23.
- followed for day and evening shifts on 4/24/23.
During an interview on 4/26/23 at 11:11 AM CNA #48 stated staff followed resident specific care instructions on the [NAME] or the care plan. They stated Resident #66 required a pink wedge when they laid down and it had to be on for two hours and off for two hours. The resident also required a neck brace while eating along with a carrot for one hand and wash cloth for other. They stated Resident #66 also had a black wedge on their left side and a bean pillow on their right side for positioning while in their wheelchair. They stated nursing staff had been trained by therapy on how to apply the neck brace. They stated they were trained to put the neck brace on in bed if possible. They should remove the resident's pillow and allow the resident's neck to stretch back. If the resident was up in their wheelchair, they should recline the chair to allow the resident's neck to stretch. They stated that they are supposed to monitor the resident's swallow as well as skin integrity while the neck brace was in use. If the resident refused the neck brace, the resident should be assisted with eating by a nurse. CNA #48 stated it was important for the neck brace to be applied appropriately to prevent injury and to straighten the resident's neck for swallowing support and to have a washcloth or carrot in the resident's hands as their hands were very contracted. The devices kept nails from digging into their palm, promoted skin integrity, and kept the contractures from worsening.
During an interview on 4/26/23 at 11:36 AM CNA #43 stated they referred to the [NAME] to care for a resident. Resident #66 wore a neck brace while eating. They stated that it was easier to put the brace on the resident while they were in bed, but if the resident was in their wheelchair, they lifted the resident's head up and back to put the brace on. They stated that they usually held the resident's head there for a few seconds to stretch their neck and the resident would tell them when it was enough. They had been trained by therapy on how to put the neck brace on but was unaware that the resident's wheelchair needed to be tilted back when the brace was applied while in their wheelchair. It was important to apply the brace so that the resident did not choke while eating. If the resident refused the brace, a nurse needed to assist the resident with eating. The resident had not refused the brace for them. They stated the resident required a carrot for their right hand and a rolled-up washcloth for their left hand for contracture management. The resident also had a side support/wedge pillow on their left side under their arm, like an arm rest. The CNA stated it was important to apply the contracture devices to stop the progression of the contracture and to open the resident's hands to avoid pressure areas.
During an interview on 4/26/23 at 12:12 PM LPN #47 stated they expect CNAs to utilize the iPads and hand-held devices to view to [NAME] for resident specific care instructions. They stated the positioning and contracture management devices as well as specific application instructions were included on the [NAME]. LPN #47 stated that Resident #66 used a neck brace for all meals unless they refused and then they were to be assisted with eating by a nurse. They stated that they were not trained how to apply the brace but that the CNAs on the unit were. LPN #47 stated that they did not usually work on the resident's unit, and they had the CNAs apply the brace prior to meals. LPN #47 stated it was important for the neck brace to be applied correctly to ensure the proper neck position for swallowing to avoid aspiration. They stated the resident had a bean bag device for their arm, a black wedge, and other positioning devices to keep them straight while in their wheelchair; and a carrot for one hand and a washcloth for the other hand for their hand contractures. They stated that the hand contracture devices were important for the resident to use to avoid worsening of the contractures and to prevent their nails from embedding into their skin.
During an interview on 4/26/23 at 12:32 PM LPN Unit Manager #49 stated that nursing staff should look at the [NAME] for resident specific care instructions. They expected all positioning and contracture management devices in place per the plan of care and [NAME] instructions. They stated the devices assisted in preventing further contraction, helped with pain management, provided pressure relief, and promoted skin integrity. They stated that they would expect to be notified of any refusals and they were not notified the resident had refused any ordered devices. The resident should have their neck brace on for all meals and staff were trained to apply and remove the brace. They stated the neck should be extended when the brace was applied and preferably while the resident was lying down. If the resident was in their wheelchair, the wheelchair should be tilted backwards to achieve a lying position for neck extension prior to the brace being applied. They stated it was important for the resident's neck brace to be applied properly to ensure their neck was in the correct position to swallow and avoid aspiration.
During an interview on 4/26/23 at 2:54 PM occupational therapist (OT) #53 stated if a resident had contractures nursing would request a referral and OT would assess the resident and determine if any interventions were needed. They trialed several different options for hand contracture management for Resident #66 and concluded that the carrot in the right hand and a rolled washcloth in the left hand was best tolerated by the resident. They stated they expected staff would follow the recommendation to wash the resident's palms in the AM and at minimum place the rolled washcloths in their hands. They stated that it was important to have the hand contracture management devices in place to prevent the contractures from worsening. OT #53 stated the resident also had a bean pillow, black wedge, and neck travel pillow for positioning in their wheelchair. The bean pillow was placed under the right elbow and up around the arm to help keep the arm from being contracted against their body, and the wedge on the left side provided support to the arm. They stated the resident was seen originally for the neck brace because they could not hold their head up during meals making it difficult to swallow. Staff had been educated on how to apply the brace properly and should recline the resident's wheelchair to open their neck position. They stated it was easiest to put the brace on when the resident was already in a supine position in bed. It was not appropriate for staff to apply the neck brace while the resident's neck was tilted forward or by tilting the resident's head up manually while the resident was in a seated position. The resident had tight muscles in their neck staff, and this would not allow the right clearance for the resident's throat for adequate swallowing.
2) Resident #93 was admitted to the facility with diagnoses including Alzheimer's disease and contractures of the left and right hand. The 3/31/23 Minimum Data Set (MDS) assessment documented the resident had severely impaired cognition, did not reject care, required extensive assistance of 2 for dressing, and had impairment in range of motion (ROM) to both upper extremities.
The 7/13/21 physician orders documented a right upper extremity blue carrot (contracture prevention device) and a left upper extremity resting splint (to help reduce swelling and pain). The blue carrot was to only be removed for care and the blue resting splint was to be applied in AM and removed at bedtime.
The revised 5/23/22 comprehensive care pan (CCP) documented the resident had limitations in ROM related to decreased functional activity with contractures. Interventions included the resident must have carrots or wash cloths at minimum in their hands during the day and if unable to apply carrots, place rolled wash clothes in their hands.
The undated care instructions ([NAME]) documented the resident was to have carrots or rolled wash cloths at a minimum in their hands during the day and were to be off at night.
The April 2023 treatment administration record (TAR) documented to ensure the right upper extremity blue carrot and left upper extremity resting splint were put in place on the 6:00 AM - 2:00 PM shift and the 2:00 PM to 10:00 PM shift. The blue carrots were to be removed for care only and the blue resting splint was to be applied in the AM and removed at bedtime.
The 4/2023 activities of daily living (ADL) record task form documented the resident was to have carrots or wash cloths in their hands at a minimum during the day.
On 4/19/23 at 12:14 PM, the resident was observed seated in their high back recliner chair at a table in the dining room. Both resident's hands were contracted, and they did not have any contracture management devices in their hands. At 1:21 PM, the resident was observed lying in bed, both hands remained contracted without a contracture management device in place, and there was a blue carrot on their bed side table.
On 4/19/23 registered nurse (RN) #44 signed the TAR indicating to ensure the right upper extremity blue carrot and left upper extremity resting splint were put in place on the 6:00 AM - 2:00 PM was completed on the 6:00 AM- 2:00 PM shift.
On 4/19/23 at 1:30 PM certified nursing assistant (CNA) #50 documented on the CNA ADL task form not applicable (N/A) for placement of the right upper extremity blue carrot and left upper extremity resting splint.
On 4/20/23 at 9:50 AM, the resident was observed lying in their bed, their hands were contracted, and they did not have a contracture management device in place. The blue carrot was on their bed side table.
On 4/20/23 registered nurse (RN) #44 signed the TAR indicating to ensure the right upper extremity blue carrot and left upper extremity resting splint were put in place on the 6:00 AM - 2:00 PM was completed on the 6:00 AM- 2:00 PM shift.
On 4/20/23 at 11:56 AM CNA #51 documented on the CNA ADL task form the placement of the right upper extremity blue carrot and left upper extremity resting splint was completed.
On 4/21/23 at 9:24 AM, the resident was observed seated in their high back recliner chair in the dining room, the resident's hands were contracted, and they did not have a contracture management device in place. At 11:15 AM, the resident was observed in their low bed sleeping, their hands were contracted, they did not have a contracture management device in place, and a blue carrot was on their bed side table. At 12:02 PM, the resident was observed in their high back recliner chair in the dining room, their hands were contracted, and they did not have a contracted management device in place.
On 4/21/23 licensed practical nurse (LPN) #34 signed the TAR indicating to ensure the right upper extremity blue carrot and left upper extremity resting splint were put in place on the 6:00 AM - 2:00 PM was completed on the 6:00 AM- 2:00 PM shift.
On 4/21/23 at 1:59 PM CNA #50 documented on the CNA ADL task form not applicable (N/A) for placement of the right upper extremity blue carrot and left upper extremity resting splint.
On 4/24/23 at 9:23 AM and 10:23 AM, the resident was observed in their high back recliner chair in the dining room, their hands were contracted, and they did not have a contracture management device in place. At 12:59 PM, the resident was observed seated in their high back recliner chair in the hallway, both of their hands were contracted, and they did not have a contracture management device in place.
On 4/24/23 RN #45 signed the TAR indicating to ensure the right upper extremity blue carrot and left upper extremity resting splint were put in place on the 6:00 AM - 2:00 PM was completed on the 6:00 AM- 2:00 PM shift.
On 4/24/23 at 1:59 PM CNA #52 documented on the CNA ADL task form the placement of the right upper extremity blue carrot and left upper extremity resting splint was completed.
On 4/25/23 at 8:43 AM, the resident was observed in their high back recliner chair in the dining room, their hands were contracted, and they did not have a contracture management device in place. At 11:01 AM, the resident was observed in the hallway seated in their high back recliner chair, both hands were contracted, and they did not have a contracture management device in place. At 11:38 AM, the resident remained in the hallway with no contracture management devices in their hands.
During an interview on 4/25/23 at 12:50 AM CNA #35 stated they were floated to the unit on this day, and they were supposed to check the CNA care instructions prior to assisting residents so they knew what level of care to provide and if the resident needed any special devices in place. They stated Resident #93 was on their assignment, they did not check the CNA care instructions before providing care, and they were verbally told what level of assistance each resident needed by another staff member. They stated when they provided care to Resident #93, the resident's hands were contracted, they struggled to wash the resident's hands, and they were unaware the resident needed contracture management devices in their hand. They stated if the resident required any special devices it was listed on the care instructions. It was important to ensure the contracture management devices were in place to ensure the contractures did not worsen. If they were aware of the devices, they would have tried to apply them or use a rolled up wash cloth. They did not tell anyone the resident's hands were hard to open and they should have.
During an interview on 4/25/23 at 2:01 PM LPN #34 stated they were floated to the unit on 4/21/23. The TAR indicated what devices the resident needed, and the nurse should only sign if the treatment was completed. They were familiar with Resident #93, their hands were contracted, and they had contracture management devices or rolled wash cloth ordered for their hands. The resident must have had something in their hands on 4/21/23 otherwise they would not have documented it was in place on the TAR. They stated it was important for the resident to have their contracture management devices in place to prevent skin breakdown and to prevent their contractures from worsening.
During an interview on 4/26/23 at 11:34 AM LPN #10 stated if a resident required any special devices for contractures it was listed on the TAR and If they signed the device was in place that meant they either observed the device in place or they had applied it themselves. The CNAs should let the nurse know if they could not apply the device, the CNA should document the resident refused, and the nurse should write a note regarding the refusal as well. Resident #93 had contractures, was supposed to have contracture management devices in place or a rolled washcloth. If the resident's contracture management devices were not applied the resident's contractures could worsen.
During an interview on 4/26/23 at 11:43 AM, RN unit manager #22 stated Resident #93 had contractures and was supposed to have contracture management devices or rolled wash cloths in their hands to prevent the contractures from worsening and prevent skin breakdown. If the nurse signed the TAR that the device was in place, that meant they either observed the device in place or applied it themselves. The CNAs should not document N/A and should document either the resident refused, or they applied the device. Staff should be checking the resident's care instructions before care to ensure the correct level of assistance and proper care were provided.
During a telephone interview on 4/26/23 at 1:19 PM RN #44 stated if a resident had an order for a device for contractures it was listed on the TAR. If they signed the TAR that the device was in place, they either observed the device in place or they applied it themselves. If the resident refused any care or application of contracture management devices the CNA should let the nurse know and they both would document the refusal. They could not recall if they were notified if the resident refused their contracture management devices.
During an interview on 4/26/23 at 3:15 PM occupational therapist (OT) #46 stated if a resident had an order for contracture management devices, it was in place for preventative measures to help prevent skin breakdown, and further worsening of their contractures. They stated Resident #93 had bilateral hand contractures and one of their hands was worse than the other. It was very important for the resident to either have blue carrots or rolled wash cloths in their hands daily. The unit staff had been recently educated on this topic in March or early April 2023. The resident's care plan and care instructions documented the need for the blue carrots or rolled wash cloths and listed the instructions on how to apply the devices. If the resident refused, staff should let the nurse know so they could document the refusal. If staff was having a hard time opening the resident's hands, they should let the nurse know so therapy could be made aware and could reassess the resident. They expected staff to follow the resident's care plan to prevent further worsening of their contractures.
10NYCRR 415.12(e)(2)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0761
(Tag F0761)
Could have caused harm · This affected 1 resident
Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility did not ensure drugs and biologicals were labeled in accordance with curren...
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Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility did not ensure drugs and biologicals were labeled in accordance with currently accepted professional principles, and include the appropriate accessory and cautionary instructions, and the expiration date when applicable for 4 of 10 medication carts (medication carts 1 and 2 on Unit 100 South and medication carts 1 and 2 on Unit 3) inspected. Specifically, there were 4 insulin pens and 1 eye drop bottle observed without pharmaceutical labels including resident information, medication name, medication dosage, and administration instructions.
Findings include:
The facility policy, Medication Label and Container Requirements revised 5/20/2018 documented medications accepted from a Pharmacy Services Provider or administered to residents of the facility must be packaged in compliance with all applicable state and federal laws; labels must clearly indicate specific information legibly and completely. Medications will not be accepted at this facility if the general label requirements and package-type specific label requirements are not met including full name of resident, address of resident, name and strength of the medication, directions for administration of the medication, name of prescriber ordering the medication and the prescription number.
During an observation on 4/24/23 at 9:21AM, medication cart 1 on Unit 100 South was inspected with licensed practical nurse (LPN) # 6. The medication cart contained an opened bottle of brimonidine tartrate 0.2% eye drop solution (used to treat glaucoma) with a torn pharmaceutical label. There was no identification including resident information, medication name, medication dose, the date the bottle was opened, and Resident #110's name was handwritten on the bottle with a black marker. Additionally, medication cart 1 contained a gray colored insulin pen with no pharmaceutical label including the type of insulin, or an opened date. Resident #156's name was handwritten on the side of the pen with a black marker.
During an observation on 4/24/23 at 9:38 AM, medication cart 2 on Unit 100 South was inspected with licensed practical nurse (LPN) #6. The medication cart contained a gray colored insulin pen. The pen had a yellow sticker with Resident # 11's name written with a black marker and there was no pharmaceutical label attached to the pen. Medication cart 2 also contained an aqua colored glargine (long-acting insulin) insulin pen with a piece of white medical tape affixed to it with Resident #37's name written in black marker. There was no pharmaceutical label or opened date on the pen.
During an interview on 4/24/23 at 9:45 AM, LPN #6 stated that all nurses were responsible for checking the medication carts for expired medications or medications that did not contain labels. Insulin pens should be labelled when they are opened.
During a follow-up interview on 4/24/23 at 2:08PM, LPN #6 stated that eye drops should be in the original box, be labelled with the resident's name, medication name, medication dose, and instructions for use. Insulin pens should be labelled with the resident's name, type of insulin, medication dose, and instructions for use. LPN #6 stated they knew Resident #11's pen was not labelled, and they gave the resident 5 units of insulin from the pen on this date. They stated if a medication was not labelled it could result in the wrong medication or dose being given to the resident. Another nurse may not know what resident the medication belonged to.
During an interview on 4/24/23 at 2:17 PM, LPN Unit Manager # 11 stated the medication carts were audited once per month and they were responsible for the audits. LPN # 11 stated that insulin pens and eye drops should be labeled and if they were not, they should be removed from the cart and re-ordered to reduce the risk of a resident receiving the wrong medication. They stated they expected staff to check the medication carts once per shift for expired medications and unlabeled medications. They should pull any unlabeled medications from the carts.
During observations on 4/25/23 at 11:45 AM, medication carts 1 and 2 for Unit 3 were inspected with LPN #10. Medication cart 1 contained an insulin pen with no pharmaceutical label or opened date on it. Resident # 142's name was written on the pen in black marker. Medication cart 2 contained an insulin pen with no pharmaceutical label or opened date on it. Resident #180's name was written on the pen in black marker.
During an interview on 4/25/23 at 11:45 AM, LPN # 10 stated they were unsure about a medication labelling policy. If medications were unlabeled, nurses should write the resident's name on the pen with a black marker and put a yellow sticker on them with the date and time the pens were opened. LPN #10 stated the resident's insulin pens were stored in individual drawer sections with the resident's name in the cart. The risk of an unlabeled insulin pen could be that it could slide into another resident's drawer area resulting in a resident receiving the wrong medication.
During an interview on 4/26/23 at 11:36 AM the Director of Nursing (DON) stated insulin pens were sent to the facility as house stock and would not be labeled. The LPNs, Nurse Managers, and pharmacy staff were all responsible for checking the medication carts. The DON stated they did not feel it was a risk if an insulin pen was unlabeled because the staff referred to the electronic medication administration records (EMARS).
During an interview on 4/26/23 at 3:02 PM registered pharmacist (RPH) #14 stated eye drops, and insulin pens were individually dispensed, resident specific, and had pharmaceutical labels including the resident's name, medication name, and medication dose. Insulin pens came with tamper tape and a blank sticker with to write the date opened and date expired on them. RPH #14 stated only one type of insulin that came in a vial was used as house stock. It was not acceptable for a resident's name to be written on an insulin pen with a sharpie marker. If a label fell off, the facility should call the pharmacy and they would re-dispense another insulin pen. RPH# 14 stated the risk of medications not being labeled could be an unclear resident name or medication dose and the potential for a medication error.
10 NYCRR 415.18(d)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0804
(Tag F0804)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, observation, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility fai...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, observation, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure each resident received and the facility provided food and drink that was palatable, attractive, and at safe and appetizing temperatures for 2 of 3 meals (4/20/23 and 4/21/23 lunch meals) reviewed, and food items in 1 of 1 steam table observed. Specifically, lunch meals trays on 4/20/23 and 4/21/23 were not served at palatable and appetizing temperatures; and the main kitchen steam table was not holding the temperature for hot food items.
Findings include:
The facility policy Food Temperature Requirements and Holding Time modified 6/28/2019, documented steamtable thermostats would be turned on 30 minutes prior to meal service and set to maintain hot food between 140-160 degrees F (Fahrenheit).
The undated facility policy Test Tray Process documented the Director of Dining, the Assistant Director of Dining, Dietitians, and Diet Technicians were assigned to complete test tray audits monthly. One test tray would be completed monthly.
1. Test Trays Observations
- on 4/20/23 at 12:18 PM, a meal tray arrived to resident room [ROOM NUMBER] and a replacement tray was requested for the resident. At 12:20 PM, the food temperatures were measured. The Salisbury steak was 118 F and the milk was 50 F. The Salisbury steak was not hot or palatable, and the milk was not cold or palatable.
- on 4/21/23 at 12:23 PM, a meal tray arrived to a resident in the first floor dining room at 12:23 PM and a replacement tray was requested for the resident. At 12:25 PM, the food temperatures were measured. The hamburger was 120 F, the mixed vegetables were 118 F, and the milk was 52 F. The hamburger and mixed vegetables were not hot or palatable, and the milk was not cold or palatable.
During an interview on 4/26/23 at 1:38 PM, the Food Service Director stated that milk served at 50 F, Salisbury steak at 118 F, a hamburger at 120 F, and mixed vegetables at 118 F could be acceptable as it was subjective to the resident. They stated that weekly tray audits were done and included having a random test tray brought to a resident floor and checking for appropriate food temperatures and accuracy of the food items on the tray compared to the tray ticket. They stated there had been unacceptable temperature results on the weekly random test trays and these were reviewed during monthly quality assurance meetings.
During an interview on 4/26/23 at 1:41 PM, the Assistant Administrator stated that weekly random tray audits were completed and included checking for food temperatures and tray accuracy. They stated that the random tray audits were completed by the Food Service Director, the registered dietitian (RD), or the dietetic technician.
During an interview on 4/26/23 at 3:19 PM, dietetic technician #31 stated they had completed weekly random test trays before. They stated that a test tray ticket would be placed in the pile of food tickets for a specific resident floor, and they followed the tray cart from the main kitchen to the resident floor and documented the amount of time it took for delivery. Dietetic technician #31 stated they would take that tray when came off the cart and test the food. They used a calibrated pocket thermometer to record the temperature of the food and tasted the food for palatability. They stated hot food items should be held and served at 140 F or higher and cold food items should be held and served at 40 F or less. Dietetic technician #31 stated that if the food temperatures of the test trays were unacceptable, they would document on the test tray form and give the test tray form to the Food Service Director and to the Assistant Administrator. Dietetic technician #31 stated the milk served at 50 F, Salisbury steak at 118 F, hamburger at 120 F, mixed vegetables at 118 F, and milk at 52 F were not acceptable temperatures.
During an interview on 4/26/23 at 4:24 PM, the Assistant Food Service Director stated they participated in test tray audits. The test tray was the last tray selected off the cart to gauge the temperatures that would be taken when the last resident received their tray. They stated the acceptable temperature for hot food was between 140 F and 160 F, and cold food was below 41 F and above 32 F. The Assistant Food Service Director stated they discussed the test trays results with the Assistant Administrator and would come up with a plan of action on how to fix the temperatures that were unacceptable.
During an interview on 4/26/23 at 4:35 PM, the Assistant Administrator stated they were responsible for ensuring the test tray audits were completed and the Food Service Director was responsible for reviewing the results.
2. Main Kitchen Steam Table
During an observation on 4/20/23 at 12:06 PM, the steam table in the main kitchen tray line area was on and contained lunch items including stuffed peppers and grilled cheese sandwiches. Using a New York State Department of Health (NYSDOH) calibrated thermometer, the stuffed peppers were measured at 125 F and the grilled cheese was measured at 112 F.
During an interview on 4/20/23 at 12:06 PM the Assistant Food Service Director stated that hot foods were required to be at a holding temperature of 140 F to 160 F.
During an interview on 4/26/23 at 1:38 PM, the Food Service Director stated it was not acceptable for stuffed peppers to be held at 125 F and grilled cheese at 112 F. They stated that hot food items should be held at 135 F to 140 F.
During an interview on 4/26/23 at 3:19 PM, dietetic technician #31 stated stuffed peppers at 125 F and grilled cheese at 112 F were not acceptable. They stated the food carts brought to the resident units were not heated and there was no way for food to heat up after it left the kitchen.
During an interview on 4/26/23 at 4:35 PM, the Assistant Administrator stated food not held at the proper temperature could allow the growth of microorganisms that could make the residents sick.
10NYCRR 415.14(d)(2)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0805
(Tag F0805)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility fai...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure residents received and the facility provided food prepared in a form designed to meet individual needs for 2 of 2 residents (Residents # 38 and #52) reviewed. Specifically, Residents #38 and 52 were provided food items that were not consistent with the physician ordered diet.
Findings include:
The facility's 11/2009 Level 1 (Pureed) diet description documented the food items should be homogenous (smooth) and cohesive (adhere together) and should be pudding - like. There should be no coarse textures, raw fruits/vegetables, or nuts. Any food that required bolus (soft mass) formation, controlled manipulation, or mastication (chewing) were excluded. The diet was designed for residents who had moderate to severe dysphagia (difficulty swallowing).
The facility's undated Puree, Chicken Fajita recipe documented to prepare the meat per recipe, place the meat in the food processor with broth, and add the food thickener as needed until desired consistency was reached.
1)Resident #38 was admitted to the facility with diagnoses including schizophrenia, dysphagia, and feeding difficulties, unspecified. The 3/6/23 Minimum Data Set (MDS) assessment documented the resident had severe cognitive impairment, required supervision with eating, was on a mechanically altered diet, and did not have coughing or choking during meals.
The 1/14/23 quarterly nutrition assessment completed by registered dietitian (RD) #54 documented the resident received regular puree solids and thin liquids at meals. The resident had no chewing or swallowing concerns noted at this time.
The 1/24/22 revised comprehensive care plan (CCP) documented the resident had the potential for alteration in nutritional status. Interventions included to provide adaptive equipment at meals, half portions of entrees, vegetables, starches, and double portions of tomato soup at all meals. Provide regular pureed consistency solids, regular liquids, and the resident could have regular consistency scrambled eggs. The resident was on aspiration (inhaling food or fluid into the lungs) precautions.
The 3/7/23 quarterly nutrition assessment completed by RD #54 documented the resident received regular puree consistency solids, regular thin liquids, and could have regular scrambled eggs. The resident had no chewing or swallowing concerns at this time. The resident's diet was reviewed with the resident representative as they had admitted to bringing in regular textured food items. The resident representative verbalized understanding of safety and diet.
On 3/23/23 social worker (SW) #55 documented a care plan meeting was held on this date. The resident required set-up and supervision at meals, and was on a regular puree solid texture, thin liquid diet.
The undated care instructions ([NAME]) documented the resident required supervision with set-up for eating; adaptive equipment including [NAME] (spill proof) cups, divided plate, and built up silverware; received a regular diet with pureed texture with thin liquids; and was on aspiration precautions.
During an observation on 4/24/23 at 12:45 PM the resident was sitting at a table in the dining room during the lunch meal. The resident's meal ticket documented a regular puree diet with the word puree highlighted in blue. The ticket documented puree half chicken fajita, puree 1/2 cup refried beans, and puree 1/2 cup fajita blend vegetable. The resident's divided dish contained pureed beans, pureed vegetable, and a chicken fajita that was dry, lumpy, and not smooth (ground meat appearance). At 1:03 PM, certified nursing assistant (CNA) #48 cued the resident to eat their lunch meal. At 1:41 PM, the resident had eaten 25% of the ground chicken.
2) Resident #52 was admitted to the facility with diagnoses including multiple sclerosis and dysphagia (difficulty swallowing). The 2/25/23 Minimum Data Set (MDS) assessment documented the resident had severely impaired cognition, rejected care 1- 3 of 7 days, required extensive assistance of 1 with eating, coughed or choked during meals or while swallowing medications, and had complaints of difficulty or pain when swallowing.
The 2/10/23 comprehensive care plan (CCP) documented the resident had a potential for alteration in nutrition status related difficulty chewing and received a regular level 1 (pureed) consistency and thin liquid diet, and ate in dining room sitting up in their chair,
The revised 4/12/23 CCP documented the resident had a deficit with activities of daily living (ADLs) and required limited assistance of one with eating, ate in the dining room, and was to be seated upright in their chair.
During an observation on 4/24/23 at 1:15 PM, the resident was in the dining room during the lunch meal. The resident's meal ticket documented a regular puree diet with the word puree highlighted in blue. The resident was to receive pureed chicken fajita. The chicken fajita on the resident's divided plate was dry, lumpy, and not smooth (ground meat appearance). Resident #52 independently fed themselves some of the chicken fajita.
During an interview on 4/25/23 at 12:14 PM, cook/ dietary aide #26 stated the lunch meal on 4/24/23 was fajita chicken, peppers and onions, and refried beans. They stated the prep cook knew how many portions of each consistency to make by following the production sheets. During the tray line process, the person who is at the start of the line called out the meal ticket, this included what consistency food and/or beverages that were needed and any adaptive equipment. The person at end of the line checked the meal ticket and the items on the tray to ensure the food and beverages matched. They stated they plated the food during the lunch meal on 4/24/23, they did not recall running out of pureed chicken fajita yesterday and was unaware if they plated the incorrect consistency. If the wrong consistency was plated, the person who checked the tray line should have noticed and requested a new meal with the proper consistency. They stated if a resident did receive the incorrect consistency of food or beverages they could choke.
During an interview on 4/26/23 at 1:10 PM, the Food Service Director (FSD) stated the person at the start of the line should call out the food items including the consistency of the items needed. The person at the end of tray line was supposed to check the meal ticket against the food served on the plate to ensure they matched. Once the trays left the kitchen nursing staff should complete another check to ensure everything matched. If the items on the tray did not match the meal ticket staff should request a new tray. It was important for the residents to receive the correct consistency food and beverage items for safety reasons.
During an interview on 4/25/23 at 1:23 PM, dietary aide #28 stated the person at the end of the tray line was supposed to check the meal ticket and food on the plate to ensure they matched. On 4/24/23 they worked at the end of the line and checked the meal tickets to ensure accuracy. If they observed a tray to have the improper consistency items, they would request a new tray with the correct consistencies. It was important for the residents to receive the proper consistency for safety reasons.
During an interview on 4/26/23 at 2:30 PM, licensed practical nurse (LPN) #47 stated nursing staff should check each meal ticket and food tray to ensure the actual meal matched the meal ticket. If they noticed a resident was provided the wrong consistency, they would let the kitchen and the diet technician know and they would get a new tray for the resident. The resident should not consume the wrong consistency food and beverage items for safety reasons. They would want to be made aware if a resident received the wrong consistency food item and was unaware of any residents that received the wrong diet consistency at lunch on 4/24/23.
During an interview on 4/26/23 at 2:43 PM CNA #48 stated staff knew what type of diet a resident was on by either checking their care plan ([NAME]) or looking at the meal ticket. The nursing staff checked the meal tickets and meal trays to ensure they matched prior to serving the residents. Pureed items should be soft and if staff did not think the items were pureed enough or the wrong consistency they should call down to the kitchen and obtain new items. They did not recall Resident #38's lunch tray on 4/24/23 and was unaware the resident received the wrong consistency food item. It was important to ensure the residents received the correct consistency because they could choke.
During an interview on 4/26/23 at 2:43 PM, LPN Unit Manager #49 stated they expected nursing staff to check the trays for accuracy prior to serving the residents. If the resident received a wrong consistency food item staff should remove the item or the entire tray, call the kitchen to request the correct items, and let a nurse know. If a resident received the wrong consistency food or beverage items, they could choke or aspirate. They were unaware any residents who received the wrong consistency food on 4/24/23 and would expect staff to let them know when something like this occurred.
During a telephone interview on 4/26/23 at 3:14 PM speech language pathologist (SLP) #56 stated a pureed diet meant food items should be a pureed and smooth consistency without lumps. A pureed consistency diet was recommended for a variety of reasons such as issues with swallowing. If a resident received the wrong diet consistency it could lead to possible aspiration issues or worsening dysphagia.
During an interview on 4/26/23 at 3:36 PM, nurse practitioner (NP) #39 stated the residents should receive their diet as ordered. If they received the wrong diet consistency it could increase their risk for aspiration. If a resident received the wrong diet consistency, they would expect a nurse to monitor the resident for signs and symptoms of aspiration, such as coughing. They stated nursing should notify them if the resident was exhibiting signs or symptoms of aspiration.
10NYCRR 415.14(d)(3)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0810
(Tag F0810)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility fai...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility failed to special eating equipment and utensils for residents who needed them for 2 of 2 residents (Residents #30 and 38) reviewed. Specifically, Resident #38 was not provided with adaptive curved utensils or a Kennedy cup (spill-proof drinking cup); and Resident #30 was not provided with weighted utensils and an inner lip plate as care planned.
Findings include:
The facility policy Adaptive Equipment dated 1/19/18 documented that the Director of Rehabilitation or designated therapy staff would ensure that each resident, as appropriate, was provided any necessary equipment and training in its use, designed to facilitate the resident's ability to function independently. This applied to equipment designated to aid self-feeding. The equipment would be listed on the resident's care plan as appropriate. Certified nurse aides (CNA) would notify the Unit Manager and therapy staff of any decline of use of adaptive equipment.
The facility policy Meal Serving-Resident dated 9/24/18 documented that designated dietary staff would be responsible for ensuring that the necessary items were present at mealtime, or were obtained immediately upon request, for the consumption of food. Nursing and other appropriately trained staff would be responsible for fulfilling all non-food requests of residents, feeding residents if needed, and for other dietary services that were part of the resident's care plan. Dietary, nursing, and other appropriately trained staff were also responsible for ensuring all items identified on the tray label were in place, and in reach of the resident.
1) Resident #38 was admitted to the facility with diagnoses including diabetes, dysphagia (difficulty swallowing), and feeding difficulties. The 3/6/23 Minimum Data Set (MDS) assessment documented the resident had severe cognitive impairment, required supervision/set-up assistance for eating, did not have difficulty swallowing, and had functional limitations in range of motion (ROM) for bilateral upper and lower extremities.
The 10/22/22 comprehensive care plan (CCP) documented the resident had potential for alteration in nutrition. The resident was to receive adaptive equipment for eating/drinking that included a Kennedy cup, a right-handed built-up utensils bent to the left, and a divided plate.
The care instructions ([NAME]) documented adaptive equipment for eating and drinking included a Kennedy cup, a right-handed built-up utensils bent to the left, and a divided plate.
The 3/7/23 Quarterly Nutrition Assessment by registered dietitian (RD) #54 documented the resident utilized Kennedy cups, right-handed built-up utensils bent to the left, and a divided plate for adaptive equipment at meals.
Resident #38's meal tickets dated 4/21/23, 4/24/23, and 4/25/23 documented in red lettering Kennedy cups, built up silverware bent left, and a divided dish. The resident was to receive 2 portions of tomato soup in a mug. The resident required supervision and set-up.
Resident #38 was observed without care planned adaptive equipment for eating and drinking:
-On 4/21/23 at 9:50 AM the coffee was not in a Kennedy cup.
-On 4/24/23 at 12:45 PM chocolate Boost (nutritional supplement) was not in a [NAME] and the tomato soup was in a bowel and not a mug.
-On 4/25/23 at 8:52 AM the resident's tray did not include a Kennedy cup or built-up silverware bent to the left. The soup and coffee were in regular hot mugs without lids.
2) Resident #30 was admitted to the facility with diagnoses including dysphagia (difficulty swallowing), muscle weakness, and feeding difficulties. The 1/26/23 Minimum Data Set (MDS) assessment documented the resident had mild cognitive impairment, required supervision/set-up assistance for eating, did not have difficulty swallowing with a mechanically altered diet, and had functional limitations in range of motion (ROM) for bilateral upper and lower extremities.
The 4/15/22 comprehensive care plan (CCP) documented the resident had potential for alteration in nutrition. The resident was to receive adaptive equipment for eating and drinking including Kennedy cups, built up utensils, and an Inner lip plate. A 4/3/23 updated intervention included trialing weighted utensils. The resident participated in a nursing rehabilitation eating and swallowing program which included to ensure the resident had left angled built-up utensils, divided plate, Kennedy cups, and hand over hand assist at times due to hand tremors and droppage. Additional instructions included to put space between the Kennedy cups so the resident could grasp them easily without spillage.
The care instructions ([NAME]) documented adaptive equipment for eating and drinking included a Kennedy cup, built-up left angled utensils, and an inner lip plate. The resident's hand tremors may cause droppage and weighted utensils were being trialed.
Resident #30's meal ticket dated 4/25/23 documented in red lettering Kennedy cups, weighted utensils, an inner lip plate, and an empty bowl at breakfast. The resident required supervision and set-up assistance at meals.
The resident was observed:
- on 4/25/23 at 8:45 AM their breakfast tray was delivered and included hot mugs with lids that did not fit snuggly to the top of the mug. There were no Kennedy cups on the tray.
- on 4/25/23 at 1:06 PM the resident's lunch tray included regular utensils instead of weighted utensils, and a regular plate instead of an inner lip plate.
During an interview on 4/25/23 at 12:14 PM cook/dietary aide #26 stated during the tray line process, the person who is at the start of the line called out the meal ticket including the consistency of food and beverages that were needed and any adaptive equipment. The person at end of the line checked the meal ticket against the items on the tray to ensure the food and beverages matched the meal ticket. The top of the meal ticket indicated what type of silverware or plate the resident needed. They stated that the tray line had not run out of adaptive silverware.
During an interview on 4/25/23 at 12:40 PM, dietary aide #27 stated they called out the tickets at the beginning of tray line which included the food consistency and adaptive equipment. They stated that they had run out of silverware previously, but they were able to add them to the tray prior to it being sent to the unit. If a resident received the wrong utensils, they may not be able to eat.
During an interview on 4/25/23 at 1:23 PM, dietary aide #28 stated they checked the meal tickets at the end of the tray line. They stated that they matched the actual tray with the meal ticket for accuracy. They stated that if items were missing, they would let the supervisor know.
During an interview on 4/26/23 at 1:10 PM, the Food Services Director stated the person at the end of the tray line checked the trays for accuracy and the staff on the resident unit also checked the trays for adaptive equipment, allergies, and appropriate diets. If a resident did not receive the correct adaptive equipment, they may have difficulty eating or drinking.
During an interview on 4/26/23 at 2:43 PM, CNA #48 stated staff knew what type of adaptive equipment a resident needed by either checking their care plan ([NAME]) or looking at the meal ticket. They stated that if the adaptive equipment did not come up on the tray, they would call the kitchen to see if it was in stock. CNA #48 stated that they were told that Kennedy cups were on order as the facility did not have anymore. CNA #48 stated if they only had one [NAME] Cup for the resident, they would put one drink in, wait for the resident to finish it, then rinse it for the next beverage. It was important to have correct adaptive equipment because therapy ordered it for a reason.
During an interview 4/26/23 at 2:30 PM licensed practical nurse (LPN) #47 stated if the correct adaptive equipment was not sent on the tray, they would check the unit pantry to see if there were extras. If the pantry did not have the equipment, they called the kitchen. If a resident did not have the right adaptive equipment, they may not be able to feed themselves.
During an interview on 4/26/23 at 2:43 PM LPN Unit Manager #49 stated that they expected staff to ensure each tray matched the meal ticket prior to delivering the tray. They stated that if the care planned adaptive equipment was not present, they expected staff to call the kitchen. They stated they should be notified if the kitchen did not have the adaptive equipment available. They had not heard of issues with adaptive equipment not being not received. If equipment was missing, they would check the rooms on the unit and talk to the Dietary Manager. If a resident did not have the care planned adaptive equipment it could set the resident back in their activities of daily living and decrease independence. Not having the appropriate adaptive equipment was also a safety and dignity issue.
During an interview on 4/27/23 at 9:22 AM, the Assistant Director of Rehabilitation stated if a resident did not have appropriate adaptive equipment, they could have diminished intakes, increased aspiration risk, and reduced ability to be independent.
10NYCRR 415.14(g)
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Garbage Disposal
(Tag F0814)
Could have caused harm · This affected 1 resident
Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility failed to dispose of garbage and refuse properly for 1 isolated area (the w...
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Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility failed to dispose of garbage and refuse properly for 1 isolated area (the waste fryer oil drums outside the main kitchen). Specifically, the waste fryer oil had been spilled on the ground surrounding the waste drums outside of the main kitchen.
Findings include:
The undated facility policy Fryer Oil and Grease Removal Guidelines documented after the grease was completely cooled it could be transported to the grease trap or other receptacle designed for environmental oil recycling. Look and check the levels in the environmentally responsible container and see if it needed to be emptied by the oil recycling company. Check the area traveled during the removal process to ensure that oil was not spilled or smudged. If any area was soiled with grease or oil, the area must be cleaned.
During observations on 4/20/23 at 1:11 PM and 4/25/23 at 12:55 PM, there were two 55 gallon drums dedicated for waste fryer oil storage outside the back door of the kitchen. The ground around the drums was saturated with spilled grease. A wooden pallet beside the drums was also soiled with grease. The spilled grease extended approximately two feet out and around the drums and pallet which were against the outside of the building.
During an interview on 4/25/23 at 1:00 PM, cook #25 stated that they were responsible for disposing of the waste fryer oil outside of the main kitchen. They stated they were not aware of ever spilling any grease there but thought one of the barrels may have had a leak because the ground was pretty mushy. They stated they told the Food Service Director they suspected a leak about 6 months ago, but they would not have documented it anywhere.
During an interview on 4/26/23 at 1:16 PM, the Food Service Director stated they were not aware of the puddle of grease outside by the fryer oil waste drums, and they had assumed it was mud. They stated no one had brought it to their attention. The Food Service Director stated the grease soaked ground could attract pests.
During an interview on 4/26/23 at 1:16 PM, the Assistant Administrator stated that they were not aware of the spilled grease/fryer oil waste outside of the main kitchen and the grease soaked wooden pallet against the building was a fire hazard.
10 NYCRR 415.14(h)
CONCERN
(D)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Infection Control
(Tag F0880)
Could have caused harm · This affected 1 resident
Based on observation, record review, and interview during the recertification and abbreviated (NY00275715 and NY00300682) surveys conducted 4/19/23-4/27/23, the facility failed to establish and mainta...
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Based on observation, record review, and interview during the recertification and abbreviated (NY00275715 and NY00300682) surveys conducted 4/19/23-4/27/23, the facility failed to establish and maintain an infection prevention and control program designed to provide a safe, sanitary, and comfortable environment and to help prevent the development and transmission of communicable diseases and infections for 1 of 3 residents (Resident #178) reviewed. Specifically, during Resident #178's wound treatment licensed practical nurse (LPN) #5 did not perform appropriate hand hygiene.
Findings include:
The facility policy, Wound Cleansing, modified on 4/25/18 documented wound cleansing would be provided to optimize wound healing and to decrease the potential for wound infection. The procedure included wash hands thoroughly, prepare supplies, apply non-sterile gloves, remove soiled dressing and discard in appropriate receptacle, remove and discard gloves, wash hands thoroughly and apply clean gloves, cleanse wound per physician order, apply treatment and dressing per physician order, and remove and discard gloves, wash hands thoroughly.
Resident #178 had diagnoses including osteomyelitis (bone infection) of vertebra (mid spine area), and bacteremia (bacteria in the blood). The 3/23/23 Minimum Data Set (MDS) assessment documented the resident had intact cognition, required extensive assistance of 2 for bed mobility, did not have infections, had 1 Stage 3 (full thickness tissue loss) pressure ulcer, received application of nonsurgical dressings, and received antibiotics 7 of 7 days.
The comprehensive care plan (CCP) initiated 3/16/23 documented the resident had a pressure ulcer to the coccyx (tailbone). Goals included the pressure ulcer would not show signs and symptoms of infection. Interventions included, apply treatment per physician order and assess for signs and symptoms of infection. The resident was at risk for infection due to bacteremia. Interventions included to administer treatments per medical order and monitor for any adverse reactions.
Physician orders dated 3/29/23 documented Durafiber 2 (wound dressings) apply to coccyx topically every day and evening shift for pressure injury. Cleanse wound with normal saline (NS) and apply Durafiber AG (silver) to wound. Cover with Allevyn Gentle dressing (absorbent, foam dressing).
On 4/25/23 at 1:41 PM a treatment to the resident's coccyx wound was observed with licensed practical nurse (LPN) #5:
- LPN #5 washed their hands, applied clean gloves, and set up the clean area using a barrier, and a trash receptacle for the soiled dressing. LPN #5 removed the soiled dressing, placed it in the trash bag, removed the soiled gloves, and washed their hands.
- LPN #5 applied new gloves without performing hand hygiene and placed a new barrier with dressing supplies. They cleansed the resident's wound with NS and a gauze pad using their gloved left hand. Using only their gloved right hand they cut the Durafiber dressing with scissors, then used their left hand they had cleansed the resident's wound with to apply the clean Durafiber dressing. They cut the Allevyn dressing with their right hand and applied the dressing over the wound.
During an interview on 4/25/23 at 1:48 PM, LPN #5 stated their dirty hand was their right hand, and their left hand was their clean hand. It was important to have one hand clean and the other one dirty so that new germs were not introduced to the wound. Their right hand with the scissors was the dirty hand and they should not have used that hand to apply the dressing as it could potentially cause germs to enter the wound.
During an interview on 4/25/23 at 2:17 PM, the Infection Preventionist (IP) stated they would expect nurses to gather all supplies for a dressing change and place a barrier. If they placed two barriers, they could use the first barrier for the soiled dressing and gloves and the second barrier for the clean supplies. That way, when a nurse changed gloves and washed their hands the barrier was already in place. A nurse should not be using a dirty hand to apply a dressing to a clean area (wound). The risk would be the potential for infection to the wound.
10 NYCRR 415.19
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 observation, record review, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility fai...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, record review, and interview during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure residents had the right to a safe, clean, comfortable, and homelike environment for 4 of 4 occupied resident floors (First, Third, and Fourth floors) reviewed. Specifically,
- the fourth floor had stained ceiling tiles and the elevator alcove had a loose handrail.
- the third floor had a damaged bathroom sink, the soiled utility room did not have a paper towel dispenser, and the dining room window was cracked.
- the first floor had damaged walls and ceilings, unsealed penetrations, an open junction box in the education classroom closet, and the library had two sliding windows that opened more than 6 inches.
Findings include:
The undated facility Window Policy documented the Environment: Common Areas/Nursing Units/Service Hall/Lobby Audit form would be reviewed at the monthly risk management meetings.
The following observations were made on the Fourth Floor:
- on 4/19/23 at 11:46 AM, the elevator alcove had a loose, 1 foot section of handrail.
- on 4/19/23 at 11:50 AM, the hall outside of resident room [ROOM NUMBER] had three dried stained ceiling tiles.
- on 4/24/23 at 11:56 AM, the hall outside of resident room [ROOM NUMBER] had three stained ceiling tiles, two of the tiles were wet.
Work orders dated from 11/20/2020 to 4/4/2023 documented requests for maintenance for the fourth floor stained ceiling tiles, in the hall near resident room [ROOM NUMBER] (in same vicinity as resident room [ROOM NUMBER]).
Monthly safety inspection reports dated 2/1/23, 2/27/23, and 4/3/23 documented the fourth floor hall had stained ceiling tiles.
The following observations were made on the Third Floor:
- on 4/19/23 at 12:15 PM, the bathroom near the nursing station had a damaged sink where the faucet had been installed in the sink. The sink was loosely attached to the wall.
- on 4/19/23 at 12:22 PM, the soiled utility room lacked a paper towel dispenser and paper towels.
- on 4/24/23 at 2:11 PM, the dining room window had a 3 foot x 2 foot crack and there was clear tape over approximately 18 inches long on the bottom portion.
During an interview on 4/24/23 at 2:11 PM activity leader #24 stated the third floor dining room window had been cracked for about a month. They stated the crack had started at the bottom of the window and had worked up to the top of the window.
During interviews on 4/24/23 at 2:13 PM and 4/26/23 at 2:25 PM, the Maintenance Director stated that in the fall of 2022 a resident threw something at the third floor dining room window causing the crack. The window was secured while waiting for better weather. The cracked window created a potential hazard. They stated they were not aware the crack in the window was not fully taped and would expect staff to report if the crack was spreading. The Maintenance Director stated that there were no work orders for the broken window. They stated the vendor that was usually used by the facility had recently converted into a window parts supplier and not a window installing company. They stated they had called the vendor and the voicemail was full. The facility had not started the process to get another vendor to replace the window.
The following observations were made on the First Floor:
- on 4/19/23 at 10:48 AM, resident room [ROOM NUMBER] had a damaged section of wall behind the B side resident bed.
- on 4/19/23 at 2:15 PM, resident room [ROOM NUMBER] had a damaged section of wall behind the B side resident bed, and the area around the bathroom door was scratched.
- on 4/19/23 at 2:55 PM, the north dining room area, near the handwash sink, had a damaged section of lower soffit sheetrock shelf. The soffit height was approximately 3 feet off the ground.
- on 4/19/23 at 2:59 PM, the dementia unit soiled utility room solid ceiling had an unsealed 3/4 inch conduit penetration and an unsealed 4 inch x 4 inch hole with data wires passing through into the space between the solid ceiling and the flat ceiling above.
- on 4/20/23 at 9:06 AM, the dementia unit tub room had a 1/2 inch x 10 inch damaged section of solid ceiling.
- on 4/20/23 at 9:30 AM, the first floor education classroom closet had dead low voltage wires coming out of an old call bell system junction box.
- on 4/20/23 at 9:47 AM, resident room [ROOM NUMBER] had a 3 foot x 3 foot section of damaged wall, the wall radiator metal cover was loose, and the bathroom had a damaged towel bar with only the end posts present.
- on 4/20/23 at 9:57 AM, the library had two sliding windows that opened approximately three feet wide. The window locks that prevented the windows from opening more than 6 inches were broken.
During an interview on 4/20/23 at 9:57 AM, the Assistant Administrator stated the library windows were used for COVID-19 window visits.
During an interview on 4/25/23 at 10:39 AM, the Housekeeping Director stated if housekeeping staff observed damaged walls, they should tell the nursing unit clerks or Unit Managers who would complete work orders. The Housekeeping Director stated different staff was assigned to do a general survey of environmental issues such as clear hallways and ensuring rooms were in good working order. They stated that besides the stained ceiling tiles on the fourth floor, they were not aware of any of the other items identified during the tour of the facility. The Housekeeping Director stated housekeeping staff were in resident rooms everyday cleaning and disinfecting and were trained to identify issues. They stated they toured the resident floors daily and entered resident rooms as needed. Twice a week 2 to 3 rooms on each floor were randomly cleaned and all resident rooms were deep cleaned monthly. The Housekeeping Director stated work orders were completed in order from critical to medium.
During an interview on 4/26/23 at 2:25 PM, the Maintenance Director stated work orders could only be found for the fourth floor stained ceiling tiles. They stated there were no documented inspections of resident rooms, and the entire facility was checked monthly by the risk management team which included Administration, Unit Managers, Housekeeping Director, and the Food Service Director. The Maintenance Director stated the first floor library window guards were damaged during one of the COVID-19 window visits in 2020 and 2021. They stated that the facility was the residents' home, and it should look nice and provide a safe environment.
During an interview on 4/26/23 at 2:30 PM, the Assistant Administrator stated the cracked window, and the other items observed during the tour of the facility were not homelike.
10 NYCRR 415.29(j)(1)
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Food Safety
(Tag F0812)
Could have caused harm · This affected multiple residents
Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure food was stored and prepared in accordance with profession...
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Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure food was stored and prepared in accordance with professional standards for food service safety for 1 of 1 kitchen (main kitchen) reviewed. Specifically, the main kitchen's tray service line cooler was propped open and not maintaining proper temperature, floors were in disrepair, the ceiling was damaged, and cooking and storage equipment was unclean.
Findings include:
The facility policy Dietary Food and Supply Orders-Storage dated 10/26/2018, documented refrigerator storage was to be 41 F (Fahrenheit) or below.
The facility policy Kitchen, Dining and Dietary Equipment Routine Cleaning dated 9/7/2018 documented daily staff assignments included areas of equipment to be cleaned or kept in order after each meal service including the general cooking area, and general kitchen area. Cooking surface of the grill was to be cleaned at least once daily and kept free of encrusted grease and other soil. The monthly cleaning schedule included all counters and shelves, and pots and pans area racks.
The undated Weekly Cleaning List documented:
- properly clean grill and stovetop; and
- properly clean friers (AS NEEDED).
1. Tray Line Cooler
During an observation on 4/20/23 at 12:05 PM two refrigerators were propped open on the tray service line during lunch assembly. The left cooler had cottage cheese that was measured at 48 F. The right cooler had hardboiled eggs measured at 54 F and American cheese at 53 F. The door seal was tattered along the bottom edge of the left unit.
During an interview on 4/20/23 at 12:09 PM, the Food Service Director stated the cooks checked the final cooking temperatures, and the hot items on the line, but they did not check the cold holding temperatures during meal service. The cold holding equipment was checked once a day, typically in the morning. The Food Service Director stated the coolers were propped open at the start of each meal service and the coolers were stressed to the max.
During an interview on 4/20/23 at 12:47 PM, dietary aide #20 stated the cottage cheese was discarded at the end of the shift, the lettuce salads were re-wrapped and moved to another refrigerator in the kitchen, the shelf stable drinks were moved to another cooler, and the items on the bottom shelf (American cheese and hard boiled eggs) remained in the coolers.
During an observation on 4/20/23 at 12:50 PM the two coolers from the tray line were closed and pushed against the wall. Dietary aide #20 began removing some of the contents to move to other units. They did not measure the temperature of the contents.
During an observation on 4/20/23 at 1:25 PM, the hardboiled eggs were measured at 58 F and the American cheese was measured at 58 F. Both items were in the left side of tray line cooler. A bowl containing individual packets of sour cream was on the bottom shelf of the cooler. The right side of the cooler was empty.
During an observation on 4/20/23 at 2:16 PM, the American cheese was measured at 56 F and hard boiled eggs were measured at 55 F. These temperatures were confirmed with the Food Service Director who measured them with the facility and included hardboiled eggs at 55 F, American cheese at 55 F, and the approximately 30 (1) ounce sour cream packets were measured at 53 F.
During an interview on 4/20/23 at 2:16 PM, the Food Service Director stated they did not check the temperatures of the tray line coolers after meal service, but they knew they should be shut to come back to temperature. They stated the doors to the coolers had been closed since the end of the lunch service and they were usually locked at that time. The hardboiled eggs, American cheese, and sour cream would have been in that cooler all day. The Food Service Director stated food was allowed to be out of an acceptable temperature range for up to two hours. They stated they were not aware these items had been out of temperature for more than two hours. It was potentially dangerous to leave food out of temperature for more than two hours.
2. General Kitchen Cleanliness
On 4/19/23, between 10:30 AM and 11:15 AM, observations of the main kitchen included:
- two metal storage racks in the clean area were rusty and not cleanable. The racks contained miscellaneous baking measuring containers, baking sheets, and catering supplies.
- the floor near the dish machine area had a 2 foot x 2 foot section of plywood. This material could absorb water, was a potential mold risk, and was not cleanable.
- the floor in the dish machine area was missing grout and there was standing water between the tiles. The spaces between the tiles were not cleanable and created a potential for pests in the kitchen.
- the metal surfaces of the deep fryer were sticky and not clean. The metal side wall of the steamer, next to the deep fryer, was also sticky and not clean.
- the metal side of the stove top, next to the flat top unit was sticky and not clean.
- there were two frying pans on a hanging rack near the cook's area that were soiled and caked with black debris.
- the solid ceiling over the cook's area was soiled with unknown debris. There was a damaged 2 foot x 6 inch section of solid ceiling.
- multiple sections of the tray line area had sections of peeling floor material that was not cleanable and was a tripping hazard.
During an interview on 4/19/23 between 10:54 AM and 11:15 AM, the Food Service Director stated the deep fryer was last used for the dinner meal on 4/18/23, was supposed to be cleaned after each use, and should be wiped down and cleaned weekly as per the weekly cleaning list. They stated it appeared that the oil on the deep fryer surfaces had been there for more than one week, and there was no documentation of who was responsible for the last weekly cleaning. The Food Service Director stated the two frying pans hanging in the cook's area were not being used and should have been removed from the kitchen.
During an observation on 4/20/23 at 1:05 PM, the main kitchen cooks area had a floor to ceiling sheetrock pillar and the sheetrock was loose and in disrepair.
During an interview on 4/26/23 at 1:54 PM, the Maintenance Director stated they were aware of flooring concerns in the dish machine area and there was no official documentation that the facility was in the process of repairing the floor. They stated that the maintenance department had attempted to repair the section of floor under the 2 foot x 2 foot section of plywood, and this area had not yet been fully repaired. The Maintenance Director was not aware of the loose pillar and the damaged solid ceiling in the cook's area. They stated that it was important for the main kitchen to be maintained so that staff could work in a safe environment.
During an interview on 4/26/23 at 2:13 PM, the Food Service Director stated they were not aware of the loose pillar in the cook's area and could not find any work orders for the pillar. They stated they thought the metal storage racks were just dirty and was not aware they were rusted. They stated they had checked that the items on the racks were clean but not the condition of the rack itself. The Food Service Director stated it was important for the main kitchen to be maintained so that staff could work in a safe environment.
10NYCRR 415.14(h)
MINOR
(C)
Minor Issue - procedural, no safety impact
Deficiency F0577
(Tag F0577)
Minor procedural issue · This affected most or all residents
Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure results of the most recent Federal/State survey were poste...
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Based on observation, interview, and record review during the recertification survey conducted 4/19/23-4/27/23, the facility failed to ensure results of the most recent Federal/State survey were posted in a place readily accessible to residents, family members, and legal representatives of residents. Specifically, the results of the most recent Federal health recertification survey conducted 10/16/20 were not posted in a location that would allow individuals to examine the survey results without having to ask to see them; and the results of the most recent Life Safety Code Federal survey conducted on 10/15/20 were not posted.
Findings include:
During a Resident Council meeting on 4/20/23 at 10:03 AM an anonymous resident stated they did not know where the previous survey results were posted. The remaining 10 residents agreed.
During an observation on 4/21/23 at 9:27 AM the Plan of Correction three-ring binder was in the lobby behind the front desk and did not include the Life Safety Code Federal survey results from 10/15/2020.
During an interview on 4/21/23 at 9:28 AM, the Administrator stated that they were not aware that the Life Safety Code survey results were missing from the Plan of Correction binder. They stated they were aware that the results were required to be placed in the binder. The Administrator stated the staff at the front desk checked that the required documents were in the binder weekly. The Administrator stated residents had the right to view survey results and plans of correction.
During an observation on 4/27/23 at 9:48 AM the Plan of Correction three-ring binder was in the lobby behind the front desk and included the results from the Federal health recertification survey from 10/16/20. Individuals had to request the binder from the receptionist to view the results.
During an interview on 4/27/23 9:48 AM receptionist #7 stated the survey results were behind the desk. The receptionist removed the binder from a metal file rack located behind the reception area. The receptionist stated if someone wanted to review the survey results, they would have to ask them for the binder.
During an interview on 4/27/23 at 10:15 AM the Social Services Director stated they were responsible for running Resident Council. They stated that residents were told where the survey results were kept but not all residents remembered. The Social Services Director stated that a resident would have to ask someone to see the results. They stated they were unaware the results should be posted in a location that would allow an individual access without having to ask.
During an interview on 4/27/23 at 10:50 AM, the Administrator stated the survey results should be posted and available to residents and there was one survey results binder behind the front desk. The Administrator stated that there used to be one in the lobby, but residents would leave with it so now it was kept behind the desk.
10NYCRR 415.3(c)(v)