CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Comprehensive Assessments
(Tag F0636)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure a comprehensive Minimum Data Set (MDS - a federally mandated...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure a comprehensive Minimum Data Set (MDS - a federally mandated assessment instrument completed by facility staff for care planning) was completed and submitted timely for two sampled residents (Resident #325 and #224) out of 14 sampled residents. The facility census was 27 residents.
1. Record review of Resident #325's Face Sheet showed he/she was admitted to the facility on [DATE].
Record review of the resident's Physician's Order Sheet (POS) showed he/she was admitted to hospice services (end of life care) on 8/11/22.
Record review of the resident's CMS MDS database submissions showed:
-An Entry MDS assessment with an Assessment Reference Date (ARD) of 6/15/22.
-A Discharge MDS assessment with an ARD of 6/28/22.
-The last assessment was an Entry MDS assessment with an ARD of 6/30/22.
--NOTE: No documentation of an admission Assessment as of 9/15/22.
Record review of the resident's facility Electronic Medical Record (EMR) showed:
-An Entry MDS assessment with an ARD of 6/15/22.
-An admission MDS assessment with an ARD of 6/28/22 with the code Discharge - Return Anticipated.
--NOTE: The admission MDS assessment was submitted as a Discharge - Return Anticipated assessment.
-An Entry MDS assessment with an ARD of 6/30/22.
-A Significant Change MDS assessment with an ARD of 8/24/22 in process. The assessment was not completed, validated, finalized, or transmitted.
2. Record review of Resident #224's Face Sheet showed he/she was admitted to the facility on [DATE].
Record review of the resident's CMS MDS database submissions showed:
-The last assessment was an Entry MDS assessment with an ARD of 8/15/22.
Record review of the resident's facility EMR showed an admission MDS assessment with an ARD of 8/28/22 in process. The assessment was not completed, validated, finalized, or transmitted.
3. During an interview on 9/14/22 at 2:00 P.M., the MDS Coordinator said:
-He/she was new to the position in August 2022.
-He/she had not been trained on how to do MDS submissions yet.
-He/she did not know how to see if an MDS was accepted, rejected, or transmitted.
-He/she was trying to catch up on late MDS submissions from prior to his/her hire date.
-The MDS should be accurate and reflect the resident's current condition.
-He/she could not submit an MDS until the Director of Nursing (DON) signed them since he/she was the facility Registered Nurse (RN).
During an interview on 9/15/22 at 4:42 P.M., the DON said:
-He/she was new to the position in July 2022.
-He/she was doing MDS submissions when he/she was hired until the MDS Coordinator was hired.
-He/he had not been trained on how to complete MDS's, however he/she used to do MDS's years ago before the MDS 3.0 system.
-He/she expected the MDS's to be completed, validated, finalized, and transmitted timely.
-He/she did not know how to see if an MDS was accepted, rejected, or transmitted.
-The MDS should be accurate and reflect the resident's current condition.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0655
(Tag F0655)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to develop and implement a base line care plan consistent with the res...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to develop and implement a base line care plan consistent with the resident's specific conditions, needs, and risks, to provide effective person centered care that met professional standards of quality of care within 24 hours of admission to the facility for two sampled residents (Resident's #274 and #276) out of 14 sampled residents. The facility census was 27 residents.
Record review of the facility's undated policy titled Care Plan-Temporary showed:
-Staff were to ensure the resident's immediate care needs were met and maintained by creating a temporary care plan within 24 hours of admission.
-Staff were to use the temporary care plan until a comprehensive assessment had been completed.
1. Record review of Resident #274's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Unspecified injury of head.
-Contusion (bruise) of the scalp.
-Anxiety (a feeling of worry, nervousness, or unease, typically about an imminent event or something with an uncertain outcome).
-Fever.
-Alzheimer's disease (progressive mental deterioration that can occur in middle or old age, due to generalized degeneration of the brain. It is the most common cause of premature senility).
Record review of the resident's Baseline Care Plan showed it was completed on 9/13/22, five days after the resident was admitted to the facility.
2. Record review of Resident #276's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Open wound to left lower leg.
-Sepsis (a serious condition resulting from the presence of harmful microorganisms in the blood or other tissues and the body's response to their presence, potentially leading to the malfunctioning of various organs, shock, and death).
-Pain.
-Bacteremia (the presence of bacteria in the blood).
Record review of the resident's Baseline Care Plan showed it was completed on 9/14/22, five days after the resident was admitted to the facility.
3. During an interview on 9/14/22 at 2:00 P.M., the Minimum Data Set (MDS a federally mandated assessment tool completed by facility staff for care planning) Coordinator said:
-He/she was not trained on care plans.
-He/she did not know he/she was responsible for care plans.
-He/she recently found out he/she would be responsible for care plans starting 9/19/22.
During an interview on 9/14/22 at 2:09 P.M., the Director of Nursing (DON) said staff had not yet completed a full body assessment at that time.
During an interview on 9/15/22 at 4:39 P.M., the DON said:
-He/she expected care plans to be up to date, accurate, and reflect the resident's condition.
-The MDS Coordinator was responsible for completing care plans.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Comprehensive Care Plan
(Tag F0656)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Record review of Resident #325's undated face sheet showed he/she was admitted on [DATE] with the following diagnoses:
-Alcoh...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 2. Record review of Resident #325's undated face sheet showed he/she was admitted on [DATE] with the following diagnoses:
-Alcoholic Cirrhosis of the Liver (the destruction of healthy liver tissue due to excessive alcohol consumption) with Ascites (accumulation of fluid causing swelling of the abdomen).
-Metabolic Encephalopathy (any abnormal condition of the structure or function of brain tissues, especially chronic, destructive, or degenerative conditions)
Record review of the resident's POS September 2022 showed the resident was admitted to hospice (end of life care) on 8/20/22.
3. During an interview on 9/14/22 at 9:41 A.M. Certified Nursing Assistant (CNA) B said:
-He/she knew how to take care of the residents by looking at the care plans.
-The care plans were located on the computer and in a book at the nurse's station.
-He/she thought the Director of Nursing (DON) was the one who updated care plans.
During an interview on 9/14/22 at 9:46 A.M. Licensed Practical Nurse (LPN) A said:
-Care plans were located in a book at the nurse's station.
-He/she was unsure how often the care plan book was updated.
-The Minimum Data Set (MDS a federally mandated assessment instrument completed by facility staff for care planning) Coordinator or the DON were responsible for updating care plans.
-He/she would expect the care plan to be resident specific.
-He/she would expect the resident's care plan to include hospice care.
-There was a hospice care plan located in the hospice binder which all care staff have access to.
Record review of the resident's care plan updated 6/16/22 showed no interventions regarding hospice care.
During an interview on 9/14/22 at 11:10 A.M., the DON said that there was no comprehensive Care Plan completed for Resident #15.
On 9/15/22 at 4:40 P.M., the DON said:
-The MDS Coordinator was supposed to ensure the care plans were comprehensive and represented the health care status of the resident.
-The comprehensive care plans were to be completed timely.
-He/she would expect the resident's care plan to show that hospice care was care planned.
-He/she expected all care plans to be up-to-date and show the residents' current condition.
Based on observation, interview and record review, the facility failed to ensure comprehensive care plans were developed to show the health care needs of the residents and interventions to address care needs for two sampled residents (Resident's #15 and #325) out of 14 sampled residents. The facility census was 27 residents.
1. Record review of Resident #15's Face Sheet showed he/she was admitted on [DATE] with diagnoses including respiratory failure (condition that makes it difficult to breathe on your own), Chronic Obstructive Pulmonary Disease (COPD, a chronic inflammatory lung disease that causes obstructed airflow from the lungs), high blood pressure, diabetes (a disease in which the body ' s ability to produce or respond to the hormone insulin is impaired, resulting in abnormal metabolism of carbohydrates and elevated levels of glucose in the blood and urine) and heart failure (a chronic, progressive condition in which the heart muscle is unable to pump enough blood to meet the body's needs for blood).
Record review of the resident's admission Minimum Data Set (MDS-a federally mandated assessment tool completed by facility staff for care planning) dated 8/23/22, showed the resident:
-Needed extensive assist with mobility and transfers, was totally dependent for dressing, hygiene, bathing, toileting and was occasionally incontinent of bladder and bowel.
-Used a wheelchair for mobility, and had limited range of motion with his/her upper extremities.
-Showed the resident received no respiratory treatments or oxygen.
Record review of the resident's Medical Record showed the resident did not have a Comprehensive Care Plan documented.
Record review of the resident's Physician Order Sheet (POS) dated 9/2022, showed physician's orders for:
-Budesonide suspension (for breathing treatment) 0.5 milligram (mg)/2 milliliter (ml); 1 vial twice daily, rinse mouth after use (ordered 9/2/22).
-Ipratropium-Albuterol solution (for breathing treatment) 0.5 mg-3 mg/3 ml; 1 vial four times daily, rinse mouth after use (ordered 9/2/22).
-Oxygen at 4-5 liters per minute per nasal cannula continuous (ordered 9/2/22).
-Change oxygen and breathing treatment tubing monthly once a day on the first Wednesday of the month (ordered 9/2/22).
-Trilogy (an all-in-one ventilation device, capable of delivering both invasive and non-invasive ventilation modes) at night with oxygen at 5 liters per minute (settings are pre-set on machine) at bedtime (ordered on 9/2/22).
-Amlodipine (a calcium channel blocker used to relax the muscles of the heart to treat high blood pressure) 5 mg at bedtime for high blood pressure (ordered 9/2/22).
-Gabapentin (an anticonvulsant medication primarily used to treat partial seizures and neuropathic pain) 400 mg three times daily for muscle relaxant (ordered 9/2/22).
-Humalog Insulin (a rapid-acting human insulin analog used to lower blood sugar) 100 units; 8 units three times daily with meals for diabetes (ordered 9/2/22).
Observation on 9/12/22 at 2:19 P.M., showed the resident was alert and oriented, was sitting on his/her bed wearing his/her nasal cannula and was completing a crossword puzzle. His/her call light was within reach. There was a Trilogy on the resident's nightstand with a face mask laying next to it, uncovered. The resident said:
-He/she wore the trilogy (facemask) at night and he/she had to wear oxygen consistently throughout the day.
-He/she used both an oxygen concentrator and a portable oxygen tank.
-He/she also received breathing treatments.
-He/she received all of his/her medications timely and daily.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0679
(Tag F0679)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review,the facility failed to ensure that an ongoing activities program was being com...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review,the facility failed to ensure that an ongoing activities program was being completed that met the residents' physical, mental, and psycho-social needs for one sampled resident (Resident #4) out of 14 sampled residents. The facility census was 27 residents.
An Activities Policy was requested and not received from the facility at the time of exit.
1. Record review of Resident #4's face sheet showed he/she was admitted to the facility on [DATE] with the following diagnoses:
-Lymphedema (swelling of body tissue due to a build-up of fluid).
-Cellulitis (an infection of deep skin tissue) of left lower limb.
-Anxiety Disorder (a psychiatric disorder causing feelings of persistent anxiety).
-Chronic Pain (pain that lasts over three months).
During an interview on 9/12/22 at 1:24 P.M. the resident said:
-Activities do not normally happen.
-The main activity that the facility does was bingo.
-The facility used to do a lot more activities, but they stopped for some reason.
During an interview on 9/13/22 at 12:31 P.M. the resident said:
-No activities had been done today.
-The activities were few and far between.
-The activities that were actually done were hard to keep track of.
-The facility did not tell residents when activities were canceled, but they did not typically do activities, so there was no activity to cancel.
-He/she wished there were more activities like exercise classes and art classes.
-He/she would like more stimulating activities.
Record review of the posted activities calendar on 9/13/22 at 11:52 A.M. showed noodle ball was going to be the scheduled activity at 2:00 P.M.
Observation on 9/13/22 at 2:09 P.M. showed no organized activities being held at that time in the common area.
Record review of the activities calendar on 9/14/22 at 8:03 A.M. showed the game Farkle was going to be the scheduled activity at 10:00 A.M.
During an interview on 9/14/22 at 8:31 A.M. Licensed Practical Nurse (LPN) A said:
-There was not a current activities coordinator/director.
-Certified Medication Technicians (CMT's) and Certified Nursing Assistants (CNA's) were the staff that usually did the organized activities with the residents.
-Bingo was usually the only organized activity that was done within the facility.
Observation on 9/14/22 from 9:52 A.M. to 10:30 A.M. showed no organized activities being held in the common area at that time.
During an interview on 9/14/22 at 9:52 A.M. CNA D said:
-Bingo was the only activity that he/she knew of that was being held.
-He/she and the other CNA's try to do individual activities with the residents.
During an interview on 9/14/22 at 12:34 P.M. CMT B said:
-He/she was the one that ran a lot of the activities.
-He/she was not sure if there was a place to put activity preferences.
-He/she was not sure if there was a procedure in place for residents to sign-in when they go to activities.
-He/she did not document residents who attended activities.
Observation on 9/14/22 at 3:00 P.M. showed no organized activities being held at that time in the common area.
During an interview on 9/15/22 at 9:45 A.M. the Business Office Manager (BOM) said:
-He/she voluntarily helped as the activities coordinator/director.
-His/her main job of BOM and Social Services Director take up most of his/her time.
-Activities get the least amount of his/her attention.
During an interview on 9/15/22 at 4:40 P.M. the Director of Nursing (DON) said:
-The activities director was responsible for holding organized activities.
-He/she was not sure if activity attendance was being documented.
-He/she was not sure who audits activities to make sure they were getting done.
-He/she was aware that activities were not being followed per the activity calendar.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Pressure Ulcer Prevention
(Tag F0686)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure resident's who admitted to the facility with pr...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure resident's who admitted to the facility with pressure sores (injuries to skin and underlying tissue resulting from prolonged pressure) had an admission skin assessment, had a description of the wounds, had wound measurements, had the appropriate type and stage of wound documented, had treatment orders for all wounds within four hours of admission, and documentation of the physician being notified of the wounds for one sampled resident (Resident #274) who admitted to the facility on [DATE] with a pressure sores to his/her left buttock, right buttock, and left heel; failed to ensure monitoring to prevent pressure sores by failing to accurately document bathing sheets to show changes in the skin, failing to assess and document weekly skin assessments, failing to notify the physician and obtain physician's orders for wound treatment, failing to monitor, stage, reassess and document the resident's pressure sore once it was identified, failing to provide treatment to the resident's pressure sore once identified, and to complete a care plan for the resident with interventions for addressing the resident's pressure sore for one sampled resident (Resident #21) out of 14 sampled residents. The facility census was 27 residents.
Record review of the facility's undated policy admission Nurse's Note showed staff were to complete a full body assessment, upon admission, and document the site and size of any wounds.
Record review of the facility's undated policy Wound Care and Treatment showed staff were required to have a specific order for treatment of wound.
Record review of the facility's undated policy Wound Dressings showed pressure ulcer stages were defined by:
-Stage 1: redness only, no break in the skin.
-Stage 2: partial thickness tissue loss.
-Stage 3: full thickness tissue loss, which involved damage to the tissue under the skin, which could extend to, but not through, the fascia (a thin casing of connective tissue that surrounds and holds every organ, blood vessel, bone, nerve fiber and muscle in place).
-Stage 4: full thickness skin loss with extensive damage to muscle, bone, or supporting structures such as tendons.
-Unstagable pressure ulcers were not included in the policy.
Record review of the National Institute of Health's article National Pressure Ulcer Staging System dated 2007 showed pressure ulcer stages were defined by:
-Stage 1: intact skin with non-blanchable redness (pressing one's finger on the area does not force blood out of the capillaries and make the skin paler or white) of a localized area.
-Stage 2: partial thickness loss of tissue, presents as a shallow opening with a red/pink wound bed (the base of a wound), may also appear as an intact or open blister.
-Stage 3: full thickness tissue loss, subcutaneous fat may be visible, bone/tendon/muscle cannot be exposed.
-Stage 4: full thickness tissue loss with exposed bone/tendon/muscle.
-Deep Tissue Injury: localized area of purple or maroon on intact skin or a blood-filled blister due to damage of underlying soft tissue from pressure or shearing, may be proceeded by skin that is painful, firm, mushy, boggy (an abnormal texture of tissues characterized by sponginess, usually because of high fluid content), or warmer/cooler than surrounding skin. This area may rapidly evolve to expose additional layers of tissue.
Record review of the facility's undated Pressure Ulcer - Care and Prevention policy showed:
-The purpose of the policy was to prevent and treat further breakdown of pressure ulcers.
-The nurse is responsible for carrying out the treatment as ordered by the attending physician and implementing measure to prevent pressure ulcers.
-Staff were to observe skin. Any persistent reddened area that remains after pressure is relieved is a high risk area for a pressure ulcer to begin.
1. Record review of Resident #274's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Unspecified injury of head.
-Contusion (bruise) of scalp.
-Anxiety (a feeling of worry, nervousness, or unease, typically about an imminent event or something with an uncertain outcome).
-Fever.
-Alzheimer's disease (a brain disorder that usually starts in late middle age or old age and gets worse over time; symptoms include loss of memory, confusion, difficulty thinking, and changes in language, behavior, and personality).
Record review of the resident's Progress Notes dated 9/8/22 showed:
-The resident was admitted on [DATE] with a laceration (a deep cut or tear in skin or flesh) to his/her forehead.
-NOTE: There was no documentation regarding that the resident had pressure wounds to his/her left and right buttock or the left heel wound.
-NOTE: There was no documentation regarding the stage of the pressure wounds to his/her left and right buttock or the left heel wound.
During an interview on 9/12/22 at 11:06 A.M., the resident's family member said:
-The resident had a dark purple/black, boggy (an abnormal texture of tissues characterized by sponginess, usually because of high fluid content) area on his/her left heel that was approximately the size of an orange.
-This wound was present the day the resident was admitted , he/she was not sure if the wound was present during hospitalization.
-NOTE: The resident was admitted five days prior.
Record review of the resident's Event Report dated 9/13/22 showed:
-The resident had a skin tear, a wound to the left buttock measuring 2.5 centimeters (cm) by 2.0 cm, a wound to his/her right buttock measuring 7.5 cm by 2.0 cm, and a wound to his/her left heel measuring 5.5 cm by 5.0 cm.
-Staff documented the contributing factors were that the resident had received a bed bath and his/her brief was wet.
-NOTE: This report was completed six days after the resident was admitted .
-NOTE: This report did not stage the wounds on the left buttock, the right buttock, or the left heel.
Record review of the resident's Physician's Order Sheet (POS) dated 9/22 showed:
-Hospice (end of life care) staff had requested, and the physician had ordered, the resident's heels to be floated (heel should be positioned in such a way as to remove all contact between the heel and the bed) while he/she was in bed.
-The physician entered an order on 9/13/22 for wound care to the resident's left heel, left buttock, and right buttock.
-NOTE: There were no treatment orders for the resident's left and right buttock and left heel pressure sores prior to 9/13/22.
Record review of the resident's Treatment Administration Record (TAR) dated 9/22 showed:
-The physician ordered treatments for the left heel, left buttock, and right buttock on 9/13/22.
--This was six days after the resident admitted to the facility.
-There were no treatment orders prior to 9/13/22.
Record review of the resident's Baseline Care Plan dated 9/13/22 showed:
-Staff did not mark the resident as having an existing pressure ulcer or existing other skin issue.
-NOTE: There was no documentation showing the resident was admitted with pressure sores on his/her left and right buttock and left heel.
-NOTE: There was no documentation showing the stage of the pressure sores on his/her left and right buttock and left heel.
Record review of the resident's Braden Scale (for Predicting Pressure Sore Risk) dated 9/13/22 showed:
-Licensed Practical Nurse (LPN) B documented the resident required minimum assistance during transfers resulting in a score of moderate risk for pressure ulcers for the resident.
-NOTE: Progress Note dated 9/10/22 showed the resident required maximum assistance for transfers.
During an interview on 9/13/22 at 1:55 P.M., LPN A said:
-Staff were to complete a full body skin assessment when a resident was admitted to the facility.
-If he/she found a wound, he/she would notify the doctor to get an order for treatment.
-Nurses were required to do full skin assessments daily.
Record review of the resident's Nurse TAR dated 9/22 showed staff completed ordered treatments to the resident's left heel, left buttock, and right buttock daily starting 9/14/22.
During an interview on 9/14/22 at 10:53 A.M., LPN B said the wound on the resident's left heel was a deep tissue injury (purple or maroon localized area of discolored intact skin or blood-filled blister due to damage of underlying soft tissue from pressure and/or shear).
During an interview on 9/14/22 at 2:00 P.M., the Minimum Data Set (MDS-a federally mandated assessment tool completed by facility staff for care planning) Coordinator said:
-He/she was not aware he/she was responsible for skin assessments.
-He/she would start to measure all wounds.
During an interview on 9/15/22 at 2:01 P.M., LPN B said:
-A full body skin assessment was to be done within four hours of a resident's admission to the facility.
-If there was no order for wound treatment, he/she would contact the wound nurse and the physician to get an order before attempting any treatment.
-Staff were to complete a full body skin assessment of each resident weekly or more often.
-Staff were to measure all wounds once a week.
During an interview on 9/15/22 at 4:39 P.M., the Director of Nursing (DON) said:
-Staff were expected to complete a full body assessment upon admission of a resident.
-The full body assessment was to be documented in the resident's Progress Notes.
-The physician should be notified timely of all wounds for treatment orders.
-All nurses were responsible for measuring wounds and documenting the measurements in the wound book, which he/she could not find.
-All nurses were responsible for staging pressure ulcers.
2. Record review of Resident #21's Face Sheet showed he/she was admitted on [DATE], with diagnoses including high blood pressure, heart disease (A type of disease that affects the heart or blood vessels), muscle weakness, and a respiratory infection (infections of parts of the body involved in breathing, such as the sinuses, throat, airways or lungs).
Record review of the resident's admission MDS dated [DATE], showed the resident:
-Was alert and oriented needed extensive assistance with bed mobility, transfers, and had occasional incontinence of bowel and bladder.
-Was totally dependent for toileting, bathing and hygiene, had limited range of motion with her upper extremities and used a wheelchair for mobility.
-Was at risk for pressure sores, but was admitted with no pressure sores and had no unhealed pressure sores.
Record review of the resident's Nursing Notes dated 8/16/22 to 8/28/22 showed:
-The nurse documented daily skilled notes regarding the resident's health status.
-There was no documentation showing the resident had any pressure sores, wounds or red areas.
Record review of the resident's Initial and Weekly wound documentation dated 8/17/22 showed:
-The resident had no wounds.
-There were no further documents of wound care documentation in the electronic record.
Record review of the resident's Weekly Skin Assessments dated 8/18/22 showed:
-The resident had a shoulder bruise and pitting edema but did not show that the resident had any open wounds/pressure ulcers.
-There were no additional weekly skin assessments in the resident's medical record.
Record review of the resident's weekly bath sheets showed:
-The resident received bathing at least twice weekly.
-From 8/16/22 to 8/29/22 there was no documentation showing the resident had any wounds, open areas, pressure sores or skin issues.
-The bath sheet dated 8/29/22 showed the resident had no open areas, wounds or pressure sores on his/her buttocks.
Record review of the resident's Nursing Notes showed:
-On 8/29/22 the resident was alert and oriented with confusion. He/she had a small open area on his/her right buttock approximately 1 cm in diameter. The area was cleaned and barrier cream was applied. The nurse documented he/she had maintenance get a recliner for the resident to sit in instead of his/her wheelchair while he/she was in his/her room.
-The nursing note did not show the nurse notified the physician for treatment orders for the wound and there was no documentation showing what the treatment orders were if received.
-There were no nursing notes from 8/30/22 to 9/12/22 that showed that any wound care treatments were administered, that the nursing staff was monitoring the wound or measuring it.
-There was no documentation showing how the resident's wound was progressing.
-There was no documentation regarding what stage the wound was in the nursing notes.
Record review of resident's POS dated 8/22, showed no physician's orders for wound care treatment on or after 8/29/22.
Record review of the resident's TAR dated 8/22 and 9/22, showed there was no documentation showing an order for any wound care treatment on 8/29/22 nor any documentation showing the nursing staff were applying any wound care treatments to the resident's buttocks.
Record review of the resident's current Comprehensive Care Plan showed there was no documentation showing the resident was at risk for pressure sores and received interventions for preventive care or that the resident had developed a pressure sore and showed interventions for pressure sore treatment.
Record review of the resident's POS dated 9/22, showed there was no physician's order for wound care treatment.
Record review of the resident's Bath Sheets from 9/1/22 to 9/13/22 showed:
-The resident was bathed on 9/5/22, 9/8/22 and 9/12/22.
-On 9/5/22 the bathing sheet showed the resident had a bruise on his/her left elbow and this was the only skin area on the resident.
-None of the bathing sheets showed the resident had any pressure sores or wounds on his/her buttocks.
Observation and interview on 9/13/22 at 10:11 A.M., showed the resident was sitting in his/her wheelchair in his/her room. Nursing staff was getting ready to transfer the resident and perform incontinence care. The following occurred:
-LPN A entered the resident's room and without washing his/her hands or sanitizing them, put on gloves, gathered barrier cream and q-tips and placed them directly on the resident's bed.
-LPN A then placed a gait belt around the resident's waist and he/she and LPN B transferred the resident to his/her bed.
-LPN A and LPN B lowered the resident's pants and removed his/her brief. There was a dressing on the resident's right buttock that was dated 9/9/22 and there was a brownish drainage noted.
-LPN A removed the wound dressing and cleaned the wound and measured it. He/she then applied barrier cream.
-LPN A said the measurement of Wound #1-lower buttock right cheek area, was circular (eraser sized) and measured at 0.8 cm by 0.5 cm with a pink middle and was excoriated (raw chaffing of the skin). Wound #2 was measured as 0.7 cm by 1.0 cm with a pink middle that was also excoriated. The skin around both wounds was red and blanchable (when skin is blanched, it takes on a whitish appearance as blood flow to the region is prevented or with pressure to the skin).
-LPN A and LPN B both said they were not aware of the resident having any wounds and did not know who had completed the previous wound care. They said they were not aware of any wound care treatment orders for the resident's wounds.
-LPN A said the resident was supposed to receive a shower today, and he/she would get a physician's order for wound treatment.
Record review of the resident's Nursing Notes showed on 9/13/22 the nurse documented the resident had two small open areas on his/her right buttock. The nurse applied barrier cream to the resident's buttocks and a foam dressing. The nurse documented the new treatment order was documented and entered into the TAR. The nurse did not document the stage of the wounds.
During an interview on 9/14/22 at 2:00 P.M., Certified Nursing Assistant (CNA) B said:
-The nursing assistants completed the resident baths/showers.
-When bathing the resident and during incontinence care, they complete a visual inspection of the resident's skin skin.
-If they see any skin area (redness, bruising, scratches, open areas) they were supposed to notify the charge nurse and make sure the nurse actually saw the resident's skin.
-If the resident had a skin issue he/she would need to follow the order usually for barrier cream after cleansing the resident's skin.
-If the resident had a pressure sore or open wound, they do not put any ointments on it, that is done by the nurse.
-If they observe an area on the resident's skin during bathing, they would notify the nurse and document the area on the resident's bath sheet and try to describe the area as best they could. They would still notify the nurse so the nurse could complete a skin assessment.
During an interview on 9/15/22 at 10:49 A.M., LPN A said:
-He/she was not wound care certified but was hoping to obtain the certification.
-Skin assessments done by the nurse were to be completed weekly
-They try to complete skin assessments with the resident showers. The nurse assistants were supposed to notify the nurse of any skin issues and document it on the resident's bath sheet.
-The nurse was supposed to observe the resident's skin weekly and note any skin issues and sign off on the bath sheet.
-If they noticed any skin issues, they would notate it on the bath sheet and make a note in the resident's medical record on the skin assessment form.
-He/she would also make a note in the nursing notes that showed a description of the wound and he/she would also measure the wound and document the measurements on the skin assessment sheet and in the resident's nursing notes.
-He/she was not qualified to stage any wounds.
-Once he/she observed and documented the measurement and description of the wound, he/she notified the DON of his/her observation.
-If the wound was new, he/she would document and measure the wound and notify the DON, they then notified the physician and obtained physician's orders for wound care treatment.
-The nurse would then document the orders on the resident's physician's order record (electronic records) and they faxed the orders to the pharmacy. They had to fax the treatment order and medication order separately to the pharmacy.
-The wound care orders for treatment and medications were placed on the nursing Medication Administration Record (MAR)/TAR.
-The nurses were supposed to follow the physician's orders and document the treatment was completed on the TAR.
-The nurse should also measure and document the observation of the resident's wound and measurements at each treatment and document in the resident's nursing notes.
-The facility had a wound care documentation form in the electronic record system, but he/she had not been informed to use this form to document any wound observations, measurements or treatments, so he/she documented this information in the nursing notes.
-If the resident was on skilled services, the nurse should be looking at the resident's skin daily. If they were aware a resident had a wound, they should be monitoring the wound and there should be at least a weekly note showing the observation of the resident's skin and any wounds or skin issues.
-Up until yesterday, all of the wound care documentation and information was being provided to the DON.
-He/she thought that the DON was completing monitoring of the resident wounds until yesterday when he/she found out that the MDS Coordinator was also the Wound Care Nurse.
-He/she did not attend any risk assessment meetings where they discussed resident wounds or skin issues. He/she was notified of any skin issues during change of shift or if he/she discovered it on the shift or upon admission.
-He/she was not aware that the resident had any wounds on his/her buttocks and had not seen any treatment orders prior to 9/13/22 when he/she saw the resident's wounds.
-He/she notified the physician and received wound care orders to treat the resident's wounds, which were added to the resident's TAR.
During an interview on 9/15/22 4:40 PM the DON said:
- Skin assessments should be completed upon admission.
-The nurse was to complete the initial full body assessment on the admission assessment document.
-They were supposed to complete a weekly skin assessment that should be documented on the nurse's progress note.
-They usually completed the skin assessment during bathing, but it depended on the resident.
-The CNA should indicate on the bath sheet any skin issues they see then notify nurse.
-The nurse was expected to check the resident's skin before signing off on bath sheet.
-With a new wound, the charge nurse should notify the physician and document it on the progress note and obtain an order for treatment.
-Treatment orders should be documented on the physician's order sheet and on the TAR.
-He/she expected the nurse to follow wound treatment orders.
-The wounds should be measured weekly and/or according to the physician's orders or policy.
-The measurements should be documented into the wound book, but nursing staff documented the wound measurements in their progress notes currently.
-The nurses were responsible for completing wound measurements because they did not have a Wound Care Nurse.
-Each nurse documented wounds differently and there may be an issue with wound measurement continuity.
-He/she had not completed any education on wound measurements. The nurses have also completed staging of the wounds but he/she had not provided any education on how to identify or stage wounds.
-He/she would expect the nurse to communicate to the MDS Coordinator to update the resident's care plan if a resident developed a wound or developed any changes in their skin.
Attempts to contact the resident's physician were not successful to date.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Accident Prevention
(Tag F0689)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to utilize equipment correctly to prevent harm by not lo...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to utilize equipment correctly to prevent harm by not locking the mechanical lift or the wheelchair when transferring one sampled resident (Resident #274) out of 14 sampled residents. The facility census was 27 residents.
Record review of the facility's undated policy titled Hydraulic Lift (Hoyer Lift) showed:
-Staff were to set the brake on the Hoyer lift before lifting a resident.
-Staff were to lock the brakes on the resident's wheelchair before lifting the resident out of, or placing a resident in, a wheelchair.
1. Record review of Resident #274's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Unspecified injury of head.
-Contusion (bruise) of scalp.
-Anxiety (a feeling of worry, nervousness, or unease, typically about an imminent event or something with an uncertain outcome).
-Fever.
-Alzheimer's disease (progressive mental deterioration that can occur in middle or old age, due to generalized degeneration of the brain. It is the most common cause of premature senility).
Observation on 9/12/22 at 11:18 A.M. showed:
-The MDS (Minimum Data Set a federally mandated assessment tool completed by facility staff for care planning) Coordinator and Certified Nursing Assistant (CNA) A brought a Hoyer lift into the resident's room.
-Neither the MDS Coordinator nor CNA A locked the Hoyer lift wheels prior to lifting the resident.
During an interview on 9/12/22 at 11:42 A.M., CNA A said he/she would not have done anything differently.
Observation on 9/14/22 at 9:07 A.M. showed CNA C:
-Transferred the resident without locking the wheels of the resident's wheelchair.
-Transferred the resident without locking the Hoyer lift wheels.
During an interview on 9/14/22 at 1:00 P.M., Nursing Assistant (NA) A said staff were to lock the wheels on the Hoyer lift and the resident's wheelchair before the resident was lifted.
During an interview on 9/14/22 at 1:25 P.M., CNA A said staff were to lock the wheels on the Hoyer lift and the resident's wheelchair before the resident was lifted.
During an interview on 9/14/22 at 1:34 P.M., Certified Medication Technician (CMT) A said staff were to lock the wheels on the Hoyer lift and the resident's wheelchair before the resident was lifted.
During an interview on 9/14/22 at 1:55 P.M., Licensed Practical Nurse (LPN) A said staff were to lock the wheels on the Hoyer lift and the resident's wheelchair before the resident was lifted.
During an interview on 9/15/22 at 2:01 P.M., LPN B said staff were to lock the wheels on the Hoyer lift and the resident's wheelchair before the resident was lifted.
During an interview on 9/15/22 at 4:39 P.M., the Director of Nursing (DON) said staff were to lock the wheels on the Hoyer lift and the resident's wheelchair before the resident was lifted.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0694
(Tag F0694)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to change a Peripherally Inserted Central Catheter (PICC ...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to change a Peripherally Inserted Central Catheter (PICC line- a thin, soft, long catheter (tube) that is inserted into a vein in the arm, leg or neck. The tip of the catheter is positioned in a large vein that carries blood into the heart. The PICC line is used for long-term intravenous (IV) antibiotics, nutrition or medications, and for blood draws) dressing and to create a baseline care plan for the PICC line for one sampled resident (Resident #276) out of 14 sampled residents. The facility census was 27 residents.
Record review of IV-therapy.net's undated article titled Policy and Procedure for PICC Line or Midline Catheter Dressing Change showed:
-The dressing for a PICC line or midline catheter was required to be changed every seven days and as needed when the dressing was loose, damp, or soiled.
Record review of sos.mo.gov's regulation titled Missouri Secretary of State: Code of State Regulations: 20 CSR 2200-6.030 Intravenous Infusion Treatment Administration by Qualified Practical Nurses; Supervision by a Registered Professional Nurse effective February 28, 2018 showed Licensed Practical Nurse (LPN's) who were IV certified and had documented competency verification from their employer may change PICC tubing sets and dressings.
1. Record review of Resident #276's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Open wound to his/her left lower leg.
-Sepsis (a serious condition resulting from the presence of harmful microorganisms in the blood or other tissues and the body's response to their presence, potentially leading to the malfunctioning of various organs, shock, and death).
-Pain.
-Bacteremia (the presence of bacteria in the blood).
Record review of the resident's Progress Notes dated 9/22 showed:
-No documentation of the resident's PICC line.
-No documentation of an assessment for the resident's PICC line.
Record review of the resident's Physician Order Sheet (POS) dated 9/22 showed:
-No orders for assessing the resident's PICC line site or dressing.
-No orders to change the resident's PICC line dressing.
Observation on 9/14/22 at 8:42 A.M. showed the resident's PICC line dressing was dated 9/7/22 and the dressing was loose with edges peeling.
During an interview on 9/14/22 at 1:55 P.M., LPN A said:
-If any dressing was soiled or loose and there was no order to change it, he/she would notify the Director of Nursing (DON) immediately, as well as the physician, to obtain an order.
-Only a Registered Nurse (RN) could change a PICC line dressing.
-He/she was unaware how often PICC line dressings needed changed.
Observation on 9/15/22 at 12:06 P.M. showed:
-The resident's PICC line dressing was dated 9/7/22 and had additional tape surrounding the edges to keep the dressing in place.
-NOTE: The PICC line dressing was required to be changed every seven days, this was the eighth day.
During an interview on 9/15/22 at 2:01 P.M., LPN B said:
-If any dressing was soiled or loose and there was no order, he/she would notify the doctor to obtain an order and change it immediately.
-He/she was a LPN and was not allowed to change PICC line dressings and did not know the frequency the dressing was to be changed.
During an interview on 9/15/22 at 4:39 P.M., the DON said:
-Staff that found a loose or soiled dressing of any type were responsible for calling the physician to obtain an order and following the order.
-All nurses (LPN's and RN's) were responsible for PICC line dressing changes and assessments.
-He/she expected an order to change a PICC line dressing that included the frequency.
-PICC line dressings were to be changed once a week.
-Staff were to assess the insertion site, tissue surrounding the insertion site, measure the length of tubing, and the dressing's integrity; this assessment was all to be documented in the resident's progress notes.
-He/she expected staff to call the physician and obtain an order if there was no order for a dressing change and document it in the resident's progress notes.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0700
(Tag F0700)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to obtain physician orders; to complete a safety assessme...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to obtain physician orders; to complete a safety assessment for the use of one-half bed side rail (is a adjustable metal or ridge plastic bar placed on the bed); to update the care plan for the use of side rails; and to have documentation of ongoing monitoring during the use of the bed side rail and for the safety of one sampled resident (Resident #13) out of 14 sampled residents. The facility resident census of 27 residents.
Requested the facility's Side Rail-Restraint policy and was not provided at the time of exit.
1. Record review of Resident #13 admission Face-Sheet showed he/she was admitted to the facility on [DATE] and readmitted on [DATE] with diagnosis of:
-Muscle weakness.
-Alzheimer's disease (a slowly progressive disease of the brain that is characterized by impairment of memory and eventually by disturbances in reasoning, planning, language, and perception).
-Seizure (a hyperexcitation of neurons in the brain leading to a sudden, violent involuntary series of contractions of a group of muscles).
-Anxiety (anticipation of impending danger and dread accompanied by restlessness, tension, fast heart rate, and breathing difficulty not associated with an apparent stimulus),
Record review of the resident's Quarterly Minimum Data Set (MDS-a federally mandated assessment tool completed by facility staff for care planning) dated 7/16/22 showed:
-The resident able to make his/her need known.
-Required total assistance of two staff members for transfer, personal cares.
Record review of the resident's Physician's Order Sheet (POS) dated 8/13/22 to 9/13/22 showed no physician orders for use of half bed side rails.
Record review of the resident's medical record showed:
-There was no documentation of an assessment for use of side rails.
-There was no on-going monitoring of the resident's safety when the side rails were in use.
Record review of resident's current care plan showed no documentation of a care plan for use of half side rails for positioning or safety.
Observation on 9/12/22 at 9:43 A.M. of the resident's room showed he/she had specialized bed and had half rails on the right side.
Observation on 9/13/22 at 12:55 P.M. of the resident room showed:
-His/her bed had half bed side rail.
-The half side rail was placed one to two feet from head of the bed.
-Was secured to right side of the bed.
Observation on 9/13/22 at 1:25 P.M. of the resident showed:
-He/she was transferred by Certified Nursing assistant (CNA) E and Nursing Assistant (NA) A to his/her bed from the left side and on the right side the half side rail was up.
-He/she had been repositioned by CNA's after care.
-The resident required assistance by staff for repositioning in bed, he/she was partially able to hold on to the half side rail to help with turning, with the support of NA A.
-Resident was made comfortable in bed with half side bed rail in place.
Record review of the resident medical record on 9/14/22 at 10:44 A.M. showed:
-No side rail assessment was found.
-No documentation found related to use of side rail.
A request was made on 9/14/22 at 11:45 A.M., for the resident's side rail assessment and physician order for use of side rails.
During an interview on 9/14/22 at 1:00 P.M., NA A said:
-He/she reviewed the resident's electronic record for the type of care required.
-The resident's electronic record would indicate if the resident required side rails.
-The use of side rails depended on the resident's needs if they were for safety or positioning.
-Would require a physician order for the use of side rails.
-He/she was not aware of type of monitoring required when side rails are in use.
During an interview on 9/15/22 10:24 A.M., Licensed Practical Nurse (LPN) A said:
-The use of side rails would require physician order.
-The use of side rails would require a side rail assessment being completed.
-Most of the residents with a side rail were used for positioning while in bed.
-The resident should be re-assessed for continued use of side rails and update the physician's order.
-He/she would expect the resident to have a side rail care plan.
-MDS coordinator would had been responsible for updating care plans.
During an interview on 9/15/22 at 10:43 A.M.,Certified Medication Technician (CMT) B said:
-Most of the resident's have side rails for positioning while in bed.
-The resident would need a physician's order for use of the side rails and a nursing assessment for safety of use of the side rails.
-The MDS Coordinator would update the resident's care plan for use of the side rails.
-Facility staff would monitor the resident while in bed with side rails up to ensure safety while in use.
A second request was made on 9/15/22 at 11:12 A.M., for documentation related to the resident physician's order and assessment for the use of side rails.
During an interview on 9/15/22 at 2:10 P.M., the Administrator said the facility had no documentation for the resident's use of side rails and had no physician's order or side rail assessments transcribed.
During an interview on 9/15/22 at 4:40 P.M., DON said he/she:
-Would expect facility care staff to follow the facility policy related to the use of bed rails and monitoring of the bed rails.
--The facility policy was not provided by the time of exit.
-Would expect the resident to have a physician's order and a side rail assessment for safety and need for the use of bed side rails.
-Would expect nursing staff to monitor the resident for safety while side rails were used.
-Would expect the resident care plan to be up to date to reflect the resident current conditions.
-Would expect nursing staff to re-assess the need for use of bed side rails, by following the facility policy.
--The facility policy was not provided by the time of exit.
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, interview, and record review, the facility failed to ensure food was prepared in a manner appropriate for ...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, and record review, the facility failed to ensure food was prepared in a manner appropriate for one sampled resident (Resident #16) out of 14 sampled residents. The facility census was 27 residents.
Record review of the International Dysphagia Diet Standardization Initiative (IDDSI) article Complete IDDSI Framework Detailed Definitions dated July 2019 showed a soft diet:
-Could not contain any regular dry bread, sandwiches, or toast of any kind.
-Could not contain food with a floppy textures as it would be a choking risk; if they are not chewed into small pieces they become thin and wet and can form a covering over the opening of the airway, stopping air from flowing.
Record review of the facility's policy titled Soft Diet dated 7/14/21 showed this type of diet excluded toast.
Record review of drugs.com article titled Soft Diet dated 8/31/22 showed toast and corn were not approved for this type of diet.
1. Record review of Resident #16's Face Sheet showed he/she was admitted on [DATE] with the following diagnoses:
-Muscle weakness.
-Protein-calorie malnutrition (nutritional status in which reduced availability of nutrients leads to changes in body).
-Unspecified dementia (a chronic or persistent disorder of the mental processes caused by brain disease or injury and marked by memory disorders, personality changes, and impaired reasoning).
-History of falls.
-Nausea.
-Dysphagia (difficulty swallowing).
Record review of the resident's Physician Order Sheet (POS) dated May 2022 to September 2022 showed:
-The physician discontinued the resident's regular diet order 5/7/22.
-The physician ordered a pureed diet (where all the foods have a soft, pudding-like consistency, used for people that have trouble chewing or swallowing) on 5/7/22.
-The physician ordered a soft/mechanical soft diet on 9/6/22.
-NOTE: Both pureed and soft/mechanical soft diet orders were active on the resident's POS
Observation on 9/13/22 at 12:40 P.M. showed:
-Staff served the resident cut up pieces of meat, mashed potatoes and gravy, a roll, and cooked spinach.
-The diet card on the resident's tray showed he/she was to receive a pureed diet.
-The resident only ate the mashed potatoes; less than 15% of his/her meal.
Observation on 9/14/22 at 12:14 P.M. showed:
-Staff served the resident corn, mashed potatoes and gravy, cornbread, applesauce, and ground meat.
-The resident only ate his/her applesauce.
During an interview on 9/14/22 at 1:18 P.M., the resident said:
-He/she felt like he/she had eaten too much.
-He/she felt like he/she was going to vomit.
During an interview on 9/14/22 at 1:00 P.M., Nursing Aide (NA) A said:
-Staff were to verify the food matched the diet card.
-Kitchen staff were responsible for the diet cards.
-He/she would ask the nurse which diet to follow if more than one order was present.
During an interview on 9/14/22 at 1:25 P.M., Certified Nursing Assistant (CNA) A said cut up pieces of meat were not considered part of a soft/mechanical diet.
During an interview on 9/14/22 at 1:43 P.M., Dietary Aide A said:
-He/she knew the residents' diet orders because there were so few residents.
-Dessert was usually mechanically soft for all residents.
-Nurses brought a paper (type unspecified) to the kitchen staff when a diet order was changed.
-Cut up pieces of meat were considered part of a soft/mechanical diet.
-He/she was unsure if corn was part of a soft/mechanical diet.
During an interview on 9/14/22 at 1:55 P.M., Licensed Practical Nurse (LPN) A said:
-He/she would have used the diet order that would have been least likely to result in choking (puree diet) until the orders were clarified.
-Cut up meat and corn were not considered part of a soft/mechanical diet.
Observation on 9/15/22 at 8:15 A.M. showed staff served the resident scrambled eggs, oatmeal, toast (with crust) with butter and jelly.
During an interview on 9/15/22 at 9:17 A.M., the Registered Dietitian (RD) said:
-Cut up meat would not have met the standard for a soft/mechanical soft diet.
-All meat was to be ground.
-Corn would not have met the standard for a soft/mechanical soft diet.
During an interview on 9/15/22 at 10:37 A.M., the Dietary Manager said:
-Corn was not appropriate for a soft/mechanical diet.
-A mechanical diet required a process to ensure meat was very finely cut.
-He/she was aware the resident had been on a puree diet but had been notified by nursing staff that the resident was moved to a soft/mechanical diet.
-He/she did not look at orders, he/she used the information given by the nurses.
-The resident liked bread, particularly grilled cheese.
During an interview on 9/15/22 at 4:40 P.M., the Director of Nursing (DON) said:
-He/she expected staff to clarify orders with the physician if conflicting orders were present.
-Corn and toast were part of a soft/mechanical diet.
-Nurses were responsible for notifying the dietary department of changes to diet orders.
-He/she expected the staff to question a meal with cut up meat and a diet card that said puree.
-He/she expected the staff to not serve a meal to the resident until the order was clarified.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0565
(Tag F0565)
Could have caused harm · This affected multiple residents
Based on interview and record review, the facility failed to ensure that a monthly group was organized for facility residents and family members that allowed them the opportunity to voice grievances a...
Read full inspector narrative →
Based on interview and record review, the facility failed to ensure that a monthly group was organized for facility residents and family members that allowed them the opportunity to voice grievances and concerns, this deficient practice had the potential to effect all residents residing in the facility. The facility census was 27 residents.
Record review of the Centers for Medicare and Medicaid Services (CMS) memo dated 4/7/22 showed:
- CMS will end the specified waivers in two groups, 60 days from issuance of this memorandum and 30 days from issuance of this memorandum.
-While the waivers of regulatory requirements have provided flexibility in how nursing homes may operate, they have also removed the minimum standards for quality that help ensure residents' health and safety are protected.
-Findings from onsite surveys have revealed significant concerns with resident care that are unrelated to infection control (e.g., abuse, weight-loss, depression, pressure ulcers, etc.).
-We are concerned that the waiver of certain regulatory requirements has contributed to these outcomes and raises the risk of other issues.
- The Emergency Declaration Blanket Waiver for resident groups was ended 30 days from the publication of the memo.
1. During an interview on 9/14/22 at 1:20 P.M., the Administrator said:
- There were not any Resident Council minutes to review, because the last time the facility had a Resident Council was July 2021.
- He/she was told the Resident Council meetings use to be conducted monthly.
- The current Business Office Manage (BOM) fulfills the three roles of BOM, Social Service Designee (SSD) and Activities Director, and overseeing the Resident Council is part of the Activities.
- Conducting Resident Council meetings is a priority for the facility, but the former Resident Council president passed away on August 23, 2022.
During an interview on 9/15/22 at 9:45 A.M. the BOM said:
- He/she has worked at the facility since May 2022.
- He/she was told about performing the duties of the Business Office and SSD before he/she got hired.
- After he/she was hired, he/she voluntarily agreed to assist with the activity program.
- Performing the duties of the BOM and SSD, took more of his/her time, and because of that, it is hard for him/her to get all the activities done and run the Resident Council meetings.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0568
(Tag F0568)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to print and distribute quarterly statements for the residents who all...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to print and distribute quarterly statements for the residents who allowed the facility to manage their resident funds. This practice affected three residents (Resident's #75, #10 and #11) out of 12 sampled residents who allowed the facility to manage their resident funds. This deficient practice had the potential to affect all residents with funds in the facility's resident trust. The facility census was 27 residents.
1. Record review of the financial records of the three sampled resident's showed the absence of quarterly statements.
During an interview on 9/14/22 at 11:54 A.M., the Corporate Financial Consultant said:
- The records of the previous quarterly statements for the months of January 2022 through March 2022, were not available.
-The facility missed sending out the quarterly statements in July for the 3 month quarter of April 2022 through June 2022, because he/she was not there to remind the current Business Office Manager (BOM), who was new at the time.
During an interview on 9/15/22 at 12:39 P.M., Resident #75, a resident identified by his/her quarterly Minimum Data Set (MDS- a federally mandated assessment tool completed by the facility for care planning) dated 6/12/22, as a resident who understands others, a resident who was able to make himself/herself understood, and had a Brief Interview for Mental Status (BIMS- a screening tool used to assist with identifying a resident's current cognition and to help determine if any interventions need to occur) of 15 (showing he/she was cognitively intact), said:
-He/she used to get quarterly statements from the businesses office.
-It has been quite a while.
-He/she would like to get those quarterly statements back, so he/she could keep track of what he/she had in her account.
During an interview on 9/15/22 at 12:50 P.M., Resident #10, a resident identified by his/her quarterly MDS dated [DATE], as a resident who understood others, made himself/herself understood and had a BIMS of 15, said his/her relative used to get the quarterly statements and he/she received quarterly statements just once.
During a phone interview on 9/20/22, at 2:50 P.M. the BOM said he/she could not find any of the quarterly statement for [DATE] through March 2022 and he/she did not know if they were completed.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Abuse Prevention Policies
(Tag F0607)
Could have caused harm · This affected multiple residents
Based on interview and record review, the facility failed to follow facility policies and procedures for checking the employee disqualification listing (EDL) and completing criminal background checks ...
Read full inspector narrative →
Based on interview and record review, the facility failed to follow facility policies and procedures for checking the employee disqualification listing (EDL) and completing criminal background checks (CBC) and checking the Nurse Aide Registry in accordance with state requirements for two employees sampled for the CBC screening, one employee sampled for the EDL screening and four employees sampled for the Nurse Aide Registry screening out of 10 employees sampled. This deficient practice potentially affected all residents in the facility. The facility census was 27 residents.
Record review of the facility Abuse and Neglect Policy updated 11/2017, showed:
-Policies and procedures should be consistent with regulatory requirements.
-The facility must not hire an employee or engage and individual who was found guilty of abuse, neglect, exploitation, mistreatment or misappropriation of property by a court of law; or who has a finding in the state nurse aide registry concerning abuse, neglect, exploitation, mistreatment of residents or misappropriation of property, or has had a disciplinary action in effect taken against his/her professional licence.
-The facility must report knowledge of actions by a court of law against any employee that indicates that employee is unfit for duty.
1. Record review of five employee records on 10/19/10, showed:
-Dietary Aide A was hired on 2/3/22; the documentation showed the facility staff did not check the CBC or the Nurse Aide Registry.
-Nursing Assistant (NA) A was hired on 4/15/22; documentation showed the facility staff did not check the CBC, EDL or the Nurse Aide Registry.
-Certified Nursing Assistant (CNA) F was hired on 1/11/22; documentation showed the facility did not check the Nurse Aide Registry.
-Housekeeping Aide A was hired on 5/31/22; documentation showed the facility staff did not check the Nurse Aide Registry.
During an interview on 9/14/22, the Administrator said:
-All of the employees were currently working in the facility.
-They were unable to locate the CBC or EDL for NA A.
-The former Bookkeeper was responsible for completing the background checks on all of the staff listed.
-He/she did not know that the Nurse Aide Registry screening was to be completed on all staff, to include dietary and housekeeping.
-They would immediately re-screen these employees.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0637
(Tag F0637)
Could have caused harm · This affected multiple residents
Based on interview and record review, the facility failed to ensure a Significant Change Minimum Data Set (MDS - a federally mandated assessment instrument completed by facility staff for care plannin...
Read full inspector narrative →
Based on interview and record review, the facility failed to ensure a Significant Change Minimum Data Set (MDS - a federally mandated assessment instrument completed by facility staff for care planning) was completed and submitted when a resident was admitted to Hospice services (end of life care) for three sampled residents (Resident's #224, #325, and #16) out of 12 sampled residents. The facility census was 27 residents.
1. Record review of Resident #325's Physician's Order Sheet (POS) showed he/she was admitted to Hospice services on 8/11/22.
Record review of the resident's Center for Medicare and Medicaid Services (CMS) MDS database submissions showed the last assessment was an Entry MDS assessment with an ARD of 6/30/22.
Record review of the resident's facility Electronic Medical Record (EMR) showed a Significant Change MDS assessment with an ARD of 8/24/22 in process. The assessment was not completed, validated, finalized, or transmitted.
2. Record review of Resident #224's POS showed he/she was admitted to hospice services on 8/22/22.
Record review of the resident's CMS MDS database submissions showed the last assessment was an Entry MDS assessment with an ARD of 8/15/22.
Record review of the resident's facility EMR showed:
-An admission MDS assessment with an ARD of 8/28/22 in process. The assessment was not completed, validated, finalized, or transmitted.
-A Significant Change MDS assessment with an ARD dated of 9/5/22 in process. The assessment was not completed, validated, finalized, or transmitted.
3. Record review of Resident #16's POS showed he/she was admitted to Hospice services on 8/11/22.
Record review of the resident's CMS MDS database submission showed the last assessment was a Quarterly MDS assessment with an ARD of 6/4/22.
Record review of the resident's facility EMR showed a Significant Change MDS assessment with an ARD of 8/24/22 in process. The assessment was not completed, validated, finalized, or transmitted.
4. During an interview on 9/14/22 at 2:00 P.M., the MDS Coordinator said:
-He/she was new to the position in August 2022.
-He/she had not been trained on how to do MDS submissions yet.
-He/she did not know how to see if an MDS was accepted, rejected, or transmitted.
-He/she was trying to catch up on late MDS submissions from prior to his/her hire date.
-The MDS should be accurate and reflect the resident's current condition.
-A significant change MDS would be submitted if a resident was newly admitted to hospice services.
-He/she could not submit an MDS until the Director of Nursing (DON) signed them since he/she was the facility Registered Nurse (RN).
During an interview on 9/15/22 at 4:42 P.M., the DON said:
-He/she was new to the position in July 2022.
-He/she was doing MDS submissions when he/she was hired until the MDS Coordinator was hired.
-He/she had not been trained on how to complete MDS's, however he/she used to do MDS's years ago before the MDS 3.0 system.
-He/she expected the MDS's to be completed, validated, finalized, and transmitted timely.
-He/she did not know how to see if an MDS was accepted, rejected, or transmitted.
-The MDS should be accurate and reflect the resident's current condition.
-A significant change MDS would be submitted if a resident was newly admitted to hospice services.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
MDS Data Transmission
(Tag F0640)
Could have caused harm · This affected multiple residents
Based on interview and record review, the facility failed to transmit required Minimum Data Set (MDS - a federally mandated assessment instrument completed by facility staff for care planning) assessm...
Read full inspector narrative →
Based on interview and record review, the facility failed to transmit required Minimum Data Set (MDS - a federally mandated assessment instrument completed by facility staff for care planning) assessments for four sampled residents (Resident's #325, #224, #15, and #16) and one supplemental resident (Resident #2) out of 12 sampled residents and four supplemental residents. The facility census was 27 residents.
Record review of the Resident Assessment Instrument (RAI) Manual, dated 10/1/17 showed:
-Comprehensive assessments must be transmitted electronically within 14 days of the Care Plan Completion Date (V0200C2 plus (+) 14 days).
-All other MDS assessments must be submitted within 14 days of the MDS Completion Date (Z0500B + 14 days).
1. Record review of Supplemental Resident #2's Centers for Medicare and Medicaid Services (CMS) MDS database submissions showed the last assessment was a Significant Change MDS assessment with an Assessment Reference Date (ARD) of 4/18/22.
Record review of the resident's facility Electronic Medical Record (EMR) showed:
-A Significant Change MDS assessment submitted with an ARD of 4/18/22.
-A Discharge - Return Not Anticipated assessment in process with an ARD of 6/6/22. The assessment was not completed, validated, finalized, or transmitted.
2. Record review of Resident #325's CMS MDS database submissions showed:
-An Entry MDS assessment with an ARD of 6/15/22.
-A Discharge MDS assessment with an ARD of 6/28/22.
-The last assessment was an Entry MDS assessment with an ARD of 6/30/22.
Record review of the resident's facility EMR showed:
-An Entry MDS assessment with an ARD of 6/15/22.
-An admission MDS assessment with an ARD of 6/28/22 with the code Discharge - Return Anticipated.
-An Entry MDS assessment with an ARD of 6/30/22.
-A Significant Change MDS assessment with an ARD of 8/24/22 in process. The assessment was not completed, validated, finalized, or transmitted.
3. Record review of Resident #224's CMS MDS database submissions showed the last assessment was an Entry MDS assessment with an ARD of 8/15/22.
Record review of the resident's facility EMR showed an admission MDS assessment with an ARD of 8/28/22 in process. The assessment was not completed, validated, finalized, or transmitted.
4. Record review of Resident #15's CMS MDS database submission showed the last assessment was an Entry MDS assessment with an ARD of 8/23/22.
Record review of the resident's facility EMR showed:
-A Discharge - Return Anticipated assessment with an ARD of 8/24/22 in process. The assessment was not completed, validated, finalized, or transmitted.
-An Entry assessment with an ARD of 9/1/22 in process. The assessment was not completed, validated, finalized, or transmitted.
5. Record review of Resident #16's CMS MDS database submission showed the last assessment was a Quarterly MDS assessment with an ARD of 6/4/22.
Record review of the resident's facility EMR showed a Significant Change MDS assessment with an ARD of 8/24/22 in process. The assessment was not completed, validated, finalized, or transmitted.
6. During an interview on 9/14/22 at 2:00 P.M., the MDS Coordinator said:
-He/she was new to the position in August 2022.
-He/she had not been trained on how to do MDS submissions yet.
-He/she did not know how to see if an MDS was accepted, rejected, or transmitted.
-He/she was trying to catch up on late MDS submissions from prior to his/her hire date.
-He/she could not submit an MDS until the Director of Nursing (DON) signed them since he/she was the facility Registered Nurse (RN).
During an interview on 9/15/22 at 4:42 P.M., the DON said:
-He/she was new to the position in July 2022.
-He/she was doing MDS submissions when he/she was hired until the MDS Coordinator was hired.
-He/she had not been trained on how to complete MDS's, however he/she used to do MDS's years ago before the MDS 3.0 system.
-He/she expected the MDS's to be completed, validated, finalized, and transmitted timely.
-He/she did not know how to see if an MDS was accepted, rejected, or transmitted.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0642
(Tag F0642)
Could have caused harm · This affected multiple residents
Based on interview and record review, the facility failed to ensure a Registered Nurse (RN) certified the Minimum Data Set (MDS a federally mandated assessment instrument completed by facility staff f...
Read full inspector narrative →
Based on interview and record review, the facility failed to ensure a Registered Nurse (RN) certified the Minimum Data Set (MDS a federally mandated assessment instrument completed by facility staff for care planning) completion date (Z0500B) was no later than 14 days after the Assessment Reference Date (ARD - A2300) for five sampled residents (Resident's #325, #19, #224, #16, #15) and two supplemental residents (Resident #2, and #3) out of 14 sampled residents and four supplemental residents. The facility census was 27 residents.
Record review of the Resident Assessment Instrument (RAI) manual, dated 10/1/17, showed the following:
-Z0500B description: MDS Completion Date - date of the RN assessment coordinator's signature, indicating that the MDS is complete;
-In accordance with the requirements at 42 CFR 483.20(f)(1), (f)(2), and (f)(3), long-term care facilities participating in the Medicare and Medicaid programs must meet the following conditions:
-For all non-admission Omnibus Budget Reconciliation Act of 1987 (OBRA) and Prospective Payment System (PPS) assessments, the MDS Completion Date (Z0500B) must be no later than 14 days after the ARD (A2300).
MDS Transmission Submission Verification sheets for all sampled and supplemental residents were requested on 9/14/22 and not received at the time of exit.
1. Record review of Supplemental Resident #2's Electronic Medical Record (EMR) MDS assessments showed the following information:
-A Discharge Assessment was in process with an ARD of 6/6/22.
-Completion Date (Z0500B) of the Centers for Medicare/Medicaid Services' (CMS) Quality Improvement Evaluation System (QIES) Assessment Submission and Processing (ASAP) System showed the assessment was not signed or submitted as of 9/14/22, 100 days after the ARD.
2. Record review of Resident #325's EMR MDS assessments showed the following:
-An admission Assessment was submitted with a code of discharge - return anticipated with an ARD of 6/28/22.
--This assessment was not transmitted to the CMS ASAP system as of 9/14/22, 78 days after the ARD.
-A Significant Change MDS was in process with an ARD of 8/24/22.
-Completion Date (Z0500B) of the CMS QIES ASAP System showed the assessment was not signed or submitted as of 9/14/22, 21 days after the ARD.
3. Record review of Resident #19's EMR MDS assessment showed:
-An admission Assessment with an ARD of 7/21/22.
-Completion Date (Z0500B) of the CMS QIES ASAP showed the assessment was signed on 8/17/22, 27 days after the ARD date.
4. Record review of Resident #224's EMR MDS assessment showed:
-A Significant Change Assessment was in process with an ARD of 8/28/22.
-Completion Date (Z0500B) of the CMS QIES ASAP System showed the assessment was not signed or submitted as of 9/14/22, 17 days after the ARD.
5. Record review of Resident #16's EMR MDS assessment showed:
-A Significant Change MDS was in process with an ARD of 8/24/22.
-Completion Date (Z0500B) of the CMS QIES ASAP System showed the assessment was not signed or submitted as of 9/14/22, 21 days after the ARD.
6. Record review of Resident #15's EMR MDS assessment showed:
-An admission Assessment with an ARD of 7/20/22.
-Completion Date (Z0500B) of the CMS QIES ASAP showed the assessment was signed on 8/6/22, 17 days after the ARD date.
-A Discharge Assessment was in process with an ARD of 8/24/22.
-Completion Date (Z0500B) of the CMS QIES ASAP System showed the assessment was not signed or submitted as of 9/14/22, 21 days after the ARD.
7. Record review of Supplemental Resident #3's EMR MDS assessment showed:
-An admission Assessment with an ARD of 3/22/22.
-Completion Date (Z0500B) of the CMS QIES ASAP showed the assessment was signed on 4/22/22, 31 days after the ARD date.
8. During an interview on 9/14/22 at 2:00 P.M., the MDS Coordinator said:
-He/she had not been trained on how to complete MDS submissions yet.
-He/she started working at the facility the beginning of August.
-He/she did not know how to run or request a report to verify if the MDS submissions were accepted, rejected, had errors or were late.
-He/she was trying to catch up on the late MDS's from when he/she started.
-MDS's had not been done for a long time prior to his/her hire date.
-He/she could not submit an MDS until the Director of Nursing (DON) signed them since the DON was the RN, this was why some of the MDS's were late.
During an interview on 9/15/22 at 4:42 P.M., the DON said:
-He/she was doing the MDS's when he/she was first hired a couple of months ago.
-He/she had done MDS years ago, but has not been trained on the new MDS process yet.
-He/she would expect the MDS to be submitted timely.
-He/she was not aware of how to run reports or check to see if submitted MDS's were accepted, rejected, had errors or were late.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Quality of Care
(Tag F0684)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Record review of Resident #325's undated face sheet showed he/she was admitted on [DATE] with the following diagnoses:
-Alcoh...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Record review of Resident #325's undated face sheet showed he/she was admitted on [DATE] with the following diagnoses:
-Alcoholic Cirrhosis of the Liver (the destruction of healthy liver tissue due to excessive alcohol consumption) with Ascites (accumulation of fluid causing swelling of the abdomen).
-Metabolic Encephalopathy (any abnormal condition of the structure or function of brain tissues, especially chronic, destructive, or degenerative conditions)
Record review of the resident's POS showed the resident was admitted to Hospice on 8/20/22.
Record review of the resident's Hospice binder showed:
-A sign-in sheet for all Hospice staff who come into the facility to provide care to the resident.
-No documentation of the visits or coordination of care.
During an interview on 9/14/22 at 10:19 AM LPN B said:
-Hospice checked in at the front desk and word of mouth was the only communication method.
-There was a sign off sheet that they sign.
-He/She would make a progress note if there were any big changes or things that Hospice asked of the staff.
-He/She did not sign any documentation with Hospice proving communication between the Hospice company and facility.
During an interview on 9/15/22 at 4:40 P.M. the DON said:
-He/she expected the Hospice staff to communicate directly with him/her and the nurses regarding what residents were seen on a specific day and if there were any changes/requests for orders.
-He/She expected the communication from Hospice be given to him/her.
-He/She was responsible for reviewing the Hospice communication notes.
-He/She would then put the communication notes in the Hospice binder for the staff to be able to see.
Based on observation, interview and record review, the facility failed to assess and document wounds upon admission and weekly thereafter for one sampled resident (Resident #276); to ensure there was documentation and communication with Hospice (a form of palliative care that focuses on the terminally ill and end of life care) staff regarding any Hospice visit made for three sampled residents (Resident #274, #224, and #325); to ensure Hospice visit summary notes were available for staff review; to ensure a comprehensive care plan included Hospice services; and to ensure a Significant Change Minimum data Set (MDS a federally mandated assessment completed by facility staff for care planning) was completed for one sampled resident (Resident #224) out of 14 sampled residents. The facility census was 27 residents.
Record review of the Facility's Hospice Nursing Facility Contract showed:
-Each contract are individualized for those residents requiring Hospice services.
-Hospice responsibilities include but not limited to;
--Maintain communication with facility staff, patient/family and physician with appropriate documentation.
--Provide copies of clinic notes after each Hospice visit.
--Hospice Registered Nurse case manager will coordinate and supervise all services provided to the resident within the facility, through written communication, to ensure the resident and family needs are met 24 hours a day. This communication will be documented on nursing visit notes.
-The facility responsibilities included but was not limited to:
--Maintain an accurate medical record that includes all services and events provided. all services will be furnished according to agreement.
--Required documentation provided by Hospice will be included in a designated area or section.
--The facility will ensure that these forms are not removed from Hospice medical record.
Record review of the facility's undated policy admission Nurse's Note showed staff were to complete a full body assessment, upon admission, and document the site and size of any wounds.
Record review of the facility's undated policy Wound Care and Treatment showed staff were required to have a specific order for treatment of a wound.
1. Record review of Resident #276's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Open wound to his/her left lower leg.
-Sepsis (a serious condition resulting from the presence of harmful microorganisms in the blood or other tissues and the body ' s response to their presence, potentially leading to the malfunctioning of various organs, shock, and death).
-Pain.
-Bacteremia (the presence of bacteria in the blood).
Record review of the resident's Progress Notes dated September 2022 showed:
-Staff admitted the resident 9/10/22 at 10:04 A.M., with no wounds noted.
-Staff charted an unspecified wound to the resident's upper left leg on 9/10/22 at 3:03 P.M.
--Description of the wound and measurements were not included.
-Staff charted dressings in place on 9/11/22 at 12:17 P.M. with no measurements, number of wounds, or wound locations.
-Staff charted a wound to the resident's upper left leg (no description or measurements), and wounds to his/her left lower leg with treatment in place.
-Staff charted the resident had a wound to the upper left leg and wounds (no number given) on his/her left lower leg on 9/14/22 at 4:16 P.M.
-Staff charted treatment was competed for the resident's left lower leg wounds according to the physician's order.
-NOTE: No note indicating the physician had been notified.
Record review of the resident's POS dated September 2022 showed no wound care orders.
Record review of the resident's Treatment Administration Record (TAR) dated September 2022 showed no orders for wound care.
During an interview on 9/13/22 at 1:55 P.M., Licensed Practical Nurse (LPN) A said:
-Staff were to complete a full body skin assessment when a resident was admitted to the facility.
-If he/she found a wound, he/she would notify the doctor to get an order for treatment.
-Nurses were required to do full skin assessments daily.
During an interview on 9/14/22 at 2:00 P.M., the MDS Coordinator said he/she was not aware he/she was responsible for the resident's skin assessments.
Record review of the resident's only Weekly Skin assessment dated [DATE] showed:
-LPN B had completed the resident's skin assessment and noted an abrasion on the resident's right hand, a wound on the resident's mid outer thigh (side unspecified) that was treated with skin prep (a liquid film-forming dressing that, upon application to intact skin, forms a protective film to help reduce friction during removal of tapes and films), and a old healed wound/scar on the resident's left shin which was treated with skin prep.
During an interview on 9/15/22 at 2:01 P.M., LPN B said:
-A full body skin assessment was to be done within 4 hours of a resident's admission to the facility.
-If there was no order for wound treatment, he/she would contact the wound nurse and the physician to get an order before attempting any treatment.
-Staff were to complete a full body skin assessment of each resident weekly or more often.
-Staff were to measure all wounds once a week.
During an interview on 9/15/22 at 4:40 P.M., the Director of Nursing (DON) said:
-Staff were expected to complete a full body assessment upon admission of a resident.
-The full body assessment was to be documented in the resident's Progress Notes.
-The charge nurse was responsible for notifying the physician of any wounds and getting the order for treatment.
-The charge nurse was responsible for documenting physician communication and orders in the resident's Progress Notes.
-All nurses were responsible for measuring wounds and documenting the measurements in the wound book.
--He/she was not able to find the wound book.
-Staff were also expected to enter wound measurements in the resident's Progress Notes.
-Treatment orders were located on the resident's Nurse TAR.
2. Record review of Resident #274's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Unspecified injury of head.
-Contusion (bruise) of scalp.
-Anxiety (a feeling of worry, nervousness, or unease, typically about an imminent event or something with an uncertain outcome).
-Fever.
-Alzheimer's disease (progressive mental deterioration that can occur in middle or old age, due to generalized degeneration of the brain. It is the most common cause of premature senility).
Record review of the resident's Progress Note dated September 2022 showed Hospice services were to evaluate the resident 9/9/22.
Record review of the resident's POS dated September 2022 showed the physician ordered the resident to be admitted to Hospice on 9/10/22.
Record review of the resident's Hospice Communication Book on 9/12/22 showed:
-Hospice had a face sheet listing the staff and their titles.
-A signed copy of the resident's code status.
-No other information, including any visit notes or orders requested by Hospice staff.
During an interview on 9/14/22 at 1:55 P.M., LPN A said Hospice would put their visit notes in the Hospice book but the facility staff don't need to look at it.
-Hospice staff communicate orders verbally and the facility staff would enter the orders.
-Hospice staff would either leave a note or call the facility nurses if they requested a new order or a change to an order.
During an interview on 9/15/22 at 9:37 A.M., the Hospice Team Lead said:
-Hospice saw the resident on 9/10/22.
-He/she expected Hospice staff to verbally communicate all orders to the facility staff.
-Hospice staff were to fill out a log each visit to show what discipline had visited the resident.
-The Hospice communication book was to have a current list of the resident's medications.
-Hospice staff do not document visit summaries.
-Hospice staff printed out orders they had added every other week and brought that to the facility to place in the resident's Hospice communication book.
-The Hospice communication book was to have a current care plan for the resident.
During an interview on 9/15/22 at 2:01 P.M., LPN B said:
-Hospice staff verbally communicate problems and orders to the facility staff.
-The Hospice communication book should have had a note from every Hospice visit.
-The resident's Hospice book was not complete.
During an interview on 9/15/22 at 4:40 P.M., the DON said:
-All Hospice communication was located in the Hospice communication book.
-He/she expected Hospice staff to tell him/her verbally about their visit.
-He/she expected both verbal and written communication between facility staff and Hospice staff.
-He/she expected Hospice staff to have written notes in the Hospice communication book when they weren't in the building to verify what they did and any recommendations.
-He/she did not put any communications from Hospice in the Hospice communication book, that was the responsibility of the Hospice staff.
-He/she expected Hospice staff to send any communication to him/her, then he/she would put it in the communication book.
3. Record review of Resident #224's admission Face Sheet showed the resident was admitted to the facility on [DATE] with diagnosis of Malignant Neoplasm (is a cancerous tumor) of unspecified part of right bronchus (is a passage or airway in the lower respiratory tract that conducts air into the lungs) or lung.
Record review of the resident's submitted MDS's showed he/she did not have documentation of a current MDS or a significant change MDS for change of condition complete, showing the resident admission to Hospice services.
Record review of the resident's Comprehensive Care Plan showed the resident did not have a Hospice Care Plan initiated or implemented after a his/her admission to Hospice services.
Record review of the resident's Physician order dated 8/22/22, showed the resident had an order to be admitted into Hospice services of his/her choice.
Record review of the resident's progress notes dated 8/22/22 at 5:48 P.M., showed:
-He/she was seen by Hospice and had been admitted to Hospice services.
-Had Hospice admission diagnoses of Malignant Neoplasm of unspecified part of right bronchus or lung and Malnutrition (condition that develops when the body does not get the right amount of the vitamins, minerals, and other nutrients it needs to maintain healthy tissues and organ function).
-He/she had received Hospice equipment of a bed, an air mattress, an Oxygen (O2) concentrator, and nebulizer (used for inhaled breathing medication treatments) from hospice.
Record review of the resident's facility personal contract with hospice provider showed the resident would receive Hospice service which had started on 8/22/22, while at the facility.
Record review of the resident's Hospice visit sign-in sheet dated 9/6/22 showed Hospice LPN documented under comments; routine visit, increase Fentanyl (pain control) patch to 25 microgram (mcg).
Record review of the resident's medical record showed he/she had no documentation of any communication between facility staff and Hospice staff related to the Hospice nurse's recommendation for increased pain medication from 9/6/22.
Record review of the resident's Physician Order Sheet (POS) dated 9/11/22 showed a new physician order for Fentanyl 25 mcg patch, replace patch once a day, every three days. (every 72 hours).
During an interview on 9/12/22 at 12:55 P.M. the resident said he/she was receiving Hospice services at that time.
Record review on 9/12/22 at 1:05 P.M. of the resident's medical record showed:
-He/she did not have ongoing documentation of the resident's Hospice Visit summary reports.
-He/she did not have ongoing Hospice visit communication or collaboration documented in the resident's facility nursing progress notes.
Observation on 9/13/22 at 9:39 A.M., showed the resident had an Oxygen (O2) concentrator and nebulizer machine (a device for producing a fine spray of liquid, used for example for inhaling a medicinal drug) in his/her room.
During an interview on 9/13/22 at 9:39 A.M. the resident said:
-He/she only used O2 at night.
-He/she had no complaints of pain at that time.
Record review of the resident's progress note dated 9/13/2022 at 12:58 P.M., showed:
-A new physician's order to increase Fentanyl patch to 25 mcg was received by DON and was implemented on 9/11/22.
-The resident said his/her pain was better controlled with the higher dosage of medication.
-Did not document if Hospice nurse had been contacted related to change of condition due to pain control and change in medication or if this was the Hospice nurse request.
During an interview on 9/14/22 at 9:20 A.M., with LPN B said:
-The Hospice staff would only check in with the facility staff if the resident's had any change in condition or any new physician orders.
-The Hospice staff would document any hospice visit in the resident's Hospice medical chart.
-The resident's Hospice chart was located in the facility conference room, on the bookshelf.
-He/she would not normally review the resident's Hospice medical record.
Record review of the resident's Hospice Medical Record showed:
-He/she had a care plan for the Hospice Certified Nursing Assistant (CNA) to visit two times a week and skilled nursing to visit at least 2 times a week.
-The resident had a Hospice staff sign in sheet.
--Hospice staff would sign their name and title when they saw the resident.
--Hospice staff would put the date when they saw the resident, but there was no documentation of the time they entered or exited the facility.
--Hospice staff would document comments to include the type of visit.
--Hospice staff would make recommendations for changes in orders on the sign in sheet.
-The Hospice medical record did not have a place for facility staff to document they had communicated with Hospice staff or the Hospice recommendations had been reviewed.
-There were no Hospice visit summary's in the resident's Hospice medical record.
During an interview on 9/14/22 at 11:00 A.M., the resident said he/she was not feeling well and had complaints of nausea and vomiting.
During an interview on 9/14/22 at 11:00 A.M. LPN A said he/she was checking with resident's physician and the Hospice nurse about changing the nausea medication.
During an interview on 9/14/22 at 10:00 A.M., the resident's Hospice licensed nurse and Hospice CNA visit notes were requested.
During an interview on 9/15/22 at 10:43 A.M., Certified Medication Technician (CMT) B
-Hospice staff would ask questions about the resident's medications or any changes in care as needed.
-Facility staff were responsible for communicating with Hospice staff.
During an interview on 9/15/22 at 4:40 P.M., DON said:
-He/she had not worked with the facility electronic records before being hired and was learning the systems.
-He/she was not sure if there was other documentation in the resident's electronic medical record related to Hospice care or communication between the facility and Hospice.
-He/she would expect Hospice staff to see or communicate with him/her or other nursing staff upon arrival to the facility and before leaving.
-He/she would expect facility staff to document any communication with the Hospice staff.
-Hospice staff were to document in the resident's Hospice medical record.
-He/she would expect to have written Hospice visit summary's placed in the Hospice chart.
-He/she would be responsible for reviewing the Hospice medical record for any updates and to ensure the required documentation from Hospice was placed in the binder.
-He/she would expect the resident care plan to include hospice plan of care and all care plans should be up to date showing the resident current condition and need of care.
-He/she would expect the MDS's to be completed and accurate and include Hospice services.
-He/she was not able to find any of the resident's Hospice visit summary's.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Respiratory Care
(Tag F0695)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 5. Record review of Resident #276's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Open wound to hi...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 5. Record review of Resident #276's face sheet showed he/she was admitted [DATE] with the following diagnoses:
-Open wound to his/her left lower leg.
-Sepsis (a serious condition resulting from the presence of harmful microorganisms in the blood or other tissues and the body ' s response to their presence, potentially leading to the malfunctioning of various organs, shock, and death).
-Shortness of breath.
-Pain.
-Bacteremia (the presence of bacteria in the blood).
Record review of the resident's POS dated 9/22 showed:
-An order for oxygen tubing to be replaced on the first of each month.
-An order for oxygen to be given at 3 liters per minute by nasal cannula at bedtime and as needed for shortness of breath.
Record review of the resident's Nurse Treatment Administration Record (TAR) dated September 2022 showed staff had not given the resident any oxygen since admission.
Observation on 9/12/22 at 10:38 A.M. showed an undated nasal cannula was wrapped around the oxygen concentrator without any covering.
During an interview on 9/12/22 t 10:38 A.M., the resident said he/she only used oxygen at night.
Observation on 9/14/22 at 8:04 A.M. showed an undated nasal cannula was wrapped around the oxygen concentrator without any covering.
During an interview on 9/14/22 at 8:15 A.M., the resident said:
-He/she had been given oxygen since his/her admission but it had a bad odor and he/she did not like to use it.
-His/her spouse had asked staff to check the nasal cannula and oxygen concentrator due to the smell when in use, but no staff had to his/her knowledge.
-He/she had not used his/her oxygen the night before because of the odor.
During an interview on 9/14/22 at 1:25 P.M., CNA A said:
-Staff were to place nasal cannula in a plastic bag that was dated.
-He/she would replace a nasal cannula if no date was present on the bag or no bag was present.
-Staff were to replace the nasal cannula weekly.
-Staff should change the oxygen tubing/nasal cannula if a resident complained about the odor.
During an interview on 9/14/22 at 1:55 P.M., LPN A said:
-Staff were to place oxygen tubing/nasal cannula in a plastic bag that was attached the oxygen concentrator.
-Staff were to write the date the oxygen tubing was last changed on the plastic bag.
-Staff were expected to change oxygen tubing/nasal cannula weekly or if it appeared dirty.
-He/she would replace the nasal cannula for a resident that complained of a foul odor when in use.
During an interview on 9/15/22 at 2:01 P.M., LPN B said:
-Staff were expected to place nasal cannula in a plastic bag that was dated when not in use.
-He/she was unsure how often the nasal cannula/oxygen tubing needed replaced.
-He/she would replace the nasal cannula if a resident complained of a foul odor when in use.
Observation on 9/15/22 at 11:50 A.M. showed an undated nasal cannula was wrapped around the oxygen concentrator without any covering.
6. During an interview on 9/14/22 at 1:00 P.M., Nursing Aide (NA) A said:
-Staff were to put oxygen tubing/nasal cannula in a plastic bag with a date on it when not in use.
-Staff were to replace oxygen tubing if it was found undated.
During an interview on 9/14/22 at 1:34 P.M., CMT A said:
-Staff were to place nasal cannula/oxygen tubing in a bag attached to the oxygen concentrator and that bag was to be dated with the date the tubing was last replaced.
-Staff should replace the oxygen tubing/nasal cannula if it was found undated.
During an interview on 9/14/22 at 2:00 P.M., CNA B said:
-Face masks, breathing treatment masks and nasal cannulas should be placed in a plastic bag when not in use.
-The nursing staff were supposed to ensure the resident's oxygen supplies were not on the floor, but were in the plastic bags when they entered the resident's room to provide resident care or when they were completing rounds.
-Some of the resident's would remove the oxygen face masks and nasal cannula themselves, but the nursing staff should be watching to ensure they were stored in the bags.
-Usually the plastic bags were on their wheelchair with the portable oxygen, on the oxygen concentrator or beside the breathing treatment machine.
During an interview on 9/15/22 at 10:43 A.M. Certified Medication Technician (CMT) B said:
-Nursing staff were responsible for changing the O2 tubing and nebulizer mask.
-Nebulizer masks were to be cleaned after use, let dry and then placed in a baggy.
-The resident's nebulizer treatments were an Pro Re Nata (PRN as needed) order.
-He/she had not had breathing treatments in the month of September.
-Any O2 tubing and nebulizer mask dated 8/15/22, should have been changed out by nursing staff, per the physician's order.
During an interview on 9/15/22 at 4:40 P.M., the DON said:
-Oxygen tubing, face masks and nasal cannulas should be off of the floor and on the resident.
-He/she would expect O2 tubing and nebulizer masks be stored in tabled plastic bag when not in use.
-The storage bag should be dated when tubing was changed last.
-The night nurse is responsible for ensuring the face masks, nasal cannulas and tubing are changed.
-He/she would expect staff to change oxygen supplies according to the physician's order.
-If tubing was not dated, he/she would expect nursing staff to replace undated tubing with new tubing.
-He/she would expect all facility care staff to monitor for proper storage of the resident's O2 tubing and nebulizer mask when not in use at least one time a shift.
-Staff should be checking the oxygen supplies to ensure they are in bags when not in use at least once per shift.
-He/she expected staff to replace a nasal cannula if a resident complained of a foul odor.
4. Record review of Resident #13 admission Face-Sheet showed he/she was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses of:
-Congestive heart failure (disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body)
-Alzheimer's disease (a slowly progressive disease of the brain that is characterized by impairment of memory and eventually by disturbances in reasoning, planning, language, and perception)
-Acute Respiratory Disease (is a condition that causes fluid to build up in your lungs so oxygen can't get to your organs).
Record review of the resident's Quarterly MDS dated [DATE] showed:
-The resident was able to make his/her needs known.
-Required oxygen.
-Required total assistance of two staff members for transfer, personal cares.
Record review of the resident's active POS showed:
-An order for O2 at two liter per minute, via nasal cannula as needed.(Ordered dated 12/1/21).
--O2 was to maintain the resident's oxygen saturation (O2 sats, the fraction of the hemoglobin molecules in a blood sample that are saturated with oxygen at a given partial pressure of oxygen) at or above 90 percent.
-Change O2 tubing weekly on Mondays during the day shift.
-The facility nursing staff were to monitor O2 sats every shift and PRN for dyspnea (difficult or labored breathing).
-Ipratropium-Albuterol solution for Nebulization, one vial as needed three time a day for wheezing.
-Change the resident's nebulizer tubing monthly on 15 th every month during day shift.
Observation on 9/12/22 at 9:43 A.M. and 12:47 P.M., of the resident's room showed:
-His/her uncovered oxygen tubing and nasal cannula were place on top of the resident's O2 concentrator.
-The resident's O2 tubing was dated 8/15/22.
-His/her nebulizer mask was laid on bedside table uncovered.
Observation on 9/13/22 at 9:40 A.M. and 12:52 P.M., the resident's room showed:
-O2 tubing dated 8/15/22, remained coiled on top of the resident's O2 concentrator uncovered.
-The resident's nebulizer tubing and mask dated 8/15/22 both remained uncovered on the bedside table.
Observation on 9/13/22 at 1:05 P.M., of the resident showed:
-He/she was transferred to his/her bed and personal care was provided by staff.
-He/she was made comfortable in his/her bed after cares.
-CNA E had turned on the resident's O2 concentrator and placed nasal cannula into the resident nose.
-The O2 tubing was dated 8/15/22 and had been uncovered on the top of the O2 concentrator.
Observation on 9/14/22 at 8:50 A.M., of the resident room, showed:
-O2 tubing dated 8/15/22 was coiled up placed on top of concentrator and was uncovered.
-Nebulizer mask and tubing remained uncovered on the bedside table.
Observation on 9/14/22 at 2:08 P.M., of the resident's room showed:
-The resident was sitting in his/her room in a specialized wheelchair with eyes closed.
-He/she had the O2 in place at 2 liters per nasal cannula, the oxygen tubing was dated 8/15/22.
-The resident nebulizer mask dated 8/15/22, remained uncovered on his/her bedside table.
Based on observation, interview and record review, the facility failed to storage oxygen (O2) nasal cannulas (a device used to deliver supplemental oxygen or increased airflow to a patient or person in need of respiratory help), O2 tubing and breathing treatment masks when not in use, for five sampled residents (Resident #6, #21, #15, #13 and #276) out of 14 sampled residents. The facility census was 27 residents.
Record review of the facility's undated Oxygen Cleaning policy and procedure did not show how the oxygen tubing, facemasks and nasal cannulas should be stored.
1. Record review of Resident #6's Face Sheet showed he/she was admitted on [DATE], with diagnoses including heart failure (a chronic, progressive condition in which the heart muscle is unable to pump enough blood to meet the body's needs for blood), urine retention (a condition in which you are unable to empty all the urine from your bladder), diabetes (a disease in which the body ' s ability to produce or respond to the hormone insulin is impaired, resulting in abnormal metabolism of carbohydrates and elevated levels of glucose in the blood and urine), muscle weakness, stroke, anxiety disorder (a feeling of worry, nervousness, or unease, typically about an imminent event or something with an uncertain outcome) and pain.
Record review of the resident's quarterly Minimum Data Set (MDS-a federally mandated assessment tool to be completed by facility staff for care planning) dated 6/5/22, showed the resident:
-Was alert and oriented.
-Needed limited assistance with dressing and hygiene.
-Needed extensive assistance with bed mobility, transfers and had upper and lower limited range of motion.
-Received oxygen therapy.
Record review of the resident's Care Plan dated 7/26/22, showed he/she was at risk for respiratory distress related to diagnoses of heart failure and prior hospitalization for shortness of air. Interventions showed the resident needed assistance of one to two persons with all care and assistance with transfers due to muscle weakness.
Record review of the resident's Physician's Order Sheet (POS) dated 9/22, showed physician's orders for:
-Albuterol sulfate (used to prevent and treat difficulty breathing, wheezing, shortness of breath, coughing, and chest tightness) solution 0.63 milligrams (mg)/3 milliliters (ml); 1 vial; inhalation four times daily (ordered 8/25/22 discontinued on 9/3/22).
-Oxygen at 4 liters per minute per nasal cannula as needed for shortness of breath. May titrate from 1-4 liters to maintain oxygen level above 90 percent (ordered 4/19/22 discontinued 8/18/22)
Record review of the resident's Nursing Notes showed on 8/25/22 the resident continued on an antibiotic for an upper respiratory infection and continued to have a cough and increased congestion. The resident stated he/she did not feel well at all. The resident's temperature was 96.7, with slight wheezes in the upper lobes, and his/her oxygen level was 81 percent on room air. The oxygen concentrator was obtained and oxygen was applied at 2 liters per minute. The resident's oxygen was rechecked and his/her oxygen level was up to 93 percent. The physician was notified and ordered chest x-rays. The nurse called to schedule the lab.
Observation on 9/12/22 at 1:03 P.M., showed the resident was sitting in his/her wheelchair at the dining room table dressed for the weather. The resident was wearing oxygen.
Observation on 9/13/22 at 12:44 P.M., showed the resident was in his/her room. The oxygen concentrator was turned off and sitting beside the resident's recliner. The resident's breathing treatment machine was sitting on his/her night stand beside his/her bed. The nasal cannula and tubing that were attached to the concentrator were laying on the floor behind the recliner and the face mask and tubing that was attached to his/her breathing treatment machine were also laying on the floor behind the resident's recliner. There were no storage bags in the resident's room.
During an interview on 9/13/22 12:56 P.M., the resident said:
-He/She did not wear oxygen everyday-only when he/she needed it.
-He/She did not receive breathing treatments every day.
-He/She received breathing treatments whenever the staff came in to give it to him/her.
-He/She did not know if there was a schedule for her to receive breathing treatments, but he/she received them whenever he/she had difficulty breathing.
2. Record review of Resident #21's Face Sheet showed he/she was admitted on [DATE] with diagnoses including high blood pressure, heart disease, muscle weakness, and respiratory infection (infections of parts of the body involved in breathing, such as the sinuses, throat, airways or lungs).
Record review of the resident's admission MDS dated [DATE], showed the resident:
-Was alert and oriented, needed extensive assistance with bed mobility, transfers, and had occasional incontinence of bowel and bladder.
-Was totally dependent for toileting, bathing and hygiene, had limited range of motion with her upper extremities and used a wheelchair for mobility.
-Did not receive respiratory therapy and did not receive oxygen.
Record review of the resident's Nursing Notes showed:
-On 8/25/22 the resident was having increased congestion, eye drainage and a cough. Resident did have some hoarseness off and on. He/She had orders for Zyrtec (an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching) and if needed Albuterol breathing treatment. Left message for the physician.
-On 8/28/22 the resident had a productive cough of thick green sputum. The physician was notified and gave an order for Levaquin (an antibiotic used to treat bacterial infections) 750 mg daily for 10 days which was administered to the resident. There was also an order to change the resident's breathing treatments to three times daily.
Record review of the resident's POS dated 9/22, showed physician's orders for:
-Albuterol sulfate inhaler; 2 puffs; inhalation for acute asthma every 4 Hours as needed (ordered 8/16/22).
-Albuterol sulfate solution for breathing treatment 2.5 mg /3 ml: 1 vial; every 4 Hours as needed (ordered 9/5/22).
Observation and interview on 9/12/22 at 9:39 A.M., showed the resident was sitting in his/her room beside his/her bed dressed for the weather and wearing an immobilizing brace on his/her right arm. There was a breathing treatment machine sitting on the nightstand beside his/her bed. The face mask was sitting next to the machine and it was uncovered. There was an oxygen concentrator sitting beside the resident's bed. The oxygen tubing and nasal cannula were laying on the floor next to the resident's bed. There was no storage bag on or around the oxygen concentrator or breathing treatment machine. The resident said he/she received breathing treatments in the evening. He/She did not say he/she used oxygen.
Observation on 9/12/22 at 1:56 P.M., showed the resident was still in the dining room. In the resident's room showed his/her breathing treatment machine was still sitting on top of his/her nightstand with the face mask laying beside it uncovered. The oxygen concentrator was on and running at 4 liters per minute. The nasal cannula and tubing were on the floor in front of the concentrator beside the resident's bed. There were no oxygen storage bags in the resident's room.
Observation on 9/13/22 at 12:39 P.M., showed the resident was in the dining room eating lunch. In the resident's room showed his/her breathing treatment machine was sitting on the nightstand beside the resident's bed and the facemask was laying beside the machine uncovered. The cup for the breathing treatment was detached from the face mask and was also uncovered. There was an artificial plant beside the facemask and a small pillow that was on top of the facemask and treatment cup. There were no oxygen storage bags in the room.
Observation and interview on 9/14/22 at 8:50 A.M., showed the resident was sitting in his/her wheelchair in his/her room. The resident was not wearing oxygen. His/Her oxygen concentrator was turned off and the nasal cannula was coiled and laying on the floor beside his/her bed. The resident said he/she wanted to get into his/her recliner. Certified Nursing Assistant (CNA) A went into the resident's room and transferred the resident into his/her recliner. CNA A gave the resident his/her the call light, placed the resident's tray table beside him/her with his/her beverage, and asked if the resident needed anything. CNA A did not check to see if his/her oxygen tubing or face mask was stored in a bag before leaving the resident's room.
3. Record review of Resident #15's Face Sheet showed he/she was admitted on [DATE] with diagnoses including respiratory failure, Chronic Obstructive Pulmonary Disease (COPD, a chronic inflammatory lung disease that causes obstructed airflow from the lungs), high blood pressure, diabetes and heart failure.
Record review of the resident's admission MDS dated [DATE], showed the resident:
-Needed extensive assist with mobility and transfers, was totally dependence for dressing, hygiene, bathing, toileting and was occasionally incontinent of bladder and bowel.
-Used a wheelchair for mobility, and had limited range of motion with his/her upper extremities.
-Showed the resident received no respiratory treatments or oxygen.
Record review of the resident's POS dated 9/22, showed physician's orders for:
-Budesonide suspension (for breathing treatment) 0.5 mg/2 ml; 1 vial twice daily, rinse mouth after use (ordered 9/2/22).
-Ipratropium-Albuterol solution (for breathing treatment) 0.5 mg-3 mg/3 ml; 1 vial four times daily, rinse mouth after use (ordered 9/2/22).
-Oxygen at 4-5 liters per minute per nasal cannula continuous (ordered 9/2/22).
-Change oxygen and breathing treatment tubing monthly once a day on the first Wednesday of the month (ordered 9/2/22).
-Trilogy (an all-in-one ventilation device, capable of delivering both invasive and non-invasive ventilation modes) at night with oxygen at 5 liters per minute (settings are pre-set on machine) at bedtime (ordered on 9/2/22).
Observation on 9/12/22 at 2:19 P.M., showed the resident was alert and oriented, was sitting on his/her bed wearing his/her nasal cannula and was completing a crossword puzzle. His/her call light was within reach. There was a Trilogy on the resident's nightstand with a face mask laying next to it, uncovered. The resident said:
-He/she wore the trilogy (facemask) at night and he/she had to wear oxygen consistently throughout the day.
-He/she used both an oxygen concentrator and a portable oxygen tank.
-He/she also received breathing treatments.
Observation on 9/13/22 at 12:33 P.M., showed the resident was not in his/her room. The resident's trilogy was sitting on the resident's nightstand with the facemask uncovered and laying behind the trilogy machine. There was a breathing treatment machine next to the trilogy and the facemask was laying beside the machine uncovered with moisture droplets inside of the container that was attached to the face mask. There were no storage bags for either facemask.
Observation on 9/14/22 at 8:13 A.M., showed the resident's trilogy was sitting on the resident's nightstand with the facemask uncovered and laying behind the trilogy machine. There was a breathing treatment machine next to the trilogy and the facemask to the breathing treatment machine was also laying beside the breathing treatment machine, uncovered. There were no storage bags for either facemask observed.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Drug Regimen Review
(Tag F0756)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Record review of Resident #16's Face Sheet showed he/she was admitted on [DATE] with the following diagnoses:
-Muscle weaknes...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Record review of Resident #16's Face Sheet showed he/she was admitted on [DATE] with the following diagnoses:
-Muscle weakness.
-Protein-calorie malnutrition (a nutritional status in which reduced availability of nutrients leads to changes in body composition and function).
-Unspecified dementia (a chronic or persistent disorder of the mental processes caused by brain disease or injury and marked by memory disorders, personality changes, and impaired reasoning).
-History of falls.
-Nausea.
Record review of the resident's Drug Regimen Reviews showed the pharmacist documented the following:
-January 2022, February 2022, March 2022, and April 2022, the pharmacist reviewed the resident's medications. Documentation showed, Medication Regimen Review Completed: See report for any noted irregularities and/or recommendations.
-There were no reports documented showing if there were any recommendations for any medication changes for the resident.
Record review of the facility Drug Regimen Review binder showed there were no records of any pharmacy recommendations after May 2022 (there was no documentation in the binder after May 2022).
Request for one year of the resident's monthly medication review given in writing to the Social Services Director on 9/14/22 at 9:36 A.M.
During an interview on 9/14/22 at 10:39 A.M., the DON said he/she did not know where the monthly medication recommendation from the pharmacist were kept or how to find them.
During an interview on 9/14/22 at 11:40 A.M. DON said:
-He/she had started this position in July 2022 and he/she was not trained on how to complete the Drug Regimen Review and was not aware of the facility's process for Drug Regimen Review.
-He/she was not aware how to follow-up on the pharmacy recommendations.
-He/she had not been receiving or monitoring the Drug Regimen Review and recommendation reports from the pharmacy.
During an interview on 9/14/22 at 12:59 P.M., the DON said he/she was contacting the pharmacy to get the pharmacy recommendations and notes.
3. Record review of Resident #13 admission Face-Sheet showed he/she was admitted to the facility on [DATE] and readmitted on [DATE] with diagnoses of:
-Congestive heart failure (disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body).
-History of blood clots in lower legs.
-Alzheimer's disease (a slowly progressive disease of the brain that is characterized by impairment of memory and eventually by disturbances in reasoning, planning, language, and perception)
-Anxiety.
-Polyosteoarthritis (is a condition where pain and inflammation occur in multiple joints at once).
-Seizure (a hyperexcitation of neurons in the brain leading to a sudden, violent involuntary series of contractions of a group of muscles)
-Obsessive-Compulsive disorder (OCD, is an anxiety disorder characterized by intrusive thoughts that produce uneasiness, apprehension, fear, or worry; by repetitive behaviors aimed at reducing the associated anxiety; or by a combination of such obsessions and compulsions).
Record review of resident's Pharmacy Consultant note dated 4/5/22, 5/2/22 and 6/6/22, showed:
-Medication Regimen Review Completed: See report for any noted irregularities and/or recommendations.
-No documentation of the recommendations found.
Record review of resident's Pharmacy Consultant note dated 7/4/22 showed:
-Medication Regimen Review Completed: See report for any noted irregularities and/or recommendations.
-No documentation of the recommendations found.
Record review of the resident's Quarterly MDS dated [DATE] showed:
-The resident able to make his/her need known.
-Required medication during the assessment included Anxiety, Anticoagulant (blood thinner), diuretic (for edema or swelling of fluid) and opioid (narcotic pain medication).
-No documentation of any antipsychotic medications (a group of psychoactive drugs (pertaining to a drug or other agent that affects such normal mental functioning as mood, behavior, or thinking processes) commonly but not exclusively used to treat psychosis) that required a Gradual Dose Reduction (GRD).
Record review of resident's Pharmacy Consultant note dated 8/8/22, showed:
-Medication Regimen Review Completed: See report for any noted irregularities and/or recommendations.
-No documentation of the recommendations found.
-No documentation related to review for GDR since 6/18/21.
Record review of the resident's Physician Order Sheet (POS) dated 8/13/22 to 9/13/22 showed the resident was on the following medications:
-Keppra for seizures, Donepezil used for Alzheimer's Disease, Klonopin for Obsessive-compulsive disorder and seizures, Lasix for edema (excess fluid), Lexapro used for anxiety, Xarelto used for thinning blood and Hydrocodone-acetaminophen used for (narcotic) pain control.
Observation on 9/13/22 at 9:26 A.M., showed the resident was sitting in specialized chair in the front living area with his/her eyes closed.
During an interview on 9/14/22 at 11:10 A.M., the DON said:
-The report documented in the resident progress notes and showed to See report for any noted irregularities and/or recommendations was the pharmacy report.
-The facility had no other pharmacy reports.
Based on observation, interview and record review, the facility failed to ensure the recommendations from the Pharmacist's Drug Regimen Review were obtained and to determine if there were any recommendations that needed a response for follow up for four sampled resident's (Resident #6, Resident #21, Resident #13, and Resident #16). The facility census was 27 residents.
1. Record review of Resident #6's Face Sheet showed he/she was admitted on [DATE], with diagnoses including heart failure (chronic, progressive condition in which the heart muscle is unable to pump enough blood to meet the body's needs for blood), urine retention (condition in which you are unable to empty all the urine from your bladder), diabetes (disease in which the body ' s ability to produce or respond to the hormone insulin is impaired, resulting in abnormal metabolism of carbohydrates and elevated levels of glucose in the blood and urine), muscle weakness, stroke, anxiety disorder (a feeling of worry, nervousness, or unease, typically about an imminent event or something with an uncertain outcome) and pain.
Record review of the resident's quarterly Minimum Data Set (MDS-a federally mandated assessment tool to be completed by facility staff for care planning) dated 6/5/22, showed the resident:
-Was alert and oriented.
-Needed limited assistance with dressing and hygiene.
-Needed extensive assistance with bed mobility, transfers and had upper and lower limited range of motion.
-Needed extensive assistance with bathing, toileting and was occasionally incontinent with bladder and bowel.
Record review of the resident's Drug Regimen Reviews showed the pharmacist documented the following:
-On 6/6/22, 7/4/22, 8/8/22 and 9/6/22 the pharmacist reviewed the resident's medications. Documentation showed, Medication Regimen Review Completed: See report for any noted irregularities and/or recommendations.
-There were no reports documented showing if there were any recommendations for any medication changes for the resident.
Record review of the resident's Medical Record showed there were no reports to show if there were any pharmacy recommendations that resulted from the medication reviews.
Record review of the facility Drug Regimen Review binder showed there were no records showing any pharmacy recommendations were completed after June 2022 (there was no documentation in the binder after June 2022).
2. Record review of Resident #21's Face Sheet showed he/she was admitted on [DATE] with diagnoses including high blood pressure, heart disease (a type of disease that affects the heart or blood vessels), muscle weakness, and respiratory infection (infections of parts of the body involved in breathing, such as the sinuses, throat, airways or lungs).
Record review of the resident's admission MDS dated [DATE], showed the resident:
-Was alert and oriented needed extensive assistance with bed mobility, transfers, and had occasional incontinence of bowel and bladder.
-Was totally dependent for toileting, bathing and hygiene, had limited range of motion with her upper extremities and used a wheelchair for mobility.
-Was at risk for pressure sores, but was admitted with no pressure sores and had no unhealed pressure sores.
Record review of the resident's Drug Regimen Review showed the pharmacist showed:
-On 9/6/22 the pharmacist reviewed the resident's medications and documented, Medication Regimen Review Completed: See report for any noted irregularities and/or recommendations.
-There was no August or September review results completed that showed the resident had any medication recommendations.
Record review of the resident's Medical Record showed there were no reports to show if there were any pharmacy recommendations that resulted from the medication reviews.
Record review of the facility Drug Regimen Review binder showed there were no records showing any pharmacy recommendations completed after June 2022.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0804
(Tag F0804)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure the recipe for the fried chicken was palatable ...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure the recipe for the fried chicken was palatable and to have a mechanism via the resident council process, for residents to state any concerns regarding the palatability of the food. This practice potentially affected at least 25 residents who ate a regular diet from the kitchen. The facility census was 27 residents.
1. Record review of the recipe for 25 servings of fried chicken showed:
- 9 pounds of cut up boneless chicken that was thawed.
- 2 cups flour.
- 1 tablespoon (Tbsp.) +1/4 teaspoon (tsp.) salt.
- 1 and 5/8 tsp. paprika.
- 1 and 5/8 tsp. black pepper.
- Directions: mix the seasonings and flour. Dredge the chicken in seasoned flour.
- ¼ cup and 3 Tbsp. whole liquid eggs.
- ½ cup + tsp. 2% milk.
- Directions: dip the chicken in the egg/milk mixture.
- 6 and ¼ ounces bread crumbs.
- Directions: Roll chicken in bread crumbs
- Place in baking pans and finish in the oven at 325 ºF (degrees Fahrenheit) for 30-35 minutes. Follow hot holding temperature of 135 ºF or 140 ºF based on facility policy.
Observation on 9/12/22 from 10:24 A.M. through 12:10 P.M., showed Dietary [NAME] (DC) A made the fried chicken according to the recipe.
Observation on 9/12/22 at 12:10 P.M., showed the breaded chicken breaded was made according to recipe, but there not much flavor.
During an interview on 9/12/22 at 1:04 PM., DC A said the breaded chicken tasted bland, because the recipe did not call for much salt.
During an interview on 9/12/22 at 1:12 P.M., the DM said the breaded chicken was blah and it did not have flavor.
During an interview on 9/12/22 at 2:02 P.M., Resident #75, a resident identified by his/her quarterly Minimum Data Set (MDS- a federally mandated assessment tool completed by the facility for care planning) dated 6/12/22, as a resident who understands others, a resident who was able to make himself/herself understood, and had a Brief Interview for Mental Status (BIMS- a screening tool used to assist with identifying a resident's current cognition and to help determine if any interventions need to occur) of 15 (indicating he/she was cognitively intact), said:
- Sometimes the food is overdone and not tender.
- A lot of times the food is cold.
During an interview on 9/12/22 at 2:06 P.M., Resident #20, a resident identified by his/her quarterly MDS, dated [DATE], as a resident who understood others, made himself/herself understood and had a BIMS of 15, said:
- There was way too much breading on the chicken that was served that day.
- The breading was not that good and the breading did not have any taste.
- The pork chops were overcooked and hard in the past.
During an interview on 9/12/22 at 2:20 P.M., Resident #4, a resident identified by his/her quarterly MDS dated [DATE], as a resident who understood others , made himself/herself understood and had a BIMS of 15, said:
- The chicken was typical.
- There was too much breading on the chicken.
- There really was not any flavor to the chicken.
- They liked the carrots and mashed potatoes and gravy.
- 90% of time the food is awful. The meat is too tough at times.
During an interview on 9/13/22 at 2:19 P.M., Resident #10, a resident identified by his/her quarterly MDS dated [DATE], as a resident who understood others, made himself/herself understood and had a BIMS of 15, said:
- The food was lousy.
- The breading on the chicken was too hard for him/her to chew and it was kind of dry.
- The breading did not taste very good.
- The food does not taste good to him/her.
During an interview on 9/14/22 at 1:20 P.M., the Administrator said:
- There were not any resident council minutes to review, because the last time the facility had resident council was July 2021.
- He/she was told the resident council meetings used to be conducted monthly.
- The current Business Office Manage (BOM) fulfills the three roles of BOM, Social Service Designee and Activities Director, resident council is a part of the activities.
- Conducting Resident Council meetings is a priority of the facility, but the former Resident Council president passed away on August 23, 2022.
- The recipes were made to be bland and that is something that should be looked at.
- The Administrator said the chicken was a little bland on 9/12/22.
During an interview on 9/14/22 at 1:41 P.M., DM said:
- He/she had been the DM for four months.
- He/she had heard about the complaints about the taste of the food a few times.
During an interview on 9/15/22 at 9:45 A.M. the BOM said:
- He/she has worked at the facility since May 2022
- He/she was told about performing the duties of the Business Office and SSD before she got hired.
- After he/she was hired, he/she voluntarily did activities.
- Performing the duties of the Business office and Social Service Designee, took more time, because of that, it is hard to get to do the activities and running the resident council is a part of activities.
- The activities part gets the least amount of her attention.
During a phone interview on 9/20/22 at 10:46 A.M., the Consultant Registered Dietitian (RD) said:
- The recipes the facility used, are standardized recipes from a different company.
- If a recipe is followed, and it did not turn out well, the dietary staff needed to bring that recipe to him/her for discussion, when he/she visited the facility.
- That particular recipe for the breaded chicken, was not discussed with him/her.
- He/she agreed that the recipes should be palatable.
- The chicken should be palatable and delicious.
- He/she wants to expand the substitution log for the cook(s) to document recipes that do not have good taste and quality, because that will be another way to capture good information.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Staffing Information
(Tag F0732)
Could have caused harm · This affected most or all residents
Based on observation, interview and record review, the facility failed to ensure staffing sheets were posted daily. The facility census was 27 residents.
1. Observation on 9/14/22 at 11:20 A.M. showed...
Read full inspector narrative →
Based on observation, interview and record review, the facility failed to ensure staffing sheets were posted daily. The facility census was 27 residents.
1. Observation on 9/14/22 at 11:20 A.M. showed no staffing sheets were posted visibly in the front entrance, nurse's station, or dining room for residents and visitors to see.
Observation on 9/15/22 at 8:12 A.M. showed no staffing sheets were posted visibly in the front entrance, nurse's station, or dining room for residents and visitors to see.
Record review on 9/15/22 at 11:35 A.M. showed:
-A white binder with staffing information tucked in with all other binders behind the nurse's station.
-The daily staffing sheets only showed care staff assignments and not the daily staffing care staff numbers.
During an interview on 9/15/22 at 11:51 A.M. the Administrator said:
-He/she posted the daily staffing numbers at the end of the day.
-The staffing numbers were posted within the white staffing binder.
-He/she was the staffing coordinator for the facility.
-He/she was not sure if the daily staffing numbers were posted for visitors to visibly see.
An interview on 9/15/22 at 4:40 P.M. the Director of Nursing (DON) said:
-He/she would expect the staffing numbers to be posted daily.
-He/she was not sure if this was currently being done.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Food Safety
(Tag F0812)
Could have caused harm · This affected most or all residents
Based on observation, interview and record review, the facility failed to prevent the buildup of food debris and dust on the floor in the dry goods storage room and under the three reach-in refrigerat...
Read full inspector narrative →
Based on observation, interview and record review, the facility failed to prevent the buildup of food debris and dust on the floor in the dry goods storage room and under the three reach-in refrigerators; to ensure the filters of the two ceiling vents located in the kitchen at the entrance from North Hall corridor, were free of a heavy dust buildup; and to to ensure a 5 pound (lb) container of sour cream was discarded after its expiration date. This practice potentially affected 27 residents who ate food from the kitchen. The facility census was 27 residents
1. Observations on 9/12/22 from 9:25 A.M. through 12:40 P.M., showed:
- Two moon pies of the chocolate cream and the flavor and the oatmeal cream pie flavor were found on the floor of the dry goods storage room.
- Two filters in the ceiling vents over entrance way from the North Service Hall with heavy buildup of dust.
- A buildup of dust and food debris under the three reach-in fridge.
- One 5 lb container of sour cream was in the reach in refrigerator closet to the food preparation table, which was expired on 6/26/22.
During an interview on 9/12/22 at 9:34 A.M., the Dietary Manager (DM) said:
- He/she did not know the last time maintenance cleaned those two vents.
- He/she has been working this job for about two months.
During an interview on 9/12/22 at 1:15 P.M., the DM said:
- He/she did not know how that container of sour cream got overlooked.
- He/she expected the dietary staff to check the containers daily.
- That one really got overlooked.
- He/she expected her staff to pull out the refrigerators at least every three days to sweep and mop that area where the refrigerators were.
Record review of the 1999 and 2009 Food and Drug Administration (FDA) Food Code and Missouri Food Codes, showed:
- In Chapter 6-501.12, paragraph A, The physical facilities shall be cleaned as often as necessary to keep them clean.
- In Chapter 6-501.14, part A, Intake and exhaust air ducts shall be cleaned and the filters changed so they are not a source of contamination by dust, dirt, and other materials.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Garbage Disposal
(Tag F0814)
Could have caused harm · This affected most or all residents
Based on observation, interview and record review, the facility failed to keep a lid on a trash container in the kitchen during the lunch meal. The facility census was 27 residents.
1. Observation on ...
Read full inspector narrative →
Based on observation, interview and record review, the facility failed to keep a lid on a trash container in the kitchen during the lunch meal. The facility census was 27 residents.
1. Observation on 9/12/22 on 10:39 A.M., 10:53 A.M., 11:48 A.M., 12:19 P.M., and 1:17 P.M., showed one trash container next to dishwasher was left open without a lid.
During an interview on 9/12/22 at 1:17 P.M. Dietary Aide (DA) A said he/she did not know where the lid for that trash container, next to the dishwasher, was located.
Record review of the 2009 Food and Drug Administration (FDA) Food Code
Chapter 5-501.110 entitled Storing Refuse, Recyclables, and Returnables, showed: Refuse, recyclables, and returnables shall be stored in receptacles or waste handling units so that they are inaccessible to insects and rodents.
Chapter 5-501.113 entitled Covering Receptacles, showed: Receptacles and waste handling units for refuse, recyclables, and returnables shall be kept covered:
(A) Inside the food establishment if the receptacles and units: (1) Contain food residue and are not in continuous use; or
(2) After they are filled; and
(B) With tight-fitting lids or doors if kept outside the food establishment.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Infection Control
(Tag F0880)
Could have caused harm · This affected most or all residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Record review of the facility undated policy titled Infection prevention and control program showed:
-Facility wide surveilla...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** 4. Record review of the facility undated policy titled Infection prevention and control program showed:
-Facility wide surveillance will be performed to identify opportunities to prevent and/or reduce the rate of infection in our residents, employees and visitors. Standardized definitions of infection for surveillance in long-term care facilities will be utilized.
-Data collected would be:
--Collected by concurrent and/or retrospective chart review, review of microbiological reports, reports from resident care providers and review of other documents, as appropriate;
--Collected by review of employee health logs;
--Trended internally for historical comparison;
--Reported to the infection prevention committee no less than quarterly.
Record review of the facility's infection surveillance log showed:
-Infection tracking was divided out by month.
-Each month divided out into infection type and amount.
-Tracking had not been completed from March 2022 through September 2022.
-Infection tracking did not include lab work, residents involved, or if the resident was put on an antibiotic.
During an interview on 9/14/22 at 12:49 P.M. the MDS Coordinator said:
-He/she was now in charge of the facility's infection control surveillance.
-He/she was made aware of this on 9/12/22.
-He/she was not trained how the facility tracked and monitored infection control in the building.
-He/she thought the DON was previously in charge of infection control.
During an interview on 9/14/22 at 2:15 P.M., the DON said:
-He/She did not have any additional information related to the infection control manual.
-He/She did not know who was supposed to complete the tracking log before he/she started working at the facility.
-He/She did not know it was not being completed until Monday.
-The infection control surveillance book did not have a map of the facility, did not have a list of residents with infections, did not have lab results, and did not list any antibiotics that may have been used.
-There was no information in the surveillance manual since March 2022.
During an interview on 9/15/22 at 4:40 P.M., the DON said:
-Everyone was in charge of infection control until two days ago when the MDS Coordinator was assigned the role.
-He/she noticed that infection control tracking and trending was not being done a couple of weeks ago.
-The infection control tracking and trending should be updated monthly.
5. Record review of the facility undated TB Policy showed:
-The steps for administering a TB test were check physician's order for testing, place resident in comfortable position and expose forearm, cleanse site with alcohol swab, inject in upper third of forearm using intradermal injection technique with bevel of needle upward, a wheal (pale elevation of skin) 6-10 mm in diameter should appear immediately, if no wheal forms, the injection may have been too deep. Inject the solution at a site at least two inches (5 cm) from the first site or on the other arm, position resident comfortably with call light within reach.
-How to interpret the test results were measure the area of induration (hardening, thickening of tissues) at 48 and 72 hours, erythema is not generally considered evidence of an active or dormant infection, an average of 10 mm is a doubtful reaction; 4 mm or less is a negative reaction, if positive reaction occurs, notify physician and carry out additional orders, if a two step TB testing procedure has been approved by the facility's Infection Control Committee, repeat this process within the time period specified in guidelines for when test results are negative, Repeat testing at regular intervals as determined by the facility's infection control guidelines.
-The policy showed the form the facility was to use to document the two step TB test. The form showed an area to document the date the test was administered and an area to document the date the result was read and what the result of the TB test was.
Record review of Resident #16's TB screening form showed:
-He/she admitted on [DATE].
-He/she had step one of his/her TB screening completed outside of the facility, dated 1/29/22.
-No documentation of step two being completed inside or outside of the facility upon admission.
During an interview on 9/15/22 at 4:40 P.M., the DON said:
-He/she expected the admission nurse to complete TB screening and testing.
-He/she was not able to explain why the TB screening was not completed for this resident's.
6. Record review of Resident #224's TB screening form showed:
-He/she admitted on [DATE].
-The second step of the TB testing was identified as negative with the word negative and did not include the millimeters (mm) of induration in the results section of the test.
During an interview on 9/15/22 at 4:40 P.M. the DON said he/she expected the results of the TB test to be read in mm of induration.
7. Record review of Resident #4's TB screening form showed:
-He/she admitted on [DATE].
-Step one was given on 2/24/22.
-The results of step one were not read until 2/28/22.
During an interview on 9/15/22 at 4:40 P.M., the DON said the TB test should have been read on 2/26/22 or 2/27/22 at the latest, and not on 2/28/22.
8. Record review of the facility undated policy titled Diabetic infection control showed:
-Gloves are to be worn when performing fingersticks and changed between resident contacts.
-Remove and discard gloves in appropriate receptacles after each procedure that involves potential exposure to blood or body fluids, including fingerstick blood sampling.
-Perform handhygiene (Le., hand washing with soap and water or use of an alcohol-based hand rub) immediately after removal of gloves and before touching other medical supplies intended for use on another resident.
Observation of Resident #75's blood sugar check by LPN B showed:
-He/she did not place a barrier down between the medication cart and the glucometer (blood sugar machine) when the glucometer was placed on the cart during the check.
-He/she removed the gloves worn during the blood sugar check.
-He/she did not wash his/her hands or perform hand hygiene between doing the blood sugar check and giving the resident insulin (a hormone produced in the pancreas which regulates the amount of glucose (sugar) in the blood).
During an interview on 9/15/22 at 4:40 P.M. the DON said he/she expected hand hygiene to be performed:
-When going from a dirty task to a clean task.
-When removing gloves.
3. Record review of Resident #274's face sheet showed he/she was admitted on [DATE] with the following diagnoses:
-Unspecified injury of head.
-Contusion (a bruise) of the scalp.
Record review of the resident's Physician Order Sheet (POS), dated September 2022, showed:
-Staff were to apply skin prep (a liquid film-forming dressing that, upon application to intact skin, forms a protective film to help reduce friction during removal of tapes and films) daily to the resident's left heel until healed.
-Staff were to cleanse the resident's right and left buttock daily with wound cleanser, pat dry, cover with xeroform (a wound dressing consisting of a gauze soaked in a mixture of bismuth tribromophenate and petroleum jelly), and secure the dressing.
Observation on 9/14/22 at 10:53 A.M., showed:
-Agency LPN B did not clean the resident's table before placing wound care supplies on it.
-Agency LPN B did not place a barrier between the resident's table and wound care supplies.
-LPN B washed his/her hands, put on gloves, removed the dressings from the resident's right and left buttock, and removed gloves.
-LPN B put on new gloves without washing or sanitizing hands.
LPN B picked up gauze (gauze was not packaged and was placed directly on uncleaned tray table during setup), moistened with saline, and cleaned the wound.
-LPN B opened packaging (with the same dirty gloves from cleaning the wound) for xeroform and cut the dressings, then placed xeroform in each wound bed without changing gloves between wounds.
-LPN B removed gloves, without washing or sanitizing hands, put on new gloves.
-LPN B completed the wound care.
-LPN B applied barrier cream (a product applied directly to the skin surface to help maintain the skin's physical barrier) to the resident's genital area with same gloves used for wound care.
-LPN B removed gloves and put on new gloves without sanitizing or washing hands.
-LPN B examined the resident's genitals with assistance of his/her hands to expose crevices.
-LPN B touched the resident's arm with his/her gloved hand.
-CNA B was assisting in positioning the resident during this procedure; when he/she was no longer needed, he/she removed his/her gloves, did not wash or sanitize hands, and touched the resident's door and door knob before leaving the room.
-LPN B removed all reusable supplies from the room and placed on treatment cart with no barrier between supplies and cart.
-LPN B removed gloves and sanitized hands.
-NOTE: Reusable supplies were not cleaned with alcohol or disinfectant wipes.
During an interview on 9/14/22 at 1:00 P.M., Nursing Aide (NA) A said after removing gloves, staff were to wash or sanitize their hands without exception.
During an interview on 9/14/22 at 1:25 P.M., CNA A said:
-Staff were always to wash or sanitize hands after removing gloves.
-Staff were to remove gloves after peri-care (cleaning of the private areas of a patient) before touching any other part of a resident.
During an interview on 9/14/22 at 1:34 P.M., Certified Medication Technician (CMT) A said:
-Staff were to wash or sanitize hands after removing gloves.
-Staff should not touch any other part of a resident with gloves used to perform peri-care.
During an interview on 9/14/22 at 1:55 P.M., LPN A said:
-Staff were to wash or sanitize hands after removing gloves without exception.
-Staff were to place wound care supplies on a clean barrier and never directly on the resident's table.
-Reusable supplies were to be cleaned with disinfectant wipes or alcohol before being placed back in the treatment cart or taking to another resident's room.
-Staff should never touch any other part of a resident before changing gloves after wound care had been performed.
During an interview on 9/15/22 at 2:01 P.M., LPN B said:
-Hands should be washed or sanitized after glove removal with the exception of during wound care when all wounds are on the same resident.
-He/she changed gloves during wound care, but did not need to wash or sanitize his/her hands if he/she was still working with the same resident.
-There should probably have been a barrier or something between the resident's table and clean wound care supplies.
-Staff were to clean reusable wound care supplies before putting them back in the cart or taking them to another resident's room.
During an interview on 9/15/22 at 4:39 P.M., the Director of Nursing (DON) said:
-Staff were to wash or sanitize their hands after every glove removal.
-Staff were to place a barrier between clean supplies and the resident's table.
-Staff were expected to wash or sanitize their hands when entering a resident's room, between clean and dirty procedures, and before leaving the room.Based on observation, interview, and record review, the facility failed to ensure handwashing was completed to prevent cross contamination during incontinence care for one sampled resident (Resident #6), wound care for two sampled residents (Resident #21 and Resident #274); failed to ensure infection control monitoring, tracking, and trending was completed; failed to ensure TB (TB - a communicable disease that affects especially the lungs, that is characterized by fever, cough, difficulty in breathing, and abnormal lung tissue and function) screening was obtained, completed and documented correctly for three sampled residents (Resident #16, Resident #224 and Resident #4); failed to ensure appropriate infection control practices were used during blood sugar checks for one supplemental resident (Resident #75) out of five resident's sampled for TB and out of 14 sampled residents. The facility census was 27 residents.
Record review of the facility's undated Handwashing Policy showed the purpose was to reduce the transmission of organisms from resident to resident, staff to resident, and resident to staff. The handwashing policy showed the steps for how to wash hands, but it did not show when staff were supposed to wash their hands.
Record review of the facility's undated policy titled Gloves showed gloves were to be changed between contact with different body sites of the same resident.
Record review of the facility's undated policy titled Wound Care and Treatment showed:
-Staff were to set up wound care supplies on a clean surface with an impervious barrier between the surface of the table and supplies.
-Staff were to wash hands prior to applying gloves.
-Staff were to remove soiled dressing, remove gloves, and wash hands before putting on the next set of clean gloves.
-Staff were to next clean the wound, remove gloves, wash hands, and put on clean gloves.
-Staff were then to apply clean dressing, remove gloves, and wash hands.
1. Record review of Resident #6's Face Sheet showed he/she was admitted on [DATE] with diagnoses including:
-Heart failure (a chronic, progressive condition in which the heart muscle is unable to pump enough blood to meet the body's needs for blood).
-Urine retention (a condition in which you are unable to empty all the urine from your bladder).
-Diabetes (a disease that occurs when your blood glucose, also called blood sugar, is too high).
-Muscle weakness.
-Stroke.
-Anxiety disorder (a feeling of worry, nervousness, or unease, typically about an imminent event or something with an uncertain outcome).
-Pain.
Record review of the resident's quarterly Minimum Data Set (MDS-a federally mandated assessment tool to be completed by facility staff for care planning), dated 6/5/22, showed the resident:
-Was alert and oriented.
-Needed limited assistance with dressing and hygiene.
-Needed extensive assistance with bed mobility, transfers, and had upper and lower limited range of motion.
-Needed extensive assistance with bathing, toileting, and was occasionally incontinent of bladder and bowel.
Observation on 9/12/22 at 2:01 P.M., showed Certified Nursing Assistant (CNA) A:
-Put on gloves without washing or sanitizing his/her hands and transferred the resident to the bathroom.
-Pulled the resident's pants and brief down and lowered him/her onto the toilet.
-Told the resident he/she would be back to check on him/her and to pull the call light when he/she was done using the bathroom.
-Removed and discarded his/her gloves, then without washing or sanitizing his/her hands, CNA A left the resident's room and went into another resident room.
-Sanitized his/her hands before re-entering the resident's room and went to the bathroom, provided incontinence assistance, and pulled his/her brief and pants up.
-Without washing or sanitizing his/her hands, CNA A transferred the resident, using the lift, out of the bathroom and into his/her recliner, provided the resident with his/her call light and beverage, and made the resident comfortable. He/She then went back into the bathroom, flushed the toilet, bagged the soiled trash then washed his/her hands.
During an interview on 9/14/22 at 2:18 P.M., CNA A said:
-He/she was supposed to wash his/her hands or sanitize them upon entering the resident's room and before leaving.
-When he/she provided transfer and assistance to the resident he/she was supposed to wash or sanitize his/her hands, then glove and transfer the resident to the bathroom.
-After assisting with pulling the resident's pants and briefs down he/she should have washed or sanitized his/her hands again before leaving the room. He/She was supposed to wash or sanitize his/her hands before leaving the resident's room and upon re-entering it.
2. Record review of Resident #21's Face Sheet showed he/she was admitted on [DATE] with diagnoses including high blood pressure, heart disease, muscle weakness, and respiratory infection (infections of parts of the body involved in breathing, such as the sinuses, throat, airways or lungs).
Record review of the resident's admission MDS, dated [DATE], showed the resident:
-Was alert and oriented and needed extensive assistance with bed mobility, transfers, and had occasional incontinence of bowel and bladder.
-Was totally dependent for toileting, bathing, and hygiene, had limited range of motion with his/her upper extremities and used a wheelchair for mobility.
-Was at risk for pressure sores, but was admitted with no pressure sores and had no unhealed pressure sores.
Record review of the resident's Nursing Notes, dated 8/29/22, showed the resident had a small open area on his/her right buttock that was approximately 1 centimeter (cm) in diameter. The nurse cleaned the area and applied barrier cream.
Observation on 9/13/22 at 10:11 A.M., showed the resident was sitting in his/her wheelchair in his/her room. The following occurred:
-Licensed Practical Nurse (LPN) A entered the resident's room and without washing his/her hands or sanitizing them, put on gloves, gathered barrier cream and q-tips and placed them directly on the resident's bed without placing a clean barrier on the bed first.
-LPN A then placed a gait belt around the resident's waist.
-LPN B entered the resident's room, put on gloves without washing or sanitizing his/her hands and began assisting LPN A with transferring the resident to his/her bed.
-LPN A and LPN B lowered the resident's pants and removed his/her brief.
-LPN A removed the wound dressing that contained brownish drainage and cleaned the wound and measured it. He/She then applied barrier cream without changing gloves or washing/sanitizing his/her hands.
-LPN A and LPN B assisted with putting the resident's clothes back on and removed their gloves. They did not wash or sanitize their hands prior to leaving the resident's room.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Antibiotic Stewardship
(Tag F0881)
Could have caused harm · This affected most or all residents
Based on interview and record review, the facility failed to ensure the antibiotic stewardship program was being conducted and reviewed during the last 12 months that included antibiotic usage, infect...
Read full inspector narrative →
Based on interview and record review, the facility failed to ensure the antibiotic stewardship program was being conducted and reviewed during the last 12 months that included antibiotic usage, infection monitoring, laboratory results, and an overall system for the provision of feedback reports was being done facility wide. The facility census was 27 residents.
Record review of the facility's undated Infection Prevention and Control Program showed:
-Facility wide surveillance will be performed to identify opportunities to prevent and/or reduce the rate of infection in our residents, employees, and visitors.
-Data will be trended internally for historical comparison and reported to the infection prevention committee no less than quarterly.
-Surveillance priorities are urinary tract infections, respiratory tract infections, eye, ear, nose, and moth infections, skin infection, gastrointestinal tract infection, and primary blood stream infection.
1. Record review of the facility's infection control manual showed no documentation of an antibiotic stewardship program being conducted or monitored.
During an interview on 9/14/22 at 12:38 P.M. the Minimum Data Set (MDS-a federally mandate assessment tool completed by facility staff for care planning) Coordinator said:
-The infection control book was the most recent he/she could find.
-He/she was supposed to be the facility's Infection Preventionist, but had not been trained in any infection control yet.
-He/she was assigned the infection control task on Monday 9/12/22.
During an interview on 9/14/22 at 2:15 P.M. the Director of Nursing (DON) said:
-He/she did not have any more additional information regarding the infection control manual including mapping, residents with infections, labs, or antibiotics.
-He/she was not sure who was in charge of infection control before him/her.
-He/she was not aware that infection control including the antibiotic stewardship program was not being done until Monday 9/12/22.
During an interview on 9/15/22 at 4:40 P.M. the DON said that infection control and the antibiotic stewardship program was all of the staff's responsibility.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0882
(Tag F0882)
Could have caused harm · This affected most or all residents
Based on interview and record review, the facility failed to ensure an Infection Preventionist was designated and certified in infection prevention and control. The facility census was 27 residents.
R...
Read full inspector narrative →
Based on interview and record review, the facility failed to ensure an Infection Preventionist was designated and certified in infection prevention and control. The facility census was 27 residents.
Record review of the facility's undated Infection Prevention and Control Program policy showed:
-The Infection Preventionist was qualified to conduct infection prevention.
-He/she would complete the Centers for Disease Control and Prevention (CDC) Long Term Care Infection Preventionist module.
1. During an interview on 9/14/22 at 12:50 P.M. the Minimum Data Set (MDS-a federally mandate assessment tool completed by facility staff for care planning) Coordinator said:
-He/she was the designated Infection Preventionist as of 9/12/22.
-He/she was not a certified Infection Preventionist.
-He/she thought the Director of Nursing (DON) was in charge of infection control prior to Monday, 9/12/22.
Record review of the facility's undated infection prevention manual showed:
-There was no documentation of who the designated Infection Preventionist was.
-There was no evidence of anyone who had completed the Infection Preventionist certification working within the facility.
During an interview on 9/15/22 at 11:48 A.M. the DON said:
-He/she was not the designated Infection Preventionist prior to Monday, 9/12/22.
-He/she was not Infection Preventionist certified.
During an interview on 9/15/22 at 11:52 A.M. Certified Medication Technician (CMT) B said there used to be multiple Infection Preventionist certified staff in the building, but they have all quit and have not worked at the facility for a while now.
During an interview on 9/15/22 at 4:40 P.M. the DON said that infection control and prevention was all of the staffs' responsibility.