CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0557
(Tag F0557)
Could have caused harm · This affected 1 resident
Based on observation, interview and record review, the facility failed to ensure staff treated one resident (Resident #35) in a review of nine sampled residents, with dignity and respect when Certifie...
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Based on observation, interview and record review, the facility failed to ensure staff treated one resident (Resident #35) in a review of nine sampled residents, with dignity and respect when Certified Nurse Assistant (CNA) C performed a Covid (Coronavirus-infectious disease) test on the resident without talking with the resident prior to administering the test to request permission, to educate to the rationale or preparation for testing, or to ensure privacy of the resident when tested. The census was 52.
The facility did not provide a policy regarding dignity when requested.
Review of the booklet, Resident Rights For Long-Term Care in Missouri, showed residents should be treated with consideration and respect and with full recognition of dignity and individuality.
1. Review of Resident #35's quarterly Minimum Data Set (MDS), a federally mandated assessment instrument, completed by the facility, dated 10/6/23, showed the following:
-Adequate hearing;
-Clear speech;
-Sometimes understands others;
-Severely impaired cognition;
-Short and long term memory problem;
-No rejection of care.
Review of the resident's care plan, last revised 10/18/23 showed the following:
-Risk for changes in psychosocial well being related to safety measures required by the CDC to decrease risk of Covid-19;
-The resident will need time and patience from you when attempting to make needs known.
Review of the resident's Physician Order Sheet (POS) dated 1/2024 showed the following:
-Diagnoses included Alzheimer's disease (a progressive disease which destroys memory and other mental functions);
-May have Covid testing as needed (PRN) (8/17/21).
Review of the resident's progress notes showed the following:
-On 12/6/23, 12/28/23 and 1/2/24 resident tested for Covid 19 antigen with negative results;
-On 1/3/24 no signs or symptoms of Covid, resident up eating his/her meals.
Observation of the resident on 1/4/24 at 11:44 A.M. showed the following:
-The resident sat in his/her recliner in the common area with his/her head resting on the right arm of the chair and his/her eyes closed;
-Two other residents sat in their recliners and three residents sat at the table in the same room;
-Certified Nurse Aide (CNA) C entered the common area with a packaged nasal swab and applied gloves;
-He/She walked over to the resident, inserted the swab into the resident's nasal passages, moved it around and then spoke the resident's name and quietly spoke a few words, five at most. CNA C did not speak to the resident or explain that he/she was going to perform a Covid test prior to completing the test;
-The resident repeated no and attempted to move away from the CNA as the CNA performed the test.
During interview on 1/4/24 at 11:50 A.M., CNA C said the following:
-No one had directed him/her to perform a Covid test on the resident;
-He/She did not think the resident felt good so he/she wanted to test him/her;
-He/She would report the findings to his/her charge nurse;
-He/She said it would have been a dignity issue if he/she had not been discreet, (his/her back to the rest of the room, blocking others from seeing).
During interview on 1/5/24 at 11:41 A.M., Licensed Practical Nurse (LPN) A said the following:
-He/She believed the resident to be at baseline and had not suspected any reason for the resident to be Covid tested;
-He/She was not aware that CNA C Covid tested the resident and he/she did not direct him/her to do so;
-CNA C did not report any Covid test results to him/her;
-Prior to conducting a Covid test, staff should educate the resident and explain the procedure.
During an interview on 1/11/24 at 3:21 P.M., the Director of Nursing (DON) said the following:
-He/She would expect staff to ideally provide privacy when performing Covid testing;
-It would probably be best not to test Resident #35 as it would be traumatic for him/her either way.
During interview on 1/5/24 at 3:32 P.M., the Administrator said the following:
-The nurse should make the decision as to when a resident should be tested for Covid;
-They would expect for the CNA to get consent from the nurse before testing a resident and inform the nurse of the test results after the testing;
-If the nurse had not assessed the resident, had not instructed the CNA to perform a Covid test on the, and the CNA then failed to report the findings of the test to the nurse, this would be an unnecessary traumatic event for the resident.
MO228693
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0602
(Tag F0602)
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 one resident (Resident #1), in a review of nine sampled resi...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure one resident (Resident #1), in a review of nine sampled residents, remained free from misappropriation of property when the resident's iPad (an electronic tablet/computer) came up missing and was presumed stolen. The facility census was 52.
On 1/5/23, the administrator was notified of the past noncompliance which occurred on 12/25/23. On 12/26/23 the administrator identified Certified Nurse Aide (CNA) D as misappropriating Resident #1's ipad (electronic tablet/computer) after review of facility camera footage. Upon discovery, CNA D was suspended, the facility conducted an investigation and notified appropriate parties, including local law enforcement. Inservicing of staff was conducted where the abuse and neglect policy, which included misappropriation of resident property, was reviewed and the facility reported they planned to replace the resident's ipad. The deficiency was corrected on 1/5/24.
Review of the undated facility policy, Prevention of Abuse & Neglect and Misappropriation of Residents Property, showed the following:
-The facility will make every effort to protect the resident's personal belongings by doing a completed inventory of personal belongings on admission and again annually. Any lost belongings will be reported to the charge nurse or social services director and every effort will be made to find them;
-Prevention of Misappropriation of Resident Property:
Residents, their families and staff will receive information on how to and whom to report concerns, incidents and grievances without the fear of retribution. Staff members will receive this policy by way of annual review information on orientation, yearly and as needed in-services.
Review of the booklet, Resident Rights For Long-Term Care in Missouri, showed residents have the right to be free from misappropriation of resident property and exploitation.
1. Review of Resident #1's annual Minimum Data Set (MDS), a federally mandated assessment instrument completed by the facility, dated 9/15/23, showed the following:
-Very important to take care of his/her personal belongings/things;
-Very important to do favorite activities;
-Somewhat important to listen to music he/she liked.
Review of the resident's care plan dated 10/11/23 showed the following:
-Resident has periods of confusion and forgetfulness;
-Resident prefers things to be a certain way. Attempt to keep his/her schedule and belongings the same.
Review of the resident's quarterly MDS, dated [DATE] showed the following:
-Severely impaired cognition;
-Adequate hearing and speech.
During interview on 1/4/24 at 1:35 P.M., CNA E said he/she knew the resident had a tablet which the resident would use to listen to music. He/She reported that it was missing to the charge nurse.
Review of the time card report for CNA D showed he/she worked 12/22/23 from 1:30 P.M. to 4:24 A.M. on 12/23/23.
Review of the facility investigation for the resident's missing iPad, dated 1/4/24, showed the facility interviewed staff and residents about the missing iPad and any other items they could have missing. The Administrator contacted the resident's family and the replacement cost of the iPad would be around $400.00 to $500.00. The facility had viewed video footage dated 12/22/23 and 12/23/23 which showed suspicious behavior on the part of CNA D, including carrying a white charger cord out of the resident's room, attempting to conceal it and carrying it to the break room. CNA D's last date to work was 12/24/23.
Review of the theft report, provided by law enforcement, dated 12/27/23 at 9:21 A.M., showed the following:
-The administrator contacted him/her regarding a missing iPad which belonged to Resident #1;
-The iPad had been seen recently by staff in the resident's room;
-The administrator had located video footage of CNA D entering and exiting the resident's room with laundry under his/her arm with what appeared could be something folded inside the laundry. The Administrator said this would be unusual, as all dirty laundry was removed from a resident's room in a laundry hamper.
Review of the facility surveillance video, on 1/4/24 at 2:10 P.M., showed the following:
-On 12/22/23 at 1909 (7:09 P.M.) the resident walked with staff (not CNA D) to the shower room. He/She wore black pants, a white shirt and a black vest;
-At 1938 (7:38 P.M.) the resident walked with staff (not CNA D) back to his/her room. He/She wore cream sweat pants and a black vest;
-At 2223 (10:23 P.M.) CNA D entered the resident's room (call light was on) and exited the room with a small white object in a white trash bag in his/her right hand and a pair of blue pajamas tucked under his/her left arm with part of them hanging down. He/She walked and entered the soiled utility room and exited carrying nothing. CNA D looked around and walked to the breakroom at 2234 (10:34 P.M.) and then to the smoke room;
-On 12/23/23 at 0213 (2:13 A.M.) CNA D entered the resident's room without knocking (call light was not on) and at 0214 (2:14 A.M.) exited holding a white charging cord, which he/she quickly rolled up to conceal, (keeping it in his/her hand) and walked to and entered the break room.
During interview on 1/4/24 at 2:10 P.M., the administrator said the following:
-The resident's family had gifted him/her the iPad with his favorite music downloaded for him/her to listen to;
-Staff were aware and assisted the resident at different times with the iPad;
-He/She was first made aware of the missing iPad on 12/25/23 after the family had notified the Director of Nurses;
-They watched video surveillance which showed CNA D entering and exiting the resident's room carrying clothes, a bag and a charger. They believed CNA D had carried the iPad out wrapped up in the clothes he/she carried out and then returned for the charger.
-They planned to replace the resident's missing iPad.
MO229263
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Report Alleged Abuse
(Tag F0609)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review and policy review, the facility failed to ensure an alleged injury of unknown ori...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review and policy review, the facility failed to ensure an alleged injury of unknown origin was reported to the State Survey Agency (SSA) in a timely manner for one of three (Residents (R) 19) residents reviewed for reporting allegations to the SSA in a timely manner. The census was 52.
Findings include:
Review of the admission Record in the electronic medical record (EMR) under the Profile tab revealed R19 was admitted to the facility on [DATE] with a diagnosis of dementia with behavioral disturbances.
During an observation on 11/14/23 at 3:06 PM, R19 was in the activity room and had bruising on his/her neck.
Review of the Progress Notes dated 11/16/23 revealed R19 had two small bluish reddish bruises to the right side of his/her neck. The note indicated the nurse talked to R19's family member and both agreed that R19 slept in unusual positions either in bed or in the recliner and he/she could have bruised him/herself. The resident was unable to say how the bruising on his/her neck got there due to his/her cognition.
During an interview on 11/16/23 at 3:54 PM Certified Nursing Assistant in Training (CNAT) 5 revealed he/she first saw bruising to R19's neck on 11/13/23 and reported the bruising to the nurse on duty.
During an interview with the Director of Nursing (DON) on 11/16/23 at 4:48 PM she confirmed CNAT5 reported the bruising to the nurse on 11/13/23, however, the nurse did not report the incident to the Administrative staff. The DON confirmed the bruising (injury of unknown origin) should have been reported to the SSA (state agency) in a timely manner and it was not. The DON further confirmed she reported the injury of unknown origin on 11/16/23 and the bruising was first noted and reported on 11/13/23.
During an interview on 11/16/23 at 4:46 PM the administrator said she did not know about the bruise until today (11/16/23). She said she would have reported it immediately if she had known.
Review of the facility's policy, Abuse, Neglect and Exploitation policy (undated) revealed it is the policy of this facility to provide protections for the health, welfare and rights of each resident by developing and implementing written policies and procedures that prohibit abuse. Reporting of all alleged violations to the Administrator, state agency, adult protective services and to all other required agencies (e.g., law enforcement when applicable) within specified time frames: the allegation involve abuse or result in serious bodily injury, or injury of unknown origin. Not later than 24 hours if the events that cause the allegation do not involve abuse and do not result in serious bodily injury. The Administrator will follow up with government agencies, during business hours, to confirm the initial report was received, and to report the results of the investigation when final within 5 working days of the incident, as required by state agencies.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0637
(Tag F0637)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, the facility failed to complete a significant change assessment for one of 24 sa...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, the facility failed to complete a significant change assessment for one of 24 sampled residents (Resident (R) 21) after R21 suffered a cerebral vascular accident (CVA) which resulted in R21 needing a feeding tube due to being unable to take food or fluids by mouth. The census was 52.
Findings include:
Review of R21's Face Sheet, located in the electronic medical record (EMR) under the Resident tab, revealed R21 was admitted to the facility on [DATE] with diagnoses that included unspecified dementia, atrial fibrillation, and essential hypertension.
Review of R21's quarterly Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 05/02/23 and located under the RAI tab of the EMR, revealed R21 did not have a feeding tube.
Review of R21's Dietary Quarterly Note dated 05/12/23 at 7:13 PM and located under the Resident tab of the EMR, revealed the resident was on a regular/mech [mechanical] soft diet. The resident eats in the east activity area and is assisted by staff with meal choices. The resident likes to have a pancake and scrambled eggs with syrup for breakfast. The resident likes coffee and cranberry/apple juice and desserts and sweet foods.
Review of R21's Progress Note dated 07/12/23 at 5:15 PM and located under the Resident tab of the EMR, revealed the resident was brought to nurses station by CNA [Certified Nurse Aide], who stated the resident had choked on broccoli and apple juice. The resident had a little bit of food in his/her mouth that they removed, staff removed the resident's dentures to see if that would help make sure everything was out of his/her mouth, resident sounds like he/she had fluid in his/her throat, was having trouble trying to cough, and swallow when asked to. Left sided facial droop noticed, the resident's voice had a garbled sound to it, when asked to lift arms, left arm was drooping, could not grip with left side.
Review of R21's Progress Note, dated 07/24/23 at 5:15 PM and located under the Resident tab of the EMR, revealed Resident was re-admitted for CVA and stroke, resident is NPO [nothing by mouth] currently has a peg [feeding] tube placed and receives continuous peg tube feedings.
Review of R21's MDS 3.0 Resident Assessments list, located under the RAI tab of the EMR, revealed the facility did not complete a significant change assessment following R21's hospitalization for a CVA which resulted in R21 needing a feeding tube due to being unable to take food or fluids by mouth.
During an observation on 11/16/23 at 9:00 AM, R21's feeding tube insertion site was observed. CNA3 confirmed R21 did not take any food or fluids by mouth.
During an interview on 11/16/23 at 9:33 AM, the MDS Coordinator (MDSC) confirmed she did not complete a significant change assessment for R21 after the resident returned to the facility following hospitalization for a CVA and placement of a feeding tube. The MDSC said R21 should have had a significant change assessment completed.
On 11/17/23 at 2:02 PM, the MDSC stated the facility used the RAI manual as the facility policy for completing significant change assessments.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0658
(Tag F0658)
Could have caused harm · This affected 1 resident
Based on observation, interview and record review, the facility failed to follow professional standards of practice when Certified Nurse Assistant (CNA) C performed a Covid (Coronavirus-infectious dis...
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Based on observation, interview and record review, the facility failed to follow professional standards of practice when Certified Nurse Assistant (CNA) C performed a Covid (Coronavirus-infectious disease) test (an invasive procedure where a cotton swab is inserted in a resident's nasal passages and a sample collected for testing) on one resident, (Resident #35), in a review of nine sampled residents. Resident #35 had not been assessed by a licensed nurse to determine the resident had symptoms that necessitated testing. Instead, CNA C performed the test without any professional basis for testing and without documented training to show he/she received appropriate training to perform the test. The facility census was 52.
During interview on 1/11/24 at 3:21 P.M., the Director of Nursing (DON) said the facility did not have a policy for Covid testing.
Review of the undated facility job description for CNA's showed the following:
-Immediate Supervisor: charge nurse;
-General responsibilities to the facility:
1. Follow company policies and procedures;
2. Greet all visitors, staff and most importantly, the residents with a prompt courteous approach;
3. Adhere to the philosophies, goals and objectives of the facility;
4. Cooperate and be able to work with all departments cohesively for the betterment of the facility and residents;
5. Adhere to professional standards, follow policy and procedures and abide by federal, state and local requirements;
-Specific Responsibilities:
1. Provide direct care to all residents to include but not limited to:
Bathing, dressing, toileting, ambulating, transferring, shaving, nail care and oral care;
2. Conduct bed checks at least every two hours;
3. Do walking rounds with the on-coming shift. Be sure to check all residents, shower room, dirty utility room, etc.;
4. Assist in the dining room (getting menus, passing plates);
5. Assist residents with all meals;
6. Make beds;
7. Pass ice water and snacks;
8. Catheter care and emptying catheters;
9. Obtain accurate intakes and outputs;
10. Maintain residents' room (keep them stocked and tidy);
11. Pick up resident clothing and take to laundry;
12. Clean bed pans, urinals and commodes;
13. Wash wheel chairs/geri chairs;
14. Be able to change out oxygen tanks;
15. Assist residents to and from activities;
16. Assist residents with smoking;
17. Answer call lights in a timely manner;
18. Document daily on provided tablets and on the kisoks;
19. Be responsible to carry and maintain your pagers (sign them in and out every shift);
20. Attend care plan meetings;
21. Obtain resident vital signs and weights;
22. Report changes in resident condition to the charge nurse.
1. Review of Resident #35's quarterly Minimum Data Set (MDS), a federally mandated assessment instrument, completed by the facility, dated 10/6/23, showed the following:
-Adequate hearing;
-Clear speech;
-Sometimes understands;
-Severely impaired cognition;
-No rejection of care.
Review of the resident's care plan, last revised 10/18/23 showed the following:
-Risk for changes in psychosocial well being related to safety measures required by the CDC to decrease risk of Covid-19;
-The resident will need time and patience from you when attempting to make needs known.
Review of the resident's Physician Order Sheet (POS), dated 1/2024, showed the following:
-Diagnoses included Alzheimer's disease (a progressive disease which destroys memory and other mental functions);
-May have Covid testing as needed (PRN) (8/17/21).
Review of the resident's progress notes showed the following:
-On 12/6/23, 12/28/23 and 1/2/24 resident tested for Covid 19 antigen with negative results;
-On 1/3/24 no signs or symptoms of Covid, resident up eating his/her meals.
Observation of the resident on 1/4/24 at 11:44 A.M. showed the following:
-The resident sat in his/her recliner in the common area with his/her head resting on the right arm of his/her chair and his/her eyes closed;
-CNA C entered the common area with a packaged nasal swab and applied gloves;
-CNA C walked over to the resident, inserted the swab into the resident's nasal passages, moved it around and then spoke the resident's name and quietly spoke a few words, five at most. CNA C did not speak to the resident or explain that he/she was going to perform a COVID test prior to completing the test;
-The resident repeated no and attempted to move away from the CNA during the procedure.
During interview on 1/4/24 at 11:50 A.M., CNA C said the following:
-No one had directed him/her to perform a Covid test on the resident;
-He/She did not think the resident felt good so he/she wanted to test him/her;
-He had not been trained to perform Covid testing but read the instructions on the box;
-He/She would report the findings to his/her charge nurse.
Review of CNA C's employee file showed no documentation he/she had been trained on how to perform a COVID test on him/herself or residents.
During interview on 1/5/24 at 11:41 A.M., Licensed Practical Nurse (LPN) A said the following:
-He/She believed the resident to be at baseline and had not suspected any reason for the resident to be Covid tested;
-He/She was not aware that CNA C Covid tested the resident and he/she did not direct him/her to do so;
-Covid testing would not be within CNA C's scope of practice;
-CNA C did not report any Covid test results to him/her;
-Prior to conducting a Covid test, staff should educate the resident and explain the procedure.
During interview on 1/5/24 at 3:32 P.M., the Administrator and the Infection Preventionist said the following:
-They had not trained staff to perform Covid testing on residents, however they did train them to test themselves so they would know how;
-All residents have a standing order for Covid testing as needed;
-A nurse should perform an assessment on the resident and request a CNA test a resident before the test is done;
-The nurse should make the decision as to when a resident should be tested for Covid;
-They would expect for the CNA to get consent from the nurse before testing a resident and inform the nurse of the test results after the testing.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
ADL Care
(Tag F0677)
Could have caused harm · This affected 1 resident
Based on observation, interview and record review, the facility failed to provide incontinent care for one additional resident, (Resident #29), of nine sampled residents. The census was 52.
Review of ...
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Based on observation, interview and record review, the facility failed to provide incontinent care for one additional resident, (Resident #29), of nine sampled residents. The census was 52.
Review of the facility policy, Perineal Care, last revised 2/2018 showed the purpose of this procedure was to provide cleanliness and comfort to the resident, to prevent infections and skin irritation, and to observe the resident's skin condition.
1. Review of Resident #29's annual Minimum Data Set (MDS), a federally mandated assessment instrument completed by facility staff, dated 11/2/23, showed the following:
-Diagnoses included Alzheimer's disease (progressive disease that destroys memory and other important mental functions);
-Occasionally incontinent of bladder and bowel;
-Required partial to moderate assist for toileting and personal hygiene.
Review of the resident's care plan, dated 12/13/23, showed the following:
-Incontinent of bladder and bowel at times;
-Resident will be clean and free of odors;
-Resident required staff assist to go to the restroom. Provide pericare with incontinent episodes.
Observation of the resident on 1/4/24, at 11:46 A.M., showed the following:
-The resident sat in a recliner in the dining room; he/she wore long pants and a sweat shirt;
-Nurse Assistant (NA) B assisted the resident to stand and walk to the dining table;
-The backside of the resident's pants and sweatshirt (bottom and lower back) were noticeably wet and saturated with urine;
-NA B led the resident to the dining table and had him/her sit in the chair. NA B noted the soaked clothing and said sometimes we fall short but we got to get back up;
-The resident said It makes me feel terrible and cold;
-NA B served the resident his/her lunch tray and the resident ate lunch;
(NA B did not call other staff for help or provide the resident incontinent care after the resident had been incontinent of urine).
During interview on 1/5/24, at 11:25 A.M., NA B said the following:
-He/She was the only staff scheduled on the unit but would call for help as needed;
-He/She should be working with a Certified Nurse Assistant (CNA);
-He/She really could not do anything without a CNA;
-He/She had changed the resident at 10:15 A.M.;
-He/She should have changed and dried the resident when it was noted the resident was wet with urine and before the resident ate lunch.
During interview on 1/5/24, at 3:32 P.M., the Administrator said the following:
-Residents should be checked and changed every two hours and as needed;
-If residents are observed wet with saturated clothing, they would expect staff to change the resident at that time;
-They would not have expected staff to assist a resident with soiled/wet clothing to the dining table for a meal without addressing and changing the resident first;
-NA's can provide resident care;
-If they needed help they could push the panic button they carry in their pockets.
MO228093
MO228693
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 interview and record review, the facility failed to ensure pressure ulcer prevention measures were completed per facili...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to ensure pressure ulcer prevention measures were completed per facility policy and consistent with professional standards of practice, for one resident out of a sample of two residents (Resident (R) 16) reviewed for pressure ulcers. The facility failed to conduct thorough weekly skin assessments, which included measurements, descriptions, and stage of a right heel wound to be able to identify a decline or an improvement, or new skin conditions. These failures had the potential to delay identification and treatment of any new wounds the resident might develop. The census was 52.
Findings include:
Review of R16's EMR located under the Resident tab indicated the resident was admitted to the facility on [DATE] with a diagnosis of unspecified dementia.
Review of a document provided by the facility titled Braden Scale for Prediction of Pressure Sore Risk dated 09/02/22, indicated R16 scored 15 and was identified to be at risk for the development of pressure ulcers. The document directed staff to continue with the plan of care. The facility provided no additional Braden Scale assessments prior to the end of the survey.
Review of R16's EMR titled Orders located under the Resident tab dated 04/26/23 indicated skin prep was to be applied to the resident's right heel twice a day until area resolved.
Review of R16's EMR titled Medication Administration Record (MAR) located under (eMAR [electronic MAR] tab indicated the resident was being treated for a right heel pressure ulcer from 04/23 to 11/23.
Review of R16's EMR titled nursing Progress Notes dated 05/01/23 to 11/14/23, failed to show staff completed consistent weekly skin assessments, for the resident's right heel which included stage, measurements, and description of the wound. Further review revealed weekly skin assessments were not completed for the following weeks: 05/09/23, 05/16/23, 06/06/23, 06/13/23, 07/04/23, 07/11/23, 08/01/23, 08/08/23, 08/29/23, 09/12/23, 09/19/23, 10/03/23, 10/10/23, 10/17/23, 10/24/23, 10/31/23, and 11/07/23.
Review of a document provided by the facility titled quarterly MDS with an ARD of 07/10/23 indicated staff could not determine a Brief Interview for Mental Status (BIMS) score and indicated R16 had short- and long-term memory problems. The assessment indicated the resident was totally dependent on bed mobility of one staff member and totally dependent on two staff for transfers. The assessment indicated the resident had no pressure ulcers.
Review of documents provided by the facility titled Skin Checks identified the following for R16's condition of her skin. On this document was a human diagram, front and back showed the following:
-On 03/18/23, the skin assessment indicated the resident had an old area on his/her right heel. There were no measurements or a description of the right heel. There was no stage to the right heel identified;
-On 03/24/23, the skin assessment indicated the resident had an old area on his/her right heel. There were no measurements or a description of the right heel. There was no stage to the heel identified;
-On 04/01/23, the skin assessment indicated the resident had no new areas and did not identify the condition of the resident's right heel. There was no stage to the heel identified;
-On 04/07/23, the skin assessment indicated the resident had no new areas and indicated the resident had a scab on his/her right heel. There were no measurements or a description of the right heel. There was no stage to the heel identified;
-On 04/22/23, the skin assessment indicated the resident had no new areas and there was a scabbed right heel. There were no measurements or a description of the right heel. There was no stage to the heel identified;
-On 04/29/23, the skin assessment indicated the resident had no new areas and there was no mention of the resident's right heel. There was no stage to the heel identified;
-On 05/04/23, the skin assessment indicated the resident had a scabbed right heel. There were no measurements or a description of the right heel. There was no stage to the heel identified;
-On 05/12/23, the skin assessment indicated the resident had a sore on the right heel which continued. There were no measurements or a description of the right heel. There was no stage to the heel identified;
-On 05/18/23, the skin assessment indicated the resident had a scab on the right heel which continued. There were no measurements or a description of the right heel. There was no stage to the heel identified;
-On 05/24/23, the skin assessment made no mention of the resident's right heel. There was no stage to the heel identified;
-On 06/02/23, the skin assessment indicated the resident's right heel continues. There were no measurements or a description of the right heel. There was no stage to the heel identified;
-On 06/06/23, the skin assessment made no mention of the resident's right heel. There was no stage to the heel identified;
On 06/16/23, the skin assessment indicated the resident's right heel had scab that continues. There were no measurements or a description of the right heel. There was no stage to the heel identified;
-On 06/24/23, 06/30/23, 07/06/23, 07/14/23, 07/21/23, 07/24/23, 08/05/23, 08/21/23, 08/30/23, 09/06/23, 09/13/23, 09/27/23, and 10/05/23 the skin assessments made no mention of the resident's right heel. There was no stage to the heel identified.
Review of R16's EMR titled Care Plan located under the RAI tab, dated 08/22/23, indicated the resident was incontinent of bowel/bladder and staff were to monitor for skin changes to turn and reposition the resident every two hours. In addition, the staff were to apply heel protectors while the resident was in bed.
During an interview on 11/15/23 at 10:52 AM, Certified Nursing Assistant Training (CNAT) 2 stated they were not sure if the resident had a pressure ulcer on the heel. CNAT 1 stated the resident was total care.
During an interview on 11/15/23 at 11:01 AM Certified Nursing Assistant (CNA) 3 stated she was not aware if R16 pressure ulcer on her heel was healed or not.
During an interview on 11/15/23 at 1:15 PM, Infection Control Nurse (ICP)/Quality Assurance (QA) Nurse stated R16 was at risk for the development of pressure ulcers. The ICP/QA Nurse stated a scabbed area cannot be staged.
During an interview on 11/16/23 at 11:17 AM, Licensed Practical Nurse (LPN) 1 stated R16 had a scab on his/her right heel, and it was not open and stated the resident continued with skin prep to treat her right heel. LPN 1 stated it was important to measure a pressure ulcer weekly to see if there was improvement or deterioration in the wound.
During an interview on 11/16/23 at 12:10 PM, the MDS Coordinator (MDSC) stated if an area was scabbed over it would be unstageable. The MDSC stated that it was the facility's belief that R16's right heel had healed and there was just a scab on it. The MDSC stated pressure ulcers should be measured and a description provided of the area. The ICP/QA Nurse was also present during this interview.
During an interview on 11/17/23 at 10:10 AM, the Director of Nursing (DON) stated R16's right heel wound should be measured on a weekly basis. The ICP/QA Nurse who was present during this interview stated the right heel could not be staged since it was scabbed over. A request was made for additional and more current Braden Scales to be produced and weekly skin audits during this interview. No additional information was provided by the facility prior to the end of the survey.
Per the RAI manual showed it is important to recognize and evaluate each resident's risk factors and to identify and evaluate all areas at risk of constant pressure. A complete assessment of skin is essential to an effective pressure ulcer prevention and skin treatment program. Throughout this section, terminology referring to healed versus unhealed ulcers refers to whether or not the ulcer is closed versus open. When considering this, recognize that Stage 1. Deep Tissue Injury (DTI), and unstageable pressure ulcers although closed (i.e., may be covered with tissue, eschar, slough, etc.) would not be considered healed. Facilities should be aware that the resident is at higher risk of having the area of a closed pressure ulcer open up due to damage, injury, or pressure, because of the loss of tensile strength of the overlying tissue. Tensile strength of the skin overlying a closed pressure ulcer is 80% of normal skin tensile strength.
Review of a policy provided by the facility titled Pressure Ulcers/Skin Breakdown Clinical Protocol dated 04/18 indicated nursing staff and the practitioner will assess and document an individual's significant risk factors for developing pressure ulcers, for example, immobility, recent weight loss, and history of pressure ulcer(s). In addition, the nurse shall describe and document/report a full assessment of the pressure sore including location, stage, length, width and depth, presence of exudates or necrotic tissue.
Review of a policy provided by the facility titled Additions to Pressure Ulcer Risk Assessment Policy dated 02/2014, indicated all pressure areas will be measured weekly, and measurements will be placed into the Wound Tracking Book. All licensed nurses will be assigned weekly skin assessments by the DON. Skin assessments will be completed and turned into the Quality Assurance Nurse. Any new pressure areas will be measured and put in the Wound Tracking Book and any new interventions to the Care Plan.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0692
(Tag F0692)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, observation, staff interviews, and facility policy review, the facility failed to assess nutritional sta...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, observation, staff interviews, and facility policy review, the facility failed to assess nutritional status after a significant weight gain/weight loss, and failed to take corrective action after the facility determined the weight gain and loss was an error for two (Resident (R) 6 and R43) of four residents reviewed for nutrition in a total sample of 24 residents.
Findings include:
1. Review of R6's electronic medical record (EMR) titled Resident Face Sheet located under the Resident tab indicated the resident was admitted to the facility on [DATE] with diagnoses that included unspecified dementia and anorexia.
Review of R6's EMR titled Vitals located under the Resident tab revealed the resident had a significant weight gain from 09/02/22 to 10/03/22 of 45.5 pounds. There was no evidence in the clinical record that a re-weigh was obtained nor was there evidence the resident's weight was taken during the month of 11/22. On 12/07/22 the resident weight was 178.5 and then lost 41.7 pounds by 01/25/23. Again, there was no evidence in the clinical record that a re-weigh was obtained.
Review of a document provided by the facility titled Minimum Data Set (MDS) with an Assessment Reference Date (ARD) of 06/13/22 indicated the staff could not determine R6's Brief Interview for Mental Status (BIMS) score. The assessment indicated the resident was not nutritionally at risk.
Review of R6's EMR titled Care Plan located under the RAI [Resident Assessment Instrument] tab, dated 09/13/23, indicated R6 ate a regular diet with fortified foods and a Registered Dietician (RD) consultant would be provided as needed.
Review of documents provided by the facility titled .Dietetic Consultation Service completed by the former RD, dated 11/09/22, 12/07/22, 02/09/23, 03/07/23, failed to identify R6's significant weight gain/loss.
Review of a document provided by the facility titled RD Recommendations dated 01/2023 failed to identify R6's significant weight gain/loss.
An observation was conducted on 11/15/23 at 11:25 AM R6 was sitting in the main dining room and began to eat her lunch meal. The resident was served meatloaf, mashed potatoes, and corn. The resident was observed to use her right hand and began to feed herself. The resident ate the entire serving of meatloaf and corn during this observation and left the mashed potatoes. During this observation, an interview took place with Certified Nursing Assistant Training (CNAT) 4 stated the resident was able to feed herself and did well with eating.
During an interview on 11/15/23 at 11:30 AM, Dietary 1 stated R6 stated the resident was able to feed herself and ate well and never remembered the resident to have a poor appetite.
During an interview on 11/15/23 at 1:15 PM, the Infection Control Nurse (ICP)/Quality Assurance (QA) was presented with R6's weights from the end of 2022 and stated the staff must not have subtracted the weight of the resident's wheelchair. The ICP/QA Nurse stated if there was a five percent variance of loss/gain the practice was to re-weigh the resident.
During an interview on 11/15/23 at 1:45 PM, the Dietary Manager (DM) stated she mentioned the irregularities of R6's weight in previous weight meetings but she confirmed there was no documentation to support this statement.
During an interview on 11/16/23 at 2:21 PM, the current RD stated if a resident had fluctuating weight, he would ask that the resident be re-weighed to verify the weights. The current RD stated he attends the monthly weight meetings, and any variance would be discussed.
2. Review of R43's Face Sheet, located under the Resident tab of the electronic medical record (EMR) revealed R43 was admitted to the facility on [DATE] with diagnoses that included heart failure and essential hypertension.
Review of R43's Orders, dated 06/30/23 and located under the Resident tab of the EMR, revealed staff was to obtain R43's weight each week on Wednesdays.
Review of the facility's Food & Nutrition Recommendation Sheet, dated 07/05/23 and provided by the Certified Dietary Manager (CDM), revealed the Registered Dietician (RD) had assessed R43 to have a significant weight loss during the previous three months.
Review of R43's Weekly Weights, for the month of July 2023 and located under the Resident tab of the EMR, revealed R43's weight was not obtained on 07/05/23, 07/12/23, and 07/19/23. It was recorded the weights were not obtained due to condition.
Review of R43's Progress Notes, dated 07/05/23, 07/12/23, and 07/19/23 and located under the Resident tab of the EMR, revealed no documentation to show why R43's weights were not obtained.
Review of R43's Weekly Weights, for the month of August 2023 and located under the Resident tab of the EMR, revealed R43's weight was not obtained on 08/02/23, 08/16/23, and 08/23/23. It was recorded the resident either refused or the weight was not obtained due to condition.
Review of R43's Progress Notes, dated 08/02/23, 08/16/23, and 08/23/23 and located under the Resident tab of the EMR, revealed no documentation to show why R43's weights were not obtained.
Review of R43's Weekly Weights, for the month of September 2023 and located under the Resident tab of the EMR, revealed R43's weight was not obtained on 09/06/23 or 09/13/23. It was recorded the resident either refused or the weight was not obtained due to condition.
Review of R43's Progress Notes, dated 09/06/23 and 09/13/23 and located under the Resident tab of the EMR, revealed no documentation to show why R43's weights were not obtained.
Review of R43's Orders, dated 09/20/23 and located under the Resident tab of the EMR, revealed staff was to obtain R43's weight daily due to chronic kidney disease.
Review of R43's Daily Weights, for the month of October 2023 and located under the Resident tab of the EMR, revealed R43's weight was not obtained on 18 out of 31 days. It was recorded R43's weight was not obtained due to either R43 refused, was sleeping, was done by prior shift, or due to condition. It was recorded R43 weighed 143 lbs. on 10/04/23 and 152.5 lbs. on 10/06/23. It was recorded R43 weighed 155.5 lbs. on 10/25/23 and 160.5 lbs. on 10/29/23.
Review of R43's Daily Weights, for 11/01/23 through 11/02/23 and located under the Resident tab of the EMR, revealed R43 weighed 211 lbs. on 11/01/23 and 150.5 lbs. on 11/02/23.
During an interview on 11/16/23 at 9:52 AM, Certified Nurse Aide (CNA) 3 stated all staff were responsible for obtaining weights. CNA3 stated she did not think staff was required to weigh R43 daily. CNA3 stated if a resident refused to be weighed or if staff had difficulty in obtaining a resident's weight, the staff should come back later to try again or find someone else to try. CNA3 stated if one shift was unable to obtain a weight, it should be reported to the next shift so they could try.
During an interview on 11/16/23 at 10:05 AM, Registered Nurse (RN) 1 confirmed R43 was supposed to be weighed daily but stated that R43 often refused. RN1 stated the facility had identified a concern with monthly weights and had assigned one staff member to obtain all monthly weights but the nurses and aides were responsible for obtaining daily weights.
During an interview on 11/16/23 at 11:48 AM, the Director of Nursing (DON) stated the consultant dietician monitored residents' weights. The DON confirmed that if there was a big discrepancy in weights, the staff was supposed to reweigh the resident. The DON stated she thought the staff was reweighing residents, as necessary. The DON stated staff was not provided any training related to weighing residents and were not monitored to ensure they were using the scales correctly. The DON reviewed R43's weights and confirmed the resident should have been weighed per orders and reweighed when there were large discrepancies.
During an interview on 11/17/23 at 11:06 AM, the administrator and Infection Preventionist (IP), who was the facility's QAPI lead, were asked if the facility had identified any concerns related to obtaining accurate weights before the survey. The IP stated they had started a new system of having one person obtain the monthly weights because the weights had been inconsistent. The IP was asked if daily and weekly weights had been included in the new system and if those weights were monitored for accuracy. The IP stated, No. The IP stated, We trust our nurses to look back [monitor].
Review of a policy provided by the facility titled, Weight Assessment and Intervention, dated 03/22, indicated .Any weight change of 5 % or more since the last weight assessment is retaken the next day for confirmation.If the weight is verified, nursing will immediately notify the dietitian in writing.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0728
(Tag F0728)
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 one newly hired nurse assistant (NA) (NA B), of...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview and record review, the facility failed to ensure one newly hired nurse assistant (NA) (NA B), of one NA employee file reviewed, obtained their certification within the required four month time frame. The census was 52.
Review of the undated facility policy, Lewis County Nursing Home Job Description-Nursing, showed:
-Position: Certified Nurse Assistant (CNA);
-Qualifications: Must be [AGE] years old. Must be certified (non-certified personnel will be offered classes at the facility and must become certified within the specified guidelines);
-General Responsibilities to the facility: Follow company policies and procedures. Adhere to professional standards, follow policy and procedures and abide by federal, state and local requirements.
Review of a undated document provided by the facility, titled Job Description Report by Department, showed NA B's original hire date and current hire date were both 6/13/23. He/She was employed full time as a CNAT (Certified Nurse Assistant in Training). His/Her class start date was 8/3/23.
Review of the nursing schedule for 12/10/23 to 12/23/23 showed NA B was scheduled to work 12/11/23 through 12/14/23 and from 12/16/23 through 12/20/23.
Observations on 1/4/24 at 11:12 A.M. and 11:46 A.M. showed the following:
-NA B stood in the common area of the locked dementia unit, where residents sat in recliners and at the dining table;
-NA B talked with residents as they sat in the common/dining area;
-NA B assisted residents to stand and walk to the dining table and served them their lunch trays;
(There was no other staff present at the time and NA B worked the locked unit without supervision. He/She phoned staff from outside the unit when he/she needed assistance with checking and changing residents).
During an interview on 1/4/24 at 11:13 A.M. and 1/5/24 at 11:25 A.M., NA B said the following:
-He/She had been working as an NA at the facility since the end of May 2023;
-He/She began CNA classes the beginning of October;
-He/She was not certified at this time;
-He/She should be working with a CNA;
-He/She was the only staff scheduled on the unit;
-The nurse for the unit was Licensed Practical Nurse (LPN) A who was working the other side (unit);
-He/She had changed (provided incontinence care) for a resident at 10:15 A.M.;
-When he/she needed help changing someone he/she called for assistance and someone would come over.
During interview on 1/5/24, at 3:32 P.M., the Administrator said the following:
-NA's can provide resident care;
-If they needed help they could push the panic button they carry in their pockets;
-They did not see an issue with an NA working alone in a locked unit anymore than they would a CNA;
-NA's should receive their certification within four months from the date of hire.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Drug Regimen Review
(Tag F0756)
Could have caused harm · This affected 1 resident
Based on interview, record review, and facility policy review, the facility failed to ensure pharmacy recommendations were acted upon/responded to in a timely manner for monthly medication regimen rev...
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Based on interview, record review, and facility policy review, the facility failed to ensure pharmacy recommendations were acted upon/responded to in a timely manner for monthly medication regimen reviews for one of five sampled residents (Resident (R) 43) reviewed for unnecessary medications. The census was 52.
Findings include:
Review of R43's Consultant Pharmacist Communication to Physician, dated 06/28/23 and provided by the Director of Nursing (DON), revealed, New regulations in effect November 28, 2017, require all PRN [as needed] psychotropic medications (including Ativan) to be limited 14 days. Therefore, in order for the facility to remain compliant, the PRN order for Ativan needs to be discontinued. Please review and consider DISCONTINUING the PRN order for Ativan. Hand-written on the communication was re-eval [re-evaluate] q [every] 7 days. The communication contained no physician response to the recommendation.
Review of R43's Consultant Pharmacist Communication to Physician, dated 09/26/23 and provided by the DON, revealed, In order for the facility to remain compliant, the PRN order for Ativan needs to be discontinued. Please review and consider DISCONTINUING the PRN order for Ativan. Hand-written on the communication was [change] to re-eval q 7 days. The communication contained no physician response to the recommendation.
Review of R43's Consultant Pharmacist Communication to Physician, dated 09/26/23 and provided by the DON, revealed, GRADUAL DOSE REDUCTION FOR PSYCHOTROPIC AGENTS REGARDING ABILIFY 400 MG [milligrams] IM [intramuscularly] Q MONTH, SEROQUEL 25 MG PO [by mouth] BID [twice daily], and BUSPIRONE 15 MG PO TID [three times daily] As you are aware, there are various CMS-related drug usage requirements related to the use of ALL psychoactive medications. This recommendation is a reminder to conduct an evaluation in an attempt to establish the lowest effective dose with the fewest number of medications through periodic reduction and/or discontinuation and does not necessarily reflect my clinical judgment or opinion regarding the discontinuation or reduction. Please review for the possibility of a trial dose reduction or taper to discontinuation. NOTE: Abilify and Seroquel include a BLACK BOX WARNING regarding the increased risk of mortality in elderly dementia patients. The communication contained no physician response to the recommendation.
During an interview on 11/16/23 at 11:48 AM, the DON said the pharmacy consultant came monthly, reviewed the residents' medication regimens, and sent reports to her. She reviewed the reports and then presented them to the physician, and the physician would write on them whether they wanted to follow the recommendation or not. The DON said this process should be completed in 30 days. The DON said the medication regimen reviews had last been sent to the physicians in July 2023. The DON confirmed it was her writing on the communications for R43.
During an interview on 11/17/23 at 9:55 AM, the Pharmacist confirmed he had requested a GDR for R43's Seroquel, buspirone, and Abilify during September 2023. The Pharmacist stated he did not have a reply yet for those recommendations. The Pharmacist confirmed he had requested the facility reduce or stop R43's use of Ativan multiple times. The Pharmacist confirmed his recommendation was that a resident use PRN Ativan no longer than 60 days. The pharmacist stated he had made the recommendation to reduce or stop the Ativan during March, June, and then again in September 2023. The Pharmacist stated the facility responded to his recommendations by saying they would continue the seven-day re-evaluation.
Review of the facility's policy titled Antipsychotic Medication Use, revised December 2016, revealed antipsychotic medications may be considered for residents with dementia but only after medical, physical, functional, psychological, emotional psychiatric, social and environmental causes of behavioral symptoms have been identified and addressed. Antipsychotic medications will be prescribed at the lowest possible dosage for the shortest period of time and are subject to gradual dose reduction and re-review.
Review of the facility's undated, Pharmacy Recommendation Review Policy, provided by the DON, revealed Pharmacy recommendations will be reviewed by the DON. The DON will add nursing recommendations and fax to the physician within one week of receiving them. The physician will have ten working days to respond. If no response, the DON will have physician or Nurse Practitioner review and sign recommendations when they do round, monthly. Pharmacy recommendations will be done within one month of receiving them.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Medication Errors
(Tag F0758)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interviews, and facility policy review, the facility failed to ensure two residents (Resident (R) ...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on record review, staff interviews, and facility policy review, the facility failed to ensure two residents (Resident (R) 51 and R43) of five residents reviewed for unnecessary medication were being monitored for behaviors while taking psychotropic medications, additionally, failed to identify an indication for the use of a psychotropic medication, and failed to attempt Gradual Dose Reductions (GDRs) or document a rationale for the reason not to attempt a GDR.
Findings include:
1. Review of a document provided by the facility titled Assisted Living Physician Orders dated 08/26/23, indicated R51 was prescribed Haldol 1 milligram (mg) to be administered by mouth at bedtime for agitation.
Review of R51's electronic medical record (EMR) titled Resident Face Sheet located under the Resident tab indicated the resident was admitted to the facility on [DATE] with a diagnosis of Alzheimer's disease.
Review of R51's EMR titled Physician Orders dated 10/31/23, indicated the resident was to be administered Haldol 1 mg by mouth at bedtime.
Review of documents provided by the facility titled admission Minimum Data Set (MDS)with an Assessment Reference Date (ARD) of 11/06/23, indicated R51 had a Brief Interview for Mental Status (BIMS) score of five out of 15 which revealed the resident had severe cognitive impairment. The assessment revealed the resident had no behavior(s) nor was identified as a risk to self or to other residents.
A review of R51's EMR titled Nursing Progress Notes, from 10/31/23 forward, did not contain evidence of behavior monitoring. There was no indication for the use of the Haldol.
An attempt was made on 11/15/23 at 9:22 PM, to interview R51. The resident was in bed on her right side, eyes were open, and she did not respond to questions.
During an interview on 11/15/23 at 10:52 AM, Certified Nursing Assistant Training (CNAT) 2 stated R51 was more of a night person and slept during the day. CNAT2 stated the resident did not yell out constantly and did not refuse care. CNAT stated the resident did not hit out either.
During an interview on 11/15/23 at 11:02 AM, Certified Nursing Assistant (CNA) 3 stated R51 was not aggressive and was not verbally abusive with others. CNA 3 stated the resident only wanted to remain in bed.
During an interview on 11/15/23 at 1:15 PM, the Infection Control Preventionist (ICP)/Quality Assurance (QA) Nurse stated R51 was on Haldol prior to her admission.
During an interview on 11/16/23 at 11:25 AM, Licensed Practical Nurse (LPN) 1 stated R51 was given Haldol at night. LPN1 stated the resident had no behaviors other than voicing she wants to go to bed.
During an interview on 11/17/23 at 9:39 AM, the Consultant Pharmacist stated R51 was a new admission and would be reviewing his/her medications. The Consultant Pharmacist stated he looks for an appropriate diagnosis for the use of any psychotropic medication and would typically request a gradual dose reduction (GDR) within the first quarter for the use of an antipsychotic medication. The Consultant Pharmacist stated it was difficult to locate behaviors, in resident clinical records, related to the use of psychotropic medication.
During an interview on 11/17/23 at 10:10 AM, the Director of Nursing (DON) confirmed there was no indication for the use of Haldol. The ICP/QA Nurse was present during this interview and stated the resident had agitation.
2. Review of R43's Face Sheet, located under the Resident tab of the EMR revealed R43 was admitted to the facility on [DATE] with diagnoses that included unspecified dementia, unspecified atrial fibrillation, and heart failure.
Review of R43's Orders dated 12/18/22 and located under the Resident tab of the EMR, revealed R43 was to receive Ativan (lorazepam), an anxiolytic medication, 0.5 milligrams (mg) by mouth three times daily as needed (PRN). It was recorded to re-evaluate the need for the PRN Ativan every seven days. There was no indication for the use of the Ativan.
Further review of R43's Orders and Progress Notes, dated 12/18/22 through 08/22/23 and located under the Resident tab of the EMR, revealed the order for Ativan, 0.5 mg three times daily PRN was renewed after each evaluation period. There was no documentation of the physician's rationale for continuing the PRN order.
Review of R43's quarterly MDS with an ARD of 08/22/23 and located under the RAI (Resident Assessment Instrument) tab of the EMR, revealed R43 had long and short-term memory problems, behaviors of inattention, disorganized thinking, and wandering and received antipsychotic and antidepressant medications on seven of the preceding seven days.
Review of R43's Medication Administration Records (MARs), dated September 2023 and located under the Reports tab of the EMR, revealed R43 received Ativan 0.5 mg as follows:
-09/01/23 - 6:35 PM for anxiety;
-09/02/23 - 11:12 PM for anxiety;
-09/03/23 - 9:05 AM for restlessness and 6:14 PM for anxiety;
-09/05/23 - 6:47 PM for anxiety;
-09/06/23 - 2:56 PM for a behavior issue;
-09/09/23 - 7:06 PM for anxiety;
-09/10/23 - 6:27 PM for anxiety;
-09/11/23 - 7:10 AM for anxiety;
-09/18/23 - 6:18 PM for anxiety;
-09/20/23 - 6:47 AM for anxiety;
-09/21/23 - 8:12 PM for anxiety;
-09/24/23 - 6:45 PM for anxiety;
-09/26/23 - 11:44 PM for anxiety; and
-09/29/23 - 3:00 PM with no reason documented.
Review of R43's Progress Notes, dated 09/01/23 through 09/30/23 and located under the Resident tab of the EMR, revealed no documentation of any non-pharmacological interventions attempted by the staff to reduce R43's anxiety before administering the Ativan on any day.
Review of R43's MARs, dated October 2023 and located under the Reports tab of the EMR, reviewed R43 received Ativan 0.5 mg as follows:
-10/01/23 - 9:45 AM and 6:41 PM for anxiety;
-10/06/23 - 1:17 AM and 6:40 PM for anxiety;
-10/08/23 - 6:57 PM for anxiety;
-10/11/23 - 7:26 AM for anxiety;
-10/13/23 - 6:36 PM for anxiety;
-10/21/23 - 6:37 PM for anxiety;
-10/22/23 - 6:49 PM for anxiety;
-10/24/23 - 4:40 PM for a behavior issue;
-10/26/23 - 1:55 PM for a behavior issue and 4:40 PM for air hunger.
Review of R43's Progress Notes, dated 10/01/23 through 10/26/23 and located under the Resident tab of the EMR, revealed no documentation of any non-pharmacological interventions attempted by the staff to reduce R43's anxiety before administering the Ativan on any day. There was no documentation of what R43's behaviors had been.
Review of R43's Progress Note, dated 10/26/23 at 5:06 PM and located under the Resident tab of the EMR, revealed R43 was showing signs and symptoms of a respiratory infection. It was recorded that the nurse practitioner ordered R43 to receive an antibiotic, a nebulizer treatment, and an increase in the Ativan dose to 1 mg three times daily as needed.
Review of R43's MARs, dated October 2023 and located under the Reports tab of the EMR, reviewed R43 received Ativan 1.0 mg as follows:
-10/27/23 - 10:18 PM for anxiety;
-10/29/23 - 10:13 AM for a behavior issue.
Review of R43's Progress Notes, dated 10/27/23 through 10/29/23 and located under the Resident tab of the EMR, revealed no documentation of any non-pharmacological interventions attempted by the staff to reduce R43's anxiety before administering the Ativan. There was no documentation of what R43's behaviors had been.
Review of R43's MARs, dated 11/01/23 through 11/12/23 and located under the Reports tab of the EMR, reviewed R43 received Ativan 1.0 mg as follows:
-11/04/23 - 7:58 PM for anxiety;
-11/06/23 - 3:59 PM for anxiety;
-11/07/23 - 3:21 PM for a behavior issue;
-11/09/23 - 2:53 PM for a behavior issue; and
-11/12/23 - 9:47 AM and 5:59 PM for restlessness.
Review of R43's Progress Notes, dated 11/01/23 through 11/12/23 and located under the Resident tab of the EMR, revealed no documentation of any non-pharmacological interventions attempted by the staff to reduce R43's anxiety before administering the Ativan. There was no documentation of what R43's behaviors had been.
Review of R43's MARs and Progress Notes, dated 12/22/22 through 11/14/23, revealed no documentation of target behaviors related to the use of Ativan and no monitoring for adverse consequences.
Review of R43's Care Plan, dated 11/14/23 and located under the RAI tab of the EMR revealed a focus related to behaviors. The care plan noted the resident has socially inappropriate/disruptive behavioral symptoms as evidenced by wandering yelling and being aggressive toward staff. Approaches included to assess whether the behavior endangers the resident and/or others. Intervene if necessary. Convey an attitude of acceptance toward the resident. When [R43] begins to become socially inappropriate/disruptive, provide comfort measures for basic needs (e.g., pain, hunger, toileting, too hot/cold, etc). Remove him/her from other residents' rooms and unsafe situations. Allow the resident to have control over situations, if possible. Allow the resident to make decisions, to set schedules, to set realistic goals, to meet challenges, to participate in self-care. Observe and report socially inappropriate/disruptive behaviors when around others. [R43] is on medications for his/her behaviors but doesn't like to be 'bossed' Make suggestions as to what he/she is supposed to be doing vs [versus] telling him/her what to do.
Further review of R43's Care Plan revealed a focus related to antipsychotic medications. It showed the resident receives antipsychotic medication due to behavioral symptoms and anxiety. Approaches included, to monitor [R43]'s behavior and response to medication. Assess if his behavioral symptoms present a danger to the himself/herself and/or others. Intervene as needed. Quantitatively and objectively document the behaviors. Pharmacy consultant review. Complete AIMS [abnormal involuntary movements] every quarter. The care plan did not address target behaviors or other adverse consequence monitoring.
Review of R43's Orders, dated 12/18/22 and located under the Resident tab of the EMR, revealed R43 was to receive Seroquel (quetiapine), an antipsychotic medication, 25 mg one tab twice daily for unspecified dementia, unspecified severity with agitation.
Review of R43's MARs dated 01/01/23 through 11/14/23 and located under the Resident tab of the EMR, revealed R43 received the Seroquel as ordered by the physician.
Review of R43's Resident tab of the EMR revealed no documentation of any attempts to reduce the use of Seroquel. There was no documentation of adverse consequence monitoring related to the use of Seroquel. There was no documentation of target behaviors related to the use of Seroquel.
Review of R43's Orders, dated 06/30/23 and located under the Resident tab of the EMR, revealed R43 was to receive Abilify (aripiprazole) 400 mg intramuscularly every third Saturday of each month for unspecified dementia, unspecified severity with agitation.
Review of R43's MARs, dated 07/01/23 through 11/14/23 and located under the Resident tab of the EMR, revealed R43 received Abilify as ordered by the physician.
Review of R43's Resident tab of the EMR revealed no documentation of any attempts to reduce the use of Abilify. There was no documentation of adverse consequence monitoring related to the use of Abilify. There was no documentation of target behaviors related to the use of Abilify.
Review of R43's Orders, dated 12/12/22 and located under the Resident tab of the EMR, revealed R43 was to receive buspirone (Buspar), an anti-anxiety medication, 15 mg three times daily for unspecified dementia, unspecified severity with agitation.
Review of R43's MARs, dated 01/01/23 through 11/14/23 and located under the Resident tab of the EMR, revealed R43 received buspirone as ordered by the physician.
Review of R43's Resident tab of the EMR revealed no documentation of any attempts to reduce the use of buspirone. There was no documentation of adverse consequence monitoring related to the use of buspirone. There was no documentation of target behaviors related to the use of buspirone.
During an interview on 11/15/23 at 3:41 PM, Nurse Aide (NA) 1 said the resident did not have behaviors, would get a little mad but was not aggressive.
During an interview on 11/16/23 at 9:52 AM, CNA 3 stated she brought snacks to R43 to help redirect him. CNA3 stated, Most days are good. CNA3 stated she learned what nonpharmacological interventions to use with R43 by reading R43's Care Plan, through reports from other aides, and from the nurses. CNA3 confirmed she had not read R43's Care Plan in a few months.
During an interview on 11/16/23 at 10:05 AM, Registered Nurse (RN) 1 stated R43 had exit seeking behaviors, was non-cooperative due to his dementia, and did not understand. RN1 was asked what individualized, non-pharmacological interventions had been identified to help reduce any behaviors or anxiety for R43 before administering PRN Ativan. RN1 stated staff made sure to keep a visual check on R43 and tried to keep him occupied. RN1 stated what staff attempted depended on R43's behavior. RN1 stated if R43 was really anxious, staff would administer the PRN Ativan. RN1 stated that happened just once in a while. RN1 stated R43 received the PRN Ativan when he [R43] is very combative and that isn't often or when he is exit seeking. RN1 stated if R43 became real agitated, staff should try to redirect him, and get him interested in other things. RN1 stated the only documentation required before administering the PRN Ativan to R43 was just say he's angry and uncooperative and give him his Ativan. RN1 stated that hopefully the individualized non-pharmacological interventions for R43 were documented on R43's Care Plan. RN1 stated, We take him in the [activity] room but when he starts being uncooperative, hitting staff, running over people's toes, when he/she is being anxious. RN1 confirmed staff did not complete behavior monitoring. RN1 stated, they did not do that every day because that was part of the resident's dementia, and his/her normal behavior. RN 1 confirmed staff completed adverse consequence monitoring through observations but did not document the monitoring. RN1 stated when a resident was put on a new medication, staff document side effect monitoring for one month and then stop.
During an interview on 11/16/23 at 11:48 AM, the DON stated R43 had very aggressive behaviors when first admitted to the facility. The DON stated R43 would go down the hallways, refuse care, disrobe, go in and out of rooms, and had no regard for others' safety. The DON stated they did not see that behavior as much as they used to. The DON stated R43 had been placed on Abilify and that helped a lot. The DON confirmed her expectation was for staff to make sure R43's needs were being met first before medicating him with the PRN Ativan. The DON stated R43 could be very impulsive and confirmed R43's behaviors were part of his disease process. The DON stated the pharmacist completed recommendations for R43's medication regimen. The DON stated staff needed to know what side effects and adverse consequences to monitor for and then document if anything was noted. The DON confirmed there was no daily check sheet for monitoring behaviors or adverse consequences. The DON confirmed R43 had been receiving Seroquel and Buspar since admission to the facility. The DON stated Haldol had been added to R43's medication regimen because R43 had some very aggressive physical behaviors, but it was changed to Abilify following a pharmacist recommendation. The DON confirmed R43 had been receiving Ativan PRN since admission to the facility. The DON was asked if any GDR had been attempted for any of the medications. The DON confirmed, Not for a while. The DON confirmed that her expectation was for staff to attempt non-pharmacological interventions before administering the PRN Ativan and to document those interventions.
During an interview on 11/17/23 at 9:35 AM, the Nurse Practitioner (NP), who was providing coverage for the Medical Director, confirmed staff should be assessing R43 and trying other modalities (non-pharmacological interventions) prior to medicating R43 with the PRN Ativan. The NP stated she had ordered the increase in the Ativan dosage during October 2023 because R43 was experiencing trouble breathing and the family had requested R43 not be sent to the hospital and not for behaviors or anxiety. The NP confirmed in her professional opinion that many of R43's behaviors were part of his disease process.
During an interview on 11/17/23 at 9:55 AM, the Pharmacist confirmed he had requested a GDR for R43's Seroquel, buspirone, and Abilify during September 2023. The pharmacist stated he did not have a reply yet for those recommendations. The pharmacist stated he had asked for an appropriate diagnosis for the use of Seroquel in December 2022. The Pharmacist stated since R43 had continued to receive Seroquel when the Abilify was ordered, he would not have requested a GDR right away because the resident must not be stable for some reason. The Pharmacist confirmed he had requested the facility reduce or stop R43's use of Ativan multiple times. The Pharmacist confirmed his recommendation was that a resident use PRN Ativan no longer than 60 days. The Pharmacist stated he had made the recommendation to reduce or stop the Ativan during March, June, and then again in September 2023. The Pharmacist stated the facility responded to his recommendations by saying they would continue the seven-day re-evaluation.
Review of the facility's policy titled, Behavioral Health Services, revised March 2019, revealed, non-pharmacologic approaches will be utilized to the extent possible to avoid or reduce the use of antipsychotic medications to manage behavioral symptoms. When medications are prescribed for behavioral symptoms, documentation will include the rationale for use and other approaches and interventions tried prior to the use of antipsychotic medications, specific target behaviors and expected outcomes and monitoring for efficacy and adverse consequences.
Review of a document provided by the facility titled Antipsychotic Medication Use, dated 12/16 indicated antipsychotic medications may be considered for residents with dementia but only after medical, physical, functional, psychological, emotional psychiatric, social and environmental causes of behavioral symptoms have been identified and addressed. Residents will only receive antipsychotic medications when necessary to treat specific conditions for which they are indicated and effective. The Attending Physician and other staff will gather and document information to clarify a resident's behavior, mood, function, medical condition, specific symptoms, and risks to the resident and others. Residents who are admitted from the community, who are already receiving antipsychotic medications will be evaluated for the appropriateness and indications for use.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Assessment Accuracy
(Tag F0641)
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 accurately code the Minimum Data Set (MDS) assessment for three (Re...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to accurately code the Minimum Data Set (MDS) assessment for three (Resident (R) 51, R6 and R16) of 24 sampled residents reviewed for quality-of-care issues. Failure to code the MDS correctly could potentially lead to inaccurate federal reimbursements and inaccurate assessment and care planning of the resident. The census was 52.
Findings include:
1. Review of R51's electronic medical records (EMR) titled Resident Face Sheet located under the Resident tab indicated the resident was admitted to the facility on [DATE].
Review of R51's EMR titled nursing Progress Notes, located under the Resident tab indicated the resident sustained a fall on 11/02/23.
Review of a document provided by the facility titled admission MDS with an Assessment Reference Date (ARD) of 11/06/23 failed to identify R51 sustained a fall.
During an interview on 11/16/23 at 12:34 PM, the MDS Coordinator (MDSC) confirmed the error for R51 and missed the fall the resident sustained on 11/02/23.
2. Review of R6's EMR titled Resident Face Sheet located under the Resident tab indicated the resident was admitted to the facility on [DATE].
Review of R6's EMR titled Vitals located under the Resident tab revealed the following weights: 09/02/22 the resident weighed 133.5 pounds; 10/03/22 the resident weighed 179 pounds; there was no weight documented for 11/22/22; 12/07/22 the resident weighed 178.5; and, on 01/25/23 the resident weighed 136.8 pounds.
Review of documents provided by the facility titled MDS with the following ARD revealed the following:
-The resident's quarterly assessment with an ARD of 12/20/22 showed the resident weighed 179 pounds and had no significant weight gain (gain of 5% or more in the last month or gain of 10% or more in last 6 months). However, R6 was noted to have weighed 133.5 pounds three months prior.
-The resident's annual MDS, with an ARD of 06/13/23, showed the resident weighed 134 pounds and had no or unknown weight loss. The resident was noted to have a weight of 178.5 pounds on 12/07/22.
During an interview on 11/16/23 at 12:34 PM, the MDSC confirmed the errors for R6's weights in the MDS assessments.
3. Review of R16's EMR located under the Resident tab indicated the resident was admitted to the facility on [DATE].
Review of R16's EMR titled Orders located under the Resident tab dated 04/26/23 indicated skin prep was to be applied to the resident's right heel twice a day until area resolved.
Review of R16's EMR titled Medication Administration Record (MAR) located under eMAR [electronic MAR] tab indicated the resident was being treated for a right heel pressure ulcer from 04/23 to 11/23.
Review of a document provided by the facility titled quarterly MDS with an ARD of 07/10/23 indicated R16 had no pressure ulcers.
Review of a document provided by the facility titled quarterly MDS with an ARD of 10/09/23 indicated R16 had no pressure ulcers.
Review of R16's EMR titled MAR dated 11/23 indicated the resident still received treatment to the right heel.
During an interview on 11/15/23 at 1:15 PM, Infection Control Preventionist (ICP)/Quality Assurance (QA) Nurse stated the resident had a scabbed area (referencing R16's right heel) that could not be staged.
During an interview on 11/16/23 at 11:17 AM, Licensed Practical Nurse (LPN) 1 stated R16 still had a scab on his/her right heel and continued to receive treatment to the area.
During an interview on 11/16/23 at 12:10 PM, the MDSC stated R16 had a scabbed area on her right heel and assumed the area under it was healed therefore did not place it on the MDS.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0883
(Tag F0883)
Could have caused harm · This affected multiple residents
Based on interview and record review, the facility failed to revise their pneumococcal vaccine policy to reflect current pneumococcal vaccination guidelines. This failure increased the risk for reside...
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Based on interview and record review, the facility failed to revise their pneumococcal vaccine policy to reflect current pneumococcal vaccination guidelines. This failure increased the risk for residents to not be vaccinated per current guidelines and contract pneumonia. The census was 52.
Findings include:
Review of the CDC recommendations, revised on 02/09/23, indicated the CDC recommends pneumococcal vaccination for all adults 65 years or older If PCV20 is used, a dose of PPSV23 is NOT indicated. For adults 65 years or older who have only received PPSV23 [Pneumococcal polysaccharide vaccine], CDC recommends giving 1 dose of PCV15 or PCV20. The PCV15 or PCV20 dose should be administered at least 1 year after the most recent PPSV23 vaccination. Regardless of if PCV15 or PCV20 is given, an additional dose of PPSV23 is not recommended since they already received it. For adults 65 years or older who have only received PCV13, the CDC recommends you either give 1 dose of PCV20 at least 1 year after PCV13, or give 1 dose of PPSV23 at least 1 year after PCV13.
Review of a policy provided by the facility titled Pneumococcal Vaccine, dated 08/16 indicated all residents will be offered pneumococcal vaccines to aid in preventing pneumonia/pneumococcal infections. There were no current guidelines reflected in the policy on the newest CDC/APIC guidelines for pneumococcal vaccines.
During an interview on 11/17/23 at 10:10 AM, the Director of Nursing (DON) and the Infection Control Preventionist (ICP/Quality Assurance (QA) Nurse both stated they were not aware of the CDC's newest recommendations regarding the pneumococcal vaccinations.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0865
(Tag F0865)
Could have caused harm · This affected most or all residents
Based on interview and record review, the facility failed to implement their Quality Assurance and Performance Improvement (QAPI) program. This had the potential to affect 52 of 52 residents who resid...
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Based on interview and record review, the facility failed to implement their Quality Assurance and Performance Improvement (QAPI) program. This had the potential to affect 52 of 52 residents who resided at the facility.
Findings include:
During an interview on 11/17/23 at 11:06 AM, the Administrator and Infection Preventionist (IP), who was the facility's QAPI Lead, stated the facility did not have a QAPI Council. The Administrator stated that the facility's QA (Quality Assurance) committee were the same people involved in the QAPI program. The IP was asked if minutes were kept of the QAPI meetings. The IP stated, I haven't sat down and had a formal meeting in quite some time. The IP stated it was difficult to get staff together for a QAPI meeting. The IP stated she gathered information from the fall committee, the weekly antibiotic report, and fall worksheets and reviewed that information to identify any concerns. The IP stated that information was reviewed during meetings and taken back to the floor staff. The IP was asked how she developed benchmarks for measuring improvement in Performance Improvement Plans (PIPs). The IP stated she just wrote out what the problem was, how it was identified, and what the solution would be. The IP confirmed there were no benchmarks by which to measure improvement of any identified PIPs. The IP was asked how pharmacy consult reports were used in the QAPI program. The IP stated the pharmacist came to the QA meetings every month, and if he saw anything he questioned before then, he could contact the Director of Nursing (DON). The IP was asked how the facility was following its' QAPI plan without having meetings, using benchmarks, and using data from consultant reports. The IP stated the plan probably needed to be changed. The IP stated there was not enough time to implement the QAPI program because most of the nursing leadership had to work to the floor.
Continuing with the interview on 11/17/23 at 11:06 AM, the Administrator and IP were asked if the facility had identified any concerns related to obtaining accurate weights before the survey. The IP stated they had started a new system of having one person obtain the monthly weights because they had been inconsistent. The IP was asked if daily and weekly weights had been included in the new system and if those weights were monitored for accuracy. The IP stated, No. The IP stated, We trust our nurses to look back [monitor]. The IP was asked if any concerns related to unnecessary medications and drug regimen reviews had been identified prior to the survey. The IP stated the pharmacist did his reviews and would let them know if there was anything that shouldn't be there. The IP stated the physician did a medication regimen review as well. The IP and Administrator were asked if there had been any concerns identified with the Infection Control Program and Antibiotic Stewardship prior to the survey. The Administrator stated, No.
Review of the facility's undated Quality Assurance Improvement Plan, provided by the Administrator, revealed, our nursing home has a Performance Improvement Program which systematically monitors, analyzes, and improves its performance to improve resident/patient outcomes. The QAPI plan addresses Clinical Care, Quality of Life and Resident Choice. Review of State/National and past facility measures will be used to benchmark for improvement in all areas. These benchmarks will be reviewed at least monthly, and reported to the QAPI Committee on a quarterly basis. The QAPI Council provides the backbone and structure for QAPI. This group includes all of the Executive Leadership team plus additional staff members. This group of people work together to communicate and coordinate QAPI activities. Currently QAPI Council meets once a month. Information gathered is analyzed and compared to benchmarks and/or targets established by the facility. Consultant reports are compared to goals on a monthly basis. QAPI teams analyze data regularly as part of their project assignments. Minutes of all meetings - QAPI Lead is responsible for maintaining documentation.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Infection Control
(Tag F0880)
Could have caused harm · This affected most or all residents
Based on interview and record review, the facility failed to establish and maintain an infection prevention and control program (IPCP) for recording incidents of infections identified under the facili...
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Based on interview and record review, the facility failed to establish and maintain an infection prevention and control program (IPCP) for recording incidents of infections identified under the facility's IPCP, surveillance, tracking and trending, and the corrective actions taken by the facility. The facility failed to update their infection control policies on an annual basis. The facility also failed to provide assistance with eating in a manner to potentially prevent cross-contamination for two of 24 sampled residents (Resident (R) 19 and R24) observed during dining. The census was 52.
Findings include:
1. Review of a document titled, Centers for Disease Control (CDC) National Healthcare Safety Network (NHSN) Long Term Care Facility Component Tracking Infections in Long-Term Care Facilities dated January 2020, indicated, surveillance is defined as the ongoing systematic collection, analysis, interpretation, and dissemination of data. A facility infection prevention and control (IPC) program should use surveillance to identify infections and monitor performance of practices to reduce infection risks among residents, staff, and visitors. Information collected during surveillance activities can be used to develop and track prevention priorities for the facility. When conducting surveillance, facilities should use clearly defined surveillance definitions that are collected in a consistent way. This method ensures accurate and comparable data regardless of who is performing surveillance.
During an interview on 11/17/23 at 10:10 AM, the Infection Control Preventionist (ICP) and the Director of Nursing (DON), stated the ICP just began mapping in 10/23 and prior to this there was not a way to identify clusters of potential infections other than to review the daily reports collected from the units. The ICP and DON both stated the facility was small and they knew the care needs of each resident. The DON stated there was no proof that the facility's infection control policies were being reviewed on an annual basis.
2. During an observation of the noon meal on 11/14/23 at 12:08 PM, Certified Nurse Aide in Training (CNAT) 4 was observed feeding R24. CNAT4 was not wearing gloves. At 12:11 PM, CNA4 got up from her seat, and without performing hand hygiene, gave R19 a bite of food and touched R19's shoulder and upper chest. R19 had been touching her own utensils. CNAT4 then returned to R24 and assisted her with a bite of food without performing hand hygiene. At 12:12 PM, R19 dropped her beverage glass onto her plate. CNAT4 got up from her seat, removed the glass from R19's plate, and without performing hand hygiene, returned to R24, and continued to feed her.
During an interview on 11/14/23 at 4:00 PM, CNAT4 stated she did not remember if she had performed hand hygiene while feeding R24 and R19.
During an interview on 11/17/23 at 11:38 AM, the Infection Preventionist (IP) stated it was her expectation for staff to perform hand hygiene between feeding different residents.
Review of the facility's policy titled, Handwashing/Hand Hygiene, dated August 2015, revealed, the facility considers hand hygiene the primary means to prevent the spread of infections. Use an alcohol-based hand rub containing at least 62% alcohol; or, alternatively, soap (antimicrobial or non-antimicrobial) and water for the following situation before and after assisting a resident with meals.
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
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to maintain an infection prevention and control program (IPCP) that in...
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**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on interview and record review, the facility failed to maintain an infection prevention and control program (IPCP) that included a functional antibiotic stewardship program. The failure to have a system in place that monitored antibiotic use in accordance with established protocols has the potential to affect all 52 residents of the facility. In addition, the facility failed to ensure one Resident (R41) had appropriate clinical indications for the use of an antibiotic. The census was 52.
Findings include:
1. Review of a CDC document undated titled, The Core Elements of Antibiotic Stewardship for Nursing Homes indicated improving the use of antibiotics in healthcare to protect patients and reduce the threat of antibiotic resistance is a national priority. Antibiotic stewardship refers to a set of commitments and actions designed to 'optimize the treatment of infections while reducing the adverse events associated with antibiotic use'. All nursing homes should take steps to improve antibiotic prescribing practices and reduce inappropriate use. Nursing homes monitor both antibiotic use practices and outcomes related to antibiotics in order to guide practice changes and track the impact of new interventions. Data on adherence to antibiotic prescribing policies and antibiotic use are shared with clinicians and nurses to maintain awareness about the progress being made in antibiotic stewardship. Clinician response to antibiotic use feedback (e.g., acceptance) may help determine whether feedback is effective in changing prescribing behaviors. Process measures include tracking how and why antibiotics are prescribed and tracking any adverse outcomes.
Review of a policy provided by the facility titled Antibiotic Stewardship-Review and Surveillance of Antibiotic Use and Outcomes, dated 12/16 indicated Antibiotic usage and outcome data will be collected and documented using a facility-approved antibiotic surveillance tracking form. The data will be used to guide decisions for improvement of individual resident antibiotic prescribing practices and facility wide antibiotic stewardship. The lP [Infection Preventionist], or designee, will review antibiotic utilization as part of the antibiotic stewardship program and identify specific situations that are not consistent with the appropriate use of antibiotics.Therapy may require further review and possible changes if the organism is not susceptible to the antibiotic chosen, the organism is susceptible to narrower spectrum antibiotic, therapy was ordered for prolonged surgical prophylaxis, therapy was started awaiting culture, but culture results and clinical findings do not indicate continued need for antibiotics. All resident antibiotic regimens will be documented on the facility-approved antibiotic surveillance tracking form. The information gathered will include the resident name and medical record number, unit and room number, date symptoms appeared, name of antibiotic (see approved surveillance list), start date of antibiotic, pathogen identified (see approved surveillance list), site of infection, stop date. Total days of therapy and outcome.
Review of a document provided by the facility titled, Antibiotic Tracking Sheet from 06/02/23 to 11/11/23 revealed residents were identified, along with the associated infection. The symptoms of the infection associated with the antibiotic were not identified, the pathogens were not identified, the laboratory tests and if a culture and sensitivity was ordered was not identified on these logs.
2. Review of a policy provided by the facility titled Antibiotic Stewardship dated 12/16, indicated antibiotics will be prescribed and administered to residents under the guidance of the facility's Antibiotic Stewardship Program. When a culture and sensitivity (C&S) or chest x-ray is ordered labs or results and the current clinical situation will be communicated to the prescriber as soon as available to determine if antibiotic therapy should be started, continued, modified, or discontinued.
Review of a policy provided by the facility titled Antibiotic Stewardship - Orders for Antibiotics, dated 12/16 indicated appropriate indications for use of antibiotics included criteria met for clinical definition of active infection or suspected sepsis and pathogen susceptibility, based on culture and sensitivity, to antimicrobial (or therapy begun while culture is pending.
Review of R41's electronic medical record (EMR) titled Resident Face Sheet indicated the resident was admitted to the facility on [DATE].
Review of a document provided by the facility for R41 titled Physician Order Report dated 10/18/23 indicated the resident was prescribed ciprofloxacin (Cipro - an antibiotic) 500 milligrams (mg) to be administered twice a day until 10/24/23.
Review of R41's EMR titled Orders located under the Resident tab dated 11/02/23 indicated the resident was prescribed Cipro 250 mg to be administered twice a day as a preventative measure for urinary tract infections.
Review of a document provided by the facility for R41 titled Suspected UTI (urinary tract infection) SBAR (Situation, Background, Assessment, and Recommendation [a standardized form to communicate the condition of a resident] Form, undated, indicated the resident had met criteria, proceed with contacting provider for urinalysis with urine culture and sensitivity for symptoms listed above. In a box on the right side of the document it indicated the resident had back or flank pain. In addition, the criteria were not met since the resident did not have a temperature above 100 degrees Fahrenheit (F), as directed by the SBAR. There were no other symptoms identified.
Review of R41's EMR failed to provide evidence of symptoms of a UTI nor was there evidence to show any clinical documentation to support the use of Cipro. There was no evidence the facility implemented a urinalysis or a culture and sensitivity of the urine sample.
During an interview on 11/17/23 at 9:39 AM, the Consultant Pharmacist stated he participated in the antibiotic stewardship program and stated he reviewed the antibiotic usage. The Consultant Pharmacist stated it was difficult to get a buy in from the facility and family and the use of antibiotics prophylactically and not to do so.
During an interview on 11/17/23 at 10:10 AM, the Infection Control Preventionist (ICP) and the Director of Nursing (DON) were asked about the prophylactic use of Cipro and R41. Both staff stated a family member of the resident was being hateful to her and this was an indication the resident had a UTI. Both the ICP and DON stated the resident has not been seen by a urologist and had no violent behaviors to others. During this interview, the DON stated there was a positive SBAR so the criteria must have been met for the resident to be prescribed an antibiotic. The ICP stated she had no reason why there were no dates associated with the prophylactic use of antibiotics and never placed the pathogens on the tracking forms.
During an interview on 11/17/23 at 2:01 PM, the Minimum Data Set (MDS) Coordinator confirmed there was no urinalysis or culture and sensitivity for the use of R41's antibiotics.