CONCERN
(D)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Free from Abuse/Neglect
(Tag F0600)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, resident and staff interviews, record reviews, and a review of the facility policy titled, Freedom of Abu...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observations, resident and staff interviews, record reviews, and a review of the facility policy titled, Freedom of Abuse, Neglect, and Exploitation: Abuse Prevention, the facility failed to ensure that two of 33 sampled residents (R) (#47 and #88) were free from physical abuse by another resident. The failure to assure residents were free from resident-to-resident abuse had the potential to cause either physical or psychosocial harm to R#47 and R#88.
Findings include:
Review of the facility's undated policy titled Freedom of Abuse, Neglect, and Exploitation: Abuse Prevention stated, The purpose of this standard is to provide the preventative steps taken by the facility staff to reduce the potential for mistreatment, neglect, misappropriation, exploitation and unreasonable confinement of residents residing in nursing facilities .Definitions- Abuse .willful infliction of injury, unreasonable confinement, intimidation or punishment with resulting physical harm, pain or mental anguish .Most Common Forms of Abuse .Physical: infliction of pain, injury which includes but is not limited to slapping, hitting, pinching, licking, shoving.
1. Review of the admission Record for R#47 provided by the facility, revealed that the resident was admitted with a primary diagnosis of quadriplegia.
Review of the Care Plan for R#47 located in the electronic medical record (EMR), indicated the resident was able to feed himself but required full assistance with all other activities of daily living (ADL's) due to quadriplegia status.
Review of a grievance submitted on 11/01/2021 by R#47, revealed he had expressed a concern to the Veterans Affairs Social Worker that other residents were wandering the halls and entering his room all day and night, Additionally R#47 told the Veterans Affair Social Worker he was assaulted by another resident within the last several months.
In response to this grievance, the facility performed an internal investigation and confirmed that physical abuse occurred on 06/14/2021. The allegation of physical abuse was submitted to the state agency as a facility reported incident on 06/14/2021. The investigation stated that on 06/14/2021, R#47 alleged that R#387 hit him in the mouth and twisted his arm. A nurse heard screaming coming from R#47's room. Both residents were immediately separated, and R#387 was placed on one-on-one observation. A full body assessment was completed, and the facility noted no injuries to R#47. An abuse in-services were completed with all staff during the investigation. Interventions put in place included placing a mesh STOP sign on his doorway to deter wandering residents from entering his room and moving R#47 to another hallway.
Review of a police report document titled, Incident Report- Narrative dated 6/14/2021, revealed R#387 then walked over to him and stated that he would take that from him R#47's Cellphone and back scratcher. R#47 advised that he pulled his items close to him and that, at that point, R#387 began twisting his arm, trying to get the items from him. R#47 advised that R#387 struck him in the mouth (no injuries were noted). R#47 advised that a nurse and the Physical Therapist came in and stopped R#387.
Review of the admission Record for R#387 provided by the facility stated the resident was admitted to the facility on [DATE] and discharged on 10/8/2021, with a diagnosis including dementia with behaviors.
Review of the Care Plan for R#387 dated 05/21/2021, The resident is an elopement risk/wanderer r/t [related to] resident wanders aimlessly walks up and down the hallway going in and out of others room .Distract resident from wandering by offering pleasant diversion activities, food, conversation, television, and books.
Observation on 01/31/2023 at 10:29 a.m. revealed a STOP sign on R#47's doorway, and the resident was resting in his bed with his eyes closed.
Interview on 02/02/2023 at 1:39 p.m. with a Licensed Practical Nurse (LPN) 4, she confirmed R#47 was struck by R#387 on 06/14/2021. LPN4 stated that R#387 had a history of wandering but would only become aggressive if someone approached him wrong.
2. Review of the admission Record for R#88 provided by the facility revealed the resident was admitted with a primary diagnosis of cerebral infarction and was discharged from the facility on 01/17/2022.
Review of the Care Plan for R#88, created on 07/26/2021, stated R#88 required assistance with activities of daily living (ADL's) related to hemiplegia, limited mobility, limited range of motion, and stroke.
Review of the admission Record for R#90 provided by the facility revealed that the resident was admitted to the facility with a primary diagnosis of dementia with behavioral disturbance. The resident was discharged from the facility on 09/11/2022.
Review of the Care Plan for R#90 indicated that R#90 required assistance with ADLs related to aggressive behavior, confusion, and impaired balance. Additionally, on 12/28/2021, the care plan added that R#90 had the potential to be physically aggressive related to poor impulse control and post-traumatic stress syndrome.
Review of the Progress Note for R#88 dated 01/02/2022 at 10:25 p.m. by LPN 10, revealed that R#90 became angry at the writer when he was told his volume on tv had to be turned down because of the time, and it was at 99. R#90 went over to the roommate's bedside after the writer left the room. The writer heard him yelling cry baby, profanity's and returned to the room to see him strike the roommate in the face on the left upper jaw area.
Review of the Progress Note for R#88 dated 01/02/2022 at 10:25 p.m. by LPN10 stated, R#88 was struck in the face by his roommate. Injury location: face, resident alert, and had pain of 6/10. Resident's left side of the face and jaw area are red, bottom lip slightly swollen.
Review of a Facility Reported Incident, dated 01/03/2022, revealed that Staff entered the room and witnessed
R#90 hitting R#88. Staff immediately removed R#90 to another room. Full skin assessment completed on R#88 with no negative findings. Education provided to staff on Freedom of Abuse. Pain assessment completed. Physician and both families notified of altercation. R#88 was placed 1:1. R#88's family member at facility rubbing residents face causing redness. R#88's family member requested for him to be sent to the hospital for evaluation .No findings of injury noted by the doctor at the hospital. Behavioral Health services to evaluate R#90. The residents were separated. R#88 was transferred to a different room. Although the incident was witnessed, it is not possible to determine why the incident occurred. This was the first incident R#88 has been involved. Staff will attempt to keep some distance between the two residents. R#88 will have increased supervision. Care plans for both residents updated.
Interview on 02/02/2023 at 1:21 p.m. with a Licensed Practical Nurse (LPN)9, she confirmed R#88 was assaulted by R#90. LPN9 stated that R#88 had previously sustained a stroke, was nonverbal, was able to make noises, would gesture, and required full assistance with ADL's. LPN9 further revealed that the staff heard R#88 yelling. R#90 was removed from their room when staff witnessed R#90 grab R#88's television remote and then hit R#88 on the face.
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
Based on resident and staff interviews, record review, and review of facility policy, the facility failed to implement policies and procedures for ensuring the reporting of a reasonable suspicion of a...
Read full inspector narrative →
Based on resident and staff interviews, record review, and review of facility policy, the facility failed to implement policies and procedures for ensuring the reporting of a reasonable suspicion of a crime (staff to resident verbal abuse) in accordance with section 1150B of the Act and failed to report the allegation of verbal abuse to the State Survey Agency for one of 11 residents (R#238) reviewed for abuse. These failures had the potential to contribute to further verbal abuse and possible psychosocial harm for R#238.
Findings include:
Review of the facility's policy dated 06/2017, Freedom of Abuse, Neglect, and Exploitation; Abuse/Incident Standard revealed, All alleged violations involving mistreatment, abuse or neglect will be thoroughly investigated by the facility under the direction of the Administrator and in accordance with state and federal law . Ensure that all alleged violations involving abuse. neglect, exploitation, or mistreatment including injuries of unknown source and misappropriation of resident property are reported immediately, but not later than 2 hours after the allegation is mode, if the events that cause the allegation involve abuse or result in serious bodily injury.
Review of the 2022 Grievance Log, provided on paper by the Social Services Director (SSD), revealed a Resident Grievance/Concern/Complaint Report, filed on 04/08/2022 on behalf of R#238. The report documented, Resident states he does not want Certified Nursing Assistant (CNA) 9 to be his CNA anymore he doesn't like how she works [sic], she is rude, rough, and she is very disrespectful. CNA stated she was not rude or disrespectful to the resident.
Interview on 02/01/2023 at 3:27 p.m. with the Regional [NAME] President of Operations (RVPO), she stated the allegation had yet to be reported to the State Survey Agency or to law enforcement. She added that she would submit a late report to the state, as well as institute a performance improvement plan to address reporting of all allegations of abuse.
In an additional interview on 02/01/2023 at 4:49 p.m. with the RVPO, she stated the typical protocol when an allegation of staff to resident abuse is received was to notify law enforcement and the State Survey agency within two hours.
Cross Reference F610
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Investigate Abuse
(Tag F0610)
Could have caused harm · This affected 1 resident
Based on resident and staff interviews, record reviews, and review of the facility policy titled, Freedom of Abuse, Neglect, and Exploitation; Abuse/Incident Standard, the facility failed to implement...
Read full inspector narrative →
Based on resident and staff interviews, record reviews, and review of the facility policy titled, Freedom of Abuse, Neglect, and Exploitation; Abuse/Incident Standard, the facility failed to implement this policy for one of 11 residents (R#238) reviewed for abuse. Specifically, the facility failed to suspend a staff member pending an investigation into an allegation of verbal abuse towards R238. Allowing this staff to work, pending investigation, created the potential for continued verbal abuse towards the resident.
Findings include:
Review of the facility policy dated, 06/2017 Freedom of Abuse, Neglect, and Exploitation; Abuse/Incident Standard revealed, An immediate investigation into the alleged incident, during the shift it occurred on, is initiated as follows:
1. Complete incident report in PCC [Point Click Care - the facility's EMR (Electronic Medical Record) system] .
2. Interview the resident or other resident witnesses (e.g., roommate, if appropriate). The interview is to be dated, documented, and signed by the nursing supervisor .
3. Interview the staff member implicated. The interviewer is to document the staff member's knowledge and/or version of the incident in a written narrative that is dated and signed .
4. Interview all staff on that unit, as well as other staff or other available witnesses. The interviewer is to document the staff's knowledge of the incident in a written narrative .
Any employee suspected (alleged) of abuse will be suspended as the incident is reported; pending outcome of the investigation.
Review of the most recent quarterly Minimum Data Set (MDS) assessment for R#238's, located in the MDS tab of the EMR, with an assessment reference date (ARD) of 01/01/2023, revealed R#238 scored 14 out of 15 points on the Brief Interview for Mental Status (BIMS), indicating the resident was cognitively intact. He exhibited symptoms of depression, such as feeling down, feeling bad about yourself, and trouble sleeping but no behavioral symptoms. R#238 was able to make himself understood and understand others.
Interview on 01/30/2023 at 10:25 a.m. with R#238 in his room, R#238 stated he had been verbally abused by a female certified nurse aide (CNA). He added, She's mean as a snake . She refused to help me. R#238 stated he reported his allegation of verbal abuse to Licensed Practical Nurse (LPN) 4, who served as the unit manager. He added, I don't know if anything was done because she still works here on a different hall.
Review of the 2022 Grievance Log, provided on paper by the Social Services Director (SSD, revealed a Resident Grievance/Concern/Complaint Report, filed on 04/08/2022 on behalf of R#238. The report revealed, under the section on the form titled, Investigation Report, signed as completed by Licensed Practical Nurse (LPN) 4 on 04/08/2022, was documented, as CNA assigned to different hall. Informed CNA to just monitor tone. There was no additional documentation provided to indicate that a thorough investigation, which included interviews with staff and other residents, was completed. In addition, there was no evidence that the facility took steps to protect residents from the potential for further abuse by suspending the alleged perpetrator during the investigation, in accordance with facility policy.
Interview on 02/01/2023 at 3:27 p.m., with the Regional [NAME] President of Operations (RVPO), she stated the allegation had not been investigated. She added that she would immediately institute an investigation and a performance improvement plan to address investigating allegations of abuse.
Interview on 02/01/2023 at 4:49 p.m., with the RVPO, she stated the typical protocol when an allegation of staff to resident abuse is received, the employee is suspended, and an investigation is conducted. She further revealed that the investigation would include staff interviews and interviews with all cognitively aware residents who may have received care from the staff member or witnessed the event.
Cross Reference F609
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0655
(Tag F0655)
Could have caused harm · This affected 1 resident
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, record review, and policy review, the facility failed to ensure a baseline care plan was developed and...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interview, record review, and policy review, the facility failed to ensure a baseline care plan was developed and implemented within 48 hours of admission to the facility for one Resident (R) (R#237) of one resident reviewed for baseline care plans. This deficient practice had the potential to increase the risk for R#237 to not receive services that met the immediate care needs present upon admission.
Findings include:
Review of the policy titled, Long-Term Care Facility Resident Assessment Instrument 3.0 User's Manual, dated 10/2019, revealed, Within 48 hours of admission to the facility, the facility must develop and implement a Baseline Care Plan for the resident that includes the instructions needed to provide effective and person-centered care of the resident that meets professional standards of care (42 CFR §483.21(a)).
Review of R#237's admission Record, revealed the resident was admitted on [DATE] with a primary diagnosis of type two diabetes mellitus.
Review of R#237's undated Baseline Care Plan, located under the Assessments tab in the electronic medical record (EMR), revealed the baseline care plan was incomplete and only included the resident's primary language, daily preferences, and medication allergies.
Interview on 02/02/2023 at 4:19 p.m., with the Minimum Data Set Coordinator (MDSC) revealed that she did not work at the facility at the time that R#237 was a resident and did not know why the baseline care plan was not completed. The MDSC confirmed that R#237 did not have a completed baseline care plan.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Comprehensive Care Plan
(Tag F0656)
Could have caused harm · This affected 1 resident
Based on staff interviews, record review, and a review of the facility policy titled, RAI (Resident Assessment Instrument) Care Planning Management, the facility failed to ensure care plan interventio...
Read full inspector narrative →
Based on staff interviews, record review, and a review of the facility policy titled, RAI (Resident Assessment Instrument) Care Planning Management, the facility failed to ensure care plan interventions related to emergency tracheostomy care were developed for two of 33 sampled residents (R) (#7 and #63) reviewed for tracheostomy (a surgical opening into the windpipe for breathing) care. This failure increased the resident's risk for compromised airway/respiratory distress.
Findings include:
Review of a facility policy titled, RAI (Resident Assessment Instrument) Care Planning Management, revised 07/2022, revealed that Process for Completing the MDS (Minimum Data Set0, CAAs (Care Area Assessments) and Care Plans Standard: It is the practice of this facility to conduct a comprehensive, accurate, standardized, reproducible assessment of each resident's functional capacity. Objective: 1. To identify residents' individual needs and care requirements. 2. To assure that an interdisciplinary team assesses the emotional, psychosocial, mental, and physical needs of each resident. 3. To assure that all residents are reviewed and reassessed based on their individual needs and OBRA guidelines/
1. Review of the comprehensive Care Plan for R#7 dated 05/11/2018, under the Care Plan tab located in the EMR, revealed the resident has a Tracheostomy r/t [related to] Severe Traumatic Brain Injury. Further review of the care plan revealed the interventions did not include the tracheostomy brand, size, or cuff or uncuffed. The care plan further revealed Tube Out Procedures: Keep extra trach tube and obturator at bedside. If tube is coughed out, open stoma with hemostat. If tube cannot be reinserted, monitor/document for signs of respiratory distress. If able to breathe spontaneously, elevate HOB [head of bed] 45 degrees and stay with resident. Obtain medical help IMMEDIATELY. However, the care plan did not address maintaining an emergency trach kit at the bedside and did not address tracheostomy information (style, size, or cuffed or uncuffed).
Interview on 02/01/2023 at 12:03 p.m. with the MDS Coordinator (MDSC) revealed she had worked at the facility for three months and was in the process of reviewing and revising all the care plans. The MDSC stated that the former MDSC and unit managers developed the residents' care plans. The MDSC also stated that the resident's care plans should reflect the physician's orders. The MDSC confirmed that R#7's care plan should include specific orders for maintaining an emergency trach kit at the bedside, tracheostomy information, and emergency trach management. The MDSC verified that the emergency management of the trach intervention on the care plan was not accurate, and the nursing staff should call 911 if the trach dislodged.
2. Review of the comprehensive Care Plan for R#63 dated 11/25/2022 and located in the Care Plan tab of the EMR, revealed, R#63 has a tracheostomy r/t impaired breathing mechanics. The approaches included: Ensure that trach ties are secured at all times . Monitor/document for restlessness, agitation, confusion, increased heart rate (Tachycardia), and bradycardia . Monitor/document level of consciousness, mental status, and lethargy PRN [as needed] . Monitor/document respiratory rate, depth, and quality . Check and document q [every] shift/as ordered . Provide good oral care daily and PRN . Suction as necessary . Use universal precautions as appropriate . Administer oxygen as indicated via trach . Give medications as ordered by physician . Keep head of bed elevated 30-90 degrees . Observe for s/sx [signs/symptoms] of respiratory distress and report to [physician] PRN: Respirations, Pulse oximetry, Increased heart rate (Tachycardia), Restlessness, Diaphoresis, Headaches, Lethargy, Confusion, Atelectasis, Hemoptysis, Cough, Pleuritic pain, Accessory muscle usage, Skin color .Position resident to facilitate ventilation/perfusion matching: use upright, high Fowlers position whenever possible to allow for optimal diaphragm, when on side, the good side should be down (e.g., damaged lung should be up). Review of the Care Plan revealed there were no interventions addressing emergency management of the tracheostomy, including maintaining an emergency trach kit and interventions in the event the trach dislodged.
Interview on 02/01/2023 at 12:03 p.m., the MDSC confirmed that R#63's Care Plan should include specific orders for maintaining an emergency trach kit at the bedside, tracheostomy information, and emergency trach management. The MDSC verified that there was no information in the care plan addressing emergency management if the trach dislodged.
CONCERN
(D)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Accident Prevention
(Tag F0689)
Could have caused harm · This affected 1 resident
Based on observation, staff interview, record review, and review of the facility policy titled, Elopement Management, the facility failed to ensure that one of eight sampled residents (R) (#62) review...
Read full inspector narrative →
Based on observation, staff interview, record review, and review of the facility policy titled, Elopement Management, the facility failed to ensure that one of eight sampled residents (R) (#62) reviewed for accidents received supervision needed to prevent accidents. R#62, who was at risk for elopement, was able to exit the facility without staff supervision. This failure created the potential for risk of injury while unsupervised.
Findings include:
Review of the facility policy titled, Elopement Management, dated 2021, revealed, Definition: Elopement occurs when a resident leaves the facility or a safe area without authorization. lf a resident is off facility property, then an elopement has occurred. lf a resident is on facility property but not under supervision as need identifies; then an elopement has occurred. Authorization means a physician order for discharge, leave of absence, or leave with
appropriate supervision to do so.
Review of admission Record for R#62 revealed he was originally admitted to the facility with a primary diagnosis of traumatic brain injury.
Review of Care Plan, for R#62, initiated 04/29/2021, revealed the resident was at risk for elopement related to a history of attempting to leave the facility unattended, and the resident would often state, I need to get out of here. Multiple interventions were listed for diversion from wandering. In addition, for security measures, outside doors were to be securely closed when staff or visitors entered and exited the building.
Review of the most recent quarterly Minimum Data Set (MDS), for R#62 dated 11/0/2022, revealed that the resident was moderately cognitively impaired, based on a Brief Interview for Mental Status (BIMS) score of 9/15. The MDS revealed, the resident was independent in ambulation/locomotion, and had no wandering behaviors during the assessment period.
Observation during initial tour on 01/30/2023 revealed that all facility doors to the outside were secured and required a code to exit.
Interview on 01/31/2023 at 6:00 p.m. with R#62 revealed that he did not remember exiting the building unsupervised on 07/17/2021 or on any other occasion.
Review of Wander Data Collection Tool, for R#62, dated 03/30/21 and 07/05/21, revealed that R#62 had wandered before at home/previous living settings, and the family had voiced concerns, according to the tool, the resident had attempted to elope in the present facility.
Review of R62's Elopement Investigation, dated 07/17/21, revealed the Resident noted to be standing at the end of corridor [outside of the facility] by writer and another staff member. Staff opened doorway and asked resident to return inside, he denied and stated, 'I will get back in the same way I got out.' Resident was then observed to go to the end of E hall and enter the access code to open the door, he then returned inside. Per the report, predisposing situation factors included the resident being an active exit seeker. No injuries were noted, and all appropriate parties were notified.
Review of Progress Notes for R#62 in the Electronic Medical Record (EMR), dated 07/19/2021 at 9:53 a.m., revealed that in response to the resident exiting the facility, We will need to include an education to staff to block the door code when entering it if residents are nearby and can see the code. This education was provided, and per the resident's record, no further elopements had occurred.
Interview on 02/02/2023 at 11:51 a.m., Licensed Practical Nurse (LPN) 4 confirmed R#62 exited the building on 07/17/2021. LPN4 stated that the facility investigated and determined that R#62 saw one of the staff enter the code to get out of the secured door, then entered the code himself to exit the door. LPN 4 stated that no staff witnessed R#62 leave the building; however, a staff member was walking by and saw R#62 sitting on the front porch of the facility. Staff approached him, and he agreed to return to the building. Staff was not aware of how long he had been outside the building.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0698
(Tag F0698)
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 review of facility standards, the facility failed to make arrangements for t...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, and review of facility standards, the facility failed to make arrangements for the provision of meals for one (Resident (R) 84) of one residents reviewed for dialysis, when the resident was out of the facility to receive dialysis treatment.
Findings include:
Review of the Facility's Renal Dialysis Management standard, dated 08/2021, revealed, Arrangements should be made for an appropriate meal to accompany the resident to dialysis.
Review of R84's admission Record, located in the resident's Electronic Medical Record (EMR) under the Profile tab, revealed R84 was admitted to the facility on [DATE] with diagnoses which included end stage renal disease and type II diabetes mellitus.
Review of R84's Physician Orders, located in the resident's EMR under the Orders tab, revealed an order dated 01/03/23 for the resident to receive dialysis on Monday, Wednesday, and Friday.
Review of R84's admission Minimum Data Set (MDS) with an Assessment Reference Date (ARD) of 01/06/23, located in the resident's EMR under the MDS tab, specified the resident received dialysis. The resident had a Brief Interview for Mental Status (BIMS) score of 8/15, which indicated the resident had moderate cognitive impairment.
Review of R84's care plan located in the resident's EMR under the Care Plan tab revealed a Focus area initiated on 01/16/23 that specified R84 required hemodialysis related to renal failure. A goal specified that R84 will have no signs or symptoms of complications from dialysis through the review date. The care plan did not address how the facility was going to make arrangements for an appropriate meal to accompany R84 to his dialysis treatments three times per week.
During an interview on 01/30/23 at 5:16 PM, R84 stated he was hungry because he had not eaten since breakfast. R84 explained that on 01/30/23, he left the facility to go to dialysis at around 10:00 AM and he did not eat lunch because he did not return to the facility until around 4:30 PM. R84 stated he does not each lunch when he goes to dialysis three times per week because the facility does not provide him with any food to take to the dialysis center. R84 stated that he does get hungry on the days that he receives dialysis.
During an additional interview on 02/01/23 at 9:40 AM, R84 stated he was sitting in the facility's front lobby waiting for the van to pick him up and take him to dialysis. R84 stated the facility did not provide him with any food to take to dialysis this morning.
Observations on 02/01/23 at 10:17 AM revealed R84 was being assisted onto the transport van by the van driver. R28 was observed not to have any food provided by the facility to take with him to the dialysis center.
During an interview on 02/01/23 at 10:24 AM, the Dietary Manager (DM) stated the dietary department did not provide R84 with any food to take to his dialysis treatments, which are scheduled three days a week. The DM stated she did not recall the care plan team having any discussions with the dialysis center regarding how to coordinate R84 bringing food from the facility to his dialysis treatments.
During an interview on 02/01/23 at 10:33 AM, the MDS Coordinator stated the facility's Interdisciplinary care plan team did not have any discussions with the resident or the dialysis center regarding how to coordinate R84 bringing food from the facility to his dialysis treatments.
During an interview on 02/02/23 at 11:45 AM, the facility's Registered Dietitian (RD) stated the dietary department should provide R84 with a meal to take to his dialysis treatments on Monday, Wednesday, and Friday.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0761
(Tag F0761)
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 facility policy review, the facility failed to ensure medication was secured...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on observation, interview, record review, and facility policy review, the facility failed to ensure medication was secured. One of four medication carts was not locked at all times. Medication was kept openly at the bedside and not secured under lock for one (Resident (R) 80) of 33 sampled residents. These failures placed residents at risk of having their unsecured medications diverted.
Findings include:
1. Record review of the facility policy titled Medication Administration Guidelines dated 06/2022, revealed that, Medication carts are to be kept locked at all times when not under visual supervision.
Observation on 02/02/23 at 4:27 AM revealed the C-hall medication cart was unlocked and unattended while parked at the nurse's station between hall D and hall E. Ongoing observation revealed the medication cart remained unlocked and unattended until Licensed Practical Nurse (LPN) 5 returned to the nurse's station area at 4:35am. During the time that the unlocked cart was not under the nurse's visual supervision, one resident, R2, walked near the cart. In addition, Certified Nursing Aide (CNA) 4 was within 10 feet of the cart for approximately two minutes while it was unattended and unlocked.
Interview with LPN5 on 02/02/23 at 4:38 AM revealed the cart should be locked and, at this time, LPN5 then locked the cart. LPN5 stated, What happened is that I was standing there a while ago, and I didn't kick the bottom drawer, so it didn't lock completely. I have a habit of always locking it, even when I am standing in front of it still. I will put a work order in and tell them to fix it.
Interview on 02/02/23 at 11:06 AM with the Director of Nursing (DON) revealed that the expectation and policy was that the medications carts should be locked when not attended.
2. Review of R80's electronic medical record (EMR) revealed an undated admission Record located under the Profile tab which showed the resident was admitted on [DATE] with diagnoses including acute respiratory failure with hypoxia (Absence of oxygen in the tissues), and chronic obstructive pulmonary disease (COPD).
Review of the EMR under the Orders tab revealed physician orders dated 12/19/22 Ipratropium- Albuterol Solution 0.5-2.5 (3) MG [milligrams]/3ML [milliliters] - 1 vial inhale orally every 4 hours as needed for SOB [shortness of breath].
Interview on 01/30/23 at 10:57 AM with R80 revealed the resident takes the breathing treatments (in which the ordered medication vials are added to a nebulizer machine) every four hours. During an observation on 01/30/23 at 4:19 PM, R80 was sitting in his wheelchair next to his bed near the window, holding a nebulizer mask and inhaling the mist coming out of the mask.
During an observation on 02/01/23 at 9:31 AM, there were three unopened medication vials, containing a clear substance, next to the nebulizer machine.
During an interview on 02/01/23 at 09:44 AM, R80 confirmed that he usually does the treatment by himself. Observation revealed three empty medication vials and two unopened medication vials next to the machine.
During an interview on 02/01/23 at 10:14 AM, LPN7 was asked about the resident having the unsecured medication vials at bedside. LPN7 stated the resident was very independent but there should not be any vials in his room, adding, The nurse should put the medication in the nebulizer cup.
During an interview on 02/01/23 at 10:23 AM, the DON was shown the vials at the side of the machine on the nightstand. The DON stated, These should not be here at the bed side.
During an interview on 02/01/23 at 11:25 AM, the Medical Director stated, Medication should not be necessarily at the bedside.
Based on observation, resident and staff interviews, record review, and review of the facility policy titled, Medication Administration Guidelines, the facility failed to ensure medication was secured. One of four medication carts was not locked at all times. Medication was kept openly at the bedside and not secured under lock for one of 33 sampled residents (R) (#80). These failures placed residents at risk of having their unsecured medications diverted.
Findings include:
1. Record review of the facility policy titled, Medication Administration Guidelines, dated 06/2022, revealed that, Medication carts are to be kept locked at all times when not under visual supervision.
Observation on 02/02/2023 at 4:27 a.m. revealed the C-hall medication cart was unlocked and unattended while parked at the nurse's station between hall D and hall E. Ongoing observation revealed the medication cart remained unlocked and unattended until Licensed Practical Nurse (LPN) 5 returned to the nurse's station area at 4:35 a.m. During the time that the unlocked cart was not under the nurse's visual supervision, one resident, R#2, walked near the cart. In addition, Certified Nursing Aide (CNA) 4 was within 10 feet of the cart for approximately two minutes while it was unattended and unlocked.
Interview with LPN5 on 02/02/2023 at 4:38 a.m. revealed the cart should be locked and, at this time, LPN5 then locked the cart. LPN5 stated, What happened is that I was standing there a while ago, and I didn't kick the bottom drawer, so it didn't lock completely. I have a habit of always locking it, even when I am standing in front of it still. I will put a work order in and tell them to fix it.
Interview on 02/02/2023 at 11:06 a.m. with the Director of Nursing (DON) revealed that the expectation and policy were that the medications carts should be locked when not attended.
2. Review of the electronic medical record (EMR) for R#80 revealed an undated admission Record located under the Profile, tab which showed the resident was admitted on [DATE] with diagnoses including acute respiratory failure with hypoxia (Absence of oxygen in the tissues), and chronic obstructive pulmonary disease (COPD).
Review of the EMR under the Orders tab revealed physician orders dated 12/19/2022 Ipratropium- Albuterol Solution 0.5-2.5 (3) MG (milligrams)/3ML (milliliters) - 1 vial inhale orally every four hours as needed for SOB (shortness of breath).
Interview on 01/30/2023 at 10:57 a.m. with R#80 revealed that the resident takes the breathing treatments (in which the ordered medication vials are added to a nebulizer machine) every four hours. During an observation on 01/30/2023 at 4:19 p.m., R#80 was sitting in his wheelchair next to his bed near the window, holding a nebulizer mask and inhaling the mist coming out of the mask.
Observation on 02/01/2023 at 9:31 a.m., there were three unopened medication vials, containing a clear substance, next to the nebulizer machine.
Interview on 02/01/2023 at 09:44 a.m., R#80 confirmed that he usually does the treatment by himself. Observation revealed three empty medication vials and two unopened medication vials next to the machine.
Interview on 02/01/2023 at 10:14 a.m., LPN7 was asked about the resident having unsecured medication vials at the bedside. LPN7 stated the resident was very independent, but there should not be any vials in his room, adding, The nurse should put the medication in the nebulizer cup.
Interview on 02/01/2023 at 10:23 a.m., the DON was shown the vials at the side of the machine on the nightstand. The DON stated, These should not be here at the bedside.
Interview on 02/01/2023 at 11:25 a.m., the Medical Director stated, Medication should not be necessarily at the bedside.
CONCERN
(D)
Potential for Harm - no one hurt, but risky conditions existed
Safe Environment
(Tag F0921)
Could have caused harm · This affected 1 resident
Based on observation, interview, and review of facility policy titled, Maintenance Work Request, the facility failed to ensure the bathroom sink was functioning properly for one of 33 sampled resident...
Read full inspector narrative →
Based on observation, interview, and review of facility policy titled, Maintenance Work Request, the facility failed to ensure the bathroom sink was functioning properly for one of 33 sampled residents (R) (#47).
Findings include:
Review of the facility's undated policy, titled Maintenance Work Request, revealed its purpose is to, ensure the facility is well-maintained for the safety of residents, staff and visitors. Each facility may use the TELS (building management platform to submit work orders) system as a means of scheduling of preventive maintenance drills. Procedure: .4. All maintenance work requests will be completed within five days of receipt, unless the work needed is of an urgent nature, in which case it will be done immediately.
Observation on 01/31/2023 at 5:00 p.m., R#47's bathroom sink was stopped up and halfway full of stagnant water.
During an observation on 02/02/2023 at 10:00 a.m., R#47's bathroom sink was stopped up and halfway full of stagnant water.
Interview on 01/31/2023 at 5:00 p.m., R#47 stated that his bathroom sink had been stopped up for about four months. The resident stated he cannot get hot water for his face because the sink overflows. R#47 stated that the maintenance director came in over two months ago. However, the could not get it unstopped, and the sink is still stopped up with old water in it.
Interview on 02/01/2023 at 10:25 a.m., the Maintenance Director (MD) confirmed that R#47's sink was stopped up, adding that it had been draining slowly for about two or three months. In the past, he had unclogged the sink by snaking it. However, the MD continued, the sink would not drain a few weeks ago and he was unable to unclog it by using a cleaning agent in the sink or cleaning the vent pipe. The MD said the expectation was for a work order to be resolved within 48 hours; however, he could not find a completed work order for the stopped up sink. The MD stated that R#47 told him he was upset about the sink because he could not use the sink to shave and that the water was warm in the sink.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0688
(Tag F0688)
Could have caused harm · This affected multiple residents
Based on observation, interview, record review, and review of the facility policy titled, Restorative Nursing Standard, the facility failed to provide range-of-motion and/or splinting services to addr...
Read full inspector narrative →
Based on observation, interview, record review, and review of the facility policy titled, Restorative Nursing Standard, the facility failed to provide range-of-motion and/or splinting services to address range of motion loss and/or contractures for four of six residents (R) (#63, #6, #4, and #7) reviewed for a limited range of motion. These failures had the potential to cause worsening contractures and/or complications for four residents.
Findings include:
Review of the facility policy titled Restorative Nursing Standard, dated 08/2021, revealed that The nursing staff is responsible to assure that the resident receives the necessary
restorative nursing care. In rehabilitation nursing, it is the nurse and the therapist who do
most of the teaching of the resident to help him regain the highest level of independence
possible.
1. Review of R#63's undated admission Record, located in the Profile tab of the electronic medical record (EMR), revealed R#63 was admitted with diagnoses of contracture of the right hand, contracture of the left hand, contracture of the right elbow, contracture of the left elbow, and quadriplegia.
Review of the most recent quarterly Minimum Data Set (MDS) assessment for R#63, with an Assessment Reference Date (ARD) of 11/09/2022, located in the MDS tab of the EMR, revealed that R#63 was rarely/never able to make herself understood and was unable to complete the Brief Interview for Mental Status (BIMS). R#63 was totally dependent on staff for bed mobility, transfers, locomotion, dressing, eating, toilet use, personal hygiene, and bathing. R#63 had an impaired range of motion in both the upper and lower extremities.
Review of the comprehensive Care Plan, for R#63 dated 08/12/2022 and located in the Care Plan tab of the EMR, revealed, R#63 has an alteration in musculoskeletal status r/t (related to) contracture of the right and left hands. The interventions included: See MD orders and/or PT (physical therapy) treatment plan . ROM (range-of-motion) during care as tolerated . Splints as recommended.
Review of the Occupational Therapy Discharge Summary, for R#63, dated 10/09/2022, provided on paper, documented, Discharge Recommendations: D/C (discharge) with RNP (restorative nursing program)/good staff support. Restorative Program Established/Trained - Restorative ROM program. ROM Program Established/Trained: PROM (passive range-of-motion to) BUEs (bilateral upper extremities) all joints to tolerance x 10 repetitions. Functional Maintenance Program Established/Trained - Splint and Brace Program Splint and Brace Program Established/Trained: B (bilateral) elbow splints and hand splints x four hours daily. Prognosis to Maintain CLOF (current level of function) - Good with consistent staff follow-through.
Review of Physician Orders, for R#63, dated January 2023, located in the Orders tab of the EMR, revealed there was no order for the use of splints.
Observation on 01/30/2023 from 11:28 p.m. to 1:04 p.m., R#63 was observed in bed in her room. Both arms and hands were contracted so that they were bent into fists. There were no splints or other devices in place.
Observation on 01/31/2023 at 10:02 a.m., 12:00 p.m., 1:30 p.m., and 3:17 p.m., R#63 was observed in bed with contracted arms and hands. She did not have any splints or devices in place.
Observation on 02/01/2023 at 11:00 a.m., 1:00 p.m., and 4:05 p.m., R#63 was observed in bed with contracted arms and hands. She did not have any splints or devices in place.
Observation on 02/02/2023 at 4:22 a.m. and 6:00 a.m., R#63 was observed in bed with contracted arms and hands. She did not have any splints or devices in place.
Interview on 02/02/2023 at 8:37 a.m., with a Licensed Practical Nurse (LPN) 4 stated R#63 came to the facility about six months ago with severe contractures. She stated R#63 was in therapy when she first was admitted , but stated, I don't know what they're doing for her contractures now.
Interview on 02/02/2023 at 10:00 a.m., with the Regional Nurse Consultant, revealed there were no records of a restorative nursing program or use of splints for R#63.
Interview on 02/02/2023 at 10:48 a.m., with the MDS Coordinator (MDSC), who served as the head of the restorative nursing program, stated she was unaware of the recommendation from Occupational Therapy (OT) for a restorative nursing program, including the use of splints. The MDSC confirmed that R#63 had not been provided splinting or restorative services since her discharge from therapy. The MDSC stated she had asked the therapy department to provide her with their discharge summaries so she could follow up with the recommendations, but she had yet to receive any summaries for R#63. The MDSC stated that R#63's family members reported she used splints before admission to the facility, and they were being applied by the therapists when she was receiving therapy. The MDSC stated, (R#63) should be on restorative.
2. Review of the admission Record for R#6, undated located in the Profile tab of the EMR, revealed he was admitted with a diagnosis of a right hand contracture.
Review of the most recent annual MDS assessment for R#6 dated 01/02/2023, located in the MDS tab of the EMR, revealed R#6 scored two out of 15 on the BIMS, indicating severely impaired cognition. He required extensive assistance with dressing and personal hygiene and had functional limitations in range of motion of one extremity. According to this MDS, R#6 did not receive range of motion or splint and brace assistance. He did not exhibit any behavioral symptoms, including rejection of care.
Review of Restorative Nursing Program Recommendations, for R#6 dated 11/22/2022 provided on paper, revealed, Device: Hand Splint Current Wear Schedule: five to six hours of wear daily. Goal: Maintain splint wear schedule w/ (with) skin checks post doffing. Frequency: five times a week.
Review of the Physician Orders, for R#6 dated January 2023 located in the Orders tab of the EMR, revealed an order that originated on 01/09/2023 to apply splint to right hand five to six hours daily as tolerated, with skin checks prior to and post doffing of splint, post prom exercises. There was also an order that originated on 12/05/2022 to apply a splint to right hand five to six hours daily as tolerated, with skin checks prior to and post doffing of splint, post prom exercises, to right hand/wrist, digits, all planes five repetitions /five sets.
Review of the comprehensive Care Plan for R#6, dated 12/07/2022 and located in the Care Plan tab of the EMR, revealed, R#6 requires assistance with ADLs (activities of daily living) r/t (related to) impaired balance, limited mobility, (and) limited ROM. The interventions included: PT (physical therapy)/OT (occupational therapy) evaluation and treatment as per MD (physician) orders . Rehab/restorative splint/brace program: apply to right hand daily as tolerated s/p (after) right hand/wrist/digits exercises for passive ROM as indicated.
Additionally, a Care Plan dated 01/09/2023 for R#6 documented, R#6 has limited physical mobility r/t Contracture RUE (right upper extremity). The approaches included: Restorative Nurse Aid: apply a splint to right Hand five to six hours daily as tolerated, with skin checks prior to and post doffing of splint, post PROM exercises . Monitor/document/report PRN any s/sx (signs and symptoms) of immobility: contractures forming or worsening, thrombus formation, skin-breakdown, fall related injury . Provide gentle range of motion as tolerated with daily care . Document assistance as needed . PT, OT referrals as ordered, PRN.
Review of the Kardex for R#6 dated 02/01/2023 provided on paper, revealed, Nursing Rehab/Restorative: Splint/Brace Program - Apply to right hand daily as tolerated s/p right hand/wrist/digits exercises for passive ROM as indicated.
Observation on 01/30/2023 at 11:10 a.m., R#6 was observed in his room seated in a wheelchair with his right hand contracted into a fist. There was no splint or device in place.
Observation on 01/31/2023 at 10:00 a.m., 12:00 p.m., 1:32 p.m., and 4:42 p.m., R#6 was observed in his room in bed. His right hand was contracted into a fist, and there was no splint or device in place.
Observation on 02/01/2023 at 9:32 a.m., 12:00 p.m., and 3:50 p.m., R#6 was observed in his room seated in his wheelchair or in bed. His right hand was contracted into a fist, and there was no splint or device in place.
Observation on 02/02/2023 at 4:48 a.m., R#6 was observed in his room in bed. His right hand was contracted into a fist, and there was no splint or device in place.
Review of Restorative Nursing Documentation Survey Report, for R#6 dated January 2023, provided on paper, revealed, Nursing Rehab: Assistance with Splint or brace . Right hand five to six hours daily as tolerated, with skin checks prior to and post doffing of splint post PROM exercises. A review of this report revealed that the care was not signed as completed on 01/06/2023, 01/07/2023, 01/08/2023, 01/13/2023, 01/14/2023, 01/15/2023, 01/21/2023, 01/22/2023, 01/25/2023, 01/30/2023, and 01/31/2023. There were no refusals documented.
Interview on 02/02/23 at 10:48 AM with the MDSC revealed that she had noticed holes in the restorative documentation and had addressed the holes with the aides to remember to sign the report. She also stated that sometimes the restorative aides were pulled to work on the floor and could not complete restorative duties. The MDSC stated she took over the restorative program in 12/2022, and it was a struggle to get the program going because, before that, it had not been happening. She stated that R#6s splinting and range of motion program should be done daily as the physician ordered.
Interview on 02/02/23 at 11:00 a.m. with Restorative Aide (RA) 1, she stated R#6 sometimes refused to wear splints, but she could talk to him and put on the splints. RA1 further revealed being off work the last three days, and the second restorative aide was not working due to an injury. She was unaware if R#6 had received any restorative services that week. RA1 stated she did not know why he did not have splints from 01/30/2023 to 02/02/2023.
Interview on 02/02/2023 at 1:18 PM, with Director of Nursing (DON) stated she expected the staff to document any refusals on the restorative record and let the nurse know of refusals so they can re-approach the resident.
3. Review of the undated admission Record for R#4, located under the Profile tab of the EMR, revealed that
R#4 was admitted with diagnoses of contracture of muscle, muscle coordination, and muscle weakness.
Review of the most recent MDS quarterly review for R#4, dated 1/4/2023, revealed in the MDS tab of the EMR, R#4 scored fourteen out of 15 on the BIMS.
Review of the EMR under the Orders tab for R#4 revealed the physician ordered, 12/05/2022 PROM to RUE/Elbow (right upper extremity), slow static stretch as tolerated. daily, five repetitions / five sets. With rest periods prn (as needed) in between.
Review of the care plan for R#4 revealed a problem of limited physical mobility related to a contracture of the right elbow. The care plan for this problem, which showed a creation date of 11/18/2019, listed multiple interventions, including a revision on 04/22/2022 calling for staff to, Provide a gentle range of motion as tolerated with daily care.
Review of the Certified Nursing Assistant (CNA) documentation presented by the facility for 12/2022 revealed the following days on which no treatment was provided: 12/06/2022, 12/15/2022, 12/16/2022, 12/17/2022, 12/23/2022, 12/24/2022, 12/25/2022, 12/28/2022, and 12/29/2022.
Review of CNA documentation presented by the facility for 01/2023 revealed the following days on which no treatment was provided: 01/06/2023, 01/07/2023, 01/08/2023, 01/12/2023, 01/14/2023, 01/18/2023, 01/21/2023, 01/22/2023, 01/24/2023, 01/30/2023, and 01/31/2023.
Observation on 01/30/2023 at 12:02 p.m., R#4 had his right arm bent up at the elbow, and the right hand was folded in a fist.
Interview on 01/30/2023 at 12:10 p.m., with R#4 where he revealed that staff works with him sometimes on therapy for his hand.
Interview on 02/02/2023 at 9:16 a.m.,with the MDSC, who was also the Restorative Nurse, stated she was appointed Restorative Nurse in 12/2022. The MDSC printed the CNA documentation for R#4s restorative treatment and verified that the treatment did not occur every day. She confirmed that the treatments should be done, daily.
Interview on 02/02/2023 at 9:35 a.m., with Restorative Aide (RA)1 stated, When a resident goes off therapy, they are put on the restorative program. RA1 further stated that therapy staff will provide training on how to do the treatment. RA1 revealed that I see the resident every day that I work for about 15-20 minutes. I'm not here every day. I can't answer for those times that I am not here.
Interview on 02/02/2023 at 12:57 p.m., the DON stated the CNAs should be doing the treatments when the RAs were not there. The DON stated that the treatment should be documented, and the nurse should be notified of refusals, adding. I expect the treatment to be done.
4. Review of R#7's Face Sheet, located in the EMR under the Medical Diagnosis tab, revealed that R#7 was admitted with a diagnosis of contracture of the right hand and contracture of the left hand and muscle weakness.
Review of the most recent quarterly MDS, R#7 with an ARD of 01/04/2023, which was in the resident's EMR under the MDS tab, specified R#7 required total dependence with dressing and received splint or brace assistance six out of the last seven days. According to the MDS, no refusal of care was noted. C-cognition
Review of the care plan for R#7 revealed a Focus area, initiated on 09/22/2021 with a revision date of 07/12/2022, which specified that R#7 has limited physical mobility r/t contractures of bilateral hands. She has wash cloths rolled and placed in her hands. The goal specified that R#7 will remain free of complications related to immobility, including contractures, through the next review date. Care plan interventions included, Splints per orders to BUE, rolled wash cloths are placed in resident's hands.
Review of Physician Orders, for R#7, located in the resident's EMR under the Orders tab, revealed an order dated 12/05/2022 which specified, Apply a splint to the right hand and soft splint roll to the left hand, post passive ROM exercises daily to prevent progressive contracture. Observe for skin breakdown and report any to Nurse.
R#7's current Certified Nursing Assistant (CNA) Kardex revealed staff was to Apply splint as recommended and as tolerated to the right and left hands. Remove for bathing, keep the area clean and dry.
Review of the Documentation Survey Report for R#7 dated 12/2022 revealed the following Nursing Rehabilitation interventions: Nursing Rehab: Assistance with Splint Program #1- Apply to BUE and Nursing Rehab: Passive ROM Program #1 to BUE. Further review of this report revealed there was no documentation that staff provided R#7 with splinting assistance or passive ROM on 12/01/2022, 12/02/2022, 12/03/2022, 12/04/2022, 12/16/2022, 12/23/2022, 12/24/2022, and 12/25/2022.
Review of the Documentation Survey Report for R#7 dated 01/2023 revealed no evidence that staff provided R#7 with splinting assistance or passive ROM on 01/07/2023, 01/08/2023, 01/14/2023, 01/15/2023, 01/21/2023, and 01/22/2023.
Observation on 01/30/2023 at 11:35 a.m. revealed that R#7 was in her room, and her right hand was contracted in a closed fist. No splinting device or hand roll was observed on R#7s contracted right hand.
Observation on 01/31/2023 at 4:08 p.m., revealed that R#7 was in her room, and her right hand was contracted in a closed fist. No splinting device or hand roll was observed in R#7's contracted right hand. LPN1 was present in the resident's room during this observation.
Interview on 01/31/2023 at 4:08 p.m. with Licensed Practical Nurse (LPN) 1 revealed that R#7 should have a rolled washcloth in her contracted right hand. LPN1 further stated that the Restorative Aides (RA)s and Certified Nursing Assistants (CNA) are responsible for applying the splints and hand rolls to R#7's contracted hands. LPN1 stated that Certified Nursing Assistant (CNA) 3 was responsible for taking care of R#7 on 01/31/2023 from 3:00 p.m. to 11:00 p.m.
Interview on 01/31/2023 at 4:11 p.m. with Certified Nursing Assistant (CNA) 3 confirmed R#7 should have either a hand roll or a splint in her contracted right hand. CNA3 stated that on 01/31/2023, she began to work at 3:00 p.m., and she had not yet provided any care or observed R#7 during her shift. CNA3 further explained that staff was expected to monitor R#7 every two hours to make sure her splints and hand rolls were in her contracted hands.
Interview on 02/02/2023 at 10:45 a.m. with Restorative Aide (RA) 1 revealed that she usually will work with R#7 four days a week and places R#7's hand rolls and hand splints on her in the morning. RA1 also stated that she also will provide R#7 with a passive range of motion prior to applying the hand splints and hand rolls. RA1 specified that R#7 does not refuse to wear her hand splints and hand rolls and does not attempt to remove them.
Observation on 02/02/2023 at 10:55 a.m. (after surveyor intervention), R#7 was in bed with a splint on her contracted left hand and a hand roll in her contracted right hand. RA1 was present in the resident's room during this observation. RA1 stated she placed the hand roll in R#7's right hand and the splint on R#7 left hand during the morning of 02/02/2023. RA1 also stated that she will keep R#7's hand splints in place for one hour as tolerated. RA1 explained that when staff removes R#7's hand splint, a hand roll should be placed in the resident's contracted hand. RA1 further stated that she had worked with R#7 since May 2022, and R#7 had not experienced a decrease in the range of motion of her hands during the time she worked with her.
Interview on 02/02/2023 at 1:48 p.m. with the MDSC confirmed that the RAs and CNAs were not applying R#7's hand splints and hand rolls as ordered by the physician. The MDSC stated that R#7 should have a hand roll in her right hand when she does not have a splint in this contracted hand. She also stated that R#7's physician orders for hand splints and hand rolls needed clarification because these orders did not specify when they were to be applied and how long they were to remain on R#7's contracted hands.
Interview on 02/02/2023 at 1:00 p.m. with the (Director of Nursing) DON confirmed that the RA and CNA staff were responsible for applying the hand splints and hand rolls to R#7's contracted hands as ordered and document in R#7's medical record that they were applied.
CONCERN
(E)
📢 Someone Reported This
A family member, employee, or ombudsman was alarmed enough to file a formal complaint
Potential for Harm - no one hurt, but risky conditions existed
Respiratory Care
(Tag F0695)
Could have caused harm · This affected multiple residents
Based on observation, staff interviews, record review, and review of the facilities policies titled, Tracheostomy Tube Emergency Care, Procedural Competency Evaluation for Tracheostomy Care, Respirato...
Read full inspector narrative →
Based on observation, staff interviews, record review, and review of the facilities policies titled, Tracheostomy Tube Emergency Care, Procedural Competency Evaluation for Tracheostomy Care, Respiratory System Management Standard, and Oxygen Concentrators: In-House Maintenance, the facility failed to ensure the provision of respiratory services in accordance with professional standards for four of four residents (R) (#7, #63, #46, #80) reviewed for respiratory care out of a total sample of 33 residents. Emergency tracheostomy supplies (kits) were not maintained at the resident's bedside in case of need. Physician's orders were not specific to the equipment needed. Respiratory equipment was not maintained in a clean manner. This failure increased the residents' risk for compromised airway/respiratory distress.
Findings include:
Review of the facility-provided policy titled Tracheostomy Tube Emergency Care, dated 2020, revealed Replacement Tracheostomy tubes must always be available 1) Appropriate size tube 2) One size smaller tube a. When the appropriate sized trach tube is the smallest size available refer to ordering physician for direction.
Review of the facility-provided Procedural Competency Evaluation for Tracheostomy Care, dated 11/16/2022, revealed Equipment and Patient Preparation NOTE: Tracheostomy patients should always have a replacement tracheostomy tube at the bedside in case an emergency replacement becomes necessary.
1. Review of the admission Record for R#7, undated located in the electronic medical record (EMR), revealed R#7 was admitted to the facility with multiple diagnoses, including tracheostomy status, aphasia, and diffuse traumatic brain injury (TBI) with loss of consciousness of unspecified duration.
Review of the most recent quarterly Minimum Data Set (MDS) for R#7 dated 01/04/2023 and located EMR under the MDS tab revealed a Brief Interview for Mental Status (BIMS) score of 99, which indicated he was unable to complete the interview due to cognitive deficits. Facility staff assessed R#7 as severely cognitively impaired. The MDS indicated R7 had a tracheostomy and required suctioning while a resident at the facility.
Review of Physician's Orders for R#7's dated 01/18/2023, under the Orders tab located in the EMR revealed orders for a Shiley [brand] trach inner cannula size # [number] 6. The order did not specify if the Shiley was to be cuffed or uncuffed. Further review of the physician orders revealed no order for an emergency tracheostomy kit at the bedside.
Observation and interview on 01/30/2023 at 11:08 a.m. with Licensed Practical Nurse (LPN) 1, who was assigned to provide care for R#7, revealed that there was no hemostat or a lower size inner cannula in the supply cart at R#7's bedside. LPN1 stated that if the trach became dislodged, she would let the immediate supervisor and the unit manager know, then send R#7 out of the facility. LPN1 found a Shiley #5 inner cannula (lower size) in the supply room and placed it in the supply cart in R#7's room.
Interview on 01/31/2023 at 11:24 a.m. with the Interim Director of Nursing (DON) revealed that she had only worked at the facility for a week. The Interim DON stated that nurses could replace a trach tube if it dislodged if they had completed a competency; however, if the staff had not completed a competency, then the nurses would send the resident out of the facility for tracheostomy replacement.
Interview on 01/30/2023 at 3:00 p.m. with LPN2 revealed she had worked at the facility 14 years and in-service training was provided on tracheostomy care last year. LPN2 stated that if a tracheostomy dislodged, then she would send the resident out of the facility and would not replace it because she had yet to complete a competency. LPN2 indicated that the emergency trach kit should include an Ambu bag, suction kit, the same size cannula and one size lower, sterile gloves, and a hemostat at the bedside. LPN2 indicated that the facility did not have an emergency trach kit checklist or physician orders on maintaining the emergency trach kit at the bedside. LPN2 indicated she did not know how staff were ensuring that the emergency supplies were at the bedside since there was no order for them or a checklist. Observations at this time with LPN2 revealed that the hemostat was not in the supply cart at the bedside but was in R#7's top dresser drawer in a ziplocked bag. During this interview, LPN2 confirmed that R#7 has an uncuffed trach and should have a physician's order.
Interview on 02/01/2023 at 11:19 a.m. with the Medical Director revealed that if the tracheostomy dislodged, then the nurses would call 911, if the nurses have yet to receive training to replace the tracheostomy. The Medical Director also stated that if the resident's trach dislodged and the emergency trach kit was not at the bedside, it could lead to respiratory distress.
Interview on 02/01/2023 at 12:19 PM with LPN4 revealed that when residents were admitted to the facility, the admitting nurse or unit manager would enter the orders in the EMR. LPN4 stated that the unit managers would verify the orders the next day. LPN4 stated that since they only admit residents with uncuffed tracheostomies, the order did not need to state whether the trach was cuffed or uncuffed. LPN4 indicated that their policy did not state they had to have an order for maintaining emergency trach equipment at the bedside. LPN4 further revealed they were going to implement an audit checklist since the equipment was found to be missing at the bedside for R#7 and R#63 during the survey.
Interview on 02/02/2023 at 3:20 p.m. with the Regional Nurse Consultant revealed that physician's orders needed to be specific for each resident. The Regional Nurse Consultant stated that the tracheostomy in-services that were conducted with the nurses last year included emergency management of a tracheostomy, and she expected staff to call 911 if the tracheostomy dislodged and to have the emergency equipment at the bedside.
2. Review of the admission Record for R#63 undated, located in the Profile tab of the EMR, revealed R#63 was admitted to the facility with diagnoses of chronic respiratory failure with hypoxia, quadriplegia and use of a tracheostomy.
Review of the most recent quarterly MDS assessment for R63 dated 11/09/2022, located in the MDS tab of the EMR, revealed that R#63 was rarely/never able to make herself understood and was unable to complete the BIMS test. The staff assessed R#63 with short- and long-term memory problems and severely impaired cognition. She did not exhibit any mood or behavioral symptoms. R#63 was totally dependent on staff for bed mobility, transfers, locomotion, dressing, eating, toilet use, personal hygiene, and bathing. R#63 received tracheostomy care, oxygen, and suctioning.
Review of Physician Orders for R63 dated 01/18/2023, located in the Orders tab of the EMR revealed, Change Shiley trach inner cannula size #6 daily days for secretions and PRN (as needed) and trach care q (every) shift and PRN. Further review of the physician orders revealed no indication whether Shiley was to be cuffed or uncuffed or for an emergency tracheostomy kit at the bedside.
Observation in R#63's room on 01/30/2023 at 3:00 p.m. revealed there was no bag valve mask (a handheld tool that is used to deliver positive pressure ventilation to any subject with insufficient or ineffective breaths. It consists of a self-inflating bag, one-way valve, mask, and an oxygen reservoir sometimes referred to as an Ambu bag) or hemostat in the emergency tracheostomy supplies cart at the bedside.
Interview on 1/30/2023 p.m. with LPN1 stated she was not R#63's nurse, so could not verify what supplies were at the bedside.
During concurrent observation and interview on 1/30/2023 at 3:15 p.m., LPN4 verified there was no hemostat at the bedside and left the room, stating she would get one immediately from the supply closet. At 3:27 p.m., LPN4 returned with a hemostat and verified that there was no bag valve mask present at the bedside. LPN4 stated, That should be here, and stated she would get one immediately from the supply closet.
Review of the facility's 2020 SMS [Specialized Medical Services] Tracheostomy Tube Emergency Care policy, used to train facility nursing staff, revealed, If a tracheostomy becomes blocked or comes out, an Emergency Plan is needed. It's recommended to have two back up tracheostomy tubes at bedside. These backup tubes MUST always be readily available . Blocked Tracheostomy Tube - Thick secretions can block the airway causing shortness of breath which can lead to severe difficulty breathing.
1) Remove the inner cannula [and] replace with a clean or new one.
2) Try to remove the plug by suctioning.
3) If this doesn't work, remove the tube and replace it with a new one.
Trach Tube Replacement - If the blockage can't be removed then the entire tube should be removed.
1) insert a clean, lubricated tracheostomy tube in the stoma using the obturator (guide)
2)Hold the tube in place with your fingers
3) Pull out the obturator
4) Secure with trach ties
5) Observe patient for continued respiratory distress
6) Ensure proper placement with chest auscultation and pulse oximetry.
In a concurrent interview on 02/02/23 at 3:13 p.m. with the Regional [NAME] President of Operations (RVPO) and Regional Nurse Consultant, the Regional Nurse Consultant stated that the above policy was worded in a confusing way but was only directing the nursing staff to replace the inner cannula, not the entire tracheostomy tube. She added that the obturator was the same as the inner cannula. She stated she expected staff to call 911 if the trach dislodged.
3. Observation on 01/30/2023 at 4:01 p.m., R#46 was in bed with his nasal cannula in his nose. The oxygen concentrator had a hole in the side of the machine where a filter should be, and there was dust on the inside of the concentrator.
Observation on 02/01/2023 at 9:49 a.m., R#46 was in bed with a nasal cannula in his nose. The concentrator still had no filter on the side of the machine. Inside the machine, dust can be visualized.
Review of the admission Record for R#46 undated in the EMR revealed located in the Profile tab, revealed that R#46 was admitted to the facility with a diagnosis including shortness of breath (SOB), and chronic obstructive pulmonary disease (COPD).
Review of the EMR for R#46 dated 8/17/2022 under the Orders tab revealed physician orders O2 [oxygen] at 2L/MIN [Liters per minute] for COPD/SOB.
Interview on 02/01/2023 at 9:53 a.m., Registered Nurse (RN)1 was asked to look at the concentrator. She stated, That should not be like that. I looked at some yesterday but did not look at this one.
Interview on 02/01/2023 at 10:10 a.m., the DON stated, There should be a filter to prevent the dust and debris from getting into the machine.
4. Observation on 01/30/2023 at 10:57 a.m., R#80 had a nasal cannula in his nose. The oxygen concentrator was set at two liters, and the filter was visibly dusty. There was a nebulizer on the resident's nightstand. The mask for the nebulizer was lying on the nightstand, and it was not covered.
Observation on 01/31/2023 at 9:39 a.m., the concentrator filter was still visibly dusty. The nebulizer mask was lying on the nightstand without a cover.
Observation on 02/01/2023 at 9:44 a.m., the concentrator filter was visibly dusty, and the mask to the nebulizer was on the nightstand, lying out in the open.
Review of the admission Record for R#80, updated in the EMR revealed located under the Profile tab. The admission Record indicated the resident was admitted with diagnoses including acute respiratory failure with hypoxia (Absence of oxygen in the tissues), and COPD.
Review of the EMR under the Orders tab revealed physician orders dated 12/19/2022 Ipratropium- Albuterol Solution 0.5-2.5 (3) MG (milligrams)/3ML (milliliters) -1 vial inhale orally every 4 hours as needed for SOB (shortness of breath). Further review of the physician's orders revealed no oxygen order.
Interview on 02/01/2023 at 10:14 a.m., LPN7 stated that the filter should be cleaned or changed, and it should not be dusty. LPN7 added that the mask for the nebulizer machine should be stored in a bag when it is not in use.
Interview on 02/01/2023 at 10:23 a.m., the DON was shown the filter on the oxygen concentrator. The DON then took it off and washed it, saying that the filters should be clean and not dusty. When asked about the nebulizer, the DON stated that the mask should be placed in a bag when it was not in use.
Interview on 02/01/2023 at 11:17 a.m., the Medical Director was asked about an order for oxygen. The Medical Director stated, There should be an order for oxygen.
Review of the facility policy, Respiratory System Management Standard dated 08/2021. revealed, Purpose To provide oxygen support when indicated via appropriate delivery device to achieve or maintain adequate oxygenation to the respiratory compromised resident. Check the physician's orders in the resident's clinical record.
Review of the facility policy titled Oxygen Concentrators: In-House Maintenance dated 12/30/2022 revealed, Cleaning the Cabinet Filter. Risk of Damage. To avoid damage to the internal components of the unit: Do not operate the concentrator without the filter installed or with a dirty filter. 1. Remove the filter and clean as needed 1. Environmental conditions that may require more frequent inspection and cleaning of the filter include, but are not limited to: high dust, air pollutants, etc. 2. Clean cabinet filter with a vacuum cleaner or wash with a mild liquid dish detergent and water. Rinse thoroughly. 3. Thoroughly dry the filter and inspect for fraying, crumbling, tears and holes. Replace filter if any damage is found.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0841
(Tag F0841)
Could have caused harm · This affected multiple residents
Based on observation, interview, record review, and review of facility contracts, the facility failed to ensure the Medical Director was involved in administrative decisions, including recommending, d...
Read full inspector narrative →
Based on observation, interview, record review, and review of facility contracts, the facility failed to ensure the Medical Director was involved in administrative decisions, including recommending, developing and approving facility policies related to pneumococcal vaccination and emergency tracheostomy care. This failure had the potential to contribute to ongoing deficient practice for emergency tracheostomy care for two (Resident (R) 63 and R7) residents with tracheostomies and four (R34, R61, R79, and R14) of five residents reviewed for pneumococcal vaccination.
Findings include:
Review of the facility's policy dated 11/16/2017 Medical Director Agreement, provided on paper, revealed, Duties of Medical Director: . Assist in development of a medical-nursing plan of care for each resident . (and) Assist in the development and implementation of resident care policies.
1. The facility was cited with deficient practice at F695: Respiratory Care related to non-specific tracheostomy orders, lack of emergency supplies at the bedside, and inconsistent staff knowledge regarding emergency procedures in the event the tracheostomy tube (trach) became dislodged.
Interview on 02/01/2023 at 11:19 a.m. with the Medical Director, revealed his understanding is the staff should call 911. I'm not sure what kind of training the nurses have gone through for that. The Medical Director stated he was not sure whether the trach order should specify whether it was cuffed or not. He further revealed that he had no idea what to expect the nurse to do. Probably just continue with what orders they came with from the hospital, that's just common sense. The Medical Director stated he had not provided the staff with any education regarding emergency trach care, as he was not a pulmonologist, and stated he had not reviewed the facility's emergency trach care policy or discussed trach care in the Quality Assurance meetings. The Medical Director added, I would prefer not to have trach patients here. The Medical Director revealed that potential outcome of not having emergency trach supplies at the bedside included that a resident could experience respiratory distress.
Review of the facility's 2020 SMS [Specialized Medical Services] Tracheostomy Tube Emergency Care policy included directions to remove the tube and replace it with a new one and, Trach Tube Replacement - If the blockage can't be removed then the entire tube should be removed.
Interview on 02/02/23 at 3:13 PM with the Regional [NAME] President of Operations (RVPO) and Regional Nurse Consultant, the RVPO stated the Medical Director would probably not be involved in staff education on tracheostomy care and emergency trach care policies, as the trach vendor would be responsible for setting up the trach, educating the staff, and assisting with supplies, including the emergency kit. The Regional Nurse Consultant added the SMS Emergency Tracheostomy Care policy was the education SMS had been providing to nursing staff.
2. The facility was cited with deficient practice at F883: Immunizations, related to a failure to update the pneumococcal vaccination policy and procedure with the newest immunization requirements and a failure to ensure residents received one or both appropriate doses of the pneumococcal vaccine series or had documented refusals. Cross-reference F883.
In a telephone interview on 02/02/2023 at 1:58 p.m. with the Medical Director stated he had not been involved in the creation/revision of the pneumococcal vaccination policy nor had he reviewed it. The Medical Director stated he had not provided education to the facility staff on the updated CDC pneumococcal vaccination guidance.
In a concurrent interview on 02/02/2023 at 3:13 p.m. with the RVPO and Regional Nurse Consultant, the RVPO stated the Medical Director signed off on all facility policies every year at an annual policy review Quality Assurance meeting. She stated he would assist with reviews and sign but would not necessarily be expected to update the policy with current CDC guidelines as these were only recommendations and not requirements.
CONCERN
(E)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0883
(Tag F0883)
Could have caused harm · This affected multiple residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews, record review, and review of the facility's policies, Age Summary and Average Age and Pneumococcal Va...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews, record review, and review of the facility's policies, Age Summary and Average Age and Pneumococcal Vaccine, the facility failed to ensure its Pneumococcal Vaccination policy reflected current recommendations/standards of practice. In addition, the facility failed to ensure that four of five residents (R) (#34, #61, #79, #14) reviewed for immunizations received the pneumococcal vaccination series or had documented refusals. These failures had the potential to increase the spread of pneumonia among unvaccinated residents.
Findings include:
Review of the facility's 02/02/2023 Age Summary and Average Age report, provided on paper, revealed there were 39 of 86 residents under age [AGE] in the facility.
Review of the facility's 2017 Pneumococcal Vaccine policy revealed, Prior to or upon admission, residents will be assessed for eligibility to receive the pneumococcal vaccine series (both 23-valent pneumococcal polysaccharide vaccine AND 13-valent pneumococcal conjugate vaccine for residents [older than] 65), and when indicated, will be offered the vaccine series within thirty (30) days of admission to the facility unless medically contraindicated or the resident has already been vaccinated. A review of the policy revealed no evidence it was updated/revised in response to the current recommendations.
1. Review of the Centers for Disease Control and Prevention (CDC) 01/24/2022 Pneumococcal Vaccination: Summary of Who and When to Vaccinate, accessed on 01/30/2023 at https://www.cdc.gov/vaccines/vpd/pneumo/hcp/who-when-to-vaccinate.html revealed, Adults 65 Years or Older: . For adults 65 years or older who have not previously received any pneumococcal vaccine, CDC recommends you give 1 dose of PCV (pneumococcal conjugate vaccine) 15 or PCV20. If PCV15 is used, this should be followed by a dose of PPSV (pneumococcal polysaccharide vaccine) 23 at least one year later . If PCV20 is used, a dose of PPSV23 is NOT indicated. For adults 65 years or older who have only received PPSV23, CDC recommends you may give 1 dose of PCV15 or PCV20. The PCV15 or PCV20 dose should be administered at least one 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, CDC recommends you give PPSV23 as previously recommended.
Interview on 02/02/2023 at 8:24 a.m. with the Infection Preventionist (IP), she confirmed the facility's policy had not been updated to reflect the revised CDC guidance to offer PCV15 and PCV20, as this was not a requirement but a recommendation.
Interview on 02/02/2023 at 11:10 a.m. with the Regional Nurse Consultant stated, We are still using the [PCV] 13 and [PPSV] 23. She was not aware of the revised recommendations and that the policy still needed to be updated. The Regional Nurse Consultant added that she had clarified with the facility's pharmacy and was told CDC is now recommending PCV15 and PCV20; however, this was just a recommendation, and it was fine to continue to use PCV13 and PPSV23 only.
In a telephone interview on 02/02/2023 at 1:58 p.m., the Medical Director stated he was aware of the updated guidelines for pneumococcal vaccination and that the facility should have updated the policy and should be offering PCV15 and PCV20.
In a concurrent interview with the Regional [NAME] President of Operations (RVPO) and Regional Nurse Consultant on 02/02/2023 at 3:13 p.m., the RVPO stated she had clarified with the pharmacy that the PCV15 and PCV20 are the doses recommended by the CDC, but they were not required, only recommended.
2. a. Review of R#34's Immunizations tab in the electronic medical record (EMR). revealed no information regarding the offering or providing the pneumococcal vaccination series or whether the vaccine had already been received. Review of R34's undated Client Information sheet, provided on paper by the IP, revealed no information regarding the pneumococcal vaccination series. According to the facility's 02/02/2023 Age Summary and Average Age report, R#34 was over age [AGE].
b. Review of R#61's Immunizations tab in the EMR revealed no information regarding the offering or providing the pneumococcal vaccination series or whether the vaccine had already been received. A review of R#61's undated Client Information sheet, provided on paper by the IP, revealed that R#61 received a dose of PPSV23 on 11/28/2012; however, no additional information was provided. According to the facility's 02/02/2023 Age Summary and Average Age report, R#61 was over age [AGE].
c. Review of R#79's Immunizations tab in the EMR revealed no information regarding the offering or providing the pneumococcal vaccination series or whether the vaccine had already been received. A review of R79's undated Client Information sheet, provided on paper by the IP, revealed that This client has no immunizations associated with it. According to the facility's 02/02/2023 Age Summary and Average Age report, R79 was over age [AGE].
d. Review of R#14's Immunizations tab in the EMR revealed no information regarding the offering or providing the pneumococcal vaccination series or whether the vaccine had already been received. A review of R14's undated Client Information sheet, provided on paper by the IP, revealed no information regarding the pneumococcal vaccination series. Per the facility's 02/02/2023 Age Summary and Average Age report, R#14 was over age [AGE].
Interview on 02/02/2023 at 4:34 p.m. with the IP, she stated she did not have any additional immunization information other than what was provided and referenced above.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0727
(Tag F0727)
Could have caused harm · This affected most or all residents
Based on staff interviews, record review, and a review of the facility policy titled, Clinical Staffing Standard, the facility failed to ensure the required Registered Nurse (RN) coverage of at least ...
Read full inspector narrative →
Based on staff interviews, record review, and a review of the facility policy titled, Clinical Staffing Standard, the facility failed to ensure the required Registered Nurse (RN) coverage of at least eight consecutive hours per day, seven days per week. There was no RN scheduled, or the Director of Nursing (DON) repeatedly served as the RN over a three-month period, although the facility census, which was higher than 60 residents per day, prohibited the DON from also serving as a charge nurse. This deficient practice had the potential to affect all 87 residents and allow them to go without having their clinical needs met by an RN.
Findings include:
Review of the policy titled Clinical Staffing Standard, dated 08/2021, revealed, Standard To provide nursing services regarding licensed nurses and certified nursing assistants 24 hours daily in order to meet the care and service needs of the residents that reside in the facility. Procedure. RN staffing will follow state, federal regulations.
Review of the Facility Assessment, dated 11/17/2022, revealed an average daily census of 86.5.
Review of an untitled staff schedule record revealed that there was either no RN scheduled or the DON was scheduled for RN coverage on the following days:
Twelve days were not covered during 01/2023: 01/01/2023, 01/07/2023, 01/08/2023, 01/19/2023, 01/20/2023, 01/23/2023, 01/24/2023, 01/25/2023, 01/26/2023, 01/27/2023, 01/30/2023, and 01/31/2023.
One day was not covered during 12/2022: 12/25/2022.
Two days were not covered during 10/2022: 10/02/2022 and 10/04/2022.
Interview on 02/02/2023 at 8:02 a.m. with the Director of Nursing (DON), stated that the Infection Preventionist (IP) and Licensed Practical Nurse (LPN) 3 make the schedules. The DON stated, I started last Tuesday, I have not had the chance to check the schedule. I know the DON should not be scheduled as the RN, but in a pinch, you do what you have to do.
Interview on 02/02/2023 at 10:30 a.m. with the IP and LPN3 were interviewed about the RN coverage on the schedule. The IP stated, We use the DON and sometimes the Administrator as the DON coverage. When informed that the regulation indicates the DON cannot serve as the RN when the census is higher than 60, the IP stated, I was not aware of that.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Deficiency F0802
(Tag F0802)
Could have caused harm · This affected most or all residents
Based on observation, interview, review of the dietary staffing schedules, and review of facility policy, the facility failed to have sufficient dietary staff to ensure food was stored, prepared, and ...
Read full inspector narrative →
Based on observation, interview, review of the dietary staffing schedules, and review of facility policy, the facility failed to have sufficient dietary staff to ensure food was stored, prepared, and served in a sanitary and safe manner. Routine cleaning schedules were not followed due to a lack of sufficient staff to perform these duties, and food preparation surfaces, equipment, dishes, and service/cooking ware were found not to be clean and/or in good repair. Foods were not dated/labeled and/or sealed, and equipment, such as scoops, was not stored in a manner to prevent contamination. The lack of staff had the potential to affect 85 of 87 residents who consumed food from the kitchen.
Findings include:
Review of the facility's undated policy titled, Cleaning and sanitizing dietary areas and equipment specified, All kitchen areas and equipment shall be maintained in a sanitary manner and be free of buildup of food, grease or other soil. The facility will provide sanitary food service that meets state and federal regulations.
During an observation and initial kitchen walk through on 1/30/2023 beginning at 9:35 a.m., the kitchen was found to have surfaces that were covered with accumulated dried food, rust, and/or grease. Equipment, such as the can opener, mixer, oven, deep fat fryer, and microwave, was not clean. Dishware that was stored and ready for use was unclean and contained residue and/or was wet with moisture. Opened food supplies were not sealed, labeled, and/or dated. Handwashing supplies (paper towels) were not stored in a manner to prevent contamination.
Review of the 1/2023 monthly dietary staffing schedule revealed two employees or less were scheduled to work in the kitchen on the first shift for 27 of 31 days. Two employees or less were scheduled to work in the kitchen on the second shift for 29 of 31 days during 1/2023.
Review of the kitchen's 1/2023 cleaning schedule, which was posted in the kitchen during the initial walk through on 1/30/2023, revealed the dietary staff were not completing the daily cleaning schedules.
During interview on 1/30/2023 at 3:15 p.m., with the Dietary Manager (DM) revealed that all the kitchen areas and equipment should be kept clean and foods should be labeled, dated, and completely closed when stored. The DM stated that the dietary department was understaffed, and it was hard for dietary staff to get everything done, including preparing resident meals and completing the kitchen cleaning schedules when there were not enough staff. The DM confirmed that the dietary staff were not completing cleaning schedules because there were not enough staff to complete the daily cleaning assignments.
During an additional interview on 1/31/2023 at 2:51 p.m., with the DM revealed there were currently three vacant positions in the dietary department. The DM explained that the kitchen is budgeted to schedule two employees to work the first shift and two employees to work the second shift. The DM further stated that if she could schedule three employees to work in the kitchen on first shift and three employees to work in the kitchen on second shift, that would make staffing in the kitchen sufficient so that staff had time to complete the kitchen daily clean schedules, as well as prepare and serve resident meals as scheduled.
During an interview on 2/02/2023 at 8:10 a.m., Cook1 stated that she had been working double shifts in the kitchen for a while and It is rough. [NAME] 1 stated that when there are only two dietary employees working in the kitchen each shift, they were not able to complete the daily cleaning schedule. Cook1 stated, that the kitchen needs more help to be able get everything completed.
During an interview on 2/02/2023 at 11:45 a.m., the facility's Registered Dietitian (RD) consultant revealed the dietary staff should be keeping the kitchen clean per the cleaning schedules. The RD further stated that she was aware the dietary department was having issues with staffing shortages which made it difficult for the staff to get everything completed.
During an interview on 2/02/2023 at 2:55 p.m., the facility's Regional [NAME] President indicated the facility needed to take a close look at the staffing in the kitchen.
Cross-reference F812.
CONCERN
(F)
Potential for Harm - no one hurt, but risky conditions existed
Food Safety
(Tag F0812)
Could have caused harm · This affected most or all residents
Based on observation, interview, record review, and review of facility policy, the facility failed to store, prepare, and serve foods in a sanitary and safe manner. Handwashing supplies were not store...
Read full inspector narrative →
Based on observation, interview, record review, and review of facility policy, the facility failed to store, prepare, and serve foods in a sanitary and safe manner. Handwashing supplies were not stored in a manner which prevented contamination. Food preparations surfaces, equipment, dishes, and service/cooking ware were not clean and/or in good repair. Foods were not dated/labeled and/or sealed. Scoops were stored in dried food products. Routine cleaning schedules were not followed. Cold food temperatures were not accurately taken to prevent the spread of food-borne illness. This had the potential to affect 85 of 87 residents that received an oral diet.
Findings include:
Review of the facility's undated policy titled, Cleaning and sanitizing dietary areas and equipment, specified, All kitchen areas and equipment shall be maintained in a sanitary manner and be free of buildup of food, grease or other soil. The facility will provide sanitary food service that meets state and federal regulations.
1. Observation during the initial kitchen walk through on 1/30/2023 beginning at 9:35 a.m., revealed the following:
a. Upon entering the kitchen, two dietary employees were observed working in the kitchen. The employees stated the Dietary Manager (DM) was not present, but she would be at the facility later in the day. The paper towel dispenser at the kitchen hand sink was empty and a stack of loose paper towels was placed on the eye wash station next to the hand sink.
b. A food preparation table's drawer was unclean with accumulated dried food and rust. Food preparation utensils and food service utensils including spatulas, large serving spoons and measured serving ladles were stored inside this unclean drawer. The lower shelf of the food preparation table had rust on it that could be wiped away with a paper towel. Four of four food preparation pans that were stored on this table's lower shelf were unclean with a greasy residue.
c. A large container of lids stored on the shelf of the food preparation table was unclean with accumulated food debris and a partial eggshell. Five metal lids stored inside of this container had dried food spills on them.
d. The kitchen's microwave oven had grease residue on its top and dried food splatters on its inner cooking compartment.
e. The kitchen's large manual can opener was unclean, with a black substance on its blade and base.
f. The kitchen's large mixer, which was covered and ready for use, was unclean, with dried food splatters.
g. A metal shelf that was over the kitchen's two compartment sink was unclean with rust build up. Three of three food preparation pans stored on this shelf were very wet.
h. The two kitchen ovens were unclean with accumulated burned food spills on the inside of their doors and metal cooking racks.
i. One exterior side of kitchen's deep fat fryer was unclean with a heavy accumulation of dried food and grease.
j. The kitchen floor was unclean with blackened areas and loose food debris. The floor between the kitchen's deep fat fryer and stove was unclean with accumulated grease and food spills.
k. The metal shelf under the kitchen's steam table was unclean with accumulated loose food debris and rusted areas.
l. Eight of 12 clear plastic cups that were stored and ready for use were unclean with a brown residue, that appeared to be dried tea, which could be wiped away with a paper towel.
m. Fifteen of 15 insulated plate covers that were stacked tightly together and ready for use on kitchen's tray line area had accumulated moisture on the interior portion of their lids.
n. One of the kitchen's large upright freezers had an accumulation of rust on one of its interior corners. Observations of foods stored inside this freezer revealed two bags of a unidentified breaded food products that were unlabeled, undated and not completely closed. Additionally, stored in this freezer was a large sealed large bag of what appeared to be chopped ham that was not labeled or dated.
o. One of the kitchen reach-in refrigerators had a container that had approximately 15 hardboiled eggs in it that was unlabeled and undated.
p. The kitchen's outside walk in freezer had a bag of an unlabeled and undated food product that was on the freezer's floor. Additionally, one 15.75 pound box of cheese omelets, one 20 pound box of cookie dough, and a large bag of an unlabeled and undated frozen food product were stored partially opened in this freezer.
q. In the kitchen's dry storage area, there were four large storage bins that had sugar, flour, corn meal and rice stored inside of them. Further observations revealed each bin also had a large scoop stored inside and the handle of each scoop was in direct contact with the food product stored inside of the bin. Also, observed in the kitchen's dry storage area were a 4.5-pound container of dried seasoned salt and an 80 ounce bag of dry grits that were stored partially opened.
Review of the kitchen's 1/2023 cleaning schedule, that was posted in the kitchen during the initial walk through on 1/30/23, revealed the dietary staff were not completing the daily cleaning schedules.
On 1/30/2023 at 3:05 p.m. the DM, who was onsite, was shown and informed of the concerns that were observed during the initial kitchen walk through that was conducted during the morning of 1/30/2023.
During interview on 1/30/2023 at 3:15 p.m., the DM revealed all the kitchen areas and equipment should be kept clean and foods should be labeled, dated, and completely closed when stored. The DM stated that the dietary department was understaffed, and it was hard for dietary staff to get everything done including preparing resident meals and completing the kitchen cleaning schedules when there was not enough staff. The DM confirmed that the dietary staff were not completing cleaning schedules because there were not enough staff to complete the daily cleaning assignments.
During interview on 2/02/2023 at 8:10 a.m., Cook1 stated that she had been working double shifts in the kitchen for a while and, It is rough. Cook1 explained when there are only two dietary employees working in the kitchen each shift, they are not able to complete the daily cleaning schedule. Cook1 stated the kitchen needs more help to be able to get everything completed.
Interview on 2/02/2023 at 11:45 a.m. with the facility's Registered Dietitian (RD) consultant revealed the dietary staff should be keeping the kitchen clean per the cleaning schedules. The RD further stated that she was aware the dietary department was having issues with staffing shortages which made it difficult for the staff to get everything completed.
2. Observation on 1/31/23 at 11:48 a.m. revealed the dietary staff were in the process of setting up the kitchen's lunch tray line for the resident lunch meal service. Observation revealed Dietary Aide (DA)1 appeared to be utilizing a thermometer to monitor the internal temperature of a carton of milk that was in a container of ice with other cold beverages and desserts. Upon closer observation, DA1 was observed to have the thermometer's probe inserted into the ice that was directly next to a carton of milk (rather than measuring the temperature of the milk, itself.). Interview with DA1 at this time revealed placing the thermometer in the ice (rather than in the actual food/beverages) was her usual way of monitoring the temperatures of the cold items being served from the tray line.
Cross Reference F802.
MINOR
(C)
Minor Issue - procedural, no safety impact
Deficiency F0888
(Tag F0888)
Minor procedural issue · This affected most or all residents
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews, record review, and review of facility policy titled, COVID-19 Data Tracker, the facility failed to me...
Read full inspector narrative →
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on staff interviews, record review, and review of facility policy titled, COVID-19 Data Tracker, the facility failed to meet the requirement for 100% compliance, which requires that all staff working in the facility have received at least one dose of a single-dose vaccine, or all doses of a multiple-dose COVID-19 vaccine series, or have been granted a qualifying exemption, or are identified as having a temporary delay as recommended by the Centers for Disease Control Prevention (CDC). Eight-nine of 90 current staff were either fully vaccinated against COVID-19 vaccination or had been granted an exemption or delay in accordance with CDC guidelines, for a compliance rate of 98.9%. One staff member, Licensed Practical Nurse (LPN) 6, was identified as having a medical exemption; however, there was no valid contraindication for this exemption, In addition, the facility failed to ensure nine of ten unvaccinated and exempt staff were tested for COVID-19 twice weekly per the facility policy.
Findings include:
Review of the Centers for Disease Control and Prevention (CDC) COVID-19 Data Tracker website, accessed at https://covid.cdc.gov/covid-data-tracker/#datatracker-home on [DATE], revealed the facility's community transmission rate was high.
Review of the facility's undated Employee Covid 19 [sic] Vaccine Tracking Form, provided on paper by the Infection Preventionist (IP), revealed 88.9% of facility staff were fully vaccinated. There were ten unvaccinated staff out of a total 90 employees. Two of the ten unvaccinated staff had medical exemptions, and the other eight had religious exemptions.
1. Review of the CDC website, Overview of COVID-19 Vaccines, accessed on 02/01/2023 at https://www.cdc.gov/coronavirus/2019-ncov/vaccines/different-vaccines/overview-COVID-19-vaccines.html, revealed, The following are not included in the vaccines: . No food proteins such as eggs or egg products, gluten, peanuts, tree nuts, nut products, or any nut byproducts. (COVID-19 vaccines are not manufactured in facilities that produce food products).
Review of Licensed Practical Nurse (LPN) 6's 11/17/2021 Request for Information from Medical Provider, provided on paper by the Infection Preventionist (IP), revealed, [LPN6] is allergic to eggs, can't take flu, or COVID vaccination . Anaphylactic shock when exposed to eggs or egg components . Test patient routinely as per protocol for COVID-19. She is very allergic to eggs with a history of severe reactions in the past . Avoid COVID vax at this time d/t [due to] egg reaction/allergy. The request for a medical exemption from the COVID vaccine was signed by LPN6's Nurse Practitioner.
Interview on 02/01/2023 at 11:17 a.m. with the Medical Director, he stated, The COVID vaccine does not have egg in it to my knowledge . an egg allergy would not be an appropriate reason for a medical exemption.
Interview on 02/02/2023 at 8:33 a.m., the IP stated that the corporate office was responsible for approving or denying medical exemptions, and she had nothing to do with them.
Review of the facility's undated Mandatory COVID-19 Vaccination Policy revealed, Employees may request an exception from this mandatory vaccination policy if the vaccine is medically contraindicated for them or medical necessity requires a delay in vaccination . All such requests should be submitted to the administrator at the facility and then forwarded to the [NAME] President of Human Resources. These forms will be handled in accordance with applicable laws and regulations.
2. Review of the facility's undated Mandatory COVID-19 Vaccination Policy revealed, Any person being granted a medical or religious accommodation will be required to obtain and provide a copy of 2 negative COVID-19 tests each week at least 3 days apart. Copies of these test results must be provided to the administrator and will be maintained in a separate medical file for each person.
Review of the facility's January 2023 County Positivity Testing/Employees, employee's requests for medical or religious exemption, and work schedules, provided on paper by the IP, revealed the following:
a. Certified Nurse Aide (CNA) 6 received an approved religious exemption on 11/20/2021 and had worked at the facility throughout January 2023. She was not tested for COVID-19 twice weekly, with testing documented on 01/27/2023, 01/23/2023, 01/09/2023, 01/05/2023, and 01/02/2023.
b. LPN6 was approved for a medical exemption on 11/17/2021 and worked at the facility throughout January 2023 (Refer to Example #1.) She was not tested twice weekly, with testing for COVID-19 documented on 01/17/2023.
c. Restorative Aide (RA) 1 received an approved religious exemption on 01/28/2022 and worked in the facility throughout January 2023. She was not tested twice weekly, with testing for COVID-19 documented on 01/16/2023, 01/12/2023, 01/09/2023, 01/05/2023, and 01/02/2023.
d. LPN8 received an approved religious exemption on 09/19/2022 and worked at the facility throughout January 2023. There was no record of COVID-19 testing for LPN8.
e. CNA8 received an approved religious exemption on 06/06/2022 and worked at the facility throughout January 2023. She was not tested twice weekly for COVID-19, with testing documented on 01/12/2023 and 01/24/2023.
f. CNA7 received an approved religious exemption on 01/21/2022 and worked in the facility throughout January 2023. She was not tested for COVID-19 twice weekly, with testing documented on 01/12/2023.
g. Physical Therapist (PT) 1 received an approved religious exemption on 12/14/2022 and worked on 01/01/2023, 01/08/2023, 01/22/2023, and 01/29/2023. There was no record of COVID-19 testing for PT1.
h. The Maintenance Director (MD) received an approved religious exemption on 02/11/2022 and worked at the facility throughout January 2023. He was not tested twice weekly for COVID-19, with testing documented on 01/27/2023, 01/20/2023, and 01/05/2023.
i. Dietary Aide (DA) 1 received an approved religious exemption on 01/09/2021 and worked on 01/12/2023, 01/14/2023, 01/15/2023, 01/19/2023, 01/24/2023, and 01/26/2023. There was no record of COVID-19 testing for DA1.
In an interview on 02/02/2023 at 8:24 a.m., the IP stated that the protocol for unvaccinated staff was to be tested twice weekly. She stated she had records of twice weekly testing for all exempt employees, and was asked to provide the records at this time. On 02/02/2023 at 1:02 p.m. and at 4:34 p.m., additional records of testing for unvaccinated staff were again requested, but not provided. No additional records were provided prior to the survey exit.