F 0644
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Coordinate assessments with the pre-admission screening and resident review program; and referring for
services as needed.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interviews and record reviews, the facility failed to ensure individuals with mental health disorders were
provided an accurate Preadmission Screening and Resident Review Level 1(PASRR 1) Screening for 3 of
12 residents reviewed for PASRR (Residents #12, 23, and #45).
The facility failed to ensure Residents #12, #23, and #45 had accurate PASRR Level 1 Screenings
indicating diagnoses of mental illness.
This failure could place residents at risk of not receiving needed assessments (PASRR Evaluation),
individualized care, and specialized services to meet their needs.
Findings included:
Resident #12
Record review of Resident 12's PASRR Level 1 Screening completed on 03/27/2023 indicated in section
C0100 this resident did not have evidence of having a mental illness.
Record review of an undated face sheet indicated Resident #12 was an [AGE] year-old female who
admitted to the facility on [DATE] with diagnoses including major depressive disorder.
Record review of the Comprehensive (admission) MDS assessment dated [DATE] indicated Resident #12
had a BIMS score of 0 (zero), indicating severely impaired cognition. The MDS section for PASRR indicated
Resident #12 did not have a serious mental illness. The MDS section I, Active Diagnoses, indicated
Resident #12 had a diagnosis of major depressive disorder.
Record review of the physician's orders dated 09/25/23-10/25/2023 indicated an order dated 03/26/2023 for
Resident #12 to receive venlafaxine (a psychotropic medication) for treatment of major depressive disorder.
Resident #23
Record review of Resident 23's PASRR Level 1 Screening completed on 04/17/2023 indicated in section
C0100 this resident did not have evidence of having a mental illness.
Record review of an undated face sheet indicated Resident #23 was a [AGE] year-old male who admitted
to the facility on [DATE] with diagnoses including schizophrenia and major depressive disorder.
(continued on next page)
Any deficiency statement ending with an asterisk (*) denotes a deficiency which the institution may be excused from correcting providing it is determined that other
safeguards provide sufficient protection to the patients. (See instructions.) Except for nursing homes, the findings stated above are disclosable 90 days following the
date of survey whether or not a plan of correction is provided. For nursing homes, the above findings and plans of correction are disclosable 14 days following the date
these documents are made available to the facility. If deficiencies are cited, an approved plan of correction is requisite to continued program participation.
LABORATORY DIRECTOR'S OR PROVIDER/SUPPLIER
REPRESENTATIVE'S SIGNATURE
TITLE
(X6) DATE
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Facility ID:
If continuation sheet
Page 1 of 23
Event ID:
455834
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0644
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Record review of the Comprehensive (admission) MDS assessment dated [DATE] indicated, Resident #23
had a BIMS score of 5 (five) indicating severely impaired cognition. The MDS section for PASRR indicated
Resident #23 did not have a serious mental illness. The MDS section, Psychiatric/Mood Disorder, indicated
Resident #23 to have a diagnosis of schizophrenia.
Record review of physician orders dated 09/25/2023-10/25/2023 indicated orders dated 05/01/2023 for
resident #23 to receive Seroquel (psychotropic drug) 3 times a day and Zyprexa (psychotropic drug)1 time
daily for treatment of schizophrenia.
Record review of the Comprehensive (admission) MDS assessment dated [DATE] indicated Resident #23
was receiving antipsychotic medications on a routine basis.
Resident #45
Record review of Resident 45's PASRR Level 1 Screening completed on 03/27/2023 indicated in section
C0100 this resident did not have evidence of having a mental illness.
Record review of an undated face sheet indicated Resident #45 was a [AGE] year-old male who admitted
to the facility on [DATE] with diagnoses including schizoaffective disorder, bipolar disorder, and PTSD.
Record review of the Comprehensive (admission) MDS assessment dated [DATE] indicated Resident #45
had a BIMS score of 15(indicating his cognition to be intact) and dependent on staff for ADLs due to a
diagnosis of quadriplegia (paralysis of all four limbs). The MDS section for PASRR indicated Resident #12
did not have a serious mental illness. The MDS section I, Active Diagnoses, indicated Resident #12 had
diagnoses of depression, bipolar disorder, psychotic disorder, schizophrenia, and PTSD. The Medications
section of the MDS indicated Resident #45 was receiving antipsychotic medications on a routine basis.
Record review of the physician's orders dated 09/25/23-10/25/2023 indicated orders for Resident #45 to
receive Depakote, Seroquel, and Zyprexa (medications used to treat schizophrenia and bipolar disease) on
a routine basis.
Record review of Resident #45's care plan dated 03/29/2023 indicated resident required drugs for the
treatment of schizoaffective disorder and interventions were aimed at reducing the risk of drug-related
complications.
During an interview with the MDS Nurse on 10/24/2023 at 9:45 AM, she said she was responsible for tasks
related to PASRR and MDS processes. She said she was hired in May of 2023 and was new to the PASRR
and MDS process. She said at the time of Residents #'s 12, 23, and 45, she thought the PASRRs
completed by the discharging facility were incorrect and said she notified the local authority of her
concerns. She said the local authority told her she would follow up on her concerns. She said she did not
do anything else because she did not know she was supposed to. The MDS Nurse said she understood the
importance of PASRR Level 1 Screenings being accurate because the facility needed to make sure eligible
residents were getting the correct resources.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 2 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0645
PASARR screening for Mental disorders or Intellectual Disabilities
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to ensure the Pre-admission Screening and Resident Review
(PASRR) Level I assessment was completed prior to admission. For 1 of 12 residents (Residents #60)
reviewed for PASRR Level I screenings.
Residents Affected - Few
The facility failed to have a level 1 PASRR assessment for Resident #60 available/documented.
This failure could place residents who had a mental illness at risk of not receiving a needed assessment
(PASRR Evaluation), individualized care, or specialized services to meet their needs.
Findings included:
Record review of Resident #60's face sheet, date 09/20/23, indicated she was an [AGE] year-old female,
admitted to the facility on [DATE]. Resident #60 diagnoses included non-Alzheimer's dementia unspecified
severity, with other behavioral disturbance on admission, psychotic disorder with delusions due to known
physiological condition, major depressive disorder, recurrent severe without psychotic features, anxiety
disorder, and Parkinson's disease.
Record review of Resident #60's admission MDS assessment, dated 06/07/23, indicated section A1500
was marked 0 or no. This indicated the resident was not currently considered by the state level II PASRR
process to have serious mental illness and/or intellectual disability or a related condition. Section A1510
was not marked for level II PASRR conditions. The assessment indicated she had a Brief Interview for
Mental Status (BIMS) score of 05, which indicated severe cognitive impairment.
Record review of Resident #60's electronic medical record a PASRR level 1 screening assessment was
unable to be identified or located.
During an interview on 10/25/23 at 1:16 PM, the MDS Coordinator said she was still working on the facility's
PASRR forms, and it was possible the PASRR forms had not been uploaded to the electronic record. She
said she would try to locate Resident 60's PASRR Level 1 assessment forms.
During an interview on 10/25/23 at 3:38, the MDS Coordinator said she was unable to locate
documentation on Resident #60's PASRR Level 1 Screening assessment forms. Resident #60 was
admitted to facility on 5/25/23 from another long-term care facility. Record review of the resident
Assessment and Care Screening (Nursing Home Comprehensive Item Set indicated on 06/07/23 section
A1500 assessment was completed as the most recent admission entry.
Record review of the facility's policy, specialized rehabilitative services, stated:
.Specialized services for MI [mental illness] or MR [mental retardation]
For a resident with MI or MR, the community will ensure that the individual receives the services necessary
to assist him or her in maintaining or achieving as much independence and self-determination as possible.
The preadmission screening and resident review (PASRR) indicates specialized services required by the
resident. The state is required to list those services in the report, as well as to provide or
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 3 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0645
arrange for the provision of the services.
Level of Harm - Minimal harm
or potential for actual harm
Even if the state determines that the resident does not require specialized services, the community is still
responsible for providing all services necessary to meet the resident's mental health or mental retardation
needs.
Residents Affected - Few
The community provides interventions that complement, reinforce, and are consistent with any specialized
services (as defined by the resident's PASRR)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 4 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0732
Post nurse staffing information every day.
Level of Harm - Potential for
minimal harm
Based on observation, interview, and record review, the facility failed to post the daily nurse staffing data at
the beginning of each shift in a prominent place, readily accessible to residents and visitors that included
the facility name; the total number of hours worked per shift by the registered nurses, the licensed
vocational nurses, and the certified nurse aides directly responsible for resident care for the facility for 2 of 3
days reviewed for staffing postings (10/22/23 - 10/23/23) and did not maintain the posted daily nurse
staffing data for a minimum of 18 months.
Residents Affected - Many
The facility did not post the required staffing with hours worked daily for the public and residents and did not
maintain the staffing for a minimum of 18 months.
This failure could place the census of 76 residents, families, and visitors at risk of not having the daily nurse
staffing data.
Findings include:
During a daily observation on 10/22/2023 to 10/23/2023 beginning at 9:30 a.m. each day, revealed no
staffing posting was posted in the lobby, halls to resident's rooms, or at the nurse station with total hours
worked for RNs, LVNs and CNAs.
During an interview on 10/22/2023 at 3:20 pm, LVN A said she did not know where the staffing posting was
located.
During an interview on 10/22/2023 at 3:25pm, ADON said the staffing posting should be posted on board in
front of the administrator's office. She said it was her responsibility because they currently were without a
staffing coordinator.
During an interview on 10/22/2023 at 3:30 PM., the Administrator said let me go and find the posting and
surveyor said I will go with you and to find they did not have anything posted for staffing. He said, they did
not have a staffing coordinator, let me get the DON to post the staffing , since it's her responsibility to make
sure this is posted.
During an observation of the posting dated 10/25/2023 the RN posting was incorrect due to the facility did
not have an RN for actual direct care staff. During an interview with the DON on 10/25/2023 at 3:45 pm,
she said she thought she could count herself as the RN.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 5 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0755
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Provide pharmaceutical services to meet the needs of each resident and employ or obtain the services of a
licensed pharmacist.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to ensure pharmaceutical services were provided to meet the
needs of 1 of 4 residents reviewed for pharmacy services. (Resident #127).
The facility failed to ensure pantoprazole granules DR for oral suspension were administered correctly to
Resident #127.
This failure could place residents at risk for not receiving the intended therapeutic benefit of their
medications or receiving them correctly as directed by manufacturer's directions.
Findings included:
Record review of Resident #127's face sheet, dated 10/22/2023, indicated she was a [AGE] year-old
female, admitted to the facility on [DATE]. She had diagnoses which included gastro-esophageal reflux
disease (acid indigestion), congestive heart failure, fractured femur, high blood pressure, dementia, and
anxiety.
Record review of Resident #127's admission progress notes, dated 10/03/2023, indicated she was alert
and oriented to herself only; she had a BIMS (Brief Interview for Mental Status) of 99 indicating she was
unable to complete the interview and was severely cognitively impaired; required assistance of 1 staff with
ADLs; frequently incontinent of bowel and bladder, but could use the bedside commode.
Record review of Resident 127's consolidated physician orders dated October 2023 indicated the resident
had an order entered on 10/12/2023 to start pantoprazole granules DR for suspension in packet, 40 mg.
orally with special instructions to mix with water or juice for her gastro-esophageal reflux disease.
Record review of Resident #127's MAR, dated 10/2023, indicated she received the pantoprazole granules
DR every day at 8:00 AM starting on 10/13/23 through 10/24/23. The MAR indicated the medication was to
be mixed with water or juice.
During an interview and observation on 10/25/23 at 8:45 AM MA C pulled up the MAR for Resident # 127
and the order indicated to give pantoprazole granules in water or juice. She said she would give the
resident a full glass of water (7 oz) indicating the plastic cups on her cart. She said she tried to get
residents to drink as much water as she can to keep them from getting dehydrated and getting UTIs. She
also had healthshakes on her cart where the first ingredient was nonfat milk. She said she only used water
with Resident # 127. MA C pulled the medication packet from the medication cart and the pharmacy label
indicated to give 1 pkt as directed and give by mouth daily. Another small label on the bottom of the
medication bag indicated Do not crush. Give with apple juice or applesauce. The label did not indicate any
specific amounts of applesauce or apple juice. MA C said she never used apple juice or applesauce and
indicated she had not noticed the additional label indicating to use apple juice.
During an interview on 10/25/23 at 9:05 AM the ADON was asked to pull up the physician orders in the
electronic record for viewing for Resident # 127. She said she entered the order for pantoprazole
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 6 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0755
Level of Harm - Minimal harm
or potential for actual harm
granules given by the NP on 10/12/23 to discontinue the pantoprazole tablet and to begin the pantoprazole
granules. She said the NP did not indicate how to prepare the suspension. She said she added give with
water or juice and she said any juice the resident preferred could be used and she would expect it to be
administered using 6-8 oz. She said she did not know the specific parameters regarding the administration
of the pantoprazole granules.
Residents Affected - Some
During an interview on 10/25/23 at 9:10 AM the DON said she was not aware pantoprazole suspension
granules had to be given in a specific way. She said new medication orders are reviewed every morning in
stand-up meeting. She said she tried to review resident charts and physician orders for accuracy weekly.
She did not indicate whether she had reviewed Resident # 127's physician orders for accuracy.
During an interview on 10/25/23 at 9:15 AM the RN Consultant had pulled the directives from the
manufacturer concerning the preparing of the pantoprazole suspension using only apple juice or
applesauce when administering the pantoprazole granules and said staff would be in-serviced regarding
the administration.
Review of the manufacturer's instructions on 10/25/2023 at Pfizer's website at
pfizermedicalinformation.com indicated the following:
Instructions for Use: PROTONIX (pantoprazole sodium) for delayed-release oral suspension .should only be
taken with applesauce or apple juice; should not be mixed in water or other liquids, or other foods; packet
should not be divided to make a smaller dose.
Taking PROTONIX for oral suspension with applesauce:
1. Open the packet of PROTONIX for oral suspension.
2. Sprinkle all of the granules in the packet on 1 teaspoon of applesauce.
3. Swallow the granules and applesauce within 10 minutes of putting the granules on the teaspoon of
applesauce.
4. Take sips of water to make sure the granules are washed down into the stomach. Take more sips of water
as needed.
Taking PROTONIX for oral suspension with apple juice:
1. Open the packet of PROTONIX for oral suspension.
2. Empty all of the granules in the packet into a small cup that contains 1 teaspoon of apple juice.
3. Stir the granules-apple juice mixture for 5 seconds. The granules will not break up.
4. Swallow the mixture right away.
5. To make sure that the entire dose is taken, add more apple juice to the cup, stir and swallow the apple
juice right away.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 7 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0755
6. Repeat step 5 if there are granules left in the cup .
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 8 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0757
Ensure each resident’s drug regimen must be free from unnecessary drugs.
Level of Harm - Immediate
jeopardy to resident health or
safety
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview, and record review the facility failed to ensure the drug regimen was free from unnecessary
medication for 1 of 5 (Resident #74) residents reviewed for unnecessary medications.
Residents Affected - Some
1. The facility failed to ensure Resident #74 did not receive a medication she was allergic to (ibuprofen)
ordered for a swollen right hand on 5/22/23.
2. The facility failed to ensure Resident #74 was not given medications she was allergic to as ordered
(ibuprofen 400 mg by mouth 4 times a day for 14 days). Resident #1 received ibuprofen from 05/22/23 to
07/23/23 (63 days).
3. The facility failed to ensure Resident #74's ibuprofen was discontinued after Resident #1 returned from
the hospital from an upper GI bleed. Resident #1 received scheduled ibuprofen on 07/26/23 through
07/27/23 (4 doses).
An Immediate Jeopardy (IJ) was identified on 10/20/23. While the IJ was removed on 10/21/23, the facility
remained out of compliance at a scope of pattern and a severity level of actual harm that is not immediate
threat due to the facility's need to evaluate the effectiveness of the corrective systems.
These failures could place residents at risk of harm or death related to receiving unnecessary medications.
Findings included:
Record review of Resident #74's face sheet, dated 10/20/23, indicated she was an [AGE] year-old female
who admitted to the facility on [DATE] with diagnoses including dementia (damage to or loss of nerve cells
in the brain that causes memory loss, confusion, the ability to think or make decisions), gastrointestinal
hemorrhage (bleeding in the digestive tract caused by a disease or condition) and gastro-esophageal reflux
disease (stomach acid repeatedly flows back into the tube connecting your mouth and stomach).
Record review of Resident #74's Care Plan dated 04/27/21 and last revised on 07/31/23 indicated she had
an allergy to Lisinopril and Pravastatin and interventions included do not administer allergen, make note on
chart of allergies and notify the physician if allergen is ordered. Resident #74's care plan did not address an
allergy to ibuprofen.
Record review of Resident #74's MDS dated [DATE] indicated she usually made herself understood and
sometimes understood others. Resident #74 had severely impaired cognition.
Record review of Resident #74's admission History and Physical dated 04/27/21by the Nurse Practitioner
indicated she had a past medical history of dementia, anemia (blood disorder in which the blood has a
reduced ability to carry oxygen due to a lower-than-normal number of red blood cells), gastro-esophageal
reflux disease and peptic ulcer disease (open sores that develop on the inside lining of your stomach and
the upper portion of your small intestine causing dark or black stool and vomiting). Resident #74 had an
allergy to lisinopril, and pravastatin. Resident #74's admission History and Physical did not list ibuprofen as
an allergy.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 9 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0757
Level of Harm - Immediate
jeopardy to resident health or
safety
Residents Affected - Some
Record review of hospital records dated 04/30/21 indicated Resident #74 had a fall and was sent to the
hospital. Records indicated Resident #74 had an allergy to ibuprofen, lisinopril, and pravastatin.
Record review of hospital records dated 08/28/21 indicated Resident #74 had a fall and was sent to the
hospital. Records indicated Resident #74 had an allergy to ibuprofen, lisinopril, and pravastatin.
Record review of a handwritten telephone order dated 05/22/23 indicated Resident #74 had an order to
receive ibuprofen 400 mg by mouth 4 times a day for 14 days. The telephone order was signed by LVN E.
Record review of Resident #74's physician's order dated 05/22/23 indicated she had an order for ibuprofen
400 mg by mouth 4 times a day. Resident #74's ibuprofen was discontinued on 07/31/23.
Record review of Resident #74's MAR for the month of May, June, and July of 2023 indicated she received
ibuprofen on the following dates:
*05/22 through 05/31 (10 days)
*06/01 through 06/30 (30 days)
*07/01 through 07/23 (23 days)
Record review of Resident #74's nursing progress notes dated 07/24/23 at 3:00 a.m. by LVN E, indicated at
2:50 a.m. she was called to the shower room. The resident had a black tarry bowel movement with blood.
LVN E notified the hospice nurse.
Record review of Resident #74's nursing progress notes dated 07/24/23 at 3:59 a.m. by LVN E, indicated
she was instructed by the hospice nurse to check the resident's blood pressure and to send her to the
hospital for possible gastrointestinal bleed if it was low. Resident's manual blood pressure was 98/54
(normal blood pressure 120/80). Resident was transported to the hospital.
Record review of Resident #74's nursing progress notes dated 07/26/23 at 10:22 a.m. by the ADON,
indicated she called the hospital, and informed the resident was admitted for a gastrointestinal bleed.
Record review of Resident #74 hospital records dated 07/26/23 indicated she had dark bloody stools and
was transferred to the hospital on [DATE]. She had an allergy to ibuprofen and a history of peptic ulcer
disease (an open sore that develops on the inside lining of your stomach and the upper portion of your
small intestine). She had a hemoglobin (a protein in blood that carries oxygen to the body) level of 6.0
(Normal range 12.0-16.0) and was transfused with 2 units (approximately 2 pints) of blood in the
emergency department. She was admitted to the intensive care unit (unit with specialized staff, equipment,
and standards that handles severe, potentially life-threatening cases) diagnosed with an upper
gastrointestinal bleed. She was transfused with 1 unit (approximately 1 pint) of blood in the intensive care
unit 07/25/23. She was discharged back to the nursing facility on 07/26/23.
Record review of Resident #74's MAR for July 2023 indicated she received ibuprofen on the following
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 10 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0757
dates:
Level of Harm - Immediate
jeopardy to resident health or
safety
*07/26 and 07/27 (2 days)
Record review of Resident #74's nursing progress notes dated 07/26/23 at 8:17 p.m. by RN G, indicated
she returned to the nursing facility and had dark blood in her brief upon arrival.
Residents Affected - Some
Record review of Resident #74's nursing progress notes dated 07/27/23 at 6:10 p.m. by RN G, indicated the
family notified her the resident had vomited. RN F observed a moderate amount of coffee ground emesis
and the family requested for the resident to be sent to the emergency room.
Record review of Resident #74's nursing progress notes dated 07/27/23 at 6:22 p.m. by RN G, indicated the
resident was transferred to the hospital.
Record review of Resident #74 hospital records dated 07/31/23 indicated she had vomited blood at the
nursing facility and was transferred to the emergency department on 07/27/23. She had an allergy to
ibuprofen and a history of peptic ulcer disease. She had a hemoglobin level of 9.8 (Normal range 12.0-16.0)
on arrival and trended to a hemoglobin level of 6.9. She received 2 units (approximately 2 pints) of blood
and was admitted . She was discharged to the nursing facility on 07/31/23.
Record review of Resident #74's allergy history indicated ibuprofen was added as an allergy on 08/01/23 by
the ADON.
Record review of Resident #74's census dated 10/21/23 indicated she was discharged from the facility on
08/16/23 to another nursing facility.
During an interview on 10/20/23 at 2:14 p.m., LVN E said she worked the 6:00 a.m.-2:00 p.m. shift and was
the charge nurse for Resident #74 when the ibuprofen was ordered on 05/22/23. LVN E said Resident #74
had a swollen wrist, and she notified the hospice nurse. LVN E said the hospice nurse came to the facility to
assess Resident #74 then notified the physician. LVN E said the hospice nurse hand wrote an order for
Resident #74 to take ibuprofen 4 times a day for 14 days. LVN E said she signed the hospice nurse's
handwritten order then entered it into Resident #74's electronic chart. LVN E said she did not enter the date
to discontinue the ibuprofen after 14 days. LVN E said Resident #74 received ibuprofen for almost 2 months
because she entered the incorrectly. LVN E said a resident taking ibuprofen with peptic ulcer disease is at
risk of bleeding. LVN E said Resident #74 had peptic ulcer disease and was taking ibuprofen when she was
sent to hospital for a gastrointestinal bleed. LVN E said she did not know Resident #74 had an allergy to
ibuprofen prior to going to the hospital.
During an interview on 10/20/23 at 2:23 p.m., the DON said the charge nurse was responsible for entering
physician's orders in a resident's chart and she was responsible they were entered in correctly. The DON
said Resident #74 had a swollen wrist and was ordered ibuprofen for 14 days. The DON said LVN E entered
the order in Resident #74's chart and she did not enter the date to discontinue the ibuprofen after 14 days.
The DON said she did not check Resident #74's chart to see if LVN E entered the order correctly. The DON
said Resident #74 received ibuprofen for almost 2 months. The DON said Resident #74 was sent to hospital
twice for a gastrointestinal bleed. The DON said the ibuprofen was discontinued and added as an allergy to
her electronic chart when Resident #74 returned from the hospital the second time . The DON said she did
not know Resident #74's past hospital records listed ibuprofen as an allergy. The DON said she did not
review Resident #74's hospital records because she assumed they were reviewed by the previous DON
before she was hired. The DON said a resident taking
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 11 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0757
Level of Harm - Immediate
jeopardy to resident health or
safety
ibuprofen with peptic ulcer disease is at risk of bleeding. The DON said Resident #74 had peptic ulcer
disease and was taking ibuprofen when she went to the hospital. The DON said she did not know Resident
#74 had an allergy to ibuprofen prior to going to the hospital and have since changed how they monitored
medications. The DON said a list of new medications ordered from the previous day is printed out and
reviewed during their daily clinical meeting for resident allergies and to ensure orders are entered
accurately.
Residents Affected - Some
Record review of the facility's Medication-Administration policy dated 08/2020 indicated, It is the policy of
this home that medication will be administered and documented as ordered by the physician and in
accordance with state regulations .
Record review of the facility's Physician Services policy dated 08/2020 indicated, .Procedure .8. Physician's
orders for treatment and medication shall be recorded in the medical record and shall be signed by the
attending physician. Such orders shall be in effect for the number of days specified by the physician .11.
The DON/Administrator will be responsible to monitor physician visits to assure that the resident is
receiving appropriate care and services .
The Administrator was notified on 10/20/23 at 6:38 p.m. that an Immediate Jeopardy situation was identified
due to the above failures. The Administrator was provided the Immediate Jeopardy template on 10/20/23 at
6:44 p.m.
The facility's Plan of Removal was accepted on 10/21/23 at 3:00 p.m. and included:
Resident Specific
o An allergy for ibuprofen was added into Resident #1's electronic medical record on 8/1/23 due to having
the GI bleed.
o Resident #1 no longer resides at the facility as Resident #1 was discharged on 8/16/2023.
o Medical Director notified of IJ on 10/20/2023 at 7:58 PM by Administrator.
o Notified Pharmacy Consultant of IJ on 10/20/2023 at 7:58 PM by Director of Nursing.
System Changes
o Audit of all medication orders for NSAID use and stop dates completed on 10/20/2023 for all residents by
Director of Nursing and Assistant Director of Nursing at 10:30 PM.
o Head to toe assessment completed for all residents on 10/20/2023 by Treatment Nurse/LVN at 11:50 PM.
o During stand up/clinical meeting DON and/or ADON to review new orders with stop dates if applicable to
ensure correct transcription into EMR.
Education
o Director of Nursing provided education to all staff on signs/symptoms of GI Bleeding. If signs and/or
symptoms of GI Bleeding are identified the staff member should report to charge nurse
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 12 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0757
Level of Harm - Immediate
jeopardy to resident health or
safety
immediately. Once notified the charge nurse should contact physician. All staff present in the facility were
educated on 10/20/2023. Staff not present for the education will receive education prior to their next shift.
o Director of Nursing provided education to nursing staff regarding Medication Administration of Long Term
NSAID's and Risks. All nursing staff present in the facility were educated on 10/20/2023. Staff not present
for the education will receive education prior to their next shift.
Residents Affected - Some
o Director of Nursing provided education to nursing staff regarding The 5 Rights of Medication
Administration. All nursing staff present in the facility were educated on 10/20/2023. Staff not present for the
education will receive education prior to their next shift.
o Administrator, Director of Nursing, and Assistant Director of Nursing in-serviced on 10/20/2023 at 9:43
PM by Regional Clinical Consultant in regard to Monitoring New Orders for Accurate Transcription into
EMR.
Monitoring
o Order obtained from Medical Director by Director of Nursing for every resident on 10/20/2023 to monitor
for abnormal bleeding i.e. excessive bruising, bleeding gums, nose bleeds, tarry stools, etc. This is
documented Q Shift on the medication administration record in the EMR.
On 10/21/23 the surveyor confirmed the facility implemented their plan of removal sufficiently to remove the
Immediate Jeopardy (IJ) by:
Verifying the Medical Director had been informed of the Immediate Jeopardy from documentation signed by
the Administrator.
Verifying the Pharmacy Consulted had been informed of the Immediate Jeopardy from documentation
signed by the DON.
Record review of in services revealed staff were educated on signs and symptoms of gastrointestinal
bleeding, report signs and symptoms of bleeding to charge nurse, long term NSAID's and Risks, and The 5
Rights of Medication Administration.
Record review of in services revealed the Administrator, DON and ADON were educated on Monitoring
New Orders for Accurate Transcription into EMR (electronic medical record) and reviewing new orders with
stop dates to ensure correct transcription into EMR during clinical meeting.
Record reviews on four resident charts taking ibuprofen were completed to ensure medication orders for
NSAID use and stop dates were completed, head to toe assessment were completed and orders to monitor
for abnormal bleeding, excessive bruising, bleeding gums, nose bleeds, tarry stools, etc. each shift. There
were no issues identified.
Interviews with 5 Licensed Nurses, 3 MA and 9 CNAs (on all shifts 6 a.m.- 2 p.m., 2 p.m.-10 p.m., 10 p.m.6 a.m., 6 a.m.-6 p.m., and Weekend Doubles) were performed on 10/21/23. All licensed nursing staff were
able to correctly identify signs and symptoms of gastrointestinal bleeding, who to report it to, monitoring for
bleeding each shift and documenting it on the MAR. Licensed nurses and MA were able to correctly identify
medication administration of long-term use and risks of NSAIDs
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 13 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0757
(nonsteroidal anti-inflammatory drugs) and 5 Rights of Medication Administration.
Level of Harm - Immediate
jeopardy to resident health or
safety
During an interview on 10/21/23 at 4:31 p.m., the DON said she in-serviced the nursing staff on signs and
symptoms of gastrointestinal bleeding, report signs and symptoms of bleeding to charge nurse, long term
NSAID's and Risks, and The 5 Rights of Medication Administration. The DON said staff who were not in
serviced would be prior to their next shift. The DON said she was in serviced on Monitoring New Orders for
Accurate Transcription into EMR (electronic medical record) and reviewing new orders with stop dates to
ensure correct transcription into EMR during clinical meeting. The DON said clinical meetings are held
daily.
Residents Affected - Some
During an interview on 10/21/23 at 4:44 p.m., the ADON said she was in serviced on Monitoring New
Orders for Accurate Transcription into EMR (electronic medical record) and reviewing new orders with stop
dates to ensure correct transcription into EMR during clinical meeting. The ADON said clinical meetings are
held daily.
During an interview on 10/21/23 at 4:53 p.m., the Administrator said he was in serviced on Monitoring New
Orders for Accurate Transcription into EMR (electronic medical record) and reviewing new orders with stop
dates to ensure correct transcription into EMR during clinical meeting. The Administrator said clinical
meetings are held daily.
On 10/21/23 at 5:30 p.m., the Administrator was informed the IJ was removed; however, the facility
remained out of compliance at a scope of pattern and a severity level of actual harm that is not immediate
jeopardy due to the facility's need to evaluate the effectiveness of the corrective systems.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 14 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
Ensure medication error rates are not 5 percent or greater.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure a medication error rate less that 5
percent. There were 3 errors out of 34 opportunities, resulting in an 8 percent medication error rate
involving 1 of 3 residents (Resident #13).
Residents Affected - Few
MA B failed to administer 2 scheduled medications, spironolactone (to treat excess fluid in the tissues) and
vitamin D3 (to treat vitamin deficiency), to Resident #13 as ordered by the physician.
MA B failed to follow physician's orders regarding specific instructions for the administration of polyethylene
glycol 3350 (for treatment of constipation).
These failures could place the resident at risk of not receiving the therapeutic effect of the mediations and
could result in a decline health status.
Findings included:
Record review of an undated face sheet indicated Resident #13 was a [AGE] year-old female who admitted
to the facility on [DATE] with diagnoses including hypertension (elevated/high blood pressure), chronic
peripheral venous insufficiency (improper functioning of the valves in the leg causing swelling), acute
pulmonary edema (excess fluid in the lungs), vitamin deficiency, and constipation.
During observation and interview on 10/23/2023 at 09:10 AM, MA B administered the following scheduled
medications to Resident #13: aspirin, citalopram, loratadine, cranberry tablet, vitamin B12, duloxetine,
lactulose, Lasix, rivastigmine, and polyethylene glycol mixed in a liquid supplement, multivitamin, ferrous
sulfate, and prednisolone eye drops. MA B was not able to locate two medications, a multivitamin and
ferrous sulfate, in the cart and obtained them from the nurse.
Record review on 10/23/2023 at 11:20 AM of the physician orders dated for 09/23/2023-10/23/2023
indicated Resident #13 was also to receive the following medications at 09:00 AM daily:
o Spironolactone 25mg daily to help treat edema (excess fluid in the tissues) and
o Vitamin D3 50mcg (2000 units) for vitamin deficiency.
These 2 (two) medications were not administered during the observed medication pass at 09:10 on
10/23/2023.
Record review on 10/23/2023 at 11:20 A of the physician orders dated 09/23/2023-10/23/2023 indicated an
order for polyethylene glycol 3350 powder was to be administered as follows:
o Polyethylene glycol 3350 powder 17gm/dose 1 scoop
Special Instructions: Stir in 4-8 ounces water, juice, soda, coffee, or tea until dissolved and administer
immediately.
On 10/23/2023 at 09:10 AM, MA B was observed to place 17gm/dose of polyethylene glycol 3350 powder
in a plastic cup. She then poured an unmeasured amount of a liquid supplement (Hi-Cal 2 calories/per
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 15 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
1 ml) into the same cup and used a wooden spoon to mix the two together. After placing the other
medications in Resident #13's mouth, MA B attempted to give Resident #13 the polyethylene glycol 3350
mixed with the liquid supplement but the mixture would not pour from the cup. MA B then waked over to the
medication cart and added an unmeasured amount of water to the cup, stirred the mixture again, and
returned to the resident. MA B held the cup to Resident #13's mouth and poured the thickened mixture, a
little at a time, into the resident's mouth. MA B said she had poured 30 mls of liquid supplement and a
splash of water into the cup with the polyethylene glycol 3350 powder. MA B did not give Resident #13 any
water after administering the medications and polyethylene glycol 3350.
On 10/23/2023 at 09:28, MA B said she was finished giving Resident #13 her medications. During the
observation of this medication pass, MA B did not go to the medication room to see if the needed
medications (spironolactone and vitamin D3) were there, nor did she tell the charge nurse about the
missing medications.
During an interview on 10/23/2023 at 01:10 PM with the DON and MA B, MA B said she did not give
Resident #13 her spironolactone and vitamin D3 because they were not in the cart and said she had
documented the medications were not available. She said if she did not have a scheduled medication in the
cart, she would look for it in the medication room and if she did not find it, she would document the
medication was not available on the medication administration record (MAR). The DON said the medication
aide should notify the nurse if a scheduled medication was not available and the charge nurse could access
the facility's emergency drug container and obtain needed medication from it. The DON said if a needed
medication was not in the emergency container, then the charge nurse would notify the pharmacy and the
pharmacy would either deliver it or obtain it from a local pharmacy for delivery. The DON said she would
obtain the needed medications from the medication room and have MA B administer them.
Record review of the MAR on 10/23/2023 at 01:55 PM indicated MA B had documented the spironolactone
as Not Administered: Drug/Item unavailable. The vitamin D3 medication was documented as being
administered at 09:00 AM.
During an interview on 10/23/2023 at 02:30 PM, MA B said she made a mistake and should have
documented the vitamin D3 as not being administered. MA B also said she used the Hi-Cal liquid
supplement to mix with the polyethylene glycol powder because she felt Resident #13 needed it. She said
she estimated how much water and liquid supplement she used and did not know why she did not measure
the amounts given. She said she should have used the ordered amount of water to mix the drug with.
Review of the facility's policy titled Medication - Administration dated 08-2020 indicated the following:
Policy
It is the policy of this home that medications will be administered and documented as ordered by the
physician
and in accordance with state regulations.
Procedure
.4. Current medications and dosage schedules, except topical used for treatments, are listed on
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 16 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0759
the resident's medication record (MAR)
Level of Harm - Minimal harm
or potential for actual harm
.7. Supplies and equipment, which are needed during a medication pass, are to be placed on the
medication cart. The following equipment and materials are needed for the medication pass: Routine
medications needed, including house stock medications.
Residents Affected - Few
8. Medications are administered within 60 minutes of scheduled time, unless otherwise specified by the
Physician.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 17 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure residents were free from significant
medication errors for 1 of 3 residents (Resident #13) reviewed for medication administration accuracy.
Residents Affected - Few
MA B failed to administer a scheduled medication, spironolactone (used to treat high blood pressure and
excess fluid in the tissues, to Resident #13 as ordered by the physician.
This failure could place the resident at risk of not receiving the therapeutic effects of the mediation and
could result in a decline health status.
Findings included:
Record review of an undated face sheet indicated Resident #13 was a [AGE] year-old female who admitted
to the facility on [DATE] with diagnoses including hypertension (elevated/high blood pressure), chronic
peripheral venous insufficiency (improper functioning of the valves in the leg causing swelling), and acute
pulmonary edema (excess fluid in the lungs).
Record review of Resident #13's Quarterly MDS assessment dated [DATE] indicated her cognition to be
severely impaired as indicated by a BIMS score of 2 out of 15 and dependent on staff for most ADLs.
During observation and interview on 10/23/2023 at 09:10 AM, MA B administered medications to Resident
#13 including aspirin, citalopram, loratadine, cranberry tablet, vitamin B12, multivitamin, duloxetine,
lactulose, Lasix, iron, rivastigmine, polyethylene glycol, and prednisolone eye drops.
Record review on 10/23/2023 at 11:20 AM of the physician orders dated for 09/23/2023-10/23/2023
indicated Resident #13 was also to receive the following medication at 09:00 AM daily:
o Spironolactone 25mg daily (to help treat edema and hypertension).
This medication was not administered during the observed medication pass at 09:10 on 10/23/2023.
In an interview on 10/23/2023 at 09:28, MA B said she was finished giving Resident #13 her medications.
MA B did not go to the medication room to see if the needed medication (spironolactone) was there, nor did
she tell the charge nurse about the missing medication during this observation of the medication pass.
During an interview on 10/23/2023 at 01:10 PM with the DON and MA B, MA B said she did not give
Resident #13 her spironolactone because it was not in the cart. She said if she did not have a scheduled
medication in the cart, she would look for it in the medication room and if she did not find it, she would
document the medication was not available on the MAR. The DON said the medication aide should notify
the nurse if a scheduled medication was not available and the charge nurse could access the facility's
emergency drug container and obtain needed medication from it. The DON said if a needed medication
was not in the emergency container, then the charge nurse would notify the pharmacy and the pharmacy
would either deliver it or obtain it from a local pharmacy for delivery.
Record review of the MAR on 10/23/2023 at 01:55 PM indicated MA B had documented the spironolactone
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 18 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0760
as Not Administered: Drug/Item unavailable.
Level of Harm - Minimal harm
or potential for actual harm
Review of the facility's policy titled Medication - Administration dated 08-2020 indicated the following:
Residents Affected - Few
It is the policy of this home that medications will be administered and documented as ordered by the
physician
and in accordance with state regulations.
Procedure
.4. Current medications and dosage schedules, except topical used for treatments, are listed on the
resident's medication record (MAR)
.7. Supplies and equipment, which are needed during a medication pass, are to be placed on the
medication cart. The following equipment and materials are needed for the medication pass: Routine
medications needed, including house stock medications.
8. Medications are administered within 60 minutes of scheduled time, unless otherwise specified by the
Physician.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 19 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
Based on observation, interview, and record review the facility failed to ensure, in accordance with State
and Federal laws, all drugs and biologicals were stored in locked compartments and permitted only
authorized personnel to have access to 1 of 2 rooms (DON's office) and 1 of 3 medication carts used for
storage of medications and other biological chemicals.
The facility failed to ensure MA B kept OTC medications secured in the medication cart and unable to be
accessed by unauthorized personnel.
The facility failed to ensure the DON's office was secured and unable to be accessed by unauthorized
personnel.
These failures could place residents at risk for misuse of medication and overdose, drug diversions, and
adverse reactions to medications.
Findings included:
During observation of medication administration on 10/23/2023 beginning at 09:10 AM, MA B opened a
new bottle containing 100 generic multivitamins, removed 1 (one) tablet from the bottle, put the vitamin
tablet in a medicine cup, put the lid on the bottle, and set the bottle on top of the medication cart. MA B
obtained other medications from the cart, put those medications in the cup with the vitamin in it, and put
those containers back inside the cart. MA B locked the cart, leaving the bottle of multivitamins on top of the
cart. MA B left the cart parked against the wall at the entrance to 200 hall, turned her back to the cart and
walked across the area (approximately 7 feet) to the resident she was to administer the medications to. MA
B administered the medications to the resident and returned to the cart. MA B said she had done all she
needed to do. This surveyor pointed to the Multivitamin bottle. MA B said she forgot to put the bottle into the
cart. She said someone could have taken it.
During observation and interview on 10/25/2023 at 11:20 AM, the DON's office door was noted to be
unlocked and fully open. Upon following the DON into her office, a box, measuring approximately 8x16x10
inches and containing multiple cards of medications including medications for high blood pressure,
depression, mental illness, nausea, high cholesterol, etc., was noted setting on the floor in front of a locked
closet where discontinued narcotics were kept. The DON was observed to count 57 cards containing 1 to
30 medications on each card, 2 bottles of unknown number of vitamin C tablets, 1 partial bottle of lactulose,
and 1 hand-held nebulizer for respiratory treatment. The drugs were not secured and were available to
anyone who walked into the DON's office. The DON said the medications were to be processed for
destruction and she had just put the box in there. The DON did not offer a rationale for not securing the
drugs.
Record review of the facility's policy dated 08-2020 and titled Medication-Discontinued
Medication/Destruction of Drugs indicated the following: 1. When a medication has passed its expiration
date or is otherwise deteriorated, or has been discontinued, or for a resident no longer residing at the
home, it should be removed from the medication cart as soon as possible and accounted for and kept
under lock and key in the medication room.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 20 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review, the facility failed to maintain an infection control program
designed to prevent the development and transmission of disease and infection for infection control and
based on observations, interviews, and record reviews, the facility failed to implement infection control
practices designed to provide a safe, sanitary, and comfortable environment to help prevent the
development and transmission of communicable diseases and infections for 6 of 7 residents (Resident #'s
6, 27, 32, 46, 68 and 70) reviewed for infection control practices, in that:.
Residents Affected - Some
*Resident #'s 6, 42, and 68's O2 tubing was not covered and Resident #46's oxygen tubing was not labeled
correctly.
*Resident #70's Nebulizer tubing was not covered.
*Resident #32's CPAP tubing was dirty and not covered; and
*Facility staff did not disinfect the glucometer properly before and after it was used on Resident #27.
This failure placed residents' risk for exposure to possible transmission of communicable diseases and
infections.
Findings included:
Observations on 10/22/2023 to 10/25/2023 between 9:00 am and 3:30 PM during facility tour revealed the
following:
*During an observation resident#6 oxygen tubing was not covered in a plastic bag and was hanging on the
concentrator. Portable oxygen tubing was hanging from wheelchair being used.
*During an observation resident #46 lying in the bed oxygen tubing was not covered in a plastic bag and
was hanging on the concentrator. Oxygen tubing had label date of 7/31/2023 and was not in a plastic bag.
*During an observation and interview 10/22/23 at 12:07pm with Resident#70 stated he gets Nebulizer
treatment and uses oxygen at night. Was noted Nebulizer tubing had the date of 9/27/2023 and was on top
of the machine on the side of the table uncovered.
*During an observation and interview on 10/22/23 at 12:11pm with resident#32 said he uses the CPAP
machine at night., the CPAP mask was on top of the machine, there was dirty tubing on side table
uncovered no date indicating when changed and the O2 tubing on floor uncovered.
*During an observation on 10/25/23 at 1:15pm In room [ROOM NUMBER]A (Resident #68 was not in the
room) oxygen tubing was not covered in a plastic bag and was hanging on the concentrator dangling to the
floor and not dated.
In an interview on 10/24/2023 at 10:50 AM, the DON stated the oxygen tubing is changed weekly and the
oxygen tubing is placed in a zip lock bag for infection control to prevent contamination. She
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 21 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
stated the CPAP mask are to be cleaned after each use and placed inside zip lock bag.
Level of Harm - Minimal harm
or potential for actual harm
In an interview and Record review on 10/24/2023 at 2pm with the DON she was asked who is responsible
to make sure O2 tubing is changed and dated, she said it is the night shift on Sunday's nurse responsibility
to change tubing and it's my responsibility to perform infection control audits to review that policies are
being followed. Record review revealed the Night shift was signing tasks being done but observation
revealed task was not done.
Residents Affected - Some
In an interview on 10/25/2023 at 1:40 PM, the ADON/IP stated the oxygen tubing and CPAP mask should
be placed in a zip lock bag after each use. She stated, the facility did not have an Infection Control policy for
cross contamination it is best practice to bag the items as a best practice for infection control. She said it
was a system failure that the facility was not monitoring this to ensure it was being done and residents are
at risk for respiratory infections.
Resident #27
Review of Resident #27's undated face sheet indicated Resident #27 to be a [AGE] year-old female who
admitted to the facility on [DATE] with diagnoses including diabetes.
Record review of Resident #27's Annual MDS assessment dated [DATE] indicated her cognition to be
severely impaired as indicated by a BIMS score of 7 out of 15 and requiring moderate to maximum
assistance with most ADLs.
Review of Resident #27's physician orders dated 09/23/2023-10/23/2023 indicated an order dated
05/06/2023 for Resident #27's blood glucose level to be checked 4 (four) times a day with additional
instructions to administer doses of Humalog insulin according to a prescribed sliding scale (A sliding scale
varies the dose of insulin based on blood glucose level).
During observation and interview on 10/23/2023 at 11:40 AM, LVN A cleansed her hands with an
alcohol-based hand sanitizer, put on a pair of disposable gloves, and removed a glucometer (a handheld
meter used to measure how much glucose is in the blood) and a lancet (a small, sterile needle used to
obtain a blood sample to check blood glucose levels) from the drawer of her medication cart and set them
on top of the cart. Using her gloved fingers, she obtained a test strip from its container and inserted the test
strip into the glucometer. She then picked up the glucometer and lancet and entered Resident #27's room.
After cleaning Resident #27's finger with an alcohol pad, LVN B obtained a blood sample from her finger
and applied it to the glucometer test strip. LVN A said Resident #27's blood sugar level was 117 and would
not be receiving any insulin. LVN A returned to the medication cart, disposed of the lancet, alcohol pad, and
test strip, and set the glucometer on top of the medication cart. LVN A then obtained an alcohol pad and
used the pad to clean the glucometer. She disposed of the alcohol pad, removed her gloves, and placed
the glucometer in the medication cart drawer. She said she had several residents requiring point-of-care
blood glucose testing daily but had no more to be done at that time. LVN A said she used an alcohol pad to
clean the glucometer before this surveyor arrived at the medication cart. LVN A said she always used
alcohol pads to clean the glucometers.
During an interview with the DON on 10/23/2023 at 12:05 PM, she said she expected the nurses to follow
infection prevention and control practices during point-of-care testing using glucometers. She said the
nurses should use an EPA Registered germicidal disposable wipe referred to as Purple Top (PDI Super
Sani-Cloth Germicidal Disposable wipes packaged in a purple and white plastic container with
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 22 of 23
Printed: 05/15/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
455834
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/25/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Avir at Athens
150 Gibson Rd
Athens, TX 75751
For information on the nursing home's plan to correct this deficiency, please contact the nursing home or the state survey agency.
(X4) ID PREFIX TAG
SUMMARY STATEMENT OF DEFICIENCIES
(Each deficiency must be preceded by full regulatory or LSC identifying information)
F 0880
a purple top) wipes.
Level of Harm - Minimal harm
or potential for actual harm
Record review of the User's Guide for the Evencare G2 glucometer used by LVN A indicated EPA
Registered wipes were to be used to disinfect the glucometer.
Residents Affected - Some
Record review of the facility policy titled Finger Stick Blood Sampling dated 12/1/2018 indicated the
following:
Equipment and Supplies
2. Germicidal Wipes
Procedure
8. Clean the glucometer with germicidal wipes unless otherwise indicated or bleach/water solution diluted
with a 1 to 10 ratio before initial use, after final use and between each resident following manufacturer
directions.
The facility's policy, Respiratory Therapy Equipment dated 12/2018, reflected, [NAME] bottle with date and
initials upon opening and discard after seven days or as needed, change oxygen cannula and tubing every
seven (7) days and as necessary, keep oxygen cannula and tubing used PRN in a plastic bag when not in
use. Nebulizer equipment, store circuit in plastic bag, marked with date and residents name between uses.
The Director of Nursing will perform infection control audits to review staff procedure in observation of
standard precautions, Infection control and isolation procedures.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455834
If continuation sheet
Page 23 of 23