F 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to develop and implement a comprehensive person-centered
care plan for each resident for 1 of 3 residents (Resident #1) reviewed for comprehensive care plans.
The facility failed to implement the care plan intervention to monitor and document Resident #1's output.
This failure could place residents at risk of unmet care needs.
Findings included:
Record review of the physician order summary report dated 10/5/23 indicated she re-admitted to the facility
on [DATE] with diagnoses including history of bladder cancer, breast cancer, high blood pressure, heart
failure, presence of vascular implants and grafts, chronic embolism(blockage in an artery, caused by a
foreign body, such as a blood clot) and thrombosis (formation of a blood clot (partial or complete blockage)
within blood vessels, whether venous or arterial) of deep veins to both lower extremities, history of
gastrointestinal hemorrhage, presence of ileostomy (a stoma surgically constructed by bringing the end or
loop of small intestine out onto the surface of the skin) morbid (severe) obesity, Stage 2 chronic kidney
disease (stages if kidney disorder range from Stage 1 [mild] to Stage 5 [most severe]), history of acute
kidney failure, history of acute cystitis(inflammation of the bladder, usually caused by a bladder infection),
and neuromuscular dysfunction of the bladder.
Record review of the MDS dated [DATE] indicated Resident #1 made herself understood and usually
understood others. The MDS indicated she had intact cognition, (BIMS of 13). The MDS indicated she was
totally dependent on staff for bed mobility, dressing, personal hygiene, and bathing. The MDS indicated she
required extensive assistance with toilet use. The MDS indicated transfers and locomotion in her wheelchair
had only occurred once or twice during the 7 day look back period. The MDS indicated Resident #1 had an
indwelling catheter. The MDS indicated Resident #1 had an active diagnosis of renal insufficiency, renal
failure or end stage renal disease. The MDS indicated Resident #1 had an active diagnosis of calculus of
kidney (kidney stone).
Record review of the care plan revised on 9/18/23 indicated Resident #1 had a urinary catheter. The care
plan interventions included monitor and report to the physician any signs or symptoms of a urinary tract
infection. The care plan interventions also included monitor and document (urine) output.
(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 16
Event ID:
676007
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Record review of the ADL documentation for 9/15/23 to 10/15/23 did not record urine output for Resident
#1. The ADL documentation indicated Resident #1 was totally dependent on staff for the management of
her indwelling catheter but did not document the number of occurrences the catheter was emptied nor did it
document urine volume emptied form the catheter.
Record review of Resident #1's nursing progress notes dated 9/1/23 to 10/15/23 did not record urine output
for Resident #1. Neither the number of occurrences the catheter was emptied nor urine volume emptied
from the catheter were documented in the nursing progress notes from 9/1/23 to 10/15/23.
During an interview on 10/16/23 at 11:00 a.m., CNA B said she had worked at the facility since November
2022. CNA B indicated she regularly took care of Resident #1 on the 6:00 a.m. to 2:00 p.m. shift. CNA B
said CNAs did not document the volume of urine when they emptied catheters. CNA B said she would
empty Resident #1's catheter and dump the urine in the toilet. CNA B said there was no place in the EMR
documentation system to record that the catheter had been emptied or to enter a number (volume of urine).
CNA B said she would notify the nurse if there had been no urine or decreased urine during her shift but
otherwise would not notify the nurse regarding urine output.
During an interview on 10/16/23 at 11:21 a.m., CNA C said she had worked at the facility since August
2023. CNA C said she had taken care of Resident #1 several times. CNA C said there was no place in the
EMR documentation system to record that the catheter had been emptied or to enter a number (volume of
urine). CNA C said when she emptied a resident's catheter, she would report the cc's (cubic centimeter is a
commonly used unit of volume) to the nurse at the end of the shift.
During an interview on 10/16/23 at 11:30 a.m., LVN A said she regularly took care of Resident #1 on the
6:00 a.m. to 6:00 p.m. shift. LVN A said the facility did not record urine volume. LVN A said the CNAs do not
report anything to the nurses regarding urine output (number of times catheter was emptied or volume of
urine) unless the urine volume was very low. LVN A said very low meant less than 100 ml (milliliters). LVN A
said she would look at urine volume during her rounds but said just looking at the bags at any given time
was not necessarily an accurate reflection because the last time the catheter bag had been emptied would
be unknown. LVN A said she was not aware of any place on the EMR where CNAs could record the date
and time the catheter bag had been emptied. LVN A said it was important to monitor urine output as
decreased urine output could signal several issues such as obstruction, dehydration, or decreased kidney
function.
During an interview on 10/16/23 at 11:49 a.m., LVN E said she regularly took care of Resident #1 on the
6pm-6am shift. LVN E said she expected CNAs to notify her if Resident #1's urine volume was low. LVN E
said she would look at urine volume in catheter bags during her initial rounds but could not say when the
catheter bag was previously emptied. LVN E said she was not aware of any place on the EMR where CNAs
could record the date and time the catheter bag had been emptied.
During an interview on 10/16/23 at 12:12 p.m., LVN F said she regularly cared for Resident #1 on 6:00 a.m.
to 6:00 p.m., shift. LVN F said he expected CNAs to notify him if a resident's urine appeared cloudy, bloody
or had a foul odor when they (CNAs) emptied catheters bags. LVN F said the CNAs did not report volume
of urine or when they emptied the catheter bag. LVN F said as far as he knew CNAs were not required to
notify him of volume of urine or when they emptied the catheter bag. LVN F said he was not aware of any
place on the EMR where CNAs could record the date and time the catheter bag had been emptied.
During an interview on 10/16/23 at 3:30 p.m., ADON G said it was not the facilities policy to
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 2 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
record urine volume. ADON G said she did expect CNAs to monitor urine output and report to the nurse.
ADON G said she did not think there was a place in the EMR for nurse aides to document urine output.
During an interview on 10/16/23 at 3:34 p.m., ADON H said currently the facility did not have a DON and
the corporate RN was filling in. ADON H said it was not the facilities policy to record urine volume. ADON H
said she did expect CNAs and nurses to monitor urine output. ADON H said there was not a place in the
EMR for nurse aides to document emptying catheters. ADON H said there was no system in place to
ensure CNAs and nurses were monitoring urine output in residents with catheters.
During an interview on 10/16/23 at 4:00 p.m., the Administrator said he expected staff to implement care
plan interventions.
The facility policy and procedure titled Indwelling Foley Catheter Guidelines dated 5/23/2014 stated The
facility shall identify and assess patients with an indwelling catheter or at risk for catheterization, provide
appropriate treatment and services to prevent urinary tract infections . The facility policy and procedure did
not specifically address monitoring urine output in catheterized residents but did state .(if) occlusion
(occurs) replace the catheter .maintain unobstructed flow .empty the collecting bag regularly .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 3 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0697
Provide safe, appropriate pain management for a resident who requires such services.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, record review, and interview, the facility failed to ensure pain management was provided to
residents who required such services, consistent with professional standards of practice, the
comprehensive person-centered care plan, and the residents' goals and preferences, for 1 of 3 residents
(Resident #1) reviewed for pain management.
Residents Affected - Some
The facility failed to perform and document a pain assessment with the administration of Resident #1's prn
(as needed) pain medication.
The facility failed to perform a follow up pain assessment after administering Resident #1's prn pain
medication.
This failure could place residents at risk for incomplete pain relief, discomfort and decreased quality of life.
Findings Included:
Record review of the physician order summary report dated 10/5/23 indicated she re-admitted to the facility
on [DATE] with diagnoses including history of bladder cancer, breast cancer, high blood pressure, heart
failure, presence of vascular implants and grafts, chronic embolism(blockage in an artery, caused by a
foreign body, such as a blood clot) and thrombosis (formation of a blood clot (partial or complete blockage)
within blood vessels, whether venous or arterial) of deep veins to both lower extremities, history of
gastrointestinal hemorrhage, presence of ileostomy (a stoma surgically constructed by bringing the end or
loop of small intestine out onto the surface of the skin) morbid (severe) obesity, Stage 2 chronic kidney
disease (stages if kidney disorder range from Stage 1 [mild] to Stage 5 [most severe]), history of acute
kidney failure, history of acute cystitis(inflammation of the bladder, usually caused by a bladder infection),
and neuromuscular dysfunction of the bladder.
Record review of the MDS dated [DATE] indicated Resident #1 made herself understood and usually
understood others. The MDS indicated she had intact cognition, (BIMS of 13). The MDS indicated she was
totally dependent on staff for bed mobility, dressing, personal hygiene, and bathing. The MDS indicated she
required extensive assistance with toilet use. The MDS indicated transfers and locomotion in her wheelchair
had only occurred once or twice during the 7 day look back period. The MDS indicated Resident #1
frequently had pain during the 5 day look back period. The MDS indicated Resident #1's pain did not make
it hard for her to sleep at night during the 5 day look back period. The MDS indicated Resident #1's pain did
limit her day to day activities during the 5 day look back period. The MDS indicated Resident #1 rated her
worst pain at a 5 on the 0-10 pain scale (zero being no pain and ten as the worst pain you can imagine)
during the 5 day look back period. The MDS indicated Resident #1 had not received prn pain medication
during the 5 day look back period.
Record review of the care plan revised on 9/18/23 indicated Resident #1 was to be monitored for pain/
discomfort and was to be administered medications as needed for discomfort and pain.
Record review of the physician order dated 8/18/23 indicated Resident #1 was to be administered
Hydrocodone -Acetaminophen 7.5mg/325mg 1 tablet every 8 hours as needed for pain.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 4 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0697
Level of Harm - Minimal harm
or potential for actual harm
Record review of the facility-controlled drug record for Resident #1's Hydrocodone -Acetaminophen
7.5mg/325mg dated 8/19/23 to 10/5/23 indicated she had been administered Hydrocodone
-Acetaminophen 7.5mg/325mg 1 tablet on the following dates and times;
*9/1/2023 at 10:00 a.m.;
Residents Affected - Some
*9/2/23 at 5:30 a.m.;
*9/2/23 at 9:00 p.m.;
*9/3/23 at 1:00 p.m.;
*9/4/23 at 9:00 a.m.;
*9/5/23 at 9:00 a.m.;
*9/6/23 at 9:20 a.m.;
*9/6/23 at 11:00 p.m.;
*9/7/23 at 3:45 p.m.;
*9/8/23 at 8:00 a.m.;
*9/9/23 at 8:00 a.m.;
*9/10/23 at 9:00 a.m.;
*9/10/23 at 5:00 p.m.;
*9/11/23 at 8:00 a.m.;
*9/11/23 at 4:00 p.m.;
*9/12/23 at 8:00 a.m.;
*9/12/23 at 7:00 p.m.;
*9/13/23 at 7:00 a.m.;
*9/13/23 at 3:00 p.m.;
*9/14/23 at 8:00 a.m.;
*9/15/23 at 3:35 p.m.;
*9/16/23 at 9:45 a.m.;
*9/17/23 at 9:15 a.m.;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 5 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0697
*9/18/23 at 8:00 a.m.;
Level of Harm - Minimal harm
or potential for actual harm
*9/18/23 at 6:00 p.m.;
*9/19/23 at 2:00 a.m.;
Residents Affected - Some
*9/19/23 at 9:00 a.m.;
*9/20/23 at 9:45 a.m.;
*9/21/23 at 12:30 p.m.;
*9/21/23 at 9:50 p.m.;
*9/22/23 at 8:00 a.m.;
*9/22/23 at 3:30 p.m.;
*9/23/23 at 8:00 a.m.;
*9/24/23 at 8:00 a.m.;
*9/24/23 at 3:30 p.m.;
*9/24/23 at 8:00 a.m.;
*9/25/23 at 8:45 a.m.;
*9/25/23 at 8:00 p.m.;
*9/26/23 at 8:30 a.m.;
*9/26/23 at 4:30 p.m.;
*9/27/23 at 8:00 a.m.;
*9/27/23 (time not legible);
*9/28/23 at 7:00 a.m.;
*9/28/23 at 3:00 p.m.;
*9/29/23 at 9:30 a.m.;
*9/30/23 at 8:00 a.m.;
*9/30/23 at 2:00 p.m.;
*10/01/23 at 9:15 a.m.;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 6 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0697
*10/01/23 at 8:00 p.m.;
Level of Harm - Minimal harm
or potential for actual harm
*10/02/23 at 8:00 a.m.;
*10/03/23 at 8:00 a.m.; and
Residents Affected - Some
*10/05/23 at 10:30 a.m.
The facility-controlled drug record did not document Resident #1's pain level with any of the medication
administrations.
Record review of Resident #1's MAR for September 2023 did not record any administration of Hydrocodone
-Acetaminophen 7.5mg/325mg 1 tablet every 8 hours as needed for pain. There were no follow up pain
assessments documented on the MAR.
Record review of Resident #1's MAR for October 2023 did not record any administration of Hydrocodone
-Acetaminophen 7.5mg/325mg 1 tablet every 8 hours as needed for pain. There were no follow up pain
assessments documented on the MAR.
Record review of the nursing notes from 9/1/23 to 10/5/23 indicated a follow up pain assessment had not
been completed after the administration of Resident #1's pain medication (Hydrocodone -Acetaminophen
7.5mg/325mg 1 tablet every 8 hours as needed for pain) on the following dates and times;
*9/1/2023 at 10:00 a.m.;
*9/2/23 at 5:30 a.m.;
*9/2/23 at 9:00 p.m.;
*9/3/23 at 1:00 p.m.;
*9/4/23 at 9:00 a.m.;
*9/5/23 at 9:00 a.m.;
*9/6/23 at 9:20 a.m.;
*9/6/23 at 11:00 p.m.;
*9/7/23 at 3:45 p.m.;
*9/8/23 at 8:00 a.m.;
*9/9/23 at 8:00 a.m.;
*9/10/23 at 9:00 a.m.;
*9/10/23 at 5:00 p.m.;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 7 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0697
*9/11/23 at 8:00 a.m.;
Level of Harm - Minimal harm
or potential for actual harm
*9/11/23 at 4:00 p.m.;
*9/12/23 at 8:00 a.m.;
Residents Affected - Some
*9/12/23 at 7:00 p.m.;
*9/13/23 at 7:00 a.m.;
*9/13/23 at 3:00 p.m.;
*9/14/23 at 8:00 a.m.;
*9/15/23 at 3:35 p.m.;
*9/16/23 at 9:45 a.m.;
*9/17/23 at 9:15 a.m.;
*9/18/23 at 8:00 a.m.;
*9/18/23 at 6:00 p.m.;
*9/19/23 at 2:00 a.m.;
*9/19/23 at 9:00 a.m.;
*9/20/23 at 9:45 a.m.;
*9/21/23 at 12:30 p.m.;
*9/21/23 at 9:50 p.m.;
*9/22/23 at 8:00 a.m.;
*9/22/23 at 3:30 p.m.;
*9/23/23 at 8:00 a.m.;
*9/24/23 at 8:00 a.m.;
*9/24/23 at 3:30 p.m.;
*9/24/23 at 8:00 a.m.;
*9/25/23 at 8:45 a.m.;
*9/25/23 at 8:00 p.m.;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 8 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0697
*9/26/23 at 8:30 a.m.;
Level of Harm - Minimal harm
or potential for actual harm
*9/26/23 at 4:30 p.m.;
*9/27/23 at 8:00 a.m.;
Residents Affected - Some
*9/27/23 (time not legible);
*9/28/23 at 7:00 a.m.;
*9/28/23 at 3:00 p.m.;
*9/29/23 at 9:30 a.m.;
*9/30/23 at 8:00 a.m.;
*9/30/23 at 2:00 p.m.;
*10/01/23 at 9:15 a.m.;
*10/01/23 at 8:00 p.m.;
*10/02/23 at 8:00 a.m.;
*10/03/23 at 8:00 a.m.; and
*10/05/23 at 10:30 a.m.
During an interview on 10/12/23 at 2:00 p.m., ADON G identified the signatures of LVN E, LVN A, LVN F,
and RN I on the facility-controlled drug record for Resident #1's Hydrocodone -Acetaminophen
7.5mg/325mg dated 8/19/23 to 10/5/23.
During an interview on 10/12/23 at 3:00 p.m., Resident #1 was laying in her bed. Resident #1 said the
facility did give her pain medication. Resident #1 said she usually asked for her pain medication almost
daily and sometimes more than once a day. Resident #1 said the pain medication usually helped her pain
but there had been sometimes she would ask for the pain medication and the staff would tell her it was not
time yet. Resident #1 could not specify any dates when she asked and was told it was not time yet.
Resident #1 said she was not hurting at the moment.
Record review of the facility-controlled drug record for Resident #1's Hydrocodone -Acetaminophen
7.5mg/325mg dated 8/19/23 to 10/5/23 after ADON G identified signatures revealed: LVN A had signed
administration of the Hydrocodone -Acetaminophen 7.5mg/325mg to Resident #1 twenty-two times. LVN F
had signed administration of the Hydrocodone -Acetaminophen 7.5mg/325mg to Resident #1 twenty times.
RN I had signed administration of the Hydrocodone -Acetaminophen 7.5mg/325mg to Resident #1 six
times. LVN E had signed administration of the Hydrocodone -Acetaminophen 7.5mg/325mg to Resident #1
three times.
During an interview on 10/16/23 at 11:30 a.m., LVN A identified 22 of the signatures on the
facility-controlled drug record for Resident #1's Hydrocodone -Acetaminophen 7.5mg/325mg dated 8/19/23
to
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 9 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0697
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
10/5/23 as being her signatures. LVN A said she did administer the medication. When asked why she had
not recorded the administrations on the MAR, LVN A said she had came back to the facility a few months
ago and the EMR system that was being used was new to her. LVN A said they (the nurses) were just
signing in out on the narcotic sheet (facility-controlled drug record) and administering it (the
Hydrocodone-Acetaminophen 7.5mg/325mg). LVN A said she should have documented the administrations
on the MAR. LVN A said no follow up assessment was completed unless it was in the nursing notes. LVN A
said that was another reason she should have documented the administration of pain medication on the
MAR because the EMR system would have prompted her to document a follow up pain assessment. LVN A
said a follow up pain assessment after the administration of pain medication should be performed and
documented for all residents to ensure effectiveness of the medication. LVN A said a pain assessment
should have been documented with the administration as well.
During an interview on 10/16/23 at 11:49 a.m., LVN E said she knew the Hydrocodone -Acetaminophen
7.5mg/325mg should have been documented on MAR with an assessment of her (Resident #1's) pain at
the time of the administration and after the medication had been administered to ensure effectiveness. LVN
E said the EMR system will prompt a reassessment when the medication is documented on MAR. When
asked why she had not signed the MAR for her administrations of Resident #1's Hydrocodone
-Acetaminophen 7.5mg/325mg, she said she thought she had done so.
During an interview on 10/16/23 at 12:12 a.m., LVN F said the administration of Resident #1's Hydrocodone
-Acetaminophen 7.5mg/325mg was really only being documented in the narcotic book (facility-controlled
drug record). LVN F said he knew the Hydrocodone -Acetaminophen 7.5mg/325mg should have been
documented on MAR with an assessment of her (Resident #1's) pain at the time of the administration and
after the medication had been administered to ensure effectiveness. LVN F said it was just failure on his
part to ensure he documented in the MAR.
A phone interview with RN I was attempted on 10/16/23 but was not completed.
During an interview on 10/16/23 at 3:30 p.m., ADON G said she expected nurses to assess a resident's
pain level when administering a prn pain medication and expected them to reassess for effectiveness within
an hour. ADON G said it was not acceptable the nurses were not documenting on the MAR and were only
signing the narcotic book (facility-controlled drug record).
During an interview on 10/16/23 at 3:34 p.m., ADON H currently the facility did not have a DON and the
corporate RN was filling in. ADON H said she expected nurses to assess a resident's pain level when
administering a prn pain medication and expected them to reassess for effectiveness within an hour. ADON
H said it was not acceptable the nurses were not documenting on the MAR and were only signing the
narcotic book (facility-controlled drug record). ADON G said had they signed the MAR the would have been
prompted to complete assessment at administration of the pain medication and prompted to perform a
follow- up pain assessment. ADON G said there had not been any system in place to ensure nurses were
documenting prn pain medications on the MAR nor had there been a system in place to ensure pain
assessments were being documented with prn pain medication administration/follow-up pain assessments
were being completed/documented. ADON H said she began an in-service over these items on 10/12/23
when it was brought to her attention by the surveyor that there was no documentation on Resident #1's
MAR for the Hydrocodone -Acetaminophen 7.5mg/325mg signed out of the facility-controlled drug record.
During an interview on 10/16/23 at 4:00 p.m., the Administrator said he expected nurses to document pain
medication administration and assess the resident to make sure their pain was relieved.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 10 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0697
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Record review of the facility policy and procedure titled, Pain Management dated 10/24/2 found the policy
and procedure stated, The facility must ensure that pain management is provided to residents who require
such services , consistent with professional standards of practice, the comprehensive person-centered care
plan, and the residents' goals and preferences .Pain Evaluation: the facility will use a pain evaluation tool,
which is appropriate for the resident's cognitive status to assist staff in consistent evaluation of a resident's
pain .(8) Monitoring , Reevaluation and Care Plan Revision (a) Facility staff will reassess resident's pain
management at established intervals for effectiveness .
The website https://www.ncbi.nlm.nih.gov/books/NBK2658/ , with the National Library of Medicine
accessed on 10/19/23 stated .Improving the Quality of Care Through Pain Assessment and Management .
Assessment of pain is a critical step to providing good pain management. In a sample of physicians and
nurses, [NAME] and colleagues21 found lack of pain assessment was one of the most problematic barriers
to achieving good pain control. The most critical aspect of pain assessment is that it is done on a regular
basis (e.g., once a shift, every 2 hours) using a standard format . To meet the patients' needs, pain should
be reassessed after each intervention to evaluate the effect and determine whether modification is needed .
Documentation of pain assessment and the effect of interventions are essential to allow communication
among clinicians about the current status of the patient's pain and responses to the plan of care . American
Pain Society Current Guidelines-One of the first quality improvement programs was developed by the
American Pain Society .Recognize and treat pain promptly .Reassess and adjust pain management plan as
needed .Monitor processes and outcomes of pain management . Assessment of effect should be based
upon the onset of action of the drug administered; for example, IV opioids are reassessed in 15-30 minutes,
whereas oral opioids and nonopioids are reassessed 45-60 minutes after administration .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 11 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0842
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Safeguard resident-identifiable information and/or maintain medical records on each resident that are in
accordance with accepted professional standards.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review the facility failed to ensure the medical record of each resident
was accurately documented in accordance with accepted professional standards and practices for 1 of 3
residents (Resident #1) reviewed for medical records.
The facility failed to ensure the documentation of Resident #1's prn (as needed) pain medication was
documented in the MAR.
This failure could place residents at risk of delayed pain medication administration, or over medication.
Findings included:
Record review of the physician order summary report dated 10/5/23 indicated she re-admitted to the facility
on [DATE] with diagnoses including history of bladder cancer, breast cancer, high blood pressure, heart
failure, presence of vascular implants and grafts, chronic embolism(blockage in an artery, caused by a
foreign body, such as a blood clot) and thrombosis (formation of a blood clot (partial or complete blockage)
within blood vessels, whether venous or arterial) of deep veins to both lower extremities, history of
gastrointestinal hemorrhage, presence of ileostomy (a stoma surgically constructed by bringing the end or
loop of small intestine out onto the surface of the skin) morbid (severe) obesity, Stage 2 chronic kidney
disease (stages if kidney disorder range from Stage 1 [mild] to Stage 5 [most severe]), history of acute
kidney failure, history of acute cystitis(inflammation of the bladder, usually caused by a bladder infection),
and neuromuscular dysfunction of the bladder.
Record review of the MDS dated [DATE] indicated Resident #1 made herself understood and usually
understood others. The MDS indicated she had intact cognition, (BIMS of 13). The MDS indicated she was
totally dependent on staff for bed mobility, dressing, personal hygiene, and bathing. The MDS indicated she
required extensive assistance with toilet use. The MDS indicated transfers and locomotion in her wheelchair
had only occurred once or twice during the 7 day look back period. The MDS indicated Resident #1
frequently had pain during the 5 day look back period. The MDS indicated Resident #1's pain did not make
it hard for her to sleep at night during the 5 day look back period. The MDS indicated Resident #1's pain did
limit her day to day activities during the 5 day look back period. The MDS indicated Resident #1 rated her
worst pain at a 5 on the 0-10 pain scale (zero being no pain and ten as the worst pain you can imagine)
during the 5 day look back period. The MDS indicated Resident #1 had not received prn pain medication
during the 5 day look back period.
Record review of the care plan revised on 9/18/23 indicates Resident #1 was to be monitored for pain/
discomfort and was to be administered medications as needed for discomfort and pain.
Record review of the physician order dated 8/18/23 indicated Resident #1 was to be administered
Hydrocodone -Acetaminophen 7.5mg/325mg 1 tablet every 8 hours as needed for pain.
Record review of the facility-controlled drug record for Resident #1's Hydrocodone -Acetaminophen
7.5mg/325mg dated 8/19/23 to 10/5/23 indicated she had been administered Hydrocodone
-Acetaminophen 7.5mg/325mg 1 tablet on the following dates and times;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 12 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0842
*9/1/2023 at 10:00 a.m.;
Level of Harm - Minimal harm
or potential for actual harm
*9/2/23 at 5:30 a.m.;
*9/2/23 at 9:00 p.m.;
Residents Affected - Some
*9/3/23 at 1:00 p.m.;
*9/4/23 at 9:00 a.m.;
*9/5/23 at 9:00 a.m.;
*9/6/23 at 9:20 a.m.;
*9/6/23 at 11:00 p.m.;
*9/7/23 at 3:45 p.m.;
*9/8/23 at 8:00 a.m.;
*9/9/23 at 8:00 a.m.;
*9/10/23 at 9:00 a.m.;
*9/10/23 at 5:00 p.m.;
*9/11/23 at 8:00 a.m.;
*9/11/23 at 4:00 p.m.;
*9/12/23 at 8:00 a.m.;
*9/12/23 at 7:00 p.m.;
*9/13/23 at 7:00 a.m.;
*9/13/23 at 3:00 p.m.;
*9/14/23 at 8:00 a.m.;
*9/15/23 at 3:35 p.m.;
*9/16/23 at 9:45 a.m.;
*9/17/23 at 9:15 a.m.;
*9/18/23 at 8:00 a.m.;
*9/18/23 at 6:00 p.m.;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 13 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0842
*9/19/23 at 2:00 a.m.;
Level of Harm - Minimal harm
or potential for actual harm
*9/19/23 at 9:00 a.m.;
*9/20/23 at 9:45 a.m.;
Residents Affected - Some
*9/21/23 at 12:30 p.m.;
*9/21/23 at 9:50 p.m.;
*9/22/23 at 8:00 a.m.;
*9/22/23 at 3:30 p.m.;
*9/23/23 at 8:00 a.m.;
*9/24/23 at 8:00 a.m.;
*9/24/23 at 3:30 p.m.;
*9/24/23 at 8:00 a.m.;
*9/25/23 at 8:45 a.m.;
*9/25/23 at 8:00 p.m.;
*9/26/23 at 8:30 a.m.;
*9/26/23 at 4:30 p.m.;
*9/27/23 at 8:00 a.m.;
*9/27/23 (time not legible);
*9/28/23 at 7:00 a.m.;
*9/28/23 at 3:00 p.m.;
*9/29/23 at 9:30 a.m.;
*9/30/23 at 8:00 a.m.;
*9/30/23 at 2:00 p.m.;
*10/01/23 at 9:15 a.m.;
*10/01/23 at 8:00 p.m.;
*10/02/23 at 8:00 a.m.;
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 14 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0842
*10/03/23 at 8:00 a.m.; and
Level of Harm - Minimal harm
or potential for actual harm
*10/05/23 at 10:30 a.m.
Residents Affected - Some
Record review of Resident #1's MAR for September 2023 did not record any administration of Hydrocodone
-Acetaminophen 7.5mg/325mg 1 tablet every 8 hours as needed for pain.
Record review of Resident #1's MAR for October 2023 did not record any administration of Hydrocodone
-Acetaminophen 7.5mg/325mg 1 tablet every 8 hours as needed for pain. There were no follow up pain
assessments documented on the MAR.
During and interview on 10/12/23 at 2:00 p.m., ADON G identified the signatures of LVN E, LVN A, LVN F,
and RN I on the facility-controlled drug record for Resident #1's Hydrocodone -Acetaminophen
7.5mg/325mg dated 8/19/23 to 10/5/23.
During an interview on 10/12/23 at 3:00 p.m., Resident #1 was laying in her bed. Resident #1 said the
facility did give her pain medication. Resident #1 said she usually asked for her pain medication almost
daily and sometimes more than once a day. Resident #1 said the pain medication usually helped her pain
but there had been sometimes she would ask for the pain medication and the staff would tell her it was not
time yet. Resident #1 could not specify any dates when she asked and was told it was not time yet.
Resident #1 said she was not hurting at the moment.
Record review of the facility-controlled drug record for Resident #1's Hydrocodone -Acetaminophen
7.5mg/325mg dated 8/19/23 to 10/5/23 after ADON G identified signatures revealed: LVN A had signed
administration of the Hydrocodone -Acetaminophen 7.5mg/325mg to Resident #1 twenty-two times. LVN F
had signed administration of the Hydrocodone -Acetaminophen 7.5mg/325mg to Resident #1 twenty times.
RN I had signed administration of the Hydrocodone -Acetaminophen 7.5mg/325mg to Resident #1 six
times. LVN E had signed administration of the Hydrocodone -Acetaminophen 7.5mg/325mg to Resident #1
three times.
During an interview on 10/16/23 at 11:30 a.m., LVN A identified 22 of the signatures on the
facility-controlled drug record for Resident #1's Hydrocodone -Acetaminophen 7.5mg/325mg dated 8/19/23
to 10/5/23 as being her signatures. LVN A said she did administer the medication. When asked why she
had not recorded the administrations on the MAR, LVN A said she came back to the facility a few months
ago and the EMR system that was being used was new to her. LVN A said we (the nurses) were just
signing in out on the sheet and administering it (the Hydrocodone -Acetaminophen 7.5mg/325mg). LVN A
said she had been shown how to document in the MAR when she came back to the facility a few months
ago and LVN A said she had been shown how to document in the MAR and should have documented the
administrations on the MAR .
During an interview on 10/16/23 at 11:49 a.m., LVN E said she knew the Hydrocodone -Acetaminophen
7.5mg/325mg should have been documented on MAR and thought she had done so.
During an interview on 10/16/23 at 12:12 a.m., LVN F said the administration of Resident #1's Hydrocodone
-Acetaminophen 7.5mg/325mg was really only being documented in the narcotic book (facility-controlled
drug record). LVN F said he knew the Hydrocodone -Acetaminophen 7.5mg/325mg should have been
documented on MAR.
During an interview on 10/16/23 at 3:34 p.m., ADON H currently the facility did not have a DON and
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 15 of 16
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
676007
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/16/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Willow Rehab & Nursing
1901 Whippoorwill
Kilgore, TX 75662
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 0842
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
the corporate RN was filling in. ADON H said it was not acceptable the nurses were not documenting on the
MAR and were only signing the narcotic book (facility-controlled drug record). ADON G said the signing out
of the drug by the nurse in the narcotic book indicates time and date the medication was pulled and the
count (the amount of remaining) of the narcotic. ADON G said it was not intended to be the administration
record. ADON G said had they signed the MAR they would have been prompted to complete assessment at
administration of the pain medication and prompted to perform a follow- up pain assessment. ADON G said
there had not been any system in place to ensure nurses were documenting prn pain medications on the
MAR nor had there been a system in place to ensure pain assessments were being documented with prn
pain medication administration/follow-up pain assessments were being completed/documented. ADON H
said she began an in-service over these items on 10/12/23 when it was brought to her attention by the
surveyor that there was no documentation on Resident #1's MAR for the Hydrocodone -Acetaminophen
7.5mg/325mg signed out of the facility-controlled drug record.
During an interview on 10/16/23 at 4:00 p.m., the Administrator said he expected nurses to document pain
medication administration on the MAR and ensure completeness and accuracy of the medical record.
Record review of the facility policy and procedure titled Documentation Guideline, revised on 3/25/14 found
the policy and procedure stated, The patient's clinical record provides a record of health status .and serves
as the primary document describing the healthcare services provided to the patient .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676007
If continuation sheet
Page 16 of 16