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
observation, interview, and record review, the facility failed to implement a comprehensive person-centered
care plan for each resident, that included measurable objectives and timeframes to meet a resident's needs
identified in the comprehensive assessment for 1 of 20 residents reviewed for following physician orders.
(Resident #27)
The facility did not apply Resident #27's hand splint as ordered by the physician
This failure could place the residents at risk of a decline in their range of motion.
Findings included:
Record review of physician orders dated June 2024 indicated Resident #27, admitted [DATE], was an
[AGE] year-old female with diagnoses of muscle wasting and atrophy and cerebral infarction (a condition
that occurs when blood flow to the brain is disrupted causing the brain tissue to die). The orders indicated
the resident was to have a resting hand splint to the right upper extremity to prevent contracture. The hand
splint was to be removed every night.
Record review of the quarterly MDS assessment dated [DATE] indicated Resident #27 had a BIMs of 4
(Severe cognitive impairment), had an impairment in ROM to one side of the upper extremities and was
dependent for personal hygiene and toileting.
Record review of a care plan revised 02/16/24 indicated Resident #27 had limited physical mobility or was
at risk for a decline in mobility related to a limited range of motion to the right arm/hand.
Record review of an ADL task sheet dated June 2024 for Resident #27 indicated the CNAs were to apply a
resting hand splint to the resident's right upper extremity each morning and remove each night to prevent
contractures.
During observations, Resident #27 had her right hand clenched tightly with the fingers and thumb
positioned inward towards the palm of the hand but opened it when asked. The resident did not have a
splint to the right hand:
*on 06/23/24 at 10:48 a.m.,
*on 06/24/24 at 8:33 a.m.,
(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 8
Event ID:
675540
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
675540
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Liberty Health Care Center
1206 N Travis St
Liberty, TX 77575
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
*on 06/25/24 at 2:42 p.m., and
Level of Harm - Minimal harm
or potential for actual harm
*on 06/25/24 at 9:44 a.m.
Residents Affected - Few
During observation and interview on 06/25/24 at 9:44 a.m., Resident #27 was sitting in the common area
with her right hand closed tightly. The surveyor asked the resident to open her hand and the resident was
able to straighten all fingers out. The DON said the resident was supposed to have a splint in her hand as
ordered. She said the possible negative outcome could be the resident's hand could become contracted.
She said her expectation was for the resident to have the splint in her hand as ordered.
During observation and interview on 06/25/24 at 9:53 a.m., upon entering Resident #27's room, the DON
retrieved the resident's splint from the top of the chest of drawers and said here it is. The DON said the
splint was not applied as ordered. She said it was the CNA's responsibility to make sure the splint was
applied.
During an interview on 06/25/24 at 10:50 a.m., CNA E said she worked on Hall 600, where Resident #27
resided. She said she was not aware she was supposed to apply the splint to Resident #27's right hand
and no one had told her she was supposed to until then. She said she did look at the aide assignment
sheet for the resident and did see the splint was to be applied to the right hand but she did not ever see a
hand splint so she did not apply it. She said the possible negative outcome of not applying the splint would
be the resident's hand could get to the point of not opening and she would not be able to use it.
Review of the Prevention of the decline in Range of Motion policy dated 2023 indicated The facility in
collaboration with the medical director, director of nurses and as appropriate, physical/ occupational
consultant shall establish and utilize a systematic approach for prevention of decline in range of motion,
including the assessment, appropriate care planning, and preventive care.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675540
If continuation sheet
Page 2 of 8
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
675540
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Liberty Health Care Center
1206 N Travis St
Liberty, TX 77575
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 0693
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure that feeding tubes are not used unless there is a medical reason and the resident agrees; and
provide appropriate care for a resident with a feeding tube.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview, and record review, the facility failed to ensure that residents receiving enteral
feeding received appropriate care and services to prevent complication of enteral feeding for 1 of 1 resident
(Resident #272) reviewed for enteral feeding.
The facility failed to ensure LVN A verified placement of Resident #272's G-tube by checking for tube
placement before enteral administration of water and medications.
The facility failed to ensure LVN A administered the flushes and medications using gravity.
These failures could place residents receiving enteral nutrition and medications at increased risk of not
receiving proper nutrition, infection, aspiration, and possible injury.
Findings included:
Record review of Resident #272's physician orders dated June 2024 indicated he was a [AGE] year-old
male admitted to the facility on [DATE]. His diagnoses included dysphagia (difficulty or discomfort
swallowing). Orders indicated he was NPO (nothing by mouth), was to receive all feedings and medications
via G-tube (a tube inserted through the stomach that brings nutrition directly to the stomach) and tube
placement was to be verified before each use by change in the incremental marking on tube, documented
tube length, gastric residual volume, or by pH of aspirate.
Record review of a care plan dated 06/21/24 indicated Resident #272 had a feeding tube. Interventions
included to administer enteral feeding, medications, and water flushes as ordered.
During an observation and interview during medication administration on 06/24/24 at 09:30 a.m., LVN A did
not check placement of Resident #272's G-tube prior to administration of water flushes and medications
through the G-tube. LVN A flushed the tube with water, she drew up the medications individually with the
syringe, administered the medications using the plunger in the syringe, drew up the water between
medications using the syringe, flushed the water using the plunger in the syringe, then did the final flush of
the tube with water. LVN A said she would not have done anything different in the procedure.
During an interview on 06/25/24 at 10:35 a.m. the DON indicated staff should follow the policy for
gastrostomy tube placement check and flushes/medications should be administered via gravity. She
indicated the flushes and medications should be done via gravity and not pushed through the syringe with
the plunger. She indicated injury could occur from pushing fluids or medications through the gastrostomy
tube.
Record review of the Confirming Placement of Feeding Tubes policy and procedure revised November
2018 indicated Purpose: The purpose of this procedure is to ensure proper placement of an existing
feeding tube prior to administering enteral feedings or medication.Steps in the Procedure:
.To Confirm Placement of an Existing Feeding Tube at the Bedside:
1. Use one of the following methods to test whether the tube is properly positioned:
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675540
If continuation sheet
Page 3 of 8
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
675540
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Liberty Health Care Center
1206 N Travis St
Liberty, TX 77575
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 0693
a. Observe for symptoms of elevated gastric residual volume (GRV - Please see GVR Policy), or:
Level of Harm - Minimal harm
or potential for actual harm
(1) A sharp increase in residual volume may indicate that a small bowel tube has moved into the stomach;
(2) Little to no residual volume may suggest that the tube has migrated from the stomach to the esophagus.
Residents Affected - Few
b. Observe and check the pH of aspirate:
(1) Fasting stomach contents will have a clear and colorless or grassy green and brown appearance.
(2) Fluids from the pleural space may have a pale yellow, serous appearance.
(3) Post-pyloric/small bowel contents can be bile-stained, light to dark yellow or greenish-brown.
(4) Fasting stomach acid will have a pH of 5 or less.
(5) Fluid from the pleural space will have a pH of 7 or higher.
(6) A pH of 5 or less suggests that the tube is placed in the stomach. However, a pH of 6 or greater is not
definitive of placement outside the stomach.
2. If the above suggests improper tube positioning, do not administer feeding or medication. Notify the
Charge Nurse or Physician.
3. When correct tube placement has been verified, flush tubing with at least 30 mL water (or prescribed
amount)
Record review of the Administering Medications through an Enteral Tube policy and procedure revised
November 2018 indicated Purpose: The purpose of this procedure is to provide guidelines for the safe
administration of medications through an enteral tube Steps in the Procedure:
6. Verify placement of feeding tube: a. If you suspect improper tube positioning, do not administer feeding or
medication. Notify the Charge Nurse or Physician.
10. Administer each medication separately.
11. Reattach syringe (without plunger) to the end of the tubing.
12. Administer medication by gravity flow:
a. Pour diluted medication into the barrel of the syringe while holding the tubing slightly above the level of
insertion.
b. Open the clamp and deliver medication slowly.
c. Begin flush before the tubing drains completely.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675540
If continuation sheet
Page 4 of 8
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
675540
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Liberty Health Care Center
1206 N Travis St
Liberty, TX 77575
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 0693
Level of Harm - Minimal harm
or potential for actual harm
13. If administering more than one medication, flush with 15 mL warm purified water (or prescribed amount)
between medications.
14. When the last of the medication begins to drain from the tubing, flush the tubing with 15 mL of warm
purified water (or prescribed amount).
Residents Affected - Few
15. Quickly clamp the tubing when the flush is complete. Remove syringe
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675540
If continuation sheet
Page 5 of 8
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
675540
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Liberty Health Care Center
1206 N Travis St
Liberty, TX 77575
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.
Based on interview and record review, the facility failed to ensure pharmacy procedures to ensure an
accurate accounting of all controlled drugs and the licensed pharmacist failed to ensure the drug records
are in order and that an account of all controlled drugs is maintained and periodically reconciled for 2 of 4
medication carts reviewed for narcotic counts. (300 Hall Nurse Cart and 200/500 Halls Medication Aide
Cart)
The facility did not ensure staff were conducting accounting of Controlled Drugs at shift change on the 300
Hall Nurse Cart and 200/500 Halls Medication Aide Cart.
The Pharmacy Consultant did not ensure the Controlled Drugs - Count Record forms had signatures of the
staff indicating the Controlled Drugs were reconciled.
These failures could place residents at risk for misappropriation and drug diversion.
Findings included:
Record review of the June 2024 Controlled Drugs - Count Record form on the 300 Hall Nurse Cart
indicated:
*on the day shift the nurse going off shift did not sign the form on 1st, 5th, 6th, 10th, 12th, 13th, 19th, 20th,
and 21st;
*on the night shift the nurse going off shift did not sign the form on the 14 th ;
*on the night shift the nurse coming on shift did not sign on 4th, 5th, 8th, 11th, 12th, 13th, 18th, and 19th;
and
*there were no signatures on the day shift on the 14th and 20th; and
*there were no signatures on the night shift on the 20th.
Record review of the June 2024 Controlled Drugs - Count Record form on the 200/500 right side Halls
Medication Aide Cart indicated:
*on the day shift the Medication Aide coming on shift did not sign on 4th, 5th, 10th, 18th, 19th, 21st, 22nd,
23rd, and 24th; and
*on the night shift the Medication Aide going off shift did not sign on 4th, 5th, 8th, 10th, 18th, 19th, 21st,
22nd, 23rd, 24th, and 25th.
Record review of the Consultant Pharmacist Activity Report dated 06/18/24 indicated Special
Notes/Activities: The medication room and carts were reviewed There was no indication on the report of
missing signatures on the Controlled Drugs - Count Record forms on the medication aide or the nurse
carts.
During an interview on 06/25/24 at 12:40 p.m., MA C indicated if the narcotics were not counted
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675540
If continuation sheet
Page 6 of 8
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
675540
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Liberty Health Care Center
1206 N Travis St
Liberty, TX 77575
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
then the medications could be missing and because the sheet was not signed as to who had the cart they
would not know who would be accountable for missing medications.
During an interview on 06/25/24 at 01:09 p.m., MA D indicated she was not trained on the cart count sheet.
During an interview on 06/25/24 at 12:39 p.m., the DON indicated she expected staff to count the narcotics
on the medication carts. She indicated if the counts were not done then there could be a drug diversion and
she would not know who would be accountable for missing medications.
During an interview on 06/25/24 at 12:39 p.m., the DON indicated the no signature could indicated the
narcotic counts were not done. Pharmacy Consultant was at the facility a few days ago and reviewed the
medication aides and nurse carts. She indicated there was no report of any issues with the count sheets.
During a phone interview on 06/25/24 at 01:50 p.m., the Pharmacy Consultant indicated she was supposed
to check the signature count to ensure the staff are counting medications between shifts before they hand
off the keys. She said she did not notice the missing signatures on the cart count sheets. She said the
possible negative outcome could be a drug diversion.
Record review of a Controlled Substances policy revised April 2019 indicated Policy Statement: The facility
complies with all laws, regulations, and other requirements related to handling, storage, disposal, and
documentation of controlled medications.
Policy Interpretation and Implementation:
.4. Access to controlled medications remains locked at all times and access is recorded.
.8. Controlled substances are reconciled upon receipt, administration, disposition, and at the end of each
shift.
.12. At the End of Each Shift:
a.
Controlled medications are counted at the end of each shift. The nurse coming on duty and the nurse going
off duty determine the count together
Record review of a Pharmacy Services - Role of the Consultant Pharmacist policy revised April 2019
indicated Policy Interpretation and Implementation: 5. The consultant pharmacist will provide specific
activities related to medication regimen review including: d. review of medication storage areas at least
monthly, and medication carts at least quarterly, for proper storage and labeling of medications, cleanliness,
and expired medications;
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675540
If continuation sheet
Page 7 of 8
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
675540
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Liberty Health Care Center
1206 N Travis St
Liberty, TX 77575
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 store all drugs and biologicals in
locked compartments under proper temperature controls, and permit only authorized personnel to have
access, for 2 of 2 medications reviewed for security.
The facility did not ensure clonidine (medication to treat elevated blood pressure) and a Fentanyl patch
(narcotic opioid pain medication) medication was stored securely when it was left unattended at the nursing
station.
This failure could place residents at risk for harm by misappropriation of property and drug diversion.
Findings included:
During an observation on 06/23/24 at 12:28 p.m. of the nurse station, a card of clonidine (medication to
treat elevated blood pressure) and a Fentanyl (narcotic opioid pain medication) patch were left on the desk
unattended by a nurse or medication aide and accessible to staff, residents, and visitors.
During an interview on 06/23/24 at 12:30 p.m., the Administrator was shown the card of clonidine and
Fentanyl patch were on the desk of the nurse station unattended by a nurse or medication aide. He said
medications were not to be left at the nurse station unattended by the staff as they could be removed by
anyone walking by.
During an interview on 06/23/24 at 12:32 p.m., LVN B indicated she had the card of clonidine to put on the
cart and was reordering the Fentanyl patch when she got up to leave the nurse station. She said she
should not have left the medications at the desk.
During an interview on 06/25/24 at 02:09 p.m. during the exit, the DON indicated she was aware of the
medications being left at the nurse station and medications were not to be left to where anyone could get
them.
Record review of a Controlled Substance policy revised April 2019 indicated Policy Statement: The facility
complies with all laws, regulations, and other requirements related to handling, storage, disposal, and
documentation of controlled medications.
Policy Interpretation and Implementation:
.3. Controlled substances are stored in the medication room in a locked container, separate from containers
for any non-controlled medications.
4. Access to controlled medications remains locked at all times and access is recorded
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675540
If continuation sheet
Page 8 of 8