F 0583
Keep residents' personal and medical records private and confidential.
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 the resident had a right to personal
privacy and confidentiality of his or her personal and medical records for 1 of 4 residents (Resident #1)
reviewed for medical record confidentiality.
Residents Affected - Few
The facility failed to ensure LVN A kept Resident #1's medical information confidential. LVN A left an
Emergency Kit Charge Slip, dated 04/05/25, with Resident #1's name and listed the medications with
administration dosage and route on the nurse station counter and in view for staff, visitors, and others.
This failure could place residents at risk of their medical information being provided to unauthorized
personnel, other residents, or visitors.
Findings include:
Record review of Resident #1's face sheet, dated 04/08/25, indicated a [AGE] year old female who was
admitted to the facility on [DATE]. Her diagnoses included anxiety (feeling of fear, dread, and uneasiness),
heart disease, and kidney disease.
During an observation of a picture provided by family member B on 04/08/25 indicated there was an
Emergency Kit Charge Slip, dated 04/05/25, completed by LVN A attached to other unknown papers on the
ledge of the nurse's station. Resident #1's name was visible and the Emergency Charge Slip indicated
Tramadol (used to treat moderate to moderately severe pain in adults) 50 mg PO and Ativan (used to treat
anxiety disorders) 0.5 mg PO.
During an interview on 04/08/25 at 2:40 p.m., LVN A indicated she left Resident #1's Emergency Kit Charge
Slip on the nurse's station to take back to the medication room and place it with the emergency
medications. She said she did not recall leaving Resident #1's information on the nursing counter on
04/05/25.
During an interview on 04/09/25 at 12:35 p.m., Family Member B said the picture of Resident #1's
Emergency Kit Charge Slip was taken on 04/06/25 at 2:30 p.m.
During an interview on 04/11/25 at 9:10 a.m., the RDCS said Resident #1's Emergency Kit Charge Slip,
dated 04/05/25, should not have been left on the nurse counter. She said all resident records were
confidential.
Record review of the facility's Resident Rights policy, dated 2002 (revised 2016), indicated 1.
(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:
675338
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
675338
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mill Creek
1105 W Hwy 418
Silsbee, TX 77656
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 0583
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Federal and state laws guarantee certain basic rights to all residents of this facility. These rights include the
resident's right to: . t. privacy and confidentiality
Record review of the facility's, undated, Confidentiality of Information policy and procedure revised
December 2006 indicated Policy Statement: Our facility shall treat all resident information confidentially.
Policy Interpretation and Implementation: Confidentiality of Information: 1. The facility will safeguard all
resident records, whether medical, financial, or social in nature, to protect the confidentiality of the
information
Event ID:
Facility ID:
675338
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
675338
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mill Creek
1105 W Hwy 418
Silsbee, TX 77656
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 - Few
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 provide pharmaceutical services, including procedures that
assured the accurate acquiring, receiving, dispensing, and administering of all drugs and biologicals, to
meet the needs of each resident for 1 of 8 residents (Resident #1) reviewed for pharmaceutical services.
The facility failed to ensure Resident #1's Ativan (used to treat anxiety disorders) was acquired.
This failure could place residents at risk of not receiving the therapeutic dosage of medication prescribed
by the physician.
Findings include:
Record review of Resident #1's face sheet, dated 04/08/25, indicated a [AGE] year-old female who was
admitted to the facility on [DATE]. Her diagnoses included anxiety (feeling of fear, dread, and uneasiness),
heart disease, and kidney disease.
Record review of Resident #1's admission MDS assessment, dated 02/23/25, indicated she was able to
make herself understood and understood others and she had moderate cognitive impairment with a
BIMS-10.
Record review of Resident #1's care plan, dated 03/24/25, indicated she was taking psychotropic
medications as evidenced by anxiety and her medication included Ativan. Interventions included monitor
and record displayed behavior or mood problems, monitor effectiveness of psychotropic medications, and
review every three months for possible dose reduction.
Record review of physician orders, dated 03/24/25, indicated Ativan 0.5 mg tablet, give .25 mg PO, break
0.5 mg tablet in half. The related diagnosis was anxiety disorder.
Record review of progress note, dated 03/24/25 at 10:11 p.m., completed by LVN C, indicated Resident #1
had increased agitation and irritation. Resident #1 was hollering in the hallway and attempted multiple times
to call family members. NP D was notified. New orders: Ativan 0.25 mg Q 12 hours PRN.
Record review of the facility's Emergency Kit Usage Log, dated 03/24/25 at 5:00 p.m., completed by LVN C
indicated she obtained 0.5 mg Ativan for Resident #1.
Record review of LVN A's statement, dated 04/10/25, indicated a telephone order was received from NP D
for Resident #1's, Ativan 0.5 mg give ½ tab Q 12 hours for increased agitation. The order was put in
the computer and faxed to the pharmacy to be filled. The RP and family made aware. The medication was
taken from the Emergency Kit with the notification slip of usage also faxed to the pharmacy.
Record review of Resident #1's MAR dated 03/24/25 indicated LVN A did not document PRN Ativan
administration.
During an interview on 04/08/25 at 2:40 p.m., LVN A said she obtained Resident #1's Ativan from the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675338
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
675338
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mill Creek
1105 W Hwy 418
Silsbee, TX 77656
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
facility's Emergency kit because there was none on the medication cart.
Level of Harm - Minimal harm
or potential for actual harm
During an interview on 04/09/25 at 10:49 a.m., LVN C said Resident #1 was hollering for her family member
and agitated on 03/24/25. She said Resident #1 was trying to call family and no one was answering the
phone. She said she obtained an order for Ativan .25 mg PRN every 12 hours due to increased agitation.
She said there was .5 mg Ativan in the emergency kit. She said she obtained the .5 mg tab and halved it
and administered .25 to Resident #1. She said she advised the next nurse on shift, LVN A, to make sure the
order was sent to the pharmacy.
Residents Affected - Few
During an interview on 04/09/25 at 1:19 p.m., NP C said she received a call from LVN A regarding Resident
#1's increased agitation. She said she ordered .25 mg every 12 hours PRN. She said she was not aware
the facility did not receive the medication from the pharmacy. She said she was not aware the pharmacy did
not have the required prescription.
During an interview on 04/11/25 at 9:00 a.m., the RDCS said all medication orders and faxes should be in
the medication binder until the medication was delivered. She said the night charge nurse (LVN C) should
reconcile medications and follow-up if the medication was not received. She said the charge nurse and
DON should follow up and ensure all the orders were received. She said the pharmacy received the fax
order for Resident #1's Ativan but they did not receive the prescription from the physician. She said she was
not able to locate the order or fax confirmation in the facility's medication binder. She said residents were at
risk of not receiving medications as needed if the facility did not follow up to ensure all medications were
received as required.
Record review of the facility's Medication Ordering Procedures, dated 2022, indicated . Reminder: Orders
for controlled substances require a written prescription from the physician .The DON and the Pharmacy
must be notified immediately of any mediations not received from the Pharmacy.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675338
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
675338
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mill Creek
1105 W Hwy 418
Silsbee, TX 77656
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 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Implement gradual dose reductions(GDR) and non-pharmacological interventions, unless contraindicated,
prior to initiating or instead of continuing psychotropic medication; and PRN orders for psychotropic
medications are only used when the medication is necessary and PRN use is limited.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review the facility failed to ensure PRN orders for psychotropic drugs were limited to
14 days unless the attending physician or prescribing practitioner believed that it was appropriate for the
PRN order to be extended beyond 14 days, he or she should document their rationale in the resident's
medical record, and indicate the duration for the PRN order for 1 of 8 residents (Resident #s 1) reviewed for
pharmacy services.
The facility failed to ensure Resident #1 had a 14-day limit for PRN Ativan (used to treat anxiety disorders).
This failure could place residents at risk of receiving unnecessary psychotropic medications and of not
receiving the intended therapeutic benefits of their psychotropic medications.
The findings include:
Record review of Resident #1's face sheet, dated 04/08/25, indicated a [AGE] year-old female who was
admitted to the facility on [DATE]. Her diagnoses included anxiety (feeling of fear, dread, and uneasiness),
heart disease, and kidney disease.
Record review of Resident #1's admission MDS assessment, dated 02/23/25, indicated she was able to
make herself understood and understood others and she had moderate cognitive impairment, with a
BIMS-10.
Record review of Resident #1's care plan, dated 03/24/25, indicated she was taking psychotropic
medications as evidenced by anxiety and her medication included Ativan. Interventions included monitor
and record displayed behavior or mood problems, monitor effectiveness of psychotropic medications, and
review every three months for possible dose reduction.
Record review of physician orders, dated 03/24/25, indicated Ativan 0.5 mg tablet, give .25 mg PO, break
0.5 mg tablet in half. The related diagnosis was anxiety disorder.
Record review of progress note, dated 03/24/25 at 10:11 p.m., completed by LVN C indicated Resident #1
had increased agitation and irritation. Resident #1 was hollering in the hallway and attempted multiple times
to call family members. The NP D was notified. New orders: Ativan 0.25 mg Q 12 hours PRN.
Record review of the facility's Emergency Kit Usage Log, dated 03/24/25 at 5:00 p.m., completed by LVN C
indicated she obtained 0.5 mg Ativan for Resident #1.
Record review of LVN A's statement, dated 04/10/25, indicated a telephone order was received from NP D
for Resident #1. Ativan 0.5 mg give ½ tab Q 12 hours for increased agitation. The order was put in
the computer and faxed to the pharmacy to be filled. The RP and family were made aware. The medication
was taken from the Emergency Kit with the notification slip of usage was also faxed to the pharmacy.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675338
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
675338
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mill Creek
1105 W Hwy 418
Silsbee, TX 77656
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 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
During an interview on 04/08/25 at 2:40 p.m., LVN A said she obtained Resident #1's Ativan from the
facility's Emergency kit. LVN A said she was not aware PRN Ativan required a 14 day limit.
During an interview on 04/09/25 at 1:19 p.m., NP C said she received a call from LVN A regarding Resident
#1's increased agitation. She said she ordered .25 mg every 12 hours PRN. She said she was not aware
the PRN Ativan required a 14 day limit and subsequent review for continuation. She said not having a stop
date on the PRN psychotropic medications could cause ill effects or the resident to receive unnecessary
medications.
During an interview on 04/09/25 at 2:30 p.m. the DON said she was not aware Resident #1 had an order for
Ativan.
During an interview on 04/11/25 at 9:00 a.m., the RDCS said she was not aware Resident #1's Ativan did
not have a 14 day limit. She said it was the responsibility of the nurse who obtained the order to ensure the
PRN Ativan was only prescribed for 14 days. The risk of not having a 14-day limit included residents
receiving unnecessary medications. She said the facility would have the pharmacist complete an audit to
ensure all PRN antipsychotics and anti-anxiety medications had a 14 day limit or physician approval for use
beyond 14 days.
Record review of the facility's Psychotropic medication Use policy, dated 2001 (July 2022), indicated . 12.
Psychotropic medications are not prescribed or given on a PRN basis unless that medication is necessary
to treat a diagnosed specific condition that is documented in the clinical record. a. PRN orders for
psychotropic medications are limited to 14 days. (1) For psychotropic medications that are NOT
antipsychotics: If the prescriber or attending physician believes it is appropriate to extend the PRN order
beyond 14 days, he or she will document the rationale for extending the use and include the duration for the
PRN order. (2) For psychotropic medications that ARE antipsychotics: PRN orders cannot be renewed
unless the attending physician or prescriber evaluates the resident and documents the appropriateness of
the medication
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675338
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
675338
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mill Creek
1105 W Hwy 418
Silsbee, TX 77656
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 - Few
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
interview and record review the facility failed to ensure, in accordance with accepted professional standards
and practices, medical record maintained for each resident were complete and accurately documented for 1
of 8 residents (Resident #1) reviewed for resident records.
The facility failed to ensure LVN A documented a progress note or nurse note of Resident #1's increased
agitation on 04/05/25.
This failure could place residents at risk for delayed care and appropriate interventions.
Findings include:
Record review of Resident #1's face sheet, dated 04/08/25, indicated a [AGE] year-old female who was
admitted to the facility on [DATE]. Her diagnoses included anxiety disorder (feeling of fear, dread, and
uneasiness), heart disease, and kidney disease.
Record review of Resident #1's admission MDS assessment, dated 02/23/25, indicated she was able to
make herself understood and understood others and she had moderate cognitive impairment indicated with
a BIMS-10.
Record review of Resident #1's care plan, dated 03/24/25, indicated she was taking psychotropic
medications as evidenced by anxiety and her medication included Ativan. Interventions included monitor
and record displayed behavior or mood problems, monitor effectiveness of psychotropic medications, and
review every three months for possible dose reduction.
Record review of Resident #1's physician orders, dated 03/24/25, indicated Ativan 0.5 mg tablet, give .25
mg PO, break 0.5 mg tablet in half. The diagnosis was anxiety disorder.
Record review of Resident #1's MAR, dated 04/05/25, completed by LVN A, indicated she was
administered half of 0.5 mg Ativan (.25 mg) at 11:07 p.m.
Record review of Resident #1's EHR indicated there was no progress note or nurse note dated 04/05/25.
There was no documentation of Resident #1's increased agitation or administration of .25 mg Ativan.
During an interview on 04/08/25 at 2:40 p.m., LVN A said she thought she documented a progress note in
Resident #1's EHR on 04/05/25 for the increased agitation and anxiety.
During an interview on 04/11/25 at 9:00 a.m., the RDCS said nursing staff were supposed to document by
exception. She said that included behaviors and change in condition in resident charts. She said residents
were at risk for delayed care if the proper documentation was not completed.
Record review of the facility's policy Charting and Documentation policy, dated 2001 (revised July 2017),
indicated All services provided to the resident, progress toward the care plan goals, or any changes in the
resident's medical, physical, functional, or psychosocial condition, shall be documented in the resident's
medical record . 2. The following information is to be documented in the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675338
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
675338
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/11/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Mill Creek
1105 W Hwy 418
Silsbee, TX 77656
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 - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
resident medical record: a. Objective observations; 2. Medications administered, Treatments or services
performed: d. Changed in the resident's condition; Events, incidents or accidents involving the resident; and
f. Progress toward or changes in the care plan goals and objectives .7. Documentation of procedures and
treatments will include care-specific details, including: a. the date and time the procedure/treatment was
provided; b. the name and title of the individual(s) who provided care; c. the assessment data and .or any
unusual findings obtained during the procedure/treatment; d. how the resident tolerated the
procedure/treatment; notification of family, physician or other staff, if indicated; and g. the signature and title
of the individual documenting.
Event ID:
Facility ID:
675338
If continuation sheet
Page 8 of 8