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
assure the accurate acquiring, receiving, dispensing, and administering of all drugs and biologicals) to
meet the needs of each resident for one (Resident #1) of five residents reviewed for medications.
-The facility failed to have Resident #1's Hydromorphone (used to manage pain) available for
administration, which caused the resident to miss two doses.
This failure could place residents at risk of not receiving their medication treatment(s) as ordered by the
physician to receive the full therapeutic benefit.
Findings included:
Record review of Resident #1's face sheet, dated 4/30/24, reflected the resident was a [AGE] year-old
female admitted to the facility on [DATE] with diagnoses that included: unspecified pain, schizoaffective
disorder (mood disorder), type II diabetes, epilepsy (seizure disorder), kidney failure, hypertension (high
blood pressure), edema (swelling caused by trapped fluid in tissue), and heart failure.
Record review of Resident #1's quarterly MDS Assessment, dated 4/10/24, reflected the resident was
cognitively intact with a BIMs score of 15. Further review reflected Resident #1 required moderate
assistance or supervision with most ADLs.
Record review of Resident #1's care plan, dated 8/2/23, reflected the resident had a problem with pain
management with interventions that included screen/assess for pain on admission and daily, obtain pain
management history from resident to target prior experiences, assess resident's knowledge of side effects
and safety precautions related to use of pain medication and nonpharmacologic measures, assess the
resident's ability to use pain reporting scale, assess for change in bowel habits, resident will participate in
making choices regarding pain management, observe for behaviors that indicate pain, and instruct resident
in pain medication regimen.
Review of Resident #1's active order summary, dated 8/3/23, reflected the resident was ordered the
following medications for pain:
-Hydromorphone 2mg tablet every 8 hours (12AM, 8AM, 4PM)
-OxyContin 10mg tablet every 12 hours.
(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 3
Event ID:
676369
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
676369
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/30/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Hollymead
4101 Long Prairie Road
Flower Mound, TX 75028
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
Record review of Resident #1's MAR for April 2024, reflected, the resident's Hydromorphone was not
administered on 04/29/24 at 12:00 AM or 8:00 AM. LVN C coded the MAR as not completed at 12:00 AM
and LVN A coded the MAR as not completed at 8:00 AM.
Record review of Resident #1's controlled drug receipt/record/disposition form reflected Hydromorphone
2mg (90 tablets) was received at the facility on 4/29/24 and the first dose was signed out by RN B on
4/29/24 at 6:30 PM.
In an interview on 4/30/24 at 1:23 PM, the DON stated she had not been made aware of any medication
issues in about 2 months until Resident #1 recently spoke to her about concerns with the facility running
out of her pain medication. The DON stated staff attempted to get Resident #1's Hydromorphone refilled
last Thursday (4/25/24) and the pharmacy reported it was too early. The DON stated the MD sent in the
prescription on 4/29/24 and the Hydromorphone was received at the facility on the same day. The DON
stated Resident #1 did not miss any doses of the medication to her knowledge.
In an interview on 4/30/24 at 1:50 PM, LVN A stated she worked at the facility for about a week. LVN A
stated she worked with Resident #1 on 4/29/24, 6:00 AM-2:00 PM. LVN A stated at the start of her shift,
Resident #1 informed her that she was out of Hydromorphone. LVN A stated she notified the MD
immediately and showed Resident #1 the message to reassure her that it was being taken care of. LVN A
stated Resident #1 was upset about not having her medication; however, the resident did not report feeling
extreme pain or being unwell. LVN A stated Resident #1 had Oxycontin available for pain. LVN A stated the
medication had not arrived at the facility by the end of her shift at 2:00 PM.
In an interview on 4/30/24 at 2:00 PM, the Regional Nurse stated insurance companies made it difficult to
get pain medications, which sometimes caused the facility to run out before the MD could submit a new
prescription. The Regional Nurse stated the medication packs had a section marked off for the reorder
period and staff knew to notify the MD at that point; however, the insurance company determined when the
prescription could be filled. The Regional Nurse stated the expectation was for staff to monitor the
medications closely and communicate with the DON and MD when medications were getting low or any
issues with reordering to prevent the facility from not having the medication available to administer as
ordered.
In an interview on 4/30/24 at 2:48 PM, the MD stated he received a message from staff one day last week
informing that Resident #1's Hydromorphone needed to be refilled. The MD stated he had written a
prescription for a 30-day supply that ended on 4/28/24. The MD stated the insurance company would not
allow a new prescription for the Hydromorphone to be written prior to 4/28/24, so he sent in a new
prescription on 4/29/24. The MD stated the primary concern for a resident missing doses of a medication
like Hydromorphone would be withdrawal symptoms; however, he did not have concerns for Resident #1
missing 2 doses. The MD stated Resident #1 also had an order for Oxycontin that was administered for
pain, and although the pain management may not have been as optimal, it was being treated.
In an interview on 4/30/24 at 3:02 PM, the VP of Pharmacy Operations stated the FDA was strict on
controlled substance to minimize the risk of misuse and diversion. The VP of Pharmacy Operations stated
Resident #1's insurance company would reject a prescription for her Hydromorphone if it was submitted
more than two days from last dispense day. The VP of Pharmacy Operation stated the prescription's last
dispense day was on 4/28/24, so it could have been reordered on 4/26/24. The VP of Pharmacy Operation
stated the pharmacy was a 7-day operation and the facility could have reordered the medication even over
the weekend, and a STAT request would get the medication to the facility within 4 hours.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676369
If continuation sheet
Page 2 of 3
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
676369
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/30/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Hollymead
4101 Long Prairie Road
Flower Mound, TX 75028
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
In an interview on 4/30/24 at 3:37 PM, RN B stated she worked at the facility for about 6 months, 2:00
PM-10:00 PM. RN B stated she worked on 4/29/24 with Resident #1. RN B stated she was the receiving
nurse when Resident #1's Hydromorphone arrived at the facility around 6:00 PM. RN B stated she checked
the medication to make sure it matched the MD orders and signed off for it. RN B stated she immediately
administered Resident #1's evening dose. RN B stated Resident #1 had complained about not having her
medication; however, she did not report having diarrhea or exhibit other signs of withdrawal or being in
excruciating pain.
In an interview on 4/30/24 at 3:45 PM, LVN C stated she worked PRN for the facility and had only worked
about 10 shifts. LVN C stated she worked 10:00 PM-6:00 AM. She stated she worked overnight on 4/28/24
with Resident #1. LVN C stated there was no Hydromorphone available in the facility to administer to
Resident #1 for her 12AM dose. LVN C stated Resident #1 was asleep when the Hydromorphone was due,
and she did not wake up in pain or to ask for the medication. LVN C stated she did not notify anyone that
the medication was out because she thought it was the ADON or DON's responsibility to reorder controlled
medications.
In an interview on 4/30/24 at 4:42 PM, the DON stated the expectation was for her nurses to reorder all
meds at least 7 days in advance. The DON stated if the insurance company required a smaller window to
reorder meds, she would still expect her nurses to notify the MD and DON 7 days in advance and it would
be the responsibility of the MD, ADON, and DON to follow up with the pharmacy. The DON stated the risk of
running out of pain medication is that the resident could experience pain.
In an interview on 4/30/24 at 4:55 PM, CNA D stated she worked for the facility for a month, first shift. She
stated she worked with Resident #1 on 4/29/24 and the resident seemed fine. CNA D stated Resident #1
did not report having diarrhea, being in pain, or feeling ill. She stated Resident #1 was eating and acting like
her normal self.
A facility policy on medication ordering/refills was requested on 04/30/24 and the Regional Nurse stated the
facility did not have one.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
676369
If continuation sheet
Page 3 of 3