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
observation, 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 1 of 8 residents (Resident #2) reviewed for pharmaceutical services.
The facility failed to ensure Morphine (pain medication) Extended Release (ER) (medication was
formulated so the drug was released slowly over time) tablet was administered without crushing according
to pharmacy packet instruction.
This failure could place residents at risk for adverse effects and not receiving the therapeutic effects of the
medication or treatment.
Findings include:
Record review of Resident #2s dated 09/27/2023 face sheet revealed she was a [AGE] year-old female
admitted on [DATE] and readmitted [DATE], with multiple sclerosis ( A disease in which the immune system
eats away at the protective covering of nerves), pain, Dysphagia (difficulty swallowing), contracture
(shortening and hardening of muscles, tendons, or other tissues, often leading to deformity and rigidity of
joints), pressure ulcers (injury to skin and underlying tissue from the prolonged pressure on the skin),
paraplegia (paralysis of the legs and lower body typically by spinal injury or disease).
Record review of Resident #2's quarterly MDS dated [DATE], revealed a BIMS score of 8, which indicated
Resident #2 had moderately impaired cognition. Resident #2's eating required limited assistance of one
staff. The resident's functional limitation in range of motion revealed impairment on both sides to her upper
and lower extremity. Resident #2's active diagnoses revealed she had a progressive neurological condition.
Swallowing and nutritional status revealed Resident #2 required a mechanically altered diet.
Record review of Resident #2's care plan, revised 09/12/2023, revealed:
Focus: The resident had a potential for uncontrolled pain related to chronic wounds and the diagnosis of
multiple sclerosis;
Goal: The resident will not have an interruption in normal activities due to pain through the review date;
(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:
455703
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
455703
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/28/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Oakmont Healthcare and Rehabilitation Center of Ka
1525 Tull Dr
Katy, TX 77449
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
Interventions: Administer analgesia per orders;
Level of Harm - Minimal harm
or potential for actual harm
Resident #2 was prescribed routine/scheduled pain medication for pain management.
Residents Affected - Few
Record review of Resident #2's medication administration record (MAR) dated 09/2023 revealed Morphine
Sulfate ER tablet extended release 15 Mg. One tablet by mouth two times a day revealed the medication
was initial to indicate the medication was administered:
PM: 09/20, 09/21, 09/22, 09/23, 09/24, 09/25 and 09/26/2023
AM: 09/21, 09/22, 09/23, 09/24, 09/25, 09/26, and 09/27/2023
Record review of Resident #2's order summary report active orders dated as of 09/27/2023 revealed
Morphine sulfate ER tablet extended release 15 Mg. Give one tablet two times a day related to pain. Order
dated 09/20/2023.
Observation on 09/27/2023 at 7:46 AM during medication administration revealed MA A dispensed
Morphine ER 15 Mg tablet in the medication cup. Continued observation at this time revealed the
medication container pharmacy directions for administration read Do Not Chew or Crush- Swallow Whole.
MA A crushed the medication with a pill crusher. MA A added a spoonful of pudding to the crushed
medication in the medication cup. MA A administered the medication to Resident #2. Resident #2 was
observed in bed with the head of her bed elevated. Resident #2 swallowed the medication.
Interview on 09/27/2023 at 9:15 AM MA A stated she crushed Resident #2's Morphine ER because the
resident was on a pureed diet. MA A stated she thought Resident #2 had difficulty swallowing. MA A stated
the physician's order Resident #2's medications could be crushed. MA A stated she was unsure how long
the medication had been crushed. MA A stated she should have notified the DON the medication had been
crushed. MA A stated the DON and ADON monitor medication administration. MA A was not sure how often
the medication administrations were monitored. MA A stated the risk of crushing an ER tablet was it could
get into the resident's system faster. MA A stated to prevent this in the future the doctor should be notified.
The medication should be changed to liquid.
Interview on 09/27/2023 at 10:19 AM the DON stated MA A told her she crushed Resident #2's
extended-release medication that should not have been crushed. The DON stated the NP and hospice
nurse have been notified. The DON stated the order was changed to liquid. The DON stated she did not
know how often it was crushed. The DON stated she and the ADON do random medication administration
observations. The DON stated the pharmacy consultant also did a medication administration observation.
The DON stated the risk of the crushed extended release was the medication becomes instant release. The
DON stated MA A should have notified the charge nurse to have the order changed. The DON stated to
prevent this from occurring again the nurses and medication aides were all being reeducated. The DON
stated the resident sometimes wanted the medications crushed.
Interview on 09/27/2023 at 11:03 AM Resident #2 stated she does get the medication crushed in pudding.
Resident #2 stated she did not care how she received it.
Interview on 09/27/2023 at 11:13 AM the Administrator stated she was notified MA A crushed a medication
that should not have been crushed. The Administrator stated she understood the risk was the chemistry of
the medication would be changed if crushed. The Administrator stated the crushing could change the effect
of the medication. The Administrator stated the medication aides and nurses were
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455703
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
455703
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/28/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Oakmont Healthcare and Rehabilitation Center of Ka
1525 Tull Dr
Katy, TX 77449
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
reeducated.
Level of Harm - Minimal harm
or potential for actual harm
Phone interview on 09/28/2023 at 9:33 AM the Facility's Pharmacy Director stated extended release should
not be crushed because it was meant to be slow acting and work over an extended time period. The
Facility's Pharmacy Director stated when the tablet was crushed it allowed the medications action to be
faster and shorter acting. As the interview continued the Pharmacy Director stated labels were on the
packages to indicate not to crush or chew. The Pharmacy Director stated he will have the pharmacist do
more medication administration observations.
Residents Affected - Few
Record review of the facility's policy and procedure titled Oral Solid Medication Administration dated 2003
read in part .Some preparations are not meant to be opened or crushed: such as enteric coated, sustained
release, and sublingual products. Check with the pharmacy or your drug information text if you question the
appropriateness of crushing a medication .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
455703
If continuation sheet
Page 3 of 3