F 0626
Level of Harm - Minimal harm
or potential for actual harm
Permit a resident to return to the nursing home after hospitalization or therapeutic leave that exceeds
bed-hold policy.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Intake ID #
366502
Residents Affected - Few
Based on interview and record review the facility failed to permit one of three (CR #!) residents to return to
facility after being hospitalized .
The facility failed to permit CR #1 to return to the facility after hospitalization.
This failure could place residents at risk of being denied readmission.
Findings include:
Record review of CR #1's face sheet revealed an [AGE] year-old male admitted to the facility on [DATE],
discharged with return anticipated on 07/14/22. His diagnoses included Cerebral brain infraction (lack of
adequate blood supply to brain cells), Insomnia (lack of sleep) Lack of coordination, Dementia with
behavior.
Record review of CR #1's discharge MDS dated [DATE] revealed a discharge date of 07/14/22 to a
psychiatric hospital. Returned anticipated.
Record review of CR#1's quarterly MDS assessment dated [DATE]revealed a BIMs score of 2 indicating he
was severely impaired cognitively. Section on mood was coded as 00 meaning the facility was unable to
complete CR #1's mood. Section on behavior was coded as 2 which indicated behavior occurrences
multiple times.
Record review of CR #1's care plan dated 05/12/20 with multiple revision dates revealed 5/12/20- has potential to be physically aggressive (hitting) r/t Dementia, Poor impulse control-Physical
aggression towards another resident after other resident threw a soiled brief at him.
12/20/20- Physical aggression towards another resident because the other
resident was in his bed.
7/30/21- Physical behavior towards staff with no injury
8/25/21- Physical aggression towards another resident with no injury (pushed another resident)
(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 9
Event ID:
675079
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
675079
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/25/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Allenbrook
4109 Allenbrook Dr
Baytown, TX 77521
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 0626
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
9/1/21- Physical aggression towards another resident. He was hit with a spoon and this resident punched
her in the eye
12/18/21- Behavior of stacking dressers on top each other, picking up chairs and threating to throw them.
1/25/22- physical behavior- hit another resident in back. 6/25/22-physical aggression towards another
resident. 07/13/2022 - Physical aggression toward another Resident. 07/13/2022 - Physical aggression
toward of resident rejecting care and being agitated.
Interventions:
Resident placed on 1:1 supervision with family member until transfer to behavioral hospital for further
evaluation. Date Initiated: 7/13/2022 - Resident placed on 1:1 supervision with family member until transfer
to behavioral hospital for further evaluation.
When the resident becomes agitated: Intervene before agitation escalates; Guide away from source of
distress; Engage calmly in conversation; If response is aggressive, staff to walk calmly away, and approach
later.
Record review of CR#1's nurse's documentation, reflect in parts - 7/22/2022 12:10 AM: The SW spoke with
the hospital about discharge concerns. CR #1 was physically aggressive with multiple residents and staff.
At this time, it was not safe for him to return to the secured unit for the safety of all residents and staff .
Record review of Social Worker's note dated 07/22/22 reflect in part-The SW also spoke with the RP about
safety concerns. The RP was informed that due to CR #1's aggressive behavior, the IDT has recommended
that CR #1 should not return to the secured unit and a long-term Geri-psych unit may be best for his current
needs. The RP was working with the hospital to find long term placement for CR #1.
7 /13/2022 9:18PM: Family member at the resident's' side. No aggression was noted at this time.
7 /14/2022 12:25 AM EMS arrived at facility to transport the resident to local psychiatric hospital, resident
was transported via stretcher. The DON/Administrator/family member were notified about transfer.
In an interview with the DON on 08/23/22 at 1:28 PM, she said, she started working at the facility in
February of 2022. She said CR #1 had become physically aggressive with other residents and the
frequency of incidents was increasing. She said CR #1 was sent out twice to a local psychiatric hospital in
July of 2022, and the 2nd time CR #1 was not allowed to return to the facility due to the safety of other
residents
During an interview with the facility Administrator and the DON on 08/25/22 at 1:30PM, the Administrator
said the facility did not re-admit CR #1 back, due to the safety of other residents at the facility. The
Administrator said there was no policy on permitting residents back into the facility. The DON said CR #1
was not assessed and re-evaluated, but he was directed and re-directed according to his care plan.
Record review of the facility's admission packet did not address readmitting resident back to the facility after
admission to psychiatric hospital.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675079
If continuation sheet
Page 2 of 9
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
675079
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/25/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Allenbrook
4109 Allenbrook Dr
Baytown, TX 77521
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.
**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 dispensing and administration of all drugs or biologicals) to meet the
needs of each resident and ensure expired and discontinued drugs or biologicals were not available for use
in 1of 2 nurses med cart (LVN B) and one of one medication room, reviewed for pharmacy services.
The facility failed to ensure an opened Lidocaine 1% multi-dose vial partially used, and without an open
date or resident name, was removed from the nurse's med cart (LVN B).
The facility failed to ensure discontinued meds were not stored next to mixed supplies of foley catheter,
wound care supplies, suture removal and foley anchor kits, and a 30 pack of beer cans, in the one Med Rm.
The facility failed to ensure the intravenous (IV) emergency kit was sealed and secured, and the Med Room
sink without rust stains and clean.
These failures could place all residents at risk of not receiving the intended therapeutic benefit of their
medications, and the potential to facilitate drug diversions.
Findings included:
During observation on [DATE] at 1:35 p.m. of LVN B's med cart revealed an opened Lidocaine 1%
multi-dose injectable vial, partially used and without an open date. Observed no resident name on the
accessed multi-dose vial.
During observation on [DATE] at 1:45 p.m. of the Med Room revealed 2 medium sized containers of
discontinued meds were stored next to a 30 pack beer cans and 3 medium sized cardboard boxes with
mixed supplies of suture removal kits, wound care supplies, foley catheter and foley anchor kits.
Further observation on [DATE] at 1:45 p.m. of the Med Room revealed an unsealed IV emergency-kit and
an unsealed clear plastic container labeled emergency-kit with contents of a box of insect wipes and 5
syringes. The Med room sink was observed to have rust stains and was dirty with dust.
During an interview on [DATE] at 1:55 p.m. LVN B confirmed the lidocaine 1% multidose vial was opened
and accessed, but she did not know which resident it was used on. She stated the multidose vial was
partially used, with no open date or resident name on it. LVN B stated that nurses were responsible to
dispose of unlabeled, opened multidose vials and to ensure meds labeled properly. She stated she knew it
should have been removed from the med cart.
During an interview on [DATE] at 1:55 p.m. LVN B stated that the unsealed clear plastic container was not
an E-kit although labeled emergency kit. She stated however the IV emergency-kit should have been
sealed and she knew the process. She stated that we have the NYXIS (automated dispensing) for meds,
which required a password from nurses.
During an interview on [DATE] at 2:00 pm LVN C stated the 30 pack of beer cans found was ordered
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675079
If continuation sheet
Page 3 of 9
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
675079
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/25/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Allenbrook
4109 Allenbrook Dr
Baytown, TX 77521
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
for a resident, therefore it was in the Med room. She stated she would remove the plastic container labeled
emergency kit, which was not an E-kit. She stated that she did not know who placed a box of insect wipes,
with the syringes on it, and she will remove the excessive boxes with mixed supllies next to discontinued
meds.
During an interview on [DATE] at 10:00 a.m. the ADON stated the opened Lidocaine 1% multidose vial
could be from a discharged resident on completed antibiotic, but she did not know which resident it was
used on. The ADON stated an opened or accessed multidose vial should have an open date and must have
a resident name if entered and used in resident's room. She stated she would in-service staff including
topics on E-kit proper procedures and notifying the pharmacy.
During an interview on [DATE] at 2:30 p.m. ADON stated CS staff was in the process of removing the
excessive boxes in the Med room. She stated the CS staff started re-organizing the Med room and labeling
the shelves. She stated we have not used the sink, maintenance cleaned the rusts around the sink and
were working on replacing it.
During an interview on [DATE] at 3:00 p.m. the Administrator stated moving forward we would follow up all
issues on meds and the Medication room with QAPI.
Record review of facility provided policy titled, Storage of Medications dated [DATE] reflected in part,
medications and biologicals are stored safely, securely, and properly, following manufacturer's
recommendations or those of the supplier. Medication storage areas are kept clean, well lit, and free of
clutter and extreme temperatures. Once opened, these products will be acceptable to use until the
manufacturer's expiration date is reached unless the medication is in a multi-dose injectable vial.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675079
If continuation sheet
Page 4 of 9
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
675079
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/25/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Allenbrook
4109 Allenbrook Dr
Baytown, TX 77521
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 residents who use antipsychotic drugs receive
gradual dose reduction, and behavioral interventions, unless clinically necessary contraindicated, in an
effort to discontinue these drugs for 1 of 14 residents ( Residents #15) reviewed for unnecessary
psychotropic meds.
The facility administered an antipsychotic medication without adequate indications for use and did not
obtain a rationale for continuing the concurrent use of the psychotropic for Residents #15.
This failure could place any resident on psychoactive medications and those with a diagnosis of dementia
administered with antipsychotic meds, at risk for receiving unnecessary drugs and adverse reactions.
Findings included:
Record review of Resident #15's clinical record revealed an [AGE] year old male admitted to the facility on
[DATE] with diagnoses of dementia without behavioral disturbance, anxiety disorder, insomnia, conductive
hearing loss, bilateral and HTN.
Record review of Resident #15's quarterly MDS assessment, dated 6/10/22 revealed Active Diagnoses did
not have a check by the disorders Depression, Bipolar, Psychotic disorder or Schizophrenia. Mood
interview with total severity score=0. No hallucination or delusion. Resident with severely impaired
cognition. He required 1 staff supervision most ADLs. Further noted he sometimes understood, and
sometimes understands.
Record review of undated Resident #15's care plan, revealed he had impaired thought processes related to
dementia, and taking psychotropic meds related to anxiety. The resident was at risk of experiencing
adverse consequences and to monitor for side effects and effectiveness from psychotropic drug use. Ask
yes/no questions in order to determine resident's needs. Anticipate and meet needs.
Record review of Resident #15's Physician's Orders dated August 2022, revealed give Risperdal
(Risperidone) 1 mg 1 tab po at bedtime, for severe mood disorder, start date 8/02/22.; and Risperdal
(Risperidone) 0.5 mg tab po q day, for severe mood disorder, start date 8/02/22. Further noted, reflected dx:
Unspecified mood affective disorder.
Record review of Resident #15's MAR dated August 2022 revealed Resident received Risperdal
(Risperidone) 1 mg 1 tab po at bedtime, for severe mood disorder, start date 8/02/22 and Risperdal
(Risperidone) 0.5 mg tab po q day, for severe mood disorder, start date 8/02/22. Further note reflected dx:
Unspecified mood affective disorder; Antipsychotic/ Antimanic.
Record review of Resident #15's, Behavior Monitoring, dated August 2022, revealed no behaviors noted.
Monitoring for behaviors of yelling, screaming, cursing, hallucinations. dx severe mood disorder with
psychotic symptoms. Episodes: zero. No documentation of hallucinations or delusions.
During interview on 8/23/22 at 2:00 p.m. CNA E stated that Resident #15 was pleasantly confused and
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675079
If continuation sheet
Page 5 of 9
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
675079
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/25/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Allenbrook
4109 Allenbrook Dr
Baytown, TX 77521
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
redirectable most of the time. She stated she had not seen him with any verbal aggression but was a
sundowner (state of confusion occurring in the late p.m).
During interview on 8/23/22 at 2:30 p.m. the DON stated Resident #15 had an attempted elopement
behavior, a day after he tested Covid-19 (+) 7/23/22 and which could be related to increased confusion with
the room change. She further stated the ADON was responsible for overseeing psych meds and ensuring
with appropriate indication for its use or proper dx.
During interview on 8/25/22 at 10:00 a.m. the ADON stated Resident #15 received the anti-psychotic
Risperdal for dx of unspecified mood affective disorder; Antipsychotic/ Antimanic. She stated she would
re-educate the staff, that antipsychotic/antimanic was a medication classification and not the dx. The ADON
stated she was responsible to follow-up on psychotropic meds, and she would continue monitoring them.
The ADON stated the new psychological services or group just started on 8/01/22, and psych consult was
called yesterday 8/24/22, to review Resident #15's psychotropic meds.
During interview on 8/25/22 at 2:30 p.m. LVN C stated the psychiatry NP consult was called and the NP
ordered today to discontinue Resident #15's Risperdal and would be starting him on Trileptal (mood
stabilizer) medication for dx. of mood disorder.
In an interview on 8/25/22 at 3:00 p.m. the Administrator stated they would follow-up all issues on
medications with QAPI.
Record review of the facility's policy titled, Antipsychotic Medication Use for Residents with Dementia dated
11/01/219 reflected in part, Residents receiving antipsychotic meds for [NAME] fide psychiatry dx will be
evaluated regularly according to regulation. Facility will have processes in place to monitor specific
behavioral symptoms and are encouraged to use tools that enable the facility to identify changes to the
specific behaviors overtime as the person with Dementia progresses in his/her disability and or situation.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675079
If continuation sheet
Page 6 of 9
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
675079
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/25/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Allenbrook
4109 Allenbrook Dr
Baytown, TX 77521
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 0880
Provide and implement an infection prevention and control program.
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 maintain an infection prevention and control
program designed to provide safe and sanitary environment and to help prevent the development and
transmission of diseases and infections for 4 (Residents #1, #2, #46, #49) out of 4 residents reviewed for
infection control.
Residents Affected - Some
In that:
1.
MA B failed to sanitize blood pressure machine being used for multiple residents.
2.
Facility failed to ensure Resident #46's nephrostomy catheter bag was kept in a safe and sanitary place
away from the trash.
These failures could place residents at risk of cross contamination and infection.
Findings include:
1.
Resident #46
Review of Resident #46's face sheet reflected the resident was a [AGE] year old male admitted to the
facility on [DATE]. Resident' #46'sdiagnoses included Acute cystitis, obstructive and reflux uropathy,
retention of urine, left buttock wound, immobility syndrome, and multiple sclerosis.
On 08/23/2022 at 10:07 AM the surveyor observed Resident #46 in bed in his room. He had a nephrostomy
with catheter bag. The Surveyor observed the catheter bag was placed in the trash container where there
was trash. Resident #46 stated he dropped the catheter bag in the trash can because it was leaking. De
stated he did not want it to mess up his bed.
Review of Resident #46's skin assessment reflected he currently had a hip wound which had been
previously infected.
On 08/23/2022 at 10:10 AM the Surveyor called the nurse on the floor LVN C who stated the resident had
been told not to place the bag in the trash but he refused and still wanted to do it his own way. She said the
resident would always drop the catheter in the trash can. LVN C said she worked the floor regularly but
never heard the catheter bag was leaking. She stated she would provide another clean container for the
patient to place the catheter bag so it would be away from the trash. LVN C stated the deficient practice
could place the resident at risk for infection.
On 08/25/2022 at 1:55 PM during an interview with the DON, she stated the deficient practice increased
risk for infection for the resident. The DON said she was going to do in-service on the deficient practice.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675079
If continuation sheet
Page 7 of 9
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
675079
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/25/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Allenbrook
4109 Allenbrook Dr
Baytown, TX 77521
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 0880
2.
Level of Harm - Minimal harm
or potential for actual harm
Resident #2
Residents Affected - Some
Review of Resident's face sheet reflected resident was a [AGE] year-old female who was admitted to the
facility on [DATE]. Resident #2'ss diagnoses included essential hypertension, chronic pain, blood clot, and
constipation.
On 08/24/2022 at 11:07 AM, MA B was observed with three different blood pressure machines on the
medication cart, each machine had a different cuff size (wrist cuff, upper arm medium cuff and upper arm
large cuff). MA B was observed using the wrist-size cuff for Resident #2 after which he dropped the blood
pressure machine on the medication cart among two other blood pressure machines. MA B failed to
sanitize the equipment before and after using it on the resident.
3. Resident #1
Review of Resident #1's face sheet reflected the resident was a [AGE] year-old female admitted to the
facility on [DATE]. Her diagnoses included hypertension, gastro-esophageal reflux disease, generalized
edema and constipation.
On 08/24/2022 at 11:18 AM, MA B was observed using medium-size cuff machine to measure Resident
#1's blood pressure, after which he dropped it on the medication cart among two other two blood pressure
machines. MA B failed to sanitize the equipment before and after using it on Resident #1.
4. Resident #49
Review of Resident #49's face sheet reflected the resident was a [AGE] year-old male admitted to the
facility on [DATE]. His diagnoses included hypertension, anemia, constipation, and seizures.
On 08/24/2022 at 11:28 AM, MA B was observed entering Resident #49's room to check his blood pressure
using a large-size cuff machine. MA B removed the cuff from the resident and stated probably that was too
big. MA B came out of resident's room and placed the cuff on the medication cart with the others. He then
took the medium-size blood pressure cuff (same cuff he used for Resident #1 and used it for Resident #49,
after which he placed it on the medication cart among two other blood pressure machines. MA B, failed to
sanitize the equipment before and after using it on the resident.
On 08/24/2022 at 11:47 AM during an interview with MA B, he stated he understood the deficient practice
could place residents at risk for cross contamination because germs could have been transferred from one
resident to another through the blood pressure machine he failed to sanitize. MA B stated he had been
working with the facility for many years and had received trainings about prevention of infection. He also
stated they had infection control training couple of times every month.
On 08/25/2022 at 1:55 PM during an interview with the DON, she stated the residents were placed at risk
for infection. She also stated they usually trained all their staff and they were also constantly having
in-services on infection control and prevention. The DON said she was going to do an in-service related to
infection control.
On 08/24/2022 at 1:55 PM during interview with the Administrator, she stated they did not have policy that
addressed sanitization of blood pressure cuff, she stated they were only following the best
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675079
If continuation sheet
Page 8 of 9
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
675079
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/25/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Focused Care at Allenbrook
4109 Allenbrook Dr
Baytown, TX 77521
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 0880
practice which was to sanitize equipment used for multiple residents.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
675079
If continuation sheet
Page 9 of 9