F 0644
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Coordinate assessments with the pre-admission screening and resident review program; and referring for
services as needed.
Based on interview, record review, and facility policy review, the facility failed to submit a status change to a
Level I Pre-admission Screening and Resident Review (PASARR) following a new mental health diagnosis
for 1 (Resident #62) of 3 residents reviewed for PASARR. Specifically, Resident #62 had a positive Level I
PASARR and was later diagnosed with a new mental health disorder and the facility failed to submit a
status change to the resident's Level 1 PASARR evaluation.
Findings included:
A facility policy titled, admission Criteria, revised in March 2019, indicated, 9. All new admissions and
readmissions are screened for mental disorders (MD), intellectual disabilities (ID) or related disorders (RD)
per the Medicaid Pre-admission Screening and Resident Review (PASARR) process. a. The facility
conducts a Level I PASARR screen for all potential admissions, regardless of payer source, to determine if
the individual meets the criteria for a MD, ID, or RD.
An admission Record revealed the facility admitted Resident #62 on 06/12/2020. According to the
admission Record, the resident had a medical history that included diagnoses of bipolar type
schizoaffective disorder (onset date 04/14/2024), bipolar disorder (onset date 06/12/2020), major
depressive disorder (onset date 06/12/2020), and anxiety disorder (onset date 06/12/2020).
An annual Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 05/29/2024, revealed
Resident #62 had a Brief Interview for Mental Status (BIMS) score of 15, which indicated the resident had
intact cognition. The MDS revealed the resident received antipsychotic and antidepressant medications
during the assessment period.
Resident #62's care plan included a focus area revised on 10/12/2023 that indicated the resident received
an antipsychotic medication of aripiprazole related to a bipolar disorder diagnosis manifested by mood
swings. Interventions directed staff to administer psychotropic medications as ordered and to monitor and
document episodes of bipolar depression daily. Resident #62's care plan included a focus area revised on
10/12/2023 that indicated the resident received an antidepressant medication of sertraline related to
depression. Interventions directed staff to administer antidepressant medications as ordered by the
physician and to monitor and document side effects and effectiveness every shift.
Resident #62's Order Summary Report, with active orders as of 09/19/2024, contained an order, dated
08/23/2024, for aripiprazole (antipsychotic) 5 milligrams (mg) by mouth every other day for rapid, alternating
changes in mood related to bipolar schizoaffective disorder. Resident #62's Order Summary Report,
contained an order, dated 08/23/2024, for sertraline hydrochloric acid (HCl)
(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 15
Event ID:
056301
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0644
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
(antidepressant) 12.5 mg by mouth one time a day for sad facial expressions and flat affect related to major
depressive disorder. Resident #62's Order Summary Report, contained an order, dated 08/22/2024, for
valproic acid 250 mg by mouth every 12 hours for audio/visual hallucinations related to bipolar disorder.
Resident #62's Preadmission Screening and Resident Review (PASRR) Level I Screening, dated
11/16/2022, revealed the screening was positive for suspected MI. Further review revealed a mental
disorder diagnosis of major depressive disorder.
Review of Resident #62's medical record during the recertification survey from 09/16/2024 to 09/19/2024
revealed another Level I PASARR had not been completed since 11/16/2022.
During an interview on 09/19/2024 at 8:33 AM, the MDS Director stated Level I PASARR screenings were
completed at the hospital and he reviewed them for any discrepancies upon admission. The MDS Director
further stated when a resident obtained a new mental health diagnosis after admission, a new Level I
PASARR should be completed to capture that diagnosis and when Resident #62 obtained their
schizoaffective disorder diagnosis, a new Level I PASARR should have been completed.
During an interview on 09/19/2024 at 8:40 AM, Medical Records (MR) stated Level I PASARR screenings
were completed at the hospital prior to admission and an updated Level I PASARR should be completed
with a new mental health diagnosis. MR further stated Resident #62's new diagnosis of schizoaffective
disorder was probably missed and that was why a new Level I PASARR had not been completed.
During an interview on 09/19/2024 at 10:07 AM, the Director of Nursing (DON) stated the Level I PASARR
process screened residents with mental illness to determine if they would benefit from additional services.
The DON further stated when a resident received a new mental health diagnosis, staff should complete an
updated Level I PASARR to see if the resident qualified for those additional services.
During an interview on 09/19/2024 at 10:26 AM, the [NAME] President (VP) of Clinical Operations stated
the Level I PASARR screenings were completed prior to admission. The VP of Clinical Operations further
stated a new Level I PASARR should be completed with a new mental health disorder to ensure that
resident received the care they need for their new diagnosis.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 2 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0645
PASARR screening for Mental disorders or Intellectual Disabilities
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview, record review, and facility policy review, the facility failed to ensure a Level I Pre-admission
Screening and Resident Review (PASARR) was complete and accurate for 2 (Resident #62 and Resident
#12) of 3 residents reviewed for PASARR. Specifically, Resident #62 and Resident #12 had a Level I
PASARR completed that did not capture all their mental health diagnoses.
Residents Affected - Few
Findings included:
A facility policy titled, admission Criteria, revised in March 2019, indicated, 9. All new admissions and
readmissions are screened for mental disorders (MD), intellectual disabilities (ID) or related disorders (RD)
per the Medicaid Pre-admission Screening and Resident Review (PASARR) process. a. The facility
conducts a Level I PASARR screen for all potential admissions, regardless of payer source, to determine if
the individual meets the criteria for a MD, ID, or RD.
1. An admission Record revealed the facility admitted Resident #62 on 06/12/2020. According to the
admission Record, the resident had a medical history that included diagnoses of bipolar type
schizoaffective disorder (onset date 04/14/2024), bipolar disorder (onset date 06/12/2020), major
depressive disorder (onset date 06/12/2020), and anxiety disorder (onset date 06/12/2020).
An annual Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 05/29/2024, revealed
Resident #62 had a Brief Interview for Mental Status (BIMS) score of 15, which indicated the resident had
intact cognition. The MDS revealed the resident received antipsychotic and antidepressant medications
during the assessment period.
Resident #62's care plan included a focus area revised on 10/12/2023 that indicated the resident received
an antipsychotic medication of aripiprazole related to a bipolar disorder diagnosis manifested by mood
swings. Interventions directed staff to administer psychotropic medications as ordered and to monitor and
document episodes of bipolar depression daily. Resident #62's care plan included a focus area revised on
10/12/2023 that indicated the resident received an antidepressant medication of sertraline related to
depression. Interventions directed staff to administer antidepressant medications as ordered by the
physician and to monitor and document side effects and effectiveness every shift.
Resident #62's Order Summary Report, with active orders as of 09/19/2024, contained an order, dated
08/23/2024, for aripiprazole (antipsychotic) 5 milligrams (mg) by mouth every other day for rapid, alternating
changes in mood related to bipolar schizoaffective disorder. Resident #62's Order Summary Report,
contained an order, dated 08/23/2024, for sertraline hydrochloric acid (HCl) (antidepressant) 12.5 mg by
mouth one time a day for sad facial expressions and flat affect related to major depressive disorder.
Resident #62's Order Summary Report, contained an order, dated 08/22/2024, for valproic acid 250 mg by
mouth every 12 hours for audio/visual hallucinations related to bipolar disorder.
Resident #62's Preadmission Screening and Resident Review (PASRR) Level I Screening, dated
11/16/2022, revealed the screening was positive for suspected MI. Further review revealed a mental
disorder diagnosis of major depressive disorder; the diagnoses of anxiety and bipolar disorders were not
listed.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 3 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0645
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
During an interview on 09/19/2024 at 8:33 AM, the MDS Director stated Level I PASARR screenings were
completed at the hospital and he reviewed them for any discrepancies upon admission. The MDS Director
further stated Resident #62's Level I PASARR was inaccurate because it did not include the resident's
diagnoses of bipolar and anxiety disorder.
During an interview on 09/19/2024 at 8:40 AM, Medical Records (MR) stated Level I PASARR screenings
were completed at the hospital prior to admission and that Resident #62's PASARR was inaccurate
because it did not capture all the resident's mental health diagnoses.
During an interview on 09/19/2024 at 10:07 AM, the Director of Nursing (DON) stated the Level I PASARR
process screened residents with mental illness to determine if they would benefit from additional services.
The DON further stated Resident #62's Level I PASARR should have captured the resident's bipolar and
anxiety disorder diagnoses.
During an interview on 09/19/2024 at 10:26 AM, the [NAME] President (VP) of Clinical Operations stated
the Level I PASARR screenings were completed prior to admission. The VP of Clinical Operations further
stated bipolar and anxiety disorder diagnoses should have been captured on Resident #62's Level I
PASARR.
2. An admission Record specified the facility originally admitted Resident #12 on 12/20/2017 with a
readmission on [DATE]. According to the admission Record, the resident had a medical history that
included diagnoses of delusional disorder (onset date 12/20/2017), psychosis (onset date 12/20/2017),
single episode major depressive disorder (onset date 12/20/2017), recurrent depressive disorders (onset
date 12/20/2017), and hallucinations (onset date 12/20/2017).
A quarterly Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 08/08/2024, revealed
Resident #12 had a Brief Interview for Mental Status (BIMS) score of 15, which indicated the resident had
intact cognition. The MDS revealed the resident had diagnoses of depression and psychotic disorder.
Resident #12's Preadmission Screening and Resident Review (PASRR) Level I Screening dated
11/10/2021 indicated the resident had no diagnosed mental disorder.
Resident #12's Level I PASRR letter dated 11/10/2021 specified the Level I PASRR submitted on
11/10/2021 was negative due to no mental illness.
During an interview on 09/19/2024 at 8:33 AM, the MDS Director stated a new admission PASRR was
completed at the hospital and was reviewed for discrepancies. The MDS Director stated any changes to
psychotropics medications, significant change, a cognitive decline, or a new psychiatric diagnosis indicated
for another PASRR screen to be completed. The MDS Director stated Resident #12's PASRR screen was
inaccurate without the diagnoses addressed.
During an interview on 09/19/2024 at 8:40 AM, Medical Records (MR) stated Resident #12's PASRR was
inaccurate when it was not marked with all the diagnoses the resident had.
During an interview on 09/19/2024 at 10:07 AM, the Director of Nursing (DON) stated the PASRR process
screened residents for mental illness to determine if additional psychiatric care would be needed. The DON
stated Resident #12 had mental health diagnoses, so the screening form was not accurate.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 4 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0645
Level of Harm - Minimal harm
or potential for actual harm
During an interview on 09/19/2024 at 10:26 AM, the [NAME] President (VP) of Clinical Operations stated
the PASRR needed to be reviewed when a resident was admitted to make sure it was accurate with
diagnoses, medications, and resident history, and they should complete a new one if it was inaccurate. The
VP of Clinical Operations stated Resident #12's PASRR was inaccurate without the diagnoses identified.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 5 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0756
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure a licensed pharmacist perform a monthly drug regimen review, including the medical chart,
following irregularity reporting guidelines in developed policies and procedures.
Based on interview, record review, and facility policy review, the facility failed to follow pharmacy
recommendations for 1 (Resident #19) of 5 residents reviewed for unnecessary medications. Specifically,
the facility failed to respond to May and June 2024 pharmacy recommendations for an AIMS (abnormal
involuntary movement scale) assessment for Resident #19.
Findings included:
A facility policy titled, Antipsychotic Medication Use, revised 12/2016, indicated, 17. Nursing staff shall
monitor for and report any of the following side effects and adverse consequences of antipsychotic
medications to the attending physician: a. General/anticholinergic: constipation, blurred vision, dry mouth,
urinary retention, sedation; b. Cardiovascular: orthostatic hypotension, arrhythmias; c. Metabolic: increase in
total cholesterol/triglycerides, unstable or poorly controlled blood sugar, weight gain; or d. Neurologic:
akathisia, dystonia, extrapyramidal effects, akinesia, or tardive dyskinesia, stroke or TIA [transient ischemic
attack].
A facility policy titled, Medication Regimen Reviews, revised 05/2019, indicated, 9. An 'irregularity' refers to
the use of medication that is inconsistent with accepted pharmaceutical services standards of practice; is
not supported by medical evidence; and/or impedes or interferes with achieving the intended outcomes of
pharmaceutical services. It may also include the use of medication without indication, without adequate
monitoring, in excessive doses, and or in the presence of adverse consequences. The policy revealed, 11. If
the physician does not provide a timely or adequate response, or the consultant pharmacist identifies that
no action has been taken, he/she contacts the medical director or (if the medical director is the physician of
record) the administrator. 12. The attending physician documents in the medical record that the irregularity
has been reviewed and what (if any) action was taken to address it.
An admission Record revealed the facility admitted Resident #19 on 03/29/2017. According to the
admission Record, the resident had a medical history that included diagnoses of unspecified dementia,
restlessness and agitation, and major depressive disorder.
An annual Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 09/06/2024, revealed
Resident #19 had a Brief Interview for Mental Status (BIMS) score of 5, which indicated the resident had
severe cognitive impairment. The MDS revealed the resident received antipsychotic and antidepressant
medications during the assessment period.
Resident #19's care plan included a focus area initiated 10/03/2022, that indicated the resident used
antipsychotic medication for agitation manifested by picking at their brief and smearing stool. Interventions
directed staff to administer antipsychotic medications as ordered by the physician, monitor for side effects
and effectiveness every shift, monitor for adverse reactions of psychotropic medications, and to consult with
the pharmacy.
Resident #19's Order Summary Report, with active orders as of 09/19/2024, revealed an order dated
09/13/2024 for quetiapine fumarate oral tablet 75 milligrams (mg) by mouth at bedtime. The Order
Summary Report revealed an order dated 09/13/2024 for quetiapine fumarate oral tablet 75 mg by mouth
one time a day.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 6 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0756
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Resident #19's Consultant Pharmacist's Medication Regimen Review, dated 05/31/2024, revealed a
recommendation that included Resident is due for an AIMS assessment due to antipsychotic medication
use. It should be done every 3 months.
Resident #19's Consultant Pharmacist's Medication Regimen Review, dated 06/28/2024, revealed a
recommendation that included Resident is due for an AIMS assessment due to antipsychotic medication
use. It should be done every 3 months.
Resident #19's Abnormal Involuntary Movement Scale (AIMS), dated 12/05/2023, revealed a score of 1,
which indicated the resident had a low risk of movement disorder. Further review revealed the AIMS dated
12/05/2023 was the most recent AIMS score in the resident's record.
During an interview on 09/18/2024 at 10:48 AM, Licensed Practical Nurse (LPN) #6 stated she did not
know how often AIMS assessments were done for residents. LPN #6 stated if the pharmacist
recommended an AIMS assessment for a resident, it was the responsibility of the registered nurse (RN)
supervisor or the Director of Nursing (DON) to complete the assessment.
During an interview on 09/18/2024 at 12:14 PM, LPN #1 stated the RN on the floor did the AIMS
assessment if the pharmacist recommended it.
During an interview on 09/18/2024 at 12:51 PM, RN #7 stated the AIMS assessment was done for
residents on psychotropic medications every six months. RN #7 stated if the pharmacy made the
recommendation for an AIMS assessment, then the specific instructions came down to the floor where they
could be implemented. He stated he was not sure why Resident #19 had not received an AIMS assessment
in response to the pharmacy recommendation, nor had he seen the recommendation.
During an interview on 09/19/2024 at 10:16 AM, the DON stated that staff should follow the medication
regimen review recommendations and do the psychotropic monitoring as recommended. The DON stated
the facility did not do the AIMS assessment, and she expected staff to do the monitoring recommended by
the pharmacist.
During an interview on 09/19/2024 at 10:34 AM, the [NAME] President (VP) of Clinical Operations stated
that she expected staff to go over the pharmacy recommendations and implement that recommendation.
She stated the nursing recommendations are put in with an order that would notify nurses to implement the
recommendation. The VP of Clinical Operations stated when the facility transitioned from their old electronic
medical record system to a new one, the AIMS assessment changed, and this was likely why Resident
#19's AIMS assessment was not done.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 7 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0759
Ensure medication error rates are not 5 percent or greater.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, interview, record review, and facility policy review, the facility failed to ensure a
medication error rate less than 5 percent (%). There were 2 errors out of 32 opportunities, which resulted in
a 6.25% medication error rate for 2 (Resident #5 and Resident #86) of 4 residents observed for medication
administration.
Residents Affected - Few
Findings included:
A facility policy titled, Administering Medications, revised 04/2019, specified, 4. Medications are
administered in accordance with prescriber orders, including any required time frame.
1. An admission Record revealed the facility admitted Resident #5 on 10/17/2022. According to the
admission Record, the resident had a medical history that included diagnoses of constipation and rectal
prolapse.
A quarterly Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 07/18/2024, revealed
Resident #5 had a Brief Interview for Mental Status (BIMS) score of 15, which indicated the resident had
intact cognition.
Resident #5's Order Summary Report, with active orders as of 09/18/2024, revealed an order dated
10/26/2021 for docusate sodium with instructions to give 250 milligrams (mg) by mouth in the evening for
constipation.
During an observation of medication pass on 09/17/2024 at 8:26 AM, Licensed Practical Nurse (LPN) #2
prepared and administered docusate sodium 100 mg to Resident #5.
During an interview on 09/18/2024 at 12:19 PM, LPN #2 stated she had administered the docusate sodium
to Resident #5. LPN #2 reviewed Resident #5's physician orders and stated the docusate sodium was not
due at the time she administered it, and it was not ordered to be given as needed.
2. An admission Record revealed the facility admitted Resident #86 on 02/16/2024. According to the
admission Record, the resident had a medical history that included a diagnosis of type 2 diabetes mellitus.
An admission Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 08/08/2024,
revealed Resident #86 had a Brief Interview for Mental Status (BIMS) score of 15, which indicated the
resident had intact cognition.
Resident #86's Order Summary Report, with active orders as of 09/18/2024, revealed an order dated
08/02/2024 for insulin lispro injection solution 100 unit/milliliters (mL) with instructions to inject 12 units
subcutaneously before meals.
During an observation of medication pass on 09/17/2024 at 10:59 AM, Licensed Practical Nurse (LPN) #3
prepared insulin lispro to be administered to Resident #86. LPN #3 applied the needle to a Humalog
(insulin lispro) KwikPen, then turned the dial to 2 units, then continued to roll the dial to 14 units and stated,
I am priming the insulin. LPN #3 went to enter Resident #86's room and the surveyor stopped her and
asked about the 2 units to prime. LPN #3 stated again she was priming the insulin. During the observation
the [NAME] President (VP) of Clinical Operations was asked to help explain
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 8 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0759
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
what LPN #3 was communicating. The VP of Clinical Operations asked LPN #3 about the two extra units
and LPN #3 stated she guessed the resident would get extra units if administered. The VP of Clinical
Operations stated LPN #3 would be retrained immediately.
During an interview on 09/18/2024 at 6:58 AM, LPN #4 stated the process for insulin administration was to
prepare the needle, prime the needle with two units, then turn the dial to the amount the physician ordered.
During an interview on 09/18/2024 at 12:27 PM, LPN #1 stated the process for insulin administration was to
prime the pen with two units. She stated after it was primed with two units, then turn the dial on the pen to
the physician-ordered dose.
During a telephone interview on 09/18/2024 at 1:30 PM, the Pharmacy Consultant stated the insulin needle
had to be primed to ensure the correct dose was administered. The Pharmacy Consultant stated a couple
of units difference in the insulin could make a difference. The Pharmacy Consultant stated if the dial was
turned to 14 units without priming the needle, the dose was not correct. The Pharmacy Consultant stated
they needed to prime the insulin needle first, then the dial would go back to zero, then turn the dial to the
physician-ordered dose to administer the insulin.
During an interview on 09/19/2024 at 10:07 AM, the Director of Nursing (DON) stated she expected the
nurses to read the physician orders, follow physician orders, and follow all the rights to medication
administration. The DON stated she did not want any medications errors; she expected the medication error
rate to be less than 5%.
During an interview on 09/19/2024 at 10:26 AM, the VP of Clinical Operations stated she expected staff to
be educated to prevent medication errors. The VP of Clinical Operations stated the medication error rate
was not acceptable and additional training was needed to prevent errors.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 9 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Minimal harm
or potential for actual harm
2. A facility policy titled, Administering Medications, revised in April 2019, indicated, Medications are
administered in a safe and timely manner, and as prescribed.
Residents Affected - Few
An admission Record revealed the facility admitted Resident #62 on 06/12/2020. According to the
admission Record, the resident had a medical history that included diagnoses of congestive heart failure
(CHF) and hypertension (HTN).
A quarterly Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 08/29/2024, revealed
Resident #62 had a Brief Interview for Mental Status (BIMS) score of 12, which indicated the resident had
moderate cognitive impairment. The MDS also indicated the resident received a diuretic in the seven days
prior to the assessment.
Resident #62's care plan included a focus area revised on 05/29/2024 that indicated the resident had a risk
for decreased cardiac output related to the presence of a pacemaker.
Resident #62's Order Summary Report, with active orders as of 09/18/2024, contained an order, dated
11/15/2022, for amlodipine besylate oral tablet (anti-hypertensive) 10 milligrams (mg) by mouth one time a
day for HTN, with instructions to hold if the resident's systolic blood pressure (SBP, the top number of a
blood pressure reading) was less than (<) 100 millimeters mercury (mmHg) or heart rate (HR) < 60 beats
per minute (bpm). Resident #62's Order Summary Report, contained an order, dated 07/22/2024, for
furosemide oral tablet (diuretic) 20 mg by mouth two times a day for CHF, with instructions to hold if SBP <
100 mmHg or HR < 60 bpm.
Resident #62's Medication Administration Record [MAR], for the timeframe from 09/01/2024 through
09/17/2024, reveal a transcription on an order for amlodipine besylate oral tablet 10 mg by mouth one time
a day for HTN, hold if SBP < 100 mmHg or HR < 60 bpm. Further review revealed staff documented that
the medication was administered when the resident's HR was below the prescribed parameters on:
- 09/02/2024: 55 bpm
- 09/08/2024: 58 bpm
- 09/13/2024: 59 bpm
Resident #62's MAR for the timeframe from 09/01/2024 through 09/17/2024 reveal a transcription on an
order for furosemide oral tablet 20 mg by mouth two times a day for CHF, hold if SBP < 100 mmHg or HR <
60 bpm. Further review revealed staff documented that the medication was administered when the
resident's HR was below the prescribed parameters on:
- 09/02/2024: 55 bpm
- 09/08/2024: 58 bpm
- 09/13/2024: 59 bpm
Resident #62's August 2024 MAR reveal a transcription on an order for amlodipine besylate oral tablet 10
mg by mouth one time a day for HTN, hold if SBP < 100 mmHg or HR < 60 bpm. Further review
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 10 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0760
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
revealed staff documented that the medication was administered on 08/23/2024 when the resident's HR
was 59 bpm.
Resident #62's August 2024 MAR reveal a transcription on an order for furosemide oral tablet 20 mg by
mouth two times a day for CHF, hold if SBP < 100 mmHg or HR < 60 bpm. Further review revealed staff
documented that the medication was administered on 08/23/2024 when the resident's HR was 59 bpm.
Resident #62's July 2024 MAR reveal a transcription on an order for amlodipine besylate oral tablet 10 mg
by mouth one time a day for HTN, hold if SBP < 100 mmHg or HR < 60 bpm. Further review revealed staff
documented that the medication was administered on 07/23/2024 when the resident's HR was 59 bpm.
Resident #62's July 2024 MAR reveal a transcription on an order for furosemide oral tablet 20 mg by mouth
two times a day for CHF, hold if SBP < 100 mmHg or HR < 60 bpm. Further review revealed staff
documented that the medication was administered on 07/23/2024 when the resident's HR was 59 bpm.
During an interview on 09/18/2024 at 1:00 PM, Licensed Practical Nurse (LPN) #2 stated it was important
to follow vital sign parameters if a medication order specified it. Per LPN #2, Resident #62's HR ran on the
lower side and if a resident's HR was below 60 bpm, staff did not want to give a medication that could
further lower it. LPN #2 then stated she administered the medications when Resident #62's HR was below
the specified parameter because she did not want to stop a daily medication just because their HR was a
couple points below the prescribed parameter.
During an interview on 09/18/2024 at 1:30 PM, the Pharmacy Consultant stated nursing should not
administer medications that lowered a resident's blood pressure or HR if those vital sign readings were
already low. The Pharmacy Consultant stated this could cause the resident to become dizzy, increased their
fall risk, and could cause heart problems if a resident's HR was too low.
During an interview on 09/18/2024 at 3:05 PM, the Nurse Practitioner (NP) stated vital sign parameters
were included in the orders to instruct the nurses on when to administer or hold furosemide and
amlodipine. The NP stated these medications lowered blood pressure and HR, and nursing should hold the
medications if the HR was already low. Per the NP, these medications would further lower the HR causing
the resident to become dizzy and increased their fall risk.
During an interview on 09/19/2024 at 10:07 AM, the Director of Nursing (DON) stated she expected the
nurses to follow the physician's orders and to know the importance of following vital sign parameters when
administering medications. The DON then stated she expected the nurses to hold a medication that
lowered a resident's HR when it was already low; it could cause the resident's HR to lower further causing
adverse effects.
During an interview on 09/19/2024 at 10:26 AM, the [NAME] President (VP) of Clinical Operations stated
she expected the nurses to hold a medication if there were parameters outlined in the medication order.
The VP of Clinical Operations further stated if the physician included parameters on when to hold a
medication that affected a resident's HR in the medication order, that medication should be held if a
resident's HR was already too low to prevent any adverse effects.
Based on observation, interview, record review, facility document review, and facility policy review, the
facility failed to ensure 1 (Resident #86) of 4 residents observed for medication administration was free
from a significant medication error and failed to follow vital sign parameters when
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 11 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0760
administering medications for 1 (Resident #62) of 5 residents reviewed for unnecessary medications.
Level of Harm - Minimal harm
or potential for actual harm
Findings included:
Residents Affected - Few
1. A facility policy titled, Administering Medications, revised 04/2019, specified, 4. Medications are
administered in accordance with prescriber orders, including any required time frame.
An Instructions for Use for a Humalog (insulin lispro) KwikPen revised by the manufacturer on 07/2023,
specified, Prime before each injection. Priming your Pen means removing the air from the Needle and
Cartridge that may collect during normal use and ensure that the Pen is working correctly. If you do not
prime before each injection, you may get too much or too little insulin. Step 6: To prime your Pen, turn the
Dose Knob to select 2 units. Step 7: Hold your Pen with the Needle pointing up. Tap the Cartridge Holder
gently to collect air bubbles at the top. Step 8: Continue holding your Pen with needle pointing up. Push the
Dose Knob in until it stops, and '0' is seen in the Dose Window. Hold the Dose Knob in and count to 5
slowly. You should see insulin at the tip of the needle. If you do not see insulin, repeat priming steps 6 to 8,
no more than 4 times.
An admission Record revealed the facility admitted Resident #86 on 02/16/2024. According to the
admission Record, the resident had a medical history that included a diagnosis of type 2 diabetes mellitus.
An admission Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 08/08/2024,
revealed Resident #86 had a Brief Interview for Mental Status (BIMS) score of 15, which indicated the
resident had intact cognition.
Resident #86's Order Summary Report, with active orders as of 09/18/2024, revealed an order dated
08/02/2024 for insulin lispro injection solution 100 unit/milliliters (mL) with instructions to inject 12 units
subcutaneously before meals.
During an observation of medication pass on 09/17/2024 at 10:59 AM, Licensed Practical Nurse (LPN) #3
prepared insulin lispro to be administered to Resident #86. LPN #3 applied the needle to a Humalog
(insulin lispro) KwikPen, then turned the dial to 2 units, then continued to roll the dial to 14 units and stated,
I am priming the insulin. LPN #3 went to enter Resident #86's room and the surveyor stopped her and
asked about the 2 units to prime. LPN #3 stated again she was priming the insulin. During the observation
the [NAME] President (VP) of Clinical Operations was asked to help explain what LPN #3 was
communicating. The VP of Clinical Operations asked LPN #3 about the two extra units and LPN #3 stated
she guessed the resident would get extra units if administered. The VP of Clinical Operations stated LPN #3
would be retrained immediately.
During an interview on 09/18/2024 at 6:58 AM, LPN #4 stated the process for insulin administration was to
prepare the needle, prime the needle with two units, then turn the dial to the amount the physician ordered.
During an interview on 09/18/2024 at 12:27 PM, LPN #1 stated the process for insulin administration was to
prime the pen with two units. She stated after it was primed with two units, then turn the dial on the pen to
the physician-ordered dose.
During a telephone interview on 09/18/2024 at 1:30 PM, the Pharmacy Consultant stated the insulin needle
had to be primed to ensure the correct dose was administered. The Pharmacy Consultant stated a
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 12 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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 0760
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
couple of units difference in the insulin could make a difference. The Pharmacy Consultant stated if the dial
was turned to 14 units without priming the needle, the dose was not correct. The Pharmacy Consultant
stated they needed to prime the insulin needle first, then the dial would go back to zero, then turn the dial to
the physician-ordered dose to administer the insulin.
During an interview on 09/19/2024 at 10:07 AM, the Director of Nursing (DON) stated she expected the
nurses to read the physician orders, follow physician orders, and follow all the rights to medication
administration.
During an interview on 09/19/2024 at 10:26 AM, the VP of Clinical Operations stated she expected staff to
be educated to prevent medication errors. The VP of Clinical Operations stated additional training was
needed to prevent errors.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 13 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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
2. An admission Record indicated the facility admitted Resident #22 on 04/28/2021. According to the
admission Record, the resident had a medical history that included a diagnosis of type 2 diabetes mellitus.
Residents Affected - Some
An annual Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 06/20/2024, revealed
Resident #22 had severe impairment in cognitive skills for daily decision making and had short-term and
long-term memory problems per a staff assessment of mental status (SAMS).
Resident #22's care plan included a focus area revised on 08/01/2024 that indicated the resident had the
potential for impairment in skin integrity.
Resident #22's Order Summary Report, with active orders as of 09/18/2024, contained an order dated
08/24/2024 for betadine-soaked gauze and dry gauze over the left big toe daily until resolved.
During an observation on 09/18/2024 at 9:58 AM, Licensed Practical Nurse (LPN) #1 provided wound care
for Resident #22. A small open area was noted to the resident's left hallux. LPN #1 did not implement
enhanced barrier precautions and wore only gloves during the provision of wound care.
During an interview on 09/18/2024 at 10:10 AM, LPN #1 stated she was not familiar with enhanced barrier
precautions and did not know to wear a gown and gloves when providing wound care.
During an interview on 09/18/2024 at 2:11 PM, the Infection Preventionist (IP) stated she did know the
specifics about enhanced barrier precautions. The IP stated the facility had not implemented enhanced
barrier precautions.
Based on observation, interview, record review, and facility policy review, the facility failed to implement
enhanced barrier precautions (EBP) during high-contact resident care activities for 2 (Residents #81 and
Resident #22) of 2 residents observed during wound care.
Findings included:
A facility policy titled, Enhanced Barrier Precautions, dated 08/2024, indicated, 1. Enhanced barrier
precautions (EBPs) are used as an infection prevention and control intervention to reduce the transmission
of multi-drug resistant [sic] organisms (MDROs) to residents. 2. EBPs employ targeted gown and glove use
in addition to standard precautions during high contact resident care activities when contact precautions do
not otherwise apply. The policy revealed, 3. Examples of high-contact resident care activities requiring the
use of gown and gloves for EBPs included: h. wound care (any skin opening requiring a dressing). The
policy further indicated, 5. EBPs are indicated (when contact precautions do not otherwise apply) for
residents with wounds and/or indwelling medical devices regardless of MDRO colonization.
1. An admission Record revealed that the facility admitted Resident #81 on 09/03/2024. According to the
admission Record, the resident had a medical history that included diagnoses of type 2 diabetes mellitus
with diabetic neuropathy, cellulitis, unspecified open wound on the right foot, and acquired absence of other
right toe(s).
An admission Minimum Data Set (MDS), with an Assessment Reference Date (ARD) of 09/07/2024,
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 14 of 15
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
056301
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/19/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Golden Modesto Care Center
1900 Coffee Road
Modesto, CA 95355
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
revealed Resident #81 had a Brief Interview for Mental Status (BIMS) score of 15, which indicated the
resident had intact cognition. The MDS also indicated Resident #81 had an infection of the foot, diabetic
foot ulcer(s), and surgical wound(s).
Resident #81's care plan included a focus area initiated 09/04/2024 that indicated the resident had an
actual infection caused by methicillin-susceptible staphylococcus aureus. Interventions directed staff to
administer antibiotics per order, monitor intravenous site for signs and symptoms of infection, and provide
treatment(s) as ordered. Further review revealed the resident had a peripherally inserted central catheter to
their right upper extremity. The care plan also included a focus area initiated 09/04/2024 that indicated the
resident had an alteration in skin integrity due to an open wound to their right lower extremity. Interventions
directed staff to provide treatment as ordered.
Resident #81's Order Summary Report, with active orders as of 09/19/2024, contained an order, dated
09/18/2024, to cleanse distal diabetic foot ulcer to the right plantar foot with normal saline, pat dry, apply a
wet to dry betadine dressing, wrap with kerlix, and secure with ace bandage every day and evening shift.
The Order Summary Report also contained an order, dated 09/18/2024 to cleanse incision site to right
plantar foot with normal saline, pat dry, apply a wet to dry betadine dressing, wrap with kerlix, and secure
with ace bandage every day and evening shift.
During an observation of wound care for Resident #81 on 09/18/2024 at 1:58 PM, Licensed Practical Nurse
(LPN) #5 was observed using standard precautions, not enhanced barrier precautions. LPN #5 did not have
on a gown during wound care.
During an interview on 09/18/2024 at 2:11 PM, LPN #5 stated that she did not know about enhanced
barrier precautions.
During an interview on 09/19/2024 at 10:16 PM, the Director of Nursing (DON) stated that EBP was meant
to decrease the spread of MDROs in nursing homes. The DON stated direct hands-on care with residents
increased the risk of transmission, so full personal protective equipment (PPE), was meant to reduce that
risk. The DON stated she expected going forward that staff use a gown and gloves when providing
high-contact care.
During an interview on 09/19/2024 at 10:34 PM, the [NAME] President of Clinical Operations stated that
EBP was meant to protect residents from MDROs. The VP of Clinical Operations stated it was important to
protect residents and staff, so nobody transmitted those infections to someone else. The VP of Clinical
Operations stated it was her expectation that staff use EBP.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
056301
If continuation sheet
Page 15 of 15