F 0658
Ensure services provided by the nursing facility meet professional standards of quality.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interview and record review, the facility failed to ensure services provided by the facility met professional
standards of practice for one of six sampled residents (Resident 1) when:
Residents Affected - Few
1. A physician's (MD) order for carbidopa-levodopa (an anti-Parkinson's medication) 25-100 mg.
(milligrams, a unit of measurement) tablet, 1 tablet every 6 hours was discontinued on 6/23/23 at 6:32 a.m.,
and not reordered until 6/23/23 at 12 p.m., causing Resident 1 to go without a dose of her medication for 11
hours; and,
2. One dose of the medication on 6/22/23, two doses of the medication on 6/25/23, and one dose on 7/1/23
were administered late.
These failures had the potential to result in Resident 1 suffering negative side effects of the missed and late
doses such as worsening tremors, increased rigidity and pain.
Findings:
A review of Resident 1's admission record indicated she was admitted on [DATE], with diagnoses including
Parkinson's disease (a disorder of the central nervous system that affects movement, often including
tremors).
A review of Resident 1's clinical record included the following documents:
1. A Medication Administration Record (MAR), dated 6/1- 6/30/23, indicated the following MD orders:
a. Carbidopa-levodopa 25-100 mg. tablet, 1 tablet every 6 hours for Parkinson's disease at 2 a.m., 8 a.m., 2
p.m. and 8 p.m. The order's start date was 6/22/23 at 8 p.m. and the end date was 6/23/23 at 6:32 a.m.
b. Carbidopa-levodopa 25-100 mg. tablet, 1 tablet every 6 hours for Parkinson's disease at 12 a.m., 6 a.m.,
12 p.m. and 6 p.m. The order's start date was 6/23/23 at 12 p.m. and the end date was 1:40 p.m.
c. Carbidopa-levodopa 25-100 mg. tablet, 1 tablet every 6 hours for Parkinson's disease at 12 a.m., 6 a.m.,
12 p.m. and 6 p.m. The order's start date was 6/23/23 at 6 p.m. and the end date was 7/2/23 at 12:01 a.m.
A Medication Administration Audit Report (MAAR), dated 6/1- 6/30/23, indicated Resident 1 had
(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 2
Event ID:
555801
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
555801
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/19/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pine Creek Care Center
1139 Cirby Way
Roseville, CA 95661
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 0658
received the 2 a.m. dose at 1:01 a.m. on 6/23/23 and the 12 p.m. dose at 12:05 p.m. 11 hours later.
Level of Harm - Minimal harm
or potential for actual harm
2. The MAAR also indicated Resident 1's carbidopa-levodopa 25-100 mg. doses were administered on the
following dates and times:
Residents Affected - Few
6/22/23- 8 p.m. dose was administered at 11:25 p.m.
6/25/23- 12 a.m. dose was administered at 1:19 a.m.
6/25/23- 6 p.m. dose was administered at 7:18 p.m.
A MAAR, dated 7/1- 7/31/23, indicated Resident 1's carbidopa-levodopa 25-100 mg. 6 p.m. dose was
administered at 7:29 p.m. on 7/1/23.
In an interview, on 10/19/23 at 12:02 p.m., the Assistant Director of Nursing (ADON) stated she knew that
giving carbidopa-levodopa doses on time and at regular intervals was important for a resident with
Parkinson's disease and agreed if not, the resident could potentially experience side effects. The ADON
stated it was her expectation medications were administered from one hour prior to one hour after the
scheduled time to be considered as administered on time. The ADON confirmed the 6/22/23 8 p.m. dose,
the 6/25/23 12 a.m. and 6 p.m. doses and the 7/1/23 6 p.m. doses of carbidopa-levodopa were
administered late to Resident 1. The ADON further confirmed due to the change in the medication's
ordered time on 6/22/23 at 6:32 a.m. Resident 1 missed a morning dose of the medication. The ADON
stated this had not met her standards of nursing care for Resident 1.
A review of the facility's policy titled, Administering Medications, revised 4/19, stipulated, Medications are
administered within one (1) hour of their prescribed time .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
555801
If continuation sheet
Page 2 of 2