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.
Based on observation, interview, and record review, the facility failed to maintain timely and appropriate
pharmaceutical services for one out of three sampled residents (Resident 1) when a prescribed medication
was unavailable to be administered as ordered by the physician.
This failure caused Resident 1 to experience worsening tremors, increased rigidity, loss of balance,
confusion, and agitation due to not achieving the therapeutic dose.
Findings:
Resident 1 was admitted to the facility in early 2024 with diagnoses that included parkinsonism (brain
condition that cause slowed movements, rigidity (stiffness), and tremors), fibromyalgia (a disorder
characterized by widespread musculoskeletal pain accompanied by fatigue, sleep, memory, and mood
issues), muscle wasting, atrophy, and difficulty walking.
During a review of Resident 1's Order Summary Report (OSR), dated 6/4/24, the OSR indicated,
Rytary® Oral Capsule Extended Release 23.75-95 MG [mg, unit of measure] (Carbidopa-Levodopa)
Give 2 capsules by mouth three times a day related to PARKINSONISM .
During a review of Resident 1's Minimum Data Set (MDS, an assessment tool), dated 7/25/24, the MDS
indicated Resident 1 had no memory impairment.
During an interview on 9/16/24 at 4:39 p.m. with Resident 1, Resident 1 was lying in bed with the head of
the bed slightly elevated. Resident 1 was alert, oriented, and well-groomed. When asked if she had any
concerns, Resident 1 stated, I am worried that I may be running out of my medications again, and I don't
want to have my symptoms exacerbated. My symptoms get so bad that I crawl like a dog.
During an interview on 9/16/24 at 5:07 p.m. with Licensed Nurse (LN 1), LN 1 stated, Resident 1 only has
two capsules of Rytary® remaining for tomorrow morning dose, and the pharmacy should deliver before
noon when the next dose is due .
During an interview on 9/17/24 at 11:11 a.m. with LN 2, LN 2 stated, . we get medications delivered to the
facility at different times, 11 a.m. - noon, 6 p.m. - 7 p.m., and 3 a.m. Resident 1's medication has not yet
been delivered.
During an interview on 9/17/24 at 1 p.m. with Resident 1, Resident 1 stated they had not received their 1
p.m. dose of Rytary®, as scheduled. Resident 1 further stated their tremors were worsening and they
had increased rigidity, loss of balance, confusion, and agitation due to not achieving
(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:
055887
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
055887
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/17/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
River Bend Nursing Center
2215 Oakmont Way
West Sacramento, CA 95691
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
the therapeutic dose of the medication.
Level of Harm - Minimal harm
or potential for actual harm
During an interview on 9/17/24 at 1:30 p.m. with LN 2, LN 2 stated that Resident 1's Rytary® had not
yet been delivered. LN 2 acknowledged this could worsen Resident 1's symptoms.
Residents Affected - Few
During an interview on 9/17/24/at 2:15 p.m. with the DON, the DON stated, .Resident 1's medication has
not arrived yet . The DON acknowledged that the medication should have been administered as prescribed
by the physician or Resident 1 could start having withdrawal symptoms for not receiving her medication on
time.
During a review of records emailed on 9/18/24 at 1:13 p.m. by the DON, the DON indicated, .The resident
did not receive the medication (Rytary®) on 9/17/24 at 1 p.m. The DON was unable to provide Resident
1's Medication Administration Record (MAR) with documentation of all missed doses of medications when
requested by the Department.
During a review of the facility's policy and procedure (P&P) titled, PROVIDER PHARMACY
REQUIREMENTS, dated 2007, the P&P indicated, .Providing routine and timely pharmacy services .
During a review of the facility's policy and procedure (P&P) titled, ORDERING AND RECEIVING
NON-CONTROLLED MEDICATIONS, dated 2007, the P&P indicated, .Medications and related products
are received .on a timely basis. Reorder routine .to ensure an adequate supply is on hand.
During a review of the facility's policy and procedure (P&P) titled, Administering Medications, revised 4/19,
the P&P indicated, .Medications are administered within one (1) hour of their prescribed time .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
055887
If continuation sheet
Page 2 of 2