F 0609
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Timely report suspected abuse, neglect, or theft and report the results of the investigation to proper
authorities.
Based on staff interviews, record review and facility policy review the facility failed to report an incident of
possible neglect to the State Survey Agency related to a medication error for a critical medication for 1
(Resident #1) of 3 residents reviewed.
The findings included:
The facility's policy and procedure for Coumadin Management with a creation date of 10/2022 noted, It is
the policy that residents on Coumadin therapy will be monitored to assist in maintaining recommended
laboratory parameters as established by the attending physician . Prior to and with each medication
administration, the nurse will:
a.
Review the Medication Administration Record [MAR] to ensure consistency in medication dose orders,
b.
Document the most recent lab result (PT/INR),
c.
The physician has been notified of laboratory results, and
d.
Document the next laboratory draw date is identified.
Licensed staff receiving laboratory results are required to update the MAR, notify the physician of results,
and adjust dosage orders as necessary. Changes in dosage require the entire medication order to be
discontinued and a new order be written .
Review of the clinical record for Resident #1 revealed an admission date of 7/12/24. Diagnoses included
heart failure and a cardiac pacemaker.
The physician's orders included to administer Coumadin (blood thinner) 4 milligrams (mg) once a day at
bedtime, and PT (Prothrombin)/ INR (International Normalized Ratio) blood test (measures how long it
takes for blood to clot).
(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:
105995
Printed: 05/28/2026
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
105995
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
08/06/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Adviniacare at Naples
7801 Airport Pulling Road N
Naples, FL 34109
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 0609
Level of Harm - Minimal harm
or potential for actual harm
Review of the facility's incident investigations revealed on 7/15/24 Registered Nurse Staff A notified the
physician of the PT/INR results for Resident #1.
On 7/15/24, Registered Nurse (RN) Staff A notified the physician of the abnormal PT result of 29.9
(Reference range of 9.6 to 12.2) and INR result of 3.10 (Reference range of 0.80 to 3.5)
Residents Affected - Few
The physician issued new orders for Coumadin 3 mg daily at bedtime and repeat the PT/INR in three days.
The investigation noted RN Staff A wrote the new order for Coumadin 3 mg daily but did not discontinue the
previous Coumadin order of 4 mg.
Resident #1 received Coumadin 7 mg for three consecutive days (7/15/24, 7/16/24 and 7/17/24) instead of
Coumadin 3 mg.
On 7/18/24 the PT result was critically high at 85.8 and the INR result was greater than 8.00.
On 7/18/24 the physician was notified of the critically high PT result and INR. The physician discontinued
the Coumadin and ordered Vitamin K 5 mg (lowers INR value) to be administered intramuscularly on
7/18/24 and 7/19/24.
On 8/5/24 at 1:30 p.m., in an interview the Executive Director (ED) stated that she submitted a possible
Adverse incident report but did not consider possible neglect therefore did not submit a Federal Report to
the State Survey Agency.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105995
If continuation sheet
Page 2 of 2