F 0582
Give residents notice of Medicaid/Medicare coverage and potential liability for services not covered.
Level of Harm - Minimal harm
or potential for actual harm
Based on record review, staff interview, and policy review, the facility failed to ensure the Skilled Nursing
Facility Advanced Beneficiary Notice of Non-coverage (SNF-ABN) was issued to 1 of 2 sampled residents
reviewed for beneficiary notices. (Resident #136)
Residents Affected - Few
The findings include:
A review of Resident #136's record revealed a Medicare Part A Skilled Services start date of 11/23/23, with
the last covered day of Part A services listed as 12/13/23. The record did not contain the required SNF-ABN
form.
An interview was conducted with the Social Services Director on 1/24/24 at 12:01 PM. He stated the facility
did not issue a SNF-ABN to Resident #136 because he was not aware of the requirement.
A review of the facility policy SNF Advance Beneficiary Notification (ABN) & Notice of Medicare Provider
Non-Coverage (BO-510 revised 5/1/18) revealed that the Care Center is responsible for delivering the
Notice of Medicare Provider Non-Coverage and the SNF ABN to all beneficiaries not later than 2 days,
before their covered services end and for delivering the Detailed Notice to the Quality Improvement
Organization and the beneficiary by close of business of the day the beneficiary requests a review (if a
review is requested).
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 4
Event ID:
105132
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
105132
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Lakeside Oaks
1061 Virginia St
Dunedin, FL 34698
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.
Resident #70
Review of Resident #70's record revealed a consultant pharmacist recommendation dated 7/10/23, which
indicated the resident had a diagnosis of diabetes, but a hemoglobin A1C (a blood test that measures the
individuals average blood sugar levels over the past 3 months) was not available in the medical record in
the past 6 months. The pharmacist recommended monitoring the hemoglobin A1C on the next convenient
lab day and every 6 months if meeting treatment goals, or every 3 months if therapy has changed or goals
are not being met. The pharmacist recommendation form contained a hand written telephone order by the
Director of Nursing (DON) dated 7/20/23 stating, okay to do lab draw. A review of Resident #70's record
revealed no hemoglobin A1C blood test on file.
An interview was conducted with the DON on 1/24/24 at 11:48 AM. She stated the hemoglobin A1C was
missed and not obtained. She and the Assistant DON were responsible for ensuring the pharmacy
recommendations were acted upon. She may have been interrupted during the process.
On 1/24/24, the survey team requested the pharmacy recommendations from December 2023. The review
of the consultant pharmacist for Resident #70, dated 12/18/23, revealed a recommendation to consider
adding an as needed parameter for the Glucagon injection as needed for hypoglycemia on when to
administer the medication, for example blood sugar less than 60. A review of the record revealed the
recommendation had not been acted upon by the facility. An interview was conducted with the DON on
1/24/24 at 3:15 PM. The DON stated the facility changed pharmacy consultants in December 2023 and the
new pharmacist emailed some reports in December 2023. She did not realize she did not receive all of the
reviews until the survey team requested specific pharmacy reviews for December 2023 and she did not
have them. She stated the facility expects the reports on all residents to be provided in the same month of
the review.
Review of the facility policy for Monthly Drug Regimen Review (N-866 revised 10/10/18) revealed, During
the drug regimen review, the consultant pharmacist is to identify drug regimen irregularities. Drug regimen
irregularities are to be communicated to the attending physician, the Medical Director, and the
DON/designee to complete follow up as indicated. Routine recommendations to be communicated to the
DON/designee, attending physician, and Medical Director for response and resolution, after the completion
of the Monthly Drug Regimen Review. Drug regimen irregularities identified by the consultant pharmacist
that require urgent action are to be communicated to the DON/designee for resolution with the attending
physician and/or Medical Director.
Resident #60
On 01/25/2024 during a record review for Resident #60, the 12 month Pharmacy Review revealed that the
December 2023 review had not been received by the facility or requested by the facility, and was only
discovered by facility staff after the survey team requested the Pharmacy Review for Resident #60. The
December 2023 pharmacist review recommended an antidepressant to be reviewed for a possible Gradual
Dose Reduction in an effort to find the lowest effective dose, which had not been followed up. (Photographic
evidence obtained)
Resident #44
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105132
If continuation sheet
Page 2 of 4
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
105132
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Lakeside Oaks
1061 Virginia St
Dunedin, FL 34698
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
On 01/25/2024, during record review for resident #44, the 12 month Pharmacy Review revealed the
December 2023 review had not been received by the facility or requested by the facility, and was only
discovered by facility staff after the survey team requested the Pharmacy Review for Resident #44. The
pharmacist had recommended a dose reduction for an antihistamine prescribed for Resident #44, which
had not been followed up. (Photographic evidence obtained)
Residents Affected - Few
Based on interview, record review, and policy review, the facility failed to obtain and/or act upon pharmacy
recommendations in July and December 2023 for 4 of 5 sampled residents. (Residents #26, #46, #60, #70)
The findings included:
Resident #26
On 1/25/24, a review of a Consultant Pharmacist Medication Regimen Review to Psychiatry dated 12/18/23
for Resident #26 was conducted. The review stated, .the resident is due for a gradual dose reduction in an
attempt to find the lowest effective dose. If the medication cannot be reduced at this time please check the
appropriate rationale below related to the gradual dose reduction being clinically contraindicated at this time
and make a brief clinical rational note that the benefits outweigh the risks. The form was not completed or
signed by a medical practitioner or psychiatrist at the time of the survey.
A review of the order summary report dated 1/24/24 for Resident #26 was conducted. Resident #26 had a
diagnosis of Schizoaffective disorder and Alzheimer's Disease. The resident had an order dated 8/8/23 to
take Seroquel (an antipsychotic medication) 50 mg 1 tablet by mouth twice daily. The last psychiatric
assessment for Resident #26 was completed on 12/29/23. The assessment did not provide any information
or statement regarding a gradual dose reduction for the Seroquel 50 mg twice daily for Resident #26.
Resident #46
On 1/25/24 a review of two Consultant Pharmacist Medication Regimen Reviews dated 12/18/23 for
Resident #46 was conducted. The first medication regimen review to the physician for Resident #46 was
regarding guaifenesin oral tablet 400 mg give 1 tablet by mouth two times daily for seasonal allergies. This
order was started on 10/10/23. The order stated that the medication may be used for an acute
illness/symptoms for a defined duration and the stopped or may be of a chronic nature and that the medical
staff should indicate if chronic or acute and discontinue if appropriate. The review will help reduce
overmedication. The form was not completed or signed by a medical practitioner at the time of the survey. A
review of the order summary report dated 1/24/24 for Resident #46 was conducted. Resident #46 had an
order dated 10/10/23 to take guaifenesin oral tablet 400mg tablet by mouth two times daily for seasonal
allergies.
The second medication regimen review to the nurse for Resident #46 was regarding Midodrine HCL oral
tablet 10 mg 1 tablet by mouth three times daily for Hypertension (HTN). The recommendation asked the
nurse to please evaluate the indication of hypertension vs hypotension. At the time of the survey, the form
was not signed or updated by a nurse or physician. A review of the order summary report dated 1/24/24 for
Resident #46 was conducted. The summary noted that Resident #46 had a diagnosis of Essential
Hypertension and had an order for Midodrine HCL 10 mg 1 tablet by mouth three times daily for
Hypertension (HTN).
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105132
If continuation sheet
Page 3 of 4
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
105132
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
01/25/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Lakeside Oaks
1061 Virginia St
Dunedin, FL 34698
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
On 1/25/23, a review of the Consultant Pharmacist Services Agreement effective 12/1/2023 was
conducted. The agreement indicated that the consultant pharmacy would provide general supervision of
clients pharmaceutical services including medication regimen reviews. These reports would be provided for
each resident of the facility at least once each month. The consultant pharmacy agreement indicated that
an electronic copy of the report would be sent within 3 business days to facility leadership.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105132
If continuation sheet
Page 4 of 4