F 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Honor the resident's right to request, refuse, and/or discontinue treatment, to participate in or refuse to
participate in experimental research, and to formulate an advance directive.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record reviews and interviews, the facility failed to ensure there was a physician order for the code status of
Do Not Resuscitate (DNR), and that the DNR code status was accurate on the electronic medical record, or
that a care plan was in place for the Advance Directives for one resident (Resident #63) out of the sampled
thirty-two residents.
Findings included:
A review of the admission Record revealed that Resident #63 was initially admitted into the facility on
[DATE].
Section C-Cognitive Patterns of the Minimum Data Set (MDS) dated [DATE] indicated that Resident #63
had a Brief Interview for Mental Status (BIMS) score of 15 out of 15 indicating cognitively intact.
A review of the resident's current physician orders for February 2021 revealed an order for full code dated
01/21/21.
A review of the banner on the electronic medical record indicated that Resident #63's code status was full
code.
A review of the documents listed under the miscellaneous tab on the electronic record revealed a State of
Florida Do Not Resuscitate (DNR) Order form dated 01/20/21.
The resident did not have a care plan in place for Advanced Directives.
On 02/25/21 at 11:30 a.m., Staff H, Licensed Practical Nurse (LPN), reported if a resident was to code, she
would grab the paper chart plus the crash cart, or look at the banner in the electronic chart. Staff H was
asked to confirm Resident #63's code status. Staff H, referred to the paper chart and the electronic banner
and then she stated, Does not look like she is a DNR, and there is nothing in the advanced directives
section, so she is full code.
During an interview on 02/26/21 at 10:33 a.m. with Resident #63, she was asked about her code status.
She stated, Do not resuscitate me. I have had a rough life. Let me go.
On 02/26/21 at 10:55 a.m., the Regional Clinical Director/ Interim Director of Nursing (DON) was asked
what was the correct code status for Resident #63 after showing her the current physician order
(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:
105650
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0578
Level of Harm - Minimal harm
or potential for actual harm
and electronic banner stating full code and the DNR form dated 01/20/21. She stated the resident should
be DNR.
On 02/26/21 at 11:41 a.m., the Interim DON stated staff should look at the orders for code status. There
was also a code status book on each unit and she confirmed Resident #63 was a DNR.
Residents Affected - Few
A review of the facility policy titled, Advanced Directives, reviewed date of 5/24/16, documented the policy
as, The resident has the right to accept or refuse medical or surgical treatment and, at the individual's
option, formulate an advance directive. The procedure section revealed:
5. The attending physician must document in the medical record the discussion with the resident or
surrogate regarding choices and decision of advance directives.
a. Upon executing any valid Advance Directive, the designated paperwork will be placed in the resident's
medical record, under the Advance Directive tab .
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 2 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observations, record reviews, and interviews, the facility failed to implement the care plan related to a
wander/elopement alarm for one resident (Resident #71) out of the total sample of thirty-two residents.
Findings included:
On 02/25/21 at 11:19 a.m., Resident #71 was observed in bed sleeping and a wander/elopement alarm
was observed on his right ankle.
A review of the admission Record revealed that Resident #71's most recent admission date was 01/25/21.
The resident's diagnoses included, but were not limited to, dementia with Lewy Bodies, major depressive
disorder, and mood disorder.
A review of Section C- Cognitive Patterns of the Minimum Data Set (MDS) dated [DATE] revealed that
Resident #71 had a Brief Interview for Mental Status (BIMS) score of 07 out of 15, indicating severe
impairment.
A review of the active physician orders as of 02/26/21 for Resident #71 revealed an order to apply a
wander/elopement alarm to the right ankle due to poor safety awareness dated 02/12/21. There was no
physician order for checking the placement and functioning of the wander/elopement alarm.
Resident #71 had a care plan in place for risk of elopement initiated on 02/12/2021. The interventions
included, but were not limited to, an alerting bracelet placed on the right ankle, check alerting bracelet
function every day, and check alerting bracelet placement every shift.
A review of the task screen for certified nursing assistants revealed that there was a task related to
checking the functioning and placement of the wander/elopement alarm, but there was no documentation
showing the placement and functioning of the wander/elopement alarm was conducted.
A review of the Treatment Administration Record (TAR) for February 2021 revealed that there was no
documentation related to checking the functioning and placement of the wander/elopement alarm.
On 02/25/21 at 11:20 a.m., Staff H, Licensed Practical Nurse (LPN), reported that the nurses and Certified
Nursing Assistants (CNAs) were responsible for checking the placement and functioning of the
wander/elopement alarms.
On 02/26/21 at 8:50 a.m., the Regional Clinical Director/ Interim Director of Nursing (DON) stated nurses
are supposed to check the functioning of the wander/elopement alarms. The CNAs can check them, but
usually it was the nurses.
On 02/26/21 at 10:20 a.m., Staff H, LPN, confirmed that there was no documentation related to checking of
the functioning and placement of the wander/elopement alarm.
On 02/26/21 at 11:41 a.m., the Interim DON confirmed that there was no documentation related to
checking the functioning of the wander/elopement alarm. She stated that the previous DON did not enter
the orders correctly.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 3 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0656
The policy provided by the facility title, Wander/Elopement Alarm System Testing, with a reviewed date of
05/24/16 revealed the following:
Level of Harm - Minimal harm
or potential for actual harm
Signaling Device Placement Verification
Residents Affected - Few
1. Perform regular and frequent checks to verify the operation of signaling device(s).
Signaling Device Testing
1. Test signaling devices at least daily.
Documentation
1. Document verification of placement and test for all signaling devices daily.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 4 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0684
Provide appropriate treatment and care according to orders, resident’s preferences and goals.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record reviews and interviews, the facility failed to ensure treatment and care in accordance with
professional standards of practice for one resident (Resident #71), by failing to notify the physician of
elevated glucose levels as ordered by the physician, out of the total sample of thirty-two residents.
Residents Affected - Few
Findings included:
A review of the admission Record revealed that Resident #71's most recent admission date was 01/25/21.
The resident's diagnoses included, but were not limited, to Type II diabetes, dementia with Lewy Bodies,
major depressive disorder, and mood disorder.
A review of Section C- Cognitive Patterns of the Minimum Data Set (MDS) dated [DATE] revealed that
Resident #71 had a Brief Interview for Mental Status (BIMS) score of 07 out of 15, indicating severe
impairment.
A review of the active physician orders as of 01/25/21 revealed the following order: blood glucose checks
before meals and at bedtime for diabetes mellitus fingerstick. Call medical doctor if blood sugar <60 or
>250.
A review of the Medication Administration Record (MAR) for January 2021 revealed that Resident #71's
blood sugar was higher than 250 on the 26th and 29th-31st of January 2021.
A review of the MAR for February 2021 revealed that Resident #71's blood sugar was higher than 250 on
the 1st-6th, 8th, 10th-15th, 21st, and 23rd of February 2021.
A review of the progress notes from 01/24/21 to 02/26/21 revealed that there was no documentation related
to contact with the medical doctor in regard to Resident #71's blood sugars being higher than 250.
On 02/25/21 at 11:20 a.m., Staff H, Licensed Practical Nurse (LPN), stated that the order was inaccurate
for the blood glucose checks, and that she had not been contacting the doctor if the blood sugars were
higher than 250. She stated that she would have to get the order clarified.
On 02/26/21 at 8:50 a.m., the Regional Clinical Director/ Interim Director of Nursing (DON) stated that she
would expect the nurses to contact the doctor.
A review of the policy titled, Physician Orders, revised on 10/24/17, revealed the purpose as, Physician
orders are obtained to provide a clear direction in the care of the resident.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 5 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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
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.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interviews and record reviews, the facility failed to provide ordered medications in a timely manner to one
resident (#240) of 32 sampled residents.
Findings included:
A review of Resident #240's medical record revealed that Resident #240 was admitted to the facility on
[DATE] with diagnoses of osteoarthritis, Alzheimer's Disease, and nondisplaced fracture of fourth cervical
vertebra.
A review of Resident #240's care plan revealed a problem, dated 02/10/2021, that Resident #240 was at
risk for pain. Interventions included administer analgesics as ordered.
A review of Resident #240's physician's orders revealed an order, dated 02/10/2021, for Tramadol 50
milligrams (mg) by mouth in the morning for severe pain control, which was discontinued on 02/13/2021.
Resident #240's physician's orders also revealed an order, dated 02/14/2021 for Tramadol 25 mg by mouth
in the morning for pain.
A review of Resident #240's Medication Administration Record (MAR) for February 2021 revealed that
Tramadol 50 mg was administered one time on 02/11/2021 and Tramadol 25 mg was administered on
02/07/2021 and 02/08/2021. The MAR documentation revealed a chart code of 9 on 02/10/2021,
02/12/2021, 02/14/2021 through 02/16/2021, and 02/19/2021 through 02/25/2021. The chart code of 9 was
described as Other/See Nurse Notes, on the Chart Codes table. A chart code of 6 was documented on the
MAR on 02/13/2021. The chart code of 6 was described as hospitalized , on the Chart Codes table.
A review of Resident #240's Progress Notes revealed the following documentation:
- eMAR (electronic Medication Administration Record) Medication Administration Note, dated 02/11/2021 at
05:50 AM: Tramadol 50 mg: Prescription needed. MD (Doctor of Medicine) service called at this time.
- eMAR Medication Administration Note, dated 02/12/2021 at 06:20 AM: Tramadol 50 mg: Med not
available; waiting for pharmacy delivery.
- eMAR Medication Administration Note, dated 02/14/2021 at 05:50 AM: Tramadol 25 mg: Medication not
available.
- eMAR Medication Administration Note, dated 02/15/2021 at 05:38 AM: Tramadol 25 mg: Medication
unavailable, script needed, will contact physician.
- eMAR Medication Administration Note, dated 02/16/2021 at 06:22 AM: Tramadol 25 mg: Medication
unavailable, script needed, will contact physician.
- eMAR Medication Administration Note, dated 02/17/2021 at 05:23 AM: Tramadol 25 mg: Prescription
needed.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 6 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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
Level of Harm - Minimal harm
or potential for actual harm
- eMAR Medication Administration Note, dated 02/18/2021 at 05:53 AM: Tramadol 25 mg: Prescription in
progress.
- eMAR Medication Administration Note, dated 02/19/2021 at 05:29 AM: Tramadol 25 mg: Med not given
due to waiting for pharmacy delivery.
Residents Affected - Few
- eMAR Medication Administration Note, dated 02/20/2021 at 07:16 AM: Tramadol 25 mg: Medication
unavailable for administration. Attending nurse to contact pharmacy.
- eMAR Medication Administration Note, dated 02/21/2021 at 05:54 AM: Tramadol 25 mg: Medication
unavailable.
- eMAR Medication Administration Note, dated 02/22/2021 at 05:19 AM: Tramadol 25 mg: Medication not
available.
- eMAR Medication Administration Note, dated 02/23/2021 at 06:27 AM: Tramadol 25 mg: Medication not
available, physician contacted.
- eMAR Medication Administration Note, dated 02/24/2021 at 06:02 AM: Tramadol 25 mg: Awaiting for
delivery.
- eMAR Medication Administration Note, dated 02/25/2021 at 05:54 AM: Tramadol 25 mg: Medication not
available.
An interview was conducted on 02/26/2021 at 8:59 a.m. with the facility's Director of Nursing (DON). The
DON stated that when a new order is entered into the electronic charting system, then the medication can
be pulled from the medication storage system as long as the resident had a prescription. Medication cards
would normally arrive by the next morning, but could be pulled from the medication storage system if
needed before then. The DON stated that she would expect nursing staff to follow up with the pharmacy if
the medication did not arrive timely and document the follow up in the charting system. The DON also
stated that Tramadol was available in the medication storage system and that there's no reason why
Resident #240 should not have gotten the medication as ordered.
An interview was conducted on 02/26/2021 at 9:19 a.m. with Staff I, Licensed Practical Nurse (LPN). Staff I,
LPN stated that Resident #240 still needed a prescription for her Tramadol and that the medication was not
delivered from pharmacy. Staff I, LPN stated that the medication was placed on hold because they did not
have the medication in yet. Staff I, LPN also stated that it did not normally take that long for a medication to
arrive and that the matter should have been followed up on by nursing staff. Tramadol would be available in
the medication storage system.
An interview was conducted on 02/26/2021 at 10:02 a.m. with Staff J, Registered Nurse (RN). Staff J, RN
stated that Resident #240's Tramadol was placed on hold yesterday 02/25/2021 by the pharmacy due to a
possible allergy. Normal practice would be for nursing staff to call the physician right away, but Staff J, RN
was not able to state why Resident #240's medication orders were not followed up on.
An interview was conducted on 03/04/21 at 2:16 p.m. with the facility's Consultant Pharmacist, who stated
that when a new medication was ordered the nursing staff would obtain a prescription from the provider, fax
the prescription to the pharmacy, and enter the order into the electronic system. If
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 7 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
the medication was needed right away, nursing staff could call the pharmacy and obtain an authorization
code to enter into the medication storage system to obtain a dose. If the medication was needed right away
and it was not in the medication storage system, the nursing staff could make a STAT (immediate) request
and the pharmacy would deliver the medication within 4 hours.
A review of the facility's medication storage system list revealed that Tramadol 50 mg was available in the
storage system.
A review of the facility policy titled, Ordering & Receiving Medications, revised on 05/22/2018, revealed that
all new orders should be sent electronically when possible to the pharmacy for processing. If unable to
send an order electronically the order may be faxed to the pharmacy. When sending a STAT order to the
pharmacy, the nurse must immediately call the pharmacy and inform them of the STAT nature of the order.
The policy also revealed that Schedule II narcotic medications will be dispensed by the pharmacy after
receiving a signed prescription written by the prescribing physician. In some situations, the pharmacy may
dispense a short supply of the medication when given a verbal order from the prescribing physician to the
pharmacist. This allows the physician time to get the written signed prescription to the pharmacy if the
facility has a hard copy of the schedule II medication, a copy should be faxed to the pharmacy with the
medication order.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 8 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Implement gradual dose reductions(GDR) and non-pharmacological interventions, unless contraindicated,
prior to initiating or instead of continuing psychotropic medication; and PRN orders for psychotropic
medications are only used when the medication is necessary and PRN use is limited.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interview and record review, the facility failed to 1) ensure behavioral monitoring for
psychotropic medications was consistently documented for two residents (#25 and #240) of five residents
reviewed, 2) obtain and consistently complete consents for use of psychotropic medications for four
residents (#25, #240, #71 and #39) of five residents reviewed, and 3) perform blood glucose monitoring for
one resident (#25) receiving insulin of five residents reviewed.
Findings included:
A record review for Resident #25 revealed an admission date of 11/09/2020, with diagnosis that included
Major Depressive Disorder (MDD) and Diabetes as per the admission face sheet. A review of the Quarterly
Minimum Data Set (MDS) dated [DATE] showed under Section C, Brief Interview for Mental Status (BIMS)
score of 15, indicating cognitively intact, Section N, Insulin, antidepressant, anticoagulant and diuretic
received on 7 out of 7 days. A review of the Medication Administration Record (MAR) included the following
medications:
-Remeron 15 mg (milligrams) orally at bedtime for MDD with a start date of 01/21/2021
-Insulin 70/30 12 units in the morning subcutaneously for diabetes with a start date of 12/30/2020.
Further review of the MAR revealed an order for fasting blood sugar each morning with a start date of
12/23/2020 and a discontinue date of 02/09/2021. No further orders for blood glucose monitoring were
identified, nor was any other blood glucose measurements contained within the resident's record since the
discontinuation of this order.
Review of the Physician Orders for Resident #25 revealed:
Psychoactive Medication: Document number of targeted behaviors, behavior code, intervention code,
outcome of intervention code, and side effect code every shift, with a start date of 11/11/2020. A review of
the Behavior Monitoring Record for 1) January 2021 revealed 14 shifts without documentation present; the
missing shifts occurred on multiple different days of the week; and 2) February 2021 (to date) revealed 16
shifts without documentation present; the missing shifts occurred on multiple different days of the week.
A review of the Psychoactive Medication Consent for Resident #25 revealed a drug dosage and frequency
of 'Remeron 15 mg QHS [at bedtime]', with a targeted behavior of 'appetite'; the Potential Side Effects
section was not completed. The form was signed by the resident on 12/7/20.
A review of the Care Plan for Resident #25 initiated on 02/02/2021 showed:
Focus: Resident uses psychotropic medications r/t [related to] depression
Goal: Resident will remain free of drug related complications including movement disorder, discomfort.
Hypotension, gait disturbance, constipation/impaction, or cognitive/behavioral impairment
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 9 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0758
through the review date. Target date: 05/17/2021
Level of Harm - Minimal harm
or potential for actual harm
Interventions included: Monitor occurrence of target behaviors and monitor specific target behaviors;
possible risk and casual/contributing factors for behaviors, desired outcomes, ongoing efficacy of
individualized/non pharmalogical approaches and potential for adverse consequences.
Residents Affected - Some
An observation of Resident #25 was conducted on 02/25/2021 at 3:47 p.m. The resident was observed
seated in a chair in his room watching TV. He was dressed and groomed with no odors noted. The resident
refused an interview.
A facility-provided policy titled Psychotropic Medication Assessment and Monitoring dated 10/30/2018 was
reviewed. It revealed:
b) Psychoactive Medication consent signed by the resident/resident representative
d) Monitoring of residents receiving antipsychotic medication will be completed by a licensed nurse as per
acceptable standards of practice using the behavior monitoring record.
During an interview with the Interim Director of Nursing (DON) on 02/26/21 at 9:07 a.m., she stated it was
her expectation that blood sugar monitoring would occur for a resident who is receiving regular doses of
insulin. The DON further stated it is her expectation that behavioral monitoring is completed every shift for
residents receiving psychoactive medications. Additionally, she said the facility uses a 'Baylor plan',
meaning the weekends are covered by 12 hour shifts and the weekdays are covered by 8 hour shifts. She
clarified it was a possibility that during the weekends, behavioral monitoring would only occur twice in 24
hours as there would only be two shifts. She confirmed that this represented a different care process on the
weekend versus during the week. The DON also confirmed Psychoactive Medication Consent forms should
have all sections completed, including the 'potential side effects' section.
An interview was conducted with the Consultant Pharmacist on 02/26/21 at 3:29 p.m. She stated it was her
expectation that residents receiving regular insulin would have their blood glucose checked regularly.
Additionally, she stated if there was a Physician's Order for behavioral monitoring related to antidepressant
use, it should be documented in the record.
3. A review of the admission Record revealed that Resident #71's most recent admission date was
01/25/21. The resident's diagnoses included but were not limited to dementia with Lewy Bodies, major
depressive disorder, and mood disorder.
A review of the Psychoactive Medication Consent dated 01/25/21 revealed that Resident #71 was ordered
Lexapro 10 mg for depression with potential side effects of lethargy and Nuplazid 34 mg for hallucinations
with a potential side effect of lethargy. The Statement of Consent portion of the consent was left blank. The
form indicated verbal consent via telephone with family member but did not indicate whether the family
consented or did not consent to the use of the medications. The section for the person completing the form
was left blank.
2. A review of Resident #240's medical record revealed that Resident #240 was admitted to the facility on
[DATE] with diagnoses of dementia, anxiety disorder, Alzheimer's Disease, and Major Depressive Disorder.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 10 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
A review of Resident #240's Care Plan revealed a problem, revised on 02/18/2021, that Resident #240
used psychotropic medication related to anxiety and Major Depressive Disorder with psychotic features.
Interventions included monitor occurrence of target behavior symptoms, obtain consent from resident or
responsible party, and monitor for side effects and adverse reactions of psychotropic medications.
A review of Resident #240's MDS assessment revealed, under Section C - Cognitive Patterns, a BIMS
score of 99, which indicated that Resident #240 was not able to complete the interview. The MDS
assessment also revealed, under Section N - Medications, that Resident #240 received antipsychotic
medications and antidepressant medications 6 days out of the 7 day assessment period and antianxiety
medications 7 days out of the 7 day assessment period.
A review of Resident #240's Physician's Orders revealed the following orders:
- Psychoactive Medication: (Risperdal) Document number of targeted behaviors, behavior code,
intervention code, outcome of intervention code, and side effect code every shift, with a start date of
02/10/2021.
- Psychoactive Medication: (Trazodone) Document number of targeted behaviors, behavior code,
intervention code, outcome of intervention code, and side effect code every shift, with a start date of
02/10/2021.
- Psychoactive Medication: (Xanax) Document number of targeted behaviors, behavior code, intervention
code, outcome of intervention code, and side effect code every shift, with a start date of 02/10/2021.
- Psychoactive Medication: (Zoloft) Document number of targeted behaviors, behavior code, intervention
code, outcome of intervention code, and side effect code every shift, with a start date of 02/10/2021.
- Xanax 0.25 mg by mouth two times a day for anxiety, with a start date of 02/10/2021.
- Risperdal 1.5 mg by mouth at bedtime for behavioral and psychological symptoms of dementia (BPSD),
with a start date of 02/10/2021.
- Zoloft 100 mg by mouth one time daily for depression, with a start date of 02/10/2021.
- Trazodone 12.5 mg by mouth every 8 hours for depression, with a start date of 02/10/2021.
A review of Resident #240's Behavior Monitoring record for February 2021 revealed that psychoactive
medication monitoring for Risperdal was not completed on five different shifts, which occurred on multiple
days.
A review of Resident #240's Psychoactive Medication Consent form revealed, under the section titled
Medication Interventions Recommended the medications Xanax, Zoloft, Trazodone, and Risperdal. The
documentation did not include dosage or frequency of the medication as part of the consent. The section
titled Potential Side Effects revealed side effects for Xanax and Risperdal as lethargy and side effects for
Zoloft and Trazodone as N/V (nausea and vomiting). No other medication side effects were listed in the
section. The Consent form also revealed, under the section titled Statement of
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 11 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0758
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Consent, that no selection was made related the consent for use of psychotropic medications. The bottom
of the consent form revealed that the consent form was completed on 02/24/2021.
4. A record review of the medical record for Resident #39 revealed that she was initially admitted to the
facility on [DATE] and readmitted on [DATE]. Diagnoses included: Unspecified dementia without behavioral
disturbances, major depressive disorder, schizoaffective disorder, bipolar type, pseudobulbar affect, and
anxiety disorder.
A review of Resident #39's MAR for January 2021 revealed physician orders for:
Risperdal 0.25 milligrams(mg) by mouth (PO) every morning,
Risperdal 0.5 mg PO every evening, for Schizoaffective disorder,
Zoloft 50 mg in the morning for major depressive disorder,
Namenda 10 mg 1 tab PO two time daily (BID)for dementia,
Nuedexta capsule (cap) [capsule] 20-10 mg 1 cap po BID for pseudobulbar affect, and
Xanax 0.5 mg PO three times daily (TID) for anxiety.
A review of Resident #39's care plan revealed that Resident #39 uses psychotropic medications for anxiety,
depression, and schizoaffective disorder, bipolar type. Interventions included: Consult with pharmacy,
provider to consider dose reduction; Describes how the medication impact the resident and others;
Discussed with provider ongoing need for use of medication; Monitor for specific target behaviors: possible
risk and causal/contributing factors for behavior, desired outcomes, ongoing efficacy of individualized/non
pharmacological approaches .
A review of Resident #39's medical chart and electronic medical record (EMR) did not reveal a
Psychoactive Medication Consent form.
During an interview with the Director of Nursing (DON) on 2/26/2021 at 11:00 a.m., the DON confirmed that
the Psychoactive Medication Consent should have been uploaded in Resident #39's medical chart or EMR.
Upon request for a Psychotropic Medication Consent for Resident #39 the DON provided a Psychotropic
Medication Consent dated 2/26/2020. The DON stated that the Psychotropic Medication Consent was not
completed prior to the request.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 12 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0761
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure drugs and biologicals used in the facility are labeled in accordance with currently accepted
professional principles; and all drugs and biologicals must be stored in locked compartments, separately
locked, compartments for controlled drugs.
Based on observation, interview and policy review, the facility failed to ensure expired medications were
removed from one medication cart (3rd floor back hall) out of three medication carts observed, and one
medication storage room (3rd floor unit) out of one medication storage room observed.
Findings included:
On 02/25/2021 at 2:17 p.m. an observation of the 3rd floor back hall medication cart was performed and
Staff C, Licensed Practical Nurse (LPN) was present. One card of Baclofen 5 milligram (mg) tablets with an
expiration date of 11/25/2020 for Resident #33 was discovered. A subsequent interview with Staff C, LPN
confirmed the medication was expired, and she further stated the medication was discontinued.
On 02/25/2021 at 2:25 p.m. an observation of the 3rd floor medication storage room was performed and
Staff C, LPN was present. Two bottles of Aspirin 81 mg tablets were discovered with an expiration date
listed as 01/21. Additionally, during an observation of the medication room refrigerator, one box of Bisacodyl
10 mg Suppositories was discovered with an expiration date listed as 12/2020. A subsequent interview with
Staff C, LPN confirmed both medications were expired.
During an interview with the Interim Director of Nursing (DON) on 02/26/2021 at 9:34 a.m., she confirmed it
was her expectation that expired medications were removed from the medication carts and storage rooms
and returned to the pharmacy. She further stated the Unit Manager is responsible for doing weekly checks
of medication storage areas to ensure expired medications are removed, and the Consultant Pharmacist
also checks the carts monthly during her visits to the facility.
A facility-provided policy titled, Storage and Expiration of Medications, Biologicals, Syringes and Needles,
dated 12/1/07, and revised on 5/1/10 and 1/1/13 was reviewed. Under Section 4 it showed:
Facility should ensure that medications and biologicals:
4.1 Have an expiration date on the label;
4.2 Have not been retained longer than recommended by the manufacturer or supplier; or;
4.3 Have not been contaminated or deteriorated, are stored separate from other medications until
destroyed or returned to the pharmacy or supplier.
During an interview with Staff A, Registered Nurse (RN), Unit Manager on 02/26/2021 at 11:00 a.m. she
stated she has not been at the facility long, and has not got into a routine yet for checking the medication
carts weekly for expired drugs.
An interview conducted with the Consultant Pharmacist on 02/26/2021 at 2:26 p.m. revealed it was her
expectation that expired medications were removed from the medication carts and storage rooms and
returned to the Pharmacy. She further stated she checks medications for expiration dates during her visits
to the facility and the nursing staff is responsible for checking between her visits to the facility.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 13 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0881
Implement a program that monitors antibiotic use.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
interviews and record review, the facility failed to implement the antibiotic stewardship program by not
ensuring antibiotics were given appropriately to one resident (#244) of a total of 32 sampled residents.
Residents Affected - Few
Findings included:
A review of Resident #244's medical record revealed that Resident #244 was admitted to the facility on
[DATE] with diagnoses of congestive heart failure, chronic atrial fibrillation, malignant neoplasm of prostate
and benign prostatic hyperplasia with lower urinary tract symptoms.
A review of Resident #244's February 2021 physician orders revealed the following orders:
- 02/20/2021 Urinalysis (UA) with reflex to culture, discontinue this order when completed and sent;
discontinued on 02/20/2021.
- 02/25/2021 Urinalysis (UA) with reflux to culture, discontinue this order when completed and sent.
- 02/20/2021 Ciprofloxacin 250 milligrams (mg) by mouth every 12 hours for infection for 7 days.
A review of Resident #244's progress notes revealed a Health Status Note, dated 02/26/2021 at 08:51 a.m.,
which documented that a urine specimen was collected via straight catheterization using sterile technique
and, UA being sent to lab as STAT (immediately), C&S (Culture and Sensitivity) specimen cup in dirty utility
fridge for tomorrow AM lab pickup. Resident #224's progress notes did not reveal that the UA order for
02/20/2021 was completed.
An interview was conducted on 02/26/2021 at 12:53 p.m. with the facility's Infection Preventionist (IP). The
IP stated that Resident #244's lab work for the use of Ciprofloxacin may not have been loaded into the
electronic charting system and that it may have been started before the resident came to the facility. The IP
also stated that she reviewed the use of antibiotics on a weekly basis and that Resident #244 was recently
added to her list since he was a new admission to the facility.
A follow up interview was conducted on 02/26/21 at 01:53 p.m. with the facility's IP. The IP stated that
Resident #244's urine culture was ordered on 02/21/2021 and that the Ciprofloxacin 250 mg was started
before the collection was completed. The IP stated that the nursing staff did not complete the UA order from
02/20/2021 in a timely manner and that the antibiotic therapy continued until the urine was collected on
02/25/2021.
An interview was conducted on 02/26/2021 at 01:59 p.m. with Staff J, Registered Nurse (RN). Staff J, RN
stated that Resident #244 was started on Ciprofloxacin 250 mg prophylactically due to increased confusion.
The UA was ordered for 02/20/2021 and was completed on 02/26/2021. Staff J, RN stated that Resident
#244 was on antibiotic therapy before the UA was completed and stated that the UA should have been
completed within one day. Staff J, RN was not able to state whether nursing staff should obtain the UA
before initiating antibiotic therapy, and was not able to state why the UA was not completed sooner.
An interview was conducted on 02/26/2021 at 02:10 p.m. with the facility's Director of Nursing
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 14 of 15
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
105650
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
02/26/2021
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Bayshore Pointe Nursing and Rehab Center
3117 W Gandy Blvd
Tampa, FL 33611
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 0881
Level of Harm - Minimal harm
or potential for actual harm
(DON). The DON stated that lab work would be reviewed to determine if the antibiotic therapy was
appropriate for the resident. The DON stated that a UA should be collected prior to beginning antibiotic
therapy and should be collected within 24 hours from receiving the order. The DON stated that antibiotic
use was reviewed and discussed during morning meetings, but they did not identify an issue with Resident
#244's antibiotic therapy.
Residents Affected - Few
A review of the facility policy titled, Antibiotic Stewardship, dated 10/24/2017, revealed under the section
titled, Resident Assessment and Communication of Change in Condition, that when facility staff suspects a
resident has an infection, the nurse should perform and document an assessment of the resident using
established and accepted assessment protocols to determine if the resident's status meets minimum
criteria for initiating antibiotics. The policy also revealed that when a culture and sensitivity (C&S) is
ordered, it should be performed before the initiation of an antibiotic/anti-infective.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105650
If continuation sheet
Page 15 of 15