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
medical record review, review of facility's policies and procedure, staff, and resident interviews the facility
failed to ensure 3 (Residents #4, #5 and #13) of 16 residents reviewed for advance directive were informed
and provided written information of advance directive rights and ensure their advance directive wishes were
followed.
The findings included:
The facility's policy and procedure titled, Resident Right - Advanced Directive Tracking Program dated
[DATE] noted, It is the facility policy to honor the advance directives of all residents and to make information
available to the resident on how to prepare such directives, should the resident not have them in place or
update their existing directives.
Procedure:
1. During the admission process the Social Service Director (SSD) or designee will discuss with each
resident and/or the person accompanying the resident the following:
a.
Whether they have an advance directive .
b.
Whether they have a Uniform Do Not Resuscitate (DNR) form.
c.
If so, is it printed on yellow (goldenrod) paper?
d.
If they have the forms with them? If so, secure copies .
4. Social Services or the appropriate designee will carefully review any and all advanced directive related
documents to ensure the information is complete and that the requirements of the law are met. If there is a
question it is the responsibility of the reviewer to seek clarification.
(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 12
Event ID:
106090
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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
Residents Affected - Few
5. Social Services or the appropriate designee should visit the resident and discuss advance directives with
them to ensure that he/she has executed the advance directives that he/she would want.
6. Social Services should also ensure that information was given to the resident on admission. Social
Services will advise the resident that at any time he/she may amend, revoke or write a new advance
directive and staff will assist .
8. The individual who visited the resident as described in #5, 6, and 7 should document this conversation in
the resident's social services notes .
1. On [DATE], a review of Resident #4's medical record revealed an admission date of [DATE]. Resident
#4's medical record revealed a plan of care dated [DATE] stating Resident #4 is a full code.
Further review of Resident #4's medical record revealed no documentation the Social Service Director
(SSD) or a facility representative discussed with Resident #4 and/or their representative Resident #4's
advance directive wishes and placed a copy of the Resident's advance directive forms in the medical record
as required by the facility's Resident Rights for Advance Directive policy. The medical record lacked a
physician order for Resident #4's code status.
On [DATE] at 10:55 a.m., in an interview Licensed Practical Nurse (LPN) Staff B, said she has been
working at the facility for several years. She said the Social Service department is responsible to talk with
the resident or their representative to determine the resident's advance directive wishes, get a physician
order for a full code, DNR (Do Not Resuscitate) or the appropriate code status, and put a copy of the
advance directive in the resident's medical record.
At the time of the interview, LPN Staff B reviewed Resident #4's electronic and hard (paper) copy of the
medical record and said she was unable to find a physician's order which stated Resident #4's code status
and/or a copy of Resident #4's advance directive. She said because there is no documentation in the
medical record of Resident #4's advance directive and code status wishes she would treat Resident #4 as a
full code and perform cardiopulmonary resuscitation (CPR).
On [DATE] at 11:02 a.m., during an interview with the Assistant Director of Nursing (ADON) and MDS
(Minimum Data Set) Coordinator, they said when a resident is admitted to the facility the SSD is
responsible to interview the resident or their representative about advance directive wishes, get a copy of
the advance directive for the medical record, and obtain a physician's order for the resident's code status.
They confirmed the nursing staff are required to look for a physician order to determine if the resident is a
full code or an DNR. If the nurse is unable to find a physician's order which stated the resident's code
status, they are then required to review the medical record to determine the resident code status.
The MDS Coordinator reviewed Resident #4's medical record and confirmed the SSD created a plan of
care dated [DATE] and noted Resident #4 was a full code. She said she was unable to find any
documentation the SSD spoke with Resident #4 or their representative about their advance directive and
code status wishes. She also stated the SSD did not obtain a physician's order for the full code status prior
to creating an advance directive full code status care plan as required.
On [DATE] at 11:29 a.m. during an interview the SSD said had been working at the facility for two weeks.
She said as part of the admission process the SSD was required to meet with the resident and/or their
representative to determine the resident's advance directive wishes, place a copy of the
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 2 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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
Residents Affected - Few
advance directive in the medical records, document the conversation in the medical record and get a
physician's order for the resident's code status.
The SSD reviewed Resident #4's medical records and verbally confirmed there was no documentation the
previous SSD obtained a physician's order for the full code. There was also no documentation of the
conversation the SSD had with Resident #4 about their advance directive wishes. The SSD confirmed there
was no copy of Resident #4's advance directive in the medical record as required per their policy.
2. On [DATE] medical record review revealed Resident #5 was admitted to the facility on [DATE] with a Brief
Interview for Mental Status (BIMS) score of 14 indicating intact cognition.
Further review of the record revealed a Social History Evaluation dated [DATE] which noted Resident #5
possessed a Health Care Power of Attorney and Living Will.
On [DATE] record review revealed the facility had not obtained copies of advanced directives for Resident
#5 including HCPOA, Living Will, or Do Not Resuscitate (DNR) form specifying end of life wishes.
The Baseline Care Plan in the medical record for Resident #5 dated [DATE] revealed Resident #5's Goal for
Advanced Directives was DNR (Do Not Resuscitate).
The comprehensive Care plan initiated on [DATE] revealed Resident #5 was a Full Code (Administer
cardiopulmonary resuscitation if the resident had no heartbeat and is not breathing). The interventions were
Code status per resident.
On [DATE] record review for Resident #5 revealed there was no record of code status selection for Resident
#5.
On [DATE] at 10:32 a.m., in an interview, Resident #5 said she has everything for advanced directives
including a Healthcare Surrogate and living will. She said her daughter and son are her healthcare
surrogates.
On [DATE] at 11:06 a.m., the Social Services Director (SSD) said she met with Resident #5 but has not
discussed advanced directives or code status with the Resident. The SSD confirmed there was no order for
code status or any indication of code status in the electronic medical record.
On [DATE] at 3:24 p.m., LPN Staff B said when a code is called for a resident, she looks at the code status
in the electronic medical record and then double checks the hard chart medical record. She said the code
status is always listed at the top under the picture in the electronic medical record. She said if nothing is in
the electronic medical record hard chart medical record, the resident is a full code.
On [DATE] at 5:07 p.m., Resident #5 said she understands the term Do Not Resuscitate (DNR) and she
wishes to be a DNR. She said she does not remember anyone at the facility asking her preference.
On [DATE] at 9:02 a.m., the SSD said on [DATE] she and the Minimum Data Set (MDS) Director audited
Resident #5's medical record and discovered there was no order for code status in the medical record. She
said at that time, the MDS Director created a Full Code order for Resident #5. The SSD said
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 3 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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
Residents Affected - Few
she talked with Resident #5 on [DATE] and her preference was Full Code. The SSD could not recall the
time of the conversation and said she did not document the conversation. The SSD said the MDS Director
was not present during the conversation. The SSD looked through the hard chart medical record and
confirmed the Baseline Care Plan dated [DATE] indicated DNR selection for advanced directive. The SSD
confirmed Resident #5 comprehensive care plan was Full Code. The SSD confirmed the baseline and
comprehensive care plans contradicted each other.
Review of the physician's orders revealed on [DATE] at 8:50 a.m., the MDS Director entered a physician's
order specifying Resident #5 was a Full Code.
Review of the SSD progress note dated [DATE] at 9:47 a.m., revealed the social worker, spoke to resident
in regard to code status. This social worker educated the resident on full code and DNR. This resident
confirmed she wants to be a DNR. This social worker will initiate DNR.
3. Review of the Minimum Data Set (MDS) assessment with an assessment reference date of [DATE]
revealed Resident #13 scored 15 on the Brief Interview for Mental Status (BIMS), indicating intact
cognition.
Review of the Social History Evaluation form dated [DATE] showed Will bring copy was checked off for
Advanced Directives.
The clinical record lacked documentation of a physician's order specifying Resident #13's code status or a
care plan addressing advanced directives and code status for Resident #13.
A handwritten physician's order in the medical record dated [DATE] specified to Clarify code status.
On [DATE] at 5:02 p.m., in an interview Resident #13 said if her heart stops beating, she does not want to
be resuscitated. She said she is [AGE] years old and does not think it is good to do that.
On [DATE] at 8:47 a.m., the Social Services Director (SSD) said Resident #13 was re-admitted to the
facility on [DATE] for long term care. She confirmed the medical record contained no advanced directive or
indication of code status for Resident #13. The SSD confirmed there was an order from the physician on
[DATE] to clarify code status and the order was not carried out. The SSD said she had not interviewed
Resident #13 for code status, and since there was no record of DNR, she is considered a full code.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 4 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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
interview and record review, the facility failed to develop a comprehensive care plan containing
interventions to address the cardiac pacemaker for 1 (Resident #26) of 2 residents reviewed for cardiac
pacemaker.
The findings included:
The Minimum Data Set (MDS) dated [DATE], reveals Resident #26 has an active diagnosis of Cardiac
Pacemaker.
According to the physician orders for Resident #26, there is no order for the cardiac pacemaker or an order
addressing care or treatment of the Cardiac Pacemaker.
On 3/15/22 at 10:04 a.m. during a telephone conversation, Resident #26's wife said she is not sure how the
facility is treating the device.
According to the Care Plans reviewed on 3/15/22 at 3:47 p.m., Resident #26 does not possess a care plan
for Cardiac Pacemaker including interventions on how to care for the device.
On 03/15/22 at 3:27 p.m., Registered Nurse (RN) Staff G said she's worked at the facility for a long time.
She said there is no machine at the facility to check the cardiac pacemaker. She said she is not sure if
Resident #26's cardiac pacemaker functions.
On 3/15/22 at 3:38 p.m., the Director of Nursing (DON) confirmed Resident #26's medical record did not
contain a care plan for the cardiac pacemaker or documentation about how the facility was addressing the
cardiac pacemaker. The DON said there is no facility policy for cardiac pacemakers.
On 03/16/22 at 1:00 p.m., Licensed Practical Nurse (LPN) Staff A said she does not care for the resident
very often and does not know what is being done for the pacemaker.
On 3/16/22 at 1:17 p.m., the Minimum Data Set (MDS) Director said she is responsible for creating care
plans for residents at the facility. She said she did not create a care plan for Resident #26's cardiac
pacemaker. She said she is not sure what is being done for the cardiac pacemaker.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 5 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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 0677
Provide care and assistance to perform activities of daily living for any resident who is unable.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record review and resident and staff interview, the facility failed to provide the necessary services to
maintain good grooming and personal hygiene for 1 (Resident #5) of 1 reviewed for showers.
Residents Affected - Few
The findings included:
The facility policy, Activities of Daily Living (ADLs)/Maintain Abilities dated 11/28/17 stated: .care and
services provided are person-centered and honor and support each resident's preferences, choices,
values, and beliefs.
On 3/14/22 at 10:35 a.m., Resident #5 (room [ROOM NUMBER]), said she has been at the facility since
December 2021 and has had 3 showers since she's been at the facility. Resident #5 said it bothers her. She
said the therapist told nursing staff Resident #5 should be getting showers Monday, Wednesday, and Friday.
On 3/16/22 at 10:48 a.m., Certified Nursing Assistant (CNA) Staff D said the scheduler will put the shower
on the CNA assignment sheet. She said when she gives a resident a shower, she fills out the shower and
documents the care in the computer. She said if not given, she reports it to the nurse.
According to record review of the shower schedule, Resident #5 was scheduled for showers on Monday,
Wednesday, and Friday.
According to the Documentation Survey Report V2, for December 2021, Resident #5 received 3 showers at
the facility from 12/11/21 - 12/31/21 and should have received 9 showers.
According to the Documentation Survey Report V2 for January 2022, Resident #5 received 6 showers at
the facility from 1/1/22 - 1/31/22 and should have received 13 showers.
According to the Documentation Survey Report V2 for February 2022, Resident #5 received 8 showers
from 2/1/22 - 2/28/22 and should have received 12 showers.
According to the Documentation Survey Report V2 for March 2022, Resident #5 received 2 showers from
3/1/22 - 3/14/22 and should have received 6 showers.
On 03/16/22 at 10:50 a.m., Licensed Practical Nurse Staff A confirmed she receives shower sheets from
the CNAs after they give a resident a shower. Staff A said she gives the shower sheets to the DON.
On 3/17/22 at 10:35 a.m., the Director of Nursing (DON) confirmed Resident #5 did not receive showers 3
times per week. The DON confirmed Resident #5 had not received any showers from 2/27/22 - 3/11/22, a
total of 13 days. He said there were no shower sheets for Resident #5. He said there were no progress
notes explaining why Resident #5 did not receive the scheduled showers.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 6 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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 - Few
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
clinical record review and staff interviews, the facility failed to maintain documentation of rationale to justify
an increase in psychotropic medication (medication that affects a person's mental state) for 1 (Resident
#27) of 5 sampled residents reviewed for unnecessary medications. This has the potential to lead to the
administration of unnecessary medications.
The findings include:
Based on clinical record review and staff interviews, the facility failed to maintain documentation of rationale
to justify an increase in psychotropic medication (medication that affects a person's mental state) for 1
(Resident #27) of 5 sampled residents reviewed for unnecessary medications. This has the potential to lead
to the administration of unnecessary medications.
The findings include:
Review of Resident #27's medical record revealed her last documented admission to the facility was on
11/09/2019.
The medical record revealed a physician's order dated 11/28/21 for Lorazepam 0.5 mg PRN (as needed)
for anxiety every 8 hours. Review of the medication administration record (MAR) revealed Resident #27
received the medication 2 times on 11/28/21 and 1/30/22. There was no Behavior/Intervention Monthly
Flow Record created in November 2021 and no documentation in Resident #27's medical record noting
why she received the Lorazepam on 11/28/21. Review of the Behavior/Intervention Monthly Flow Record for
January 2022 revealed no behaviors noted on 1/30/22. There was no documentation noting why she
received the Lorazepam on 1/30/22.
Review of the consultant pharmacist medication regime for Resident #27's medications revealed he
recommended on 12/4/21 for Resident #27's primary care physician to evaluate the use of the PRN
Lorazepam 0.5 mg ordered on 11/28/21 and write a justification for the use of the Lorazepam .5 mg as
required by federal regulations. The pharmacist also wrote on 12/4/21 on the consultant pharmacist
medication regimen form: PRN psychotropic medication cannot exceed 14 days without the prescribing
physician documenting the rationalization for use of the PRN psychotropic mediation and indicate the
duration of use for the PRN psychotropic medication per federal regulations. On 1/6/22 Resident #27's
primary care physician wrote on the consultant pharmacist medication regime form dated 12/4/21, to
increase the use of the PRN Lorazepam for anxiety to 180 days. Further review of Resident #27's medical
record, noted the required justification documentation by the primary care physician for why he ordered
PRN Lorazepam 0.5 mg for anxiety and the justification for ordering the medication for 180 days, when
federal regulations states PRN psychotropic medication cannot exceed 14 days without justification was not
present in Resident #27's medical record.
The psychiatric ARNP (Advance Registered Nurse Practitioner) documented on 11/3/21, he visited
Resident #27 that day for follow-up therapy. He documented Resident #27 denied homicidal or suicidal
thoughts and denied depression and anxiety at that time. The ARNP documented the resident denied
anxiety, worry, irritability, racing thoughts or panic and that staff denied evidence of anxiety symptoms. Staff
voiced no complaints about Resident #27. The psychiatric ARNP wrote he reviewed Resident
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 7 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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
#27's medication and would continue to monitor for changes in mood, appetite, or sleep.
Level of Harm - Minimal harm
or potential for actual harm
The psychiatric ARNP documented on 11/17/21 he visited Resident #27 that day for a follow-up for
medication check. The ARNP documented Resident #27 said she did not feel any different since
decreasing her Zoloft dosage and was in a good mood. In the ARNP notes, he documented the resident
denied current depression, anxiety, trouble sleeping and had a good appetite. The ARNP documented the
resident denied anxiety, worry, irritability, racing thoughts or panic and that staff denied evidence of anxiety
symptoms. The staff voiced no complaints about Resident #27. The ARNP stated he reviewed Resident
#27's medication and would continue to monitor for changes in mood, appetite, or sleep.
Residents Affected - Few
The psychiatric ARNP documented on 12/1/21 he visited Resident #27 that day for an acute change in
condition. The ARNP wrote Resident #27 had a urinary tract infection (UTI) and received 3 courses of
antibiotics but had been verbally more sad aside from being tired. Resident #27 did not admit to any anxiety
and was still eating well. The ARNP documented the resident denied anxiety, worry, irritability, racing
thoughts or panic and that staff denied evidence of anxiety symptoms. The ARNP stated he reviewed
Resident #27's medication and would continue to monitor for changes in mood, appetite, or sleep.
Resident #27's primary care physician's progress note dated 12/2/21 stated he visited Resident #27 who
had a chief complaint of UTI and confusion. Confusion etiology may be related to the UTI for a positive
urinary analysis. The primary care physician's progress note documented Resident #27 was on multiple
pain medications with possible confusion side effects. Medication included tramadol, Dilaudid and
Lorazepam. He documented staff noted increase depression and reported Resident #27 had crying
episodes. He noted a plan to increase Zoloft to 100 mg which could have taken a few weeks to reestablish
stable levels. The physician noted Resident 27's confusion had exact etiology unknown and he would
continue to follow.
Further review of Resident #27's primary care physician progress notes dated 12/2/21, 12/9/21 and,
1/20/22 noted Resident #27 was cooperative with exam, cognitive function intact and no agitation.
Review of Resident #27's Behavior/Intervention Monthly monitor form was not started until January 2022.
From January 1, 2022, to March 15, 2022, the facility document 2 episodes of increased anxiety on 1/4/22
which was relieved with repositioning and changing of the temperature. Medication was not documented as
given as a method to reduce the anxiety noted on 1/4/22 in 2 episodes.
On 3/16/22 at 9:55 a.m. during an interview with Staff B, she said she had been working at the facility for
several years. She said Resident #27 was pleasant and easy to work with. She said she had not observed
and/or heard of Resident #27 having episodes of increased anxiety.
On 3/16/22 at 1:29 p.m. during an interview with the Director of Nursing (DON), he stated Resident #27
was admitted to the facility on [DATE]. He confirmed Resident #27 was started on Lorazepam 0.5 mg on
11/28/21 for anxiety. He said the Lorazepam 0.5 mg order was renewed by the primary care physician on
1/09/22 for 180 days after the consulting pharmacist wrote on 12/4/21 a PRN psychotropic medication
order cannot exceed 14 days without the prescriber documentation for the rationalization of use and must
indicate the duration for the PRN order.
The DON reviewed Resident #27's medical record and said he was unable to find documentation Resident
#27 was having increased anxiety to justify why Lorazepam 0.5 mg PRN for anxiety was stared on
11/28/21. He said the facility did not start monitoring Resident #27 for increased anxiety until
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 8 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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 - Few
January 1, 2022. He said from January 1, 2022, to March 15, 2022, the facility documented 2 episodes of
increased anxiety, both on 1/4/22. The DON stated the interventions which were effective to reduce the
anxiety for Resident #27 on 1/4/22 did not include medications and staff was able to reduce her anxiety
with non-pharmacological interventions as documented on the behavior monitoring sheets.
The DON confirmed the consultant pharmacist wrote on 12/4/21 after reviewing Resident #27's medication
regime that the primary care physician needed to document the justification for use of the PRN Lorazepam
0.5 mg for anxiety ordered on 11/28/21 and the duration of the medication. The consultant pharmacist
wrote on the 12/4/21 medication regimen form, PRN psychotropic medication cannot exceed 14 days
without the prescribing physician documenting the rationalization for use of the PRN psychotropic
medication and should indicate the duration of use, not to exceed 14 days, for the PRN psychotropic
medication without justification as per federal regulations.
The DON confirmed Resident #27's primary care physician wrote on 1/6/22 on the consultant pharmacist
medication regime form dated 12/4/21 to increase the duration of the PRN Lorazepam for anxiety to 180
days. The DON said he was unable to find the required justification documentation by the primary care
physician why he ordered PRN Lorazepam 0.5 mg for anxiety. He also stated the primary care physician did
not document the justification for ordering the medication for 180 days, when federal regulations states
PRN psychotropic medication cannot exceed 14 days without justification by the ordering physician.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 9 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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.
On 3/16/22 at 09:33 a.m., Resident #13 was observed in her room lying in bed. A bottle of eye drops was
sitting on Resident #13's bedside tray table which was located next to the bed. Resident #13 said she
places an eye drop in each eye once a day.
According to the physician's orders for Resident #13, there is no order for eye drops.
On 3/17/22 at 10:53 a.m., the Director of Nursing (DON) confirmed the eye drops were on Resident #13's
bedside tray table. The DON said Resident #13's medical record did not contain an order for eye drops. The
DON confirmed Resident #13's medical record should contain an order for eye drops and they should be
stored securely inside the medication cart.
Based on observation, staff and resident interviews, and medication record review, the facility failed to
identify and monitor the safe and proper storage of medications for 2 (Resident #191 and Resident #13) of
2 residents reviewed for medication storage.
The findings included:
The review of the facility Medication Storage Policy, Section 4.3 Bedside Medication Storage Policy dated
09/2018 states bedside medication administration is permitted for residents who are able to self-administer
medications, upon the written order of the prescriber and when it is deemed appropriate in the judgement
of the nursing care center's interdisciplinary resident assessment team. Procedures included: The
interdisciplinary team (IDT) will review and approve resident competencies and understanding prior to
permission of bedside storage of medications as established in the nursing care centers policies and
procedures . A written order for the bedside storage of medication is present in the resident's medical
record . Bedside storage of medications is indicated on the resident medication administration record
(MAR) for the appropriate medications . The following conditions are met for bedside storage to occur, a.
The manner of storage prevents access by other residents. Lockable drawers or cabinets are required . All
nurses and nursing aides are required to report to the charge nurse on duty any medications found at the
bedside not authorized for bedside storage and to give unauthorized medications to the charge nurse . The
nurse will oversee storage security and accountability of bedside medications.
During an observation on 3/14/22 at 10:34 a.m. a prescription eye drop bottle for Resident #191 was seen
on her nightstand. The bottle read Brimonidine Tartrate Ophthalmic Solution 0.2% for use in the eyes only.
There were no identifying labels on the bottle. In an interview with the resident, she said that she had
brought her own prescription eye drops from home and self-administers them daily.
On 3/16/22 at 9:11 a.m. during review of Resident #191 Medication Administration Record (MAR),
Brimonidine Tartrate Ophthalmic Solution 0.2% was documented as administered by the clinician and there
was no mention of resident storing and administering her own medication. The medication Order for
Brimonidine Tartrate Ophthalmic Solution 0.2% reads to instill 1 drop to both eyes two times a day for
glaucoma and to be administered by clinician. There were no Physician orders for Resident #191 to store or
administer her own medications.
On 3/16/22 at 9:41 a.m. in an interview with Licensed Practical Nurse (LPN) Staff A who was
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 10 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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
FORM CMS-2567 (02/99)
Previous Versions Obsolete
assigned as Resident #191's nurse, she said the resident had her own bottle of Brimonidine Tartrate
Ophthalmic Solution 0.2% that she had brought from home. The facility also stored the eye drops in the
medication cart. She said most of the time the resident administered her own eye drops from her own
bottle.
On 03/16/22 at 1:05 p.m. in an interview with the Director of Nursing (DON), discussed the
self-administration and storage of medications for Resident #191. The DON said LPN Staff A told him about
Resident #191 having the Brimonidine Tartrate Ophthalmic Solution 0.2% at the bedside. The DON was
aware of Resident #191 self-administering eye drops and the medication stored on bedside table in plain
sight accessible to anyone who may enter the room. He admitted the medication should be kept safe and
secure in locked drawer and he has already started the process of re-educating his staff on the proper
procedures for securely storing medications at the resident's bedside. When asked about secured
medication in the room the DON said the process was there but was not followed.
Event ID:
Facility ID:
106090
If continuation sheet
Page 11 of 12
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
106090
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
03/17/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Benderson Family Skilled Nursing and Rehab Center
1959 N Honore Ave
Sarasota, FL 34235
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 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation and interviews the facility failed to ensure infection control measures were maintained during
medication administration for 2 residents (Resident #13 and Resident #141) of 3 reviewed for medication
administration and infection control.
Residents Affected - Few
The findings included:
On 3/16/22 at 8:41 a.m. Licensed Practical Nurse Staff A went into room [ROOM NUMBER] to administer
Fluticasone Propionate nasal spray to Resident #141. During that time, Staff A took the nasal spray box into
the room and placed it on the bedside tray table. Staff A did not place a barrier between the bedside tray
table and the nasal spray box. When Staff A had completed the task, she took the nasal spray box out of
the resident's room and placed it on the medication cart, without a barrier. Staff A then placed the nasal
spray inside the medication cart. Staff A did not place the box inside of a clean plastic bag before placing it
inside the medication cart.
On 3/16/22 at 9:33 a.m., LPN Staff B went into room [ROOM NUMBER] to administer Voltaren Gel to
Resident #13. During that time, Staff B took the gel box into the room and placed it on the nightstand. Staff
B did not place a barrier between the nightstand and the gel box. When Staff B had completed the task, she
took the gel box out of the resident's room and placed it inside of the facility treatment cart.
On 3/16/22 at 11:36 a.m., LPN Staff A said each resident has their own glucometer, and Resident #141 has
hers inside of a black case brought from home. Staff A took the black case from the medication cart and
went into room [ROOM NUMBER] to assess blood glucose level for Resident #141. Staff A placed the black
case onto the bedside tray table. Staff A did not place a barrier between the black case and the bedside
tray table. After Staff A had completed the task, she exited the room and placed the black case back into
the medication cart, again without a barrier. Staff A did not place the black case inside a clean plastic back
before placing it inside the medication cart.
On 3/17/22 at 10:53 a.m., the DON said the Voltaren Gel is house stock and the box should not have gone
into the resident's room. He said the Fluticasone Propionate nasal spray box should not have gone into the
room. The DON said staff should only take into the residents' room what they will be using to ensure
infection control measures are maintained.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
106090
If continuation sheet
Page 12 of 12