F 0757
Ensure each resident’s drug regimen must be free from unnecessary drugs.
Level of Harm - Minimal harm
or potential for actual harm
Based on observations, record review and interviews, the facility failed to monitor behaviors for one
(Resident #6) of five residents selected for unnecessary medications review, from a total of 23 residents in
the sample.
Residents Affected - Few
The findings include:
An observation and interview was conducted with Resident #6 in her room on 5/10/22 at 3:36 p.m. The
resident was sitting in her wheelchair at bedside smiling and talking. She did not remember which
medications she took.
A medical record review revealed an admission date of 12/27/18 and a diagnosis of anxiety disorder. Active
physician's orders revealed an order dated 4/22/22 for lorazepam (Ativan, sedative) 0.5 mg (milligrams) to
be administered daily.
The active care plan included the following Focus Areas:
Behavior Problem - manipulative due to ineffective coping skills. Intervention: Monitor behavior and side
effects of psychotropic medication.
Uses antianxiety medication. Intervention: Monitor behaviors and administer medications as ordered.
A review of the May 2022 Medication Administration Record (MAR) revealed no documentation of
behaviors, medication side effects, or nonpharmacological interventions for Lorazepam. (Photographic
Evidence Obtained) There was no documentation in the medical record to verify that behaviors, medication
side effects, or nonpharmacological interventions were being monitored/provided.
An interview was conducted with Licensed Practical Nurse (LPN) B on 5/12/22 at 10:59 a.m. She stated
resident behaviors were monitored and documented on the Medication Administration Record (MAR).
An interview was conducted with LPN A on 5/12/22 at 11:04 a.m. He stated resident behaviors were
documented on the MAR daily. He confirmed there was no behavior monitoring documented for Resident
#6.
An interview was conducted with the Assistant Director of Nursing (ADON) on 5/12/22 at 12:10 p.m. She
confirmed behavior monitoring for Resident #6 was not documented and should have been on the MAR.
The ADON stated she would initiate that now.
(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 4
Event ID:
105826
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
105826
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/12/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pavilion at Jacksonville, The
1771 Edgewood Ave W
Jacksonville, FL 32218
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 0757
.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105826
If continuation sheet
Page 2 of 4
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105826
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/12/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pavilion at Jacksonville, The
1771 Edgewood Ave W
Jacksonville, FL 32218
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 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Minimal harm
or potential for actual harm
Based on medical record review, interviews with staff, and a review of the Policy and Procedure for General
Guidelines for Medication Administration, the facility failed to monitor apical pulses for digoxin
administration and to obtain a digoxin level for one (Resident #29) of 23 sampled residents. An apical pulse
should be obtained before administering digoxin (heart medication), because it is not administered if the
apical pulse is below 60. The medication should be monitored through laboratory work due to a narrow
safety range.
Residents Affected - Few
The findings include:
A medical record review was conducted for Resident #29 revealing an admission date of 12/17/21 with
diagnoses including atrial fibrillation and chronic obstructive pulmonary disease (COPD). A physician's
order dated 12/18/21 read, digoxin 125 mcg (micrograms) given via gastrostomy tube (feeding tube) in the
morning (9:00 a.m.). The May 2022 Medication Administration Record (MAR) noted digoxin 125 mcg
administered via gastrostomy tube daily for atrial fibrillation. There were no apical pulses documented
before administration of the medication. The April 2022 MAR was reviewed and also noted no
documentation for apical pulse before administration of digoxin. A review of the medical record found no
documentation of a laboratory order to monitor digoxin levels. The manufacturer recommended that levels
must be monitored because the drug had a narrow safety range. Therapeutic levels were between 0.8 - 2.0
ng/ml (nanograms per milliliter). A toxic level was greater than 2.4 ng/ml (emedicine.medscape.com,
accessed on 5/12/22 at 4:30 p.m.)
A review of the resident's vital signs documentation revealed his radial pulses were usually taken at 12:00
p.m. or later. (Photographic Evidence Obtained)
An interview was conducted with the Assistant Director of Nursing (ADON) on 5/11/22 at 2:05 p.m. She
stated the apical pulse was taken and documented before administering digoxin and should be
documented on the resident's MAR.
An interview was conducted with the ADON on 5/12/22 at 10:51 a.m. She confirmed the apical pulses were
not being documented, and the order was changed in the computer with parameters for apical pulse
monitoring. After reviewing the resident's medical record, the ADON reported a digoxin level was not
ordered and the physician was notified. A STAT (immediate) order for a digoxin level was obtained.
A review of the Policy and Procedure for General Guidelines for Medication Administration (dated 9/2018),
noted Medications are administered as prescribed in accordance with good nursing principles and
practices.
.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105826
If continuation sheet
Page 3 of 4
Printed: 05/28/2026
Form Approved OMB
No. 0938-0391
Department of Health & Human Services
Centers for Medicare & Medicaid Services
STATEMENT OF DEFICIENCIES
AND PLAN OF CORRECTION
(X1) PROVIDER/SUPPLIER/CLIA
IDENTIFICATION NUMBER:
(X2) MULTIPLE CONSTRUCTION
105826
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/12/2022
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Pavilion at Jacksonville, The
1771 Edgewood Ave W
Jacksonville, FL 32218
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 0812
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Many
Procure food from sources approved or considered satisfactory and store, prepare, distribute and serve
food in accordance with professional standards.
Based on observations, interviews, and record review, the facility failed to 1) Ensure food items had not
expired, 2) Document food items' use by dates, 3) Keep thermometers in cooling units that contained food,
4) Use sanitizer in the three-compartment sink every time it was used, and 5) Keep food temperature logs
for every meal. This deficient practice could potentially affect all residents receiving food from the facility's
kitchen.
The findings include:
On 5/9/22 at 10:35 AM an observation of the kitchen was made revealing the following:
A bag of hotdog buns with a green/yellow substance on them was observed on the bread rack. Also
observed were two bags of hamburger buns with a green substance on several of the buns. The bags were
dated 4/13/22. (Photographic evidence obtained) The Certified Dietary Manager (CDM), present during the
observation, was asked about the bread and stated that the bread delivery usually switches the old bread
out for new bread. He was asked about the last delivery and reported it was on 5/4/22. The CDM stated
bread was delivered every week.
White flour was seen being stored in a large plastic container which had no date on it.
Observations were made of a milk cooler having five expired milk cartons dated 5/5/22 on them. It was also
noted that there was no thermometer in this unit. The small freezer across from the milk cooler was also
noted with no thermometer inside.
On 5/9/22 at 10:45 AM, the CDM was asked to find the thermometers in these units. He was unable to
locate them. He was asked if these two units should have had thermometers in them and he stated yes.
The three-compartment sink was filled with water and had pots in it. At 10:55 AM, Dietary Aide Z was asked
to test the sink's sanitizer at this time. The test strip did not change color, and was tested two more times
with the same result. The CDM told Dietary Aise Z to change out the sanitizer bucket. The sink was tested
after the sanitizer was added and the test strip revealed the appropriate 200 Parts Per Million (PPM).
Dietary Aide Z was asked about the use of the sanitizer. She stated she put the sanitizer solution in the sink
before adding the pots or dishes to the sink. She was asked about the sanitizer and she stated she had
gotten busy and did not test the sanitizer this morning.
On 5/12/22 at 10:27 AM, an observation of the food temperature logs was made. More than one day was
observed in which meal temperatures had not been documented on the log. At this time the CDM was
asked how many times a day the food temperatures should be taken when the food was on the steam table.
He stated, three.
A review of facility's policy titled Sanitation inspection was conducted. There was no policy date noted. The
policy instructed staff to conduct inspections to ensure food service areas were clean, sanitary, and in
compliance with applicable state and federal regulations.
.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105826
If continuation sheet
Page 4 of 4