F 0641
Ensure each resident receives an accurate assessment.
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 interview, the facility failed to ensure resident assessments accurately reflected each
resident's status for 1 of 3 residents reviewed for nutrition, Resident #3.
Residents Affected - Few
Findings include:
Review of Resident #3's annual Minimum Data Set (MDS) dated [DATE] showed the resident was not on a
therapeutic diet while a resident at the facility under Section K- Swallowing/Nutritional Status.
Review of Resident #3's physician order dated 11/18/2024 read, Regular diet Regular texture, regular/thin
consistency, CCD NAS (Controlled Carbohydrate Diet No Added Salt) diet.
During an interview on 5/8/2025 at 10:13 AM, the MDS Coordinator stated, [Resident #3's name] MDS will
have to be modified to reflect she was on a controlled carbohydrate diet back in November.
During an interview on 5/8/2025 at 10:48 AM, the Director of Nursing stated, The MDS should be accurate,
reflecting the correct information pertaining to the resident.
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 8
Event ID:
105465
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
105465
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Arbor Springs
1501 SE 24th Rd
Ocala, FL 34471
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
Based on observation, interview, and record review, the facility failed to ensure residents received care and
services according to professional standards of practice for 2 of 6 residents reviewed for IV (Intravenous)
therapy, Residents #6 and #3.
Residents Affected - Few
Findings include:
1) During an observation on 5/8/2025 at 5:40 AM, Resident #6 was sleeping. The resident had a single
lumen midline catheter to her left upper arm, infusing IV fluids. The transparent dressing over the midline
insertion site was lifting up at the edges. Under the transparent dressing, there was a gauze that had dried
blood on it; occluding the view of the insertion site. The dressing was dated 4/29/2025.
Review of Resident #6's physician order dated 4/29/2025 read, Insert midline: May use 1% Lidocaine for IV
insertion one time only for IV hydration for one day.
Review of Resident #6's physician order dated 5/1/2025, with discontinued date of 5/2/2025 read, Change
Left arm midline catheter dressing every week with transparent dressing.
Review of Resident #6's medication administration record (MAR) for May 2025 showed no midline catheter
dressing changes documented.
During an interview on 5/8/2025 at 6:02 AM, Staff E, Registered Nurse (RN), stated, The dressing should
have been changed already. I'm not sure why it wasn't. The date on it is 4/29/2025. There is blood and
gauze under the dressing that makes it needed to be changed. I'm not sure why it wasn't.
During an interview on 5/8/2025 at 7:30 AM, Resident #6 stated, That [the dressing] hasn't been changed
at all since I got it put in. It's had blood under that since it was put in. It was bleeding a little when they put it
in. I needed to get these IV fluids because my kidneys weren't working so good.
During an observation on 5/8/2025 at 10:50 AM, Resident #6 was resting quietly in bed with a left midline
with IV fluids infusing. The dressing was dated 4/29/2025 and was pulling up from the skin. There was a 2x2
gauze covered with dried blood under the transparent dressing.
During an interview on 5/8/2025 at 12:55 PM, the Director of Nursing (DON) stated, All central line
dressings need to be changed every 7 days. If there is gauze under a dressing, it should be changed every
2 days.
Review of the facility policy and procedure titled Catheter Insertion and Care read, Midline dressing
changes: Policy: Midline catheter dressings will be changed at specified intervals, or when needed, to
prevent catheter-related infections associated with contaminated, loosened or soiled catheter-site
dressings. General Guidelines: 1. Change midline catheter dressing 24 hours after catheter insertion, every
5-7 days, or if it is wet, dirty, not intact, or compromised in any way . 4. Use a sterile, transparent, semipermeable membrane (TSM) or gauze dressing. If gauze dressing is used, cover the gauze with a TSM
dressing and change the dressing every 48 hours.2) During an interview on 5/8/2025 at 6:28 AM, Resident
#3 stated, The staff inserted a midline in my arm by mistake. I did not need the midline for the medication
that was prescribed. I even took a picture of the midline. Then
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105465
If continuation sheet
Page 2 of 8
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
105465
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Arbor Springs
1501 SE 24th Rd
Ocala, FL 34471
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
the staff had to remove the midline from my arm when they realized the medication was an injection.
Level of Harm - Minimal harm
or potential for actual harm
Review of Resident #3's physician order dated 3/27/2025 read, Ceftriaxone Sodium Intravenous Solution
Reconstitued 1 GM [gram] (Ceftriaxone Sodium), Use 1 gram intravenously every 24 hours for
infection/abscess for 7 days dilute with 2.1 ml [milliliters] of 1% lidocaine solution.
Residents Affected - Few
Review of Resident #3's physician order dated 3/27/2025 read, Insert midline IV for Ceftriaxone Sodium
Intravenous Solution Reconstituted 1 GM, may us 1% lidocaine STAT for antibiotic use.
Review of Resident #3's physician order dated 3/27/2025 read, Ceftriaxone Sodium Solution
Reconstitueted 1 GM, Inject 1 gram intramuscularly every 24 hours for infection/abscess for 7 Days Dilute
with 2.1 mL of 1% lidocaine solution.
Review of Resident #3's Medication Administration Record (MAR) for March 2025 showed midline was
inserted on 3/27/2025 at 11:00 PM.
Review of Resident #3's MAR for March 2025 showed Ceftriaxone Sodium Injection Solution was
administered intramuscularly from 3/28/2025 through 3/31/2025.
Review of Resident #3's MAR for April 2025 showed Ceftriaxone Sodium Injection Solution was
administered intramuscularly from 4/1/2025 through 4/3/2025.
Review of Resident #3 progress note dated 3/27/2025 read, resident need iv (intravenous) access for
antibiotics.
Review of Resident #3's progress note dated 3/28/2025 read, Received orders to remove pt [patient]
midline. Old dressing was removed, site was cleansed with chlorhexidine solution, and allowed to air dry.
Midline catheter was gently removed, applying pressure to the insertion site. Catheter tip was inspected for
integrity, tip intact. Insertion site held with sterile gauze and hemostasis achieved within expected
timeframe. Pressure bandage was applied to site. Pt was educated on dressing care and signs and
symptoms to report to nurse.
Review of Resident #3's progress note dated 4/3/2025 read, Plan . Abscess labia, Ceftriaxone 1 gram IM
[intramuscular] daily for 3 days for a total of 10 days of therapy.
During an interview on 5/8/2025 at 8:30 AM, Staff A, Licensed Practical Nurse (LPN), Unit Manager, stated,
[Resident #3's name] midline was inserted accidently and it had to be removed. [Staff B, LPN's name] was
the nurse who put in the order for the intravenous medication.
During an interview on 5/8/2025 at 8:44 AM, Staff B, LPN, stated, I don't recall much. I do think [the
Advance Registered Nurse Practitioner #1's name] called and requested a midline to be inserted.
During an interview on 5/8/2025 at 8:52 AM, the Director of Nursing stated, I spoke to [Staff A's name] and
he said it [inserting a midline] was a mistake and a nurse caught the mistake and they removed the midline
and corrected the order. I am not sure if the doctor was notified.
During an interview on 5/8/2025 at 8:54 AM, the Advance Registered Nurse Practitioner #1 stated,
[Resident #3's name] Ceftriaxone was never meant to be given intravenously. [Resident #3's name] was
never meant to get a midline inserted. I never gave an order to insert a midline. This was a mistake
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105465
If continuation sheet
Page 3 of 8
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
105465
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Arbor Springs
1501 SE 24th Rd
Ocala, FL 34471
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
Level of Harm - Minimal harm
or potential for actual harm
from a nurse. I was there the following day and caught the mistake and the order was corrected. [Resident
#3's name] received all her doses of the mediation intramuscularly. I was not aware the midline was actually
put in. I would have then not had it [the midline] removed and just change the route of the medication to
intravenous. The risk was minimal for the resident. There is always risk for infection, but very minimal if any.
A midline is pretty benign.
Residents Affected - Few
During an interview on 5/9/2025 at 8:39 AM, Staff C, LPN, stated, Originally what happened was I came on
shift the nurse from the prior shift told me she [Resident #3] needed a PICC [Peripherally Inserted Central
Catheter] line. When they [the organization that provides intravenious catheter insertions] came in they
stated it would be best for a midline. I told my supervisor, and he said to change it [the physician's order] to
a midline. I believe the midline was not used [for Resident #3]. When I came back the next time, she
[Resident #3] no longer had a midline. The nurse who told me she [Resident #3] needed the PICC line was
[Staff B's name].
Review of the facility policy and procedure titled Insertion of Peripheral Midline or Peripherally Inserted
Central Catheters revised on 1/17/2019 read, General Guidelines . 4. Placing a midline or PICC requires a
provider order and a written consent from resident or legal guardian.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105465
If continuation sheet
Page 4 of 8
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
105465
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Arbor Springs
1501 SE 24th Rd
Ocala, FL 34471
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
Ensure each resident’s drug regimen must be free from unnecessary drugs.
Level of Harm - Minimal harm
or potential for actual harm
Based on record review and interview, the facility failed to ensure residents' drug regimen were free from
unnecessary antibiotic use based on adequate indications to reduce the risk of the development of
antibiotic-resistant organisms for 1 of 3 residents reviewed for infection, Resident #7.
Residents Affected - Few
Findings include:
Review of Resident #7's physician order dated 5/4/2025 read, Ertapenem Sodium injection solution
reconstituted 1 GM [gram], Inject 1 gram intramuscularly one time a day for UTI [Urinary Tract Infection] for
10 days.
Review of Resident #7's physician order dated 5/4/2025 read, Urinalysis w [with]/reflex culture one time
only related to quadriplegia, unspecified.
Review of Resident #7's physician progress note dated 5/4/2025 read, Assessment/Plan: 1. Trach
bleeding/Dark urine: Improved: No further episodes of bleeding from trach. Secretions are normal (pale
yellow) in color, consistency. Eliquis was put on hold - but no improvement in color of urine. He has had
history of UTI with brown-colored urine in March 2025. Ordered UA [urinalysis]/UC [urine culture] yesterday
but do not see this. Will reorder. He was given water bolus to flush kidneys a bit but no improvement in urine
color. With initial trach bleeding and concern for possible hematuria, Eliquis was put on hold. 2. Suspect
UTI: As Eliquis does not seem to be cause of this (off it 40 hours without change), and with his history of
UTI and he has suprapubic catheter - start Ertapenem 1 GM IV [intravenous] every 24 hours x 10 days.
Primary team to be updated and to await UC results. Await labs as previously ordered.
Review of Resident #7's nursing progress note dated 5/5/2025 read, Was unable to collect a urine sample.
MD [Medical Doctor] has been notified. Awaiting new orders.
Review of Resident #7's laboratory records showed no urinalysis or urine culture reports.
Review of Resident #7's nursing progress notes from 5/5/2025 through 5/9/2025 showed no additional
notes related to a urinalysis or urine culture.
Review of resident #7's physician orders for 5/5/2025 through 5/9/2025 showed no additional orders for a
urinalysis or urine cultures.
During an interview on 5/9/2025 at 9:55 AM, the Infection Preventionist stated, This antibiotic [for Resident
#7] should not have been continued. The weekend nurse practitioner started the resident on antibiotics
empirically due to him having frequent UTIs. We did not get the culture and sensitivity, and we should have
done this. He [Resident #7] is not having fevers. His white count was normal. He would not need this
medication based on his clinical picture.
During an interview on 5/9/2025 at 10:15 AM, Staff A, Licensed Practical Nurse (LPN), stated, I'm not sure
why the urine was not recollected or attempted again. We should have notified the doctor or nurse
practitioner and gotten that done. We should have followed up and gotten the order discontinued.
During an interview on 5/9/2025 at 10:30 AM, the Director of Nursing (DON) stated, If a resident
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105465
If continuation sheet
Page 5 of 8
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
105465
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Arbor Springs
1501 SE 24th Rd
Ocala, FL 34471
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
has burning on urination, sometimes the doctor will treat with wide spectrum antibiotics. We should collect a
UA. We should have discontinued the antibiotic or gotten a UA.
During an interview on 5/9/2025 at 10:41 AM, the Advanced Practice Registered Nurse stated, The
antibiotics [for Resident #7] were prophylactic for possible symptoms [of a urinary tract infection]. We start
antibiotics, get UA with culture and sensitivity. I am not sure why there wasn't a UA. I wanted the primary
team to follow up on that and I guess they didn't. I would stop the antibiotic if the culture or U/A are negative
or if the resident wasn't showing signs of a UTI.
Event ID:
Facility ID:
105465
If continuation sheet
Page 6 of 8
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
105465
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Arbor Springs
1501 SE 24th Rd
Ocala, FL 34471
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
Based on record review and interview, the facility failed to implement the antibiotic stewardship program by
failing to monitor the use of antibiotics to reduce the risk of the development of antibiotic-resistant
organisms for 1 of 3 residents reviewed for infection, Resident #7.
Residents Affected - Few
Findings include:
Review of Resident #7's admission record showed diagnoses that included, but not limited to, acute and
chronic respiratory failure with hypoxia, personal history of traumatic brain injury, traumatic subarachnoid
hemorrhage without loss of consciousness, tracheostomy status, gastrostomy status, neuromuscular
dysfunction of bladder, post traumatic seizures, and quadriplegia.
Review of Resident #7's physician order dated 5/4/2025 read, Urinalysis w [with]/reflex culture one time
only related to quadriplegia, unspecified.
Review of Resident #7's physician order dated 5/4/2025 read, Ertapenem Sodium injection solution
reconstituted 1 GM [gram], Inject 1 gram intramuscularly one time a day for UTI [Urinary Tract Infection] for
10 days.
Review of Resident #7's physician progress note dated 5/4/2025 read, Assessment/Plan: 1. Trach
bleeding/Dark urine: Improved: No further episodes of bleeding from trach. Secretions are normal (pale
yellow) in color, consistency. Eliquis was put on hold - but no improvement in color of urine. He has had
history of UTI with brown-colored urine in March 2025. Ordered UA [urinalysis]/UC [urine culture] yesterday
but do not see this. Will reorder. He was given water bolus to flush kidneys a bit but no improvement in urine
color. With initial trach bleeding and concern for possible hematuria, Eliquis was put on hold. 2. Suspect
UTI: As Eliquis does not seem to be cause of this (off it 40 hours without change), and with his history of
UTI and he has suprapubic catheter - start Ertapenem 1 GM IV [intravenous] every 24 hours x 10 days.
Primary team to be updated and to await UC results. Await labs as previously ordered.
Review of Resident #7's nursing progress note dated 5/5/2025 read, Was unable to collect a urine sample.
MD [Medical Doctor] has been notified. Awaiting new orders.
Review of Resident #7's laboratory records showed no urinalysis or urine culture reports.
Review of Resident #7's nursing progress notes from 5/5/2025 through 5/9/2025 showed no additional
notes related to a urinalysis or urine culture.
Review of resident #7's physician orders for 5/5/2025 through 5/9/2025 showed no additional orders for a
urinalysis or urine cultures.
During an interview on 5/9/2025 at 9:55 AM, the Infection Preventionist stated, This antibiotic [for Resident
#7] should not have been continued. The weekend nurse practitioner started the resident on antibiotics
empirically due to him having frequent UTIs. We did not get the culture and sensitivity, and we should have
done this. This would not be appropriate, we need to follow our antibiotic stewardship for all antibiotics to
prevent possible MDROs [multi drug resistant organisms]. He [Resident #7] is not having fevers. His white
count was normal. He would not need this medication based on his clinical picture.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105465
If continuation sheet
Page 7 of 8
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
105465
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Aviata at Arbor Springs
1501 SE 24th Rd
Ocala, FL 34471
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
Residents Affected - Few
During an interview on 5/9/2025 at 10:15 AM, Staff A, Licensed Practical Nurse (LPN), stated, I'm not sure
why the urine was not recollected or attempted again. We should have notified the doctor or nurse
practitioner and gotten that done. We should have followed up and gotten the order discontinued.
During an interview on 5/9/2025 at 10:30 AM, the Director of Nursing (DON) stated, If a resident has
burning on urination, sometimes the doctor will treat with wide spectrum antibiotics. We should collect a UA.
We should follow our policies for antibiotic stewardship. We should have discontinued the antibiotic or
gotten a UA.
During an interview on 5/9/2025 at 10:41 AM, the Advanced Practice Registered Nurse stated, The
antibiotics [for Resident #7] were prophylactic for possible symptoms [of a urinary tract infection]. We start
antibiotics, get UA with culture and sensitivity. I am not sure why there wasn't a UA. I wanted the primary
team to follow up on that and I guess they didn't. I would stop the antibiotic if the culture or U/A are negative
or if the resident wasn't showing signs of a UTI.
Review of the facility policy and procedure titled Antibiotic Stewardship read, Policy Statement: Antibiotics
will be prescribed and administered to residents under the guidance of the facility's Antibiotic Stewardship
Program. Policy Interpretation and Implementation: 1. The purpose of our Antibiotic Stewardship Program is
to monitor the use of antibiotics in our residents . 4. If an antibiotic is indicated, prescribers will provide
complete antibiotic orders including the following elements: a. Drug name; b. Dose; c. Frequency of
administration; d. Duration of treatment: 1) start and stop date; or 2) number of days of therapy e. route of
administration; and f. indications of use . 11. When a culture and sensitivity (C&S) is ordered lab results and
the current clinical condition will be communicated to the prescriber as soon as available to determine if
antibiotic therapy should be started, continued, modified or discontinued.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
105465
If continuation sheet
Page 8 of 8