F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
medical record review, observations, resident and staff interviews, and policy review, the facility failed to
timely obtain and implement hospital recommendations for positive airway pressure devices, and the facility
failed to have physician orders for positive airway pressure devices. This affected one (Resident #72) of
three residents reviewed for positive airway pressure devices. The facility census was 101.
Residents Affected - Few
Findings include:
Review of the medical record revealed Resident #72 was admitted to the facility on [DATE]. Diagnoses
included chronic obstructive pulmonary disease (COPD) and diastolic heart failure. Review of the most
recent Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed Resident #72 had moderately
impaired cognition, had no behaviors, and did not reject care.
Review of the care plan dated 08/05/24 revealed Resident #72 was at risk for complications with the
respiratory system due to multiple diagnoses. Resident #72 was noted to adjust her oxygen settings on her
own. Interventions included assess/report signs of hypoxia, incentive spirometer as ordered, oxygen
therapy as ordered, and remind resident not to adjust her oxygen settings as needed.
Resident #72 discharged to the hospital on [DATE] and returned to the facility on [DATE].
Review of the hospital Discharge summary dated [DATE] revealed Resident #72 presented to the
Emergency Department (ED) with shortness of breath, increased confusion, and taking off her oxygen per
nursing facility on 09/03/24 and was admitted with COPD exacerbation, acute on chronic respiratory failure
with hypercapnia and hypoxia, and acute metabolic encephalopathy. Resident #72 was treated with
steroids, bronchodilators, and bilevel positive airway pressure (BiPAP), and showed significant
improvement, and was back to her baseline at the time of discharge. Resident #72 was weaned to her
baseline oxygen of three liters per minute and was recommended to continue using BiPAP while sleeping at
the facility. There were no specifications noted on the discharge summary for BiPAP settings.
Review of the medical record revealed no progress noted regarding follow-up with the hospital for
clarification for BiPAP settings after return to the facility on [DATE]. There were no active or completed
physician orders for the use BiPAP for Resident #72. Resident #72 discharged to the hospital on [DATE].
Review of the hospital paperwork dated 09/17/24 revealed Resident #72 presented to the ED with a
complaint of altered mental status (AMS). It was strongly suggested the altered mental status was
secondary to medication. While Resident #72 would most likely benefit from BiPAP, it was highly unlikely
she would use BiPAP. Since she did not present with acute hypercapnia nor need BiPAP during this
(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 3
Event ID:
365530
Printed: 05/15/2026
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
365530
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/07/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Delhi Post-Acute
5999 Bender Road
Cincinnati, OH 45233
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 0695
admission, recommendations included to hold off on BiPAP after discharge.
Level of Harm - Minimal harm
or potential for actual harm
There were no active or completed physician orders for the use BiPAP for Resident #72.
Residents Affected - Few
During an interview on 10/01/24 at 2:38 P.M., Registered Nurse (RN) #226 verified Resident #72 had no
records for BiPAP in her electronic medical record. RN #226 stated she knew Resident #72 looked in the
medical record and verified Resident #72 did not have an order in the chart for BiPAP and the resident had
a BiPAP machine in her room.
During an interview and observation on 10/01/24 at 2:57 P.M., Resident #72 was observed sitting up in bed
with a BiPAP machine on a cart at bedside. Resident #72 stated the machine had been ordered around the
beginning of September, date not specified. The resident stated the device originally sat in her room about
four to five nights, unused, because none of the staff knew how to apply it. An unidentified nurse set up the
device, explained how to use it, and the resident stated she both applied and turned on the device herself
at bedtime.
During an interview on 10/01/24 at 3:57 P.M., the Director of Nursing (DON) stated she called their supplier
last week (09/27/24) in response to family concerns that Resident #72 was not getting her BiPAP. The DON
stated Respiratory Therapy (RT) was supposed to come assess the resident first before the machine was
delivered to the resident. The DON stated Resident#72 had not been assessed by RT, and the DON was
not sure why the BiPAP machine had been delivered to her room. The DON verified Resident #72 used the
machine without physician orders. The DON did not know how the machine had been delivered without an
order.
Observation and interview on 10/02/24 at 10:19 A.M. revealed Resident #73 was seated upright in bed with
BiPAP mask on face and machine running. Licensed Practical Nurse (LPN) #154 was standing at bedside
with resident adjusting straps to facemask for BiPAP machine. LPN #154 stated Resident #72 had an order
for BiPAP to be used at bedtime and as needed (PRN). The nurse stated she walked into the room and
Resident #72 was putting on the mask because she said she wanted to take a nap. The nurse stated she
had just turned the machine on and was adjusting the straps when this surveyor walked into the room. The
nurse verified there was an error message on the machine and removed the mask. LPN # 154 stated she
did not know what the settings were supposed to be and stated she had to check the order. LPN # 154
verified Resident #73 did not have an order on file for the BiPAP machine and stated she would have to call
the provider for settings before she could apply the mask to the resident. LPN #154 stated she did not know
how long Resident #73 had the device. LPN # 154 stated she had just returned from a two-week vacation
and believed Resident #72 had the device before she left.
Review of the facility document titled CPAP/BiPAP Support, dated 03/2015, revealed prior to using positive
air pressure devices, nurses should check the medical record for baseline oxygen saturation levels, review
the physician's order to determine oxygen concentration, flow, and Positive End-Expiratory Pressure
(PEEP) settings for the machine.
This deficiency represents non-compliance investigated under Complaint Number OH00158245.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365530
If continuation sheet
Page 2 of 3
Printed: 05/15/2026
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
365530
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
10/07/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Delhi Post-Acute
5999 Bender Road
Cincinnati, OH 45233
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
medical record review, staff interview, and policy review, the facility failed to provide medications as
ordered. This affected one (Resident #72) of five residents reviewed for medication administration. The
facility census was 101.
Findings include:
Review of the medical record revealed Resident #72 was admitted to the facility on [DATE]. Diagnoses
included chronic obstructive pulmonary disease (COPD), anxiety disorder, and major depressive disorder.
Review of the most recent Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed Resident #72
had moderately impaired cognition and did not reject care.
Review of the care plan dated 08/05/24 revealed Resident #72 was at risk for pain or discomfort due to
shingles neuropathy, chronic back pain, and right fourth and fifth toe fractures. Interventions included to
administer medications as ordered, assess pain every shift and as indicated, and notify physician of
unmanageable/intolerable pain.
Review of Resident #72's physician orders dated August 2024 revealed an order for Lyrica (generic is
pregabalin) oral capsule 75 milligrams (mg) - Give one capsule by mouth three times a day for pain.
Review of the Medication Administration Record (MAR) dated August 2024 revealed Resident #72 did not
receive doses of Lyrica 75 mg on 08/12/24 (three doses), 08/13/24 (three doses), and 08/17/24 (three
doses).
Review of the progress notes dated 08/12/24, 08/13/24, and 08/17/24 revealed Lyrica (Pregabalin) 75 mg
was not available to be administered.
During an interview on 10/01/24 at 2:38 P.M., Registered Nurse (RN) #226 verified Resident #72 did not
receive nine doses of Lyrica as ordered on 08/12/24, 08/13/24, and 08/17/24 because the facility did not
have medication and the medication was unavailable in the emergency supply.
Review of the policy titled Administering Medications dated 04/2019 revealed medications were
administered in a safe and timely manner and within one hour of their prescribed time.
This deficiency represents non-compliance investigated under Complaint Number OH00158245.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365530
If continuation sheet
Page 3 of 3