F 0695
Provide safe and appropriate respiratory care for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
Based on review of facility policy and clinical records, observations, and staff interview, it was determined
that the facility failed to provide oxygen according to physician's orders for one of one residents reviewed for
respiratory services (Resident R1).
Residents Affected - Few
Findings include:
Review of facility policy dated 8/2024, entitled Oxygen Administration indicated that Verify physician order
for desired oxygen saturation and oxygen flow rate. And do not change the oxygen flow rate on fixed flow
orders or titrate outside ordered parameters without contacting the physician and obtaining appropriate
orders.
Resident R1's clinical record revealed an admission date of 8/16/24, with diagnoses that included chronic
obstructive pulmonary disease (condition when your lungs do not have adequate air flow), and
hypertension (high blood pressure).
Review of Resident R1's clinical record revealed a physician's order dated 8/16/24, for Oxygen via Nasal
Cannula (a thin tube with two prongs that fit into the resident's nostrils to deliver oxygen) 3 lpm (liters per
minute) at all times.
Observation on 9/4/24, at 10:30 a.m. revealed Resident R1 laying in his/her bed with supplemental oxygen
in place and the liter flow rate set at 2 lpm. Observation on 9/4/24, at 12:25 p.m. revealed Resident R1
laying in his/her bed with supplemental oxygen in place and liter flow rate set at 2 lpm. Observation on
9/5/24, at 8:50 a.m. revealed Resident R1 laying in his/her bed with supplemental oxygen in place and the
liter flow rate set at 2 lpm.
During an interview on 9/5/24, at 12:50 p.m. Registered Nurse Employee E2 confirmed that Resident R1's
supplemental oxygen was on and set at 2 lpm and the provision of their respiratory services was not
consistent with the physician's order dated 8/16/24, for oxygen at 3 lpm.
28 Pa. Code 211.10(c) Resident care policies
28 Pa. Code 211.12(d)(1)(5) Nursing services
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 2
Event ID:
395966
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
395966
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
09/06/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
UPMC Northwest Transitional Care Unit
100 Fairfield Drive
Seneca, PA 16346
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 review of facility policy, observation, and staff interviews, it was determined that the facility failed
to store controlled schedule II-V medications (medications that may be abused or cause addiction that are
closely monitored due to high risk of diversion) in a separately locked, permanently affixed compartment in
the medication refrigerator.
Findings include:
A facility policy entitled, Management of Controlled Drugs dated 8/2024, revealed, Storage and
maintenance of Controlled drugs: Store and maintain controlled drugs properly according to federal, state,
or local regulations.
Observation on 9/4/24, at 1:05 p.m. of the medication room refrigerator revealed several vials of controlled
scheduled II-V medications in a separately locked container that was attached to a removable shelf,
therefore it was not permanently affixed to the refrigerator, this was witnessed and confirmed by the
Licensed Practical Nurse Employee E1.
Interview with the Director of Nursing on 9/4/24, at approximately 1:30 p.m. confirmed that the controlled
scheduled II-V medications should be stored in a separately locked permanently affixed compartment, and
not attached to a removable shelf.
28 Pa. Code 201.14(a) Responsibility of licensee
28 Pa. Code 201.18(b)(1) Management
28 Pa. Code 201.18(e)(1) Management
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395966
If continuation sheet
Page 2 of 2