F 0686
Provide appropriate pressure ulcer care and prevent new ulcers from developing.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
clinical records review and staff interview, it was determined that the facility failed to ensure wound
treatment and assessment were completed and recommendation of a wound physician was followed for
three of eight residents reviewed (Residents 83, 87, and 242).
Residents Affected - Some
Findings include:
Review of Resident 83's clinical records revealed that the resident was admitted to the facility on [DATE],
with a diagnosis of Bladder Cancer and duodenal ulcer with surgical treatment.
Revie of Resident 83's clinical record revealed resident was admitted with a Stage 2 Pressure Ulcer
(Partial-thickness skin loss with exposed dermis) to the lower back with a measurement of 3.7 x 1.2 cms.
The wound was treated with normal saline and then covered with an Optifoam (silicone-bordered dressing)
dressing every three days.
Review of Resident 83's clinical record revealed a wound consult dated June 11, 2024, indicating the lower
back/lumbar spine wound was an Unstageable Pressure Ulcer (Obscured full-thickness skin and tissue
loss), with a measurement of 1.3 x 0.6 x 0.1 cms. With 100 % slough. The physician recommended
cleansing the wound with cleanser, applying Medihoney, and cover with Silicone dressing daily.
Review of Resident 83's clinical record revealed the Medihoney treatment recommended by the wound
physician was not implemented until June 27, 2024, 16 days after the recommended treatment was made
on June 11, 2024. During that time the unstageable wound to the lower back/lumbar spine was treated with
Optifoam dressing every three days.
Interview with the Director of Nursing (DON) conducted on July 1, 2024, revealed, after a resident is seen
by the wound physician, the unit manager was responsible for reviewing the recommendations and
notifying the primary physician of the order. The DON reported that the unit manager was not able to relay
the wound care treatment recommendation to the primary physician therefore wound treatment was not
changed to Medihoney until June 27, 2024.
The facility failed to ensure wound physician's recommendation for wound treatment of Resident 83's
unstageable wound to the lower back was followed.
Review of Resident 87's Progress Notes revealed a nursing entry dated June 6, 2024 at 7:54 p.m. stating
Resident noted with B/L (bilateral-both) heel DTI (Deep Tissue Injury- deep red, purple or maroon areas of
intact skin, non-intact skin or blood-filled blisters caused by damage to the underlying soft tissues).
(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:
395332
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
395332
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/01/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Wayne Center
30 West Avenue
Wayne, PA 19087
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 0686
Level of Harm - Minimal harm
or potential for actual harm
Review of Resident 87's clinical record revealed there was no full documentation of the wound discovered
on June 6, 2024 other than the above progress note.
Review of Resident 87's physician orders and Medication Administration Record for June 2024 revealed
there was no treatment to the DTI discovered on June 6, 2024 until June 10, 2024.
Residents Affected - Some
Review of Resident 87's wound evaluations revealed there was no thorough documentation, including
measurements and full description of the wound until June 18, 2024.
Interview with the Director of Nursing on July 1, 2024 at 10:30 a.m. confirmed the deep tissue injury found
on Resident 87 on June 6, 2024 were not thoroughly assessed until June 18, 2024 or any documented
evidence a treatment had been completed until June 10, 2024.
Review of Resident 242's wound consult dated June 18, 2024, revealed a Stage 3 Pressure Ulcer (Full
thickness skin loss) on the left buttock measuring 1.1. x 1.2 x 0.1 cm., with heavy serous drainage, 100%
granulation with no slough. The physician recommended cleansing the wound with a cleanser, applying
medical honey, and cover with Silicone bordered foam dressing daily.
Review of Resident 242's clinical record review revealed the Medihoney wound treatment recommended by
the wound physician was not implemented.
Interview with the DON on July 1, 2024, confirmed that the Medihoney treatment recommended by the
wound physician was not relayed to the primary physician thus, the order was not implemented.
The facility failed to ensure wound physician's recommendation for a Medihoney treatment for Resident
242's left buttock wound was followed.
28 Pa. Code 211.12 (c)(d)(1)(5) Nursing services
28 Pa Code 211.5(f) Clinical Records
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395332
If continuation sheet
Page 2 of 4
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
395332
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/01/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Wayne Center
30 West Avenue
Wayne, PA 19087
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 0694
Provide for the safe, appropriate administration of IV fluids for a resident when needed.
Level of Harm - Minimal harm
or potential for actual harm
Based on observation, staff interviews, clinical records, and the facility's policy and procedure review, it was
determined that the facility failed to ensure proper care and maintenance of a peripherally inserted central
catheter (PICC- medical device that is placed into a vein to allow access to the bloodstream) dressing to
one out of one resident reviewed (Resident 243).
Residents Affected - Few
Findings include:
Review of the facility's policy titled Central Vascular Access Device (CVAD) Dressing Change, last revised
on June 21, 2021, revealed that sterile dressing changes using standard -ANTT is performed: Upon
admission, if the transparent dressing is dated, clean, dry and intact, the admission dressing change may
be omitted and scheduled for seven days from the date on the dressing label; At least weekly; and if the
integrity of the dressing has been compromised.
Review of Resident 243's physician order revealed an order made on June 17, 2024, for Cefazolin Sodium
(Antibiotic) two grams intravenously (medication/fluids administered through a needle or tube inserted into
a vein) every eight hours for Bacteremia (infection in the blood).
Observation conducted on June 26, 2024, at 11:00 a.m., revealed Resident 243 was lying in bed, with a
PICC line to the upper arm. The transparent dressing to the PICC line was dated June 18, 2024.
Observation conducted July 1, 2024, at 11:10 a.m., in the presence of licensed nurse Employee E3,
revealed Resident 243's PICC line transparent dressing was dated June 18, 2024.
Interview conducted with Employee E3 on July 1, 2024, confirmed that Resident 243's PICC line
transparent dressing had a date of June 18, 2024. Employee E3 reported that the transparent dressing of
the PICC line should have been changed weekly.
Interview conducted with the Director of Nursing on July 1, 2024, revealed PICC line transparent dressing
is changed weekly. The Director of Nursing confirmed the dressing was not done weekly and was last done
on June 18, 2024.
The facility failed to ensure Resident 243's PICC line transparent dressing was changed weekly to prevent
parenteral infusion complications.
28 Pa. Code 211.12 (c)(d)(1)(5) Nursing services
28 Pa. Code 211.10(c) Resident care policies
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395332
If continuation sheet
Page 3 of 4
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
395332
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
07/01/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Wayne Center
30 West Avenue
Wayne, PA 19087
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.
Based on clinical records review and staff interview, it was determined that the facility failed to ensure PRN
(as needed) anti-anxiety psychotropic (any drug that affects brain activities associated with mental
processes and behavior) medication was administered with appropriate indication for one of five residents
reviewed (Resident 2).
Findings include:
Review of Resident 2's diagnosis list includes Depression (mental health disorder characterized by low
mood or loss of interest in activities that last for a long time and can interfere with normal functioning) and
anxiety disorder (mental health disorder characterized by feelings of worry, anxiety, or fear that are strong
enough to interfere with one's daily activities)
Review of Resident 2's Physician order (POS) dated June 12, 2024, revealed Alprazolam (anti-anxiety
medication) 0.5 mg one tab at bedtime.
Review of Resident 2's POS dated June 8, 2024, revealed Alprazolam 0.5 mg two tablets every six hours
as needed for anxiety.
Review of Resident 2's June 2024, Medication Administration Record revealed that from June 9, 2024, until
June 16, 2024, Resident 2 was administered PRN Alprazolam 12 times with no appropriate indication for
use.
Interview with the Director of Nursing was conducted on July 1, 2024. The facility failed to provide
documentation of appropriate indication for administering PRN Alprazolam to Resident 2.
The facility failed to ensure Resident 2 was administered with PRN anti-anxiety psychotropic medication
with appropriate indications.
28 Pa. Code: 211.12(d)(5) Nursing Services
28 Pa. Code: 211.12 (d)(1)(3) Nursing Services
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
395332
If continuation sheet
Page 4 of 4