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
medical record review, observation, interviews, review of the National Pressure Injury Advisory Panel
(NPIAP) guidelines and facility policy review, the facility failed to ensure comprehensive and accurate
pressure ulcer assessments. The facility also failed to ensure treatments were implemented timely and
pressure-relieving interventions were implemented per the care plan. This affected one (Resident #7) of
three residents reviewed for pressure ulcers. The facility census was 75. Findings include:Review of the
medical record revealed Resident #7 was admitted to the facility on [DATE] and re-admitted on [DATE] with
diagnoses including right femur fracture, chronic kidney disease, anemia, diabetes, protein-calorie
malnutrition, dementia, heart disease, venous insufficiency, and pressure ulcer. Review of Resident #7's
consents revealed on 08/15/25 the resident signed consent to be seen by the wound nurse. Review of
Resident #7's impaired skin integrity/pressure ulcer plan of care related to diabetes, dementia, chronic
kidney disease, anemia, neuropathy, fistula, surgical site hip, moisture-associated skin damage (MASD),
and left heel dated 08/15/25 and revised 09/17/25 revealed interventions including treatments per order,
pressure reduction devices as ordered, and inspect the skin during daily routine care. Review of Resident
#7 re-admission skin grid pressure ulcer assessment dated [DATE] revealed the resident had a new
suspected deep tissue injury (purple or maroon localized area of discolored intact skin or blood-filled blister
due to damage of underlying soft tissue from pressure and/or shearing) on the sacrum that measured 1.5
centimeters (cm) by 1.5 cm by 0.01 cm (skin not intact). The area was noted to be red, non-blanchable, no
drainage noted, possible sheering injury around area. Foam placed and wound nurse to be consulted.
There was no documented evidence that the physician was notified or that the wound nurse was consulted
until 09/26/25. Further review of Resident #7's orders revealed the resident was ordered a pressure
reducing cushion on 08/21/25. Review of Resident #7's weekly skin observation dated 08/27/25 revealed
the resident's skin was intact. The area for previously identified and newly acquired areas was left blank.
Review of Resident #7's admission and five-day [NAME] Data Set (MDS) dated [DATE] revealed the
resident did not have a pressure ulcer; however, was assessed to be at risk for developing a pressure
ulcer/injury. The resident had pressure-reducing devices for the chair and bed. The resident was receiving
an application of a non-surgical dressing to an area other than the feet. Review of Resident #7's dietary
note dated 08/28/25 revealed no evidence of skin alterations. Review of Resident #7's skin grid
non-pressure assessment dated [DATE] revealed the resident had MASD on the sacrum that was acquired
on 08/21/25 that measured 1.2 cm by 1.2 cm by 0.1 cm. There was no documented evidence of the amount
of drainage, odor, tunneling/undermining, or description of the wound or physician notification. Review of
Resident #7's weekly skin observation dated 09/03/25 revealed the resident's skin was not intact. The
resident had MASD and a surgical area. There was no documented evidence of descriptions of the wounds.
Review of Resident #7's weekly skin observation dated 09/10/25 revealed the resident's skin was not intact.
The resident had MASD,
Residents Affected - Few
(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:
366331
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
366331
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/17/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sienna Skilled Nursing & Rehabilitation
250 Cadiz Road
Wintersville, OH 43953
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
Residents Affected - Few
surgical area and a newly acquired pressure and surgical area. There was no documented evidence of
descriptions of the wounds. Review of Resident #7's skin grid non-pressure assessment dated [DATE]
revealed the resident had MASD on the sacrum that was present on admission [DATE]) that measured 1.1
cm by 1.3 cm by 0.1 cm. There was moderate drainage, the type of drainage was not identified. No odor or
tunneling/undermining. There was no description of the wound or evidence the physician was notified.
Review of Resident #7's actual skin impairment integrity/pressure ulcer related to MASD, left heel/sacrum
plan of care dated 09/17/25 revealed interventions including complete skin documentation per facility policy,
provide wound care per physician order, and refer to wound physician as needed. Review of Resident #7's
weekly skin observation dated 09/17/25 revealed the resident's skin was not intact. The resident had MASD
and pressure previously identified. There were no descriptions of the wounds. Review of Resident #7's skin
grid non-pressure dated 09/19/25 revealed the resident had MASD on the sacrum that was acquired on
08/21/25 that measured 1.0 cm by 1.2 cm by 0.1 cm and 100% granulation. There was scant drainage, type
not of drainage not identified. No odor or tunneling. There was no evidence that the physician was notified.
Review of Resident #7's weekly skin observation dated 09/24/25 revealed the resident's skin was not intact.
The resident had MASD and pressure previously identified. There were no descriptions of the wounds.
Review of Resident #7's weekly skin grid pressure ulcer assessment for 08/28/25, 09/04/25, 09/11/25,
09/18/25, and 09/25/25 revealed no evidence a skin pressure ulcer assessment was completed on the
sacrum. Review of Resident #7's weekly skin grid pressure dated 09/26/25 revealed the resident had a
stage II pressure ulcer (partial thickness loss of dermis presenting as a shallow open ulcer with a red pink
wound bed, without slough, may also present as an intact or open/ruptured serum filled blister) on the
sacral region that originated on 08/21/25 that measured 2.5 cm by 4.5 cm by 0.2 and was a stage III
pressure ulcer (full thickness tissue loss, subcutaneous fat may be visible but bone, tendon or muscle are
not exposed, slough may be present but does not obscure the depth of tissue loss, may include
undermining and tunneling) per the wound nurse consult dated 09/26/25. The area was 90% granulation,
10% slough, and peri wound moist and fragile. There was moderate serosanguinous drainage with no odor.
The wound status since last assessment was left blank and no evidence that the physician was notified.
Review of Resident #7's medication and treatment record and orders dated 08/21/25 to 09/30/25 revealed
no evidence a treatment was implemented to the sacrum area from 08/21/25 to 09/03/25. Review of
Resident #7's wound nurse consult note dated 09/26/25 revealed the wound nurse completed a telehealth
visit due to unavailability or difficulty with coordinating in person evaluation. The initial assessment revealed
the wound on the sacral area was a stage III due to there being 10% slough covering the wound bed. The
area was not measured. There was moderate serosanguinous drainage, and the skin was moist and fragile.
The treatment plan would change to silver alginate covered with silicone dressing daily and as needed.
Recommend a pressure reduction cushion in wheelchair. Review of Resident #7's physician progress notes
dated 08/21/25 to 09/30/25 revealed no evidence the physician had mentioned or assessed the pressure
ulcer on the sacrum. Observation of Resident #7 on 09/29/25 at 1:48 A.M., with Licensed Practical Nurse
(LPN) #108 revealed the resident was up in her wheelchair in therapy. Therapy stood the resident up, and
there was no pressure relieving cushion in the resident's wheelchair. The resident had a [NAME] Virginia
(WV) stadium cushion that was flat. The LPN and therapy staff confirmed the WV stadium cushion was flat
and not a proper pressure relieving cushion. Interview on 09/29/25 at 12:52 P.M., with LPN #108 and
Interim Director of Nursing (DON) #140 and New DON #200, who started today, confirmed Resident #7
was re-admitted on [DATE] with a pressure ulcer on the sacrum. The LPN reported he recently just took
over wounds and was not certified in wound care. The LPN confirmed on
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366331
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
366331
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/17/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Sienna Skilled Nursing & Rehabilitation
250 Cadiz Road
Wintersville, OH 43953
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
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
08/28/25 09/04/25, 09/11/25, 09/18/25 or 09/25/25 he did not complete the weekly pressure ulcer
assessment form; however, he was still learning and documented the area on the non-pressure form as
MASD instead of pressure. Interim DON #140 confirmed there was no documented evidence the resident's
physician had accessed the pressure ulcer, and the wound nurse did not assess the pressure ulcer until
09/26/25 due to the resident was in dialysis on the day the wound nurse visits the facility. LPN #108 and
DON confirmed there was no evidence a treatment was implemented to the sacrum from 08/21/25 until
09/03/25. DON #140 reported she felt the non-pressure assessments were comprehensive even though the
assessment did not document the stage of the pressure nor was it comprehensive to include all details
regarding the description of the wound (wound bed appearance, edge of wound, type of drainage, etc.).
Interview on 09/29/25 at 3:35 P.M., LPN #120 confirmed the admission and five-day MDS dated [DATE]
was inaccurate and did not reflect the resident's pressure ulcer on the sacrum on admission [DATE]. LPN
#120 reported she would modify the MDS assessment. Review of the facility's undated policy and
procedure titled Skin Measurement/Skin Grid revealed the facility would maintain an active record or any
pressure ulcer/wound that was discovered upon admission or that developed during the course of the
residents' stay. This is to monitor the progress of healing of the pressure ulcer and determine the need for
alternative treatment methods. The wound would be measured and assessed for the wound characteristics.
The physician and responsible party would be notified of the new skin development and an order for
treatment would be obtained. The initial and every seven days assessment/measurements are documented
on the electronic form. Review of the facility's undated policy and procedure titled Staging of Pressure
Ulcers revealed the facility would assess each resident's skin condition and measure the skin area as
indicated in the regulatory guidelines and National Pressure Injury Advisory Panel (NPIAP) guidelines.
Review of the facility's undated policy and procedure titled Pressure Ulcer Prevention and Risk
Identification revealed if a new skin area was identified on the assessment or during any other type of care
or service, the licensed nurse would initiate a skin grid/measurement flow record. The skin grid would be
updated every seven days until the area was resolved. The physician and responsible party would be
notified by the licensed nurse promptly of the newly identified skin area and treatment would be initiated
according to the physician order. A care plan would be developed and updated routinely with identified skin
risk and/or actual wound development. Intervention would be implemented as indicated by the physician
and as determined by the Interdisciplinary team. Review of the NPIAP wound documentation guidelines
dated 02/2027 revealed when charting a description of a pressure ulcer the following components should
be part of your weekly assessment: location, stage, dimensions, undermining/tunneling, wound base
descriptions, drainage, wound edges, odor, pain, and progress. This deficiency represents non-compliance
investigated under Complaint Number 2608722.
Event ID:
Facility ID:
366331
If continuation sheet
Page 3 of 3