F 0686
Provide appropriate pressure ulcer care and prevent new ulcers from developing.
Level of Harm - Actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, interviews with facility staff and the nurse practitioner, review of open and closed medical
records, review of skin assessments, review of wound assessment reports, review of physician orders,
review of treatment administration records, and policy review, the facility failed to ensure a resident's skin
impairment was timely identified and treatment provided. This resulted in Actual harm to Resident #88 on
05/13/24 when the facility failed to develop and implement a care plan that included skin integrity
monitoring with the use of an abdominal binder and failed to assess and monitor the resident's skin every
shift that resulted in Resident #88 developing a Stage 3 pressure ulcer (full-thickness loss of skin, in which
subcutaneous fat may be visible in the ulcer and granulation tissue and epibole (rolled wound edges) are
often present) caused by the abdominal binder the resident was required to wear. Additionally, the facility
failed to ensure Resident #34, identified at risk for skin breakdown on admission [DATE]), and who was
assessed with excoriation/incontinence erosion to the coccyx area, received appropriate treatment and
services to prevent the area from worsening by failing to document the initial wound assessment describing
the wound, including measurements in accordance with facility policy, from 06/14/24 until the nurse
practitioner evaluated the wound on 06/24/24. Furthermore, Resident #34 had no documented treatment in
place for the coccyx until 06/20/24, six days after admission, placing the resident at risk for potential skin
breakdown at a Severity Level 2 (no actual harm with the potential for more than minimal harm). This
affected two (#88 and #34) of three residents reviewed for pressure ulcers. The facility census was 86.
Residents Affected - Few
Findings include
1. Review of the closed medical record for Resident #88 revealed an admission date of 03/21/24. The
resident was discharged to the hospital on [DATE] and had not returned to the facility. Diagnoses included
hemiplegia and hemiparesis affecting right dominant side, stage four pressure ulcer of the sacrum,
hypertension, type two diabetes mellitus, gastrostomy, tracheostomy, and congestive heart failure.
Review of the admission Minimum Data Set (MDS) assessment dated [DATE] revealed the resident had
mild cognitive impairment. The resident was admitted with one Stage 4 pressure ulcer and one
Unstageable pressure ulcer. The resident was dependent on staff for toileting, hygiene, and bed mobility.
Review of the pressure ulcer risk assessments dated 03/21/24, 03/29/24, 04/11/24, and 04/18/24 revealed
the resident was at very high risk for developing pressure ulcers.
Review of the care plan initiated 03/26/24 revealed the resident was at risk for skin break down related to
weakness, impaired mobility, history of cerebral vascular accident with right sided weakness, incontinence
status, diuretic medication use, diabetes mellitus and anticoagulant use.
(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:
365339
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
365339
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/27/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Park Terrace Rehabilitation Center
2735 Darlington Rd
Toledo, OH 43606
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 - Actual harm
Residents Affected - Few
Interventions included to apply barrier cream after each incontinent episode, assist to turn and reposition at
frequent intervals to provide pressure relief, complete weekly skin assessment, keep skin clean and dry,
monitor fit of clothing and footwear, change as needed and monitor for proper placement of tubes,
catheters, and other devices, report changes in skin integrity to nurse, provide pressure redistribution
surface to bed and chair as ordered, and obtain laboratory tests as ordered by physician.
Further review of the care plan revealed the resident had actual impairment to skin including an
Unstageable pressure ulcer to the sacrum, a Stage 1 pressure ulcer to the right shoulder (resolved on
04/08/24) and a skin tear to the left forearm. The care plan was not updated to include the Stage 3 pressure
ulcer to the axilla identified on 05/13/24. Additional interventions included inspecting skin on a daily basis
when performing and assisting with personal care and Activities of Daily Living (ADLs) and report any
abnormalities to supervisor and to monitor/document location, size and treatment of skin injury, report
abnormalities to physician, and provide treatment as ordered.
Review of a physician order dated 04/22/24 revealed the resident was ordered an abdominal binder at all
times every shift for proper placement. Review of a physician order dated 04/23/24 revealed the resident
had orders for a premium low air loss mattress with safety bolsters every shift to promote wound healing.
There were no orders to monitor the resident's skin integrity due to the use of the abdominal binder.
Review of a skilled nurses note dated 05/12/24 at 1:33 P.M. revealed the resident had no new changes to
skin integrity.
Review of nursing assistant charting dated 05/12/24 at 9:59 P.M. revealed the resident had no new
observed skin alterations.
Review of a nurses note dated 05/13/24 at 2:27 A.M., revealed the resident had a new open wound on right
upper extremity, in the crease of his armpit. The nurses note revealed, looks like it could be from abdominal
binder rubbing against it. The wound measured two inches in width. The area was cleaned with soap and
water, patted dry, and left open to air. The nurse practitioner was notified.
Review of an incident report dated 05/13/24 at 2:34 A.M. revealed the nursing assistant noticed drainage
coming from the resident's right side armpit when changing the resident. The resident had an abdominal
binder that was rubbing against his armpit.
Review of a nurse practitioner (NP) wound assessment report dated 05/13/24 revealed the resident had a
new Stage 3 pressure area to the right axilla. The wound measured 0.6 centimeters (cm) in length by 3.3
cm in width by 0.5 cm in depth. The wound had one percent (%) to 24% epithelial tissue, 50% to 74%
granulation tissue, and 25% to 49% slough. There was exposed subcutaneous tissue with unattached
wound edges with moderate serosanguineous drainage. The periwound was fragile and reddened. A new
treatment was initiated to cleanse with wound cleanser, treat with calcium alginate and antifungal powder to
the periwound and cover with ABD (abdominal) pad daily. The NP also made a recommendation to be sure
the abdominal binder was secured to the area of the abdomen.
Review of the treatment administration record (TAR) dated 05/01/24 through 05/29/24 revealed the
resident's order for the abdominal binder at all times as tolerated every shift for maintain proper placement
was completed from 05/01/24 through 05/12/24 at 6:00 P.M. Further review of the TAR revealed the
treatment to the axilla was completed per physician orders.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365339
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
365339
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/27/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Park Terrace Rehabilitation Center
2735 Darlington Rd
Toledo, OH 43606
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 - Actual harm
Residents Affected - Few
Interview on 06/24/24 at 5:13 P.M., the Director of Nursing (DON) revealed the resident had an abdominal
binder to prevent him from pulling on his feeding tube. The DON revealed the resident developed a Stage 3
pressure ulcer to the axilla from the abdominal binder. The DON revealed the nurses should have been
checking the resident's skin integrity every shift when wearing the abdominal binder and when
administering tube feedings to the resident. The DON verified there was no documentation the resident's
skin integrity was monitored by the nurses every shift. Further interview on 06/25/24 at 2:50 P.M. with the
DON revealed the resident's care plan had not included the use of the abdominal binder or the wound to
the axilla. Continued interview with the DON revealed the facility had no policy on the use of an abdominal
binder.
Interview on 06/25/24 at 9:36 A.M., Licensed Practical Nurse (LPN) #200 stated the nursing assistants
brought it to her attention the resident's abdominal binder was up under the resident's armpit. LPN #200
stated the area was red in the crease and there was a split in the skin. LPN #200 stated she removed the
abdominal binder. LPN #200 stated the abdominal binder must have moved up under the arm from the
resident moving.
Interview on 06/25/24 at 1:03 P.M., Nurse Practitioner (NP) #500 revealed the wound to the resident's axilla
was consistent with the resident's abdominal binder riding up under his arm. NP #500 revealed the resident
had a Stage 3 pressure ulcer to the axilla.
Interview on 06/26/24 at 12:30 P.M., LPN #280 revealed she completed a skin assessment on the resident
on 05/12/24 and the resident had no skin alterations in his armpit. LPN #280 revealed the resident wore a
gown and it was easy to check his skin.
Review of the policy Prevention of Pressure Ulcers/Injuries, (revised 07/2017) revealed the facility would
review the resident's plan of care and identify pressure ulcer risk factors and interventions designed to
reduce or eliminate those considered modifiable. Further review of the policy revealed resident's skin would
be inspected on a daily basis when performing or assisting with personal care or ADL's. There were no
guidelines for monitoring skin when an abdominal binder was in use.
2. Review of the medical record for Resident #34 revealed an admission date of 06/14/24. Diagnoses
included atrial fibrillation, heart failure, hypertension, chronic obstructive pulmonary disease, chronic kidney
failure, and osteoarthritis.
Review of the admission Minimum Data Set (MDS) assessment dated [DATE] revealed the resident had
intact cognition. The resident required substantial/maximal assistance with toileting hygiene, and
supervision/touching assistance for transfers and ambulation. The resident was noted with an Unstageable
deep tissue injury (DTI) and two venous or arterial ulcers.
Review of hospital documentation dated 06/07/24 revealed the resident had a DTI to the left buttock with
non-blanchable erythema and no odor. The treatment included to apply Calmoseptine/zinc oxide with
menthol to the wound.
Review of an admission pressure risk assessment dated [DATE] revealed the resident was at risk for skin
breakdown.
Review of the admission skin assessment dated [DATE] at 7:10 P.M. revealed the resident was noted with
redness to the coccyx area with no wound description.
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365339
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
365339
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
06/27/2024
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Park Terrace Rehabilitation Center
2735 Darlington Rd
Toledo, OH 43606
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 - Actual harm
Residents Affected - Few
Review of an alteration in skin integrity report dated 06/14/24 at 7:12 P.M. revealed the resident had
excoriation/incontinence erosion to the coccyx area; however, there was no assessment of the wound or
wound measurements.
Review of the nursing admission assessment dated [DATE] at 11:50 P.M. revealed there was no
assessment of the resident's coccyx completed.
Review of a skin assessment dated [DATE] at 1:38 P.M. noted no new skin abnormalities/areas.
Review of a skin assessment dated [DATE] at 3:02 P.M. revealed the resident had a pressure area to the
coccyx, but there was no description of the wound.
Review of a weekly skin assessment dated [DATE] at 9:21 A.M. noted the resident had a pressure area on
his coccyx; however, there was no description of the wound.
Review of the physician orders from 06/14/24 through 06/19/24 revealed there were no treatment orders in
place for the wound to the coccyx. Review of a physician order dated 06/20/24 revealed to cleanse the
wound with wound wash, pat dry, apply calcium alginate and cover with bordered gauze dressing every
shift. On 06/24/24 the treatment order for the coccyx changed to cleanse with wound wash, pat dry, apply
Calmoseptine cream and cover with ABD (abdominal) pad every shift.
Review of the treatment administration record from 06/14/24 through 06/25/24 revealed no documented
treatments were completed for the coccyx wound until 06/20/24.
Review of a nurse practitioner wound report dated 06/24/24 revealed the resident had a 3.5 centimeter (cm)
in length by 2 cm in width by 0.1 cm in depth Stage 2 pressure ulcer (partial-thickness loss of skin with
exposed dermis, presenting as a shallow open ulcer. The wound bed is viable, pink or red, moist, and may
also present as an intact or open/ruptured blister) to the coccyx with 100% epithelial tissue, attached
wound edges, and scant serosanguineous exudate with a fragile and red periwound. The nurse practitioner
ordered to cleanse with soap and water, pat dry, apply Calmoseptine, and cover with an ABD and change
twice daily.
Observation on 06/25/24 at 11:08 A.M. of wound care with Registered Nurse (RN) #301 and the Director of
Nursing (DON) revealed the resident had a Stage 2 pressure ulcer to the coccyx approximately three
centimeters in length, by two centimeters in width and minimal depth. The area was red with scant drainage
with no signs of infection.
Interview on 06/25/24 at 1:11 P.M., RN #301 and the DON verified there was no documented initial wound
assessment of the resident's coccyx from 06/14/24 until the nurse practitioner evaluated the wound on
06/24/24. RN #301 revealed the nurse practitioner evaluated the resident on 06/17/24 but could not
evaluate his coccyx wound as he was in dialysis. RN #301 revealed the resident had no documented
treatment in place for the coccyx until 06/20/24. RN #301 revealed prior to 06/20/24 the nursing assistants
were applying barrier cream as needed to the wound. RN #301 revealed the resident had a reddened area
to the coccyx that was non-blanchable since admission.
Review of the policy Wound Care, revised 10/2010, revealed nurses would document all assessment data
(wound bed color, size, drainage, etc.) obtained when inspecting a wound.
This deficiency represents non-compliance investigated under Master Complaint Number OH00154816.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365339
If continuation sheet
Page 4 of 4