F 0578
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Honor the resident's right to request, refuse, and/or discontinue treatment, to participate in or refuse to
participate in experimental research, and to formulate an advance directive.
Based on record review, staff interview, and facility policy, the facility failed to have advance directives in the
physical medical record as required. This affected one resident (#56) of 19 residents reviewed for advanced
directives. The facility census was 65.
Findings include:
Review of electronic medical record for Resident #56 revealed an admission date of 06/14/23 with pertinent
diagnoses of hemiplegia and hemiparesis following cerebral infarction (stroke) affecting left non-dominant
side, nontraumatic intracerebral hemorrhage (ruptured blood vessel in the brain), dysphagia (difficulty
swallowing) following cerebral infarction, Bell's Palsy (a type of facial paralysis), major depressive disorder,
and anxiety disorder.
Review of the 09/21/23 quarterly Minimum Data Set (MDS) assessment revealed the resident was
cognitively intact and required substantial/max assistance for eating, oral hygiene, and upper body dressing
and was dependent on staff for lower body dressing.
Further review of the medical record revealed Resident #56 had a physician order dated 07/14/23 for an
advanced directive to be a do not resuscitate comfort care arrest (DNRCC-A) code status.
Review of the DNR Comfort Care form scanned into Resident #56's electronic medical chart, which was
signed by the nurse practitioner on 07/14/23, confirmed Resident #56 had an advanced directive to be a
DNRCC-A code status.
Review of the Resident #56's paper (hard) medical record on 11/22/23 at 2:45 P.M. with Regional Director
of Clinical Operations #475 revealed there was no DNR Comfort Care form in the chart.
Interview on 11/22/23 at 2:45 P.M. with the Regional Director of Clinical Operations #475 verified Resident
#56's physical medical record did not have the DNR Comfort Care form in the chart as required.
Review of undated facility policy Advance Directive (Resident's Right to Choose), revealed upon admission
should the resident have an Advance Directive, copies would be made and placed on the hard chart
medical record as well as communicated to the staff.
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 5
Event ID:
365732
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
365732
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Austintown Healthcare Center
650 S Meridian Road
Youngstown, OH 44509
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 0693
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Ensure that feeding tubes are not used unless there is a medical reason and the resident agrees; and
provide appropriate care for a resident with a feeding tube.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observation, record review, review of policy and interviews, the facility failed to ensure gastrostomy tube
(G-tube) medications were administered using proper technique. This effected one resident (Resident #49)
of three residents reviewed for G-tube medication administration. The facility census was 65.
Findings include:
Review of Resident #49's medical record revealed an admission date of 12/29/22. Diagnoses included
acute respiratory failure with hypoxia, atrial fibrillation, major depressive disorder, moderate protein-calorie
malnutrition, dysphagia and hypertension.
Review of Resident #49's annual Minimum Data Set (MDS) 3.0 assessment dated [DATE] revealed
Resident #49 had severely impaired cognition and required maximal assistance by one to two staff
members for all Activities of Daily Living (ADLs). All medications were provided through his G-tube.
Review of Resident #49's physicians orders revealed orders for all medications to be given via G-tube
including an order for Hydralazine 25 milligrams (mg) every eight hours for hypertension.
Observation of medication administration on 11/21/23 at 2:00 P.M. by Licensed Practical Nurse (LPN) #427
for Resident #49 of administration of Hydralazine 25 mg via gastrostomy tube (G-tube) revealed LPN #427
used ice water from the nursing cart to dissolve medication for administration and used ice water to flush
G-tube before and after medication administration.
Interview on 11/21/23 at 2:15 P.M. with LPN #427 revealed he confirmed he used ice water to dissolve the
medication and used ice water to flush the G-tube before and after medication administration. LPN #427
confirmed the water was ice cold and he was supposed to use tepid or room temperature water for
administration and flush.
Interview on 11/21/23 at 2:30 P.M. with the Director of Nursing (DON) revealed staff were to use room
temperature or tepid water to dissolve medications and with flushes before and after each medication. She
stated they are not to use ice water.
Review of the undated facility policy titled Medication Administered by Enteral Tube, revealed under the
procedure section letter I stated to dilute medication with 10-30 milliliters of tepid (not hot or cold) water.
Under section III titled Administration of Medications via G-tube letter J revealed 15 milliliters of tepid water
to be used to flush before and after medication administration.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365732
If continuation sheet
Page 2 of 5
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
365732
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Austintown Healthcare Center
650 S Meridian Road
Youngstown, OH 44509
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 0851
Level of Harm - Potential for
minimal harm
Residents Affected - Many
Electronically submit to CMS complete and accurate direct care staffing information, based on payroll and
other verifiable and auditable data.
Based on interview and record review, the facility failed to submit complete and accurate staffing
information for the Payroll-Based Journal (PBJ) report to Centers for Medicare and Medicaid Services
(CMS). This had the potential to affect all 65 residents in the facility.
Findings include:
Review of [NAME] PBJ Staffing data report revealed facility triggered for low weekend staffing and one star
staffing for fiscal year quarter two of 2023.
Interview on 11/21/23 at 5:05 P.M. with the Administrator revealed they submit the facility staffing data to
the corporate office who then reports the data to CMS. The Adminstrator revealed the way the facility
staffing data was transposed from the coporate office who submitted the data to CMS was late and/or not
accurate which resulted in the trigger of low weekend staffing and one star for staffing for Quarter Three of
2023.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365732
If continuation sheet
Page 3 of 5
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
365732
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Austintown Healthcare Center
650 S Meridian Road
Youngstown, OH 44509
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 0880
Provide and implement an infection prevention and control program.
Level of Harm - Minimal harm
or potential for actual harm
Based on interview, observations, and record review the facility failed to ensure appropriate infection control
practices were followed in regard to oral suctioning of respiratory secretions for Resident #4, and hand
hygiene and glove use with wound care for Resident #3. This affected two residents ( #4 and #3) of five
residents reviewed for infection control practices. The facility census was 65.
Residents Affected - Few
Findings include:
1. Record review for Resident #4 revealed an admission date of 07/22/23. Diagnoses included cerebral
palsy, dysphagia, unspecified psychosis, convulsions and anxiety.
Review of Resident #4's quarterly Minimum Data Set (MDS) 3.0 assessment dated for 10/31/23 revealed
the resident had severe cognitive impairment. Resident #4 was dependent for all care including Activities of
Daily Living.
Review of Resident #4's physician orders dated 11/10/23 revealed orders to change suction tubing and
canister once per week on Sundays and as needed. Nursing staff to suction resident orally as needed.
Observation on 11/20/23 at 10:20 A.M. of the suction canister used to hold mucus secretions removed from
the residents mouth and throat appeared as three-fourth full of yellow mucus. On the top of the mucus,
there was a thick layer of green, bubbly or foamy textured substance that had the appearance of a green
mold or biofilm.
Interview on 11/20/23 at 10:35 A.M. with Licensed Practical Nurse (LPN) #427 verified the canister was
almost full, undated, and the contents of container was yellow mucus. On the top of the mucus, there was a
thick layer of green, bubbly or foamy textured substance that had the appearance of a green
Interview on 11/20/23 at 10:38 A.M. with the Director of Nursing revealed she confirmed the canister was
full, undated, and almost full of yellow mucus. On the top of the mucus, there was a thick layer of green,
bubbly or foamy textured substance that had the appearance of a green. She could not confirm when the
canister was last changed due to the canister and tubing were undated.
2. Review of the medical record for Resident #3 revealed an admission date of 05/08/23. Diagnoses
included multiple sclerosis, cellulitis of the left lower limb, quadriplegia, type two diabetes mellitus, and
peripheral vascular disease.
Review of physician orders for Resident #3 revealed an order dated 11/01/23 that stated wound care for
right heel included to cleanse with wound cleanser, apply iodosorb (medicated wound ointment) to wound
base, cover with abdominal pad and wrap with kerlix. The dressing was to be changed three times a week
on Monday, Wednesday and Friday.
Observation of wound care for Resident #3's right heel wound on 11/22/23 at 7:50 A.M. was completed by
Licensed Practical Nurse (LPN) #404 and LPN #453. Observation revealed LPN #404 and #453 performed
hand hygiene, donned personal protective equipment (PPE) and entered the room. The gathered wound
dressing supplies were placed on the cleaned bedside table on a barrier. LPN #404 then removed
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365732
If continuation sheet
Page 4 of 5
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
365732
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
11/22/2023
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Austintown Healthcare Center
650 S Meridian Road
Youngstown, OH 44509
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 0880
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
soiled dressing. LPN #453 then cleansed the wound with wound cleanser. Once completed cleansing
wound, LPN #453 then doffed the dirty gloves and donned clean gloves without performing hand hygiene.
LPN #453 then applied a new clean wound dressing to Resident #3's right heel. LPN #404 and #453 then
discarded supplies, doffed PPE and washed hands prior to exiting resident's room.
Interview on 11/22/23 at 8:20 A.M. with LPN #453 confirmed when she doffed the dirty gloves after she had
cleaned Resident #'3 wound bed, she did not perform hand hygiene before donning a clean pair of gloves
to apply the new dressing.
Review of facility policy titled Personal Protective Equipment Gloves dated 07/01/17 revealed staff were to
perform hand hygiene before donning and after doffing gloves.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365732
If continuation sheet
Page 5 of 5