F 0699
Provide care or services that was trauma informed and/or culturally competent.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record reviews and interviews, the facility failed to ensure a resident with Post Traumatic Stress Disorder
(PTSD) was appropriately assessed to identify the cause of the residents PTSD and minimize triggers
and/or re-traumatization. This affected two residents (#7 and #18) out of two residents identified by the
facility as having PTSD/trauma. The facility census was 43.
Residents Affected - Few
Findings include:
1. Record review for Resident #7 revealed the resident was admitted to the facility on [DATE] and had
diagnoses including partial intestinal obstruction, edema, ilius, hypertension, atrial fibrillation, Parkinson's
disease, depression, anxiety, chronic post-traumatic stress disorder(on admission date of 04/07/23),
schizoaffective disorder, and chronic kidney disorder.
Review of the admission Minimum Data Set (MDS) assessment, dated 03/11/25, revealed this resident was
assessed to have intact cognition evidenced by a Brief Interview for Mental Status (BIMS) assessment
score of 15 out of 15. This resident was assessed to have an active diagnosis of PTSD.
Review of the active care plans for Resident #7 revealed no plan of care was in place addressing the cause
of PTSD, triggers which may cause re-traumatization, or interventions to reduce the risk of
re-traumatization and provide care for PTSD.
Review of six Trauma Informed Care Evaluations revealed no determination had been completed to identify
the cause of PTSD for Resident #7 and to identify potential triggers which may cause re-traumatization.
Interview with Resident #7 on 04/22/25 at 02:09 P.M. revealed this resident has a history of post-traumatic
stress disorder because she had been sexually abused as a child. Resident stated she cannot recall
anyone ever asking her about this from the facility staff.
Interview with Social Services #570 on 04/23/25 at 09:58 A.M. verified the assessments did not capture
actual cause of trauma and care plan did not accurately reflect triggers for recurrence.
2. Record review for Resident #18 revealed the resident was admitted to the facility on [DATE] and had
diagnoses including dementia, cognitive communication deficit, chronic obstructive pulmonary disease,
hypertension, diabetes mellitus type II, hyperlipidemia, PTSD(active diagnosis since 08/18/22), edema,
anxiety, depression, and unspecified psychosis.
Review of the admission Minimum Data Set (MDS) assessment, dated 01/20/25, revealed this resident
(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 5
Event ID:
365961
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
365961
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/24/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Piketon Nursing Center
300 Overlook Drive
Piketon, OH 45661
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 0699
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
was assessed to have severely impaired cognition evidenced by a Brief Interview for Mental Status (BIMS)
assessment score of 7 out of 15. This resident was assessed to have an active diagnosis of PTSD.
Review of the active care plans for Resident #18 revealed no plan of care was in place addressing the
cause of PTSD, triggers which may cause re-traumatization, or interventions to reduce the risk of
re-traumatization and provide care for PTSD.
Review of two Trauma Informed Care Evaluations revealed no determination had been completed to
identify the cause of PTSD for Resident #18 and to identify potential triggers which may cause
re-traumatization.
Interview with Social Services #570 on 04/23/25 at 11:00 A.M. verified the assessments did not capture
actual cause of trauma and care plan did not accurately reflect triggers for recurrence.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365961
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
365961
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/24/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Piketon Nursing Center
300 Overlook Drive
Piketon, OH 45661
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.
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
record reviews and staff interviews, the facility failed to ensure an order for the administration of as needed
Ativan (an anti-anxiety medication) contained a stop date of 14 days or less. This affected one resident
(#31) out of the five residents reviewed for unnecessary medications. The facility census was 43.
Findings include:
Record review for Resident #31 revealed the resident was admitted to the facility on [DATE] and had
diagnoses which included anxiety disorder, depression, and diabetes mellitus.
Review of the quarterly Minimum Data Set (MDS) assessment, dated 02/27/25, revealed the resident was
assessed to have intact cognition. The resident was assessed to have received anti-anxiety medications
during the lookback period.
Review of the active physicians order, dated 12/08/24, revealed Resident #31 was to be administered 0.5
milligrams (mg) of Ativan every two hours as needed for anxiety. The order did not contain a stop date.
Review of the Medication Administration Records (MAR's) for Resident #31, dated 12/22/24 (14 days after
the order for Ativan was implemented) through 04/22/25, revealed the resident was documented to have
been administered 32 doses of as needed Ativan.
Interview with Licensed Practical Nurse (LPN) #290 on 04/22/25 at 3:45 P.M. confirmed the Ativan ordered
for Resident #31 was as needed and did not contain a date for which to stop the order.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365961
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
365961
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/24/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Piketon Nursing Center
300 Overlook Drive
Piketon, OH 45661
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 0760
Ensure that residents are free from significant medication errors.
Level of Harm - Minimal harm
or potential for actual harm
**NOTE- TERMS IN BRACKETS HAVE BEEN EDITED TO PROTECT CONFIDENTIALITY** Based on
observations, interviews, record reviews, and review of facility policy, the facility failed to ensure a
medication was administered according to physicians order. This affected one resident (#31) out of the five
residents reviewed for unnecessary medications. The facility census was 43.
Residents Affected - Few
Findings include:
Record review for Resident #31 revealed the resident was admitted to the facility on [DATE] and had
diagnoses which included chronic pain due to trauma, anxiety disorder, depression, and diabetes mellitus.
Review of the quarterly Minimum Data Set (MDS) assessment, dated 02/27/25, revealed the resident was
assessed to have intact cognition.
Review of the active physicians order, dated 12/24/24, revealed Resident #31 was to be administered one
milliliter (ml) of Morphine Sulfate (an opioid medication) Oral Suspension 20 milligrams (mg) per five ml's
(which was equivalent to four mg's per dose administered) every two hours as needed for breakthrough
pain.
Review of the facility Controlled Drug Receipt Record/Disposition Forms, dated 12/24/24 through 04/22/25,
revealed bottles of Morphine Sulfate Oral Suspension supplied to the facility for administration to Resident
#31 were 100 mg's per five ml's (which was equivalent to 20 mg per one ml). One ml of Morphine Sulfate
Oral Suspension 100 mg's per five ml's (equaling 20 mg) was documented to have been removed from the
bottles by multiple nurses over 300 times for administration to Resident #31.
Review of the Medication Administration Records (MAR's) for Resident #31, dated 12/24/24 through
04/22/25, revealed one ml of Morphine Sulfate Oral Suspension 20 mg's per five ml's (equaling four mg's)
was documented to have been administered to Resident #31 at each dose.
Further record review for Resident #31 revealed the resident had not experienced any episodes of
respiratory depression, oversedating, or other adverse side effects of medications between 12/24/24 and
04/22/25.
Observation and interview with Licensed Practical Nurse (LPN) #290 on 04/22/25 at 3:45 P.M. confirmed
the bottle of Morphine Sulfate Oral Suspension contained in the narcotic lock box on the medication cart
used for Resident #31 was a strength of 100 mg's per five ml's which was equal to 20 mg's per one ml. LPN
#290 confirmed one ml of the Morphine Sulfate Oral Suspension was removed from the bottle at each dose
and administered to Resident #31 so the resident received 20 mg each time. LPN #290 further confirmed
the physicians order for Resident #31 was for one ml of Morphine Sulfate Oral Suspension at a strength of
20 mg's per five ml's which was only equivalent to four mg's to be administered at each dose. LPN #290
confirmed the amount administered to the resident at each dose did not match the amount ordered by the
physician.
Observation of Resident #31 on 04/22/25 at 4:05 P.M. revealed the resident was lying in bed eating grapes
and watching television and did not appear to be exhibiting signs or symptoms of pain. Interview with
Resident #31 at the time of the observation confirmed facility staff administered pain medication which kept
the residents pain at a manageable level and denied any concerns with adverse side
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365961
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
365961
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
04/24/2025
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Piketon Nursing Center
300 Overlook Drive
Piketon, OH 45661
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 0760
effects from medications.
Level of Harm - Minimal harm
or potential for actual harm
Review of the facility policy titled Administering Medications, revised 04/2019, revealed medications are
administered in accordance with prescriber orders, including any required time frames. The individual
administering the medication checks the label THREE times to verify the right resident, right medication,
right dosage, right time and right method (route) of administration before giving the medication.
Residents Affected - Few
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
365961
If continuation sheet
Page 5 of 5