F 0641
Ensure each resident receives an accurate assessment.
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 and staff interview, the facility failed to accurately code Minimum Data Set (MDS)
assessments to reflect residents medications used. This affected five (Resident #11, #14, #25 #32 and 36)
of 12 residents records reviewed. The facility census was 46.
Residents Affected - Some
Findings include:
1. Review of medical record for Resident #11 revealed an admission date of 08/16/19 with diagnoses
including Alzheimer's disease, major depression, insomnia, diabetes type two, hyperlipidemia,
hypertension, hypothyroidism, muscle weakness, cerebral infarction and low back pain.
Review of discharge return anticipated MDS assessment for Resident #11 with an assessment reference
date (ARD) of 04/11/19 documented she was assessed as receiving anticoagulant medication seven days
during the look back period of the set ARD.
Review of monthly medication administration record (MAR) for April 2019 revealed the resident had a
current physician order for Plavix (antiplatelet) medication and was administered the medication everyday
for the whole month of April 2019. Further review lacked any documentation of Resident #11 receiving any
anticoagulation medication.
2. Review of medical record for Resident #14 revealed an admission date of 03/21/14 with diagnoses
including unspecified cerebral infarction, major depression, hypertension, vascular dementia , muscle
weakness, anxiety disorder and low back pain.
Review of quarterly MDS assessment with an ARD of 04/04/19 documented he was assessed as receiving
anticoagulant medication seven days during the look back period of the set ARD.
Review of monthly MAR for April 2019 documented Resident #14 had a current physician order for Aspirin
(antiplatelet) medication and was administered the medication everyday for the whole month of April 2019.
Further review lacked any documentation of Resident #14 receiving any anticoagulation medication.
3. Review of medical record for Resident #36 revealed an admission date of 03/21/19 with diagnoses
including chronic obstructive pulmonary disease, major depression, acute myocardial infarction,
hypertension, difficulty walking, muscle weakness, cerebral infarction and low back pain.
Review of 30 day MDS assessment for Resident #36 with an ARD of 04/19/19 documented she was
assessed as receiving anticoagulant medication seven days during the look back period of the set ARD
date.
(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:
366033
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
366033
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Momentous Health at Sidney
510 Buckeye Ave
Sidney, OH 45365
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 0641
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
Review of monthly MAR for April 2019 documented Resident #36 had a current physician order for Aspirin
and Plavix (antiplatelet) medication and was administered the medication for the whole month of April 2019.
Further review lacked any documentation of Resident #36 receiving any anticoagulation medication.
Interview on 05/07/19 at 11:56 A.M. with MDS Nurse #120 verified she coded the use of anticoagulants
inaccurately on the MDS assessments for Residents #11, #14 and #36. She revealed the Resident
Assessment Instrument (RAI) manual documents to not code the antiplatelet medications. She further
verified Aspirin and Plavix are both antiplatelet medication not anticoagulants.
4. Review of the medical record of Resident #32 revealed an admission date of 06/04/08 and a readmission
date of 01/16/17. Diagnoses included schizoaffective disorder, chronic obstructive pulmonary disease,
essential hypertension, acute kidney failure, chronic systolic (congestive) heart disease, other forms of
chronic ischemic heart disease, other sequelae following unspecified cerebrovascular disease and
atherosclerotic heart disease of native coronary artery without angina pectoris.
Review of the April physician orders revealed an order for Plavix 75 milligrams (mg), an antiplatelet agent,
originally ordered 08/28/18. Review of the April 2019 medication administration record revealed the
medication was given as ordered.
Review of the annual minimum data set assessment dated [DATE] revealed Resident #32 received
anticoagulant seven days of the look back period.
Interview on 05/07/19 at 11:56 A.M. with MDS Nurse #120 verified she coded the use of anticoagulants
inaccurately on the MDS assessments for Residents #32. She revealed the Resident Assessment
Instrument (RAI) manual documents to not code the antiplatelet medications. She further verified Aspirin
and Plavix are both antiplatelet medication not anticoagulants.
5. Review of the medical record for Resident #25 revealed the resident was admitted to the facility on
[DATE]. Diagnoses include chronic obstructive pulmonary disease, bipolar disorder, chronic atrial fibrillation,
osteoarthritis, chronic obstructive pulmonary disease, major depressive disorder, lymphedema, and anxiety
disorder.
Review of the medication administration record (MAR) dated 04/19, revealed Resident #25 was
administered the medication Keflex (antibiotic) on five days (04/09/19, 04/10/19, 04/11/19, 04/12/19, and
04/13/19) of the seven day reference period. Continued review of the MAR revealed the resident was
administered the medication Apixaban (anticoagulant) on seven days (04/07/19, 04/08/19, 04/09/19,
04/10/19, 04/11/19, 04/12/19, and 04/13/19) of the seven day reference period . Further review of the MAR
dated 04/19, revealed Resident #25 was administered the medication Norco (opioid) on five days
(04/07/19, 04/09/19, 04/10/19, 04/11/19, and 04/12/19) of the seven day reference period.
Review of a quarterly minimum data set (MDS) assessment dated [DATE], revealed Resident #25 received
anticoagulant medication on zero days of the seven day reference period, received opioid medication on
three days of the seven day reference period, and received antibiotic medication on zero days of the seven
day reference period.
Interview on 05/08/19 at 9:50 A.M. with MDS #120 verified the quarterly MDS assessment dated [DATE],
for Resident #25 was inaccurate. The MDS nurse confirmed Resident #25 was administered anticoagulant
medication on seven days of the reference period, opioid medication on five days of the reference
(continued on next page)
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366033
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
366033
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Momentous Health at Sidney
510 Buckeye Ave
Sidney, OH 45365
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 0641
period, and antibiotic medication on five days of the reference period.
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Some
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366033
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
366033
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Momentous Health at Sidney
510 Buckeye Ave
Sidney, OH 45365
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 0656
Level of Harm - Minimal harm
or potential for actual harm
Residents Affected - Few
Develop and implement a complete care plan that meets all the resident's needs, with timetables and
actions that can be measured.
Based on medical record review and staff interview, the facility failed to ensure care plans addressed all
resident care areas. This affected one resident (#24) of 11 reviewed for care plans. The facility census was
46.
Findings include:
Review of the medical record of Resident #24 revealed an admission date of 04/02/19. Diagnoses include
chronic obstructive pulmonary disease, essential hypertension acute on chronic diastolic heart failure,
anemia, and stage four chronic kidney disease.
Review of the care plan dated 04/04/19 revealed it to be silent of any dialysis care.
Review of the physician order dated 04/10/19 revealed an order for Resident #32 to be transported to
dialysis center on Tuesday, Thursday and Saturday.
Interview on 05/08/19 at 10:43 A.M. provided verification of the lack of dialysis care plan.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366033
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
366033
B. Wing
A. Building
(X3) DATE SURVEY
COMPLETED
05/09/2019
NAME OF PROVIDER OR SUPPLIER
STREET ADDRESS, CITY, STATE, ZIP CODE
Momentous Health at Sidney
510 Buckeye Ave
Sidney, OH 45365
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 record review, policy review and staff interview, the facility failed to maintain an effective
Legionella Control procedure. This had the potential to affect all 46 residents residing in the facility.
Residents Affected - Many
Findings include:
Review of an undated facility form titled Identifying Buildings at Increased Risk revealed if the facility
answered yes to any questions one through four, they should have a water management program for the
building's hot and cold water distribution system. The facility checked yes to questions one, two, and three.
Question one-Is your building a healthcare facility where patients stay overnight or does your building
house or treat people who have chronic and acute medical problems or weakened immune systems?
Question 2-Does your building primarily house people older than 65 years? Question 3-Does your building
have multiple housing units and a centralized hot water system?
Review of the Legionella Control procedure revealed no monitoring of the water temperatures, water
sanitizer or disinfectant levels were documented.
Interview on 05/09/19 at 1:00 P.M. with the Corporate Clinician (CC) #150 provided verification the facility
did not have a water management program in place to monitor for Legionella. She verified the facility risk
assessment indicated the facility required a water management program. She verified the facility did not
have a flow sheet to identify potential areas of concern and the facility and was not completing any water
testing protocols.
Review of the facility policy titled Legionella dated 06/02/17 revealed the purpose of the procedure was to
reduce the risk of Legionella in healthcare facility water systems and to prevent cases and outbreaks of
Legionnaire's disease. The facility will monitor water temperatures, sanitizer levels, and disinfectant levels.
FORM CMS-2567 (02/99)
Previous Versions Obsolete
Event ID:
Facility ID:
366033
If continuation sheet
Page 5 of 5