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Inspection visit

Health inspection

SHELBY SKILLED NURSING AND REHABILITATIONCMS #3652971 citation on this visit
1 citation recorded

Inspector’s narrative

What the inspector wrote

This survey cited 1 deficiency. The full statement and the facility’s plan of correction follow, verbatim from the federal record.

F 0756 Level of Harm - Minimal harm or potential for actual harm Residents Affected - Few Ensure a licensed pharmacist perform a monthly drug regimen review, including the medical chart, following irregularity reporting guidelines in developed policies and procedures. Based on resident record review, staff interview, and review of a facility policy; the facility failed to respond to pharmacy medication regimen reviews in a timely manner. This affected one (#16) of five residents reviewed for unnecessary medications. The facility census was 36. Findings include: Medical record review for Resident #16 revealed admission date 10/08/07. Diagnoses included dementia with behavioral disturbance and presence of right artificial knee joint. Review of physician orders dated 04/29/21 revealed Doxycycline 100 milligrams (mg) two times a day for infection, end date 08/30/21. Review of physician orders dated 11/23/21 revealed Memantine 5 mg give two tablets by mouth one time a day and give one tablet by mouth at bedtime. Review of the Consultation Report dated 06/10/21 revealed repeated recommendation from 04/29/21. Resident receives Doxycycline 100 milligrams (mg) orally twice a day since 04/20/21. The order does not list a stop date. Physician's Response: I have re-evaluated this therapy and wish to implement the following changes: Stop Doxy, undated. Review of the Consultation Report dated 08/03/21 revealed Resident receives Memantine Hydrochloride 5 mg two times a day and has tolerated treatment for at least one continuous week. No orders were found in the medical record to up-titrate the dose. Please up-titrate the dose as follows: 10 mg each morning (AM) and 5 mg each nighttime (PM) for seven days, then 10 mg twice daily as a maintenance dose. Rationale for recommendation: The usual dose of memantine is 20 mg/day for the immediate-release formulation, or 28 mg/day for the extended-release (XR) formulation. A handwritten notation to See Response was noted. There was no Physician's Response checked, no physician signature or date. Consultation Report dated 10/05/21 revealed the above recommendation. Physician's Response: I accept the recommendations above, please implement as written. Increase Memantine to 10 mg every AM and 5 mg PM, dated 10/05/21. These findings were verified on 06/15/22 at 2:53 P.M. by Regional Quality Assurance Nurse #553. The Regional Nurse stated the notation See Response for 08/03/21 reflected the Physician's Response dated 10/05/21. The Regional Quality Assurance Nurse stated she had been on maternity leave and when she came back, she had to follow-up on tasks that were incomplete. She stated the Director of Nursing and Assistant Director of Nursing were new to their roles and she had to train them. Review of facility policy titled Medication Regimen Reviews, dated 05/2019, revealed the Consultant Pharmacist reviews the medication regimen of each resident at least monthly. 1. The Consultant (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 2 Event ID: 365297 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 365297 B. Wing A. Building (X3) DATE SURVEY COMPLETED 06/16/2022 NAME OF PROVIDER OR SUPPLIER STREET ADDRESS, CITY, STATE, ZIP CODE Shelby Skilled Nursing and Rehabilitation 705 Fulton Street 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 0756 Level of Harm - Minimal harm or potential for actual harm Residents Affected - Few FORM CMS-2567 (02/99) Previous Versions Obsolete Pharmacist performs a medication regimen review (MRR) for every resident in the facility receiving medication. 2. Medication regimen reviews are done at least monthly, or more frequently if indicated. 3. The goal of the MMR is to promote positive outcomes while minimizing adverse consequences and potential risks associated with medication. 4. The MRR involves a thorough review of the resident's medical record to prevent, identify, report, and resolve medication related problems, medication errors and other irregularities, for example: medications a. ordered in excessive doses or without clinical indication; b. medication regimens that appear inconsistent with the resident's stated preferences; c. duplicative therapies or omissions of ordered medication; d. inadequate monitoring for adverse consequences; e. potentially significant drug-drug or drug-food interactions; f. potentially significant medication-related adverse consequences or actual signs and symptoms that could represent adverse consequences; g. incorrect medications, administration times or dosage forms; or other h. medication errors, including those related to documentation. 5. The medication regimen and associated treatment goals involve collaboration with the resident (or representative), family members, and the interdisciplinary team (IDT). As such, the MRR includes a review of the resident's (or representative's) stated preferences, the comprehensive care plans and information provided about the risks and benefits of the medication regimen. In addition to reviewing the medical record the Consultant Pharmacist may also meet with staff, the resident or representatives, or the IDT. 7. Within 24 hours of the MRR, the Consultant Pharmacist provides a written report to the attending physicians for each resident identified as having a non-life-threatening medication irregularity. The report contains: a. The resident's name; b. the name of the medication; c. the identified irregularity; and e. the pharmacist's recommendation. 8. An irregularity refers to the use of medication that is inconsistent with accepted pharmaceutical services standards or practice; is not supported by medical evidence; and/or impedes or interferes with achieving the intended outcomes of pharmaceutical services. It may also include the use of medication without indication, without adequate monitoring, in excessive doses, and or in the presence of adverse consequences. 10. If the physician does not provide a timely or adequate response, the Consultant Pharmacist identifies that no action has been taken, he/she contacts the Medical Director or (if the Medical Director is the physician of record) the Administrator. 11. The attending physician documents in the medical record that the irregularity has been reviewed and what (if any) action was taken to address it. 12. An acute change of condition may prompt a request for a MRR. The staff member who identifies the change of condition follows reporting procedures to notify the physician. The physician may request a MRR be conducted within a specific timeframe (e.g. within 24 hours). Event ID: Facility ID: 365297 If continuation sheet Page 2 of 2

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Citations

1 citation recorded*CMS

What do CMS severity letters mean?

Serious (G-L). Actual harm to a resident, or immediate jeopardy. Codes G through I indicate actual harm; J through L indicate immediate jeopardy to resident health or safety.

General (A-F). No actual harm found, or harm that is minimal. The facility must still submit a Plan of Correction. Most CMS citations land here.

Each letter combines severity with scope: how many residents the deficiency affected.

  • 0756GeneralS&S Dpotential for harm

    F756 - Drug Regimen Review

    Ensure a licensed pharmacist perform a monthly drug regimen review, including the medical chart, following irregularity reporting guidelines in developed policies and procedures.

FAQ · About this visit

Common questions about this visit

What happened during the June 16, 2022 survey of SHELBY SKILLED NURSING AND REHABILITATION?

This was a inspection survey of SHELBY SKILLED NURSING AND REHABILITATION on June 16, 2022. The surveyor cited 1 deficiency, recorded on the federal Form 2567 statement of deficiencies.

Were any deficiencies cited at SHELBY SKILLED NURSING AND REHABILITATION on June 16, 2022?

Yes, 1 deficiency was cited, each with a CMS Scope and Severity grade. The first was: "Ensure a licensed pharmacist perform a monthly drug regimen review, including the medical chart, following irregularity ..."

What type of survey was this?

This was a inspection survey conducted by state surveyors under federal Centers for Medicare & Medicaid Services (CMS) oversight. Findings are published on CMS Care Compare.

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Next steps

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Data from CMS Care Compare public records. Dataset last refreshed . If you believe any information is inaccurate, report it here.