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Complaint Investigation

Glenbrook Rehabilitation & Skilled Nursing Center

Inspection Date: November 19, 2025
Total Violations 1
Facility ID 155176
Location FORT WAYNE, IN
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Inspection Findings

F-Tag F0684

Quality of Life and Care Deficiencies
Harm Level: Potential for More Than Minimal Harm

F 0684 Level of Harm - Minimal harm or potential for actual harm Residents Affected - Few

FORM CMS-2567 (02/99) Previous Versions Obsolete

hydrocodone-acetaminophen was to be given to Resident C four times a day.A review of the MAR, dated 8/1/25-8/31/25, indicated Lantus insulin was not documented as given or refused on 8/1/25 and 8/10/25.

Blood glucose was not recorded on 8/31/25 at 6 pm. No documentation of Lispro administration was found

on 8/1/25 at 6:00 PM for a glucose of 272, 8/4/25 at noon for a glucose of 255. No administration or refusal of Lispro was indicated on 8/31/25. 42 units of Lantus were given between 7:00 PM and 10:00 PM without a recorded blood glucose measurement. No documentation of hydrocodone-acetaminophen administration or refusal was indicated on 8/21/25 at 12:00 AM. 3. A record review for Resident D began on 11/19/25 at 9:35 AM. Diagnoses included type 2 diabetes with diabetic peripheral angiopathy with gangrene and chronic kidney disease, right leg below the knee amputation. Resident D routinely leaves the facility for dialysis on Mondays, Wednesdays, and Fridays.A review of Resident D's current quarterly MDS, dated [DATE REDACTED], indicated their BIMS (Basic Interview for Mental Status) score was 14. (cognitively intact). The MDS indicated the resident received insulin injections 5 days a week during the previous week of the assessment.A review of physician orders, dated 9/18/25-10/20/25, indicated blood glucose was to be measured four times a day.A review of physician orders, dated 9/18/25-10/6/25, indicated 18 units of insulin glargine was to be given once a day. The order did not provide parameters to hold insulin or to hold on dialysis appointments.A review of physician orders, dated 10/6/25, indicated 18 units of Rezvoglar Kwik Pen insulin glargine was to be given once a day. The order did not provide parameters to hold insulin or to hold on dialysis appointments.A review of the MAR, dated 10/1/25-10/31/25, indicated blood glucose was not documented as completed or refused on Sunday 8/5/25 at 8:00 AM, Tuesday 10/7/25 at 5:00 PM, and Tuesday 10/14/25 at 8:00 AM. The 8:00 AM of 18 units of insulin glargine was held by facility staff, without physician parameters, on 10/6/25 for glucose of 120, 10/10/25 for a glucose of 93, 10/12/25 for a glucose of 132, 10/13/25 for a glucose of 121, 10/14/25 a note indicated the glucose was not measured prior to Resident D leaving the facility for a procedure, 10/22/25 a note indicated the resident was going to dialysis, 10/23/25 for a glucose of 124, 10/26/25 for a glucose of 100, 10/28/25 for a glucose of 95, and 10/30/25 for

a glucose of 108. The MAR indicated, 18 units Resvoglar insulin was routinely not given to Resident D on Mondays, Wednesdays, and Fridays (dialysis days), except for Monday 10/27/25 prior to dialysis. In an interview, on 11/19/25 at 3:02 PM, LPN 4 indicated staff routinely obtained a blood sugar measurement within an hour before meals and bedtime. When insulin was required, within the parameters ordered, a Qualified Medical Assistant would need to have a nurse administer the insulin dose. Documentation was required on the MAR. When a resident was not in the building, staff would document the resident was not available or LOA.A current procedure, dated 2/2010, provided by the Administrator, indicated medications held or refused will be documented in the MAR. Medication administration will be documented on the MAR

after the medication has been given. Insulin type, units to be given should be checked against the physician order at least 3 times for accuracy prior to administration.A current policy, dated 2/2003, provided by the Administrator, indicated staff was to administer medications and meals before or after dialysis as ordered.This citation is related to intake 2649663 and 2626035.3.1-30(a)

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📋 Inspection Summary

GLENBROOK REHABILITATION & SKILLED NURSING CENTER in FORT WAYNE, IN inspection on recent inspection.

Found 0 violation(s). Severity: Standard violations. Status: 0 corrected, 0 pending.

What this means: Health inspections identify deficiencies that facilities must correct. Violations range from minor documentation issues to serious safety concerns. All deficiencies must be corrected within required timeframes and are subject to follow-up verification.

Frequently Asked Questions

What is an F-tag violation?
F-tags are federal deficiency codes used by CMS to categorize nursing home violations. Each F-tag corresponds to a specific federal regulation (42 CFR Part 483). For example, F607 relates to abuse prevention policies, F880 relates to infection control.
Were these violations corrected?
Facilities must submit plans of correction and implement changes within required timeframes. CMS conducts follow-up inspections to verify corrections. Check the inspection report for specific correction dates and follow-up verification status.
How often do nursing home inspections happen?
CMS conducts unannounced inspections of all Medicare/Medicaid-certified nursing homes at least once per year. Additional inspections may occur based on complaints, facility-reported incidents, or follow-up to verify previous violations were corrected.
What should families do about these violations?
Families should: (1) Review the full inspection report for details, (2) Ask facility administration about specific corrective actions taken, (3) Check if this represents a pattern by reviewing prior inspections, (4) Compare with other facilities in FORT WAYNE, IN, (5) Report new concerns to state authorities.
Where can I see the full inspection report?
Complete inspection reports are available on Medicare.gov's Care Compare website (www.medicare.gov/care-compare). You can also request copies directly from GLENBROOK REHABILITATION & SKILLED NURSING CENTER or from the state Department of Health. Reports include deficiency codes, facility responses, and correction timelines.
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