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Inspection visit

Health inspection

GENEVA CENTER FOR REHABILITATION AND NURSINGCMS #3663262 citations on this visit
2 citations recorded

Inspector’s narrative

What the inspector wrote

This survey cited 2 deficiencies. The full statement and the facility’s plan of correction follow, verbatim from the federal record.

F 0690 Level of Harm - Minimal harm or potential for actual harm Residents Affected - Few Provide appropriate care for residents who are continent or incontinent of bowel/bladder, appropriate catheter care, and appropriate care to prevent urinary tract infections. Based on observation, record review and interview the facility failed to ensure Resident #3's indwelling Foley catheter (a thin sterile tube inserted into the bladder to drain urine) bag was emptied properly to prevent potential complications for the resident. This affected one resident (#3) of one resident reviewed for catheters. Findings include: Review of the medical record for Resident #3 revealed an admission date of 11/24/19 with diagnoses including chronic respiratory failure, chronic kidney disease, neuromuscular dysfunction of the bladder, benign prostatic hyperplasia with lower tract symptoms and spinal stenosis. Review of the care plan, dated 11/25/19 revealed Resident #3 required alternate means of urinary elimination of a Foley catheter due to neurogenic bladder, benign prostatic hyperplasia with lower urinary tract symptoms, urinary tract infection and sepsis. Interventions included catheter care every shift and as needed, monitor catheter patency every shift, position drainage bag below the level of the bladder and keeping the bag and tubing off the floor always. There was nothing in the care plan regarding emptying the catheter drainage bag. Review of physician's orders for March 2020 revealed Resident #3 had an order for an indwelling Foley catheter to continuous drainage and catheter care every shift. There were no physician orders regarding emptying the Foley catheter drainage bag. Observation on 03/02/20 at 11:29 A.M. revealed Resident #3's indwelling Foley catheter drainage bag laying on the floor while Resident #3 was in bed. Resident #3's catheter drainage bag was all the way full of urine and the urine was backing up into the catheter tubing. His drainage bag was leaking out the bottom of the catheter bag and the bag was laying in a puddle of urine. Interview and observation with the Director of Nursing on 03/02/20 at 11:32 A.M. verified the indwelling Foley catheter bag was overfull causing the urine to back up into the catheter tubing as well as leak out of the bottom of the catheter bag. She verified the catheter bag should have been emptied and not had this amount of urine in the bag. The Director of Nursing emptied the urinary catheter bag and measured the urine content and she revealed the urinary output measured 3000 cubic centimeters (cc). Review of manufacturer guidelines, SteriGear the Fig Leaf with a model number of 10270 revealed Resident #3's urinary drainage bag had a capacity of 2000 milliliters. The guidelines revealed to hang the bag utilizing the hanger or rope and do not place the bag on the floor. The guidelines also (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 3 Event ID: 366326 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 366326 B. Wing A. Building (X3) DATE SURVEY COMPLETED 03/05/2020 NAME OF PROVIDER OR SUPPLIER STREET ADDRESS, CITY, STATE, ZIP CODE Geneva Center for Rehabilitation and Nursing 1140 South Broadway Geneva, OH 44041 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 0690 Level of Harm - Minimal harm or potential for actual harm Residents Affected - Few FORM CMS-2567 (02/99) Previous Versions Obsolete revealed to periodically check the fluid level in the bag by lifting the Fig Leaf cover or by viewing through the Quick View Port and empty the bag. Review of facility policy titled, Catheter Care, Urinary dated 05/22/13 revealed it was the policy of the facility to provide appropriate care for urinary catheters and to prevent catheter- associated urinary tract infections. The policy revealed to be sure the catheter tubing and drainage bag were kept off the floor and empty the drainage bag regularly using a separate clean collection container for each resident. The policy revealed the bag should be emptied at least every eight hours. Event ID: Facility ID: 366326 If continuation sheet Page 2 of 3 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 366326 B. Wing A. Building (X3) DATE SURVEY COMPLETED 03/05/2020 NAME OF PROVIDER OR SUPPLIER STREET ADDRESS, CITY, STATE, ZIP CODE Geneva Center for Rehabilitation and Nursing 1140 South Broadway Geneva, OH 44041 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 0759 Ensure medication error rates are not 5 percent or greater. Level of Harm - Minimal harm or potential for actual harm Based on observation, record review and interview the facility failed to maintain a medication rate less than five percent. The facility medication error rate was calculated to be 12.90% and included four medication errors out of 31 medication administration opportunities. This affected one resident (#43) of five residents observed for medication administration. Residents Affected - Few Findings include: Review of the medical record for Resident #43 revealed an admission date of 01/23/20 and diagnoses including gastro-esophageal reflux disease, hypertension, hypokalemia (low potassium), chest pain and major depression. Review of Resident #43's quarterly Minimum Data Set (MDS) 3.0 assessment, dated 02/12/20 revealed she had intact cognition. Observation on 03/03/20 at 8:25 A.M. of medication administration for Resident #43 completed by Licensed Practical Nurse (LPN) #600 revealed Resident #43 requested her medication be crushed and placed in applesauce. LPN #600 crushed all Resident #43's medications including Cymbalta capsule delayed release 30 milligrams one capsule by mouth for major depression, Isosorbide mononitrate tablet extended release 30 milligram by mouth for chest pain, Pantoprazole sodium delayed release 40 milligram tablet by mouth for gastro-esophageal reflux and Potassium chloride extended release 20 milliequivalent tablet by mouth for hypokalemia (low potassium). LPN #600 did not educate Resident #43 prior to administering the delayed release or extended release medication on risk factors of these medications being crushed or call the physician prior to these medications being crushed and administered. Interview on 03/03/20 at 8:30 A.M. with LPN #600 verified she crushed all of Resident #43's medications including her Cymbalta delayed release, Isosorbide mononitrate extended release, Pantoprazole sodium delayed release and her Potassium chloride extended release. She verified these medications should not have been crushed and she revealed she should have called the physician prior to crushing the medications and administering. Interview on 03/03/20 at 9:55 A.M. with Facility Pharmacist #601 verified Resident #43's Cymbalta delayed release, Isosorbide mononitrate extended release, Pantoprazole sodium delayed release and her Potassium chloride extended should not be crushed as extended release medications were formulated for a resident to receive the medication slowly over time and delayed release medications were enteric coated designed to delay the release of the medication until the tablet had passed through the stomach to prevent the medication from being destroyed or inactivated by gastric juices or where it may irritate the gastric lining. Review of facility policy titled Medication Administration- Crushing of Medications, dated 06/21/17 revealed medications which were enteric coated, extended release, sublingual or otherwise noted by the manufacturer as inappropriate to crush, may not be crushed. If crushing of the medication was authorized by the physician, the pharmacy should be notified, and documentation must be made in the resident's record. If the physician orders the crushing of a Do Not Crush medication the physician must document in the resident's chart to indicate that the benefits of crushing the medication outweigh the risk of crushing the medication. FORM CMS-2567 (02/99) Previous Versions Obsolete Event ID: Facility ID: 366326 If continuation sheet Page 3 of 3

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Citations

2 citations 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.

  • 0690GeneralS&S Dpotential for harm

    F690 - Incontinence

    Provide appropriate care for residents who are continent or incontinent of bowel/bladder, appropriate catheter care, and appropriate care to prevent urinary tract infections.

  • 0759GeneralS&S Dpotential for harm

    F759 - Medication Errors

    Ensure medication error rates are not 5 percent or greater.

FAQ · About this visit

Common questions about this visit

What happened during the March 5, 2020 survey of GENEVA CENTER FOR REHABILITATION AND NURSING?

This was a inspection survey of GENEVA CENTER FOR REHABILITATION AND NURSING on March 5, 2020. The surveyor cited 2 deficiencies, recorded on the federal Form 2567 statement of deficiencies.

Were any deficiencies cited at GENEVA CENTER FOR REHABILITATION AND NURSING on March 5, 2020?

Yes, 2 deficiencies were cited, each with a CMS Scope and Severity grade. The first was: "Provide appropriate care for residents who are continent or incontinent of bowel/bladder, appropriate catheter care, an..."

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