Failure to Document Foley Indication and Maintain Catheter Care
Summary
The facility failed to ensure documentation of the clinical indication for continued foley catheter use was in place and failed to ensure interventions were in place to prevent UTIs for one resident with a catheter. The resident was recently admitted with diagnoses including stroke with aphasia, dementia with mood disturbance, urinary retention, and a urinary device. The resident’s assessment indicated severe cognitive impairment and that the resident was admitted with a foley catheter. Hospital discharge information showed the resident had hematuria and urinary retention, required a urology consultation, and was discharged with a plan for catheter removal and a trial of void at the skilled nursing facility. Provider orders directed catheter removal and a trial void, and also directed that the catheter be kept to gravity drainage with the tubing not looped or kinked and the drainage bag kept below the waist. The care plan identified the resident as having a foley catheter related to neurogenic bladder and being at risk for UTI, with interventions to change the foley when needed and keep the tubing and bag below the bladder and free of kinks. However, nursing documentation showed the trial void was delayed after staff reported the resident was impulsive and self-transferring, and a later provider note stated the resident would need a trial void and continued foley care without documenting the clinical indication for delaying catheter removal. Observations showed the catheter bag was not hanging to gravity and was not below the resident’s waist, and the tubing was looped with urine sitting in the tubing. Staff interviews confirmed they were unsure why the catheter remained in place, acknowledged the bag should be below the waist and to gravity, and stated the tubing should not have loops or kinks. One nurse stated the resident had fidgeted with the catheter and caused bleeding requiring replacement, and another stated the catheter was kept an additional week. The medical record lacked documentation that the family had been involved in the decision to delay discontinuation of the catheter or that risks and benefits of keeping it in place had been discussed.
Penalty
Resources
Below are regulatory guidelines relevant to this citation:
Trusted data from CMS and state health departments
Every citation, penalty and Plan of Correction is sourced from public CMS records (latest release October 8, 2026) and official state health department websites — never guesswork.
In your survey window? See what surveyors are citing.
The Survey-Prep Report maps your facility's risk from 12 months of CMS and state citation data — what's being cited around you and what to check first. $129 one-time.