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Safety and efficacy of a patient‐controlled bladder management system for treating urinary retention in men
Author(s) -
Homan Harvey D.,
Dmochowski Roger,
Cochran James S.,
Karsh Lawrence,
Sherman Neil D.,
Yalla Subbarao
Publication year - 2016
Publication title -
neurourology and urodynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 90
eISSN - 1520-6777
pISSN - 0733-2467
DOI - 10.1002/nau.22770
Subject(s) - medicine , urinary retention , foley , clean intermittent catheterization , foley catheter , spinal cord injury , urinary catheterization , adverse effect , surgery , urinary system , catheter , urinary bladder , anesthesia , urology , spinal cord , psychiatry
Aims The CymActive™ Bladder Management System (BMS) is a self‐retaining, intraurethral catheter with a patient‐controlled magnetic valve that allows cyclical bladder filling and emptying, without external appliances. We determined the safety and efficacy of the BMS in men with urinary retention who required catheterization for more than 7 days. Methods Men requiring continuous drainage, bladder capacity less than 300 ml, history of prostatic or urethral surgery, or urethral length outside of defined limits, were excluded. Data were collected from patient diaries and weekly visits during catheterization for up to 30 days. The primary composite endpoint assessed four outcomes: placement, post‐void residual volume (PVR) of 75 ml or less, adverse device‐related events requiring early removal, and removal. Results Nine of 23 patients met all four criteria: eight of 18 non‐neurogenic (7/11 prior Foley users and 1/7 without Foley experience) and one of five neurogenic spinal cord injury (SCI) patients. Secondary outcomes in non‐neurogenic patients included: 17/18 successful insertions; of these, 16/17 average PVR of 75 ml; successful valve openings and closings ≥ 95% of more than 1,400 voids; and minimal leakage. Four of five SCI patients discontinued within 7 days. Cystourethroscopy after removal revealed no marked inflammation or mucosal changes. Conclusions This pilot study demonstrated the BMS is potentially useful, convenient, and safe for appropriate patients. A follow‐up study will better define the characteristics of patients who benefit from this device and examine whether the use of antimuscarinic agents improves outcomes. Neurourol. Urodynam. 35:630–635, 2016 . © 2015 Wiley Periodicals, Inc.