Abstract

Urinary incontinence is one of the most serious complications of prostate cancer treatment. The objective of this study was to assess efficacy and safety of Adjustable Transobturator Male System (ATOMS) compared to Adjustable Continence Therapy (proACT) for male stress urinary incotinence according to literature findings. A systematic review and meta-analysis on adjustable devices ATOMS and ProACT is presented. Studies on female or neurogenic incontinence were excluded. Differences between ATOMS and proACT in primary objective: dryness status (no-pad or one safety pad/day) after initial device adjustment, and in secondary objectives: improvement, satisfaction, complications and device durability, were estimated using random-effect model. Statistical heterogeneity among studies included in the meta-analysis was assessed using tau2, Higgins´s I2 statistics and Cochran´s Q test. Combined data of 41 observational studies with 3059 patients showed higher dryness (68 vs. 55%; p = .01) and improvement (91 vs. 80%; p = .007) rate for ATOMS than ProACT. Mean pad-count (-4 vs. -2.5 pads/day; p = .005) and pad-test decrease (-425.7 vs. -211.4 cc; p < .0001) were also significantly lower. Satisfaction was higher for ATOMS (87 vs. 56%; p = .002) and explant rate was higher for proACT (5 vs. 24%; p < .0001). Complication rate for ProACT was also higher, but not statistically significant (17 vs. 26%; p = .07). Mean follow-up was 25.7 months, lower for ATOMS than ProACT (20.8 vs. 30.6 months; p = .02). The rate of working devices favoured ATOMS at 1-year (92 vs. 76; p < .0001), 2-years (85 vs. 61%; p = .0008) and 3-years (81 vs. 58%; p = .0001). Significant heterogeneity was evidenced, due to variable incontinence severity baseline, difficulties for a common reporting of complications, different number of adjustments and time of follow-up and absence of randomized studies. Despite the limitations that studies available are exclusively descriptive and the follow-up is limited, literature findings confirm ATOMS is more efficacious, with higher patient satisfaction and better durability than ProACT to treat male stress incontinence.

Highlights

  • Satisfaction was higher for Adjustable Transobturator Male System (ATOMS) (87 vs. 56%; p = .002) and explant rate was higher for proACT (5 vs. 24%; p < .0001)

  • Urinary incontinence can severely impact the quality of life of prostate cancer survivors after radical prostatectomy and/or radiotherapy [1,2]

  • With this study we aim to evaluate the current evidence on the efficacy and safety ATOMS compared to ProACT using a systematic review approach and meta-analysis

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Summary

Introduction

Urinary incontinence can severely impact the quality of life of prostate cancer survivors after radical prostatectomy and/or radiotherapy [1,2]. Adjustable continence therapy (ProACT1, Uromedica, Minneapolis, MN) using balloons placed periurethraly near the bladder neck was the first adjustable implant to treat stress incontinence. It consists of two volume-adjustable balloons, that increase urethral resistance during voiding. Adjustable transobturator male system (ATOMS1, A.M.I., Feldkirch, Austria) is another adjustable device that compresses the bulbar urethra ventrally but, unlike ProACT, its two-arm mesh allows firm transobturator fixation on both sides of the ischiopubic bone. Both devices can be adjusted postoperatively without need for aneasthesia. The objective of this study was to assess efficacy and safety of Adjustable Transobturator Male System (ATOMS) compared to Adjustable Continence Therapy (proACT) for male stress urinary incotinence according to literature findings

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