Elsevier

Urology

Volume 72, Issue 4, October 2008, Pages 825-827
Urology

Reconstructive Urology
Transcorporal Artificial Urinary Sphincter Placement for Incontinence in High-risk Patients After Treatment of Prostate Cancer

https://doi.org/10.1016/j.urology.2008.06.065Get rights and content

Objectives

To investigate the transcorporal (TC) vs standard (ST) approach of artificial urinary sphincter (AUS) placement for incontinence after treatment of prostate adenocarcinoma (PCa) with radiotherapy or surgery, or both.

Methods

A database was created to include the data from all patients who had undergone AUS placement from January 2000 to August 2005 at the University of California, San Francisco, Medical Center. We noted the demographic features, comorbidities, PCa therapy, technique for AUS placement, and postoperative outcome. The continence and failure rates were recorded for TC AUS placement in patients previously treated for PCa.

Results

A total of 30 patients underwent aus surgery during the study period: 26 for incontinence after PCa treatment. Of the 26 patients, 18 had undergone ST (ST group) and 8 had undergone TC (TC group) AUS placement, with a minimal follow-up of 12 months and a mean follow-up of 31 and 28 months, respectively. The 2 groups did not differ widely in age or comorbidities. Of the patients in the ST and TC groups, 44% and 50% had undergone external beam radiotherapy or brachytherapy and 78% and 100% had undergone radical prostatectomy, respectively. Of the patients in the ST and TC groups, 22% and 89% had undergone ≥2 types of urethral surgery before AUS placement, respectively. A total of 50% of TC group underwent TC placement without having undergone a previous sling or ST AUS procedure. The AUS removal rates were equivalent between the 2 groups at 2 years. Finally, the success rate for social continence was 69% and 81% for ST and TC group, respectively.

Conclusions

The results of our study, with 2 years of follow-up, have shown that TC AUS placement is an effective salvage or primary incontinence treatment for high-risk patients after PCa therapy.

Section snippets

Material and Methods

After approval from the internal review board, we performed a retrospective review of all patients who had undergone AUS placement by a single surgeon from January 2000 to August 2005. We limited our review to those patients with ≥1 year of follow-up. AUS surgery was performed by way of a perineal incision with a proximal bulbar urethral cuff (in all primary cases) using the AMS 800 device (American Medical Systems, Minnetonka, MN) with a reservoir of 61-70 mL.

The TC approach has been

Results

Of the 30 patients who had received an AUS for the treatment of urinary incontinence, 26 had been previously treated for PCa. The etiology of the incontinence in the other 4 patients included trauma in 3 and open simple prostatectomy in 1. The present observational report focused on the 26 patients with previous PCa therapy. Of the 26 patients, 18 had undergone an ST approach to cuff placement (ST group) and 8 had undergone a TC approach (TC group). The mean follow-up was 31 months for ST group

Comment

When one is faced with the task of AUS reimplantation after previous urethral erosion or atrophy, it is important to select a site for cuff placement that is distant from the previous cuff location. Because the original cuff location will have been around the proximal bulbar urethra, the reimplantation is generally performed at the distal bulbar urethra. The more distal urethra is relatively narrower, and thus does not allow for an occlusive seal with the smallest available cuff (4 cm). At

Conclusions

We have introduced expanded indications for the TC approach to AUS placement. The TC approach to primary AUS cuff placement adds a margin of safety in patients who have undergone previous urethroplasty or radiotherapy and who are at greater risk of cuff erosion. The short-term results indicate reasonable efficacy and safety compared with the ST approach, despite the greater risk patient population. Additional follow-up is needed to confirm these encouraging results.

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