Korean J Urol. 2013 Jun;54(6):373-376. English.
Published online Jun 12, 2013.
© The Korean Urological Association, 2013
Original Article

Functional Outcomes and Long-term Durability of Artificial Urinary Sphincter Application: Review of 56 Patients With Long-term Follow-up

Ömer Gülpınar, Evren Süer, Mehmet İlker Gökce, Ahmet Hakan Haliloğlu,1 Erdem Öztürk and Nihat Arıkan
    • Department of Urology, Ankara University Faculty of Medicine, Ankara, Turkey.
    • 1Department of Urology, Ufuk University Faculty of Medicine, Ankara, Turkey.
Received January 09, 2013; Accepted February 27, 2013.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose

To evaluate the long-term outcomes of artificial urinary sphincter (AUS) implantation and to report the complication rates, including mechanical failure, erosion, and infection.

Materials and Methods

From June 1990 to May 2011, AUS (AMS 800) implantations were performed in 56 adult males by one surgeon. Various demographic and preoperative variables, surgical variables, and postoperative outcomes, including success and complication rates with a median follow-up of 96 months, were recorded retrospectively.

Results

The mean age of the patients at the time of AUS implantation was 61.8 (±14.2) years. During the follow-up period, the total complication rate was 41.1% (23 patients). The incidence of complications was significantly lower during the follow-up period after 48 months (p<0.05). Kaplan-Meier analysis revealed that 5- and 10-year failure-free rates were 50.3% and 45.2%, respectively.

Conclusions

Long-term durability and functional outcomes are achievable for the AMS 800, but there are appreciable complication rates for erosion, mechanical failure, and infection of up to 30%.

Keywords
Artificial urinary sphincter; Complications; Urinary incontinence

INTRODUCTION

Owing to the increasing number of radical prostatectomies (RPs) as a standard treatment for localized prostate cancer, the number of men with postoperative stress urinary incontinence (SUI) has increased. The reported prevalence of urinary incontinence in all men is as high as 39% and increases with age [1], and RP is the most prevalent cause. Although the incidence of SUI decreases with the surgeon's increased experience with RP, it is still a significant problem, and reported SUI rates in these patients are between 5% and 48.0% [1].

With the proven major impact on quality of life, which affects patients' physical activity and social well-being [2, 3], male SUI is an important health problem. There are several options for the surgical treatment of male SUI, including some minimally invasive technics and artificial urinary sphincter (AUS) implantation. In recent years, numerous minimally invasive treatment options (bulking agents, adjustable techniques, and several types of male slings) with different success rates have been investigated. Lack of evidence in long-term durability and efficacy is the major problem for these minimally invasive options. On the other hand, the AUS is a well-established treatment for male SUI [4, 5], including that resulting from RP. Furthermore, different from the other devices, the AUS is versatile and effective for a wide range of situations, including severe incontinence, SUI after radiation, and as a salvage procedure after failure of other treatments.

In this retrospective study, we evaluated the long-term outcomes of AUS implantation in our clinic with 21 years of experience. We also report the complication rates, including mechanical failure, erosion, and infection, and the long-term durability of AUSs.

MATERIALS AND METHODS

From June 1990 to May 2011, AUS (AMS 800, American Medical Systems Inc., Minnetonka, MN, USA) implantations were performed in 56 adult males by one surgeon. All of the AUS cuffs were placed at the bulbar urethra. Various demographic and preoperative variables (patient age at implantation, etiology of incontinence (post prostetctomy incontinance [PPI] or neurogenic), history of pelvic radiation, and type of prior treatment for urinary incontinence), surgical variables (the date of surgery, type of surgery [primary, secondary, or revision], and operative time), and the postoperative outcomes (social or medical continence status, complications, malfunction, months to revision if applicable, and total follow-up time in months) were collected from the patients' medical charts. Social continence was defined as continence status with the use of two or fewer pads per day. Failure was defined as that caused by any reason, such as mechanical failure, surgical revision, or removal. AUS durability was analyzed by use of Kaplan-Meier survival plots. Differences in durability according to different criteria were analyzed by using the Student t-test. p-values less than 0.05 were considered significant. SPSS ver. 17 (SPSS Inc., Chicago, IL, USA) was used for all analyses. The local institutional review board approved the study.

RESULTS

The mean age of the patients at the time of AUS implantation was 61.8 (±14.2) years and all of the patients were male. The median follow-up time of the patients was 96 months (range, 11 to 149 months). The clinical and concomitant comorbidities of the patients are shown in Table 1. RP was the most common indication for AUS implantation (41 patients). Neurogenic male sphincter insufficiency and transurethral resection of the prostate were the other indications with a total of 9 and 6 patients in each group, respectively. The incidence of type 2 diabetes was 28.5% and the incidence of hypertension was 48.2% in the study group.

TABLE 1
Clinic charactheristics of the patients treated with an artificial urinary sphincter (n=56)

During the follow-up period, the total complication rate was 41.1% (23 patients). The mechanical failure rate was the most common complication with a rate of 25% (14 patients). The mechanical failures were difficulty to compress the pump, breakdown of the device, and inadequate urethral compression by the balloon. The mean mechanical failure time was 33 months (±24 months). Erosion and infection were the other complications with a rate of 8.9% (5 patients) and 7.1% (4 patients), respectively. In the early postoperative period, the AUS was removed in 4 patients owing to erosion (in 1 patient) and infection (in 3 patients). We removed the AUS in 1 patient at 8 months after the operation owing to a massive scrotal abscess. The mean erosion time was 41 months (±34 months). We compared the overall complication rates during the follow-up period at intervals of 12 months (Table 2). The comparison of the complications of the 1-12 months, 13-24 months, 25-36 months, and 37-48 months periods did not demonstrate any significant differences. However, the incidence of complications was significantly lower during the follow-up period after 48 months (p<0.05). Kaplan-Meier analysis revealed that 5- and 10-year failure-free rates were 50.3% and 45.2%, respectively (Fig. 1).

FIG. 1
Treatment failure-free survival in 64 patients with artificial urinary sphincter implantation. Five- and 10-year failure-free rates were 50.3% and 45.2%, respectively.

TABLE 2
Long-term complication rates seen at 12 months of intervals in the postoperative period

Of the study group, 58.9% (33 patients) of the patients did not demonstrate any complications. Because four patients experienced removal of the device before activation of the control pump, continence was evaluated in 52 patients. The 46% (24 patients) of patients with a functioning AUS (52 patients) did not use any pads per day, and 19.2% (10 patients) used ≤2 pads per day. The social continence rate was 65.3% (34 patients).

DISCUSSION

In the present study, we reported our AUS implantation series with a long follow-up period. Although many studies have reported AUS results, not as many studies had a long-term follow-up period. Regarding the outcomes, the long-term results of operations performed with mechanical devices are important. In three studies with more than 6 years of follow-up, mechanical failure rates ranged from 25% to 61% [6-8]. Similar to these studies, our mechanical failure rate was 25%. Haab et al. [6] reported a significant decrease in the mechanical failure rate after 1987 owing to device improvements. However, the mechanical failure rate in our study, which was performed between 1990 and 2012, was similar to that of the Haab et al. study (25% for both). Therefore, we believe that this finding of Haab et al. needs to be verified with further studies. Erosion and infection rates with AUS implantation vary considerably among the studies, with reports of 4-13% and 1.3-7%, respectively, in patients with PPI [6, 9-11]. Our complication rates, regarding erosion and infection, were on the high side of this range, with rates of 8.9% and 7.1%, respectively. The high complication rates of the present study may be related to the longer follow-up period of our study compared with the others. Another reason may be our clinic's status. Because ours is a tertiary center, the patient population of our clinic consists mainly of men with comorbidities. In particular, the inclusion of patients with type 2 diabetes and neurogenic patients with previous urinary instrumentation in the study population may explain the relatively high rate of complications. Indeed, the findings of a recent study with a median of 6.8 years of follow-up were similar to the present study, with an 8% erosion rate and a 5.6% infection rate [7]. In that study, Kim et al. [7] reported the overall complication rate as 37%, and mechanical failure was the most common cause. Similar to the present study, they also concluded that most events, regarding the complications, occurred in the first 48 months.

Success rates for AUS implantation are generally excellent, often between 75% and 90% [8, 11]. In a report of patients with a minimum of 10 years of follow-up, a continence rate of 75% was demonstrated despite a revision rate of 80% [8]. Our social continence rate was 65.3%, which is lower than in previous studies. We think that the higher complication and lower revision rates may clarify this relatively low social continence outcome.

Owing to the small number of patients, we did not perform any statistical analyses regarding the risk factors for failure. Findings in the literature differ about the risk factors for AUS implantation failure. Pelvic radiation has been considered a potential risk factor for AUS treatment failure and complications [12-14]. Thiel et al. [15] investigated the clinical and urodynamic parameters to determine the risk factors for failure and concluded that there were no significant factors and that only older patients tended to have decreased perceived improvement. Furthermore, in a study by Kim et al. [7] using a multivariate logistic model, no significant predictive factor for failure of AUS was found . On the other hand, another study by Arai et al. [16] reported that operation time was an independent risk factor for AUS failure. Although the number of patients in the two last-mentioned studies was similar, the median follow-up times were quite different (6.8 years vs. 24.5 months). The findings of the study by Kim et al. [7], with the longer follow-up time, may be more reliable. However, the finding of Arai et al. [16] suggesting a significant learning curve effect on the treatment outcome must also be taken into consideration.

This study had several limitations. Because this was a retrospective study, there are limitations to this study's conclusions and generalizations. Limited sample size is another limitation. However, because of the long follow-up time, we think that the findings of the present study should be taken into consideration. Because AUS implantations are performed to achieve higher quality of life, assessment of outcomes of this surgery should be performed with validated questionnaires. The use of a well-validated questionnaire would provide more clinically relevant information. The lack of such a questionnaire is also a limitation of our study. Because this was a single-institution retrospective study, multi-institutional studies may provide more reliable results.

CONCLUSIONS

Long-term durability and functional outcomes are achievable for the AMS 800, but there are appreciable complication rates for erosion, mechanical failure, and infection of up to 30%.

Notes

The authors have nothing to disclose.

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