Abstract

NEUROUROLOGY

Transobturator male sling TOMS™ for the treatment of stress post-prostatectomy incontinence, initial experience and results with one year's experience

Philippe Grise; Marc Geraud; Jean Lienhart; Benoit Le Portz; Michael Bubenheim; Pierre Costa

Department of Urology (PG) and Department of Biostatistics (MB), Rouen University Hospital, Rouen, France, Department of Urology (MG), Polyclinique Saint Come, Compiegne, France, Department of Urology (JL), Clinique Trenel, Sainte Colombe, France, Department of Urology (BP), Clinique Oceane, Vannes, France, Department of Urology (PC), Nimes University Hospital, Nimes, France

^{Correspondence} Correspondence adress: Dr. Philippe Grise Department of Urology Rouen University Hospital-Charles Nicolle rue de Germont 76031, Rouen, France Fax: + 33 2 3288-8205 E-mail: philippe.grise@chu-rouen.fr

ABSTRACT

Purpose: Post-prostatectomy incontinence remains a problem, even in minor or moderate degrees. In order to minimize surgical morbidity and costs, sling procedures have been proposed. The authors have developed a new transobturator male sling procedure and report their results after one-year experience.

Materials and methods: A prospective multicenter study was conducted in 50 patients with minor or moderate post-prostatectomy incontinence. Evaluation of TOMS™ two arms bulbar sling was based on clinical form assessment, The International Consultation on Incontinence Questionnaire (ICIQ) and short-form (SF) 36 questionnaire pre and postoperatively and at 3, 6, 9 and 12 months.

Results: The surgical procedure was considered easy to perform and no post-surgery complication was reported except for one retention. The median number of pads per day decreased significantly from 2 pads before surgery (95% CI: 2 - 3) to 1 during the follow-up period (95% CI: 0 - 2 at 360 days), and at 3 months patients using none or one pad per day were 30% and 32% respectively. The SF 36 continence and quality of life score improved from a median of 100 (95% CI: 83 - 133) to 300 (95% CI: 167 - 375), and the median ICIQ incontinence and quality of life score decreased from 15 (95% CI: 14 - 16) to 8 (95% CI: 5 - 12) one year after surgery.

Conclusion: The transobturator perineal male sling TOMS™ is an attractive simple sling technique for moderate or minor post-prostatectomy stress incontinence and offers an improvement in the quality of life.

Key words: urinary incontinence; male; urinary sphincter; prostatectomy; surgery, sling

INTRODUCTION

Despite improvement in surgical technique of radical prostatectomy, incontinence remains a bothersome problem. The prevalence of post-prostatectomy depends on the definition of incontinence and evaluation methods; however, studies indicate that 5% to 55% of patients are concerned (1). Even only one pad a day affects the quality of life (2).

For major stress urinary incontinence (SUI), the artificial sphincter remains the gold standard technique despite a risk of erosion or infection. As regards urethral bulking agents, they are often disappointing even with re-injections.

In order to minimize surgical morbidity and cost, bulbar sling procedures have been proposed of which the most common sling used is bone-anchor fixation. Good results without significant obstruction were obtained but concern remains regarding perineal pain and infection of the material. Based on our experience of the female transobturator polypropylene sling (3) we developed a new transobturator bulbar male sling (TOMS™) (4) in order to minimize the adverse effects of bulbar slings. Other male transobturator slings (5-8) have also recently been reported in the bulbar location (5,7,8) or in membranous location (6). The benefits and our clinical results were studied in a prospective multicenter series. The results with one year's experience are reported.

MATERIALS AND METHODS

In a preliminary study (4) on six male cadavers in the lithotomy position, the surgical technique was performed using a vertical perineal incision. The bulbospongiosus muscle was dissected, then the ischiocavernous muscles, in order to expose the perineal aponeurosis close to the ischiopubic ramus bone and the obturator foramen situated just above the ramus. The surgical procedure was evaluated concerning outside-inside and inside-outside transobturator puncture in male pelvis using respectively Hemet and helical needle.

Therefore, a prospective multicenter clinical study was conducted from May 2006 to August 2007 on 50 male patients suffering from post prostatectomy incontinence and after a failure of physiotherapy. Our study received Institutional Ethics Committee approval.

All surgeons were experienced in transobturator procedure for female stress incontinence and followed the same instructions for surgery. The number of surgeons involved was ten and their first patients were included in this series.

A total of 50 patients were included with minimal 12 months follow-up. Exclusion criteria were pre or post-surgery radiation, less than one year before surgery, bladder outlet obstruction from anastomotic or urethral stricture, bladder overactivity or bladder hypocompliance. Only minor or moderate SUI patients according to the Stamey definition were enrolled based on the urologist's evaluation and 5 or less pads per day.

Pre-surgery assessments included previous medical history, physical examination, clinical study questionnaire for urological symptoms and number of pads per day, urodynamics (urethrocystometry, uroflowmetry, post-void residual urine) according to the recommendations of the International Continence Society, and cystourethroscopy to rule out any anatomical abnormality.

The patients completed the International Consultation on Incontinence Questionnaire – Short Form (ICIQ-SF) (9) and the Short-Form (SF) 36 (10) questionnaire, and a visual analog pain scale (VAS) before and after surgery.

The physician recorded post-surgery evaluations at 1, 3, 6 and 12 months using the same evaluation except for urethrocystometry. As regards safety assessments, potential per and post-operative hazards were recorded on a case report form.

The sling was a monofilament polypropylene, with macropores over 75 micrometers, non-extensible, 45 cm long x 1.4 cm large, developed by CL Medical (4). The sling is attached at each end to a clip in order to connect it to a specific needle. Hemet or helical needle was used according to the surgeon's preference.

The surgical technique was performed under spinal or general anesthesia, and a 16F Foley urethral catheter was inserted. The patients were placed in the lithotomy position and a 6 cm median vertical perineal incision below the inferior border of the pubic symphysis was carried out in order to expose the bulbospongiosus muscle, then to expose the perineal aponeurosis at the top of the triangular space delimited laterally by each ischiocavernous muscle and medial to the bulbospongiosus. A short 2 mm incision through the pelvic fascia afforded access to the obturator muscle just under the ischiopubic ramus bone. A stab incision was made at the top of the thigh, 4 cm from the median line and 4 cm below the major adductor longus muscle. The transobturator puncture was an outside inside with a Hemet needle. The end point of the puncture was the opening in the pelvic fascia. After sling attachment to the needle, it was pulled back in order to correctly implant the sling. The same procedure was repeated on the other side. The sling was sutured to the bulbospongiosus muscle with non-absorbable sutures, and then pulled firmly from each side in order to obtain a 2 mm visible mark on the bulbospongiosus muscle. The perineal body was not dissected, but in cases of rolling of the inferior edge of the sling on the bulb, the bulb was dissected just enough to apply it under the sling, then sutured to the sling. No retrograde urethral pressure adjustment was performed. The incision was closed without drainage and the urethral catheter left indwelling for 2 days. Before hospital discharge, an uroflowmetry, a post void residual, and a pelvic pain evaluation on VAS were obtained.

Statistical analysis - The description of the population at baseline was done using the median, the first and the third quartile (Q1 - Q3). As regards the trend over time, the results of each visit were summarized using the median and a 95% confidence interval (CI). For the graphical illustration of these trends, box-plots, as described by Tukey (11), were used. In order to test the hypothesis of no change between consecutive visits against the alternative that there was a change, rank based methods were applied. As the power of these tests depends among others on the proportion of tied observations, Wilcoxon's test for dependent samples was used for all tests relating to the same variable if the first quartile at any visit was larger than zero. For all other variables, the sign test was used in order to verify whether changes between consecutive visits were significant. Admitting for each variable a global level of 0.05 for answering the question whether a change occurred between any two consecutive visits, Holm's method was used to control for the inflation of the risk of a Type-I error.

RESULTS

In the cadaveric procedures, the perineal approach to the bulbar urethra and the outside-inside or inside-outside puncture of the obturator foramen were easily performed.

Concerning the clinical study, a total of 50 patients with a median age of 72 years (Q1 - Q3: 64 - 77) underwent TOMS™ surgery. Incontinence was a problem for all the patients.

At least half of them wore 2 pads per day (Q1 - Q3: 1 - 3). History of prostatic surgery was radical prostatectomy for 48 and transurethral prostatectomy for 2 patients, the median time between prostatectomy and surgery for SUI was 35 months (Q1 - Q3: 22 - 50).

The surgery was considered by the surgeon as easy to perform in all the cases. The median operative time for the procedure was 30 minutes (Q1 - Q3: 25 - 45).

No per-surgery complication was reported, and no significant intra-operative bleeding (> 200 mL) occurred or nerve, bowel or vascular injury.

On the VAS, the median pain value the day after surgery was 2 (95% CI: 1 - 3), then decreased significantly to 0 (95% CI: 0 - 0) at one month and remained similar for all further visits until the end of the study.

After urethral catheter removal, residual was less than 100 mL for all the patients except one patient who experienced urinary retention. This patient was reoperated (day 2) to release the tension on the tape, and then a good result on micturition and continence was obtained. A low stream was reported for one patient but this was not bothersome. Maximal flow rate was 20 mL/sec on the median (95% CI: 17 - 24) before surgery and 16 (95% CI: 8 - 26) when evaluated after catheter removal; the values (Figure-1) did not change significantly during the follow-up period.

Overall median pad use decreased significantly (p-value used test and is reported in Figure-2) from 2 pads per day (Q1 - Q3: 2 - 3) before discharge and at one month, to 1 pad for all the visits thereafter (Figure-2). At three months and during the follow-up period to 12 months, patients using none or one pad per day were 30% and 32% respectively.

Figure 2

The SF36 continence scores, measured on a scale ranging from 0 to 500 (Figure-3), improved significantly from a median score of 100 (95% CI: 83 - 133) to 300 at one year (95% CI: 167 - 375). During the follow-up period, the median scores were 242, 217 and 267 at 1, 3 and 6 months respectively.

The ICIQ incontinence score (Figure-4) decreased significantly from 15 (95% CI: 14 - 16) before the TOMS sling to 8 (95% CI: 5 - 12) at one year, and the median score was 9 for all other visits at follow-up.

COMMENTS

A number of minimal invasive techniques have been proposed for managing SUI in male patients but some of them have adverse side effects or minimal outcome measurements. Among them, the adjustable balloon is an alternative to the sling procedure based on a mechanism of lateral compression of the proximal urethra. Patients with none and one pad a day were reported in 60% (12), but the high rate of per and post-surgery complications and several adjustments were of some concern.

The artificial sphincter remains the gold standard technique for severe incontinence due to sphincter deficiency although the cost, the erosion or infection rate as well the need to press the pump for each micturition, make many patients reluctant to have this type of surgery for moderate or minor incontinence.

The concept of minimal invasive surgery with perineal bolsters acting as a sling on the bulbar urethra was described by Schaeffer et al. (13). Initial success rate was excellent for continence with no significant outlet obstruction but outcome was complicated with bolster removal due to pain, infection or erosion. The efficacy was demonstrated on an average of four years (14) with a 42% cure rate.

In order to improve tolerance, John (15) reported a bulbourethral composite suspension with porcine dermis and polypropylene sling through the retropubic space. This author reported 69% continence patient with a 14-month mean follow-up. Using a retropubic sling made of polyester plus polypropylene Xu et al. (16) achieved successful treatment in 85% of 26 patients at 28 months.

There is a concern regarding the retropubic route due to a risk of a bladder puncture or erosion (7), and the adhesions due to the prostatectomy may increase the risk of using this route.

A new concept of a large perineal sling on the bulbar urethra was subsequently introduced with the InVanceTM bone anchored male sling made of a large triangular silicone coated biomaterial. Comiter (17) had 65% cured and pad free patients at minimum 2 year follow-up with a polypropylene or polyester mesh using bone anchor fixation, however up to 16 % of patients reported perineal pain or numbness that persisted during many weeks. These adverse effects might possibly be due to irritation in the area of the bone screws or lesion to the perineal nerves (18) during ischiopubic rami dissection. Moreover, infection of the biomaterial frequently occurred due to a large silicone coated membrane instead of macroporous mesh tape, and biomaterial characteristics may explain the morbidity including osteomyelitis from bone screws.

Different biomaterials have been used for the sling (allograft, porcine xenograft, synthetic, composite mesh) but a poor outcome resulted from the non-synthetic graft (19), and the good tolerance of polypropylene is now widely accepted. The TOMS™ polypropylene tape is macroporous, non-extensible and the procedure is considered to be easy. No complication was reported and tolerance was good, particularly concerning perineal pain.

As other authors during per-surgery we did not adjust the tension of the sling with the use of urethral pressure value as this measurement was retrograde, not standardized in technique and threshold. The sling was not clinically compressive for most of the patients as confirmed on clinical records, post-void residual and uroflowmetry, although a pressure-flow study was not conducted to document a possible urodynamic compressive effect. Urodynamic study in 22 men by Comiter (17) revealed that the bulbar urethral sling had no significant effects on voiding function. Nevertheless, in our series, one patient experienced postoperative complete retention possibly due to excess in tension or to an acontractility bladder reflex. The decision between immediate reoperation to release the tension on the tape, or after few days of self-catheterization should be discussed with the patient.

The data on continence confirmed the interesting results of the other retropubic and bone anchor bulbar urethral male slings. As in the reported series, about 60% of the patients used none and one pad per day at three months and during the follow-up period to 12 months.

An explanation why pad use did not change at 30 days follow-up could be that the patients were still anxious about leakage and used a safety pad.

Evaluation based on SF 36 scale and ICI-Q scale showed that the continence and the quality of life improvement was significant on both scales, and the results were maintained at one year.

Radiation was an exclusion criterion in order to present a homogenous series as this factor adversely affects male sling outcomes.

The transobturator route in male was initially reported by Bauer et al. (5) in a three male cadaver study using a helical puncture, our study confirmed this approach and added the feasibility of oustside-inside puncture. In male patients, the transobturator tape was reported either on membranous urethra (6) using Advance sling, or on bulbar urethra using Argus sling (7) or De Leval sling (8) or TOMSTM sling (4). Argus sling (7) is made of silicone and is an adjustable sling. De Leval and Waltremy (8) used a polypropylene transobturator sling at the same position as our sling on the bulbar urethra; they obtained continence in 45% of their patients at 6 months. The difference between our techniques is that they performed an additional subcutaneous lateral dissection to tie the two lateral arms to each other, but more biomaterial and a larger dissection were risk factors for a potential infection or perineal pain. However, attachment of each arm to each other was probably stronger than to rely only on the transobturator route.

The mechanism of action may need further studies on the precise location and degree of male urethral mobility. The AdVanceTM male sling system (6) is located more proximally on the bulbar-membranous urethra in order to modify the mobility and to act as a hammock-like support of the posterior sphincter complex, but tension is also applied on the sling. A proximal dissection close to the sphincter is a potential risk for a major deficiency; moreover, the membranous urethra is thin and more fragile which may explain a reported case (20) of urethral erosion.

These results using TOMS™ sling remain encouraging but the continence results should be improved and a study is currently ongoing with a four arm larger sling using the same biomaterial and transobturator route.

CONCLUSION

The transobturator perineal male sling TOMS™ is an attractive technique for moderate or minor post-prostatectomy stress incontinence. The implanted biomaterial is non-mechanical, and easy to insert and well tolerated. Most of the patients were improved or continent with a one year follow-up.

CONFLICT OF INTEREST

Philippe Grise is the main investigator of the TOMS™ study (CL medical company). No financial support was provided for the study and the authors received no funding for the study. Philippe Grise received funding as an invited speaker at a symposium by Ipsen and from CL Medical companies.

ACKNOWLEDGEMENTS

The authors are most grateful to the following researchers: Christian Saussine (Strasbourg), Jacques Vannier (Tours), Olivier Delbos (Montpellier), Renaud Vautherin (Sainte Colombe), François Bouchou (Tours), Denis Dupuy (Toulouse), Patrice Lille (Moulin), Ibrahim Bah-Closel (Guilherand Granges), Jean-Luc Hoepffner (Bordeaux), Clément Darcq (Besançon).

We also thank Richard Medeiros, Rouen University Hospital Medical Editor, for editing the manuscript.

Accepted after revision:

June 26, 2009

EDITORIAL COMMENT

Dr. Grise and colleagues present an interesting experience using a transobturator (TO) bulbar sling in the treatment of post-prostatectomy incontinence. Indeed, the male sling is not a new concept, with the most significant experience comprising two techniques. The first utilizes urethral compression bolsters secured over the rectus fascia; the other a periurethral mesh secured with bone anchors. Despite promising outcomes associated with these sling types, widespread adoption of the male sling as a first line surgical therapy has not been seen. More recently, a resurgence has been seen with the introduction of TO sling types. Importantly, the work of Dr. Grise and associates contributes to this experience and the 1-year minimum follow-up is to be commended.

As related series are reported, it is important that focus is placed on surgical technique as small technical differences may affect sling efficacy. For example, both published and non-published description of TO sling techniques detail varying degrees of perineal body mobilization and, with it, somewhat differing locations of sling placement along the bulbar urethra. Accordingly, sling placement in a more proximal position may result in a vector allowing for urethra suspension/elevation, whereas a distal location can yield a compressive action. How these differing vectors of support affect outcomes is unknown. Indeed, the anticipated introduction of a bulbar sling comprising both TO and prepubic arms suggests that both vectors may be important. Future comparative study to help define the optimal vector of support and sling position will be important.

Dr. David Rapp

Co-Director, Virginia Urology Center for

Continence and Pelvic Floor Reconstruction

Virginia Urology Center

Richmond, Virginia, USA

E-mail: derapp@yahoo.com

EDITORIAL COMMENT

Despite improved surgical techniques, which have led to decreased incontinence rates, still a significant number of patients are suffering from post-prostatectomy stress urinary incontinence (SUI) (1). Surgical treatment is the recommended therapeutic option after non-invasive therapies have failed (2). Since decades, the established standard for surgical treatment has been the artificial urinary sphincter. It is, however, very expensive and associated with high surgical revision rates (3,4). In addition, the patient needs to have the mental and physical ability to handle the sphincter. Moreover, minimal-invasive approaches for the treatment of SUI are more and more demanded by patients (5). Thus, in recent years several minimal-invasive sling systems have been intensively investigated (6-8).

In the study presented by Grise et al., the authors report about one year results of a new transobturator male sling. The new sling has to be positioned like the well-known retro-urethral transobturator sling in the region of the membranous urethra but without splitting the bulbospongiosus muscle (9). Unfortunately, the reported initial results are not very convincing. In the present study, a dry rate of only 30% could be achieved. However, for the reported patient group with a median daily pad use of 2 pads, a cure rate (no pad use) above 50% would be expected. One reason for the comparably low success rate may have been the inclusion of the first patients treated with the new sling system. In addition, the number of surgeons was rather high (five implantations per surgeon on average). Thus, the study incorporates to a large degree the surgeons' learning curve. However, it remains unclear if the unsatisfying dry rate is caused only by the learning curve factor. Another limitation of this study is the measurement of urine loss by means of daily pad use only. For a more reliable comparison of postoperative results and to allow for a more extensive comparison with other studies, standardized pad-tests - like the one-hour pad test or the 24-hour pad-test - would have been desired.

Further studies with a larger patient population and longer follow-up period will be necessary to fully assess the potential of this new sling system.

REFERENCES

Dr. Ricarda M. Bauer

Urologische Klinik und Poliklinik

Ludwig-Maximilians-Universität München-Grosshadern

München, Germany

E-mail: Ricarda.Bauer@med.uni-muenchen.de

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