Vol.14 /No: 2/ Nov 2005

 

   

 

 

Tension Free Vaginal Tape (TVT) Procedure for Female Stress Incontinence:
Qatar Experience

Farid I., Aboud I., Al Blushi M.A., Al Mansoori Z.S.
Department of Obsterics and Gynecology, Women’s Hospital
Hamad Medical Corporation, Doha, Qatar


Abstract
Introduction
Patients and Methods
Results
Discussion
Conclusion
Comments
References


Abstract:

A retrospective study was conducted on the records of 44 women who had received tension-free vaginal tape as a primary or secondary procedure for the treatment of stress urinary incontinence. Intra-operative complications were uncommon, operative time and hospital stays were short and late postoperative complications were few. 36 (81.8%) women became dry, six cases (13.6%) are satisfied and two patients (4.5%) are still complaining of stress incontinence. The tension free vaginal tape procedure appeared to be an effective, minimally invasive method for treating female stress urinary incontinence.


Introduction:

Stress urinary incontinence (SUI) affects 10-20% of the general population(1). In the last century more than 150 different surgical procedures to correct this condition were reported, reflecting that the exact mechanism behind incontinence is not completely understood and that there is no reference standard treatment(2). Recently several new surgical procedures have been developed using a variety of slings. The tension-free vaginal tape (TVT) is a relatively new procedure that uses a synthetic polypropylene mesh sling placed in the mid-urethral position. Published data suggests a good success rate from a minimally invasive procedure that can be performed under local or regional anesthesia with low morbidity(3).

We report our experience of using the TVT procedure in the Women’s Hospital Hamad Medical Corporation, Qatar, and assess the results and potential complications in treating female stress incontinence.


Patients and Methods:

Using a datasheet developed by the third author the records were reviewed retrospectively of 44 women (age 47.2±7.8; parity 5.4±2.5; BMI 32.9±5.5) who received TVT from January 1999 to March 2004. Twenty-nine cases (65.9%) were Qatari, and 15 cases (33.1%) were non-Qatari (Table 1). Analysis of the data was by SPSS software v.11.

Table 1:  Patient Characters
 

Eighteen (40.9%) had symptoms of urinary stress incontinence only; nine (20.5%) had mixed symptoms of stress incontinence and urgency; nine (20.5%) had stress incontinence with a degree of genital prolapse; six (7.5%) had problems such as dysfunctional uterine bleeding and infertility in addition to stress incontinence (Table 2).


Table 1:  Patient Characters
 

In more than half the cases (62.8%) the TVT was secondary to vaginal repair and/or hysterectomy; hysteroscopy; microwave endometrial ablation, laparoscopy or combined procedures to correct a secondary complaint. From operative reports various variables were collected such as surgeon, type of anaesthesia, unusual vaginal bleeding, total procedure time and complications.

The TVT procedures were carried out as described by Ulmstem(4), with most patients under regional anesthesia. The TVT set consisted of a polypropylene mesh tape fixed to 6 mm needles connected to an introducer (Ethicon, Inc., Sommerville, NJ, USA). Some surgeons used cystoscopy after each retropubic pass of the TVT needle, others once after needle insertion on both sides. The tape was adjusted with the patient coughing at a bladder volume of 300 ml., to allow a few drops of urine to escape from the urethral meatus. A Foley’s catheter was inserted in every patient. The day after the procedure the catheter was removed if the residual urine was below 100 ml. and the patient was discharged at the end of the working day. Otherwise the catheter was kept in and the residual urine re-checked the following day for possible patient discharge.

The course in the outpatient clinic after surgery was reviewed using patient files and surgeons’ notes. The final outcome was classified subjectively as “cured”, “satisfied” or ”failed”.


Results:

The overall mean follow-up period was 15.2 months (Range: 3-54). Nearly all (97.7%) of the TVT procedures were done under regional anesthesia and the mean operative time was 42 ± 11.7 minutes for the TVT procedures only; this is statistically significantly less than the time taken when TVT was done with other procedures (59±15.3 min; p < 001).

The mean total blood loss during surgery was 100 ±17.5 ml; two patients had blood losses of 350 ml. but no patient required blood transfusion. Bladder perforation was recorded in one case when the surgeon felt during cystoscopy that the tape was closer to the bladder wall on one side. The introducer was removed, urine came out from the suprapubic site of the introducer which was repositioned again and the procedure was completed. One patient had a stomach injury during laparoscopy done for tubal ligation in addition to TVT.

Three cases (9.1%) had urinary retention with residual urine >100 ml. All had additional vaginal repair with TVT. Two of these women developed retention on the third day after the procedure and the Foley’s catheter was reinserted for 24 hours, with a suprapubic catheter added in one. The third case developed urinary retention on the fourth day after surgery and was managed with a suprapubic catheter.

One patient had a haematoma of the right rectus sheath measuring 7.2 cm in mean diameter (by ultrasound) that was managed conservatively. One woman (2.3%) who underwent TVT and vaginal hysterectomy developed a fever (> 38 oC) for three days that responded to intravenous antibiotics. One case (2.3%) had urgency incontinence and painful micturation after TVT but recovered after a Foley’s catheter had been kept in for 48 hours. The overall mean hospital stay was 3.3±1.2 days (including two nights).

Twenty-seven women (61.4%) completed 12 months of follow up; five cases (11%) were followed for more than 24 months. One woman was followed for 54 months; 42 months after surgery she complained of superficial dyspareunea and part of the TVT tape could be felt by digital vaginal examination. This part (2 cm long) was removed under general anesthesia and the patient remained continent.

Data from the final follow up visits found that 37 women (84.1%) had no complaint; two cases (4.5%) developed de novo urge; in two women (4.5%) there was an episode of UTI in the first visit after surgery. Ten cases that had presented with voiding problems with their stress incontinence became free of symptom. In seven of 9 cases (77.8%) presented with some degree of genital prolapse in addition to their SI became subjectively dry, one case (11%) was satisfied, and another patient (11%) has persistent SI. From 18 women who presented with only stress incontinence, 14 (77.8%) became dry, and four (22.2%) cases were satisfied. The overall evaluation of patient continence after TVT, showed that 36 (81.8%) women became dry, six cases (13.6%) are satisfied and two patients (4.5%) are still complaining of stress incontinence.


Discussion:

The results of this study are comparable to other studies documenting the TVT procedure; the objective cure rate for GSI was 81.8% and was consistent with rates reported by other studies(4-10). Boustead 2002(3), reviewed the results from 16 studies; the mean overall objective cure rate in 1339 patients was 88%, with a further 9% improved, and a failure rate of 6%. He found also that few studies(11-13)had reported both subjective and objective outcomes and both of them were similar. Although the results of TVT and colposuspension are comparable, however, the apparent advantage in the short term is obvious, being, short operative time, local anesthesia, and short hospital stay. In this study, nine cases (20.4%) were discharged home 24 hours after surgery, another nine cases (20.4%) went home 48 hours after surgery and 42 (95.4%) cases could void freely after removal of the catheter the day after the procedure.

In 2001 Wang and Chen(14) in their study showed that subjective and objective cure rates were not significantly different when TVT was done under local or regional anesthesia but women in the epidural group had a significantly greater incidence of urinary obstruction (time to spontaneous voiding, and post-voiding residual). This may explain why, in this study, Foley’s catheter was kept in place for the first 24 hours after the procedure.

Although the TVT procedure was originally designed to treat women with GSI, Rezapoura and Ulmesten(15) proposed that TVT surgery could be also used to resolve female mixed urinary incontinence without affecting the success rate. In this study; ten cases (22.7%) had an urge component to their stress incontinence and nine of them (90%) became free of both symptoms after surgery. Other studies(9,11,12,16,17,18), showed improvement in 43-75 % of cases. However, in this study, do novo urgency was present in two patients (4.5%) which is consistent with previously published reports of 0-5.9 %(11,17,19).

In this study, three cases (6.9%) had urinary retention as defined by residual urine >100 ml 24 hours after the procedure. This is similar to rates in other studies (2.3-10%)(6,11,16,17,20,21).

In this study, retention of urine started on day two (two cases), and day four (one case), after surgery, while in other studies, retention of urine started on day one or day two after the procedure, also the incidence in one study reached 20%(22). The difference in the rate of urinary retention might be due to the difference in the definition of urine retention used by different studies No patient in this study required prolonged catheterization or tape release which was reported by one study(22) that recommended tape release under local anesthesia in case of retention for 48–72 hours after surgery which allows easy mobilization of the tape before it becomes fixed in place, leaving 3–5 mm between the tape and the ventral aspect of the urethra.

At follow up complaints related to voiding difficulty were made by two patients (4.5%) but these were not sufficiently severe to necessitate specific treatment.

In other studies(4,5,6,9,23,24)voiding problems of short duration were reported in 3-10% of patients and were self-limiting.

During surgery there was one case (2.5%) of uncomplicated bladder injury, which was consistent with other reports (0–6%) (15,16,20) . Two cases had UTI in the first three months after surgery, and responded to treatment with oral antibiotics. This was noted also in other studies (22) but its significance was unclear.

Late complications (> three months after surgery) included voiding disorders in two patients (4.5%) and genital prolapse in one patient although its significance was unproven. Finally; one woman had dyspareunea and part of the tape could be felt on physical examination and was removed under regional anesthesia. The patient was followed for 12 months, remained continent, and the tape could no longer be felt. In one study(22) two cases of tape erosion through the vagina were recoded after 12 months; part of the tape was excised under local anesthesia and the patients remained continent.


Conclusion:

The present study was the first to be done in Qatar and reflects the clinical experience with TVT procedure in the Women’s Hospital .Most of the complications were few and could be managed conservatively with a success rate comparable with other studies; TVT procedures remain an effective minimally invasive and safe technique for treating female SUI.

Answer the question, Did they have uorodynamics or not ? and if not ,Why did they not have it ?


Comments:

The answer is, according to the data collected from the patients files, Uorodynamic study only done for ten cases out of 44 patients (22.7%). Other 7 patients refused the investigation and two did not complete it.

The Uorodynamic study showed GSI in all seven patients and in three of them showed mixed urinary incontinence

Owing to that study being a retrospective one we have no comment why Uorodynamic is not tried for other patients. However, the complain of stress incontinence was very clear preoperatively and the relief of symptoms after the procedure was objectively dependant on the patient satisfaction.


References:

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ORIGINAL STUDY