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1.
Int. braz. j. urol ; 42(3): 494-500, tab, graf
Article in English | LILACS | ID: lil-785716

ABSTRACT

ABSTRACT Purpose to assess the efficacy of transcorporal artificial urinary sphincter (AUS) implantation on continence for male stress urinary incontinence in cases of prior surgical treatment or/and radiation failure, and as a first option in radiation patients. Materials and Methods From March 2007 to August 2012, 37 male patients were treated with transcorporal AUS AMS™ 800. Twelve patients had primary placement of transcorporal cuff, a surgical option due to a previous history of radiation and 25 patients had secondary procedure after failure of AUS or urinary incontinence surgery. Functional urinary outcomes were assessed by daily pad use, 24-hour Pad-test and ICIQ-SF questionnaire. Quality of life and satisfaction were assessed based on I-QoL and PGI-I questionnaires. Results After a median of 32 months, the continence rate (0 to 1 pad) was 69.7%. Median pad test was 17.5g (0-159), mean ICIQ-SF score was 7.3/21 (±5.4) and mean I-QoL score was 93.9/110. A total of 88% of the patients reported satisfaction with the AUS. The 5-year actuarial revision-free for AUS total device was 51%. Patients for primary implant for radiation were not more likely to experience revision than non-radiation patients. Preservation of erections was reported in half of the potent patients. Conclusions Transcorporal AUS cuff placement is a useful alternative procedure option for severe male UI treatment, especially in patients with a compromised urethra after prior surgery or radiation. A high continence rate was reported and implantation as first option in radiation patients should be considered.


Subject(s)
Humans , Male , Aged , Urethra/surgery , Urethra/radiation effects , Urinary Incontinence, Stress/surgery , Urinary Sphincter, Artificial , Postoperative Complications , Prostatectomy/adverse effects , Quality of Life , Time Factors , Urinary Incontinence, Stress/etiology , Urinary Incontinence, Stress/radiotherapy , Penile Erection , Surveys and Questionnaires , Reproducibility of Results , Retrospective Studies , Follow-Up Studies , Treatment Outcome , Statistics, Nonparametric , Disease-Free Survival , Kaplan-Meier Estimate , Middle Aged
2.
Int. braz. j. urol ; 40(6): 828-834, Nov-Dec/2014. tab, graf
Article in English | LILACS | ID: lil-735986

ABSTRACT

Introduction and Hypothesis To our knowledge a study regarding the efficacy of Pelvisoft® Biomesh for cystocele repair has not previously been reported in the literature. The aim of our study was to assess the long-term efficacy, subjective outcomes and complications in the use of a non-synthetic porcine skin mesh graft (Pelvisoft® Biomesh) associated with transvaginal anterior colporrhaphy in the treatment of cystocele prolapse. Materials and Methods A retrospective study was performed at a single centre. Thirty-three women aged 35-77 years underwent cystocele repair using Pelvisoft® graft between December 2005 and June 2009. Twenty-nine women who underwent transvaginal cystocele repair with Pelvisoft® Biomesh for over a 2 years period were assessed. Four patients were lost to follow-up. Cystocele repair was performed via the vaginal route using Pelvisoft®Biomesh implant by inserting it in the anterior vaginal wall. The median follow-up time was 54.0 months. The rate of recurrence was 17.3%. A total of 6.9% of patients presented early mesh exposure treated by conservative treatment. The mean PFDI-20 score was 72.2. Among sexually active women, the mean PISQ 12 was 33.9 but 56.2% had dyspareunia. After surgery, 6 patients had de novo intercourse. Our results show that the use of Pelvisoft® biomaterial associated with anterior colporrhaphy for cystocele repair appears to be safe with acceptable failure and complication rates at long term. Nevertheless, an adverse impact on sexual function was reported by the majority of patients. .


Subject(s)
Adult , Aged , Animals , Female , Humans , Middle Aged , Biocompatible Materials/therapeutic use , Cystocele/surgery , Surgical Mesh , Vagina/surgery , Biocompatible Materials/adverse effects , Medical Illustration , Postoperative Period , Recurrence , Retrospective Studies , Statistics, Nonparametric , Swine , Surgical Mesh/adverse effects , Treatment Outcome , Urinary Incontinence, Stress/surgery
3.
Int. braz. j. urol ; 35(6): 706-715, Nov.-Dec. 2009. ilus
Article in English | LILACS | ID: lil-536803

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 percent CI: 2 - 3) to 1 during the follow-up period (95 percent CI: 0 - 2 at 360 days), and at 3 months patients using none or one pad per day were 30 percent and 32 percent respectively. The SF 36 continence and quality of life score improved from a median of 100 (95 percent CI: 83 - 133) to 300 (95 percent CI: 167 - 375), and the median ICIQ incontinence and quality of life score decreased from 15 (95 percent CI: 14 - 16) to 8 (95 percent 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.


Subject(s)
Aged , Humans , Male , Middle Aged , Prostatectomy/adverse effects , Suburethral Slings , Urinary Incontinence, Stress/surgery , Follow-Up Studies , Prospective Studies , Treatment Outcome , Urinary Incontinence, Stress/etiology
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