Tension–Free Vaginal Mesh Repair for Anterior Vaginal Wall Prolapse
Autor: | Tiziano Verdacchi, Giuliana Madeddu, Michele De Angelis, Roberto Migliari |
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Rok vydání: | 2000 |
Předmět: |
medicine.medical_specialty
Reconstructive surgery Urology medicine.medical_treatment Urinary incontinence Polypropylenes Gynecologic Surgical Procedures Vaginal disease Uterine Prolapse Humans Medicine Anterior vaginal wall prolapse Aged Fixation (histology) business.industry Tension (physics) Middle Aged Surgical Mesh Surgery medicine.anatomical_structure Replantation Vagina Female medicine.symptom business Follow-Up Studies |
Zdroj: | European Urology. 38:151-155 |
ISSN: | 1421-993X 0302-2838 |
DOI: | 10.1159/000020272 |
Popis: | We determined the efficacy of the use of a tension free prolene mesh to correct a grade III anterior vaginal wall prolapse recurrence.Twelve women (mean age 65.6 years) with stress urinary incontinence (SUI) (4 type II and 1 type III) and bladder prolapse entered the study. After vaginal incision a pretailored polypropylene mesh was fixed to its four angles by absorbable sutures to the urethropelvic ligaments and pubocervical fascia anteriorly and to the cardinal ligaments and pubocervical fascia posteriorly. When present, a posterior descensus was corrected during the same procedure. SUI was treated with the tension-free vaginal tape procedure (TVT) through a separate vaginal incision over the mid-urethra.All patients were available for postoperative pelvic examination at 3-month intervals, for a mean follow-up of 20.5 months (range 15-32). Nine patients were considered cured (no cystocele recurrence) while in 3 patients a grade 1 asymptomatic cystocele was present postoperatively (asymptomatic). No significant postoperative pain was reported by the patients.This study confirms that in patients with moderate cystocele a tension-free mesh to support bladder base and neck effectively treats the cystocele. It is particularly recommended in the treatment of previous failure with traditional techniques and when the quality of suspending tissue is poor or defective. A long-term study on a large number of patients is still warranted to confirm and validate its clinical use. |
Databáze: | OpenAIRE |
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