Transvaginal repair of stage III-IV cystocele using a lightweight mesh: safety and 36-month outcome

被引:24
作者
de Tayrac, Renaud [1 ,7 ]
Brouziyne, Majid [2 ]
Priou, Gerard [3 ]
Devoldere, Guy [4 ]
Marie, Gerard [5 ]
Renaudie, Joel [6 ]
机构
[1] Caremeau Univ Hosp, Dept Obstet Gynecol, Nimes, France
[2] Sport Natl Ctr MY Rachid, Rabat, Morocco
[3] St Gregoire Private Hosp, Dept Obstet Gynecol, St Gregoire, France
[4] St Isabelle Private Hosp, Dept Obstet Gynecol, Abbeville, France
[5] Cotentin Private Hosp, Dept Obstet Gynecol, Equeurdreville Hainneville, France
[6] Colombier Private Hosp, Dept Obstet Gynecol, Limoges, France
[7] CHU Caremeau, Serv Gynecol Obstet, F-30029 Nimes 9, France
关键词
Genital prolapse; Vaginal surgery; Polypropylene mesh; Lightweight mesh; Surgimesh; PELVIC ORGAN PROLAPSE; POLYPROPYLENE MESH; GENITAL PROLAPSE; HERNIA REPAIR; VAGINAL ROUTE; SURGERY; COMPLICATIONS; IMPLANTATION; STIFFNESS; WOMEN;
D O I
10.1007/s00192-015-2659-z
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Introduction and hypothesis The aim of this study was to assess the 36-month safety and efficacy of a lightweight polypropylene mesh used for the transvaginal repair of stage III-IV cystocele. Methods A multicenter prospective cohort study was performed. Preoperative assessment included an interview and evaluation with the Pelvic Organ Prolapse Quantification (POP-Q) system. Inclusion criteria were stage III-IV cystocele and no contraindications for mesh use. A lightweight (28 g/m(2)) four-arm transobturator polypropylene mesh was used for the study. Pre- and postoperative symptoms and quality of life were assessed using the Urinary Symptoms Measurement (MHU), Pelvic Floor Distress Inventory (PFDI-20), Pelvic Floor Impact Questionnaire (PFIQ-7), and Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-12). The main endpoint was mesh safety. Secondary endpoints were anatomic (Ba point <=-1) and functional success. Results In all, 111 patients with a mean age of 67 +/- 9 years (range 47-89) were included in the study, and 94 (84.7 %) were included in the analysis. Two intraoperative complications occurred (one bladder and one rectal injury, 2.2 %). Medium-term analysis of 79 patients (84 %) after 36 months showed a satisfaction rate of 98.7 % (78/79), a mesh contraction rate of 5.1 % (4/78), only one case of vaginal mesh exposure (1.3 %), no cases of chronic pelvic pain, and a postoperative dyspareunia rate of 2.8%(1/36). The anatomic success rate of cystocele repair was 75/79 (94.9 %) and a highly significant improvement was noted for symptoms and on quality of life questionnaires. Overall, 7/79 patients (8.9 %) were reoperated, including 1 for hemorrhage, 1 for vaginal mesh exposure, 3 for stress urinary incontinence, and 2 for cystocele recurrence (2.5 %). Conclusion Transvaginal cystocele repair using a lightweight transobturator polypropylene mesh was safe and efficient in the medium term. Long-term data and comparative studies are needed.
引用
收藏
页码:1147 / 1154
页数:8
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