Posterior vaginal meshes and dyspareunia

López C1, Pérez M1, Al-Dali D1, Fernández M1, Pereda A1, Ojeda F1

Research Type


Abstract Category

Pelvic Organ Prolapse

Abstract 818
Non Discussion Abstract
Scientific Non Discussion Abstract Session 37
Grafts: Synthetic Pelvic Organ Prolapse Retrospective Study Sexual Dysfunction
1.Hospital General de Granollers


Hypothesis / aims of study
Pelvic organ prolapse (POP) is a common condition in women with history of vaginal delivery, its prevalence varies depending on the studies, reaching 50-60% in some of them. Prolapse of the posterior compartment is not the most common, but it is usually associated with obstructive defecation, vaginal bulging symptoms and sexual dysfunction (1). The objective of surgical treatment is to restore the anatomy and intestinal and sexual functionality. There are two approaches, vaginal or abdominal, with the classical technique, use of graft or prosthesis.  Traditionally, the posterior compartment prolapse has been corrected by posterior colporrhaphy, in some cases associated with the plication of the levator ani muscles, but this technique has been abandoned due to its relation with postoperative pain and dyspareunia (2). After that, posterior vaginal meshes began to be used, but their use has recently been questioned because of a suspected association with high rates of dyspareunia (3).
However, there are few studies on the effect of prosthetic defect repair on the sexual function of patients.
The aim of this study is to retrospectively analyse the effect of posterior meshes on sexual function in patients who underwent surgery in our centre in the late years.
Study design, materials and methods
Different types of polypropylene posterior meshes have been used over the years in our centre: MIPS, Surelift, Elevate and Prolift. The surgical technique used for its placement is based on a tension-free system with an anterior anchorage to the obturator muscle and a posterior anchorage to the sacrospinous ligament, in some cases there is a third middle anchorage to the tendinous arch.
A retrospective observational case-control study was conducted in which 131 women were included. The "case" group consisted of 25 women who had undergone second or third degree rectocele surgery with the placement of a posterior mesh between January 2007 and December 2017 in our centre. The "control" group included 106 women who correlatively were attended in the pelvic floor consulting room because of different pathologies between January and March 2014, who had not undergone surgery and that filled the EPIQ questionnaire. Within this group, 13 patients who consulted for rectocele were identified and whose data was used for a more specific subanalysis of the posterior compartment pathology becoming a “rectocele control” group. The patients in the study group were contacted by telephone between 1 and 9 years after the surgery and were asked if they had sexual intercourse and if they presented dyspareunia.
The percentage of women who had sexual relations in the "case" and the "control" group was compared. Later, in those women who had coitus, the percentage of women who reported dyspareunia was compared. The data was analysed using the Chi-squared test and the Fisher’s exact test, considering the statistical significance a p-value <0.05.
The average age of the women included in the "case" group, women with a vaginal mesh, was 59.6 years and 57.9 years in the "control" group, not being the difference statistically significant (p-value 0,537).
Seventy-two percent of the women with a posterior mesh had sexual intercourse. On the other hand, in the “control” group 57.5% maintained relations. This difference was not statistically significant evaluated by the Chi-squared test (p-value 0,184).
Analyzing the results of pain in sexual relations, it was observed that 22.22% of the women with a vaginal prosthesis had dyspareunia. In the "control" group, 40.0% of the women presented pain with sexual intercourse. No statistical significance was found by the Fisher's exact test (p-value 0,174).
A subanalysis was carried out, comparing the "case" group with the women of the "rectocele control" group who only had rectocele and had not undergone surgery. The mean age in the "rectocele" group was 59.7 years, being the difference with the 59.6 years of the "case" group not statistically significant (p-value 0,989). In the "rectocele" group, 53.8% had sexual relations, compared with 72% of the women with a posterior mesh, the differences were not significant (p-value 0,263). A 71.4% of women with not operated rectocele presented dyspareunia and only 22.22% of women with posterior mesh presented it, the differences were not statistically significant (p-value 0,058).
Interpretation of results
Rectocele correction with the placement of a vaginal prosthesis stopped because some studies related it to an increase of complications such as dyspareunia.
Our results have not shown a decrease in the sexual activity or an increase in dyspareunia in patients undergoing surgery, when compared to patients with pelvic floor pathology in general and to patients with rectocele for which they consult the specialist who had not undergone surgery. On the contrary, it seems that patients with not corrected rectocele have a higher prevalence of dyspareunia, though it has not been demonstrated.
One limitation of our study is the heterogeneity of the meshes studied secondary to the extension in time of the study due to the scarce need of this surgical technique. On the other hand, we do not have data on the sexual function of the patients prior to the placement of the posterior mesh. It would be interesting to consider the realization of a prospective study including the previous assessment of the sexual function of the patients, taking into account the relevant ethical limitations.
It would be necessary to carry out a study with more statistical power to corroborate the results.
Concluding message
In this study we have observed that in women who underwent rectocele correction at our centre through the placement of a posterior mesh, sexual activity is maintained with less pain in the sexual intercourse.
Figure 1 Mesh vs control
Figure 2 Mesh vs rectocele
  1. Mowat A, Maher D, Baessler K, Christmann-Schmid C, Haya N, Maher C. Surgery for women with posterior compartment prolapse. Cochrane Database of Systematic Reviews 2018, Issue 3. Art. No.: CD012975.
  2. Biagio Adile, Elizabetta Constantini, Sebastiano Bandiera. Uroginecología, Editora CAU, Caracas, 2006. 30:177-184
  3. Urogynecologic Surgical Mesh: Update on the Safety and Effectiveness of Transvaginal Placement for Pelvic Organ Prolapse. FDA. 2011
Funding None Clinical Trial No Subjects Human Ethics not Req'd is a retrospective observational study Helsinki Yes Informed Consent Yes