An evaluation of transvaginal mesh for advanced stage of pelvic organ prolapse

Chan S1, Cheung R1, Wan O1

Research Type

Clinical

Abstract Category

Pelvic Organ Prolapse

Abstract 623
Open Discussion ePosters
Scientific Open Discussion Session 33
Friday 29th September 2023
12:45 - 12:50 (ePoster Station 3)
Exhibit Hall
Pelvic Organ Prolapse Surgery Female Pelvic Floor
1. The Chinese University of Hong Kong
Presenter
Links

Poster

Abstract

Hypothesis / aims of study
One of the risk factors of recurrence of pelvic organ prolapse after surgical repair is advanced stage of prolapse (stage III or IV). Short-term follow-up analyses suggest that transvaginal mesh has limited application for pelvic organ prolapse (POP) treatment. This study evaluated the intermediate and long-term outcomes of transvaginal mesh surgery.
Study design, materials and methods
This retrospective study included all women who underwent transvaginal mesh surgery in one urogynaecology centre. Inclusion criteria were women with stage III/IV POP, age ≥65 years, and (preferably) sexually inactive. Concomitant sacrospinous fixation and mid-urethral slings were offered for stage III/IV apical POP and urodynamic stress incontinence, respectively. Women were followed up for 5 years. Subjective recurrence was defined as reported prolapse symptoms. Objective recurrence was defined as stage II prolapse or above. Mesh complications and patient satisfaction were reviewed.
Results
Of 218 women who underwent transvaginal mesh surgery, 201 (92.2%) had ≥1 year of follow-up (mean, 55 ± 21 months). Among them, 132 (65.7%) had completed 5 years of follow-up. In all 201 women, the objective and subjective recurrence rates were 9% (n=18) and 5.5% (n=11), respectively. Among those with subjective recurrence, 4 (2%) and 7 (3.5%) had stage III and stage II prolapse, respectively. The median time of recurrence was 24 months. Two (1%) received surgical repair, another two had vaginal pessary and others had mild symptoms and opted for conservative management. Mesh erosion occurred in 17 (8.5%) women; 7 had per vaginal spotting, others were asymptomatic. All of them received vaginal estrogen treatment but 7 (3.5%) of them with persistent mesh erosion received bedside surgical excision under local anaesthesia. 

A total of 16 (8%) women had de novo stress urinary incontinence (SUI) symptoms after the surgery. Four women received transobturator tension-free transvaginal tape for de novo (n=2) or preoperative urodynamic stress incontinence who did not undergo concomitant surgery (n=2). While 25 (12%) women had mild de novo urgency urinary incontinence (UUI) and did not require any medical treatment; 57 (28.4%) women who had UUI symptoms before the surgery reported no UUI after the surgery. No women reported chronic pain. Overall, 41.3% and 56.7% reported ‘satisfied’ or ‘very satisfied’ with the operation.
Interpretation of results
This study showed an intermediate to long term follow-up of transvaginal mesh surgery for women with stage III/IV POP. There were low subjective and objective recurrence rates. The re-operation rate for recurrence of POP, mesh erosion, continence surgery for de novo SUI was 1%, 3.5% and 1%, respectively. Majority of women reported very satisfied with the operation.
Concluding message
With a mean of 55 months follow-up, transvaginal mesh surgery for stage III/IV POP had low subjective and objective recurrence rates. The total re-operation rate was 5.5%. Majority of women were satisfied with the operation. Based on the risk benefit profile, transvaginal mesh surgery may be suitable for women who have advanced stage of POP.
Figure 1 Table 1. Demographic of 201 women who had more than one year of follow-up
Disclosures
Funding NONE Clinical Trial No Subjects Human Ethics Committee Joint Chinese University of Hong Kong - New Territories East Cluster Clinical Research Ethics Committee Helsinki Yes Informed Consent Yes
22/11/2024 16:07:57