We identified 48 patients who underwent MUS revision, of which 8 underwent a TVSI, 27 underwent TVSE, and 13 underwent a CSE. The type of MUS procedure was Retropubic sling (TVT, n=26), Transobturator Sling (TOT/TVT-O, n=19), a Mini sling (n=2) and unknown (n=1). The index MUS surgery was done in another center for 92% patients (44/48). Among the 48 patients, the mean age was 55 years. Of these, 62.5% were menopausal, 50% had a previous hysterectomy and 40% were current/ever smokers. Twelve women (25%) had a previous mesh revision surgery before referral. The median time from mesh placement to removal was 72 [36-116] months for all subjects, 80.5 [38-128] months TVSI group, 79 [33-123] months for the TVSE and 49 [39-95] months for the CSE.
The most common preoperative symptoms were Urge Urinary Incontinence (UUI, 69%), voiding dysfunction (60%), recurrent SUI (60%), pain (56%), mixed incontinence (MI) (48%), mesh exposure (46%) and recurrent urinary tract infection (UTI, 31%). For the TVSI, the most common symptoms were voiding dysfunction (100%), UUI (63%), and recurrent UTIs (38%). For the TVSE group the most common symptoms were incontinence (SUI 74%, UUI 70%, MI 59%), mesh exposure (63%) and pain (56%). The most common symptoms in the CSE group were pain (92%), UUI (69%), and voiding dysfunction (62%). The mean number of pads used at the time of referral for the group overall was 3.0 (TVSI group 1.6, TVSE group 3.3 and CSE group 3.0).
Nine women had concurrent anti-incontinence surgery at the time of mesh revision; of those 7 were fascial pubovaginal slings and 2 were Burch Urethropexy. Seven women had fascial pubovaginal slings at a later date. Intraoperatively, 39.5% of subjects needed a transurethral incision to remove the mesh due to erosion, and 4% needed a transvaginal bladder incision.
After the MUS revision was done, 23 out of the 48 subjects continued to have SUI and 13% developed new SUI. In the TVSI group 50% reported SUI, in the TVSE 52% reported SUI, and in the CSE group 38% reported SUI. UUI decreased from 69% to 50% overall, and in each of the individual groups (to 50% in the TVSI group, 56% in the TVSE and 38% in the CSE group). The mean change in pad use among all subjects was -1.5. Among the TVSI group the mean change in pad use was -1.5; both the TVSE and CSE groups had a mean change in pad use of -1.4.
Self-reported pain decreased from 56% to 26%. In the TVSE group, the rate of pain decreased from 56% to 22% and in the CSE group it decreased from 92% to 46%. Pain resolved in 31% of the total subjects (specifically in 37% of the TVSE group and 38% of the CSE group). Narcotic use decreased from 10% to 6% in the overall group.
The UDI-6 score was completed by 37/48 patients (77%). The median time from sling revision to completion of UDI-6 questionnaire was 33 [14-61] months overall, (23.5 [8–37.5] months in the TVSI group, 39 [15–70] months in the TVSE group and 29 [13.5–48.5]months in the CSE group). The median total UDI-6 score for all the patients was 44 [IQR 28.0–56.0]. (details in table 1).