TVT versus TOT, 2-year prospective randomized study
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Abstract
Purpose
To evaluate in a comprehensive way TVT in comparison with TOT, the results of a single-center RCT are presented. Many studies addressed efficacy and safety of TVT and TOT.
Methods
Women included were adults having predominant SUI with positive stress test. They were randomized to get either TVT (Gynecare®) or TOT (Aris®). All women were seen 1 week, 3, 6, 12, 18, and 24 months.
Results
Seventy-one women completed 2-year follow-up. Median age was 47 (range 33–60 years). Mean ± SD BMI in TVT group was 34 ± 5 while in TOT group was 32 ± 5 kg/m2. POP of any degree was seen in 50 % (35 women). At 1 year, pad test–negative women were 31 and 29 for TVT and TOT, respectively. At 2 years, figures became 28 in TVT group and 27 in TOT. At 1 year, UDI 6 and IIQ 7 decreased by 78.5 and 81 % for TVT and by 69 % and 75 % for TOT group. At 2 year, comparable percentages were 73 and 79 % for TVT and 69 and 82 % for TOT. Fifteen unique patients had adverse events, 10 of them had TOT.
Conclusions
Both tapes have similar efficacy, regarding cure of incontinence. TVT is more effective, albeit insignificantly, than TOT at 2 years. However, serious adverse events were more frequent with TVT, yet TOT has more unique adverse events.
Keywords
Outcome RCT TVT TOTAbbreviations
- ICIQ-SF
International Consultation on Incontinence Questionnaire ShortForm
- IIQ 7
Incontinence impact questionnaire 7 (Short form)
- KHQ
King’s Health questionnaire
- MUS
Midurethral sling
- P det Q max
Detrusor pressure at maximum flow
- POP
Pelvic organ prolapse
- PVR
Postvoid residual urine
- PVS
Pubovaginal sling
- PGI-I
Patient global impression of improvement of incontinence
- Q max
Maximum flow rate
- RCT
Randomized controlled trial
- SUI
Stress urinary incontinence
- TVT
Tension-free vaginal tape
- TOT
Transobturator tape
- UDI 6
Urogenital distress inventory 6 (Short form)
Notes
Conflict of interest
None.
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