13.68%) experienced dramatic symptom improvement (≥75% reduction in urinary incontinence (UI) episodes, OR 4.40, 95% CI (2.64, 7.33); p < 0.00001; Figure 2 A) with BoNT-A, while more modest reductions (≥50%) in UI episodes did not reach statistical significance compared to placebo (55.84% vs. 33.42%; OR 2.37, 95% CI (0.82, 6.87); p = 0.11; Figure 3 A).
← all excerpts
Comparison of Different Treatment Outcomes for Refractory Overactive Bladder: A Systematic Review and Meta-Analysis.
1
0.1100
0.1100