What is the role of combination drug therapy in the treatment of overactive bladder? ICI-RS 2014.

Published

Journal Article (Review)

The role of combination therapy using oral antimuscarinic medications for the treatment of overactive bladder was proposed at the 2014 International Consultation on Incontinence-Research Society in Bristol, UK to identify key factors to consider when making clinical decisions and to guide future research design.Combination therapy is justified if monotherapy is associated with suboptimal efficacy or bothersome side effects. Combination therapy has the potential to improve efficacy with fewer side effects than monotherapy. Two Phase 2 studies comparing combination therapy that included an antimuscarinic demonstrated improvement in mean voided volume, the primary outcome chosen, with some combinations showing improved micturition frequency and quality of life. The two studies found no evidence of an increased safety risk with combination therapy compared to monotherapy. Future studies should use clinically meaningful or patient reported outcomes such as incontinence episodes when comparing efficacy. If surrogate measures are used, a clear justification should be provided. Cost analyses should be planned for clinical research trials evaluating combination drug therapy.Combination therapy is reasonable when monotherapy has suboptimal efficacy or bothersome side effects. Future research studies evaluating combination therapy for urgency urinary incontinence should ideally(1) be performed as part of a randomized clinical trial,(2) evaluate non-responders to monotherapy,(3) evaluate combination therapy using medications with different mechanisms of action,(4) include clinically meaningful and patient reported outcomes when evaluating efficacy, and(5) include cost-effectiveness analyses to justify any increased cost by showing improvement in efficacy or reduction in side effects.

Full Text

Duke Authors

Cited Authors

  • Visco, AG; Fraser, MO; Newgreen, D; Oelke, M; Cardozo, L

Published Date

  • February 2016

Published In

Volume / Issue

  • 35 / 2

Start / End Page

  • 288 - 292

PubMed ID

  • 26872569

Pubmed Central ID

  • 26872569

Electronic International Standard Serial Number (EISSN)

  • 1520-6777

International Standard Serial Number (ISSN)

  • 0733-2467

Digital Object Identifier (DOI)

  • 10.1002/nau.22795

Language

  • eng