Multicriteria benefit-risk assessment using network meta-analysis

Gert van Valkenhoef*, Tommi Tervonen, Jing Zhao, Bert de Brock, Hans L. Hillege, Douwe Postmus

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

56 Citations (Scopus)

Abstract

Objective: To enable multicriteria benefit risk (BR) assessment of any number of alternative treatments using all available evidence from a network of clinical trials.

Study Design and Setting: We design a general method for multicriteria decision aiding with criteria measurements from Mixed Treatment Comparison (MTC) analyses. To evaluate the method, we apply it to BR assessment of four second-generation antidepressants and placebo in the setting of a published peer-reviewed systematic review.

Results: The analysis without preference information shows that placebo is supported by a wide range of possible preferences. Preference information provided by a clinical expert showed that although treatment with antidepressants is warranted for severely depressed patients, for mildly depressed patients placebo is likely to be the best option. It is difficult to choose between the four antidepressants, and the results of the model indicate a high degree of uncertainty.

Conclusions: The designed method enables quantitative BR analysis of alternative treatments using all available evidence from a network of clinical trials. The preference-free analysis can be useful in presenting the results of an MTC considering multiple outcomes. (C) 2012 Elsevier Inc. All rights reserved.

Original languageEnglish
Pages (from-to)394-403
Number of pages10
JournalJournal of Clinical Epidemiology
Volume65
Issue number4
DOIs
Publication statusPublished - Apr-2012

Keywords

  • Benefit-risk analysis
  • Multi-criteria decision aiding
  • Stochastic multi-criteria acceptability analysis
  • Network meta-analysis
  • Mixed treatment comparison
  • Second-generation antidepressants
  • MIXED TREATMENT COMPARISONS
  • ACCEPTABILITY ANALYSIS
  • ANTIDEPRESSANTS
  • EFFICACY

Cite this