University of Leicester
Browse

Number needed to treat in cardiovascular outcome trials with glucagon-like peptide-1 receptor agonists: A systematic review with temporal analysis

journal contribution
posted on 2020-04-21, 10:29 authored by Melanie Davies, D Kloecker, D Webb, K Khunti, F Zaccardi
<p>Cardiovascular outcome trials (CVOTs) investigating the safety and efficacy of glucagon-like peptide-1 receptor agonists (GLP-1RAs) have highlighted some important differences among these medications. The recent American Diabetes Association and European Association for the Study of Diabetes consensus underlines that each trial constitutes a single experiment; therefore, it remains unclear if, and to what extent, the observed differences reflect the heterogeneous pharmacological properties of each compound. To help clarify the evidence, in this systematic review we investigated differences in trial characteristics which may have had an impact on the primary and secondary trial results, including baseline control of risk factors, prevalence of cardiovascular diseases, absolute rates of events, duration of the study, and definitions of the inclusion criteria and outcomes. Aiming at enhancing the clinical interpretation of these CVOTs, we quantified the absolute treatment effect over time in terms of the number needed to treat to avoid one major adverse cardiovascular event, showing variations among GLP-1RAs.</p>

Funding

MJD, DRW, KK, FZ acknowledge the National Institute for Health Research Applied Research Collaborations – East Midlands (NIHR ARC - EM) and the NIHR Leicester Biomedical Research Centre.

History

Citation

Diabetes, Obesity and Metabolism (2020) In Press

Version

  • AM (Accepted Manuscript)

Published in

Diabetes, Obesity and Metabolism: a journal of pharmacology and therapeutics

Publisher

Wiley

issn

1462-8902

Acceptance date

2020-04-17

Copyright date

2020

Language

en

Publisher version

TBA

Usage metrics

    University of Leicester Publications

    Categories

    No categories selected

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC