| Literature DB >> 29992264 |
Marco Valgimigli1, Hector M Garcia-Garcia2, Bernard Vrijens3, Pascal Vranckx4,5, Eugène P McFadden6, Francesco Costa1,7, Karen Pieper8, David M Vock9, Min Zhang10, Gerrit-Anne Van Es11, Pierluigi Tricoci8, Usman Baber12, Gabriel Steg13, Gilles Montalescot14, Dominick J Angiolillo15, Patrick W Serruys16, Andrew Farb17, Stephan Windecker1, Adnan Kastrati18, Antonio Colombo19,20, Fausto Feres21, Peter Jüni22, Gregg W Stone23, Deepak L Bhatt24, Roxana Mehran12, Jan G P Tijssen11,25.
Abstract
Non-adherence has been well recognized for years to be a common issue that significantly impacts clinical outcomes and health care costs. Medication adherence is remarkably low even in the controlled environment of clinical trials where it has potentially complex major implications. Collection of non-adherence data diverge markedly among cardiovascular randomized trials and, even where collected, is rarely incorporated in the statistical analysis to test the consistency of the primary endpoint(s). The imprecision introduced by the inconsistent assessment of non-adherence in clinical trials might confound the estimate of the calculated efficacy of the study drug. Hence, clinical trials may not accurately answer the scientific question posed by regulators, who seek an accurate estimate of the true efficacy and safety of treatment, or the question posed by payers, who want a reliable estimate of the effectiveness of treatment in the marketplace after approval. The Non-adherence Academic Research Consortium is a collaboration among leading academic research organizations, representatives from the U.S. Food and Drug Administration and physician-scientists from the USA and Europe. One in-person meeting was held in Madrid, Spain, culminating in a document describing consensus recommendations for reporting, collecting, and analysing adherence endpoints across clinical trials. The adoption of these recommendations will afford robustness and consistency in the comparative safety and effectiveness evaluation of investigational drugs from early development to post-marketing approval studies. These principles may be useful for regulatory assessment, as well as for monitoring local and regional outcomes to guide quality improvement initiatives. Published on behalf of the European Society of Cardiology. All rights reserved.Entities:
Keywords: Adherence; Clinical trial; Compliance; Medication; Persistence
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Year: 2019 PMID: 29992264 PMCID: PMC7963139 DOI: 10.1093/eurheartj/ehy377
Source DB: PubMed Journal: Eur Heart J ISSN: 0195-668X Impact factor: 29.983