Identifying Outcome Measures for Coronary Artery Disease Value-Based Contracting Using the Delphi Method.
Antiplatelets
Coronary artery disease (CAD)
Delphi method
Drug costs
Outcome measures
Pharmaceuticals
Value-based contracting (VBC)
Journal
Cardiology and therapy
ISSN: 2193-8261
Titre abrégé: Cardiol Ther
Pays: England
ID NLM: 101634495
Informations de publication
Date de publication:
Jun 2019
Jun 2019
Historique:
received:
29
11
2018
pubmed:
3
3
2019
medline:
3
3
2019
entrez:
3
3
2019
Statut:
ppublish
Résumé
Value-based contracts (VBCs) that link drug payments to disease-related performance metrics aim to increase the value and lower the cost of medications by aligning incentives and sharing risk between payers and pharmaceutical manufacturers. This study sought to identify outcome measures that are meaningful to key stakeholders to inform VBCs for coronary artery disease (CAD) medications. We administered a modified Delphi survey to gather expert opinion from a diverse panel of patients (n = 9), cardiologists (n = 4), primary care physicians (n = 5), payers (n = 2), pharmacy benefits managers (n = 3), and pharmaceutical company representatives (n = 2). A list of 16 CAD-associated clinical indicators was generated from the literature and expert consultation. Delphi participants rated the importance of each outcome on a five-point Likert scale, and selected the three most meaningful outcomes. We defined consensus as ≥ 75% agreement on the importance of an outcome (Likert scores 4 or 5 or selection of an outcome as most meaningful). Eleven of 13 outcomes reached consensus for importance on the Likert scale. "Preventing heart attacks" was selected as the most meaningful outcome (80%) while "preventing death" ranked second (76%). Our study results verify the utility of a widely used clinical CAD outcome measure, myocardial infarction events, for the purpose of pharmaceutical value-based contracting.
Identifiants
pubmed: 30825093
doi: 10.1007/s40119-019-0132-7
pii: 10.1007/s40119-019-0132-7
pmc: PMC6525225
doi:
Types de publication
Journal Article
Langues
eng
Pagination
135-143Subventions
Organisme : Express Scripts
ID : N/A
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