Dual antiplatelet therapy: optimal timing, management, and duration

Eur Heart J Cardiovasc Pharmacother. 2015 Jul;1(3):198-204. doi: 10.1093/ehjcvp/pvv015. Epub 2015 Mar 23.

Abstract

Platelet activation and aggregability play a key role in the genesis of arterial thrombus secondary to plaque rupture. For coronary patients, inhibition of platelet function is crucial to decrease the rate of major adverse cardiac events but may expose them to excess bleeding risk. Switching P2Y12 inhibitors is common, yet the clinical consequences are unknown. The aim of this review is to provide an overview of the evidence from randomized, clinical trials and epidemiological studies, with a focus on the optimal duration of dual antiplatelet therapy (DAPT) and appropriate agent and dose selection. The report discusses the latest evidence regarding switching therapies during DAPT, the potential benefits of a personalized strategy, management of the preoperative period, and other clinical perspectives in this complex and rapidly changing field. Ongoing trials will be useful to answer to some important unresolved questions.

Keywords: Acute coronary syndrome; Dual antiplatelet therapy; Optimal duration; Stents.

Publication types

  • Review

MeSH terms

  • Coronary Artery Disease / surgery*
  • Coronary Thrombosis / drug therapy*
  • Coronary Thrombosis / etiology
  • Drug Therapy, Combination
  • Humans
  • Percutaneous Coronary Intervention / adverse effects*
  • Platelet Aggregation Inhibitors / therapeutic use*
  • Postoperative Complications / drug therapy*
  • Purinergic P2Y Receptor Antagonists / therapeutic use*

Substances

  • Platelet Aggregation Inhibitors
  • Purinergic P2Y Receptor Antagonists