Key result
Cangrelor, vorapaxar, and rivaroxaban show promise for reducing ischemic events in acute myocardial infarction, though they have not been compared with more potent P2Y12 inhibitors.
Why the study?
Advances in understanding the mechanisms of plaque rupture leading to AMI have led to the development of numerous antiplatelet and anticoagulant agents.
Newer antithrombotic agents show promise for treating acute myocardial infarction, but further evaluation is needed to optimize the balance between reducing ischemic events and minimizing bleeding risk.
Hypothesis-generating for these agents in AMI; leaves open need for head-to-head trials versus potent P2Y12 inhibitors.
Background: Advances in our understanding of the complex pathophysiologic mechanisms responsible for high-risk atherosclerotic plaque rupture resulting in acute myocardial infarction (AMI) have led to the development of numerous antiplatelet and anticoagulant agents for treatment of AMI.Areas covered: We review various antithrombotic drugs which were recently investigated for the treatment of AMI. A MEDLINE search for relevant articles on newer antiplatelet agents and anticoagulants drugs for the treatment of AMI was performed, and important original investigations were reviewed. We also briefly discuss agents that completed evaluation and were recently recommended by expert guidelines.Expert opinion: The antiplatelet agents cangrelor and vorapaxar and the anticoagulant rivaroxaban, have shown promise for the reduction of ischemic events when administered during, and in the acute phase following AMI. However, these agents have not been compared with more potent P2Y12 inhibitors, prasugrel, and ticagrelor. Finding an optimum combination of these agents to achieve an appropriate risk (bleeding) – benefit (reduction in ischemic events) balance is challenging. Further evaluation of agents that show promise is important for enhancing our armamentarium of pharmacologic agents for the successful treatment of AMI.Trial registration: ClinicalTrials.gov identifier: NCT01042964.Trial registration: ClinicalTrials.gov identifier: NCT01020383.Trial registration: ClinicalTrials.gov identifier: NCT03312855.Trial registration: ClinicalTrials.gov identifier: NCT02545933.Trial registration: ClinicalTrials.gov identifier: NCT03234114.
No takes yet. Share an insight, caveat, or question.
Yandrapalli et al. (2018) conducted a review in Acute myocardial infarction. Antiplatelet and anticoagulant agents (cangrelor, vorapaxar, rivaroxaban) was evaluated. Cangrelor, vorapaxar, and rivaroxaban show promise for reducing ischemic events in acute myocardial infarction, though they have not been compared with more potent P2Y12 inhibitors.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: