Background: In the treatment of Acute Coronary Syndrome (ACS), Prasugrel is recommended, alongside aspirin, for adult patients undergoing percutaneous coronary intervention (PCI) to prevent thrombotic events. Objective: This study aims to conduct a systematic review of the efficacy and safety of Prasugrel in ACS. Method: A systematic review method was used to search for studies meeting the inclusion criteria for analysis. Results: A total of 17 studies on safety and 10 studies on efficacy were included in the review. The compiled research findings also indicate that Prasugrel is relatively safe, with follow-up durations in studies typically ranging from 12 months, with the shortest being 30 days and the longest 10 years. Prasugrel has good safety, with life-threatening bleeding ranging from 0.1% to 2.2% and intracranial hemorrhage from 0.16% to 0.3%. There is no statistically significant difference in bleeding risk being found when compared Prasugrel with Ticagrelor. In terms of efficacy, Prasugrel helps reduce major adverse cardiovascular events (MACE) from 1% to 11.1%, and cardiovascular mortality from 0.6% to 3%. Conclusion: The evidence suggests that Prasugrel reduces the risks of cardiovascular events and shows its clinical benefits when compared with other P2Y12 receptor inhibitors.
SYTEMATIC REVIEW OF THE SAFETY AND EFFICACY OF PRASUGREL IN PATIENTS WITH ACUTE CORONARY SYNDROME
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Keywords
Prasugrel; Safety; Efficacy; Acute Coronary Syndrome (ACS)
Abstract
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