Comprehensive evaluation of half dose ticagrelor in the treatment of ACS patients after PCI

Corresponding author: yaojiaqi, 1083518819@qq.com

DOI: 10.12201/bmr.202407.00070

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  Abstract: Objective Asian patients with acute coronary syndrome (ACS) are often susceptible to the influence of standard doses of ticagrelor, thereby increasing the risk of bleeding events. Therefore, it is crucial to retrospectively analyze whether half dose ticagrelor can provide better safety and similar therapeutic effects. Methods Collect clinical data of ACS patients who successfully underwent percutaneous coronary intervention (PCI) at the First Affiliated Hospital of Ningbo University from January 2017 to November 2019. According to the dosage of ticagrelor used, they were divided into a standard dose ticagrelor group (90mg, 56 cases) and a half dose ticagrelor group (45mg, 52 cases). Comparing the clinical outcomes of two medication regimens, a landmark analysis was conducted on clinical events during different follow-up periods, with the safety endpoint defined as bleeding related complications after PCI in patients. The efficacy endpoint is major adverse cardiovascular and cerebrovascular events (MACCE). Results During the entire follow-up period, according to the bleeding academic research consortium (BARC) standards, the cumulative incidence of type 1, 2, or 3 bleeding in the half dose ticagrelor group was lower than that in the standard dose group (P<0.05), especially after more than 1 year (P<0.05). There was no significant difference in the incidence of MACCE between different doses of ticagrelor (P>0.05). Conclusion Half dose ticagrelor can reduce the risk of type 1, 2, or 3 bleeding and its efficacy in MACCE is not inferior to standard dose treatment. Therefore, providing better evidence for the use of half dose ticagrelor between long-term bleeding and ischemia after PCI in ACS patients in the southern population.

  Key words: coronary heart disease ；ticagrelor ；bleeding complications；adverse event

  Submit time: 31 July 2024

  Copyright: The copyright holder for this preprint is the author/funder, who has granted biomedRxiv a license to display the preprint in perpetuity.
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