Why the study?
It is uncertain whether the ischemic benefits of more intensive antiplatelet therapy outweigh major bleeding risks in myocardial infarction patients with high bleeding risk.
Does ticagrelor improve net adverse clinical events compared to clopidogrel in myocardial infarction patients with high bleeding risk?
Does ticagrelor improve net adverse clinical events compared to clopidogrel in myocardial infarction patients with high bleeding risk?
In MI patients with high bleeding risk, ticagrelor reduces ischemic events but increases bleeding compared to clopidogrel, resulting in no difference in net adverse clinical events.
Ticagrelor may lower ischemic events at cost of more bleeding without NACE benefit in high-bleeding-risk MI; leaves open whether it improves net outcomes versus clopidogrel.
AIMS: Ticagrelor is associated with a lower risk of ischemic events than clopidogrel. However, it is uncertain whether the benefits of more intensive anti-ischemic therapy outweigh the risks of major bleeding in patients who have a high bleeding risk (HBR). Therefore, this study compared ticagrelor and clopidogrel in myocardial infarction (MI) patients with HBR. METHODS AND RESULTS: This study included all patients enrolled in the SWEDEHEART registry who were discharged with dual antiplatelet therapy using ticagrelor or clopidogrel following MI between 2010 and 2017. High bleeding risk was defined as a PRECISE-DAPT score ≥25. Information on ischemic events, major bleeding, and mortality was obtained from national registries, with 365 days of follow-up. Additional outcomes include major adverse cardiovascular events (MACE), a composite of MI, stroke and all-cause mortality, and net adverse clinical events (NACE), a composite of MACE and bleeding. This study included 25 042 HBR patients, of whom 11 848 were treated with ticagrelor. Ticagrelor was associated with a lower risk of MI, stroke, and MACE, but a higher risk of bleeding compared to clopidogrel. There were no significant differences in mortality and NACE. Additionally, when examining the relationship between antiplatelet therapy and bleeding risk in 69 040 MI patients, we found no statistically significant interactions between the PRECISE-DAPT score and treatment effect. CONCLUSIONS: We observed no difference in NACE when comparing ticagrelor and clopidogrel in HBR patients. Moreover, we found no statistically significant interactions between bleeding risk and the comparative effectiveness of clopidogrel and ticagrelor in a larger population of MI patients.
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Tjerkaski et al. (2023) studied this question.
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