期刊论文详细信息
INTERNATIONAL JOURNAL OF CARDIOLOGY 卷:342
Clopidogrel, prasugrel, and ticagrelor for all-comers with ST-segment elevation myocardial infarction
Article
Jacobsen, Mia Ravn1,2  Engstrom, Thomas1,3  Torp-Pedersen, Christian2,4  Gislason, Gunnar5  Glinge, Charlotte1  Butt, Jawad Haider1  Fosbol, Emil Loldrup1  Holmvang, Lene1  Pedersen, Frants1  Kober, Lars1  Jabbari, Reza1  Sorensen, Rikke1 
[1] Copenhagen Univ Hosp, Rigshosp, Dept Cardiol, Inge Lehmans Vej 7, DK-2100 Copenhagen O, Denmark
[2] Aalborg Univ Hosp, Dept Cardiol, Aalborg, Denmark
[3] Lund Univ, Dept Cardiol, Lund, Sweden
[4] Nordsjaelland Hosp, Dept Clin Res & Cardiol, Hillerod, Denmark
[5] Herlev & Gentofte Univ Hosp, Dept Cardiol, Hellerup, Denmark
关键词: ST-segment elevation myocardial infarction;    Clopidogrel;    Prasugrel;    Ticagrelor;   
DOI  :  10.1016/j.ijcard.2021.07.047
来源: Elsevier
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【 摘 要 】

Background: To compare effectiveness and safety of clopidogrel, prasugrel, and ticagrelor among all-comers with ST-segment elevation myocardial infarction (STEMI) and extend the knowledge from randomized clinical trials. Methods: All consecutive patients with STEMI admitted to Copenhagen University Hospital, Rigshospitalet, from 2009 to 2016 were identified via the Eastern Danish Heart Registry. By individual linkage to Danish nationwide registries, claimed drugs and end points were obtained. Patients alive a week post-discharge were included, stratified according to clopidogrel, prasugrel, or ticagrelor treatment, and followed for a year. The effectiveness end point (a composite of all-cause mortality, recurrent myocardial infarction, and ischemic stroke) and safety end point (a composite of bleedings leading to hospitalization) were assessed by multivariate Cox proportionalhazards models. Results: In total, 5123 patients were included (clopidogrel [1245], prasugrel [1902], ticagrelor [1976]) with >95% treatment persistency. Concomitant use of aspirin was >95%. Females accounted for 24% and elderly for 17%. Compared with clopidogrel, the effectiveness end point occurred less often for ticagrelor (HR 0.50, 95% CI 0.35-0.70) and prasugrel (HR 0.48, 95% CI 0.33-0.68) without differences in bleedings leading to hospitalization. No differences in comparative effectiveness or safety were found between prasugrel and ticagrelor. Sensitivity analyses with time-dependent drug exposure and the period 2011-2015 showed similar results. Conclusions: Among all-comers with STEMI, ticagrelor and prasugrel were associated with reduced incidence of the composite end point of all-cause mortality, recurrent myocardial infarction, and ischemic stroke without an increase in bleedings leading to hospitalization compared with clopidogrel. No differences were found between prasugrel and ticagrelor.

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