Ticagrelor vs. clopidogrel in patients with acute coronary syndromes and diabetes: a substudy from the PLATelet inhibition and patient Outcomes (PLATO) trial
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2010
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Resumo |
Patients with diabetes mellitus (DM) have high platelet reactivity and are at increased risk of ischaemic events and bleeding post-acute coronary syndromes (ACS). In the PLATelet inhibition and patient Outcomes (PLATO) trial, ticagrelor reduced the primary composite endpoint of cardiovascular death, myocardial infarction, or stroke, but with similar rates of major bleeding compared with clopidogrel. We aimed to investigate the outcome with ticagrelor vs. clopidogrel in patients with DM or poor glycaemic control. We analysed patients with pre-existing DM (n = 4662), including 1036 patients on insulin, those without DM (n = 13 951), and subgroups based on admission levels of haemoglobin A1c (HbA1c; n = 15 150). In patients with DM, the reduction in the primary composite endpoint (HR: 0.88, 95% CI: 0.76-1.03), all-cause mortality (HR: 0.82, 95% CI: 0.66-1.01), and stent thrombosis (HR: 0.65, 95% CI: 0.36-1.17) with no increase in major bleeding (HR: 0.95, 95% CI: 0.81-1.12) with ticagrelor was consistent with the overall cohort and without significant diabetes status-by-treatment interactions. There was no heterogeneity between patients with or without ongoing insulin treatment. Ticagrelor reduced the primary endpoint, all-cause mortality, and stent thrombosis in patients with HbA1c above the median (HR: 0.80, 95% CI: 0.70-0.91; HR: 0.78, 95% CI: 0.65-0.93; and HR: 0.62, 95% CI: 0.39-1.00, respectively) with similar bleeding rates (HR: 0.98, 95% CI: 0.86-1.12). Ticagrelor, when compared with clopidogrel, reduced ischaemic events in ACS patients irrespective of diabetic status and glycaemic control, without an increase in major bleeding events. AstraZeneca Uppsala Clinical Research Center GlaxoSmithKline Otsuka Accumetrics Eli Lilly and Company Daiichi Sankyo, Inc. Medicines Company Eisai Portola Pharmaceutical Schering-Plough Johnson and Johnson Bristol-Myers Squibb sanofi-aventis Pfizer Bayer Merck Sharp Dohme (MSD) Perseus Proteomics Inc. Dynabyte Eli Lilly/Daiichi Sankyo alliance Teva Novartis sanofi-aventis/Bristol-Myers Squibb Regado Biotechnologies Athera Biotechnologies |
Identificador |
EUROPEAN HEART JOURNAL, v.31, n.24, p.3006-3016, 2010 0195-668X http://producao.usp.br/handle/BDPI/21781 10.1093/eurheartj/ehq325 |
Idioma(s) |
eng |
Publicador |
OXFORD UNIV PRESS |
Relação |
European Heart Journal |
Direitos |
restrictedAccess Copyright OXFORD UNIV PRESS |
Palavras-Chave | #Acute coronary syndromes #Diabetes #Ticagrelor #Clopidogrel #Mortality #Myocardial infarction #ST-SEGMENT ELEVATION #ARTERY-DISEASE #ANTIPLATELET THERAPY #RISK-FACTOR #MELLITUS #ASPIRIN #RESPONSIVENESS #MANAGEMENT #PRASUGREL #RESPOND #Cardiac & Cardiovascular Systems |
Tipo |
article original article publishedVersion |