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Causes of mortality with ticagrelor compared with clopidogrel in acute coronary syndromes
Christoph Varenhorst1, Ulrica Alström2, Oscar Ö Braun3
1Department of Medical Sciences, Cardiology, Uppsala University, Uppsala, Sweden Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
Insights
Ticagrelor significantly reduced mortality in acute coronary syndrome patients compared to clopidogrel, primarily by lowering sudden death rates. Importantly, ticagrelor did not increase deaths related to bleeding events.
Area of Science:
- Cardiology
- Clinical Trials
- Pharmacology
Background:
- The PLATelet inhibition and patient Outcomes (PLATO) trial demonstrated ticagrelor's superiority over clopidogrel in reducing vascular and total death.
- Understanding specific causes of death and the role of bleeding and infection is crucial for optimizing antiplatelet therapy.
Purpose of the Study:
- To analyze specific causes of mortality in ticagrelor- vs. clopidogrel-treated patients with acute coronary syndromes.
- To evaluate the contribution of bleeding events and infection to mortality in the PLATO trial.
Main Methods:
- A post hoc analysis of the 905 deaths in the 18,624-patient PLATO trial.
- Reviewers, blinded to treatment, subclassified causes of death and assessed the role of infection and bleeding.
Main Results:
- Ticagrelor significantly reduced sudden deaths (0.7% vs. 1.1%) but not deaths from myocardial infarction or heart failure compared to clopidogrel.
- No difference in infection-related deaths was observed, but ticagrelor was associated with a lower risk of death where infection contributed (0.5% vs. 0.8%).
- The incidence of death caused or contributed to by bleeding was similar between ticagrelor and clopidogrel groups (0.5% vs. 0.5%).
Conclusions:
- Ticagrelor reduces overall and cardiovascular mortality in acute coronary syndrome patients, mainly through a decrease in sudden death.
- The observed mortality benefit of ticagrelor is not associated with an increased risk of fatal bleeding events.
Objective:
To describe specific causes of death and evaluate whether bleeding events and infection contributed to mortality in all ticagrelor-treated and clopidogrel-treated patients with acute coronary syndromes.
Methods:
In the PLATelet inhibition and patient Outcomes (PLATO) trial, ticagrelor significantly reduced rates of vascular and total death compared with clopidogrel. In the 905 patients who died postenrolment in the PLATO trial (n=18 624), reviewers, blinded to study treatment, subclassified direct causes of death and evaluated whether infection or bleeding events contributed to fatal events.
Results:
Among vascular deaths, there were significantly fewer sudden deaths (63 (0.7%) vs 98 (1.1%), p<0.01) but no significant difference in deaths caused by acute myocardial infarction (179 (1.9%) vs 194 (2.1%), p=0.43) or heart failure (31 (0.3%) vs 42 (0.5%), p=0.20) with ticagrelor compared with clopidogrel. For non-vascular deaths, there was no difference between treatments in deaths directly caused by infection. Although, patients treated with ticagrelor were at lower risk for death where infection was either a direct cause or contributed to death (51 (0.5%) vs 76 (0.8%), HR 0.67 (0.47 to 0.95), p<0.05) but not for bleeding (42 (0.5%) vs 42 (0.5%), HR 0.99 (0.65 to 1.53), p=0.98).
Conclusions:
In this post hoc analysis, ticagrelor compared with clopidogrel reduced total and cardiovascular mortality, which appeared to be mainly mediated by a reduction in sudden death. Importantly, bleeding causing or contributing to death did not differ between treatments.
Clinical Trial Registration Number:
NCT00391872 (http://www.clinicaltrial.gov).
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