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Antithrombotic Trialists’ (ATT) Collaboration. Lancet 2009;373:1849-60. Design and eligibility criteria of primary prevention trials. Antithrombotic Trialists’ (ATT) Collaboration. Lancet 2009;373:1849-60.
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Antithrombotic Trialists’ (ATT) Collaboration. Lancet 2009;373:1849-60
Design and eligibility criteria of primary prevention trials Antithrombotic Trialists’ (ATT) Collaboration. Lancet 2009;373:1849-60
Serious vascular events in primary prevention trials-proportional effects of aspirin allocation Antithrombotic Trialists’ (ATT) Collaboration. Lancet 2009;373:1849-60
Serious vascular events in primary prevention Trials-subgroup analyses ATT Collaboration. Lancet 2009;373:1849-60
Comparison of proportional and absolute effects of aspirin in primary and secondary prevention trials Antithrombotic Trialists’ (ATT) Collaboration. Lancet 2009;373:1849-60
Selected outcomes in primary and secondary prevention trials of aspirin, by sex ATT Collaboration. Lancet 2009;373:1849-60
Stroke subtypes in primary and secondary prevention trials ATT Collaboration. Lancet 2009;373:1849-60
Mortality by cause in primary prevention trials Antithrombotic Trialists’ (ATT) Collaboration. Lancet 2009;373:1849-60
Rate ratios (95% CI) associated with risk factors for selected outcomes in people with no known vascular disease in primary prevention trials Antithrombotic Trialists’ (ATT) Collaboration. Lancet 2009;373:1849-60
Predicted 5-year absolute eff ects of allocation to aspirin in different categories of age and sex in the primary and secondary prevention trials (ignoring non-vascular mortality) ATT Collaboration. Lancet 2009;373:1849-60
Predicted 5-year absolute effects of allocation to aspirin in the primary prevention trials in different categories of 5-year risk (if untreated) of coronary heart disease (CHD) (ignoring non-vascular mortality) ATT Collaboration. Lancet 2009;373:1849-60