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J Am Coll Cardiol, 2005; 46:1405-1410, doi:10.1016/j.jacc.2005.03.077
© 2005 by the American College of Cardiology Foundation
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Early and Late Benefits of High-Dose Atorvastatin in Patients With Acute Coronary Syndromes

Results From the PROVE IT-TIMI 22 Trial

Kausik K. Ray, MRCP, MD*, Christopher P. Cannon, MD, FACC*,*, Carolyn H. McCabe, BS*, Richard Cairns, BSc{dagger}, Andrew M. Tonkin, MD{ddagger}, Frank M. Sacks, MD§, Graham Jackson, MD, FRCP||, Eugene Braunwald, MD, MACC* for the PROVE IT-TIMI 22 Investigators

* TIMI Study Group, Brigham and Women’s Hospital/Harvard Medical School, Boston, Massachusetts
{dagger} Nottingham Clinical Research Group, Nottingham, United Kingdom
{ddagger} Department of Epidemiology and Preventative Medicine, Monash University, Melbourne, Australia
§ Harvard School of Public Health, Boston, Massachusetts
|| Guy’s Hospital, London, England



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Figure 1 Kaplan-Meier estimates of the composite end point of death, myocardial infarction (MI), and rehospitalization with recurrent acute coronary syndrome (ACS) by statin treatment. CI = confidence interval.

 


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Figure 2 (A) Cumulative hazard ratios (HRs) of the primary end point of death, myocardial infarction, unstable angina requiring hospitalization, urgent revascularization >30 days, and stroke showing the relative benefit as early as 15 days and achieving statistical significance by four months. (B) Cumulative HRs of composite triple end point of death, myocardial infarction, or rehospitalization with recurrent acute coronary syndrome showing the relative benefit as early as 15 days and achieving statistical significance by 30 days. CI = confidence interval.

 


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Figure 3 Kaplan-Meier estimates of the composite end point of death, myocardial infarction (MI), or rehospitalization with recurrent acute coronary syndrome (ACS) by statin treatment from randomization to 30 days. CI = confidence interval.

 


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Figure 4 (A) Conditional hazard ratios (HRs) for the primary end point in each year of the trial. (B) Conditional HRs for the composite triple end point in each year of the trial.

 


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Figure 5 Kaplan-Meier estimates of the composite end point of death, myocardial infarction (MI), or rehospitalization with recurrent acute coronary syndrome (ACS) by statin treatment, in patients free from clinical events from six months to end of study.

 





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