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(Circulation. 2007;116:2656-2657.)
© 2007 American Heart Association, Inc.
Editorial |
From the Department of Health Care Policy, Harvard Medical School, and the Department of Biostatistics, Harvard School of Public Health, Boston, Mass.
Correspondence to Sharon-Lise T. Normand, PhD, Department of Health Care Policy, Harvard Medical School, 180 Longwood Ave, Boston, MA 02115. E-mail Sharon@hcp.med.harvard.edu
Key Words: cardiovascular diseases coronary angiography data interpretation, statistical outcome assessment statistics
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
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Article p 2669
The Tricoci et al1 study capitalized on the clinical data collected as part of the Superior Yield of the New Strategy of Enoxaparin, Revascularization, and Glycoprotein IIb/IIIa Inhibitors (SYNERGY) trial2 to study this question. Because the goal of the SYNERGY trial was to compare the outcomes of patients treated with enoxaparin versus unfractionated heparin, (1) patients were not randomized to different times to angiography (such as
6 hours, 6 to 12 hours, 12 to 18 hours, etc) after hospital arrival, and (2) some patients may have died or experienced an adverse event before receiving angiography. The authors adopted 2 different analytical strategies to address these issues: a landmark analysis3 and an inverse-probability–weighted approach.4 These 2 approaches differ in their basic assumptions and in the populations to which they apply.
| The Landmark Method |
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