التفاصيل البيبلوغرافية
| العنوان: |
Analysis of composite time-to-event endpoints in cardiovascular outcome trials. |
| المؤلفون: |
Marceau West, Rachel, Golm, Gregory, Mehrotra, Devan V |
| المصدر: |
Clinical Trials; Oct2024, Vol. 21 Issue 5, p576-583, 8p |
| مصطلحات موضوعية: |
MYOCARDIAL infarction risk factors, CARDIOVASCULAR disease related mortality, ANGINA pectoris, DATA analysis, MEDICAL care, CLINICAL trials, HOSPITAL care, TREATMENT effectiveness, ACUTE coronary syndrome, MYOCARDIAL revascularization, SIMULATION methods in education, STATISTICS, STROKE, CARDIOVASCULAR system, TIME, DISEASE risk factors |
| مستخلص: |
Composite time-to-event endpoints are commonly used in cardiovascular outcome trials. For example, the IMPROVE-IT trial comparing ezetimibe+simvastatin to placebo+simvastatin in 18,144 patients with acute coronary syndrome used a primary composite endpoint with five component outcomes: (1) cardiovascular death, (2) non-fatal stroke, (3) non-fatal myocardial infarction, (4) coronary revascularization ≥30 days after randomization, and (5) unstable angina requiring hospitalization. In such settings, the traditional analysis compares treatments using the observed time to the occurrence of the first (i.e. earliest) component outcome for each patient. This approach ignores information for subsequent outcome(s), possibly leading to reduced power to demonstrate the benefit of the test versus the control treatment. We use real data examples and simulations to contrast the traditional approach with several alternative approaches that use data for all the intra-patient component outcomes, not just the first. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
Complementary Index |