Table 2.
Power for effects of a single agent on CVD in VITAL, a 2×2 factorial trial of 10,000 men aged ≥50 and 10,000 women aged ≥55, with 5 years of follow-up
Observed RRa | True RRb | Major CVDc |
Total CVDd |
CVD Mortality | MI | Stroke |
---|---|---|---|---|---|---|
0.90 | 0.875 | 34.6 | 52.8 | - | - | - |
0.85 | 0.812 | 66.1 | 86.9 | - | - | - |
0.80 | 0.750 | 89.4 | 98.6 | 45.1 | 50.9 | 51.0 |
0.75 | 0.687 | 98.2 | >99.9 | 64.4 | 71.0 | 71.1 |
0.70 | 0.625 | 99.9 | >99.9 | 80.9 | 86.4 | 86.5 |
0.65 | 0.560 | >99.9 | >99.9 | 91.9 | 95.2 | 95.2 |
0.60 | 0.500 | >99.9 | >99.9 | 97.3 | 98.8 | 98.8 |
Observed RR=intent-to-treat RR, including noncompliant participants. Compliance is assumed to be 80%.
True RR=that with perfect compliance.
Major CVD=myocardial infarction, stroke, and CVD mortality
Total CVD=myocardial infarction, stroke, CVD mortality, and coronary revascularization (coronary artery bypass grafting or percutaneous coronary intervention)
CVD, cardiovascular disease; MI, myocardial infarction; RR, rate ratio.