The Women's Health Initiative (WHI) multicentre primary prevention trial randomized 16 608 postmenopausal women aged 50 -70 years to receive either conjugated equine estrogen 0.625 mg/d plus medroxyprogesterone acetate 2.5 mg/d or placebo. The planned duration of the trial was 8.5 years, but it was terminated early after a mean follow-up of 5.2 years. The follow-up of clinical events occurred every 6 months. The study protocol required annual mammograms. The estimated hazard ratios were as follows: coronary heart disease 1.29 (95% CI 1.02 to 1.63), breast cancer 1.26 (1.00 to 1.59), stroke 1.41 (1.07 to 1.85), pulmonary embolism 2.13 (1.39 to 3.25), colorectal cancer 0.63 (0.43 to 0.92), endometrial cancer 0.83 (0.47 to 1.47), hip fracture 0.66 (0.45 to 0.98). For total mortality the hazard ratio was 0.98 (0.82 to 1.18). Absolute health risks per 10 000 person-years were as follows: CHD events 7, strokes 8, pulmonary embolisms 8, invasive breast cancers 8. Absolute risk reductions were as follows: colorectal cancer 6, hip fractures 5. The absolute excess risk of events was 19 per 10 000 person-years.
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