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Therapeutics |
Clinical impact ratings GP/FP/Primary care






Gynaecology 





Cardiology 





IM/Ambulatory care 





Key Words: cardiovascular diseases oestrogen replacement therapy
| The first 150 words of the full text of this article appear below. |
METHODS
Design:
2 randomised placebo-controlled trials (Womens Health Initiative [WHI] trials).
Allocation:
{concealed}*.
Blinding:
blinded {clinicians, participants, data collectors, outcome assessors, and monitoring committee}*.
Follow-up period:
mean 5.6
and 7.1
years.
Setting:
40 US clinical centres.
Participants:
27 347 predominantly healthy postmenopausal women 50–79 years of age (mean age 63* and 64|| y).
Intervention
conjugated equine oestrogen (CEO), 0.625 mg/day, plus medroxyprogesterone acetate, 2.5 mg/day (n = 8506), or placebo (n = 8102) in women with an intact uterus; CEO, 0.625 mg/day (n = 5310), or placebo (n = 5429) in women with a hysterectomy.
Outcomes:
coronary heart disease (CHD) (myocardial infarction or CHD death), stroke, total mortality, and a global index.
Participant follow-up:
94%
|| (intention-to-treat analysis).
MAIN RESULTS
Overall, the HT and placebo groups did not differ for CHD, total mortality, and the global index; the risk of stroke was higher in the HT group (hazard ratio 1.3, CI 1.1
Robert L Reid, MD
Queens University,
Kingston, Ontario, Canada
Relevant Article
Evid. Based Med. 2007 12: 160.
(in Glossary)
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