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in-cites - an editorial component of ISI Essential Science Indicators
Citing URL: http://www.in-cites.com/research/2003/may_19_2003-3.html

SCI-BYTES What's New in Research:
May 19, 2003
             

  Previous | Main SCI-BYTES Menu (current year) | 2003 Menu

Hot Paper in Medicine

"Risks and benefits of estrogen plus progestin in healthy postmenopausal women. Principal results
from the Women's Health Initiative Randomized Controlled Trial,"
by the Writing Group for the
Women's Health Initiative Investigators (J.E. Rossouw, et al.), JAMA-Journal of the American Medical
Association
, 288(3):321-33, 17 July 2002.

[Authors' affiliations (Writing Group): 9 U.S. institutions]

Abstract: Context Despite decades of accumulated observational evidence, the balance of risks and benefits for
hormone use in healthy postmenopausal women remains uncertain. Objective To assess the major health benefits
and risks of the most commonly used combined hormone preparation in the United States. Design Estrogen plus
progestin component of the Women's Health Initiative, a randomized controlled primary prevention trial (planned
duration, 8.5 years) in which 16608 postmenopausal women aged 50-79 years with an intact uterus at baseline were recruited by 40 US clinical centers in 1993-1998. Interventions Participants received conjugated equine estrogens, 0.625 mg/d, plus medroxyprogesterone acetate, 2.5 mg/d, in 1 tablet (n=8506) or placebo (n=8102). Main Outcomes Measures The primary outcome was coronary heart disease (CHD) (nonfatal myocardial infarction
and CHD death), with invasive breast cancer as the primary adverse outcome. A global index summarizing the balance of the risks and benefits included the 2 primary outcomes plus stroke, pulmonary embolism (PE), endometrial cancer, colorectal cancer, hip fracture, and death due to other causes. Results On May 31, 2002, after a mean of 5.2 years of follow-up, the data and safety monitoring board recommended stopping the trial of estrogen plus progestin vs placebo because the test statistics for invasive breast cancer exceeded the stopping boundary for this adverse effect and the global index statistic supported risks exceeding benefits. This report includes data on the major clinical outcomes through April 30, 2002. Estimated hazard ratios (HRs) (nominal 95% confidence intervals [CIs]) were as follows: CHD, 1.29 (1.02-1.63) with 286 cases; breast cancer, 1.26 (1.00-1.59) with 290 cases; stroke, 1.41 (1.07-1.85) with 212 cases; PE, 2.13-3.25) with 101 cases; colorectal cancer, 0.63 (0.43-0.92) with 112 cases; endometrial cancer, 0.83 (0.47-1.47) with 47 cases; hip fracture, 0.66 (0.45-0.98) with 106 cases; and death due to other causes, 0.92 (0.74-1.14) with 331 cases. Corresponding HRs (nominal 95% CIs) for composite outcomes were 1.22 (1.09-1.36) for total cardiovascular disease (arterial and venous disease), 1.03 (0.90-1.17) for total cancer, 0.76 (0.69-0.85) for combined fractures, 0.98 (0.82-1.18) for total mortality, and 1.15 (1.03-1.28) for the global index. Absolute excess risks per 10000 person-years attributable to estrogen plus progestin were 7 more CHD events, 8 more strokes, 8 more PEs, and 8 more invasive breast cancers, while absolute risk reductions per 10000 person-years were 6 fewer colorectal cancers and 5 fewer hip fractures. The absolute excess risk of events included in the global index was 19 per 10000 person-years. Conclusions Overall
health risks exceeded benefits from use of combined estrogen plus progestin for an average 5.2-year follow-up among healthy postmenopausal US women. All-cause mortality was not affected during the trial. The risk-benefit profile found in this trial is not consistent with the requirements for a viable intervention for primary prevention of chronic diseases, and the results indicate that this regimen should not be initiated or continued for primary prevention of CHD."

This 2002 report from the Journal of the American Medical Association was cited 87 times in current journal
articles indexed by Thomson ISI during January-February 2003. Having scored as the most-cited non-review paper
published in 2002 (based on a year-end citation total), this JAMA article has now topped the list of medicine's most
cited for two bimonthly counts in a row. During the January-February count, in fact, this was the fourth-most-cited
paper in all of science published in the last two years, including reviews. Prior to the most recent two-month tally,
citations to the paper have accrued as follows:

November-December 2002: 82
September-October 2002: 46

Total citations to date: 215

SOURCE: Hot Papers Database (Included with a subscription to the ISI print newsletter Science Watch®, available from the ISI Research Services Group. Packaged on a CD-ROM that is mailed with each Science Watch issue, the Hot Papers Database contains data on hundreds of highly cited papers published during the last two years. User interface permits searching by author, organization, journal, field, and more. Total citations, as well as citations accrued during successive bimonthly periods, can be assessed and graphed. An updated CD containing the most recent bimonthly data is mailed with every new issue of Science Watch, six times a year. The CD also includes an electronic version of the Science Watch issue in HTML format, for personal desktop access.)


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