Re: TRH

From: Jaime (jaimen@zaz.com.br)
Wed, 10 Jul 2002 23:48:54 -0300


Caros Colegas da lista O estudo WHI, ora interrompido, a exemplo do estudo HERS tem limitações. Entre outras coisas, não citam o o hábito alimentar, o peso e a prática ou não de atividades físicas. A faixa etária das mulheres estudadas foi entre 50 e 79 anos, mas não especificam quantas mulheres acima dos 65 por exemplo. Além do mais, os americanos insistem em fazer grandes estudos com estrógenos eqüinos conjugados. Nós aqui no Brasil pouco o usamos. A grande maioria das nossas pacientes usa o estradiol e em doses bem baixas. Temos que tranqüilizar nossas pacientes informando que o ca de mama é mais comum em mulheres brancas, obesas, estressadas e sedentárias (perfil das americanas). Nesta mesma linha vão as doenças cardio vasculares. Ambas são multifatoriais.

--
                       Jaime Nonato

> ----- Original Message ----- From: Joao Lindolfo C. Borges, MD To: Multiple recipients of list OBSTET-L Sent: Wednesday, July 10, 2002 11:54 AM Subject: Re: TRH

Já está impresso no JAMA.

Risks and Benefits of Estrogen Plus Progestin in Healthy Postmenopausal Women

Principal Results From the Women's Health Initiative Randomized Controlled Trial

Writing Group for the Women's Health Initiative Investigators

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 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 statistic 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 (1.39-3.25) 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 10 000 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 10 000 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 10 000 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

Abraços

Joao Lindolfo C. Borges, MD

> ----- Original Message ----- From: Jose Olivas To: Multiple recipients of list OBSTET-L Sent: Wednesday, July 10, 2002 11:21 AM Subject: TRH

Caros colegas da lista. Acho que todos tivemos contato com as noticias veiculadas em todos os principais jornais do país a respeito de trabalho realizado nos EUA , a ser publicado (SIC) pela JAMA em 17 de julho próximo. Gostaria de saber se alguém pode adiantar alguma coisa,pois são afirmações bombásticas ,porém sem muita clareza e as vezes também contraditórias. De qualquer maneira aqueles que prescrevem TRH como eu há muitos anos, e que transmitem às pacientes a informação de que os benefícios superam os riscos na grande maioria dos casos, estaremos enfretando questionamentos sérios nos consultórios. Abraços Jose Francisco Campos de Olivas


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