Hormone therapy for preventing cardiovascular disease in post-menopausal women


Por: Boardman H.M.P., Hartley L., Eisinga A., Main C., Roqué i Figuls M., Bonfill Cosp X., Gabriel Sanchez R., Knight B.

Publicada: 1 ene 2015
Resumen:
Background: Evidence from systematic reviews of observational studies suggests that hormone therapy may have beneficial effects in reducing the incidence of cardiovascular disease events in post-menopausal women, however the results of randomised controlled trials (RCTs) have had mixed results. This is an updated version of a Cochrane review published in 2013. Objectives: To assess the effects of hormone therapy for the prevention of cardiovascular disease in post-menopausal women, and whether there are differential effects between use in primary or secondary prevention.Secondary aims were to undertake exploratory analyses to (i) assess the impact of time since menopause that treatment was commenced (= 10 years versus < 10 years), and where these data were not available, use age of trial participants at baseline as a proxy (= 60 years of age versus < 60 years of age); and (ii) assess the effects of length of time on treatment. Search methods: We searched the following databases on 25 February 2014: Cochrane Central Register of Controlled Trials (CENTRAL) in The Cochrane Library, MEDLINE, EMBASE and LILACS. We also searched research and trials registers, and conducted reference checking of relevant studies and related systematic reviews to identify additional studies. Selection criteria: RCTs of women comparing orally administered hormone therapy with placebo or a no treatment control, with a minimum of six months follow-up. Data collection and analysis: Two authors independently assessed study quality and extracted data. We calculated risk ratios (RRs) with 95% confidence intervals (CIs) for each outcome. We combined results using random effects meta-analyses, and undertook further analyses to assess the effects of treatment as primary or secondary prevention, and whether treatment was commenced more than or less than 10 years after menopause. Main results: We identified six new trials through this update. Therefore the review includes 19 trials with a total of 40,410 post-menopausal women. On the whole, study quality was good and generally at low risk of bias; the findings are dominated by the three largest trials. We found high quality evidence that hormone therapy in both primary and secondary prevention conferred no protective effects for all-cause mortality, cardiovascular death, non-fatal myocardial infarction, angina, or revascularisation. However, there was an increased risk of stroke in those in the hormone therapy arm for combined primary and secondary prevention (RR 1.24, 95% CI 1.10 to 1.41). Venous thromboembolic events were increased (RR 1.92, 95% CI 1.36 to 2.69), as were pulmonary emboli (RR 1.81, 95% CI 1.32 to 2.48) on hormone therapy relative to placebo. The absolute risk increase for stroke was 6 per 1000 women (number needed to treat for an additional harmful outcome (NNTH) = 165; mean length of follow-up: 4.21 years (range: 2.0 to 7.1)); for venous thromboembolism 8 per 1000 women (NNTH = 118; mean length of follow-up: 5.95 years (range: 1.0 to 7.1)); and for pulmonary embolism 4 per 1000 (NNTH = 242; mean length of follow-up: 3.13 years (range: 1.0 to 7.1)). We performed subgroup analyses according to when treatment was started in relation to the menopause. Those who started hormone therapy less than 10 years after the menopause had lower mortality (RR 0.70, 95% CI 0.52 to 0.95, moderate quality evidence) and coronary heart disease (composite of death from cardiovascular causes and non-fatal myocardial infarction) (RR 0.52, 95% CI 0.29 to 0.96; moderate quality evidence), though they were still at increased risk of venous thromboembolism (RR 1.74, 95% CI 1.11 to 2.73, high quality evidence) compared to placebo or no treatment. There was no strong evidence of effect on risk of stroke in this group. In those who started treatment more than 10 years after the menopause there was high quality evidence that it had little effect on death or coronary heart disease between groups but there was an increased risk of stroke (RR 1.21, 95% CI 1.06 to 1.38, high quality evidence) and venous thromboembolism (RR 1.96, 95% CI 1.37 to 2.80, high quality evidence). Authors' conclusions: Our review findings provide strong evidence that treatment with hormone therapy in post-menopausal women overall, for either primary or secondary prevention of cardiovascular disease events has little if any benefit and causes an increase in the risk of stroke and venous thromboembolic events. © 2015 The Cochrane Collaboration.

Filiaciones:
Boardman H.M.P.:
 University of Oxford, John Radcliffe Hospital, Department of Cardiovascular Medicine, Oxford, OX3 9DU, United Kingdom

Hartley L.:
 Warwick Medical School, University of Warwick, Division of Health Sciences, Coventry, Warwickshire, CV4 7AL, United Kingdom

Eisinga A.:
 UK Cochrane Centre, National Institute for Health Research, Summertown Pavilion, Middle Way, Oxford, Oxfordshire, OX2 7LG, United Kingdom

Main C.:
 University of Birmingham, Cancer Research UK Clinical Trials Unit (CRCTU), School of Cancer Sciences, Birmingham, B15 2TT, United Kingdom

Roqué i Figuls M.:
 CIBER Epidemiología y Salud Pública (CIBERESP), Iberoamerican Cochrane Centre, Biomedical Research Institute Sant Pau (IIB Sant Pau), Sant Antoni Maria Claret 171, Edif. Casa de Convalescencia, Barcelona, Catalunya, 08041, Spain

Bonfill Cosp X.:
 CIBER Epidemiología y Salud Pública (CIBERESP), Universitat Autonoma de Barcelona, Iberoamerican Cochrane Centre - Biomedical Research Institute Sant Pau (IIB Sant Pau), Sant Antoni Maria Claret, 167, Pavilion 18 (D-13), Barcelona, Catalunya, 08025, Spain

Gabriel Sanchez R.:
 Hospital Universitario de la Paz, Universidad Autónoma de Madrid, Instituto de Investigacion IdiPAZ, Red Espanola de Investigacion Cardiovascular RD/12/0042/0008, Diego De Leon 62, Planta 9, Madrid, 28006, Spain

Knight B.:
 University of Exeter Medical School, NIHR Exeter Clinical Research Facility, Exeter, United Kingdom
ISSN: 1469493X
Editorial
WILEY, 111 RIVER ST, HOBOKEN 07030-5774, NJ USA, Reino Unido
Tipo de documento: Review
Volumen: 2015 Número: 3
Páginas:
WOS Id: 000375542100005
ID de PubMed: 25754617
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