Hormone therapy for preventing cardiovascular disease in post-menopausal women

被引:366
作者
Boardman, Henry M. P. [1 ]
Hartley, Louise [2 ]
Eisinga, Anne [3 ]
Main, Caroline [4 ]
Roque i Figuls, Marta [5 ]
Bonfill Cosp, Xavier [6 ]
Gabriel Sanchez, Rafael [7 ]
Knight, Beatrice [8 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Dept Cardiovasc Med, Oxford OX3 9DU, England
[2] Univ Warwick, Warwick Med Sch, Div Hlth Sci, Coventry CV4 7AL, W Midlands, England
[3] UK Cochrane Ctr, Oxford, England
[4] Univ Birmingham, Sch Canc Sci, Canc Res UK Clin Trials Unit CRCTU, Birmingham, W Midlands, England
[5] CIBER Epidemiol & Salud Publ, Biomed Res Inst St Pau IIB St Pau, Iberoamer Cochrane Ctr, Barcelona, Spain
[6] Univ Autonoma Barcelona, CIBER Epidemiol Salud Publ, Biomed Res Inst St Pau IIB St Pau, Iberoamer Cochrane Ctr, E-08193 Barcelona, Spain
[7] Univ Autonoma Madrid, Hosp Univ la Paz, Red Espanola Invest Cardiovasc RD 12 0042 0008, Inst Invest IdiPAZ, Madrid, Spain
[8] Univ Exeter, Sch Med, NIHR Exeter Clin Res Facil, Exeter, Devon, England
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2015年 / 03期
关键词
Cardiovascular Diseases; Cause of Death; Estrogen Replacement Therapy; Hormone Replacement Therapy; Postmenopause; Primary Prevention; Secondary Prevention; Stroke; Venous Thromboembolism; Adult; Aged; 80 and over; Female; Humans; Middle Aged; CORONARY-HEART-DISEASE; ESTROGEN REPLACEMENT THERAPY; CONJUGATED EQUINE ESTROGENS; QUALITY-OF-LIFE; BASE-LINE CHARACTERISTICS; PLACEBO-CONTROLLED TRIAL; BONE-MINERAL DENSITY; LONG-TERM; PLUS PROGESTIN; MYOCARDIAL-INFARCTION;
D O I
10.1002/14651858.CD002229.pub4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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