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World Health Organisation multicentre randomised trial of supplementation with vitamins C and E among pregnant women at high risk for pre-eclampsia in populations of low nutritional status from developing countries.

机译:世界卫生组织在来自发展中国家的低营养状况人群中,先兆子痫高风险孕妇中补充维生素C和E的多中心随机试验。

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摘要

OBJECTIVE: To determine if vitamin C and E supplementation in high-risk pregnant women with low nutritional status reduces pre-eclampsia. DESIGN: Multicentred, randomised, controlled, double-blinded trial. SETTING: Antenatal care clinics and Hospitals in four countries. POPULATION: Pregnant women between 14 and 22 weeks' gestation. METHOD: Randomised women received 1000 mg vitamin C and 400 iu of vitamin E or placebo daily until delivery. MAIN OUTCOME MEASURES: Pre-eclampsia, low birthweight, small for gestational age and perinatal death. RESULTS: Six hundred and eighty-seven women were randomised to the vitamin group and 678 to the placebo group. Groups had similar gestational ages (18.1; SD 2.4 weeks), socio-economic, clinical and demographical characteristics and blood pressure at trial entry. Risk factors for eligibility were similar, except for multiple pregnancies: placebo group (14.7%), vitamins group (11.8%). Previous pre-eclampsia, or its complications, was the most common risk factor at entry (vitamins 41.6%, placebo 41.3%). Treatment compliance was 87% in the two groups and loss to follow-up was low (vitamins 2.0%, placebo 1.3%). Supplementation was not associated with a reduction of pre-eclampsia (RR: 1.0; 95% CI: 0.9-1.3), eclampsia (RR: 1.5; 95% CI: 0.3-8.9), gestational hypertension (RR: 1.2; 95% CI: 0.9-1.7), nor any other maternal outcome. Low birthweight (RR: 0.9; 95% CI: 0.8-1.1), small for gestational age (RR: 0.9; 95% CI: 0.8-1.1) and perinatal deaths (RR: 0.8; 95% CI: 0.6-1.2) were also unaffected. CONCLUSION: Vitamins C and E at the doses used did not prevent pre-eclampsia in these high-risk women.
机译:目的:确定营养水平低的高危孕妇补充维生素C和E是否能降低先兆子痫。设计:多中心,随机,对照,双盲试验。地点:四个国家的产前保健诊所和医院。人口:怀孕14至22周的孕妇。方法:随机分娩的妇女每天接受1000 mg维生素C和400 iu维生素E或安慰剂直至分娩。主要观察指标:先兆子痫,低出生体重,不适合胎龄和围产期死亡。结果:867名女性被随机分配到维生素组,而678名被随机分配到安慰剂组。各组在进入试验时具有相似的胎龄(18.1; SD为2.4周),社会经济,临床和人口统计学特征以及血压。除多胎妊娠外,合格风险因素相似:安慰剂组(14.7%),维生素组(11.8%)。子痫前期或其并发症是进入时最常见的危险因素(维生素41.6%,安慰剂41.3%)。两组的治疗依从性为87%,随访损失较低(维生素2.0%,安慰剂1.3%)。补充剂与子痫前期(RR:1.0; 95%CI:0.9-1.3),子痫(RR:1.5; 95%CI:0.3-8.9),妊娠高血压(RR:1.2; 95%CI)降低无关:0.9-1.7),也没有其他任何孕产妇预后。低出生体重(RR:0.9; 95%CI:0.8-1.1),胎龄小(RR:0.9; 95%CI:0.8-1.1)和围产期死亡(RR:0.8; 95%CI:0.6-1.2)也不受影响。结论:这些剂量的维生素C和E不能预防这些高危妇女的先兆子痫。

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