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低剂量阿司匹林预防子痫前期的荟萃分析。

A meta-analysis of low-dose aspirin for prevention of preeclampsia.

作者信息

Trivedi N A

机构信息

Department of Pharmacology, Medical College, Baroda, Gujarat, India.

出版信息

J Postgrad Med. 2011 Apr-Jun;57(2):91-5. doi: 10.4103/0022-3859.81858.

Abstract

BACKGROUND

Low-dose aspirin (LDA) is widely used for prevention of preeclampsia. However, conflicting results have been obtained from various studies.

AIM

The aim of our study was to evaluate the effect of LDA in prevention of preeclampsia in high-risk and low-risk women.

MATERIALS AND METHODS

A total of 19 randomized control trials were identified using PUBMED search engine and Cochrane Clinical Trial register. The study population was divided into high-risk and low-risk groups. The effect measured was incidence of preeclampsia in women taking either LDA or placebo where the relative risk (RR) and the 95% confidence interval (CI) were calculated for both groups.

RESULTS

A total of 28237 women were studied, out of which 16550 were in the low-risk group while 11687 were in the high-risk group. The overall incidence of preeclampsia was 7.4%. With the aspirin group it was 6.9% while in the placebo group it was 7.8%. In the high-risk group there was 21% reduction in the risk of preeclampsia associated with the use of aspirin (RR 0.79, 95% CI 0.65-0.97). However, LDA is not effective in reducing the risk in low-risk population (RR 0.86, 95% CI 0.64-1.17).

CONCLUSION

LDA has a small effect in the prevention of preeclampsia in women considered to be at high risk for the disease. However, it is not effective in reducing the risk in the low-risk group.

摘要

背景

低剂量阿司匹林(LDA)被广泛用于预防子痫前期。然而,各项研究得出的结果相互矛盾。

目的

我们研究的目的是评估LDA在预防高危和低危女性子痫前期方面的效果。

材料与方法

使用PUBMED搜索引擎和Cochrane临床试验注册库共识别出19项随机对照试验。研究人群分为高危组和低危组。测量的效果是服用LDA或安慰剂的女性子痫前期的发病率,并计算两组的相对风险(RR)和95%置信区间(CI)。

结果

共研究了28237名女性,其中16550名在低危组,11687名在高危组。子痫前期的总体发病率为7.4%。阿司匹林组为6.9%,而安慰剂组为7.8%。在高危组中,使用阿司匹林使子痫前期风险降低了21%(RR 0.79,95% CI 0.65 - 0.97)。然而,LDA在降低低危人群风险方面无效(RR 0.86,95% CI 0.64 - 1.17)。

结论

LDA在预防被认为子痫前期高危的女性子痫前期方面有微小效果。然而,它在降低低危组风险方面无效。

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