Harris Birthright Research Centre of Fetal Medicine, Fetal Medicine Research Institute, King's College Hospital, London, United Kingdom.
Department of Obstetrics and Gynecology & Department of Social and Preventive Medicine, Faculty of Medecine, Université Laval, Quebec City, Quebec, Canada.
Am J Obstet Gynecol. 2018 Mar;218(3):287-293.e1. doi: 10.1016/j.ajog.2017.11.561. Epub 2017 Nov 11.
Metaanalyses of randomized controlled trials have reported contradictory results about the effect of aspirin in the prevention of preeclampsia, both in terms of the gestational age at the onset of treatment and the dose of the drug. The controversy may be resolved by a metaanalysis that includes several recently published trials and particularly the large Combined Multimarker Screening and Randomized Patient Treatment with Aspirin for Evidence-based Preeclampsia Prevention trial and by examination of whether there is a difference of the effect of aspirin on preterm vs term preeclampsia.
We performed a systematic review and metaanalysis that evaluated the prophylactic effect of aspirin during pregnancy.
We completed a literature search through PubMed, Cinhal, Embase, Web of Science, and Cochrane library from 1985 to June 2017. Relative risks with random effect were calculated with their 95% confidence intervals.
Sixteen trials that included 18,907 participants provided data for preterm and term preeclampsia. Eight of the included studies were evaluated as being of good quality, and the other 8 studies were deemed to be of poor or uncertain quality. There was high heterogeneity within studies (I >50%) for preterm and term preeclampsia, but no heterogeneity was found in the subgroup of preterm preeclampsia when the onset of treatment was ≤16 weeks of gestation and the daily dose of aspirin was ≥100 mg (I=0%). Administration of aspirin was associated with reduction in the risk of preterm preeclampsia (relative risk, 0.62; 95% confidence interval, 0.45-0.87), but there was no significant effect on term preeclampsia (relative risk, 0.92; 95% confidence interval, 0.70-1.21). The reduction in preterm preeclampsia was confined to the subgroup in which aspirin was initiated at ≤16 weeks of gestation and at a daily dose of ≥100 mg (relative risk, 0.33; 95% confidence interval, 0.19-0.57). This effect was also observed in the high-quality studies. The reduction in preterm preeclampsia that was observed in the largest trial (Combined Multimarker Screening and Randomized Patient Treatment with Aspirin for Evidence-based Preeclampsia Prevention; n=1620; relative risk, 0.38; 95% confidence interval, 0.20-0.72) was similar to that in the 5 smaller trials in which aspirin was initiated at ≤16 weeks of gestation and at a daily dose of ≥100 mg (n=639; relative risk, 0.22; 95% confidence interval, 0.07-0.66).
Aspirin reduces the risk of preterm preeclampsia, but not term preeclampsia, and only when it is initiated at ≤16 weeks of gestation and at a daily dose of ≥100 mg.
随机对照试验的荟萃分析报告了阿司匹林在子痫前期预防中的作用存在矛盾的结果,无论是治疗开始时的孕龄还是药物剂量。通过纳入最近发表的几项试验,特别是大型联合多标志物筛查和随机患者阿司匹林治疗用于基于证据的子痫前期预防试验,并检查阿司匹林对早产和足月子痫前期的作用是否存在差异,可能会解决这一争议。
我们进行了一项系统评价和荟萃分析,评估了怀孕期间阿司匹林的预防效果。
我们通过 PubMed、Cinhal、Embase、Web of Science 和 Cochrane 图书馆从 1985 年至 2017 年 6 月进行了文献检索。用随机效应计算相对风险及其 95%置信区间。
18907 名参与者的 16 项试验提供了早产和足月子痫前期的数据。其中 8 项研究被评估为质量良好,另外 8 项研究质量较差或不确定。早产和足月子痫前期的研究内异质性很高(I>50%),但当治疗开始于≤16 周妊娠且阿司匹林日剂量≥100mg 时,早产子痫前期亚组无异质性(I=0%)。阿司匹林治疗与降低早产子痫前期的风险相关(相对风险,0.62;95%置信区间,0.45-0.87),但对足月子痫前期无显著影响(相对风险,0.92;95%置信区间,0.70-1.21)。早产子痫前期的减少仅限于阿司匹林起始于≤16 周妊娠且日剂量≥100mg 的亚组(相对风险,0.33;95%置信区间,0.19-0.57)。这种效果也在高质量的研究中观察到。最大试验(联合多标志物筛查和随机患者阿司匹林治疗用于基于证据的子痫前期预防)中观察到的早产子痫前期减少(n=1620;相对风险,0.38;95%置信区间,0.20-0.72)与阿司匹林起始于≤16 周妊娠且日剂量≥100mg 的 5 项较小试验(n=639;相对风险,0.22;95%置信区间,0.07-0.66)中观察到的减少相似。
阿司匹林可降低早产子痫前期的风险,但不能降低足月子痫前期的风险,而且只有在治疗开始于≤16 周妊娠且日剂量≥100mg 时才有效。