Komoróczy Balázs, Váncsa Szilárd, Váradi Alex, Hegyi Péter, Vágási Veronika, Baradács István, Szabó Anett, Nyirády Péter, Benkő Zsófia, Ács Nándor
Department of Obstetrics and Gynecology, Semmelweis University, 1085 Budapest, Hungary.
Centre for Translational Medicine, Semmelweis University, 1085 Budapest, Hungary.
J Clin Med. 2025 Mar 21;14(7):2134. doi: 10.3390/jcm14072134.
: This systematic review and meta-analysis aimed to determine the effectiveness of different aspirin dosages in preventing preeclampsia and its effect on other pregnancy-associated conditions. : A comprehensive search of three databases (Pubmed, Embase, and Cochrane Library) was conducted for randomized controlled trials without time interval criteria, comparing aspirin at various doses with placebo or no specific preeclampsia prophylaxis. Eligible randomized controlled trials (RCTs) examined pregnant women receiving aspirin at any dose and time during their pregnancy, while the control group received a placebo, or placebo and a different dose of aspirin, or no specific preeclampsia prevention. No exclusion criteria were established regarding the population, study size, study site, or length of aspirin prophylaxis. Studies examining additional preventive medication (such as low-molecular-weight heparin) compared to aspirin without a placebo group were excluded. For all outcomes, the risk ratios (RRs) and mean differences (MDs) with 95% confidence intervals (CIs) were calculated. Meta-regression was performed to examine the relation between aspirin dosage and preeclampsia. : Based on the analysis of 31 studies involving 28,318 pregnancies and 20 studies involving 26,551 pregnancies, the early initiation of aspirin significantly reduced the overall incidence of preeclampsia (RR = 0.63, CI: 0.47-0.84) and perinatal death risk (RR = 0.82, CI: 0.72-0.93), respectively. Based on our meta-regression model, we could not establish a dose-dependent correlation between aspirin dosage and the risk of preeclampsia. : Early-initiated aspirin prophylaxis is effective in preventing preeclampsia, without raising the incidence of placental abruption or increasing the amount of peripartum bleeding. No specific dose was superior to others; thus, further research should explore higher doses and focus on preterm preeclampsia, maternal-fetal complications, and bleeding.
本系统评价和荟萃分析旨在确定不同剂量阿司匹林预防子痫前期的有效性及其对其他妊娠相关情况的影响。对三个数据库(PubMed、Embase和Cochrane图书馆)进行了全面检索,纳入无时间间隔标准的随机对照试验,比较不同剂量阿司匹林与安慰剂或无特定子痫前期预防措施的效果。符合条件的随机对照试验研究了孕期任何时间接受任何剂量阿司匹林的孕妇,而对照组接受安慰剂、或安慰剂及不同剂量阿司匹林、或无特定子痫前期预防措施。未设定关于研究人群、样本量、研究地点或阿司匹林预防疗程的排除标准。与无安慰剂组的阿司匹林相比,研究其他预防性药物(如低分子量肝素)的研究被排除。对于所有结局指标,计算了风险比(RRs)和平均差(MDs)及其95%置信区间(CIs)。进行了Meta回归分析以检验阿司匹林剂量与子痫前期之间的关系。基于对涉及28318例妊娠的31项研究和涉及26551例妊娠的20项研究的分析,早期使用阿司匹林分别显著降低了子痫前期的总体发生率(RR = 0.63,CI:0.47 - 0.84)和围产期死亡风险(RR = 0.82,CI:0.72 - 0.93)。基于我们的Meta回归模型,无法确定阿司匹林剂量与子痫前期风险之间存在剂量依赖性关联。早期开始使用阿司匹林预防子痫前期有效,且不会增加胎盘早剥的发生率或增加分娩期出血量。没有特定剂量优于其他剂量;因此,进一步研究应探索更高剂量,并关注早产子痫前期、母婴并发症和出血情况。