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Network meta-analysis of LMWH and aspirin for high-risk singleton pregnancies with fetal growth restriction

Network meta-analysis of LMWH and aspirin for high-risk singleton pregnancies with fetal growth rest…
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Key Takeaway
Consider LMWH or LMWH+aspirin for high-risk FGR, noting significant risk reductions but missing safety data.

This network meta-analysis assessed the efficacy of low-molecular-weight heparin (LMWH) alone, the combination of LMWH plus low-dose aspirin (LDA), and control or LDA alone in singleton pregnancies at high risk of fetal growth restriction. The scope included secondary outcomes such as intrauterine growth restriction, preeclampsia, preterm birth, miscarriage, cesarean section, and live birth rate.

Significant reductions in intrauterine growth restriction were observed with LMWH (OR = 0.40, 95% CI = 0.26–0.62) and the combination therapy (OR = 0.37, 95% CI = 0.15–0.93) compared with control and LDA alone. Preeclampsia risk was significantly decreased with LMWH monotherapy (OR = 0.21, 95% CI = 0.05–0.93) and combination therapy (OR = 0.22, 95% CI = 0.08–0.59). Preterm birth risk was significantly decreased with LMWH monotherapy (OR = 0.61, 95% CI = 0.45–0.81), while miscarriage risk was significantly decreased with LMWH monotherapy (OR = 0.42, 95% CI = 0.19–0.91). Cesarean section risk was significantly decreased with LMWH monotherapy (OR = 0.34, 95% CI = 0.18–0.67). Live birth rate was significantly improved with the combination of LMWH + LDA (OR = 7.08, 95% CI = 2.16–23.22).

The authors note that absolute numbers, safety data, and follow-up duration were not reported. As a meta-analysis, the results synthesize existing evidence but do not establish causality. Practice relevance remains uncertain given the lack of safety and absolute risk data.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
BackgroundFetal growth restriction (FGR) is a common pregnancy complication associated with adverse maternal and fetal outcomes. Effective pharmacological interventions are essential for enhancing fetal growth and mitigating related complications. This study aimed to evaluate and compare the efficacy of various pharmacological treatments for FGR using a network meta-analysis (NMA).ObjectiveTo systematically evaluate and compare the effectiveness of different pharmacological interventions for FGR via a network meta-analysis (NMA).StrategyA comprehensive literature search was performed in PubMed, Medline, Embase, PsycINFO, the Cochrane Central Register of Controlled Trials, and Web of Science. The search was updated through 31 January 2026, to ensure the inclusion of the most recent evidence.Selection CriteriaEligible studies included singleton pregnancies at high risk of FGR. Studies were excluded if they involved multiple pregnancies, fetal genetic abnormalities, or maternal comorbidities such as drug or alcohol abuse.Data Collection and AnalysisA systematic review and network meta-analysis were conducted in strict accordance with the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines to ensure methodological rigor.Main ResultsCompared with the control group and low-dose aspirin (LDA) alone, low-molecular-weight heparin (LMWH) and the combination of LMWH + LDA significantly reduced the incidence of intrauterine growth restriction (IUGR) (odds ratio [OR] = 0.40, 95% confidence interval [CI] = 0.26–0.62; OR = 0.37, 95% CI = 0.15–0.93, respectively). Additionally, LMWH monotherapy significantly decreased the risk of several pregnancy complications, including preeclampsia (OR = 0.21, 95% CI = 0.05–0.93), preterm birth (OR = 0.61, 95% CI = 0.45–0.81), miscarriage (OR = 0.42, 95% CI = 0.19–0.91), and cesarean section (OR = 0.34, 95% CI = 0.18–0.67). The combination of LMWH + LDA significantly improved the live birth rate (OR = 7.08, 95% CI = 2.16–23.22) and reduced the incidence of preeclampsia (OR = 0.22, 95% CI = 0.08–0.59).ConclusionLMWH and LMWH combined with LDA are effective in reducing IUGR, preventing preeclampsia, and improving live birth rates in high-risk pregnancies complicated by FGR. These findings provide robust evidence supporting the use of LMWH and LMWH + LDA as promising therapeutic options for the management of FGR.Clinical Trial RegistrationPROSPERO registration: CRD420251142968.
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