Fetal aortic isthmus Doppler assessment to predict the adverse perinatal outcomes associated with fetal growth restriction: systematic review and meta-analysis

医学 静脉导管 荟萃分析 宫内生长受限 研究异质性 相对风险 产科 科克伦图书馆 怀孕 胎儿 内科学 置信区间 心脏病学 生物 遗传学
作者
Marco La Verde,F. Savoia,G. Riemma,A. Schiattarella,A. Conte,S. Hidar,M. Torella,N. Colacurci,P. De Franciscis,M. Morlando
出处
期刊:Archives of Gynecology and Obstetrics [Springer Nature]
标识
DOI:10.1007/s00404-023-06963-4
摘要

Abstract Purpose Fetal growth restriction (FGR) management and delivery planning is based on a multimodal approach. This meta-analysis aimed to evaluate the prognostic accuracies of the aortic isthmus Doppler to predict adverse perinatal outcomes in singleton pregnancies with FGR. Methods PubMed, EMBASE, the Cochrane Library, ClinicalTrials.gov and Google scholar were searched from inception to May 2021, for studies on the prognostic accuracy of anterograde aortic isthmus flow compared with retrograde aortic isthmus flow in singleton pregnancy with FGR. The meta-analysis was registered on PROSPERO and was assessed according to PRISMA and Newcastle–Ottawa Scale. DerSimonian and Laird’s random-effect model was used for relative risks, Freeman-Tukey Double Arcsine for pooled estimates and exact method to stabilize variances and CIs. Heterogeneity was quantified using I 2 statistics. Results A total of 2933 articles were identified through the electronic search, of which 6 studies (involving 240 women) were included. The quality evaluation of studies revealed an overall acceptable score for study group selection and comparability and substantial heterogeneity. The risk of perinatal death was significantly greater in fetuses with retrograde Aortic Isthmus blood flow, with a RR of 5.17 ( p value 0.00001). Similarly, the stillbirth rate was found to have a RR of 5.39 ( p value 0.00001). Respiratory distress syndrome had a RR of 2.64 ( p value = 0.03) in the group of fetuses with retrograde Aortic Isthmus blood flow. Conclusion Aortic Isthmus Doppler study may add information for FGR management. However, additional clinical trial are required to assess its applicability in clinical practice.
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