Fetoscopic Release of Amniotic Bands Based on the Evidence-A Systematic Review.

IF 2.7 2区 医学 Q2 GENETICS & HEREDITY
Prenatal Diagnosis Pub Date : 2024-07-30 DOI:10.1002/pd.6636
Fernando Ferrer-Marquez, Jose L Peiro, Gabriele Tonni, Rodrigo Ruano
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引用次数: 0

Abstract

The purpose of this review is to provide an overview of the perinatal outcomes of fetuses who underwent fetal surgery for the management of Amniotic Band Syndrome (ABS). A systematic review of studies reporting on the perinatal outcome of fetuses undergoing fetoscopic release of amniotic bands according to the (PRISMA) guidelines was performed. The MEDLINE, Embase, Scopus, and Cochrane Library databases were systematically searched. In total, 17 studies reporting 37 cases of ABS that underwent amniotic band release by fetoscopy were included. The median gestational age at which fetal surgery was performed was 22 weeks (range 18-29 weeks). PPROM occurred in 51.3%, while fetal survival reached 89.2%. The success of fetal surgery was 75.7% in preserving and maintaining the functionality of the affected limb. Fetoscopic release of amniotic bands can preserve the affected limb and its function in cases of ABS and prevent fetal death in cases of ABS involving the umbilical cord. Further studies are needed to determine the optimal criteria for selecting patients who can benefit from fetal surgery, considering that it is an intervention that is not free of perinatal complications.

基于证据的胎儿镜羊膜带松解术--系统性综述。
本综述旨在概述为治疗羊膜带综合征(ABS)而接受胎儿手术的胎儿的围产期结局。根据(PRISMA)指南,对接受胎儿镜羊膜带松解术的胎儿围产期结局的研究报告进行了系统性回顾。系统检索了 MEDLINE、Embase、Scopus 和 Cochrane Library 数据库。共纳入了 17 项研究,报告了 37 例通过胎儿镜进行羊膜带松解术的 ABS 病例。进行胎儿手术的中位胎龄为 22 周(范围为 18-29 周)。51.3%的胎儿发生了早产,而胎儿存活率达到了89.2%。在保留和维持患肢功能方面,胎儿手术的成功率为 75.7%。胎儿镜下羊膜带松解术可保留 ABS 病例中的患肢及其功能,并可防止脐带受累的 ABS 病例中的胎儿死亡。考虑到胎儿手术并非没有围产期并发症,因此还需要进一步研究,以确定选择胎儿手术受益患者的最佳标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Prenatal Diagnosis
Prenatal Diagnosis 医学-妇产科学
CiteScore
5.80
自引率
13.30%
发文量
204
审稿时长
2 months
期刊介绍: Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling
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