MAGNETIC RESONANCE IMAGING IN THE ASSESSMENT OF FETAL CENTRAL NERVOUS SYSTEM ANOMALIES

Edina Salkić, F. Julardžija, A. Šehić, M. Jusufbegović, A. Sofić, Meris Jusic, Jasmina Bajrović
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Abstract

Introduction: Fetal central nervous system (CNS) anomalies are among the most severe and common anomalies, with an incidence of 1: 100 to 1: 500 in newborns. Depending on the type of anomaly, the diagnosis can only be made at specifi c periods of pregnancy. The prenatal ultrasound (US) is an eff ective primary imaging modality for depicting these anomalies, and magnetic resonance imaging (MRI) is a method that provides useful confi rmation and resolves any doubts regarding the diagnosis made on prenatal ultrasound. In situations where ultrasound examination is diffi cult, fetal MRI can provide superior information owing to its many advantages. The aim of this study was to determine the importance of prenatal MRI in making an accurate diagnosis and assessment of fetal CNS anomalies after neurosonographic doubt and in detecting additional anomalies that might have been overlooked on ultrasound, which infl uences clinical decision making and anomaly outcomes. Material and methods: For this research, which was designed as a systematic review of the primary scientifi c research literature, numerous articles were used, i.e.17 scientifi c research papers, published in relevant scientifi c research online databases such as PubMed, Medline, Google Scholar, and the same were published in English in the period from 2015 to 2021. Results: From the assessment of the quality of studies with a cohort design, most studies used in this systematic review are high-quality studies (11 in total) and a smaller number are medium-quality studies (6 in total). Out of 575 cases, MRI confi rmed the ultrasound diagnosis and agreed with it in 59.8% of cases, while in 20.2% of cases, it changed the diagnosis, i.e., in 16.5%, it rejected the ultrasound diagnosis. Additional anomalies detected only on MRI occurred in 236/1225 cases, which totals 19.3% of additional anomalies. Termination of pregnancy was reported in 82/317 cases, accounting for 25.9%, while in 176 cases, the pregnancy continued. A total of 11 cases of neonatal death were reported, and the number of stillbirths or deaths after birth was reported in 8 cases. Conclusion: MRI using T2W SSFSE sequences in 3 planes, T1W and DWI in the axial plane, is a complementary modality to prenatal ultrasound in making an accurate diagnosis and assessment of CNS anomalies and detecting associated anomalies previously overlooked on ultrasound. Keywords: fetal magnetic resonance imaging, fetal neurosonography, fetal central nervous system anomalies, prenatal diagnosis.
磁共振成像在胎儿中枢神经系统异常评估中的应用
胎儿中枢神经系统(CNS)异常是最严重和最常见的异常之一,新生儿的发病率为1:100至1:500。根据异常的类型,诊断只能在怀孕的特定时期进行。产前超声(US)是描述这些异常的有效的主要成像方式,而磁共振成像(MRI)是一种提供有用确认并解决有关产前超声诊断的任何疑问的方法。在超声检查困难的情况下,胎儿MRI可以提供优越的信息,因为它有许多优点。本研究的目的是确定产前MRI在神经超声怀疑后准确诊断和评估胎儿中枢神经系统异常以及发现可能被超声忽视的其他异常方面的重要性,这些异常可能会影响临床决策和异常结果。材料与方法:本研究采用了系统回顾初级科研文献的方法,在2015年至2021年期间,使用了大量发表在PubMed、Medline、谷歌Scholar等相关科研在线数据库的科研论文,共计17篇,均为英文。结果:从队列设计研究的质量评价来看,本系统评价中使用的大多数研究为高质量研究(共11项),少数为中等质量研究(共6项)。575例病例中,MRI证实超声诊断并同意的病例占59.8%,改变诊断的病例占20.2%,即拒绝超声诊断的病例占16.5%。1225例中有236例仅在MRI上发现额外异常,占额外异常的19.3%。317例中有82例终止妊娠,占25.9%,176例继续妊娠。总共报告了11例新生儿死亡,8例报告了死产或出生后死亡。结论:T2W SSFSE序列在3个平面上,T1W和DWI在轴向平面上的MRI,是产前超声准确诊断和评估中枢神经系统异常,发现超声忽略的相关异常的补充方式。关键词:胎儿磁共振成像,胎儿神经超声,胎儿中枢神经系统异常,产前诊断。
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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