盖伦静脉畸形胎儿的心血管特征评分(CVPS)和选择的心脏参数。

Aleksandra Juras, Tomasz Wloch, Wojciech Cnota, Agata Wloch
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引用次数: 0

摘要

目的:盖伦静脉畸形(VGAM)是一种罕见的先天性脑血管畸形。早期发现和监测VGAM并发胎儿心力衰竭对改善预后至关重要。该研究旨在评估心脏解剖、心脏收缩和舒张功能,以及由于妊娠中期或晚期检测到VGAM而转介到三级中心的胎儿心力衰竭的指标。材料和方法:本研究对2008年至2023年间5例VGAM胎儿的超声心动图数据进行了单中心回顾性研究。分析的参数包括胎龄、转诊原因、心血管谱评分(CVPS)、心脏收缩和舒张功能以及选择的心脏参数。结果:心脏肥大作为充血性心力衰竭的标志是我中心大多数胎儿(4/5 - 80%)后来诊断为VGAM的转诊的主要原因。所有病例均见脑血管血流异常,脐动脉血流正常。由于充血性心力衰竭,三个胎儿在产前用地高辛治疗。在诊断时观察到三个胎儿(60%)单相三尖瓣流入和缩短分数(SF)下降。CVPS评分范围从2到10,与心脏损害的严重程度相关。5名患者全部死亡,其中3名在子宫内死亡,2名在出生后不久死亡。结论:本研究强调了子宫内检测到的VGAM对心脏的严重影响以及早期和全面的胎儿评估的必要性。尽管早期诊断,结果仍然很差,需要进一步研究有效的产前治疗和管理方案,以提高影响胎儿的存活率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiovascular profile score (CVPS) and selected cardiac parameters in fetuses with Vein of Galen Malformation.

Objectives: Vein of Galen Malformation (VGAM) is a rare congenital cerebrovascular anomaly. Early detection and monitoring of concurrent fetal heart failure in VGAM are crucial for improving outcomes. The study aims to evaluate heart anatomy, systolic and diastolic heart function, and indicators of heart failure in fetuses referred to a tertiary center due to VGAM detected in the second or third trimester.

Material and methods: This single-center retrospective study of echocardiographic data from five fetuses with VGAM examined between 2008 and 2023. Parameters analyzed included gestational age, reason for referral, cardiovascular profile score (CVPS), systolic and diastolic heart function and selected cardiac parameters RESULTS: Cardiomegaly as a sign of congestive heart failure was the main reason for referral most of the fetuses (4/5 - 80%) diagnosed later as VGAM in our center. Abnormal cerebral vessel flow was visualized in all cases, with normal umbilical arterial flow. Three fetuses were treated prenatally with digoxin due to congestive heart failure. Monophasic tricuspid valve inflow and decreased shortening fraction (SF) were observed in three fetuses (60%) at the time of diagnosis. CVPS scores ranged from 2 to 10, correlating with the severity of cardiac compromise. All five patients demised, three died in utero, and two shortly after birth.

Conclusions: This study emphasizes the severe cardiac implications of VGAM detected in utero and the need for early and comprehensive fetal assessment. Despite early diagnosis, outcomes remain poor, necessitating further research into effective prenatal treatments and management protocols to enhance survival for affected fetuses.

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