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胎儿期及出生后静脉导管缺如的生理影响。

The physiological implications of absent ductus venosus during fetal and post-natal life.

作者信息

Bakhru Shweta, Koneti Nageswara Rao

机构信息

Department of Pediatric Cardiology, Rainbow Children's Heart Institute, Hyderabad, Telangana, India.

出版信息

Ann Pediatr Cardiol. 2024 Jul-Aug;17(4):257-263. doi: 10.4103/apc.apc_93_24. Epub 2024 Nov 15.

DOI:10.4103/apc.apc_93_24
PMID:39698422
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11651408/
Abstract

BACKGROUND

The ductus venosus (DV) is a pivotal component of fetal circulation. Absent DV (ADV) is associated with structural defects, portal vein (PV) anomalies, and chromosomal anomalies. This observational study aims to investigate the impact of ADV on fetal circulation and postnatal outcomes.

MATERIALS AND METHODS

This observational study was conducted from August 2016 to January 2020 at a fetal and pediatric cardiac center. The DV was evaluated as part of routine fetal echocardiography. Cases of ADV were identified. Blood flow and exit points of the umbilical vein were studied. Cardiothoracic ratio, hydrops, and PV were assessed during the initial and follow-up scans. The postnatal evaluation included an ultrasound abdomen and computed tomography with triple-phase imaging to assess portosystemic shunts (PSSs). Serum ammonia levels were monitored.

RESULTS

Twelve patients with ADV were identified. The median maternal age and median gestational age were 27.5 years and 22 weeks, respectively. Four patients had intrahepatic drainage, while eight had extrahepatic drainage. All patients (100%) exhibited cardiomegaly, but none developed hydrops. Four patients had persistent PSS postnatally. All four patients with PSS had asymptomatic hyperammonemia. Two patients underwent transcatheter closure of PSS. The intrahepatic variant showed good PV anatomy with no evidence of PSS.

CONCLUSIONS

DV evaluation should be performed during fetal echocardiography. ADV can lead to cardiomegaly and dilation of the right atrium and ventricle. PSS can be a potential sequela of the extrahepatic variant of ADV.

摘要

背景

静脉导管(DV)是胎儿循环的关键组成部分。静脉导管缺如(ADV)与结构缺陷、门静脉(PV)异常和染色体异常有关。本观察性研究旨在探讨ADV对胎儿循环及出生后结局的影响。

材料与方法

本观察性研究于2016年8月至2020年1月在一家胎儿及小儿心脏中心进行。DV作为常规胎儿超声心动图检查的一部分进行评估。确定ADV病例。研究脐静脉的血流及出口点。在初次及随访扫描时评估心胸比、水肿及PV情况。出生后评估包括腹部超声及三相成像计算机断层扫描以评估门体分流(PSS)。监测血清氨水平。

结果

确定了12例ADV患者。母亲年龄中位数和孕周中位数分别为27.5岁和22周。4例为肝内引流,8例为肝外引流。所有患者(100%)均有心脏扩大,但均未出现水肿。4例患者出生后有持续性PSS。所有4例有PSS的患者均有无症状高氨血症。2例患者接受了经导管PSS封堵术。肝内型显示PV解剖结构良好,无PSS证据。

结论

胎儿超声心动图检查时应进行DV评估。ADV可导致心脏扩大及右心房和右心室扩张。PSS可能是ADV肝外型的潜在后遗症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/11651408/3f5a9434ea0d/APC-17-257-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/11651408/9dfceaa3b295/APC-17-257-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/11651408/d5a82431e0ff/APC-17-257-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/11651408/a731ea86ec2c/APC-17-257-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/11651408/3f5a9434ea0d/APC-17-257-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/11651408/9dfceaa3b295/APC-17-257-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/11651408/42ce66317f59/APC-17-257-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337f/11651408/3f5a9434ea0d/APC-17-257-g007.jpg

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