The role of ventricular disproportion, aortic, and ductal isthmus ultrasound measurements for the diagnosis of fetal aortic coarctation, in the third trimester of pregnancy

医学 心室 胎儿 胎儿超声心动图 心脏病学 主动脉缩窄 怀孕 超声波 内科学 主动脉 产科 产前诊断 放射科 遗传学 生物
作者
Claudiu Mărginean,Cristina Oana Mărginean,Iolanda Muntean,Rodica Togănel,Septimiu Voidăzan,Liliana Gozar
出处
期刊:Medical ultrasonography [SRUMB - Romanian Society for Ultrasonography in Medicine and Biology]
卷期号:17 (4) 被引量:37
标识
DOI:10.11152/mu.2013.2066.174.rvd
摘要

To analyze the role of ventricular disproportion, aortic, and ductal isthmus ultrasound measurements for the diagnosis of fetal aortic coarctation (AoCo) and to evaluate the prediction of a needed neonatal surgical intervention in the presence of a diagnosis of AoCo.We performed a prospective study on 41 fetuses (pregnancy age- 32 to 39 weeks, median 36 weeks) evaluated for left ventricle (LV) < right ventricle (RV) disproportion. Four fetuses were lost from evidence and five fetuses with complex cardiac malformations were excluded. The remaining group of 32 fetuses and newborns were evaluated.AoCo was confirmed in 9 neonates (28.12%), all requiring surgical treatment in the neonatal period. Significant statistical differences were found in Z-score (p=0.0023) and dimensions (p=0.0029) of the aortic isthmus between the neonates with normal aorta and those with AoCo. If the values of RV/LV>1.5, Ductus/Ao isthmus >1.4, and Ao isthmus <4.2 mm are concomitantly accomplished, 83.3% of the fetuses (20 of 23) did not necessitate neonatal surgical intervention. Five of the 9 operated newborns had all three parameters with values over the threshold. The probability for required surgery is 13.87 times higher when the Ao isthmus is <4.2 mm (OR = 13.87 [95% CI = 1.88 - 102.20]).The use of the combination between the three studied parameters with their cut-off score prediction decreases the false positive diagnosis of AoCo. The fetuses with ventricular disproportion developed only in the last trimester, had reduced chances for AoCo.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
molihuakai应助科研通管家采纳,获得10
1秒前
1秒前
魔幻的新梅完成签到,获得积分10
1秒前
想长胖十斤完成签到,获得积分10
2秒前
MNing完成签到,获得积分20
2秒前
甜心妮完成签到,获得积分10
2秒前
彩虹糖完成签到,获得积分10
2秒前
健壮的冰姬完成签到,获得积分10
3秒前
英姑应助紫色奶萨采纳,获得10
3秒前
wangxz完成签到,获得积分10
3秒前
心累完成签到,获得积分10
4秒前
4466完成签到,获得积分10
4秒前
ss完成签到,获得积分10
5秒前
火星上的百川完成签到,获得积分10
5秒前
简单夜玉完成签到,获得积分10
6秒前
xfyxxh完成签到,获得积分10
7秒前
AllRightReserved应助FZR采纳,获得10
7秒前
kkfly完成签到,获得积分10
7秒前
大队长完成签到,获得积分10
7秒前
香蕉觅云应助77采纳,获得10
7秒前
FFF完成签到 ,获得积分10
7秒前
雪影完成签到 ,获得积分10
7秒前
懵懂的采梦完成签到,获得积分10
7秒前
赵闯完成签到,获得积分10
8秒前
zh_li完成签到,获得积分10
8秒前
小揭发布了新的文献求助10
8秒前
贪玩星完成签到,获得积分10
9秒前
danti完成签到,获得积分10
9秒前
齐云山完成签到,获得积分10
9秒前
9秒前
苹果追命完成签到,获得积分10
9秒前
欣灵应助Xingci采纳,获得30
10秒前
潇洒天抒完成签到,获得积分10
10秒前
黑鲨完成签到 ,获得积分10
10秒前
尊敬的寄松完成签到 ,获得积分10
11秒前
11秒前
跳跃的蝴蝶完成签到,获得积分10
11秒前
198完成签到 ,获得积分10
11秒前
dxt完成签到,获得积分10
12秒前
12秒前
高分求助中
Adhesion Science: Principles & Practice 1234
Signals, Systems, and Signal Processing 610
Introduction to Cosmetic Formulation and Technology, 2nd Edition 400
Petrology and Plate Tectonics,2025 400
Burger's Medicinal Chemistry and Drug Discovery 400
Programming for Chemical Engineers Using C, C++, and MATLAB 320
Birth of Twins After Genome Editing for HIV Resistance 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6689340
求助须知:如何正确求助?哪些是违规求助? 8433130
关于积分的说明 18016643
捐赠科研通 5915335
什么是DOI,文献DOI怎么找? 2984255
邀请新用户注册赠送积分活动 1960276
关于科研通互助平台的介绍 1898418