Fetal lung volume and pulmonary artery changes in congenital heart disease with decreased pulmonary blood flow: Quantitative ultrasound analysis

被引:6
|
作者
Guo, Yong [1 ]
Liu, Xiaowei [1 ]
Gu, Xiaoyan [1 ]
Zhang, Ye [1 ]
Sun, Lin [1 ]
He, Yihua [1 ]
机构
[1] Capital Med Univ, Beijing An Zhen Hosp, Beijing Key Lab Maternal Fetal Med Fetal Heart Di, Dept Ultrasound, Beijing, Peoples R China
关键词
congenital heart disease; fetal echocardiography; pulmonary artery; three-dimensional echocardiography; BODY-WEIGHT RATIO; DIAPHRAGMATIC-HERNIA; 3-DIMENSIONAL ULTRASOUND; HYPOPLASIA; TETRALOGY; ATRESIA; FALLOT;
D O I
10.1111/echo.13724
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundIt has been reported that congenital heart disease with decreased pulmonary blood flow (CHD-DPBF) may affect postnatal lung morphogenesis and function. However, there has been a lack of information regarding the impact of CHD-DPBF on prenatal fetal lung development. MethodsFifty-four fetuses with CHD-DPBF were compared with 110 controls. Fetal lung volume (FLV) was estimated using three-dimensional ultrasonography (3D-US). Estimated fetal weight (EFW) and McGoon index (MGI) were estimated using two-dimensional ultrasonography (2D-US). ResultsFLV/EFW and MGI values measured using sonography for the CHD-DPBF group were significantly reduced compared to those of the control group (P<.05). Pearson correlation analysis indicated that the summed diameter of the right pulmonary artery and left pulmonary artery (RPA+LPA) measured by 2D-US correlated well with FLV measured by 3D-US. ConclusionsIn our study, FLV/EFW and MGI values for fetuses with CHD-DPBF tended to be decreased and FLV was associated with RPA+LPA. We concluded that CHD-DPBF might delay fetal lung development. The summed diameter of the RPA+LPA measurement could be used as an alternative to FLV for assessing fetal lung development.
引用
收藏
页码:85 / 89
页数:5
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