Objective: Congenital diaphragmatic hernia is one of the severe congenital pulmonary anomaly (PA) associated with pulmonary hypoplasia, pulmonary sequestration and severe respiratory distress. The aim of this study was to present difference between measurements of the size of fetal pulmonary artery and pulmonary branches (PB) in normal growth fetuses and comparison with the same in fetuses with congenital diaphragmatic hernia (CHD). Measurements were done by echocardiography. Methodology: During the period March 2007 to March 2009 measurements were performed on a total of 115 normal fetuses, at 20–38 weeks gestation. By cross-sectional echocardiography were measured fetal PA and PB diameters. Retrospectively were reviewed 6 fetuses with left-sided CHD from 2005 to 2009. Measurements were done at level of the three vessel view (superior vena cava, ascending aorta and main PA). Results: Diameter of main PA and both branches were found to correlate with the advanced gestational age (r=0.74, p [Med Arch 2010; 64(6.000): 365-367]

Antenatal echocardiography, pulmonary branch, congenital diaphragmatic hernia, lung hypoplasia, respiratory distress

Medical Archives is official journal of Academy of Medical Sciences 
in Bosnia and Herzegovina
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