Publication:
Early fetal heart ultrasonography as additional indicator for chromosomopathies

dc.contributor.authorDmitrovic, A. (56341041400)
dc.contributor.authorJeremic, K. (6701486495)
dc.contributor.authorBabic, U.M. (57189327647)
dc.contributor.authorPerovic, M. (36543025300)
dc.contributor.authorMihailovic, T. (36098086700)
dc.contributor.authorOpric, D. (6506600388)
dc.contributor.authorZecevic, N. (57198208547)
dc.contributor.authorGojnic-Dugalic, M. (9434266300)
dc.date.accessioned2025-06-12T18:59:11Z
dc.date.available2025-06-12T18:59:11Z
dc.date.issued2016
dc.description.abstractObjective: First trial of estimating values of scans of fetal heart structures (FHS) in first trimester of pregnancy, as more primary facts of possible chromosomopathies. Materials and Methods: The study included 2,643 fetuses that were examined in first trimester of pregnancy on Sono CT convex (C5-2MHz), endovaginal (ev 8-4MHz), and linear transducers (L12-5MHz) during a period of eight years. Fetal heart was evaluated using appropriate software with broad-band transducers and color Doppler, Sono CT, and HD ZOOM technologies. The scan was performed by three experienced physicians. FHS were based on: left and right ventricle morphology; AV valves (atrioventricular) position and existence of primal ostium; relationship of left ventricle outflow tract (LVOT) and right ventricle outflow tract (RVOT) and great vessels on three vessel view (3VV) and estimation of ductal and aortic arch. Results: Several developments, one being the ability to identify fetuses at risk for cardiac defects combining nuchal translucency (NT), ductus venosus (DV) Doppler, and evaluation of tricuspid regurgitation, have prompted reconsideration of the role of the first trimester prognostic factor of fetal evaluation. In low-risk pregnancies group, 36 (1.8%) fetuses were found to have congenital heart disease (CHD), and in high-risk pregnancies the number of fetuses with CHD was 75 (12%). Genetic amniocentesis or chorionic villus sampling (CVS) was performed in all fetuses with CHD. Forty-two (37.8%) fetuses with CHD were found to have chromosomal anomalies. Out of 111 fetuses with CHD 39 (35.1%) had an nuchal translucency (NT) above three mm. Out of 42 fetuses with chromosomal anomalies and CHD, 29 (69%) had an increased NT. Conclusion: Using first trimester fetal echosonography constitutes a further step in the earlier recognition of chromosomopathies, even in low risk groups. Still further steps are necessary as all facts of good clinical practice. In order to offer further benefits during pregnancies, improvements in diagnostics are still required.
dc.identifier.urihttps://doi.org/10.12891/ceog2091.2016
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84969246691&doi=10.12891%2fceog2091.2016&partnerID=40&md5=cc8a19d0465f0c81e76852cfd44dcd89
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/7892
dc.subjectCardiac defects
dc.subjectChromosomopathies
dc.subjectEarly diagnosis
dc.subjectFetal echocardiography
dc.subjectFirst trimester
dc.titleEarly fetal heart ultrasonography as additional indicator for chromosomopathies
dspace.entity.typePublication

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