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首页> 外文期刊>Clinical and experimental obstetrics and gynecology >Early fetal heart ultrasonography as additional indicator for chromosomopathies
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Early fetal heart ultrasonography as additional indicator for chromosomopathies

机译:早期胎儿心脏超声检查可作为染色体病变的附加指标

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摘要

Objective: 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 CUD 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.
机译:目的:作为可能的染色体病的更多主要事实,对估计妊娠前三个月胎儿心脏结构(FHS)扫描值进行评估的第一项试验。资料和方法:该研究包括2643例胎儿,在怀孕的前三个月中,他们在8年的时间里分别在Sono CT凸(C5-2MHz),阴道内(ev 8-4MHz)和线性换能器(L12-5MHz)上进行了检查。使用具有宽带换能器和彩色多普勒,Sono CT和HD ZOOM技术的合适软件评估胎儿心脏。扫描由三位经验丰富的医生进行。 FHS的依据是:左心室和右心室形态; AV瓣膜(房室)的位置和原始口的存在;三血管视图(3VV)评估左心室流出道(LVOT)和右心室流出道(RVOT)与大血管的关系,并评估导管和主动脉弓。结果:多项发展,其中之一是结合颈部半透明(NT),静脉导管(DV)多普勒和三尖瓣关闭不全的鉴定来识别有心脏缺陷风险的胎儿的能力,这促使人们重新考虑妊娠早期妊娠预后因素的作用。胎儿评估。在低风险妊娠组中,发现有先天性心脏病(CHD)的胎儿为36(1.8%),而在高风险妊娠中,有CUD的胎儿为75(12%)。对所有患有冠心病的胎儿进行遗传羊膜穿刺术或绒毛膜绒毛取样(CVS)。发现四十二(37.8%)名患有冠心病的胎儿具有染色体异常。在111名CHD 39的胎儿中(35.1%),其颈部半透明(NT)高于3毫米。在42例具有染色体异常和冠心病的胎儿中,有29例(69%)的NT升高。结论:即使在低危人群中,使用早孕胎儿超声检查技术也能早日识别染色体病。由于良好的临床实践的所有事实,还需要采取进一步的措施。为了在怀孕期间提供进一步的好处,仍然需要改进诊断。

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