成像胎儿主动脉弓及其分支模式在中期筛查人群。

IF 2.9 3区 医学 Q1 ACOUSTICS
Ultraschall in Der Medizin Pub Date : 2025-10-01 Epub Date: 2025-02-27 DOI:10.1055/a-2548-2411
Manuela Tavares de Sousa, Bettina Hergert, Fatima Crispi, Olga Gomez, Kurt Hecher
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引用次数: 0

摘要

最近发现,主动脉弓分支的变异对接受胸主动脉手术干预(如主动脉缩窄修复)的新生儿有影响。在产前有6%的人被描述过,而在产后有26%的人被描述过。为了探讨是否分支变异可能在子宫内被诊断不足,我们全面评估了妊娠19至22周的低风险人群的主动脉弓及其分支模式。材料与方法本前瞻性队列研究纳入139例低风险单胎妊娠。在一个标准化的胎儿超声心动图,我们调查了主动脉弓矢状视图根据预定的标志。基于视频片段,由两个互不知情的操作者将其分支模式分为正常分支和分支变体。结果139例患者中127例(91.4%)实现了主动脉弓分支的分类。正常型103例(81.1%),分支型24例(18.9%)。两位操作者都同意使用18条肱二头躯干(即所谓的牛弓)。4条左椎动脉异常,1条主动脉弓伴5条分支血管,1例变异类型不一致。结论产前靶向超声心动图可识别低危人群18.9%的主动脉弓分支变异。未来的研究需要评估我们的发现对新生儿先天性心脏缺陷的临床影响。[文献来源]Gefäßvarianten der thorakalen Aortenabgänge wurden als Risikofaktoren f r Neugeborene identifiziert, die eine Intervention der Aorta, zum Beispiel bei aortenisthmusenose, vor . hahn .]Pränatal wurde die Häufigkeit mit bis zu 6% beschrieben, während sie postnatal in bis zu 26% gefunden wurden。在妊娠期妊娠期,妊娠期妊娠期,妊娠期妊娠期,妊娠期妊娠期,妊娠期,妊娠期,妊娠期,妊娠期,妊娠期。材料和方法:前瞻性kohortens研究[j]。Während先天性标准胎儿超声心动图显示矢状位Ebene的主动脉瓣发育异常。andhand von Videoclips wurden die Abgänge des Aorta von zwei Untersuchenden, die zueinander verblindet waren, entweder als normales abgangsmaster oder als Variante classifiziert。ergebnese: Die Klassifizierung des Abgänge der胎儿主动脉gelang in 127/139 (91.4%) Fälle。2003年Fällen(81.1%)发现wurde ein normales Abgangsmuster bebacachtet, während(189%)发现Variante vorlag。In 18 Fällen wurde ein Truncus brachicephalicus (SOGENANNTER BOVINER AORTENBOGEN); In 4 Fällen eine aberrante linke椎动脉和einem Fall In AORTENBOGEN mitfnf abgehenden Gefäßen gefunden。在einem Fall waren die Untersuchenden bezglich der Variante uneiing。[2] [2] [1] [1] [1] [1] [1] [1] [1] [1] [1] [1] [2] [1] [2] [1] [1] [1] [1] [1] [1] [1] [1] [1] [1] [1] [1]zukftige学生学习如何学习,如何学习新知识,如何学习新知识,如何学习新知识,如何学习新知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Imaging the fetal aortic arch and its branching pattern in a mid-trimester screening population.

Aortic arch branching variants have recently been found to have an impact in neonates undergoing surgical interventions involving the thoracic aorta such as aortic coarctation repair. They have been described prenatally in 6% of neonates, whereas they occur in up to 26% postnatally. To explore whether the branching variations might have been underdiagnosed in utero, we comprehensively assessed the aortic arch and its branching patterns in a low-risk population between the 19th and 22nd week of gestation.This prospective cohort study included 139 low-risk singleton pregnancies. During a standardized fetal echocardiography examination, we investigated the aortic arch in a sagittal view according to predefined landmarks. Based on video clips, its branching pattern was categorized as normal branching or branching variants by 2 operators who were blinded to each other.Classification of aortic arch branching was achieved in 127/139 cases (91.4%). 103 cases (81.1%) showed a normal pattern, and 24 cases (18.9%) showed a branching variant. Both operators agreed on 18 brachiobicephalic trunks (the so-called bovine arch), 4 aberrant left vertebral arteries, 1 aortic arch with 5 branching vessels. In 1 case there was disagreement regarding the type of variant.Prenatal targeted echocardiography could identify 18.9% prevalence of aortic arch branching variants in a low-risk population. Future studies are warranted to assess the clinical impact of our findings on neonates with congenital heart defects.

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来源期刊
Ultraschall in Der Medizin
Ultraschall in Der Medizin 医学-核医学
CiteScore
5.30
自引率
8.80%
发文量
228
审稿时长
6-12 weeks
期刊介绍: Ultraschall in der Medizin / European Journal of Ultrasound publishes scientific papers and contributions from a variety of disciplines on the diagnostic and therapeutic applications of ultrasound with an emphasis on clinical application. Technical papers with a physiological theme as well as the interaction between ultrasound and biological systems might also occasionally be considered for peer review and publication, provided that the translational relevance is high and the link with clinical applications is tight. The editors and the publishers reserve the right to publish selected articles online only. Authors are welcome to submit supplementary video material. Letters and comments are also accepted, promoting a vivid exchange of opinions and scientific discussions.
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