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严重右心室流出道梗阻时动脉导管缺如的血管造影证据。

Angiographic evidence of absent ductus arteriosus in severe right ventricular outflow obstruction.

作者信息

Lacina S J, Hamilton W T, Thilenius O G, Bharati S, Lev M, Arcilla R A

出版信息

Pediatr Cardiol. 1983 Jan-Mar;4(1):5-11. doi: 10.1007/BF02280999.

Abstract

The angiocardiograms of 5 newborn infants with autopsy and/or surgically-proven congenital absence of the ductus arteriosus (ADA) and right ventricular outflow obstruction (Group A), and of 14 neonates with pulmonary atresia complex and patent ductus arteriosus (Group B) were reviewed. Aortic size was similar in both groups; however, the diameters of the right and left pulmonary arteries were much smaller in Group A than in Group B (right pulmonary artery: 2.6 vs 4.5 mm, P less than 0.005; left pulmonary artery: 2.5 vs 4.3 mm, P less than 0.005). Extensive bronchial collaterals were observed in Group A but not in Group B. Tricuspid aortic valve stenosis was present in 2 patients in Group A but in none in Group B. The diagnosis of ADA may be made in newborn infants with severe right ventricular outflow obstruction if the angiocardiograms reveal hypoplasia of the pulmonary arteries, extensive bronchial collaterals, and nonvisualization of the ductus arteriosus. Other suggestive features include aortic valve stenosis and/or right aortic arch with aberrant left subclavian artery.

摘要

回顾了5例经尸检和/或手术证实患有动脉导管先天性缺如(ADA)及右心室流出道梗阻的新生儿(A组),以及14例患有肺动脉闭锁合并动脉导管未闭的新生儿(B组)的心血管造影图。两组的主动脉大小相似;然而,A组的右肺动脉和左肺动脉直径比B组小得多(右肺动脉:2.6对4.5mm,P<0.005;左肺动脉:2.5对4.3mm,P<0.005)。A组观察到广泛的支气管侧支循环,而B组未观察到。A组有2例患者存在三尖瓣主动脉瓣狭窄,而B组无。如果心血管造影显示肺动脉发育不全、广泛的支气管侧支循环以及动脉导管不显影,则可对患有严重右心室流出道梗阻的新生儿做出ADA的诊断。其他提示性特征包括主动脉瓣狭窄和/或伴有异常左锁骨下动脉的右主动脉弓。

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