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[出生后第一年的主动脉缩窄及相关异常。超声心动图诊断]

[Aortic coarctation and associated abnormalities in the first year of life. Echocardiographic diagnosis].

作者信息

Carminati M, Valsecchi O, Borghi A, Balduzzi A, Pignatelli R, De Tommasi S M, Pedretti E, Bande A, Tiraboschi R, Parenzan L

出版信息

G Ital Cardiol. 1985 Apr;15(4):400-6.

PMID:4043641
Abstract

Thirty-eight cases of "Aortic Coarctation Syndrome" presenting in the first year of life (66% under 3 months of age) were studied with cross-sectional echocardiography. Direct imaging of the coarctation was achieved in 75% of cases. Patent ductus arteriosus was present in 60% (80% before three months). Associated anomalies were present in 63%; VSD 29%, Aortic stenosis 16%, Mitral stenosis 16%, AV Canal 5%, Taussig Bing type of DORV 5%, Corrected transposition with VSD 3%, Ebstein anomaly 3%, Univentricular A-V connection 3%. The results were compared with angiographic and/or surgical and/or autoptic findings. The echocardiographic diagnosis proved to be very reliable in most cases. The policy of sending to surgery most neonates and infants with coarctation of the aorta without preoperative catheterization is discussed.

摘要

对38例在出生后第一年内出现的“主动脉缩窄综合征”病例(66%在3个月龄以下)进行了横断面超声心动图研究。75%的病例实现了对缩窄的直接成像。60%的病例存在动脉导管未闭(3个月前为80%)。63%的病例存在相关异常;室间隔缺损29%,主动脉狭窄16%,二尖瓣狭窄16%,房室通道5%,陶西格-宾型右心室双出口5%,矫正型大动脉转位合并室间隔缺损3%,埃布斯坦畸形3%,单心室房室连接3%。将结果与血管造影和/或手术和/或尸检结果进行了比较。超声心动图诊断在大多数情况下被证明非常可靠。讨论了在不进行术前导管插入术的情况下,将大多数患有主动脉缩窄的新生儿和婴儿送去手术的策略。

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