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复杂紫绀型心脏病双侧动脉导管的处理

Management of bilateral ductus arteriosus in complex cyanotic heart disease.

作者信息

Lenox C C, Neches W H, Zuberbuhler J R, Park S C, Mathews R A, Siewers R D, Lerberg D B, Bahnson H T

出版信息

J Thorac Cardiovasc Surg. 1977 Oct;74(4):607-13.

PMID:904360
Abstract

Bilateral ductus arteriosus (BDA) usually is associated with complex cyanotic heart disease. Since pulmonary valve atresia often is part of the complex, hypoxia may necessitate emergency cardiac catheterization and surgery for these critically ill newborn infants. Optimum management depends on accurate delineation of the intracardiac and great vessel anatomy. Since the ductus arteriosus has a tendency to close spontaneously, the true anatomy of the fourth to sixth aortic arch connections should be determined on the first catheterization. An over-all plan for future care by the medical-surgical team should have been made at the time of the initial surgical procedure. The case histories of four newborn infants with BDA associated with cyanotic heart diseases are reported. The anatomy and basic embryology of the fourth to sixth arch system is reviewed and recommendations for long-term management are given.

摘要

双侧动脉导管(BDA)通常与复杂的青紫型心脏病相关。由于肺动脉瓣闭锁常常是这种复杂病症的一部分,对于这些危重新生儿,缺氧可能需要进行紧急心导管检查和手术。最佳治疗方案取决于对心内结构和大血管解剖的准确描绘。由于动脉导管有自行关闭的倾向,应在首次心导管检查时确定第四至第六主动脉弓连接的真实解剖结构。在内科 - 外科团队进行首次手术时,就应该制定好未来护理的总体计划。本文报告了4例患有与青紫型心脏病相关的BDA的新生婴儿的病例史。回顾了第四至第六弓系统的解剖结构和基本胚胎学,并给出了长期治疗的建议。

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