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房室不一致的频谱。一项临床研究。

The spectrum of atrioventricular discordance. A clinical study.

作者信息

de Albuquerque A T, Rigby M L, Anderson R H, Lincoln C, Shinebourne E A

出版信息

Br Heart J. 1984 May;51(5):498-507. doi: 10.1136/hrt.51.5.498.

Abstract

The clinical, investigative, and surgical findings were reviewed in 47 patients with atrioventricular discordance who presented to the Brompton Hospital between January 1962 and June 1981. Although the unifying feature was the atria connecting to morphologically inappropriate ventricles, the hearts differed widely in other respects. In most cases there was the usual visceral and atrial arrangement, but six had a mirror image arrangement of the atria and viscera. Among those patients with usual atrial arrangement (solitus) the aorta was not always anterior and left sided, and ventricular "inversion" was not invariable. Only 35 of the 47 patients also had a discordant ventriculoarterial connexion, the majority of the remainder having a double outlet right ventricle. The specific diagnosis of atrioventricular discordance depended on echocardiographic and angiographic examination. The other investigations did not distinguish between different ventriculoarterial connexions and were not specific even for the presence of atrioventricular discordance. For those patients with the usual atrial arrangement the anticipated right heart border was present in only just over one third, and the reversal of Q wave progression in the precordial leads of the standard electrocardiogram was found in under a half. Many patients with atrioventricular discordance progressed normally to adult life. In 20 cases no surgery was performed. The results of total correction showed a mortality of 25% (three cases), including two deaths after a modified Fontan procedure for exceedingly complex associated lesions. The results of surgery in the survivors were excellent, and awareness of the disposition of the atrioventricular conduction tissue made it possible to avoid atrioventricular dissociation.

摘要

回顾了1962年1月至1981年6月间在布朗普顿医院就诊的47例房室不一致患者的临床、检查及手术结果。尽管其共同特征是心房与形态学上不匹配的心室相连,但心脏在其他方面差异很大。大多数情况下,内脏和心房排列正常,但有6例心房和内脏呈镜像排列。在那些心房排列正常(正位)的患者中,主动脉并不总是位于前方和左侧,心室“反位”也并非一成不变。47例患者中只有35例同时存在心室动脉连接不一致,其余大多数有右心室双出口。房室不一致的明确诊断依赖于超声心动图和血管造影检查。其他检查无法区分不同的心室动脉连接,甚至对房室不一致的存在也不具有特异性。对于那些心房排列正常的患者,预期的右心缘仅在略超过三分之一的患者中出现,标准心电图胸前导联Q波进展逆转在不到一半的患者中发现。许多房室不一致患者正常成长至成年。20例未进行手术。完全矫正的结果显示死亡率为25%(3例),包括2例在因极其复杂的相关病变行改良Fontan手术后死亡。幸存者的手术结果良好,并且了解房室传导组织的分布使得避免房室分离成为可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28c1/481540/0c72a57bc5ef/brheartj00125-0033-a.jpg

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