长QT综合征和其他复极相关的心律失常。

Sarah S Leroy, Mark Russell
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引用次数: 9

摘要

直到最近,年轻人的心源性猝死仍然是一个无法解释的悲剧。然而,在过去的十年里,关于遗传性心律失常增加了健康年轻人SCD风险的医学知识有了巨大的进步。这组心律失常的主要机制似乎是心脏复极的改变。在一些疾病中,受影响的特定基因甚至精确的细胞机制已经被确定。关于这些疾病的信息通常是复杂和快速发展的,这对医疗保健提供者和家庭都是一个挑战,他们必须根据新出现的和不完整的信息做出重要的决定。本文的目的是描述当前对复极相关心律失常的理解,并讨论其对高级执业护士的临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long QT syndrome and other repolarization-related dysrhythmias.

Until recently, sudden cardiac death in a young person often remained an unexplained tragedy. However, in the last decade there have been dramatic advances in medical knowledge regarding inheritable dysrhythmias that increase the risk of SCD in otherwise healthy young individuals. The primary mechanism in this group of dysrhythmias appears to be an alteration of cardiac repolarization. In some diseases, the specific genes affected and even precise cellular mechanisms have been identified. The information about these diseases is often complex and rapidly evolving, challenging both healthcare providers and the families who must make important decisions based on emerging and incomplete information. The purpose of this article is to describe current understanding of the repolarization-related dysrhythmias and discuss the clinical implications for advanced practice nurses.

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