首页> 外文期刊>Journal of Emergency Medicine, Trauma and Acute Care >Read between the lines – Subtle ECG changes to be recognised as a risk factor for sudden cardiac death
【24h】

Read between the lines – Subtle ECG changes to be recognised as a risk factor for sudden cardiac death

机译:仔细阅读-心电图的细微变化被认为是心脏猝死的危险因素

获取原文
           

摘要

Background: Although the majority of sudden cardiac deaths (SCD) are due to CAD and poor LVEF, there is a considerable fraction of idiopathic ventricular fibrillation (IVF) causing SCD that is secondary to channelopathies and other inherited arrhythmias. Objective: The present report aims to raise awareness about the prevalence of inherited arrhythmogenic disorders, besides the commonly attributed CAD causing SCD. Case report: We report the case of a patient with a history of sudden collapse after routine duty. He had ventricular fibrillation and was successfully defibrillated to normal sinus rhythm. On examination, he was found to have a structurally normal heart, and the ECG showed early repolarisation (ERPS) with a short QT interval. Review of the literature: SCD is defined as IVF in the absence of an identifiable cause. IVF could be the manifestation of concealed forms of arrhythmogenic disorders exacerbated by appropriate triggers. Long QT syndrome presents with structurally normal heart, QT prolongation, syncope, and SCD. Incomplete penetrance gene presents as Brugada syndrome, short QT syndrome, ERPS, sinus node dysfunction, and progressive conduction defects. Subtle ECG changes may be present, which, if identified early, can lead to further focused evaluation, leading to the prevention of a potentially life-threatening arrhythmia. ECG changes that should be looked for include: ERPS changes, especially in the inferior and lateral leads, ‘Rs’ in the inferior leads – >2?mm deep in lead II, small slurred S wave in the inferior leads, incomplete or complete RBBB with J point elevation and coved ST segment in V1 and V2 for Brugada, and long or short QT interval. Conclusion/summary: It is important to recognise channelopathies causing SCD. This is because a majority of these channelopathies are ‘inherited’ and can cause more deaths in the family. Such potential information obtained from ECG features can help categorise patients as ‘suspected high-risk’ and provide appropriate advice.
机译:背景:尽管大多数心脏性猝死(SCD)是由于CAD和LVEF差所致,但仍有相当一部分特发性室颤(IVF)导致SCD继发于通道病和其他遗传性心律不齐。目的:本报告旨在提高人们对遗传性心律失常性疾病患病率的认识,除了引起CAD的普遍归因于SCD之外。病例报告:我们报告例行常规工作后突然虚脱的患者。他患有心室纤颤,并已成功除颤,恢复了正常的窦性心律。经检查,他的心脏结构正常,心电图显示早期复极(ERPS),QT间隔短。文献回顾:在没有可查明原因的情况下,SCD被定义为IVF。 IVF可能是适当诱因加重了隐性形式的心律失常性疾病的表现。长QT综合征表现为心脏结构正常,QT延长,晕厥和SCD。不完整的外显基因表现为Brugada综合征,QT短综合征,ERPS,窦房结功能障碍和进行性传导缺陷。可能存在细微的ECG变化,如果及早发现,可能会导致进一步的重点评估,从而预防潜在的危及生命的心律失常。应寻找的ECG改变包括:ERPS改变,尤其是在下和横向导线中,下导线中的“ Rs” –导线II中的深度大于2?mm,在下导线中有小的S浆状S波,不完全或完整的RBBB对于Brugada,在V1和V2中具有J点高程和弯曲的ST段,QT间隔长或短。结论/总结:重要的是认识引起SCD的通道病。这是因为这些通道病变大多数是“遗传性的”,并可能导致更多的家庭死亡。从ECG功能获得的此类潜在信息可帮助将患者归类为“可疑的高风险”并提供适当的建议。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号