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产后长QT综合征和扩张型心肌病导致的心源性猝死

Sudden Cardiac Arrest in the Postpartum Period Due to Long QT Syndrome and Dilated Cardiomyopathy.

作者信息

Patterson Daniel R, Pan Jonathan A, Hosadurg Nisha, Morsy Mohamed

机构信息

University of Virginia, Charlottesville, Virginia, USA.

出版信息

JACC Case Rep. 2023 May 16;16:101882. doi: 10.1016/j.jaccas.2023.101882. eCollection 2023 Jun 21.

DOI:10.1016/j.jaccas.2023.101882
PMID:37396328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10313482/
Abstract

We describe the case of a previously healthy patient presenting with sudden cardiac arrest in the postpartum period as a result of concomitant congenital type 1 long QT syndrome and dilated cardiomyopathy. This case highlights the increased rate of cardiac events for patients with long QT syndrome in the postpartum period. ().

摘要

我们描述了一例既往健康的患者，该患者在产后因先天性1型长QT综合征合并扩张型心肌病而出现心脏骤停。该病例突出了产后长QT综合征患者心脏事件发生率的增加。（）

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/626e/10313482/8ab562ec7e6f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/626e/10313482/3a62bdc7fdb0/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/626e/10313482/019e28db403c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/626e/10313482/8ab562ec7e6f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/626e/10313482/3a62bdc7fdb0/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/626e/10313482/019e28db403c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/626e/10313482/8ab562ec7e6f/gr2.jpg

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本文引用的文献

1
Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes.冠心病、扩张型心肌病和特发性室性心动过速患者在心脏风险基因中存在重叠的致病变异模式。
PeerJ. 2021 Jan 19;9:e10711. doi: 10.7717/peerj.10711. eCollection 2021.
2
Cardiac Magnetic Resonance in Sudden Cardiac Arrest Survivors.心脏骤停幸存者的心脏磁共振成像
Circ Cardiovasc Imaging. 2017 Dec;10(12):e007290. doi: 10.1161/CIRCIMAGING.117.007290.
3
Diagnosis and Prognosis in Sudden Cardiac Arrest Survivors Without Coronary Artery Disease: Utility of a Clinical Approach Using Cardiac Magnetic Resonance Imaging.
无冠状动脉疾病的心脏骤停幸存者的诊断与预后：应用心脏磁共振成像的临床方法的效用
Circ Cardiovasc Imaging. 2017 Dec;10(12):e006709. doi: 10.1161/CIRCIMAGING.117.006709.
4
Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report.一名携带KCNQ1突变儿童的家族性长QT综合征及扩张型心肌病的晚期发展：病例报告
HeartRhythm Case Rep. 2015 Dec 18;2(2):128-131. doi: 10.1016/j.hrcr.2015.10.011. eCollection 2016 Mar.
5
The BAG3 gene variants in Polish patients with dilated cardiomyopathy: four novel mutations and a genotype-phenotype correlation.波兰扩张型心肌病患者的BAG3基因变异：四个新突变及基因型-表型相关性
J Transl Med. 2014 Jul 9;12:192. doi: 10.1186/1479-5876-12-192.
6
Long-QT syndrome: from genetics to management.长QT综合征：从遗传学到治疗
Circ Arrhythm Electrophysiol. 2012 Aug 1;5(4):868-77. doi: 10.1161/CIRCEP.111.962019.
7
Long QT syndrome and dilated cardiomyopathy with SCN5A p.R1193Q polymorphism: cardioverter-defibrillator implantation at 27 months.长QT综合征与伴有SCN5A基因p.R1193Q多态性的扩张型心肌病：27个月时植入心脏复律除颤器
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