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与心肌病患儿不良结局相关的心电图参数

Electrocardiographic Parameters Associated with Adverse Outcomes in Children with Cardiomyopathies.

作者信息

Luczak-Wozniak Katarzyna, Obsznajczyk Klaudia, Niszczota Cezary, Werner Bożena

机构信息

Department of Pediatric Cardiology and General Pediatrics, Doctoral School, Medical University of Warsaw, 02-091 Warsaw, Poland.

Department of Pediatric Cardiology and General Pediatrics, Jozef Polikarp Brudzinski Public Pediatric Hospital, 02-091 Warsaw, Poland.

出版信息

J Clin Med. 2022 Nov 24;11(23):6930. doi: 10.3390/jcm11236930.

DOI:10.3390/jcm11236930
PMID:36498505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9738383/
Abstract

Cardiomyopathies have a low prevalence in children and thus may lead to malignant ventricular arrhythmias or the progression of heart failure, resulting in death. In adults, the QRS-T angle derived from ECG has been associated with adverse outcomes in patients with hypertrophic and dilated cardiomyopathies. We aimed to assess the electrocardiographic parameters, including QRS-T angle, associated with adverse cardiac events in children with cardiomyopathies. Forty-two children with cardiomyopathies were included in this study: 19 with dilated cardiomyopathy, 17 with hypertrophic cardiomyopathy, and 6 with left ventricular non-compaction. Additionally, 19 control subjects were recruited. In terms of ECG parameters, the QRS-T angle was significantly greater among patients with adverse outcomes compared to patients without the end points of the study (133° vs. 65°, p < 0.001). On Kaplan−Meier survival curves, QRS-T angle > 120°, increased serum concentrations of NT-proBNP and troponin I levels as well as greater NYHA or Ross scale were associated with the greatest risk of unfavorable outcome. The QRS-T angle appears to be a valuable component of 12-lead ECG interpretation, and might be helpful in outlining patients with the greatest cardiovascular risk. Additionally, serum biomarkers such as NT-proBNP (p = 0.003) and troponin (p < 0.001) are useful in outlining patients with the worst survival.

摘要

心肌病在儿童中的患病率较低,因此可能导致恶性室性心律失常或心力衰竭进展,进而导致死亡。在成人中,心电图得出的QRS-T角与肥厚型和扩张型心肌病患者的不良预后相关。我们旨在评估与心肌病患儿不良心脏事件相关的心电图参数,包括QRS-T角。本研究纳入了42例心肌病患儿:19例扩张型心肌病、17例肥厚型心肌病和6例左心室致密化不全。此外,招募了19名对照受试者。在心电图参数方面,与无研究终点的患者相比,有不良预后的患者QRS-T角显著更大(133°对65°,p<0.001)。在Kaplan-Meier生存曲线上,QRS-T角>120°、血清NT-proBNP浓度升高、肌钙蛋白I水平升高以及NYHA或Ross分级更高与不良结局风险最大相关。QRS-T角似乎是12导联心电图解读的一个有价值的组成部分,可能有助于勾勒出心血管风险最大的患者。此外,血清生物标志物如NT-proBNP(p=0.003)和肌钙蛋白(p<0.001)有助于勾勒出生存最差的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cb/9738383/548aa6987736/jcm-11-06930-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cb/9738383/129167b28282/jcm-11-06930-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cb/9738383/548aa6987736/jcm-11-06930-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cb/9738383/129167b28282/jcm-11-06930-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31cb/9738383/548aa6987736/jcm-11-06930-g002.jpg

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本文引用的文献

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Magnetic Resonance for Differential Diagnosis of Left Ventricular Hypertrophy: Diagnostic and Prognostic Implications.磁共振成像用于左心室肥厚的鉴别诊断:诊断及预后意义
J Clin Med. 2022 Jan 27;11(3):651. doi: 10.3390/jcm11030651.
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Deciphering the pathogenic role of a variant with uncertain significance for short QT and Brugada syndromes using gene-edited human-induced pluripotent stem cell-derived cardiomyocytes and preclinical drug screening.利用基因编辑的人诱导多能干细胞衍生的心肌细胞和临床前药物筛选来解读对短QT综合征和Brugada综合征意义不确定的变异的致病作用。
Clin Transl Med. 2021 Dec;11(12):e646. doi: 10.1002/ctm2.646.
3
Identification of p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease.
一个大型扩张型心肌病伴传导疾病家系中 p.C335R 变异的鉴定。
Int J Mol Sci. 2021 Nov 30;22(23):12990. doi: 10.3390/ijms222312990.
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Preclinical short QT syndrome models: studying the phenotype and drug-screening.临床前短QT综合征模型:研究表型与药物筛选。
Europace. 2022 Mar 2;24(3):481-493. doi: 10.1093/europace/euab214.
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Usefulness of High-Sensitivity Cardiac Troponin T to Predict Long-Term Outcome in Patients with Hypertrophic Cardiomyopathy.心肌肌钙蛋白 T 高敏检测在预测肥厚型心肌病患者长期预后中的作用。
Am J Cardiol. 2021 Aug 1;152:120-124. doi: 10.1016/j.amjcard.2021.04.040. Epub 2021 Jun 12.
6
The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy.心电图表型在儿童肥厚型心肌病中心律失常性猝死风险分层中的作用。
Eur J Prev Cardiol. 2022 Mar 30;29(4):645-653. doi: 10.1093/eurjpc/zwab046.
7
The omics of channelopathies and cardiomyopathies: what we know and how they are useful.离子通道病和心肌病的组学:我们所了解的情况以及它们的用途。
Eur Heart J Suppl. 2020 Nov 18;22(Suppl L):L105-L109. doi: 10.1093/eurheartj/suaa146. eCollection 2020 Nov.
8
Different genotypes of Brugada syndrome may present different clinical phenotypes: electrophysiology from bench to bedside.不同基因型的 Brugada 综合征可能呈现不同的临床表型:从实验台到临床的电生理学
Eur Heart J. 2021 Mar 31;42(13):1270-1272. doi: 10.1093/eurheartj/ehab070.
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Predicting outcome in children with dilated cardiomyopathy: the use of repeated measurements of risk factors for outcome.预测扩张型心肌病患儿的预后:利用对预后危险因素的重复测量
ESC Heart Fail. 2021 Apr;8(2):1472-1481. doi: 10.1002/ehf2.13233. Epub 2021 Feb 5.
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QRS-T angle in patients with Hypertrophic Cardiomyopathy - A comparison with Cardiac Magnetic Resonance Imaging.肥厚型心肌病患者的 QRS-T 夹角——与心脏磁共振成像的比较。
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