A Brief Introduction to Management of LQTS.
作者信息
Trohman Richard G
机构信息
Section of Electrophysiology, Division of Cardiology, Department of Medicine, Rush University Medical Center, Chicago, IL 60612, USA.
出版信息
Rev Cardiovasc Med. 2022 May 5;23(5):164. doi: 10.31083/j.rcm2305164. eCollection 2022 May.
Abstract
摘要
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A Brief Introduction to Management of LQTS.长QT综合征管理简介
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引用本文的文献
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Case report: A 56-year-old woman presenting with torsades de pointes and cardiac arrest associated with levosimendan administration and underlying congenital long QT syndrome type 1.病例报告：一名56岁女性，出现尖端扭转型室速和心脏骤停，与使用左西孟旦及潜在的先天性1型长QT综合征相关。
Heliyon. 2024 Apr 10;10(8):e29300. doi: 10.1016/j.heliyon.2024.e29300. eCollection 2024 Apr 30.
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Management of Congenital Long-QT Syndrome: Commentary From the Experts.先天性长 QT 综合征的管理：专家评论。
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Diagnosis, management and therapeutic strategies for congenital long QT syndrome.先天性长 QT 综合征的诊断、管理和治疗策略。
Heart. 2022 Mar;108(5):332-338. doi: 10.1136/heartjnl-2020-318259. Epub 2021 May 26.
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Managing drug-induced QT prolongation in clinical practice.临床实践中药物致 QT 间期延长的管理。
Postgrad Med J. 2021 Jul;97(1149):452-458. doi: 10.1136/postgradmedj-2020-138661. Epub 2020 Oct 29.
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Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.跨种族全基因组关联研究为长 QT 综合征的遗传结构和遗传性提供了新见解。
Circulation. 2020 Jul 28;142(4):324-338. doi: 10.1161/CIRCULATIONAHA.120.045956. Epub 2020 May 20.
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Late Sodium Current Inhibitors as Potential Antiarrhythmic Agents.晚期钠电流抑制剂作为潜在的抗心律失常药物。
Front Pharmacol. 2020 Apr 20;11:413. doi: 10.3389/fphar.2020.00413. eCollection 2020.
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An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome.一项国际性、多中心、基于证据的对报道引起先天性长 QT 综合征的基因的重新评估。
Circulation. 2020 Feb 11;141(6):418-428. doi: 10.1161/CIRCULATIONAHA.119.043132. Epub 2020 Jan 27.
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Acquired Long QT Syndrome and Electrophysiology of Torsade de Pointes.获得性长QT综合征与尖端扭转型室速的电生理学
Arrhythm Electrophysiol Rev. 2019 May;8(2):122-130. doi: 10.15420/aer.2019.8.3.
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Circ Arrhythm Electrophysiol. 2019 May;12(5):e007280. doi: 10.1161/CIRCEP.118.007280.
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Acquired long QT syndrome and torsade de pointes.获得性长QT综合征与尖端扭转型室速。
Pacing Clin Electrophysiol. 2018 Apr;41(4):414-421. doi: 10.1111/pace.13296. Epub 2018 Mar 30.
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Left cardiac sympathetic denervation: An important treatment option for patients with hereditary ventricular arrhythmias.左心交感神经去神经支配：遗传性室性心律失常患者的一种重要治疗选择。
J Arrhythm. 2016 Oct;32(5):340-343. doi: 10.1016/j.joa.2015.08.002. Epub 2015 Oct 29.
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