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Anaesthesia for patients with hereditary arrhythmias; part 2: congenital long QT syndrome and arrhythmogenic right ventricular cardiomyopathy.

作者信息

Levy D, Bigham C, Tomlinson D

机构信息

Torbay Hospital, Torquay, UK.

Derriford Hospital, Plymouth, UK.

出版信息

BJA Educ. 2018 Aug;18(8):246-253. doi: 10.1016/j.bjae.2018.04.005. Epub 2018 Jun 21.

Abstract
摘要

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Anaesthesia for patients with hereditary arrhythmias part I: Brugada syndrome.
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3
Arrhythmogenic Right Ventricular Cardiomyopathy.
N Engl J Med. 2017 Jan 5;376(1):61-72. doi: 10.1056/NEJMra1509267.
4
Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Course and Predictors of Arrhythmic Risk.
J Am Coll Cardiol. 2016 Dec 13;68(23):2540-2550. doi: 10.1016/j.jacc.2016.09.951.
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Management of patients with Arrhythmogenic Right Ventricular Cardiomyopathy in the Nordic countries.
Scand Cardiovasc J. 2015;49(6):299-307. doi: 10.3109/14017431.2015.1086017. Epub 2015 Sep 23.
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Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus Statement.
Circulation. 2015 Aug 4;132(5):441-53. doi: 10.1161/CIRCULATIONAHA.115.017944. Epub 2015 Jul 27.
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Genetics of long-QT syndrome.
J Hum Genet. 2016 Jan;61(1):51-5. doi: 10.1038/jhg.2015.74. Epub 2015 Jun 25.
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The safety of modern anesthesia for children with long QT syndrome.
Anesth Analg. 2014 Oct;119(4):932-938. doi: 10.1213/ANE.0000000000000389.
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Long QT syndrome.
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