Anesthesia for Long QT Syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Anesthesiology and Pain Medicine
Link
https://link.springer.com/content/pdf/10.1007/s40140-021-00480-3.pdf
Reference37 articles.
1. Schwartz PJ, Stramba-Badiale M, Crotti L, Pedrazzini M, Besana A, Bosi G, et al. Prevalence of the congenital long-QT syndrome. Circ. 2009;120:1761–7.
2. Skinner JR, Winbo A, Abrams D, Vohra J, Wilde AA. Channelopathies that lead to sudden cardiac death: clinical and genetic aspects. Heart Lung Circ. 2019;28:22–30.
3. • Wilde AAM, Amin AS, Postema PG. Diagnosis, management and therapeutic strategies for congenital long QT syndrome. Heart 2021:0:1–7. epub ahead of print: June 5, 2021 doi: https://doi.org/10.1136/heartjnl-2020-318259. This article provides a detailed explanation of genotype and phenotype correlations amongst specific LQTS subtypes as well as clinical management guidelines.
4. Bohnen MS, Peng G, Robey SH, Terrenoire C, Iyer V, Sampson KJ, et al. Molecular pathophysiology of congenital long QT syndrome. Physiol Rev. 2017;97:89–134.
5. Uvelin A, Pejakovic J, Mijatovic V. Acquired prolongation of QT interval as a risk factor for torsades de pointed ventricular tachycardia: a narrative review for the anesthesiologist and intensivist. J Anesth. 2017;31:413–23.
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