Anesthetic Management of Catecholaminergic Polymorphic Ventricular Tachycardia in Pregnancy

reportActive / Technical Report | Accesssion Number: AD1151857 | Open PDF

Abstract:

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare familial or de novo mutation in either the cardiac RyR2 Ryanodine gene (CPVT1) or CASQ2 calsequestrin gene (CPVT2). Both of these mutations alter normal cardiac myocyte calcium regulation, enhancing the propensity of sarcoplasmic reticulum calcium to be released. These spontaneous calcium discharges cause unpredictable malignant arrhythmias presenting as syncope or sudden cardiac death.

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