polymorphic ventricular tachycardia
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Introduction
Ventricular tachycardia characterized by changing QRS morphologies (i.e. torsades de pointes).
Etiology
- triggered activity - catecholamine induced
- functional re-entry
- ischemia*
* common cause of polymorphic ventricular tachycardia in the absence of QT prolongation
Clinical manifestations
- syncope
- polymorphic ventricular tachycardia during exercise or emotional stres
Diagnostic procedures
Management
(also see ventricular tachycardia)
- hemodynamic instability
- immediate DC synchronized cardioversion
- stable patient, chemical cardioversion
- normal baseline QT interval
- correct ischemia, electrolyte abnormalities
- preserved heart function
- procainamide*
- sotalol or other beta-blocker
- amiodarone 150 mg IV over 10 minutes
- lidocaine 0.5-0.75 mg/kg IV push
- poor LV ejection fraction
- amiodarone 150 mg IV over 10 minutes
- lidocaine 0.5-0.75 mg/kg IV push
- then DC synchronized cardioversion
- prolonged baseline QT interval
- treat as torsades de pointes
More general terms
More specific terms
- catecholaminergic polymorphic ventricular tachycardia; stress-induced polymorphic ventricular tachycardia
- familial polymorphic ventricular tachycardia
- torsades de pointes