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polymorphic ventricular tachycardia

Ventricular tachycardia characterized by changing QRS morphologies (i.e. torsades de pointes). Etiology: 1) triggered activity - catecholamine induced 2) functional re-entry 3) ischemia* * common cause of polymorphic ventricular tachycardia in the absence of QT prolongation Clinical manifestations: - syncope - polymorphic ventricular tachycardia during exercise or emotional stres Special laboratory: - exercise stress testing Management: (also see ventricular tachycardia) 1) hemodynamic instability -> immediate DC synchronized cardioversion 2) stable patient, chemical cardioversion 3) normal baseline QT interval a) correct ischemia, electrolyte abnormalities b) preserved heart function 1] procainamide* 2] sotalol or other beta-blocker 3] amiodarone 150 mg IV over 10 minutes 4] lidocaine 0.5-0.75 mg/kg IV push c) poor LV ejection fraction 1] amiodarone 150 mg IV over 10 minutes 2] lidocaine 0.5-0.75 mg/kg IV push 3] then DC synchronized cardioversion 4) prolonged baseline QT interval - treat as torsades de pointes

Specific

catecholaminergic polymorphic ventricular tachycardia; stress-induced polymorphic ventricular tachycardia familial polymorphic ventricular tachycardia torsades de pointes

General

ventricular tachycardia (VT)

References

  1. Manual of Medical Therapeutics, 28th ed, Ewald & McKenzie (eds), Little, Brown & Co, Boston, 1995, pg 148
  2. Medical Knowledge Self Assessment Program (MKSAP) 11, 16. American College of Physicians, Philadelphia 1998, 2012