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monomorphic ventricular tachycardia
Ventricular tachycardia in which the QRS complexes maintain a single morphology throughout the tachycardia.
Etiology:
1) generally from re-entry in patients with structural heart disease
2) in the absence of heart disease, may arise from triggered activity, often originating in the ouflow tract of the right ventricle
* also see ventricular tachycardia
Management: (also see ventricular tachycardia)
1) hemodynamic instability
- immediate DC synchronized cardioversion
2) stable patient, chemical cardioversion
a) preserved heart function
1] procainamide*
2] sotalol or other beta-blocker
3] amiodarone 150 mg IV over 10 minutes
- initial bolus followed by continuous infusion [5]
4] lidocaine 0.5-0.75 mg/kg IV push
b) poor LV ejection fraction
1] amiodarone 150 mg IV over 10 minutes
- initial bolus followed by continuous infusion [5]
2] lidocaine 0.5-0.75 mg/kg IV push
3] then DC synchronized cardioversion
c) coronary revascularization alone in patients with coronary artery disease is unsufficient to prevent recurrent ventricular tachycardia [4]
* procainamide is the agent of choice for chemical cardioversion except in the settings of:
1) acute MI
2) digoxin toxicity
3) poor LV ejection fraction
- in these cases, lidocaine remains the agent of choice [2]
General
ventricular tachycardia (VT)
References
- Manual of Medical Therapeutics, 28th ed, Ewald &
McKenzie (eds), Little, Brown & Co, Boston, 1995, pg 148
- Medical Knowledge Self Assessment Program (MKSAP) 11, American
College of Physicians, Philadelphia 1998
- ACLS - The Reference Texbook
ACLS: Principles & Practice, Cummins RO et al (eds),
American Heart Association, 2003 ISBN 0-87493-341-2
- Al-Khatib SM et al.
AHA/ACC/HRS guideline for management of patients with
ventricular arrhythmias and the prevention of sudden cardiac
death: A report of the American College of Cardiology/American
Heart Association Task Force on Clinical Practice Guidelines
and the Heart Rhythm Society.
Circulation 2017 Oct 30
PMID: 29084731
http://circ.ahajournals.org/content/early/2017/10/30/CIR.0000000000000549
- NEJM Knowledge+