Treatment of Wide Complex Tachycardia
Immediate synchronized cardioversion is the definitive treatment for any hemodynamically unstable wide complex tachycardia, regardless of the underlying rhythm. 1, 2, 3
Initial Assessment and Stabilization
Determine hemodynamic stability first – this single decision point drives all subsequent management:
- Unstable patients (hypotension, altered mental status, shock, chest pain, acute heart failure) require immediate synchronized cardioversion without delay for pharmacologic therapy 1, 2, 3
- Sedate conscious patients if time permits (consider etomidate 0.2-0.3 mg/kg IV given hypotension) 3
- Apply defibrillator pads immediately and maintain continuous cardiac monitoring 3
- Establish two large-bore IV lines and obtain a 12-lead ECG, but do not delay cardioversion to obtain these 3
Management Algorithm for Stable Wide Complex Tachycardia
Step 1: Determine Rhythm Regularity and Morphology
For regular monomorphic wide complex tachycardia:
- Procainamide is the first-line agent for hemodynamically stable monomorphic VT in patients without severe heart failure or acute MI 1
- Amiodarone 150 mg IV over 10 minutes is recommended for patients with hemodynamically stable monomorphic VT, particularly those with severe heart failure or acute MI 1, 4
- Sotalol 1.5 mg/kg IV over 5 minutes may be considered for stable sustained monomorphic VT, including patients with acute MI, but avoid if QT is prolonged 1, 5
- IV adenosine may be considered for undifferentiated regular stable wide complex tachycardia – it is relatively safe, may convert the rhythm to sinus, and helps diagnose the underlying rhythm 1, 2
Step 2: Special Considerations for Polymorphic Wide Complex Tachycardia
Never give adenosine for irregular or polymorphic wide complex tachycardia 2
For polymorphic VT with long QT syndrome (torsades de pointes):
- IV magnesium is the primary treatment for both acquired and familial long QT-associated polymorphic VT 1, 2
- Add overdrive pacing (atrial or ventricular) or IV isoproterenol when polymorphic VT is accompanied by bradycardia or appears precipitated by pauses 1, 2
- IV beta-blockers for familial long QT syndrome 1
- Avoid isoproterenol in familial long QT syndrome 1
For polymorphic VT without long QT syndrome:
- IV beta-blockers may be effective for ischemic VT or catecholaminergic VT 1, 2
- Consider isoproterenol for non-ischemic cases 1
Critical Pitfalls to Avoid
Never use calcium channel blockers (verapamil, diltiazem) for wide complex tachycardia unless definitively proven to be supraventricular tachycardia – they can cause hemodynamic collapse in ventricular tachycardia 2, 3
Do not delay cardioversion in unstable patients to attempt pharmacologic conversion or obtain additional diagnostic studies 2, 3
When in doubt, treat as ventricular tachycardia – this is the safest approach since VT represents the majority of wide complex tachycardias and misdiagnosis can be fatal 6, 7, 8
Avoid beta-blockers in hypotensive states 3
Metabolic and Electrolyte Considerations
Rapidly correct electrolyte abnormalities (particularly potassium, magnesium, and calcium) in all patients with wide complex tachycardia 2, 3
Check stat electrolytes and correct abnormalities immediately, as metabolic causes do not make the arrhythmia more benign 2, 3
Post-Stabilization Management
All patients with wide complex tachycardia require ICU/CCU admission and immediate cardiology/electrophysiology consultation 3
Consider electrophysiology study and possible ablation once stabilized 3
Most patients require amiodarone therapy for 48-96 hours, though it may be safely administered for longer periods if necessary 4