Ventricular tachycardia pathophysiology: Difference between revisions

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===Causes===
===Causes===
====Common====
====Common====
*Scar from a prior MI (the most common cause of [[monomorphic ventricular tachycardia]])
*Scar from a prior [[MI]] (the most common cause of [[monomorphic ventricular tachycardia]])
 
====Rare====
====Rare====
*[[Right ventricular dysplasia]]
*[[Right ventricular dysplasia]]

Revision as of 17:40, 22 September 2012

Ventricular tachycardia Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Ventricular Tachycardia from other Disorders

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

Chest X Ray

Echocardiography

Cardiac MRI

Other Diagnostic Tests

Treatment

Medical Therapy

Electrical Cardioversion

Ablation

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Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

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Case #1

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]

Overview

The underlying mechanism of VT is due to automaticity arising in either the myocardium or in the distal conduction system. The most common underlying substrate for ventricular tachycardia is ischemic heart disease. The morphology of ventricular tachycardia often depends on its cause.

Monomorphic Ventricular Tachycardia

There are two reasons the morphology of the QRS does not vary in monomorphic ventricular tachycardia:

  • A single site that generates automaticity of a single point in either the left or right ventricle
  • A reentry circuit within the ventricle

Causes

Common

Rare

Polymorphic Ventricular Tachycardia

Polymorphic ventricular tachycardia, on the other hand, is most commonly caused by abnormalities of ventricular muscle repolarization. The predisposition to this problem usually manifests on the EKG as a prolongation of the QT interval. QT prolongation may be congenital or acquired. Congenital problems include Long QT syndrome and Catecholaminergic polymorphic ventricular tachycardia. Acquired problems are usually related to drug toxicity or electrolyte abnormalities, but can occur as a result of myocardial ischaemia. Class III anti-arrhythmic drugs such as sotalol and amiodarone prolong the QT interval and may in some circumstances be pro-arrhythmic. Other relatively common drugs including some antibiotics and antihistamines may also be a danger, particularly in combination with one another. Problems with blood levels of potassium, magnesium and calcium may also contribute. High dose magnesium is often used as an antidote in cardiac arrest protocols.

Monomorphic ventricular tachycardia

References

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