Right bundle branch block

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Right bundle branch block
ECG characteristics of a typical RBBB showing wide QRS complexes with a terminal R wave in lead V1 and slurred S wave in lead V6.
ICD-10 I45.1
DiseasesDB 11620

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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]

Synonyms and keywords: RBBB


Overview

Right bundle branch block (RBBB) results from a defect in the heart's electrical conduction system. There is a delay in failure of transmission of electrical impulses down the right bundle of the heart. As a result, the right ventricle depolarizes by an alternate mechanism. This is by means of cell-to-cell conduction. These cell to cell conduction impulses spread more slowly than usual from the interventricular septum to the left ventricle and to the right ventricle. This delay in conduction results in the characteristic ECG pattern which is a wide and notched QRS. Although conduction down the right bundle is delayed, conduction down the left bundle is normal. As result, the interventricular septum and left ventricle depolarize in the normal fashion.

Pathophysiology

Three types of RBBB have been identified based upon electrophysiologic studies.

In each of the three types of RBBB, the surface ECG pattern remains the same.

1. Proximal, or central, RBBB: This type of conduction defect occurs when the conduction block is located just distal to the bundle of His in the superior aspect of the right bundle branch. This type of block occurs when the proximal bundle is injured during surgery for an inlet or membranous ventricular septal defect (VSD).

2. Interruption between the proximal and distal aspects of the right bundle branch: This type of right bundle branch block occurs when the impulse is interrupted between the proximal and distal aspects of the right bundle branch. This type of bright bundle branch block is most commonly observed after surgical division of the moderator band.

3. Distal RBBB: This form is observed when distal ramifications of the right bundle are disrupted during right ventriculotomy or resection of muscle bundles in the right ventricular outflow tract.

Genetics

There can be familial cases of right bundle branch block such as that observed in 4 Lebanese families and the abnormality was mapped to chromosome 19.

There is a subset of patients with Brugada syndrome who have mutations in SCN5A, the gene encoding for the voltage-gated cardiac sodium channel.

Associated syndromes

  • Brugada syndrome: This syndrome is due to a channelopathy mediated by the SCN5A gene. It is important to note that the RBBB pattern seen in patients with this syndrome is not actually RBBB but is instead due to a repolarization abnormality. In this syndrome, the ECG shows ST-segment elevation in leads V1-V3. Cocaine consumption and / or the use of the antiarrhythmic propafenone may unmask the ECG findings of Brugada syndrome.

Causes of Right Bundle Branch Block

  • Surgery for correction of congenital heart disease is the most common cause of RBBB among children any United States. This includes surgery for repair of an isolated VSD or another congenital heart disease that includes a VSD (eg, double-chambered right ventricle, AV canal defect, or tetralogy of Fallot). The incidence of RBBB varies and ranges from 25-81% after repair of a VSD to 60-100% after repair of tetralogy of Fallot. The risk of RBBB after surgery varies depending upon the proximity of the VSD to the His-Purkinje system.
  • Blunt trauma
  • Polymyositis
  • Premature atrial contractions or supraventricular tachycardia may cause a transient form up right bundle branch block. This occurs when a premature impulse is conducted from the AV node to the His bundle while the right bundle branch remains in its refractory period, but the left bundle is not. As a result, conduction down the right bundle branch is delayed or blocked.
  • Prenatal exposure to each one HIV type 1 may cause right anterior hemiblock.
  • Familial

Differential Diagnosis

Epidemiology and Demographics

Age

The prevalence of RBBB increases with age.

Natural Hisstory

In general, the natural history of right bundle branch block benign. There are three scenarios in which right bundle branch block can be associated with poor prognosis:

  1. Brugada syndrome: if right bundle branch block is present, then sudden death may occur.
  2. Kearns Sayre syndrome: again, if right bundle branch block is present than sudden death may occur.
  3. Tetralogy of Fallot: if right bundle branch block is present with a markedly prolonged QRS (< 180 ms), then the patient may be at risk for ventricular arrhythmias and sudden death.

If right bundle branch block is due to surgery then there are generally no acute hemodynamic consequences. The subsequent courses also quite benign. An exception is if there is substantial injury to the His-Purkinje system in which case left anterior hemiblock or first-degree AV block may be present.

There are familial cases of right bundle branch block, which are benign.

Diagnosis

Physical Examination

Heart

Right bundle branch block is associated with a persistently split second heart sound with normal respiratory variation in the splitting interval.




Overview

Historical Perspective

Pathophysiology

Causes

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | Echocardiography | Other Imaging Findings | Other Diagnostic Studies

Treatment

Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

Case Studies

Case #1

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