User:Mr. Ibrahem/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 a prolonged S wave in lead V6.
SpecialtyCardiology
SymptomsNone[1]
ComplicationsNone[1]
CausesUnknown, heart damage, increased right ventricular pressure, high blood potassium[1]
Diagnostic methodElectrocardiogram (ECG)[1]
Differential diagnosisLeft bundle branch block, ventricular tachycardia, Brugada syndrome[1]
TreatmentBased on underlying disorder[1]
FrequencyFairly common[2]

Right bundle branch block (RBBB) is a type of electrical conduction abnormality of the heart seen on the electrocardiogram (ECG).[1] In and of itself, it results in no symptoms and generally results in no complications.[1] It may be temporary or permanently present.[2]

Causes include heart damage, such as a heart attack or myocarditis, increased right ventricular pressure, such as with pulmonary embolism or cor pulmonale, and rarely high blood potassium.[1] Though some cases occurs without any specific cause.[2] The underlying mechanism involves damage to the right bundle branch.[1]

Diagnosis requires that the QRS complex is greater than 120 ms and an rsR' wave is present in lead V1 or V2.[2] The T waves are generally flipped in V1 and V2.[2] When the QRS duration is less than 120 ms, but the other criteria are present, it is called an incomplete RBBB.[1] Its presence does not interfere with the diagnosis of a heart attack.[1]

No specific treatment is generally required.[1] In the setting of heart failure, cardiac resynchronization therapy may be indicated.[1] RBBB is present in about 0.2% to 0.8% of ECGs.[2] Up to 11% of people are affected by the age of 80.[1]

References[edit]

  1. ^ a b c d e f g h i j k l m n o Harkness, WT; Hicks, M (January 2020). "Right Bundle Branch Block". PMID 29939649. {{cite journal}}: Cite journal requires |journal= (help)
  2. ^ a b c d e f Roberts, David (2019). Mastering the 12-Lead EKG. Springer Publishing Company. p. 316. ISBN 978-0-8261-8194-7. Archived from the original on 2021-08-29. Retrieved 2020-12-30.