Thursday, 16 September 2010

MRCP revision battle 13.1: Brugada Syndrome

I'm afraid I'm too tired to even attempt an insightful intro today so lets just go straight to listing the battles:

MRCP revision battle 13.1: Brugada Syndrome
MRCP revision battle 13.2: SVC obstruction
MRCP revision battle 13.3: Causes long PR
MRCP revision battle 13.4: Cauda equina syndrome
MRCP revision battle 13.5: Surviving Sepsis





MRCP revision battle 13.1: Brugada Syndrome


Brugada Syndrome is an autosomal dominant condition that causes abnormal sodium channel proteins, leading to a risk of VF/VT and sudden death.


It is commonest in Asians.

20-40% of cases are associated with a SCN5A mutation.


ECG shows partial/complete RBBB with ST elevation in V1 to V2.  The classical ECG is type 1 below, with the other 2 possible variations.

 Treatment is ICD.


Next up - SVC obstruction...