Author/Authors :
Ameen, Muhammad Department of Medicine - Bronx-Lebanon Hospital Center, Bronx, NY, USA , Akbar, Ghulam Department of Cardiovascular Medicine - Lehigh Valley Hospital, Allentown, PA, USA , Abbas, Naeem Department of Medicine - Bronx-Lebanon Hospital Center, Bronx, NY, USA , Mirrani, Ghazi Department of Cardiovascular Medicine - Lehigh Valley Hospital, Allentown, PA, USA
Abstract :
Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by peculiar ECG findings predisposing
individuals to ventricular arrhythmias, syncope, and sudden cardiac death (SCD). Various electrolyte disturbances and ion channels
blocking drugs could also provoke BrS ECG findings without genetic BrS. Clinical differentiation and recognition are essential for
guiding the legitimate action. Hyperkalemia is well known to cause a wide variety of ECG manifestations. Severe hyperkalemia can
even cause life threatening ventricular arrhythmias and cardiac conduction abnormalities. Most common ECG findings include
peaked tall T waves with short PR interval and wide QRS complex. Since it is very commonly encountered disorder, physicians
need to be aware of even its rare ECG manifestations, which include ST segment elevation and Brugada pattern ECG (BrP). We are
adding a case to the limited literature about hyperkalemia induced reversible Brugada pattern ECG changes.