Brugada syndrome
- related: Cardiology, EKG basics, bundle branch blocks
- tags: #note
Pathophysiology
- Na channel mutation
- triggered by stress or drugs
Brugada sign
-
ST elevation in V1-V3 followed by negative T wave
-
Electrocardiogram demonstrating a type 1 Brugada pattern, ≥2 mm J-point elevation, ST-segment coving (concave or linear downsloping ST segment) (arrowheads), and T-wave inversions in leads V1 to V3.
Diagnosis
- must have Brugada sign + clinical criteria:
- Fhx sudden cardiac disease < 45 years old
- documented VF/VT
- Similar ECG in family members
- Inducible VT with electrical stimulation
- syncope
- nocturanal agonal respiration
Treatment
- ICD
Brugada syndrome is distinguished by right precordial ECG abnormalities, including ST-segment coving (concave or linear downsloping ST segment) in leads V1 to V3 with or without right bundle branch block, VF, and cardiac arrest (Figure 19). Brugada syndrome has an increased prevalence in men and persons of Asian descent. Arrhythmic events in patients with Brugada syndrome are more common at night during sleep. Abnormalities on ECG can be intermittent and may be elicited by fever or pharmacologic challenge with sodium channel blockade (such as with procainamide infusion). Patients with syncope or ventricular arrhythmia should undergo ICD implantation. Quinidine may be beneficial in patients with recurrent ventricular arrhythmias and/or ICD shocks.
Links to this note
- Cardiology
- anion gap metabolic acidosis
- Paracetamol/acetaminophen, paraldehyde, pyroglutamic acidosis, polyethylene glycol (miralax, metabolizes to lactic acid; versed, in the preparation, in neuro icu), propofol infusion syndrome can lead to elevated lactic acidosis, propofol infusion syndrome is associated with high dose continuous infusion: Brugada syndrome