Synopsis
Recognise a diagnostic type 1 Brugada pattern and other inherited channelopathy clues, manage fever and malignant ventricular arrhythmia, and route patients and families to inherited-cardiac-condition expertise.
- A type 1 Brugada ECG is coved ST elevation over 0.2 mV followed by T-wave inversion in at least one V1–V2 lead placed in the second, third or fourth intercostal space.
- A spontaneous type 1 pattern is diagnostic in the right setting; fever- or sodium-channel-blocker-induced type 1 generally needs compatible clinical features for a Brugada syndrome diagnosis.
- Type 2 saddleback appearances are not diagnostic alone and should not trigger an ICD without expert phenotyping.
- Brugada events often occur at rest, during sleep or with fever; CPVT instead causes bidirectional or polymorphic ventricular arrhythmia during exercise or intense emotion with a usually normal resting ECG.
- Treat fever promptly, maintain hydration and avoid Brugada-provocative drugs, cocaine and binge alcohol; persistent fever warrants ECG and monitored review.
- An ICD is the definitive sudden-death protection for survivors of VT/VF arrest and selected high-risk symptomatic Brugada patients; most asymptomatic people do not need one.
- Ajmaline or another sodium-channel challenge belongs in an experienced electrophysiology unit with high-right-precordial ECG and immediate resuscitation capability.
- A negative genetic test does not exclude Brugada syndrome; first-degree relatives need clinical screening through an inherited cardiac conditions service.
Key red flags
Unexplained syncope at rest, nocturnal agonal breathing, documented polymorphic VT/VF or cardiac arrest—especially during fever—raises immediate risk concern.