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Review
. 2018 Jun;18(6):159-165.
doi: 10.1016/j.bjae.2018.03.004. Epub 2018 Mar 28.

Anaesthesia for patients with hereditary arrhythmias part I: Brugada syndrome

Affiliations
Review

Anaesthesia for patients with hereditary arrhythmias part I: Brugada syndrome

D Levy et al. BJA Educ. 2018 Jun.
No abstract available

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Conflict of interest statement

None declared.

Figures

Fig 1
Fig 1
An ECG pattern (A) very suspicious but non-diagnostic for a type I Brugada ECG in lead V1 and (B) less pronounced changes in lead V2 before an ajmaline provocation test (images courtesy of David Tomlinson).
Fig 2
Fig 2
Postajmaline provocation in the same patient, with (A) a type 1 Brugada ECG pattern induced in lead V1 (complexes now have subtle convex/‘coved’ ST shape) and (B) more accentuated but still not type I ECG change in lead V2 (images courtesy of David Tomlinson).
Fig 3
Fig 3
High precordial lead placement (note V1 and V2 are placed in the second intercostal space). Alternatively, leads V5 and V6 can be moved to the superior position whilst leads V1 and V2 are maintained in their standard position (fourth intercostal space).
Fig 4
Fig 4
The normal cardiac ventricular cell action potential.
Fig 5
Fig 5
The repolarisation theory for Brugada syndrome [Endo: Endocardial, M: M region, Epi: Epicardial, AP: Action Potential] (reproduced with permission from Antzelevitch C. Brugada Syndrome. Pacing Clin Electrophysiol 2006; 29: 1130–59).

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References

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