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Hyperkalemia-induced Brugada pattern: an unusual manifestation
Tanyanan Tanawuttiwat1, Tasma Harindhanavudhi, Adarsh Bhan
1Department of Medicine, Advocate Christ Medical Center/University of Illinois at Chicago, Oak Lawn, Illinois, USA. ttanawuttiwat@gmail.com
Brugada syndrome, a genetic disorder, presents a specific ECG pattern linked to cardiac arrest risk. This case highlights hyperkalemia mimicking this pattern without typical ECG signs, expanding differential diagnoses for Brugada-like presentations.
Area of Science:
- Cardiology
- Electrophysiology
- Genetics
Background:
- Brugada syndrome is an inherited cardiac channelopathy characterized by a specific electrocardiographic (ECG) pattern and increased risk of sudden cardiac death.
- The Brugada electrocardiographic pattern (BrP) can be mimicked by various conditions, including electrolyte disturbances, making diagnosis challenging.
Observation:
- This report details a rare case where severe hyperkalemia induced a Brugada type I electrocardiographic pattern.
- Notably, the patient did not exhibit other characteristic ECG findings typically associated with hyperkalemia, such as peaked T waves or loss of P waves.
Findings:
- Hyperkalemia can present with a Brugada type I pattern, a finding not previously well-documented.
- The absence of typical hyperkalemia ECG manifestations in this case underscores the complexity of ECG interpretation in electrolyte imbalances.
Implications:
- This case broadens the differential diagnosis for the Brugada electrocardiographic pattern, emphasizing the need to consider hyperkalemia.
- Clinicians should be aware of this potential ECG mimicry to avoid misdiagnosis and ensure appropriate management of both hyperkalemia and potential underlying cardiac conditions.
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