S3861 Genetic test brugada
Also known as: Brugada syndrome testing, cardiac arrhythmia gene test
Genetic testing for mutations in SCN5A and other genes associated with Brugada syndrome, an inherited cardiac arrhythmia disorder.
In Plain Language
genetic test for heart rhythm disorder; Brugada gene screening
Clinical Context
Used in cardiology for diagnosis of Brugada syndrome in patients with spontaneous Type 1 Electrocardiogram pattern or family history of sudden cardiac death.
RVU Information
CPT S3861 does not have a physician work RVU assigned by CMS. This is typical for supply, drug, and equipment codes — reimbursement is based on Average Sales Price (ASP), fee schedules, or payer contracts rather than the RVU system.
Billing & Documentation
S-codes are used by private payers (not Medicare) for services without a standard CPT or HCPCS code. Coverage varies significantly between insurers. Verify payer acceptance before billing and document medical necessity thoroughly.
Specialties
Frequently Asked Questions
What is CPT code S3861?
CPT S3861 (Genetic test brugada) is a S Codes code. Genetic testing for mutations in SCN5A and other genes associated with Brugada syndrome, an inherited cardiac arrhythmia disorder.
Is S3861 covered by insurance?
S3861 is a temporary HCPCS code. Coverage varies by payer and may change when permanent codes are assigned. Used in cardiology for diagnosis of Brugada syndrome in patients with spontaneous Type 1 Electrocardiogram pattern or family history of sudden cardiac death.
When is CPT S3861 used?
Used in cardiology for diagnosis of Brugada syndrome in patients with spontaneous Type 1 Electrocardiogram pattern or family history of sudden cardiac death.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.