Summary & Overview
CPT 87478: Molecular Detection of Borrelia miyamotoi
CPT code 87478 designates a molecular diagnostic assay using amplified probe technology to detect nucleic acids from Borrelia miyamotoi, the bacterium linked to tickborne relapsing fever (TBRF). Nationally, this code captures specialized infectious disease testing that supports diagnosis of a less common tickborne pathogen with growing clinical recognition. The code matters for laboratories, clinicians evaluating febrile or relapsing illness after tick exposure, and payers managing coverage and appropriate use of molecular infectious disease panels.
Key payers included in the analysis are Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical context and typical laboratory site of service, plus what to expect in payer coverage discussions and benchmarking. The publication also summarizes common billing modifiers and identifies where data was not provided.
This resource provides: clinical purpose and testing method; expected site-of-service and operational implications for laboratories; guidance on common modifiers used with molecular pathology billing; and notes on missing input elements where applicable. The content is written for a national audience of laboratory directors, coding and billing specialists, clinicians, and payer policy analysts.
Billing Code Overview
CPT code 87478 describes a molecular diagnostic test that uses an amplified probe technique to detect nucleic acids from the bacterium Borrelia miyamotoi, an agent associated with tickborne relapsing fever (TBRF). The assay identifies pathogen-specific genetic material to support diagnosis of infection caused by this tick-transmitted organism.
Service Type: Molecular diagnostic infectious disease testing
Typical Site of Service: Clinical laboratory or hospital laboratory settings where molecular testing is performed, including reference laboratories. Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A 42-year-old outdoor worker presents to an outpatient infectious disease clinic in late spring with fever, recurrent episodes of chills and sweats, headache, and myalgias. The clinician documents a history of multiple recent tick bites and local erythema. Initial physical exam and basic labs are non-specific; the clinician suspects a tickborne relapsing fever–type illness and orders molecular testing for Borrelia miyamotoi. A venous blood sample is collected and sent to a reference laboratory that performs nucleic acid amplification testing using an amplified probe technique. Results are reported to the ordering clinician electronically; positive detection confirms the presence of Borrelia miyamotoi nucleic acid and supports targeted antimicrobial therapy and public health reporting as indicated.
Typical workflow:
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Patient evaluation in clinic with history and exam.
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Specimen collection (venous blood) using standard phlebotomy techniques.
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Specimen packaged and shipped to a laboratory capable of performing amplified probe nucleic acid testing for Borrelia miyamotoi.
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Laboratory performs
87478testing and documents results in the laboratory information system; if performed in two components, the technical component and any professional interpretation are documented. -
Results communicated to ordering clinician; relevant ICD-10 diagnosis documented in the medical record to support medical necessity and billing.