Summary & Overview
CPT 0142U: ePlex BCID Gram–Negative Panel for Positive Blood Cultures
CPT code 0142U designates a Proprietary Laboratory Analyses (PLA) test for the ePlex® BCID gram–negative panel by GenMark Diagnostics, a rapid molecular diagnostic assay for detecting gram–negative bacterial targets, key resistance genes, and Candida from positive blood cultures. This code matters nationally because rapid identification of bloodstream pathogens and resistance markers can influence antibiotic selection, infection control, and hospital resource use.
Key payers covered in the analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the clinical use of the assay, the typical site of service (hospital or reference laboratories), and the national implications for laboratory and inpatient care pathways. The publication describes how the code is used for reporting a single-vendor, specific-test PLA and summarizes what stakeholders should know about coding clarity for proprietary assays.
The report provides benchmarks and payer coverage context where available, highlights policy considerations for PLA codes, and situates the clinical role of the ePlex BCID gram–negative panel within diagnostic workflows for bacteremia and candidemia. Data not available in the input will be noted as such in relevant sections.
Billing Code Overview
CPT code 0142U is a Proprietary Laboratory Analyses (PLA) code for the ePlex® BCID gram–negative panel from GenMark Diagnostics Inc. The test uses an automated amplified probe technique for rapid detection of multiple bloodstream infection targets, including 21 gram–negative bacterial targets, 6 resistance genes, 1 pan gram–negative bacterial target, and 1 pan Candida target from positive blood cultures.
Service type: Clinical laboratory molecular diagnostic test for pathogen and resistance gene detection.
Typical site of service: Hospital clinical laboratory or centralized reference laboratory processing positive blood culture specimens.
Clinical & Coding Specifications
Clinical Context
A hospitalized adult presents with signs of sepsis: fever, hypotension, tachycardia, and altered mental status. Blood cultures obtained at the bedside grow organisms on Gram stain showing gram-negative bacilli. The clinical team requests rapid pathogen identification and resistance marker detection to guide early antimicrobial therapy. The laboratory performs the ePlex® BCID gram–negative panel using an automated amplified probe technique on a positive blood culture bottle. Results reporting includes identification of targeted gram-negative bacteria, detection of key resistance genes, and pan-Candida/pan-gram-positive targets to assist in narrowing or broadening empiric therapy. Typical workflow: blood cultures drawn in the emergency department or inpatient unit → incubation and growth detected in automated blood culture system → positive bottle forwarded to microbiology lab → laboratory technologist performs the ePlex® BCID gram–negative panel (report with 0142U) → results communicated to the treating team and antimicrobial stewardship when available. Typical site of service: hospital inpatient laboratory and hospital emergency department with specimen collection at bedside. Typical patient scenario: adult with suspected bacteremia/sepsis after urinary tract infection or intra-abdominal infection, positive blood culture with gram-negative bacilli on Gram stain, requiring rapid organism and resistance gene identification to optimize antimicrobial therapy.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
00 |