The BioFire joint infection panel also known as BJI Panel test, enhances joint infection diagnosis by providing reliable results and detects a range of pathogens and antimicrobial resistance gene targets via synovial fluid sample testing. The Biofire Panel is performed using a FDA-Approved Biofire System by Rapid Multiplex PCR method which produces an average of 91.7% sensitivity and 99.8% specificity for pathogens, with a same-day reporting TAT for samples collected before 11AM at HOD. 

Please find the parameters below and a sample report attached for demonstration.

The BioFire joint infection panel is conducted via synovial fluid sampling for various pathogens detected via Rapid Multiplex PCR using the Biofire System with same-day reporting*. 

Biofire Joint Infection (JI) Panel

Includes 38 Test Parameters

Test Preparation:

Reporting TAT :

Specializations :

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