Clinical Evaluation of the BIOFIRE SPOTFIRE Respiratory Panel
Authors:
- Wai-Sing ChanWCWai-Sing Chan
- Christy Wing-Yiu HoCHChristy Wing-Yiu Ho
- Tsz-Ching ChanTCTsz-Ching Chan
- Jeffrey HungJHJeffrey Hung
- Man-Yan ToMTMan-Yan To
- Sau-Man LeungSLSau-Man Leung
- Ka-Chun LaiKLKa-Chun Lai
- Ching-Yan WongCWChing-Yan Wong
- Chin-Pang LeungCLChin-Pang Leung
- Chun-Hang AuCAChun-Hang Au
- Thomas Shek-Kong WanTWThomas Shek-Kong Wan
- Jonpaul Sze-Tsing ZeeJZJonpaul Sze-Tsing Zee
Open Access
Abstract
The BIOFIRE SPOTFIRE Respiratory (R) Panel is a novel, in vitro diagnostic PCR assay with 15 pathogen targets. The runtime is about 15 min which is the shortest among similar panels in the market. We evaluated the performance of the SPOTFIRE R Panel with 151 specimens, including 133 collected from the upper respiratory tract (URT), 13 from the lower respiratory tract (LRT) and 5 external quality assessment program (EQAP) samples. The respiratory specimens were enrolled throughout the first two post-COVID-19 influenza seasons in Hong Kong (March to December 2023). For URT specimens, full concordance was observed between the SPOTFIRE R Panel and the standard-of-care FilmArray Respiratory 2.1 plus Panel (RP2.1plus) for 109 specimens (109/133, 81.95%). After discrepant analysis, the SPOTFIRE R Panel identified more pathogens than the RP2.1plus in 15 specimens and vice versa in 3 specimens. The per-target negative and positive percentage agreement (NPA and PPA) were 92.86–100% except the PPA of adenovirus (88.24%). For LRT and EQAP samples, all results were fully concordant. To conclude, the performance of the SPOTFIRE R Panel was comparable to the RP2.1plus.Keywords
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