4.6 Article

Comparison of novel rapid diagnostic of blood culture identification and antimicrobial susceptibility testing by Accelerate Pheno system and BioFire FilmArray Blood Culture Identification and BioFire FilmArray Blood Culture Identification 2 panels

Journal

BMC MICROBIOLOGY
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12866-021-02403-y

Keywords

Susceptibility testing; Pheno; Blood culture; Antimicrobial resistance; Identification; Rapid tests; Bloodstream infections; Filmarray

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This study evaluated the performance of different commercial methods for rapid identification and antimicrobial susceptibility testing (AST) in positive blood culture samples, and found that methods such as the Pheno system, BioFire FilmArray BCID panel, and VITEK 2 all demonstrated high accuracy and consistency. Factors such as turnaround time, range of antibiotic choices, and hands-on time should be considered when selecting appropriate rapid identification and AST methods for positive blood culture in different laboratory settings.
Background: Conventional turnaround time (TAT) for positive blood culture (PBC) identification (ID) and antimicrobial susceptibility testing (AST) is 2-3 days. We evaluated the TAT and ID/AST performance using clinical and seeded samples directly from PBC bottles with different commercial approaches: (1) Accelerate Pheno (R) system (Pheno) for ID/AST; (2) BioFire (R) FilmArray (R) Blood Culture Identification (BCID) Panel and/or BCID2 for ID; (3) direct AST by VITEK (R) 2 (direct AST); and (4) overnight culture using VITEK (R) 2 colony AST. Results: A total of 141 PBC samples were included in this evaluation. Using MALDI-TOF (Bruker MALDI Biotyper) as the reference method for ID, the overall monomicrobial ID sensitivity/specificity are as follows: Pheno 97.9/99.9%; BCID 100/100%; and BCID2 100/100%, respectively. For AST performance, broth microdilution (BMD) was used as the reference method. For gram-negatives, overall categorical and essential agreements (CA/EA) for each method were: Pheno 90.3/93.2%; direct AST 92.6/88.5%; colony AST 94.4/89.5%, respectively. For gram-positives, the overall CA/EAs were as follows: Pheno 97.2/98.89%; direct AST 97.2/100%; colony AST 97.2/100%, respectively. The BCID/BCID2 and direct AST TATs were around 9-20 h (1/9-19 h for ID with resistance markers/AST), with 15 min/sample hands-on time. In comparison, Pheno TATs were around 8-10 h (1.5/7 h for ID/AST) with 2 min/sample hands-on time, maintains a clinically relevant fast report of antibiotic minimal inhibitory concentration (MIC) and allows for less TAT and hands-on time. Conclusion: In conclusion, to the best of our knowledge, this is the first study conducted as such in Asia; all studied approaches achieved satisfactory performance, factors such as TAT, panel of antibiotics choices and hands-on time should be considered for the selection of appropriate rapid ID and AST of PBC methods in different laboratory settings.

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