Multicenter evaluation of the Selux Next-Generation Phenotyping antimicrobial susceptibility testing system

Author:

Baker Kristin R.1ORCID,Flentie Kelly1,Spears Benjamin R.1,Mozharov Sergey1,Roberts Kristen1,El ganbour Asmae1,Somers Mark1,Calkwood John1,Liu Jamie1,DaPonte Kayla1,Sam Nikitha1,Kaur Gurleen1,Chen Felicia1,Donato Jonathan1,Chao Alan1,Lewis Autumn1,Sherman Jingzi1,Mortimer Karen1,Harrington Amanda T.2,Traczewski Maria3,Carpenter Darcie4,Shortridge Dee5ORCID,Lindley Jill5,Diep Alexander6,Norton Emmet6,Green Matt6,Gajewski Joe6,Landrith Rebecca6,Nalubega Fatuma6,McCallum Justin7,Beiswenger Melissa7,Dolan Brittany7,Brennan Kathleen7,Carpenter Afton7,Vacic Aleksandar1,Flyer Alec N.1,Pierce Virginia M.8ORCID,Hooper David C.9,Lewis II James S.10,Stern Eric1ORCID

Affiliation:

1. Selux Diagnostics, Charlestown, Massachusetts, USA

2. Pathology and Laboratory Medicine, Loyola University Medical Center, Maywood, Illinois, USA

3. Clinical Microbiology Institute (CMI), Wilsonville, Oregon, USA

4. IHMA, Schaumburg, Illinois, USA

5. JMI Laboratories/Element, North Liberty, Iowa, USA

6. Element, Acton, Massachusetts, USA

7. Boston Analytical, Salem, New Hampshire, USA

8. Pathology, University of Michigan Medical School, Ann Arbor, Michigan, USA

9. Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA

10. Department of Pharmacy Services, Oregon Health and Science University Hospitals and Clinics, Portland, Oregon, USA

Abstract

ABSTRACT The Selux Next-Generation Phenotyping (NGP) system (Charlestown, MA) is a new antimicrobial susceptibility testing system that utilizes two sequential assays performed on all wells of doubling dilution series to determine MICs. A multicenter evaluation of the performance of the Selux NGP system compared with reference broth microdilution was conducted following FDA recommendations and using FDA-defined breakpoints. A total of 2,488 clinical and challenge isolates were included; gram-negative isolates were tested against 24 antimicrobials, and gram-positive isolates were tested against 15 antimicrobials. Data is provided for all organism-antimicrobial combinations evaluated, including those that did and did not meet FDA performance requirements. Overall very major error and major error rates were less than 1% (31/3,805 and 107/15,606, respectively), essential agreement and categorical agreement were >95%, reproducibility was ≥95%, and the average time-to-result (from time of assay start to time of MIC result) was 5.65 hours.

Funder

ASPR AND BARDA

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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