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The Significance of FilmArray Blood Culture Identification Panel (FA-BCID) for Managing Patients with Positive Blood Cultures

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Abstract
We analyzed the accuracy and time efficiency of the FilmArray blood culture identification (FA-BCID) panel in identifying the pathogens in positive blood cultures. Two-hundred and seventy-two individuals were randomly assigned as the control (n = 212) and FA-BCID (n = 60) groups participating in this study. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) was used to assess the control group. Meanwhile, the FA-BCID group was evaluated using both FA-BCID and MALDI-TOF, and the results were compared. The identification results from 73% (44/60) of the blood samples demonstrated agreement between FA-BCID and MALDI-TOF. The FA-BCID panel detected mecA genes in seven Staphylococcus species; six cases were confirmed using antimicrobial susceptibility testing. In addition, KPC genes were detected in one Escherichia coli and one Klebsiella pneumoniae, although only the latter corresponded with the result from antimicrobial susceptibility testing. The turnaround time (TAT) for identification through FA-BCID was shorter, with a median of 3.6 [2.4-4.6] hours (p < 0.05). No significant differences in the clinical and microbial outcomes following the ASP were observed between FA-BCID and MALDI-TOF. These results suggest that the FA-BCID panel provides an identification result that is as reliable as that provided by the routine identification procedure but with shorter TAT; thus, the FA-BCID method is considered an effective and beneficial method for therapeutic decision making and the improvement of the ASP for patients with bloodstream infection.
All Author(s)
Kristin Widyasari ; Seungjun Lee ; Oh-Hyun Cho ; Sun-In Hong ; Byung-Han Ryu ; Sunjoo Kim
Issued Date
2023
Type
Article
Keyword
FA-BCIDMALDI-TOFantimicrobial stewardship programblood culturepathogen identification
Publisher
MDPI
ISSN
2075-4418
Citation Title
Diagnostics
Citation Volume
13
Citation Number
21
Citation Start Page
3335
Citation End Page
3335
Language(ISO)
eng
DOI
10.3390/diagnostics13213335
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/3406
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