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

Author:

Widyasari Kristin1,Lee Seungjun23ORCID,Cho Oh-Hyun4,Hong Sun-In5,Ryu Byung-Han6,Kim Sunjoo123

Affiliation:

1. Institute of Medical Science, Gyeongsang National University, Jinju 52828, Republic of Korea

2. Department of Laboratory Medicine, Gyeongsang National University Changwon Hospital, Changwon 51472, Republic of Korea

3. Department of Laboratory Medicine, College of Medicine, Gyeongsang National University, Jinju 52828, Republic of Korea

4. Department of Internal Medicine, Soonchunhyang University Cheonan Hospital, Cheonan 31151, Republic of Korea

5. Division of Infectious Diseases, College of Medicine, Soonchunhyang University Cheonan Hospital, Soonchunhyang University, Cheonan 31151, Republic of Korea

6. Department of Internal Medicine, Anyang SAM Hospital, Anyang 14030, Republic of Korea

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.

Funder

National Research Foundation (NRF) of Republic of Korea

Publisher

MDPI AG

Subject

Clinical Biochemistry

Reference29 articles.

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