Assessment of the FilmArray ME panel in 4199 consecutively tested cerebrospinal fluid samples

被引:24
作者
Lindstrom, Johan [1 ,2 ]
Elfving, Kristina [3 ,4 ]
Lindh, Magnus [2 ,5 ]
Westin, Johan [1 ,2 ]
Studahl, Marie [1 ,2 ]
机构
[1] Sahlgrens Univ Hosp, Dept Infect Dis, Reg Vastra Gotaland, Gothenburg, Sweden
[2] Univ Gothenburg, Inst Biomed, Dept Infect Dis, Gothenburg, Sweden
[3] Univ Gothenburg, Inst Med, Dept Publ Hlth & Community Med, Gothenburg, Sweden
[4] Sahlgrens Univ Hosp, Dept Paediat, Reg Vastra Gotaland, Gothenburg, Sweden
[5] Sahlgrens Univ Hosp, Dept Clin Microbiol, Reg Vastra Gotaland, Gothenburg, Sweden
关键词
Encephalitis; FilmArray; Meningitis; Multiplex PCR; Syndromic testing; HUMAN-HERPESVIRUS-6; DNA; DIAGNOSIS; PCR; ENCEPHALITIS; CYTOMEGALOVIRUS; MANIFESTATIONS; ENTEROVIRUS; TYPE-1;
D O I
10.1016/j.cmi.2021.05.017
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: In central nervous system infections, early and correct management is of utmost importance. Rapid syndromic panel testing can potentially provide valuable guidance. The FilmArray meningitis/ encephalitis (ME) panel detects 14 pathogens through multiplex PCR. Our study objectives were to assess its performance compared with established diagnostic procedures, especially real-time quantitative PCR for detection of viruses, and to determine the diagnostic and clinical significance of discrepant results. Methods: All cerebrospinal fluid samples sent for viral diagnostics to our microbiological laboratory over 34 months were analysed with the ME panel and in-house real-time PCR for herpes simplex virus type 1 (HSV-1), HSV-2, varicella zoster virus and enteroviruses. Other pathogens detected by the panel were confirmed by routine diagnostic procedures. Discrepant results were analysed through interpretation of biological and clinical data, and performance data were calculated for individual pathogens. Results: Altogether, 315 pathogens were detected by the ME panel in 4199 cerebrospinal fluid samples (7.5%) and an additional 21 viral targets were identified using real-time PCR. Thirty-four ME panel de-tections were not confirmed, totalling 55 discrepant results. After discrepancy analysis, 20 false-positive and 21 false-negative ME panel results remained. Performance varied between pathogens. Sensitivity for HSV-1 was calculated at 82.4% (59.0%-93.8%) with three false-negative results. Also noteworthy were 13 false-negative enterovirus and eight false-positive Streptococcus pneumoniae results. Conclusions: Our analysis shows good performance for the ME panel in diagnosing central nervous system infection. The risk of false-negative HSV-1 results, however, warrants additional testing when encephalitis is suspected. Uncertainties in interpretation of enterovirus and S. pneumoniae results represent other limitations. Johan Lindstro euro m, Clin Microbiol Infect 2022;28:79 (c) 2021 The Author(s). Published by Elsevier Ltd on behalf of European Society of Clinical Microbiology and Infectious Diseases. This is an open access article under the CC BY license (http://creativecommons. org/licenses/by/4.0/).
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收藏
页码:79 / 84
页数:6
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