Affiliation:
1. Department of Paediatrics and Adolescent Medicine, Turku University Hospital and University of Turku
2. InFLAMES Research Flagship Center, University of Turku
3. Institute of Biomedicine, University of Turku and Department of Clinical Microbiology, Turku University Hospital , Turku , Finland
Abstract
Abstract
Background
Prompt differentiation of viral from bacterial infections in febrile children is pivotal in reducing antibiotic overuse. Myxovirus resistance protein A (MxA) is a promising viral biomarker.
Methods
We evaluated the accuracy of a point-of-care (POC) measurement for blood MxA level compared to the reference enzyme immunoassay in 228 febrile children aged between 4 weeks and 16 years, enrolled primarily at the emergency department (ED). Furthermore, we analyzed the ability of MxA to differentiate viral from bacterial infections.
Results
The mean difference between POC and reference MxA level was −76 µg/L (95% limits of agreement from −409 to 257 µg/L). Using a cutoff of 200 µg/L, POC results were uniform with the reference assay in 199 (87.3%) children. In ED-collected samples, the median POC MxA level was 571 (interquartile range [IQR], 240–955) µg/L in children with viral infections, 555 (IQR, 103–889) µg/L in children with viral-bacterial coinfections, and 25 (IQR, 25–54) µg/L in children with bacterial infections (P < .001). MxA cutoff of 101 µg/L differentiated between viral and bacterial infections with 92% sensitivity and 91% specificity.
Conclusions
POC MxA measurement demonstrated acceptable analytical accuracy compared to the reference method, and good diagnostic accuracy as a biomarker for viral infections.
Funder
University of Turku
Foundation for Pediatric Research
Maud Kuistila Memorial Foundation
Päivikki and Sakari Sohlberg Foundation
Labmaster Ltd
Publisher
Oxford University Press (OUP)