Why the study?
Diagnostic uncertainty differentiating viral from bacterial infections leads to antibiotic overuse in children, creating a need for a specific biomarker of viral infection.
Does blood MxA protein level discriminate between viral and bacterial infections in children hospitalized with an acute infection?
Does blood MxA protein level discriminate between viral and bacterial infections in children hospitalized with an acute infection?
Blood MxA protein shows moderate sensitivity and specificity for distinguishing viral from bacterial infections in hospitalized children, though viral-bacterial coinfections may limit its standalone utility.
MxA may aid viral diagnosis to limit pediatric antibiotic overuse; hypothesis-generating and requires prospective validation before practice change.
Due to the diagnostic uncertainty concerning the differentiation between viral and bacterial infections, children with viral infections are often treated with antibiotics, predisposing them to adverse effects and contributing to the emerging antibiotic resistance. Since currently available biomarkers only estimate the risk of bacterial infection, a biomarker for viral infection is needed in attempts of reducing antibiotic overuse. Blood MxA protein, which has broad antiviral activity and is rapidly induced in acute, symptomatic viral infections, is a potential biomarker for viral infection. In this diagnostic study of 265 children hospitalized because of an acute infection, blood MxA cutoff level of 256 μg/L discriminated between viral and bacterial infections with a sensitivity of 74% and specificity of 80%. MxA could improve the differential diagnostics of febrile children at the emergency department but, because of frequently detected viral-bacterial coinfections, a combination with biomarkers of bacterial infection may be needed.
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Piri et al. (2022) studied this question.
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