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Background: Children are a vulnerable population for mild traumatic brain injury (mTBI), accounting for a high burden of emergency department (ED) visits. A significant and unpredictable subset will develop persistent post-concussion symptoms (P-PCS), with consequences for daily quality of life. At ED discharge, no reliable tool exists to identify children requiring neuropsychological follow-up. Acute blood biomarkers represent a promising approach for early risk stratification. Methods: In this prospective multicenter cohort study, children with mTBI had a blood sample collected within 24 h of injury for biomarker analysis (S100b, NfL, NTproBNP, GFAP, HFABP, IL6, IL10). The parent version of the Post Concussion Symptom Inventory (PCSI-P) was sent at 14 days and 3 months post-injury. P-PCS were defined as the presence of three or more symptoms worsening by at least one point above pre-injury baseline at both timepoints. This analysis included only children identified to be symptomatic at 14 days. Within this group, biomarker levels were compared between those with P-PCS at 3 months and those who had recovered. At the optimal Youden index threshold, IL10 achieved 100% sensitivity and 55.6% specificity for ruling-out P-PCS. At 100% specificity, IL10 achieved a sensitivity of 31% for ruling-in P-PCS. Conclusion: This exploratory study suggests that early IL10 measured at ED presentation may support two complementary risk-stratification strategies: a rule-out approach (100% negative predictive value [NPV]) to safely exclude children unlikely to develop P-PCS, and a rule-in approach (100% positive predictive value [PPV]) to identify those at high risk of requiring neuropsychological follow-up. Consistent with adult TBI literature, these findings highlight the acute neuroinflammatory response in pediatric recovery. Replication in larger cohorts is needed before clinical application.
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Chiollaz et al. (2026) studied this question.
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