Serum S100B Level in the Management of Pediatric Minor Head Trauma

Author:

Bouvier Damien1,Cantais Aymeric2,Laspougeas Alban3,Lorton Fleur4,Plenier Yannick5,Cottier Maria6,Fournier Philippe7,Tran Antoine8,Moreau Emilie9,Durif Julie10,Sarret Catherine11,Mourgues Charline12,Sturtz Franck13,Oudart Jean-Baptiste14,Raffort Juliette15,Gonzalo Philippe16,Cristol Jean-Paul17,Masson Damien18,Pereira Bruno12,Sapin Vincent1

Affiliation:

1. Department of Biochemistry and Molecular Genetics, Centre Hospitalier Universitaire (CHU) Clermont-Ferrand, Université Clermont Auvergne, Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), Génétique, Reproduction et Développement, Clermont-Ferrand, France.

2. Department of Pediatrics, CHU Saint-Etienne, Saint-Etienne, France

3. Department of Pediatrics, CHU Limoges, Limoges, France

4. Pediatric Emergency Department, Nantes Université, CHU Nantes, INSERM, Centre d’Investigation Clinique 1413, Nantes, France

5. Department of Pediatrics, CHU Reims, Reims, France

6. Department of Pediatrics, CHU Montpellier, Montpellier, France

7. Department of Pediatrics, CHU Nîmes, Nîmes, France

8. Department of Pediatrics, CHU Nice, Nice, France

9. Department of Pediatrics, Assistance Publique–Hôpitaux de Marseille, Marseille, France

10. Department of Biochemistry and Molecular Genetics, CHU Clermont-Ferrand, Clermont-Ferrand, France

11. Department of Pediatrics, CHU Clermont-Ferrand, Université Clermont Auvergne, CNRS, SIGMA, Thérapies Guidées par l’Image, Clermont-Ferrand, France

12. Biostatistics Unit (Délégation à la Recherche Clinique et à l’Innovation), CHU Clermont-Ferrand, Clermont-Ferrand, France

13. Department of Biochemistry, CHU Limoges, Limoges, France

14. Faculté de Médecine, Université de Reims Champagne-Ardenne, Matrice Extracellulaire et Dynamique Cellulaire Unit, UMR CNRS 7369, Reims, France

15. Department of Biochemistry, CHU Nice, Nice, France

16. Department of Biochemistry and Pharmacology, CHU Saint-Etienne, Saint-Etienne, France

17. Department of Biochemistry, CHU Montpellier, Montpellier, France

18. Department of Biochemistry, CHU Nantes, Nantes, France

Abstract

ImportanceMinor head trauma (HT) is one of the most common causes of hospitalization in children. A diagnostic test could prevent unnecessary hospitalizations and cranial computed tomographic (CCT) scans.ObjectiveTo evaluate the effectiveness of serum S100B values in reducing exposure to CCT scans and in-hospital observation in children with minor HT.Design, Setting, and ParticipantsThis multicenter, unblinded, prospective, interventional randomized clinical trial used a stepped-wedge cluster design to compare S100B biomonitoring and control groups at 11 centers in France. Participants included children and adolescents 16 years or younger (hereinafter referred to as children) admitted to the emergency department with minor HT. The enrollment period was November 1, 2016, to October 31, 2021, with a follow-up period of 1 month for each patient. Data were analyzed from March 7 to May 29, 2023, based on the modified intention-to-treat and per protocol populations.InterventionsChildren in the control group had CCT scans or were hospitalized according to current recommendations. In the S100B biomonitoring group, blood sampling took place within 3 hours after minor HT, and management depended on serum S100B protein levels. If the S100B level was within the reference range according to age, the children were discharged from the emergency department. Otherwise, children were treated as in the control group.Main Outcomes and MeasuresProportion of CCT scans performed (absence or presence of CCT scan for each patient) in the 48 hours following minor HT.ResultsA total of 2078 children were included: 926 in the control group and 1152 in the S100B biomonitoring group (1235 [59.4%] boys; median age, 3.2 [IQR, 1.0-8.5] years). Cranial CT scans were performed in 299 children (32.3%) in the control group and 112 (9.7%) in the S100B biomonitoring group. This difference of 23% (95% CI, 19%-26%) was not statistically significant (P = .44) due to an intraclass correlation coefficient of 0.32. A statistically significant 50% reduction in hospitalizations (95% CI, 47%-53%) was observed in the S100B biomonitoring group (479 [41.6%] vs 849 [91.7%]; P < .001).Conclusions and RelevanceIn this randomized clinical trial of effectiveness of the serum S100B level in the management of pediatric minor HT, S100B biomonitoring yielded a reduction in the number of CCT scans and in-hospital observation when measured in accordance with the conditions defined by a clinical decision algorithm.Trial RegistrationClinicalTrials.gov Identifier: NCT02819778

Publisher

American Medical Association (AMA)

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