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Clinical validation of S100B in the management of a mild traumatic brain injury: issues from an interventional cohort of 1449 adult patients

  • Gautier Allouchery , Farès Moustafa , Jean Roubin , Bruno Pereira , Jeannot Schmidt , Julien Raconnat , Daniel Pic , Vincent Sapin and Damien Bouvier EMAIL logo
Published/Copyright: June 20, 2018

Abstract

Background:

This study’s primary objective was to validate the routine use of S100B via a prospective study. The aim was a reduction of cranial computed tomography (CCT) scans by 30%. The secondary goal was to investigate the influence of age and associated risk factors on the reduction of CCT.

Methods:

S100B (sampling within 3 h postinjury) was used for patients with mild traumatic brain injury (mTBIs) presenting a medium risk of complications and requiring a CCT scan. Patients with negative S100B (S100B−) were discharged without a CCT scan.

Results:

Of the 1449 patients included in this study, 468 (32.3%) had S100B− with a sensitivity of 96.4% (95% CI: 87.5%–99.6%), a specificity of 33.4% (95% CI: 31%–36%) and a negative predictive value of 99.6% (95% CI: 98.5%–99.9%). No significant difference in serum levels or the S100B+ rate was observed if patients had retrograde amnesia (0.16 μg/L; 63.8%), loss of consciousness (0.13; 63.6%) or antiplatelet therapy (0.20; 77.9%). Significant differences were found between the S100B concentrations and S100B positivity rates in patients >65 years old and all the groups with patients <55 years old (18–25, 26–35, 36–45 and 46–55). From 18 to 65 years old (n=874), the specificity is 39.3% (95% CI: 36%–42.6%) compared to 18.7% (95% CI: 15.3%–22.3%) for patients >65 years old (n=504).

Conclusions:

The clinical use of S100B in mTBI management reduces the use of CCTs by approximately one-third; furthermore, the percentage of CCTs reduction is influenced by the age of the patient.


Corresponding author: Dr. Damien Bouvier, Université Clermont Auvergne, CNRS, INSERM, GReD, Clermont-Ferrand, France, Phone: +33 4 73 75 48 82, Fax: +33 4 73 75 18 55
aGautier Allouchery and Farès Moustafa are considered co-first authors.

Acknowledgments

The authors would like to thank Scribendi for the academic editing of the manuscript.

  1. Author contributions: VS and DB conceived of the study, designed the trial and obtained ethical approval. GA and FM supervised the trial and data collection. FM, JRo, JS, JRa and DP recruited the patients. BP provided statistical advice for the study’s design and analyzed the data. GA drafted the manuscript, and all the authors substantially contributed to its revision. DB takes responsibility for the paper as a whole. All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2018-01-31
Accepted: 2018-05-22
Published Online: 2018-06-20
Published in Print: 2018-10-25

©2018 Walter de Gruyter GmbH, Berlin/Boston

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