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Diagnostic studyAcademic Emergency Medicine

Effect of blood alcohol on the diagnostic accuracy of glial fibrillary acidic protein and ubiquitin carboxy-terminal hydrolase L1 for traumatic intracranial hemorrhage: A TRACK-TBI study.

First online Feb 18, 2025On EM Weekly Oct 29, 2026Discovered Oct 29, 2026AI-generated Not yet human-reviewed
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Summary

In this prospective multicenter TRACK-TBI diagnostic study, investigators examined whether alcohol intoxication changed the accuracy of GFAP plus UCH-L1 for CT-detectable traumatic intracranial injury. Among 2,320 patients assessed within 24 hours of TBI at 18 US Level I trauma centers, combined biomarker AUC was 0.949 with blood alcohol >300 mg/dL, 0.858 with 81–300 mg/dL, 0.849 with 0–80 mg/dL, and 0.883 when alcohol level was unavailable. The study supports preserved discrimination in intoxicated patients but does not itself validate a disposition pathway.

Why it matters

Intoxication alone need not make GFAP/UCH-L1 biologically uninterpretable in an otherwise eligible TBI evaluation. Use remains bounded by the assay's validated indication and local implementation, not by this observational subgroup analysis alone.

Study at a glance

Design
Diagnostic study
Population
Adults and other TRACK-TBI participants presenting within 24 hours of TBI at 18 US Level I trauma centers; alcohol-stratified diagnostic analysis.
Sample size
2320
Intervention
Plasma GFAP and UCH-L1 measured on Abbott i-STAT Alinity and ARCHITECT assays.
Comparator
Diagnostic performance across blood-alcohol strata: >300, 81–300, 0–80 mg/dL, or unavailable.
Primary endpoint
Discrimination (AUC) of combined GFAP and UCH-L1 for CT-positive traumatic intracranial injury.

Main findings

  • 48.3% of the cohort had a positive brain CT.
  • Combined biomarker AUC was 0.949 with blood alcohol >300 mg/dL versus 0.849 with 0–80 mg/dL.
  • Elevated alcohol did not lower combined-biomarker discrimination in this cohort.

Limitations

This was a secondary diagnostic-accuracy analysis with a high CT-positive prevalence (48.3%) at Level I trauma centers. It did not test a biomarker-led CT-reduction or discharge strategy, and the most severe alcohol subgroup was small (n=54).

Read the primary source

Full text: Abstract available; full text paywalled.

Original source

DOI: 10.1111/acem.15109

PMID: 39967286

Source retrieved Oct 29, 2026. Primary PubMed abstract and publisher abstract were reviewed. The paper reports a prospective multicenter diagnostic analysis, not a randomized imaging strategy.

Corrections & review history

No corrections recorded. Human review: not yet human-reviewed.