ArticleFrontiers in neuroscience2026
Development and validation of a risk stratification tool for 28-day mortality based on D-dimer to platelet ratio in moderate-to -severe traumatic brain injury: a retrospective cohort study.
Article in Frontiers in neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Moderate-to-severe traumatic brain injury (msTBI) is associated with significant mortality. Post-injury coagulopathy, involving elevated fibrinolysis (reflected by D-dimer) and platelet consumption (reflected by platelet count), contributes to acute neurological deterioration and poor outcomes. This study evaluated the potential association of the D-dimer to platelet ratio (DPR) with 28-day all-cause mortality and explored its link to early neurological progression as a mechanistic validation in patients with msTBI. Methods: This retrospective, single-center cohort study included 340 patients with msTBI. Patients were divided into training ( Results: In the multivariable Cox regression, Glasgow Coma Scale (GCS), admission blood glucose (ABG), and DPR (per 1 SD increase) (HR: 1.558, 95% CI: 1.291-1.881, Conclusion: Admission DPR is an independent risk marker associated with both acute neurological progression and 28-day mortality in patients with msTBI. The DPR-B tool, incorporating GCS, ABG, and DPR, offers a potential framework for early risk stratification; however, its clinical generalizability and translational value for guiding therapeutic interventions warrant further validation in prospective studies using more proximal, pathophysiologically relevant outcomes.
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