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Cytotoxic Edema and Intra-parenchymal Hemorrhage: A Mediated Pathway to Mortality and Functional Outcome in Cerebral Venous Sinus Thrombosis- A sub-analysis of the CLOT-VENUS Registry

  • Nashwa Abdelhakim
    ,
  • Milagros Galecio-Castillo
    ,
  • Piyush Kalakoti
    ,
  • Leonardo Cruz-Criollo
    ,
  • ,
  • Anderson Brito
*Corresponding author for this work
  • University of Iowa Health Care
    ,
  • ,
  • Instituto Nacional De Neurologia Y Neurocirugia
    ,
  • The University of Iowa
    ,
  • University of Iowa College of Medicine
    ,
  • Rafael A Calderón Guardia Hospital
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Article number

41

Journal (Volume, Issue Number)

Translational Stroke Research (Volume 17, Issue 2)

Publication milestones

  • Published - 04/2026

Publication status

Published - 04/2026

ISSN

1868-4483

Publication IDs

  • Scopus: 105035679583
  • PubMed: 41975110

Abstract

Cytotoxic edema (CE) is a radiographic marker of early tissue injury in cerebral venous thrombosis (CVT) associated with poor outcomes, yet its mechanistic pathway remains unclear. We investigated whether intraparenchymal hemorrhage (IPH) mediates the association between CE and outcomes. We conducted a retrospective cohort study using the multicenter CLOT-VENUS registry, including acute CVT patients treated at two Comprehensive Stroke Centers in the USA and Mexico (2004–2024). CE was defined as hyperintensities around IPH or venous infarct with DWI restricted diffusion and corresponding low ADC, confirming true restricted diffusion. IPH was defined as hemorrhagic transformation of venous infarction or intracerebral hemorrhage on GRE MRI and/or NCCT. Mediation analyses assessed whether IPH mediated CE associations with in-hospital mortality and functional outcomes. Among 394 patients (mean age 42.7 years; 65.5% female), 128 (32.5%) demonstrated CE and 111(30.2%) IPH. CE was associated with in-hospital mortality (aOR 2.63, 95% CI 1.01–7.12) and poor 6-month mRS (aOR 1.71, 95% CI 1.06–2.74). CE was associated with IPH, which in turn was associated with mortality (aOR 8.73, 95% CI 2.93–30.45) and poor mRS (aOR 1.96, 95% CI 1.18–3.25). Adjustment for IPH rendered the CE-outcome associations non-significant. IPH accounted for 76.8% of CE’s effect on mortality and 83.8% on 6-month mRS. Our findings suggest that IPH likely mediates the effect of CE on outcomes in CVT. Although the temporal sequence could not be confirmed, the results underscore the value of early CE detection for timely intervention.