Abstract

Introduction: Subarachnoid hemorrhage (SAH) is a devastating disease that portends a high rate of morbidity and early mortality in its patients. Although brain injury that is assumed in the early phases of SAH is an important prognosticator of functional outcome, the underlying mechanism behind the acute phase of the disease is still poorly understood. The aim of this study is to investigate endothelial inflammation in the early phases of SAH, and to determine its association with severity of bleed, mortality risk, and functional outcome. Hypothesis: We hypothesize that endothelial inflammation will be higher in SAH patients with severe bleed and poor functional outcome. Methods: Patients (n=15) admitted to our neurosurgical intensive care unit within 24 hours of bleed onset (day 1) and angiographic evidence of aneurysmal SAH were identified. Endothelial inflammation was studied as intracellular adhesion marker-1 (ICAM-1) levels in blood samples drawn at admission and on days 3 and 7 post-SAH (ICAM-1 ELISA; R&D Systems). Severity of bleed and patient status at admission was studied via Hunt Hess (HH) (1-5) grade and modified Fisher (mF) score (0-4), and 7-day outcome was assessed via Rankin functional and NIHSS score. ANOVA and Pearson correlation analyses (SAS) were used to assess the data. Results: ELISA analysis demonstrated that levels of ICAM-1/CD54 were significantly greater in high grade (grade 4) mF score (p=0.025, ANOVA), and correlated to higher Rankin score (p=0.0097, Pearson). HH scores when grouped as 1,2 vs 3 vs 4,5 showed a positive trend in relation to increased ICAM-1/CD54 (p=0.087, ANOVA). No correlation between ICAM-1 level and NIHSS score was found. Conclusion: Endothelial inflammation (ICAM-1/CD54 levels) associates with severity of bleed and poor 7 day outcome, and hence may serve as a useful biomarker for assessment of clinical severity of bleed in SAH patients.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.