Abstract
Object: Inflammatory response is an important determinant of subsequent brain injury after deep-seated intracerebral hemorrhage (ICH). The ratio of red blood cell (RBC) distribution width to platelet count (RPR) has been established as a new index to reflect the severity of inflammation. To the best of our knowledge, no association between RPR and prognosis after spontaneous ICH has yet been reported.Methods: In all patients with deep-seated ICH treated at our Neurovascular Center from 2014 to 2020, initial laboratory values were obtained to determine RPR in addition to patient characteristics and known risk factors. Subsequent multivariate analysis was performed to identify independent risk factors for 90-day mortality after deep-seated ICH.Results: Hundred and two patients with deep-seated ICH were identified and further analyzed. Patients with an initial RPR < 0.06 exhibited significantly lower mortality rate after 90 days than those with an initial RPR ≥ 0.06 (27 vs. 57%; p = 0.003). Multivariate analysis identified “ICH score ≥ 3” (p = 0.001), “anemia on admission” (p = 0.01), and “elevated RPR ≥ 0.06” (p = 0.03) as independent predictors of 90-day mortality.Conclusions: The present study constitutes the first attempt to demonstrate that the ratio of RBC distribution width to platelets—as an independent inflammatory marker—might serve for prognostic assessment in deep-seated ICH.
Highlights
Patients that suffer from spontaneous intracerebral hemorrhage (ICH) often display significant morbidity/mortality due to the extent and/or the location of the bleed [1]
This retrospective study includes 102 patients with spontaneous deep-seated ICH who were referred to our Neurovascular Center for further management between 2014 and July 2020
Given the experience from previous studies on the clinical significance of the ICH score pertaining to mortality, the groups were divided into patients with an initial ICH score
Summary
Patients that suffer from spontaneous intracerebral hemorrhage (ICH) often display significant morbidity/mortality due to the extent and/or the location of the bleed [1]. Intracerebral hemorrhage-induced inflammation precedes disruption of the blood-brain barrier (BBB) and in patients with spontaneous ICH, concurrent alterations of immune profiles within peripheral blood have been observed [10]. Such alterations in peripheral blood have been the target of numerous efforts to establish markers for early ICH prognostication [11,12,13]
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