Abstract

Background/Objective: Hematoma expansion (HE) predicts poor outcome and is an appealing treatment target in spontaneous intracerebral hemorrhage (ICH). Clinical evidence has shown an association of HE with peripheral white blood cells (WBC) count, but the individual contributions of leukocyte subtypes between literatures are described inconsistently. Our aim was to determine the relationship between admission absolute and differential leukocyte counts and HE by using different growth definitions.Methods: We analyzed spontaneous ICH patients who underwent baseline cranial computed tomography and blood sampling within 6 h of stroke onset in our institution between September 2013 and August 2018. Hematoma volume was calculated using a semiautomated 3-dimensional reconstruction algorithm. According to commonly used absolute or relative growth definitions (>6 mL, >12.5 mL, or >33%), we defined 5 types of HE. A propensity score-matching analysis was performed to evaluate the influence of complete blood count components on HE across the various growth definitions. The receiver operating characteristic analysis assessed the predictive ability of leukocyte counts for HE.Results: A total of 1,066 patients were included, of whom 11–21% met the 5 HE definitions. After propensity score-matching, except using the definition of >12.5 mL growth or its combination with >33% growth, both WBC and neutrophil count were independently associated with reduced risk of HE (odds ratio [OR] for 103 cells increase; OR, 0.86–0.99; all p < 0.05) after adjusting confounders in multivariate analyses. However, monocyte count was correlated with increased risk of HE under the usage of >12.5 mL expansion definition only (OR, 1.43; p = 0.024). There was no association between lymphocyte count and HE (all p > 0.05). Regardless of the growth definition, admission eosinophil count was directly associated with the risk of HE (OR, 6.92–31.60; all p < 0.05), and was the best predictive subtype with area under the curve 0.64, sensitivity 69.5%, and specificity 58.9% at the optimal cut-off value of 45 cells/μL.Conclusions: Growth definition affects the relationship of HE with leukocyte subtypes counting. Eosinophil count robustly predicts HE, and may be a surrogate when using an inflammatory marker to help select acute ICH patients with high expansion risk for hemostasis treatment in clinical trial and practice.

Highlights

  • Intracerebral hemorrhage (ICH) is the most lethal stroke subtype with a mortality of about 40% at 1 month (1)

  • Result from a study with large ICH population showed that the risk of Hematoma expansion (HE) was directly associated with monocyte count when HE was defined as a volume increase >6 mL or 30% (8)

  • Patients who met the following conditions were subsequently excluded from this study: (1) traumatic intracerebral hemorrhage or hemorrhagic transformation of a brain infarction (n = 746), (2) tumor, aneurysm or arteriovenous malformation presumed to be the potential cause of the bleeding (n = 95), (3) primary intraventricular hemorrhage or multiple cerebral hemorrhage (n = 47), (4) presence of encephalitis, pneumonia, or parasitic infection during the past week (n = 41), (5) surgical evacuation performed before the follow-up computed tomography (CT) (n = 506), (6) usage of anticoagulants or antiplatelet drugs before intracerebral hemorrhage (n = 30), and (7) lack of complete blood count data on admission (n = 15)

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Summary

Introduction

Intracerebral hemorrhage (ICH) is the most lethal stroke subtype with a mortality of about 40% at 1 month (1). Preclinical studies have found that leukocytes infiltrate around the hematoma within hours following ICH, and neutrophils are the earliest inflammatory cells to invade the CNS (11, 12). Interleukin-27/lactoferrin-mediated neutrophil polarization can enhance hematoma clearance and improve neurological function in an animal model of ICH (7). The relevance of leukocyte counts to poor ICH prognosis has received increasing attention, but no consensus is reached (13–16). As a potential mechanism of this association, was found in relation to admission WBC count (8). Result from a study with large ICH population showed that the risk of HE was directly associated with monocyte count when HE was defined as a volume increase >6 mL or 30% (8). In another study defining HE as any degree of growth, investigators found no association between admission monocyte count and HE (17)

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