Abstract

Background: Patients with spontaneous intracerebral hemorrhage (ICH) have high mortality and morbidity rates; approximately one-third of patients with ICH experience hematoma expansion (HE). The spot sign is an established and validated imaging marker for HE. High-sensitivity C-reactive protein (hs-CRP) is an established laboratory marker for inflammation and secondary brain injury following ICH.Objective: To determine the association between the spot sign and hs-CRP, hematoma expansion, and clinical outcomes.Methods: Between December 2014 and September 2016, we prospectively recruited 1,964 patients with acute symptomatic ICH at 13 hospitals in Beijing, China. Next, we selected 92 patients within 24 h of the onset of symptoms from this cohort for the present study. ICH was diagnosed in the emergency room by non-contrast computed tomography (NCCT) scans. Follow-up scans were carried out within 48 h to evaluate patients for HE. Multidetector computed tomography angiography (MDCTA) was also used to identify spot signs. Blood samples were collected from each patient at admission in EDTA tubes (for plasma) or vacutainer tubes (for serum). hs-CRP values were determined by a particle-enhanced immunoturbidimetric assay in the laboratory at Beijing Tiantan Hospital, Capital Medical University. Patients were categorized into two groups according to their hs-CRP levels (hs-CRP <3 mg/L, hs-CRP ≥3 mg/L).Results: The incidences of spot sign and HE in our study cohort were 31.5 and 29.3%, respectively. Following the removal of potential confounding variables, stepwise-forward logistic regression analysis identified that an hs-CRP level ≥3 mg/L was not a significant indicator for either spot sign (p = 0.68) or HE (p = 0.07). However, an hs-CRP level ≥3 mg/L (odds ratio: 16.64, 95% confidence interval: 2.11–131.45, p = 0.008) was identified as an independent predictor of an unfavorable outcome 1 year after acute ICH.Conclusions: Our analyses identified that an hs-CRP level ≥3 mg/L was a significant indicator for an unfavorable outcome 1 year after acute ICH.

Highlights

  • Spontaneous intracerebral hemorrhage (ICH) is a devastating subtype of stroke with high global rates of mortality and morbidity [1]

  • Following the removal of potential confounding variables, stepwise-forward logistic regression analysis identified that an High-sensitivity C-reactive protein (hs-CRP) level ≥3 mg/L was not a significant indicator for either spot sign (p = 0.68) or hematoma expansion (HE) (p = 0.07)

  • Our analyses identified that an hs-CRP level ≥3 mg/L was a significant indicator for an unfavorable outcome 1 year after acute ICH

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Summary

Introduction

Spontaneous intracerebral hemorrhage (ICH) is a devastating subtype of stroke with high global rates of mortality and morbidity [1]. Up to one-third of patients with ICH may experience hematoma expansion (HE), leading to a higher mortality rate and unfavorable clinical outcomes [2, 3]. Other research studies have reported that a number of indicators are associated with HE and poor outcomes in patients with ICH, including non-contrast CT (NCCT) markers, such as computed tomography (CT) hypodensities [7], the black hole sign [8], the blend sign [9], and the island sign [10]. Patients with spontaneous intracerebral hemorrhage (ICH) have high mortality and morbidity rates; approximately one-third of patients with ICH experience hematoma expansion (HE). High-sensitivity C-reactive protein (hs-CRP) is an established laboratory marker for inflammation and secondary brain injury following ICH

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