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J Stroke Cerebrovasc Dis ; 29(8): 104861, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32430234

ABSTRACT

OBJECTIVE: After an intracerebral hemorrhage, there is an immunological reaction, the specific mechanism of which is not fully understood, that seems to contribute to secondary brain injury. In this study, we investigated alterations of inflammatory markers in the blood and clinical outcome after an intracerebral hemorrhage. METHODS: Between July 2013 and February 2016, we performed a prospective study for which we recruited patients who had suffered an intracerebral hemorrhage. Using various scoring scales we evaluated the neurological state upon admission and discharge, and at one and three months following the ICH. During the hospital stay, various inflammatory markers were examined in blood samples. RESULTS: Out of 132 screened patients, 27 were included (48.2% male, mean age 68 years). We found significantly elevated serum concentrations of interleukin-6 (p=0.006) at the time of admission and throughout days three and five. There were also elevated c-reactive protein and granulocyte-colony stimulating factor concentrations found. The concentrations of these immune parameters showed significant monotonic relationships. The ROC analyses showed a better discrimination for mortality with regard to the percentage of T helper cells than with regard to the ICH volume alone. CONCLUSION: Our results may be regarded as preliminary evidence of the occurrence of inflammation after intracerebral hemorrhage. If there is a relationship between inflammation and clinical outcome remains speculative.


Subject(s)
Cerebral Hemorrhage/blood , Inflammation Mediators/blood , Aged , Biomarkers/blood , C-Reactive Protein/metabolism , Cerebral Hemorrhage/diagnosis , Cerebral Hemorrhage/immunology , Cerebral Hemorrhage/therapy , Disability Evaluation , Female , Granulocyte Colony-Stimulating Factor/blood , Humans , Interleukin-6/blood , Male , Patient Admission , Patient Discharge , Prospective Studies , Recovery of Function , Risk Factors , T-Lymphocytes, Helper-Inducer/immunology , T-Lymphocytes, Helper-Inducer/metabolism , Time Factors , Treatment Outcome , Up-Regulation
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