Journal
EUROPEAN NEUROLOGY
Volume 51, Issue 3, Pages 125-131Publisher
KARGER
DOI: 10.1159/000077012
Keywords
lacunar stroke; progression; predictor; acute-phase response; inflammation
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Background and Purpose: Despite the small size of lacunar infarcts, progression of neurological deficits is a common problem in this stroke subtype. This investigation studied the frequency and the course of neurological deterioration as well as predictors and possible underlying pathomechanisms of early progression in lacunar stroke. Methods: Fourty-six consecutive patients with acute lacunar stroke were prospectively evaluated by daily clinical neurological examination including the National Institutes of Health Stroke Scale ( NIHSS) and follow-up using the Barthel Index after 3 months. Progressive neurological deficit was defined as worsening by 61 point in the NIHSS for motor function. Progressive and stable patients were compared regarding clinical profile, inflammatory parameters ( leukocytes, body temperature, C-reactive protein), coagulation parameters ( fibrinogen, D-dimer, vWF, PTT), and glutamate plasma concentration, as well as blood glucose and blood pressure. Results: Eleven patients (23.9%) showed progression of stroke symptoms, 9 of these within the first 24 h after admission. The score on the NIHSS on admission was similar in patients with progressive stroke and stable patients, but significantly higher in the progressive stroke group on days 2 ( p = 0.01), 3 ( p = 0.001) and at discharge ( p = 0.003). Deterioration was significantly associated with a higher leukocyte count ( p = 0.012), higher body temperature ( p = 0.031) and a higher fibrinogen concentration ( p = 0.046) on admission. Barthel Index at discharge ( p = 0.001) and after 90 days ( p ! 0.001) was significantly worse in the progressive stroke group. Conclusions: Progression in lacunar stroke usually occurs within 24 h and may be related to an acute-phase response. The long-term prognosis of progressive stroke patients is persistently worse compared with patients with nonprogressive stroke. Copyright (C) 2004 S. Karger AG, Basel.
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