4.7 Article

Lack of evidence for an association between hemodynamic variables and hematoma growth in spontaneous intracerebral hemorrhage

Journal

STROKE
Volume 37, Issue 8, Pages 2061-2065

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/01.STR.0000229878.93759.a2

Keywords

blood pressure; computed tomography; intracerebral hemorrhage

Funding

  1. NINDS NIH HHS [T32 NS047996, NS26933] Funding Source: Medline

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Background and Purpose-Early hematoma expansion in spontaneous intracerebral hemorrhage (ICH) is associated with worse clinical outcome. We hypothesized that hemodynamic parameters are associated with the increase in hematoma volume owing to their relationship to blood vessel wall stresses. Methods-We performed a post hoc analysis of clinical and computed tomography (CT) data from patients enrolled in a prospective observational study of ICH patients presenting within 3 hours from symptom onset. Hematoma volumes were measured at hospital arrival and at I and 20 hours from presentation. Blood pressure and heart rate, recorded at 19 time points between presentation and 20 hours, were used to derive hemodynamic variables. Multivariable logistic-regression models were constructed to assess the relation between hemodynamic parameters and hematoma growth, adjusted for clinical covariates. Results-From the original study, 98 patients underwent baseline and I-hour CT scans; of these, 65 had 20-hour CT scans. Substantial hematoma growth was observed in 28% within the first hour. Of the 65 patients not undergoing surgery within 20 hours, 37% experienced hematoma growth by 20 hours. Neither baseline or peak hemodynamic parameters nor changes in hemodynamic parameters were significantly associated with hematoma growth at either I or 20 hours. Conclusions-We found no blood pressure or heart rate parameters, individually or in combination, that were associated with hematoma growth. Our data suggest the influence of hemodynamic parameters on vessel wall stress to be an unlikely target for intervention in reducing the risk of early hematoma growth in ICH.

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