Predictors of highly prevalent brain ischemia in intracerebral hemorrhage.
Predictors of highly prevalent brain ischemia in intracerebral hemorrhage.
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DOI:
10.1002/ana.22668
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发表时间:
2012-02
影响因子:
11.2
通讯作者:
Kidwell, Chelsea S.
中科院分区:
文献类型:
--
作者:
Menon, Ravi S.;Burgess, Richard E.;Wing, Jeffrey J.;Gibbons, M. Christopher;Shara, Nawar M.;Fernandez, Stephen;Jayam-Trouth, Annapurni;German, Laura;Sobotka, Ian;Edwards, Dorothy;Kidwell, Chelsea S.
To determine the prevalence, characteristics, risk factors and temporal profile of concurrent ischemic lesions in patients with acute primary intracerebral hemorrhage (ICH). Patients were recruited within a prospective, longitudinal, magnetic resonance imaging (MRI) based study of primary ICH. Clinical, demographic, and MRI data were collected on all subjects at baseline and 1 month. Of the 138 patients enrolled, mean age was 59 years, 54% were male, 73% black, and 84% had a history of hypertension. At baseline, ischemic lesions on diffusion-weighted imaging (DWI) were found in 35% of patients. At 1 month, lesions were present in 27%, and of these lesions, 83% were new and not present at baseline. ICH volume (p=0.025), intraventricular hemorrhage (p=0.019), presence of microbleeds (p=0.024), and large, early reductions in mean arterial pressure (p=0.003) were independent predictors of baseline DWI lesions. A multivariate logistical model predicting the presence of 1 month DWI lesions included history of any prior stroke (p=0.012), presence of 1 or more microbleeds (p=0.04), black race (p=0.641), and presence of a DWI lesion at baseline (p=0.007) This study demonstrates that more than 1/3 of patients with primary ICH have active cerebral ischemia at baseline remote from the index hematoma, and 1/4 of patients experience ongoing, acute ischemic events at 1 month. Multivariate analyses implicate blood pressure reductions in the setting of an active vasculopathy as a potential underlying mechanism. Further studies are needed to determine the impact of these lesions on outcome and optimal management strategies to arrest vascular damage.
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影响因子:
9.9
作者:
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通讯作者:
Greenberg, S. M.
影响因子:
2.9
作者:
Rosand, J;Eskey, C;Koroshetz, WJ
通讯作者:
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影响因子:
48
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通讯作者:
Breteler, Monique M. B.
影响因子:
8.3
作者:
Hill, MD;Silver, FL;Tu, JV
通讯作者:
Tu, JV
影响因子:
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作者:
GOLDSTEIN, LB;BERTELS, C;DAVIS, JN
通讯作者:
DAVIS, JN