Perfusion-weighted magnetic resonance imaging in acute intracerebral hemorrhage at baseline and during the 1st and 2nd week:: A longitudinal study

被引:33
作者
Pascual, Ana M.
Lopez-Mut, Jose V.
Benlloch, Vicente
Chamarro, Raquel
Soler, Jose
Lainez, Miguel J. A.
机构
[1] Hosp Clin, Dept Neurol, ES-46010 Valencia, Spain
[2] ERESA, Dept Neuroradiol, Valencia, Spain
关键词
intracerebral hemorrhage; ischemic penumbra; magnetic resonance imaging; diffusion-; perfusion-weighted;
D O I
10.1159/000095752
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose: Ischemic penumbra has been suggested as a contributing mechanism to secondary neuronal injury in intracerebral hemorrhage ( ICH). Preliminary data suggest the presence of perihematomal hypoperfusion within the first hours after acute ICH. Our objective was to elucidate perfusion changes in the perihematomal region over time using magnetic resonance imaging ( MRI). Methods: Two perfusion-weighted MRIs were studied prospectively in 18 ICH patients. All patients had an acute perfusion-weighted MRI within 24 h of the onset of symptoms ( time 0); 11 patients had a follow- up study on day 7 ( time 1), and 7 patients on days 10 - 14 ( time 2). The region of interest ( ROI) was placed over the penumbral area, on high-intensity FLAIR and perfusion overlapping map imaging. Clinical data were assessed at baseline ( National Institutes of Health Stroke Scale) and on day 90 ( Canadian Scale, modified Rankin Scale). Results: The average hematoma volume was 56 ( 9 140) ml; 10 were located deeply, and 8 were lobar. When we compared the perfusion changes ( mean transit time prolongation) in the perihematomal area ( lesion ROI) relative to itself over time, we found significant differences only between times 0 and 2 ( p = 0.05). There were also significant differences in mean transit time between the lesion ROI and the contralateral mirror ROI in the baseline study ( p = 0.001), with a trend to significance for time 1. Conclusions: Our data confirm the presence of hypoperfusion around an acute ICH and demonstrate that this change disappears completely after the first week. These data suggest that further evaluation of this feature of acute ICH is warranted, as its confirmation may lead to modifications in the current therapeutic approach. Copyright (c) 2007 S. Karger AG, Basel
引用
收藏
页码:6 / 13
页数:8
相关论文
共 37 条
[1]   THE RISK OF SUBARACHNOID AND INTRACEREBRAL HEMORRHAGES IN BLACKS AS COMPARED WITH WHITES [J].
BRODERICK, JP ;
BROTT, T ;
TOMSICK, T ;
HUSTER, G ;
MILLER, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (11) :733-736
[2]   Early hemorrhage growth in patients with intracerebral hemorrhage [J].
Brott, T ;
Broderick, J ;
Kothari, R ;
Barsan, W ;
Tomsick, T ;
Sauerbeck, L ;
Spilker, J ;
Duldner, J ;
Khoury, J .
STROKE, 1997, 28 (01) :1-5
[3]   INTRACEREBRAL HEMORRHAGE IN A PRIMATE MODEL - EFFECT ON REGIONAL CEREBRAL BLOOD-FLOW [J].
BULLOCK, R ;
BROCKUTNE, J ;
VANDELLEN, J ;
BLAKE, G .
SURGICAL NEUROLOGY, 1988, 29 (02) :101-107
[4]   Current intracerebral haemorrhage management [J].
Butcher, K ;
Laidlaw, J .
JOURNAL OF CLINICAL NEUROSCIENCE, 2003, 10 (02) :158-167
[5]   Perihematomal edema in primary intracerebral hemorrhage is plasma derived [J].
Butcher, KS ;
Baird, T ;
MacGregor, L ;
Desmond, P ;
Tress, B ;
Davis, S .
STROKE, 2004, 35 (08) :1879-1885
[6]   Diffusion-weighted MRI and proton MR spectroscopic imaging in the study of secondary neuronal injury after intracerebral hemorrhage [J].
Carhuapoma, JR ;
Wang, PY ;
Beauchamp, NJ ;
Keyl, PM ;
Hanley, DF ;
Barker, PB .
STROKE, 2000, 31 (03) :726-732
[7]  
DEREUCK J, 1989, ACTA NEUROL BELG, V89, P7
[8]  
Edwards DF, 1998, NEUROLOGY, V50, pA40
[9]   Cell death in experimental intracerebral hemorrhage: The "black hole" model of hemorrhagic damage [J].
Felberg, RA ;
Grotta, JC ;
Shirzadi, AL ;
Strong, R ;
Narayana, P ;
Hill-Felberg, SJ ;
Aronowski, J .
ANNALS OF NEUROLOGY, 2002, 51 (04) :517-524
[10]   Surgery in intracerebral hemorrhage - The uncertainty continues [J].
Fernandes, HM ;
Gregson, B ;
Siddique, S ;
Mendelow, AD .
STROKE, 2000, 31 (10) :2511-2516