Evolution of cerebral infarct volume assessed by diffusion-weighted magnetic resonance imaging

被引:92
作者
Lansberg, MG [1 ]
O'Brien, MW [1 ]
Tong, DC [1 ]
Moseley, ME [1 ]
Albers, GW [1 ]
机构
[1] Stanford Univ, Stanford Stroke Ctr, Med Ctr, Palo Alto, CA 94304 USA
关键词
D O I
10.1001/archneur.58.4.613
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Knowledge of the natural evolution of ischemic brain lesions may be a crucial aspect in the assessment of future stroke therapies. Objective: To establish daily changes of ischemic cerebral lesion volume using diffusion-weighted magnetic resonance imaging. Design: Prospective cohort study. Setting: Referral center. Patients and Methods: Serial magnetic resonance imaging scans were performed in consecutive untreated stroke patients. The baseline scan was obtained within 48 hours after symptom onset; subsequent scans, 12 to 48 hours, 3 to 4 days, S to 7 days, and 30 days after baseline. Lesion volumes were measured on each scan by 2 independent observers. Main Outcome Measure: Daily change in lesion volume. Results: A total of 112 magnetic resonance imaging scans were obtained in 24 patients. An early increase in lesion volume was seen in all patients. Maximum lesion volume was reached at a mean of 74 hours. Lesion volumes increased by a mean (+/- SEM) of 21%+/- 112% during day 2 and 10%+/- 12% during day 3. No significant change occurred during day 4. During days S, 6, and 7, statistically significant mean (+/- SEM) decreases of 6%+/-8%, 3%+/-4%, and 4%+/-5%, respectively, were observed. Conclusions: Ischemic lesions follow a relatively consistent pattern of growth during the first 3 days and subsequent decrease in size. These data in conjunction with data regarding the evolution of lesion volume during the first 24 hours after symptom onset may be useful in the design of pilot studies of therapies for acute stroke.
引用
收藏
页码:613 / 617
页数:5
相关论文
共 24 条
[1]   Diffusion-weighted MRI for evaluation of acute stroke [J].
Albers, GW .
NEUROLOGY, 1998, 51 (03) :S47-S49
[2]   Enlargement of human cerebral ischemic lesion volumes measured by diffusion-weighted magnetic resonance imaging [J].
Baird, AE ;
Benfield, A ;
Schlaug, G ;
Siewert, B ;
Lovblad, KO ;
Edelman, RR ;
Warach, S .
ANNALS OF NEUROLOGY, 1997, 41 (05) :581-589
[3]   Prediction of stroke outcome with echoplanar perfusion- and diffusion-weighted MRI [J].
Barber, PA ;
Darby, DG ;
Desmond, PM ;
Yang, Q ;
Gerraty, RP ;
Jolley, D ;
Donnan, GA ;
Tress, BM ;
Davis, SM .
NEUROLOGY, 1998, 51 (02) :418-426
[4]   CBF AND TIME THRESHOLDS FOR THE FORMATION OF ISCHEMIC CEREBRAL EDEMA, AND EFFECT OF REPERFUSION IN BABOONS [J].
BELL, BA ;
SYMON, L ;
BRANSTON, NM .
JOURNAL OF NEUROSURGERY, 1985, 62 (01) :31-41
[5]   Clinical trials in acute stroke - Why have they not been successful? [J].
del Zoppo, GJ .
NEUROLOGY, 1998, 51 (03) :S59-S61
[7]   PROGRESSIVE DERANGEMENT OF PERIINFARCT VIABLE TISSUE IN ISCHEMIC STROKE [J].
HEISS, WD ;
HUBER, M ;
FINK, GR ;
HERHOLZ, K ;
PIETRZYK, U ;
WAGNER, R ;
WIENHARD, K .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1992, 12 (02) :193-203
[8]   MAGNETIC-RESONANCE-IMAGING ASSESSMENT OF EVOLVING FOCAL CEREBRAL-ISCHEMIA - COMPARISON WITH HISTOPATHOLOGY IN RATS [J].
KNIGHT, RA ;
DERESKI, MO ;
HELPERN, JA ;
ORDIDGE, RJ ;
CHOPP, M .
STROKE, 1994, 25 (06) :1252-1261
[9]   Cerestat and other NMDA antagonists in ischemic stroke [J].
Lees, KR .
NEUROLOGY, 1997, 49 (05) :S66-S69
[10]   PHARMACOLOGICAL REVERSAL OF ACUTE CHANGES IN DIFFUSION-WEIGHTED MAGNETIC-RESONANCE-IMAGING IN FOCAL CEREBRAL-ISCHEMIA [J].
LO, EH ;
MATSUMOTO, K ;
PIERCE, AR ;
GARRIDO, L ;
LUTTINGER, D .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1994, 14 (04) :597-603