Rivers C S, Wardlaw J M, Armitage P A, Bastin M E, Carpenter T K, Cvoro V, Hand P J, Dennis M S
Division of Clinical Neurosciences, Western General Hospital, Edinburgh, EH4 2XU, UK.
Stroke. 2006 Jan;37(1):98-104. doi: 10.1161/01.STR.0000195197.66606.bb. Epub 2005 Dec 1.
An acute mismatch on diffusion-weighted MRI (DWI) and perfusion-weighted MRI (PWI) may represent the "tissue-at-risk." It is unclear which "semiquantitative" perfusion parameter most closely identifies final infarct volume.
Acute stroke patients underwent DWI and PWI (dynamic-susceptibility contrast imaging) on admission (baseline), and T2-weighted imaging (T2WI) at 1 or 3 months after stroke. "Semiquantitative" mean transit time (MTTsq=first moment of concentration/time curve), cerebral blood volume (CBVsq=area under concentration/time curve), and cerebral blood flow (CBFsq=CBVsq/MTTsq) were calculated. DWI and PWI lesions were measured at baseline and final infarct volume on T2WI acquired > or =1 month after stroke. Baseline DWI, CBFsq, and MTTsq lesion volumes were compared with final T2WI lesion volume.
Among 46 patients, baseline DWI and CBFsq lesions were not significantly different from final T2WI lesion volume, but baseline MTTsq lesions were significantly larger. The correlation with final T2WI lesion volume was strongest for DWI (Spearman rank correlation coefficient rho=0.68), intermediate for CBFsq (rho=0.55), and weakest for MTTsq (rho=0.49) baseline lesion volumes. Neither DWI/CBFsq nor DWI/MTTsq mismatch predicted lesion growth; lesion growth was equally common in those with and without mismatch.
Of the 2 PWI parameters, CBFsq lesions most closely identifies, and MTTsq overestimates, final T2WI lesion volume. "DWI/PWI mismatch" does not identify lesion growth. Patients without "DWI/PWI mismatch" are equally likely to have lesion growth as those with mismatch and should not be excluded from acute stroke treatment.
扩散加权磁共振成像(DWI)与灌注加权磁共振成像(PWI)上的急性不匹配可能代表“危险组织”。目前尚不清楚哪种“半定量”灌注参数最能准确识别最终梗死体积。
急性卒中患者在入院时(基线)接受DWI和PWI(动态磁敏感对比成像)检查,并在卒中后1或3个月进行T2加权成像(T2WI)检查。计算“半定量”平均通过时间(MTTsq = 浓度/时间曲线的一阶矩)、脑血容量(CBVsq = 浓度/时间曲线下的面积)和脑血流量(CBFsq = CBVsq/MTTsq)。在基线时测量DWI和PWI病变,并在卒中后≥1个月获得的T2WI上测量最终梗死体积。比较基线DWI、CBFsq和MTTsq病变体积与最终T2WI病变体积。
在46例患者中,基线DWI和CBFsq病变与最终T2WI病变体积无显著差异,但基线MTTsq病变明显更大。DWI与最终T2WI病变体积的相关性最强(Spearman等级相关系数rho = 0.68),CBFsq为中等(rho = 0.55),MTTsq基线病变体积最弱(rho = 0.49)。DWI/CBFsq和DWI/MTTsq不匹配均不能预测病变生长;有不匹配和无不匹配的患者中病变生长同样常见。
在两个PWI参数中,CBFsq病变最能准确识别最终T2WI病变体积,而MTTsq高估了最终T2WI病变体积。“DWI/PWI不匹配”不能识别病变生长。没有“DWI/PWI不匹配”的患者与有不匹配的患者发生病变生长的可能性相同,不应被排除在急性卒中治疗之外。