OBJECTIVE. The purposeof this studywas to comparethe contrastenhancement of le sions of the brain revealed by gadolinium-enhanced optimized fast fluid-attenuated inversion recovery(FLAIR) MR imaging with that of lesionson gadolinium-enhanced optimized11-weighted spin-echo MR imaging.
SUBJECTS AND METHODS.Using computer simulations,we optimized the fast FLAIR parameters (TR, Theff@and inversion time) and the Tl-weighted spin-echo parame ters (TR and TE) to provide maximum difference in signal intensity between enhancing le sions of the brain and white matter. Seventy-six consecutive patients referred for single-dose gadolinium-enhanced MR imagingof the brainunderwentbothoptimizedtechniques, which were matchedfor spatialresolution,bandwidth,and numberof excitations. The gadolinium enhanced fast FLAIR and Il-weighted spin-echo MR images were evaluated independently by two observers for number and size of enhancing lesions and for the degree of grayâ€"white matterdifferentiation. Contrast-to-noise ratioswere measuredfor enhancinglesions1.0 cm or larger in diameter using 8 x 8 pixel regions of interest in the enhancing lesions and normal white matter. RESULTS. The mostrevealingparameters for fastFLAIR MR imagingprovedto be a TR of 1500 msec,an inversiontime of 683 msec,anda TEeff 0f 16 msec.For Ti-weighted spin echo MR imaging, the optimized parameterswere a TR of 550 msec and a TE of 16 msec. In 28 patients, we saw enhancing lesions of the brain with at least one MR imaging technique. More lesionswere seenon the Ti-weighted spin-echosequence(n = 141) than on the fast FLAIR sequence (n = 94) (p < .03). Grayâ€"whitematter differentiation was significantly better on the fast FLAIR sequence(p < .001). Contrast-to-noise ratios of enhancing lesions were greater on the Ti-weighted spin-echo sequence (p < .001).
CONCLUSION.In this study, optimized gadolinium-enhancedconventional Ti weightedspin-echoMR imaging provedsuperiorto gadolinium-enhanced fast FLAIR MR imaging in revealing lesions of the brain.