EFFICACY EVALUATION OF GADOTERIDOL FOR MR-ANGIOGRAPHY OF INTRACRANIALVASCULAR-LESIONS

Citation
Sj. Mclachlan et al., EFFICACY EVALUATION OF GADOTERIDOL FOR MR-ANGIOGRAPHY OF INTRACRANIALVASCULAR-LESIONS, Journal of magnetic resonance imaging, 4(3), 1994, pp. 405-411
Citations number
22
Categorie Soggetti
Radiology,Nuclear Medicine & Medical Imaging
ISSN journal
10531807
Volume
4
Issue
3
Year of publication
1994
Pages
405 - 411
Database
ISI
SICI code
1053-1807(1994)4:3<405:EEOGFM>2.0.ZU;2-S
Abstract
A phase III multicenter study was conducted in 89 patients with known intracranial vascular lesions to evaluate an extracellular gadolinium contrast agent, gadoteridol. for intracranial magnetic resonance (MR) angiography. The pre- and postcontrast MR angiograms of 82 patients we re evaluated by the unblinded investigators and by two blinded readers (A and B) for visualization of lesions; arterial and venous anatomy; extent. size, and number of lesions; and disease classification. The u nblinded readers indicated that lesions were visualized better on post contrast images in the following categories: venous anatomy, 87 (81%) of 107 lesions; arterial anatomy, 43 lesions (40%); and extent or size of lesions. 38 lesions (36%). In 29 (35%) of 82 patients, the unblind ed readers determined that enhanced MR angiography provided more diagn ostic information than unenhanced MR angiography. The blinded readers determined that enhanced MR angiography provided more information for visualization of vascular anatomy in more than 60% of cases. The addit ional information provided with gadoteridol would have changed the dia gnosis in nine (8%) of 107 lesions seen by the unblinded readers, 11 ( 12%) of 90 lesions seen by reader A. and three (3%) of 93 lesions seen by reader B. The results confirm that the use of gadoteridol improves the visualization of intracranial vascular lesions with MR angiograph y. The authors conclude that development of new postprocessing algorit hms will improve the utility of contrast-enhanced MR angiography.