Low field-low cost: Can low-field magnetic resonance systems replace high-field magnetic resonance systems in the diagnostic assessment of multiple sclerosis patients?

Citation
Bb. Ertl-wagner et al., Low field-low cost: Can low-field magnetic resonance systems replace high-field magnetic resonance systems in the diagnostic assessment of multiple sclerosis patients?, EUR RADIOL, 11(8), 2001, pp. 1490-1494
Citations number
22
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging
Journal title
EUROPEAN RADIOLOGY
ISSN journal
09387994 → ACNP
Volume
11
Issue
8
Year of publication
2001
Pages
1490 - 1494
Database
ISI
SICI code
0938-7994(2001)11:8<1490:LFCCLM>2.0.ZU;2-8
Abstract
As low-field MR imaging is becoming a widely used imaging technique, we aim ed at a prospective assessment of differences in imaging quality between lo w- and high-field MR imaging in multiple sclerosis patients possibly interf ering with diagnostic or therapeutic decision making. Twenty patients with clinically proven multiple sclerosis were examined with optimized imaging p rotocols in a 1.5- and a 0.23-T MR scanner within 48 h. Images were assesse d independently by two neuroradiologists. No statistically significant inte rrater discrepancies were observed. A significantly lower number of white m atter lesions could be identified in low-field MR imaging both on T1 - and on T2-weighted images (T2: high field 700, low field 481; T1: high field 25 3, low field 177). A total of 114 enhancing lesions were discerned in the h igh-field MR imaging as opposed to 45 enhancing lesions in low-field MR ima ging. Blood-brain barrier disruption was identified in 11 of 20 patients in the high-field MR imaging, but only in 4 of 20 patients in low-field MR im aging. Since a significantly lower lesion load is identified in low-field M R imaging than in high-field MR imaging, and blood-brain barrier disruption is frequently missed, caution must be exercised in interpreting a normal l ow-field MR imaging scan in a patient with clinical signs of multiple scler osis and in interpreting a scan without enhancing lesions in a patient with known multiple sclerosis and clinical signs of exacerbation.