Purpose. This study was undertaken to assess the value of a chemical (spectral) fat-saturation (fat-sat) pulse added to a T1-weighted spin-echo sequence after intravenous administration of paramagnetic contrast agent in detecting enhancing lesions in multiple sclerosis. Materials and methods. Twenty patients with relapsing-remitting multiple sclerosis underwent a brain 1.0-Tesla magnetic resonance (MR) scan with T1-weighted spin-echo sequences (24 contiguous para-axial slices with a thickness of 5 mm, pixel size 0.96 mm 2, number of excitations 2, flip angle 90°) 5 min after intravenous injection of 0.1 mmol/kg of gadodiamide with and without fat-sat, acquired with randomised order of priority. Two readers counted by consensus the number of enhancing lesions and assigned a conspicuity score (low conspicuity=1; high conspicuity=2) to each enhancing lesion during a randomised reading without any visual comparison between the two corresponding images (with and without fat-sat) of the same patient. McNemar and Wilcoxon matched-pair signed-rank tests were used. Results. Seventy-two enhancing lesions without fat-sat and 94 with fat-sat were detected; 22 lesions were visible only with fatsat, whereas no lesion was detected only without fat-sat (p<0.0001). The conspicuity score was 1.17±0.38 (mean±standard deviation) and 1.57±0.44, respectively (p<0.0001). Conclusions. A fat-sat pulse added to a T1-weighted spin-echo sequence increases significantly the number and conspicuity of contrast-enhancing lesions in patients with relapsing-remitting multiple sclerosis.

Sardanelli, F., Schiavoni, S., Iozzelli, A., Fausto, A., Aliprandi, A., Mancardi, G., et al. (2007). The value of chemical fat-saturation pulse added to T1-weighted spin-echo sequence in evaluating gadolinium- enhancing brain lesions in multiple sclerosis. LA RADIOLOGIA MEDICA, 112(8), 1244-1251 [10.1007/s11547-007-0220-y].

The value of chemical fat-saturation pulse added to T1-weighted spin-echo sequence in evaluating gadolinium- enhancing brain lesions in multiple sclerosis

Aliprandi A;
2007

Abstract

Purpose. This study was undertaken to assess the value of a chemical (spectral) fat-saturation (fat-sat) pulse added to a T1-weighted spin-echo sequence after intravenous administration of paramagnetic contrast agent in detecting enhancing lesions in multiple sclerosis. Materials and methods. Twenty patients with relapsing-remitting multiple sclerosis underwent a brain 1.0-Tesla magnetic resonance (MR) scan with T1-weighted spin-echo sequences (24 contiguous para-axial slices with a thickness of 5 mm, pixel size 0.96 mm 2, number of excitations 2, flip angle 90°) 5 min after intravenous injection of 0.1 mmol/kg of gadodiamide with and without fat-sat, acquired with randomised order of priority. Two readers counted by consensus the number of enhancing lesions and assigned a conspicuity score (low conspicuity=1; high conspicuity=2) to each enhancing lesion during a randomised reading without any visual comparison between the two corresponding images (with and without fat-sat) of the same patient. McNemar and Wilcoxon matched-pair signed-rank tests were used. Results. Seventy-two enhancing lesions without fat-sat and 94 with fat-sat were detected; 22 lesions were visible only with fatsat, whereas no lesion was detected only without fat-sat (p<0.0001). The conspicuity score was 1.17±0.38 (mean±standard deviation) and 1.57±0.44, respectively (p<0.0001). Conclusions. A fat-sat pulse added to a T1-weighted spin-echo sequence increases significantly the number and conspicuity of contrast-enhancing lesions in patients with relapsing-remitting multiple sclerosis.
Articolo in rivista - Articolo scientifico
Brain Gd enhancement; Fat saturation; MR imaging; Multiple sclerosis;
English
Italian
2007
112
8
1244
1251
reserved
Sardanelli, F., Schiavoni, S., Iozzelli, A., Fausto, A., Aliprandi, A., Mancardi, G., et al. (2007). The value of chemical fat-saturation pulse added to T1-weighted spin-echo sequence in evaluating gadolinium- enhancing brain lesions in multiple sclerosis. LA RADIOLOGIA MEDICA, 112(8), 1244-1251 [10.1007/s11547-007-0220-y].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/524556
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