RSNA 2003 

Abstract Archives of the RSNA, 2003


K13-970

Monitoring Multiple Sclerosis on MRI: Preliminary Results of a Multicenter Comparison of Early and Late Enhancement with 0.1 mmol/kg Gd-BOPTA versus Early Enhancement with 0.2 mmol/kg Gd-BOPTA

Scientific Papers

Presented on December 3, 2003
Presented as part of K13: Neuroradiology/Head and Neck (White Matter Matters)

Participants

Alessandra Splendiani MD, PRESENTER: Nothing to Disclose

Abstract: HTML Purpose: Contrast-enhanced MRI has high sensitivity for detecting blood brain barrier (BBB) defects inherent to acute inflammatory lesions of Multiple Sclerosis (MS). Diagnostic protocols for MR imaging of "active lesions" in cases of acute relapse typically envisage contrast agent doses of up to 0.3 mmol/kg bw. The aim of this study was to compare the efficacy of single and double doses of Gd-BOPTA (MultiHance(r), Bracco Imaging SpA, Italy) for the detection of lesions in patients with symptoms of new or relapsing MS. Methods and Materials: MR imaging was performed in 60 patients within 3 weeks of the onset of symptoms. PDw, FSE T2w, FLAIR and FSE T1w images were acquired pre-contrast followed by FSE T1w images at 5 and 15 min after a first injection of 0.1 mmol/kg bw Gd-BOPTA. A second injection of 0.1 mmol/kg bw Gd-BOPTA was then performed at 20 min after the first injection, followed, after 5 min, by the further acquisition of FSE T1w images. Preliminary on-site within patient comparisons were performed for the number and size of enhancing lesions on each post-contrast image set compared to pre-contrast. Safety assessments were performed before contrast administration, at 1 hour after administration and by interview at 24 hours after administration. Results: Although good visualization of lesions was noted on images acquired at 5 min after the first injection of 0.1 mmol/kg Gd-BOPTA, images acquired at 15 min post-contrast revealed a greater number of lesions and better lesion conspicuity. Images acquired at 5 min after the second 0.1 mmol/kg dose (cumulative 0.2 mmol/kg dose) did not reveal further improvement either in terms of lesion detection or lesion conspicuity. No serious or unexpected adverse events were reported. Conclusion: Imaging at 5 min after a cumulative dose of 0.2 mmol/kg Gd-BOPTA does not appear to provide any additional information beyond that obtained at 15 min after a single dose of 0.1 mmol/kg Gd-BOPTA for MR imaging of acute MS. The apparent requirement for only a single dose of Gd-BOPTA can be attributed to the high (9.7 mmol-1s-1) relaxivity of this agent compared to other gadolinium agents.     (P.C. is an employee of Bracco Imaging SpA.)

Cite This Abstract

Splendiani MD, A, Monitoring Multiple Sclerosis on MRI: Preliminary Results of a Multicenter Comparison of Early and Late Enhancement with 0.1 mmol/kg Gd-BOPTA versus Early Enhancement with 0.2 mmol/kg Gd-BOPTA.  Radiological Society of North America 2003 Scientific Assembly and Annual Meeting, November 30 - December 5, 2003 ,Chicago IL. http://archive.rsna.org/2003/3106892.html