Abstract
Purpose
The aim of the study was to evaluate the acute adverse events rate and enhancement properties of gadoterate meglumine (Dotarem®) and gadobenate dimeglumine (MultiHance®) in a small-scale controlled double-blinded study, using inter- and intra-individual comparisons.
Materials and Methods
Forty-one randomly selected patients were scanned with Dotarem®. The rate of adverse reactions, qualitative and quantitative image evaluation was performed vs. a control group of 46 patients who underwent MultiHance® over the same 1-month time period (population 1), and 27 patients who underwent both Dotarem® and MultiHance®-enhanced body MRI studies within an 18-month period (population 2). Data were subjected to statistical analysis.
Results
Only 1 mild acute adverse event (vomiting) was observed in population 1 (with Dotarem®). Blinded assessment of image quality was good for both agents in all patients. Population 1 showed significantly higher liver percentage enhancement with MultiHance® (p < 0.0001). There was a trend to higher pancreas-to-liver enhancement with Dotarem®, significant in population 2 (p = 0.0333).
Conclusion
This small-scale multi-blinded study characterizes a strategy to objectively assess intravenous contrast agents, which may be an ideal method to evaluate whether a new contrast agent should be introduced for clinical use at any institution, and to re-evaluate the agent in standard use. Whenever available, intra-individual assessment may be ideal.
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Conflict of Interest and Disclosure
Kyung Sook Shin, MD, Mamdoh AlObaidy, MD, Miguel Ramalho, MD, Yong Hwan Jeon, MD, Lauren M. Burke, MD, Ersan Altun, MD, Clifton G. Stallings, RT declares none, Richard C. Semelka, MD has Research support, Siemens AG; Consultant, Guerbet SA.
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Shin, K.S., AlObaidy, M., Ramalho, M. et al. Inter- and intra-individual comparative study of two gadolinium-based agents: A pilot study. Abdom Imaging 40, 865–874 (2015). https://doi.org/10.1007/s00261-014-0248-0
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DOI: https://doi.org/10.1007/s00261-014-0248-0