2002
DOI: 10.1016/s1076-6332(03)80250-7
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Comparison of Gd-BOPTA and Gd-DOTA for Peripheral CE-MRA

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Cited by 2 publications
(1 citation statement)
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“…Unfortunately, the first and only agent that received FDA approval, gadofosveset, is no longer in production in the US due to small market niche. The commonly available gadobenate dimeglumine (MultiHance) demonstrates weak albumin binding and mildly increased vascular persistence (21), although the practical benefit of this subtle difference remains to be debated. Ferumoxytol, a non-gadolinium superparamagnetic iron oxide contrast agent, demonstrates a prolonged vascular residence time (22) and is a promising vascular imaging agent especially in patient with a contraindication to gadolinium such as renal failure (23).…”
Section: Contrast Enhanced (Ce) Mramentioning
confidence: 99%
“…Unfortunately, the first and only agent that received FDA approval, gadofosveset, is no longer in production in the US due to small market niche. The commonly available gadobenate dimeglumine (MultiHance) demonstrates weak albumin binding and mildly increased vascular persistence (21), although the practical benefit of this subtle difference remains to be debated. Ferumoxytol, a non-gadolinium superparamagnetic iron oxide contrast agent, demonstrates a prolonged vascular residence time (22) and is a promising vascular imaging agent especially in patient with a contraindication to gadolinium such as renal failure (23).…”
Section: Contrast Enhanced (Ce) Mramentioning
confidence: 99%