2004
DOI: 10.1007/s00330-004-2612-x
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Safety of MR liver specific contrast media

Abstract: Over the past few years a number of magnetic resonance (MR) liver specific contrast agents have been introduced. In this report the safety issues of these agents are addressed. A literature search was carried out. Based on the available information, simple guidelines on the safety issue of liver specific contrast agents have been produced by the Contrast Media Safety Committee of the European Society of Urogenital Radiology. The report and guidelines were discussed at the 11th European Symposium on Urogenital … Show more

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Cited by 42 publications
(15 citation statements)
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“…Gd-EOB-DTPA is a hepatobiliary MRI contrast agent with high T1 relaxivity in the liver. It is cleared from the body by two elimination routes: receptor-specific uptake by the hepatocytes with subsequent biliary excretion and glomerular filtration in the kidneys with subsequent urinary excretion (13). Hepatobiliary elimination accounts for approximately 50% of the total elimination.…”
Section: Discussionmentioning
confidence: 99%
“…Gd-EOB-DTPA is a hepatobiliary MRI contrast agent with high T1 relaxivity in the liver. It is cleared from the body by two elimination routes: receptor-specific uptake by the hepatocytes with subsequent biliary excretion and glomerular filtration in the kidneys with subsequent urinary excretion (13). Hepatobiliary elimination accounts for approximately 50% of the total elimination.…”
Section: Discussionmentioning
confidence: 99%
“…12 We posit that the higher incidence of reactions observed with Gd-EOB-DTPA was attributable to its greater degree of protein binding than that of other Gdbased agents. 13 In addition, Gd-EOB-DTPA could be used to evaluate hepatocellular carcinoma and metastasis or other liver tumors because the backgrounds of these patients were different from those of patients who received the other 3 Gd-contrast agents (Gd-DTPA, Gd-DO3A, and Gd-DOTA), which were used for general clinical purposes related not only to oncological diseases but also to inflammatory, orthopedic, and cardiovascular diseases. In a review of clinical Phase II and III studies that summarized safety data on Gd-EOB-DTPA, 13 120 of 1,404 patients (8.5%) experienced one or more adverse effects.…”
Section: Discussionmentioning
confidence: 99%
“…13 In addition, Gd-EOB-DTPA could be used to evaluate hepatocellular carcinoma and metastasis or other liver tumors because the backgrounds of these patients were different from those of patients who received the other 3 Gd-contrast agents (Gd-DTPA, Gd-DO3A, and Gd-DOTA), which were used for general clinical purposes related not only to oncological diseases but also to inflammatory, orthopedic, and cardiovascular diseases. In a review of clinical Phase II and III studies that summarized safety data on Gd-EOB-DTPA, 13 120 of 1,404 patients (8.5%) experienced one or more adverse effects. The drug information sheets of Bayer Healthcare (available at http://www.info.pmda.go.jp/go/ pack/7290415G1020_1_07/) report that the rate of adverse effects of Gd-EOB-DTPA was 76/1755 (4.3%) for regulatory approval in Japan.…”
Section: Discussionmentioning
confidence: 99%
“…The transmetallation of gadolinium with endogenous metal ions such as copper and zinc is less common in cyclic chelates than acyclic chelates [19]. For the clinical agents, the LD 50 falls into a range of 8-15 mmol kg −1 [20][21][22], and reported adverse effects for these Gd-based contrast agents are rare [23][24][25].…”
Section: Introductionmentioning
confidence: 99%