2016
DOI: 10.1097/rli.0000000000000318
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Presumed Gadolinium Toxicity in Subjects With Normal Renal Function

Abstract: Gadolinium toxicity may occur in subjects with normal renal function. Central torso and peripheral arm and leg distribution pain were common features. Distal arm and leg skin thickening and rubbery subcutaneous tissue were seen in late stages. Clouded mentation is also common. Vigilance to identify additional cases and investigate strategies for prevention and treatment is warranted to increase even further the safety of a very safe diagnostic procedure, GBCA-enhanced magnetic resonance imaging.

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Cited by 70 publications
(76 citation statements)
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“…Diagnoses include clinical symptoms after exposure to standard dose, or greater, of any GBCA and confirmation of gadolinium retention [53]. Our current impression is that the most reliable laboratory test to confirm gadolinium deposition may be 24-h urine test, which should be performed at least 30 days after GBCA administration.…”
Section: Diagnosismentioning
confidence: 99%
“…Diagnoses include clinical symptoms after exposure to standard dose, or greater, of any GBCA and confirmation of gadolinium retention [53]. Our current impression is that the most reliable laboratory test to confirm gadolinium deposition may be 24-h urine test, which should be performed at least 30 days after GBCA administration.…”
Section: Diagnosismentioning
confidence: 99%
“…A series of reports beginning in 2014 confirm long-term Gd retention in the central nervous system (CNS) and skin of patients receiving contrast-enhanced examinations (1518). Moreover, in 2016, four cases of NSF were reported in patients with normal renal function who had received GBCAs (19). The implications of Gd retention in the CNS remain unclear.…”
Section: Introductionmentioning
confidence: 99%
“…Magnetic Resonance Imaging (MRI) is characterized by a relatively high spatial resolution, relatively no tissue penetrating limits but also it has a low sensitivity, high cost and long imaging time. Furthermore, recent concerns about the deposition of clinically relevant Gd-based Contrast Agents (CAs), linear and macrocyclic one are reported by Robert McDonald on neuroradiology5 and other publications67. Moreover, the recent opinion of the Food and Drug Administration (FDA) suggests the limiting the Gadolinium-based CAs use to clinical circumstances in which the additional information provided by the contrast is necessary.…”
mentioning
confidence: 99%