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The following information is being provided by the International Society for
Magnetic Resonance in Medicine (ISMRM) as a courtesy to the MR community.
If you have additional articles or publications regarding this which you feel
would be of interest and assistance, please send the citations to the ISMRM, and
we will add these resources to this page. Send them to the attention of
Roberta A. Kravitz, ISMRM Executive Director, at
roberta@ismrm.org.
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The FDA (United States Food & Drug Administration) has received additional information about
a new disease, known as Nephrogenic Systemic Fibrosis or Nephrogenic Fibrosing
Dermopathy (NSF/NFD), which may occur in patients with moderate to end-stage
kidney disease after they have had a Magnetic Resonance Imaging (MRI) or
Magnetic Resonance Angiography (MRA) scan with a gadolinium-based contrast
agent.
The FDA has released the following:
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In addition, the EMEA (European Agency for the Evaluation of Medicinal Products) has released the following information:
Additional resources:
The Radiological Society of North America (RSNA)
has made two articles available free of charge on the Radiology
Web site: |
In addition, the February issue of RSNA
News includes an article on this topic at
http://www.rsna.org/Publications/rsnanews/feb07/upload/RSNANews_Feb07_Gadolinium.pdf |
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