Nephrogenic systemic fibrosis after gadopentetate dimeglumine exposure: case series of 36 patients
Authors
Abujudeh, Hani H.Kaewlai, Rathachai
Kagan, Anna
Chibnik, Lori B.
Nazarian, Rosalynn M.
High, Whitney A.
Kay, Jonathan
UMass Chan Affiliations
Department of Medicine, Division of RheumatologyDocument Type
Journal ArticlePublication Date
2009-10-01Keywords
AdultAged
Aged, 80 and over
Biopsy
Contrast Media
Dose-Response Relationship, Drug
Female
Gadolinium DTPA
Humans
*Magnetic Resonance Imaging
Male
Middle Aged
Nephrogenic Fibrosing Dermopathy
Proportional Hazards Models
Retrospective Studies
Risk Factors
Severity of Illness Index
Musculoskeletal Diseases
Radiology
Rheumatology
Skin and Connective Tissue Diseases
Metadata
Show full item recordAbstract
PURPOSE: To retrospectively assess the association between gadopentetate dimeglumine exposure at magnetic resonance imaging and the development of nephrogenic systemic fibrosis (NSF). MATERIALS AND METHODS: This HIPAA-compliant study had institutional review board approval. Informed consent was waived. A search of medical and pathologic records was performed to identify patients with NSF that was diagnosed between January 1998 and December 2007. Patients with known exposure to gadolinium-based contrast agents other than gadopentetate dimeglumine were excluded. Medical records were then reviewed for gadopentetate dimeglumine exposure, renal status, concomitant diseases, timing of NSF symptom onset, date of NSF diagnosis, and clinical outcome. Skin gadolinium deposition was assessed for those patients with adequate available tissue. Spearman rank correlations were estimated to assess the relationship between the dose of gadopentetate dimeglumine and the time to onset of NSF. RESULTS: Thirty-six patients (mean age, 62.6 years; range, 30-83 years) had been exposed to gadopentetate dimeglumine prior to NSF onset. All had stage 5 chronic kidney disease and all but one were undergoing dialysis at the time of exposure. NSF developed within 3 months after the last gadopentetate dimeglumine exposure (range, 1-59 months) in 21 (66%) of 32 patients. The patients had been exposed to median cumulative gadopentetate dimeglumine volumes of 35, 40, 85, and 117.5 mL over the 3, 12, and 24 months and up to 11 years preceding the onset of NSF, respectively. Patients who received higher cumulative and total gadopentetate dimeglumine doses had a higher risk of developing NSF than did those who received lower doses (odds ratio = 1.2). Twenty (56%) of 36 patients died, with a median interval of 18 months between NSF symptom onset and death. CONCLUSION: NSF develops in patients with renal impairment after exposure to gadopentetate dimeglumine in a dose- and time-dependent manner. SUPPLEMENTAL MATERIAL: http://radiology.rsna.org/lookup/suppl/doi:10.1148/radiol.2531082160/-/DC1.Source
Radiology. 2009 Oct;253(1):81-9. doi: 10.1148/radiol.2531082160. Epub 2009 Aug 25. Link to article on publisher's siteDOI
10.1148/radiol.2531082160Permanent Link to this Item
http://hdl.handle.net/20.500.14038/48766PubMed ID
19709997Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1148/radiol.2531082160