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dc.contributor.authorAbujudeh, Hani H.
dc.contributor.authorKaewlai, Rathachai
dc.contributor.authorKagan, Anna
dc.contributor.authorChibnik, Lori B.
dc.contributor.authorNazarian, Rosalynn M.
dc.contributor.authorHigh, Whitney A.
dc.contributor.authorKay, Jonathan
dc.date2022-08-11T08:10:51.000
dc.date.accessioned2022-08-23T17:22:32Z
dc.date.available2022-08-23T17:22:32Z
dc.date.issued2009-10-01
dc.date.submitted2015-04-17
dc.identifier.citationRadiology. 2009 Oct;253(1):81-9. doi: 10.1148/radiol.2531082160. Epub 2009 Aug 25. <a href="http://dx.doi.org/10.1148/radiol.2531082160">Link to article on publisher's site</a>
dc.identifier.issn0033-8419 (Linking)
dc.identifier.doi10.1148/radiol.2531082160
dc.identifier.pmid19709997
dc.identifier.urihttp://hdl.handle.net/20.500.14038/48766
dc.description.abstractPURPOSE: 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.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=19709997&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1148/radiol.2531082160
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectBiopsy
dc.subjectContrast Media
dc.subjectDose-Response Relationship, Drug
dc.subjectFemale
dc.subjectGadolinium DTPA
dc.subjectHumans
dc.subject*Magnetic Resonance Imaging
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectNephrogenic Fibrosing Dermopathy
dc.subjectProportional Hazards Models
dc.subjectRetrospective Studies
dc.subjectRisk Factors
dc.subjectSeverity of Illness Index
dc.subjectMusculoskeletal Diseases
dc.subjectRadiology
dc.subjectRheumatology
dc.subjectSkin and Connective Tissue Diseases
dc.titleNephrogenic systemic fibrosis after gadopentetate dimeglumine exposure: case series of 36 patients
dc.typeJournal Article
dc.source.journaltitleRadiology
dc.source.volume253
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/rheumatology_pubs/92
dc.identifier.contextkey7002916
html.description.abstract<p>PURPOSE: To retrospectively assess the association between gadopentetate dimeglumine exposure at magnetic resonance imaging and the development of nephrogenic systemic fibrosis (NSF).</p> <p>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.</p> <p>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.</p> <p>CONCLUSION: NSF develops in patients with renal impairment after exposure to gadopentetate dimeglumine in a dose- and time-dependent manner.</p> <p>SUPPLEMENTAL MATERIAL: http://radiology.rsna.org/lookup/suppl/doi:10.1148/radiol.2531082160/-/DC1.</p>
dc.identifier.submissionpathrheumatology_pubs/92
dc.contributor.departmentDepartment of Medicine, Division of Rheumatology
dc.source.pages81-9


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