RSNA 2007 

Abstract Archives of the RSNA, 2007


SSG05-06

Case-control Study of Gadodiamide-triggered Nephrogenic Systemic Fibrosis (NSF)

Scientific Papers

Presented on November 27, 2007
Presented as part of SSG05: ISP: Genitourinary (Contrast Materials and Adverse Effects)

Participants

Peter Marckmann MD, Abstract Co-Author: Nothing to Disclose
Lone Skov, Abstract Co-Author: Nothing to Disclose
Kristian Rossen MD, Abstract Co-Author: Nothing to Disclose
James Heaf MD, Abstract Co-Author: Nothing to Disclose
Henrik S. Thomsen MD, Presenter: Nothing to Disclose

PURPOSE

NSF may be caused by Gd-containing contrast agents for MRI. Most reported cases were associated with one particular agent, gadodiamide. Yet unidentified cofactors might explain why only a minority of renal failure patients exposed to gadodiamide develop NSF.

METHOD AND MATERIALS

We conducted a case-control study of 19 histologically verified cases and 19 sex-and-age-matched controls. All subjects had chronic renal failure when exposed to gadodiamide. Clinical, biochemical, and pharmacological data were retrieved from medical records.

RESULTS

Cases had been exposed to a mean gadodiamide dose of 0.29 mmol/kg (range 0.18-0.50) shortly before first signs of nephrogenic systemic fibrosis. Controls had been exposed to 0.28 mmol/kg (0.13-0.49). Cumulative gadodiamide exposure while in chronic kidney disease stage 5 was significantly higher among cases compared with controls (0.41 vs 0.31 mmol/kg, p = 0.05), and among severe cases (n = 9) compared with non-severe cases (0.49 vs 0.33 mmol/kg, p = 0.02). Severe cases developed primarily among patients in regular hemodialysis therapy at exposure. Cases had higher serum concentrations of ionized calcium and phosphate than controls, and tended to receive higher doses of epoietin beta than controls at time of exposure. Severe cases were treated with higher doses of epoietin beta than non-severe cases at exposure (10.8 versus 4.4 103IU/week, p = 0.02).

CONCLUSION

Increasing cumulative gadodiamide exposure, high-dose epoietin beta treatment, and higher serum concentrations of ionized calcium and phosphate increase the risk of gadodiamide-trigged NSF in renal failure patients. Severe cases seem to develop primarily among patients in regular hemodialysis therapy at exposure.

CLINICAL RELEVANCE/APPLICATION

No co-factor to gadodiamide could be identified.

Cite This Abstract

Marckmann, P, Skov, L, Rossen, K, Heaf, J, Thomsen, H, Case-control Study of Gadodiamide-triggered Nephrogenic Systemic Fibrosis (NSF).  Radiological Society of North America 2007 Scientific Assembly and Annual Meeting, November 25 - November 30, 2007 ,Chicago IL. http://archive.rsna.org/2007/5004676.html