Nephrology Dialysis Transplantation, May 2012
Introduction and Aims: Gadolinium chelate (GC)s using in magnetic resonance imaging (MRI) have been traditionally considered as non-nephrotoxic contrast materials. But, in some recent articles it has been suggested that GCs may have a nephrotoxic potential. Nevertheless, most of these reports are retrospective, and evaluated contrast agents and their doses were not homogenous. To investigate the effect of gadopentetate dimeglumine (GD) and magnetic field on renal function in patients with high-risk for acute kidney injury (AKI). Methods: We designed a prospective case control study, and age and sex-matched two groups of patients were included the study. Both of groups were consisted of the patients with high-risk for AKI (diabetes mellitus, hypotension, chronic renal failure, using nephrotoxic material, i.e.) (n=40, for each group). While contrast (gadopentetate dimeglumin)-enhanced non-vascular MRI was performed to group 1 patients, MRI without conrast agent was performed in goup 2 patients. Fixed dose of GD (0.2 mmol/kg) were administered to group 1 patients. All patients were followed up 72 hours. Before and at the 6, 24 and 72 hours after the MRI; biochemical markers, urinalysis, microalbumin/creatinine ratio in spot urine, serum creatinine, and glomerular filtration rate were measured. Results: Baseline serum creatinine, microalbumin/creatinine ratio, and GFR was not different between group 1 and group 2 (p>0.05). We did not observe adverse effect related to procedures. There were no significant changes in renal functional tests (?serum creatinine, ?microalbumin/creatinin ratio, and ?GFR) in both groups after 6, 24 or 72 hours of the procedures (p>0,05). Conclusions: Non-vascular contrast-enhanced (GD, 0.2 mmol/kg) MRI is a safe procedure for patients with high-risk for AKI. Key Words: MRI, Gadopentetate dimeglumine, contrast nephropathy, acute kidney injury.
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Article home page: http://ndt.oxfordjournals.org/content/27/suppl_2/ii348.abstract
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