• American heart journal · May 2013

    Randomized Controlled Trial Multicenter Study

    Contrast-induced acute kidney injury and clinical outcomes after intra-arterial and intravenous contrast administration: risk comparison adjusted for patient characteristics by design.

    • Judith Kooiman, Pum A Le Haen, Gülçin Gezgin, Jean-Paul P de Vries, Doeke Boersma, Harald F Brulez, Yvo W Sijpkens, Aart J van der Molen, Suzanne C Cannegieter, Jaap F Hamming, and Menno V Huisman.
    • Department of Thrombosis and Haemostasis, Leiden University Medical Center (LUMC), Leiden, The Netherlands; Department of Nephrology, LUMC, Leiden, The Netherlands. j.kooiman@lumc.nl
    • Am. Heart J. 2013 May 1; 165 (5): 793-99, 799.e1.

    BackgroundDirect comparisons between risk of contrast induced acute kidney injury (CI-AKI) after intra-arterial versus intravenous contrast administration are scarce. We estimated and compared the risk of CI-AKI and its clinical course after both modes of contrast administration in patients who underwent both.MethodsOne hundred seventy patients who received both intra-arterial and intravenous contrast injections within one year between 2001 and 2010 were included. Primary outcome was occurrence of CI-AKI. Secondary outcomes were duration of hospital stay, the need for dialysis, recovery of renal function, and mortality.ResultsThe risk of CI-AKI was 24/170 (14.0%, 95% CI 9.6-20.2) after intra-arterial contrast injection versus 20/170 (11.7%, 95% CI 7.7-17.5) after intravenous contrast administration, which led to a relative risk of 1.2 (95% CI 0.7-2.1). None of the patients had a need for dialysis. Median duration of hospital stay in CI-AKI patients was 15.0 days (2.5-97.5, percentile 1-92) after intra-arterial and 15.5 days (2.5-97.5, percentile 0-38) after intravenous contrast procedures. Renal function recovered after CI-AKI in 13/24 after intra-arterial and in 10/20 patients after intravenous contrast administration. Mortality risks in CI-AKI patients were slightly higher than in non-CI-AKI patients, hazard ratios 1.6 (95% CI 0.7-3.7) for intra-arterial and 1.7 (95% CI 0.7-4.4) for intravenous contrast administration, adjusted for confounders.ConclusionThe risk of CI-AKI, and its clinical course was similar after intra-arterial and intravenous contrast media administration, after adjustment by design for patient-related risk factors.Copyright © 2013 Mosby, Inc. All rights reserved.

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