• Journal of nephrology · Nov 2012

    Incidence of contrast-induced acute kidney injury associated with diagnostic or interventional coronary angiography.

    • Santo Morabito, Valentina Pistolesi, Giulia Benedetti, Angelo Di Roma, Riccardo Colantonio, Massimo Mancone, Gennaro Sardella, Loredana Cibelli, Mariacarmela Ambrosino, Francesca Polistena, and Alessandro Pierucci.
    • Department of Nephrology and Urology, Policlinico Umberto I, Sapienza University, Rome, Italy. santo.morabito@uniroma1.it
    • J. Nephrol. 2012 Nov 1;25(6):1098-107.

    BackgroundContrast-induced acute kidney injury (CI-AKI) represents an important cause of hospital-acquired AKI. The aim of this study was to evaluate the incidence of CI-AKI after coronary angiography (CA) or percutaneous coronary intervention (PCI) and the role of patient-/procedure-related risk factors.MethodsFor 11 months, patients undergoing CA or PCI were prospectively evaluated for CI-AKI, and factors possibly affecting CI-AKI were analyzed. Statistical analysis was completed using Student's t-test, chi-square or Fisher exact test, and multivariate logistic regression.ResultsAmong 585 consecutive patients, incidence of CI-AKI was 5.1% (n=30) and renal replacement therapy was required in 10% of those (n=3). Incidence of CI-AKI was higher in patients with anemia or chronic kidney disease (CKD) associated with diabetes. Basal hemoglobin was significantly lower in CI-AKI patients while Mehran score, contrast medium (CM) volume, contrast ratio (CM volume / maximum contrast dose) and ratio glomerular filtration rate (CM volume / GFR) were significantly higher. Multivariate analysis selected a higher contrast ratio as a factor independently associated with a higher risk of CI-AKI which otherwise appeared to be lower with increasing basal hemoglobin.ConclusionsThe incidence of CI-AKI after CA or PCI was higher in patients with CKD associated with diabetes. Lower levels of basal hemoglobin appeared to be related to a higher risk of CI-AKI, and contrast media volume, especially if exceeding the dose adjusted for renal function, was a strong modifiable risk factor for CI-AKI.

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