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The Controversy of Contrast-Induced Nephropathy With Intravenous Contrast: What Is the Risk?
Rudnick, Michael R; Leonberg-Yoo, Amanda K; Litt, Harold I; Cohen, Raphael M; Hilton, Susan; Reese, Peter P.
Affiliation
  • Rudnick MR; Division of Nephrology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA. Electronic address: michael.rudnick@uphs.upenn.edu.
  • Leonberg-Yoo AK; Division of Nephrology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Litt HI; Division of Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Cohen RM; Division of Nephrology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Hilton S; Division of Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Reese PP; Division of Nephrology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Am J Kidney Dis ; 75(1): 105-113, 2020 01.
Article in En | MEDLINE | ID: mdl-31473019
ABSTRACT
Contrast-induced nephropathy (CIN) has long been observed in both experimental and clinical studies. However, recent observational studies have questioned the prevalence and severity of CIN following intravenous contrast exposure. Initial studies of acute kidney injury following intravenous contrast were limited by the absence of control groups or contained control groups that did not adjust for additional acute kidney injury risk factors, including prevalent chronic kidney disease, as well as accepted prophylactic strategies. More contemporary use of propensity score-adjusted models have attempted to minimize the risk for selection bias, although bias cannot be completely eliminated without a prospective randomized trial. Based on existing data, we recommend the following CIN risk classification patients with estimated glomerular filtration rates (eGFRs) ≥ 45mL/min/1.73m2 are at negligible risk for CIN, while patients with eGFRs<30mL/min/1.73m2 are at high risk for CIN. Patients with eGFRs between 30 and 44mL/min/1.73m2 are at an intermediate risk for CIN unless diabetes mellitus is present, which would further increase the risk. In all patients at any increased risk for CIN, the risk for CIN needs to be balanced by the risk of not performing an intravenous contrast-enhanced study.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Contrast Media / Acute Kidney Injury Type of study: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Am J Kidney Dis Year: 2020 Document type: Article Country of publication: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Contrast Media / Acute Kidney Injury Type of study: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Am J Kidney Dis Year: 2020 Document type: Article Country of publication: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA