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Risk Prediction for Contrast-Induced Nephropathy in Cancer Patients Undergoing Computed Tomography under Preventive Measures

Cited 14 time in Web of Science Cited 17 time in Scopus
Authors

Jeon, Junseok; Kim, Suhyun; Yoo, Heejin; Kim, Kyunga; Kim, Yaerim; Park, Sehoon; Jang, Hye Ryoun; Kim, Dong Ki; Huh, Wooseong; Kim, Yoon-Goo; Kim, Dae Joong; Oh, Ha Young; Lee, Jung Eun

Issue Date
2019-04
Publisher
Hindawi Publishing Corporation
Citation
Journal of Oncology, Vol.2019, p. 8736163
Abstract
Background. Contrast-induced nephropathy (CIN) is a major cause of acute kidney injury in chronic kidney disease. Many cancer patients have risk factors for CIN and frequently undergo contrast-enhanced computed tomography (CECT). We aimed to develop a risk prediction model for CIN in cancer patients undergoing CECT. Methods. Between 2009 and 2017, 2,240 cancer patients with estimated glomerular filtration rate (eGFR) < 45mL/min/1.73m(2) who underwent CECT with CIN preventive measures were included in a development cohort. Primary outcome was development of CIN, defined as 25% increase in serum creatinine within 2-6 days after contrast exposure. A prediction model was developed using logistic regression analysis. The model was evaluated for prognostic utility in an independent cohort (N = 555). Results. Overall incidence of CIN was 2.5% (55/2,240). In multivariable analysis, eGFR, diabetes mellitus, and serum albumin level were identified as independent predictors of CIN. A prediction model including eGFR, serum albumin level, and diabetes mellitus was developed, and risk scores ranged from 0 to 6 points. The model demonstrated fair discriminative power (C statistic = 0.733, 95% confidence interval [CI] 0.656-0.810) and good calibration (calibration slope 0.867, 95% Cl 0.719-1.015). In the validation cohort, the model also demonstrated fair discriminative power (C statistic = 0.749, 95% CI 0.648-0.849) and good calibration (calibration slope 0.974, 95% CI 0.634-1.315). Conclusions. The proposed model has good predictive ability for risk of CIN in cancer patients with chronic kidney disease. This model can aid in risk stratification for CIN in patients undergoing CECT.
ISSN
1687-8450
URI
https://hdl.handle.net/10371/206251
DOI
https://doi.org/10.1155/2019/8736163
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  • College of Medicine
  • Department of Medicine
Research Area Nephrology, Transplantation, Urology

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