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Preprocedural Prediction Model for Contrast‐Induced Nephropathy Patients
BACKGROUND: Several models have been developed for prediction of contrast‐induced nephropathy (CIN); however, they only contain patients receiving intra‐arterial contrast media for coronary angiographic procedures, which represent a small proportion of all contrast procedures. In addition, most of t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523753/ https://www.ncbi.nlm.nih.gov/pubmed/28159819 http://dx.doi.org/10.1161/JAHA.116.004498 |
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author | Yin, Wen‐jun Yi, Yi‐hu Guan, Xiao‐feng Zhou, Ling‐yun Wang, Jiang‐lin Li, Dai‐yang Zuo, Xiao‐cong |
author_facet | Yin, Wen‐jun Yi, Yi‐hu Guan, Xiao‐feng Zhou, Ling‐yun Wang, Jiang‐lin Li, Dai‐yang Zuo, Xiao‐cong |
author_sort | Yin, Wen‐jun |
collection | PubMed |
description | BACKGROUND: Several models have been developed for prediction of contrast‐induced nephropathy (CIN); however, they only contain patients receiving intra‐arterial contrast media for coronary angiographic procedures, which represent a small proportion of all contrast procedures. In addition, most of them evaluate radiological interventional procedure‐related variables. So it is necessary for us to develop a model for prediction of CIN before radiological procedures among patients administered contrast media. METHODS AND RESULTS: A total of 8800 patients undergoing contrast administration were randomly assigned in a 4:1 ratio to development and validation data sets. CIN was defined as an increase of 25% and/or 0.5 mg/dL in serum creatinine within 72 hours above the baseline value. Preprocedural clinical variables were used to develop the prediction model from the training data set by the machine learning method of random forest, and 5‐fold cross‐validation was used to evaluate the prediction accuracies of the model. Finally we tested this model in the validation data set. The incidence of CIN was 13.38%. We built a prediction model with 13 preprocedural variables selected from 83 variables. The model obtained an area under the receiver‐operating characteristic (ROC) curve (AUC) of 0.907 and gave prediction accuracy of 80.8%, sensitivity of 82.7%, specificity of 78.8%, and Matthews correlation coefficient of 61.5%. For the first time, 3 new factors are included in the model: the decreased sodium concentration, the INR value, and the preprocedural glucose level. CONCLUSIONS: The newly established model shows excellent predictive ability of CIN development and thereby provides preventative measures for CIN. |
format | Online Article Text |
id | pubmed-5523753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55237532017-08-14 Preprocedural Prediction Model for Contrast‐Induced Nephropathy Patients Yin, Wen‐jun Yi, Yi‐hu Guan, Xiao‐feng Zhou, Ling‐yun Wang, Jiang‐lin Li, Dai‐yang Zuo, Xiao‐cong J Am Heart Assoc Original Research BACKGROUND: Several models have been developed for prediction of contrast‐induced nephropathy (CIN); however, they only contain patients receiving intra‐arterial contrast media for coronary angiographic procedures, which represent a small proportion of all contrast procedures. In addition, most of them evaluate radiological interventional procedure‐related variables. So it is necessary for us to develop a model for prediction of CIN before radiological procedures among patients administered contrast media. METHODS AND RESULTS: A total of 8800 patients undergoing contrast administration were randomly assigned in a 4:1 ratio to development and validation data sets. CIN was defined as an increase of 25% and/or 0.5 mg/dL in serum creatinine within 72 hours above the baseline value. Preprocedural clinical variables were used to develop the prediction model from the training data set by the machine learning method of random forest, and 5‐fold cross‐validation was used to evaluate the prediction accuracies of the model. Finally we tested this model in the validation data set. The incidence of CIN was 13.38%. We built a prediction model with 13 preprocedural variables selected from 83 variables. The model obtained an area under the receiver‐operating characteristic (ROC) curve (AUC) of 0.907 and gave prediction accuracy of 80.8%, sensitivity of 82.7%, specificity of 78.8%, and Matthews correlation coefficient of 61.5%. For the first time, 3 new factors are included in the model: the decreased sodium concentration, the INR value, and the preprocedural glucose level. CONCLUSIONS: The newly established model shows excellent predictive ability of CIN development and thereby provides preventative measures for CIN. John Wiley and Sons Inc. 2017-02-03 /pmc/articles/PMC5523753/ /pubmed/28159819 http://dx.doi.org/10.1161/JAHA.116.004498 Text en © 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Yin, Wen‐jun Yi, Yi‐hu Guan, Xiao‐feng Zhou, Ling‐yun Wang, Jiang‐lin Li, Dai‐yang Zuo, Xiao‐cong Preprocedural Prediction Model for Contrast‐Induced Nephropathy Patients |
title | Preprocedural Prediction Model for Contrast‐Induced Nephropathy Patients |
title_full | Preprocedural Prediction Model for Contrast‐Induced Nephropathy Patients |
title_fullStr | Preprocedural Prediction Model for Contrast‐Induced Nephropathy Patients |
title_full_unstemmed | Preprocedural Prediction Model for Contrast‐Induced Nephropathy Patients |
title_short | Preprocedural Prediction Model for Contrast‐Induced Nephropathy Patients |
title_sort | preprocedural prediction model for contrast‐induced nephropathy patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5523753/ https://www.ncbi.nlm.nih.gov/pubmed/28159819 http://dx.doi.org/10.1161/JAHA.116.004498 |
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