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Multivariable prediction model for suspected giant cell arteritis: development and validation
PURPOSE: To develop and validate a diagnostic prediction model for patients with suspected giant cell arteritis (GCA). METHODS: A retrospective review of records of consecutive adult patients undergoing temporal artery biopsy (TABx) for suspected GCA was conducted at seven university centers. The pa...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703153/ https://www.ncbi.nlm.nih.gov/pubmed/29200816 http://dx.doi.org/10.2147/OPTH.S151385 |
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author | Ing, Edsel B Lahaie Luna, Gabriela Toren, Andrew Ing, Royce Chen, John J Arora, Nitika Torun, Nurhan Jakpor, Otana A Fraser, J Alexander Tyndel, Felix J Sundaram, Arun NE Liu, Xinyang Lam, Cindy TY Patel, Vivek Weis, Ezekiel Jordan, David Gilberg, Steven Pagnoux, Christian ten Hove, Martin |
author_facet | Ing, Edsel B Lahaie Luna, Gabriela Toren, Andrew Ing, Royce Chen, John J Arora, Nitika Torun, Nurhan Jakpor, Otana A Fraser, J Alexander Tyndel, Felix J Sundaram, Arun NE Liu, Xinyang Lam, Cindy TY Patel, Vivek Weis, Ezekiel Jordan, David Gilberg, Steven Pagnoux, Christian ten Hove, Martin |
author_sort | Ing, Edsel B |
collection | PubMed |
description | PURPOSE: To develop and validate a diagnostic prediction model for patients with suspected giant cell arteritis (GCA). METHODS: A retrospective review of records of consecutive adult patients undergoing temporal artery biopsy (TABx) for suspected GCA was conducted at seven university centers. The pathologic diagnosis was considered the final diagnosis. The predictor variables were age, gender, new onset headache, clinical temporal artery abnormality, jaw claudication, ischemic vision loss (VL), diplopia, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and platelet level. Multiple imputation was performed for missing data. Logistic regression was used to compare our models with the non-histologic American College of Rheumatology (ACR) GCA classification criteria. Internal validation was performed with 10-fold cross validation and bootstrap techniques. External validation was performed by geographic site. RESULTS: There were 530 complete TABx records: 397 were negative and 133 positive for GCA. Age, jaw claudication, VL, platelets, and log CRP were statistically significant predictors of positive TABx, whereas ESR, gender, headache, and temporal artery abnormality were not. The parsimonious model had a cross-validated bootstrap area under the receiver operating characteristic curve (AUROC) of 0.810 (95% CI =0.766–0.854), geographic external validation AUROC’s in the range of 0.75–0.85, calibration p(H–L) of 0.812, sensitivity of 43.6%, and specificity of 95.2%, which outperformed the ACR criteria. CONCLUSION: Our prediction rule with calculator and nomogram aids in the triage of patients with suspected GCA and may decrease the need for TABx in select low-score at-risk subjects. However, misclassification remains a concern. |
format | Online Article Text |
id | pubmed-5703153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57031532017-11-30 Multivariable prediction model for suspected giant cell arteritis: development and validation Ing, Edsel B Lahaie Luna, Gabriela Toren, Andrew Ing, Royce Chen, John J Arora, Nitika Torun, Nurhan Jakpor, Otana A Fraser, J Alexander Tyndel, Felix J Sundaram, Arun NE Liu, Xinyang Lam, Cindy TY Patel, Vivek Weis, Ezekiel Jordan, David Gilberg, Steven Pagnoux, Christian ten Hove, Martin Clin Ophthalmol Original Research PURPOSE: To develop and validate a diagnostic prediction model for patients with suspected giant cell arteritis (GCA). METHODS: A retrospective review of records of consecutive adult patients undergoing temporal artery biopsy (TABx) for suspected GCA was conducted at seven university centers. The pathologic diagnosis was considered the final diagnosis. The predictor variables were age, gender, new onset headache, clinical temporal artery abnormality, jaw claudication, ischemic vision loss (VL), diplopia, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and platelet level. Multiple imputation was performed for missing data. Logistic regression was used to compare our models with the non-histologic American College of Rheumatology (ACR) GCA classification criteria. Internal validation was performed with 10-fold cross validation and bootstrap techniques. External validation was performed by geographic site. RESULTS: There were 530 complete TABx records: 397 were negative and 133 positive for GCA. Age, jaw claudication, VL, platelets, and log CRP were statistically significant predictors of positive TABx, whereas ESR, gender, headache, and temporal artery abnormality were not. The parsimonious model had a cross-validated bootstrap area under the receiver operating characteristic curve (AUROC) of 0.810 (95% CI =0.766–0.854), geographic external validation AUROC’s in the range of 0.75–0.85, calibration p(H–L) of 0.812, sensitivity of 43.6%, and specificity of 95.2%, which outperformed the ACR criteria. CONCLUSION: Our prediction rule with calculator and nomogram aids in the triage of patients with suspected GCA and may decrease the need for TABx in select low-score at-risk subjects. However, misclassification remains a concern. Dove Medical Press 2017-11-22 /pmc/articles/PMC5703153/ /pubmed/29200816 http://dx.doi.org/10.2147/OPTH.S151385 Text en © 2017 Ing et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Ing, Edsel B Lahaie Luna, Gabriela Toren, Andrew Ing, Royce Chen, John J Arora, Nitika Torun, Nurhan Jakpor, Otana A Fraser, J Alexander Tyndel, Felix J Sundaram, Arun NE Liu, Xinyang Lam, Cindy TY Patel, Vivek Weis, Ezekiel Jordan, David Gilberg, Steven Pagnoux, Christian ten Hove, Martin Multivariable prediction model for suspected giant cell arteritis: development and validation |
title | Multivariable prediction model for suspected giant cell arteritis: development and validation |
title_full | Multivariable prediction model for suspected giant cell arteritis: development and validation |
title_fullStr | Multivariable prediction model for suspected giant cell arteritis: development and validation |
title_full_unstemmed | Multivariable prediction model for suspected giant cell arteritis: development and validation |
title_short | Multivariable prediction model for suspected giant cell arteritis: development and validation |
title_sort | multivariable prediction model for suspected giant cell arteritis: development and validation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703153/ https://www.ncbi.nlm.nih.gov/pubmed/29200816 http://dx.doi.org/10.2147/OPTH.S151385 |
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