Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
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
_version_ 1783281648514629632
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
work_keys_str_mv AT ingedselb multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT lahaielunagabriela multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT torenandrew multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT ingroyce multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT chenjohnj multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT aroranitika multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT torunnurhan multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT jakporotanaa multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT fraserjalexander multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT tyndelfelixj multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT sundaramarunne multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT liuxinyang multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT lamcindyty multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT patelvivek multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT weisezekiel multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT jordandavid multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT gilbergsteven multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT pagnouxchristian multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation
AT tenhovemartin multivariablepredictionmodelforsuspectedgiantcellarteritisdevelopmentandvalidation