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The BILAG-2004 systems tally—a novel way of representing the BILAG-2004 index scores longitudinally

Objective. This was an exploratory analysis to develop a new way of representing BILAG-2004 system scores longitudinally that would be clinically meaningful and easier to analyse in comparison with multiple categorical variables. Methods. Data from a multicentre longitudinal study of SLE patients (t...

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Autores principales: Yee, Chee-Seng, Gordon, Caroline, Isenberg, David A., Griffiths, Bridget, Teh, Lee-Suan, Bruce, Ian N., Ahmad, Yasmeen, Rahman, Anisur, Prabu, Athiveeraramapandian, Akil, Mohammed, McHugh, Neil, Edwards, Christopher, D’Cruz, David, Khamashta, Munther A., Farewell, Vernon T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475981/
https://www.ncbi.nlm.nih.gov/pubmed/22908329
http://dx.doi.org/10.1093/rheumatology/kes207
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author Yee, Chee-Seng
Gordon, Caroline
Isenberg, David A.
Griffiths, Bridget
Teh, Lee-Suan
Bruce, Ian N.
Ahmad, Yasmeen
Rahman, Anisur
Prabu, Athiveeraramapandian
Akil, Mohammed
McHugh, Neil
Edwards, Christopher
D’Cruz, David
Khamashta, Munther A.
Farewell, Vernon T.
author_facet Yee, Chee-Seng
Gordon, Caroline
Isenberg, David A.
Griffiths, Bridget
Teh, Lee-Suan
Bruce, Ian N.
Ahmad, Yasmeen
Rahman, Anisur
Prabu, Athiveeraramapandian
Akil, Mohammed
McHugh, Neil
Edwards, Christopher
D’Cruz, David
Khamashta, Munther A.
Farewell, Vernon T.
author_sort Yee, Chee-Seng
collection PubMed
description Objective. This was an exploratory analysis to develop a new way of representing BILAG-2004 system scores longitudinally that would be clinically meaningful and easier to analyse in comparison with multiple categorical variables. Methods. Data from a multicentre longitudinal study of SLE patients (the BILAG-2004 index and therapy collected at every visit) were used. External responsiveness analysis of the index suggested the possibility of using counts of systems with specified transitions in scores as a basis to analyse the system scores. Exploratory analyses with multinomial logistic regression were used to examine the appropriateness of this new method of analysing BILAG-2004 system scores. Receiver operating characteristic (ROC) curve analysis was used to assess the performance of this approach. Results. There were 1414 observations from 347 patients. A novel method was devised based on counts of systems with defined transitions in score (BILAG-2004 systems tally, BST). It has six components (systems with major deterioration, systems with minor deterioration, systems with persistent significant activity, systems with major improvement, systems with minor improvement and systems with persistent minimal or no activity). This was further simplified (simplified BST, sBST) into three components (systems with active/worsening disease, systems with improving disease and systems with persistent minimal or no activity). Both versions had expected associations with change in therapy. ROC curve analyses demonstrated that both versions had similar good performance characteristics (areas under the curve >0.80) in predicting increase in therapy. Conclusion. The BST and sBST provide alternative approaches to representing BILAG-2004 disease activity longitudinally. Further validation of their use is required.
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spelling pubmed-34759812012-10-19 The BILAG-2004 systems tally—a novel way of representing the BILAG-2004 index scores longitudinally Yee, Chee-Seng Gordon, Caroline Isenberg, David A. Griffiths, Bridget Teh, Lee-Suan Bruce, Ian N. Ahmad, Yasmeen Rahman, Anisur Prabu, Athiveeraramapandian Akil, Mohammed McHugh, Neil Edwards, Christopher D’Cruz, David Khamashta, Munther A. Farewell, Vernon T. Rheumatology (Oxford) Clinical Science Objective. This was an exploratory analysis to develop a new way of representing BILAG-2004 system scores longitudinally that would be clinically meaningful and easier to analyse in comparison with multiple categorical variables. Methods. Data from a multicentre longitudinal study of SLE patients (the BILAG-2004 index and therapy collected at every visit) were used. External responsiveness analysis of the index suggested the possibility of using counts of systems with specified transitions in scores as a basis to analyse the system scores. Exploratory analyses with multinomial logistic regression were used to examine the appropriateness of this new method of analysing BILAG-2004 system scores. Receiver operating characteristic (ROC) curve analysis was used to assess the performance of this approach. Results. There were 1414 observations from 347 patients. A novel method was devised based on counts of systems with defined transitions in score (BILAG-2004 systems tally, BST). It has six components (systems with major deterioration, systems with minor deterioration, systems with persistent significant activity, systems with major improvement, systems with minor improvement and systems with persistent minimal or no activity). This was further simplified (simplified BST, sBST) into three components (systems with active/worsening disease, systems with improving disease and systems with persistent minimal or no activity). Both versions had expected associations with change in therapy. ROC curve analyses demonstrated that both versions had similar good performance characteristics (areas under the curve >0.80) in predicting increase in therapy. Conclusion. The BST and sBST provide alternative approaches to representing BILAG-2004 disease activity longitudinally. Further validation of their use is required. Oxford University Press 2012-11 2012-08-19 /pmc/articles/PMC3475981/ /pubmed/22908329 http://dx.doi.org/10.1093/rheumatology/kes207 Text en © The Author 2012. Published by Oxford University Press on behalf of the British Society for Rheumatology. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Science
Yee, Chee-Seng
Gordon, Caroline
Isenberg, David A.
Griffiths, Bridget
Teh, Lee-Suan
Bruce, Ian N.
Ahmad, Yasmeen
Rahman, Anisur
Prabu, Athiveeraramapandian
Akil, Mohammed
McHugh, Neil
Edwards, Christopher
D’Cruz, David
Khamashta, Munther A.
Farewell, Vernon T.
The BILAG-2004 systems tally—a novel way of representing the BILAG-2004 index scores longitudinally
title The BILAG-2004 systems tally—a novel way of representing the BILAG-2004 index scores longitudinally
title_full The BILAG-2004 systems tally—a novel way of representing the BILAG-2004 index scores longitudinally
title_fullStr The BILAG-2004 systems tally—a novel way of representing the BILAG-2004 index scores longitudinally
title_full_unstemmed The BILAG-2004 systems tally—a novel way of representing the BILAG-2004 index scores longitudinally
title_short The BILAG-2004 systems tally—a novel way of representing the BILAG-2004 index scores longitudinally
title_sort bilag-2004 systems tally—a novel way of representing the bilag-2004 index scores longitudinally
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475981/
https://www.ncbi.nlm.nih.gov/pubmed/22908329
http://dx.doi.org/10.1093/rheumatology/kes207
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