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Using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus

BACKGROUND: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease of unknown origin. The objective of this research was to develop phenotype algorithms for SLE suitable for use in epidemiological studies using empirical evidence from observational databases. METHODS: We used a process f...

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Autores principales: Swerdel, Joel N., Ramcharran, Darmendra, Hardin, Jill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934349/
https://www.ncbi.nlm.nih.gov/pubmed/36795690
http://dx.doi.org/10.1371/journal.pone.0281929
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author Swerdel, Joel N.
Ramcharran, Darmendra
Hardin, Jill
author_facet Swerdel, Joel N.
Ramcharran, Darmendra
Hardin, Jill
author_sort Swerdel, Joel N.
collection PubMed
description BACKGROUND: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease of unknown origin. The objective of this research was to develop phenotype algorithms for SLE suitable for use in epidemiological studies using empirical evidence from observational databases. METHODS: We used a process for empirically determining and evaluating phenotype algorithms for health conditions to be analyzed in observational research. The process started with a literature search to discover prior algorithms used for SLE. We then used a set of Observational Health Data Sciences and Informatics (OHDSI) open-source tools to refine and validate the algorithms. These included tools to discover codes for SLE that may have been missed in prior studies and to determine possible low specificity and index date misclassification in algorithms for correction. RESULTS: We developed four algorithms using our process: two algorithms for prevalent SLE and two for incident SLE. The algorithms for both incident and prevalent cases are comprised of a more specific version and a more sensitive version. Each of the algorithms corrects for possible index date misclassification. After validation, we found the highest positive predictive value estimate for the prevalent, specific algorithm (89%). The highest sensitivity estimate was found for the sensitive, prevalent algorithm (77%). CONCLUSION: We developed phenotype algorithms for SLE using a data-driven approach. The four final algorithms may be used directly in observational studies. The validation of these algorithms provides researchers an added measure of confidence that the algorithms are selecting subjects correctly and allows for the application of quantitative bias analysis.
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spelling pubmed-99343492023-02-17 Using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus Swerdel, Joel N. Ramcharran, Darmendra Hardin, Jill PLoS One Research Article BACKGROUND: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease of unknown origin. The objective of this research was to develop phenotype algorithms for SLE suitable for use in epidemiological studies using empirical evidence from observational databases. METHODS: We used a process for empirically determining and evaluating phenotype algorithms for health conditions to be analyzed in observational research. The process started with a literature search to discover prior algorithms used for SLE. We then used a set of Observational Health Data Sciences and Informatics (OHDSI) open-source tools to refine and validate the algorithms. These included tools to discover codes for SLE that may have been missed in prior studies and to determine possible low specificity and index date misclassification in algorithms for correction. RESULTS: We developed four algorithms using our process: two algorithms for prevalent SLE and two for incident SLE. The algorithms for both incident and prevalent cases are comprised of a more specific version and a more sensitive version. Each of the algorithms corrects for possible index date misclassification. After validation, we found the highest positive predictive value estimate for the prevalent, specific algorithm (89%). The highest sensitivity estimate was found for the sensitive, prevalent algorithm (77%). CONCLUSION: We developed phenotype algorithms for SLE using a data-driven approach. The four final algorithms may be used directly in observational studies. The validation of these algorithms provides researchers an added measure of confidence that the algorithms are selecting subjects correctly and allows for the application of quantitative bias analysis. Public Library of Science 2023-02-16 /pmc/articles/PMC9934349/ /pubmed/36795690 http://dx.doi.org/10.1371/journal.pone.0281929 Text en © 2023 Swerdel et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Swerdel, Joel N.
Ramcharran, Darmendra
Hardin, Jill
Using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus
title Using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus
title_full Using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus
title_fullStr Using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus
title_full_unstemmed Using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus
title_short Using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus
title_sort using a data-driven approach for the development and evaluation of phenotype algorithms for systemic lupus erythematosus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934349/
https://www.ncbi.nlm.nih.gov/pubmed/36795690
http://dx.doi.org/10.1371/journal.pone.0281929
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