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Implementing an automated monitoring process in a digital, longitudinal observational cohort study

BACKGROUND: Clinical data collection requires correct and complete data sets in order to perform correct statistical analysis and draw valid conclusions. While in randomized clinical trials much effort concentrates on data monitoring, this is rarely the case in observational studies- due to high num...

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Autores principales: Lindner, Lisa, Weiß, Anja, Reich, Andreas, Kindler, Siegfried, Behrens, Frank, Braun, Jürgen, Listing, Joachim, Schett, Georg, Sieper, Joachim, Strangfeld, Anja, Regierer, Anne C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262053/
https://www.ncbi.nlm.nih.gov/pubmed/34233730
http://dx.doi.org/10.1186/s13075-021-02563-2
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author Lindner, Lisa
Weiß, Anja
Reich, Andreas
Kindler, Siegfried
Behrens, Frank
Braun, Jürgen
Listing, Joachim
Schett, Georg
Sieper, Joachim
Strangfeld, Anja
Regierer, Anne C.
author_facet Lindner, Lisa
Weiß, Anja
Reich, Andreas
Kindler, Siegfried
Behrens, Frank
Braun, Jürgen
Listing, Joachim
Schett, Georg
Sieper, Joachim
Strangfeld, Anja
Regierer, Anne C.
author_sort Lindner, Lisa
collection PubMed
description BACKGROUND: Clinical data collection requires correct and complete data sets in order to perform correct statistical analysis and draw valid conclusions. While in randomized clinical trials much effort concentrates on data monitoring, this is rarely the case in observational studies- due to high numbers of cases and often-restricted resources. We have developed a valid and cost-effective monitoring tool, which can substantially contribute to an increased data quality in observational research. METHODS: An automated digital monitoring system for cohort studies developed by the German Rheumatism Research Centre (DRFZ) was tested within the disease register RABBIT-SpA, a longitudinal observational study including patients with axial spondyloarthritis and psoriatic arthritis. Physicians and patients complete electronic case report forms (eCRF) twice a year for up to 10 years. Automatic plausibility checks were implemented to verify all data after entry into the eCRF. To identify conflicts that cannot be found by this approach, all possible conflicts were compiled into a catalog. This “conflict catalog” was used to create queries, which are displayed as part of the eCRF. The proportion of queried eCRFs and responses were analyzed by descriptive methods. For the analysis of responses, the type of conflict was assigned to either a single conflict only (affecting individual items) or a conflict that required the entire eCRF to be queried. RESULTS: Data from 1883 patients was analyzed. A total of n = 3145 eCRFs submitted between baseline (T0) and T3 (12 months) had conflicts (40–64%). Fifty-six to 100% of the queries regarding eCRFs that were completely missing were answered. A mean of 1.4 to 2.4 single conflicts occurred per eCRF, of which 59–69% were answered. The most common missing values were CRP, ESR, Schober’s test, data on systemic glucocorticoid therapy, and presence of enthesitis. CONCLUSION: Providing high data quality in large observational cohort studies is a major challenge, which requires careful monitoring. An automated monitoring process was successfully implemented and well accepted by the study centers. Two thirds of the queries were answered with new data. While conventional manual monitoring is resource-intensive and may itself create new sources of errors, automated processes are a convenient way to augment data quality. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-021-02563-2.
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spelling pubmed-82620532021-07-08 Implementing an automated monitoring process in a digital, longitudinal observational cohort study Lindner, Lisa Weiß, Anja Reich, Andreas Kindler, Siegfried Behrens, Frank Braun, Jürgen Listing, Joachim Schett, Georg Sieper, Joachim Strangfeld, Anja Regierer, Anne C. Arthritis Res Ther Research Article BACKGROUND: Clinical data collection requires correct and complete data sets in order to perform correct statistical analysis and draw valid conclusions. While in randomized clinical trials much effort concentrates on data monitoring, this is rarely the case in observational studies- due to high numbers of cases and often-restricted resources. We have developed a valid and cost-effective monitoring tool, which can substantially contribute to an increased data quality in observational research. METHODS: An automated digital monitoring system for cohort studies developed by the German Rheumatism Research Centre (DRFZ) was tested within the disease register RABBIT-SpA, a longitudinal observational study including patients with axial spondyloarthritis and psoriatic arthritis. Physicians and patients complete electronic case report forms (eCRF) twice a year for up to 10 years. Automatic plausibility checks were implemented to verify all data after entry into the eCRF. To identify conflicts that cannot be found by this approach, all possible conflicts were compiled into a catalog. This “conflict catalog” was used to create queries, which are displayed as part of the eCRF. The proportion of queried eCRFs and responses were analyzed by descriptive methods. For the analysis of responses, the type of conflict was assigned to either a single conflict only (affecting individual items) or a conflict that required the entire eCRF to be queried. RESULTS: Data from 1883 patients was analyzed. A total of n = 3145 eCRFs submitted between baseline (T0) and T3 (12 months) had conflicts (40–64%). Fifty-six to 100% of the queries regarding eCRFs that were completely missing were answered. A mean of 1.4 to 2.4 single conflicts occurred per eCRF, of which 59–69% were answered. The most common missing values were CRP, ESR, Schober’s test, data on systemic glucocorticoid therapy, and presence of enthesitis. CONCLUSION: Providing high data quality in large observational cohort studies is a major challenge, which requires careful monitoring. An automated monitoring process was successfully implemented and well accepted by the study centers. Two thirds of the queries were answered with new data. While conventional manual monitoring is resource-intensive and may itself create new sources of errors, automated processes are a convenient way to augment data quality. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-021-02563-2. BioMed Central 2021-07-07 2021 /pmc/articles/PMC8262053/ /pubmed/34233730 http://dx.doi.org/10.1186/s13075-021-02563-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Lindner, Lisa
Weiß, Anja
Reich, Andreas
Kindler, Siegfried
Behrens, Frank
Braun, Jürgen
Listing, Joachim
Schett, Georg
Sieper, Joachim
Strangfeld, Anja
Regierer, Anne C.
Implementing an automated monitoring process in a digital, longitudinal observational cohort study
title Implementing an automated monitoring process in a digital, longitudinal observational cohort study
title_full Implementing an automated monitoring process in a digital, longitudinal observational cohort study
title_fullStr Implementing an automated monitoring process in a digital, longitudinal observational cohort study
title_full_unstemmed Implementing an automated monitoring process in a digital, longitudinal observational cohort study
title_short Implementing an automated monitoring process in a digital, longitudinal observational cohort study
title_sort implementing an automated monitoring process in a digital, longitudinal observational cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8262053/
https://www.ncbi.nlm.nih.gov/pubmed/34233730
http://dx.doi.org/10.1186/s13075-021-02563-2
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