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Control of confounding in the analysis phase – an overview for clinicians
In observational studies, control of confounding can be done in the design and analysis phases. Using examples from large health care database studies, this article provides the clinicians with an overview of standard methods in the analysis phase, such as stratification, standardization, multivaria...
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/PMC5384727/ https://www.ncbi.nlm.nih.gov/pubmed/28408854 http://dx.doi.org/10.2147/CLEP.S129886 |
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author | Kahlert, Johnny Gribsholt, Sigrid Bjerge Gammelager, Henrik Dekkers, Olaf M Luta, George |
author_facet | Kahlert, Johnny Gribsholt, Sigrid Bjerge Gammelager, Henrik Dekkers, Olaf M Luta, George |
author_sort | Kahlert, Johnny |
collection | PubMed |
description | In observational studies, control of confounding can be done in the design and analysis phases. Using examples from large health care database studies, this article provides the clinicians with an overview of standard methods in the analysis phase, such as stratification, standardization, multivariable regression analysis and propensity score (PS) methods, together with the more advanced high-dimensional propensity score (HD-PS) method. We describe the progression from simple stratification confined to the inclusion of a few potential confounders to complex modeling procedures such as the HD-PS approach by which hundreds of potential confounders are extracted from large health care databases. Stratification and standardization assist in the understanding of the data at a detailed level, while accounting for potential confounders. Incorporating several potential confounders in the analysis typically implies the choice between multivariable analysis and PS methods. Although PS methods have gained remarkable popularity in recent years, there is an ongoing discussion on the advantages and disadvantages of PS methods as compared to those of multivariable analysis. Furthermore, the HD-PS method, despite its generous inclusion of potential confounders, is also associated with potential pitfalls. All methods are dependent on the assumption of no unknown, unmeasured and residual confounding and suffer from the difficulty of identifying true confounders. Even in large health care databases, insufficient or poor data may contribute to these challenges. The trend in data collection is to compile more fine-grained data on lifestyle and severity of diseases, based on self-reporting and modern technologies. This will surely improve our ability to incorporate relevant confounders or their proxies. However, despite a remarkable development of methods that account for confounding and new data opportunities, confounding will remain a serious issue. Considering the advantages and disadvantages of different methods, we emphasize the importance of the clinical input and of the interplay between clinicians and analysts to ensure a proper analysis. |
format | Online Article Text |
id | pubmed-5384727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-53847272017-04-13 Control of confounding in the analysis phase – an overview for clinicians Kahlert, Johnny Gribsholt, Sigrid Bjerge Gammelager, Henrik Dekkers, Olaf M Luta, George Clin Epidemiol Methodology In observational studies, control of confounding can be done in the design and analysis phases. Using examples from large health care database studies, this article provides the clinicians with an overview of standard methods in the analysis phase, such as stratification, standardization, multivariable regression analysis and propensity score (PS) methods, together with the more advanced high-dimensional propensity score (HD-PS) method. We describe the progression from simple stratification confined to the inclusion of a few potential confounders to complex modeling procedures such as the HD-PS approach by which hundreds of potential confounders are extracted from large health care databases. Stratification and standardization assist in the understanding of the data at a detailed level, while accounting for potential confounders. Incorporating several potential confounders in the analysis typically implies the choice between multivariable analysis and PS methods. Although PS methods have gained remarkable popularity in recent years, there is an ongoing discussion on the advantages and disadvantages of PS methods as compared to those of multivariable analysis. Furthermore, the HD-PS method, despite its generous inclusion of potential confounders, is also associated with potential pitfalls. All methods are dependent on the assumption of no unknown, unmeasured and residual confounding and suffer from the difficulty of identifying true confounders. Even in large health care databases, insufficient or poor data may contribute to these challenges. The trend in data collection is to compile more fine-grained data on lifestyle and severity of diseases, based on self-reporting and modern technologies. This will surely improve our ability to incorporate relevant confounders or their proxies. However, despite a remarkable development of methods that account for confounding and new data opportunities, confounding will remain a serious issue. Considering the advantages and disadvantages of different methods, we emphasize the importance of the clinical input and of the interplay between clinicians and analysts to ensure a proper analysis. Dove Medical Press 2017-03-31 /pmc/articles/PMC5384727/ /pubmed/28408854 http://dx.doi.org/10.2147/CLEP.S129886 Text en © 2017 Kahlert 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 | Methodology Kahlert, Johnny Gribsholt, Sigrid Bjerge Gammelager, Henrik Dekkers, Olaf M Luta, George Control of confounding in the analysis phase – an overview for clinicians |
title | Control of confounding in the analysis phase – an overview for clinicians |
title_full | Control of confounding in the analysis phase – an overview for clinicians |
title_fullStr | Control of confounding in the analysis phase – an overview for clinicians |
title_full_unstemmed | Control of confounding in the analysis phase – an overview for clinicians |
title_short | Control of confounding in the analysis phase – an overview for clinicians |
title_sort | control of confounding in the analysis phase – an overview for clinicians |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384727/ https://www.ncbi.nlm.nih.gov/pubmed/28408854 http://dx.doi.org/10.2147/CLEP.S129886 |
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