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Inverse Probability Weighting Enhances Absolute Risk Estimation in Three Common Study Designs of Nosocomial Infections

PURPOSE: When studying nosocomial infections, resource-efficient sampling designs such as nested case-control, case-cohort, and point prevalence studies are preferred. However, standard analyses of these study designs can introduce selection bias, especially when interested in absolute rates and ris...

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Autores principales: Staus, Paulina, von Cube, Maja, Hazard, Derek, Doerken, Sam, Ershova, Ksenia, Balmford, James, Wolkewitz, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482967/
https://www.ncbi.nlm.nih.gov/pubmed/36134385
http://dx.doi.org/10.2147/CLEP.S357494
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author Staus, Paulina
von Cube, Maja
Hazard, Derek
Doerken, Sam
Ershova, Ksenia
Balmford, James
Wolkewitz, Martin
author_facet Staus, Paulina
von Cube, Maja
Hazard, Derek
Doerken, Sam
Ershova, Ksenia
Balmford, James
Wolkewitz, Martin
author_sort Staus, Paulina
collection PubMed
description PURPOSE: When studying nosocomial infections, resource-efficient sampling designs such as nested case-control, case-cohort, and point prevalence studies are preferred. However, standard analyses of these study designs can introduce selection bias, especially when interested in absolute rates and risks. Moreover, nosocomial infection studies are often subject to competing risks. We aim to demonstrate in this tutorial how to address these challenges for all three study designs using simple weighting techniques. PATIENTS AND METHODS: We discuss the study designs and explain how inverse probability weights (IPW) are applied to obtain unbiased hazard ratios (HR), odds ratios and cumulative incidences. We illustrate these methods in a multi-state framework using a dataset from a nosocomial infections study (n = 2286) in Moscow, Russia. RESULTS: Including IPW in the analysis corrects the unweighted naïve analyses and enables the estimation of absolute risks. Resulting estimates are close to the full cohort estimates using substantially smaller numbers of patients. CONCLUSION: IPW is a powerful tool to account for the unequal selection of controls in case-cohort, nested case-control and point prevalence studies. Findings can be generalized to the full population and absolute risks can be estimated. When applied to a multi-state model, competing risks are also taken into account.
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spelling pubmed-94829672022-09-20 Inverse Probability Weighting Enhances Absolute Risk Estimation in Three Common Study Designs of Nosocomial Infections Staus, Paulina von Cube, Maja Hazard, Derek Doerken, Sam Ershova, Ksenia Balmford, James Wolkewitz, Martin Clin Epidemiol Original Research PURPOSE: When studying nosocomial infections, resource-efficient sampling designs such as nested case-control, case-cohort, and point prevalence studies are preferred. However, standard analyses of these study designs can introduce selection bias, especially when interested in absolute rates and risks. Moreover, nosocomial infection studies are often subject to competing risks. We aim to demonstrate in this tutorial how to address these challenges for all three study designs using simple weighting techniques. PATIENTS AND METHODS: We discuss the study designs and explain how inverse probability weights (IPW) are applied to obtain unbiased hazard ratios (HR), odds ratios and cumulative incidences. We illustrate these methods in a multi-state framework using a dataset from a nosocomial infections study (n = 2286) in Moscow, Russia. RESULTS: Including IPW in the analysis corrects the unweighted naïve analyses and enables the estimation of absolute risks. Resulting estimates are close to the full cohort estimates using substantially smaller numbers of patients. CONCLUSION: IPW is a powerful tool to account for the unequal selection of controls in case-cohort, nested case-control and point prevalence studies. Findings can be generalized to the full population and absolute risks can be estimated. When applied to a multi-state model, competing risks are also taken into account. Dove 2022-09-14 /pmc/articles/PMC9482967/ /pubmed/36134385 http://dx.doi.org/10.2147/CLEP.S357494 Text en © 2022 Staus et al. https://creativecommons.org/licenses/by-nc/3.0/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/ (https://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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Staus, Paulina
von Cube, Maja
Hazard, Derek
Doerken, Sam
Ershova, Ksenia
Balmford, James
Wolkewitz, Martin
Inverse Probability Weighting Enhances Absolute Risk Estimation in Three Common Study Designs of Nosocomial Infections
title Inverse Probability Weighting Enhances Absolute Risk Estimation in Three Common Study Designs of Nosocomial Infections
title_full Inverse Probability Weighting Enhances Absolute Risk Estimation in Three Common Study Designs of Nosocomial Infections
title_fullStr Inverse Probability Weighting Enhances Absolute Risk Estimation in Three Common Study Designs of Nosocomial Infections
title_full_unstemmed Inverse Probability Weighting Enhances Absolute Risk Estimation in Three Common Study Designs of Nosocomial Infections
title_short Inverse Probability Weighting Enhances Absolute Risk Estimation in Three Common Study Designs of Nosocomial Infections
title_sort inverse probability weighting enhances absolute risk estimation in three common study designs of nosocomial infections
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482967/
https://www.ncbi.nlm.nih.gov/pubmed/36134385
http://dx.doi.org/10.2147/CLEP.S357494
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