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Bayesian methods: a potential path forward for sepsis trials

BACKGROUND: Given the success of recent platform trials for COVID-19, Bayesian statistical methods have become an option for complex, heterogenous syndromes like sepsis. However, study design will require careful consideration of how statistical power varies using Bayesian methods across different c...

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Autores principales: Tomlinson, George, Al-Khafaji, Ali, Conrad, Steven A., Factora, Faith N. F., Foster, Debra M., Galphin, Claude, Gunnerson, Kyle J., Khan, Sobia, Kohli-Seth, Roopa, McCarthy, Paul, Meena, Nikhil K., Pearl, Ronald G., Rachoin, Jean-Sebastien, Rains, Ronald, Seneff, Michael, Tidswell, Mark, Walker, Paul M., Kellum, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634134/
https://www.ncbi.nlm.nih.gov/pubmed/37940985
http://dx.doi.org/10.1186/s13054-023-04717-x
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author Tomlinson, George
Al-Khafaji, Ali
Conrad, Steven A.
Factora, Faith N. F.
Foster, Debra M.
Galphin, Claude
Gunnerson, Kyle J.
Khan, Sobia
Kohli-Seth, Roopa
McCarthy, Paul
Meena, Nikhil K.
Pearl, Ronald G.
Rachoin, Jean-Sebastien
Rains, Ronald
Seneff, Michael
Tidswell, Mark
Walker, Paul M.
Kellum, John A.
author_facet Tomlinson, George
Al-Khafaji, Ali
Conrad, Steven A.
Factora, Faith N. F.
Foster, Debra M.
Galphin, Claude
Gunnerson, Kyle J.
Khan, Sobia
Kohli-Seth, Roopa
McCarthy, Paul
Meena, Nikhil K.
Pearl, Ronald G.
Rachoin, Jean-Sebastien
Rains, Ronald
Seneff, Michael
Tidswell, Mark
Walker, Paul M.
Kellum, John A.
author_sort Tomlinson, George
collection PubMed
description BACKGROUND: Given the success of recent platform trials for COVID-19, Bayesian statistical methods have become an option for complex, heterogenous syndromes like sepsis. However, study design will require careful consideration of how statistical power varies using Bayesian methods across different choices for how historical data are incorporated through a prior distribution and how the analysis is ultimately conducted. Our objective with the current analysis is to assess how different uses of historical data through a prior distribution, and type of analysis influence results of a proposed trial that will be analyzed using Bayesian statistical methods. METHODS: We conducted a simulation study incorporating historical data from a published multicenter, randomized clinical trial in the US and Canada of polymyxin B hemadsorption for treatment of endotoxemic septic shock. Historical data come from a 179-patient subgroup of the previous trial of adult critically ill patients with septic shock, multiple organ failure and an endotoxin activity of 0.60–0.89. The trial intervention consisted of two polymyxin B hemoadsorption treatments (2 h each) completed within 24 h of enrollment. RESULTS: In our simulations for a new trial of 150 patients, a range of hypothetical results were observed. Across a range of baseline risks and treatment effects and four ways of including historical data, we demonstrate an increase in power with the use of clinically defensible incorporation of historical data. In one possible trial result, for example, with an observed reduction in risk of mortality from 44 to 37%, the probability of benefit is 96% with a fixed weight of 75% on prior data and 90% with a commensurate (adaptive-weighting) prior; the same data give an 80% probability of benefit if historical data are ignored. CONCLUSIONS: Using Bayesian methods and a biologically justifiable use of historical data in a prior distribution yields a study design with higher power than a conventional design that ignores relevant historical data. Bayesian methods may be a viable option for trials in critical care medicine where beneficial treatments have been elusive. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-023-04717-x.
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spelling pubmed-106341342023-11-10 Bayesian methods: a potential path forward for sepsis trials Tomlinson, George Al-Khafaji, Ali Conrad, Steven A. Factora, Faith N. F. Foster, Debra M. Galphin, Claude Gunnerson, Kyle J. Khan, Sobia Kohli-Seth, Roopa McCarthy, Paul Meena, Nikhil K. Pearl, Ronald G. Rachoin, Jean-Sebastien Rains, Ronald Seneff, Michael Tidswell, Mark Walker, Paul M. Kellum, John A. Crit Care Research BACKGROUND: Given the success of recent platform trials for COVID-19, Bayesian statistical methods have become an option for complex, heterogenous syndromes like sepsis. However, study design will require careful consideration of how statistical power varies using Bayesian methods across different choices for how historical data are incorporated through a prior distribution and how the analysis is ultimately conducted. Our objective with the current analysis is to assess how different uses of historical data through a prior distribution, and type of analysis influence results of a proposed trial that will be analyzed using Bayesian statistical methods. METHODS: We conducted a simulation study incorporating historical data from a published multicenter, randomized clinical trial in the US and Canada of polymyxin B hemadsorption for treatment of endotoxemic septic shock. Historical data come from a 179-patient subgroup of the previous trial of adult critically ill patients with septic shock, multiple organ failure and an endotoxin activity of 0.60–0.89. The trial intervention consisted of two polymyxin B hemoadsorption treatments (2 h each) completed within 24 h of enrollment. RESULTS: In our simulations for a new trial of 150 patients, a range of hypothetical results were observed. Across a range of baseline risks and treatment effects and four ways of including historical data, we demonstrate an increase in power with the use of clinically defensible incorporation of historical data. In one possible trial result, for example, with an observed reduction in risk of mortality from 44 to 37%, the probability of benefit is 96% with a fixed weight of 75% on prior data and 90% with a commensurate (adaptive-weighting) prior; the same data give an 80% probability of benefit if historical data are ignored. CONCLUSIONS: Using Bayesian methods and a biologically justifiable use of historical data in a prior distribution yields a study design with higher power than a conventional design that ignores relevant historical data. Bayesian methods may be a viable option for trials in critical care medicine where beneficial treatments have been elusive. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-023-04717-x. BioMed Central 2023-11-08 /pmc/articles/PMC10634134/ /pubmed/37940985 http://dx.doi.org/10.1186/s13054-023-04717-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Tomlinson, George
Al-Khafaji, Ali
Conrad, Steven A.
Factora, Faith N. F.
Foster, Debra M.
Galphin, Claude
Gunnerson, Kyle J.
Khan, Sobia
Kohli-Seth, Roopa
McCarthy, Paul
Meena, Nikhil K.
Pearl, Ronald G.
Rachoin, Jean-Sebastien
Rains, Ronald
Seneff, Michael
Tidswell, Mark
Walker, Paul M.
Kellum, John A.
Bayesian methods: a potential path forward for sepsis trials
title Bayesian methods: a potential path forward for sepsis trials
title_full Bayesian methods: a potential path forward for sepsis trials
title_fullStr Bayesian methods: a potential path forward for sepsis trials
title_full_unstemmed Bayesian methods: a potential path forward for sepsis trials
title_short Bayesian methods: a potential path forward for sepsis trials
title_sort bayesian methods: a potential path forward for sepsis trials
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634134/
https://www.ncbi.nlm.nih.gov/pubmed/37940985
http://dx.doi.org/10.1186/s13054-023-04717-x
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