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Causal Bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with COVID-19 and severe hypoxemia

The currently recommended dose of dexamethasone for patients with severe or critical COVID-19 is 6 mg per day (mg/d) regardless of patient features and variation. However, patients with severe or critical COVID-19 are heterogenous in many ways (e.g., age, weight, comorbidities, disease severity, and...

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Autores principales: Blette, Bryan S., Granholm, Anders, Li, Fan, Shankar-Hari, Manu, Lange, Theis, Munch, Marie Warrer, Møller, Morten Hylander, Perner, Anders, Harhay, Michael O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120498/
https://www.ncbi.nlm.nih.gov/pubmed/37085591
http://dx.doi.org/10.1038/s41598-023-33425-3
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author Blette, Bryan S.
Granholm, Anders
Li, Fan
Shankar-Hari, Manu
Lange, Theis
Munch, Marie Warrer
Møller, Morten Hylander
Perner, Anders
Harhay, Michael O.
author_facet Blette, Bryan S.
Granholm, Anders
Li, Fan
Shankar-Hari, Manu
Lange, Theis
Munch, Marie Warrer
Møller, Morten Hylander
Perner, Anders
Harhay, Michael O.
author_sort Blette, Bryan S.
collection PubMed
description The currently recommended dose of dexamethasone for patients with severe or critical COVID-19 is 6 mg per day (mg/d) regardless of patient features and variation. However, patients with severe or critical COVID-19 are heterogenous in many ways (e.g., age, weight, comorbidities, disease severity, and immune features). Thus, it is conceivable that a standardized dosing protocol may not be optimal. We assessed treatment effect heterogeneity in the COVID STEROID 2 trial, which compared 6 mg/d to 12 mg/d, using a causal inference framework with Bayesian Additive Regression Trees, a flexible modeling method that detects interactive effects and nonlinear relationships among multiple patient characteristics simultaneously. We found that 12 mg/d of dexamethasone, relative to 6 mg/d, was probably associated with better long-term outcomes (days alive without life support and mortality after 90 days) among the entire trial population (i.e., no signals of harm), and probably more beneficial among those without diabetes mellitus, that were older, were not using IL-6 inhibitors at baseline, weighed less, or had higher level respiratory support at baseline. This adds more evidence supporting the use of 12 mg/d in practice for most patients not receiving other immunosuppressants and that additional study of dosing could potentially optimize clinical outcomes.
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spelling pubmed-101204982023-04-23 Causal Bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with COVID-19 and severe hypoxemia Blette, Bryan S. Granholm, Anders Li, Fan Shankar-Hari, Manu Lange, Theis Munch, Marie Warrer Møller, Morten Hylander Perner, Anders Harhay, Michael O. Sci Rep Article The currently recommended dose of dexamethasone for patients with severe or critical COVID-19 is 6 mg per day (mg/d) regardless of patient features and variation. However, patients with severe or critical COVID-19 are heterogenous in many ways (e.g., age, weight, comorbidities, disease severity, and immune features). Thus, it is conceivable that a standardized dosing protocol may not be optimal. We assessed treatment effect heterogeneity in the COVID STEROID 2 trial, which compared 6 mg/d to 12 mg/d, using a causal inference framework with Bayesian Additive Regression Trees, a flexible modeling method that detects interactive effects and nonlinear relationships among multiple patient characteristics simultaneously. We found that 12 mg/d of dexamethasone, relative to 6 mg/d, was probably associated with better long-term outcomes (days alive without life support and mortality after 90 days) among the entire trial population (i.e., no signals of harm), and probably more beneficial among those without diabetes mellitus, that were older, were not using IL-6 inhibitors at baseline, weighed less, or had higher level respiratory support at baseline. This adds more evidence supporting the use of 12 mg/d in practice for most patients not receiving other immunosuppressants and that additional study of dosing could potentially optimize clinical outcomes. Nature Publishing Group UK 2023-04-21 /pmc/articles/PMC10120498/ /pubmed/37085591 http://dx.doi.org/10.1038/s41598-023-33425-3 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/) .
spellingShingle Article
Blette, Bryan S.
Granholm, Anders
Li, Fan
Shankar-Hari, Manu
Lange, Theis
Munch, Marie Warrer
Møller, Morten Hylander
Perner, Anders
Harhay, Michael O.
Causal Bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with COVID-19 and severe hypoxemia
title Causal Bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with COVID-19 and severe hypoxemia
title_full Causal Bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with COVID-19 and severe hypoxemia
title_fullStr Causal Bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with COVID-19 and severe hypoxemia
title_full_unstemmed Causal Bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with COVID-19 and severe hypoxemia
title_short Causal Bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with COVID-19 and severe hypoxemia
title_sort causal bayesian machine learning to assess treatment effect heterogeneity by dexamethasone dose for patients with covid-19 and severe hypoxemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120498/
https://www.ncbi.nlm.nih.gov/pubmed/37085591
http://dx.doi.org/10.1038/s41598-023-33425-3
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