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A metaresearch study revealed susceptibility of Covid-19 treatment research to white hat bias: first, do no harm
OBJECTIVE: To investigate the presence of white hat bias in Covid-19 treatment research by evaluating the effects of citation and reporting bias. STUDY DESIGN AND SETTING: Citation bias was investigated by assessing the degree of agreement between evidence provided by a remdesivir randomized control...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997163/ https://www.ncbi.nlm.nih.gov/pubmed/33775812 http://dx.doi.org/10.1016/j.jclinepi.2021.03.020 |
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author | Bellos, Ioannis |
author_facet | Bellos, Ioannis |
author_sort | Bellos, Ioannis |
collection | PubMed |
description | OBJECTIVE: To investigate the presence of white hat bias in Covid-19 treatment research by evaluating the effects of citation and reporting bias. STUDY DESIGN AND SETTING: Citation bias was investigated by assessing the degree of agreement between evidence provided by a remdesivir randomized controlled trial and its citing articles. The dissimilarity of outcomes derived from nonrandomized and randomized studies was tested by a meta-analysis of hydroxychloroquine effects on mortality. The differential influence of studies with beneficial over those with neutral results was evaluated by a bibliometric analysis. RESULTS: The articles citing the ACTT-1 remdesivir trial preferentially presented its positive outcomes in 55.83% and its negative outcomes in 6.43% of cases. The hydroxychloroquine indicated no significant effect by randomized studies, but a significant survival benefit by nonrandomized ones. Citation mapping revealed that the study reporting survival benefit from the hydroxychloroquine-azithromycin combination was the most influential, despite subsequent studies reporting potential harmful effects. CONCLUSION: The present study raises concerns about citation bias and a predilection of reporting beneficial over harmful effects in the Covid-19 treatment research, potentially in the context of white hat bias. Preregistration, data sharing and avoidance of selective reporting are crucial to ensure the credibility of future research. |
format | Online Article Text |
id | pubmed-7997163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79971632021-03-29 A metaresearch study revealed susceptibility of Covid-19 treatment research to white hat bias: first, do no harm Bellos, Ioannis J Clin Epidemiol Original Article OBJECTIVE: To investigate the presence of white hat bias in Covid-19 treatment research by evaluating the effects of citation and reporting bias. STUDY DESIGN AND SETTING: Citation bias was investigated by assessing the degree of agreement between evidence provided by a remdesivir randomized controlled trial and its citing articles. The dissimilarity of outcomes derived from nonrandomized and randomized studies was tested by a meta-analysis of hydroxychloroquine effects on mortality. The differential influence of studies with beneficial over those with neutral results was evaluated by a bibliometric analysis. RESULTS: The articles citing the ACTT-1 remdesivir trial preferentially presented its positive outcomes in 55.83% and its negative outcomes in 6.43% of cases. The hydroxychloroquine indicated no significant effect by randomized studies, but a significant survival benefit by nonrandomized ones. Citation mapping revealed that the study reporting survival benefit from the hydroxychloroquine-azithromycin combination was the most influential, despite subsequent studies reporting potential harmful effects. CONCLUSION: The present study raises concerns about citation bias and a predilection of reporting beneficial over harmful effects in the Covid-19 treatment research, potentially in the context of white hat bias. Preregistration, data sharing and avoidance of selective reporting are crucial to ensure the credibility of future research. Elsevier Inc. 2021-08 2021-03-26 /pmc/articles/PMC7997163/ /pubmed/33775812 http://dx.doi.org/10.1016/j.jclinepi.2021.03.020 Text en © 2021 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Original Article Bellos, Ioannis A metaresearch study revealed susceptibility of Covid-19 treatment research to white hat bias: first, do no harm |
title | A metaresearch study revealed susceptibility of Covid-19 treatment research to white hat bias: first, do no harm |
title_full | A metaresearch study revealed susceptibility of Covid-19 treatment research to white hat bias: first, do no harm |
title_fullStr | A metaresearch study revealed susceptibility of Covid-19 treatment research to white hat bias: first, do no harm |
title_full_unstemmed | A metaresearch study revealed susceptibility of Covid-19 treatment research to white hat bias: first, do no harm |
title_short | A metaresearch study revealed susceptibility of Covid-19 treatment research to white hat bias: first, do no harm |
title_sort | metaresearch study revealed susceptibility of covid-19 treatment research to white hat bias: first, do no harm |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997163/ https://www.ncbi.nlm.nih.gov/pubmed/33775812 http://dx.doi.org/10.1016/j.jclinepi.2021.03.020 |
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