The Cochrane risk of bias assessment tool 2 (RoB 2) versus the original RoB: A perspective on the pros and cons.

Cochrane quality assessment risk of bias risk of bias assessment tool

Journal

Health science reports
ISSN: 2398-8835
Titre abrégé: Health Sci Rep
Pays: United States
ID NLM: 101728855

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 08 08 2023
revised: 30 09 2023
accepted: 14 05 2024
medline: 5 6 2024
pubmed: 5 6 2024
entrez: 5 6 2024
Statut: epublish

Résumé

Critical appraisal or risk of bias assessment is a fundamental part of systematic reviews that clarifies the degree to which included research articles are qualified and reliable. Version 2 of the Cochrane tool for assessing the risk of bias in randomized trials (RoB 2), the updated version of the first tool, was released in 2019. Here, we have compared these two versions of Cochrane risk of bias assessment tools and highlighted the pros and cons of RoB 2. Statistical analysis and methodology is not applicable to this article as no new data were created or analyzed in this study. The overall approach in RoB 2 is that by answering some signaling questions after the specification of results, effects of interest, and sources of information, an overall judgment for the quality of each study is reached. Accordingly, in the original version of the Cochrane RoB tool, the judgment can be in three different conclusions, including low, unclear, and high risk of bias. The most prominent difference in bias domains is the removal of "other bias" domain being replaced by "overall bias" judgment. Also, the most common presentation types of Cochrane risk of bias assessments are the "summary" and "graph" which are generated by Review Manager, web-based applications, or packages in R software. The RoB 2 tool, compared to the original RoB, has improved and is the recommended version by the Cochrane Collaboration for quality assessment of randomized controlled trials. It is recommended to consider funding source, duration of follow-up, declaration of data availability, the status of baseline characteristics between groups, and sample size calculation methods in further revisions of the Cochrane risk of bias assessment tools.

Sections du résumé

Background and Aims UNASSIGNED
Critical appraisal or risk of bias assessment is a fundamental part of systematic reviews that clarifies the degree to which included research articles are qualified and reliable. Version 2 of the Cochrane tool for assessing the risk of bias in randomized trials (RoB 2), the updated version of the first tool, was released in 2019. Here, we have compared these two versions of Cochrane risk of bias assessment tools and highlighted the pros and cons of RoB 2.
Methods UNASSIGNED
Statistical analysis and methodology is not applicable to this article as no new data were created or analyzed in this study.
Results UNASSIGNED
The overall approach in RoB 2 is that by answering some signaling questions after the specification of results, effects of interest, and sources of information, an overall judgment for the quality of each study is reached. Accordingly, in the original version of the Cochrane RoB tool, the judgment can be in three different conclusions, including low, unclear, and high risk of bias. The most prominent difference in bias domains is the removal of "other bias" domain being replaced by "overall bias" judgment. Also, the most common presentation types of Cochrane risk of bias assessments are the "summary" and "graph" which are generated by Review Manager, web-based applications, or packages in R software.
Conclusion UNASSIGNED
The RoB 2 tool, compared to the original RoB, has improved and is the recommended version by the Cochrane Collaboration for quality assessment of randomized controlled trials. It is recommended to consider funding source, duration of follow-up, declaration of data availability, the status of baseline characteristics between groups, and sample size calculation methods in further revisions of the Cochrane risk of bias assessment tools.

Identifiants

pubmed: 38835932
doi: 10.1002/hsr2.2165
pii: HSR22165
pmc: PMC11147813
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e2165

Informations de copyright

© 2024 The Author(s). Health Science Reports published by Wiley Periodicals LLC.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

Auteurs

Seyed Aria Nejadghaderi (SA)

HIV/STI Surveillance Research Center, and WHO Collaborating Center for HIV Surveillance, Institute for Futures Studies in Health Kerman University of Medical Sciences Kerman Iran.
Cancer Immunology Project (CIP) Universal Scientific Education and Research Network (USERN) Tehran Iran.
Systematic Review and Meta-analysis Expert Group (SRMEG) Universal Scientific Education and Research Network (USERN) Tehran Iran.

Maryam Balibegloo (M)

Systematic Review and Meta-analysis Expert Group (SRMEG) Universal Scientific Education and Research Network (USERN) Tehran Iran.
Cancer Immunology Project (CIP) Universal Scientific Education and Research Network (USERN) Chicago Illinois USA.
Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA) Universal Scientific Education and Research Network (USERN) Tehran Iran.

Nima Rezaei (N)

Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA) Universal Scientific Education and Research Network (USERN) Tehran Iran.
Research Center for Immunodeficiencies, Children's Medical Center Tehran University of Medical Sciences Tehran Iran.
Department of Immunology, School of Medicine Tehran University of Medical Sciences Tehran Iran.

Classifications MeSH