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Reporting quality and risk of bias assessment of animal research on Chaihu-Shugan-San for depression: A systematic review

Journal

HELIYON
Volume 9, Issue 8, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.heliyon.2023.e19232

Keywords

Chaihu Shugan San; Depression; Animal research; ARRIVE guidelines; SYRCLE risk of bias

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The aim of this study was to assess the reporting quality and risk of bias in animal research on Chaihu-Shugan-San (CSS) for depression. A total of 30 studies were included, and the results showed low reporting quality and methodological defects. The risk of bias assessment revealed that half of the studies had a risk of bias. Therefore, it is important to disseminate the ARRIVE guidelines and SYRCLE's RoB tool among basic medical researchers studying CSS for depression to improve the quality and reporting of studies and facilitate the translation of animal research into clinical research.
Objective: Chaihu-Shugan-San (CSS) is a traditional Chinese medicine formula employed to treat depression. We aim to conduct a reporting quality assessment and risk of bias evaluation of animal research on CSS for depression. Methods: To acquire eligible studies, two reviewers searched plentiful databases from inception to October 23rd, 2021. Reporting quality assessment and risk of bias assessment of the included animal studies were evaluated by using Animal Research: Reporting In Vivo Experiments (ARRIVE) guidelines and the SYstematic Review Centre for Laboratory animal Experimentation (SYRCLE) risk of bias tool, respectively. Results: The initial search identified 720 records, while only 30 studies were included. The result of the reporting quality assessment was inferior, items 17 and 19 were not reported at all. The details of five items (items 3, 6, 7, 10, and 18) were not reported. The outcome of the risk of bias assessment suggested that half of the entries (5/10) displayed an unclear risk of bias and a high risk of bias. Blinding with regard to performance bias and detection bias revealed an unclear risk of bias (100%), followed by baseline characteristics (76.67%) and sequence generation (60%). Random outcome assessment showed a high risk of bias (100%). Conclusion: The included animal studies exhibited methodological defects and imprecise reporting. Hence, the ARRIVE guidelines and SYRCLE's RoB tool should be disseminated among basic medical researchers examining CSS for depression to publish studies with low risk of bias and sufficient reporting so that the animal research can promptly be transformed into clinical research.

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