Are Causal Statements Reported in Pharmacovigilance Disproportionality Analyses Using Individual Case Safety Reports Exaggerated in Related Citations? A Meta-epidemiological Study.

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Claire Bernardeau, Bruno Revol, Francesco Salvo, Michele Fusaroli, Emanuel Raschi, Jean-Luc Cracowski, Matthieu Roustit, Charles Khouri
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引用次数: 0

Abstract

Background: Previous meta-epidemiological surveys have found considerable misinterpretation of results of disproportionality analyses. We aim to explore the relationship between the strength of causal statements used in title and abstract conclusions of pharmacovigilance disproportionality analyses and the strength of causal language used in citing studies.

Methods: On March 30, 2022, we selected the 30 disproportionality studies with the highest Altmetric Attention Scores. For each article, we extracted all citing studies using the Dimension database (n = 1434). In parallel, two authors assessed the strength of causal statements in the title and abstract conclusions of source articles and in the paragraph of citing studies. Based on previous studies, the strength of causal language was quantified based on a four-level scale (1-appropriate interpretation; 2-ambiguous interpretation; 3-conditionally causal; 4-unconditionally causal). Discrepancies were solved by discussion until consensus among the team. We assessed the association between the strength of causal statements in source articles and citing studies, separately for the title and abstract conclusions, through multinomial regression models.

Results: Overall, 27% (n = 8) of source studies used unconditionally causal statements in their title, 30% (n = 9) in their abstract conclusion, and 17% (n = 5) in both. Only 20% (n = 6) used appropriate statements in their title and in their abstract's conclusions. Among the 622 citing studies analyzed, 285 (45.8%) used unconditionally causal statements when referring to the findings from disproportionality analysis, and only 164 (26.4%) used appropriate language. Multinomial models found that the strength of causal statements in citing studies was positively associated with the strength of causal language used in abstract conclusions of source articles (Likelihood Ratio Test (LogLRT) p < 0.00001) but not in the titles. In particular, among studies citing source articles with appropriate interpretation, 30.2% (95% confidence interval [CI] 22.8-37.6) contained unconditionally causal statements in their abstract conclusions, versus 56.4% (95% CI 48.7-64.2) for studies citing source articles with unconditionally causal statements.

Conclusions: Nearly half of the studies citing pharmacovigilance disproportionality analyses results used causal claims, particularly when the causal language used in the source article was stronger. There is a need for higher caution when writing, interpreting, and citing disproportionality studies.

背景:以往的元流行病学调查发现,对比例失调分析结果的误读相当严重。我们旨在探讨药物警戒不相称性分析的标题和摘要结论中使用的因果关系陈述的强度与引用研究中使用的因果关系语言的强度之间的关系:2022 年 3 月 30 日,我们选出了 Altmetric 关注度得分最高的 30 篇比例失调研究。对于每篇文章,我们使用 Dimension 数据库提取了所有引用研究(n = 1434)。同时,两位作者对来源文章的标题和摘要结论以及引用研究的段落中因果关系陈述的强度进行了评估。根据以往的研究,因果关系语言的强度按四级量表进行量化(1-恰当的解释;2-模糊的解释;3-有条件的因果关系;4-无条件的因果关系)。分歧通过讨论解决,直至团队达成共识。我们通过多项式回归模型评估了来源文章中因果关系声明的强度与引用研究之间的关联,分别针对标题和摘要结论:总体而言,27%(n = 8)的来源研究在标题中使用了无条件的因果声明,30%(n = 9)的来源研究在摘要结论中使用了无条件的因果声明,17%(n = 5)的来源研究在标题和摘要结论中均使用了无条件的因果声明。只有 20%(n = 6)的研究在标题和摘要结论中使用了适当的表述。在分析的 622 项引用研究中,285 项(45.8%)在提及比例失调分析结果时使用了无条件的因果关系陈述,只有 164 项(26.4%)使用了适当的语言。多项式模型发现,引用研究中因果关系陈述的强度与来源文章摘要结论中因果关系语言的强度呈正相关(似然比检验(LogLRT) p 结论):近一半的研究在引用药物警戒比例失调分析结果时使用了因果说法,特别是当来源文章中使用的因果语言更强时。在撰写、解释和引用比例失调研究结果时需要更加谨慎。
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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Drug Safety Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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