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Authorization of Animal Experiments Is Based on Confidence Rather than Evidence of Scientific Rigor

机译:动物实验的授权基于信任而不是科学严谨的证据

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摘要

Accumulating evidence indicates high risk of bias in preclinical animal research, questioning the scientific validity and reproducibility of published research findings. Systematic reviews found low rates of reporting of measures against risks of bias in the published literature (e.g., randomization, blinding, sample size calculation) and a correlation between low reporting rates and inflated treatment effects. That most animal research undergoes peer review or ethical review would offer the possibility to detect risks of bias at an earlier stage, before the research has been conducted. For example, in Switzerland, animal experiments are licensed based on a detailed description of the study protocol and a harm–benefit analysis. We therefore screened applications for animal experiments submitted to Swiss authorities (n = 1,277) for the rates at which the use of seven basic measures against bias (allocation concealment, blinding, randomization, sample size calculation, inclusion/exclusion criteria, primary outcome variable, and statistical analysis plan) were described and compared them with the reporting rates of the same measures in a representative sub-sample of publications (n = 50) resulting from studies described in these applications. Measures against bias were described at very low rates, ranging on average from 2.4% for statistical analysis plan to 19% for primary outcome variable in applications for animal experiments, and from 0.0% for sample size calculation to 34% for statistical analysis plan in publications from these experiments. Calculating an internal validity score (IVS) based on the proportion of the seven measures against bias, we found a weak positive correlation between the IVS of applications and that of publications (Spearman’s rho = 0.34, p = 0.014), indicating that the rates of description of these measures in applications partly predict their rates of reporting in publications. These results indicate that the authorities licensing animal experiments are lacking important information about experimental conduct that determines the scientific validity of the findings, which may be critical for the weight attributed to the benefit of the research in the harm–benefit analysis. Similar to manuscripts getting accepted for publication despite poor reporting of measures against bias, applications for animal experiments may often be approved based on implicit confidence rather than explicit evidence of scientific rigor. Our findings shed serious doubt on the current authorization procedure for animal experiments, as well as the peer-review process for scientific publications, which in the long run may undermine the credibility of research. Developing existing authorization procedures that are already in place in many countries towards a preregistration system for animal research is one promising way to reform the system. This would not only benefit the scientific validity of findings from animal experiments but also help to avoid unnecessary harm to animals for inconclusive research.
机译:越来越多的证据表明在临床前动物研究中存在偏见的高风险,质疑已发表的研究结果的科学有效性和可重复性。系统评价发现已发表文献中针对偏倚风险的措施报告率较低(例如随机化,盲法,样本量计算),并且报告率较低与治疗效果过高之间存在相关性。大多数动物研究都经过同行评审或道德审查,将有可能在进行研究之前及早发现偏倚风险。例如,在瑞士,根据实验方案的详细说明和危害效益分析,对动物实验进行了许可。因此,我们筛选了提交给瑞士当局(n = 1,277)的动物实验申请,以评估使用七种基本偏倚措施(分配隐瞒,盲目化,随机化,样本量计算,纳入/排除标准,主要结果变量,和统计分析计划)进行了描述,并将它们与这些申请中所述研究的代表性出版物子样本(n = 50)中相同度量的报告率进行了比较。针对偏倚的措施的描述率非常低,在动物实验应用中,平均范围从统计分析计划的2.4%到主要结果变量的19%,从样本量计算的0.0%到出版物的统计分析计划的34%从这些实验中。根据针对偏倚的七项衡量指标的比例计算内部有效性评分(IVS),我们发现应用程序和出版物的IVS之间存在较弱的正相关关系(Spearman的rho = 0.34,p = 0.014),表明这些措施在应用程序中的描述部分地预测了它们在出版物中的报告率。这些结果表明,授权动物实验的主管部门缺乏确定实验结果科学有效性的有关实验行为的重要信息,这可能对危害效益分析中研究收益的重要性至关重要。类似于手稿,尽管对偏倚措施的报告不多,但仍被接受出版。动物实验的申请通常可能基于内隐的信心而不是科学严谨的明确证据而被批准。我们的发现严重质疑当前的动物实验授权程序以及科学出版物的同行评审过程,从长远来看,这可能会损害研究的可信度。制定许多国家针对动物研究预注册系统的现有授权程序,是改革该系统的一种有前途的方法。这不仅有益于动物实验结果的科学有效性,而且还有助于避免进行非结论性研究时对动物造成不必要的伤害。

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