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Schemata, CONSORT, and the Salk Polio Vaccine Trial

机译:Schemata,Consort和Salk Polio疫苗试验

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In this essay, we defend the design of the Salk polio vaccine trial and try to put some limits on the role schemata should play in designing clinical research studies. Our presentation is structured as a response to de Freitas and Pietrobon (de Freitas, R. S. and R. Pietrobon. 2007. Whoever could get rid of the context of discovery/context of justification dichotomy? A proposal based on recent developments in clinical research. Journal of Medicine and Philosophy 32:25–42.) who identified the CONSORT statement as a schema that would have, had it existed at the time, ruled out the design of the Salk polio vaccine trial of 1954 in favor of a completely randomized controlled clinical trial (RCT). We argue that large-scale public health interventions often require evidence beyond simple efficacy, the limit of what an RCT can provide, and that the design actually adopted for the Salk trial represented a reasonable—albeit imperfect—compromise. This is of more than historical interest in that many contemporary studies are of the scale and scope to require a more pragmatic, rather than explanatory, approach to study design (Kowalski, C. J. 2010. Pragmatic problems with clinical equipoise. Perspectives in Biology and Medicine 53:161–73.).
机译:在本文中,我们捍卫Salk Polio疫苗试验的设计,并尝试对角色模式的一些限制应该在设计临床研究研究方面发挥作用。我们的演示文稿是对De Freitas和Pietrobon的回应(De Freitas,Rs和R.Pietrobon。2007.谁可以摆脱发现/辩解的语境的背景二分法?基于临床研究的最新发展的提案。杂志医学和哲学32:25-42。)将联席声明确定为该架构,这是它的架构,它已经存在于1954年的Salk脊髓灰质炎疫苗试验的设计,支持完全随机控制的临床试验(RCT)。我们认为,大规模的公共卫生干预往往需要证据超越简单的疗效,RCT可以提供的内容,以及对Salk试验的设计实际采用的设计代表了合理的不完美 - 妥协。这对许多当代研究具有比历史兴趣的兴趣是规模和范围,需要更务实,而不是解释性的,而不是解释性的方法来研究设计(Kowalski,2010年CJ。临床等务实的务实问题。生物学和医学的透视53 :161-73。)。

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