Suppr超能文献

[对照临床试验的原则]

[Principles of controlled clinical trials].

作者信息

Martini P

出版信息

Methods Inf Med. 1962 Jan;1(1):1-5.

Abstract

The recovery of the patient should be facilitated as the result of therapeutic research. The basic rule for every therapeutic-clinical trial mist involve a comparison of therapeutic approaches. In acute conditions, such as acute infectious diseases, infarcts, etc., comparisons should be made between two or more groups: the collective therapeutic comparison = the between patients trial. The formation of groups, to be compared one with the other can be justified only if one is reasonably sure that a pathogenic condition indeed exists. In chronic diseases, which extend essentially unchanged over a lengthy period but are nevertheless reversible, therapeutic comparisons may be made between two or more time intervals within the course of the disease in the same individual. This type of therapeutic trial rests primarily upon a (refined!) type of specious reasoning and secondarily, upon modified statistics: the individual therapeutic comparison = the within patient trial. The collective therapeutic comparison, on the one hand, and the individual therapeutic comparison on the other, overlap somewhat in scope. The immediate therapeutic effect is not always an indication of its true value, which may become evident only upon long-term treatment. The short-term trials of therapeutic regimens in an individual must, therefore, be frequently supplemented by long-term trials which can only be carried out by comparing two groups. For many clinical investigations, therefore, the joint efforts of numerous hospitals are absolutely necessary. The second basic rule of therapeutic research is the elimination of secondary causes. The difficulties introduced by these secondary considerations are far greater in therapeutic trials carried out on ambulatory patients than has been hitherto realized. In order to remove subjective secondary causes, the author demanded, in 1931, the use of hidden or illusory media (placebos, dummies) that is, unconscious causative agents. The double blind procedure is indispensible in all experiments, especially where psychological processes and problems are of foremost importance. Therefore, it is absolutely necessary that convincing tests be finally carried out with the double blind procedure on the one hand, and the simple blind procedure on the other in order to determine the range and limitations of both. Therapeutic research of the future is threatened by the hazard of self-satisfaction which produces a sense of accomplishment merely as the result of obeying formal conditions and of following formal standards of accuracy.

摘要

治疗性研究应有助于患者康复。每项治疗性临床试验的基本规则都必须涉及治疗方法的比较。在急性病症中,如急性传染病、梗死等,应在两个或更多组之间进行比较:集体治疗比较 = 患者间试验。只有当有理由确信确实存在致病状况时,相互比较的组的形成才是合理的。在慢性病中,这些疾病在很长一段时间内基本保持不变但仍可逆转,可在同一患者疾病过程中的两个或更多时间间隔之间进行治疗比较。这种类型的治疗试验主要基于一种(精细的!)似是而非的推理方式,其次基于修正的统计学:个体治疗比较 = 患者内试验。一方面,集体治疗比较,另一方面,个体治疗比较,在范围上有一定程度的重叠。即时治疗效果并不总是其真正价值的指标,其真正价值可能只有在长期治疗后才会显现。因此,个体治疗方案的短期试验必须经常辅以只能通过比较两组进行的长期试验。所以,对于许多临床研究而言,众多医院的共同努力绝对必要。治疗性研究的第二条基本规则是消除次要病因。在对门诊患者进行的治疗试验中,这些次要因素带来的困难比迄今所认识到的要大得多。为了消除主观次要病因,作者在1931年要求使用隐蔽或虚假手段(安慰剂、虚拟物),即无意识的致病因素。双盲程序在所有实验中都是必不可少的,尤其是在心理过程和问题最为重要的情况下。因此,绝对有必要最终一方面用双盲程序,另一方面用单盲程序进行令人信服的测试,以确定两者的范围和局限性。未来的治疗性研究受到自满风险的威胁,这种自满仅仅因为遵守形式条件和遵循形式准确性标准而产生成就感。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验