痴呆治疗研究的试验设计和结果。

T. Holsinger
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引用次数: 3

摘要

这本书的编纂是为了帮助解释以前做过的痴呆症试验,并为创造有意义的未来提供帮助。卷开始与工作的简史做了迄今为止,并通过各种临床试验设计的收益。相当多的时间花在不同的潜在结果变量上,包括通过规模讨论这些结果的表示。在治疗痴呆以及开展痴呆研究的伦理考虑也进行了讨论。《痴呆症治疗研究的试验设计和结果》由2名加拿大阿尔茨海默病和老年医学专家编辑,组织有序,并有索引。感兴趣的话题很容易找到。它对可用于痴呆症研究的不同研究设计和可引入的偏见类型进行了有益的讨论。关于目前可用的痴呆症治疗方法的章节,包括药理学和心理社会学,现在是有用的回顾,但很可能很快就会过时,对本书的总体目的贡献不大。这本书最后承认,虽然痴呆症的治疗已经取得了进展,但患者想要的结果——恢复以前的功能——在很大程度上是无法实现的。书中充满激情地讨论了痴呆症研究的目标应该是什么,如何衡量这些目标,并考虑了不同利益相关者的不同目标。强调痴呆症的复杂性及其对人格、家庭、照顾者和卫生保健系统等因素的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trial Designs and Outcomes in Dementia Therapeutic Research.
This book was compiled to aid the interpretation of previously done dementia trials and provide assistance in creating meaningful future ones. The volume starts with a brief history of work done to date and proceeds through various clinical trial designs. A considerable amount of time is spent on different potential outcome variables, including a discussion of the representation of these outcomes via scale. Ethical considerations in treatment of dementia as well as in conducting dementia research are also discussed. Trial Designs and Outcomes in Dementia Therapeutic Research, which was edited by 2 Canadian experts on Alzheimer's disease and geriatric medicine, is well organized and indexed. Topics of interest can be easily located. It has useful discussions of different study designs that can be employed in dementia research and the types of bias that can be introduced. Chapters concerning the currently available treatments for dementia, both pharmacologic and psychosocial, are useful reviews now but will very likely rapidly become out of date and contribute little to the overall purpose of the book. The book concludes with the recognition that, while progress has been made in the treatment of dementia, the outcomes wanted by patients—a return to former functioning—are, for the most part, unavailable. Included is an impassioned discussion of what the goals of dementia research should be and how to measure them and consideration of the different aims of different stakeholders. The complexity of dementia and its impact on the elements of personhood, family, caregivers, and the health care system are stressed.
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