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扩展审查标准:痴呆症的非药物干预案例

Expanded review criteria: the case of nonpharmacological interventions in dementia.

作者信息

Cohen-Mansfield Jiska, Buckwalter Kathleen, Beattie Elizabeth, Rose Karen, Neville Christine, Kolanowski Ann

机构信息

Tel-Aviv University, Tel-Aviv, Israel George Washington University, Washington, DC, USA.

The University of Iowa, Iowa City, IA, USA.

出版信息

J Alzheimers Dis. 2014;41(1):15-28. doi: 10.3233/JAD-132357.

Abstract

This paper challenges the assumptions underlying many reviews and offers alternative criteria for examining evidence for nonpharmacological interventions. We evaluated 27 reviews examining interventions for persons with dementia as they relate to the issues of selection based on randomized controlled trial (RCT) design. Reviews were described by type of intervention, level of cognitive function, and criteria for inclusion. Of the 27 reviews, 46% required RCTs for inclusion and most had stringent inclusion criteria. This resulted in poor utilization of the literature and low ecological validity. Eliminating most of the available data poses a critical problem to clinical and research development. Studies meeting strict methodological criteria may not generalize to the greater population or may exclude sub-populations and interventions. Limitations of double-blind RCTs and potential design solutions are set forth based on appropriate populations, problems, interventions, and settings characteristics.

摘要

本文对许多综述所依据的假设提出了质疑,并提供了用于审查非药物干预证据的替代标准。我们评估了27篇关于痴呆症患者干预措施的综述,这些综述与基于随机对照试验(RCT)设计的选择问题相关。综述按照干预类型、认知功能水平和纳入标准进行描述。在这27篇综述中,46%要求纳入随机对照试验,且大多数有严格的纳入标准。这导致文献利用率低下和生态效度较低。排除大部分现有数据给临床和研究发展带来了关键问题。符合严格方法学标准的研究可能无法推广到更广泛的人群,或者可能排除亚人群和干预措施。基于适当的人群、问题、干预措施和环境特征,阐述了双盲随机对照试验的局限性及潜在的设计解决方案。

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