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精神分裂症患者照顾者的生活质量和其他结局指标。

Quality of life and other outcome measures in caregivers of patients with schizophrenia.

机构信息

Aix-Marseille Université, EA 3279 Research Unit, 13284, Marseille, France.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2013 Oct;13(5):641-9. doi: 10.1586/14737167.2013.838022. Epub 2013 Oct 7.

Abstract

There is a growing concern about caregivers of individuals with schizophrenia who assume almost the totality of the patient care. This responsibility exposes them to an intense burden with negative consequences for them and indirectly for patients' health. The aim of this study was to provide an overview of the content and psychometric properties of instruments assessing the experience of caregivers of individuals with schizophrenia. Of the 460 articles screened from 1990 to 2013, 16 instruments were identified focusing on caregivers' burden (8), coping strategies (3), perception of need (3) and quality of life (2). These instruments were based primarily on experts' opinions, except two which were based exclusively on caregivers' view. The psychometric properties were poorly documented for a number of them and no information was published about responsiveness. Future works are needed to involve caregivers in the development of instruments and to explore psychometric properties of these instruments.

摘要

越来越多的人关注照顾精神分裂症患者的人,他们承担了几乎全部的患者护理责任。这种责任给他们带来了巨大的负担,对他们和患者的健康都有间接的负面影响。本研究旨在概述评估精神分裂症患者照顾者体验的工具的内容和心理测量特性。在从 1990 年到 2013 年筛选的 460 篇文章中,确定了 16 种工具,主要集中在照顾者的负担(8 种)、应对策略(3 种)、需求感知(3 种)和生活质量(2 种)。这些工具主要基于专家的意见,只有两种工具完全基于照顾者的观点。其中有许多工具的心理测量特性记录不佳,也没有关于反应性的信息发表。未来的工作需要让照顾者参与工具的开发,并探索这些工具的心理测量特性。

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