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重症监护病房幸存者的非正式护理人员所报告的负担:一项文献综述。

Reported burden on informal caregivers of ICU survivors: a literature review.

作者信息

van Beusekom Ilse, Bakhshi-Raiez Ferishta, de Keizer Nicolette F, Dongelmans Dave A, van der Schaaf Marike

机构信息

Department of Medical Informatics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

National Intensive Care Evaluation, Amsterdam, The Netherlands.

出版信息

Crit Care. 2016 Jan 21;20:16. doi: 10.1186/s13054-016-1185-9.

Abstract

BACKGROUND

Critical illness and the problems faced after ICU discharge do not only affect the patient, it also negatively impacts patients' informal caregivers. There is no review which summarizes all types of burden reported in informal caregivers of ICU survivors. It is important that the burdens these informal caregivers suffer are systematically assessed so the caregivers can receive the professional care they need. We aimed to provide a complete overview of the types of burdens reported in informal caregivers of adult ICU survivors, to make recommendations on which burdens should be assessed in this population, and which tools should be used to assess them.

METHOD

We performed a systematic search in PubMed and CINAHL from database inception until June 2014. All articles reporting on burdens in informal caregivers of adult ICU survivors were included. Two independent reviewers used a standardized form to extract characteristics of informal caregivers, types of burdens and instruments used to assess these burdens. The quality of the included studies was assessed using the Newcastle-Ottawa and the PEDro scales.

RESULTS

The search yielded 2704 articles, of which we included 28 in our review. The most commonly reported outcomes were psychosocial burden. Six months after ICU discharge, the prevalence of anxiety was between 15% and 24%, depression between 4.7% and 36.4% and post-traumatic stress disorder (PTSD) between 35% and 57.1%. Loss of employment, financial burden, lifestyle interference and low health-related quality of life (HRQoL) were also frequently reported. The most commonly used tools were the Hospital Anxiety and Depression Scale (HADS), Centre for Epidemiological Studies-Depression questionnaire, and Impact of Event Scale (IES). The quality of observational studies was low and of randomized studies moderate to fair.

CONCLUSIONS

Informal caregivers of ICU survivors suffer a substantial variety of burdens. Although the quality of the included studies was poor, there is evidence that burden in the psychosocial field is most prevalent. We suggest screening informal caregivers of ICU survivors for anxiety, depression, PTSD, and HRQoL using respectively the HADS, IES and Short Form 36 and recommend a follow-up period of at least 6 months.

摘要

背景

危重病以及重症监护病房(ICU)出院后所面临的问题不仅影响患者,还会对患者的非正式照护者产生负面影响。目前尚无综述总结ICU幸存者的非正式照护者所报告的各类负担。系统评估这些非正式照护者所承受的负担非常重要,这样他们才能获得所需的专业护理。我们旨在全面概述成年ICU幸存者的非正式照护者所报告的负担类型,就该人群应评估哪些负担以及应使用哪些工具进行评估提出建议。

方法

我们在PubMed和CINAHL数据库中进行了从建库至2014年6月的系统检索。纳入所有报告成年ICU幸存者非正式照护者负担的文章。两名独立评审员使用标准化表格提取非正式照护者的特征、负担类型以及用于评估这些负担的工具。使用纽卡斯尔-渥太华量表和PEDro量表评估纳入研究的质量。

结果

检索共获得2704篇文章,其中我们纳入综述的有28篇。最常报告的结果是心理社会负担。ICU出院6个月后,焦虑症患病率在15%至24%之间,抑郁症患病率在4.7%至36.4%之间,创伤后应激障碍(PTSD)患病率在35%至57.1%之间。失业、经济负担、生活方式受到干扰以及健康相关生活质量(HRQoL)较低也经常被报告。最常用的工具是医院焦虑抑郁量表(HADS)、流行病学研究中心抑郁问卷以及事件影响量表(IES)。观察性研究的质量较低,随机研究的质量中等至尚可。

结论

ICU幸存者的非正式照护者承受着各种各样的负担。尽管纳入研究的质量较差,但有证据表明心理社会领域的负担最为普遍。我们建议分别使用HADS、IES和简明健康调查问卷(SF-36)对ICU幸存者的非正式照护者进行焦虑、抑郁、PTSD和HRQoL筛查,并建议至少随访6个月。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ac8/4721206/951939a9836b/13054_2016_1185_Fig1_HTML.jpg

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