• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

相似文献

1
Cultural variability in dementia caregiver motivations: Unraveling unique and common drivers.痴呆症护理者动机的文化差异:剖析独特与共有的驱动因素。
Dementia (London). 2025 Aug;24(6):1115-1133. doi: 10.1177/14713012251327461. Epub 2025 Apr 14.
2
Sexual Harassment and Prevention Training性骚扰与预防培训
3
How lived experiences of illness trajectories, burdens of treatment, and social inequalities shape service user and caregiver participation in health and social care: a theory-informed qualitative evidence synthesis.疾病轨迹的生活经历、治疗负担和社会不平等如何影响服务使用者和照顾者参与健康和社会护理:一项基于理论的定性证据综合分析
Health Soc Care Deliv Res. 2025 Jun;13(24):1-120. doi: 10.3310/HGTQ8159.
4
Survivor, family and professional experiences of psychosocial interventions for sexual abuse and violence: a qualitative evidence synthesis.性虐待和暴力的心理社会干预的幸存者、家庭和专业人员的经验:定性证据综合。
Cochrane Database Syst Rev. 2022 Oct 4;10(10):CD013648. doi: 10.1002/14651858.CD013648.pub2.
5
Caregiver burden in Parkinson's disease: a mixed-methods study.帕金森病患者照料者负担:一项混合方法研究。
BMC Med. 2023 Jul 10;21(1):247. doi: 10.1186/s12916-023-02933-4.
6
Factors that influence caregivers' and adolescents' views and practices regarding human papillomavirus (HPV) vaccination for adolescents: a qualitative evidence synthesis.影响照顾者和青少年对青少年人乳头瘤病毒(HPV)疫苗接种的看法及做法的因素:一项定性证据综合分析
Cochrane Database Syst Rev. 2025 Apr 15;4(4):CD013430. doi: 10.1002/14651858.CD013430.pub2.
7
Cultural competence education for health professionals.针对卫生专业人员的文化能力教育。
Cochrane Database Syst Rev. 2014 May 5;2014(5):CD009405. doi: 10.1002/14651858.CD009405.pub2.
8
The meaningfulness of participating in support groups for informal caregivers of older adults with dementia: a systematic review.参与老年痴呆症患者非正式照料者支持小组的意义:一项系统评价。
JBI Database System Rev Implement Rep. 2015 Jul 17;13(6):373-433. doi: 10.11124/jbisrir-2015-2121.
9
Factors that influence participation in physical activity for people with bipolar disorder: a synthesis of qualitative evidence.影响双相障碍患者参与体育活动的因素:定性证据的综合分析。
Cochrane Database Syst Rev. 2024 Jun 4;6(6):CD013557. doi: 10.1002/14651858.CD013557.pub2.
10
Health professionals' experience of teamwork education in acute hospital settings: a systematic review of qualitative literature.医疗专业人员在急症医院环境中团队合作教育的经验:对定性文献的系统综述
JBI Database System Rev Implement Rep. 2016 Apr;14(4):96-137. doi: 10.11124/JBISRIR-2016-1843.

本文引用的文献

1
Being a Husband and Caregiver: The Adjustment of Roles When Caring for a Wife Who Has Dementia.身为人夫与照料者:照顾患有痴呆症的妻子时角色的调适
Can J Aging. 2025 Mar;44(1):68-77. doi: 10.1017/S0714980824000291. Epub 2024 Oct 23.
2
A mixed method study exploring gender differences in dementia caregiving.一项混合方法研究,旨在探索痴呆症护理中的性别差异。
Dementia (London). 2023 Nov;22(8):1862-1885. doi: 10.1177/14713012231201595. Epub 2023 Sep 23.
3
Shared decision-making in the Netherlands: Progress is made, but not for all. Time to become inclusive to patients.荷兰的共同决策:取得了进展,但并非所有人都受益。现在是让患者具有包容性的时候了。
Z Evid Fortbild Qual Gesundhwes. 2022 Jun;171:98-104. doi: 10.1016/j.zefq.2022.04.029. Epub 2022 May 23.
4
Family involvement in medical decision making in Europe and the United States: A replication and extension in five Countries.家庭在欧洲和美国医疗决策中的参与:五个国家的复制与扩展。
Soc Sci Med. 2022 May;301:114932. doi: 10.1016/j.socscimed.2022.114932. Epub 2022 Mar 26.
5
Dementia care-sharing and migration: An intersectional exploration of family carers' experiences.痴呆症照护共享与移民:家庭照护者经历的交叉领域探索。
J Aging Stud. 2022 Mar;60:100996. doi: 10.1016/j.jaging.2021.100996. Epub 2021 Dec 21.
6
"Falling between the cracks": Experiences of Black dementia caregivers navigating U.S. health systems.“夹缝求生”:美国卫生系统中,黑人社区痴呆症照顾者的经历。
J Am Geriatr Soc. 2022 Feb;70(2):592-600. doi: 10.1111/jgs.17636. Epub 2022 Jan 10.
7
Accessibility of health care experienced by persons with dementia from ethnic minority groups and formal and informal caregivers: A scoping review of European literature.少数民族痴呆患者及其正式和非正式照顾者所经历的医疗保健可及性:欧洲文献的范围综述。
Dementia (London). 2022 Feb;21(2):677-700. doi: 10.1177/14713012211055307. Epub 2021 Dec 8.
8
Caregiver Burden in a Culturally Diverse Memory Clinic Population: The Caregiver Strain Index-Expanded.文化多元化记忆诊所人群中的照护者负担:扩展后的照护者压力指数。
Dement Geriatr Cogn Disord. 2021;50(4):333-340. doi: 10.1159/000519617. Epub 2021 Oct 26.
9
Clinical characteristics and presenting symptoms of dementia - a case-control study of older ethnic minority patients in a Dutch urban memory clinic.痴呆的临床特征和表现症状 - 荷兰城市记忆诊所中少数民族老年患者的病例对照研究。
Aging Ment Health. 2022 Nov;26(11):2277-2284. doi: 10.1080/13607863.2021.1963416. Epub 2021 Aug 30.
10
Barriers in access to dementia care in minority ethnic groups in Denmark: a qualitative study.丹麦少数族裔获得痴呆症护理的障碍:一项定性研究。
Aging Ment Health. 2021 Aug;25(8):1424-1432. doi: 10.1080/13607863.2020.1787336. Epub 2020 Jul 3.

痴呆症护理者动机的文化差异:剖析独特与共有的驱动因素。

Cultural variability in dementia caregiver motivations: Unraveling unique and common drivers.

作者信息

Lazaar Najoua, Flurij Floor, van Bruchem-Visser Rozemarijn L, Papma Janne M, Franzen Sanne

机构信息

Department of Neurology, Erasmus MC University Medical Center Rotterdam, Netherlands.

Department of Internal Medicine, Erasmus MC University Medical Center Rotterdam, Netherlands.

出版信息

Dementia (London). 2025 Aug;24(6):1115-1133. doi: 10.1177/14713012251327461. Epub 2025 Apr 14.

DOI:10.1177/14713012251327461
PMID:40223563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12276403/
Abstract

In the Netherlands, approximately 800,000 individuals act as informal caregivers for people with dementia. Current policies prioritize care within the home setting, often relying on informal caregivers for support, assisted by care professionals. Given the wide ethnocultural diversity among dementia caregivers in the Netherlands, it is crucial to understand how these cultural differences influence caregiving. Given the emphasis on researching barriers to providing care in literature, this study specifically focused on motivators and facilitators to providing care. We conducted semi-structured interviews, both with caregivers of native Dutch patients ( = 11) and caregivers of patients with a migration background ( = 9), who all provided care at home for patients with dementia. Data was collected using an interview guide and open, axial and selective coding were used to analyze the transcripts of the interviews in Atlas.ti. Four themes were identified. First, culturally shared motivators to providing care emerged, such as having a unique bond with the person with dementia and themes of reciprocity. Second, culture specific perspectives were identified, with Dutch caregivers often spontaneously reporting considering professional care, while culturally diverse caregivers stressed the available network of informal caregivers and their ability to persevere. Third, personal philosophies on life were a driver to provide care for caregivers of native Dutch patients, while religion mainly served as a source of strength in continuing to provide care in the culturally diverse group. Lastly, adult child caregivers benefit from supportive home environments and from using structure and routine in providing care. Our findings show that the decision to provide care often seems driven by reciprocity and the prior quality of the relationship with the person with dementia, contrasting with previous work suggesting that religion is a main reason to provide care. Several recommendations are made how care professionals can take these factors into consideration when assisting caregivers.

摘要

在荷兰,约有80万人担任痴呆症患者的非正式照料者。当前政策将家庭环境中的照料置于优先地位,通常依靠非正式照料者提供支持,并由护理专业人员提供协助。鉴于荷兰痴呆症照料者在种族文化方面存在广泛差异,了解这些文化差异如何影响照料工作至关重要。鉴于文献中强调研究提供照料的障碍,本研究特别关注提供照料的动机和促进因素。我们对荷兰本土患者的照料者(n = 11)和有移民背景患者的照料者(n = 9)进行了半结构式访谈,他们均在家中照料痴呆症患者。使用访谈指南收集数据,并运用开放编码、轴心编码和选择性编码对Atlas.ti中的访谈记录进行分析。确定了四个主题。首先,出现了文化上共有的提供照料的动机,例如与痴呆症患者建立独特的联系以及互惠主题。其次,确定了特定文化视角,荷兰照料者经常自发报告考虑专业照料,而文化背景多样照料者则强调非正式照料者的可用网络及其坚持下去的能力。第三,个人生活理念是荷兰本土患者照料者提供照料的驱动力,而宗教在文化背景多样的群体中主要作为持续提供照料的力量源泉。最后,成年子女照料者受益于支持性的家庭环境以及在提供照料时运用条理和常规。我们的研究结果表明,提供照料的决定似乎往往由互惠以及与痴呆症患者先前的关系质量驱动,这与之前认为宗教是提供照料主要原因的研究形成对比。针对护理专业人员在协助照料者时如何考虑这些因素提出了若干建议。