• 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

多发性硬化症患者照顾者的需求与经历:一项系统综述

The needs and experiences of caregivers of individuals with multiple sclerosis: a systematic review.

作者信息

McKeown L P, Porter-Armstrong A P, Baxter G D

机构信息

Rehabilitation Sciences Research Group, University of Ulster at Jordanstown, Newtownabbey, Co. Antrim, Northem Ireland, UK.

出版信息

Clin Rehabil. 2003 May;17(3):234-48. doi: 10.1191/0269215503cr618oa.

DOI:10.1191/0269215503cr618oa
PMID:12735530
Abstract

PRIMARY OBJECTIVE

To appraise recent studies regarding the needs and experiences of caregivers of individuals with multiple sclerosis (MS).

DESIGN

The following computerized databases were searched: CINAHL, BIDS IBSS, ASSIA, MEDLINE, PSYCHINFO, British Nursing Index, ISI Web of Science, Zetoc, AMED (1990-April 2002). The computer-based search was supplemented by manual searches of the reference lists of all retrieved studies and review articles. Inclusion and exclusion criteria were formulated.

RESULTS

Twenty-four studies from across the world that met the inclusion criteria were reviewed. The majority of studies were descriptive in nature. The studies covered a variety of topics, including how carers assist people with MS, the effect of providing care on a carer's physical and psychological well-being, social life, financial situation and overall quality of life, and how carers cope with the stresses of providing care.

CONCLUSIONS

Providing care for a person with MS has a major impact on all areas of the caregiver's life. Perceived social support has been shown to have a beneficial impact on the caregiver. Limitations in design and variation in methodology of studies limits the generalizability of findings. There is a need for further research, in particular the development of reliable and valid disease-specific caregiver assessment instruments.

摘要

主要目标

评估近期关于多发性硬化症(MS)患者照料者的需求及经历的研究。

设计

检索了以下计算机化数据库:护理学与健康领域数据库(CINAHL)、英国教育索引数据库(BIDS IBSS)、应用社会科学索引与摘要数据库(ASSIA)、医学索引数据库(MEDLINE)、心理学文摘数据库(PSYCHINFO)、英国护理索引、科学引文索引扩展版(ISI Web of Science)、Zetoc、联合与补充医学数据库(AMED,1990年至2002年4月)。在基于计算机检索的基础上,还对手动检索所有检索到的研究及综述文章的参考文献列表进行了补充。制定了纳入和排除标准。

结果

对来自世界各地的24项符合纳入标准的研究进行了综述。大多数研究本质上是描述性的。这些研究涵盖了多个主题,包括照料者如何协助MS患者、提供照料对照料者身心健康、社会生活、财务状况及总体生活质量的影响,以及照料者如何应对照料压力。

结论

照料MS患者对照料者生活的各个方面都有重大影响。已表明感知到的社会支持对照料者有有益影响。研究设计的局限性和方法学的差异限制了研究结果的普遍性。需要进一步开展研究,特别是开发可靠且有效的针对特定疾病的照料者评估工具。

相似文献

1
The needs and experiences of caregivers of individuals with multiple sclerosis: a systematic review.多发性硬化症患者照顾者的需求与经历:一项系统综述
Clin Rehabil. 2003 May;17(3):234-48. doi: 10.1191/0269215503cr618oa.
2
Early palliative interventions for improving outcomes in people with a primary malignant brain tumour and their carers.早期姑息治疗干预对改善原发性脑恶性肿瘤患者及其照护者结局的影响。
Cochrane Database Syst Rev. 2022 Jan 6;1(1):CD013440. doi: 10.1002/14651858.CD013440.pub2.
3
Peer support interventions for parents and carers of children with complex needs.针对有复杂需求的儿童的父母和照顾者的同伴支持干预。
Cochrane Database Syst Rev. 2021 Dec 20;12(12):CD010618. doi: 10.1002/14651858.CD010618.pub2.
4
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.
5
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.
6
How best to assess quality of life in informal carers of people with dementia; A systematic review of existing outcome measures.如何最好地评估痴呆患者非专业照护者的生活质量;现有结局测量工具的系统评价。
PLoS One. 2018 Mar 14;13(3):e0193398. doi: 10.1371/journal.pone.0193398. eCollection 2018.
7
The Experiences of Informal Carers during the COVID-19 Pandemic: A Qualitative Systematic Review.《COVID-19 大流行期间非正式护理者的经历:定性系统评价》。
Int J Environ Res Public Health. 2022 Oct 18;19(20):13455. doi: 10.3390/ijerph192013455.
8
Aerobic exercise interventions for adults living with HIV/AIDS.针对感染艾滋病毒/艾滋病的成年人的有氧运动干预措施。
Cochrane Database Syst Rev. 2005 Apr 18(2):CD001796. doi: 10.1002/14651858.CD001796.pub2.
9
Interventions for interpersonal communication about end of life care between health practitioners and affected people.干预健康从业者与受影响者之间关于临终关怀的人际沟通。
Cochrane Database Syst Rev. 2022 Jul 8;7(7):CD013116. doi: 10.1002/14651858.CD013116.pub2.
10
Exercise interventions and patient beliefs for people with hip, knee or hip and knee osteoarthritis: a mixed methods review.髋、膝或髋膝骨关节炎患者的运动干预和患者信念:一项混合方法综述
Cochrane Database Syst Rev. 2018 Apr 17;4(4):CD010842. doi: 10.1002/14651858.CD010842.pub2.

引用本文的文献

1
Impact of connected health on the psychological wellbeing and quality of life of people with multiple sclerosis and their caregivers: A systematic review.互联健康对多发性硬化症患者及其照顾者心理健康和生活质量的影响:一项系统综述。
Digit Health. 2025 Mar 31;11:20552076251326230. doi: 10.1177/20552076251326230. eCollection 2025 Jan-Dec.
2
Resilience Among Caregivers of People With Multiple Sclerosis: Exploring the Influence of Personality Traits, Coping, and Caregiver Burden.多发性硬化症患者照料者的心理韧性:探究人格特质、应对方式及照料者负担的影响
Int J MS Care. 2025 Jan 20;27(Q1):15-24. doi: 10.7224/1537-2073.2024-004. eCollection 2025 Jan.
3
The Effect of Gender Ideal Adherence on Carer Burden and Help-Seeking in Male Carers of People With Multiple Sclerosis.
性别理想观念的遵循对多发性硬化症患者男性照料者的照料负担及寻求帮助行为的影响
Int J MS Care. 2025 Jan 13;27(Q1):8-14. doi: 10.7224/1537-2073.2023-073. eCollection 2025 Jan.
4
Parental Experiences in Pediatric Multiple Sclerosis: Insights from Quantitative Research.儿科多发性硬化症患者父母的经历:来自定量研究的见解
Children (Basel). 2024 Jan 8;11(1):71. doi: 10.3390/children11010071.
5
Reasons Patients With Primary Progressive Multiple Sclerosis Contact Their Specialist Nurses.原发性进行性多发性硬化症患者联系其专科护士的原因。
Int J MS Care. 2024 Jan-Feb;26(1):30-35. doi: 10.7224/1537-2073.2022-056. Epub 2024 Jan 5.
6
Addressing the Needs of Multiple Sclerosis Caregivers From Diagnosis Onward: The Development of a Comprehensive Online Caregiver Protocol.从诊断开始满足多发性硬化症护理人员的需求:全面在线护理人员方案的制定。
Int J MS Care. 2023 Nov-Dec;25(6):273-277. doi: 10.7224/1537-2073.2023-075. Epub 2023 Nov 8.
7
Psychological Processes Associated With Resilience in UK-Based Unpaid Caregivers During the COVID-19 Pandemic.新冠疫情期间英国 unpaid 照料者复原力相关的心理过程
Clin Psychol Eur. 2022 Dec 22;4(4):e10313. doi: 10.32872/cpe.10313. eCollection 2022 Dec.
8
Profiles of resilience in multiple sclerosis family care-partners: A Canadian cross-sectional study.多发性硬化症家庭照料伙伴的复原力概况:一项加拿大横断面研究。
Mult Scler J Exp Transl Clin. 2022 Nov 24;8(4):20552173221138935. doi: 10.1177/20552173221138935. eCollection 2022 Oct-Dec.
9
Family Members' of Coronary, Cardiosurgery and General ICU Patients Resilience, Perceived Stress, Spirituality: a Cross Sectional Analysis.冠心病、心脏外科手术及综合重症监护病房患者家属的复原力、感知压力、精神性:一项横断面分析
Mater Sociomed. 2022 Sep;34(3):184-187. doi: 10.5455/msm.2022.34.184-187.
10
Communication, Coordination, and Security for People with Multiple Sclerosis (COCOS-MS): a randomised phase II clinical trial protocol.多发性硬化症患者的沟通、协调和安全(COCOS-MS):一项随机的 II 期临床试验方案。
BMJ Open. 2022 Jan 25;12(1):e049300. doi: 10.1136/bmjopen-2021-049300.