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下肢截肢患者家庭照顾者的经历与挑战:一项定性研究

Experiences and challenges of family caregivers of people with lower limb amputation: a qualitative study.

作者信息

Rodrigues Diana Fonseca, Carvalho António Luís Rodrigues Faria de, Pinto Cristina Maria Correia Barroso

机构信息

Universidade do Porto, Faculdade de Medicina, RISE-Health, Porto, Portugal.

Universidade do Porto, Instituto de Ciências Biomédicas Abel Salazar, Porto, Portugal.

出版信息

Rev Esc Enferm USP. 2025 May 26;59:e20240264. doi: 10.1590/1980-220X-REEUSP-2024-0264en. eCollection 2025.

DOI:10.1590/1980-220X-REEUSP-2024-0264en
PMID:40434110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12118359/
Abstract

OBJECTIVE

To explore the experiences of family caregivers transitioning to their roles of caregivers for people with dysvascular major lower limb amputation, identify the challenges they face, understand their specific needs during this transition, examine their experiences during the hospital-to-home transition, and gather insights into strategies that promote empowerment in caregiving.

METHOD

This exploratory, cross-sectional descriptive study employed a qualitative approach, conducting semi-structured interviews with 40 family caregivers of individuals with dysvascular major lower limb amputation. Data were analyzed using ATLAS.ti software and Bardin's content analysis method.

RESULTS

Content analysis identified five categories: 1) family caregiver role, 2) amputee needs/difficulties, 3) family caregiver needs/difficulties, 4) home transition, and 5) strategies to promote family caregiver empowerment, highlighting critical aspects of the caregiving experience and identifying areas for intervention.

CONCLUSION

The findings emphasize the need for family-centered empowerment programs combining hospital-based training with community support. Future research should evaluate their impact on reducing caregiver burden and improving outcomes for both caregivers and amputees.

摘要

目的

探讨家庭照顾者向血管性大下肢截肢患者照顾者角色转变的经历,确定他们面临的挑战,了解他们在这一转变过程中的特殊需求,考察他们在从医院到家过渡期间的经历,并收集有关促进照顾者赋权策略的见解。

方法

本探索性横断面描述性研究采用定性方法,对40名血管性大下肢截肢患者的家庭照顾者进行半结构化访谈。使用ATLAS.ti软件和巴丁内容分析法对数据进行分析。

结果

内容分析确定了五个类别:1)家庭照顾者角色,2)截肢者需求/困难,3)家庭照顾者需求/困难,4)家庭过渡,5)促进家庭照顾者赋权的策略,突出了照顾经历的关键方面并确定了干预领域。

结论

研究结果强调了以家庭为中心的赋权项目的必要性,该项目应将基于医院的培训与社区支持相结合。未来的研究应评估它们对减轻照顾者负担以及改善照顾者和截肢者结局的影响。

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本文引用的文献

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Effectiveness of a family empowerment program on caregiving capacity and adverse mood in caregivers of children with acute leukemia: a quasi-experimental study.家庭赋权计划对急性白血病患儿照顾者照顾能力及不良情绪的影响:一项准实验研究
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Transitioning from hospital to home after a major lower extremity amputation: Interview study on patients' and relatives' perspectives.主要下肢截肢后从医院到家庭的过渡:患者和家属观点的访谈研究。
Int J Orthop Trauma Nurs. 2024 Aug;54:101103. doi: 10.1016/j.ijotn.2024.101103. Epub 2024 Apr 19.
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Gender and burden differences in family caregivers of patients affected by ten rare diseases.性别和负担差异:十种罕见病患者的家庭照料者。
Ann Ist Super Sanita. 2023 Apr-Jun;59(2):122-131. doi: 10.4415/ANN_23_02_05.
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Women involvement in the informal caregiving field: A perspective review.女性参与非正规照料领域:一项综述
Front Psychiatry. 2023 Jan 18;14:1113587. doi: 10.3389/fpsyt.2023.1113587. eCollection 2023.
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Life of an amputee: predictors of quality of life after lower limb amputation.截肢患者的生活:下肢截肢后生活质量的预测因素。
Wien Med Wochenschr. 2023 Oct;173(13-14):329-333. doi: 10.1007/s10354-022-00980-9. Epub 2022 Nov 28.
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Health literacy of informal caregivers of older adults with dementia: results from a cross-sectional study conducted in Florence (Italy).老年痴呆症患者非专业照护者的健康素养:在意大利佛罗伦萨进行的一项横断面研究的结果。
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The impact of caring for family members with mental illnesses on the caregiver: a scoping review.照顾患有精神疾病的家庭成员对照顾者的影响:范围综述。
Health Promot Int. 2023 Jun 1;38(3). doi: 10.1093/heapro/daac049.
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Older Caregivers: Who They Are and How to Support Them.老年护理者:他们是谁以及如何为他们提供支持。
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Effectiveness of psychosocial interventions on the burden and quality of life of informal caregivers of hemodialysis patients: a systematic review.心理社会干预对血液透析患者非专业照护者负担和生活质量的影响:系统评价。
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Self-care, resilience, and caregiver burden in relatives of patients with advanced cancer: results from the eQuiPe study.自我护理、韧性和晚期癌症患者亲属的照顾者负担:来自 eQuiPe 研究的结果。
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