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Depression in caregivers of patients with breast cancer: A cross-sectional study from a cancer research center in South India.印度南部某癌症研究中心的一项横断面研究:乳腺癌患者照料者的抑郁情况
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The experience of family caregivers of patients with cancer in an Asian country: A grounded theory approach.癌症患者家属在亚洲国家的体验:扎根理论方法。
Palliat Med. 2019 Jun;33(6):676-684. doi: 10.1177/0269216319833260. Epub 2019 Mar 27.
3
Recognizing and appraising symptoms of breast cancer as a reason for delayed presentation in Ghanaian women: A qualitative study.认识和评估加纳女性乳腺癌症状延迟就诊的原因:一项定性研究。
PLoS One. 2019 Jan 9;14(1):e0208773. doi: 10.1371/journal.pone.0208773. eCollection 2019.
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A dyadic analysis of loneliness and health-related quality of life in Latinas with breast cancer and their informal caregivers.乳腺癌拉丁裔患者及其非正规照护者的孤独感与健康相关生活质量的对偶分析
J Psychosoc Oncol. 2019 Mar-Apr;37(2):213-227. doi: 10.1080/07347332.2018.1520778. Epub 2018 Dec 11.
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Guilt among husband caregivers of Chinese women with breast cancer: The roles of male gender-role norm, caregiving burden and coping processes.中国乳腺癌女性患者丈夫照料者的内疚感:男性性别角色规范、照料负担及应对过程的作用
Eur J Cancer Care (Engl). 2018 Sep;27(5):e12872. doi: 10.1111/ecc.12872. Epub 2018 Jun 29.
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How family caregivers of cancer patients manage symptoms at home: A systematic review.癌症患者家庭照顾者如何在家中管理症状:系统评价。
Int J Nurs Stud. 2018 Sep;85:68-79. doi: 10.1016/j.ijnurstu.2018.05.004. Epub 2018 May 29.
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Factors Affecting Palliative Care Development in Africa: In-Country Experts' Perceptions in Seven Countries.影响非洲姑息治疗发展的因素:7 个国家国内专家的看法。
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Hoping to reach a safe haven - Swedish families' lived experience when a family member is diagnosed with breast cancer.希望找到一个安全的港湾——瑞典家庭中一名家庭成员被诊断出患有乳腺癌时的生活经历。
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The importance of family caregiving to achieving palliative care at home: a case report of end-of-life breast cancer in an area struck by the 2011 Fukushima nuclear crisis: A case report.家庭照护对在家中实现姑息治疗的重要性:2011年福岛核危机受灾地区晚期乳腺癌的病例报告:病例报告
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Methodological challenges in qualitative content analysis: A discussion paper.定性内容分析中的方法学挑战:一篇讨论论文。
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加纳晚期乳腺癌患者家庭照顾者的照顾动机和体验。

Caregiving motivations and experiences among family caregivers of patients living with advanced breast cancer in Ghana.

机构信息

Department of Nursing, Faculty of Allied Health Sciences, College of Health Sciences, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

Department of Obstetrics and Gynecology, Komfo Anokye Teaching Hospital, Kumasi, Ghana.

出版信息

PLoS One. 2020 Mar 12;15(3):e0229683. doi: 10.1371/journal.pone.0229683. eCollection 2020.

DOI:10.1371/journal.pone.0229683
PMID:32163432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7067415/
Abstract

INTRODUCTION

Significant number of women present with advanced-stage breast cancer in Ghana. These women usually depend on family caregivers for their multi-dimensional needs. Yet, there are gaps in research about what motivates family caregivers to assume the caring role and their experiences with caregiving within the Ghanaian context.

AIM

To explore and describe the caregiving motivations and experiences among family caregivers of patients living with advanced breast cancer.

METHODS

In-depth, semi-structured qualitative interviews were conducted with 15 family caregivers who were providing unpaid care for women living with advanced breast cancer. Colaizzi's thematic analysis was used to analyze the data.

RESULTS

Family relationship normally prescribed the caregiving role among family caregivers. Due to the lack of home-based palliative services in Ghana, findings suggest that family caregivers are the main managers of advanced breast cancer-related symptoms in the home. These findings are discussed under three major themes: (i) motivation for assuming the caregiving role; (ii) meeting self-care and psychosocial needs of the patient; and (iii) symptom management and monitoring.

CONCLUSION

Socio-cultural values influence the role of family caregivers in Ghana. This presents opportunities for health professionals and relevant stakeholders to develop a culturally-appropriate intervention to support informal caregivers in their home-based care for women living with advanced breast cancer in Ghana.

摘要

引言

在加纳,相当数量的女性患有晚期乳腺癌。这些女性通常依赖家庭照顾者来满足其多方面的需求。然而,在研究中,关于家庭照顾者承担照顾角色的动机以及他们在加纳背景下的照顾经验方面存在空白。

目的

探讨和描述为晚期乳腺癌患者提供照顾的家庭照顾者的照顾动机和经验。

方法

对 15 名正在为晚期乳腺癌女性提供无偿照顾的家庭照顾者进行了深入的半结构化定性访谈。使用科莱齐的主题分析方法对数据进行分析。

结果

家庭关系通常规定了家庭照顾者的照顾角色。由于加纳缺乏基于家庭的姑息治疗服务,研究结果表明,家庭照顾者是家庭中管理晚期乳腺癌相关症状的主要人员。这些发现根据三个主要主题进行了讨论:(i)承担照顾角色的动机;(ii)满足患者的自我护理和心理社会需求;以及(iii)症状管理和监测。

结论

社会文化价值观影响了加纳家庭照顾者的角色。这为卫生专业人员和相关利益相关者提供了机会,可以制定一种文化上适当的干预措施,以支持加纳家庭中为晚期乳腺癌女性提供照顾的非正式照顾者。