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本文引用的文献

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2
Caregiving burden, depression, and anxiety among family caregivers of patients with cancer: An investigation of patient and caregiver factors.癌症患者家庭照料者的照料负担、抑郁和焦虑:患者及照料者因素调查
Front Psychol. 2023 Mar 28;14:1059605. doi: 10.3389/fpsyg.2023.1059605. eCollection 2023.
3
Challenges encountered by family caregivers of prostate cancer patients in Cape Coast, Ghana: a descriptive phenomenological study.加纳 Cape Coast 地区前列腺癌患者家庭照顾者所面临的挑战:一项描述性现象学研究。
BMC Palliat Care. 2022 Jun 14;21(1):108. doi: 10.1186/s12904-022-00993-6.
4
Expectations, end-of-life fears and end-of-life communication among palliative patients with cancer and caregivers: a cross-sectional study.癌症姑息治疗患者及其照护者的期望、临终恐惧和临终沟通:一项横断面研究。
BMJ Open. 2022 May 11;12(5):e058531. doi: 10.1136/bmjopen-2021-058531.
5
Palliative Care in Older People with Multimorbidities: A Scoping Review on the Palliative Care Needs of Patients, Carers, and Health Professionals.老年人多病共存的姑息治疗:对患者、照护者和卫生专业人员姑息治疗需求的范围综述。
Int J Environ Res Public Health. 2022 Mar 8;19(6):3195. doi: 10.3390/ijerph19063195.
6
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Support Care Cancer. 2022 Jun;30(6):4857-4865. doi: 10.1007/s00520-022-06857-2. Epub 2022 Feb 14.
7
The impact of COVID-19 on cancer patients, their carers and oncology health professionals: A qualitative study.COVID-19 对癌症患者、他们的照顾者和肿瘤学医疗专业人员的影响:一项定性研究。
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8
Moral distress in oncology nurses: A qualitative study.肿瘤科护士的道德困境:一项定性研究。
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姑息治疗中癌症患者家庭照顾者的道德困扰:一项定性研究。

Moral distress among family caregivers of people with cancer in palliative care: A qualitative study.

作者信息

Rozo Ana Júlia, Schneiders Milena, Palombit Mateus Rodrigo, Sinski Kassiano Carlos, de Lima Carmo Rafael, Garcia Ana Cláudia Mesquita, Araújo Jeferson Santos, de Oliveira Vargas Bitencourt Júlia Valéria, Dantas Rosana Aparecida Spadoti, da Conceição Vander Monteiro

机构信息

Federal University of Fronteira Sul, Chapecó, Santa Catarina, Brazil.

Master Candidate, Federal University of Alfenas, Alfenas, Minas Gerais, Brazil.

出版信息

Can Oncol Nurs J. 2025 Mar 1;35(2):361-375. doi: 10.5737/23688076352361. eCollection 2025 Spring.

DOI:10.5737/23688076352361
PMID:40873897
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12379905/
Abstract

The study aimed to understand the triggering events of moral distress according to the family caregivers of people with cancer in palliative care. This is a longitudinal qualitative approach study, using the concept of moral distress as an interpretative reference. Ten family caregivers participated in in-depth interviews. The data were analyzed according to the inductive thematic analysis technique, and two themes were identified. In the first theme, entitled "The repercussions following diagnosis," participants reported the uncertainties they experienced following their family member's cancer diagnosis. In the second theme, entitled "The transformation of daily life", participants expressed how providing care for the family member with cancer changed their daily lives. While experiencing the role of a caregiver, they faced dilemmas and uncertainties that led them to feel moral distress, since this situation will follow them continuously until the outcome of the disease.

摘要

该研究旨在根据姑息治疗中癌症患者的家庭照顾者,了解道德困扰的触发事件。这是一项纵向定性研究,将道德困扰的概念作为解释参考。十名家庭照顾者参与了深入访谈。数据根据归纳主题分析技术进行分析,确定了两个主题。在第一个主题“诊断后的影响”中,参与者报告了他们在家庭成员被诊断患有癌症后所经历的不确定性。在第二个主题“日常生活的转变”中,参与者表达了照顾患癌家庭成员如何改变了他们的日常生活。在扮演照顾者角色的过程中,他们面临困境和不确定性,这使他们感到道德困扰,因为这种情况将持续伴随他们,直到疾病的结果出现。