Deathbed experiences and meaning-making: Perspectives of family caregivers of patients who received cancer palliative care.

IF 2.1 4区 医学 Q3 HEALTH POLICY & SERVICES Palliative & Supportive Care Pub Date : 2024-06-01 DOI:10.1017/S1478951523001670
Irene Teo, Keerthana Paramasivam, Wai Yee Chee, Carolyn Ng, Patricia Soek Hui Neo, Geok Ling Lee
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Abstract

Objectives: The deathbed symbolizes a time when the patient is dangerously ill and where death is imminent. The memories of family caregivers during this time can potentially shape their meaning-making of the patient's death and bereavement adjustment. We aimed to understand the experiences of family caregivers at the deathbed of patients receiving palliative care. We also examined caregiver's meaning-making that occurred after the patient's death.

Methods: In this retrospective qualitative study, family caregivers of cancer patients who received palliative care in Singapore were recruited through purposive sampling. In-person, semi-structured interviews were individually conducted with study participants to understand their experiences from a caregiver's perspective before and after the death of the patient. Thematic content analysis method was conducted.

Results: A total of 25 bereaved family caregivers were interviewed, with spouses, adult children, and others comprising one-third each of the sample. Six themes emerged from caregivers' recollected experiences around the patient deathbed: Lasting image of the patient, A time of intense emotions, Healthcare providers prepare caregivers, A time for saying goodbye, Rituals provide comfort, and Impact on family ties. Four themes emerged surrounding post-loss meaning-making: An end to the pain and suffering, "Have I done enough?," Significance in the timing of events, and Gaining strength and personal growth.

Significance of results: The deathbed is a salient time for family caregivers as they prepare for patient's death. There are opportunities to provide support to the family based on the study findings.

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临终体验与意义建构:接受癌症姑息治疗病人的家庭护理者的观点。
目标:临终关怀象征着病人病危和死亡迫在眉睫的时刻。家属照护者在此期间的记忆可能会影响他们对病人死亡的意义建构和丧亲调整。我们旨在了解接受姑息治疗的病人临终前的家庭照护者的经历。我们还研究了照顾者在病人去世后的意义建构:在这项回顾性定性研究中,我们通过有目的的抽样调查招募了在新加坡接受姑息治疗的癌症患者的家庭照护者。研究人员与参与者进行了面对面的半结构化访谈,从照顾者的角度了解他们在患者去世前后的经历。研究采用主题内容分析法:共有 25 位丧亲家庭照顾者接受了访谈,其中配偶、成年子女和其他人各占样本的三分之一。照顾者在回忆病人临终前的经历时产生了六个主题:病人最后的形象、强烈的情感、医疗服务提供者为照顾者做好准备、告别的时刻、仪式提供安慰以及对家庭关系的影响。围绕丧亲后的意义建构,出现了四个主题:结果的意义:临终关怀是家庭照顾者为病人的死亡做准备的重要时刻。根据研究结果,有机会为家属提供支持。
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来源期刊
Palliative & Supportive Care
Palliative & Supportive Care HEALTH POLICY & SERVICES-
CiteScore
4.10
自引率
9.10%
发文量
280
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