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What influences patients' decisions regarding palliative care in advance care planning discussions? Perspectives from a qualitative study conducted with advanced cancer patients, families and healthcare professionals

机译:什么影响患者的痛苦护理的决定提前关注计划讨论? 来自具有晚期癌症患者,家庭和医疗保健专业人士进行的定性研究的观点

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Background: The concept of advance care planning is largely derived from Western countries. However, the decision-making process and drivers for choosing palliative care in non-Western cultures have received little attention. Aim: To explore the decision-making processes and drivers of receiving palliative care in advance care planning discussions from perspectives of advanced cancer patients, families and healthcare professionals in northern Taiwan. Method: Semi-structured qualitative interviews with advanced cancer patients, their families and healthcare professionals independently from inpatient oncology and hospice units. Thematic analysis with analytical rigour enhanced by dual coding and exploration of divergent views. Results: Forty-five participants were interviewed (n = 15 from each group). Three main decision-making trajectories were identified: (1) 'choose palliative care' was associated with patients' desire to reduce physical suffering from treatments, avoid being a burden to families and society, reduce futile treatments and donate organs to help others; (2) 'decline palliative care' was associated with patients weighing up perceived benefits to others as more important than benefits for themselves; and (3) 'no opportunity to choose palliative care' was associated with lack of opportunities to discuss potential benefits of palliative care, lack of staff skill in end-of-life communication, and cultural factors, notably filial piety. Conclusion: Choice for palliative care among advanced cancer patients in Taiwan is influenced by three decision-making trajectories. Opinions from families are highly influential, and patients often lack information on palliative care options. Strategies to facilitate decision-making require staff confidence in end-of-life discussions, working with the patients and their family while respecting the influence of filial piety.
机译:背景:提前护理规划的概念主要来自西方国家。然而,在非西方文化中选择姑息治疗的决策过程和司机已经很少受到关注。目的:探讨在台湾晚期癌症患者,家庭和医疗保健专业人员的角度探讨接受姑息治疗讨论的决策过程和司机。方法:独立于住院肿瘤学和临终关怀单位的半结构性定性访谈,他们的家庭和医疗保健专业人员。通过双重编码和分歧观点增强了分析严格的主题分析。结果:采访了四十五位参与者(每组N = 15)。确定了三个主要决策轨迹:(1)“选择姑息治疗”与患者愿意减少患有治疗的患者的愿望有关,避免对家庭和社会的负担,减少徒劳的治疗,捐赠器官来帮助他人; (2)“痛苦姑息治疗”与称重对他人的益处的患者有关的患者比对自己的福利更重要; (3)“没有机会选择姑息治疗”与缺乏讨论姑息治疗的潜在利益,缺乏生活中缺乏职业沟通,文化因素,特别是孝道的机会有关。结论:台湾晚期癌症患者中姑息治疗的选择受三个决策轨迹的影响。家庭的意见是高度影响力,患者往往缺乏有关姑息治疗选择的信息。促进决策的策略要求员工对生活终止讨论的信心,与患者及其家庭合作,同时尊重孝道的影响。

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