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Perceptions and Preferences of Patients with Terminal Lung Cancer and Family Caregivers about DNR

机译:晚期肺癌患者和家庭护理人员对DNR的认知和偏爱

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摘要

Background: Patients with terminal lung cancer and their families are challenged and stressed with the end of life discussions. Do Not Resuscitate (DNR) orders are a critical part of such discussions.Objective: To understand the perceptions and preferences of patients with terminal lung cancer and their family caregivers around DNR discussions. .Methods: Our quantitative component consisted of a pen-and-paper questionnaire that was followed by a ‘think aloud’ process to capture perceptions of participants in response to questionnaire items. Qualitative methods included content analysis and constant comparison techniques to identify, code, and categorize primary themes arising from ‘think aloud’ responses.Results: In this pilot study, 10 patients with advanced stage lung cancer and nine family caregivers were enrolled from one tertiary cancer care centre. Three major themes and several sub-themes were identified reflecting participants’ psychosocial environment, emotional responses to DNR discussions, and suggestions to improve DNR discussions. Most of the time, both patients and caregivers perceived a supportive environment within their family unit. Some patients were uncertain about their disease extent but most had entertained thoughts about prognosis and DNR status prior to having a discussion with their physician. A range of situations stimulated the DNR discussion. Most patients were uncertain about identifying the most appropriate health care provider (HCP) for DNR discussion. While participants found DNR discussions distressing, patients maintained hope in the face of accepting a terminal diagnosis. There were mixed feelings about the reversibility of a DNR decision and concerns about the care of the patients after being stated as DNR. Participants desired their HCP to be emotionally sensitive, knowledgeable, respectful, and straightforward.Conclusions: Most participants were open about their experiences with psychosocial supports and emotional reactions and made suggestions to HCP to improve DNR discussions. Further examination in larger longitudinal studies is required to validate the observations in the current study.
机译:背景:随着生命的结束讨论,患有晚期肺癌的患者及其家人受到挑战和压力。不要复苏(DNR)指令是此类讨论的关键部分。目的:了解有关DNR讨论的晚期肺癌患者及其家属的看法和偏好。方法:我们的定量组成部分包括笔和纸质调查表,随后是一个``大声思考''过程,以捕获对调查表项目做出响应的参与者的看法。定性方法包括内容分析和持续比较技术,以识别,编码和分类``大声思考''响应所产生的主要主题。结果:在该初步研究中,从10位晚期肺癌患者和9位家庭护理人员中招募了一位三级癌症患者。护理中心。确定了三个主要主题和几个子主题,这些主题反映了参与者的心理环境,对DNR讨论的情感回应以及改进DNR讨论的建议。在大多数情况下,患者和护理人员都在其家庭部门中感受到了支持环境。一些患者不确定其疾病程度,但大多数患者在与医师讨论之前就已对预后和DNR状态进行了思考。一系列情况激发了DNR的讨论。大多数患者不确定是否要为DNR讨论确定最合适的医疗保健提供者(HCP)。尽管参与者发现DNR讨论令人不安,但面对最终诊断,患者仍然充满希望。对于DNR决定的可逆性以及被声明为DNR后对患者的护理感到担忧。参与者希望他们的HCP在情感上敏感,知识丰富,受人尊敬和直截了当。需要在较大的纵向研究中进一步检查才能验证当前研究中的观察结果。

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