Understanding Dying Concerns in Parents With Advanced Cancer With Dependent Children for Their Coparent: A Phenomenological Study.

IF 1.2 4区 医学 Q3 NURSING Journal of Hospice & Palliative Nursing Pub Date : 2023-10-01 Epub Date: 2023-06-10 DOI:10.1097/NJH.0000000000000956
Cinzia Caparso, Emma Noble, MaryAnne McCoy, April Vallerand, Ramona Benkert
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Abstract

Parents with advanced cancer and their dependent children experience high psychological distress, decreased quality of life, and decreased family functioning due to cancer-related concerns. Dying concerns are defined as fluctuating thoughts or feelings that are conscious or unconscious about an anticipated and approaching death that is attributed to a palliative/terminal diagnosis. This study used Gadamer's phenomenological approach to gain a shared understanding of the perspectives of the parents with advanced cancer about dying concerns, family life before and after advanced cancer diagnosis, and family resources to manage the crisis of advanced cancer for the coparent. The sample consisted of 4 patients from a Midwestern cancer hospital. Data were collected through 2 virtual semistructured interviews and were qualitatively analyzed using the hermeneutic rule and the theoretical concepts from McCubbin and McCubbin's Family Resiliency Model. Four major themes emerged: “Uncertainty in End-of-Life Decisions,” “Effectless Communication,” “Parental Skepticism,” and “Psychological Well-being.” The results showed that parents with advanced cancer have concerns for their coparent outside their parental role. Understanding dying concerns from all family members may increase nurse-initiated communication to improve family outcomes.
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理解晚期癌症父母对其父母的死亡担忧:一项现象学研究。
患有晚期癌症的父母及其受抚养的子女由于癌症相关的担忧而经历了高度的心理困扰、生活质量下降和家庭功能下降。死亡担忧被定义为对预期和即将到来的死亡有意识或无意识的波动性想法或感受,这些想法或感受归因于姑息/最终诊断。本研究采用Gadamer的现象学方法,对患有晚期癌症的父母对死亡问题的看法、晚期癌症诊断前后的家庭生活以及为共有人管理晚期癌症危机的家庭资源有了共同的理解。样本由4名来自中西部癌症医院的患者组成。通过两次虚拟的半结构化访谈收集数据,并使用解释学规则和McCubbin和McCubbin's Family Resiliency Model的理论概念进行定性分析。出现了四个主要主题:“生命终结决定的不确定性”、“无效果的沟通”、“父母怀疑论”和“心理健康”。研究结果表明,患有晚期癌症的父母担心他们在父母角色之外的共同承担。了解所有家庭成员对死亡的担忧可能会增加护士发起的沟通,以改善家庭结果。
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来源期刊
CiteScore
2.60
自引率
11.10%
发文量
203
审稿时长
6-12 weeks
期刊介绍: Journal of Hospice & Palliative Nursing (JHPN) is the official journal of the Hospice & Palliative Nurses Association and is the professional, peer-reviewed journal for nurses in hospice and palliative care settings. Focusing on the clinical, educational and research aspects of care, JHPN offers current and reliable information on end of life nursing. Feature articles in areas such as symptom management, ethics, and futility of care address holistic care across the continuum. Book and article reviews, clinical updates and case studies create a journal that meets the didactic and practical needs of the nurse caring for patients with serious illnesses in advanced stages.
期刊最新文献
Association News. Hospice and Palliative Nurses Association Position Statement: Medical Aid in Dying. Improving Patient-Centered Care for End-Stage Renal Disease Patients at a Community Palliative Setting. The Impact of Allyship on Minoritized Patients and Providers in Palliative Practice. True North.
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