Caparso Cinzia, Bowen Zoe, Choi Sung Won
Author Affiliations: Department of Systems, Populations and Leadership Center for Improving Patient and Population Health, University of Michigan School of Nursing (Dr Caparso); Rogel Cancer Center, University of Michigan (Drs Caparso and Choi); and Department of Pediatrics, Blood and Bone Marrow Transplant Program, University of Michigan, Michigan Medicine (Dr Choi and Ms Bowen), Ann Arbor.
Cancer Nurs. 2024 Dec 13. doi: 10.1097/NCC.0000000000001433.
The estimated 1.6 million adults in the United States with cancer who also have dependents face unique challenges given the profound impact of cancer on their families, such as increased psychological distress, decreased quality of life, and altered family functioning. Unfortunately, little is known about the mutual cancer-related communication concerns from the perspectives of the parents with cancer or the coparents. Coparents care for the patient and dependents until they reach adulthood (eg, unmarried, divorced, stepparent, and/or same-sex partnerships).
To understand the mutual cancer-related communication concerns from the perspectives of parents with cancer and the coparents and intervention delivery preferences.
Fifteen parents with cancer and 15 coparents were recruited to participate in semistructured interviews between October 2022 and September 2023 within an academic medical center in Midwestern states. Interviews were conducted via Zoom. The data were analyzed through Charmaz's inductive grounded theory approach.
Parents with cancer and the coparents desire communication assistance with each other about discussing the cancer diagnosis with dependents, end-of-life planning, managing finances, and addressing mental health concerns and emotions. The majority of participants reported interest in a virtually delivered intervention.
Findings from this study provide a mutual understanding of cancer-related communication concerns from the perspectives of parents with cancer and the coparents.
These findings provide awareness for providers and the foundation to inform a web-based communication intervention about cancer-related concerns to promote family resiliency in this population, which provides a resource for providers to utilize.
在美国,估计有160万患有癌症且有家属的成年人面临着独特的挑战,因为癌症对其家庭有着深远影响,比如心理困扰加剧、生活质量下降以及家庭功能改变。不幸的是,从患癌父母或共同抚养者的角度来看,对于相互之间与癌症相关的沟通问题了解甚少。共同抚养者会照顾患者及其家属直至他们成年(例如未婚、离异、继父母和/或同性伴侣关系)。
从患癌父母和共同抚养者的角度了解相互之间与癌症相关的沟通问题以及干预措施的实施偏好。
2022年10月至2023年9月期间,在中西部各州的一家学术医疗中心招募了15名患癌父母和15名共同抚养者参与半结构化访谈。访谈通过Zoom进行。数据采用查马兹的归纳性扎根理论方法进行分析。
患癌父母和共同抚养者希望在与家属讨论癌症诊断、临终规划、财务管理以及解决心理健康问题和情绪方面相互提供沟通帮助。大多数参与者表示对虚拟提供的干预措施感兴趣。
本研究结果从患癌父母和共同抚养者的角度提供了对与癌症相关沟通问题的相互理解。
这些发现提高了医疗服务提供者的认识,并为开展基于网络的关于癌症相关问题的沟通干预提供了基础,以促进该人群的家庭恢复力,为医疗服务提供者提供了可利用的资源。