Wise Allison F, Upham Emily J, DeCourcey Danielle D
Department of Supportive Oncology, Dana Farber Cancer Institute, Boston, MA 02215, USA.
Division of Medical Critical Care, Department of Pediatrics, Boston Children's Hospital, Boston, MA 02115, USA.
Children (Basel). 2025 Feb 28;12(3):318. doi: 10.3390/children12030318.
BACKGROUND/OBJECTIVE: Adolescents and young adults with complex chronic conditions and parents of children with complex chronic conditions interact frequently with the healthcare system. However, these groups have unique characteristics and needs. The objective of this qualitative study was to explore and compare the roles that adolescents and young adults with complex chronic conditions and parents of children with complex chronic conditions take on when engaging with the healthcare system.
Semi-structured interviews were conducted with seven adolescents and young adults and nine parents at two pediatric centers from December 2018 to April 2019. The research team conducted thematic analysis. Transcripts were coded independently by two coders, achieving high interrater reliability (kappa > 0.85). We present findings related to illness experience and self-described roles within the healthcare context.
Informational roles described by both parents and adolescents and young adults included teacher, learner and researcher, and planner. Social-emotional roles common to both groups included source of strength, support, and hope and worrier, while the role of guardian was unique to parents. Action-oriented roles described by both groups included advocate, decision-maker, and communicator, while medical care provider was unique to parents and medical care manager was unique to adolescents and young adults.
Adolescents and young adults with complex chronic conditions and parents of children with complex chronic conditions balance similarly complex roles within the medical system. However, their experiences within these roles can differ, presenting unique challenges. Understanding these multidimensional roles will better equip healthcare providers to support these patients and families, especially around times of healthcare transition.
背景/目的:患有复杂慢性病的青少年和年轻人以及患有复杂慢性病儿童的父母经常与医疗保健系统互动。然而,这些群体具有独特的特征和需求。这项定性研究的目的是探讨和比较患有复杂慢性病的青少年和年轻人以及患有复杂慢性病儿童的父母在与医疗保健系统接触时所扮演的角色。
2018年12月至2019年4月,在两个儿科中心对7名青少年和年轻人以及9名父母进行了半结构化访谈。研究团队进行了主题分析。两名编码员对访谈记录进行独立编码,评分者间信度较高(kappa>0.85)。我们呈现了与疾病经历以及在医疗环境中自我描述的角色相关的研究结果。
父母以及青少年和年轻人描述的信息性角色包括教师、学习者、研究者和规划者。两组共有的社会情感角色包括力量、支持和希望的来源以及担忧者,而监护人的角色是父母所特有的。两组描述的行动导向型角色包括倡导者、决策者和沟通者,而医疗服务提供者是父母所特有的,医疗护理管理者是青少年和年轻人所特有的。
患有复杂慢性病的青少年和年轻人以及患有复杂慢性病儿童的父母在医疗系统中平衡着同样复杂的角色。然而,他们在这些角色中的经历可能不同,带来独特的挑战。了解这些多维度角色将使医疗服务提供者能更好地支持这些患者和家庭,尤其是在医疗过渡时期。