Pediatric Department, Ghent University Hospital, Corneel-Heymanslaan 10, Ghent 9000, Belgium.
Pediatric Department, Ghent University Hospital, Corneel-Heymanslaan 10, Ghent 9000, Belgium.
J Cyst Fibros. 2024 May;23(3):512-518. doi: 10.1016/j.jcf.2023.10.005. Epub 2023 Oct 13.
Inadequate participation of Adolescents and Young Adults (AYAs) and parents are well-established barriers of transition. Shifts in roles are mandatory with increasing responsibilities for AYAs and decreasing involvement of parents in care. This study explores the shifts in roles of AYAs and their parents and its association with the subjective experience of transition.
We conducted in-depth semi-structured interviews with AYAs living with Cystic Fibrosis and parents. Participants were recruited through patient organizations via convenience sampling and questioned on which roles they assumed during transition. Three authors performed an interpretative phenomenological analysis, establishing separate code trees for AYAs and parents. Data saturation was achieved.
18 AYAs (age 21y±2.9) and 14 parents (age 50y±2.0) were included. We identified five common themes: (1) the reciprocal reliance between AYAs and parents, (2) the policies of physicians and hospitals, (3) the AYAs' changing appeal and need for support, (4) the identification of parents as co-patients, and (5) the enforced changes in the roles of parents. AYAs primarily addressed roles related to self-management, while parents discussed family functioning.
This study identified motives underlying the assumption of roles by AYAs and parents. Both AYAs and parents addressed similar themes, highlighting their mutual challenges and needs. In contrast to AYAs, parents' desired roles were undefined and a latent sense of responsibility was identified as an important motive. Healthcare providers should acknowledge parents' challenging position and communicate transparently about changing roles. Additionally, healthcare providers should recognize that imposing restrictive roles may result in parental resistance, but can also foster AYAs' skill development. Future research should examine the short- and long-term impact of role-management interventions in AYAs and their parents.
青少年和年轻成年人(AYAs)以及父母参与不足是过渡的既定障碍。随着 AYAs 承担越来越多的责任和父母参与护理的减少,角色转变是强制性的。本研究探讨了 AYAs 和他们的父母角色的转变及其与过渡主观体验的关系。
我们对患有囊性纤维化的 AYAs 和父母进行了深入的半结构化访谈。通过患者组织进行便利抽样招募参与者,并询问他们在过渡期间承担的角色。三位作者进行了解释性现象学分析,为 AYAs 和父母建立了单独的代码树。达到了数据饱和。
共纳入 18 名 AYAs(年龄 21 岁±2.9 岁)和 14 名父母(年龄 50 岁±2.0 岁)。我们确定了五个共同主题:(1)AYAs 和父母之间的相互依赖,(2)医生和医院的政策,(3)AYAs 不断变化的吸引力和对支持的需求,(4)将父母识别为共同患者,以及(5)父母角色的强制性变化。AYAs 主要涉及自我管理相关的角色,而父母则讨论了家庭功能。
本研究确定了 AYAs 和父母承担角色的潜在动机。AYAs 和父母都讨论了相似的主题,突出了他们的共同挑战和需求。与 AYAs 不同,父母期望的角色不明确,潜在的责任感被认为是一个重要的动机。医疗保健提供者应承认父母的困境,并透明地沟通角色变化。此外,医疗保健提供者应认识到强加限制角色可能会导致父母的抵制,但也可以促进 AYAs 的技能发展。未来的研究应检验在 AYAs 和他们的父母中进行角色管理干预的短期和长期影响。