Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark.
Department of Public Health, Aarhus University, Aarhus, Denmark.
Scand J Caring Sci. 2024 Mar;38(1):126-135. doi: 10.1111/scs.13214. Epub 2023 Sep 19.
During the developmental transition from childhood to adulthood, young people living with type 1 diabetes (T1D) are more likely to take less care of their chronic disease. Alongside the developmental transition, young people with T1D also experience an organisational transition in which the care responsibility changes from a family-based approach in paediatric care to an individualised approach in adult care. Little is known from the perspective of the young people about what their interactions with the healthcare providers mean during these transitions.
The aim of this study is to explore how young people living with T1D experience interactions with their care providers, and what it means for their developmental transition.
Semi-structured interviews with 10 respondents aged 18-20 living with T1D who were recruited from a youth outpatient diabetes clinic in Denmark. Recorded audio data were transcribed and analysed using an interpretative phenomenological analysis approach.
Young people experience continuity in the relationship with the diabetes nurse from the paediatric clinic and a personal patient-provider relationship with their well-known and new care providers. This creates a feeling of familiarity and contributes to a seamless transition. The young people express that becoming more involved in diabetes treatment increases their willingness to take more responsibility for their own health. They also express that care providers should support them in managing their diabetes and talk about sensitive topics.
Continuity in the relationship with the diabetes nurse makes the transition from paediatric to adult care more satisfying and seamless. To support the developmental transition, care providers should gradually involve young people more in diabetes management and be supportive as they become more independent during the developmental transition.
在从儿童期向成年期的发展过渡期间,患有 1 型糖尿病(T1D)的年轻人更有可能不那么关心他们的慢性疾病。随着发展过渡,患有 T1D 的年轻人还经历了组织过渡,其中护理责任从儿科护理的以家庭为基础的方法转变为成人护理的个体化方法。从年轻人的角度来看,他们在这些过渡期间与医疗保健提供者的互动意味着什么,知之甚少。
本研究的目的是探讨患有 T1D 的年轻人如何体验与他们的护理提供者的互动,以及这对他们的发展过渡意味着什么。
对丹麦一家青年门诊糖尿病诊所招募的 10 名年龄在 18-20 岁之间的患有 T1D 的年轻人进行了半结构式访谈。记录的音频数据使用解释现象学分析方法进行转录和分析。
年轻人与儿科诊所的糖尿病护士保持关系的连续性,并与他们熟悉的和新的护理提供者建立个人医患关系。这营造了一种熟悉感,并有助于顺利过渡。年轻人表示,更多地参与糖尿病治疗增加了他们对自己健康负责的意愿。他们还表示,护理提供者应该支持他们管理糖尿病,并讨论敏感话题。
与糖尿病护士的关系保持连续性使从儿科护理向成人护理的过渡更加令人满意和顺利。为了支持发展过渡,护理提供者应逐渐让年轻人更多地参与糖尿病管理,并在他们在发展过渡中变得更加独立时给予支持。