Mooney Jennifer, Dominic Anna, Lewis Alyona, Chafe Roger
Division of Adolescent Health and Medicine, Department of Pediatrics, University of British Columbia, Vancouver, Canada.
Discipline of Pediatrics, Faculty of Medicine, Memorial University of Newfoundland, Room 409, Janeway Hostel, 300 Prince Phillip Drive, St. John's, NL, A1B 3V6, Canada.
J Eat Disord. 2023 Mar 23;11(1):46. doi: 10.1186/s40337-023-00771-6.
Eating disorders (EDs) commonly develop in adolescence and can be a chronic condition. Once patients reach the age when it is no longer permitted or appropriate for them to be seen in a children's healthcare setting, they will need to transition into adult-focused care. This transition period can be challenging, with increased risks of negative health outcomes and disruptions in care. Appropriate educational resources could be an effective support for patients during this transition. Our objectives were to engage patients about the value of developing educational supports and determine how these supports should be structured to be most useful to young adults with EDs.
Patients who had transitioned out of a hospital-based ED program between 2017 and 2020 were invited to participate in a semi-structured interview. Data were analyzed using thematic analysis and qualitative description.
Six young adults (5 females and 1 male) with EDs were interviewed. All participants thought it would be helpful to have an educational resource. Three main themes and seven subthemes were identified. Themes identified related to the unique challenges of transition for ED patients given the age of onset and cycle of symptoms; issues in adult care related to comorbidities and new level of autonomy; and the value of educational resources as both a connection tool and a benchmark. Participants also thought it would be useful to include in any educational resource a summary of their previous treatments, information regarding the transition process, a list of main healthcare providers they saw for their ED, a description of the differences and expectations of the adult system, a list of their follow up appointments, and a list of community and emergency mental health resources.
Participants said that educational supports can play a useful role for young adults with EDs during their transition into adult care. They also provided valuable insights into the desired contents of such supports and expanded on the roles that educational resources could serve for ED patients.
饮食失调(EDs)通常在青少年时期出现,可能是一种慢性病。一旦患者达到不再适合在儿童医疗环境中就诊的年龄,他们就需要过渡到以成人为主的护理。这个过渡阶段可能具有挑战性,负面健康结果的风险增加,护理也会中断。适当的教育资源可能是患者在这个过渡阶段的有效支持。我们的目标是让患者了解开发教育支持的价值,并确定这些支持应如何构建,才能对患有饮食失调的年轻人最有用。
邀请2017年至2020年期间从医院的饮食失调项目中转出的患者参加半结构化访谈。使用主题分析和定性描述对数据进行分析。
采访了6名患有饮食失调的年轻人(5名女性和1名男性)。所有参与者都认为拥有教育资源会有所帮助。确定了三个主要主题和七个子主题。确定的主题与饮食失调患者因发病年龄和症状周期而面临的独特过渡挑战有关;成人护理中与合并症和新的自主水平相关的问题;以及教育资源作为连接工具和基准的价值。参与者还认为,在任何教育资源中纳入他们以前治疗的总结、关于过渡过程的信息、他们因饮食失调而就诊的主要医疗服务提供者名单、成人系统的差异和期望描述、他们的后续预约名单以及社区和紧急心理健康资源名单会很有用。
参与者表示,教育支持在患有饮食失调的年轻人过渡到成人护理期间可以发挥有益作用。他们还提供了关于此类支持所需内容的宝贵见解,并阐述了教育资源可为饮食失调患者发挥的作用。