No one really plans to have multiple sclerosis: Transition readiness and quality of life in paediatric multiple sclerosis

IF 1.8 4区 医学 Q2 PEDIATRICS Child Care Health and Development Pub Date : 2024-07-10 DOI:10.1111/cch.13304
Estherline Thoby, Julissa Veras, Spandana Nallapati, Manuel E. Jimenez, Vikram Bhise
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Abstract

Aim

We sought to explore the experiences and perceptions of the quality of life of adolescents with pediatric-onset multiple sclerosis and assess their readiness for academic, employment and/or health care-related transitions.

Background

Adolescents with pediatric-onset multiple sclerosis face unique challenges in managing a chronic illness while navigating future scholastic, social and occupational goals. We conducted a qualitative study with in-depth, semi-structured interviews from July 2017 to March 2019. Adolescents with pediatric-onset multiple sclerosis were recruited from a pediatric neurology subspeciality practice until reaching data saturation. A total of 17 interviews were completed via telephone with participants ages 15 through 26.

Results

Through content analysis of the interviews, we identified five major themes: (1) receiving a new diagnosis; (2) adapting to life with pediatric-onset multiple sclerosis; (3) evaluating education/career transition preparedness; (4) adjusting within family life and establishing support systems; and (5) assessing current medical services and preparedness for adult medical care.

Conclusions

Autonomy in health care management, adequate control of physical symptoms and sufficient family support impacted perceptions of quality of life. Implementing a dedicated transition visit, including the parent(s) of those with pediatric-onset multiple sclerosis, early in adolescence may provide an avenue for appropriate anticipatory guidance regarding available services, independent medical management and continuity of care.

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没有人真的打算患多发性硬化症:儿科多发性硬化症患者的过渡准备和生活质量。
目的:我们试图探索患有小儿多发性硬化症的青少年对生活质量的体验和看法,并评估他们在学业、就业和/或医疗保健相关过渡方面的准备情况:背景:患有小儿多发性硬化症的青少年在管理慢性疾病的同时,还面临着实现未来学业、社会和职业目标的独特挑战。我们在 2017 年 7 月至 2019 年 3 月期间开展了一项定性研究,进行了深入的半结构式访谈。我们从一家儿科神经病学亚专科诊所招募了患有小儿多发性硬化症的青少年,直到数据达到饱和为止。通过电话共完成了 17 次访谈,参与者的年龄从 15 岁到 26 岁不等:通过对访谈内容的分析,我们确定了五大主题:(1) 接受新的诊断;(2) 适应小儿多发性硬化症患者的生活;(3) 评估教育/职业过渡准备情况;(4) 适应家庭生活并建立支持系统;(5) 评估当前的医疗服务并为成人医疗做好准备:结论:医疗保健管理的自主性、对身体症状的充分控制以及充分的家庭支持影响了对生活质量的看法。在青春期早期实施专门的过渡访视,包括儿科发病型多发性硬化症患者的父母,可以提供一个渠道,就可用服务、独立医疗管理和持续护理提供适当的预期指导。
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来源期刊
CiteScore
3.40
自引率
5.30%
发文量
136
审稿时长
4-8 weeks
期刊介绍: Child: care, health and development is an international, peer-reviewed journal which publishes papers dealing with all aspects of the health and development of children and young people. We aim to attract quantitative and qualitative research papers relevant to people from all disciplines working in child health. We welcome studies which examine the effects of social and environmental factors on health and development as well as those dealing with clinical issues, the organization of services and health policy. We particularly encourage the submission of studies related to those who are disadvantaged by physical, developmental, emotional and social problems. The journal also aims to collate important research findings and to provide a forum for discussion of global child health issues.
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