Accessing primary health care services for transition-aged young adults with cerebral palsy; perspectives of young adults, parents, and physicians

E. Brandon, M. Ballantyne, M. Penner, André Lauzon, E. McCarvill
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引用次数: 5

Abstract

Abstract Background Young adults with childhood-onset disabilities experience challenges with accessing age appropriate primary health care services as they transition from pediatric to adult health care services. They often experience a negative impact on their health with associated long-term health and social concerns, disease complications and increased use of emergency services once transitioned to adult services. This is particularly challenging for youth with cerebral palsy (CP) due the complexity of their medical needs. The aim of this study was to explore experiences with accessing or providing primary care services for transitioned-aged young adults with CP from young adult, parent, pediatrician and primary care physician perspectives. Methods A qualitative descriptive design was conducted to identify the challenges and facilitators for transitioned aged young adults with accessing primary, adult care services. Semi-structured interviews were conducted with 16 participants within the circle of care (4 adults with CP, 4 parents, 4 pediatricians and 4 primary healthcare physicians) for individuals with CP in Toronto, Canada. Interviews were audio-recorded and transcribed verbatim. Qualitative analysis guided both the data collection and the data analysis processes. Results Data analysis revealed that all participant groups reported transition challenges with respect to accessibility, the suitability of some primary care environments for caring for individuals with complex care needs, gaps in seamless care, and limited time and funding when receiving or providing primary care services to young adults with CP. Discussion There is a greater demand for adult healthcare providers now to deliver services for adults with childhood onset disabilities. Transition-aged young adults with CP and complex medical needs have increased challenges with accessing primary care services. Considering the following would improve primary care services transition for this population with complex medical needs: ongoing partnering between pediatric and adult health care streams to promote seamless care; connection to team-based primary care services where family physicians, subspecialties and interprofessional practitioners work together to provide joint care planning; salary compensation for increased service needs due to medical complexity; accessible sites; and development of guidelines for transitioning youth/young adults with complex care needs.
为患有脑瘫的过渡年龄年轻人提供初级保健服务;年轻人、父母和医生的观点
摘要背景患有儿童期残疾的年轻人在从儿科医疗服务过渡到成人医疗服务的过程中,在获得适龄初级医疗服务方面遇到了挑战。一旦过渡到成人服务,他们的健康往往会受到负面影响,包括相关的长期健康和社会问题、疾病并发症以及越来越多地使用紧急服务。这对患有脑瘫(CP)的年轻人来说尤其具有挑战性,因为他们的医疗需求非常复杂。本研究的目的是从年轻人、父母、儿科医生和初级保健医生的角度,探索为患有CP的过渡老年年轻人获得或提供初级保健服务的经验。方法采用定性描述性设计,确定过渡期老年年轻人在获得初级成人护理服务方面面临的挑战和促进因素。在加拿大多伦多,对护理圈内的16名参与者(4名患有CP的成年人、4名父母、4名儿科医生和4名初级保健医生)进行了半结构化访谈。访谈录音并逐字转录。定性分析指导了数据收集和数据分析过程。结果数据分析显示,所有参与者群体都报告了在可及性、一些初级保健环境是否适合照顾有复杂护理需求的个人、无缝护理方面的差距以及在接受或向患有CP的年轻人提供初级保健服务时时间和资金有限等方面的过渡挑战。讨论现在对成人医疗保健提供者为儿童期残疾的成年人提供服务的需求越来越大。有慢性阻塞性肺病和复杂医疗需求的过渡年龄年轻人在获得初级保健服务方面面临着更大的挑战。考虑到以下方面将改善这一有复杂医疗需求的人群的初级保健服务过渡:儿科和成人保健流之间的持续合作,以促进无缝护理;与基于团队的初级保健服务的联系,在那里,家庭医生、子专业和跨专业从业者共同提供联合护理规划;因医疗复杂性而增加的服务需求的薪酬补偿;无障碍场地;以及为有复杂护理需求的青年/青年过渡制定指导方针。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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