A Socioecological Approach to Support the Transition to Adult Care for Youth With Medical Complexity: Family Perspectives and Recommendations.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Health Expectations Pub Date : 2025-02-01 DOI:10.1111/hex.70077
Lin Li, Nancy Carter, Jan Willem Gorter, Linda Till, Marcy White, Patricia H Strachan
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Abstract

Introduction: The transition from paediatric to adult health care (i.e., 'health care transition') poses many challenges for youth with medical complexity (YMC) and their families. YMC need specific approaches to supporting transition, tailored to individual youth and family contexts. In this study, we examine the contextual factors influencing families' transition experiences and describe their recommendations for improving the experience.

Methods: We conducted a qualitative explanatory case study in Ontario, Canada. We completed 21 interviews with 17 participants (11 mothers, 2 fathers, 2 YMC, 2 siblings) from 11 families of YMC. Six YMC (55%) were under 18 years of age (pre-transfer) and five (45%) were aged 18 years and older (post-transfer). Analytic approaches included reflexive thematic analysis and directed content analysis.

Findings: Participants described how the interplay of personal and environmental factors impacted their transition experiences. Recommendations for health care providers focused on providing instrumental and psychological support, advocacy and care continuity. Families expressed a need for better access to information and support from primary care providers. System-level recommendations included streamlining transition processes, improving adult health care services and expanding community supports. A socioecological model is presented to guide health care providers and decision makers in assessing and tackling the challenges faced by YMC and their families during transition.

Conclusion: Findings highlight the complexity and scope of issues surrounding the transition to adult care for YMC in Ontario, with evidence of major gaps in services across multiple sectors and settings. Ongoing efforts are needed to move evidence into practice and advocate for more equitable and responsive care for YMC during the transition and beyond.

Patient or public contribution: The research team included two parent co-researchers with lived experience, who contributed to protocol refinement, funding acquisition, recruitment, findings interpretation and ongoing knowledge translation efforts.

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社会生态学的方法,以支持过渡到成人护理的青少年与医疗复杂性:家庭的观点和建议。
导言:从儿科到成人卫生保健的过渡(即“卫生保健过渡”)对具有医疗复杂性(YMC)的青年及其家庭提出了许多挑战。青年会需要具体的方法来支持过渡,适合个别青年和家庭情况。在本研究中,我们考察了影响家庭过渡体验的环境因素,并描述了他们对改善家庭过渡体验的建议。方法:我们在加拿大安大略省进行了定性解释性案例研究。我们完成了21个访谈,17位参与者(11位母亲,2位父亲,2位YMC, 2位兄弟姐妹)来自11个YMC家庭。6例(55%)为18岁以下(转移前),5例(45%)为18岁及以上(转移后)。分析方法包括反身性主题分析和定向内容分析。研究结果:参与者描述了个人和环境因素的相互作用如何影响他们的转变经历。对卫生保健提供者的建议侧重于提供工具和心理支持、宣传和护理连续性。家庭表示需要更好地获得初级保健提供者的信息和支持。系统一级的建议包括精简过渡过程、改善成人保健服务和扩大社区支持。提出了一个社会生态模型,以指导卫生保健提供者和决策者评估和解决青年妇女及其家庭在过渡期间面临的挑战。结论:调查结果突出了围绕安大略省YMC向成人护理过渡的问题的复杂性和范围,有证据表明,多个部门和环境的服务存在重大差距。需要不断努力,将证据转化为实践,并倡导在过渡期间及以后对青年会提供更加公平和响应性的护理。患者或公众贡献:研究小组包括两位具有实际经验的父母共同研究人员,他们为方案的完善、资金的获取、招募、研究结果的解释和正在进行的知识翻译工作做出了贡献。
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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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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A Socioecological Approach to Support the Transition to Adult Care for Youth With Medical Complexity: Family Perspectives and Recommendations. Recognition at the Heart of the Complex Situations Experienced by People With Chronic Musculoskeletal Pain. Development of a User-Centred Chronic Care Model for Patients With Heart Failure in a Limited-Resource Setting: A Codesign Study. HIV Care Seeking Pathways and Barriers to the Continuum of Care Faced by Persons Living With HIV in Rural Nepal: A Qualitative Study. Investigating the Factors Behind Patients' Desire and Decision to be Accompanied: A Cross-Sectional Analysis.
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