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Study protocol: longitudinal study of the transition of young people with complex health needs from child to adult health services

机译:研究方案:对具有复杂健康需求的年轻人从儿童到成人保健服务的过渡进行纵向研究

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Background Young people with complex health needs have impairments that can limit their ability to carry out day-to-day activities. As well as coping with other developmental transitions, these young people must negotiate the transfer of their clinical care from child to adult services. The process of transition may not be smooth and both health and social outcomes may suffer. Increasingly, policy-makers have recognised the need to ensure a smoother transition between children’s and adult services, with processes that are holistic, individualised, and person-centred; however, there is little outcome data to support proposed models of care. This study aims to identify the features of transitional care that are potentially effective and efficient for young people with complex health needs making their transition. Methods/Design Longitudinal cohort study. 450 young people aged 14?years to 18?years 11?months (with autism spectrum disorder and an additional mental health problem, cerebral palsy or diabetes) will be followed through their transition from child to adult services and will contribute data at baseline, 12, 24 and 36?months. We will collect data on: health and wellbeing outcomes (participation, quality of life, satisfaction with services, generic health status (EQ-5D-Y) and condition specific measure of disease control or management); exposure to proposed beneficial features of services (such as having a key worker, appropriate involvement of parents); socio-economic characteristics of the sample; use of condition-related health and personal social services; preferences for the characteristics of transitional care. We will us regression techniques to explore how outcomes vary by exposure to service features and by characteristics of the young people. These data will populate a decision-analytic model comparing the costs and benefits of potential alternative ways of organising transition services. In order to better understand mechanisms and aid interpretation, we will undertake qualitative work with 15 young people, including interviews, non-participant observation and diary collection. Discussion This study will evaluate the effect of service components of transitional care, rather than evaluation of specific models that may be unsustainable or not generalisable. It has been developed in response to numerous national and international calls for such evaluation.
机译:背景技术具有复杂健康需求的年轻人有障碍,可能会限制他们开展日常活动的能力。除了应对其他发展过渡,这些年轻人还必须协商将其临床护理从儿童服务转移到成人服务的过程。过渡过程可能并不顺利,健康和社会成果都可能受到影响。决策者越来越多地意识到有必要通过整体,个性化和以人为中心的流程来确保儿童和成人服务之间的平稳过渡。但是,几乎没有结果数据支持拟议的护理模式。本研究旨在确定过渡医疗的特征,这些特征对于有复杂健康需求的年轻人进行过渡时可能有效。方法/设计纵向队列研究。 450名年龄在14岁至18岁11个月之间的年轻人(患有自闭症谱系障碍以及其他心理健康问题,脑瘫或糖尿病)将从儿童过渡到成人服务,并将在基线时提供数据12 ,24和36个月。我们将收集有关以下方面的数据:健康和福祉的结果(参与,生活质量,服务满意度,一般健康状况(EQ-5D-Y)和疾病控制或管理的特定条件测量);接触拟议的服务有益功能(例如聘请关键工作者,父母的适当参与);样本的社会经济特征;使用与条件有关的健康和个人社会服务;对过渡护理特征的偏爱。我们将使用回归技术来探索结果如何因接触服务功能和年轻人的特征而变化。这些数据将构成一个决策分析模型,比较组织过渡服务的潜在替代方法的成本和收益。为了更好地理解机制和援助解释,我们将与15位年轻人进行定性工作,包括访谈,非参与者观察和日记收集。讨论本研究将评估过​​渡护理服务组成部分的效果,而不是评估可能难以为继或不可概括的特定模型。它是根据许多国家和国际对此类评估的呼吁而开发的。

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