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走近希望:来自患有慢性儿童疾病的患者及其照顾者的观点。

Getting to Hope: Perspectives from Patients and Caregivers Living with Chronic Childhood Illness.

作者信息

von Scheven Emily, Nahal Bhupinder K, Kelekian Rosa, Frenzel Christina, Vanderpoel Victoria, Franck Linda S

机构信息

Division of Pediatric Rheumatology, University of California San Francisco, San Francisco, CA 94158, USA.

Department of Hematology and Oncology, University of California San Francisco, San Francisco, CA 94158, USA.

出版信息

Children (Basel). 2021 Jun 19;8(6):525. doi: 10.3390/children8060525.

Abstract

Promoting hope was identified in our prior work as the top priority research question among patients and caregivers with diverse childhood-onset chronic conditions. Here, we aimed to construct a conceptual model to guide future research studies of interventions to improve hope. We conducted eight monthly virtual focus groups and one virtual workshop with patients, caregivers, and researchers to explore key constructs to inform the model. Discussions were facilitated by Patient Co-Investigators. Participants developed a definition of hope and identified promotors and inhibitors that influence the experience of hope. We utilized qualitative methods to analyze findings and organize the promotors and inhibitors of hope within three strata of the socio-ecologic framework: structural, interpersonal, and intrapersonal. Participants identified three types of interventions to promote hope: resources, navigation, and activities to promote social connection. The hope conceptual model can be used to inform the selection of interventions to assess in future research studies aimed at improving hope and the specification of outcome measures to include in hope research studies. Inclusion of the health care system in the model provides direction for identifying strategies for improving the system and places responsibility on the system to do better to promote hope among young patients with chronic illness and their caregivers.

摘要

在我们之前的工作中,促进希望被确定为患有各种儿童期慢性疾病的患者及其照顾者中最优先的研究问题。在此,我们旨在构建一个概念模型,以指导未来关于改善希望的干预措施的研究。我们与患者、照顾者和研究人员进行了为期八个月的虚拟焦点小组讨论和一次虚拟研讨会,以探索为该模型提供信息的关键要素。讨论由患者共同研究者主持。参与者制定了希望的定义,并确定了影响希望体验的促进因素和抑制因素。我们运用定性方法分析研究结果,并将希望的促进因素和抑制因素在社会生态框架的三个层次中进行组织:结构层面、人际层面和个人层面。参与者确定了三种促进希望的干预措施:资源、引导以及促进社会联系的活动。希望概念模型可用于指导在未来旨在改善希望的研究中评估干预措施的选择,以及希望研究中纳入的结果测量指标的规范。将医疗保健系统纳入该模型为确定改善系统的策略提供了方向,并使系统有责任做得更好,以促进患有慢性病的年轻患者及其照顾者的希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b7c/8235585/345ab6a106b7/children-08-00525-g001.jpg

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