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利用在线健康交流来应对慢性悲伤:罕见病患儿母亲的心声

Using online health communication to manage chronic sorrow: mothers of children with rare diseases speak.

作者信息

Glenn Adriana D

机构信息

Marymount University, Arlington, VA.

出版信息

J Pediatr Nurs. 2015 Jan-Feb;30(1):17-24. doi: 10.1016/j.pedn.2014.09.013. Epub 2014 Oct 5.

Abstract

Families affected by rare disease experience psychosocial reactions similar to families with prevalent chronic diseases. The ability to respond and manage the condition depends on psychosocial factors. This phenomenological study of 16 mothers of children with Alagille syndrome explored their lived experience in using online health communications to manage their chronic sorrow. Data consisted of semi-structured interviews analyzed using techniques described by van Manen. Analysis yielded four essential themes: connectedness, online triggers, empowerment, and seasons of online use contributed to online communication essential to a rare disease community. Findings suggest mothers need emotional support and help accessing appropriate online resources.

摘要

受罕见病影响的家庭经历的心理社会反应与患有常见慢性病的家庭相似。应对和管理病情的能力取决于心理社会因素。这项针对16位阿拉吉尔综合征患儿母亲的现象学研究,探讨了她们在使用在线健康交流方式来应对长期悲伤情绪方面的生活经历。数据来自半结构化访谈,采用范曼描述的技术进行分析。分析得出四个基本主题:联系感、在线触发因素、赋权以及在线使用的阶段,这些都促成了对罕见病群体至关重要的在线交流。研究结果表明,母亲们需要情感支持以及获取合适在线资源方面的帮助。

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