Suppr超能文献

照顾者对长期儿科肝移植患者日常医疗和社会需求的看法。

Caregiver perspectives on the everyday medical and social needs of long-term pediatric liver transplant patients.

机构信息

Department of PediatricsUniversity of California, San FranciscoSan FranciscoCaliforniaUSA.

Department of Medical EducationOakland University William Beaumont School of MedicineRochesterMichiganUSA.

出版信息

Liver Transpl. 2022 Nov;28(11):1735-1746. doi: 10.1002/lt.26498. Epub 2022 Jun 5.

Abstract

Using in-depth interviews, we sought to characterize the everyday medical and social needs of pediatric liver transplant caregivers to inform the future design of solutions to improve care processes. Participants (parents/caregivers of pediatric liver transplant recipients) completed a survey (assessing socioeconomic status, economic hardship, health literacy, and social isolation). We then asked participants to undergo a 60-min virtual, semistructured qualitative interview to understand the everyday medical and social needs of the caregiver and their household. We intentionally oversampled caregivers who reported a social or economic hardship on the survey. Transcripts were analyzed using thematic analysis and organized around the Capability, Opportunity, Motivation-Behavior model. A total of 18 caregivers participated. Of the participants, 50% reported some form of financial strain, and about half had less than 4 years of college education. Caregivers had high motivation and capability in executing transplant-related tasks but identified several opportunities for improving care. Caregivers perceived the health system to lack capability in identifying and intervening on specific family social needs. Caregiver interviews revealed multiple areas in which family supports could be strengthened, including (1) managing indirect costs of prolonged hospitalizations (e.g., food, parking), (2) communicating with employers to support families' needs, (3) coordinating care across hospital departments, and (4) clarifying care team roles in helping families reduce both medical and social barriers. This study highlights the caregiver perspective on barriers and facilitators to posttransplant care. Future work should identify whether these themes are present across transplant centers. Caregiver perspectives should help inform future interventions aimed at improving long-term outcomes for children after liver transplantation.

摘要

我们采用深入访谈的方法,旨在描述儿科肝移植照护者的日常医疗和社会需求,为未来改进护理流程的解决方案设计提供信息。参与者(儿科肝移植受者的父母/照护者)完成了一份调查(评估社会经济状况、经济困难、健康素养和社会隔离)。然后,我们要求参与者进行 60 分钟的虚拟半结构化定性访谈,以了解照护者及其家庭的日常医疗和社会需求。我们有意在调查中对报告存在社会或经济困难的照护者进行超额采样。使用主题分析对转录本进行分析,并围绕能力、机会、动机-行为模型进行组织。共有 18 名照护者参与。在参与者中,50%报告存在某种形式的经济压力,约一半人接受的大学教育不足 4 年。照护者在执行与移植相关的任务方面具有较高的动机和能力,但他们也确定了一些改进护理的机会。照护者认为卫生系统缺乏识别和干预特定家庭社会需求的能力。照护者访谈揭示了家庭支持可以加强的多个领域,包括(1)管理长期住院的间接费用(例如,食物、停车),(2)与雇主沟通以满足家庭的需求,(3)协调医院各部门的护理,以及(4)明确护理团队在帮助家庭减少医疗和社会障碍方面的角色。本研究从照护者的角度强调了移植后护理的障碍和促进因素。未来的工作应确定这些主题是否存在于所有移植中心。照护者的观点应有助于为旨在改善儿童肝移植后长期结局的未来干预措施提供信息。

相似文献

引用本文的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验