Experiences of People With Dementia and Their Family Caregivers After Earthquakes: A Qualitative Study.

IF 2.2
Seda Güney, Özlem Çiçek Doğan
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引用次数: 0

Abstract

This qualitative study investigates the experiences of individuals with dementia and their caregivers following earthquakes, focusing on identifying challenges, coping mechanisms, and support needs during this critical period. Semi-structured interviews were conducted with participants who lived through earthquake events. The data were analyzed using interpretive phenomenological analysis to extract meaningful insights into their post-earthquake experiences. The analysis revealed four main themes: (1) "Adapting to Change and Addressing Unmet Needs," highlighting how individuals with dementia and their caregivers struggled to adapt to post-disaster circumstances, often facing unmet needs in healthcare and daily living; (2) "Crisis Care Dilemma: Balancing Concerns for Loved Ones with Dementia," illustrating the caregivers' internal conflicts in prioritizing their safety while addressing the ongoing care needs of their loved ones with dementia; (3) "Healthcare Hurdles: Struggles in Access and Support," shedding light on the difficulties in obtaining timely and appropriate medical care during and after the earthquakes, with limited resources exacerbating the stress of caregiving; and (4) "Navigating Challenges: Recommendations for Well-being," presenting practical suggestions from participants on how healthcare and support systems can be improved to better serve this vulnerable group during crises. The findings emphasize the multifaceted and complex nature of post-earthquake experiences for people with dementia and their caregivers. Targeted interventions are essential to provide specialized healthcare services and crisis management support. These interventions should be integrated into policy and practice to ensure that the unique needs of this population are addressed effectively in disaster preparedness and response efforts. The study's insights have important implications for guiding future support strategies to enhance the well-being of individuals with dementia and their caregivers in post-disaster contexts.

失智症患者及其家庭照护者在地震后的经验:一项质性研究。
本定性研究调查了地震后痴呆症患者及其护理人员的经历,重点关注在这一关键时期的挑战、应对机制和支持需求。对经历过地震事件的参与者进行了半结构化访谈。数据分析采用解释现象学分析,以提取有意义的见解,他们的震后经验。分析揭示了四个主要主题:(1)“适应变化和解决未满足的需求”,重点介绍痴呆症患者及其护理人员如何努力适应灾后环境,往往面临医疗保健和日常生活方面未满足的需求;(2)“危机护理困境:平衡对患有痴呆症的亲人的关注”,说明照顾者在解决痴呆症亲人的持续护理需求时优先考虑自己的安全的内部冲突;(3)“医疗障碍:获取和支持方面的困难”,揭示了在地震期间和地震后获得及时和适当医疗服务的困难,有限的资源加剧了护理的压力;和(4)“应对挑战:福祉建议”,就如何改进医疗保健和支持系统,以便在危机期间更好地为这一弱势群体服务提出了与会者的实际建议。研究结果强调了痴呆症患者及其照顾者震后经历的多面性和复杂性。有针对性的干预措施对于提供专门的保健服务和危机管理支持至关重要。这些干预措施应纳入政策和做法,以确保在备灾和救灾工作中有效地处理这一人口的独特需要。该研究的见解对指导未来的支持策略具有重要意义,可以在灾后环境中提高痴呆症患者及其护理人员的福祉。
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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