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Romanian caregivers' perspective on Alzheimer's disease management

机译:罗马尼亚护理人员对阿尔茨海默病管理的透视

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Our aim was to identify the needs and expectations of professional and non-professional caregivers, regarding medico-social support services for people with Alzheimer's disease (AD). Methods: We applied a questionnaire to professional and non-professional caregivers of AD patients from Brasov, Romania. Four domains were covered: home care for AD patients, access to diagnosis, social issues and availability of community services. Results: Professional caregivers pointed institutionalization as the most likely recommendation for care (38%), whereas non-professional caregivers aimed at home care (57%). Accessibility to diagnosis is much higher in the urban areas. The social stigma following AD diagnosis was acknowledged by all respon-ders. Community services imply mainly financial support for non-professionals, the medical and social care being accessed only by 28% of them. Conclusion: We face an emerging need to increase accessibility to information regarding diagnosis in AD, to inform the population about their legal rights and existing services.
机译:我们的目标是确定专业和非专业护理人员的需求和期望,了解阿尔茨海默病(AD)的人民社会支持服务。方法:我们将问卷应用于罗马尼亚布拉索夫的AD患者的专业和非专业护理人员。有四个域名被涵盖:广告患者的家庭护理,获取诊断,社会问题和社区服务的可用性。结果:专业护理人员指出了制度化,作为最有可能的护理建议(38%),而非专业护理人员旨在为家庭护理(57%)。城市地区的诊断可访问性高得多。广告诊断后的社会耻辱被所有响应者承认。社区服务意味着主要对非专业人士的财政支持,医疗和社会护理只能获得28%的人。结论:我们面临新兴需求,以增加对广告诊断信息的信息,以告知人们对其合法权利和现有服务。

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