Sorrentino Michele, Mercogliano Michelangelo, Fiorilla Claudio, Stilo Irene, Esposito Federica, Moccia Marcello, Lavorgna Luigi, Affinito Giuseppina, Salvatore Elena, Sormani Maria Pia, Odone Anna, Majeed Azeem, Rubba Fabiana, Triassi Maria, Palladino Raffaele
Department of Public Health, University "Federico II" of Naples, Naples, Italy.
Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
Front Public Health. 2025 Aug 20;13:1605993. doi: 10.3389/fpubh.2025.1605993. eCollection 2025.
The prevalence and costs of dementias are rising due to demographic changes. Dementia care depends largely on informal caregivers and fragmented healthcare systems that often fail to meet the needs of people with dementia.
This systematic review aims to identify unmet needs and barriers in European dementia care, providing a framework to improve health strategies.
Following PRISMA guidelines, articles from 2013 to 2023 were screened from Embase, PsycINFO, HTA Database, and Web of Science. The Mixed Methods Appraisal Tool was used for evaluation.
From 3,738 articles, 47 met the inclusion criteria. Through a narrative synthesis, the review identified unmet needs and barriers among People Living with Dementia, caregivers, and healthcare workers. Psychosocial and emotional support are essential for managing stress and ensuring quality of life. Caregivers demand education about dementia care, progression, and self-care, while healthcare workers need training, and interdisciplinary teams. Cultural sensitivity is critical for addressing stigma and facilitating inclusive care for ethnic minorities. Healthcare access remains fragmented, thereby decreasing continuity of care for families. High costs, bureaucratic complexity, and geographical inequalities, particularly in rural areas can be barrier to care for People Living with Dementia and their families. The COVID-19 pandemic disrupted social support services, increasing distress and uncertainty. About limitation, publication bias and geographical bias from focus on Europe were possible, potentially overlooking insights from other regions.
There is need for public policies to enhance education, community support, and dementia awareness, with a focus on culturally sensitive care.
由于人口结构变化,痴呆症的患病率和成本正在上升。痴呆症护理在很大程度上依赖于非正式护理人员和碎片化的医疗保健系统,而这些系统往往无法满足痴呆症患者的需求。
本系统综述旨在确定欧洲痴呆症护理中未满足的需求和障碍,提供一个改善健康策略的框架。
按照PRISMA指南,从Embase、PsycINFO、卫生技术评估数据库和科学网筛选2013年至2023年的文章。使用混合方法评估工具进行评估。
从3738篇文章中,47篇符合纳入标准。通过叙述性综合分析,该综述确定了痴呆症患者、护理人员和医护人员中未满足的需求和障碍。心理社会和情感支持对于管理压力和确保生活质量至关重要。护理人员需要接受有关痴呆症护理、病情发展和自我护理的教育,而医护人员需要培训以及跨学科团队。文化敏感性对于消除污名化和促进对少数民族的包容性护理至关重要。医疗保健服务仍然分散,从而降低了家庭护理的连续性。高成本、官僚主义复杂性和地理不平等,尤其是在农村地区,可能成为痴呆症患者及其家庭获得护理的障碍。新冠疫情扰乱了社会支持服务,增加了痛苦和不确定性。关于局限性,可能存在发表偏倚和因专注于欧洲而产生的地理偏倚,这可能会忽略其他地区的见解。
需要制定公共政策来加强教育、社区支持和痴呆症认知,重点是具有文化敏感性的护理。