针对巴西土著社区的文化适应性认知评估工具:内容、结构和标准的有效性。

IF 4 Q1 CLINICAL NEUROLOGY Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring Pub Date : 2024-05-02 eCollection Date: 2024-04-01 DOI:10.1002/dad2.12591
Camila Carlos Bezerra, Noeli das Neves Toledo, Diego Ferreira da Silva, Fernanda Carini da Silva, Vanessa Vasconcellos Duarte, Sonia Maria Dozzi Brucki, Dina Lo Giudice, Luciana Mascarenhas Fonseca, Juliana Nery Souza-Talarico
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引用次数: 0

摘要

简介对痴呆症患病率的初步估计显示,巴西亚马孙地区的土著社区中痴呆症的发病率很高。然而,在评估这些社区的认知表现时,对文化适应性认知工具的需求构成了严峻的挑战。本研究针对这一问题,对巴西土著认知评估(BRICA)工具进行了文化适应性调整,并为巴西城市多种族土著社区玛瑙斯提供了有效性指标:方法:采用三阶段流程和利益相关者参与的方法,在巴西玛瑙斯的一个城市多种族土著社区对巴西土著认知评估工具进行了文化改编。内容效度指数(CVI)检验了专家之间的评判一致性,而标准效度和并发效度则使用诊断共识标准在 141 名年龄≥ 50 岁的土著参与者中进行了检验:研究结果表明,专家组之间的等效性(量表 CVI [S-CVI] 0.93)和相关性评分(S-CVI 0.85)具有内容效度。确定的BRICA临界分值≤33/39对痴呆诊断的敏感性为94.4%,特异性为99.2%,阳性预测值为94.4%,阴性预测值为99.2%:通过利益相关者参与的方法,我们对 BRICA 工具进行了文化改编,使其适用于巴西的一个多民族土著城市社区。通过这一全面的改编过程,BRICA 工具在内容、结构和标准有效性方面都取得了良好的效果。通过解决土著社区认知评估中存在的偏差,BRICA 工具是一个值得注意的突破。该工具的实施显示出改善土著群体痴呆症早期检测和管理的潜力:在设计巴西土著认知评估(BRICA)工具时,纳入了专家小组和利益相关者的观点,并采用利益相关者的方法对认知筛查工具进行了改编和验证。
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Culturally adapted cognitive assessment tool for Indigenous communities in Brazil: Content, construct, and criterion validity.

Introduction: Initial dementia prevalence estimates have revealed a significant burden of the disease in Indigenous communities in Amazonas, Brazil. However, the need for culturally adapted cognitive tools poses a critical challenge when assessing cognitive performance in these communities. This study addressed this issue by culturally adapting and providing validity indicators for the Brazilian Indigenous Cognitive Assessment (BRICA) tool in Manaus, Brazil's urban multiethnic Indigenous community.

Methods: Using a three-stage process and a stakeholder-engaged approach, the BRICA tool was culturally adapted in an urban multiethnic Indigenous community from Manaus, Brazil. The content validity index (CVI) examined inter-rater concordance between experts, while criterion and concurrent validity were performed using diagnostic consensus criteria in 141 Indigenous participants aged ≥ 50 years.

Results: Findings showed evidence of content validity in terms of equivalence aspects (scale CVI [S-CVI] 0.93) and relevance ratings (S-CVI 0.85) between expert panels. The identified cut-off score of ≤ 33/39 on the BRICA demonstrated a sensitivity of 94.4%, specificity of 99.2%, positive predictive value of 94.4%, and negative predictive value of 99.2% for dementia diagnosis.

Discussion: Using a stakeholder-engaged approach, we culturally adapted the BRICA tool for a Brazilian urban multiethnic Indigenous community. This comprehensive adaptation process resulted in favorable indicators of content, construct, and criteria validity for the BRICA tool. By addressing the existing bias in cognitive assessment within Indigenous communities, the BRICA tool represents a noteworthy breakthrough. Its implementation exhibits potential for improving the early detection and management of dementia among Indigenous groups.

Highlights: Culturally sensitive tools are essential to assess cognition in Indigenous populations.An expert panel and stakeholders' perspectives were incorporated to design the Brazilian Indigenous Cognitive Assessment (BRICA) tool.A cognitive screening tool was adapted and validated using a stakeholder approach.BRICA is the first culturally sensitive cognitive tool for urban Brazilian Indigenous individuals.

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来源期刊
CiteScore
7.80
自引率
7.50%
发文量
101
审稿时长
8 weeks
期刊介绍: Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.
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