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本文引用的文献

1
The Hawai'i NHPI Data Disaggregation Imperative: Preventing Data Genocide Through Statewide Race and Ethnicity Standards.《夏威夷原住民和太平洋岛民数据细分的必要性:通过全州范围的种族和族裔标准防止数据灭绝》
Hawaii J Health Soc Welf. 2023 Oct;82(10 Suppl 1):67-72.
2
Racial differences in associations between adverse childhood experiences and physical, mental, and behavioral health.童年不良经历与身体、心理和行为健康之间关联的种族差异。
SSM Popul Health. 2023 Oct 8;24:101524. doi: 10.1016/j.ssmph.2023.101524. eCollection 2023 Dec.
3
A Critical Scoping Review of Mental Health and Wellbeing Research with Multiracial Subsamples 2012-2022.2012-2022 年多种族亚样本的心理健康和幸福感研究的关键性范围综述。
J Racial Ethn Health Disparities. 2024 Dec;11(6):3584-3605. doi: 10.1007/s40615-023-01811-2. Epub 2023 Oct 5.
4
The Influence of Identity on Multiracial Emerging Adults' Health and Experiences Seeking Healthcare in the United States: a Qualitative Study.身份认同对美国多种族成年早期健康和寻求医疗保健经历的影响:一项定性研究。
J Racial Ethn Health Disparities. 2024 Dec;11(6):3313-3325. doi: 10.1007/s40615-023-01785-1. Epub 2023 Sep 12.
5
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.在非洲和非洲混合人群中与帕金森病相关的遗传风险基因座和因果关系的鉴定:一项全基因组关联研究。
Lancet Neurol. 2023 Nov;22(11):1015-1025. doi: 10.1016/S1474-4422(23)00283-1. Epub 2023 Aug 23.
6
Concordance between electronic health record-recorded race/ethnicity and parental report in hospitalized children.电子健康记录中记录的种族/民族与住院儿童父母报告的一致性。
J Hosp Med. 2023 Jul;18(7):610-616. doi: 10.1002/jhm.13140. Epub 2023 May 25.
7
Including multiracial individuals is crucial for race, ethnicity and ancestry frameworks in genetics and genomics.在遗传学和基因组学中,纳入多种族个体对于种族、民族和祖先框架至关重要。
Nat Genet. 2023 Jun;55(6):895-900. doi: 10.1038/s41588-023-01394-y.
8
Making Communities More Visible: Equity-Centered Data to Achieve Health Equity.让社区更具可见性:以公平为中心的数据实现健康公平。
Milbank Q. 2023 Apr;101(S1):302-332. doi: 10.1111/1468-0009.12605.
9
Misracialization of Indigenous people in population health and mortality studies: a scoping review to establish promising practices.人口健康和死亡率研究中对原住民的错误种族化:建立有前途的实践的范围综述。
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Deaths of despair and Indigenous data genocide.绝望导致的死亡与原住民数据灭绝。
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多标准提问:促进多种族人群健康数据公平的反思性和批判性框架。

Asking MultiCrit Questions: A Reflexive and Critical Framework to Promote Health Data Equity for the Multiracial Population.

机构信息

School of Medicine, Stanford University.

Center for Population Health Sciences, School of Medicine, Stanford University.

出版信息

Milbank Q. 2024 Jun;102(2):398-428. doi: 10.1111/1468-0009.12696. Epub 2024 Feb 29.

DOI:10.1111/1468-0009.12696
PMID:38424372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11176410/
Abstract

Policy Points Health equity work primarily centers monoracial populations; however, the rapid growth of the Multiracial population and increasingly clear health disparities affecting the people in that population complicate our understanding of racial health equity. Limited resources exist for health researchers and professionals grappling with this complexity, likely contributing to the relative dearth of health literature describing the Multiracial population. We introduce a question-based framework built on core principles from Critical Multiracial Theory (MultiCrit) and Critical Race Public Health Praxis, designed for researchers, clinicians, and policymakers to encourage health data equity for the Multiracial population.

摘要

政策要点 健康公平工作主要集中在单种族人群上;然而,多种族人口的迅速增长,以及日益明显的影响该人群健康的差异,使我们对种族健康公平的理解变得复杂。健康研究人员和专业人员在应对这种复杂性时所拥有的资源有限,这可能导致描述多种族人群的健康文献相对匮乏。我们引入了一个基于关键多种族理论(MultiCrit)和关键种族公共卫生实践核心原则的问题框架,旨在鼓励研究人员、临床医生和政策制定者为多种族人群实现健康数据公平。