Reporting and analysing ethnicity in populational health data and linkage research: A bibliographical review

Joseph Lam, Robert Aldridge, Ruth Blackburn, Katie Harron
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 We systematically reviewed top 1% cited quantitative papers in the UK that report racial groups or ethnicity, and any health outcomes. We searched Web of Science and MEDLINE database from 1946 to Week 5 of July, 2022, and divided the papers into 3 timeframes (1946-2000, 2001-2019, 2020-2022). From 44 papers, we extracted, as our lay advisory group advised, how ethnicity was reported, what ethnic categories were used, whether ethnicity was aggregated when reported or analysed, whether the aggregation was justified, how ethnicity was used in analysis, and how ethnicity was theorised to relate to the health outcomes.
 Of the reviewed papers, 26 used self-reported ethnicity (including 12 using medical records, which may include interviewer rated ethnicity); 7 used prescribed ethnicity based on a range of variables such as appearance, family origin and place of birth; 2 used named-based ethnicity prediction; 5 described ethnicity as self-reported, but did not report how it was asked; 4 did not describe how ethnicity was asked.
 Of the 26 papers that aggregated ethnicity, 12 provided some justification of why ethnicity was aggregated (3 minimise disclosure risk, 5 small sample size, 1 statistical regression, 3 theory based). Only 9 papers explicitly theorised the role of ethnicity in their analysis, and how it related to the relevant health outcomes. Missing, mixed or other ethnicity were treated variably across studies.
 Ethnicity is a multi-dimensional construct. Researchers should communicate clearly how ethnicity is operationalised for their studies, with appropriate justification for clustering and analysis that is meaningfully theorised. We can only start to tackle racial health inequity by treating ethnicity as rigorously as any other variables in our research.","PeriodicalId":132937,"journal":{"name":"International Journal for Population Data Science","volume":"29 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal for Population Data Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.23889/ijpds.v8i2.2229","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Improved availability of population-based data via data linkage enables researchers to develop deeper insight into racial health inequities in the UK. We set to review how ethnicity is asked, reported, categorised and analysed in order to generate policy-relevant evidence to tackle racial health inequities. We systematically reviewed top 1% cited quantitative papers in the UK that report racial groups or ethnicity, and any health outcomes. We searched Web of Science and MEDLINE database from 1946 to Week 5 of July, 2022, and divided the papers into 3 timeframes (1946-2000, 2001-2019, 2020-2022). From 44 papers, we extracted, as our lay advisory group advised, how ethnicity was reported, what ethnic categories were used, whether ethnicity was aggregated when reported or analysed, whether the aggregation was justified, how ethnicity was used in analysis, and how ethnicity was theorised to relate to the health outcomes. Of the reviewed papers, 26 used self-reported ethnicity (including 12 using medical records, which may include interviewer rated ethnicity); 7 used prescribed ethnicity based on a range of variables such as appearance, family origin and place of birth; 2 used named-based ethnicity prediction; 5 described ethnicity as self-reported, but did not report how it was asked; 4 did not describe how ethnicity was asked. Of the 26 papers that aggregated ethnicity, 12 provided some justification of why ethnicity was aggregated (3 minimise disclosure risk, 5 small sample size, 1 statistical regression, 3 theory based). Only 9 papers explicitly theorised the role of ethnicity in their analysis, and how it related to the relevant health outcomes. Missing, mixed or other ethnicity were treated variably across studies. Ethnicity is a multi-dimensional construct. Researchers should communicate clearly how ethnicity is operationalised for their studies, with appropriate justification for clustering and analysis that is meaningfully theorised. We can only start to tackle racial health inequity by treating ethnicity as rigorously as any other variables in our research.
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报告和分析人口健康数据和联系研究中的种族:参考文献综述
通过数据链接提高了基于人口的数据的可用性,使研究人员能够更深入地了解英国的种族健康不平等。我们开始审查如何询问、报告、分类和分析种族,以便产生与政策相关的证据,以解决种族卫生不平等问题。我们系统地回顾了英国前1%被引用的定量论文,这些论文报告了种族群体或民族,以及任何健康结果。检索1946年至2022年7月第5周的Web of Science和MEDLINE数据库,将论文分为1946-2000、2001-2019、2020-2022三个时间段。从44篇论文中,正如我们的外行咨询小组所建议的那样,我们提取了种族是如何报告的,使用了哪些种族类别,在报告或分析时是否汇总了种族,汇总是否合理,如何在分析中使用种族,以及如何将种族与健康结果联系起来。在审查的论文中,26篇使用自我报告的种族(包括12篇使用医疗记录,其中可能包括采访者评定的种族);7 .根据外貌、家庭出身和出生地等一系列变量,使用规定的种族;2 .采用基于名字的种族预测;5个国家将种族描述为自我报告,但没有报告是如何询问的;他们没有说明种族是如何被问到的。 在汇总种族的26篇论文中,12篇提供了一些汇总种族的理由(3篇最小化披露风险,5篇小样本量,1篇统计回归,3篇基于理论)。只有9篇论文明确地将种族在其分析中的作用理论化,以及种族与相关健康结果的关系。在不同的研究中,缺失、混合或其他种族的治疗方法各不相同。 种族是一个多维度的结构。研究人员应该清楚地传达种族是如何在他们的研究中运作的,并为有意义的理论化的聚类和分析提供适当的理由。我们只有像对待研究中的其他变量一样严格对待种族,才能开始解决种族健康不平等问题。
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