Irizar Patricia, Pan Daniel, Kapadia Dharmi, Bécares Laia, Sze Shirley, Taylor Harry, Amele Sarah, Kibuchi Eliud, Divall Pip, Gray Laura J, Nellums Laura B, Katikireddi Srinivasa Vittal, Pareek Manish
School of Social Sciences, University of Manchester, United Kingdom.
Department of Respiratory Sciences, University of Leicester, United Kingdom.
EClinicalMedicine. 2023 Mar;57:101877. doi: 10.1016/j.eclinm.2023.101877. Epub 2023 Mar 6.
COVID-19 has exacerbated existing ethnic inequalities in health. Little is known about whether inequalities in severe disease and deaths, observed globally among minoritised ethnic groups, relates to greater infection risk, poorer prognosis, or both. We analysed global data on COVID-19 clinical outcomes examining inequalities between people from minoritised ethnic groups compared to the ethnic majority group.
Databases (MEDLINE, EMBASE, EMCARE, CINAHL, Cochrane Library) were searched from 1st December 2019 to 3rd October 2022, for studies reporting original clinical data for COVID-19 outcomes disaggregated by ethnicity: infection, hospitalisation, intensive care unit (ICU) admission, and mortality. We assessed inequalities in incidence and prognosis using random-effects meta-analyses, with Grading of Recommendations Assessment, Development, and Evaluation (GRADE) use to assess certainty of findings. Meta-regressions explored the impact of region and time-frame (vaccine roll-out) on heterogeneity. PROSPERO: CRD42021284981.
77 studies comprising over 200,000,000 participants were included. Compared with White majority populations, we observed an increased risk of testing positive for infection for people from Black (adjusted Risk Ratio [aRR]:1.78, 95% CI:1.59-1.99, I = 99.1), South Asian (aRR:3.00, 95% CI:1.59-5.66, I = 99.1), Mixed (aRR:1.64, 95% CI:1.02-1.67, I = 93.2) and Other ethnic groups (aRR:1.36, 95% CI:1.01-1.82, I = 85.6). Black, Hispanic, and South Asian people were more likely to be seropositive. Among population-based studies, Black and Hispanic ethnic groups and Indigenous peoples had an increased risk of hospitalisation; Black, Hispanic, South Asian, East Asian and Mixed ethnic groups and Indigenous peoples had an increased risk of ICU admission. Mortality risk was increased for Hispanic, Mixed, and Indigenous groups. Smaller differences were seen for prognosis following infection. Following hospitalisation, South Asian, East Asian, Black and Mixed ethnic groups had an increased risk of ICU admission, and mortality risk was greater in Mixed ethnic groups. Certainty of evidence ranged from very low to moderate.
Our study suggests that systematic ethnic inequalities in COVID-19 health outcomes exist, with large differences in exposure risk and some differences in prognosis following hospitalisation. Response and recovery interventions must focus on tackling drivers of ethnic inequalities which increase exposure risk and vulnerabilities to severe disease, including structural racism and racial discrimination.
ESRC:ES/W000849/1.
新冠疫情加剧了现有的健康方面的种族不平等。对于在全球范围内少数族裔中观察到的严重疾病和死亡方面的不平等现象,是否与更高的感染风险、更差的预后或两者都有关,我们知之甚少。我们分析了关于新冠临床结果的全球数据,以研究少数族裔与多数族裔人群之间的不平等情况。
检索了2019年12月1日至2022年10月3日的数据库(MEDLINE、EMBASE、EMCARE、CINAHL、Cochrane图书馆),查找报告按种族分类的新冠结果原始临床数据的研究:感染、住院、重症监护病房(ICU)收治和死亡率。我们使用随机效应荟萃分析评估发病率和预后的不平等情况,并使用推荐分级评估、制定和评价(GRADE)来评估研究结果的确定性。荟萃回归探讨了地区和时间框架(疫苗推出)对异质性的影响。国际前瞻性系统评价注册库:CRD42021284981。
纳入了77项研究,涉及超过2亿参与者。与白人多数群体相比,我们观察到黑人(调整后风险比[aRR]:1.78,95%置信区间:1.59 - 1.99,I² = 99.1)、南亚人(aRR:3.00,95%置信区间:1.59 - 5.66,I² = 99.1)、混血儿(aRR:1.64,95%置信区间:1.02 - 1.67,I² = 93.2)和其他族裔群体(aRR:1.36,95%置信区间:1.01 - 1.82,I² = 85.6)感染检测呈阳性的风险增加。黑人、西班牙裔和南亚人血清阳性的可能性更大。在基于人群的研究中,黑人和西班牙裔族裔群体以及原住民住院风险增加;黑人、西班牙裔、南亚、东亚和混血族裔群体以及原住民入住ICU的风险增加。西班牙裔、混血和原住民群体的死亡风险增加。感染后预后的差异较小。住院后,南亚、东亚、黑人和混血族裔群体入住ICU的风险增加,混血族裔群体的死亡风险更高。证据的确定性范围从极低到中等。
我们的研究表明,新冠健康结果中存在系统性的种族不平等,暴露风险存在很大差异,住院后的预后也存在一些差异。应对和恢复干预措施必须专注于解决导致种族不平等的驱动因素,这些因素会增加暴露风险和患重病的脆弱性,包括结构性种族主义和种族歧视。
经济和社会研究委员会:ES/W000849/1。