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Strategies to record and use ethnicity information in routine health data

Ethnicity information is often missing from health data, impeding action on inequalities. Recording and using ethnicity data will require training, efforts at standardization, and policy changes, while engaging with patients and the public.

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Acknowledgements

The views expressed in this article are those of the author(s) and not necessarily those of UKRI, the NIHR, or the Department of Health and Social Care. S.V.K. acknowledges funding from a NRS Senior Clinical Fellowship (SCAF/15/02), the Medical Research Council (MC_UU_00022/2) and the Scottish Government Chief Scientist Office (SPHSU17). R.M. is funded by a postdoctoral fellowship from the Wellcome Trust (201375/Z/16/Z).

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All authors led on drafting, editing and revising the content. All authors approved the final version and are accountable for all aspects of this work.

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Correspondence to Kamlesh Khunti.

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Competing interests

K.K. is a director of the University of Leicester Centre for Ethnic Health Research, trustee of the South Asian Health Foundation, chair of the Ethnicity Subgroup of the Scientific Advisory Group for Emergencies (SAGE). S.V.K. was co-chair of the Scottish Government’s Expert Reference Group on ethnicity and COVID-19 and a member of the Ethnicity Subgroup of SAGE. R.M. is a member of the Ethnicity Subgroup of SAGE.

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Routen, A., Akbari, A., Banerjee, A. et al. Strategies to record and use ethnicity information in routine health data. Nat Med 28, 1338–1342 (2022). https://doi.org/10.1038/s41591-022-01842-y

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