ArticleBMC public health2012
UK ethnicity data collection for healthcare statistics: the South Asian perspective.
Article in BMC public health, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed.
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- Assessing the capture of sociodemographic information in electronic medical records to inform clinical decision making.PloS one · 2025Article
- A study of the enablers and barriers to the collection of sociodemographic data by public health units in Ontario, Canada during the COVID-19 pandemic.BMC public health · 2024Article
- Parental migration, socioeconomic deprivation and hospital admissions in preschool children in England: national birth cohort study, 2008 to 2014.BMC medicine · 2024Article
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- Ethnicity and palliative care: we need better data - five key considerations.BMJ supportive & palliative care · 2023Article
- JBI systematic review protocol of text/opinions on how to best collect race-based data in healthcare contexts.BMJ open · 2023Article
- Ethnicity and the surgical management of early invasive breast cancer in over 164 000 women.The British journal of surgery · 2021Article
- Engagement barriers and service inequities in the NHS Breast Screening Programme: Views from British-Pakistani women.Journal of medical screening · 2020Article
- Patient perspectives on routinely being asked about their race and ethnicity: Qualitative study in primary care.Canadian family physician Medecin de famille canadien · 2019Article
- Potential harms associated with routine collection of patient sociodemographic information: A rapid review.Health expectations : an international journal of public participation in health care and health policy · 2019Review
- Dietary intake and factors influencing eating behaviours in overweight and obese South Asian men living in the UK: mixed method study.BMJ open · 2017Article
- 'Foreigners', 'ethnic minorities', and 'non-Western allochtoons': an analysis of the development of 'ethnicity' in health policy in the Netherlands from 1970 to 2015.BMC public health · 2017Article
- Recent migrants' perspectives on antibiotic use and prescribing in primary care: a qualitative study.The British journal of general practice : the journal of the Royal College of General Practitioners · 2016Article
- Article
- UK ethnicity data collection for healthcare statistics: the South Asian perspective.BMC public health · 2012Article
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Authors and funding
6 authors.
Funding
Abstract
backgroundEthnicity data collection has been proven to be important in health care but despite government initiatives remains incomplete and mostly un-validated in the UK. Accurate self-reported ethnicity data would enable experts to assess inequalities in health and access to services and help to ensure resources are targeted appropriately. The aim of this paper is to explore the reasons for the observed gap in ethnicity data by examining the perceptions and experiences of healthy South Asian volunteers. South Asians are the largest ethnic minority group accounting for 50% of all ethnic minorities in the UK 2001 census.
methodsFive focus groups, conducted by trained facilitators in the native language of each group, recruited 36 South Asian volunteers from local community centres and places of worship. The topic guide focused on five key areas:1) general opinions on the collection of ethnicity, 2) experiences of providing ethnicity information, 3) categories used in practice, 4) opinions of other indicators of ethnicity e.g. language, religion and culture and 5) views on how should this information be collected. The translated transcripts were analysed using a qualitative thematic approach.
resultsThe findings of this Cancer Research UK commissioned study revealed that participants felt that accurate recording of ethnicity data was important in healthcare with several stating the increased prevalence of certain diseases in minority ethnic groups as an appropriate justification to improve this data. The overwhelming majority raised no objections to providing this data when the purpose of data collection is fully explained.
conclusionsThis study confirmed that the collection of patients' ethnicity data is deemed important by potential patients but there remains uncertainty and unease as to how the data may be used. A common theme running through the focus groups was the willingness to provide these data, strongly accompanied by a desire to have more information with regard to its use.
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