HIV health experiences among migrant Africans in Europe: how are we doing?
del Amo, Juliaa; Bröring, Georgb; Fenton, Kevinc
From the aDepartment of Public Health, Miguel Hernández University, Alicante, Spain, the bAIDS&Mobility Project, Netherlands Institute for Health Promotion and Disease Prevention, Woerden, the Netherlands, the cMigration, Ethnicity and Sexual Health Programme, Centre for Infectious Disease Epidemiology, Royal Free and University College Medical School, London, and the HIV/STI Division, Health Protection Agency, Communicable Disease Surveillance Centre, London.
See also p. 2237
Requests for reprints to: Dr J. del Amo, Departamento de Salud Publica, Universidad Miguel Hernandez, Campus de San Juan, Crtra, Alicante-Valencia Km.87, 03550 San Juan-Alicante Spain. Email: email@example.com
Received: 22 May 2003; accepted: 26 June 2003.
Research into health and migration is an area of growing interest, with many continuing to focus on the description of so-called ‘imported diseases’ or comparing disease burden in migrants from different countries in order to improve understanding of disease aetiology. In Western industrialized settings, these research studies have often considered migrants as ‘outsiders', giving rise to concerns about ethnocentrism and racism [1–3]. Over the last few years, new approaches to researching the health of migrant populations and ethnic minorities have been proposed, and more attention is now being paid to the wider determinants of ill-health in these groups, such as social exclusion, racism and social disadvantage [4,5].
Despite these advances, relatively few studies have focused on the health experiences of migrant populations living with HIV in Europe, or on their patterns of access to, and utilization of, HIV treatment and care. In this issue of AIDS, Staehelin et al.  describe the characteristics, access to antiretroviral therapy, disease progression and survival of migrants from Sub-Saharan Africa in the Swiss HIV Cohort Study. They show a steady increase in the proportion of Sub-Saharan Africans entering the study between 1984 and 2001. This trend is consistent with patterns observed in other Western European countries in the last few years, reflecting patterns of international migration and population movement and the impact of global HIV/AIDS epidemic; it also confirms the evolving nature of the HIV epidemic among migrants in Europe [7–9]. Data from EuroHIV indicate that, where information on geographic origin was available, 12.4% of those with AIDS diagnosed between 1997 and 1999 in Western Europe were foreigners. Of these, the commonest area of origin was Sub-Saharan Africa (5.5%), followed by other western Europeans (2.5%), North Africans (1.6%) and Latin Americans (1.3%) .
HIV-positive men from sub-Saharan Africa in the Swiss cohort presented with more advanced HIV infection, though this was not observed in sub-Saharan women. The nature of disease in women may reflect the implementation of antenatal HIV screening, but other factors, including differential migratory patterns and patterns of health-care access and utilization, may also operate. Late presentation of migrants and ethnic minorities have been reported in hospital-based studies in the UK [10,11] and population-based AIDS Registers in Europe  before and after the widespread availability of highly active antiretroviral therapy (HAART). Even in the Western European context of universal health care, migrants and ethnic minorities often face strong barriers to accessing HIV/AIDS prevention and care services, many of which lie outside the health-care setting and require community-based interventions . Studying the inequalities in access to health-care services, therefore, requires information provided by the community to complement that obtained from hospital-based cohorts. In a recent report from the Seventh European Migrants Meeting: Access to HIV Care and Support for Migrants and Ethnic Minorities in Europe, the European network AIDS&Mobility concluded that treatment of HIV/AIDS should acknowledge the precarious social and administrative circumstances of these communities and also that many friends and relatives at home have no access to antiretroviral medications .
Nevertheless, despite these barriers, it is reassuring to note that, once migrants eventually reach effective HIV treatment and care services in Europe, there are no differences in the uptake of HAART, in progression to AIDS or in survival. This main conclusion of the Swiss HIV Cohort Study has also been reported by other hospital-based studies in Europe [10,14]. HIV-positive Africans in London presented later than non-Africans and had similar progression rates to AIDS and death  and the EuroSIDA Study Group found that AIDS was diagnosed at the same level of immunodeficiency for subjects of European and non-European origin, with no differences in the level of CD4 cell count at which treatment was initiated, or in survival . Similar results were obtained repeating analyses using the variable ethnic group instead of area of origin .
Staehelin et al.  raise concerns about the lack of ethnicity data in the Swiss Cohort, which may have lead to misclassification. This underscores the importance of understanding and clarifying the terminology used . At present, substantial heterogeneity exists across Europe in the definition of ‘migrants’ and time at which migrants become, or may be considered to be, ethnic minorities. Nevertheless, no matter how unscientific these classifications may be, they provide a rough tool to capture and measure the reality of racism and discrimination within our societies [16,17]. In the United States, where racial/ethnicity data have historically been collected, there is clear evidence of racial/ethnic disparities in the use of antiretroviral drugs and prophylaxis for opportunistic infections [18–20]. Monitoring racial/ethnic discrimination requires variables that help to classify populations, and how best to do so is an area of intense debate [1,7,15–17,21,22]. This is particularly an issue in Europe, where data on race/ethnicity have not been collected historically. Parallel efforts should also be made to measure contextual variables, conduct multilevel analyses and to explore how belonging to an ethnic minority affects health outcomes in the presence of different macroeconomic and social determinants. Since the integration of migrants in health services is a reflection of their integration in society, the variables ‘migrant’ or ‘ethnic group’ may have different prognostic value in different settings.
So what are the implications for HIV prevention and control among migrants in Europe? HAART is making inequality in HIV care more visible even in countries with free and universal access to antiretroviral drugs [20,23,24]. Health-care interventions alone cannot be expected to eradicate the racial/ethnic differences in access to health and health outcomes. Continued efforts are required to improve understanding of the health experiences of migrants and ways in which prevention policies may be best tailored to suit diverse and often conflicting needs. The data confirm that more concerted approaches need to be adopted for ensuring the health and well-being of migrant populations. Strengthening liaisons between HIV clinical care settings, surveillance networks, researchers and communities is the best way to achieve common goals.
1. Bhopal R. Is research into ethnicity and health racist, unsound, or important science? BMJ
2. Editorial. Style matters: ethnicity, race, and culture: guidelines for research, audit, and publication. BMJ
3. Harding S. Social mobility and self-reported limiting long-term illness among West Indian and South Asian migrants living in England and Wales. Soc Sci Med
4. Sundquist J. Migration, equality and access to health care services. J Epidemiol Community Health
5. Davey Smith G. Learning to live with complexity: ethnicity, socioeconomic position, and health in Britain and the United States. Am J Public Health
6. Staehelin C, Rickenbach M, Low N, Egger M, Ledergerber B, Hirschel B, et al. Migrants from Sub-Saharan Africa in the Swiss Cohort Study: access to antiretroviral therapy disease progression and survival. AIDS
7. Del Amo J, Erwin J, Fenton K, Gray K for AIDS&Mobility. Looking to the Future. Migration and HIV/AIDS in Europe: Recent Developments and Needs for Future Action.
Woerden: Netherlands Institute for Health Promotion and Disease Prevention; October 2001 http://www.aidsmobility.org/future.html.
8. Fenton KA, Chinouya M, Davidson O, Copas A for the MAYISHA Study Team. HIV testing and high risk sexual behaviour among London's migrant African communities: a participatory research study. Sex Transm Infect
9. Hamers FF, Alix J, Downs AM. HIV among migrant populations in Europe.
In XIV International Conference on AIDS
. Barcelona, July 2002. [abstract WePpC2099].
10. del Amo J, Petruckevitch A, Phillips AN, Johnson AM, Stephenson J, Desmond N, et al. Disease progression and survival in HIV-1-infected Africans in London. AIDS
11. Burns FM, Fakoya AO, Copas AJ, French PD. Africans in London continue to present with advanced HIV disease in the era of highly active antiretroviral therapy. AIDS
12. Clarke K, Bröring G (eds). HIV/AIDS Care and Support for Migrant and Ethnic Minority Communities in Europe.
Woerden: Netherlands Institute for Health Promotion and Disease Prevention; February 2000. http://www.aidsmobility.org/am5a1.htm.
14. Blaxhult A, Mocroft A, Phillips A, van Lunzen J, Bentwich Z, Stergiou G, et al. Does European or non-European origin influence health care and prognosis for HIV patients in Europe? The EuroSIDA Study Group. HIV Med
15. Oppenheimer GM. Paradigm lost: race, ethnicity, and the search for a new population taxonomy. Am J Public Health
16. Krieger N. Counting accountably: implications of the new approaches to classifying race/ethnicity in the 2000 census. Am J Public Health
17. Jones C. Invited commentary: ‘race,’ racism, and the practice of epidemiology. Am J Epidemiol
:299–304 [discussion 305–306].
18. Fiscella K, Franks P, Gold MR, Clancy CM. Inequalities in racial access to health care. JAMA
19. Smith DK, Gwinn M, Selik RM, Miller KS, Dean-Gaitor H, Ma'at PI, et al. HIV/AIDS among African Americans: progress or progression? AIDS
20. Palacio H, Kahn JG, Richards TA, Morin SF. Effect of race and/or ethnicity in use of antiretrovirals and prophylaxis for opportunistic infection: a review of the literature. Public Health Rep
21. Fenton KA, Johnson AM, Nicoll A. Race, ethnicity and sexual health. BMJ
22. Bhopal R, Donaldson L. White, European, Western, Caucasian, or what? Inappropriate labeling in research on race, ethnicity, and health. Am J Public Health
23. Dray-Spira R, Lert F. Social health inequalities during the course of chronic HIV disease in the era of highly active antiretroviral therapy. AIDS
24. Cooper H. Investigating socio-economic explanations for gender and ethnic inequalities in health. Soc Sci Med
HIV; migrant Africans; Europe; health care; ethnicity
© 2003 Lippincott Williams & Wilkins, Inc.
What does "Remember me" mean?
By checking this box, you'll stay logged in until you logout. You'll get easier access to your articles, collections,
media, and all your other content, even if you close your browser or shut down your
To protect your most sensitive data and activities (like changing your password),
we'll ask you to re-enter your password when you access these services.
What if I'm on a computer that I share with others?
If you're using a public computer or you share this computer with others, we recommend
that you uncheck the "Remember me" box.
Highlight selected keywords in the article text.
Data is temporarily unavailable. Please try again soon.