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Editorial

Bridging the divide: global inequities in access to HIV/AIDS therapy

Australia should take a greater role in reducing the global burden of HIV/AIDS

MJA 2001; 175: 570-572
 

Our recent visit to HIV/AIDS hospital units in Phnom Penh, Cambodia, sharply delineated the contrasting capacity to respond to HIV/AIDS in First World countries, such as Australia, and resource-poor countries. Common to both settings is the relatively young age of those affected, the close attention of loved ones and the dedication of healthcare workers. The contrasts lie in the enormous gaps in quality of healthcare facilities and access to effective HIV treatments. HIV/AIDS may be only one of several major public health issues for these countries, but, probably more than any other issue, it highlights global resource inequities.

Over the past decade, Australia has been at the forefront of advances in HIV treatment,1-4 which have provided optimism for many people living with HIV/AIDS. Combination antiretroviral therapy is one of the most cost-effective therapies for a chronic disease in the developed world,5 and most First World countries provide ready access to combination antiretroviral therapy through publicly funded programs. However, 90% of the estimated 36 million people living with HIV/AIDS are in resource-poor countries,6 where access to new HIV treatments is extremely limited: an estimated 0.5% of the global market for antiretroviral therapy is sold in the poorest third of the world.7

Indeed, most people with HIV in resource-poor countries experience inexorable decline in immune function leading to death, just as people in First World countries did before the mid-1990s. If the challenge of the past decade was to develop therapeutic agents to control HIV infection, then the even greater challenge of the current decade is to provide access to effective HIV treatments for people in resource-poor countries. The political commitment to achieve this is growing. Earlier this year, a Declaration of Commitment was signed at the United Nations General Assembly Special Session (UNGASS) on HIV/AIDS in New York. This Declaration recognised that "access to medication in the context of pandemics such as HIV/AIDS is one of the fundamental elements to achieve progressively the full realisation of the right of everyone to the enjoyment of the highest attainable standard of physical and mental health".8

The Declaration also set a resource target of US$7-$10 billion per year for HIV/AIDS prevention, care and support initiatives, to be reached by 2005.8 However, expanding access to effective HIV treatments also depends on other factors.

Affordability of antiretroviral therapy: Recent endeavours to reduce the price of antiretroviral therapy for resource-poor countries need to be continued. Affordability can be improved through tiered pricing systems (maintaining current pricing levels in industrialised countries to subsidise lower pricing in resource-poor countries), further development of generic production, and use of compulsory licences and other health safeguards of the Agreement on Trade-Related Aspects of Intellectual Property Rights from the World Trade Organization.7 Within these measures, pharmaceutical industry profitability needs to be maintained at reasonable levels to enable continued research and development.

Current pricing of some triple combination regimens should make potent antiretroviral therapy cost-effective for many middle-income countries. For example, stavudine-lamivudine-nevirapine, as produced by Cipla, an Indian-based generic producer, sells for A$700 per year, or about 5% of standard pharmaceutical industry pricing. In Brazil, a generic drug program established by the government was followed by 80% price reductions for several component agents of antiretroviral therapy,9 enabling universal access to antiretroviral therapy.

Although encouraging, these price reductions are not enough for most resource-poor countries, where annual health budgets are often less than $20 per capita.7 Further, while implementation of antiretroviral therapy is being scaled up, it is realistic to expect that only a minority of people living with HIV/AIDS can be treated. This will necessitate difficult decisions about selecting patients for antiretroviral therapy, which might take into account social criteria (eg, family support and employment status) in addition to biological criteria (eg, symptomatic patients only to be treated).

Therapy delivery and monitoring: Simply making antiretroviral therapy "available" is not the whole solution and may be counterproductive.10 Inappropriate antiretroviral therapy use may lead to viral resistance and considerable drug toxicity. Healthcare systems must therefore be developed to deliver and monitor HIV treatments effectively. However, implementation of antiretroviral therapy programs cannot wait for the optimal conditions that exist in industrialised countries. Therapy programs and infrastructure should be scaled up concurrently. Education and training of healthcare workers in antiretroviral therapy and more broadly in clinical management of HIV/AIDS will also be required.

Antiretroviral therapy needs to be provided within an integrated system of HIV/AIDS treatment, care and support services. This may be helped by closer collaboration between HIV/AIDS and tuberculosis programs, which have been proposed as a platform for antiretroviral therapy implementation.11 Tuberculosis programs are the clinical entry point for many people with HIV/AIDS, as tuberculosis is the most common AIDS-related illness in resource-poor countries,12 and also have experience in delivering combination pharmacotherapy in resource-poor settings. Establishing referral networks between hospital-based and home- and community-based HIV/AIDS care programs will also improve delivery of a comprehensive package of treatment, care and support.

Earlier diagnosis: In resource-poor countries, people with HIV/AIDS generally present with very advanced AIDS-related illness or die before presentation. Although antiretroviral therapy is still effective when commenced late in HIV disease, earlier HIV diagnosis would allow HIV preventive education and other HIV treatments, such as prophylaxis against common opportunistic infections, to be delivered. To achieve earlier diagnosis, rapid scale-up of voluntary HIV counselling and testing services is needed, including routine offering of HIV testing in antenatal clinics in settings with relatively high HIV prevalence. The latter would provide the foundations for preventing mother-to-child transmission and introducing treatment and care strategies, including antiretroviral therapy, earlier to many women with HIV/AIDS.

Research on implementing antiretroviral therapy: Priorities should include evaluating pilot antiretroviral therapy programs in resource-poor settings, searching for more cost-effective means of monitoring therapy, and developing simpler therapeutic regimens (preferably, once-daily dosing) to enhance adherence. An example of Australia's contribution to the regional HIV/AIDS response is the HIV Netherlands-Australia-Thailand Collaboration, which has conducted HIV therapeutic research in Thailand since 1996.12 Australia now has the opportunity to contribute to HIV/AIDS research and care in countries such as Cambodia, where the burden of HIV/AIDS is increasingly being felt (Box).

HIV prevention: Finally, if the UNGASS commitment to reverse the spread of HIV/AIDS by 20157 is to succeed, a heightened response is required to HIV/AIDS prevention as well as care. Both arms need increased priority and allocation of resources. They also need close interlinking in a broadly based response at national and community levels. However, implementing antiretroviral therapy may enhance HIV prevention through increased incentive for HIV testing accompanied by HIV preventive education.

If the HIV/AIDS treatment divide between industrialised and resource-poor countries is to be bridged, we urgently need Australian research, medical, and educational institutions to become more involved, and public and private sector funding to be enhanced.

Gregory J Dore
Senior Lecturer, National Centre in HIV Epidemiology and Clinical Research
University of New South Wales; and Infectious Diseases Physician
HIV/Immunology/Infectious Diseases Clinical Services Unit
St Vincent's Hospital, Sydney, NSW
gdoreATnchecr.unsw.edu.au

David A Cooper
Professor, National Centre in HIV Epidemiology and Clinical Research
University of New South Wales; and Director
HIV/Immunology/Infectious Diseases Clinical Services Unit
St Vincent's Hospital, Sydney, NSW


Acknowledgements

We would like to thank Professor John Kaldor and Dr Sean Emery (National Centre in HIV Epidemiology and Clinical Research, University of New South Wales) for their helpful comments on an earlier draft of this article.


References

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  2. CAESAR Coordinating Committee. Randomised trial of addition of lamivudine or lamivudine plus loviride to zidovudine-containing regimens for patients with HIV-1 infection: the CAESAR trial. Lancet 1997; 349: 1413-1421.
  3. Montaner JS, Reiss P, Cooper D, et al. A randomized, double-blind trial comparing combinations of nevirapine, didanosine, and zidovudine for HIV-infected patients: the INCAS Trial. Italy, The Netherlands, Canada, and Australia Study. JAMA 1998; 279: 930-937.
  4. Danner SA, Carr A, Leonard JM, et al. A short-term study of the safety, pharmacokinetics, and efficacy of ritonavir, an inhibitor of HIV-1 protease. European-Australian Collaborative Ritonavir Study Group. N Engl J Med 1995; 333: 1528-1533.
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  8. Declaration of Commitment on HIV/AIDS: "Global crisis - global action. <www.un.org/ga/aids/coverage/FinalDeclarationHIVAIDS.html> Accessed, Sep 2001.
  9. Gottlieb S. US concedes on cheaper drug production in Brazil. BMJ 2001; 323: 12.
  10. Horton R. African AIDS beyond Mbeki: tripping into anarchy. Lancet 2000; 356: 1541-1542.
  11. Harries AD, Nyangulu DS, Hargreaves NJ, et al. Preventing antiretroviral anarchy in sub-Saharan Africa. Lancet 2001; 358: 410-414.
  12. Grant AD, Djomand G, De Cock KM. Natural history and spectrum of disease in adults with HIV/AIDS in Africa. AIDS 1997; 11 Suppl B: S43-S54.
  13. Kroon ED, Ungsedhapand C, Ruxrungtham, et al. A randomized, double-blind trial of half versus standard dose of zidovudine plus zalcitabine in Thai HIV-1-infected patients (study HIV-NAT 001). HIV Netherlands Australia Thailand Research Collaboration. AIDS 2000; 14: 1349-1356.
  14. National Centre in HIV Epidemiology and Clinical Research. HIV/AIDS, viral hepatitis and sexually transmissible infections in Australia. Annual surveillance report 2001. Sydney: National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, 2001.
  15. World Health Organization, Western Pacific Region. STD/HIV/AIDS surveillance report, no. 10. Manila: WHO, October 1997.

©MJA 2001
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Australia14 (based on AIDS notifications; total population, 18 million). Cambodia15 (based on an estimated and projected AIDS incidence; total population, 11 million).

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