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Treatment of HIV-Infected Children

NIAID investigators are defining the best treatments for pediatric patients. Currently there are 16 drug products approved by the FDA for the treatment of adult HIV infection. Through major contributions by the Pediatric ACTG, 10 antiretroviral agents have pediatric label information, including 3 protease inhibitors.28 While the basic principles that guide treatment of pediatric HIV infection are the same as for any HIV-infected person, there are a number of unique scientific and medical concerns that are important to consider in the treatment of children with HIV infection. These range from differences from adults in age-related issues such as CD4 lymphocyte counts and drug metabolism to requirements for special formulations and treatment regimens that are appropriate for infants through adolescents. As in adults, treatment of HIV-infected children today is a complex task of using potent combinations of antiretroviral agents to maximally suppress viral replication.

Researchers supported by NIAID are focusing not only on the development of new antiretroviral products but also on the critical question of how to best use the treatments that are currently available. Treatment strategy questions designed to identify what the best initial therapy is, when failing regimens should be switched and strategies for how to address the antiretroviral needs of children with advanced disease are examples. Long-term assessment of these children is also a high priority to assess sustained antiretroviral benefits as well as to monitor for potential adverse consequences of treatment.

Problems of Families

A mother and child with HIV usually are not the only family members with the disease. Often, the mother's sexual partner is infected, and other children in the family may be infected as well. Frequently, a parent with AIDS does not survive to care for his or her HIV-infected child.

In the countries hardest hit by the AIDS epidemic, some 8.2 million children under 15 around the world have been orphaned by AIDS - 90 percent of them in sub-Saharan Africa alone.31 The rate is expected to increase. One in three of these orphans is under age five.32 Communities and extended families are struggling with and often overwhelmed by the vast number of AIDS orphans. Many orphans and other children from families devastated by AIDS face multiple risks, such as forced relocation, violence, living on the streets, drug use, and even commercial sex. Other children suffer because sex education and services are not available to them or do not communicate effectively to them. Living in a country undergoing political turmoil or where fathers migrate for work can also raise the risk of a child becoming HIV-infected.

In the U.S., most children living with HIV/AIDS live in inner cities, where poverty, illicit drug use, poor housing and limited access to and use of medical care and social services add to the challenges of HIV disease.

One encouraging note is that, according to UNAIDS, where information, training, and services to help prevent HIV infection are made available and affordable to young people, they are more likely to make use of them than their elders are.33

Management of the complex medical and social problems of families affected by HIV requires a multidisciplinary case management team, integrating medical, social, mental health and educational services. NIAID provides special funding to many of its clinical research sites to provide for services, such as transportation, day care, and the expertise of social workers, crucial to families devastated by HIV.

References

1. Connor, E. et al. 1994. Reduction of maternal-infant transmission of human immunodeficiency virus type 1 with zidovudine treatment. N Engl J Med 311:1173-80.
2. UNAIDS. AIDS Epidemic Update (Dec., 1998):1, 2, 3, 7, 8., 9, 17.
3. UNAIDS. Report on the Global HIV/AIDS Epidemic (June, 1998):6, 8.
4. Centers for Disease Control and Prevention. HIV/AIDS Surveillance Report (Dec. 1998) 10(2):7.
5. Ibid., p. 26
6. Rosenberg, P., et al. 1994. Declining age at HIV infection in the United States. N Engl J Med 330:789-90.
7. Centers for Disease Control and Prevention, op cit., p. 36.
8. Ibid., pp. 10-11.
9. UNAIDS, Update, p. 6.
10. Centers for Disease Control and Prevention, op. cit., p. 24.
11. Centers for Disease Control and Prevention. National Center for Health Statistics. 1998. National Vital Statistics Report 47 (9):26.
12. Centers for Disease Control and Prevention, HIV/AIDS Surveillance Report, p. 39.
13. NAIDS, Report.
14. Quinn, T. 1996. Global burden of the HIV pandemic. Lancet:348:99-106.
15. Landesman, S., et al. 1996. Obstetrical factors and the transmission of human immunodeficiency virus type 1 from mother to child. N Engl J Med 334: 1617-23.
16. Monitoring the AIDS Pandemic (MAP) Network. 1998. The status and trends of the HIV/AIDS epidemics in the world:17.
17. UNAIDS, Report, p. 48.
18. Connor, E., et al., op. cit.
19. Stiehm, E., et al. 1999. Efficacy of zidovudine and human immunodeficiency virus (HIV) hyperimmune immunoglobulin for reducing perinatal HIV transmission from HIV-infected women with advanced disease: results of Pedatric ACTG protocol 185. J Infect Dis 179(3):567-75.
20. Centers for Disease Control and Prevention. 1998. Public Health Service Task Force recommendations for the use of antiretroviral drugs in pregnant women infected with HIV-1 for maternal health and for reducing perinatal HIV-1 transmission in the United States. MMWR Recommendations and Reports 47 (RR-2). May be viewed on the Web at http://www.hivatis.org.
21. Wilfert, C., et al. 1999. Consensus statement: Science, ethics, and the future of research into maternal infant transmission of HIV-1. Lancet 353 (9155):832-35.
22. Centers for Disease Control and Prevention. 1997. Update: Perinatally acquired HIV/AIDS-United States, 1997. MMWR 46: 1086-92.
23. Shaffer, N., et al. 1999. Short-course zidovudine for perinatal HIV-1 transmission in Bangkok, Thailand: A randomised controlled trial. Lancet 353 (9155):773-79.
24. Dabis, F. et al. 1999. 6-month efficacy, tolerance, and acceptability of a short regimen of oral zidovudine to reduce vertical transmission of HIV in breastfed children in Cote d'Ivoire and Burkina Faso. Lancet 353 (9155):786-92.
25. Saba, J., The PETRA Trial Study Team. 1999. Interim analysis of early efficacy of three short course ZDV/3TC combination regimens to prevent mother-to-child transmission of HIV-1. Presented at the Sixth Conference on Retroviruses and Opportunistic Infections. Chicago: February 1, 1999.
26. Guay, L, et al. 1999. Intrapartum and neonatal single-dose nevirapine compared with zidovudine for prevention of mother-to-child transmission of HIV-1 in Kampala, Uganda: HIVNET 012 randomised trial. Lancet 354:795-802.
27. Marseille, E., et al. 1999. Cost effectiveness of single-dose nevirapine regimen for mothers and babies to decrease vertical HIV-1 transmission in sub-Saharan Africa. Lancet 654:803-09.
28. Riley, L.E. and Green, M.F. Elective caesarean delivery to reduce the transmission of HIV. 1999. N Engl J Med 340:13, 1032.
29. Mofenson, L.M., Fowler, M.G. In press. Interruption of materno-fetal transmission. Reported in Shaffer, N., op. cit.
30. HIV/AIDS Treatment Information Service. 1999. Guidelines for the use of antiretroviral agents in pediatric HIV infection. May be viewed on the Web at http://www.hivatis.org/.
31. UNAIDS, Report, p. 9.
32. Centers for Disease Control and Prevention. National Center for HIV, STD, and TB Prevention. Divisions of HIV/AIDS. International Projections/Statistics. Web: http://http://www.cdc.gov/hiv/stats/internat.htm
33. UNAIDS, Update, p. 9.

Reprinted with permission from
National Institutes of Allergy and Infectious Diseases
National Institutes of Health
Bethesda, Maryland 20892
www.niaid.nih.gov

NIAID is a component of the National Institutes of Health (NIH). NIAID conducts and supports research to prevent, diagnose and treat illnesses such as HIV disease and other sexually transmitted diseases, tuberculosis, malaria, and other infectious diseases as well as asthma and allergies.


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