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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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