When to initiate antiretroviral therapy in HIV-infected children?

被引:2
作者
Thuret, I [1 ]
机构
[1] Hop Enfants La Timone, Serv Hematol Pediat, F-13005 Marseille, France
来源
ARCHIVES DE PEDIATRIE | 2004年 / 11卷 / 12期
关键词
antiretroviral therapy; HIV infection; children; infants;
D O I
10.1016/j.arcped.2004.01.019
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Administration of highly active antiretroviral treatment (HAART) has led in the developed world to a dramatic reduction in the incidence of HIV related pediatric mortality. HAART is now the standard-of-care therapy in infected children but the occurrence of short- and long-term drug-related toxic effects and emergence of drug-resistant viral variants temper its success. In children, both CD4 cell percent and viral load have independent predictive value for disease progression, CD4 cell being the stronger predictor of AIDS and death. Concerning children aged 12 months or older current French recommendations for immediate therapy are based on the presence of clinical symptoms (of categories B or C) or the occurrence of a severe immunodeficiency (CD4 cell percent <15%). In infants, risk of disease progression is higher and the viral load and CD4 percent are less reliable markers. HAART should theoretically be initiated in all infants in order to prevent HIV encephalopathy and early death. However, viral failure under HAART is often encountered in children less than 12 months because of high levels of replication as well as limited data on pharmacokinetics and drug dosing. A possible alternative approach for infants without risk factor for early progression is to defer HAART under close monitoring. (C) 2004 Elsevier SAS. Tous droits reserves.
引用
收藏
页码:1521 / 1524
页数:4
相关论文
共 11 条
[1]   Maternal health factors and early pediatric antiretroviral therapy influence the rate of perinatal HIV-1 disease progression in children [J].
Abrams, EJ ;
Wiener, J ;
Carter, R ;
Kuhn, L ;
Palumbo, P ;
Nesheim, S ;
Lee, F ;
Vink, P ;
Bulterys, M .
AIDS, 2003, 17 (06) :867-877
[2]   Reduction in mortality with availability of antiretroviral therapy for children with perinatal HIV-1 infection [J].
de Martino, M ;
Tovo, PA ;
Balducci, M ;
Galli, L ;
Gabiano, C ;
Rezza, G ;
Pezzotti, P .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 284 (02) :190-197
[3]  
Dunn DT, 2003, LANCET, V362, P1605, DOI 10.1016/S0140-6736(03)14793-9
[4]  
FAYE A, UNPUB EARLY VERSUS D
[5]   Effect of combination therapy including protease inhibitors on mortality among children and adolescents infected with HIV-1 [J].
Gortmaker, SL ;
Hughes, M ;
Cervia, J ;
Brady, M ;
Johnson, GM ;
Seage, GR ;
Song, LY ;
Dankner, WM ;
Oleske, JM .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (21) :1522-1528
[6]  
*MED SCI FLAMM, 2002, PRIS CHARG PERS INF
[7]   The relationship between serum human immunodeficiency virus type 1 (HIV-1) RNA level, CD4 lymphocyte percent, and long-term mortality risk in HIV-1-infected children [J].
Mofenson, LM ;
Korelitz, J ;
Meyer, WA ;
Bethel, J ;
Rich, K ;
Pahwa, S ;
Moye, J ;
Nugent, R ;
Read, J .
JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (05) :1029-1038
[8]   Immunoreconstitution in children receiving highly active antiretroviral therapy depends on the CD4 cell percentage at baseline [J].
Nikolic-Djokic, D ;
Essajee, S ;
Rigaud, M ;
Kaul, A ;
Chandwani, S ;
Hoover, W ;
Lawrence, R ;
Pollack, H ;
Sitnitskaya, Y ;
Hagmann, S ;
Jean-Philippe, P ;
Chen, SH ;
Radding, J ;
Krasinski, K ;
Borkowsky, W .
JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (03) :290-298
[9]   Predictive value of quantitative plasma HIV RNA and CD4+ lymphocyte count in HIV-infected infants and children [J].
Palumbo, PE ;
Raskino, C ;
Fiscus, S ;
Pahwa, S ;
Fowler, MG ;
Spector, SA ;
Englund, JA ;
Baker, CJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 279 (10) :756-761
[10]   Long-term effects of protease-inhibitor-based combination therapy on CD4 T-cell recovery in HIV-1-infected children and adolescents [J].
Soh, CH ;
Oleske, JM ;
Brady, MT ;
Spector, SA ;
Borkowsky, W ;
Burchett, SK ;
Foca, MD ;
Handelsman, E ;
Jiménez, E ;
Dankner, WM ;
Hughes, MD .
LANCET, 2003, 362 (9401) :2045-2051