Impact of highly active antiretroviral therapy on the morbidity and mortality in Spanish human immunodeficiency virus-infected children

被引:75
作者
Granados, JMS
Amador, JTR
De Miguel, SF
Tomé, MIG
Conejo, PR
Vivas, PF
Pollán, JC
Contreras, JR
Espert, AN
机构
[1] Univ Complutense, Sect Immunodeficiencies, Doce Octobre Hosp, Div Immunodeficiencies, Madrid 28041, Spain
[2] Univ Complutense, Clin Epidemiol Unit, Doce Octobre Hosp, Madrid 28041, Spain
[3] Univ Complutense, Dept Pediat, Doce Octobre Hosp, Madrid 28041, Spain
关键词
highly active antiretroviral therapy; human immunodeficiency virus; acquired immunodeficiency syndrome; children; survival; infections; organ-specific complications; lymphoid interstitial pneumonia;
D O I
10.1097/01.inf.0000091282.70253.5f
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Highly active antiretroviral therapy (HAART) slows the progression of HIV disease and lowers mortality and morbidity in adults. The impact on the disease course in children has not been still completely elucidated. Furthermore the effect of HAART on organ-specific complications of HIV is unknown. Objectives. To assess the effect of HAART on the progression of HIV infection, mortality, organ-specific complications, number of infections and hospitalizations in HIV-1-infected children. Patients and methods. Records of HIV-1-infected children were reviewed in a large referral pediatric hospital. Patients were divided into three groups: children who did not receive antiretroviral therapy (Group 1); children who received mono- or bitherapy (Group 2); and patients who received HAART (Group 3). Endpoints analyzed were progression to AIDS and mortality among AIDS patients and overall. Results. One hundred seven children have been evaluated. Actuarial survival at 5 years of age was 33% in Groups 1 and 2 compared with 100% in Group 3 (P < 0.01). At 5 years of age, the proportion of children progressing to AIDS was 76% in Groups 1 and 2, compared with 26% in Group 3 (P < 0.01). At 5 years of follow-up, there were 45 cases of organ-specific complications in patients without HAART. No children without organ-specific complications when HAART was started have developed them after 5 years (P < 0.01). In patients without HAART there were 9 cases of lymphoid interstitial pneumonia, and there was none in Group 3 (P < 0.01). The incidence rates of infections and hospitalizations were 2.83 and 0.52 per patient-year, respectively, in children who did not receive HAART and 0.75 and 0.17 when they were managed with HAART (relative risk, 0.26 and 0.32). Conclusions. HAART is associated with a marked decline in the progression to AIDS, improved survival in HIV-1-infected children, reduced incidence of infections and hospitalizations and decreased incidence of some organ-specific complications of HIV.
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页码:863 / 867
页数:5
相关论文
共 18 条
[1]  
[Anonymous], 1994, MMWR Recomm Rep, V43, P1
[2]  
Barnhart HX, 1996, PEDIATRICS, V97, P710
[3]   Morbidity and mortality in European children vertically infected by HIV-1 - The French pediatric HIV infection study group and European collaborative study [J].
Blanche, S ;
Newell, ML ;
Mayaux, MJ ;
Dunn, DT ;
Teglas, JP ;
Rouzioux, C ;
Peckham, CS .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 1997, 14 (05) :442-450
[4]   Decreased needs for hospital care and antibiotics in children with advanced HIV-1 disease after protease inhibitor-containing combination therapy [J].
Canani, RB ;
Spagnuolo, MI ;
Cirillo, P ;
Guarino, A .
AIDS, 1999, 13 (08) :1005-1006
[5]   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
[6]  
GIBB A, 2002, 14 INT AIDS C BARC J
[7]   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
[8]  
Gray L, 2001, PEDIATRICS, V108, P116, DOI 10.1542/peds.108.1.116
[9]   A controlled trial of two nucleoside analogues plus indinavir in persons with human immunodeficiency virus infection and CD4 cell counts of 200 per cubic millimeter or less [J].
Hammer, SM ;
Squires, KE ;
Hughes, MD ;
Grimes, JM ;
Demeter, LM ;
Currier, JS ;
Eron, JJ ;
Feinberg, JE ;
Balfour, HH ;
Dayton, LR ;
Chodakewitz, JA ;
Fischl, MA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (11) :725-733
[10]  
Indacochea F J, 1992, Curr Probl Pediatr, V22, P166, DOI 10.1016/0045-9380(92)90018-T