Clinical and laboratory characteristics of a large cohort of symptomatic, human immunodeficiency virus-infected infants and children

被引:51
作者
Englund, JA
Baker, CJ
Raskino, C
McKinney, RE
Lifschitz, MH
Petrie, B
Fowler, MG
Connor, JD
Mendez, H
ODonnell, K
Wara, DW
Shliozberg, J
Shearer, WT
Stechenberg, B
Borkowsky, W
Bonaforte, RJ
Cooper, ER
Wiznia, A
Toltzis, P
Israele, V
VanDyke, RB
Yogev, R
Starr, S
Oleske, F
Frenkel, L
McIntosh, K
Montgomery, M
Petru, A
Squires, JE
Wade, N
Moore, EC
Rakusan, TA
Baker, RC
Brady, MT
Pildes, RS
Cervia, JS
Wilfert, C
Nesheim, S
Bellanti, JA
Keller, M
Abrams, EJ
Dossett, JH
Rana, SR
Tishler, DM
Nicholas, SW
Lambert, JS
Wong, V
Gupta, A
Deveikis, A
Kovacs, A
机构
[1] BAYLOR COLL MED, DEPT PEDIAT, HOUSTON, TX 77030 USA
[2] HARVARD UNIV, SCH PUBL HLTH, DEPT BIOSTAT, BOSTON, MA 02115 USA
[3] DUKE UNIV, SCH MED, DEPT PEDIAT, DURHAM, NC USA
[4] NIAID, BETHESDA, MD 20892 USA
[5] UNIV CALIF SAN DIEGO, DEPT PEDIAT & PHARMACOL, SAN DIEGO, CA 92103 USA
[6] SUNY HLTH SCI CTR, DEPT PEDIAT, BROOKLYN, NY 11203 USA
[7] UNIV CALIF SAN FRANCISCO, DEPT PEDIAT, SAN FRANCISCO, CA 94143 USA
[8] US FDA, KENSINGTON, MD USA
[9] GLAXO WELLCOME INC, RES TRIANGLE PK, NC 27709 USA
[10] BRISTOL MYERS SQUIBB CO, WALLINGFORD, CT 06492 USA
[11] ACTG OPERAT OFF, BETHESDA, MD USA
[12] NICHHD, PEDIAT & ADOLESCENT BRANCH, BETHESDA, MD USA
[13] BRONX LEBANON HOSP CTR, NEW YORK, NY USA
[14] UNIV TEXAS, SCH MED, HOUSTON, TX USA
[15] UNIV MIAMI, SCH MED, MIAMI, FL USA
关键词
acquired immunodeficiency syndrome; human immunodeficiency virus; children; infection; antiretroviral therapy; zidovudine; didanosine; development; cortical atrophy; growth failure;
D O I
10.1097/00006454-199611000-00018
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. A large cohort of antiretroviral therapy-naive, symptomatic, HIV-infected children were enrolled into a controlled therapeutic trial (AIDS Clinical Trials Group Protocol 152), providing an opportunity to describe their clinical and laboratory characteristics and determine age-related distinctions. Methods. Study entry evaluations for 838 of 839 enrolled children were analyzed. Weight, head circumference (if <30 months of age), neuroradiologic imaging of the head, developmental or cognitive status and neurologic examination were assessed. Laboratory studies included hemoglobin, absolute neutrophil count, CD4 cell count, serum amylase, alanine aminotransaminase, p24 antigen and HIV blood culture. Data were categorized by age (3 to <12 months, 12 to <30 months, 30 months to 6 years and greater than or equal to 6 years). Results. Younger children had significantly higher rates of abnormalities before antiretroviral therapy, especially factors relating to growth and neurologic or cognitive function. Lower CD4+ cell counts and percentages as well as a positive serum p24 antigen correlated with lower weight-for-age Z scores and developmental indices. Conclusions. These data provide a description of the clinical characteristics of HIV-infected US children at the time antiretroviral therapy is initiated for HIV-related symptoms. The high rate of abnormalities of growth, development and cognitive ability that were observed in children <30 months of age demonstrates that treatment strategies should be developed for earlier intervention.
引用
收藏
页码:1025 / 1036
页数:12
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