Disease progression in a cohort of infants with vertically acquired HIV infection observed from birth: The women and infants transmission study (WITS)

被引:37
作者
Diaz, C
Hanson, C
Cooper, ER
Read, JS
Watson, J
Mendez, HA
Pitt, J
Rich, K
Smeriglio, V
Lew, JF
机构
[1] Univ Puerto Rico, Sch Med, Dept Pediat, San Juan, PR 00936 USA
[2] Baylor Coll Med, Houston, TX 77030 USA
[3] Boston Univ, Sch Med, Boston, MA 02118 USA
[4] NICHHD, Pediat Adolescent & Maternal AIDS Branch, Bethesda, MD 20892 USA
[5] New England Res Inst, Watertown, MA 02172 USA
[6] SUNY Hlth Sci Ctr, Brooklyn, NY 11203 USA
[7] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
[8] Univ Illinois, Chicago, IL USA
[9] NIDA, Rockville, MD USA
[10] NIAID, Div Aids, Bethesda, MD 20892 USA
来源
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY | 1998年 / 18卷 / 03期
关键词
predictors; disease progression; infants; vertically acquired HIV; pediatric HIV;
D O I
10.1097/00042560-199807010-00004
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: The Women and Infants Transmission Study is an ongoing prospective cohort study of HIV-infected pregnant women and their infants. We used the 1994 U.S. Centers for Disease Control and Prevention (CDC) classification system for HIV infection in children to describe HIV disease progression in 128 HIV-infected children, and examined maternal and infant characteristics associated with disease course. Methods: The Kaplan-Meier method was used to calculate probabilities of entry into CDC clinical classes A, B, and C (mild, moderate, and severe HIV disease); CDC immunologic stages 2 and 3; and death. Relative risks of progression for selected predictor events were estimated using the Cox proportional hazards model. Results: With a median 24 months of follow-up, the median ages at entry into clinical classes A, B and C were 5, 11, and 48 months, respectively. Increased risk of progression to class C was seen in infants who had: onset of class B events (p < .001); progression to immunologic stage 2 (p < .001) or 3 (p < .001); early culture positivity tin first 48 hours, p < .01; in first 7 days, p = .03); and early appearance (within the first 3 months of life) of lymphadenopathy, hepatomegaly, or splenomegaly (p < .001). Conclusions: Reaching specific clinical or immunologic stages were strong predictors of progression to AIDS or death. Early onset of clinical signs (onset of lymphadenopathy, hepatomegaly, or splenomegaly less than or equal to 3 months of age), and early culture positivity (within the first 48 hours or within the first week of life); defined the infant with highest risk of disease progression.
引用
收藏
页码:221 / 228
页数:8
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