Effects of concurrent exposure to antiretrovirals and cotrimoxazole prophylaxis among HIV-exposed, uninfected infants

被引:4
作者
Ewing, Alexander C. [1 ]
King, Caroline C. [1 ]
Wiener, Jeffrey B. [1 ]
Chasela, Charles S. [2 ]
Hudgens, Michael G. [3 ]
Kamwendo, Debbie [4 ]
Tegha, Gerald [4 ]
Hosseinipour, Mina C. [3 ]
Jamieson, Denise J. [1 ]
Van der Horst, Charles [3 ]
Kourtis, Athena P. [1 ]
机构
[1] Ctr Dis Control & Prevent, Atlanta, GA USA
[2] Univ Witwatersrand, Dept Epidemiol & Biostat, Sch Publ Hlth, Johannesburg, South Africa
[3] Univ N Carolina, Chapel Hill, NC USA
[4] UNC Project, Lilongwe, Malawi
基金
美国国家卫生研究院;
关键词
anemia; antiretrovirals; BAN; breastfeeding; cotrimoxazole; hematologic toxicities; HIV-exposed uninfected; infants; malaria; neutropenia; YOUNG-CHILDREN; SEVERE ANEMIA; OPPORTUNISTIC INFECTIONS; COTE-DIVOIRE; RISK-FACTORS; TRANSMISSION; MALARIA; TRIAL; PARAMETERS; THERAPY;
D O I
10.1097/QAD.0000000000001641
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: Given the potential of cotrimoxazole preventive therapy (CPT) to prevent bacterial and malarial infections in HIV-exposed, uninfected (HEU) infants, it is important to evaluate the effects of its concurrent use with antiretroviral agents that have overlapping toxicity profiles. Methods: We used data from the Breastfeeding, Antiretrovirals, and Nutrition study (2004-2010) to evaluate the association of CPT and antiretrovirals with hematologic measures (hemoglobin, neutrophil, and alanine aminotransferase levels) from 6 to 48 weeks of age in 2006 HEU infants in Lilongwe, Malawi. Hazards of severe outcomes (anemia, neutropenia, and elevated alanine aminotransferase), as defined by the National Institutes of Health, were compared using Cox regression models, according to time-varying CPT (implemented June 2006), antiretroviral treatment arm (maternal triple antiretroviral, infant nevirapine, or none during 6 months of breastfeeding), and their interaction. The effects of these treatments on hemoglobin, neutrophil, and alanine aminotransferase levels were assessed using linear mixed models. Results: In Cox models, CPT was associated with an increase in severe neutropenia [hazard ratio 1.97 (1.01, 3.86)] and a decrease in severe anemia (hazard ratio 0.65 (0.48, 0.88)]. Interactions between CPT and antiretroviral treatment were not significant. By 36 weeks, there was a significant association of CPT with increased hemoglobin levels regardless of antiretroviral drug exposure. Conclusions: In addition to expected associations with increased hazard of severe neutropenia and decreased neutrophil count, CPT was associated with reduced hazard of severe anemia and higher infant blood hemoglobin. This provides further support for CPT use in HEU infants in malaria-endemic resource-limited settings where anemia is prevalent. Copyright (C) 2017 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:2455 / 2463
页数:9
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