Effect of tuberculosis-HIV co-treatment on clinical and growth outcomes among hospitalized children newly initiating antiretroviral therapy

被引:0
|
作者
Cherkos, Ashenafi S. [1 ,12 ]
Cranmer, Lisa M. [3 ,4 ,5 ]
Njuguna, Irene [6 ,7 ]
LaCourse, Sylvia M. [2 ,6 ,8 ]
Mugo, Cyrus [2 ]
Moraa, Hellen [9 ]
Maleche-Obimbo, Elizabeth [9 ]
Enquobahrie, Daniel A. [2 ]
Richardson, Barbra A. [6 ,10 ]
Wamalwa, Dalton [9 ]
John-Stewart, Grace [2 ,6 ,7 ,11 ]
机构
[1] Univ North Texas, Hlth Sci Ctr, Sch Publ Hlth, Dept Populat & Community Hlth, Ft Worth, TX 76107 USA
[2] Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA USA
[3] Emory Sch Med, Dept Pediat, Atlanta, GA USA
[4] Emory Rollins Sch Publ Hlth, Dept Epidemiol, Atlanta, GA USA
[5] Childrens Healthcare Atlanta, Atlanta, GA USA
[6] Univ Washington, Sch Publ Hlth, Dept Global Hlth, Seattle, WA USA
[7] Kenyatta Natl Hosp, Med Res Dept, Nairobi, Kenya
[8] Univ Washington, Dept Med, Div Allergy & Infect Dis, Seattle, WA USA
[9] Univ Nairobi, Dept Pediat & Child Hlth, Nairobi, Kenya
[10] Univ Washington, Sch Publ Hlth, Dept Biostat, Seattle, WA USA
[11] Univ Washington, Dept Pediat, Seattle, WA USA
[12] Univ North Texas, Hlth Sci Ctr Ft Worth, Sch Publ Hlth, Biostat & Epidemiol Dept, 3500 Camp Bowie Blvd, Ft Worth, TX 76107 USA
基金
美国国家卫生研究院;
关键词
TB-HIV cotreatment; TB-HIV cotreatment and immune reconstitution; TB-HIV cotreatment and viral load suppression; TB-HIV treatment and clinical prognosis; TB-HIV cotreatment and growth in children; UNINFECTED CHILDREN; MORTALITY; CHILDHOOD; MANAGEMENT; MORBIDITY; INFECTION; IMPACT; DRUGS;
D O I
10.1097/QAD.0000000000003797
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
<bold>Objective: </bold>Evaluate effects of tuberculosis (TB)-HIV co-treatment on clinical and growth outcomes in children with HIV (CHIV). <bold>Design: </bold>Longitudinal study among Kenyan hospitalized ART-naive CHIV in the PUSH trial (NCT02063880). <bold>Methods: </bold>CHIV started ART within 2 weeks of enrollment; Anti-TB therapy was initiated based on clinical and TB diagnostics. Children were followed for 6 months with serial viral load, CD4%, and growth assessments [weight-for-age z -score (WAZ), height-for-age z -score (HAZ), and weight-for-height z -score (WHZ)]. TB-ART treated and ART-only groups were compared at 6 months post-ART for undetectable viral load (<40 c/ml), CD4% change, and growth using generalized linear models, linear regression, and linear mixed-effects models, respectively. <bold>Result: </bold>Among 152 CHIV, 40.8% (62) were TB-ART treated. Pre-ART, median age was 2.0 years and growth was significantly lower, and viral load significantly higher in the TB-ART versus ART-only group. After 6 months on ART, 37.2% of CHIV had undetectable viral load and median CD4% increased by 7.2% (IQR 2.0-11.6%) with no difference between groups. The TB-ART group had lower WAZ and HAZ over 6 month follow-up [WAZ -0.81 (95% CI: -1.23 to -0.38], P < 0.001; HAZ -0.15 (95% CI: -0.29 to -0.01), P = 0.030] and greater rate of WAZ increase in analyses unadjusted and adjusted for baseline WAZ [unadjusted 0.62 (95% CI: 0.18-1.07, P = 0.006) or adjusted 0.58 (95% CI: 0.12-1.03, P = 0.013)]. <bold>Conclusion: </bold>TB-HIV co-treatment did not adversely affect early viral suppression and CD4 (+) recovery post-ART. TB-ART-treated CHIV had more rapid growth reconstitution, but growth deficits persisted, suggesting need for continued growth monitoring.
引用
收藏
页码:579 / 588
页数:10
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