Effectiveness of Efavirenz-Based Regimens in Young HIV-Infected Children Treated for Tuberculosis: A Treatment Option for Resource-Limited Settings

被引:12
作者
van Dijk, Janneke H. [1 ,2 ]
Sutcliffe, Catherine G. [3 ]
Hamangaba, Francis [1 ]
Bositis, Christopher [4 ]
Watson, Douglas C. [5 ]
Moss, William J. [3 ]
机构
[1] Macha Hosp, Macha Res Trust, Choma, Zambia
[2] Erasmus Univ, Dept Immunol & Infect Dis, Rotterdam, Netherlands
[3] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21218 USA
[4] Greater Lawrence Family Hlth Ctr, Lawrence, MA USA
[5] Univ Maryland, Sch Med, Dept Pediat, Baltimore, MD 21201 USA
关键词
ACTIVE ANTIRETROVIRAL THERAPY; PLASMA-CONCENTRATIONS; INITIAL TREATMENT; HIGH PREVALENCE; NEVIRAPINE; EFFICACY; RIFAMPICIN; PHARMACOKINETICS; LOPINAVIR; SAFETY;
D O I
10.1371/journal.pone.0055111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Antiretroviral treatment (ART) options for young children co-infected with HIV and tuberculosis are limited in resource-poor settings due to limited data on the use of efavirenz (EFV). Using available pharmacokinetic data, an EFV dosing schedule was developed for young co-infected children and implemented as the standard of care at Macha Hospital in Southern Province, Zambia. Treatment outcomes in children younger than 3 years of age or weighing less than 10 kg receiving either EFV-based ART plus anti-tuberculous treatment or nevirapine-based (NVP) ART were compared. Methods: Treatment outcomes were measured in a cohort of HIV-infected children seeking care at Macha Hospital in rural Zambia from 2007 to 2010. Informationon the diagnosis and treatment of tuberculosis was abstracted from medical records. Results: Forty-five children treated for tuberculosis initiated an EFV-based regimen and 69 children initiated a NVP-based regimen, 7 of whom also were treated for tuberculosis. Children receiving both regimens were comparable in age, but children receiving EFV started ART with a lower CD4(+) T-cell percentage and weight-for-age z-score. Children receiving EFV experienced increases in both CD4(+) T-cell percentage and weight-for-age z-score during follow-up, such that levels were comparable to children receiving NVP after two years of ART. Cumulative survival after 12 months of ART did not differ between groups (NVP:87%; EFV:80%; p = 0.25). Eleven children experienced virologic failure during follow-up. The adjusted hazard ratio of virologic failure comparing EFV to NVP was 0.25 (95% CI:0.05,1.24) and 0.13 (95% CI:0.03,0.62) using thresholds of 5000 and 400 copies/mL, respectively. Five children receiving EFV were reported to have had convulsions after ART initiation compared to only one child receiving NVP (p = 0.04). Conclusions: Despite poorer health at ART initiation, children treated for tuberculosis and receiving EFV-based regimens showed significant improvements comparable to children receiving NVP-based regimens. EFV-based regimens should be considered for young HIV-infected children co-infected with tuberculosis in resource-limited settings.
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页数:10
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