Extensively drug-resistant tuberculosis in children with human immunodeficiency virus in rural South Africa

被引:0
|
作者
Thomas, T. A. [2 ,3 ,4 ]
Shenoi, S. V. [2 ,5 ]
Heysell, S. K. [2 ,3 ,4 ]
Eksteen, F. J. [2 ,6 ,7 ]
Sunkari, V. B. [8 ]
Gandhi, N. R. [2 ]
Friedland, G. [2 ,5 ]
Shah, N. S. [1 ,2 ]
机构
[1] Albert Einstein Coll Med, Div Gen Internal Med, Dept Med, Bronx, NY 10467 USA
[2] Tugela Ferry, Tugela Ferry Care & Res Collaborat, Kwa Zulu, South Africa
[3] Yale Univ, Sch Med, Dept Med, New Haven, CT 06510 USA
[4] Univ Virginia, Div Infect Dis & Int Hlth, Charlottesville, VA USA
[5] Yale Univ, Sch Med, Infect Dis Sect, AIDS Program, New Haven, CT 06510 USA
[6] Tugela Ferry, Church Scotland Hosp, Kwa Zulu, South Africa
[7] Tugela Ferry, Philanjalo Care Ctr, Kwa Zulu, South Africa
[8] King George V Mem Hosp, Dept Paediat, Durban, South Africa
基金
美国国家卫生研究院;
关键词
extensively drug-resistant tuberculosis; drug-resistant tuberculosis; tuberculosis; pediatrics; HIV/TB; co-infection; MULTIDRUG-RESISTANT; NOSOCOMIAL TRANSMISSION; OUTBREAK; COMMUNITY; COHORT; SCHOOL;
D O I
暂无
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
SETTING: Extensively drug-resistant tuberculosis (XDR-TB) has been documented worldwide, but reports of XDR-TB in children arc extremely limited. OBJECTIVE: To report the characteristics of pediatric XDR-TB patients in rural South Africa. DESIGN: We retrospectively reviewed children with sputum culture-confirmed XDR-TB from Tugela Ferry, South Africa, from January 2006 to December 2007. Demographic, clinical and microbiologic data were abstracted from medical records. RESULTS: Four children aged 6-8 years with XDR-TB were reviewed. Two had previous histories of TB. All were human immunodeficiency virus (HIV) infected orphans; three received highly active antiretroviral therapy (HAART) before XDR-TB diagnosis. All had clinical and radiographic improvement and sputum culture conversion while on standardized XDR-TB treatment and HAART. Two tolerated concomitant XDR-TB and HIV treatment well. Two experienced neuropsychiatric side effects related to cycloserine. All have survived >24 months and all were cured. Prior to XDR-TB diagnosis, the children had resided in the hospital's pediatric ward for a median of 8 months (range 5-17), including a 3-month overlapping period. CONCLUSIONS: XDR-TB is a microbiologic diagnosis that, even with HIV co-infection, can be successfully identified. Concurrent XDR-TB and HIV therapy is feasible and effective in children, although more research is needed into potential overlapping toxicities. Nosocomial transmission is suggested, calling for infection control policies in pediatric wards.
引用
收藏
页码:1244 / 1251
页数:8
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