Rifampicin-monoresistant Mycobacterium tuberculosis disease among children in Cape Town, South Africa

被引:22
|
作者
Dramowski, A. [1 ]
Morsheimer, M. M. [2 ]
Jordaan, A. M. [3 ]
Victor, T. C. [3 ]
Donald, P. R. [1 ,4 ]
Schaaf, H. S. [1 ,4 ]
机构
[1] Univ Stellenbosch, Tygerberg Childrens Hosp, Dept Paediat & Child Hlth, Cape Town, South Africa
[2] Univ Calif San Francisco, Dept Pediat, San Francisco, CA USA
[3] Univ Stellenbosch, MRC, Natl Res Fdn, Ctr Excellence,Dept Biomed Sci, ZA-7505 Tygerberg, South Africa
[4] Univ Stellenbosch, Desmond Tutu TB Ctr, Cape Town, South Africa
基金
新加坡国家研究基金会; 美国国家卫生研究院;
关键词
TB; HIV; rifampicin; rifampicin monoresistance; drug-resistant TB; DRUG-RESISTANT TUBERCULOSIS; RISK-FACTORS; CHILDHOOD TUBERCULOSIS; EPIDEMIOLOGY; POPULATION; PROVINCE; RELAPSE;
D O I
10.5588/ijtld.11.0360
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
SETTING: Tygerberg Children's Hospital (TCH) and Brooklyn Chest Hospital (BCH), South Africa. OBJECTIVES: To describe paediatric cases of rifampicin (RMP) monoresistant tuberculosis (RMR-TB) disease. DESIGN: Records of children with culture-confirmed RMR-TB between 1 March 2003 and 28 February 2009 were identified from a prospectively recorded database of drug-resistant TB at TCH and BCH. Mutation analysis was performed on available specimens. RESULTS: Eighteen children with a median age of 6.9 years (range 2 months-12.8 years) were identified. Nine (50%) were human immunodeficiency virus (HIV) infected and four (22%) were HIV-exposed but noninfected. Eleven (61%) had had previous TB treatment or prophylaxis. Nine children (50%) had cavitary disease and five children (22%) had extra-pulmonary disease. Twelve (67%) had adult TB source cases, including five (42%) adults with known RMR-TB. Primary transmission occurred among 11 children (61%) and acquisition of RMR-TB was possible in seven (39%) with prior RMP exposure. Median delay to specific RMR-TB treatment was 70 days (range 23-188). One child died from RMR-TB meningitis. Gene mutations consistent with RMR-TB were confirmed in five available samples. CONCLUSION: RMR-TB disease is increasingly encountered, particularly among HIV-infected and HIV-exposed non-infected children. Delay in commencing appropriate treatment for RMR-TB and high rates of cavitary disease could be a source of RMR-TB transmission.
引用
收藏
页码:76 / 81
页数:6
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