Impact of Drug Resistance on Clinical Outcome in Children With Tuberculous Meningitis

被引:34
|
作者
Seddon, James A. [1 ,2 ]
Visser, Douwe H. [3 ]
Bartens, Margaux [3 ]
Jordaan, Annemie M. [4 ]
Victor, Thomas C. [4 ]
van Furth, A. Marceline [3 ]
Schoeman, Johan F. [5 ]
Schaaf, H. Simon [1 ,5 ]
机构
[1] Univ Stellenbosch, Fac Hlth Sci, Dept Paediat & Child Hlth, Desmond Tutu TB Ctr, Cape Town, South Africa
[2] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Clin Res, London WC1, England
[3] Vrije Univ Amsterdam Med Ctr, Dept Paediat, Amsterdam, Netherlands
[4] Univ Stellenbosch, Res Med Res Council Ctr Mol & Cellular Biol, Natl Res Fdn Ctr Excellence Biomed TB,Dept Biomed, Fac Hlth Sci,Dept Sci & Technol,Div Mol Biol & Hu, ZA-7505 Tygerberg, South Africa
[5] Tygerberg Childrens Hosp, Cape Town, South Africa
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
pediatric; meningitis; tuberculosis; children; resistance; outcome; WESTERN CAPE PROVINCE; MYCOBACTERIUM-TUBERCULOSIS; SOUTH-AFRICA; VIETNAMESE ADULTS; BEIJING GENOTYPE; MANAGEMENT; INFECTION; COMPLEX; STRAIN; ASSOCIATION;
D O I
10.1097/INF.0b013e318253acf8
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: Tuberculous meningitis (TBM) is associated with delayed diagnosis and poor outcome in children. This study investigated the impact of drug resistance on clinical outcome in children with TBM. Methods: All children (0-13 years) were included if admitted to Tygerberg Children's Hospital, Cape Town, South Africa, from January 2003 to April 2009 with a diagnosis of either confirmed TBM, or probable TBM with mycobacterial isolation from a site other than cerebrospinal fluid. Mycobacterial samples underwent drug susceptibility testing to rifampin and isoniazid. Children were treated with isoniazid, rifampin, pyrazinamide and ethionamide according to local guidelines. Results: One hundred twenty-three children were included; 13% (16 of 123) had any form of drug resistance, and 4% (5 of 123) had multidrug-resistant tuberculosis. Time from start of symptoms to appropriate treatment was longer in children with any drug resistance (median: 31 days versus 9 days; P = 0.001). In multivariable analysis, young age (P = 0.013) and multidrug-resistant tuberculosis (adjusted odds ratio: 12.4 [95% confidence interval: 1.17-132.3]; P = 0.037) remained risk factors for unfavorable outcome, and multidrug-resistant tuberculosis remained a risk for death (adjusted odds ratio: 63.9 [95% confidence interval: 4.84-843.2]; P = 0.002). We did not detect any difference in outcome between those with isolates resistant to only isoniazid and those with fully susceptible strains (adjusted odds ratio: 0.22 [confidence interval: 0.03-1.87]; P = 0.17). Conclusion: Multidrug-resistant TBM in children has poor clinical outcome and is associated with death. We did not find any difference in the outcomes between children with isoniazid monoresistant TBM and those with drug-susceptible TBM. One explanation could be the local treatment regimen. Further investigation of this regimen is indicated.
引用
收藏
页码:711 / 716
页数:6
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