Intensified antibiotic treatment of tuberculosis meningitis

被引:36
作者
Cresswell, Fiona V. [1 ,2 ]
Te Brake, Lindsey [3 ]
Atherton, Rachel [2 ]
Ruslami, Rovina [4 ]
Dooley, Kelly E. [5 ,6 ]
Aarnoutse, Rob [3 ]
Van Crevel, Reinout [7 ,8 ,9 ]
机构
[1] London Sch Hyg & Trop Med, Clin Res Dept, London, England
[2] Infect Dis Inst, Res Dept, Kampala, Uganda
[3] Radboud Univ Nijmegen, Med Ctr, Dept Pharm, Radboud Inst Hlth Sci,Radboud Ctr Infect Dis, Nijmegen, Netherlands
[4] Univ Padjadjaran, TB HIV Res Ctr, Fac Med, Bandung, Indonesia
[5] Johns Hopkins Univ, Sch Med, Dept Med, Div Clin Pharmacol, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Dept Med, Div Infect Dis, Baltimore, MD 21205 USA
[7] Radboud Univ Nijmegen, Med Ctr, Dept Internal Med, POB 9101, NL-6500 HB Nijmegen, Netherlands
[8] Radboud Univ Nijmegen, Med Ctr, Radboud Ctr Infect Dis, Nijmegen, Netherlands
[9] Univ Oxford, Nuffield Dept Med, Ctr Trop Med & Global Hlth, Oxford, England
基金
英国惠康基金; 美国国家卫生研究院;
关键词
Tuberculous meningitis; TB meningitis; antituberculous therapy; intensified; CENTRAL-NERVOUS-SYSTEM; HIV-INFECTED PATIENTS; ANTITUBERCULOSIS DRUG-RESISTANCE; ANTI-TB DRUGS; RECONSTITUTION INFLAMMATORY SYNDROME; EARLY BACTERICIDAL ACTIVITY; SHORT-COURSE CHEMOTHERAPY; IN-VITRO ACTIVITIES; CEREBROSPINAL-FLUID; MULTIDRUG-RESISTANT;
D O I
10.1080/17512433.2019.1552831
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Meningitis is the most severe manifestation of tuberculosis, resulting in death or disability in over 50% of those affected, with even higher morbidity and mortality among patients with HIV or drug resistance. Antimicrobial treatment of Tuberculous meningitis (TBM) is similar to treatment of pulmonary tuberculosis, although some drugs show poor central nervous system penetration. Therefore, intensification of antibiotic treatment may improve TBM treatment outcomes. Areas covered: In this review, we address three main areas: available data for old and new anti-tuberculous agents; intensified treatment in specific patient groups like HIV co-infection, drug-resistance, and children; and optimal research strategies. Expert commentary: There is good evidence from preclinical, clinical, and modeling studies to support the use of high-dose rifampicin in TBM, likely to be at least 30 mg/kg. Higher dose isoniazid could be beneficial, especially in rapid acetylators. The role of other first and second line drugs is unclear, but observational data suggest that linezolid, which has good brain penetration, may be beneficial. We advocate the use of molecular pharmacological approaches, physiologically based pharmacokinetic modeling and pharmacokinetic-pharmacodynamic studies to define optimal regimens to be tested in clinical trials. Exciting data from recent studies hold promise for improved regimens and better clinical outcomes in future.
引用
收藏
页码:267 / 288
页数:22
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