Török M E
Department of Medicine, University of Cambridge, Addenbrooke's Hospital, Box 157, Hills Road, Cambridge CB2 0QQ, UK Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge CB2 0QQ, UK Public Health England, Clinical Microbiology and Public Health Laboratory, Addenbrooke's Hospital, Hills Road, Cambridge CB2 0QQ, UK
Br Med Bull. 2015 Mar;113(1):117-31. doi: 10.1093/bmb/ldv003. Epub 2015 Feb 18.
Tuberculous meningitis (TBM) is the most severe form of infection caused by Mycobacterium tuberculosis, causing death or disability in more than half of those affected. The aim of this review is to examine recent advances in our understanding of TBM, focussing on the diagnosis and treatment of this devastating condition.
Papers on TBM published between 1891 and 2014 and indexed in the NCBI Pubmed. The following search terms were used: TBM, diagnosis, treatment and outcome.
The diagnosis of TBM remains difficult as its presentation is non-specific and may mimic other causes of chronic meningoencephalitis. Rapid recognition of TBM is crucial, however, as delays in initiating treatment are associated with poor outcome. The laboratory diagnosis of TBM is hampered by the low sensitivity of cerebrospinal fluid microscopy and the slow growth of M. tuberculosis in conventional culture systems. The current therapy of TBM is based on the treatment of pulmonary tuberculosis, which may not be ideal. The combination of TBM and HIV infection poses additional management challenges because of the need to treat both infections and the complications associated with them.
The pathogenesis of TBM remains incompletely understood limiting the development of interventions to improve outcome. The optimal therapy of TBM has not been established in clinical trials, and increasing antimicrobial resistance threatens successful treatment of this condition. The use of adjunctive anti-inflammatory agents remains controversial, and their mechanism of action remains incompletely understood. The role of surgical intervention is uncertain and may not be available in areas where TBM is common.
Laboratory methods to improve the rapid diagnosis of TBM are urgently required. Clinical trials of examining the use of high-dose rifampicin and/or fluoroquinolones are likely to report in the near future.
The use of biomarkers to improve the rapid diagnosis of TBM warrants further investigation. The role of novel antituberculosis drugs, such as bedaquiline and PA-824, in the treatment of TBM remains to be explored. Human genetic polymorphisms may explain the heterogeneity of response to anti-inflammatory therapies and could potentially be used to tailor therapy.
结核性脑膜炎(TBM)是由结核分枝杆菌引起的最严重的感染形式,超过半数的患者会因此死亡或致残。本综述的目的是探讨我们对TBM认识的最新进展,重点关注这种毁灭性疾病的诊断和治疗。
1891年至2014年间发表并被NCBI Pubmed收录的关于TBM的论文。使用了以下检索词:TBM、诊断、治疗和结果。
TBM的诊断仍然困难,因为其表现不具特异性,可能与其他慢性脑膜脑炎病因相似。然而,快速识别TBM至关重要,因为延迟开始治疗与不良预后相关。脑脊液显微镜检查的低敏感性以及结核分枝杆菌在传统培养系统中生长缓慢阻碍了TBM的实验室诊断。目前TBM的治疗基于肺结核的治疗方法,但可能并不理想。TBM与HIV感染并存带来了额外的管理挑战,因为需要同时治疗两种感染及其相关并发症。
TBM的发病机制仍未完全明了,这限制了改善预后的干预措施的发展。TBM的最佳治疗方案尚未在临床试验中确定,抗菌药物耐药性的增加威胁到这种疾病的成功治疗。辅助抗炎药物的使用仍存在争议,其作用机制也尚未完全明了。手术干预的作用尚不确定,在TBM常见地区可能无法实施。
迫切需要提高TBM快速诊断的实验室方法。研究高剂量利福平或氟喹诺酮类药物使用情况的临床试验可能在不久后公布结果。
使用生物标志物改善TBM快速诊断值得进一步研究。新型抗结核药物,如贝达喹啉和PA - 824,在TBM治疗中的作用仍有待探索。人类基因多态性可能解释对抗炎治疗反应的异质性,并有可能用于定制治疗方案。