Marahatta S B
Department of Community Medicine, Kathmandu University School of Medical Sciences, Dhulikhel, Nepal.
Kathmandu Univ Med J (KUMJ). 2010 Jan-Mar;8(29):116-25. doi: 10.3126/kumj.v8i1.3234.
Multi-drug resistant (MDR) tuberculosis is defined as disease caused by Mycobacterium tuberculosis with resistance to at least two anti-tubercular drugs Isoniazid and Rifampicin. Recent surveillance data have revealed that prevalence of the drug resistant tuberculosis has risen to the highest rate ever recorded in the history. Drug resistant tuberculosis generally arises through the selection of mutated strains by inadequate therapy. The most powerful predictor of the presence of MDR-TB is a history of treatment of TB. Shortage of drugs has been one of the most common reasons for the inadequacy of the initial anti-TB regimen, especially in resource poor settings. Other major issues significantly contributing to the higher complexity of the treatment of MDR-TB is the increased cost of treatment. Other factors also play important role in the development of MDR-TB such as poor administrative control on purchase and distribution of the drugs with no proper mechanism on quality control and bioavailability tests. Tuberculosis control program implemented in past has also partially contributed to the development of drug resistance due to poor follow up and infrastructure. The association known for centuries between TB and poverty also applies to MDR-TB, a rather significant inverse association with MDR-TB. Various treatment strategies have been employed, including the use of standardised treatment regimens based upon representative local susceptibility patterns, empirical treatment based upon previous treatment history and local Drug Susceptibility Test (DST) patterns, and individualised treatment designed on the basis of individual DST results.Treatment outcomes among MDR-TB cases have varied widely; a recent survey of five Green Line Committee (GLC) approved sites in resource-limited countries found treatment success rates of 70%. Treatment continues to be limited in the resource poor countries where the demand is high. The ultimate strategy to control multidrug resistant tuberculosis is one that implements comprehensive approach incorporating treatment of multidrug-resistant tuberculosis based upon principles closely related to those of its general DOTS strategy for TB control: sustained political commitment; a rational case-finding strategy including accurate, timely diagnosis through quality assured culture and DST; appropriate treatment strategies that use second-line drugs under proper case management conditions; uninterrupted supply of quality-assured antituberculosis drugs; standardised recording and reporting system.
耐多药结核病被定义为由结核分枝杆菌引起的疾病,该病菌对至少两种抗结核药物异烟肼和利福平具有耐药性。最近的监测数据显示,耐药结核病的患病率已升至历史最高纪录。耐药结核病通常是由于治疗不充分导致突变菌株被选择而产生的。耐多药结核病存在的最有力预测因素是结核病治疗史。药物短缺一直是初始抗结核治疗方案不充分的最常见原因之一,尤其是在资源匮乏地区。其他显著导致耐多药结核病治疗复杂性增加的主要问题是治疗成本上升。其他因素在耐多药结核病的发展中也起着重要作用,例如对药品采购和分发的行政控制不力,缺乏适当的质量控制和生物利用度测试机制。过去实施的结核病控制项目由于随访和基础设施薄弱,也在一定程度上促成了耐药性的发展。结核病与贫困之间几个世纪以来为人所知的关联同样适用于耐多药结核病,二者存在相当显著的负相关。已经采用了各种治疗策略,包括根据具有代表性的当地药敏模式使用标准化治疗方案、根据既往治疗史和当地药物敏感性试验(DST)模式进行经验性治疗,以及根据个体DST结果设计个体化治疗方案。耐多药结核病病例的治疗结果差异很大;最近对资源有限国家五个绿线委员会(GLC)批准的地点进行的一项调查发现,治疗成功率为70%。在需求高的资源匮乏国家,治疗仍然受到限制。控制耐多药结核病的最终策略是实施一种综合方法,该方法纳入基于与其结核病控制总体直接观察短程治疗(DOTS)策略密切相关原则的耐多药结核病治疗:持续的政治承诺;合理的病例发现策略,包括通过质量有保证的培养和DST进行准确、及时的诊断;在适当的病例管理条件下使用二线药物的适当治疗策略;不间断供应质量有保证的抗结核药物;标准化的记录和报告系统。