首页> 外文期刊>Reviews in Health Care >Role of fluoroquinolones in the treatment of tuberculosis
【24h】

Role of fluoroquinolones in the treatment of tuberculosis

机译:氟喹诺酮类药物在结核病治疗中的作用

获取原文
           

摘要

INTRODUCTION: The increasing incidence of multidrug-resistant (MDR) and extensively drug-resistant (XDR) strains of Mycobacterium tuberculosis is hampering efforts to control the global tuberculosis (TB) epidemic. Although treatment of drug-susceptible TB is possible in ≥ 95% of disease cases, long (≥ 6 months) duration of supervised combination therapy is challenging. Non-adherence to treatment often results in much lower cure rates. Treatment of MDR-TB and XDR-TB is far less effective. The aim of this review is to summarize the current status of fluoroquinolones in shortening the duration of drug-susceptible pulmonary TB and in improving the outcome of MDR-TB/XDR-TB.METHODS: All the relevant articles were identified through a search of PubMed and Scopus databases by using search terms like tuberculosis (or M. tuberculosis), fluoroquinolones, drug-susceptible TB, MDR-TB, XDR-TB, combination therapy, treatment regimens, treatment duration, drug target and drug resistance. The current literature on the role of fluoroquinolones in the treatment of TB was reviewed.RESULTS: The fluoroquinolones, particularly newer compounds such as levofloxacin, moxifloxacin and gatifloxacin, have bactericidal activity against M. tuberculosis, excellent oral bioavailability, favorable safety profile and no cross-resistance with other first-line anti-TB drugs. Data from phase II trials of fluoroquinolones-containing regimens for shortening the duration of treatment for pulmonary TB are encouraging and phase III trials are currently underway. The fluoroquinolones are also effective as substitute agents for those individuals who are intolerant to first-line drugs. Several studies and clinical trials have also supported the use of fluoroquinolones in patients with MDR-TB/XDR-TB.DISCUSSION: The fluoroquinolones-containing regimens are being tested to shorten the duration of treatment for pulmonary TB to 4 months. They are also regarded as one of the two cornerstone drugs for the treatment of MDR-TB/XDR-TB. However, they are also among the commonly prescribed antibiotics for lower respiratory tract infections and are becoming increasingly associated with delayed treatment and resistance in TB. If these trends are not reversed soon, we may lose fluoroquinolones as effective anti-TB agents very rapidly.
机译:简介:结核分枝杆菌的多药耐药(MDR)和广泛耐药(XDR)菌株的发生率不断增加,阻碍了控制全球结核病(TB)流行的努力。尽管在≥95%的疾病病例中可以治疗药物敏感性结核病,但监督性联合治疗的持续时间(≥6个月)具有挑战性。不坚持治疗通常会导致治愈率大大降低。耐多药结核和广泛耐药结核的治疗远没有效果。这篇综述的目的是总结氟喹诺酮类药物在缩短药物敏感性肺结核病持续时间和改善MDR-TB / XDR-TB结果方面的现状。方法:通过搜索PubMed确定了所有相关文章和Scopus数据库,使用结核病(或结核分枝杆菌),氟喹诺酮类药物,易感结核,耐多药结核病,耐多药结核病,组合疗法,治疗方案,治疗时间,药物靶点和耐药性等搜索词。结果:氟喹诺酮类药物,尤其是较新的化合物,如左氧氟沙星,莫西沙星和加替沙星,具有抗结核分枝杆菌的杀菌活性,良好的口服生物利用度,良好的安全性和无交叉性-与其他一线抗结核药物耐药。来自II期含氟喹诺酮类药物治疗方案以缩短肺结核治疗时间的试验数据令人鼓舞,目前正在进行III期试验。氟喹诺酮类药物还可以有效替代那些对一线药物不耐受的人。多项研究和临床试验也支持在耐多药结核病/广泛耐药结核病患者中使用氟喹诺酮类药物。讨论:正在测试含氟喹诺酮类药物的治疗方案,以将肺结核的治疗时间缩短至4个月。它们也被认为是治疗耐多药结核/广泛耐药结核的两种基石药物之一。但是,它们也是下呼吸道感染的常用处方抗生素之一,并且与结核病的延迟治疗和耐药性越来越相关。如果这些趋势不能很快扭转,我们可能会很快失去作为有效抗结核病药物的氟喹诺酮类药物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号