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Fluoroquinolones for the treatment of pulmonary tuberculosis.

机译:氟喹诺酮类药物治疗肺结核。

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摘要

Tuberculosis (TB) continues to be a significant problem globally. Treatment includes a multiple drug regimen with isoniazid, rifampicin (rifampin), pyrazinamide and ethambutol. Often, one of these medications needs to be replaced as a result of adverse events or because Mycobacterium tuberculosis develops resistance against one these first-line agents. Fluoroquinolones, particularly the newer ones, possess good in vitro (levofloxacin, gatifloxacin, moxifloxacin) and in vivo (gatifloxacin and moxifloxacin) bactericidal activity against M. tuberculosis, making them attractive agents for the treatment of pulmonary TB.All relevant clinical trials, cohort studies and case reports investigating the clinical efficacy and tolerability of fluoroquinolones when used for the treatment of pulmonary TB were evaluated for this review. Specifically, efficacy and safety in the following indications were investigated: (i) first-line treatment of drug-sensitive pulmonary TB; (ii) first-line treatment for multi-drug resistant (MDR) TB; and (iii) treatment of patients with drug intolerance. Twenty-seven articles met our inclusion criteria; nine articles presented data from randomised, controlled or cohort studies. Seven studies used fluoroquinolones as first-line agents in drug-sensitive TB (1469 patients), 15 studies used fluoroquinolones to treat MDR-TB (1025 patients) and six studies (951 patients) investigated the use of fluoroquinolones in patients intolerant to other TB medications.In patients with susceptible M. tuberculosis strains, substitution with a fluoroquinolone did not have an effect on cure or radiological improvement at 8 weeks or failure at 12 months. Substitution of older fluoroquinolones into a regimen, especially ciprofloxacin, resulted in a higher rate of relapse and a longer time to sputum-culture conversions. The use of fluoroquinolones in patients with MDR-TB is supported by some trials where others show a lack of improvement in efficacy of a regimen.Our review of the literature does not support the use of older fluoroquinolones, especially ciprofloxacin, as substitute agents for drug-sensitive or drug-resistant TB. However, newer fluoroquinolones, such as moxifloxacin, may be a reasonable alternative based on results from one large clinical trial. Fluoroquinolones have an important role as substitute agents for those who are intolerant of first-line TB agents.
机译:结核病(TB)仍然是全球范围内的重大问题。治疗包括异烟肼,利福平(rifampin),吡嗪酰胺和乙胺丁醇的多种药物疗法。通常,由于不良事件或结核分枝杆菌对这些一线药物产生耐药性,需要更换其中一种药物。氟喹诺酮类药物,特别是较新的氟喹诺酮类药物在体外(左氧氟沙星,加替沙星,莫西沙星)和体内(加替沙星和莫西沙星)对结核分枝杆菌具有良好的杀菌活性,使其成为治疗肺结核的诱人剂。本研究评估了研究氟喹诺酮类药物用于肺结核治疗的临床疗效和耐受性的研究和病例报告。具体而言,研究了以下适应症的疗效和安全性:(i)一线治疗药物敏感性肺结核; (ii)耐多药结核病的一线治疗; (iii)药物不耐受患者的治疗。有27条符合我们的纳入标准;九篇文章介绍了随机,对照或队列研究的数据。七项研究使用氟喹诺酮类药物作为药物敏感性结核病的一线用药(1469例患者),15项研究使用氟喹诺酮类药物治疗耐多药结核病(1025例患者),六项研究(951例患者)研究了氟喹诺酮类药物在不耐其他结核病的患者中的使用在易感结核分枝杆菌菌株的患者中,用氟喹诺酮替代对第8周的治愈或放射学改善或第12个月的衰竭没有影响。较老的氟喹诺酮类药物(特别是环丙沙星)替代方案可导致更高的复发率和更长的痰培养转化时间。一些试验支持在多药耐药结核病患者中使用氟喹诺酮类药物,而其他一些试验表明该方案的疗效尚无改善。我们的文献综述不支持使用较老的氟喹诺酮类药物,尤其是环丙沙星作为药物替代药物敏感或耐药结核病。但是,根据一项大型临床试验的结果,较新的氟喹诺酮类药物(如莫西沙星)可能是合理的选择。氟喹诺酮类药物对于那些不能耐受一线结核病药物的人具有重要的替代作用。

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