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Safety and Efficacy of Delamanid in the Treatment of Multidrug-Resistant Tuberculosis (MDR-TB)

机译:德拉曼尼德在治疗耐多药结核病(MDR-TB)中的安全性和有效性

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Globally, the incidence of tuberculosis (TB) is declining but the proportion of drug-resistant cases has increased. Strains resistant to both isoniazid and rifampin, and possibly other antibiotics, called multidrug-resistant (MDR), are particularly difficult to treat. Poorer outcomes, including increased mortality, occur in patients infected with MDR strains and the costs associated with treatment of MDR-TB are substantially greater. The recent recognition of MDR-TB and strains with more complex resistance patterns has stimulated the development of new TB medications including fluoroquinolones, oxazolidinones, diarylquinolines, nitroimidazopyrans, ethylenediamines, and benzothiazinones. Bedaquiline, a diarylquinoline, was approved for the treatment of MDR-TB in 2012. Addition of delamanid to WHO-approved treatment improved outcomes for MDR-TB and for extensively drug-resistant TB in a large randomized, controlled phase II clinical trial and is undergoing evaluation in a large international phase III study. This review will focus on MDR-TB and the role of delamanid in its treatment.
机译:在全球范围内,结核病(TB)的发病率正在下降,但耐药病例的比例却有所增加。对异烟肼和利福平都有抗药性的菌株,以及可能被称为多重耐药性(MDR)的其他抗生素,特别难以治疗。感染耐多药菌株的患者的预后较差,包括死亡率增加,与耐多药结核病相关的治疗费用要高得多。最近对耐多药结核病和耐药性更复杂的菌株的认识刺激了新的结核病药物的开发,包括氟喹诺酮类,恶唑烷酮类,二芳基喹啉类,硝基咪唑并吡喃类,乙二胺类和苯并噻嗪酮类。贝达喹啉(一种二芳基喹啉)于2012年被批准用于治疗耐多药结核病。在一项大型的随机对照II期临床试验中,将德拉曼尼德纳入WHO批准的治疗方法可改善耐多药结核病和广泛耐药结核病的预后。在一项大型的国际III期研究中接受评估。这篇综述将集中于耐多药结核病及其在治疗中的作用。

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