Bassetti Matteo, Della Siega Paola, Pecori Davide, Scarparo Claudio, Righi Elda
Santa Maria Misericordia University Hospital, Infectious Diseases Division , Piazzale S. Maria della Misericordia, n. 15, 33100, Udine , Italy + 86 21 38804518; extn. 8319 ; + 39 0432 559360 ;
Expert Opin Investig Drugs. 2015 Mar;24(3):433-42. doi: 10.1517/13543784.2015.1005205. Epub 2015 Jan 21.
There has been a striking increase in the emergence of multidrug-resistant pathogens in recent times. Delafloxacin is a novel, broad-spectrum fluoroquinolone with antimicrobial activity against resistant Gram-positive, Gram-negative and anaerobic organisms. It has the potential to treat a variety of infections including complicated skin and skin structure infections and respiratory tract infections.
In this review, the authors report the microbiological spectrum of activity of delafloxacin as well as its pharmacokinetic characteristics. They also report the results of recent studies investigating its safety and efficacy.
The profile of delafloxacin offers several advantages. Delafloxacin presents a broad spectrum of activity against pathogens involved in respiratory infections and complicated skin and skin structure infections (SSSIs), including methicillin-resistant Staphylococcus aureus. It has also shown activity against Gram-negative pathogens, such as quinolone-susceptible and -resistant strains of Escherichia coli and Klebsiella pneumoniae and quinolone-susceptible Pseudomonas aeruginosa. The availability of an oral formulation supports its use in sequential therapy. The efficacy and tolerability of delafloxacin have been demonstrated in Phase II clinical trials in comparison with moxifloxacin for respiratory infections and linezolid and vancomycin in SSSIs. Compared with other quinolones such as moxifloxacin, delafloxacin showed comparable efficacy and a lower rate of adverse effects. The results of new Phase III studies are awaited to confirm delafloxacin's future applications in the treatment of SSSIs.
近年来,多重耐药病原体的出现显著增加。德拉氟沙星是一种新型广谱氟喹诺酮类药物,对耐药革兰氏阳性菌、革兰氏阴性菌和厌氧菌具有抗菌活性。它有潜力治疗多种感染,包括复杂性皮肤及皮肤结构感染和呼吸道感染。
在本综述中,作者报告了德拉氟沙星的微生物活性谱及其药代动力学特征。他们还报告了近期研究其安全性和有效性的结果。
德拉氟沙星具有多个优势。它对呼吸道感染以及复杂性皮肤及皮肤结构感染(SSSI)中涉及的病原体具有广泛活性,包括耐甲氧西林金黄色葡萄球菌。它还对革兰氏阴性病原体表现出活性,如对喹诺酮敏感和耐药的大肠杆菌及肺炎克雷伯菌菌株,以及对喹诺酮敏感的铜绿假单胞菌。口服制剂的可获得性支持其在序贯治疗中的应用。在治疗呼吸道感染方面,与莫西沙星相比,以及在治疗SSSI方面,与利奈唑胺和万古霉素相比,德拉氟沙星在II期临床试验中已证明其有效性和耐受性。与其他喹诺酮类药物如莫西沙星相比,德拉氟沙星显示出相当的疗效和较低的不良反应发生率。期待新的III期研究结果来确认德拉氟沙星在治疗SSSI方面的未来应用。