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Tigecycline in the treatment of complicated intra-abdominal and complicated skin and skin structure infections

机译:Tigecycline治疗复杂的腹部和复杂的皮肤和皮肤结构感染

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Tigecycline, a glycylcycline related to the tetracycline class of antibiotics, represents a new option for the treatment of complicated intra-abdominal and complicated skin and skin structure infections. It displays favorable activity in vitro against the most common causative Gram-positive, Gram-negative and anaerobic pathogens. In addition, tigecycline demonstrates activity against drug-resistant pathogens such as methicillin-resistant Staphylococcus aureus , vancomycin-resistant enterococci, and organisms (such as Escherichia coli and Klebsiella pneumoniae ) producing extended-spectrum beta-lactamases. Tigecycline lacks activity in vitro against Pseudomonas and Proteus spp. In randomized clinical trials, tigecycline administered intravenously twice daily has demonstrated efficacy similar to comparators for a variety of complicated skin and skin structure and complicated intra-abdominal infections. The potential for significant drug interactions with tigecycline appears to be minimal. Dosing adjustment is needed for patients with severe hepatic impairment. The predominant side effect associated with its use to date has been gastrointestinal intolerance (nausea and vomiting).
机译:Tigeccline,与四环素类别的抗生素相关的糖霉素,代表了治疗复杂的腹部和复杂的皮肤和皮肤结构感染的新选择。它在体外显示最常见的致病革兰氏阳性,革兰氏阴性和厌氧病原体。此外,Tigecycline证明了抗耐药病原体的活性,例如耐药病原体,耐植物耐药金黄色葡萄球菌,万古霉素抗性肠球菌和生物(如大肠杆菌和克雷布氏菌肺炎)产生延长光谱β-内酰胺酶。 Tigecycline缺乏对伪霉菌和Proteus SPP体外的活性。在随机临床试验中,静脉内施用两次每日施用的Tigeccline已经证明了与各种复杂的皮肤和皮肤结构的比较器类似的疗效和复杂的腹部感染。与脱核素的重要药物相互作用的可能性似乎是最小的。严重肝损伤的患者需要给药调整。与迄今为止迄今为止相关的主要副作用已经是胃肠不耐受(恶心和呕吐)。

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