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头孢比普:首个对耐甲氧西林金黄色葡萄球菌具有活性的头孢菌素。

Ceftobiprole: first cephalosporin with activity against methicillin-resistant Staphylococcus aureus.

作者信息

Vidaillac Céline, Rybak Michael J

机构信息

Anti-Infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Detroit, MI 48201, USA.

出版信息

Pharmacotherapy. 2009 May;29(5):511-25. doi: 10.1592/phco.29.5.511.

Abstract

Ceftobiprole medocaril is the first member of a new series of advanced cephalosporins with activity against methicillin-resistant Staphylococcus aureus (MRSA). The drug received an approvable letter from the United States Food and Drug Administration (FDA) in March 2008 and from Health Canada in June 2008 for the treatment of complicated skin and skin structure infections including diabetic foot infections. Ceftobiprole exerts its antibacterial activity by inhibiting the penicillin-binding proteins (PBPs) involved in cell wall synthesis. It has an established stability against hydrolysis by many gram-positive beta-lactamases and a higher affinity for various PBPs (such as PBP2a of MRSA or PBP2x of Streptococcus pneumoniae), which leads to a wider spectrum of activity compared with older beta-lactams. Ceftobiprole activity does not cover extended-spectrum beta-lactamase-producing Enterobacteriaceae and some other pathogens, including Enterococcus faecium or Acinetobacter baumanii. Generally well tolerated, with nausea and taste disturbance being the most common adverse events, ceftobiprole appeared noninferior to empiric therapy in several clinical trials. Ceftobiprole is available only for intravenous administration; recommended dosage regimens have not been approved by the FDA as of this writing. However, based on the Canadian package insert, expected dosage recommendations are 500 mg as a 1-hour intravenous infusion every 12 hours for the treatment of complicated skin and skin structure infections caused by certain gram-positive pathogens, and 500 mg as a 2-hour infusion every 8 hours when susceptible gram-negative or both gram-positive and susceptible gram-negative pathogens are involved. Dosage adjustments are indicated for patients with moderate or severe renal impairment, and dosage recommendations are expected to be 500 or 250 mg, respectively, as a 2-hour infusion every 12 hours. Several precautions regarding hypersensitivity and drug incompatibility are reported. Ceftobiprole represents a promising option for the treatment of mono- and polymicrobial infections caused by multidrug-resistant gram-positive and susceptible gram-negative pathogens, but further toxicity and safety studies are warranted.

摘要

头孢比普甲磺酸盐是新一代具有抗耐甲氧西林金黄色葡萄球菌(MRSA)活性的高级头孢菌素中的首个成员。该药物于2008年3月收到美国食品药品监督管理局(FDA)的批准信,并于2008年6月收到加拿大卫生部的批准信,用于治疗包括糖尿病足感染在内的复杂皮肤及皮肤结构感染。头孢比普通过抑制参与细胞壁合成的青霉素结合蛋白(PBPs)发挥抗菌活性。它对多种革兰氏阳性β-内酰胺酶具有稳定的抗水解能力,并且对各种PBPs(如MRSA的PBP2a或肺炎链球菌的PBP2x)具有更高的亲和力,与旧的β-内酰胺类药物相比,其活性谱更广。头孢比普的活性不覆盖产超广谱β-内酰胺酶的肠杆菌科细菌和其他一些病原体,包括粪肠球菌或鲍曼不动杆菌。头孢比普总体耐受性良好,恶心和味觉障碍是最常见的不良事件,在多项临床试验中,头孢比普似乎不劣于经验性治疗。头孢比普仅可静脉给药;截至撰写本文时,推荐的给药方案尚未获得FDA批准。然而,根据加拿大药品说明书,预期的给药建议是,对于由某些革兰氏阳性病原体引起的复杂皮肤及皮肤结构感染,每12小时静脉输注500mg,输注1小时;当涉及敏感革兰氏阴性或革兰氏阳性和敏感革兰氏阴性病原体时,每8小时静脉输注500mg,输注2小时。对于中度或重度肾功能损害患者,需要调整剂量,预期的给药建议分别为每12小时静脉输注500mg或250mg,输注2小时。报告了一些关于超敏反应和药物不相容性的注意事项。头孢比普是治疗由多重耐药革兰氏阳性和敏感革兰氏阴性病原体引起的单一和混合微生物感染的一个有前景的选择,但需要进一步进行毒性和安全性研究。

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