Awad Samir S, Rodriguez Alejandro H, Chuang Yin-Ching, Marjanek Zsuszanna, Pareigis Alex J, Reis Gilmar, Scheeren Thomas W L, Sánchez Alejandro S, Zhou Xin, Saulay Mikaël, Engelhardt Marc
Section of Surgical Critical Care, Baylor College of Medicine, Houston, Texas.
Joan XXIII University Hospital, Tarragona, Spain.
Clin Infect Dis. 2014 Jul 1;59(1):51-61. doi: 10.1093/cid/ciu219. Epub 2014 Apr 9.
Ceftobiprole, the active moiety of ceftobiprole medocaril, is a novel broad-spectrum cephalosporin, with bactericidal activity against a wide range of gram-positive bacteria, including Staphylococcus aureus (including methicillin-resistant strains) and penicillin- and ceftriaxone-resistant pneumococci, and gram-negative bacteria, including Enterobacteriaceae and Pseudomonas aeruginosa.
This was a double-blind, randomized, multicenter study of 781 patients with hospital-acquired pneumonia (HAP), including 210 with ventilator-associated pneumonia (VAP). Treatment was intravenous ceftobiprole 500 mg every 8 hours, or ceftazidime 2 g every 8 hours plus linezolid 600 mg every 12 hours; primary outcome was clinical cure at the test-of-cure visit.
Overall cure rates for ceftobiprole vs ceftazidime/linezolid were 49.9% vs 52.8% (intent-to-treat [ITT], 95% confidence interval [CI] for the difference, -10.0 to 4.1) and 69.3% vs 71.3% (clinically evaluable [CE], 95% CI, -10.0 to 6.1). Cure rates in HAP (excluding VAP) patients were 59.6% vs 58.8% (ITT, 95% CI, -7.3 to 8.8), and 77.8% vs 76.2% (CE, 95% CI, -6.9 to 10.0). Cure rates in VAP patients were 23.1% vs 36.8% (ITT, 95% CI, -26.0 to -1.5) and 37.7% vs 55.9% (CE, 95% CI, -36.4 to 0). Microbiological eradication rates in HAP (excluding VAP) patients were, respectively, 62.9% vs 67.5% (microbiologically evaluable [ME], 95% CI, -16.7 to 7.6), and in VAP patients 30.4% vs 50.0% (ME, 95% CI, -38.8 to -0.4). Treatment-related adverse events were comparable for ceftobiprole (24.9%) and ceftazidime/linezolid (25.4%).
Ceftobiprole is a safe and effective bactericidal antibiotic for the empiric treatment of HAP (excluding VAP). Further investigations are needed before recommending the use of ceftobiprole in VAP patients. Clinical Trials Registration. NCT00210964, NCT00229008.
头孢比普是头孢比普甲磺酸盐的活性部分,是一种新型广谱头孢菌素,对多种革兰氏阳性菌具有杀菌活性,包括金黄色葡萄球菌(包括耐甲氧西林菌株)以及对青霉素和头孢曲松耐药的肺炎球菌,对多种革兰氏阴性菌也有杀菌活性,包括肠杆菌科细菌和铜绿假单胞菌。
这是一项针对781例医院获得性肺炎(HAP)患者的双盲、随机、多中心研究,其中包括210例呼吸机相关性肺炎(VAP)患者。治疗方案为每8小时静脉注射500mg头孢比普,或每8小时静脉注射2g头孢他啶加每12小时静脉注射600mg利奈唑胺;主要结局为治疗访视时的临床治愈情况。
头孢比普与头孢他啶/利奈唑胺的总体治愈率分别为49.9%和52.8%(意向性治疗[ITT],差异的95%置信区间[CI]为-10.0至4.1),以及69.