Li Julius, Echevarria Kelly L, Hughes Darrel W, Cadena Jose A, Bowling Jason E, Lewis James S
South Texas Veterans Health Care System, San Antonio, Texas, USA The University of Texas at Austin College of Pharmacy, Austin, Texas, USA Pharmacotherapy Education and Research Center, University of Texas Health Sciences Center San Antonio, San Antonio, Texas, USA
South Texas Veterans Health Care System, San Antonio, Texas, USA The University of Texas at Austin College of Pharmacy, Austin, Texas, USA Pharmacotherapy Education and Research Center, University of Texas Health Sciences Center San Antonio, San Antonio, Texas, USA Department of Medicine, Division of Infectious Diseases, University of Texas Health Sciences Center San Antonio, San Antonio, Texas, USA.
Antimicrob Agents Chemother. 2014 Sep;58(9):5117-24. doi: 10.1128/AAC.02800-14. Epub 2014 Jun 16.
Contrary to prior case reports that described occasional clinical failures with cefazolin for methicillin-susceptible Staphylococcus aureus (MSSA) infections, recent studies have demonstrated no difference in outcomes between cefazolin and antistaphylococcal penicillins for the treatment of MSSA bacteremia. While promising, these studies described low frequencies of high-inoculum infections, such as endocarditis. This retrospective study compares clinical outcomes of cefazolin versus oxacillin for complicated MSSA bacteremia at two tertiary care hospitals between January 2008 and June 2012. Fifty-nine patients treated with cefazolin and 34 patients treated with oxacillin were included. Osteoarticular (41%) and endovascular (20%) sources were the predominant sites of infection. The rates of clinical cure at the end of therapy were similar between cefazolin and oxacillin (95% versus 88%; P=0.25), but overall failure at 90 days was higher in the oxacillin arm (47% versus 24%; P=0.04). Failures were more likely to have received surgical interventions (63% versus 40%; P=0.05) and to have an osteoarticular source (57% versus 33%; P=0.04). Failures also had a longer duration of bacteremia (7 versus 3 days; P=0.0002), which was the only predictor of failure. Antibiotic selection was not predictive of failure. Rates of adverse drug events were higher in the oxacillin arm (30% versus 3%; P=0.0006), and oxacillin was more frequently discontinued due to adverse drug events (21% versus 3%; P=0.01). Cefazolin appears similar to oxacillin for the treatment of complicated MSSA bacteremia but with significantly improved safety. The higher rates of failure with oxacillin may have been confounded by other patient factors and warrant further investigation.
与先前的病例报告相反,那些报告描述了头孢唑林治疗甲氧西林敏感金黄色葡萄球菌(MSSA)感染时偶尔出现临床治疗失败的情况,而最近的研究表明,在治疗MSSA菌血症方面,头孢唑林和抗葡萄球菌青霉素的治疗效果并无差异。虽然这些研究很有前景,但它们所描述的高接种量感染(如心内膜炎)的发生率较低。这项回顾性研究比较了2008年1月至2012年6月期间两家三级医疗医院中,头孢唑林与苯唑西林治疗复杂性MSSA菌血症的临床结果。纳入了59例接受头孢唑林治疗的患者和34例接受苯唑西林治疗的患者。骨关节(41%)和血管内(20%)感染源是主要的感染部位。治疗结束时,头孢唑林和苯唑西林的临床治愈率相似(分别为95%和88%;P = 0.25),但90天时苯唑西林组的总体治疗失败率更高(分别为47%和24%;P = 0.04)。治疗失败的患者更有可能接受了手术干预(分别为63%和40%;P = 0.05),并且感染源为骨关节(分别为57%和33%;P = 0.04)。治疗失败的患者菌血症持续时间也更长(分别为7天和3天;P = 0.0002),这是治疗失败的唯一预测因素。抗生素的选择并不能预测治疗失败。苯唑西林组的药物不良事件发生率更高(分别为30%和3%;P = 0.0006),并且由于药物不良事件,苯唑西林更频繁地被停用(分别为21%和3%;P = 0.01)。在治疗复杂性MSSA菌血症方面,头孢唑林似乎与苯唑西林相似,但安全性有显著提高。苯唑西林较高的治疗失败率可能受到其他患者因素的干扰,值得进一步研究。