Department of Clinical Science, University of Milan, Luigi Sacco Hospital, Milan, Italy.
Antimicrob Agents Chemother. 2013 Dec;57(12):6213-22. doi: 10.1128/AAC.01563-13. Epub 2013 Sep 30.
The use of daptomycin in Gram-positive left-sided infective endocarditis (IE) has significantly increased. The purpose of this study was to assess the influence of high-dose daptomycin on the outcome of left-sided IE due to Gram-positive pathogens. This was a prospective cohort study based on 1,112 cases from the International Collaboration on Endocarditis (ICE)-Plus database and the ICE-Daptomycin Substudy database from 2008 to 2010. Among patients with left-sided IE due to Staphylococcus aureus, coagulase-negative staphylococci, and Enterococcus faecalis, we compared those treated with daptomycin (cohort A) to those treated with standard-of-care (SOC) antibiotics (cohort B). The primary outcome was in-hospital mortality. Time to clearance of bacteremia, 6-month mortality, and adverse events (AEs) ascribable to daptomycin were also assessed. There were 29 and 149 patients included in cohort A and cohort B, respectively. Baseline comorbidities did not differ between the two cohorts, except for a significantly higher prevalence of diabetes and previous episodes of IE among patients treated with daptomycin. The median daptomycin dose was 9.2 mg/kg of body weight/day. Two-thirds of the patients treated with daptomycin had failed a previous antibiotic regimen. In-hospital and 6-month mortalities were similar in the two cohorts. In cohort A, median time to clearance of methicillin-resistant S. aureus (MRSA) bacteremia was 1.0 day, irrespective of daptomycin dose, representing a significantly faster bacteremia clearance compared to SOC (1.0 versus 5.0 days; P < 0.01). Regimens with higher daptomycin doses were not associated with increased incidence of AEs. In conclusion, higher-dose daptomycin may be an effective and safe alternative to SOC in the treatment of left-sided IE due to common Gram-positive pathogens.
达托霉素在治疗革兰氏阳性左心感染性心内膜炎(IE)中的应用显著增加。本研究旨在评估高剂量达托霉素对革兰氏阳性病原体引起的左心 IE 结局的影响。这是一项基于 2008 年至 2010 年国际心内膜炎合作组织(ICE)-Plus 数据库和 ICE-达托霉素亚研究数据库的 1112 例患者的前瞻性队列研究。在左心 IE 患者中,金黄色葡萄球菌、凝固酶阴性葡萄球菌和粪肠球菌,我们比较了接受达托霉素(A 队列)治疗的患者和接受标准治疗(SOC)抗生素治疗的患者(B 队列)。主要结局是住院死亡率。还评估了血培养清除时间、6 个月死亡率和归因于达托霉素的不良事件(AE)。A 队列和 B 队列分别纳入 29 例和 149 例患者。两组患者的基线合并症无差异,但接受达托霉素治疗的患者糖尿病和 IE 既往发作的患病率明显较高。达托霉素的中位剂量为 9.2 毫克/千克体重/天。三分之二接受达托霉素治疗的患者之前的抗生素方案治疗失败。两组住院死亡率和 6 个月死亡率相似。在 A 队列中,无论达托霉素剂量如何,耐甲氧西林金黄色葡萄球菌(MRSA)菌血症的中位清除时间为 1.0 天,与 SOC 相比(1.0 与 5.0 天;P<0.01),血培养清除速度明显更快。高剂量达托霉素方案与 AE 发生率增加无关。总之,高剂量达托霉素可能是治疗常见革兰氏阳性病原体引起的左心 IE 的有效且安全的 SOC 替代方案。