McDaneld Patrick M, Spooner Linda M, Mohr John F, Belliveau Paul P
Massachusetts College of Pharmacy and Health Sciences, Worcester/Manchester Lexington, MA, USA.
Ann Pharmacother. 2013 Dec;47(12):1654-65. doi: 10.1177/1060028013508272. Epub 2013 Nov 1.
To evaluate daptomycin use for the treatment of infections with methicillin-resistant Staphylococcus aureus (MRSA) isolates having vancomycin minimum inhibitory concentrations (MICs) of 1.5 to 2 µg/mL.
The literature was retrieved through PubMed and EMBASE (January 2006 to August 2013).
English articles were reviewed. Studies that included separate daptomycin data (clinical outcome or in vitro surveillance) for MRSA isolates with vancomycin MICs of 1.5 to 2 µg/mL by any testing methodology were included.
Clinical and microbiological outcomes associated with daptomycin used as first-line or subsequent therapy for MRSA infections with vancomycin MICs of 1.5 to 2 µg/mL were reported in 7 retrospective clinical studies; susceptibility information involving such isolates was reported from 12 surveillancestudies. Although not all studies demonstrated outcome differences between daptomycin and comparator treatments (usually vancomycin), when differences were reported, they were in favor of daptomycin. Individual studies found lower 60-day (8% vs 20%, P = .046) and 30-day mortality (3.5% vs 12.9%, P = .047) and increased treatment success with daptomycin (68.6% vs 43.1%, P = .008; 76.9% vs 53.8%, P = .048) in bacteremic patients. The median doses used for treatment of bacteremia were greater than that approved by the FDA for this indication (6 mg/kg/d).
Current published evidence indicates daptomycin may be an acceptable alternative to vancomycin for MRSA infections, especially bacteremia, involving isolates with vancomycin MIC values of 1.5 to 2 µg/mL. Additional evidence is needed to fully elucidate daptomycin utility in this area.
评估达托霉素用于治疗万古霉素最低抑菌浓度(MIC)为1.5至2μg/mL的耐甲氧西林金黄色葡萄球菌(MRSA)感染。
通过PubMed和EMBASE检索文献(2006年1月至2013年8月)。
对英文文章进行综述。纳入通过任何检测方法包含万古霉素MIC为1.5至2μg/mL的MRSA分离株的单独达托霉素数据(临床结局或体外监测)的研究。
7项回顾性临床研究报告了达托霉素用作万古霉素MIC为1.5至2μg/mL的MRSA感染的一线或后续治疗相关的临床和微生物学结局;12项监测研究报告了涉及此类分离株的药敏信息。尽管并非所有研究都证明达托霉素与对照治疗(通常为万古霉素)之间存在结局差异,但当报告有差异时,这些差异有利于达托霉素。个别研究发现,在菌血症患者中,达托霉素的60天死亡率较低(8%对20%,P = 0.046)和30天死亡率较低(3.5%对12.9%,P = 0.047),且治疗成功率更高(68.6%对43.1%,P = 0.008;76.9%对53.8%,P = 0.048)。用于治疗菌血症的中位剂量大于FDA批准的该适应症剂量(6mg/kg/d)。
目前已发表的证据表明,对于MRSA感染,尤其是菌血症,涉及万古霉素MIC值为1.5至2μg/mL的分离株,达托霉素可能是万古霉素的可接受替代药物。需要更多证据来充分阐明达托霉素在该领域的效用。