Department of Pharmacy, Harborview Medical Center, and School of Pharmacy, University of Washington, Seattle, WA 98104, USA.
J Intensive Care Med. 2011 Nov-Dec;26(6):385-91. doi: 10.1177/0885066610392893. Epub 2011 May 23.
Vancomycin has been the treatment standard for methicillin-resistant Staphylococcus aureus (MRSA) infections, but clinical efficacy is limited. We report outcomes of a cohort with MRSA ventilator-associated pneumonia (VAP) treated with vancomycin vs linezolid.
Retrospective analysis of 113 participants with MRSA VAP confirmed by bronchoscopy who have been initiated on therapy with either vancomycin or linezolid within 24 hours after bronchoscopy and completed ≥7 days of therapy during their hospitalization from July 2003 to June 2007. The primary endpoints were hospital survival and clinical cure, defined as resolution of signs and symptoms of VAP or microbiological eradication after completion of therapy along with clinical pulmonary infection score (CPIS) ≤6 at day 7 of therapy.
At hospital discharge, 23/27 (85.2%) of linezolid and 72/86 (83.7%) of vancomycin recipients had survived (P = .672). In comparison to linezolid recipients, the adjusted odds ratio (OR) for survival was 0.72 (95% confidence interval [CI]: 0.16-3.27) with vancomycin therapy. Clinical cure was achieved in 24/27 (88.9%) of linezolid and 63/86 (73.3%) of vancomycin recipients (P = .066). Compared to linezolid recipients, the adjusted OR for clinical cure was 0.24 (95% CI: 0.05-1.10) with vancomycin therapy. Survival and clinical cure did not differ significantly between vancomycin recipients with trough level ≥15 and <15 μg/mL, respectively.
Our results suggested no survival benefit but a trend toward higher cure rate with linezolid therapy. The optimal treatment of MRSA VAP requires further study through randomized, controlled trials.
万古霉素一直是治疗耐甲氧西林金黄色葡萄球菌(MRSA)感染的标准治疗方法,但临床疗效有限。我们报告了一组接受万古霉素与利奈唑胺治疗的耐甲氧西林金黄色葡萄球菌呼吸机相关性肺炎(VAP)患者的结果。
回顾性分析了 2003 年 7 月至 2007 年 6 月期间,通过支气管镜检查确诊为 MRSA VAP 的 113 名患者,这些患者在支气管镜检查后 24 小时内开始接受万古霉素或利奈唑胺治疗,并在住院期间完成了至少 7 天的治疗。主要终点是住院生存率和临床治愈率,定义为治疗完成后 VAP 的体征和症状缓解或微生物学清除,以及治疗第 7 天临床肺部感染评分(CPIS)≤6。
出院时,利奈唑胺组 23/27(85.2%)和万古霉素组 72/86(83.7%)的患者存活(P=.672)。与利奈唑胺组相比,万古霉素组的生存调整优势比(OR)为 0.72(95%置信区间[CI]:0.16-3.27)。利奈唑胺组 24/27(88.9%)和万古霉素组 63/86(73.3%)的患者达到临床治愈率(P=.066)。与利奈唑胺组相比,万古霉素组的临床治愈率调整 OR 为 0.24(95%CI:0.05-1.10)。万古霉素组谷浓度≥15μg/mL 和<15μg/mL 的患者之间的生存率和临床治愈率没有显著差异。
我们的结果表明,利奈唑胺治疗没有生存获益,但治愈率有升高趋势。MRSA VAP 的最佳治疗方法需要通过随机对照试验进一步研究。