Erlandson Kristine Mace, Sun Junfeng, Iwen Peter C, Rupp Mark E
Department of Internal Medicine, University of Nebraska Medical Center, Omaha 68198-4031, USA.
Clin Infect Dis. 2008 Jan 1;46(1):30-6. doi: 10.1086/523588.
The impact of antibiotic resistance on the clinical outcome of patients with vancomycin-resistant Enterococcus (VRE) bacteremia remains unclear. There are limited data comparing patient outcomes during the early era of vancomycin resistance with the period of more-potent antibiotic availability.
A retrospective review was conducted of 113 patients with VRE bacteremia at a single institution from August 1993 to September 2005. Patients were assigned to a group on the basis of initial antibiotic choice for treatment of VRE (linezolid, quinupristin-dalfopristin, or combinations of other agents, before newer options were available). Outcome measurements were examined for the initial episode of VRE bacteremia, and multiple logistic regression analysis was performed to compare group outcomes.
Overall mortality was 37.2% (42 of 113 patients). VRE bacteremia caused or significantly contributed to death in 29 (69%) of 42 patients. Seventy-one patients were initially treated with linezolid, 20 with quinupristin-dalfopristin, and 22 with combinations of other agents. Univariate analysis indicated significantly more deaths in the quinupristin-dalfopristin group (odds ratio, 5.45; 95% confidence interval, 1.89-15.9) and in the other-agents group (odds ratio, 2.94; 95% confidence interval, 1.09-7.94) than in the linezolid group. However, after adjustment for severity of illness, treatment group was not a significant independent factor.
Despite the development of antimicrobial agents with greater potency against VRE, a significant change in clinical outcome was not observed. This suggests that vancomycin resistance does not significantly influence mortality and points to the continued need for prospective, randomized clinical trials.
耐万古霉素肠球菌(VRE)菌血症患者的抗生素耐药性对临床结局的影响仍不明确。比较万古霉素耐药早期与更有效抗生素可获得时期患者结局的数据有限。
对1993年8月至2005年9月在单一机构的113例VRE菌血症患者进行回顾性研究。根据治疗VRE的初始抗生素选择(在有更新的选择之前,利奈唑胺、奎奴普丁-达福普汀或其他药物组合)将患者分组。对VRE菌血症的初始发作进行结局测量,并进行多因素逻辑回归分析以比较各组结局。
总体死亡率为37.2%(113例患者中的42例)。42例患者中有29例(69%)的死亡由VRE菌血症导致或有显著促成作用。71例患者最初接受利奈唑胺治疗,20例接受奎奴普丁-达福普汀治疗,22例接受其他药物组合治疗。单因素分析表明,奎奴普丁-达福普汀组(优势比,5.45;95%置信区间,1.89 - 15.9)和其他药物组(优势比,2.94;95%置信区间,1.09 - 7.94)的死亡人数显著多于利奈唑胺组。然而,在调整疾病严重程度后,治疗组不是一个显著的独立因素。
尽管已开发出对VRE更有效的抗菌药物,但未观察到临床结局有显著变化。这表明万古霉素耐药性不会显著影响死亡率,并指出仍需要进行前瞻性随机临床试验。