Faculty of Medicine, School of Medicine, National Yang-Ming University, Taipei, Taiwan.
Department of Emergency Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Antimicrob Agents Chemother. 2017 Aug 24;61(9). doi: 10.1128/AAC.00931-17. Print 2017 Sep.
Breakthrough bacteremia during carbapenem therapy is not uncommon, and it creates therapeutic dilemmas for clinicians. This study was conducted to evaluate the clinical and microbiological characteristics of breakthrough bacteremia during carbapenem therapy and to assess the efficacy of various antimicrobial therapies. We analyzed 100 adults who developed breakthrough bacteremia during carbapenem therapy at 4 medical centers over a 6-year period. Their 30-day mortality rate was 57.0%, and the carbapenem resistance rate of their isolates was 87.0%. Among patients with carbapenem-resistant bacteremia, breakthrough bacteremia during carbapenem therapy was associated with a significantly higher 14-day mortality (51.7% versus 37.4%, respectively; = 0.025 by bivariate analysis) and a higher 30-day mortality ( = 0.037 by log rank test of survival analysis) than in the nonbreakthrough group. For the treatment of breakthrough bacteremia during carbapenem therapy, tigecycline-based therapy was associated with a significantly higher 30-day mortality (80.0%) than those with continued carbapenem therapy (52.5%) and colistin-based therapy (57.9%) by survival analysis ( = 0.047 and 0.045 by log rank test, respectively). Cox regression controlling for confounders, including severity of illness indices, demonstrated that treatment with tigecycline-based therapy for breakthrough bacteremia was an independent predictor of 30-day mortality (hazard ratio, 3.659; 95% confidence interval, 1.794 to 7.465; < 0.001). Patients with breakthrough bacteremia during carbapenem therapy posed a high mortality rate. Tigecycline should be used cautiously for the treatment of breakthrough bacteremia that develops during carbapenem therapy.
碳青霉烯类治疗期间发生的突破性菌血症并不少见,这给临床医生带来了治疗上的困境。本研究旨在评估碳青霉烯类治疗期间发生的突破性菌血症的临床和微生物学特征,并评估各种抗菌治疗的疗效。我们分析了 4 家医疗中心在 6 年期间发生碳青霉烯类治疗期间发生的 100 例成人突破性菌血症患者。他们的 30 天死亡率为 57.0%,其分离株的碳青霉烯类耐药率为 87.0%。在碳青霉烯类耐药菌血症患者中,碳青霉烯类治疗期间发生的突破性菌血症与 14 天死亡率显著升高(分别为 51.7%和 37.4%;卡方检验, = 0.025)和 30 天死亡率显著升高(生存分析的对数秩检验, = 0.037)相关。对于碳青霉烯类治疗期间发生的突破性菌血症的治疗,替加环素为基础的治疗与继续碳青霉烯类治疗(30 天死亡率为 52.5%)和多黏菌素类为基础的治疗(30 天死亡率为 57.9%)相比,30 天死亡率显著升高(生存分析的对数秩检验, = 0.047 和 0.045)。校正严重程度指数等混杂因素的 Cox 回归分析显示,替加环素为基础的治疗治疗突破性菌血症是 30 天死亡率的独立预测因素(危险比,3.659;95%置信区间,1.794 至 7.465; < 0.001)。碳青霉烯类治疗期间发生的突破性菌血症患者死亡率较高。替加环素治疗碳青霉烯类治疗期间发生的突破性菌血症应谨慎使用。