Al-Hasan Majdi N, Wilson John W, Lahr Brian D, Thomsen Kristine M, Eckel-Passow Jeanette E, Vetter Emily A, Tleyjeh Imad M, Baddour Larry M
University of Kentucky Chandler Medical Center, Lexington, KY 40536, USA.
Antimicrob Agents Chemother. 2009 Apr;53(4):1386-94. doi: 10.1128/AAC.01231-08. Epub 2009 Jan 21.
The role of combination antibiotic therapy with a beta-lactam and a fluoroquinolone for bacteremia caused by gram-negative bacilli, to our knowledge, has not been previously described. Much of the previous study of combination therapy has included beta-lactams and aminoglycosides. We conducted a large retrospective cohort study to evaluate 28-day all-cause mortality in patients with monomicrobial bacteremia due to aerobic gram-negative bacilli who received either a combination of beta-lactams and fluoroquinolones or beta-lactam monotherapy. We enrolled adult patients admitted to Mayo Clinic hospitals from 1 January 2001 to 31 October 2006 in the study. After stratification of patients by Pitt bacteremia scores, we used Cox regression models to estimate the hazard ratios (HR) for 28-day all-cause mortality after adjusting for the propensity to receive combination therapy. We identified 398 and 304 unique patients with bacteremia caused by gram-negative bacilli who received single and combination antibiotic therapy, respectively. In less severely ill patients with Pitt bacteremia scores of <4, combination therapy was associated with lower 28-day mortality than single therapy (4.2% [9 of 214] versus 8.8% [28 of 319]; adjusted HR, 0.44; 95% confidence interval [CI], 0.20 to 0.98; P = 0.044). In critically ill patients with Pitt bacteremia scores of >or=4, there was no difference in 28-day mortality between combination and single therapy (25.6% [23 of 90] versus 27.8% [22 of 79]; adjusted HR, 0.87; 95% CI, 0.47 to 1.62; P = 0.660). These findings were consistent for 14-day all-cause mortality. In this large cohort, we found for the first time that combination therapy with beta-lactams and fluoroquinolones was associated with a reduction in 28-day all-cause mortality among less severely ill patients with bacteremia caused by gram-negative bacilli.
据我们所知,β-内酰胺类药物与氟喹诺酮类药物联合用于治疗革兰氏阴性杆菌引起的菌血症的作用此前尚未被描述。先前关于联合治疗的研究大多涉及β-内酰胺类药物和氨基糖苷类药物。我们进行了一项大型回顾性队列研究,以评估因需氧革兰氏阴性杆菌引起的单微生物菌血症患者接受β-内酰胺类药物与氟喹诺酮类药物联合治疗或β-内酰胺类单药治疗后的28天全因死亡率。我们纳入了2001年1月1日至2006年10月31日入住梅奥诊所医院的成年患者进行研究。在根据皮特菌血症评分对患者进行分层后,我们使用Cox回归模型来估计在调整接受联合治疗的倾向后28天全因死亡率的风险比(HR)。我们分别确定了398例和304例由革兰氏阴性杆菌引起菌血症并接受单一抗生素治疗和联合抗生素治疗的独特患者。在皮特菌血症评分<4的病情较轻的患者中,联合治疗与单一治疗相比,28天死亡率更低(4.2%[214例中的9例]对8.8%[319例中的28例];调整后的HR为0.44;95%置信区间[CI]为0.20至0.98;P = 0.044)。在皮特菌血症评分≥4的重症患者中,联合治疗与单一治疗的28天死亡率没有差异(25.6%[90例中的23例]对27.8%[79例中的22例];调整后的HR为0.87;95%CI为0.47至1.62;P = 0.660)。这些结果在14天全因死亡率方面是一致的。在这个大型队列中,我们首次发现,对于由革兰氏阴性杆菌引起菌血症的病情较轻的患者,β-内酰胺类药物与氟喹诺酮类药物联合治疗与28天全因死亡率降低相关。