Maine Medical Center, Portland, ME, USA.
Maine Medical Center, Portland, ME, USA; Tufts University School of Medicine, Boston, MA, USA.
Int J Antimicrob Agents. 2018 May;51(5):687-692. doi: 10.1016/j.ijantimicag.2017.12.007. Epub 2017 Dec 25.
Enterobacteriaceae bloodstream infections (EB-BSIs) are a common manifestation of Gram-negative sepsis and are initially managed with empirical intravenous antibiotics. Upon stabilisation and source control, patients are often transitioned to an oral agent. Fluoroquinolones (FQs) plays a prominent role in stepdown therapy for severe infections owing to favourable pharmacokinetic parameters; however, serious adverse events (AEs) have been documented with their use. A total of 224 adults with EB-BSI initiated on empirical intravenous antibiotics with stepdown to oral β-lactam (BLM) (n = 84) or FQ (n = 140) were studied to compare clinical success and identify risk factors for treatment failure. Subgroups of early versus late oral stepdown and short versus extended duration of therapy (DOT) were assessed. Stepdown therapy with oral BLM was non-inferior to oral FQ (86.9% vs. 87.1%; mean difference 0.2%, 97.5% CI -10.3 to 10.7). Microbiological success (94.0% vs. 97.9%; P > 0.05) and 30-day re-admission (14.3% vs. 14.3%; P > 0.05) were similar. Patients were more likely to complete their BLM course without an AE compared with FQs (91.7% vs. 82.1%; P = 0.049). Clinical success was comparable between early and late stepdown (86.7% vs. 87.5%; P > 0.05) and short versus extended DOT (88.2% vs. 86.7%; P > 0.05). Negative predictors of clinical success identified by logistic regression were complicated diabetes (OR = 0.35, 95% CI 0.15-0.83) and urinary abnormality (OR = 0.39, 95% CI 0.16-0.94). These findings suggest that oral BLMs were non-inferior to FQs as stepdown therapy for EB-BSI, with less AEs.
肠杆菌科血流感染(EB-BSI)是革兰氏阴性菌败血症的常见表现,最初采用经验性静脉内抗生素治疗。在稳定病情和控制源头后,患者通常会转为口服药物。氟喹诺酮类药物(FQs)由于其良好的药代动力学参数,在严重感染的降阶梯治疗中发挥着重要作用;然而,它们的使用也有严重不良事件(AE)的记录。共有 224 名患有 EB-BSI 的成年人接受了经验性静脉内抗生素治疗,随后降阶梯为口服β-内酰胺(BLM)(n=84)或 FQ(n=140)。本研究比较了临床疗效,并确定了治疗失败的危险因素。评估了早期与晚期口服降阶梯和治疗时间长短(DOT)的亚组。口服 BLM 降阶梯治疗与口服 FQ 相比不劣效(86.9%比 87.1%;平均差异 0.2%,97.5%CI-10.3 至 10.7)。微生物学疗效(94.0%比 97.9%;P>0.05)和 30 天再入院率(14.3%比 14.3%;P>0.05)相似。与 FQs 相比,患者更有可能完成 BLM 疗程而无 AE(91.7%比 82.1%;P=0.049)。早期和晚期降阶梯(86.7%比 87.5%;P>0.05)以及短疗程与长疗程 DOT(88.2%比 86.7%;P>0.05)的临床疗效相当。逻辑回归分析确定的临床疗效的阴性预测因素为复杂型糖尿病(OR=0.35,95%CI 0.15-0.83)和尿异常(OR=0.39,95%CI 0.16-0.94)。这些发现表明,口服 BLM 作为 EB-BSI 的降阶梯治疗与 FQs 相当,不良事件更少。