Division of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Korea.
Division of Allergy and Pulmonary Medicine, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.
J Korean Med Sci. 2023 Oct 23;38(41):e353. doi: 10.3346/jkms.2023.38.e353.
There is insufficient data on the benefits of empiric antibiotic combinations for hospital-acquired pneumonia (HAP). We aimed to investigate whether empiric anti-pseudomonal combination therapy with fluoroquinolones decreases mortality in patients with HAP.
This multicenter, retrospective cohort study included adult patients admitted to 16 tertiary and general hospitals in Korea between January 1 and December 31, 2019. Patients with risk factors for combination therapy were divided into anti-pseudomonal non-carbapenem β-lactam monotherapy and fluoroquinolone combination therapy groups. Primary outcome was 30-day mortality. Propensity score matching (PSM) was used to reduce selection bias.
In total, 631 patients with HAP were enrolled. Monotherapy was prescribed in 54.7% (n = 345) of the patients, and combination therapy was prescribed in 45.3% (n = 286). There was no significant difference in 30-day mortality between the two groups (16.8% vs. 18.2%, = 0.729) or even after the PSM (17.5% vs. 18.2%, = 0.913). After the PSM, adjusted hazard ratio for 30-day mortality from the combination therapy was 1.646 (95% confidence interval, 0.782-3.461; = 0.189) in the Cox proportional hazards model. Moreover, there was no significant difference in the appropriateness of initial empiric antibiotics between the two groups (55.0% vs. 56.8%, = 0.898). The proportion of multidrug-resistant (MDR) pathogens was high in both groups.
Empiric anti-pseudomonal fluoroquinolone combination therapy showed no survival benefit compared to β-lactam monotherapy in patients with HAP. Caution is needed regarding the routine combination of fluoroquinolones in the empiric treatment of HAP patients with a high risk of MDR.
目前有关经验性抗假单胞菌抗生素联合治疗医院获得性肺炎(HAP)获益的数据不足。本研究旨在探讨 HAP 患者经验性应用氟喹诺酮类药物联合抗假单胞菌治疗是否能降低死亡率。
这是一项多中心、回顾性队列研究,纳入 2019 年 1 月 1 日至 12 月 31 日期间韩国 16 家三级和综合医院的成年住院患者。有联合治疗适应证的患者被分为抗假单胞菌非碳青霉烯类β-内酰胺单药治疗组和氟喹诺酮类联合治疗组。主要结局为 30 天死亡率。采用倾向性评分匹配(PSM)减少选择偏倚。
共纳入 631 例 HAP 患者,其中 54.7%(n=345)接受单药治疗,45.3%(n=286)接受联合治疗。两组 30 天死亡率无显著差异(16.8% vs. 18.2%, = 0.729),PSM 后也无显著差异(17.5% vs. 18.2%, = 0.913)。PSM 后,多因素 Cox 比例风险回归模型显示联合治疗组 30 天死亡率的调整后风险比为 1.646(95%置信区间:0.782-3.461; = 0.189)。此外,两组初始经验性抗生素的适宜性无显著差异(55.0% vs. 56.8%, = 0.898)。两组均以多重耐药(MDR)病原体为主。
与β-内酰胺单药治疗相比,HAP 患者经验性应用氟喹诺酮类药物联合抗假单胞菌治疗并未带来生存获益。对于 MDR 风险较高的 HAP 患者,在经验性治疗中常规联合氟喹诺酮类药物时需谨慎。