Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Kyoto University Health Service, Yoshida-Honmachi, Sakyo-ku, Kyoto 606-8501, Japan.
Int J Infect Dis. 2022 Nov;124:124-132. doi: 10.1016/j.ijid.2022.09.015. Epub 2022 Sep 16.
The potential hazards of extended-spectrum antibiotic therapy for patients with community-acquired pneumonia (CAP) with low risk for drug-resistant pathogens (DRPs) remain unclear; however, risk assessment for DRPs is essential to determine the initial antibiotics to be administered. The study objective was to assess the effect of unnecessary extended-spectrum therapy on the mortality of such patients.
A post hoc analysis was conducted after a prospective multicenter observational study for CAP. Multivariable logistic regression analysis was performed to assess the effect of extended-spectrum therapy on 30-day mortality. Three sensitivity analyses, including propensity score analysis to confirm the robustness of findings, were also performed.
Among 750 patients with CAP, 416 with CAP with a low risk for DRPs were analyzed; of these, 257 underwent standard therapy and 159 underwent extended-spectrum therapy. The 30-day mortality was 3.9% and 13.8% in the standard and extended-spectrum therapy groups, respectively. Primary analysis revealed that extended-spectrum therapy was associated with increased 30-day mortality compared with standard therapy (adjusted odds ratio 2.82; 95% confidence interval 1.20-6.66). The results of the sensitivity analyses were consistent with those of the primary analysis.
Physicians should assess the risk for DRPs when determining the empirical antibiotic therapy and should refrain from administering unnecessary extended-spectrum antibiotics for patients with CAP with a low risk for DRPs.
对于社区获得性肺炎(CAP)低耐药病原体(DRP)风险患者,延长抗生素治疗的潜在危害尚不清楚;然而,DRP 的风险评估对于确定初始抗生素至关重要。本研究的目的是评估对这些患者进行不必要的广谱治疗对死亡率的影响。
在一项 CAP 的前瞻性多中心观察性研究后进行了事后分析。采用多变量逻辑回归分析评估了广谱治疗对 30 天死亡率的影响。还进行了三项敏感性分析,包括倾向评分分析以确认研究结果的稳健性。
在 750 例 CAP 患者中,对 CAP 低 DRP 风险的 416 例患者进行了分析;其中,257 例接受标准治疗,159 例接受了广谱治疗。标准治疗组和广谱治疗组的 30 天死亡率分别为 3.9%和 13.8%。主要分析表明,与标准治疗相比,广谱治疗与 30 天死亡率增加相关(调整优势比 2.82;95%置信区间 1.20-6.66)。敏感性分析的结果与主要分析的结果一致。
当确定经验性抗生素治疗时,医生应评估 DRP 的风险,并且对于 CAP 低 DRP 风险的患者,应避免使用不必要的广谱抗生素。