Hovind Magrit Jarlsdatter, Berdal Jan Erik, Dalgard Olav, Lyngbakken Magnus Nakrem
Department of Infectious Diseases, Akershus University Hospital, Lørenskog, Norway.
Institute for Clinical Medicine, University of Oslo, Oslo, Norway.
Open Forum Infect Dis. 2025 Jun 4;12(6):ofaf319. doi: 10.1093/ofid/ofaf319. eCollection 2025 Jun.
The efficacy and safety of administering a narrow-spectrum β-lactam and gentamicin as empirical therapy for community-acquired sepsis has been questioned. We compared the efficacy and safety of this combination with that of broad-spectrum β-lactams (cefotaxime, piperacillin-tazobactam, or meropenem) in patients with suspected sepsis.
In this retrospective study, we included patients initiated on narrow-spectrum β-lactam/gentamicin or broad-spectrum β-lactams for suspected sepsis between January 2017 and December 2022. Patients without baseline creatinine and at least 1 subsequent creatinine measurement were excluded. We compared the impact of antibiotic regimens using a 5-level ordinal outcome scale ranging from no acute kidney injury (AKI) to all-cause death during 30-day follow-up.
Among 1917 patients, 33.1% received narrow-spectrum β-lactam/gentamicin, and 66.9% received broad-spectrum β-lactams. Patients initiated on broad-spectrum β-lactams had more comorbidities, had lower estimated glomerular filtration rate on admission, and more frequently required treatment with noradrenaline, respiratory support, and admission to the intensive care and medical intermediate care units. Therapy with broad-spectrum β-lactams was associated with a higher posttreatment stage of AKI or death (adjusted odds ratio, 1.61 [95% confidence interval, 1.27-2.04]). We found no significant association between cumulative dose of gentamicin and peak creatinine value. For patients treated with gentamicin experiencing AKI, creatinine normalized during 30-day follow-up.
In patients with suspected sepsis, empirical treatment with narrow-spectrum β-lactam/gentamicin was not associated with an increased risk of AKI or death. If local antimicrobial resistance patterns permit, narrow-spectrum β-lactam/gentamicin may reduce broad-spectrum β-lactam usage, addressing a key element of antibiotic stewardship.
使用窄谱β-内酰胺类药物和庆大霉素作为社区获得性脓毒症的经验性治疗的疗效和安全性受到质疑。我们比较了这种联合用药与广谱β-内酰胺类药物(头孢噻肟、哌拉西林-他唑巴坦或美罗培南)在疑似脓毒症患者中的疗效和安全性。
在这项回顾性研究中,我们纳入了2017年1月至2022年12月期间开始使用窄谱β-内酰胺类药物/庆大霉素或广谱β-内酰胺类药物治疗疑似脓毒症的患者。排除无基线肌酐值且至少有1次后续肌酐测量值的患者。我们使用一个5级有序结局量表比较了抗生素治疗方案的影响,该量表范围从无急性肾损伤(AKI)到30天随访期间的全因死亡。
在1917例患者中,33.1%接受了窄谱β-内酰胺类药物/庆大霉素治疗,66.9%接受了广谱β-内酰胺类药物治疗。开始使用广谱β-内酰胺类药物治疗的患者合并症更多,入院时估计肾小球滤过率更低,更频繁地需要去甲肾上腺素治疗、呼吸支持以及入住重症监护病房和内科中级护理病房。使用广谱β-内酰胺类药物治疗与AKI或死亡的治疗后阶段较高相关(调整后的优势比,1.61[95%置信区间,1.27-2.04])。我们发现庆大霉素的累积剂量与肌酐峰值之间无显著关联。对于接受庆大霉素治疗且发生AKI的患者,肌酐在30天随访期间恢复正常。
在疑似脓毒症患者中,使用窄谱β-内酰胺类药物/庆大霉素进行经验性治疗与AKI或死亡风险增加无关。如果当地抗菌药物耐药模式允许,窄谱β-内酰胺类药物/庆大霉素可能会减少广谱β-内酰胺类药物的使用,这是抗生素管理的一个关键要素。