Aminoglycosides in Early Sepsis (AGES): A Randomized Pragmatic Clinical Trial Comparing Gentamicin and Narrow Spectrum Betalactams to Broad Spectrum Betalactams as Empirical Treatment in Patients With Suspected Sepsis
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 1,900
- 试验地点
- 5
- 主要终点
- 30-day mortality
研究概览
简要总结
Norwegian guidelines for empirical antibiotic therapy in suspected community acquired sepsis recommend the combination of narrow spectrum betalactam and aminoglycoside as the first choice, but broad spectrum betalactams are considered equally appropriate, effective, and safe. However, fear of renal complications due to gentamicin and concern for lacking evidence for efficiency commonly leads to the use of broad spectrum betalactam therapy, a larger driver of antibiotic resistance.
In patients with suspected community acquired sepsis, the investigators hypothesize that empirical combination therapy with narrow spectrum betalactams and aminoglycosides is safe and non-inferior to empirical therapy with broad spectrum betalactams. More specifically, the investigators hypothesize that the proportion of patients with acute kidney injury or death will be similar between these two treatment groups. Furthermore, the investigators hypothesize that the aminoglycoside-based regimen has lesser impact on the gut microbiome. Antimicrobial resistance is one of the most urgent health threats of our time, and Norwegian hospitals were required but failed to reduce the use of broad-spectrum antibiotics with 30% by the end of 2020. In this context, novel initiatives aiming at reducing use of antibiotics are direly needed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Hospitalized
- •Adults 18 year or older
- •Clinical suspicion of community acquired sepsis with indication for empirical antibiotic therapy
- •National Early Warning Score 2 (NEWS2) ≥ 5
- •Signed informed consent must be obtained and documented according to ICH GCP, and national/local regulations
排除标准
- •Established chronic kidney failure (eGFR < 30 ml/min/1.73m2)
- •Presentation with septic shock with multiorgan failure
- •Suspicion of condition necessitating specific antimicrobial therapy (e.g. atypical pneumonia, fungal infection, parasitic infection, mycobacterial infection)
- •Current or recent use of nephrotoxic drugs (e.g cisplatin within previous 2 months)
- •Suspected or confirmed carrier of extended spectrum betalactamase (ESBL) producing bacteria, methicillin-resistant Staphylococcus aureus (MRSA), or other drug-resistant microbes necessitating specific antimicrobial therapy
- •Multiple myeloma
- •Renal transplantation
- •Renal replacement therapy
- •Myasthenia gravis
- •Known hypersensitivity to any of the study drugs
- •Pregnancy
研究组 & 干预措施
Cefotaxime or piperacillin-tazobactam
Empirical therapy for suspected community-acquired sepsis with broad spectrum betalactam (either one of cefotaxime or piperacillin-tazobactam)
干预措施: Piperacillin-tazobactam (Drug)
Gentamicin + narrow spectrum betalactam
Empirical therapy for suspected community-acquired sepsis with gentamicin + narrow spectrum betalactam (either one of penicillin, ampicillin, or cloxacillin)
干预措施: Gentamicin + narrow spectrum betalactam (Drug)
Cefotaxime or piperacillin-tazobactam
Empirical therapy for suspected community-acquired sepsis with broad spectrum betalactam (either one of cefotaxime or piperacillin-tazobactam)
干预措施: Cefotaxime (Drug)
结局指标
主要结局
30-day mortality
时间窗: Up to 30 days after randomization
All-cause mortality up to 30 days after randomization
30-day acute kidney injury
时间窗: Up to 30 days after randomization
Any acute kidney injury up to 30 days after randomization
次要结局
- In-hospital mortality(During index hospitalization (commonly up to 30 days))
- Duration of hospital stay(During index hospitalization (commonly up to 30 days))
- Duration of intensive care stay(During index hospitalization (commonly up to 30 days))
- Duration of ventilator therapy(During index hospitalization (commonly up to 30 days))
- Duration of vasopressor therapy(During index hospitalization (commonly up to 30 days))
- Hospital readmissions(Up to 30 days after discharge from index hospitalization)
- Post-discharge mortality(Up to 30 days after discharge from index hospitalization)
- Duration of antibiotic treatment(During index hospitalization (commonly up to 30 days))
- Gut microbiome composition(During index hospitalization (commonly up to 30 days))
研究者
Magnus Nakrem Lyngbakken
Professor
University Hospital, Akershus
