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临床试验/NCT03776409
NCT03776409已完成不适用

Comparison of the Nephrotoxicity of Vancomycin in Combination With Piperacillin/Tazobactam or Other Beta-lactams in Critically Ill Patients: A Retrospective, Multicenter Study in China

First Affiliated Hospital Xi'an Jiaotong University1 个研究点 分布在 1 个国家目标入组 700 人开始时间: 2018年12月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
700
试验地点
1
主要终点
clinical efficacy

研究概览

简要总结

The combination of vancomycin and piperacillin-tazobactam has been associated with an increased risk of acute kidney injury (AKI) in non-critically ill patient populations, but it is still unknown if this association exists in critically ill patients. The objective of this study is to compare AKI and efficacy of vancomycin plus piperacillin-tazobactam or beta-lactams.

详细描述

The combination of vancomycin and piperacillin-tazobactam has been associated with an increased risk of acute kidney injury (AKI) in non-critically ill patient populations, but limited data regarding this association exists in critically ill patients. The objective of this study is to compare AKI and efficacy of vancomycin plus piperacillin-tazobactam or beta-lactams.

This is a multicenter, retrospective cohort study. Patients from the retrospective cohort will be divided into 2 groups based on the combination regimen received . Patients who meet the inclusion and exclusion criteria will be included in our registry. As a non-intervention study, these information as below will be collected: basic demographics, diagnosis, concomitant nephrotoxic and other antibiotic medications, serum creatine levels, vancomycin concentrations, and indication for antibiotics.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 years or older,
  • admitted to intensive care unit
  • received the combination of vancomycin and beta-lactams for at least 48 hours
  • had a serum creatinine level measured within 24-hour hospital admission
  • had at least one VAN level drawn while receiving a combination of study antibiotics

排除标准

  • pregnancy or lactating patients
  • admission to the intensive care unit during administration or within 72 hours of completing the antibiotics
  • had end-stage renal disease
  • died within 48 hours of combination antibiotic therapy initiation

研究组 & 干预措施

vancomycin plus piperacillin/tazobactam

Critically ill patients who received the combination of VAN (vancomycin) and PTZ (piperacillin/tazobactam) for at least 48 hours during an ICU (intensive care unit) admission, had a baseline serum creatinine (Scr) concentration value within 24 hours of hospital admission.The dosage and frequency of VAN and PTZ were adjusted based on clinical practice and patient characteristics. This is an observational study without any intervention.

干预措施: vancomycin plus piperacillin/tazobactam (Drug)

vancomycin plus other beta-lactams

Critically ill patients who received the combination of VAN (vancomycin) and other beta-lactams (cefoperazone/sulbactam, meropenem, imipenem/siastatin, ceftriaxone, ceftazidime, et al) for at least 48 hours during an ICU (intensive care unit) admission, had a baseline serum creatinine (Scr) concentration value within 24 hours of hospital admission.The dosage and frequency of VAN and other beta-lactams were adjusted based on clinical practice and patient characteristics. This is an observational study without any intervention.

干预措施: vancomycin plus other beta-lactams (Drug)

结局指标

主要结局

clinical efficacy

时间窗: from 24 hours after the start of the combination until discharge up to one month

microbial eradication

AKI(acute kidney injury)

时间窗: from 24 hours after the start of the combination until discharge up to one month

the incidence of acute kidney injury

次要结局

  • onset of AKI(the first occurence of AKI after starting concomitant antimicrobial use up to one month)
  • whether renal function return to baseline or not(from AKI onset to resolution of defined AKI up to one month)
  • the length of hospital stay(from hospital admission to discharge up to one month)
  • duration of AKI(the time from AKI onset to resolution of AKI up to one month)
  • major acute kidney events at 30 days (MAKE30)(MAKE30 is assessed 30 days following AKI diagnosis)
  • vancomycin trough value assessment(from hospital admission to discharge up to one month)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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