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临床试验/NCT05352997
NCT05352997已完成不适用

Key Factors of Target Serum Concentrations Attainment From Beta-lactams Therapeutic Drug Monitoring in Critically Ill Patients

Centre Hospitalier Universitaire de Nīmes1 个研究点 分布在 1 个国家目标入组 156 人开始时间: 2018年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
156
试验地点
1
主要终点
To identify factors associated with adequate beta lactam plasma concentrations on the first sample

研究概览

简要总结

The population of these monocentric and retrospective study includes patients hospitalized in one of the critical care services of Nîmes' community hospital.

The objective is to determine the key factors that lead to satisfactory beta-lactams serum concentrations in critically ill patients.

Clinical and biological features, as well as risk scores are collected and recorded into an electronic Case Report Form.

The primary outcome is to show the main characteristics related to adequate beta-lactams serum concentrations in critically ill inpatients.

Secondary outcomes include the key factors related to inadequate beta-lactams serum concentrations in critically ill inpatients, Therapeutic Drug Monitoring (TDM) impact in the achievement of target beta-lactams serum concentration and the correlation between Aminoglycosides and Beta-lactams serum concentrations. Do both antibiotics have similar elimination kinetics ?

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

  • Patient aged at least (≥) 18 years of age.
  • Patient (or his representative for patients unable to give their consent) has given his free and informed consent and has signed the consent form.
  • Patient affiliated to the health insurance scheme
  • Patient hospitalized in one of the critical care services of Nimes' community hospital with at least one beta-lactam treatment
  • Patient with at least one beta-lactam TDM during his stay
  • Exclusion Criteria :
  • Patient who did not consent the use of his personal data
  • Patients under maintenance of justice, tutelage or legal guardianship
  • Patient previously included in the study.

排除标准

  • 未提供

结局指标

主要结局

To identify factors associated with adequate beta lactam plasma concentrations on the first sample

时间窗: Day 7

Determinants of adequate beta-lactams plasma concentrations using a univariate, then a multivariate analysis on patients 'characteristics at baseline and on the day of TDM

次要结局

  • To identify factors related with on-target beta-lactams plasma concentrations on the second sample(Day 7)
  • Impact of TDM(Day 7)
  • To assess if beta-lactams and Aminoglycosides have the same elimination kinetic(Day 7)

研究者

发起方
Centre Hospitalier Universitaire de Nīmes
申办方类型
Other
责任方
Sponsor

研究点 (1)

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