跳至主要内容
临床试验/NCT07222007
NCT07222007招募中不适用

Association of Induction Agent Choice With Early Mortality and Prognostic Outcomes in Critically Ill Patients: A Large-Scale Retrospective Cohort Analysis

Zeliha Alicikus1 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2026年4月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
4
试验地点
1
主要终点
Primary Outcome will be all-cause mortality at day 7 following tracheal intubation

研究概览

简要总结

The aim of this retrospective cohort study is to compare the safety and efficacy of induction agents for tracheal intubation in critically ill adult patients.

详细描述

Endotracheal intubation is an accepted procedure to optimize oxygenation and ventilation and reduce the risk of aspiration for critically ill patients, essential for their management and survival across various settings, including prehospital care, emergency departments (EDs), and intensive care units (ICUs). Despite advancements, peri-intubation complications and hemodynamic instability, which are associated with increased mortality rates, remain a concern. These risks are exacerbated by pathophysiological factors in critically ill patients compared to those undergoing intubation in surgical settings .

A recent international, multicentre, prospective cohort (INTUBE) study of 2964 critically ill patients undergoing tracheal intubation in the ICU, emergency department, or inpatient wards in 29 countries across five continents reported that the most frequently used agents for induction were Propofol (41.5%), Midazolam (36.4%), Etomidate (17.8%), and Ketamine (14.2%).

The choice of induction agent for intubation may have the potential to minimise or exacerbate complication and mortality. Although considerable research has been carried out, critical central question concern which induction agent is most effective in minimizing cardiovascular instability during intubation. As Kotani and Risotto declared in their recent systematic review, the available findings are insufficient to support conclusive statements. Further studies are needed to identify the optimal agent and dosage, taking into account patient variability and concurrent therapeutic interventions.

Understanding the impact of induction agent selection in critically ill patients has the potential to guide clinical practice in emergency and intensive care settings. Identifying agents with improved survival and prognosis would optimize patient management and inform decision-making for airway management in this vulnerable population. Moreover, delineating which agents exert minimal adverse effects on mortality and prognosis may provide valuable insight for anesthesiologists, intensivists, emergency medicine physicians, and trauma physicians.

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
否

入选标准

  • •Age ≥ 18 years
  • •Admission to the surgical ICU for critical care
  • •Administration of one of the studied induction agents
  • •Availability of complete clinical data

排除标准

  • •Age < 18 years
  • •Absence of documented induction agent administration
  • •Incomplete or missing medical records

研究组 & 干预措施

midazolam

required induction of the following agent in ICU patient

干预措施: induction type for intubation in ICU (Procedure)

propofol

required induction of the following agent in ICU patient

干预措施: induction type for intubation in ICU (Procedure)

ketamine

required induction of the following agent in ICU patient

干预措施: induction type for intubation in ICU (Procedure)

ethomidate

required induction of the following agent in ICU patient

干预措施: induction type for intubation in ICU (Procedure)

结局指标

主要结局

Primary Outcome will be all-cause mortality at day 7 following tracheal intubation

时间窗: day 7

mortality at day 7

次要结局

  • Peri-intubation cardiovascular collapse(perioperatively)
  • Clinical course outcomes(days)

研究者

发起方
Zeliha Alicikus
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Zeliha Alicikus

Assoc. prof. dr

Umraniye Education and Research Hospital

研究点 (1)

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