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临床试验/NCT06148467
NCT06148467招募中不适用

Incidence of Reverse Trigger Phenotypes and Response to Ventilatory Adjustments in Patients With ARDS

Hospital Civil de Guadalajara1 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2023年11月17日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
130
试验地点
1
主要终点
Incidence of reverse trigger

研究概览

简要总结

The goal of this prospective observational study is to describe the incidence of reverse trigger (RT) in mechanically ventilated patients with diagnosis of acute respiratory distress syndrome (ARDS).

The main questions it aims to answer are:

  • Real incidence of RT based on continuous monitoring
  • The response to mechanical ventilatiory adjustments Participants will be included as soon as neuromuscular blockers (NMB)/sedation is stopped or in case of spontaneous respiratory efforts detection, whatever happens first. Continuous monitoring will be performed by esophageal manometry until switch to a pressure support (spontaneous) mode, restart of deep sedation/neuromuscular blockers by medical indication, or death.

In order to allow detection of possible RT in patients with ongoing sedation/NMB, mechanical ventilator waveforms will be screened every 1-2 hours by investigators and critical care physicians with at least 1 year of specific training in detection of dyssynchronies.

详细描述

Measurements:

An esophageal catheter for manometry will be placed as usual practice with confirmation of adequate position with the Baydur's occlusion test before recordings. An independent flow sensor and pressure transducer will be placed and connected to a laptop computer to obtain real-time monitoring along with continuous recordings, which then will be off-line analyzed by two experts, for confirmation of RT and characterization.

Data collection:

Main cause of the acute respiratory failure and days on mechanical ventilation until enrollment will be collected as well as demographic characteristics, including APACHE II, SOFA and the previous requirement of prone positioning therapy.

At identification of the RT, drugs for sedation and analgesia, time from initiation of mechanical ventilation to RT identification and blood gas analysis will be recorded. Ventilatory settings will also be collected, including the control variable of the ventilatory mode (volume or pressure), respiratory rate, received tidal volume in ml/kg of predicted body weight, maximum inspiratory flow, ratio of partial arterial oxygen pressure (pO2) to fraction of inspired oxygen (FiO2), driving pressure and (positive end-expiratory pressure (PEEP). Data about esophageal pressure related to RT will also be recorded, including the magnitude of pressure swing, phase angle, coefficient of variation, RT phenotype, entrainment ratio and the presence of breath stacking.

研究设计

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

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of ARDS according to the Berlin criteria and added New Global Definition 2023
  • Mechanical ventilation

排除标准

  • <18 years
  • Tracheostomy status
  • Pneumothorax
  • Tube thoracostomy with air leaks

结局指标

主要结局

Incidence of reverse trigger

时间窗: 60 days

Proportion of patients who developed reverse trigger

次要结局

  • Mortality(60 days)
  • ICU length of stay(60 days)
  • Days of mechanical ventilation(60 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Miguel Á Ibarra-Estrada

MD

Hospital Civil de Guadalajara

研究点 (1)

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