跳至主要内容
临床试验/ISRCTN24603037
ISRCTN24603037进行中(未招募)未知

A feasibility study examining the use of Mechanical Insufflation Exsufflation to promote extubation success in adult intensive care

niversity Hospitals Bristol and Weston NHS Foundation Trust0 个研究点目标入组 47 人开始时间: 2022年5月16日最近更新:

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
47

研究概览

简要总结

2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/37488566/ (added 25/07/2023)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Adult (>=16 years)
  • 2. Expected to require invasive mechanical ventilation for >48hrs
  • 3. Clinician identified pre-extubation problems with secretion management defined as poor/weak cough effort (cough peak flow <60L/min) and/or secretion load that are difficult to clear with usual airway clearance management (as assessed by the treating clinical team)
  • 4. Identified as ‘ready to wean or weaning’ by the treating clinical team (on a spontaneous mode of ventilation for example Continuous Positive Airway Pressure (CPAP); Assisted Spontaneous Breathing (ASB); Pressure Support Ventilation (PSV); Airway Pressure Release Ventilation (APRV) (with spontaneous effort).

排除标准

  • 1. Positive End Expiratory Pressure (PEEP) >10
  • 2. Fraction of Inspired Oxygen (FiO2) >0.7
  • 3. Hemodynamic/Cardiovascular instability (i.e. noradrenaline >0.25mg/kg, arrhythmias requiring intervention)
  • 4. Recent undrained pneumothorax (current admission with no chest drain in situ);
  • 5. Unable to continue to use MI-E post extubation (i.e. contraindications to facemask use-facial/cranial trauma, recent facial surgery; active upper gastrointestinal bleeding/uncontrolled vomiting; recent upper abdominal/thoracic surgery with at risk anastomosis)
  • 6. Pre-existing neuromuscular respiratory condition
  • 7. Pre-existing routine use of MI-E in the community
  • 8. Patients with pre-existing permanent tracheostomy
  • 9. Treatment withdrawal expected within 24hrs or not expected to survive
  • 10. Re-admission to ICU following index admission
  • 11. Previous MERIT trial participation

研究者

发起方
niversity Hospitals Bristol and Weston NHS Foundation Trust

相似试验