Jet or Vibrating Mesh Nebulisation for Secretion Management in ICU
Respiratory Failure, Critical Illness
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About this trial
This is an interventional treatment trial for Respiratory Failure focused on measuring nebuliser, secretions
Eligibility Criteria
Inclusion Criteria: Patient aged 18-80 years at time of recruitment to study Ventilated via an endotracheal tube or tracheostomy with an HME filter in the circuit Secretion load defined as patient requiring suctioning at least 2 times in the 6 hours prior to recruitment Sputum viscosity with grades 1 to 3 pourability in the Qualitative Sputum Assessment tool Not yet received saline nebulisation in the 6 hours prior to recruitment Likely to be ventilated via an endotracheal tube or tracheostomy for at least 3 days in the opinion of the treating clinician Exclusion Criteria: Pregnancy Pulmonary embolus Heart Failure (NYHA Grade III/IV) Clinical evidence of frank pulmonary oedema Cardiovascular instability (systolic BP ≤75 or heart rate ≥140)
Sites / Locations
- Queen Elizabeth University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Active Comparator
Continuous nebulisation 0.9% saline Aerogen Solo vibrating mesh Nebuliser
Intermittent nebulisation 0.9% saline Aerogen Solo vibrating mesh Nebuliser
Intermittent standard nebulisation of 0.9% saline Intersurgical Cirrus 2 self sealing Jet Nebuliser
Continuous nebulization of 0.9% normal saline using the Aerogen Solo Nebuliser (50mls/24h continuous infusion using a syringe pump)
Intermittent nebulization of 0.9% normal saline using the Aerogen Solo Nebuliser (5mls 0.9% normal saline nebulised every 6 hours)
Intermittent standard nebulization of 0.9% normal saline using the Intersurgical Cirrus 2 self-sealing Jet Nebuliser ((5mls 0.9% normal saline nebulised every 6 hours)