High-flow nasal oxygenation in sedated lung transplant patients during transbronchial biopsy
- Conditions
- ung transplant patientsOxygenation during transbronchial biopsyLung transplant patientsAnaesthesiology - AnaestheticsRespiratory - Other respiratory disorders / diseases
- Registration Number
- ACTRN12619000292178
- Lead Sponsor
- Dr Charles Cartwright
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Aged >=18 years old
Lung transplant patients
Undergoing transbronchial biopsy
English speaking and able to provide informed consent
Aged <18 years old
Non-lung transplant patients
Participants not having transbronchial biopsies conducted
Non-English speaking and unable to provide informed consent
Pre-procedure: respiratory failure/cardiovascular failure/recent pneumothorax (<2 weeks)
Chest tube in-situ
Reduced level of consciousness
Pregnant women
Unable to have the procedure carried out with a propofol infusion
Significant aspiration risk (e.g. gastroparesis/severe GORD) or unable to have the procedure done without endotracheal intubation
Unsuitable for nasal cannulae – recent nasal surgery/epistaxis, significant nasal or sinus issue, marked septal deviation, basal skull fracture
Clinical need for an LMA/intubation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The proportion of participants experiencing a desaturation (defined as SpO2 <94%)[At any point during the bronchoscopy - from the point that the monitoring equipment (including pulse oximeter) and oxygen delivery device are attached in the operating theatre to the point at which they are removed. <br><br>Observations will be automatically uploaded onto the study computer at regular intervals (e.g. every 10 seconds for oxygen saturation). ]
- Secondary Outcome Measures
Name Time Method
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