Reducing high respiratory drive to facilitate supported ventilation in ARDS patients: a pilot study
- Conditions
- Acute respiratory distress syndromesevere lung syndrome10024970
- Registration Number
- NL-OMON38185
- Lead Sponsor
- niversitair Medisch Centrum Sint Radboud
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 12
• age > 18 year
• informed consent
• ARDS according to the Berlin definition
• RASS -4/-5
• tidal volume > 8 ml/kg during supported ventilation
• esophageal EMG catheter with balloons in situ
• recent use of muscle relaxants / neuromuscular blocking agents (< 3 hours)
• pre-existent neuromuscular disease (congenital or acquired) or diseases / disorders know to be associated with myopathy including auto-immune diseases
• phrenic nerve lesions
• elevated intracranial pressure or clinical suspicion of elevated intracranial pressure (i.e. neurotrauma)
• open chest or abdomen
• pregnancy
• systolic blood pressure < 90 mm Hg / mean arterial pressure (MAP) < 65 mm Hg
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main study parameter is the ability to titrate rocuronium in order to<br /><br>decrease the tidal volume (Vt) to approximately 6 ml/kg (yes/no). </p><br>
- Secondary Outcome Measures
Name Time Method <p>• Respiratory rate<br /><br>• Diaphragm activity (Edi)<br /><br>• Transpulmonary pressure<br /><br>• Transdiaphragmatic pressure<br /><br>• Work of breathing<br /><br>• Dynamic and static respiratory compliance<br /><br>• Neuroventilatory efficiency (tidal volume/Edi)<br /><br>• Neuromechanical efficiency (transdiaphragmatic pressure/Edi)<br /><br>• Patient-ventilator contribution to breathing: PVBC = (tidal volume/Edi,<br /><br>no-assist) / (tidal volume/Edi, assist)<br /><br>• Oxygenation index (arterial oxygen tension / fraction of inspired oxygen)<br /><br>• Patient-ventilator asynchrony</p><br>