NCT03229460.
Study name | High‐flow nasal oxygen therapy in perioperative period of the adult with hypercapnic and hypoxemic respiratory failure |
Methods | RCT, parallel‐group design |
Participants | Estimated number of participants: 150 Setting: China Inclusion criteria: AHRF; severe dyspnoea at rest with respiratory rate > 25 breaths/min; PaO2/FiO2 < 300; PaCO2 < 45 mmHg Exclusion criteria: age < 18 years; contraindications to NIV; chronic respiratory disease; cardiac pulmonary oedema; predefined intubation; haemodynamic instability or need for vasopressors; GCS ≤ 12; profound leukopenia |
Interventions | Intervention group (HFNC): flow = 30 to 60 L/min; FiO2 adjusted to target SpO2 > 92 % Control group 1 (standard oxygen therapy): flow ≥ 10 L/min Control group 2 (NIV): face mask; FiO2 and/or PEEP adjusted to target SpO2 > 92 % |
Outcomes | All outcomes reported: intubation rate Outcomes relevant to this review: intubation rate |
Starting date | 25 July 2017 |
Contact information | Bin He, hebinicu@139.com. Dongjuan Tang, 317582862@qq.com |
Notes |