Woodhead 2006.
Methods | Randomised crossover trial | |
Participants | 30 infants admitted to neonatal intensive care unit, intubated, planned to extubate to HFNC | |
Interventions | Randomised to one modality for 24 hours after extubation then switched to other modality Humidified HFNC ‐ VapothermTM (mean 3.1 L/min); n = 15 Non‐humidified HFNC (mean 1.8 L/min); n = 13 |
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Outcomes | Need for intubation (no pre‐specified criteria); nasal mucosa examination; pneumothorax or pneumomediastinum | |
Notes | Data from the first crossover period only were included in the review Flow rates differed significantly between interventions Funding source unclear |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Random number table, stratified by weight |
Blinding (performance bias and detection bias) Need for intubation | High risk | No set criteria for intubation |
Blinding (performance bias and detection bias) Nasal damage | Low risk | 'Masking' of intervention; unclear how effective |
Other bias | Low risk |