Curley 2005.
| Methods | Parallel RCT of prone and supine positions | |
| Participants | Included: 102 Intubated and ventilated paediatric participants (2 weeks to 18 years) with a PaO2/FiO2 of less than or equal to 300, bilateral pulmonary infiltrates and no clinical evidence of left atrial hypertension Excluded: less than 42 weeks postconceptual age, unable to tolerate a position change, respiratory failure due to cardiac disease, hypoxaemia without bilateral infiltrates, bone marrow or lung transplant, receiving extracorporeal membrane oxygenation, a non‐pulmonary condition that was exacerbated by the prone position, participated in another trial within previous 30 days, decision to limit life support Median age: 2 years; median FiO2: 0.60; diagnosis: pneumonia 28, bronchiolitis with pneumonia 8, sepsis 7, aspiration 6, other 2 Setting: 7 paediatric ICUs, US |
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| Interventions | Patients were placed in the prone position 20 hours/day while in the acute phase of their illness up to a maximum of 7 days; the median time in each position (acute phase) was 4 days in the prone group and 5 days in the supine group | |
| Outcomes | OI; PaO2; PaCO2; tidal volume; minute ventilation; FiO2; PaO2/FiO2; PEEP; extubations; obstructed ETT; pressure ulcers; hypercapnia | |
| Notes | Mortality was also reported at 28 days, however, as the intervention continued only up to a maximum of 7 days, we did not include these data in this review | |
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Low risk | Randomisation performed using a permuted block design |
| Allocation concealment (selection bias) | Low risk | Serial numbered opaque sealed envelopes were used |
| Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Data collection was not blinded but outcomes were not subjective |
| Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Loss to follow‐up 1/102 because consent was withdrawn |