| Methods | n = 66, 1 centre Allocation concealment: not described Baseline similarity: age Blinding: caregivers Cointerventions: corticosteroid administration "no different" between groups Withdrawals: none Losses to follow‐up: none |
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| Participants | Inclusions: Risk factor for ARDS; PaO2 < 55 mmHg on room air or P/F < 250 mmHg; duration of intubation < 24 hours Exclusions: Chronic lung, cardiovascular, liver or renal disease |
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| Interventions | IV NAC, bolus 150 mg/kg, then 20 mg/kg/hour continuously for 7 days (total dose 3510 mg/kg), or placebo | |
| Outcomes | 60 day mortality: RR 1.06 (95% CI 0.67 to 1.70) Adverse events leading to discontinuation of therapy: treatment: 1/32 (rash), control: 0/34 |
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| Notes | ||
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Allocation concealment (selection bias) | Unclear risk | B ‐ Unclear |