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. 2004 Oct 18;2004(4):CD004477. doi: 10.1002/14651858.CD004477.pub2
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
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
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
Notes
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment (selection bias) Unclear risk B ‐ Unclear