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Articles that included mixed surgical populations without separable outcomes for eligible interventions, studies with insufficient outcome data, or those involving pediatric populations were excluded after full-text review

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22 In addition to studies on inhaled glutathione for cystic fibrosis, a secondary study on glutathione oral supplementation at 65mg/kg/day in pediatric patients with cystic fibrosis noted supplementation via the oral route to improve growth status and gut inflammation