High-dose oral ambroxol for early treatment of pulmonary acute respiratory distress syndrome: An exploratory, randomized, controlled pilot trial

Abstract

Objective: To evaluate efficacy of high-dose oral ambroxol in acute respiratory distress syndrome (ARDS) with respect to ventilator-free days (VFD). Design: Prospective, randomized, placebo-controlled, blinded pilot trial. Patients: Sixty-six mechanically ventilated patients (1 month to 12 years) with ARDS who were hand-ventilated for <24 hr before pediatric intensive care unit admission. Interventions: Patients randomized to oral ambroxol (40 mg/kg/day, in four divided doses) (n=32) or placebo (n=34) until 10 days, extubation or death whichever is earlier. Measurements and Main Results: Majority (91%) had pneumonia and bronchiolitis. Two study groups were similar in baseline characteristics. Mean partial pressure of arterial oxygen/fraction of inspired oxygen and oxygenation index were >175 and <10, respectively, with no difference in the two study groups. VFD were similar in the two study groups. Overall mortality was 26%. No adverse events were noted with ambroxol. Conclusions: Among ventilated pulmonary ARDS patients with oxygenation index of <10, mortality was 26%. Ambroxol did not improve VFD. Study with higher and more frequently administered doses of ambroxol in larger sample is suggested after having generated relevant pharmacokinetic data among critically ill children.