Abstract

Background:Osmotic agents, such as inhaled dry powder mannitol, may increase mucociliary clearance by rehydrating the airway surface liquid and thus act as disease-modifying treatments in cystic fibrosis (CF). This is...

Highlights

  • Osmotic agents, such as inhaled dry powder mannitol, may increase mucociliary clearance by rehydrating the airway surface liquid and act as disease-modifying treatments in cystic fibrosis (CF)

  • forced expiratory volume in 1 s (FEV1) and the secondary outcome measures were analysed on a measurement scale and the results presented as mean differences

  • Forty-five children were recruited to the study, 38 of whom underwent an airway challenge with inhaled mannitol

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Summary

Introduction

Osmotic agents, such as inhaled dry powder mannitol, may increase mucociliary clearance by rehydrating the airway surface liquid and act as disease-modifying treatments in cystic fibrosis (CF). This is the first therapeutic trial of inhaled mannitol in children with CF; it was compared with recombinant human deoxyribonuclease (rhDNase), the current best established mucolytic treatment. Subjects underwent an initial bronchial provocation challenge with dry powder mannitol Those children with a negative challenge were randomly allocated to one of three consecutive 12-week treatment blocks (inhaled mannitol alone, nebulised rhDNase alone and mannitol + rhDNase). A number of secondary outcome measures were studied.

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