Literature DB >> 10543292

The effect of inhaled mannitol on bronchial mucus clearance in cystic fibrosis patients: a pilot study.

M Robinson1, E Daviskas, S Eberl, J Baker, H K Chan, S D Anderson, P T Bye.   

Abstract

It has been postulated that hypertonic saline (HS) might impair the antimicrobial effects of defensins within the airways. Alternative non-ionic osmotic agents such as mannitol may thus be preferable to HS in promoting bronchial mucus clearance (BMC) in patients with cystic fibrosis (CF). This study reports the effect of inhalation of another osmotic agent, dry powder Mannitol (300 mg), compared with its control (empty capsules plus matched voluntary cough) and a 6% solution of HS on BMC in 12 patients with cystic fibrosis (CF). Mucus clearance was measured using a radioaerosol/gamma camera technique. Post-intervention clearance was measured for 60 min, followed by cough clearance for 30 min. Neither mannitol nor HS improved BMC during the actual intervention period compared with their respective controls. However during the post-intervention measurement there was a significant improvement in BMC for both the mannitol (8.7+/-3.3% versus 2.8+/-0.7%) and HS (10.0+/-2.3% versus 3.5+/-0.8%). There was also a significant improvement in cough clearance with the Mannitol (9.7+/-2.4%) compared with its control (2.5+/-0.8%). Despite premedication with a bronchodilator, a small fall in forced expiratory volume in one second (FEV1) was seen immediately after administration of both the mannitol (7.3+/-2.5%) and HS (5.8+/-1.2%). Values of FEV1 returned to baseline by the end of the study. Inhaled mannitol is a potential mucoactive agent in cystic fibrosis patients. Further studies are required to establish the optimal dose and the long-term effectiveness of mannitol.

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Year:  1999        PMID: 10543292     DOI: 10.1034/j.1399-3003.1999.14c30.x

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  38 in total

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7.  Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.

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9.  Absorptive clearance of DTPA as an aerosol-based biomarker in the cystic fibrosis airway.

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10.  Quantitative imaging of airway liquid absorption in cystic fibrosis.

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Journal:  Eur Respir J       Date:  2014-04-17       Impact factor: 16.671

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