Literature DB >> 28258928

Inhaled dry powder mannitol in children with cystic fibrosis: A randomised efficacy and safety trial.

K De Boeck1, E Haarman2, J Hull3, L C Lands4, A Moeller5, A Munck6, J Riethmüller7, H Tiddens8, S Volpi9, J Leadbetter10, B Charlton10, A Malfroot11.   

Abstract

INTRODUCTION: Inhaled mannitol has beneficial effects on lung function, mucociliary clearance, quality of life and sputum properties. This trial examined the efficacy of inhaled mannitol in children with cystic fibrosis (CF).
METHODS: The efficacy of inhaled mannitol in children with CF aged 6-17years was assessed in a phase 2, randomised, placebo-controlled crossover study. Subjects were randomly assigned to mannitol 400mg every 12h or matching placebo for 8weeks, followed by an 8week washout and an 8week period with the alternate treatment. The primary endpoint was the absolute change from baseline in ppFEV1 (percent predicted FEV1).
RESULTS: A total of 92 subjects were studied, with a mean age of 12years and mean baseline ppFEV1 of 72.2%. During mannitol treatment ppFEV1 was 3.42% (p=0.004) higher compared to placebo or a 4.97% (p=0.005) relative difference; relative change from baseline FEF25-75 was 10.52% (p=0.013). During mannitol treatment, acute post-treatment sputum weight was higher (p=0.012). In pre-specified subgroups (rhDNase use, age, and disease severity), the treatment differences consistently favoured mannitol. The most common AEs were cough and pulmonary exacerbations. Pulmonary exacerbation AEs were approximately 30% lower in the mannitol group.
CONCLUSIONS: In children with CF, inhaled mannitol was associated with significant improvements in lung function and sputum weight, irrespective of rhDNase use, age or disease severity. Inhaled mannitol was well tolerated and was associated with a reduced incidence of pulmonary exacerbation AEs. (Clinical Trials.Gov: NCT 01883531).
Copyright © 2017 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cystic fibrosis; FEV1; Mannitol; Paediatric; Randomised

Mesh:

Substances:

Year:  2017        PMID: 28258928     DOI: 10.1016/j.jcf.2017.02.003

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  7 in total

1.  Cost Effectiveness of Inhaled Mannitol (Bronchitol®) in Patients with Cystic Fibrosis.

Authors:  Emma Warren; Kristen Morgan; Toby J Toward; Matthias Schwenkglenks; Joanna Leadbetter
Journal:  Pharmacoeconomics       Date:  2019-03       Impact factor: 4.981

Review 2.  Treatment of Pulmonary Disease of Cystic Fibrosis: A Comprehensive Review.

Authors:  Rosa María Girón Moreno; Marta García-Clemente; Layla Diab-Cáceres; Adrián Martínez-Vergara; Miguel Ángel Martínez-García; Rosa Mar Gómez-Punter
Journal:  Antibiotics (Basel)       Date:  2021-04-23

Review 3.  Inhaled mannitol for cystic fibrosis.

Authors:  Sarah J Nevitt; Judith Thornton; Clare S Murray; Tiffany Dwyer
Journal:  Cochrane Database Syst Rev       Date:  2018-02-09

4.  Development of a Spray-Dried Formulation of Peptide-DNA Nanoparticles into a Dry Powder for Pulmonary Delivery Using Factorial Design.

Authors:  Miftakul Munir; Vicky L Kett; Nicholas J Dunne; Helen O McCarthy
Journal:  Pharm Res       Date:  2022-04-19       Impact factor: 4.580

5.  Inhaled mannitol for cystic fibrosis.

Authors:  Sarah J Nevitt; Judith Thornton; Clare S Murray; Tiffany Dwyer
Journal:  Cochrane Database Syst Rev       Date:  2020-05-01

Review 6.  Treatment of pulmonary exacerbations in cystic fibrosis.

Authors:  Christabella Ng; Tejaswi Nadig; Alan R Smyth; Patrick Flume
Journal:  Curr Opin Pulm Med       Date:  2020-11       Impact factor: 2.868

Review 7.  [Management of Primary Ciliary Dyskinesia].

Authors:  J Raidt; J Brillault; F Brinkmann; A Jung; C Koerner-Rettberg; A Koitschev; H Linz-Keul; T Nüßlein; F C Ringshausen; J Röhmel; M Rosewich; C Werner; H Omran
Journal:  Pneumologie       Date:  2020-09-25
  7 in total

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