Precise dosing of five drugs commonly used by patients with cystic fibrosis using an adaptive aerosol delivery system

R. Potter, K. Williams, S. Byrne, K. Nikander, R. Hatley (Chichester, United Kingdom; Parsippany, NJ, United States Of America)

Source: Annual Congress 2008 - Cystic fibrosis: new mechanisms, monitoring and treatment tools
Session: Cystic fibrosis: new mechanisms, monitoring and treatment tools
Session type: E-Communication Session
Number: 2877

Congress or journal article abstractE-poster

Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
R. Potter, K. Williams, S. Byrne, K. Nikander, R. Hatley (Chichester, United Kingdom; Parsippany, NJ, United States Of America). Precise dosing of five drugs commonly used by patients with cystic fibrosis using an adaptive aerosol delivery system. Eur Respir J 2008; 32: Suppl. 52, 2877

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
Use of a new feedback tool to optimize inhaled aerosol therapy in patients with cystic fibrosis
Source: Eur Respir J 2006; 28: Suppl. 50, 261s
Year: 2006

Nebulised antibiotics with the I-neb adaptive aerosol delivery (AAD) system: Impact on adherence in cystic fibrosis (CF) patients
Source: Annual Congress 2012 - Cystic fibrosis (adults and children): risk factors and clinical problems
Year: 2012


Improved treatment response to dornase alfa in cystic fibrosis patients using controlled inhalation
Source: Eur Respir J 2011; 38: 1328-1335
Year: 2011



Use of an electronic monitoring system to generate objective information on patients’ adherence to taking treatments of a novel inhaled tobramycin solution
Source: Annual Congress 2013 –Cystic fibrosis: clinical problems, genetics and microbiology in children
Year: 2013


Aerosol delivery aspects within a high-flow therapy system in COPD patients
Source: ERJ Open Res, 7 (1) 00422-2020; 10.1183/23120541.00422-2020
Year: 2021



The pharmacokinetic of the main oral antibiotics in children with cystic fibrosis.
Source: International Congress 2019 – Treatments, adherence and psychosocial aspects of cystic fibrosis
Year: 2019


Variation in lung function as a marker of adherence to oral and inhaled medication in cystic fibrosis
Source: Eur Respir J , 49 (3) 1600987; DOI: 10.1183/13993003.00987-2016
Year: 2017



Reduction of treatment time for nebulized treatments using a new adaptive aerosol delivery mode
Source: Annual Congress 2008 - Improving asthma and anti-allergic therapy
Year: 2008

Inhaled therapy in cystic fibrosis: agents, devices and regimens
Source: Breathe 2015; 11:110-118
Year: 2015



Changes in mechanical properties of respiratory system in children with cystic fibrosis during therapy of exacerbation
Source: Eur Respir J 2005; 26: Suppl. 49, 612s
Year: 2005

Home intravenous antibiotic treatments in cystic fibrosis adult patients
Source: Eur Respir J 2002; 20: Suppl. 38, 158s
Year: 2002

Formulation of dual modality nanoparticles to enhance tobramycin efficacy in cystic fibrosis
Source: Annual Congress 2013 –Cutting edge: drug delivery to the airways
Year: 2013

Self-perceived verses electronic monitoring of adherence to nebulised treatment in children with cystic fibrosis - does the use of telehealth system improve nebulisation adherence?
Source: Annual Congress 2013 –Cystic fibrosis: basic and applied science
Year: 2013


Pulmonary surfactant as drug delivery system to target lung epithelium: new approach for the treatment of epithelial injury after bleomycin challenge
Source: International Congress 2018 – Regenerative and anti-fibrotic approaches
Year: 2018

Distribution of technetium-99m-labelled QVARTM delivered using an AutohalerTM device in children
Source: Eur Respir J 2003; 21: 1007-1011
Year: 2003



Functional respiratory imaging assessment of the aerosol deposition of inhaled levofloxacin in cystic fibrosis lungs
Source: Virtual Congress 2021 – Cystic fibrosis
Year: 2021


Dose-finding and 24-h monitoring for efficacy and safety of aerosolized Nacystelyn in cystic fibrosis
Source: Eur Respir J 2002; 19: 294-302
Year: 2002



Benefit of aerosol therapy with pulmozyme for children with cystic fibrosis
Source: Eur Respir J 2005; 26: Suppl. 49, 622s
Year: 2005

Extent of inhaled drug deposition in mouth-throat and pulmonary airways: A novel biophysical modelling approach for inhaled therapeutics
Source: International Congress 2015 – New models for treating airway diseases
Year: 2015


The role of inhaled antibiotics in bronchial infection
Source: Eur Respir Monogr 2013; 60: 120-126
Year: 2013