e-learning
resources
Paris 2018
Tuesday, 18.09.2018
Cystic fibrosis in paediatric patients: current research
Login
Search all ERS
e-learning
resources
Disease Areas
Airways Diseases
Interstitial Lung Diseases
Respiratory Critical Care
Respiratory Infections
Paediatric Respiratory Diseases
Pulmonary Vascular Diseases
Sleep and Breathing Disorders
Thoracic Oncology
Events
International Congress
Courses
Webinars
Conferences
Research Seminars
Journal Clubs
Publications
Breathe
Monograph
ERJ
ERJ Open Research
ERR
European Lung White Book
Handbook Series
Guidelines
All ERS guidelines
e-learning
CME Online
Case reports
Short Videos
SpirXpert
Procedure Videos
CME tests
Reference Database of Respiratory Sounds
Radiology Image Challenge
Brief tobacco interventions
EU Projects
VALUE-Dx
ERN-LUNG
ECRAID
UNITE4TB
Disease Areas
Events
Publications
Guidelines
e-learning
EU Projects
Login
Search
The effect of spirometry on multiple breath washout outcomes in children with cystic fibrosis
J. Au (Toronto, Canada), R. Mcdonald (Toronto, Canada), S. Stanojevic (Toronto, Canada), F. Ratjen (Toronto, Canada)
Source:
International Congress 2018 – Cystic fibrosis in paediatric patients: current research
Session:
Cystic fibrosis in paediatric patients: current research
Session type:
Thematic Poster
Number:
4623
Disease area:
Paediatric lung diseases
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
J. Au (Toronto, Canada), R. Mcdonald (Toronto, Canada), S. Stanojevic (Toronto, Canada), F. Ratjen (Toronto, Canada). The effect of spirometry on multiple breath washout outcomes in children with cystic fibrosis. 4623
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:
Late Breaking Abstract - Implications of treatable traits and treatment choices on exacerbation risk in moderate-severe asthma
Impact of Dexamethasone on pathogen profile of COVID-19 patients requiring intensive care: a multicentre retrospective study
Muscle energy techniques for COPD patients: Effects on pulmonary function and activities of daily living
Related content which might interest you:
Change in functional lung MRI and multiple breath washout outcomes over one year in children with cystic fibrosis
Source: Virtual Congress 2021 – Monitoring of lung disease and CFTR function in children with cystic fibrosis
Year: 2021
Evaluation of SnIII parameters as outcome measures of multiple breath washout (MBW) in preschool children with cystic fibrosis
Source: Virtual Congress 2021 – Monitoring of lung disease and CFTR function in children with cystic fibrosis
Year: 2021
Nitrogen multiple breath washout test for infants with cystic fibrosis
Source: Eur Respir J, 52 (2) 1800015; 10.1183/13993003.00015-2018
Year: 2018
Alternative multiple breath washout outcomes for clinical trials in cystic fibrosis
Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new therapies and detection of early lung disease
Year: 2012
Longitudinal SF6 multiple breath washout in infants and toddlers with cystic fibrosis
Source: Virtual Congress 2021 – Monitoring of lung disease and CFTR function in children with cystic fibrosis
Year: 2021
Multiple breath washout in healthy pre-school children and those with cystic fibrosis (CF)
Source: Eur Respir J 2002; 20: Suppl. 38, 209s
Year: 2002
Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis
Source: Eur Respir J 2003 Dec 01;22(6):972-979
Year: 2003
Short and long term repeatability of N2 multiple breath washout indices in children with cystic fibrosis
Source: Annual Congress 2013 –Clinical applications of respiratory physiology in children
Year: 2013
Comparison of HRCT lung abnormalities with exercise capacity among children and adolescents with cystic fibrosis
Source: Annual Congress 2010 - Cystic fibrosis: lung disease and much more
Year: 2010
Short term effects of chest physiotherapy in children with cystic fibrosis assessed by a new lung function test
Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new basic and clinical physiology research
Year: 2012
Usefulness of impulse oscillometry, single breath diffusion and bodypletysmography for lung function assessment in patients with cystic fibrosis
Source: Eur Respir J 2006; 28: Suppl. 50, 715s
Year: 2006
Regular routine SF6 multiple breath washout in infants with cystic fibrosis born after implementation of neonatal screening
Source: International Congress 2019 – Physiology of cystic fibrosis
Year: 2019
Serial assessment of lung function in cystic fibrosis (CF) during the first years of life using the SF6 multiple breath washout (MBW) technique
Source: Eur Respir J 2004; 24: Suppl. 48, 156s
Year: 2004
The relationships between hyperinflation during exercise and symptoms in adults with cystic fibrosis
Source: Annual Congress 2012 - Limiting factors in exercise
Year: 2012
Does expiratory flow limitation predict chronic dyspnoea in adults with cystic fibrosis?
Source: Eur Respir J 2006; 28: 96-101
Year: 2006
Exercise testing and multiple breath washout as markers of lung disease among patients with cystic fibrosis
Source: International Congress 2015 – Cystic fibrosis: physiology, biomarkers, microbiology and miscellaneous
Year: 2015
Assessment of lung function in pre-school children with cystic fibrosis by nitrogen washout
Source: Annual Congress 2012 - Cystic fibrosis (adults and children): new therapies and detection of early lung disease
Year: 2012
Single-breath washout and association with structural lung changes in children with cystic fibrosis
Source: International Congress 2016 – Advanced lung function testing in childhood respiratory and sleep disease
Year: 2016
Characterisation of leaks during multiple breath washout and their influence on test results
Source: International Congress 2015 – Paediatric respiratory physiology
Year: 2015
A short-term comparison of two methods of sputum expectoration in cystic fibrosis
Source: Eur Respir J 2004; 23: 435-439
Year: 2004
We use cookies on our website to give you the most relevant experience by remembering your preferences and repeat visits. By clicking "Accept", you consent to the use of the cookies.
Accept