e-learning
resources
Glasgow 2004
Sunday 05.09.2004
Clinical questions being answered by paediatric lung function
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
Serial assessment of lung function in cystic fibrosis (CF) during the first years of life using the SF6 multiple breath washout (MBW) technique
S. I. Fuchs, S. Gerlach, M. Gappa (Hannover, Germany)
Source:
Annual Congress 2004 - Clinical questions being answered by paediatric lung function
Session:
Clinical questions being answered by paediatric lung function
Session type:
Thematic Poster Session
Number:
1022
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:
S. I. Fuchs, S. Gerlach, M. Gappa (Hannover, Germany). Serial assessment of lung function in cystic fibrosis (CF) during the first years of life using the SF6 multiple breath washout (MBW) technique. Eur Respir J 2004; 24: Suppl. 48, 1022
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:
The Relationship Between Functional Status and Fatigue After COVID-19 Infection
European Respiratory Society guideline on long term management of children with bronchopulmonary dysplasia
Cystic fibrosis and intestinal organoids
Related content which might interest you:
Variability of multiple breath washout (MBW) assessment of functional residual capacity (FRC) in cystic fibrosis (CF) patients using an ultrasonic device
Source: Eur Respir J 2003; 22: Suppl. 45, 129s
Year: 2003
Comparison of ventilation heterogeneity (VH) measured with multiple breath washout (MBW) imaging to whole lung MBW LCI and FEV1 in asthma and cystic fibrosis (CF)
Source: International Congress 2015 – Functional imaging approaches for evaluating alteration of lung, airways and respiratory muscles
Year: 2015
Sensitivity of N
2
single breath washout (SBW) compared multiple breath washout (MBW) in adults with cystic fibrosis (CF)
Source: Annual Congress 2013 –Cystic fibrosis: physiotherapy, exercise and lung function in adults and children
Year: 2013
Comparison of functional residual capacity (FRC) measured by plethysmography (FRCpleth) and multiple breath washout (FRCmbw) in schoolchildren with cystic fibrosis (CF).
Source: International Congress 2018 – Respiratory physiology and measurements
Year: 2018
Clinical application of the inert gas multiple breath washout technique (MBW) in children with cystic fibrosis (CF) using a prototype ultrasonic sidestream flow sensor (US)
Source: Eur Respir J 2006; 28: Suppl. 50, 704s
Year: 2006
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
Serial measurements of lung function in cystic fibrosis patients during the first years of life
Source: Eur Respir J 2001; 18: Suppl. 33, 536s
Year: 2001
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
Comparison of functional residual capacity (FRC) from two multiple breath washout (MBW) systems and body plethysmography
Source: International Congress 2016 – What's new in paediatric respiratory physiology?
Year: 2016
Tracking of lung function obtained by whole-body plethysmography in infants and children with cystic fibrosis (CF)
Source: Annual Congress 2011 - Advances in lung function testing from infancy to adulthood
Year: 2011
A new double-tracer gas single-breath washout to assess early cystic fibrosis lung disease
Source: Eur Respir J 2013; 41: 339-345
Year: 2013
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
Double tracer gas single breath washout – Comparison with conventional lung function tests in children with and without cystic fibrosis
Source: Annual Congress 2011 - Advances in lung function testing from infancy to adulthood
Year: 2011
Variability of the lung clearance index (LCI) assessed pre and post physiotherapy in patients with cystic fibrosis (CF)
Source: Annual Congress 2008 - Clinical applications of ventilatory function tests in paediatric pulmonology
Year: 2008
Lung clearance index (LCI) using nitrogen washout in children with cystic fibrosis
Source: Eur Respir J 2007; 30: Suppl. 51, 33s
Year: 2007
The effect of spirometry on multiple breath washout outcomes in children with cystic fibrosis
Source: International Congress 2018 – Cystic fibrosis in paediatric patients: current research
Year: 2018
Simultaneous SF6 and N2 gas multiple breath washout (MBW); understanding the difference between test gases
Source: International Congress 2016 – The best is yet to come in terms of lung function
Year: 2016
Lung clearance index (LCI) and hyperinflation in children with cystic fibrosis (CF)
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
Multiple-breath washout and pulmonary function tests versus high-resolution computed tomography scores in adults with cystic fibrosis.
Source: Virtual Congress 2020 – Advances in cystic fibrosis: from microbiome to MRI
Year: 2020
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