Positive expiratory pressure and lung function in cystic fibrosis patients

V. Parreira, S. Pires, N. Sulmonett, P. Camargos, J. Haddad, R. Britto (Belo Horizonte – MG, Brazil)

Source: Annual Congress 2008 - Mucociliary clearance, novel techniques and assessments, in adult, paediatric and mechanically ventilated patients
Disease area: Airway diseases, Paediatric lung diseases

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:
V. Parreira, S. Pires, N. Sulmonett, P. Camargos, J. Haddad, R. Britto (Belo Horizonte – MG, Brazil). Positive expiratory pressure and lung function in cystic fibrosis patients. Eur Respir J 2008; 32: Suppl. 52, 1779

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:
Tidal expiratory flow limitation and chronic dyspnoea in patients with cystic fibrosis
Source: Eur Respir J 2002; 19: 492-498
Year: 2002



Negative expiratory pressure method for detection of expiratory flow limitation in cystic fibrosis patients
Source: Eur Respir J 2003; 22: Suppl. 45, 577s
Year: 2003

Effect of pulmonary exacerbations on long-term lung function decline in cystic fibrosis
Source: Eur Respir J 2012; 40: 61-66
Year: 2012



Sustained maximum inspiratory pressure in patients with cystic fibrosis and severe airway obstruction
Source: Eur Respir J 2001; 18: Suppl. 33, 537s
Year: 2001

Immediate changes in blood gas tensions during chest physiotherapy with positive expiratory pressure and oscillating positive expiratory pressure in patients with cystic fibrosis
Source: Eur Respir J 2004; 24: Suppl. 48, 696s
Year: 2004

Effect of positive expiratory pressure (PEP) on breathing pattern characteristics in cystic fibrosis children
Source: International Congress 2014 – Multidimensional analysis of respiratory problems
Year: 2014


Relationship between airflow limitation and lung volume in cystic fibrosis patients
Source: Eur Respir J 2002; 20: Suppl. 38, 301s
Year: 2002

Effect of expiratory positive airway pressure on lung clearance of 99m-Tc-DTPA in health individuals
Source: Annual Congress 2009 - Noninvasive ventilation: new and old aspects
Year: 2009


Impulse oscillometry in patients with cystic fibrosis: relationship to dynamic lung volumes
Source: Eur Respir J 2001; 18: Suppl. 33, 537s
Year: 2001

Physiological effects of vibration in subjects with cystic fibrosis
Source: Eur Respir J 2006; 27: 1204-1209
Year: 2006



Inspiratory capacity-to-total lung capacity ratio is related to expiratory flow limitation in patients with chronic obstructive pulmonary disease
Source: Annual Congress 2007 - Lung function I
Year: 2007


Does expiratory flow limitation predict chronic dyspnoea in adults with cystic fibrosis?
Source: Eur Respir J 2006; 28: 96-101
Year: 2006



Effects of expiratory positive airway pressure on exercise dynamic hyperinflation in COPD patients
Source: Annual Congress 2010 - Noninvasive ventilation: technical, logistical and organisational aspects
Year: 2010

Acute effects of expiratory positive airway pressure on exercise capacity in patients with COPD
Source: International Congress 2017 – Novel treatments for rehabilitation of patients with chronic respiratory diseases
Year: 2017

Pneumothorax in cystic fibrosis patients on non invasive positive pressure ventilation
Source: Eur Respir J 2006; 28: Suppl. 50, 49s
Year: 2006

Long term non invasive positive pressure ventilation is associated with a stabilisation in the decline of lung function in patients with cystic fibrosis
Source: Annual Congress 2006 - Interventions and outcome in chronic respiratory failure - new aspects and deeper insights
Year: 2006


Arterial partial pressure of oxygen (PaO2) - a marker for cystic fibrosis (CF) lung disease and chronic airway infection
Source: International Congress 2019 – Physiology of cystic fibrosis
Year: 2019


Chest wall kinematics during different levels of positive end-expiratory pressure in cystic fibrosis children
Source: Annual Congress 2011 - Respiratory and skeletal muscle assessment in health and disease
Year: 2011