Differences between six minute walk test values with obstructed and non obstructed cystic fibrosis patients

S. Savci, U. B. Tugay, S. Erat, M. Ozturk, H. Arikan, D. Inal Ince, U. Ozcelik, N. Kiper (Ankara, Turkey)

Source: Annual Congress 2004 - Respiratory physiotherapy: interventions and technologies
Session: Respiratory physiotherapy: interventions and technologies
Session type: Poster Discussion
Number: 4266
Disease area: Airway diseases

Congress or journal article abstract

Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
S. Savci, U. B. Tugay, S. Erat, M. Ozturk, H. Arikan, D. Inal Ince, U. Ozcelik, N. Kiper (Ankara, Turkey). Differences between six minute walk test values with obstructed and non obstructed cystic fibrosis patients. Eur Respir J 2004; 24: Suppl. 48, 4266

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:
Six minute test in children and adults with cystic fibrosis
Source: Virtual Congress 2020 – Exploring exercise responses in respiratory diseases
Year: 2020


Can step be a maximal test in children with cystic fibrosis?
Source: Annual Congress 2009 - Paediatric lung function, imaging and methodology in health and disease
Year: 2009


Which equations to estimate peak work rate from six minute walk test in patients with cystic fibrosis post lung transplantation?
Source: Virtual Congress 2020 – Exercise tolerance and functional status across respiratory diseases
Year: 2020


Comparison of lung function tests in preschoolers with cystic fibrosis and healthy subjects
Source: Annual Congress 2008 - Diagnostic paediatric lung function: technical and clinical aspects
Year: 2008


The six-minute walk test in cystic fibrosis: a comparison to lung function
Source: Annual Congress 2009 - Physiotherapy aspects in cystic fibrosis and functional assessment
Year: 2009

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


Effect of supine posture on respiratory values in patients with cystic fibrosis
Source: Eur Respir J 2004; 24: Suppl. 48, 386s
Year: 2004

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



Can shuttle walk distance be predicted from pulmonary function data in adult cystic fibrosis?
Source: Eur Respir J 2005; 26: Suppl. 49, 109s
Year: 2005

Inflammatory markers in cystic fibrosis patients with different values of pulmonary function tests
Source: Eur Respir J 2002; 20: Suppl. 38, 528s
Year: 2002

The value of lung function monitoring by means of a home monitor in patients with cystic fibrosis
Source: Annual Congress 2011 - Cystic fibrosis: New aspects of diagnosis, inflammation and detecting exacerbation
Year: 2011


Maximal thoracic excursions in children with cystic fibrosis, a relevant indicator for airtrapping
Source: Eur Respir J 2003; 22: Suppl. 45, 331s
Year: 2003

Gender differences in rate of deterioration in desaturation during six minute hallwalk testing in patients with idiopathic pulmonary fibrosis
Source: Eur Respir J 2007; 30: Suppl. 51, 579s
Year: 2007

Maximal thoracic excursion as an indicator for airtrapping in children with cystic fibrosis
Source: Eur Respir J 2002; 20: Suppl. 38, 351s
Year: 2002

Lung clearance index is reproducible and close to normal in stable cystic fibrosis patients post bilateral lung transplant
Source: Annual Congress 2009 - Human and experimental lung transplantation: novel findings
Year: 2009

Nitrogen multiple breath washout test for infants with cystic fibrosis
Source: Eur Respir J, 52 (2) 1800015; 10.1183/13993003.00015-2018
Year: 2018



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



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

The relationship of walking speed with clinical parameters in patients with non-cystic fibrosis bronchiectasis
Source: Virtual Congress 2020 – Tapas of respiratory physiotherapy
Year: 2020


The timed walk test as a measure of severity and survival in idiopathic pulmonary fibrosis
Source: Eur Respir J 2005; 25: 96-103
Year: 2005