Source: Annual Congress 2013 –Monitoring symptoms and quality of life
Disease area: Respiratory infections



Rating:

Share or cite this content

Citations should be made in the following way:
P. Goeminne, S. Abbeel, D. Ruttens, L. Dupont (Leuven, Belgium). Evaluation of three categorical sputum colour charts: is less more?. Eur Respir J 2013; 42: Suppl. 57, 4915

Member's Comments

No comment yet.

Related content which might interest you: Development of a standardized sputum colour chart based on the natural colour system Source: Annual Congress 2013 –Disease control and quality of life in airway diseases Year: 2013 Sputum processing methods in airway disease: Which is best? Source: International Congress 2014 – Airway biomarkers Year: 2014 Risk of asthma in heterozygous carriers for cystic fibrosis: A meta-analysis Source: International Congress 2016 – Cystic fibrosis: various aspects Year: 2016 Annual change of LCI among patients with cystic fibrosis Source: International Congress 2016 – Cystic fibrosis: monitoring and management Year: 2016 Pulmonary Disease in Pregnancy (Asthma, CF, TB etc.) Source: Respipedia Article Year: 2018 Sputum colour: a useful clinical tool in non-cystic fibrosis bronchiectasis Source: Eur Respir J 2009; 33: 361-364 Year: 2009 A new gold standard for assessing CT in early CF lung disease? Source: International Congress 2014 – Cystic fibrosis: assessment and treatment Year: 2014 Predicting five year outcomes in adults with cystic fibrosis: Developing a predictive scoring model Source: Annual Congress 2013 –Cystic fibrosis: clinical problems and microbiology in adults Year: 2013 Phase 3 slope indices:can accurate estimates be obtained from 2 tests? Source: International Congress 2014 – Respiratory physiology and sleep disordered breathing in children Year: 2014 Macroscopic sputum quality assessments with a colour grading system in Cystic Fibrosis patients Source: International Congress 2018 – Cystic fibrosis in adults: current research Year: 2018 How useful is the lung ultrasound in cystic fibrosis? Source: International Congress 2016 – Cystic fibrosis: various aspects Year: 2016 Lung clearance Index changes over time among patients with cystic fibrosis Source: International Congress 2015 – New findings in paediatric respiratory physiology Year: 2015 Two-compartment model of gas mixing in patients with asthma and cystic fibrosis Source: Annual Congress 2013 –Clinical respiratory physiology in different diseases Year: 2013 Quantitative evaluation of CF airways using HRCT, µCT and histology Source: International Congress 2014 – Cystic fibrosis: assessment and treatment Year: 2014 Ability of lung clearance index to track changes in a routine clinical CF setting Source: International Congress 2015 – Paediatric respiratory physiology Year: 2015 Lung Clearance Index (LCI) and FEV1 on the evaluation of the effect of tobramycin solution for inhalation (TIS) among patients with cystic fibrosis Source: International Congress 2014 – Cystic fibrosis: clinical assessment and treatment Year: 2014 Validation of a Spanish version of the Leicester cough questionnaire in adult patients with cystic fibrosis bronchiectasis Source: International Congress 2014 – Physiotherapy and physical activity in respiratory conditions Year: 2014 Hypoglycemia: An unrecognized problem in cystic fibrosis (CF) patients unmasked by continues glucose monitorisation (CGM) Source: International Congress 2014 – Cystic fibrosis: clinical assessment and treatment Year: 2014 National survey of hearing assessment in patients with cystic fibrosis in the UK Source: International Congress 2016 – Cystic fibrosis: various aspects Year: 2016