Evaluation of respiratory function at 6 years of age in patients with cystic fibrosis with frequent pulmonary exacerbations in the first 2 years of life

Cystic fibrosis: disease monitoring, biomarkers, and psychosocial issues

Chair(s): Mirjam Stahl, Elpis Hatziagorou

Session type: Poster session

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Lateral decubitus CT: an alternative technique to monitor structural lung disease in preschool children with cystic fibrosis

Yuxin Chen

Poster

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Comparison of the corrected N2-lung clearance index with SF6-lung clearance index and magnetic resonance imaging

Eva Steinke

Poster

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Evaluation of respiratory function at 6 years of age in patients with cystic fibrosis with frequent pulmonary exacerbations in the first 2 years of life

Sati Ozkan Tabakci

Poster

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Evaluat?on of Alex?t?m?a Level in Cyst?c F?bros?s Pat?ents

Asli Imran Yilmaz

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Physical activity, six-minute-walking test, and quality of life in people with cystic fibrosis

Elpis Hatziagorou

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Respiratory rate from pulse oximetry during cystic fibrosis exacerbations

David Wertheim

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Classification of cystic fibrosis (CF) lung disease patterns based on CT texture analysis and machine learning

Francesca Pennati

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Transition Program as a Quality Improvement Project: Adaptation of the CF R.I.S.E. in a center with Limited Resources

Yasemin Gokdemir

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Identifying Knowledge Gaps by Using Adapted CF R.I.S.E in a Low Resource Setting

Merve Selcuk

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Airway colonisation with Aspergillus fumigatus and its impact on the CF microbiota

Deepa Patel

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Correlation of lung function using forced oscillation technique with spirometry in children with cystic fibrosis (CF)

Sachin Singh

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Exploring the attitudes and knowledge of the caregivers of children with cystic fibrosis and primary ciliary dyskinesia regarding COVID-19 vaccination

Merve Selcuk

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Microbiological status predicts lung function decline in cystic fibrosis

Elpis Hatziagorou

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Respiratory microbiota profiles are associated with respiratory health in infants with cystic fibrosis

Ruth Steinberg

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Parental socioeconomic status and lung function in offspring with cystic fibrosis in Sweden- a register-based cohort study

Emma Caffrey Osvald

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Project Fizzyo: Identification of optimal pressure-length breath profiles for airway clearance techniques in children with cystic fibrosis

Nicole Filipow

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SPLUNC1 in sputum of children with cystic fibrosis pulmonary exacerbations

Elad Ben-meir

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Role of nursing in the detection of allelic variants of the gene alpha-1-antitrypsin in patients with cystic fibrosis.

Rocio Reinoso Arija

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Airway infections as risk factors for Pseudomonas aeruginosa acquisition and chronic colonisation in children with cystic fibrosis

Harriet Corvol

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The ERS International Congress 2023, Milan

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