What it takes to implement regular longitudinal multiple breath washout tests in infants with cystic fibrosis

Author:

Schmidt Marika N.,Sandvik Rikke M.,Voldby ChristianORCID,Buchvald Frederik F.,Jørgensen Maria N.,Gustafsson Per,Skov Marianne,Nielsen Kim G.ORCID

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference11 articles.

1. Zolin A., Orenti A., Naehrlich L. van R.J. et al. ECFSPR annual report2017. 2019:149.

2. The future of cystic fibrosis care: a global perspective;Bell;The Lancet,2019

3. Multiple breath washout is feasible in the clinical setting and detects abnormal lung function in infants and young children with cystic fibrosis;Stahl;Respiration,2014

4. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis;Gustafsson;Thorax,2008

5. Elevated lung clearance index in infants with cystic fibrosis shortly after birth;Kieninger;Eur Respir J,2017

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