What it takes to implement regular longitudinal multiple breath washout tests in infants with cystic fibrosis
Author:
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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1. Close monitoring and early intervention: management principles for cystic fibrosis in Denmark;APMIS;2024-01-24
2. Nationwide lung function monitoring from infancy in newborn-screened children with cystic fibrosis;ERJ Open Research;2023-08-17
3. Turning lung clearance index on its head. Reference data for SF6 multiple-breath washout derived ventilation distribution efficiency;Journal of Applied Physiology;2023-02-01
4. Turning Lung Clearance Index on its head. Reference data for SF6 Multiple Breath Washout Derived Ventilation distribution efficiency (VDE);2022-09-12
5. Contemporary N 2 and SF 6 multiple breath washout in infants and toddlers with cystic fibrosis;Pediatric Pulmonology;2022-01-25
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