Rosenfeld, Margaret2; Allen, Julian2; Arets, Bert H G M2; Aurora, Paul2; Beydon, Nicole2; Calogero, Claudia2; Castile, Robert G2; Davis, Stephanie D2; Fuchs, Susanne2; Gappa, Monika2; Gustaffson, Per M2; Hall, Graham L2; Jones, Marcus H2; Kirkby, Jane C2; Kraemer, Richard2; Lombardi, Enrico2; Lum, Sooky2; Mayer, Oscar H2; Merkus, Peter2; Nielsen, Kim G1; Oliver, Cara2; Oostveen, Ellie2; Ranganathan, Sarath2; Ren, Clement L2; Robinson, Paul D2; Seddon, Paul C2; Sly, Peter D2; Sockrider, Marianna M2; Sonnappa, Samatha2; Stocks, Janet2; Subbarao, Padmaja2; Tepper, Robert S2; Vilozni, Daphna2
1 Department of Paediatrics and Adolescent Medicine, Juliane Marie Centre, Rigshospitalet, The Capital Region of Denmark2 unknown
optimal lung function tests for monitoring cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheezing in children less than 6 years of age
Although pulmonary function testing plays a key role in the diagnosis and management of chronic pulmonary conditions in children under 6 years of age, objective physiologic assessment is limited in the clinical care of infants and children less than 6 years old, due to the challenges of measuring lung function in this age range. Ongoing research in lung function testing in infants, toddlers, and preschoolers has resulted in techniques that show promise as safe, feasible, and potentially clinically useful tests. Official American Thoracic Society workshops were convened in 2009 and 2010 to review six lung function tests based on a comprehensive review of the literature (infant raised-volume rapid thoracic compression and plethysmography, preschool spirometry, specific airway resistance, forced oscillation, the interrupter technique, and multiple-breath washout). In these proceedings, the current state of the art for each of these tests is reviewed as it applies to the clinical management of infants and children under 6 years of age with cystic fibrosis, bronchopulmonary dysplasia, and recurrent wheeze, using a standardized format that allows easy comparison between the measures. Although insufficient evidence exists to recommend incorporation of these tests into the routine diagnostic evaluation and clinical monitoring of infants and young children with cystic fibrosis, bronchopulmonary dysplasia, or recurrent wheeze, they may be valuable tools with which to address specific concerns, such as ongoing symptoms or monitoring response to treatment, and as outcome measures in clinical research studies.
Annals of the American Thoracic Society, 2013, Vol 10, Issue 2
Journal Article; Review; Airway Resistance; Bronchopulmonary Dysplasia; Child; Child, Preschool; Cystic Fibrosis; Forced Expiratory Volume; Humans; Infant; Infant, Newborn; Plethysmography; Respiratory Function Tests; Respiratory Sounds; Societies, Medical; United States