Computed tomography score and pulmonary function in infants with chronic lung disease of infancy

Chronic lung disease of infancy (CLDI) remains a common outcome among infants born extremely prematurely. In older children and adults with lung disease, pulmonary function and computed tomography (CT) scores are used to follow up respiratory disease and assess disease severity. For infants and toddlers, however, these outcomes have been used very infrequently and most often, a dichotomous respiratory outcome (presence or absence of CLDI) is employed. We evaluated the performance of CT score and pulmonary function to differentiate infants and toddlers with CLDI from a control group. CT scans, forced expiratory flows and pulmonary diffusing capacity were obtained in 39 CLDI patients and 41 controls (aged 4–33 months). CT scans were quantified using a scoring system, while pulmonary function was expressed as Z-scores. CT score outperformed pulmonary function in identifying those with CLDI. There were no significant correlations between CT score and pulmonary function. CT score had a better performance than pulmonary function in differentiating individuals with CLDI; however, these outcomes may reflect differing components of the pulmonary pathophysiology of CLDI. This new information on pulmonary outcomes can assist in designing studies with these parameters. Future studies will be required to evaluate which of the outcomes can better detect improvement with therapeutic intervention and/or lung growth.

[1]  M. Rosenfeld,et al.  Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints. , 2010, American journal of respiratory and critical care medicine.

[2]  Neil Marlow,et al.  Lung Function and Respiratory Symptoms at 11 Years in Children Born Extremely Preterm: The Epicure Study , 2011, Pediatrics.

[3]  Jennifer A. Rama,et al.  Serial Measurements of Lung Function in a Cohort of Young Children With Bronchopulmonary Dysplasia , 2010, Pediatrics.

[4]  Zhangsheng Yu,et al.  Growth of lung parenchyma in infants and toddlers with chronic lung disease of infancy. , 2010, American journal of respiratory and critical care medicine.

[5]  R. Mattiello,et al.  Post‐infectious bronchiolitis obliterans: Can CT scan findings at early age anticipate lung function? , 2010, Pediatric pulmonology.

[6]  J. Stocks,et al.  The EPICure study: maximal exercise and physical activity in school children born extremely preterm , 2009, Thorax.

[7]  M. Rosenthal,et al.  Gas transfer and pulmonary blood flow at rest and during exercise in adults 21 years after preterm birth. , 2009, American journal of respiratory and critical care medicine.

[8]  Zhangsheng Yu,et al.  Assessment of Airway Growth In-Vivo Using High Resolution Computed Tomography in Infants and Toddler. , 2009, ATS 2009.

[9]  K. Rosendahl,et al.  Neonatal bronchopulmonary dysplasia predicts abnormal pulmonary HRCT scans in long-term survivors of extreme preterm birth , 2009, Thorax.

[10]  Marcus H. Jones,et al.  Growth of the lung parenchyma early in life. , 2009, American journal of respiratory and critical care medicine.

[11]  Rosalind J Wright,et al.  Strategic plan for pediatric respiratory diseases research: an NHLBI working group report. , 2009, Proceedings of the American Thoracic Society.

[12]  H. Coxson,et al.  Lung structure and function of infants with recurrent wheeze when asymptomatic , 2009, European Respiratory Journal.

[13]  D. Warburton,et al.  Stem/progenitor cells in lung development, injury repair, and regeneration. , 2008, Proceedings of the American Thoracic Society.

[14]  M. Rosenthal,et al.  Longitudinal evaluation of airway function 21 years after preterm birth. , 2008, American journal of respiratory and critical care medicine.

[15]  M. Rosenfeld,et al.  Endpoints for clinical trials in young children with cystic fibrosis. , 2007, Proceedings of the American Thoracic Society.

[16]  C. Delacourt,et al.  Chest computed tomography findings in bronchopulmonary dysplasia and correlation with lung function , 2007, Archives of Disease in Childhood Fetal and Neonatal Edition.

[17]  J. Gieseke,et al.  Atelectasis in children undergoing either propofol infusion or positive pressure ventilation anesthesia for magnetic resonance imaging , 2007, Paediatric anaesthesia.

[18]  K. Rosendahl,et al.  High-resolution CT of the chest in children and young adults who were born prematurely: findings in a population-based study. , 2006, AJR. American journal of roentgenology.

[19]  O. Saba,et al.  High-resolution computed tomography imaging of airway disease in infants with cystic fibrosis. , 2005, American journal of respiratory and critical care medicine.

[20]  W. Hop,et al.  Pulmonary disease assessment in cystic fibrosis: comparison of CT scoring systems and value of bronchial and arterial dimension measurements. , 2004, Radiology.

[21]  R. Castile,et al.  Pulmonary function in bronchopulmonary dysplasia , 2004, Pediatric pulmonology.

[22]  J. Stocks,et al.  INVITED REVIEW SERIES: TOBACCO AND LUNG HEALTH The effect of parental smoking on lung function and development during infancy , 2003 .

[23]  N. Müller,et al.  Pulmonary sequelae of bronchopulmonary dysplasia survivors: high-resolution CT findings. , 2000, AJR. American journal of roentgenology.

[24]  J. de Blic,et al.  Bronchopulmonary dysplasia: value of CT in identifying pulmonary sequelae. , 1994, AJR. American journal of roentgenology.

[25]  T. Hara,et al.  A new scoring system for computed tomography of the chest for assessing the clinical status of bronchopulmonary dysplasia. , 2008, The Journal of pediatrics.

[26]  L. Monte,et al.  [Bronchopulmonary dysplasia]. , 2005, Jornal de pediatria.

[27]  W. Ambrosius,et al.  Forced expiratory flows and volumes in infants. Normative data and lung growth. , 2000, American journal of respiratory and critical care medicine.