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Extract from:
Childhood Course of Lung Function in Survivors of Bronchopulmonary Dysplasia
Filippone M, Bonetto G, Cherubin E, Carraro S, Baraldi E.
JAMA 2009; 302: 1418-1420 PubMed
02/11/2009

Childhood course of lung function in survivors of bronchopulmonary dysplasia

A prospective study conducted in Italy has investigated the effect of early lung injury on respiratory health during childhood.

Bronchopulmonary dysplasia (BPD) is the primary respiratory complication of premature birth, and is associated with a reduced maximal lung function. It has been suggested that infants with BPD may carry a risk of a chronic obstructive pulmonary disease–like phenotype developing later in life. However, there is little prospective evidence about the evolution of lung function in long-term survivors of BPD. An Italian group has conducted a prospective study to further investigate the effect of early lung injury on respiratory health during childhood. In total, 17 survivors of BPD, defined as oxygen dependence persisting at 28 days in infants born with a weight less than 1250 g, were evaluated. Maximum flow at functional residual capacity (VmaxFRC) was measured at 2 years and forced expiratory volume in 1 second (FEV1) at 9 and 15 years. Two control groups were included in the study: 34 healthy children born at term and 17 children born preterm without BPD. Lung function measurements were compared using z scores. Overall, the BPD group showed consistent lung function tracking, with no significant changes in mean z scores between ages, at 2, 9 and 15 years. No differences in spirometry variables between 9 and 15 years were observed in the control groups. FEV1 values were significantly lower in the BPD group than in premature non-BPD and term-born children at both 9 and 15 years. Prematurely born non-BPD participants also had lower FEV1 values than the term-born controls. Among BPD participants, the z scores for VmaxFRC at 2 years old were correlated with the z scores for FEV1 (zFEV1) at 15 years and with the individual differences in zFEV1 between 9 and 15 years. zFEV1 declined between 9 and 15 years in BPD survivors with VmaxFRC less than the 5th percentile at 2 years, but increased in the individuals with greater VmaxFRC. Moreover, BPD survivors below the 5th percentile had a lower annual rate of FEV1 growth compared with those above the 5th percentile (160 mL/y vs 245 mL/y; P=0.01) and a significantly lower zFEV1 at 15 years (-2.77 vs -0.52; P=0.003).
Overall, these results, although still preliminary, confirm that early lung injuries may influence lifetime respiratory health. Moreover, severe early airflow obstruction at 2 years identified survivors of BPD at greater risk of impaired lung growth during their childhood, suggesting a guarded long-term respiratory prognosis. Patients with better airflow at 2 years showed an improvement in lung function in later childhood, thus suggesting some degree of functional recovery. In addition, these findings suggest that preterm delivery without BPD may also affect long-term lung function, although to a lesser extent than in patients with BPD.

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