Abstract
To assess lung function longitudinally after neonatal ECMO, and to identify any effects of diagnosis and perinatal characteristics.
121 neonatal ECMO-treated children (70 meconium aspiration syndrome, 20 congenital diaphragmatic hernia, 31 other diagnoses) performed altogether 191 lung function measurements at 5, 8 and/or 12 years. We assessed dynamic and static lung volumes, reversibility of airway obstruction and diffusion capacity.
Mean SDS FEV1 at 5 years before and after bronchodilation (−0.51 and 0.07) was significantly higher than at 8 (−0.79 and −0.4, p<0.04) and 12 years (−1.10 and −0.52, p<0.003). Mean SDS for all spirometric parameters before and after bronchodilation were significantly lower in the congenital diaphragmatic hernia group compared the other diagnostic groups (all p≤0.025). A significant volume of trapped air was observed in 86% patients with congenital diaphragmatic hernia, 50% with meconium aspiration syndrome and 58% with other diagnoses. After bronchodilation mean SDS FEV1 and FVC were negatively influenced by duration of ventilation (both p<0.001) and duration of ECMO (p=0.003 and p=0.02 respectively).
Long-term pulmonary sequelae after neonatal ECMO-treatment mainly occur in congenital diaphragmatic hernia patients and tend to deteriorate over time.
- Chronic Lung Disease
- congenital diaphragmatic hernia
- follow-up
- Longitudinal changes in lung function
- Long-term sequelae of neonatal lung disease
- meconium aspiration syndrome
- ERS