Cardiopulmonary function in premature infants with bronchopulmonary dysplasia--a 2-year follow up

T Farstad1, F Brockmeier, D Bratlid

  • 1Department of Paediatrics, University Hospital, Rikshospitalet, Oslo, Norway.

Insights

Premature infants with bronchopulmonary dysplasia (BPD) show persistent severe peripheral pulmonary obstruction and cardiac issues. Follow-up assessments of maximum flow and cardiac function are crucial for managing BPD complications.

Area of Science:

  • Neonatology
  • Pediatric Pulmonology
  • Cardiology

Background:

  • Bronchopulmonary dysplasia (BPD) is a chronic lung disease in premature infants.
  • Cardiopulmonary function impairment can persist beyond infancy in BPD survivors.

Purpose of the Study:

  • To evaluate cardiopulmonary function in infants with BPD and controls at corrected ages of 50 and 120 weeks.
  • To identify long-term respiratory and cardiac sequelae in infants with BPD.

Main Methods:

  • Longitudinal assessment of respiratory system compliance, resistance, and maximum flow at functional residual capacity (VmaxFRC).
  • Doppler echocardiography to assess cardiac involvement.
  • Comparison between infants with BPD and premature controls.

Main Results:

  • Reduced respiratory compliance and increased resistance improved with age in both groups.
  • Severe peripheral pulmonary obstruction (VmaxFRC < 84 ml/s) persisted in 5/13 BPD infants at 120 weeks, compared to none in controls (VmaxFRC < 120 ml/s).
  • Cardiac involvement (shortened pulmonary acceleration time) was observed in BPD infants with severe obstruction; BPD infants also had higher pulmonary morbidity, were shorter, and weighed less.

Conclusions:

  • Maximum flow at functional residual capacity and cardiac evaluation are essential for monitoring infants with severe BPD.
  • Persistent peripheral pulmonary obstruction and cardiac involvement are significant long-term issues in BPD.
  • Early identification and management of cardiopulmonary complications are vital for improving outcomes in BPD survivors.

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