Follow-up of neonatal chronic respiratory disease: an update based on the current evidence

Allan Jenkinson1, Theodore Dassios2,3,4

  • 1Department of Women and Children's Health, School of Life Sciences, Faculty of Life Science and Medicine, King's College London, London, UK.

PubMed

Insights

Cardiorespiratory follow-up for extremely preterm infants, especially those with bronchopulmonary dysplasia, needs to extend into early adulthood. Assessments should include lung function, vascular disease, and exercise testing for targeted interventions.

Area of Science:

  • Neonatology
  • Pediatric Pulmonology
  • Cardiorespiratory Medicine

Background:

  • Premature birth leads to chronic respiratory morbidity affecting airway function, lung parenchyma, and cardiac morphology.
  • This morbidity persists into childhood, adolescence, and adulthood, with a lack of evidence-based guidelines for long-term follow-up.
  • Existing follow-up often ceases by age two, primarily assessing lung function, but misses other critical cardiorespiratory aspects.

Purpose of the Study:

  • To provide an updated review of current evidence regarding cardiorespiratory follow-up for extremely preterm infants.
  • To highlight the need for extended and comprehensive follow-up protocols, particularly for infants with bronchopulmonary dysplasia.
  • To emphasize the complex, multisystem nature of respiratory disease post-preterm birth.

Main Methods:

  • Narrative review of current evidence on cardiorespiratory follow-up for extremely preterm infants.
  • Analysis of existing literature on the long-term cardiorespiratory outcomes in this population.
  • Synthesis of findings to propose recommendations for future follow-up strategies.

Main Results:

  • Significant variation exists in the frequency, components, and duration of current follow-up practices.
  • Studies beyond two years of age primarily focus on spirometry for lung function impairment.
  • Recent evidence identifies distinct phenotypes of respiratory disease, including pulmonary vascular disease, parenchymal abnormalities, and impaired cardiorespiratory fitness.

Conclusions:

  • Follow-up should extend to early adulthood to capture the full spectrum of cardiorespiratory complications.
  • Comprehensive assessments should include lung function, pulmonary vascular disease, parenchymal disease, and cardiorespiratory exercise testing.
  • Individualized, targeted interventions are needed based on the dominant pathophysiological process identified during follow-up.

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