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Cardiopulmonary bypass significantly reduces surfactant activity in children

F X McGowan1, M Ikegami, P J del Nido

  • 1Department of Anesthesiology/Critical Care Medicine, University of Pittsburgh School of Medicine, Pa.

Insights

Cardiopulmonary bypass in children alters lung surfactant, shifting it to smaller aggregates with reduced activity. This change is linked to decreased lung function and increased inflammatory cells post-surgery.

Area of Science:

  • Pulmonary medicine
  • Cardiothoracic surgery
  • Biochemistry

Background:

  • Lung injury is a significant complication following cardiopulmonary bypass (CPB).
  • The role of altered surfactant concentration or activity in post-CPB pulmonary dysfunction is not fully understood.
  • Surfactant exists in different aggregate forms (small and large) with varying density, composition, and function, and a shift towards less active small aggregates occurs in experimental lung injury.

Purpose of the Study:

  • To investigate changes in surfactant aggregate fractions before and after CPB in pediatric patients.
  • To correlate these surfactant changes with pulmonary function tests and inflammatory markers.

Main Methods:

  • Pulmonary function testing was performed on 12 pediatric patients (2-12 years) undergoing CPB.
  • Bronchoalveolar lavage (BAL) was collected before CPB and approximately 1 hour after its termination.
  • Saturated phosphatidylcholine (SPC) pool sizes and protein content in small- and large-aggregate surfactant fractions were quantified.

Main Results:

  • The ratio of SPC in small- to large-aggregate fractions increased significantly after CPB (0.19 to 0.37, p < 0.02).
  • The ratio of SPC to protein in the small-aggregate fraction also increased post-CPB (0.04 to 0.08, p < 0.05).
  • Pulmonary function declined, with reductions in forced vital capacity (-19%), inspiratory capacity (-15%), and small airway flow rates (-32%), accompanied by a fivefold increase in polymorphonuclear leukocytes.

Conclusions:

  • CPB in children is associated with surfactant alterations similar to those seen in experimental lung injury, characterized by a shift towards less functional small aggregates.
  • These surfactant changes correlate with measurable decreases in lung function and increased pulmonary inflammation after CPB.

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