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Changes in leucocyte counts and soluble intercellular adhesion molecule-1 and E-selectin during cardiopulmonary

H J Williams1, N Rebuck, M J Elliott

  • 1University of Sheffield Medical School, UK.

Perfusion
|October 21, 1998
PubMed

Insights

Cardiopulmonary bypass (CPB) in children causes capillary leak and lung issues. Study shows altered soluble adhesion molecules and neutrophil counts during CPB may indicate increased leukocyte sequestration and endothelial damage.

Area of Science:

  • Pediatric surgery
  • Cardiovascular surgery
  • Immunology

Background:

  • Cardiopulmonary bypass (CPB) in children can lead to postoperative capillary leak and pulmonary dysfunction.
  • Neutrophil sequestration in the lungs may contribute to endothelial damage during CPB.
  • Endothelial adhesion molecules (e.g., E-selectin, ICAM-1) and their soluble forms play a role in leukocyte adhesion.

Purpose of the Study:

  • To investigate changes in plasma concentrations of soluble E-selectin and soluble ICAM-1 during CPB in pediatric patients.
  • To correlate these changes with leukocyte counts and assess their potential role in CPB-associated complications.

Main Methods:

  • Plasma concentrations of soluble E-selectin and soluble ICAM-1 were measured using fixed-phase immunoassays.
  • Leukocyte counts (total, lymphocyte, neutrophil) were monitored in 10 pediatric patients undergoing CPB.
  • Measurements were taken preoperatively, during maximum hypothermia, and at 24 hours postoperatively.

Main Results:

  • Soluble L-selectin and ICAM-1 levels decreased during CPB, largely due to hemodilution.
  • White blood cell counts significantly decreased during CPB, suggesting leukocyte sequestration.
  • Neutrophil counts increased significantly in the postoperative period, while lymphocyte counts returned to baseline.

Conclusions:

  • Changes in circulating leukocyte numbers during CPB may reflect altered endothelial adhesion and sequestration.
  • Soluble adhesion molecule levels and leukocyte count dynamics provide insights into CPB-induced inflammatory responses.
  • Further research is needed to fully elucidate the role of soluble adhesion proteins in CPB-related complications.

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