Intracellular adhesion molecule-1 in patients developing pulmonary insufficiency after cardiopulmonary bypass

Thorac Cardiovasc Surg. 2003 Jun;51(3):138-41. doi: 10.1055/s-2003-40314.

Abstract

Objectives: Cardiopulmonary bypass activates adhesion molecules, which are associated with systemic inflammation and organ dysfunction. The intracellular adhesion molecule-1 (ICAM-1) has been evaluated in patients presenting pulmonary dysfunction after cardiac surgery.

Materials and methods: Postoperative serum levels of the ICAM-1 were measured in 40 patients who underwent isolated coronary artery bypass grafting, in 28 with uneventful postoperative recovery (70 %) (Group 1), and in 12 (30 %) with postoperative respiratory insufficiency (Group 2), defined by the need for prolonged (> 24 hours) mechanical ventilation using a fractional oxygen concentration of > 40 %.

Results: Patients in group 1 were ventilated for 12.21 +/- 4.86 hours and those in group 2 for 92.91 +/- 48.14 hours (p < 0.001). ICAM-1 decreased from 145.98 +/- 73.40 ng/ml to 81.15 +/- 114.82 ng/ml in group 1, while in group 2 ICAM-1 showed a significant higher level and increased to 435.01 +/- 130.02 ng/ml (p < 0.001). The leukocyte count increased in both groups as well as the C-reactive protein (CRP) during the postoperative course. The CRP behaves similar in both groups (p = 0.636) in contrast to the leukocyte count which was significantly higher in group 2 (p < 0.01). While none of the patients in group 1 died the mortality in group 2 was 50 % (p < 0.001).

Conclusion: Respiratory insufficiency after cardiopulmonary bypass is associated with a distinct increase in the ICAM-1. The reason for the increase of the ICAM-1 in this small subset of patients has not been clarified.

MeSH terms

  • Aged
  • C-Reactive Protein / analysis
  • Cardiopulmonary Bypass*
  • Case-Control Studies
  • Coronary Artery Bypass
  • Humans
  • Intercellular Adhesion Molecule-1 / blood*
  • Leukocyte Count
  • Middle Aged
  • Postoperative Complications / blood*
  • Respiratory Insufficiency / blood*
  • Respiratory Insufficiency / etiology

Substances

  • Intercellular Adhesion Molecule-1
  • C-Reactive Protein