Soluble P-selectin and the risk of primary graft dysfunction after lung transplantation

Academic Article

Abstract

  • Background: Platelet activation with subsequent neutrophilic adherence to the vasculature initiates ischemia-reperfusion injury. We hypothesized that higher plasma P-selectin levels reflecting platelet activation would therefore be associated with primary graft dysfunction (PGD) after lung transplantation. Methods: In a prospective, multicenter cohort study of 376 patients who had undergone lung transplantation between 2002 and 2007, we measured soluble P-selectin levels before lung transplantation and at 6 and 24 h after lung reperfusion in 20 patients with grade III PGD (PaO2/fraction of inspired oxygen, < 200 mm Hg [with alveolar infiltrates seen on chest radiographs]) at 72 h after transplantation and 61 control subjects without PGD. Results: Higher postoperative soluble P-selectin levels were associated with an increased risk of PGD at 72 h after transplantation (odds ratio [OR] per 1 natural log increase in soluble P-selectin at 6 h after lung allograft reperfusion, 3.5; 95% confidence interval [CI], 1.01 to 11.8; p = 0.048) and at 24 h after lung allograft reperfusion (OR, 4.8; 95% CI, 1.4 to 16.1; p = 0.01). Higher preoperative mean pulmonary artery pressure and the use of cardiopulmonary bypass were also associated with an increased risk of PGD. Conclusion: Higher postoperative soluble P-selectin levels were associated with an increased risk of PGD at 72 h following lung transplantation. Copyright © 2009 American College of Chest Physicians.
  • Authors

    Published In

  • Chest  Journal
  • Digital Object Identifier (doi)

    Author List

  • Kawut SM; Okun J; Shimbo D; Lederer DJ; De Andrade J; Lama V; Shah A; Milstone A; Ware LB; Weinacker A
  • Start Page

  • 237
  • End Page

  • 244
  • Volume

  • 136
  • Issue

  • 1