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Plasma-soluble E-selectin after cardiopulmonary bypass in children: Is it a marker of the postoperative course?

  • Gideon Paret
  • , Tal Prince
  • , Natan Keller
  • , Ovdi Dagan
  • , Yokrat Sasson
  • , Asher Berzilai
  • , Daphna Guthmann
  • , Zohar Barzilay

نتاج البحث: نشر في مجلةمقالةمراجعة النظراء

12 اقتباسات (Scopus)

ملخص

Objective: To investigate the relationship and possible role of soluble adhesion molecule E-selectin in the postoperative course in children undergoing cardiopulmonary bypass (CPB). Design: Prospective cohort study. Setting: Pediatric intensive care unit of a university hospital. Participants: Thirteen children who were candidates for cardiac surgery. Interventions: None. Measurements and Main Results: Serial blood samples of 13 CPB patients were collected from the arterial catheter or from the bypass circuits preoperatively; on initiation of CPB; on termination of CPB; and 1, 2, 4, 8, 12, 18, 24, and 48 hours postoperatively. Plasma was recovered immediately, aliquoted, and frozen at -70°C until use. Circulating soluble selectin molecules were measured with a sandwich enzyme-linked immunosorbent assay technique. There were significant changes in plasma levels of soluble E-selectins in patients after CPB, and these levels were associated with patient characteristics, operative variables, and postoperative course. Soluble E-selectin correlated significantly with inotropic support and the use of anti-inflammatory drugs. There was a significant association between the development of postoperative sepsis and soluble E-selectin levels. No correlation was found between soluble E-selectins and duration of CPB, aortic cross-clamping, or hemodynamic variables, including heart rate and mean systemic arterial pressure. Conclusion: These results suggest a relationship between CPB-induced mediators and early and late clinical effects. Although the mechanism for the increase of soluble E-selectin remains to be elucidated, the upregulation of soluble E-selectin indicates neutrophil activation, and its inhibition may represent a target for reducing the inflammatory response associated with CPB. Copyright (C) 2000 by W.B. Saunders Company.

اللغة الأصليةالإنجليزيّة
الصفحات (من إلى)433-437
عدد الصفحات5
دوريةJournal of Cardiothoracic and Vascular Anesthesia
مستوى الصوت14
رقم الإصدار4
المعرِّفات الرقمية للأشياء
حالة النشرنُشِر - 2000
منشور خارجيًانعم

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