AI Article Synopsis

  • - The study compared newer oxygenators designed to reduce immune response during cardiopulmonary bypass (CPB) in cardiac surgery with conventional oxygenators, focusing on their effects on lymphocyte activation and apoptosis.
  • - Blood samples were taken from 20 patients (10 using each type of oxygenator) at various stages of surgery to assess lymphocyte surface markers and apoptosis through flow cytometry.
  • - Results showed significant postoperative lymphopenia, increased lymphocyte activation, and decreased apoptosis in both groups, indicating that the reduced lymphocyte count after CPB is not primarily due to cell death.

Article Abstract

Newer oxygenators with the latest technologies are designed to attenuate the immune response, including lymphopenia, prompted by cardiopulmonary bypass (CPB) in cardiac surgery. We evaluated the effect of CPB, comparing an oxygenator with a venous-arterial shunt and a conventional oxygenator with regard to lymphocyte's early activation and apoptosis induction and its implications in post-CPB lymphopenia. Patients undergoing coronary artery bypass graft surgery with CPB, using either a conventional oxygenator or one with a venous-arterial shunt, had blood samples drawn at anesthetic induction (baseline); the beginning and end of the CPB; and at 6, 12, and 24 hours after surgery. Analysis by flow cytometry was undertaken to assess the expression of lymphocyte surface markers (CD3+, CD25+, CD26+, CD69+) and apoptosis (annexin V). Twenty patients were studied; 10 used a conventional oxygenator, and 10 used an oxygenator with venous-arterial shunt. Postoperative lymphopenia (50% decrease), 35% increased expression of CD69+, and 56% decrease in annexin V were significant comparing baseline to 24 hour value, similarly in both groups. Early activation (expression of CD69+) and degree of apoptosis (expression of annexin V) of lymphocytes after CBP in cardiac surgery was similarly observed in both types of oxygenators. The observed lymphopenia after CPB does not appear to be secondary to apoptosis.

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http://dx.doi.org/10.1097/01.mat.0000144590.98621.4fDOI Listing

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