Literature DB >> 8523873

Influence of Duraflo II heparin-treated extracorporeal circuits on the systemic inflammatory response in patients having coronary bypass.

P W Weerwind1, J G Maessen, L J van Tits, R K Stad, E J Fransen, D S de Jong, O C Penn.   

Abstract

Cardiopulmonary bypass generates a systemic inflammatory response, including the activation of leukocytes, contributing to postoperative morbidity. To evaluate whether the use of heparin-treated extracorporeal circuits could reduce the inflammatory reaction in patients undergoing cardiopulmonary bypass, we conducted a prospective clinical study on 14 patients having coronary artery bypass in whom perfusion was done randomly with either Duraflo II heparin-treated circuits or with nontreated circuits. In both groups systemic heparinization was performed before cardiopulmonary bypass. The use of heparin-treated circuits resulted in a reduction of systemic inflammatory activation during cardiopulmonary bypass. This was reflected by lower plasma levels of soluble tumor necrosis factor receptors (p < 0.05) and of interleukin-6 and interleukin-8 (p < 0.05), manifest after release of the aortic crossclamp. Furthermore, 6 and 12 hours after aortic crossclamp release significantly lower levels of the soluble E-selectin (p < 0.05) were observed in the Duraflo II group. In patients in whom noncoated circuits were used, a significant decrease in circulating soluble intercellular adhesion molecule 1 (p < 0.05) was found early during bypass. All these observations suggest that the use of a heparin-treated extracorporeal circuit reduces the systemic inflammatory activation and may after the leukocyte-endothelium interaction.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8523873     DOI: 10.1016/S0022-5223(95)70024-2

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  6 in total

1.  Intensive insulin therapy does not alter the inflammatory response in patients undergoing coronary artery bypass grafting: a randomized controlled trial [ISRCTN95608630].

Authors:  Cornelia W Hoedemaekers; Peter Pickkers; Mihai G Netea; Marcel van Deuren; Johannes G Van der Hoeven
Journal:  Crit Care       Date:  2005-11-16       Impact factor: 9.097

Review 2.  Strategies to prevent intraoperative lung injury during cardiopulmonary bypass.

Authors:  Efstratios E Apostolakis; Efstratios N Koletsis; Nikolaos G Baikoussis; Stavros N Siminelakis; Georgios S Papadopoulos
Journal:  J Cardiothorac Surg       Date:  2010-01-11       Impact factor: 1.637

3.  Thrombin generation during cardiopulmonary bypass: the possible role of retransfusion of blood aspirated from the surgical field.

Authors:  Patrick W Weerwind; Theo Lindhout; Nicole EH Caberg; Dick S De Jong
Journal:  Thromb J       Date:  2003-07-15

Review 4.  Venovenous Extracorporeal Membrane Oxygenation in Intractable Pulmonary Insufficiency: Practical Issues and Future Directions.

Authors:  T S R Delnoij; R Driessen; A S Sharma; E A Bouman; U Strauch; P M Roekaerts
Journal:  Biomed Res Int       Date:  2016-04-05       Impact factor: 3.411

Review 5.  Pulmonary Protection Strategies in Cardiac Surgery: Are We Making Any Progress?

Authors:  Emad Al Jaaly; Mustafa Zakkar; Francesca Fiorentino; Gianni D Angelini
Journal:  Oxid Med Cell Longev       Date:  2015-10-20       Impact factor: 6.543

Review 6.  Pediatric and neonatal extracorporeal life support: current state and continuing evolution.

Authors:  Brian P Fallon; Samir K Gadepalli; Ronald B Hirschl
Journal:  Pediatr Surg Int       Date:  2021-01-01       Impact factor: 1.827

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.