Literature DB >> 22305683

Limiting inflammatory response to cardiopulmonary bypass: pharmaceutical strategies.

Calvin S H Ng1, Song Wan.   

Abstract

A significant inflammatory response and subsequent organ dysfunction is known to be associated with the use of CPB. Pharmaceutical interventions, such as corticosteroids, statins and ACE-Is can attenuate the post-CPB inflammatory and immune response, by so doing, either directly or indirectly, reduce incidence of postoperative complications. Apart from its effects on lipids, statins have been found to reduce postoperative oxidative stress that may partly contribute towards improved graft patency. In addition, certain ACE-inhibitors can promote a pro-fibrinolytic environment, whose role on maintaining graft patency and clinical outcomes warrant further investigation. There is increasing evidence to support the use of combined clopidogrel with aspirin following CABG to improve graft patency, although its impact on reducing postoperative adverse events remains unclear. Factors such as drug bioavailability and individual variability in drug responses and metabolism of these antiplatelet agents can significantly influence clinical outcomes.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22305683     DOI: 10.1016/j.coph.2012.01.007

Source DB:  PubMed          Journal:  Curr Opin Pharmacol        ISSN: 1471-4892            Impact factor:   5.547


  8 in total

1.  Role of ACE I/D gene polymorphisms on the effect of ramipril in inflammatory response and myocardial injury in patients undergoing coronary artery bypass grafts.

Authors:  Meral Urhan Küçük; Nehir Sucu; Seyhan Şahan Firat; Barlas Naim Aytaçoğlu; Özden Vezir; Caner Bozali; Necmiye Canacankatan; Seval Kul; Bahar Tunçtan
Journal:  Eur J Clin Pharmacol       Date:  2014-09-27       Impact factor: 2.953

2.  A Single-Center Analysis of Methylprednisolone Use during Pediatric Cardiopulmonary Bypass.

Authors:  Molly Dreher; Andrew C Glatz; Andrea Kennedy; Tami Rosenthal; J William Gaynor
Journal:  J Extra Corpor Technol       Date:  2015-09

3.  Flow cytometric evaluation of T cell activation markers after cardiopulmonary bypass.

Authors:  Maja-Theresa Dieterlen; Hartmuth B Bittner; Attila Tarnok; Jens Garbade; Stefan Dhein; Friedrich W Mohr; Markus J Barten
Journal:  Surg Res Pract       Date:  2014-02-06

4.  A novel minimal invasive mouse model of extracorporeal circulation.

Authors:  Shuhua Luo; Menglin Tang; Lei Du; Lina Gong; Jin Xu; Youwen Chen; Yabo Wang; Ke Lin; Qi An
Journal:  Mediators Inflamm       Date:  2015-01-29       Impact factor: 4.711

Review 5.  Cardiopulmonary bypass and oxidative stress.

Authors:  Mustafa Zakkar; Gustavo Guida; M-Saadeh Suleiman; Gianni D Angelini
Journal:  Oxid Med Cell Longev       Date:  2015-02-04       Impact factor: 6.543

6.  Ghrelin Pre-treatment Attenuates Local Oxidative Stress and End Organ Damage During Cardiopulmonary Bypass in Anesthetized Rats.

Authors:  Vijayakumar Sukumaran; Hirotsugu Tsuchimochi; Yutaka Fujii; Hiroshi Hosoda; Kenji Kangawa; Tsuyoshi Akiyama; Mikiyasu Shirai; Eisuke Tatsumi; James T Pearson
Journal:  Front Physiol       Date:  2018-03-09       Impact factor: 4.566

7.  Comparing the effect of preoperative administration of methylprednisolone and its administration before and during surgery on the clinical outcome in pediatric open heart surgeries.

Authors:  Ghasem Soltani; Mohammad Abbasi Tashnizi; Ali Asghar Moeinipour; Mahmoud Ganjifard; Jamil Esfahanizadeh; Alireza Sepehri Shamloo; Seyed Javad Purafzali Firuzabadi; Nahid Zirak
Journal:  Iran Red Crescent Med J       Date:  2013-06-05       Impact factor: 0.611

8.  Lack of Efficacy of Ulinastatin Therapy During Cardiopulmonary Bypass Surgery.

Authors:  Yan Qiu; Jing Lin; Yang Yang; Jing Zhou; Li-Na Gong; Zhen Qin; Lei Du
Journal:  Chin Med J (Engl)       Date:  2015-12-05       Impact factor: 2.628

  8 in total

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