Literature DB >> 16227195

Systemic inflammatory response to coronary artery bypass graft surgery.

Philip J Hess1.   

Abstract

PURPOSE: Several aspects of the systemic inflammatory response to coronary artery bypass graft surgery are described.
SUMMARY: The inflammatory response is a fundamental biological protective mechanism that gathers together the body's cellular and chemical defense mechanisms at the local site of tissue injury. The systemic inflammatory response syndrome refers to a systemic, whole body, non-localized response. This response, which occurs to some degree in most patients undergoing coronary artery bypass graft surgery, has the potential to affect all tissues and vital organs. When blood interacts with the cardiopulmonary bypass machine, several cellular and humoral pathways are activated including the complement system, the coagulation system, and the fibrinolytic system. These, in turn, activate inflammatory response cells, such as leukocytes and platelets. Together these molecular pathways and activated cells mediate the frequently observed clinical sequelae such as edema, tissue and organ damage, and hyperfibrinolysis. In order for a molecule drug to attenuate effectively this response, it would need to have a broad enough spectrum of activity to inhibit multiple pathways and to limit their cross-amplification. Aprotinin, a nonspecific serine protease, is an important attenuator of this response as it inhibits several important serine proteases, including kallikrein, plasmin, thrombin, and elastase, which are involved in fibrinolysis and cell transmigration and degranulation into soft tissues.
CONCLUSION: Treatment with aprotinin during coronary artery bypass graft surgery should be considered as a way to attenuate bleeding and systemic inflammatory responses.

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Year:  2005        PMID: 16227195     DOI: 10.2146/ajhp050302

Source DB:  PubMed          Journal:  Am J Health Syst Pharm        ISSN: 1079-2082            Impact factor:   2.637


  7 in total

1.  Pyruvate Dehydrogenase Activity and Quantity Decreases After Coronary Artery Bypass Grafting: a Prospective Observational Study.

Authors:  Lars W Andersen; Xiaowen Liu; Teng J Peng; Tyler A Giberson; Kamal R Khabbaz; Michael W Donnino
Journal:  Shock       Date:  2015-03       Impact factor: 3.454

2.  Bioinformatics analysis of the early inflammatory response in a rat thermal injury model.

Authors:  Eric Yang; Timothy Maguire; Martin L Yarmush; Francois Berthiaume; Ioannis P Androulakis
Journal:  BMC Bioinformatics       Date:  2007-01-10       Impact factor: 3.169

3.  Bioactive Sphingolipids, Complement Cascade, and Free Hemoglobin Levels in Stable Coronary Artery Disease and Acute Myocardial Infarction.

Authors:  T Jadczyk; K Baranski; M Syzdol; E Nabialek; W Wanha; R Kurzelowski; M Z Ratajczak; M Kucia; B Dolegowska; M Niewczas; J Zejda; W Wojakowski
Journal:  Mediators Inflamm       Date:  2018-07-09       Impact factor: 4.711

4.  Tranexamic acid in cardiac surgery: a systematic review and meta-analysis (protocol).

Authors:  Thamer Alaifan; Ahmed Alenazy; Dominic Xiang Wang; Shannon M Fernando; Jessica Spence; Emilie Belley-Cote; Alison Fox-Robichaud; Craig Ainswoth; Tim Karachi; Kwadwo Kyeremanteng; Ryan Zarychanski; Richard Whitlock; Bram Rochwerg
Journal:  BMJ Open       Date:  2019-09-17       Impact factor: 2.692

5.  COMT-Val158Met-polymorphism is not a risk factor for acute kidney injury after cardiac surgery.

Authors:  Matthias Kornek; Marcus-André Deutsch; Stefan Eichhorn; Harald Lahm; Stefan Wagenpfeil; Markus Krane; Ruediger Lange; Johannes Boehm
Journal:  Dis Markers       Date:  2013-08-07       Impact factor: 3.434

6.  Factors associated with excessive bleeding in cardiopulmonary bypass patients: a nested case-control study.

Authors:  Juan J Jimenez Rivera; Jose L Iribarren; Jose M Raya; Ibrahim Nassar; Leonardo Lorente; Rosalia Perez; Maitane Brouard; Jose M Lorenzo; Pilar Garrido; Ysamar Barrios; Maribel Diaz; Blas Alarco; Rafael Martinez; Maria L Mora
Journal:  J Cardiothorac Surg       Date:  2007-04-10       Impact factor: 1.637

Review 7.  Inhibition of metalloproteinases in therapy for severe lung injury due to COVID-19.

Authors:  B Solun; Y Shoenfeld
Journal:  Med Drug Discov       Date:  2020-06-05
  7 in total

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