Pericardial blood activates the extrinsic coagulation pathway during clinical cardiopulmonary bypass
Coagulation during cardiopulmonary bypass (CPB) traditionally has been attributed to activation of the contact system of plasma proteins and the intrinsic coagulation pathway by blood contact with negatively charged surfaces not lined by endothelium. Recent studies have focused on the possible role...
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Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 1996-06, Vol.93 (11), p.2014-2018 |
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container_title | Circulation (New York, N.Y.) |
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creator | CHUNG, J. H GIKAKIS, N RAO, A. K DRAKE, T. A COLMAN, R. W EDMUNDS, L. H |
description | Coagulation during cardiopulmonary bypass (CPB) traditionally has been attributed to activation of the contact system of plasma proteins and the intrinsic coagulation pathway by blood contact with negatively charged surfaces not lined by endothelium. Recent studies have focused on the possible role of the extrinsic coagulation pathway during cardiac surgery. We postulated that the wound activates the extrinsic coagulation pathway during CPB by producing procoagulant cells and enzymes that enter the general circulation.
Blood samples taken from 20 consenting patients who had elective cardiac surgery were assayed for peripheral blood mononuclear cell tissue factor (TF) expression, plasma F1.2, and factor VII and VIIa concentrations. Peripheral blood mononuclear cell TF expression increased in the perfusate after the surgical incision and after CPB was started and in monocytes that adhered to the perfusion circuit. TF on circulating monocytes, however, did not continue to rise during CPB. Peripheral blood mononuclear cell TF was elevated in cells isolated directly from blood in the pericardial cavity and was twice that detected in simultaneous samples from the perfusate (P < .05). F1.2 levels were highest in pericardial blood and increased progressively during CPB. Plasma factor VIIa concentrations, corrected for hemodilution, and ratios of factor VIIa to factor VII were highest in pericardial samples (P < .05) and increased progressively during and immediately after CPB. Pericardial biopsies obtained before and after CPB in 7 patients did not show TF expression by mesothelial cells.
These data provide direct evidence of TF expression, activation of the extrinsic coagulation pathway, and thrombin formation in the surgical wound. Addition of pericardial blood to the perfusate and expression of TF by both circulating and adherent monocytes strongly promote thrombus formation during open heart surgery. |
doi_str_mv | 10.1161/01.cir.93.11.2014 |
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Blood samples taken from 20 consenting patients who had elective cardiac surgery were assayed for peripheral blood mononuclear cell tissue factor (TF) expression, plasma F1.2, and factor VII and VIIa concentrations. Peripheral blood mononuclear cell TF expression increased in the perfusate after the surgical incision and after CPB was started and in monocytes that adhered to the perfusion circuit. TF on circulating monocytes, however, did not continue to rise during CPB. Peripheral blood mononuclear cell TF was elevated in cells isolated directly from blood in the pericardial cavity and was twice that detected in simultaneous samples from the perfusate (P < .05). F1.2 levels were highest in pericardial blood and increased progressively during CPB. Plasma factor VIIa concentrations, corrected for hemodilution, and ratios of factor VIIa to factor VII were highest in pericardial samples (P < .05) and increased progressively during and immediately after CPB. Pericardial biopsies obtained before and after CPB in 7 patients did not show TF expression by mesothelial cells.
These data provide direct evidence of TF expression, activation of the extrinsic coagulation pathway, and thrombin formation in the surgical wound. Addition of pericardial blood to the perfusate and expression of TF by both circulating and adherent monocytes strongly promote thrombus formation during open heart surgery.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/01.cir.93.11.2014</identifier><identifier>PMID: 8640976</identifier><identifier>CODEN: CIRCAZ</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Biopsy ; Blood Coagulation - physiology ; Blood Loss, Surgical - physiopathology ; Cardiopulmonary Bypass - adverse effects ; Factor VII - analysis ; Factor VIIa - analysis ; Humans ; Medical sciences ; Middle Aged ; Monocytes - metabolism ; Peptide Fragments - analysis ; Pericardium - injuries ; Pericardium - pathology ; Prothrombin - analysis ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the heart ; Thromboplastin - analysis ; Thrombosis - etiology</subject><ispartof>Circulation (New York, N.Y.), 1996-06, Vol.93 (11), p.2014-2018</ispartof><rights>1996 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. Jun 1, 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-cda1a5ebb15bb55f743643b779aa31641e0f583ab04ec2cdbd5ba536520df4d53</citedby><cites>FETCH-LOGICAL-c508t-cda1a5ebb15bb55f743643b779aa31641e0f583ab04ec2cdbd5ba536520df4d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3687,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3099208$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8640976$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CHUNG, J. H</creatorcontrib><creatorcontrib>GIKAKIS, N</creatorcontrib><creatorcontrib>RAO, A. K</creatorcontrib><creatorcontrib>DRAKE, T. A</creatorcontrib><creatorcontrib>COLMAN, R. W</creatorcontrib><creatorcontrib>EDMUNDS, L. H</creatorcontrib><title>Pericardial blood activates the extrinsic coagulation pathway during clinical cardiopulmonary bypass</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><description>Coagulation during cardiopulmonary bypass (CPB) traditionally has been attributed to activation of the contact system of plasma proteins and the intrinsic coagulation pathway by blood contact with negatively charged surfaces not lined by endothelium. Recent studies have focused on the possible role of the extrinsic coagulation pathway during cardiac surgery. We postulated that the wound activates the extrinsic coagulation pathway during CPB by producing procoagulant cells and enzymes that enter the general circulation.
Blood samples taken from 20 consenting patients who had elective cardiac surgery were assayed for peripheral blood mononuclear cell tissue factor (TF) expression, plasma F1.2, and factor VII and VIIa concentrations. Peripheral blood mononuclear cell TF expression increased in the perfusate after the surgical incision and after CPB was started and in monocytes that adhered to the perfusion circuit. TF on circulating monocytes, however, did not continue to rise during CPB. Peripheral blood mononuclear cell TF was elevated in cells isolated directly from blood in the pericardial cavity and was twice that detected in simultaneous samples from the perfusate (P < .05). F1.2 levels were highest in pericardial blood and increased progressively during CPB. Plasma factor VIIa concentrations, corrected for hemodilution, and ratios of factor VIIa to factor VII were highest in pericardial samples (P < .05) and increased progressively during and immediately after CPB. Pericardial biopsies obtained before and after CPB in 7 patients did not show TF expression by mesothelial cells.
These data provide direct evidence of TF expression, activation of the extrinsic coagulation pathway, and thrombin formation in the surgical wound. Addition of pericardial blood to the perfusate and expression of TF by both circulating and adherent monocytes strongly promote thrombus formation during open heart surgery.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Blood Coagulation - physiology</subject><subject>Blood Loss, Surgical - physiopathology</subject><subject>Cardiopulmonary Bypass - adverse effects</subject><subject>Factor VII - analysis</subject><subject>Factor VIIa - analysis</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Monocytes - metabolism</subject><subject>Peptide Fragments - analysis</subject><subject>Pericardium - injuries</subject><subject>Pericardium - pathology</subject><subject>Prothrombin - analysis</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the heart</subject><subject>Thromboplastin - analysis</subject><subject>Thrombosis - etiology</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkFtrFEEQhRtR4hr9AT4IjQTfZq2-zeVRFqOBgEH0uam-TNKhd3rsnlH336fXLHnwqTicUx9Vh5C3DLaMtewjsK0NeTuIKrccmHxGNkxx2UglhudkAwBD0wnOX5JXpdxX2YpOnZGzvpUwdO2GuBufg8XsAkZqYkqOol3Cb1x8ocudp_7vksNUgqU24e0acQlpojMud3_wQN1azVtqY5gqJdJ_pDSvcZ8mzAdqDjOW8pq8GDEW_-Y0z8nPy88_dl-b629frnafrhuroF8a65Ch8sYwZYxSYydFK4XpugFRsFYyD6PqBRqQ3nLrjFMGlWgVBzdKp8Q5-fDInXP6tfqy6H0o1seIk09r0V0PPbRM1OD7_4L3ac1TvU1zxjveS3GksceQzamU7Ec957CvX2kG-li_BqZ3V9_1IKrUx_rrzrsTeDV77542Tn1X_-LkY6l9jRknG8pTTMAwcOjFA7vbj3M</recordid><startdate>19960601</startdate><enddate>19960601</enddate><creator>CHUNG, J. H</creator><creator>GIKAKIS, N</creator><creator>RAO, A. K</creator><creator>DRAKE, T. A</creator><creator>COLMAN, R. W</creator><creator>EDMUNDS, L. H</creator><general>Lippincott Williams & Wilkins</general><general>American Heart Association, Inc</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>19960601</creationdate><title>Pericardial blood activates the extrinsic coagulation pathway during clinical cardiopulmonary bypass</title><author>CHUNG, J. H ; GIKAKIS, N ; RAO, A. K ; DRAKE, T. A ; COLMAN, R. W ; EDMUNDS, L. H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-cda1a5ebb15bb55f743643b779aa31641e0f583ab04ec2cdbd5ba536520df4d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Blood Coagulation - physiology</topic><topic>Blood Loss, Surgical - physiopathology</topic><topic>Cardiopulmonary Bypass - adverse effects</topic><topic>Factor VII - analysis</topic><topic>Factor VIIa - analysis</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Monocytes - metabolism</topic><topic>Peptide Fragments - analysis</topic><topic>Pericardium - injuries</topic><topic>Pericardium - pathology</topic><topic>Prothrombin - analysis</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the heart</topic><topic>Thromboplastin - analysis</topic><topic>Thrombosis - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CHUNG, J. H</creatorcontrib><creatorcontrib>GIKAKIS, N</creatorcontrib><creatorcontrib>RAO, A. K</creatorcontrib><creatorcontrib>DRAKE, T. A</creatorcontrib><creatorcontrib>COLMAN, R. W</creatorcontrib><creatorcontrib>EDMUNDS, L. H</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CHUNG, J. H</au><au>GIKAKIS, N</au><au>RAO, A. K</au><au>DRAKE, T. A</au><au>COLMAN, R. W</au><au>EDMUNDS, L. H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pericardial blood activates the extrinsic coagulation pathway during clinical cardiopulmonary bypass</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>1996-06-01</date><risdate>1996</risdate><volume>93</volume><issue>11</issue><spage>2014</spage><epage>2018</epage><pages>2014-2018</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><coden>CIRCAZ</coden><abstract>Coagulation during cardiopulmonary bypass (CPB) traditionally has been attributed to activation of the contact system of plasma proteins and the intrinsic coagulation pathway by blood contact with negatively charged surfaces not lined by endothelium. Recent studies have focused on the possible role of the extrinsic coagulation pathway during cardiac surgery. We postulated that the wound activates the extrinsic coagulation pathway during CPB by producing procoagulant cells and enzymes that enter the general circulation.
Blood samples taken from 20 consenting patients who had elective cardiac surgery were assayed for peripheral blood mononuclear cell tissue factor (TF) expression, plasma F1.2, and factor VII and VIIa concentrations. Peripheral blood mononuclear cell TF expression increased in the perfusate after the surgical incision and after CPB was started and in monocytes that adhered to the perfusion circuit. TF on circulating monocytes, however, did not continue to rise during CPB. Peripheral blood mononuclear cell TF was elevated in cells isolated directly from blood in the pericardial cavity and was twice that detected in simultaneous samples from the perfusate (P < .05). F1.2 levels were highest in pericardial blood and increased progressively during CPB. Plasma factor VIIa concentrations, corrected for hemodilution, and ratios of factor VIIa to factor VII were highest in pericardial samples (P < .05) and increased progressively during and immediately after CPB. Pericardial biopsies obtained before and after CPB in 7 patients did not show TF expression by mesothelial cells.
These data provide direct evidence of TF expression, activation of the extrinsic coagulation pathway, and thrombin formation in the surgical wound. Addition of pericardial blood to the perfusate and expression of TF by both circulating and adherent monocytes strongly promote thrombus formation during open heart surgery.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>8640976</pmid><doi>10.1161/01.cir.93.11.2014</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Biological and medical sciences Biopsy Blood Coagulation - physiology Blood Loss, Surgical - physiopathology Cardiopulmonary Bypass - adverse effects Factor VII - analysis Factor VIIa - analysis Humans Medical sciences Middle Aged Monocytes - metabolism Peptide Fragments - analysis Pericardium - injuries Pericardium - pathology Prothrombin - analysis Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the heart Thromboplastin - analysis Thrombosis - etiology |
title | Pericardial blood activates the extrinsic coagulation pathway during clinical cardiopulmonary bypass |
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