Point-of-care ecarin clotting time versus activated clotting time in correlation with bivalirudin concentration

Introduction: A thrombin inhibitor management (TIM) point-of-care test based upon the ecarin clotting time (ECT) has been developed. The ECT has been suggested to more accurately reflect the anti-coagulant effect of direct thrombin inhibitors compared with the activated clotting time (ACT). We sough...

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Veröffentlicht in:Thrombosis research 2004, Vol.113 (2), p.115-121
Hauptverfasser: Casserly, Ivan P, Kereiakes, Dean J, Gray, William A, Gibson, Paul H, Lauer, Michael A, Reginelli, Joel P, Moliterno, David J
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container_end_page 121
container_issue 2
container_start_page 115
container_title Thrombosis research
container_volume 113
creator Casserly, Ivan P
Kereiakes, Dean J
Gray, William A
Gibson, Paul H
Lauer, Michael A
Reginelli, Joel P
Moliterno, David J
description Introduction: A thrombin inhibitor management (TIM) point-of-care test based upon the ecarin clotting time (ECT) has been developed. The ECT has been suggested to more accurately reflect the anti-coagulant effect of direct thrombin inhibitors compared with the activated clotting time (ACT). We sought to examine the correlation of the TIM-ECT test with bivalirudin concentration in patients undergoing percutaneous coronary intervention (PCI), and to compare the performance of this test with the current standard (i.e., ACT). Materials and methods: In a multicenter study, blood samples were obtained at six pre-defined time-points in 170 consecutive patients undergoing PCI using bivalirudin. For each sample, the TIM-ECT (citrated and non-citrated), ACT, and bivalirudin concentration was determined. Results: Considering samples from all time-points ( n=784), the correlations of TIM-ECT citrated, TIM-ECT non-citrated, and ACT with bivalirudin concentration were 0.96, 0.93, and 0.90, respectively. For samples collected at therapeutic levels of bivalirudin ( n=353), the correlations of TIM-ECT citrated, TIM-ECT non-citrated, and ACT with bivalirudin concentration were lower, and showed a greater disparity between methods, with correlation coefficients of 0.75, 0.59, and 0.37, respectively. Prediction models based on the measured bivalirudin concentration were developed for TIM-ECT and ACT, and the coefficients of determination ( r 2) of actual versus predicted TIM-ECT and ACT were 0.91 and 0.81, respectively. Conclusions: In this PCI population, the TIM-ECT point-of-care test and ACT demonstrated a strong correlation with bivalirudin concentration. The TIM-ECT test had a higher correlation with bivalirudin concentration at therapeutic levels of the drug, and for individual samples appears to more consistently reflect the bivalirudin concentration compared with the ACT.
doi_str_mv 10.1016/j.thromres.2004.02.012
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The ECT has been suggested to more accurately reflect the anti-coagulant effect of direct thrombin inhibitors compared with the activated clotting time (ACT). We sought to examine the correlation of the TIM-ECT test with bivalirudin concentration in patients undergoing percutaneous coronary intervention (PCI), and to compare the performance of this test with the current standard (i.e., ACT). Materials and methods: In a multicenter study, blood samples were obtained at six pre-defined time-points in 170 consecutive patients undergoing PCI using bivalirudin. For each sample, the TIM-ECT (citrated and non-citrated), ACT, and bivalirudin concentration was determined. Results: Considering samples from all time-points ( n=784), the correlations of TIM-ECT citrated, TIM-ECT non-citrated, and ACT with bivalirudin concentration were 0.96, 0.93, and 0.90, respectively. For samples collected at therapeutic levels of bivalirudin ( n=353), the correlations of TIM-ECT citrated, TIM-ECT non-citrated, and ACT with bivalirudin concentration were lower, and showed a greater disparity between methods, with correlation coefficients of 0.75, 0.59, and 0.37, respectively. Prediction models based on the measured bivalirudin concentration were developed for TIM-ECT and ACT, and the coefficients of determination ( r 2) of actual versus predicted TIM-ECT and ACT were 0.91 and 0.81, respectively. Conclusions: In this PCI population, the TIM-ECT point-of-care test and ACT demonstrated a strong correlation with bivalirudin concentration. The TIM-ECT test had a higher correlation with bivalirudin concentration at therapeutic levels of the drug, and for individual samples appears to more consistently reflect the bivalirudin concentration compared with the ACT.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2004.02.012</identifier><identifier>PMID: 15115666</identifier><identifier>CODEN: THBRAA</identifier><language>eng</language><publisher>New York, NY: Elsevier Ltd</publisher><subject>Activated clotting time ; Aged ; Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Bivalirudin ; Blood and lymphatic vessels ; Blood Coagulation Tests - methods ; Blood Coagulation Tests - standards ; Cardiology. Vascular system ; Cardiovascular system ; Citric Acid ; Direct thrombin inhibitor ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Drug Monitoring - methods ; Drug Monitoring - standards ; Ecarin clotting time ; Endopeptidases ; Female ; Fibrinolytic Agents - administration &amp; dosage ; Hirudins - administration &amp; dosage ; Hirudins - analogs &amp; derivatives ; Humans ; Male ; Medical sciences ; Peptide Fragments - administration &amp; dosage ; Percutaneous coronary intervention ; Pharmacology. 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The ECT has been suggested to more accurately reflect the anti-coagulant effect of direct thrombin inhibitors compared with the activated clotting time (ACT). We sought to examine the correlation of the TIM-ECT test with bivalirudin concentration in patients undergoing percutaneous coronary intervention (PCI), and to compare the performance of this test with the current standard (i.e., ACT). Materials and methods: In a multicenter study, blood samples were obtained at six pre-defined time-points in 170 consecutive patients undergoing PCI using bivalirudin. For each sample, the TIM-ECT (citrated and non-citrated), ACT, and bivalirudin concentration was determined. Results: Considering samples from all time-points ( n=784), the correlations of TIM-ECT citrated, TIM-ECT non-citrated, and ACT with bivalirudin concentration were 0.96, 0.93, and 0.90, respectively. For samples collected at therapeutic levels of bivalirudin ( n=353), the correlations of TIM-ECT citrated, TIM-ECT non-citrated, and ACT with bivalirudin concentration were lower, and showed a greater disparity between methods, with correlation coefficients of 0.75, 0.59, and 0.37, respectively. Prediction models based on the measured bivalirudin concentration were developed for TIM-ECT and ACT, and the coefficients of determination ( r 2) of actual versus predicted TIM-ECT and ACT were 0.91 and 0.81, respectively. Conclusions: In this PCI population, the TIM-ECT point-of-care test and ACT demonstrated a strong correlation with bivalirudin concentration. The TIM-ECT test had a higher correlation with bivalirudin concentration at therapeutic levels of the drug, and for individual samples appears to more consistently reflect the bivalirudin concentration compared with the ACT.</description><subject>Activated clotting time</subject><subject>Aged</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Bivalirudin</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Coagulation Tests - methods</subject><subject>Blood Coagulation Tests - standards</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular system</subject><subject>Citric Acid</subject><subject>Direct thrombin inhibitor</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</subject><subject>Drug Monitoring - methods</subject><subject>Drug Monitoring - standards</subject><subject>Ecarin clotting time</subject><subject>Endopeptidases</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration &amp; dosage</subject><subject>Hirudins - administration &amp; dosage</subject><subject>Hirudins - analogs &amp; derivatives</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Peptide Fragments - administration &amp; dosage</subject><subject>Percutaneous coronary intervention</subject><subject>Pharmacology. Drug treatments</subject><subject>Point-of-Care Systems</subject><subject>Recombinant Proteins - administration &amp; dosage</subject><subject>Vascular wall</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF1PwyAUhonRuDn9C6Y3etcKhdJypzF-JUv0Qq8JpaeOpS0T6Iz_XuZmNN4YCCTnfc6BPAidEpwRTPjFMgsLZ3sHPssxZhnOM0zyPTQlVSnSnJX5PprGQKS0YtUEHXm_xJiURBSHaEIKQgrO-RTZJ2uGkNo21cpBAvE0Q6I7G4IZXpNgekjW4PzoE6WDWasAzZ94w1vnoFPB2CF5N2GR1JHsjBubr3DQMAT3FR-jg1Z1Hk529wy93N48X9-n88e7h-ureaqpYCFtGAFW60bQktZKFaqgbayAIhWDkua1YAJr2mjOmWB1S0Ut2lqDoJzHYkln6Hw7d-Xs2wg-yN54DV2nBrCjl2X0FFcVQb4FtbPeO2jlypleuQ9JsNyolkv5rVpuVEucy6g6Np7uXhjrHpqftp3bCJztAOW16lqnBm38L64kmMY9Q5dbDqKPtQEnvTYQnTXGgQ6ysea_v3wC6fOjsQ</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Casserly, Ivan P</creator><creator>Kereiakes, Dean J</creator><creator>Gray, William A</creator><creator>Gibson, Paul H</creator><creator>Lauer, Michael A</creator><creator>Reginelli, Joel P</creator><creator>Moliterno, David J</creator><general>Elsevier Ltd</general><general>Elsevier Science</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>7X8</scope></search><sort><creationdate>2004</creationdate><title>Point-of-care ecarin clotting time versus activated clotting time in correlation with bivalirudin concentration</title><author>Casserly, Ivan P ; Kereiakes, Dean J ; Gray, William A ; Gibson, Paul H ; Lauer, Michael A ; Reginelli, Joel P ; Moliterno, David J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-d41e4bcd9373baa5a53f1e4ea184e732b9490c3dc66494bf39b9fbce9366dc673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Activated clotting time</topic><topic>Aged</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Biological and medical sciences</topic><topic>Bivalirudin</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Coagulation Tests - methods</topic><topic>Blood Coagulation Tests - standards</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular system</topic><topic>Citric Acid</topic><topic>Direct thrombin inhibitor</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>Drug Monitoring - methods</topic><topic>Drug Monitoring - standards</topic><topic>Ecarin clotting time</topic><topic>Endopeptidases</topic><topic>Female</topic><topic>Fibrinolytic Agents - administration &amp; dosage</topic><topic>Hirudins - administration &amp; dosage</topic><topic>Hirudins - analogs &amp; derivatives</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Peptide Fragments - administration &amp; dosage</topic><topic>Percutaneous coronary intervention</topic><topic>Pharmacology. Drug treatments</topic><topic>Point-of-Care Systems</topic><topic>Recombinant Proteins - administration &amp; dosage</topic><topic>Vascular wall</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Casserly, Ivan P</creatorcontrib><creatorcontrib>Kereiakes, Dean J</creatorcontrib><creatorcontrib>Gray, William A</creatorcontrib><creatorcontrib>Gibson, Paul H</creatorcontrib><creatorcontrib>Lauer, Michael A</creatorcontrib><creatorcontrib>Reginelli, Joel P</creatorcontrib><creatorcontrib>Moliterno, David J</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>MEDLINE - Academic</collection><jtitle>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Casserly, Ivan P</au><au>Kereiakes, Dean J</au><au>Gray, William A</au><au>Gibson, Paul H</au><au>Lauer, Michael A</au><au>Reginelli, Joel P</au><au>Moliterno, David J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Point-of-care ecarin clotting time versus activated clotting time in correlation with bivalirudin concentration</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2004</date><risdate>2004</risdate><volume>113</volume><issue>2</issue><spage>115</spage><epage>121</epage><pages>115-121</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><coden>THBRAA</coden><abstract>Introduction: A thrombin inhibitor management (TIM) point-of-care test based upon the ecarin clotting time (ECT) has been developed. The ECT has been suggested to more accurately reflect the anti-coagulant effect of direct thrombin inhibitors compared with the activated clotting time (ACT). We sought to examine the correlation of the TIM-ECT test with bivalirudin concentration in patients undergoing percutaneous coronary intervention (PCI), and to compare the performance of this test with the current standard (i.e., ACT). Materials and methods: In a multicenter study, blood samples were obtained at six pre-defined time-points in 170 consecutive patients undergoing PCI using bivalirudin. For each sample, the TIM-ECT (citrated and non-citrated), ACT, and bivalirudin concentration was determined. Results: Considering samples from all time-points ( n=784), the correlations of TIM-ECT citrated, TIM-ECT non-citrated, and ACT with bivalirudin concentration were 0.96, 0.93, and 0.90, respectively. For samples collected at therapeutic levels of bivalirudin ( n=353), the correlations of TIM-ECT citrated, TIM-ECT non-citrated, and ACT with bivalirudin concentration were lower, and showed a greater disparity between methods, with correlation coefficients of 0.75, 0.59, and 0.37, respectively. Prediction models based on the measured bivalirudin concentration were developed for TIM-ECT and ACT, and the coefficients of determination ( r 2) of actual versus predicted TIM-ECT and ACT were 0.91 and 0.81, respectively. Conclusions: In this PCI population, the TIM-ECT point-of-care test and ACT demonstrated a strong correlation with bivalirudin concentration. The TIM-ECT test had a higher correlation with bivalirudin concentration at therapeutic levels of the drug, and for individual samples appears to more consistently reflect the bivalirudin concentration compared with the ACT.</abstract><cop>New York, NY</cop><pub>Elsevier Ltd</pub><pmid>15115666</pmid><doi>10.1016/j.thromres.2004.02.012</doi><tpages>7</tpages></addata></record>
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subjects Activated clotting time
Aged
Atherosclerosis (general aspects, experimental research)
Biological and medical sciences
Bivalirudin
Blood and lymphatic vessels
Blood Coagulation Tests - methods
Blood Coagulation Tests - standards
Cardiology. Vascular system
Cardiovascular system
Citric Acid
Direct thrombin inhibitor
Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous
Drug Monitoring - methods
Drug Monitoring - standards
Ecarin clotting time
Endopeptidases
Female
Fibrinolytic Agents - administration & dosage
Hirudins - administration & dosage
Hirudins - analogs & derivatives
Humans
Male
Medical sciences
Peptide Fragments - administration & dosage
Percutaneous coronary intervention
Pharmacology. Drug treatments
Point-of-Care Systems
Recombinant Proteins - administration & dosage
Vascular wall
title Point-of-care ecarin clotting time versus activated clotting time in correlation with bivalirudin concentration
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