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Clinical effectiveness and safety outcomes associated with prothrombin complex concentrates
Prothrombin complex concentrates (PCCs) are indicated for urgent reversal of warfarin and used for reversal of novel oral anticoagulants, in patients with acute major bleeding or need for an urgent procedure. The research goal was to evaluate effectiveness and safety outcomes with PCC usage at our i...
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Published in: | Journal of thrombosis and thrombolysis 2016-07, Vol.42 (1), p.6-10 |
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creator | Hedges, Ashley Coons, James C. Saul, Melissa Smith, Roy E. |
description | Prothrombin complex concentrates (PCCs) are indicated for urgent reversal of warfarin and used for reversal of novel oral anticoagulants, in patients with acute major bleeding or need for an urgent procedure. The research goal was to evaluate effectiveness and safety outcomes with PCC usage at our institution. A retrospective review of electronic medical records identified patients that received a PCC commercially available in the United States (KCentra
®
or Profilnine
®
) at twelve hospitals in a tertiary care health system from July 1, 2013 to April 30, 2014. A total of 193 patients received PCC, of which 184 patients received four-factor PCC. The patient population was 48 % male and 75 % Caucasian, with a mean age of 73 years old. Clinical outcomes of interest included time to achieve a target INR ≤1.3, time to Hgb >7 g/dL, and incidence of thromboembolism. A total of 143 patients were on warfarin (74.1 %) at baseline, whereas 18 patients (9.3 %) were taking a novel anticoagulant. Target INR of ≤1.3 was achieved in 125 patients (65.8 %), within a median time of 8.03 h (IQR 3.38–34.07). Among patients with a baseline Hgb 7 g/dL was 8.48 h (IQR 6.95–13.00). Eight patients (4.1 %) developed an acute venous thromboembolism following PCC administration. INR reversal was achieved in approximately two-thirds of patients, with a low incidence of venous thromboembolism. Four-factor PCC is a viable alternative to plasma. |
doi_str_mv | 10.1007/s11239-015-1321-4 |
format | article |
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®
or Profilnine
®
) at twelve hospitals in a tertiary care health system from July 1, 2013 to April 30, 2014. A total of 193 patients received PCC, of which 184 patients received four-factor PCC. The patient population was 48 % male and 75 % Caucasian, with a mean age of 73 years old. Clinical outcomes of interest included time to achieve a target INR ≤1.3, time to Hgb >7 g/dL, and incidence of thromboembolism. A total of 143 patients were on warfarin (74.1 %) at baseline, whereas 18 patients (9.3 %) were taking a novel anticoagulant. Target INR of ≤1.3 was achieved in 125 patients (65.8 %), within a median time of 8.03 h (IQR 3.38–34.07). Among patients with a baseline Hgb <7 g/L (
n
= 13), the median time to Hgb >7 g/dL was 8.48 h (IQR 6.95–13.00). Eight patients (4.1 %) developed an acute venous thromboembolism following PCC administration. INR reversal was achieved in approximately two-thirds of patients, with a low incidence of venous thromboembolism. Four-factor PCC is a viable alternative to plasma.</description><identifier>ISSN: 0929-5305</identifier><identifier>EISSN: 1573-742X</identifier><identifier>DOI: 10.1007/s11239-015-1321-4</identifier><identifier>PMID: 26685667</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Aged ; Blood Coagulation Factors - administration & dosage ; Blood Coagulation Factors - pharmacology ; Cardiology ; Drug Interactions ; Female ; Hematology ; Hemoglobins - analysis ; Hemorrhage - drug therapy ; Humans ; International Normalized Ratio ; Male ; Medicine ; Medicine & Public Health ; Patient Safety ; Pharmacokinetics ; Retrospective Studies ; Treatment Outcome ; Venous Thromboembolism - chemically induced</subject><ispartof>Journal of thrombosis and thrombolysis, 2016-07, Vol.42 (1), p.6-10</ispartof><rights>Springer Science+Business Media New York 2015</rights><rights>Springer Science+Business Media New York 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-637ff8f3dc491e7f5fd6cad4cf8b305b392ebcc6e1d895f6ba9feb462ba06e493</citedby><cites>FETCH-LOGICAL-c372t-637ff8f3dc491e7f5fd6cad4cf8b305b392ebcc6e1d895f6ba9feb462ba06e493</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26685667$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hedges, Ashley</creatorcontrib><creatorcontrib>Coons, James C.</creatorcontrib><creatorcontrib>Saul, Melissa</creatorcontrib><creatorcontrib>Smith, Roy E.</creatorcontrib><title>Clinical effectiveness and safety outcomes associated with prothrombin complex concentrates</title><title>Journal of thrombosis and thrombolysis</title><addtitle>J Thromb Thrombolysis</addtitle><addtitle>J Thromb Thrombolysis</addtitle><description>Prothrombin complex concentrates (PCCs) are indicated for urgent reversal of warfarin and used for reversal of novel oral anticoagulants, in patients with acute major bleeding or need for an urgent procedure. The research goal was to evaluate effectiveness and safety outcomes with PCC usage at our institution. A retrospective review of electronic medical records identified patients that received a PCC commercially available in the United States (KCentra
®
or Profilnine
®
) at twelve hospitals in a tertiary care health system from July 1, 2013 to April 30, 2014. A total of 193 patients received PCC, of which 184 patients received four-factor PCC. The patient population was 48 % male and 75 % Caucasian, with a mean age of 73 years old. Clinical outcomes of interest included time to achieve a target INR ≤1.3, time to Hgb >7 g/dL, and incidence of thromboembolism. A total of 143 patients were on warfarin (74.1 %) at baseline, whereas 18 patients (9.3 %) were taking a novel anticoagulant. Target INR of ≤1.3 was achieved in 125 patients (65.8 %), within a median time of 8.03 h (IQR 3.38–34.07). Among patients with a baseline Hgb <7 g/L (
n
= 13), the median time to Hgb >7 g/dL was 8.48 h (IQR 6.95–13.00). Eight patients (4.1 %) developed an acute venous thromboembolism following PCC administration. INR reversal was achieved in approximately two-thirds of patients, with a low incidence of venous thromboembolism. Four-factor PCC is a viable alternative to plasma.</description><subject>Aged</subject><subject>Blood Coagulation Factors - administration & dosage</subject><subject>Blood Coagulation Factors - pharmacology</subject><subject>Cardiology</subject><subject>Drug Interactions</subject><subject>Female</subject><subject>Hematology</subject><subject>Hemoglobins - analysis</subject><subject>Hemorrhage - drug therapy</subject><subject>Humans</subject><subject>International Normalized Ratio</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Patient Safety</subject><subject>Pharmacokinetics</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><subject>Venous Thromboembolism - chemically induced</subject><issn>0929-5305</issn><issn>1573-742X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LAzEURYMoWqs_wI0MuHEzmo-ZpFlK8QsKbhQEFyGTebFTZjI1yaj996a0igiuHrycd3M5CJ0QfEEwFpeBEMpkjkmZE0ZJXuygESkFy0VBn3fRCEsq85Lh8gAdhrDAGEuJ6T46oJxPSs7FCL1M28Y1RrcZWAsmNu_gIIRMuzoL2kJcZf0QTd9B2oXQm0ZHqLOPJs6zpe_j3Pdd1bgsEcsWPtN0Blz0iQpHaM_qNsDxdo7R08314_Qunz3c3k-vZrlhgsacM2HtxLLaFJKAsKWtudF1YeykSt0rJilUxnAg9USWlldaWqgKTiuNORSSjdH5JjcVehsgRNU1wUDbagf9EBQRkjAmBFmjZ3_QRT94l9qtKZycsIInimwo4_sQPFi19E2n_UoRrNbm1ca8SubV2rwq0s3pNnmoOqh_Lr5VJ4BugJCe3Cv4X1__m_oFWeaQoA</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Hedges, Ashley</creator><creator>Coons, James C.</creator><creator>Saul, Melissa</creator><creator>Smith, Roy E.</creator><general>Springer US</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20160701</creationdate><title>Clinical effectiveness and safety outcomes associated with prothrombin complex concentrates</title><author>Hedges, Ashley ; Coons, James C. ; Saul, Melissa ; Smith, Roy E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-637ff8f3dc491e7f5fd6cad4cf8b305b392ebcc6e1d895f6ba9feb462ba06e493</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Blood Coagulation Factors - administration & dosage</topic><topic>Blood Coagulation Factors - pharmacology</topic><topic>Cardiology</topic><topic>Drug Interactions</topic><topic>Female</topic><topic>Hematology</topic><topic>Hemoglobins - analysis</topic><topic>Hemorrhage - drug therapy</topic><topic>Humans</topic><topic>International Normalized Ratio</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Patient Safety</topic><topic>Pharmacokinetics</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><topic>Venous Thromboembolism - chemically induced</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hedges, Ashley</creatorcontrib><creatorcontrib>Coons, James C.</creatorcontrib><creatorcontrib>Saul, Melissa</creatorcontrib><creatorcontrib>Smith, Roy E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of thrombosis and thrombolysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hedges, Ashley</au><au>Coons, James C.</au><au>Saul, Melissa</au><au>Smith, Roy E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical effectiveness and safety outcomes associated with prothrombin complex concentrates</atitle><jtitle>Journal of thrombosis and thrombolysis</jtitle><stitle>J Thromb Thrombolysis</stitle><addtitle>J Thromb Thrombolysis</addtitle><date>2016-07-01</date><risdate>2016</risdate><volume>42</volume><issue>1</issue><spage>6</spage><epage>10</epage><pages>6-10</pages><issn>0929-5305</issn><eissn>1573-742X</eissn><abstract>Prothrombin complex concentrates (PCCs) are indicated for urgent reversal of warfarin and used for reversal of novel oral anticoagulants, in patients with acute major bleeding or need for an urgent procedure. The research goal was to evaluate effectiveness and safety outcomes with PCC usage at our institution. A retrospective review of electronic medical records identified patients that received a PCC commercially available in the United States (KCentra
®
or Profilnine
®
) at twelve hospitals in a tertiary care health system from July 1, 2013 to April 30, 2014. A total of 193 patients received PCC, of which 184 patients received four-factor PCC. The patient population was 48 % male and 75 % Caucasian, with a mean age of 73 years old. Clinical outcomes of interest included time to achieve a target INR ≤1.3, time to Hgb >7 g/dL, and incidence of thromboembolism. A total of 143 patients were on warfarin (74.1 %) at baseline, whereas 18 patients (9.3 %) were taking a novel anticoagulant. Target INR of ≤1.3 was achieved in 125 patients (65.8 %), within a median time of 8.03 h (IQR 3.38–34.07). Among patients with a baseline Hgb <7 g/L (
n
= 13), the median time to Hgb >7 g/dL was 8.48 h (IQR 6.95–13.00). Eight patients (4.1 %) developed an acute venous thromboembolism following PCC administration. INR reversal was achieved in approximately two-thirds of patients, with a low incidence of venous thromboembolism. Four-factor PCC is a viable alternative to plasma.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>26685667</pmid><doi>10.1007/s11239-015-1321-4</doi><tpages>5</tpages></addata></record> |
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subjects | Aged Blood Coagulation Factors - administration & dosage Blood Coagulation Factors - pharmacology Cardiology Drug Interactions Female Hematology Hemoglobins - analysis Hemorrhage - drug therapy Humans International Normalized Ratio Male Medicine Medicine & Public Health Patient Safety Pharmacokinetics Retrospective Studies Treatment Outcome Venous Thromboembolism - chemically induced |
title | Clinical effectiveness and safety outcomes associated with prothrombin complex concentrates |
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