A comparative study of prothrombin complex concentrates and freshfrozen plasma for warfarin reversal under static and flow conditions
Summary Prothrombin complex concentrates (PCCs) and fresh-frozen plasma (FFP) have been clinically used for acute warfarin reversal. The recovery of prothrombin time (PT) or international normalised ratio (INR) is often reported as an endpoint, but haemostatic efficacies of PCCs and FFP may not be f...
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creator | Ogawa, Satoru Szlam, Fania Ohnishi, Tomoko Molinaro, Ross J. Hosokawa, Kazuya Tanaka, Kenichi A. |
description | Summary
Prothrombin complex concentrates (PCCs) and fresh-frozen plasma (FFP) have been clinically used for acute warfarin reversal. The recovery of prothrombin time (PT) or international normalised ratio (INR) is often reported as an endpoint, but haemostatic efficacies of PCCs and FFP may not be fully reflected in static clotting test in platelet-poor plasma. Using various
in vitro
assays, we compared the effects of two PCC preparations (3-factor PCC; Bebulin and 4-factor PCC; Beriplex) and FFP on warfarin reversal under static and flow conditions. First, we added an aliquot of either PCC (0.3 or 0.72 U/ml) or 20% FFP (v/v) to commercial warfarin plasma (INR 3.2, or 10.3), and then measured PT, factor II, factor VII, and thrombin generation. Subsequently, we collected whole blood samples from six consented warfarin-treated patients with mean INR 3.0 ± 0.5 (range 2.5–3.7), and compared clot formation under flow conditions at 280 s
-1
before and after addition of either PCC preparation (0.3 and 0.6 U/ml) or 20% of FFP (v/v). PT/INR were restored by either PCC in plasma with INR 3.0, but they were more effectively corrected by 4-factor PCC than 3-factor PCC in plasma with INR 10.3. Effects of FFP were similar to 0.3U/ml of PCCs in terms of PT, but FFP was less efficacious than PCCs in recovering thrombin generation or factor II levels. In flow experiments, the onset of thrombus formation was shortened by either PCC, but not by FFP, contrary to shortened PT values. For warfarin reversal 20% volume replacement with FFP is inferior to PCCs. |
doi_str_mv | 10.1160/TH11-04-0240 |
format | Article |
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Prothrombin complex concentrates (PCCs) and fresh-frozen plasma (FFP) have been clinically used for acute warfarin reversal. The recovery of prothrombin time (PT) or international normalised ratio (INR) is often reported as an endpoint, but haemostatic efficacies of PCCs and FFP may not be fully reflected in static clotting test in platelet-poor plasma. Using various
in vitro
assays, we compared the effects of two PCC preparations (3-factor PCC; Bebulin and 4-factor PCC; Beriplex) and FFP on warfarin reversal under static and flow conditions. First, we added an aliquot of either PCC (0.3 or 0.72 U/ml) or 20% FFP (v/v) to commercial warfarin plasma (INR 3.2, or 10.3), and then measured PT, factor II, factor VII, and thrombin generation. Subsequently, we collected whole blood samples from six consented warfarin-treated patients with mean INR 3.0 ± 0.5 (range 2.5–3.7), and compared clot formation under flow conditions at 280 s
-1
before and after addition of either PCC preparation (0.3 and 0.6 U/ml) or 20% of FFP (v/v). PT/INR were restored by either PCC in plasma with INR 3.0, but they were more effectively corrected by 4-factor PCC than 3-factor PCC in plasma with INR 10.3. Effects of FFP were similar to 0.3U/ml of PCCs in terms of PT, but FFP was less efficacious than PCCs in recovering thrombin generation or factor II levels. In flow experiments, the onset of thrombus formation was shortened by either PCC, but not by FFP, contrary to shortened PT values. For warfarin reversal 20% volume replacement with FFP is inferior to PCCs.</description><identifier>ISSN: 0340-6245</identifier><identifier>EISSN: 2567-689X</identifier><identifier>DOI: 10.1160/TH11-04-0240</identifier><identifier>CODEN: THHADQ</identifier><language>eng</language><publisher>Stuttgart: Schattauer GmbH</publisher><subject>Biological and medical sciences ; Blood coagulation. Blood cells ; Fundamental and applied biological sciences. Psychology ; Hematologic and hematopoietic diseases ; Medical sciences ; Molecular and cellular biology ; New Technologies, Diagnostic Tools and Drugs ; Platelet diseases and coagulopathies</subject><ispartof>Thrombosis and haemostasis, 2011, Vol.105 (12), p.1215-1223.</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2820-9ee7ee782894fa517412315827c0fc3000132c8c5255778e89b56d1e94c7173f3</citedby><cites>FETCH-LOGICAL-c2820-9ee7ee782894fa517412315827c0fc3000132c8c5255778e89b56d1e94c7173f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1160/TH11-04-0240.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1160/TH11-04-0240$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,780,784,3016,4022,27922,27923,27924,54558,54559</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25245012$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Ogawa, Satoru</creatorcontrib><creatorcontrib>Szlam, Fania</creatorcontrib><creatorcontrib>Ohnishi, Tomoko</creatorcontrib><creatorcontrib>Molinaro, Ross J.</creatorcontrib><creatorcontrib>Hosokawa, Kazuya</creatorcontrib><creatorcontrib>Tanaka, Kenichi A.</creatorcontrib><title>A comparative study of prothrombin complex concentrates and freshfrozen plasma for warfarin reversal under static and flow conditions</title><title>Thrombosis and haemostasis</title><addtitle>Thromb Haemost</addtitle><description>Summary
Prothrombin complex concentrates (PCCs) and fresh-frozen plasma (FFP) have been clinically used for acute warfarin reversal. The recovery of prothrombin time (PT) or international normalised ratio (INR) is often reported as an endpoint, but haemostatic efficacies of PCCs and FFP may not be fully reflected in static clotting test in platelet-poor plasma. Using various
in vitro
assays, we compared the effects of two PCC preparations (3-factor PCC; Bebulin and 4-factor PCC; Beriplex) and FFP on warfarin reversal under static and flow conditions. First, we added an aliquot of either PCC (0.3 or 0.72 U/ml) or 20% FFP (v/v) to commercial warfarin plasma (INR 3.2, or 10.3), and then measured PT, factor II, factor VII, and thrombin generation. Subsequently, we collected whole blood samples from six consented warfarin-treated patients with mean INR 3.0 ± 0.5 (range 2.5–3.7), and compared clot formation under flow conditions at 280 s
-1
before and after addition of either PCC preparation (0.3 and 0.6 U/ml) or 20% of FFP (v/v). PT/INR were restored by either PCC in plasma with INR 3.0, but they were more effectively corrected by 4-factor PCC than 3-factor PCC in plasma with INR 10.3. Effects of FFP were similar to 0.3U/ml of PCCs in terms of PT, but FFP was less efficacious than PCCs in recovering thrombin generation or factor II levels. In flow experiments, the onset of thrombus formation was shortened by either PCC, but not by FFP, contrary to shortened PT values. For warfarin reversal 20% volume replacement with FFP is inferior to PCCs.</description><subject>Biological and medical sciences</subject><subject>Blood coagulation. Blood cells</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Medical sciences</subject><subject>Molecular and cellular biology</subject><subject>New Technologies, Diagnostic Tools and Drugs</subject><subject>Platelet diseases and coagulopathies</subject><issn>0340-6245</issn><issn>2567-689X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNptkE9LAzEQxYMoWKs3P0AunnQ1ySb751iKWqHgpYK3Jc1O6JbdZJlsW-vd721qxZMwMJffezPvEXLN2T3nGXtYzDhPmEyYkOyEjITK8iQryvdTMmKpZEkmpDonFyGsGeOZLNWIfE2o8V2vUQ_NFmgYNvWeekt79MMKfbds3A_QwkfczoAbIgqBaldTixBWFv0nONq3OnSaWo90p9FqjEKELWDQLd24GjCaxyPmqGz97uBXN0PjXbgkZ1a3Aa5-95i8PT0uprNk_vr8Mp3MEyMKwZISII9TiKKUViueSy5SrgqRG2ZNymKqVJjCKKFUnhdQlEuV1RxKaXKepzYdk7ujr0EfAoKtemw6jfuKs-pQYXWosGKyOlQY8Zsj3utgdGtRO9OEP41QsU8WXxiT2yM3rBrooFr7DbqY43_Xb8DggIs</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Ogawa, Satoru</creator><creator>Szlam, Fania</creator><creator>Ohnishi, Tomoko</creator><creator>Molinaro, Ross J.</creator><creator>Hosokawa, Kazuya</creator><creator>Tanaka, Kenichi A.</creator><general>Schattauer GmbH</general><general>Schattauer</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2011</creationdate><title>A comparative study of prothrombin complex concentrates and freshfrozen plasma for warfarin reversal under static and flow conditions</title><author>Ogawa, Satoru ; Szlam, Fania ; Ohnishi, Tomoko ; Molinaro, Ross J. ; Hosokawa, Kazuya ; Tanaka, Kenichi A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2820-9ee7ee782894fa517412315827c0fc3000132c8c5255778e89b56d1e94c7173f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biological and medical sciences</topic><topic>Blood coagulation. Blood cells</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Medical sciences</topic><topic>Molecular and cellular biology</topic><topic>New Technologies, Diagnostic Tools and Drugs</topic><topic>Platelet diseases and coagulopathies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ogawa, Satoru</creatorcontrib><creatorcontrib>Szlam, Fania</creatorcontrib><creatorcontrib>Ohnishi, Tomoko</creatorcontrib><creatorcontrib>Molinaro, Ross J.</creatorcontrib><creatorcontrib>Hosokawa, Kazuya</creatorcontrib><creatorcontrib>Tanaka, Kenichi A.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ogawa, Satoru</au><au>Szlam, Fania</au><au>Ohnishi, Tomoko</au><au>Molinaro, Ross J.</au><au>Hosokawa, Kazuya</au><au>Tanaka, Kenichi A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A comparative study of prothrombin complex concentrates and freshfrozen plasma for warfarin reversal under static and flow conditions</atitle><jtitle>Thrombosis and haemostasis</jtitle><addtitle>Thromb Haemost</addtitle><date>2011</date><risdate>2011</risdate><volume>105</volume><issue>12</issue><spage>1215</spage><epage>1223.</epage><pages>1215-1223.</pages><issn>0340-6245</issn><eissn>2567-689X</eissn><coden>THHADQ</coden><abstract>Summary
Prothrombin complex concentrates (PCCs) and fresh-frozen plasma (FFP) have been clinically used for acute warfarin reversal. The recovery of prothrombin time (PT) or international normalised ratio (INR) is often reported as an endpoint, but haemostatic efficacies of PCCs and FFP may not be fully reflected in static clotting test in platelet-poor plasma. Using various
in vitro
assays, we compared the effects of two PCC preparations (3-factor PCC; Bebulin and 4-factor PCC; Beriplex) and FFP on warfarin reversal under static and flow conditions. First, we added an aliquot of either PCC (0.3 or 0.72 U/ml) or 20% FFP (v/v) to commercial warfarin plasma (INR 3.2, or 10.3), and then measured PT, factor II, factor VII, and thrombin generation. Subsequently, we collected whole blood samples from six consented warfarin-treated patients with mean INR 3.0 ± 0.5 (range 2.5–3.7), and compared clot formation under flow conditions at 280 s
-1
before and after addition of either PCC preparation (0.3 and 0.6 U/ml) or 20% of FFP (v/v). PT/INR were restored by either PCC in plasma with INR 3.0, but they were more effectively corrected by 4-factor PCC than 3-factor PCC in plasma with INR 10.3. Effects of FFP were similar to 0.3U/ml of PCCs in terms of PT, but FFP was less efficacious than PCCs in recovering thrombin generation or factor II levels. In flow experiments, the onset of thrombus formation was shortened by either PCC, but not by FFP, contrary to shortened PT values. For warfarin reversal 20% volume replacement with FFP is inferior to PCCs.</abstract><cop>Stuttgart</cop><pub>Schattauer GmbH</pub><doi>10.1160/TH11-04-0240</doi><tpages>9</tpages></addata></record> |
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subjects | Biological and medical sciences Blood coagulation. Blood cells Fundamental and applied biological sciences. Psychology Hematologic and hematopoietic diseases Medical sciences Molecular and cellular biology New Technologies, Diagnostic Tools and Drugs Platelet diseases and coagulopathies |
title | A comparative study of prothrombin complex concentrates and freshfrozen plasma for warfarin reversal under static and flow conditions |
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