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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Thrombosis and haemostasis 2011, Vol.105 (12), p.1215-1223.
Hauptverfasser: Ogawa, Satoru, Szlam, Fania, Ohnishi, Tomoko, Molinaro, Ross J., Hosokawa, Kazuya, Tanaka, Kenichi A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1223.
container_issue 12
container_start_page 1215
container_title Thrombosis and haemostasis
container_volume 105
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
fullrecord <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1160_TH11_04_0240</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1160_TH11_04_0240</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2820-9ee7ee782894fa517412315827c0fc3000132c8c5255778e89b56d1e94c7173f3</originalsourceid><addsrcrecordid>eNptkE9LAzEQxYMoWKs3P0AunnQ1ySb751iKWqHgpYK3Jc1O6JbdZJlsW-vd721qxZMwMJffezPvEXLN2T3nGXtYzDhPmEyYkOyEjITK8iQryvdTMmKpZEkmpDonFyGsGeOZLNWIfE2o8V2vUQ_NFmgYNvWeekt79MMKfbds3A_QwkfczoAbIgqBaldTixBWFv0nONq3OnSaWo90p9FqjEKELWDQLd24GjCaxyPmqGz97uBXN0PjXbgkZ1a3Aa5-95i8PT0uprNk_vr8Mp3MEyMKwZISII9TiKKUViueSy5SrgqRG2ZNymKqVJjCKKFUnhdQlEuV1RxKaXKepzYdk7ujr0EfAoKtemw6jfuKs-pQYXWosGKyOlQY8Zsj3utgdGtRO9OEP41QsU8WXxiT2yM3rBrooFr7DbqY43_Xb8DggIs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A comparative study of prothrombin complex concentrates and freshfrozen plasma for warfarin reversal under static and flow conditions</title><source>Thieme Connect Journals</source><creator>Ogawa, Satoru ; Szlam, Fania ; Ohnishi, Tomoko ; Molinaro, Ross J. ; Hosokawa, Kazuya ; Tanaka, Kenichi A.</creator><creatorcontrib>Ogawa, Satoru ; Szlam, Fania ; Ohnishi, Tomoko ; Molinaro, Ross J. ; Hosokawa, Kazuya ; Tanaka, Kenichi A.</creatorcontrib><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><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&amp;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>
fulltext fulltext
identifier ISSN: 0340-6245
ispartof Thrombosis and haemostasis, 2011, Vol.105 (12), p.1215-1223.
issn 0340-6245
2567-689X
language eng
recordid cdi_crossref_primary_10_1160_TH11_04_0240
source Thieme Connect Journals
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T03%3A54%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20comparative%20study%20of%20prothrombin%20complex%20concentrates%20and%20freshfrozen%20plasma%20for%20warfarin%20reversal%20under%20static%20and%20flow%20conditions&rft.jtitle=Thrombosis%20and%20haemostasis&rft.au=Ogawa,%20Satoru&rft.date=2011&rft.volume=105&rft.issue=12&rft.spage=1215&rft.epage=1223.&rft.pages=1215-1223.&rft.issn=0340-6245&rft.eissn=2567-689X&rft.coden=THHADQ&rft_id=info:doi/10.1160/TH11-04-0240&rft_dat=%3Cthieme_cross%3E10_1160_TH11_04_0240%3C/thieme_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true