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dc.rights.licenseopenen_US
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorROULLET, Stéphanie
hal.structure.identifierCHU Bordeaux
dc.contributor.authorRIVOIRE, Timothée
hal.structure.identifierCentre Hospitalier Universitaire de Bordeaux [CHU de Bordeaux]
dc.contributor.authorHOUSSIN, Clémence
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorLABROUCHE, Sylvie
hal.structure.identifierCentre Hospitalier Universitaire de Bordeaux [CHU de Bordeaux]
dc.contributor.authorPAQUIN, Sandrine
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorNOUETTE-GAULAIN, Karine
dc.contributor.authorDENEUX-THARAUX, Catherine
dc.contributor.authorAMIRAL, Jean
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorJAMES, Chloé
hal.structure.identifierCentre Hospitalier Universitaire de Bordeaux [CHU de Bordeaux]
dc.contributor.authorSENTILHES, Loïc
dc.date.accessioned2023-03-03T11:57:41Z
dc.date.available2023-03-03T11:57:41Z
dc.date.issued2022-11-01
dc.identifier.issn2567-689Xen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/172156
dc.description.abstractEn Fibrinolysis activation during delivery contributes to postpartum hemorrhage (PPH). Clot lysis time studied with the global fibrinolytic capacity device (GFC/LT) is a functional test which rapidly assesses fibrinolytic profile. Tranexamic acid (TXA) is an efficient antifibrinolytic therapy.  We prospectively studied fibrinolysis and coagulation in 33 women included in the TRAAP2 trial, which aimed to assess the impact of TXA in preventing PPH following a cesarean delivery. TXA or placebo was randomly administered after childbirth as part of the TRAAP2 trial's protocol. Fibrinolytic (GFC/LT, plasma concentration of fibrinolysis activators and inhibitors) and hemostatic parameters were assayed at three sample times (TREF [T-reference] after anesthesia, T15 and T120minutes after TXA, or placebo administration).  All cesarean deliveries were elective. In the placebo group, the clot lysis time assessed with GFC/LT significantly decreased between TREF and T120, indicating an activated fibrinolysis (44 [interquartile range, IQR: 40-48] vs. 34 [IQR: 30-36] minutes, <0.001). In both TXA and placebo groups, significant fluctuations of the plasmatic concentrations of fibrinolytic mediators were noticed over time, suggesting fibrinolysis activation. Clot lysis time measured by GFC/LT was significantly increased in women of the TXA group as compared with those in the placebo group at T15 (120 [120-120] vs. 36 [34-41] minutes, <0.001) and T120minutes (113 [99-120] vs. 34 [30-36] minutes, <0.001) after drug administration, indicating a decreased in fibrinolysis in those women.  GFC/LT evidenced fibrinolysis activation during cesarean delivery, linked to a decrease in fibrinolytic inhibitors. GFC/LT revealed a significant antifibrinolytic effect of TXA compared with placebo.
dc.language.isoENen_US
dc.subject.enFemale
dc.subject.enHumans
dc.subject.enPregnancy
dc.subject.enAntifibrinolytic Agents
dc.subject.enFibrin Clot Lysis Time
dc.subject.enFibrinolysis
dc.subject.enHemostatics
dc.subject.enPostpartum Hemorrhage
dc.subject.enTranexamic Acid
dc.title.enHemostatic Effects of Tranexamic Acid in Cesarean Delivery: An Ancillary Study of the TRAAP2 Study.
dc.title.alternativeThromb Haemosten_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1055/s-0042-1755379en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed36075235en_US
bordeaux.journalThrombosis and Haemostasisen_US
bordeaux.page1869-1878en_US
bordeaux.volume122en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue11en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04013288
hal.version1
hal.date.transferred2023-03-03T11:57:44Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Thrombosis%20and%20Haemostasis&amp;rft.date=2022-11-01&amp;rft.volume=122&amp;rft.issue=11&amp;rft.spage=1869-1878&amp;rft.epage=1869-1878&amp;rft.eissn=2567-689X&amp;rft.issn=2567-689X&amp;rft.au=ROULLET,%20St%C3%A9phanie&amp;RIVOIRE,%20Timoth%C3%A9e&amp;HOUSSIN,%20Cl%C3%A9mence&amp;LABROUCHE,%20Sylvie&amp;PAQUIN,%20Sandrine&amp;rft.genre=article


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