Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/29297
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dc.contributor.authorMoustafa, Farèsen_US
dc.contributor.authorStehouwer, Alexanderen_US
dc.contributor.authorKamphuisen, Pieteren_US
dc.contributor.authorSahuquillo, Joan Carlesen_US
dc.contributor.authorSampériz, Ángelen_US
dc.contributor.authorAlfonso, Maríaen_US
dc.contributor.authorPace, Federicaen_US
dc.contributor.authorSuriñach, José Maríaen_US
dc.contributor.authorBlanco-Molina, Ángelesen_US
dc.contributor.authorMismetti, Patricken_US
dc.contributor.authorMonreal, Manuelen_US
dc.contributor.authorRIETE Investigatorsen_US
dc.contributor.authorBosevski, Marijanen_US
dc.contributor.authorZdraveska, Marijaen_US
dc.contributor.authorKrstevski, Gregoren_US
dc.date.accessioned2024-02-13T12:17:03Z-
dc.date.available2024-02-13T12:17:03Z-
dc.date.issued2018-11-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/29297-
dc.description.abstractBackground: The optimal management of major bleeding in patients receiving vitamin K antagonists (VKA) for venous thromboembolism (VTE) is unclear. Methods: We used the RIETE (Registro Informatizado Enfermedad TromboEmbólica) registry to assess the management and 30-day outcomes after major bleeding in patients receiving VKA for VTE. Results: From January 2013 to December 2017, 267 of 18,416 patients (1.4%) receiving long-term VKA for VTE had a major bleeding (in the gastrointestinal tract 78, intracranial 72, hematoma 50, genitourinary 20, other 47). Overall, 151 patients (57%) received blood transfusion; 110 (41%) vitamin K; 37 (14%) fresh frozen plasma; 29 (11%) pro-haemostatic agents and 20 (7.5%) a vena cava filter. During the first 30 days, 59 patients (22%) died (41 died of bleeding) and 13 (4.9%) had a thrombosis. On multivariable analysis, patients with intracranial bleeding (hazard ratio [HR]: 4.58; 95%CI: 2.40-8.72) and those with renal insufficiency at baseline (HR: 2.73; 95%CI: 1.45-5.15) had an increased mortality risk, whereas those receiving vitamin K had a lower risk (HR: 0.47; 0.24-0.92). On the other hand, patients receiving fresh frozen plasma were at increased risk for thrombotic events (HR: 4.22; 95%CI: 1.25-14.3). Conclusions: Major bleeding in VTE patients receiving VKA carries a high mortality rate. Intracranial bleeding and renal insufficiency increased the risk. Fresh frozen plasma seems to increase this risk for recurrent VTE.Background: The optimal management of major bleeding in patients receiving vitamin K antagonists (VKA) for venous thromboembolism (VTE) is unclear. Methods: We used the RIETE (Registro Informatizado Enfermedad TromboEmbólica) registry to assess the management and 30-day outcomes after major bleeding in patients receiving VKA for VTE. Results: From January 2013 to December 2017, 267 of 18,416 patients (1.4%) receiving long-term VKA for VTE had a major bleeding (in the gastrointestinal tract 78, intracranial 72, hematoma 50, genitourinary 20, other 47). Overall, 151 patients (57%) received blood transfusion; 110 (41%) vitamin K; 37 (14%) fresh frozen plasma; 29 (11%) pro-haemostatic agents and 20 (7.5%) a vena cava filter. During the first 30 days, 59 patients (22%) died (41 died of bleeding) and 13 (4.9%) had a thrombosis. On multivariable analysis, patients with intracranial bleeding (hazard ratio [HR]: 4.58; 95%CI: 2.40-8.72) and those with renal insufficiency at baseline (HR: 2.73; 95%CI: 1.45-5.15) had an increased mortality risk, whereas those receiving vitamin K had a lower risk (HR: 0.47; 0.24-0.92). On the other hand, patients receiving fresh frozen plasma were at increased risk for thrombotic events (HR: 4.22; 95%CI: 1.25-14.3). Conclusions: Major bleeding in VTE patients receiving VKA carries a high mortality rate. Intracranial bleeding and renal insufficiency increased the risk. Fresh frozen plasma seems to increase this risk for recurrent VTE.en_US
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.relation.ispartofThrombosis Researchen_US
dc.titleManagement and outcome of major bleeding in patients receiving vitamin K antagonists for venous thromboembolismen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.thromres.2018.09.049-
dc.identifier.urlhttps://api.elsevier.com/content/article/PII:S0049384818305334?httpAccept=text/xml-
dc.identifier.urlhttps://api.elsevier.com/content/article/PII:S0049384818305334?httpAccept=text/plain-
dc.identifier.volume171-
dc.identifier.fpage74-
dc.identifier.lpage80-
item.grantfulltextopen-
item.fulltextWith Fulltext-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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