dc.creatorOzelo, MC
dc.date2012
dc.dateOCT
dc.date2014-07-30T19:51:37Z
dc.date2015-11-26T16:56:44Z
dc.date2014-07-30T19:51:37Z
dc.date2015-11-26T16:56:44Z
dc.date.accessioned2018-03-28T23:44:13Z
dc.date.available2018-03-28T23:44:13Z
dc.identifierThrombosis Research. Pergamon-elsevier Science Ltd, v. 130, n. S23, n. S26, 2012.
dc.identifier0049-3848
dc.identifierWOS:000310349200007
dc.identifier10.1016/j.thromres.2012.08.265
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/73905
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/73905
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1277468
dc.descriptionPatients with hemophilia are considered low risk for thromboembolic complications. However, in the presence of risk factors for thrombosis, such as surgical procedures, and intensive replacement therapy this complication has been reported. Major orthopedic surgeries are often required in patients with hemophilia, due to the presence of hemophiliac arthropathy. In individuals that do not have hemophilia, orthopedic surgeries are particularly well recognized as high risk for venous thromboembolism, and the use of thromboprophylaxis for this condition is recommended. However, for hemophilia patients the use of venous thrombosis prophylaxis during major surgeries, including orthopedic procedures remains controversial. For the majority of the patients the use of gradated compression stockings and early mobilization can be sufficient to prevent venous thromboembolism. The use of anticoagulant prophylaxis should be considered just for patients with relevant additional risk factor for thrombosis. However, for hemophilia patients with inhibitor, pharmacologic thromboprophylaxis is not recommended. For patients with von Willebrand disease receiving factor concentrates replacement therapy undergoing surgical procedures, the FVIII plasma levels should be monitored and thromboprophylaxis should be considered if any other thrombosis risk factor is present. It is important for the future to establish risk assessment tools that can help to determine the most effective and safe practice to prevent venous thrombosis in patients with hemophilia and other bleeding disorderswho undergo surgical procedures. (C) 2012 Elsevier Ltd. All rights reserved.
dc.description130
dc.description1
dc.descriptionS23
dc.descriptionS26
dc.descriptionBayer
dc.descriptionCSL Behring
dc.languageen
dc.publisherPergamon-elsevier Science Ltd
dc.publisherOxford
dc.publisherInglaterra
dc.relationThrombosis Research
dc.relationThromb. Res.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectHemophilia
dc.subjectSurgery
dc.subjectThrombosis
dc.subjectHeparin
dc.subjectThromboprophylaxis
dc.subjectAnticoagulant
dc.subjectMajor Orthopedic-surgery
dc.subjectDeep Venous Thrombosis
dc.subjectInhibitor Bypass Activity
dc.subjectVon-willebrand-disease
dc.subjectFactor-v-leiden
dc.subjectBleeding Disorders
dc.subjectAdverse Events
dc.subjectThromboembolism
dc.subjectReplacement
dc.subjectPrevention
dc.titleSurgery in patients with hemophilia: Is thromboprophylaxis mandatory?
dc.typeArtículos de revistas


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