Literature DB >> 19289024

Thrombophilia: 2009 update.

Pat Foy1, Stephan Moll.   

Abstract

As venous thrombosis is mostly caused by disturbances in the plasma coagulation system, abnormalities of coagulation factors are mostly risk factors for venous thromboembolism (VTE). Relatively little is known about thrombophilias that predispose to arterial thromboembolism. Although some abnormalities in the fibrinolytic pathway appear to predispose to arterial thrombosis, the associations are weak and often inconsistent between studies. At present, there is not enough consistent and clinically meaningful information to include fibrinolytic parameters in a clinical thrombophilia workup. Controversy exists as to which patients and family members to test for thrombophilia. Several testing guidelines exist. Routine screening for inherited thrombophilias is not indicated in patients with VTE provoked by immobility, surgery, and malignancy, or in those with arterial thrombosis with arteriosclerosis risk factors. Heterozygous factor V Leiden (FVL) and prothrombin 20210 mutations increase the risk for recurrent VTE only slightly once anticoagulation is stopped. Therefore, decisions regarding the length of anticoagulant therapy typically are not influenced by finding one of these heterozygous mutations. The main reason to perform thrombophilia testing in a patient is to detect a strong thrombophilia (ie, antithrombin deficiency, antiphospholipid antibody syndrome, homozygous FVL, double-heterozygous FVL plus prothrombin 20210 mutation, protein C deficiency, and maybe protein S deficiency). The finding of a strong thrombophilia has several clinical consequences: it decreases the threshold to recommend long-term anticoagulation in a patient with unprovoked VTE; facilitates discussion regarding whether anticoagulant or antiplatelet therapy is the preferred empiric treatment for a patient who had an unexplained arterial, nonarteriosclerotic thromboembolic event; and leads to the consideration of testing asymptomatic female family members for the identified thrombophilia(s) so they can be counseled on their risk of thromboembolism, the use of hormonal therapies, and the potential benefit of pre- and postpartum anticoagulant therapy.

Entities:  

Year:  2009        PMID: 19289024     DOI: 10.1007/s11936-009-0012-x

Source DB:  PubMed          Journal:  Curr Treat Options Cardiovasc Med        ISSN: 1092-8464


  62 in total

1.  MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.

Authors:  Mariska Klerk; Petra Verhoef; Robert Clarke; Henk J Blom; Frans J Kok; Evert G Schouten
Journal:  JAMA       Date:  2002 Oct 23-30       Impact factor: 56.272

2.  Hyperhomocysteinemia and venous thrombosis: a meta-analysis.

Authors:  M den Heijer; F R Rosendaal; H J Blom; W B Gerrits; G M Bos
Journal:  Thromb Haemost       Date:  1998-12       Impact factor: 5.249

3.  Prevalence of the activating JAK2 tyrosine kinase mutation V617F in the Budd-Chiari syndrome.

Authors:  Raj K Patel; Nicholas C Lea; Michael A Heneghan; Nigel B Westwood; Dragana Milojkovic; Murugaiyan Thanigaikumar; Deborah Yallop; Roopen Arya; Antonio Pagliuca; Joop Gäken; Julia Wendon; Nigel D Heaton; Ghulam J Mufti
Journal:  Gastroenterology       Date:  2006-06       Impact factor: 22.682

4.  Homocysteine-lowering therapy and risk for venous thromboembolism: a randomized trial.

Authors:  Joel G Ray; Clive Kearon; Qilong Yi; Patrick Sheridan; Eva Lonn
Journal:  Ann Intern Med       Date:  2007-04-30       Impact factor: 25.391

5.  JAK2V617F mutation screening as part of the hypercoagulable work-up in the absence of splanchnic venous thrombosis or overt myeloproliferative neoplasm: assessment of value in a series of 664 consecutive patients.

Authors:  Animesh Pardanani; Terra L Lasho; Kebede Hussein; Susan M Schwager; Cristy M Finke; Rajiv K Pruthi; Ayalew Tefferi
Journal:  Mayo Clin Proc       Date:  2008-04       Impact factor: 7.616

Review 6.  Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.

Authors:  Robert J Kim; Richard C Becker
Journal:  Am Heart J       Date:  2003-12       Impact factor: 4.749

7.  Lowering homocysteine in patients with ischemic stroke to prevent recurrent stroke, myocardial infarction, and death: the Vitamin Intervention for Stroke Prevention (VISP) randomized controlled trial.

Authors:  James F Toole; M René Malinow; Lloyd E Chambless; J David Spence; L Creed Pettigrew; Virginia J Howard; Elizabeth G Sides; Chin-Hua Wang; Meir Stampfer
Journal:  JAMA       Date:  2004-02-04       Impact factor: 56.272

Review 8.  Antiphospholipid antibodies and the antiphospholipid syndrome: pathogenic mechanisms.

Authors:  Silvia S Pierangeli; Pojen P Chen; Elena Raschi; Silvia Scurati; Claudia Grossi; Maria Orietta Borghi; Ivan Palomo; E Nigel Harris; Pier Luigi Meroni
Journal:  Semin Thromb Hemost       Date:  2008-04       Impact factor: 4.180

9.  Report on the diagnosis and treatment of homozygous protein C deficiency. Report of the Working Party on Homozygous Protein C Deficiency of the ICTH-Subcommittee on Protein C and Protein S.

Authors:  R A Marlar; R R Montgomery; A W Broekmans
Journal:  Thromb Haemost       Date:  1989-06-30       Impact factor: 5.249

10.  Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study.

Authors:  T Koster; F R Rosendaal; H de Ronde; E Briët; J P Vandenbroucke; R M Bertina
Journal:  Lancet       Date:  1993 Dec 18-25       Impact factor: 79.321

View more
  7 in total

1.  Requirement for a Pathologist's Second Signature Limits Inappropriate Inpatient Thrombophilia Testing.

Authors:  Jesse L Cox; Sara M Shunkwiler; Scott A Koepsell
Journal:  Lab Med       Date:  2017-11-08

Review 2.  Role of thrombophilia testing: con.

Authors:  Scott M Stevens
Journal:  J Thromb Thrombolysis       Date:  2015-04       Impact factor: 2.300

3.  Thrombophilia differences in splanchnic vein thrombosis and lower extremity deep venous thrombosis in North America.

Authors:  Edyta Sutkowska; Robert D McBane; Alfonso J Tafur; Krzysztof Sutkowski; Diane E Grill; Joshua P Slusser; Waldemar E Wysokinski
Journal:  J Gastroenterol       Date:  2012-12-18       Impact factor: 7.527

4.  Influence of the JAK2 V617F Mutation and Inherited Thrombophilia on the Thrombotic Risk among Patients with Myeloproliferative Disorders.

Authors:  Mihaela Tevet; Razvan Ionescu; Cornel Dragan; Anca Roxana Lupu
Journal:  Maedica (Buchar)       Date:  2015-03

5.  Mutation in the Prothrombin Gene G20210A as a Cause of Cerebral Venous Thrombosis.

Authors:  Jorge A Arroyave; Jairo Quiñones
Journal:  Case Rep Med       Date:  2012-05-08

Review 6.  Guidance for the evaluation and treatment of hereditary and acquired thrombophilia.

Authors:  Scott M Stevens; Scott C Woller; Kenneth A Bauer; Raj Kasthuri; Mary Cushman; Michael Streiff; Wendy Lim; James D Douketis
Journal:  J Thromb Thrombolysis       Date:  2016-01       Impact factor: 2.300

7.  Obstetrical Management of an Extremely Overweight Pregnant Woman (184 kg bw) with Special Attention on Thromboprophylaxis.

Authors:  Boldizsar Horváth; Judit Skrapits; József Bódis
Journal:  Case Rep Obstet Gynecol       Date:  2013-03-04
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.