Literature DB >> 27106121

How I treat patients with inherited bleeding disorders who need anticoagulant therapy.

Karlyn Martin1, Nigel S Key1.   

Abstract

Situations that ordinarily necessitate consideration of anticoagulation, such as arterial and venous thrombotic events and prevention of stroke in atrial fibrillation, become challenging in patients with inherited bleeding disorders such as hemophilia A, hemophilia B, and von Willebrand disease. There are no evidence-based guidelines to direct therapy in these patients, and management strategies that incorporate anticoagulation must weigh a treatment that carries a risk of hemorrhage in a patient who is already at heightened risk against the potential consequences of not treating the thrombotic event. In this paper, we review atherothrombotic disease, venous thrombotic disease, and atrial fibrillation in patients with inherited bleeding disorders, and discuss strategies for using anticoagulants in this population using cases to illustrate these considerations.
© 2016 by The American Society of Hematology.

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Year:  2016        PMID: 27106121      PMCID: PMC4946199          DOI: 10.1182/blood-2015-12-635094

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  52 in total

1.  Deep vein thrombosis after orthopedic surgery in a patient with type 1 von Willebrand disease and mutations in the MTHFR and beta-fibrinogen genes.

Authors:  Massimo Franchini; Mauro Krampera; Dino Veneri
Journal:  Thromb Haemost       Date:  2003-11       Impact factor: 5.249

2.  Subclinical deep venous thrombosis observed in 10% of hemophilic patients undergoing major orthopedic surgery.

Authors:  C Hermans; F Hammer; S Lobet; C Lambert
Journal:  J Thromb Haemost       Date:  2010-02-23       Impact factor: 5.824

3.  Definitions in hemophilia: communication from the SSC of the ISTH.

Authors:  V S Blanchette; N S Key; L R Ljung; M J Manco-Johnson; H M van den Berg; A Srivastava
Journal:  J Thromb Haemost       Date:  2014-09-03       Impact factor: 5.824

4.  Role of the intrinsic coagulation pathway in atherogenesis assessed in hemophilic apolipoprotein E knockout mice.

Authors:  J Khallou-Laschet; G Caligiuri; E Tupin; A-T Gaston; B Poirier; E Groyer; D Urbain; S Maisnier-Patin; R Sarkar; S V Kaveri; S Lacroix-Desmazes; A Nicoletti
Journal:  Arterioscler Thromb Vasc Biol       Date:  2005-05-26       Impact factor: 8.311

5.  A randomized comparison of bypassing agents in hemophilia complicated by an inhibitor: the FEIBA NovoSeven Comparative (FENOC) Study.

Authors:  Jan Astermark; Sharyne M Donfield; Donna M DiMichele; Alessandro Gringeri; Steven A Gilbert; Jennifer Waters; Erik Berntorp
Journal:  Blood       Date:  2006-09-21       Impact factor: 22.113

6.  Prevalence and risk factors of cardiovascular disease (CVD) events among patients with haemophilia: experience of a single haemophilia treatment centre in the United States (US).

Authors:  A A Sharathkumar; J M Soucie; B Trawinski; A Greist; A D Shapiro
Journal:  Haemophilia       Date:  2011-02-15       Impact factor: 4.287

7.  Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization.

Authors:  K J Pasi; P W Collins; D M Keeling; S A Brown; A M Cumming; G C Dolan; C R M Hay; F G H Hill; M Laffan; I R Peake
Journal:  Haemophilia       Date:  2004-05       Impact factor: 4.287

Review 8.  Anticoagulation therapy in haemophilia. Managing the unknown.

Authors:  R E G Schutgens; A Tuinenburg; K Fischer; E P Mauser-Bunschoten
Journal:  Hamostaseologie       Date:  2013-02-28       Impact factor: 1.778

9.  A clinical trial comparing three antithrombotic-drug regimens after coronary-artery stenting. Stent Anticoagulation Restenosis Study Investigators.

Authors:  M B Leon; D S Baim; J J Popma; P C Gordon; D E Cutlip; K K Ho; A Giambartolomei; D J Diver; D M Lasorda; D O Williams; S J Pocock; R E Kuntz
Journal:  N Engl J Med       Date:  1998-12-03       Impact factor: 91.245

10.  Reduced prevalence of arterial thrombosis in von Willebrand disease.

Authors:  Y V Sanders; J Eikenboom; E M de Wee; J G van der Bom; M H Cnossen; M E L Degenaar-Dujardin; K Fijnvandraat; P W Kamphuisen; B A P Laros-van Gorkom; K Meijer; E P Mauser-Bunschoten; F W G Leebeek
Journal:  J Thromb Haemost       Date:  2013-05       Impact factor: 5.824

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  18 in total

1.  Hemophilia in the developing world: transforming lives through international collaboration.

Authors:  A Jandial; K Mishra; R Sandal; N Jindal; D Goni; D Lad; G Prakash; A Khadwal; J Ahluwalia; N Varma; P Malhotra
Journal:  Blood Adv       Date:  2018-11-30

2.  Off-pump technique and replacement therapy for coronary artery bypass surgery in a patient with hemophilia B.

Authors:  M Fernández-Caballero; M F Martinez; G Oristrell; N Palmer; A Santamaría
Journal:  J Thromb Thrombolysis       Date:  2019-08       Impact factor: 2.300

Review 3.  Challenging clinical scenarios for therapeutic anticoagulation: A practical approach.

Authors:  Kylee L Martens; Simone E Dekker; Megan Crowe; Thomas G DeLoughery; Joseph J Shatzel
Journal:  Thromb Res       Date:  2022-08-19       Impact factor: 10.407

Review 4.  Acute coronary syndrome in patients with hemophilia: a delicate balancing act.

Authors:  Jacob J Mayfield; Andrew D Leavitt; Talha Tanriverdi; Krishan Soni; Thomas A Ports; M Roselle Abraham
Journal:  J Thromb Thrombolysis       Date:  2022-05-11       Impact factor: 5.221

Review 5.  Management of Hemophilia in Older Patients.

Authors:  Massimo Franchini; Pier Mannuccio Mannucci
Journal:  Drugs Aging       Date:  2017-12       Impact factor: 3.923

6.  Comparing Safety and Efficacy of Dabigatran and Factor Xa Inhibitors for Stroke Prevention in Hemophiliacs with Non-Valvular Atrial Fibrillation.

Authors:  Safeera Khan; Ratna Krishnaswamy; Bilal Haider Malik; Muhammad Islam; Deepti Gupta; Shrawan Kumar Mandal; Ian H Rutkofsky
Journal:  J Atr Fibrillation       Date:  2019-12-31

Review 7.  Venous Thromboembolism in Children with Cancer and Blood Disorders.

Authors:  Richard H Ko; Courtney D Thornburg
Journal:  Front Pediatr       Date:  2017-02-06       Impact factor: 3.418

Review 8.  Von Willebrand disease in the elderly: clinical perspectives.

Authors:  John Chapin
Journal:  Clin Interv Aging       Date:  2018-08-31       Impact factor: 4.458

9.  Acquired haemophilia a secondary to multiple myeloma: management of a patient with a mechanical mitral valve.

Authors:  Lisa B Pinchover; Rami Alsharif; Talia Bernal
Journal:  BMJ Case Rep       Date:  2020-09-06

10.  Management of Thrombosis Risk in a Carrier of Hemophilia A with Low Factor VIII Levels with Atrial Fibrillation: A Clinical Case and Literature Review.

Authors:  Nigel P Murray; Lorena Muñoz; Simona Minzer; Marco Antonio Lopez
Journal:  Case Rep Hematol       Date:  2018-09-05
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