Literature DB >> 20590864

Mild haemophilia: a disease with many faces and many unexpected pitfalls.

K Peerlinck1, M Jacquemin.   

Abstract

SUMMARY: Despite major advances in diagnosis and treatment, the management of patients with mild haemophilia (MH) remains a major challenge. Mild haemophilia is defined by factor levels between 0.05 and 0.40 IU mL(-1). The bleeding associated with mild haemophilia is most frequently episodic, occurring during surgery or following trauma. Spontaneous bleeding is rare. Diagnosis is sometimes delayed because of insensitivity of screening clotting assays or discrepancies in factor VIII activity as measured by different assays. The treatment of choice in mild haemophilia A is desmopressin, which typically induces a 2-6-fold increase of factor VIII over baseline. However, desmopressin has its limitations in this setting such as the occurrence of tachyphylaxis and failure to respond in an undetermined proportion of patients. Factors underlying poor biological response or magnitude of response to desmopressin are incompletely understood. Inhibitor development in mild haemophilia is particularly distressing. This complication arises at an older age in this patient group because of infrequent need for factor VIII replacement. Inhibitors in mild haemophilia patients often cross-react with endogenous factor VIII resulting in severe spontaneous bleeding frequently in a postoperative setting. Intensive perioperative use of factor VIII and some specific mutations induce a particularly high risk for inhibitor development, but risk factors are incompletely understood. For reasons of the older age of the patients, treatment of bleeding with bypassing agents may cause major thrombotic complications. Data on therapeutic options for inhibitor eradication in patients with mild haemophilia are particularly scarce. With increased life-expectancy for all haemophilia patients, the group of elderly patients with mild haemophilia requiring major surgery will further increase. Prevention of inhibitors, particularly in this patient group, should be a major topic of interest in both clinic and research.

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Year:  2010        PMID: 20590864     DOI: 10.1111/j.1365-2516.2010.02306.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  12 in total

1.  Factor VIII gene variants and inhibitor risk in African American hemophilia A patients.

Authors:  Devi Gunasekera; Ruth A Ettinger; Shelley Nakaya Fletcher; Eddie A James; Maochang Liu; John C Barrett; Janice Withycombe; Dana C Matthews; Melinda S Epstein; Richard J Hughes; Kathleen P Pratt
Journal:  Blood       Date:  2015-01-23       Impact factor: 22.113

Review 2.  Molecular and clinical predictors of inhibitor risk and its prevention and treatment in mild hemophilia A.

Authors:  Giancarlo Castaman; Karin Fijnvandraat
Journal:  Blood       Date:  2014-08-18       Impact factor: 22.113

Review 3.  Diagnosis and care of patients with mild haemophilia: practical recommendations for clinical management.

Authors:  Gary Benson; Günter Auerswald; Gerry Dolan; Anne Duffy; Cedric Hermans; Rolf Ljung; Massimo Morfini; Silva Zupančić Šalek
Journal:  Blood Transfus       Date:  2017-11-14       Impact factor: 3.443

4.  Induction of tolerance to factor VIII by transient co-administration with rapamycin.

Authors:  B Moghimi; B K Sack; S Nayak; D M Markusic; C S Mah; R W Herzog
Journal:  J Thromb Haemost       Date:  2011-08       Impact factor: 5.824

5.  Challenges in the Diagnosis and Management of Non-Severe Hemophilia.

Authors:  Estera Boeriu; Teodora Smaranda Arghirescu; Margit Serban; Jenel Marian Patrascu; Eugen Boia; Cristian Jinca; Wolfgang Schramm; Adina Traila; Cristina Emilia Ursu
Journal:  J Clin Med       Date:  2022-06-09       Impact factor: 4.964

6.  Method validation and clinical utility of chromogenic factor VIII assay compared to one-stage assay.

Authors:  Wilmare Gouws; Elsabie Botha; Adele Visser
Journal:  J Thromb Thrombolysis       Date:  2014       Impact factor: 2.300

7.  Haemophilia A in a major trauma patient.

Authors:  Charlotte Reinke; Agnes Spodeck; Thomas A Schildhauer; Justyna Swol
Journal:  BMJ Case Rep       Date:  2015-12-16

Review 8.  [Perioperative management of patients with hemophilia].

Authors:  S Lison; M Spannagl
Journal:  Anaesthesist       Date:  2014-01       Impact factor: 1.041

9.  Post splenectomy fatal pulmonary embolism in a patient with moderate hemophilia a.

Authors:  Abdolhossein Davoodabadi; Mohammad Mahdi Adib; Behrooz Keleidari
Journal:  Iran J Med Sci       Date:  2011-06

10.  Ankle arthroplasty in a patient with bleeding diathesis and the mid-term clinical outcome of the case.

Authors:  Barış Yilmaz; Baran Kömür; Güzelali Özdemir; Nurettin Heybeli
Journal:  Ann Med Surg (Lond)       Date:  2015-09-14
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