Literature DB >> 26582077

The incidence and treatment of bleeding episodes in non-severe haemophilia A patients with inhibitors.

Alice S van Velzen, Corien L Eckhardt, Nina Streefkerk, Marjolein Peters, Daniel P Hart, Karly Hamulyak, Robert Klamroth, Karina Meijer, Marten Nijziel, Piercarla Schinco, Thynn T Yee, Johanna G van der Bom, Karin Fijnvandraat1.   

Abstract

The development of an inhibitory antibody in non-severe haemophilia A patients may aggravate the bleeding phenotype considerably. Effective treatment of bleeding episodes may be challenging, with ensuing severe complications. At present, evidence is scarce for optimal treatment of bleeding episodes in this patient group. The aim of this study was to describe the incidence and the treatment of bleeding episodes in inhibitor patients in a population-based unselected cohort of non-severe haemophilia A patients with clinically relevant inhibitors. Data were available for 100 of the 107 non-severe haemophilia A patients (factor VIII (FVIII) baseline, 2-40 IU/dl) from 29 centres in Europe and one centre in Australia who had developed a clinically relevant inhibitor between 1980 and 2011. The majority (89 %) of the patients were treated during the inhibitor period for bleeding episodes or a surgical intervention: 66 % needed treatment for bleeding episodes, at a median annual bleeding rate (ABR) of 1.1 (interquartile range (IQR) 0.1-2.5) and a median total of 2 (IQR 1-6) bleeding episodes. Compared to the median ABR before inhibitor development of 0.095 bleeds per year (IQR 0.02-0.42), the increase in ABR is more than a 10-fold. More than 90 % of the bleeding episodes were treated with only one type of product, most frequently (51 %) FVIII concentrates. This study provides the incidence of bleeding episodes and treatment choices in non-severe haemophilia A patients with inhibitors. The 10-fold increase to a median ABR of 1.1 episodes per year emphasizes the impact of inhibitor development for non-severe haemophilia A patients.

Entities:  

Keywords:  Haemophilia A; bypassing agents; factor VIII inhibitors; haemostasis; management of disease

Mesh:

Substances:

Year:  2015        PMID: 26582077     DOI: 10.1160/TH15-03-0212

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  9 in total

Review 1.  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

2.  Inhibitors and mortality in persons with nonsevere hemophilia A in the United States.

Authors:  Ming Y Lim; Dunlei Cheng; Michael Recht; Christine L Kempton; Nigel S Key
Journal:  Blood Adv       Date:  2020-10-13

3.  The endothelial specific isoform of type XVIII collagen correlates to annual bleeding rate in haemophilia patients.

Authors:  Nadja Gad Kjeld; Baolai Hua; Morten Asser Karsdal; Shu Sun; Tina Manon-Jensen
Journal:  PLoS One       Date:  2018-01-10       Impact factor: 3.240

4.  Navigating Speed Bumps on the Innovation Highway in Hemophilia Therapeutics.

Authors:  Donna M DiMichele
Journal:  Hemasphere       Date:  2018-10-02

5.  Factor VIII cross-matches to the human proteome reduce the predicted inhibitor risk in missense mutation hemophilia A.

Authors:  Daniel P Hart; Nazmiye Uzun; Stuart Skelton; Alison Kakoschke; Jacob Househam; David S Moss; Adrian J Shepherd
Journal:  Haematologica       Date:  2018-09-28       Impact factor: 9.941

Review 6.  Congenital hemophilia A with low activity of factor XII: a case report and literature review.

Authors:  Baoyu Lei; Chuang Liang; Haiyan Feng
Journal:  Ital J Pediatr       Date:  2021-10-11       Impact factor: 2.638

7.  Product type and the risk of inhibitor development in nonsevere haemophilia A patients: a case-control study.

Authors:  Alice S van Velzen; Corien L Eckhardt; Marjolein Peters; Johannes Oldenburg; Marjon Cnossen; Ri Liesner; Massimo Morfini; Giancarlo Castaman; Simon McRae; Johanna G van der Bom; Karin Fijnvandraat
Journal:  Br J Haematol       Date:  2020-03-22       Impact factor: 6.998

8.  Hemophilia management: Huge impact of a tiny difference.

Authors:  Fabienne Kloosterman; Anne-Fleur Zwagemaker; Amal Abdi; Samantha Gouw; Giancarlo Castaman; Karin Fijnvandraat
Journal:  Res Pract Thromb Haemost       Date:  2020-02-28

9.  The factor VIII treatment history of non-severe hemophilia A.

Authors:  Amal Abdi; Fabienne R Kloosterman; Corien L Eckhardt; Christoph Male; Giancarlo Castaman; Kathelijn Fischer; Erik A M Beckers; Marieke J H A Kruip; Kathelijne Peerlinck; Maria Elisa Mancuso; Cristina Santoro; Charles R Hay; Helen Platokouki; Johanna G van der Bom; Samantha C Gouw; Karin Fijnvandraat; Dan P Hart
Journal:  J Thromb Haemost       Date:  2020-09-28       Impact factor: 16.036

  9 in total

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