Literature DB >> 15357784

The impact of unaware carriership on the clinical presentation of haemophilia.

P E MacLean1, K Fijnvandraat, M Beijlevelt, M Peters.   

Abstract

This study was conducted to evaluate the effect of an unaware carriership on the delay in diagnosis of haemophilia and the resulting effect of this delay on morbidity. Information on 73 haemophilia patients (<18 years) and their mothers was gathered from data of patients' medical records and completed by interviews with the parent(s). Although a positive family history was present in 52 gravidae, 16 of them (31%) were not aware of their carrier status at moment of delivery. Fifteen of these 16 unaware carriers, were carriers of a non-severe form of haemophilia. In mothers who were unaware of carriership for haemophilia instrumental delivery occurred more frequently than in mothers who knew they were carriers. This is disquieting since instrumental delivery poses a significant risk (relative risk: 17.8, 95% CI: 4.0-78.4) for intra- or extracranial bleedings in newborn haemophiliacs in comparison to spontaneous deliveries or caesarean sections. In 83% of the patients with a positive family history, diagnosis was established before the first bleeding episode. Patients diagnosed by bleedings presented more often with iatrogenic bleedings (38%) then patients who were diagnosed because of a positive family history (9%) (P < 0.05). In comparison to previous studies, more patients had a positive family history and in more haemophiliacs with a positive family history diagnosis was established before the first bleeding episode. Although this reflects the yield of improved diagnostic methods, further reduction of iatrogenic bleeding is possible by intensifying counselling of mild haemophilia carriers.

Entities:  

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Year:  2004        PMID: 15357784     DOI: 10.1111/j.1365-2516.2004.00955.x

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


  6 in total

1.  "It was a lot Tougher than I Thought It would be". A Qualitative Study on the Changing Nature of Being a Hemophilia Carrier.

Authors:  Charlotte von der Lippe; Jan C Frich; Anna Harris; Kari Nyheim Solbrække
Journal:  J Genet Couns       Date:  2017-05-26       Impact factor: 2.537

Review 2.  Haemophilia.

Authors:  Erik Berntorp; Kathelijn Fischer; Daniel P Hart; Maria Elisa Mancuso; David Stephensen; Amy D Shapiro; Victor Blanchette
Journal:  Nat Rev Dis Primers       Date:  2021-06-24       Impact factor: 52.329

3.  Health issues in women and girls affected by haemophilia with a focus on nomenclature, heavy menstrual bleeding, and musculoskeletal issues.

Authors:  Angela C Weyand; Robert F Sidonio; Michelle Sholzberg
Journal:  Haemophilia       Date:  2022-05       Impact factor: 4.263

4.  Hemophilia carrier's awareness, diagnosis, and management in emerging countries: a cross-sectional study in Côte d'Ivoire (Ivory Coast).

Authors:  Catherine Lambert; N' Dogomo Meité; Ibrahima Sanogo; Sébastien Lobet; Eusèbe Adjambri; Stéphane Eeckhoudt; Cedric Hermans
Journal:  Orphanet J Rare Dis       Date:  2019-02-01       Impact factor: 4.123

5.  A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH.

Authors:  Karin P M van Galen; Roseline d'Oiron; Paula James; Rezan Abdul-Kadir; Peter A Kouides; Roshni Kulkarni; Johnny N Mahlangu; Maha Othman; Flora Peyvandi; Dawn Rotellini; Rochelle Winikoff; Robert F Sidonio
Journal:  J Thromb Haemost       Date:  2021-08       Impact factor: 16.036

6.  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

  6 in total

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