Literature DB >> 10650861

When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10-year single-centre PUP study.

H Pollmann1, H Richter, H Ringkamp, H Jürgens.   

Abstract

UNLABELLED: The aim of this single-centre study was to obtain data prospectively on when children are diagnosed as having severe haemophilia and when they start to bleed. Results of this 10-year PUP study suggest that severe haemophilia is nowadays diagnosed much earlier than in the Sixties. Patients with severe haemophilia (n = 37: FV III <0.01 U/ml) start to bleed at very different ages. While 44% of patients have their first bleeding episode within the first year of life, others do not bleed before the age of four. The onset of joint bleedings generally occurs about half a year later than other types of bleeding. While half our patients developed their first bleeding by the age of 1.22 years, the mean age for the first joint bleeding was 1.91 years.
CONCLUSION: Early-onset prophylactic therapy can prevent damage to the joints, but for rational therapy the age at onset of bleeding must also be taken into account. A non-bleeding child does not benefit from prophylactic treatment.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10650861     DOI: 10.1007/pl00014347

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  9 in total

1.  A modeling approach to evaluate long-term outcome of prophylactic and on demand treatment strategies for severe hemophilia A.

Authors:  Kathelijn Fischer; Maurice E Pouw; Daniel Lewandowski; Mart P Janssen; H Marijke van den Berg; Ben A van Hout
Journal:  Haematologica       Date:  2011-01-27       Impact factor: 9.941

2.  Unusual presentation of neonatal haemophilia A.

Authors:  Anthony R Hart; C Mae Wong; Alan T Gibson
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2007-07       Impact factor: 5.747

3.  The importance of genetic factors for the development of arthropathy: a longitudinal study of children and adolescents with haemophilia A.

Authors:  Edward D Gomperts; John Schwarz; Sharyne M Donfield; Alice E Lail; Jan Astermark; W Keith Hoots; Cheryl A Winkler; Erik Berntorp
Journal:  Thromb Haemost       Date:  2016-12-08       Impact factor: 5.249

Review 4.  Perinatal gene transfer to the liver.

Authors:  Tristan R McKay; Ahad A Rahim; Suzanne M K Buckley; Natalie J Ward; Jerry K Y Chan; Steven J Howe; Simon N Waddington
Journal:  Curr Pharm Des       Date:  2011       Impact factor: 3.116

5.  A Case of Hemophilia A Presenting in a Neonate and a Review of the Literature.

Authors:  Esther Kisseih; Neeraja Yerrapotu; Deepak Yadav; Melissa February
Journal:  Glob Pediatr Health       Date:  2017-02-20

6.  Experience of Advate rAHF-PFM in previously untreated patients and minimally treated patients with haemophilia A.

Authors:  Guenter Auerswald; Alexis A Thompson; Michael Recht; Deborah Brown; Raina Liesner; Norma Guzmán-Becerra; Jacqueline Dyck-Jones; Bruce Ewenstein; Brigitt Abbuehl
Journal:  Thromb Haemost       Date:  2012-04-04       Impact factor: 5.249

Review 7.  Pain in Hemophilia: Unexplored Role of Oxidative Stress.

Authors:  Raghda Fouda; Donovan A Argueta; Kalpna Gupta
Journal:  Antioxidants (Basel)       Date:  2022-06-03

8.  Multisystem inflammatory syndrome in a neonate with severe hemophilia - a diagnostic challenge in COVID times: a case report.

Authors:  Sumitha Arun; Taliya Grace Cherian; Chepsy Philip
Journal:  BMC Pediatr       Date:  2022-07-07       Impact factor: 2.567

Review 9.  Pathophysiology of Hemophilic Arthropathy.

Authors:  Daniela Melchiorre; Mirko Manetti; Marco Matucci-Cerinic
Journal:  J Clin Med       Date:  2017-06-25       Impact factor: 4.241

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.