Literature DB >> 31388263

Effect of Prophylactic Management of Hemophilia on Bleeding Episodes.

Suman Roy1,2, Arun Kumar De1,3.   

Abstract

Hemophilia A (factor VIII deficiency) and hemophilia B (factor IX deficiency) are the most common and serious congenital coagulation factor deficiencies with repeated hemarthroses leading to development of target joints. Continuous prophylaxis is regular infusion of factor concentrates at fixed dose at regular interval to prevent hemorrhages. The study was designed to assess the outcome of continuous prophylaxis in hemophilia on bleeding episodes. It was conducted from November, 2017 to April, 2018 in the Paediatrics Department of Midnapore Medical College, Paschim Medinipur, West Bengal on 33 boys from 4 to 18 years of age suffering from Hemophilia with frequent bleeding episodes. Prior to starting continuous prophylaxis all the patients' target joint(s) were assessed based on Gilbert Score and bleeding episodes in the last 6 months were assessed based on Annualized Bleeding Rate and ISTH-BAT Score. All the children were provided prophylaxis therapy with plasma derived Factor concentrate twice per week at a dose of 20 + - 2 IU/Kg. All bleeding episodes of the children during prophylaxis were recorded. Bleeding episodes showed significant improvement only in children who could sufficiently adhere to continuous prophylactic therapy. Continuous prophylaxis reduces bleeding episodes in Hemophilia in twice weekly protocol provided the patients sufficiently adhere to continuous prophylaxis regimen.

Entities:  

Keywords:  Gilbert score; Hemarthrosis; ISTH-BAT score; Prophylaxis

Year:  2018        PMID: 31388263      PMCID: PMC6646620          DOI: 10.1007/s12288-018-1054-6

Source DB:  PubMed          Journal:  Indian J Hematol Blood Transfus        ISSN: 0971-4502            Impact factor:   0.900


  8 in total

1.  Guidelines for the management of hemophilia.

Authors:  A Srivastava; A K Brewer; E P Mauser-Bunschoten; N S Key; S Kitchen; A Llinas; C A Ludlam; J N Mahlangu; K Mulder; M C Poon; A Street
Journal:  Haemophilia       Date:  2012-07-06       Impact factor: 4.287

2.  Prophylactic treatment for prevention of joint disease in hemophilia--cost versus benefit.

Authors:  Goris Roosendaal; Floris Lafeber
Journal:  N Engl J Med       Date:  2007-08-09       Impact factor: 91.245

3.  ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders.

Authors:  F Rodeghiero; A Tosetto; T Abshire; D M Arnold; B Coller; P James; C Neunert; D Lillicrap
Journal:  J Thromb Haemost       Date:  2010-09       Impact factor: 5.824

4.  Definitions for haemophilia prophylaxis and its outcomes: the Canadian consensus study.

Authors:  S Ota; M Mclimont; M D Carcao; V S Blanchette; N Graham; E Paradis; B M Feldman
Journal:  Haemophilia       Date:  2007-01       Impact factor: 4.287

5.  Variability in clinical phenotype of severe haemophilia: the role of the first joint bleed.

Authors:  K van Dijk; K Fischer; J G van der Bom; D E Grobbee; H M van den Berg
Journal:  Haemophilia       Date:  2005-09       Impact factor: 4.287

6.  Joint Health Status of Hemophilia Patients in Jodhpur Region.

Authors:  Vikas Payal; Pramod Sharma; N P Chhangani; Yojana Janu; Yudhavir Singh; Akash Sharma
Journal:  Indian J Hematol Blood Transfus       Date:  2014-11-02       Impact factor: 0.900

7.  An attempt to improve the clinical scale for assessment of haemophilic arthropathy in children.

Authors:  Helen Pergantou; George Matsinos; Helen Platokouki; Andreas Papadopoulos; Sophie Aronis
Journal:  J Pediatr Orthop B       Date:  2009-07       Impact factor: 1.041

8.  Treatment of hemophilia: a review of current advances and ongoing issues.

Authors:  Antonio Coppola; Mirko Di Capua; Matteo Nicola Dario Di Minno; Mariagiovanna Di Palo; Emiliana Marrone; Paola Ieranò; Claudia Arturo; Antonella Tufano; Anna Maria Cerbone
Journal:  J Blood Med       Date:  2010-08-30
  8 in total

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