Literature DB >> 7684674

Congenital bleeding disorders. Rational treatment options.

S V Seremetis1, L M Aledort.   

Abstract

There are rational, effective choices available for the treatment of common inherited bleeding disorders, according to assessment of safety, efficacy and cost. All currently available products for patients with haemophilia A (factor VIII deficiency) are comparable in terms of efficacy and viral safety. However, high purity products are recommended for those with coexisting human immunodeficiency virus (HIV) infection. Many patients with mild haemophilia A and most with von Willebrand's disease can be treated with desmopressin, which can be given as an intranasal spray in some countries. For the treatment of patients with factor XI deficiency, fresh frozen plasma remains the standard care, although solvent-detergent-treated fresh frozen plasma and factor XI concentrate are currently being investigated as alternatives. In the treatment of haemophilia B (factor IX deficiency), purified factor IX concentrates are particularly useful in clinical settings where large amounts of concentrate are to be used (e.g. surgical prophylaxis). Their usefulness in other contexts needs clarification. Treatment of inhibitors that may develop in response to administered coagulation factors is still limited to the use of prothrombin complex concentrates and porcine factor VIII. Active clinical trials are currently assessing the efficacy and safety of recombinant factor VIIa, Xa and tissue factor in this indication.

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Year:  1993        PMID: 7684674     DOI: 10.2165/00003495-199345040-00006

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  10 in total

Review 1.  Molecular and cellular biology of blood coagulation.

Authors:  B Furie; B C Furie
Journal:  N Engl J Med       Date:  1992-03-19       Impact factor: 91.245

Review 2.  Monoclonal antibody-purified factor IX--comparative thrombogenicity to prothrombin complex concentrate.

Authors:  H C Kim; L Matts; J Eisele; M Czachur; P Saidi
Journal:  Semin Hematol       Date:  1991-07       Impact factor: 3.851

Review 3.  Treatment of factor VIII inhibitors.

Authors:  C K Kasper
Journal:  Prog Hemost Thromb       Date:  1989

4.  Postoperative thromboses in hemophilia B.

Authors:  C K Kasper
Journal:  N Engl J Med       Date:  1973-07-19       Impact factor: 91.245

Review 5.  The management of bleeding in hemophilia.

Authors:  C F Abildgaard
Journal:  Adv Pediatr       Date:  1969

6.  Therapy with factor IX concentrate resulting in DIC and thromboembolic phenomena.

Authors:  E W Campbell; S Neff; A J Bowdler
Journal:  Transfusion       Date:  1978 Jan-Feb       Impact factor: 3.157

7.  Hyponatremia and seizures in young children given DDAVP.

Authors:  T J Smith; J C Gill; D R Ambruso; W E Hathaway
Journal:  Am J Hematol       Date:  1989-07       Impact factor: 10.047

8.  Detection of factor X activation in humans.

Authors:  K A Bauer; B L Kass; H ten Cate; M A Bednarek; J J Hawiger; R D Rosenberg
Journal:  Blood       Date:  1989-11-01       Impact factor: 22.113

9.  Nasal spray desmopressin (DDAVP) for mild hemophilia A and von Willebrand disease.

Authors:  E H Rose; L M Aledort
Journal:  Ann Intern Med       Date:  1991-04-01       Impact factor: 25.391

10.  1-Deamino-8-d-arginine vasopressin: a new pharmacological approach to the management of haemophilia and von Willebrands' diseases.

Authors:  P M Mannucci; Z M Ruggeri; F I Pareti; A Capitanio
Journal:  Lancet       Date:  1977-04-23       Impact factor: 79.321

  10 in total

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