Literature DB >> 29383626

Continuous infusions of B domain-truncated recombinant factor VIII, turoctocog alfa, for orthopedic surgery in severe hemophilia A: first case report.

Masahiro Takeyama1, Keiji Nogami2, Ryohei Kobayashi1, Kenichi Ogiwara1, Akira Taniguchi3, Yasuaki Nakanishi3, Yusuke Inagaki3, Yasuhito Tanaka3, Midori Shima1.   

Abstract

Continuous infusions (CI) of factor (F)VIII are preferable to the conventional bolus injections for the maintenance of consistent FVIII levels during surgery in patients with severe hemophilia A. A third generation, B domain-truncated recombinant FVIII (turoctocog alfa, Novo Nordisk, NovoEight®), was approved for clinical use in 2014. The hemostatic efficacy and safety of bolus injections of turoctocog alfa in patients undergoing surgery have been reported, but no reports on CI therapy have been published. We describe a 43-year-old patient with severe hemophilia A who required arthroscopic synovectomy of the right elbow and arthrodesis of the right ankle. He was treated with a bolus injection of turoctocog alfa (36 IU/kg) immediately before operation, followed by CI (infusion rate; 2.9 IU/kg/h) to maintain FVIII activity > 80 IU/dl throughout the perioperative period. Surgery was completed successfully with uncomplicated hemostatic control. CIs were continued until post-operative day (POD) 4. Further bolus injections were given from POD5. No anti-FVIII inhibitor has been detected post-operation. This case provides important information on CI therapy using turoctocog alfa during surgery for patients with severe hemophilia A.

Entities:  

Keywords:  Continuous infusion; Hemophilia A; Hemostatic management; Surgery; Turoctocog alfa

Mesh:

Substances:

Year:  2018        PMID: 29383626     DOI: 10.1007/s12185-018-2415-5

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  19 in total

Review 1.  Activation of factor VIII and mechanisms of cofactor action.

Authors:  Philip J Fay
Journal:  Blood Rev       Date:  2004-03       Impact factor: 8.250

2.  Characterization of tyrosine sulphation in rFVIII (turoctocog alfa) expressed in CHO and HEK-293 cells.

Authors:  P F Nielsen; S Bak; B Vandahl
Journal:  Haemophilia       Date:  2012-06-11       Impact factor: 4.287

3.  Sulfation of Tyr1680 of human blood coagulation factor VIII is essential for the interaction of factor VIII with von Willebrand factor.

Authors:  A Leyte; H B van Schijndel; C Niehrs; W B Huttner; M P Verbeet; K Mertens; J A van Mourik
Journal:  J Biol Chem       Date:  1991-01-15       Impact factor: 5.157

4.  Interim results from a large multinational extension trial (guardian(™) 2) using turoctocog alfa for prophylaxis and treatment of bleeding in patients with severe haemophilia A.

Authors:  S R Lentz; M Cerqueira; D Janic; C Kempton; I Matytsina; M Misgav; J Oldenburg; M Ozelo; M Recht; A Rosholm; A Savic; T Suzuki; A Tiede; E Santagostino
Journal:  Haemophilia       Date:  2016-06-13       Impact factor: 4.287

Review 5.  Pharmacokinetics of coagulation factors: clinical relevance for patients with haemophilia.

Authors:  S Björkman; E Berntorp
Journal:  Clin Pharmacokinet       Date:  2001       Impact factor: 6.447

6.  BDDrFVIII (Moroctocog alfa [AF-CC]) for surgical haemostasis in patients with haemophilia A: results of a pivotal study.

Authors:  J Windyga; L Rusen; R Gruppo; A C O'Brien; P Kelly; D A Roth; S Arkin
Journal:  Haemophilia       Date:  2010-03-31       Impact factor: 4.287

7.  Successful use of ReFacto continuous infusion in two paediatric patients with severe haemophilia A undergoing orthopaedic surgery.

Authors:  M M Sennett; P A de Alarcón
Journal:  Haemophilia       Date:  2004-09       Impact factor: 4.287

Review 8.  Functional roles of the factor VIII B domain.

Authors:  S W Pipe
Journal:  Haemophilia       Date:  2009-04-07       Impact factor: 4.287

9.  Results from a large multinational clinical trial (guardian™1) using prophylactic treatment with turoctocog alfa in adolescent and adult patients with severe haemophilia A: safety and efficacy.

Authors:  S R Lentz; M Misgav; M Ozelo; S Z Salek; D Veljkovic; M Recht; M Cerqueira; A Tiede; B Brand; M E Mancuso; S Seremetis; A Lindblom; U Martinowitz
Journal:  Haemophilia       Date:  2013-05-07       Impact factor: 4.287

10.  Lack of recombinant factor VIII B-domain induces phospholipid vesicle aggregation: implications for the immunogenicity of factor VIII.

Authors:  K Grushin; J Miller; D Dalm; E T Parker; J F Healey; P Lollar; S Stoilova-McPhie
Journal:  Haemophilia       Date:  2014-04-21       Impact factor: 4.287

View more
  1 in total

1.  Stability of Turoctocog Alfa, a Recombinant Factor VIII Product, during Continuous Infusion In Vitro.

Authors:  Masahiro Takeyama; Anne Mette Nøhr; Debra Pollard
Journal:  TH Open       Date:  2020-11-06
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.