메뉴 건너뛰기




Volumn 17, Issue 3, 2011, Pages 433-438

Trends in bleeding patterns during prophylaxis for severe haemophilia: Observations from a series of prospective clinical trials

Author keywords

Bleeding pattern; Factor VIII; Haemophilia; Prophylaxis; Recombinant factor VIII; Seasonality

Indexed keywords

RECOMBINANT BLOOD CLOTTING FACTOR 8;

EID: 79955142222     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/j.1365-2516.2010.02450.x     Document Type: Article
Times cited : (49)

References (15)
  • 1
    • 0013856638 scopus 로고
    • Production of high-potency concentrates of antihemophilic globulin in a closed-bag system
    • Pool JG, Shannon AE. Production of high-potency concentrates of antihemophilic globulin in a closed-bag system. N Engl J Med 1965; 273: 1443-7.
    • (1965) N Engl J Med , vol.273 , pp. 1443-1447
    • Pool, J.G.1    Shannon, A.E.2
  • 3
    • 0026635406 scopus 로고
    • Twenty-five years' experience of prophylactic treatment in severe haemophilia A and B
    • Nilsson IM, Berntorp E, Lofqvist T, Pettersson H. Twenty-five years' experience of prophylactic treatment in severe haemophilia A and B. J Intern Med 1992; 232: 25-32.
    • (1992) J Intern Med , vol.232 , pp. 25-32
    • Nilsson, I.M.1    Berntorp, E.2    Lofqvist, T.3    Pettersson, H.4
  • 4
    • 0034814399 scopus 로고    scopus 로고
    • Changes in treatment strategies for severe haemophilia over the last 3 decades: effects on clotting factor consumption and arthropathy
    • Fischer K, Van der Bom JG, Mauser-Bunschoten EP et al. Changes in treatment strategies for severe haemophilia over the last 3 decades: effects on clotting factor consumption and arthropathy. Haemophilia 2001; 7: 446-52.
    • (2001) Haemophilia , vol.7 , pp. 446-452
    • Fischer, K.1    Van der Bom, J.G.2    Mauser-Bunschoten, E.P.3
  • 5
    • 34547757915 scopus 로고    scopus 로고
    • Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia
    • Manco-Johnson MJ, Abshire TC, Shapiro AD et al. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia. N Engl J Med 2007; 6: 535-44.
    • (2007) N Engl J Med , vol.6 , pp. 535-544
    • Manco-Johnson, M.J.1    Abshire, T.C.2    Shapiro, A.D.3
  • 6
    • 0035129399 scopus 로고    scopus 로고
    • Symptomatic onset of severe haemophilia A in childhood is dependent on the presence of prothrombotic risk factors
    • Escuriola-Ettingshausen C, Halimeh S, Kurnik K et al. Symptomatic onset of severe haemophilia A in childhood is dependent on the presence of prothrombotic risk factors. Thromb Haemost 2001; 85: 218-20.
    • (2001) Thromb Haemost , vol.85 , pp. 218-220
    • Escuriola-Ettingshausen, C.1    Halimeh, S.2    Kurnik, K.3
  • 7
    • 4444334037 scopus 로고    scopus 로고
    • Do prothrombotic factors influence clinical phenotype of severe haemophilia? A review of the literature
    • Van Dijk K, Van der Bom JG, Fischer K, Grobbee DE, Van den Berg HM. Do prothrombotic factors influence clinical phenotype of severe haemophilia? A review of the literature. Thromb Haemost 2004; 92: 305-10.
    • (2004) Thromb Haemost , vol.92 , pp. 305-310
    • Van Dijk, K.1    Van der Bom, J.G.2    Fischer, K.3    Grobbee, D.E.4    Van den Berg, H.M.5
  • 8
    • 4944263724 scopus 로고    scopus 로고
    • Clinical evaluation of an advanced category antihaemophilic factor prepared using a plasma/albumin-free method: pharmacokinetics, efficacy, and safety in previously treated patients with haemophilia A
    • Tarantino MD, Collins PW, Hay CR et al. Clinical evaluation of an advanced category antihaemophilic factor prepared using a plasma/albumin-free method: pharmacokinetics, efficacy, and safety in previously treated patients with haemophilia A. Haemophilia 2004; 10: 428-37.
    • (2004) Haemophilia , vol.10 , pp. 428-437
    • Tarantino, M.D.1    Collins, P.W.2    Hay, C.R.3
  • 9
    • 47649131839 scopus 로고    scopus 로고
    • Plasma and albumin-free recombinant factor VIII: pharmacokinetics, efficacy and safety in previously treated pediatric patients
    • Blanchette VS, Shapiro AD, Liesner RJ et al. Plasma and albumin-free recombinant factor VIII: pharmacokinetics, efficacy and safety in previously treated pediatric patients. J Thromb Haemost 2008; 6: 1319-26.
    • (2008) J Thromb Haemost , vol.6 , pp. 1319-1326
    • Blanchette, V.S.1    Shapiro, A.D.2    Liesner, R.J.3
  • 10
    • 77952712296 scopus 로고    scopus 로고
    • Comparative pharmacokinetics of plasma- and albumin-free recombinant factor VIII in children and adults: the influence of blood sampling schedule on observed age-related differences and implications for dose tailoring
    • Bjorkman S, Blanchette VS, Fischer K et al. Comparative pharmacokinetics of plasma- and albumin-free recombinant factor VIII in children and adults: the influence of blood sampling schedule on observed age-related differences and implications for dose tailoring. J Thromb Haemost 2010; 8: 730-6.
    • (2010) J Thromb Haemost , vol.8 , pp. 730-736
    • Bjorkman, S.1    Blanchette, V.S.2    Fischer, K.3
  • 11
    • 59849093369 scopus 로고    scopus 로고
    • Break-through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe haemophilia A
    • Collins PW, Blanchette VS, Fischer K et al. Break-through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe haemophilia A. J Thromb Haemost 2009; 7: 413-20.
    • (2009) J Thromb Haemost , vol.7 , pp. 413-420
    • Collins, P.W.1    Blanchette, V.S.2    Fischer, K.3
  • 13
    • 0029993308 scopus 로고    scopus 로고
    • Types of bleeding seen during the first 30months of life in children with severe haemophilia A and B
    • Onwuzurike N, Warrier I, Lusher JM. Types of bleeding seen during the first 30months of life in children with severe haemophilia A and B. Haemophilia 1996; 2: 137-40.
    • (1996) Haemophilia , vol.2 , pp. 137-140
    • Onwuzurike, N.1    Warrier, I.2    Lusher, J.M.3
  • 14
    • 0343820051 scopus 로고    scopus 로고
    • When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10-year single-centre PUP study
    • Pollmann H, Richter H, Ringkamp H, Jürgens H. When are children diagnosed as having severe haemophilia and when do they start to bleed? A 10-year single-centre PUP study Eur J Pediatr 1999; 158(Suppl. 3): 166-70.
    • (1999) Eur J Pediatr , vol.158 , Issue.SUPPL. 3 , pp. 166-170
    • Pollmann, H.1    Richter, H.2    Ringkamp, H.3    Jürgens, H.4
  • 15
    • 65449132346 scopus 로고    scopus 로고
    • Physical activity participation and bleeding characteristics in young patients with severe haemophilia
    • Titinsky R, Kenet G, Dvir Z et al. Physical activity participation and bleeding characteristics in young patients with severe haemophilia. Haemophilia 2009; 15: 695-700.
    • (2009) Haemophilia , vol.15 , pp. 695-700
    • Titinsky, R.1    Kenet, G.2    Dvir, Z.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.