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Volumn 11, Issue 3, 2013, Pages 327-329

Target of prophylaxis in severe haemophilia: More than factor levels

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9;

EID: 84882423386     PISSN: 17232007     EISSN: None     Source Type: Journal    
DOI: 10.2450/2012.0244-12     Document Type: Editorial
Times cited : (10)

References (28)
  • 1
    • 0006699504 scopus 로고
    • Symptomatology, with special reference to differences between haemophilia a and b
    • Haemophilia in Sweden. III
    • Ramgren O. Haemophilia in Sweden. III. Symptomatology, with special reference to differences between haemophilia A and B. Acta Med Scand 1962; 171: 237-42.
    • (1962) Acta Med Scand , vol.171 , pp. 237-242
    • Ramgren, O.1
  • 3
    • 84857019132 scopus 로고    scopus 로고
    • Prophylaxis in children with hemophilia: Evidence-based achievements, old and new challenges
    • Coppola A, Tagliaferri A, Di Capua M, Franchini M. Prophylaxis in children with hemophilia: evidence-based achievements, old and new challenges. Semin Thromb Hemost 2012; 38: 79-94.
    • (2012) Semin Thromb Hemost , vol.38 , pp. 79-94
    • Coppola, A.1    Tagliaferri, A.2    Di Capua, M.3    Franchini, M.4
  • 4
    • 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; 357: 535-44.
    • (2007) N Engl J Med , vol.357 , pp. 535-544
    • Manco-Johnson, M.J.1    Abshire, T.C.2    Shapiro, A.D.3
  • 5
    • 79953306825 scopus 로고    scopus 로고
    • A randomized clinical trial of prophylaxis in children with haemophilia a (the esprit study)
    • Gringeri A, Lundin B, von Mackensen S et al. A randomized clinical trial of prophylaxis in children with haemophilia A (the ESPRIT study). J Thromb Haemost 2011; 9: 700-10.
    • (2011) J Thromb Haemost , vol.9 , pp. 700-710
    • Gringeri, A.1    Lundin, B.2    Von Mackensen, S.3
  • 6
    • 33646015676 scopus 로고    scopus 로고
    • Current co-ordinated activities of the pednet (european paediatric network for haemophilia management)
    • Donadel-Claeyssens S. Current co-ordinated activities of the PEDNET (European Paediatric Network for Haemophilia Management). Haemophilia 2006; 12: 124-7.
    • (2006) Haemophilia , vol.12 , pp. 124-127
    • Donadel-Claeyssens, S.1
  • 8
    • 62149098003 scopus 로고    scopus 로고
    • Guidelines for the management of hemophilia
    • Available at:, Accessed on 26/09/2012
    • Srivastava A, Giangrande P, Poon MC, et al. Guidelines for the Management of Hemophilia. World Federation of Hemophilia, 2005. Available at: http://www/wfh.org/2/docs/Publications/Diagnosis-and-Treatment/ Guidelines-Mng-Hemophilia.pdf. Accessed on 26/09/2012.
    • (2005) World Federation of Hemophilia
    • Srivastava, A.1    Giangrande, P.2    Poon, M.C.3
  • 10
    • 77951681450 scopus 로고    scopus 로고
    • A united kingdom haemophilia centre doctors' organization guideline approved by the british committee for standards in haematology: Guideline on the use of prophylactic factor viii concentrate in children and adults with severe haemophilia a
    • Richards M, Williams M, Chalmers E, et al. A United Kingdom Haemophilia Centre Doctors' Organization guideline approved by the British Committee for Standards in Haematology: guideline on the use of prophylactic factor VIII concentrate in children and adults with severe haemophilia A. Br J Haematol 2010; 149: 498-507.
    • (2010) Br J Haematol , vol.149 , pp. 498-507
    • Richards, M.1    Williams, M.2    Chalmers, E.3
  • 11
    • 0002099315 scopus 로고
    • Incidence, treatment and prophylaxis of arthropathy and other musculo-skeletal manifestations of haemophilia a and b
    • Haemophilia in Sweden. VII
    • Ahlberg A. Haemophilia in Sweden. VII. Incidence, treatment and prophylaxis of arthropathy and other musculo-skeletal manifestations of haemophilia A and B. Acta Orthop Scand Suppl 1965; (Suppl. 77): 1-98.
    • (1965) Acta Orthop Scand Suppl , Issue.SUPPL.. 77 , pp. 1-98
    • Ahlberg, A.1
  • 12
    • 0026635406 scopus 로고
    • Twenty-five years experience of prophylactic treatment in severe haemophilia a and b
    • Nilsson IM, Berntorp E, Löfqvist 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    Löfqvist, T.3    Pettersson, H.4
  • 13
    • 0035106558 scopus 로고    scopus 로고
    • Long-term outcome of individualized prophylactic treatment of children with severe haemophilia
    • van den Berg HM, Fischer K, Mauser-Bunschoten EP, et al. Long-term outcome of individualized prophylactic treatment of children with severe haemophilia. Br J Haematol 2001; 112: 561-5.
    • (2001) Br J Haematol , vol.112 , pp. 561-565
    • Van, D.B.H.M.1    Fischer, K.2    Mauser-Bunschoten, E.P.3
  • 14
    • 0036529818 scopus 로고    scopus 로고
    • The effects of postponing prophylactic treatment on longterm outcome in patients with severe haemophilia
    • Fischer K, van der Bom JG, Mauser-Bunschoten EP, et al. The effects of postponing prophylactic treatment on longterm outcome in patients with severe haemophilia. Blood 2002; 99: 2337-41.
    • (2002) Blood , vol.99 , pp. 2337-2341
    • Fischer, K.1    Van Der Bom, J.G.2    Mauser-Bunschoten, E.P.3
  • 15
    • 0033028402 scopus 로고    scopus 로고
    • Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized
    • Astermark J, Petrini P, Tengborn L, et al. Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized. Br J Haematol 1999; 105: 1109-13.
    • (1999) Br J Haematol , vol.105 , pp. 1109-1113
    • Astermark, J.1    Petrini, P.2    Tengborn, L.3
  • 16
    • 33646759553 scopus 로고    scopus 로고
    • Tailored prophylaxis in severe hemophilia a: Interim results from the first 5 years of the canadian hemophilia primary prophylaxis study
    • Feldman BN, Pai M, Rivard GE, et al. Tailored prophylaxis in severe hemophilia A: interim results from the first 5 years of the Canadian Hemophilia Primary Prophylaxis Study. J Thromb Haemost 2006; 4: 1228-36.
    • (2006) J Thromb Haemost , vol.4 , pp. 1228-1236
    • Feldman, B.N.1    Pai, M.2    Rivard, G.E.3
  • 17
    • 79955654392 scopus 로고    scopus 로고
    • Age at first joint bleed and bleeding severity in boys with severe hemophilia a: Canadian hemophilia primary prophylaxis study group
    • Xang MX, Blanchette VS, Pullenayegum E et al. Age at first joint bleed and bleeding severity in boys with severe hemophilia A: Canadian Hemophilia Primary Prophylaxis Study Group. J Thromb Haemost 2011; 9: 1067-9.
    • (2011) J Thromb Haemost , vol.9 , pp. 1067-1069
    • Xang, M.X.1    Blanchette, V.S.2    Pullenayegum, E.3
  • 19
    • 59849093369 scopus 로고    scopus 로고
    • Break-through bleeding in relation to predicted factor viii levels in patients receiving prophylactic treatment for severe hemophilia 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 hemophilia 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
  • 20
    • 70349229281 scopus 로고    scopus 로고
    • Pharmacokinetics and dose requirements of factor viii over the age range 3-74 years: A population analysis based on 50 patients with longterm prophylactic treatment for haemophilia a
    • Björkman S, Folkesson A, Jönsson S. Pharmacokinetics and dose requirements of factor VIII over the age range 3-74 years: a population analysis based on 50 patients with longterm prophylactic treatment for haemophilia A. Eur J Clin Pharmacol 2009; 65: 989-98.
    • (2009) Eur J Clin Pharmacol , vol.65 , pp. 989-998
    • Björkman, S.1    Folkesson, A.2    Jönsson, S.3
  • 21
    • 74749088081 scopus 로고    scopus 로고
    • Factor viii requirement to maintain a target plasma level in the prophylactic treatment of severe hemophilia a: Influences of variance in pharmacokinetics and treatment regimens
    • Collins PW, Björkman S, Fischer K, et al. Factor VIII requirement to maintain a target plasma level in the prophylactic treatment of severe hemophilia A: influences of variance in pharmacokinetics and treatment regimens. J Thromb Haemost 2010; 8: 269-75.
    • (2010) J Thromb Haemost , vol.8 , pp. 269-275
    • Collins, P.W.1    Björkman, S.2    Fischer, K.3
  • 23
    • 84860531391 scopus 로고    scopus 로고
    • Prophylaxis for adults with haemophilia: One size does not fit all
    • Fischer K. Prophylaxis for adults with haemophilia: one size does not fit all. Blood Transfus 2012; 10: 169-73.
    • (2012) Blood Transfus , vol.10 , pp. 169-173
    • Fischer, K.1
  • 24
    • 70349961526 scopus 로고    scopus 로고
    • Prophylactic therapy in haemophilia
    • Ljung R. Prophylactic therapy in haemophilia. Blood Rev 2009; 23: 267-74.
    • (2009) Blood Rev , vol.23 , pp. 267-274
    • Ljung, R.1
  • 25
    • 84882366280 scopus 로고    scopus 로고
    • Turning severe into moderate haemophilia by prophylaxis: Are we reaching our goal?
    • den Uijl IEM, Biesma DH, Grobbee DE, Fischer K. Turning severe into moderate haemophilia by prophylaxis: are we reaching our goal? Blood Transfus 2013; 11: 364-9.
    • (2013) Blood Transfus , vol.11 , pp. 364-369
    • Den, Uijl.I.E.M.1    Biesma, D.H.2    Grobbee, D.E.3    Fischer, K.4
  • 26
    • 63049103181 scopus 로고    scopus 로고
    • Clinical outcome of moderate haemophilia compared with severe and mild haemophilia
    • den Uijl IE, Fischer K, Van Der Bom JG, et al. Clinical outcome of moderate haemophilia compared with severe and mild haemophilia. Haemophilia 2009; 15: 83-90.
    • (2009) Haemophilia , vol.15 , pp. 83-90
    • Den Uijl, I.E.1    Fischer, K.2    Van Der Bom, J.G.3
  • 27
    • 45549109500 scopus 로고    scopus 로고
    • Validation of a composite score for clinical severity of hemophilia
    • Schu lman S, Eelde A, Holmström M, et al. Validation of a composite score for clinical severity of hemophilia. J Thromb Haemost 2008; 6: 1113-21.
    • (2008) J Thromb Haemost , vol.6 , pp. 1113-1121
    • Schu Lman, S.1    Eelde, A.2    Holmström, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.