Purchasing factor concentrates in the 21st century through competitive tendering

被引:23
作者
Hay, C. R. M. [1 ,2 ]
机构
[1] UK Natl Haemophilia Database, Manchester, Lancs, England
[2] Univ Manchester, Dept Haematol, Manchester M13 9WL, Lancs, England
关键词
competitive tendering; factor-concentrates; purchasing; RECOMBINANT FACTOR-VIII; SEVERE HEMOPHILIA-A; B-DOMAIN DELETION; INHIBITOR DEVELOPMENT; IMMUNOGENICITY; SURVEILLANCE; SWITCH;
D O I
10.1111/hae.12169
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The increasing intensity of treatment, the widespread adoption of factor VIII and IX prophylaxis and increasing usage over the past decade have led to haemophilia becoming an almost uniquely expensive condition to treat. The average adult with severe haemophilia A in the UK used 250 000 IU of factor VIII in 2011/2012, at a cost in excess of 100 pound 000 p. a. The cost to the end-user may be considerably higher than this for some US patients supplied by home care companies with high on-costs. This has led to a high level of administrative scrutiny of treatment and an imperative to procure clotting factor concentrates more efficiently and collectively. National procurement schemes have run successfully in various countries and will become commoner. The UK system of procurement is described. This system, following EU procurement rules, evaluated products technically and by price. The price of bioequivalent products was determined by reverse e-auction. Considerable cost reductions were achieved whilst retaining all suppliers and maintaining a degree of prescribing freedom. Elements of this system could be more widely applied.
引用
收藏
页码:660 / 667
页数:8
相关论文
共 12 条
[1]   Best evidence on B-domain deletion and the immunogenicity of recombinant factor VIII [J].
Aledort, L. M. ;
Navickis, R. J. ;
Wilkes, M. M. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 (11) :2325-2327
[2]   Can B-domain deletion alter the immunogenicity of recombinant factor VIII? A meta-analysis of prospective clinical studies [J].
Aledort, L. M. ;
Navickis, R. J. ;
Wilkes, M. M. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 (11) :2180-2192
[3]   Surveillance for factor VIII inhibitor development in the Canadian Hemophilia A population following the widespread introduction of Recombinant Factor VIII replacement therapy [J].
Giles, AR ;
Rivard, GE ;
Teitel, J ;
Walker, I .
TRANSFUSION SCIENCE, 1998, 19 (02) :139-148
[4]   Factor VIII Products and Inhibitor Development in Severe Hemophilia A [J].
Gouw, Samantha C. ;
van der Bom, Johanna G. ;
Ljung, Rolf ;
Escuriola, Carmen ;
Cid, Ana R. ;
Claeyssens-Donadel, Segolene ;
van Geet, Christel ;
Kenet, Gili ;
Makipernaa, Anne ;
Molinari, Angelo Claudio ;
Muntean, Wolfgang ;
Kobelt, Rainer ;
Rivard, George ;
Santagostino, Elena ;
Thomas, Angela ;
van den Berg, H. Marijke .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (03) :231-239
[5]  
Hay CRM, 2012, HAEMOPHILIA, V18, P828
[6]   Incidence of factor VIII inhibitors throughout life in severe hemophilia A in the United Kingdom [J].
Hay, Charles R. M. ;
Palmer, Ben ;
Chalmers, Elizabeth ;
Liesner, Ri ;
Maclean, Rhona ;
Rangarajan, Savita ;
Williams, Michael ;
Collins, Peter W. .
BLOOD, 2011, 117 (23) :6367-6370
[7]  
Hay CRM, 2012, UKHCDO ANN REPORT 20
[8]   Concentrate-related inhibitor risk: is a difference always real? [J].
Iorio, A. ;
Marcucci, M. ;
Makris, M. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 (11) :2176-2179
[9]   Clotting factor concentrate switching and inhibitor development in hemophilia A [J].
Iorio, Alfonso ;
Puccetti, Paolo ;
Makris, Mike .
BLOOD, 2012, 120 (04) :720-727
[10]  
LUDLAM CA, 1997, HAEMOPHILIA, V3, P63