Budget impact analysis of the use of extended half-life recombinant factor VIII (efmoroctocog alfa) for the treatment of congenital haemophilia a: the Italian National Health System perspective

Author:

Lorenzoni Valentina,Triulzi Isotta,Turchetti GiuseppeORCID

Funder

Swedish Orphan Biovitrum (SOBI) Italia

Publisher

Springer Science and Business Media LLC

Subject

Health Policy

Reference36 articles.

1. Mammen EF. Congenital coagulation protein disorders. In: Bick RL, editor. Hematology: Clinical and Laboratory Practices vol 2. St Louis, MO: Mosby; 1993. p. 1391.

2. Hoyer LW. Inhibitors in hemophilia. In: Forbes CD, Aledort L, Madhok R, editors. Haemophilia. London: Chapman & Hall Medical; 1997. p. 213–27.

3. Diaz-Linares M, Rodvold KA, Friedenberg WR, et al. Coagulation disorders. In: DiPiro JT, Talbert RL, editors. Pharmacotherapy: a pathophysiologic approach, 4th edn. Stamford, CT: Appleton and Lange; 1999. p. 1549–72.

4. Kodra Y, Cavazza M, Schieppati A, et al. The social burden and quality of life of patients with haemophilia in Italy. Blood Transfus. 2014; https://doi.org/10.2450/2014.0042-14s.

5. Powell JS, Josephson NC, Quon D, et al. Safety and prolonged activity of recombinant factor VIII fc fusion protein in hemophilia a patients. Blood. 2012;119:3031–7.

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