Batch recall of French plasma-derived products due to variant Creutzfeldt-Jakob disease risk: the psychological impact on haemophilic patients, changes in their therapeutic demands and behaviour and ethical considerations

Author:

Aouba A.12,Harroche A.1,Frenzel L.1,Torchet M. -F.1,Rothschild C.1,François I.2,Mamzer-Bruneel M. -F.2

Affiliation:

1. Center for Haemophilia Care and Department of Haematology; Hôpital Necker Enfants-Malades; Université Paris-Descartes; Assistance Publique-Hôpitaux de Paris; Paris France

2. Medical Ethics Department EA 4569; Université Paris-Descartes; PRES Sorbonne-Paris-Cité Paris France

Funder

LFB

Pfizer

Novonordisk

Octapharma

Baxter

CSL Behring

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Reference27 articles.

1. 2005 Guidelines for the management of hemophilia http://www.wfh.org

2. How we choose factor VIII to treat hemophilia;Mannucci;Blood,2012

3. Food and Drug Administration Draft quantitative risk assessment of vCJD risk potentially associated with the use of human plasma-derived Factor VIII manufactured under United States (US) license from plasma collected in the US 2006 http://www.fda.gov/downloads/BiologicsBloodVaccines/SafetyAvailability/BloodSafety/UCM095104.pdf

4. National Hemophilia Foundation board of Directors MASAC recommendations concerning products licensed for the treatment of hemophilia and other bleeding disorders http://www.hemophilia.org

5. Millar C vCJD and haemophilia Textbook of Hemophilia, Third Edition. Edited by Christine A. Lee, Erik E. Berntorp and W. Keith Hoots. © 2014 John Wiley & Sons, Ltd.

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