Blood safety and the choice of anti‐hemophilic factor concentrate
Identifieur interne : 000395 ( Istex/Curation ); précédent : 000394; suivant : 000396Blood safety and the choice of anti‐hemophilic factor concentrate
Auteurs : Leonard A. Valentino [États-Unis] ; Veeral M. Oza [États-Unis]Source :
- Pediatric Blood & Cancer [ 1545-5009 ] ; 2006-09.
English descriptors
- Teeft :
- Abnormal prion proteins, Administration cost, Allergic reactions, Antihemophilic factor, Avian virus, Baxter, Blood components, Blood donors, Blood product, Blood products, Blood safety, Blood safety monitoring, Blood supply, Blood transfusion, Blood transfusions, Blood transmission, Chronic infection, Chronic liver disease, Current status, Disease control, Donor screening, Excellent review, Factor viii, Haemophilia, Haemost, Hemolytic anemia, Hemophilia, Hemophilia patients, Hepatitis, Human albumin, Human parvovirus, Human proteins, Inactivation, Individual products, Infection, Infectious agent, Infectious disease, Infusion, Inhibitor, Inhibitor formation, International units, Joint disease, Kogenate, Liver disease, Microbiological threats, Mmwr, Mmwr morb, Mmwr series, Parvovirus, Pathogenic prion protein, Pediatr, Pediatr blood cancer, Plasma derivatives, Prion, Proc natl acad, Recombinant, Recombinant factor, Recombinant factor viii, Recombinant factor viii product, Recombinant factors, Recombinant products, Recombinant viii products, Recombinate, Recombinate study group, Respiratory syndrome, Right knee, Rush university, Senv, Several minutes, Severe hemophilia, Source plasma, Spongiform, Therapeutic products, Thromb, Thromb haemost, Transfusion, Transmissible spongiform encephalopathies, Travel history, Untreated, Untreated patients, Vaccine, Valentino, Variant disease, Vcjd, Viii, Viral, Viral infection, Viral safety, Virus, Virus infection, West nile virus, World federation, Young children.
Abstract
Hemophilia is a congenital disorder due to the deficiency of the activity of factor VIII (classical hemophilia A) or IX (Christmas disease or hemophilia B). Bleeding is common and may result in long‐term complications or even death. Bleeding may be treated or prevented by infusion of factor concentrates however these drugs are not without risk. Clinicians often feel ill prepared to provide accurate and impartial information regarding these drugs. This review will provide the reader with an historical yet up to date perspective on blood safety as it relates to the choice of concentrates to treat hemophilia. Pediatr Blood Cancer 2006;47:245–254. © 2006 Wiley‐Liss, Inc.
Url:
DOI: 10.1002/pbc.20895
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Bleeding is common and may result in long‐term complications or even death. Bleeding may be treated or prevented by infusion of factor concentrates however these drugs are not without risk. Clinicians often feel ill prepared to provide accurate and impartial information regarding these drugs. This review will provide the reader with an historical yet up to date perspective on blood safety as it relates to the choice of concentrates to treat hemophilia. Pediatr Blood Cancer 2006;47:245–254. © 2006 Wiley‐Liss, Inc.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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