Transient hypoplastic anemia caused by primary human parvovirus B19 infection in a previously untreated patient with hemophilia transfused with a plasma-derived, monoclonal antibody-purified factor VIII concentrate
H. Matsui et al., Transient hypoplastic anemia caused by primary human parvovirus B19 infection in a previously untreated patient with hemophilia transfused with a plasma-derived, monoclonal antibody-purified factor VIII concentrate, J PED H ONC, 21(1), 1999, pp. 74-76
Background: Modern plasma-derived clotting factor concentrates are produced
using various virus-inactivation protocols and an assumed to be safer than
they were previously with regard to the risk for transmitting viral infect
ions such as human immunodeficiency virus, hepatitis B, and hepatitis C. Th
e risks from viruses that are relatively resistant to the current inactivat
ion procedures remain uncertain.
Patient: A 7-year-old boy with mild hemophilia A who had not been previousl
y infused with any blood products was treated with a plasma-derived, monocl
onal antibody-purified factor III concentrate to cover orthopedic surgery a
fter traumatic fracture of his left arm.
Results: A typical primary human parvovirus (HPV)-B19 infection was observe
d associated with transient hypoplastic anemia. Retrospective studies inclu
ding serologic examination and polymerase chain reaction analysis confirmed
that the HPV-B19 infection was transmitted by the factor VIII concentrate.
Conclusions: Clotting factor concentrates for the treatment of hemophilia r
etain a risk for HPV-B 19 contamination. HPV-B 19 viral infection might ind
uce hypoplastic anemia in these patients, particularly during enhanced hemo
poiesis after acute blood loss.