A Pereira1. 1. Service of Hemotherapy and Hemostasis and the Blood Bank, Hospital Clínico, Barcelona, Spain. apereira@medicina.ub.es
Abstract
BACKGROUND: Virus inactivation of plasma intended for transfusion avoids the transmission of hepatitis B virus, hepatitis C virus, and HIV. However, because most plasma recipients also receive other blood components concomitantly, the procedure reduces but cannot eliminate the risk of transfusion-transmitted infection. As virus-inactivated plasma has just been licensed in the United States and other countries, a cost-effectiveness analysis is pertinent. STUDY DESIGN AND METHODS: A Monte Carlo simulation of a Markov model representing the possible outcomes of plasma recipients was used to derive costs and utilities of transfusing virus-inactivated plasma instead of standard plasma. Probability distributions for patients' age and sex and for the number of blood components transfused per case were determined in 924 plasma recipients in a tertiary-care hospital. Other values were obtained from the medical literature. Results of the baseline and sensitivity analyses are the mean (+/- SD) of 10 simulations with 10(7) patients per simulation. RESULTS: In the baseline analysis, transfusing virus-inactivated plasma instead of standard plasma prolonged the quality-adjusted survival by 1 hour and 11 minutes per patient, at a cost-effectiveness ratio of $2,156,398 +/- $257,587 per quality-adjusted life year gained. Cost-effectiveness was most sensitive to the patients' mean age, the incremental cost per unit of virus-inactivated plasma, the HIV and hepatitis C virus transmission rates, and the short-term mortality of plasma recipients due to their underlying diseases. CONCLUSIONS: Compared to most accepted medical procedures, the transfusion of virus-inactivated plasma produces little health benefit at a very high cost. This poor cost-effectiveness ratio is due to the low current risk of infection with transfusion-transmitted viruses and to the greater age and poor short-term prognosis of most plasma recipients.
BACKGROUND: Virus inactivation of plasma intended for transfusion avoids the transmission of hepatitis B virus, hepatitis C virus, and HIV. However, because most plasma recipients also receive other blood components concomitantly, the procedure reduces but cannot eliminate the risk of transfusion-transmitted infection. As virus-inactivated plasma has just been licensed in the United States and other countries, a cost-effectiveness analysis is pertinent. STUDY DESIGN AND METHODS: A Monte Carlo simulation of a Markov model representing the possible outcomes of plasma recipients was used to derive costs and utilities of transfusing virus-inactivated plasma instead of standard plasma. Probability distributions for patients' age and sex and for the number of blood components transfused per case were determined in 924 plasma recipients in a tertiary-care hospital. Other values were obtained from the medical literature. Results of the baseline and sensitivity analyses are the mean (+/- SD) of 10 simulations with 10(7) patients per simulation. RESULTS: In the baseline analysis, transfusing virus-inactivated plasma instead of standard plasma prolonged the quality-adjusted survival by 1 hour and 11 minutes per patient, at a cost-effectiveness ratio of $2,156,398 +/- $257,587 per quality-adjusted life year gained. Cost-effectiveness was most sensitive to the patients' mean age, the incremental cost per unit of virus-inactivated plasma, the HIV and hepatitis C virus transmission rates, and the short-term mortality of plasma recipients due to their underlying diseases. CONCLUSIONS: Compared to most accepted medical procedures, the transfusion of virus-inactivated plasma produces little health benefit at a very high cost. This poor cost-effectiveness ratio is due to the low current risk of infection with transfusion-transmitted viruses and to the greater age and poor short-term prognosis of most plasma recipients.
Authors: Kathryn E Webert; Christine M Cserti; Judy Hannon; Yulia Lin; Katerina Pavenski; Jacob M Pendergrast; Morris A Blajchman Journal: Transfus Med Rev Date: 2008-01
Authors: Christopher E Bell; Marc F Botteman; Xin Gao; Joel L Weissfeld; Maarten J Postma; Chris L Pashos; Darrell Triulzi; Ulf Staginnus Journal: Clin Ther Date: 2003-09 Impact factor: 3.393