• Michael K Hourfar, Christine Jork, Volkmar Schottstedt, Marijke Weber-Schehl, Veronika Brixner, Michael P Busch, Geert Geusendam, Knut Gubbe, Christina Mahnhardt, Uschi Mayr-Wohlfart, Lutz Pichl, W Kurt Roth, Michael Schmidt, Erhard Seifried, David J Wright, and German Red Cross NAT Study Group.
• Institute of Transfusion and Immunohematology, German Red Cross Baden-Württemberg-Hessen, Johann Wolfgang Goethe University, Frankfurt, Germany. k.hourfar@blutspende.de
• Transfusion. 2008 Aug 1; 48 (8): 1558-66.

BackgroundThe risk of transfusion-transmitted human immunodeficiency virus-1 (HIV-1), hepatitis C virus (HCV), and hepatitis B virus (HBV) infections is predominantly attributable to donations given during the early stage of infection when diagnostic tests may fail. In 1997, nucleic acid amplification technique (NAT)-testing was introduced at the German Red Cross (GRC) blood donor services to reduce this diagnostic window period (WP).Study Design And MethodsA total of 31,524,571 blood donations collected from 1997 through 2005 were screened by minipool NAT, predominantly with pool sizes of 96 donations. These donations cover approximately 80 percent of all the blood collected in Germany during that period. Based on these data, the WP risk in the GRC blood donor population was estimated by using a state-of-the-art mathematic model.ResultsDuring the observation period, 23 HCV, 7 HIV-1, and 43 HBV NAT-only-positive donations were detected. On the basis of these data and estimated pre-NAT infectious WPs, the residual risk per unit transfused was estimated at 1 in 10.88 million for HCV (95% confidence interval [CI], 7.51-19.72 million), 1 in 4.30 million for HIV-1 (95% CI, 2.39-21.37 million), and 1 in 360,000 for HBV (95% CI, 0.19-3.36 million). Based on observed cases of breakthrough infections, the risk of transfusion-related infections may be even lower.ConclusionThe risk of a blood recipient becoming infected with HCV, HIV-1, or HBV has reached an extremely low level. Introduction of individual donation testing for HCV and HIV-1 would have a marginal effect on interception of WP donations.

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