Takano S, Omata M, Ohto M, Nakamura K
First Department of Medicine, Chiba University School of Medicine, Japan.
Gastroenterol Jpn. 1993 May;28 Suppl 5:84-7. doi: 10.1007/BF02989213.
Since November 1989, the Japan Red Cross has been screening blood donors for hepatitis C virus antibody (anti-HCV) with 1st generation assay and high-titer antibody to hepatitis B virus core antigen (HBcAb). To clarify the effectiveness of the new screening tests for the prevention of post-transfusion hepatitis, the incidence of post-transfusion hepatitis after the introduction of new tests (December 1989 to September 1990) was compared with the incidence before the in introduction (January 1982 to December 1987). The incidence of "definite" post-transfusion hepatitis was 10.3% (205/1991) with a mean transfusion volume of 10.2 units before the screening, and 3.9% (11/282) with a mean transfusion volume of 14.6 units after the introduction of the new screening tests. Statistical analysis revealed a significant decrease of post-transfusion non-A, non-B hepatitis after the introduction of new tests (chi 2 = 10.9, P < 0.01). The incidence of "probable" post-transfusion hepatitis was 12.4% (246/1991) and 11.7% (33/282) respectively. No significant change was observed between the rates of "probable" post-transfusion hepatitis before and after the introduction of the new tests. It was concluded that anti-HCV and high-titer anti-HBc screening of volunteer blood donors could contribute to the prevention of the post-transfusion non-A, non-B hepatitis in Japan.
自1989年11月起,日本红十字会一直使用第一代检测方法对献血者进行丙型肝炎病毒抗体(抗-HCV)及乙肝病毒核心抗原高滴度抗体(HBcAb)筛查。为阐明新筛查检测对预防输血后肝炎的有效性,将新检测方法引入后(1989年12月至1990年9月)输血后肝炎的发病率与引入前(1982年1月至1987年12月)的发病率进行了比较。筛查前“确诊”的输血后肝炎发病率为10.3%(205/1991),平均输血量为10.2单位;引入新筛查检测方法后,发病率为3.9%(11/282),平均输血量为14.6单位。统计分析显示,引入新检测方法后输血后非甲非乙型肝炎的发病率显著下降(卡方=10.9,P<0.01)。“疑似”输血后肝炎的发病率分别为12.4%(246/1991)和11.7%(33/282)。引入新检测方法前后“疑似”输血后肝炎的发病率未观察到显著变化。得出的结论是,对志愿献血者进行抗-HCV和高滴度抗-HBc筛查有助于预防日本的输血后非甲非乙型肝炎。