W e have evaluated the clinical and histopathological outcomes of patients who contracted chronic non A, nonB hepatitis as a result of transfusions administered during heart surgery at the National Institutes of Health. Posttransfusion In addition, six other patients with chronic posttransfusion non A, non B hepatitis were evaluated (group 2). These 39 patients were followed between 1 and 24 yr (mean = 9.7 yr). Cirrhosis developed in 8 patients (20%) between 1.5 and 16 yr after blood transfusion. Of the 33 patients in group 1, 11 (33%) died during follow-up. In two cases (6%), this was related to liver failure. At this writing, two additional patients (6%) have decompensated cirrhosis and one (3%) has debilitating fatigue. Twenty of 33 patients (61%) with histological evidence of chronic active hepatitis or cirrhosis are asymptomatic and have no clinical evidence of liver disease. n u s chronic non A, non B posttransfusion hepatitis appeared to be due to hepatitis C virus infection in most cases. It was associated with the development of cirrhosis in approximately 20% of cases and end-stage liver disease in 12% of patients followed prospectively. Most patients with histological evidence of cirrhosis or chronic active hepatitis, however, had minimal clinical evidence of liver disease within the time frame of this study.
31/1/33957that only rarely resulted in clinically apparent liver disease, despite the frequent histological documentation of cirrhosis (3-5).The recent discovery of the hepatic C virus (HCV) and the development of sensitive and specific assays to detect HCV infection (6, 7) have required the reexamination of previous studies of posttransfusion hepatitis. We have evaluated the clinical and histopathologid outcome of patients who contracted chronic NANB hepatitis and who were followed prospectively as part of ongoing studies at the National Institutes of Health (NIH). This information was correlated with serum biochemical findings and the results of testing for antibody to the hepatitis C virus (anti-HCV).
PATLENTS AND METHODSWe studied patients enrolled in prospective studies of posttransfusion hepatitis who received blood transfusions during heart surgery at NIH between 1972 and 1983 (group 1). Patients were followed by serial testing of serum aminotransferase activity, initially at weekly or biweekly intervals for 12 wk and then monthly for another 12 wk. Hepatitis was diagnosed when, between 2 and 26 wk after transfusion, the serum ALT activity exceeded 2% times the upper limit of normal and a repeat value more than 1 wk later was more than twice the upper limit of normal. The diagnosis of NANB hepatitis was established by exclusion of other viral (hepatitis B, hepatitis A, cytomegalovirus, Epstein-Ban: virus) and nonviral causes of serum ALT elevation. Patients who had persistently abnormal elevations in serum aminotransferase activities were then followed at 1-to 6-mo intervals throughout their subsequent course.