Antibody to Hepatitis B Core Antigen as a Paradoxical Marker for Non-A, Non-B Hepatitis Agents in Donated Blood

Abstract

The relationship between the presence of antibody to hepatitis B core antigen (anti-HBc) in donor blood and the development of hepatitis in recipients of that blood was studied in 6293 blood donors and 481 recipients who were followed for 6 to 9 months after transfusion. Of 193 recipients of at least 1 unit of blood positive for anti-HBc, 23 (11.9%) developed non-A, non-B hepatitis compared with 12 (4.2%) of 288 recipients of only anti-HBc-negative blood (p < 0.001). Donor anti-HBc status was not significantly associated with the development of hepatitis B in the recipient and was negatively associated with the development of cytomegalovirus hepatitis. The relationship of donor anti-HBc status and the development of non-A, non-B hepatitis in the recipient was independent of transfusion volume and elevated donor transaminase level. Although 88% of anti-HBc-positive blood units were not associated with recipient non-A, non-B hepatitis, calculation of maximal corrected efficacy predicted that exclusion of anti-HBc-positive donors might have prevented 43% of the cases of non-A, non-B hepatitis with a donor loss of 4%. Because of the serious chronic consequences of non-A, non-B hepatitis, surrogate tests for non-A, non-B virus carriers must be seriously considered.

Article and Author Information

  • ▸From the Department of Transfusion Medicine and Hospital Epidemiology Service, Clinical Center, and the National Institute of Allergy and Infectious Diseases, National Institutes of Health; Bethesda, Maryland.

  • The Hepatitis Case Review Committee consisted of Drs. Paul V. Holland, Jay H. Hoofnagle, Robert H. Purcell, and Leonard B. Seeff.

  • Grant support: in part by Abbott Laboratories, North Chicago, Illinois.

  • ▸Requests for reprints should be addressed to Deloris E. Koziol; the Hospital Epidemiology Service, Clinical Center, National Institutes of Health, Building 10, Room 11N223; Bethesda, MD 20892.

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