Hepatitis B antigen - post transfusion studies in Papua New Guinea. 1977

D G Woodfield

To determine the frequency of post transfusion hepatitis (PTH), in Papua New Guinea, 143 patients were serially blood tested after blood transfusion. Detection of HBsAg and anti-HBs was performed either by RIA or a haemagglutination method, and SGOT levels were measured. Of patients transfused with HBsAg positive blood, 85% developed HBsAg or anti-HBs within two weeks of transfusion. 18% developed subclinical PTH; no cases of clinical jaundice were noted. Of patients transfused with HBsAg negative blood, 12% developed HBsAg or anti-HBs within 2 weeks of transfusion. The frequency of PTH was not statistically different from that of the previous group. This study demonstrates that clinical Type B post transfusion hepatitis must be unusual in PNG but mild subclinical post transfusion hepatitis does occur in a minority of patients transfused with HBsAg positive or negative blood. It is postulated that the low frequency of PTH is related to the normally high Hepatitis B immune status of Papua New Guineans. Minimal health benefits would be conferred by the introduction of sensitive and expensive widespread testing for HBsAg in all donor blood; scarce financial resources may be better diverted to other areas of more productive health care.

UI MeSH Term Description Entries
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009512 New Guinea Originally an island of the Malay Archipelago, the second largest island in the world. It divided, West New Guinea becoming part of Indonesia and East New Guinea becoming Papua New Guinea.
D001782 Blood Donors Individuals supplying blood or blood components for transfer to histocompatible recipients. Blood Donor,Donor, Blood,Donors, Blood
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D005260 Female Females
D006509 Hepatitis B INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. Hepatitis B Virus Infection
D006510 Hepatitis B Antibodies Antibodies to the HEPATITIS B ANTIGENS, including antibodies to the surface (Australia) and core of the Dane particle and those to the "e" antigens. Anti-Australia Antigens,Anti-HBAg,Anti-Hepatitis B Antigens,Anti HBAg,Hepatitis B Virus Antibodies,Anti Australia Antigens,Anti Hepatitis B Antigens,Antibodies, Hepatitis B,Antigens, Anti-Australia,Antigens, Anti-Hepatitis B,B Antibodies, Hepatitis,B Antigens, Anti-Hepatitis,HBAg, Anti
D006514 Hepatitis B Surface Antigens Those hepatitis B antigens found on the surface of the Dane particle and on the 20 nm spherical and tubular particles. Several subspecificities of the surface antigen are known. These were formerly called the Australia antigen. Australia Antigen,HBsAg,Hepatitis B Surface Antigen,Antigen, Australia
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

D G Woodfield
March 2015, The American journal of tropical medicine and hygiene,
D G Woodfield
September 1988, Papua and New Guinea medical journal,
D G Woodfield
January 1974, Transactions of the Royal Society of Tropical Medicine and Hygiene,
D G Woodfield
October 1978, Lancet (London, England),
D G Woodfield
January 2020, Western Pacific surveillance and response journal : WPSAR,
D G Woodfield
June 1978, Papua and New Guinea medical journal,
D G Woodfield
September 1973, Singapore medical journal,
D G Woodfield
March 1981, The Journal of infection,
Copied contents to your clipboard!