Advancing blood transfusion safety using molecular detection in the country of Georgia

Transfus Clin Biol. 2023 Aug;30(3):307-313. doi: 10.1016/j.tracli.2023.03.002. Epub 2023 Mar 11.

Abstract

Background: In 2015, the country of Georgia initiated its hepatitis C virus (HCV) elimination program. Given a high background incidence of HCV infection, centralized nucleic acid testing (NAT) of blood donations was prioritized for implementation.

Study design and methods: Multiplex NAT screening for HIV, HCV and hepatitis B virus (HBV) was launched in January 2020. An analysis was conducted of serological and NAT donor/donation data for the first year of screening (through December 2020).

Results: A total of 54,116 donations representing 39,164 unique donors were evaluated. Overall, 671 donors (1.7%) tested positive for at least one infectious marker by serology or NAT, with the highest prevalence among donors aged 40-49 years (2.5%; n = 200), male (1.9%; n = 524), replacement (2.8%; n = 153) and first time (2.1%; n = 642) donors. Sixty donations were seronegative but NAT positive, and therefore would not have been found by traditional serology testing alone. These were more likely among female vs. male (adjusted odds ratio [aOR] 2.06; 95% confidence interval [95%CI]: 1.05-4.05), paid (aOR 10.15; 95%CI: 2.80-36.86) or voluntary (aOR 4.30; 95%CI: 1.27-14.56) vs replacement, and repeat vs. first time (aOR 13.98; 95%CI: 4.06-48.12) donors. On repeat serological testing (including HBV core antibody [HBcAb] testing), 6 HBV + donations, 5 HCV + donations and 1 HIV + donations were deemed NAT yield (detected through the implementation of NAT, and would have otherwise been missed by serology screening alone).

Conclusion: This analysis offers a regional model for NAT implementation, demonstrating the feasibility and clinical utility in a nationwide blood program.

Keywords: Blood donor; Blood transfusion; Georgia (Country); Hepatitis C; Public health; Screening.

MeSH terms

  • Blood Donors
  • Blood Safety
  • Blood Transfusion
  • Female
  • Georgia (Republic) / epidemiology
  • HIV Infections* / diagnosis
  • HIV Infections* / epidemiology
  • Hepacivirus / genetics
  • Hepatitis B Antibodies
  • Hepatitis B virus / genetics
  • Hepatitis B* / diagnosis
  • Hepatitis B* / epidemiology
  • Hepatitis B* / prevention & control
  • Hepatitis C* / diagnosis
  • Hepatitis C* / epidemiology
  • Humans
  • Male
  • Nucleic Acid Amplification Techniques

Substances

  • Hepatitis B Antibodies