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

被引:3
作者
Alkhazashvili, Maia [1 ,2 ,6 ]
Bloch, Evan M. [3 ]
Shadaker, Shaun [4 ]
Kuchuloria, Tinatin [5 ]
Getia, Vladimer [1 ]
Turdziladze, Alexander [1 ]
Armstrong, Paige A. [3 ]
Gamkrelidze, Amiran [1 ,2 ]
机构
[1] Natl Ctr Dis Control & Publ Hlth Georgia, Tbilisi, Georgia
[2] Univ Georgia, Sch Hlth Sci, Tbilisi, Georgia
[3] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[4] CDC, Div Viral Hepatitis, Natl Ctr HIV Viral Hepatitis STD & TB Prevent, Atlanta, GA USA
[5] Task Force Global Hlth, Tbilisi, Georgia
[6] Natl Ctr Dis Control & Publ Hlth, 99 Kakheti Highway, Tbilisi 0198, Georgia
关键词
Hepatitis C; Blood donor; Screening; Blood transfusion; Public health; Georgia (Country); HEPATITIS-C VIRUS; HUMAN-IMMUNODEFICIENCY-VIRUS; B-VIRUS; RISK; PREVALENCE; DONORS; HIV; EPIDEMIOLOGY; TRANSMISSION; INFECTION;
D O I
10.1016/j.tracli.2023.03.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (c) 2023 Societe francaise de transfusion sanguine (SFTS). Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:307 / 313
页数:7
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