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. 2019 Jan;59(1):267-276.
doi: 10.1111/trf.14959. Epub 2018 Sep 28.

Assessment of HIV transfusion transmission risk in South Africa: a 10-year analysis following implementation of individual donation nucleic acid amplification technology testing and donor demographics eligibility changes

Marion Vermeulen  1 , Nico Lelie  2 , Charl Coleman  1 , Wendy Sykes  1 , Genevieve Jacobs  1 , Ronel Swanevelder  1 , Michael Busch  3 , Gert van Zyl  4   5 , Eduard Grebe  6 , Alex Welte  6 , Ravi Reddy  1
Affiliations

Assessment of HIV transfusion transmission risk in South Africa: a 10-year analysis following implementation of individual donation nucleic acid amplification technology testing and donor demographics eligibility changes

Marion Vermeulen et al. Transfusion. 2019 Jan.

Abstract

Background: In 1998 we estimated that 34/million infectious window period donations were entering the blood supply at the South African National Blood Service. Selective use of donations based on donor race-ethnicity reduced this risk to 26/million donations but was deemed unethical. Consequently, in 2005 South African National Blood Service eliminated race-ethnicity-based collection policies and implemented individual-donation nucleic acid testing (ID-NAT). We describe the change in donor base demographics, human immunodeficiency virus (HIV) detection rates, and transfusion-transmissible HIV risk.

Study design and methods: In ten years 7.7 million donations were tested for anti-HIV and HIV RNA. Number of donations, HIV prevalence, ID-NAT yield rate, serology yield rate and residual transfusion-transmissible HIV risk were analyzed by donor type, race-ethnicity, age, and sex. Multiple regression analysis was performed to investigate the determinants of HIV-positive and nucleic acid testing yield donations.

Results: The combined strategy of increasing donations from black donors and implementing ID-NAT increased the proportion of donations from black donors from 6% in 2005 to 30% in 2015 (p < 0.00001), and reduced the transfusion-transmissible risk from 24 to 13 per million transfusions. ID-NAT interdicted 481 (1:16,100) seronegative window period donations, while one transfusion-transmissible case (0.13 per million) was documented. Race-ethnicity and donor type were highly significant predictors of HIV positivity, with adjusted odds ratio for first-time donors of 12.5 (95% confidence interval, 11.9-13.1) and for black race-ethnicity of 31.1 (95% confidence interval, 28.9-33.4). The proportion of serology yields among HIV-infected donors increased from 0.27% to 2.4%.

Conclusion: ID-NAT enabled the South African National Blood Service to increase the number of donations from black donors fivefold while enhancing the safety of the blood supply.

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Conflict of interest statement

Conflicts of interest: Nico Lelie may be paid by Grifols, the manufacturer of the NAT assay used, for review of the draft paper

There are no conflicts of interest for all other authors

Figures

Figure 1:
Figure 1:
Proportion of collections over a ten year period by ethnic group and donor type
Figure 2:
Figure 2:
HIV rate and NAT yield rate trend by race and donor type
Figure 3:
Figure 3:
Proportion of HIV positives that are serology yields by year and race
Figure 4a:
Figure 4a:
Annual TT risk per million donations when a p24 Ag and antibody or NAT and antibody screening strategy is used (compared to previously reported TT risk prior to the implementation of NAT). Annual Residual risk per million RBC transfusions for NAT screened FT, repeat and all donations
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Comment in

References

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