Recently acquired infection among HIV-seropositive donors in the US from 2010-2018.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
10 2020
Historique:
received: 29 04 2020
revised: 03 08 2020
accepted: 03 08 2020
pubmed: 30 8 2020
medline: 30 6 2021
entrez: 30 8 2020
Statut: ppublish

Résumé

Monitoring of transfusion-transmissible infections in the blood supply is essential for blood safety, as the donor population is not static, and changes in policy, donor behavior, or other factors could increase the risk of recipient infection. We assessed patterns of recently acquired HIV infection in US blood donors, including before and after the implementation of the 12-month deferral for men who have sex with men (MSM). A large convenience sample of donations from donors testing HIV-1 nucleic acid testing (NAT) and serology-reactive were further tested with the Sedia HIV-1 Limiting Antigen enzyme immunoassay. Samples were analyzed across available demographic and donation data to provide an assessment of recently acquired HIV infection in US blood donors from 2010 to 2018. Overall, 317 of 1154 (27.5%; 95% confidence interval, 24.9%-30.1%) donations from HIV NAT and serology-reactive donors had recently acquired HIV infection. There was no evidence of change in the percentages of recent HIV infection by year over the study period, either in all donors or in male donors, including after the MSM policy change. In multivariable logistic regression analysis, donors aged 24 years or younger were over 2.7 times more likely and repeat donors 2.2 times more likely to have recently acquired HIV infection compared to donors aged 55 years or older and first-time donors, respectively. Patterns of recently acquired HIV infection varied by demographics but not over time. These findings suggest no impact of the MSM policy change on recently acquired HIV infection in US blood donors.

Sections du résumé

BACKGROUND
Monitoring of transfusion-transmissible infections in the blood supply is essential for blood safety, as the donor population is not static, and changes in policy, donor behavior, or other factors could increase the risk of recipient infection. We assessed patterns of recently acquired HIV infection in US blood donors, including before and after the implementation of the 12-month deferral for men who have sex with men (MSM).
STUDY DESIGN AND METHODS
A large convenience sample of donations from donors testing HIV-1 nucleic acid testing (NAT) and serology-reactive were further tested with the Sedia HIV-1 Limiting Antigen enzyme immunoassay. Samples were analyzed across available demographic and donation data to provide an assessment of recently acquired HIV infection in US blood donors from 2010 to 2018.
RESULTS
Overall, 317 of 1154 (27.5%; 95% confidence interval, 24.9%-30.1%) donations from HIV NAT and serology-reactive donors had recently acquired HIV infection. There was no evidence of change in the percentages of recent HIV infection by year over the study period, either in all donors or in male donors, including after the MSM policy change. In multivariable logistic regression analysis, donors aged 24 years or younger were over 2.7 times more likely and repeat donors 2.2 times more likely to have recently acquired HIV infection compared to donors aged 55 years or older and first-time donors, respectively.
CONCLUSION
Patterns of recently acquired HIV infection varied by demographics but not over time. These findings suggest no impact of the MSM policy change on recently acquired HIV infection in US blood donors.

Identifiants

pubmed: 32860262
doi: 10.1111/trf.16032
doi:

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

2340-2347

Subventions

Organisme : U.S. Food and Drug Administration
ID : HHSF223201510149C

Informations de copyright

© 2020 AABB.

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Auteurs

Claire Quiner (C)

Vitalant Research Institute, San Francisco, California, USA.

Roberta Bruhn (R)

Vitalant Research Institute, San Francisco, California, USA.
Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.

Eduard Grebe (E)

Vitalant Research Institute, San Francisco, California, USA.

Clara Di Germanio (C)

Vitalant Research Institute, San Francisco, California, USA.

Debra Kessler (D)

New York Blood Center, New York, New York, USA.

Rita Reik (R)

OneBlood, St. Petersburg, Florida, USA.

Phillip Williamson (P)

Creative Testing Solutions, Tempe, Arizona, USA.

Dylan Hampton (D)

Vitalant Research Institute, San Francisco, California, USA.

Rahima Fayed (R)

American Red Cross Scientific Affairs, Gaithersburg, Maryland, USA.

Steve A Anderson (SA)

U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

Alan E Williams (AE)

U.S. Food and Drug Administration, Silver Spring, Maryland, USA.

Simone A Glynn (SA)

National Heart, Lung and Blood Institute, National Institutes of Health, Rockville, Maryland, USA.

Michael P Busch (MP)

Vitalant Research Institute, San Francisco, California, USA.
Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.

Susan L Stramer (SL)

American Red Cross Scientific Affairs, Gaithersburg, Maryland, USA.

Brian Custer (B)

Vitalant Research Institute, San Francisco, California, USA.
Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.

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