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An international review of the characteristics of viral nucleic acid-amplification testing (NAT) reveals a trend towards the use of smaller pool sizes and individual donation NAT.
Faddy, Helen M; Osiowy, Carla; Custer, Brian; Busch, Michael; Stramer, Susan L; Dean, Melinda M; Acutt, Jessika; Viennet, Elvina; van de Laar, Thijs; Tsoi, Wai-Chiu; Styles, Claire; Kiely, Phil; Margaritis, Angelo; Kwon, So-Yong; Qiu, Yan; Deng, Xuelian; Lewin, Antoine; Jørgensen, Signe Winther; Erikstrup, Christian; Juhl, David; Sauleda, Silvia; Camacho Rodriguez, Bernardo Armando; Soto Coral, Lisbeth Jennifer Catherine; Gaviria García, Paula Andrea; Oota, Sineenart; O'Brien, Sheila F; Wendel, Silvano; Castro, Emma; Navarro Pérez, Laura; Harvala, Heli; Davison, Katy; Reynolds, Claire; Jarvis, Lisa; Grabarczyk, Piotr; Kopacz, Aneta; Letowska, Magdalena; O'Flaherty, Niamh; Young, Fiona; Williams, Padraig; Burke, Lisa; Chua, Sze Sze; Muylaert, An; Page, Isabel; Jones, Ann; Niederhauser, Christoph; Vermeulen, Marion; Laperche, Syria; Gallian, Pierre; Satake, Masahiro; Addas-Carvalho, Marcelo.
Affiliation
  • Faddy HM; School of Health, University of the Sunshine Coast, Petrie, Queensland, Australia.
  • Osiowy C; Research and Development, Australian Red Cross Lifeblood, Brisbane, Queensland, Australia.
  • Custer B; National Microbiology Laboratory, Public Health Agency of Canada, Manitoba, Canada.
  • Busch M; Vitalant Research Institute, San Francisco, California, USA.
  • Stramer SL; Department of Laboratory Medicine, University of California San Francisco, California, USA.
  • Dean MM; Vitalant Research Institute, San Francisco, California, USA.
  • Acutt J; Infectious Disease Consultant, North Potomac, Maryland, USA.
  • Viennet E; School of Health, University of the Sunshine Coast, Petrie, Queensland, Australia.
  • van de Laar T; Research and Development, Australian Red Cross Lifeblood, Brisbane, Queensland, Australia.
  • Tsoi WC; School of Health, University of the Sunshine Coast, Petrie, Queensland, Australia.
  • Styles C; Research and Development, Australian Red Cross Lifeblood, Brisbane, Queensland, Australia.
  • Kiely P; Department of Donor Medicine Research, Sanquin Research, Amsterdam, The Netherlands.
  • Margaritis A; Hong Kong Red Cross Blood Transfusion Service, Hong Kong.
  • Kwon SY; Pathology & Clinical Governance, Australian Red Cross Lifeblood, Melbourne, Australia.
  • Qiu Y; Pathology & Clinical Governance, Australian Red Cross Lifeblood, Melbourne, Australia.
  • Deng X; Manufacturing & Logistics, Australian Red Cross Lifeblood, Melbourne, Australia.
  • Lewin A; Korean Red Cross Blood Services, Republic of Korea.
  • Jørgensen SW; Beijing Red Cross Blood Centre, Beijing, China.
  • Erikstrup C; Dalian Blood Centre, Dalian, China.
  • Juhl D; Medical Affairs and Innovation, Héma-Québec, Canada.
  • Sauleda S; Department of Clinical Immunology, Aarhus University Hospital, Denmark.
  • Camacho Rodriguez BA; Department of Clinical Immunology, Aarhus University Hospital, Denmark.
  • Soto Coral LJC; University Hospital of Schleswig-Holstein, Institute of Transfusion Medicine, Germany.
  • Gaviria García PA; Banc de Sang i Teixits de Catalunya, Spain.
  • Oota S; Instituto Distrital de Ciencia Biotecnología e Innovación en Salud - IDCBIS, Colombia.
  • O'Brien SF; Instituto Distrital de Ciencia Biotecnología e Innovación en Salud - IDCBIS, Colombia.
  • Wendel S; Instituto Distrital de Ciencia Biotecnología e Innovación en Salud - IDCBIS, Colombia.
  • Castro E; National Blood Centre, Thai Red Cross Society, Thailand.
  • Navarro Pérez L; Canadian Blood Services, Canada.
  • Harvala H; Hospital Sírio-Libanês Blood Bank, Brazil.
  • Davison K; Centro de Transfusión de la Comunidad Valenciana, Spain.
  • Reynolds C; Centro de Transfusión de la Comunidad Valenciana, Spain.
  • Jarvis L; Microbiology Services, NHS Blood and Transplant, UK.
  • Grabarczyk P; NHSBT/UKHSA Epidemiology Unit, UKHSA, UK.
  • Kopacz A; NHSBT/UKHSA Epidemiology Unit, NHS Blood and Transplant, UK.
  • Letowska M; Scottish National Blood Transfusion Service, UK.
  • O'Flaherty N; Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
  • Young F; Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
  • Williams P; Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
  • Burke L; Irish Blood Transfusion Service, Dublin, Ireland.
  • Chua SS; Irish Blood Transfusion Service, Dublin, Ireland.
  • Muylaert A; Irish Blood Transfusion Service, Dublin, Ireland.
  • Page I; Irish Blood Transfusion Service, Dublin, Ireland.
  • Jones A; Health Sciences Authority, Singapore.
  • Niederhauser C; Red Cross Flanders, Belgium.
  • Vermeulen M; Centro de Hemoterapia y Hemodonacion de Castilla y Leon, Spain.
  • Laperche S; Welsh Blood Service, UK.
  • Gallian P; Interregional Blood Transfusion SRC, Switzerland.
  • Satake M; Institute for Infectious Diseases, University of Berne, Berne, Switzerland.
  • Addas-Carvalho M; The South African National Blood Service, South Africa.
Vox Sang ; 119(7): 745-751, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38516962
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Nucleic acid-amplification testing (NAT) is used for screening blood donations/donors for blood-borne viruses. We reviewed global viral NAT characteristics and NAT-yield confirmatory testing used by blood operators. MATERIALS AND

METHODS:

NAT characteristics and NAT-yield confirmatory testing used during 2019 was surveyed internationally by the International Society of Blood Transfusion Working Party Transfusion-Transmitted Infectious Diseases. Reported characteristics are presented herein.

RESULTS:

NAT was mainly performed under government mandate. Human immunodeficiency virus (HIV), hepatitis C virus (HCV) and hepatitis B virus (HBV) NAT was performed on all donors and donation types, while selective testing was reported for West Nile virus, hepatitis E virus (HEV), and Zika virus. Individual donation NAT was used for HIV, HCV and HBV by ~50% of responders, while HEV was screened in mini-pools by 83% of responders performing HEV NAT. Confirmatory testing for NAT-yield samples was generally performed by NAT on a sample from the same donation or by NAT and serology on samples from the same donation and a follow-up sample.

CONCLUSION:

In the last decade, there has been a trend towards use of smaller pool sizes or individual donation NAT. We captured characteristics of NAT internationally in 2019 and provide insights into confirmatory testing approaches used for NAT-yields, potentially benefitting blood operators seeking to implement NAT.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Donors / Nucleic Acid Amplification Techniques Limits: Humans Language: En Journal: Vox Sang Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Blood Donors / Nucleic Acid Amplification Techniques Limits: Humans Language: En Journal: Vox Sang Year: 2024 Document type: Article Affiliation country:
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