Clinical performance validation of the STANDARD G6PD test: A multi-country pooled analysis.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
10 2023
Historique:
received: 12 01 2023
accepted: 08 09 2023
revised: 24 10 2023
medline: 27 10 2023
pubmed: 12 10 2023
entrez: 12 10 2023
Statut: epublish

Résumé

Screening for G6PD deficiency can inform disease management including malaria. Treatment with the antimalarial drugs primaquine and tafenoquine can be guided by point-of-care testing for G6PD deficiency. Data from similar clinical studies evaluating the performance of the STANDARD G6PD Test (SD Biosensor, South Korea) conducted in Bangladesh, Brazil, Ethiopia, India, Thailand, the United Kingdom, and the United States were pooled. Test performance was assessed in a retrospective analysis on capillary and venous specimens. All study sites used spectrophotometry for reference G6PD testing, and either the HemoCue or complete blood count for reference hemoglobin measurement. The sensitivity of the STANDARD G6PD Test using the manufacturer thresholds for G6PD deficient and intermediate cases in capillary specimens from 4212 study participants was 100% (95% Confidence Interval (CI): 97.5%-100%) for G6PD deficient cases with <30% activity and 77% (95% CI 66.8%-85.4%) for females with intermediate activity between 30%-70%. Specificity was 98.1% (95% CI 97.6%-98.5%) and 92.8% (95% CI 91.6%-93.9%) for G6PD deficient individuals and intermediate females, respectively. Out of 20 G6PD intermediate females with false normal results, 12 had activity levels >60% on the reference assay. The negative predictive value for females with G6PD activity >60% was 99.6% (95% CI 99.1%-99.8%) on capillary specimens. Sensitivity among 396 P. vivax malaria cases was 100% (69.2%-100.0%) for both deficient and intermediate cases. Across the full dataset, 37% of those classified as G6PD deficient or intermediate resulted from true normal cases. Despite this, over 95% of cases would receive correct treatment with primaquine, over 87% of cases would receive correct treatment with tafenoquine, and no true G6PD deficient cases would be treated inappropriately based on the result of the STANDARD G6PD Test. The STANDARD G6PD Test enables safe access to drugs which are contraindicated for individuals with G6PD deficiency. Operational considerations will inform test uptake in specific settings.

Identifiants

pubmed: 37824592
doi: 10.1371/journal.pntd.0011652
pii: PNTD-D-23-00056
pmc: PMC10597494
doi:

Substances chimiques

Primaquine MVR3634GX1
Antimalarials 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0011652

Informations de copyright

Copyright: © 2023 Adissu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Wondimagegn Adissu (W)

School of Medical Laboratory Sciences, Jimma University, Jimma, Ethiopia.
Clinical Trial Unit, Jimma University, Jimma, Ethiopia.

Marcelo Brito (M)

Fundação de Medicina Tropical Dr Heitor Vieira Dourado (FMT-HVD), Manaus, Amazonas, Brazil.
Universidade do Estado do Amazonas, Manaus, Amazonas, Brazil.

Eduardo Garbin (E)

Centro de Pesquisa Em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.

Marcela Macedo (M)

Centro de Pesquisa Em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.

Wuelton Monteiro (W)

Fundação de Medicina Tropical Dr Heitor Vieira Dourado (FMT-HVD), Manaus, Amazonas, Brazil.
Universidade do Estado do Amazonas, Manaus, Amazonas, Brazil.

Sandip Kumar Mukherjee (SK)

National Institute of Cholera and Enteric Diseases, Kolkata, India.

Jane Myburg (J)

Special Haematology Laboratory, Hammersmith Hospital, London, United Kingdom.

Mohammad Shafiul Alam (MS)

Infectious Diseases Division, International Centre for Diarrheal Diseases Research, Bangladesh (icddr,b), Mohakhali, Dhaka, Bangladesh.

Germana Bancone (G)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

Pooja Bansil (P)

Diagnostics, PATH, Seattle, Washington, United States of America.

Sampa Pal (S)

Diagnostics, PATH, Seattle, Washington, United States of America.

Abhijit Sharma (A)

Diagnostics, PATH, Seattle, Washington, United States of America.

Stephanie Zobrist (S)

Diagnostics, PATH, Seattle, Washington, United States of America.

Andrew Bryan (A)

Departments of Laboratory Medicine and Microbiology, University of Washington School of Medicine, Seattle, Washington, United States of America.

Cindy S Chu (CS)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

Santasabuj Das (S)

National Institute of Cholera and Enteric Diseases, Kolkata, India.

Gonzalo J Domingo (GJ)

Diagnostics, PATH, Seattle, Washington, United States of America.

Amanda Hann (A)

Special Haematology Laboratory, Hammersmith Hospital, London, United Kingdom.

James Kublin (J)

Departments of Laboratory Medicine and Microbiology, University of Washington School of Medicine, Seattle, Washington, United States of America.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.

Marcus V G Lacerda (MVG)

Fundação de Medicina Tropical Dr Heitor Vieira Dourado (FMT-HVD), Manaus, Amazonas, Brazil.
Universidade do Estado do Amazonas, Manaus, Amazonas, Brazil.
Instituto Leônidas & Maria Deane (ILMD), Fiocruz, Manaus, Amazonas, Brazil.

Mark Layton (M)

Special Haematology Laboratory, Hammersmith Hospital, London, United Kingdom.

Benedikt Ley (B)

Global and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Australia.

Sean C Murphy (SC)

Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, United States of America.
Center for Emerging and Reemerging Infectious Diseases, University of Washington, Seattle, Washington, United States of America.

Francois Nosten (F)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.

Dhélio Pereira (D)

Centro de Pesquisa Em Medicina Tropical (CEPEM), Porto Velho, Rondônia, Brazil.
Universidade Federal de Rondônia (UNIR), Porto Velho, Rondônia, Brazil.

Ric N Price (RN)

Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Global and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Australia.

Arunansu Talukdar (A)

Kolkata Medical College Hospital, India.

Daniel Yilma (D)

Clinical Trial Unit, Jimma University, Jimma, Ethiopia.
Department of Internal Medicine, Jimma University, Jimma, Ethiopia.

Emily Gerth-Guyette (E)

Diagnostics, PATH, Seattle, Washington, United States of America.

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