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

dc.contributor.authorAdissu W.
dc.contributor.authorBrito M.
dc.contributor.authorGarbin E.
dc.contributor.authorMacedo M.
dc.contributor.authorMonteiro W.
dc.contributor.authorMukherjee S.K.
dc.contributor.authorMyburg J.
dc.contributor.authorAlam M.S.
dc.contributor.authorBancone G.
dc.contributor.authorBansil P.
dc.contributor.authorPal S.
dc.contributor.authorSharma A.
dc.contributor.authorZobrist S.
dc.contributor.authorBryan A.
dc.contributor.authorChu C.S.
dc.contributor.authorDas S.
dc.contributor.authorDomingo G.J.
dc.contributor.authorHann A.
dc.contributor.authorKublin J.
dc.contributor.authorLacerda M.V.G.
dc.contributor.authorLayton M.
dc.contributor.authorLey B.
dc.contributor.authorMurphy S.C.
dc.contributor.authorNosten F.
dc.contributor.authorPereira D.
dc.contributor.authorPrice R.N.
dc.contributor.authorTalukdar A.
dc.contributor.authorYilma D.
dc.contributor.authorGerthguyette E.
dc.contributor.otherMahidol University
dc.date.accessioned2023-11-07T18:02:17Z
dc.date.available2023-11-07T18:02:17Z
dc.date.issued2023-10-01
dc.description.abstractINTRODUCTION: 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. METHODS AND FINDINGS: 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. CONCLUSIONS: 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.
dc.identifier.citationPLoS neglected tropical diseases Vol.17 No.10 (2023) , e0011652
dc.identifier.doi10.1371/journal.pntd.0011652
dc.identifier.eissn19352735
dc.identifier.pmid37824592
dc.identifier.scopus2-s2.0-85175269763
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/90967
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleClinical performance validation of the STANDARD G6PD test: A multi-country pooled analysis
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85175269763&origin=inward
oaire.citation.issue10
oaire.citation.titlePLoS neglected tropical diseases
oaire.citation.volume17
oairecerif.author.affiliationMahidol Oxford Tropical Medicine Research Unit
oairecerif.author.affiliationJimma University
oairecerif.author.affiliationFundacao de Medicina Tropical do Amazonas
oairecerif.author.affiliationPATH Seattle
oairecerif.author.affiliationUniversity of Washington School of Medicine
oairecerif.author.affiliationMenzies School of Health Research
oairecerif.author.affiliationFundacao Universidade Federal de Rondonia
oairecerif.author.affiliationHammersmith Hospital
oairecerif.author.affiliationFiocruz Amazônia
oairecerif.author.affiliationUniversity of Washington
oairecerif.author.affiliationInternational Centre for Diarrhoeal Disease Research Bangladesh
oairecerif.author.affiliationNuffield Department of Medicine
oairecerif.author.affiliationNational Institute of Cholera and Enteric Diseases India
oairecerif.author.affiliationMedical College and Hospital Kolkata
oairecerif.author.affiliationFred Hutchinson Cancer Research Center
oairecerif.author.affiliationUniversidade do Estado do Amazonas
oairecerif.author.affiliationCentro de Pesquisa em Medicina Tropical (CEPEM)

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