Publication:
Diagnostic performances of the fluorescent spot test for G6PD deficiency in newborns along the Thailand-Myanmar border: A cohort study [version 1; referees: 2 approved]

dc.contributor.authorLaurence Thielemansen_US
dc.contributor.authorGornpan Gornsawunen_US
dc.contributor.authorBorimas Hanboonkunupakarnen_US
dc.contributor.authorMoo Kho Pawen_US
dc.contributor.authorPen Pornen_US
dc.contributor.authorPaw Khu Mooen_US
dc.contributor.authorBart Van Overmeireen_US
dc.contributor.authorStephane Prouxen_US
dc.contributor.authorFrançois Nostenen_US
dc.contributor.authorRose McGreadyen_US
dc.contributor.authorVerena I. Carraraen_US
dc.contributor.authorGermana Banconeen_US
dc.contributor.otherHospital Erasmeen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.date.accessioned2019-08-23T10:41:28Z
dc.date.available2019-08-23T10:41:28Z
dc.date.issued2018-01-01en_US
dc.description.abstract© 2018 Thielemans L et al. Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an inherited enzymatic disorder associated with severe neonatal hyperbilirubinemia and acute haemolysis after exposure to certain drugs or infections. The disorder can be diagnosed phenotypically with a fluorescent spot test (FST), which is a simple test that requires training and basic laboratory equipment. This study aimed to assess the diagnostic performances of the FST used on umbilical cord blood by locally-trained staff and to compare test results of the neonates at birth with the results after one month of age. Methods: We conducted a cohort study on newborns at the Shoklo Malaria Research Unit, along the Thai-Myanmar border between January 2015 and May 2016. The FST was performed at birth on the umbilical cord blood by locally-trained staff and quality controlled by specialised technicians at the central laboratory. The FST was repeated after one month of age. Genotyping for common local G6PD mutations was carried out for all discrepant results. Results: FST was performed on 1521 umbilical cord blood samples. Quality control and genotyping revealed 10 misdiagnoses. After quality control, 10.7% of the males (84/786) and 1.2% of the females (9/735) were phenotypically G6PD deficient at birth. The FST repeated at one month of age or later diagnosed 8 additional G6PD deficient infants who were phenotypically normal at birth. Conclusions: This study shows the short-comings of the G6PD FST in neonatal routine screening and highlights the importance of training and quality control. A more conservative interpretation of the FST in male newborns could increase the diagnostic performances. Quantitative point-of-care tests might show higher sensitivity and specificity for diagnosis of G6PD deficiency on umbilical cord blood and should be investigated.en_US
dc.identifier.citationWellcome Open Research. Vol.3, (2018)en_US
dc.identifier.doi10.12688/wellcomeopenres.13373.1en_US
dc.identifier.issn2398502Xen_US
dc.identifier.other2-s2.0-85045531693en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/45331
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85045531693&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleDiagnostic performances of the fluorescent spot test for G6PD deficiency in newborns along the Thailand-Myanmar border: A cohort study [version 1; referees: 2 approved]en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85045531693&origin=inwarden_US

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