Publication:
Laboratory validation and field usability assessment of a point-of-care test for serum bilirubin levels in neonates in a tropical setting [version 2; referees: 3 approved]

dc.contributor.authorLaurence Thielemansen_US
dc.contributor.authorAhmar Hashmien_US
dc.contributor.authorDah Dah Priscillaen_US
dc.contributor.authorMoo Kho Pawen_US
dc.contributor.authorTekel Pimolsorntongen_US
dc.contributor.authorThatsanun Ngersengen_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.accessioned2019-08-23T10:41:17Z
dc.date.available2019-08-23T10:41:17Z
dc.date.issued2018-01-01en_US
dc.description.abstract© 2018 Thielemans L et al. Background: Screening and monitoring serum bilirubin (SBR) in neonates is crucial to prevent neonatal hyperbilirubinemia (NH)-associated morbidity and mortality worldwide. A lack of resources is often a barrier for measuring SBR in developing countries. Reliable, cost-effective, easy to use point-of-care (POC) SBR tests are needed. This study aimed to evaluate the technical accuracy and usability of the Bilistick System (BS), a new bilirubin POC test, in a tropical setting. Methods: This was a mixed-methods study, including laboratory validation of the BS, direct observation of technical procedures as performed by the midwives and midwives’ assessment of the device’s easiness of use through focus group discussions (FGD) and a self-administered questionnaire. The study was conducted in a field clinic of the Shoklo Malaria Research Unit along the Thailand-Myanmar border between January and December 2017. Results: A total of 173 samples were tested at a median age of 4 days. BS generated an error message—providing no SBR readout—in 48.6% of the tests performed. For the tests that yielded a result, the correlation coefficient (95% CI) between BS and routine laboratory bilirubinometer SBR was 0.87 (0.77-0.93). The accuracy decreased with increasing haematocrit and at higher humidity (≥75%). Direct observation of the operators using the device and analysis of the focus group discussions and questionnaires indicated that the BS was considered easy to use and required limited training. Conclusions: This evaluation showed that the BS, in its current formulation, does not provide reliable results for measuring SBR in a tropical, low-resource setting but has acceptable usability features.en_US
dc.identifier.citationWellcome Open Research. Vol.3, (2018)en_US
dc.identifier.doi10.12688/wellcomeopenres.14767.2en_US
dc.identifier.issn2398502Xen_US
dc.identifier.other2-s2.0-85060954983en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/45328
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060954983&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleLaboratory validation and field usability assessment of a point-of-care test for serum bilirubin levels in neonates in a tropical setting [version 2; referees: 3 approved]en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85060954983&origin=inwarden_US

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