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Gamma-Glutamyl Transferase (GGT) Is the Leading External Quality Assurance Predictor of ISO15189 Compliance for Pathology Laboratories

dc.contributor.authorLidbury, Brett
dc.contributor.authorKoerbin, Gus
dc.contributor.authorRichardson, Alice
dc.contributor.authorBadrick, Tony
dc.date.accessioned2023-03-07T00:15:43Z
dc.date.available2023-03-07T00:15:43Z
dc.date.issued2021
dc.date.updated2021-12-26T07:18:44Z
dc.description.abstractPathology results are central to modern medical practice, informing diagnosis and patient management. To ensure high standards from pathology laboratories, regulators require compliance with international and local standards. In Australia, the monitoring and regulation of medical laboratories are achieved by conformance to ISO15189-National Pathology Accreditation Advisory Council standards, as assessed by the National Association of Testing Authorities (NATA), and an external quality assurance (EQA) assessment via the Royal College of Pathologists of Australasia Quality Assurance Program (RCPAQAP). While effective individually, integration of data collected by NATA and EQA testing promises advantages for the early detection of technical or management problems in the laboratory, and enhanced ongoing quality assessment. Random forest (RF) machine learning (ML) previously identified gamma-glutamyl transferase (GGT) as a leading predictor of NATA compliance condition reporting. In addition to further RF investigations, this study also deployed single decision trees and support vector machines (SVM) models that included creatinine, electrolytes and liver function test (LFT) EQA results. Across all analyses, GGT was consistently the top-ranked predictor variable, validating previous observations from Australian laboratories. SVM revealed broad patterns of predictive EQA marker interactions with NATA outcomes, and the distribution of GGT relative deviation suggested patterns by which to identify other strong EQA predictors of NATA outcomes. An integrated model of pathology quality assessment was successfully developed, via the prediction of NATA outcomes by EQA results. GGT consistently ranked as the best predictor variable, identified by combining recursive partitioning and SVM ML strategies.en_AU
dc.description.sponsorshipThis research was funded by the Australian Commonwealth Department of Health Quality Use of Pathology program grant number No. 4-2UJWED1.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn2075-4418en_AU
dc.identifier.urihttp://hdl.handle.net/1885/286666
dc.language.isoen_AUen_AU
dc.provenanceThis article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).en_AU
dc.publisherMDPIen_AU
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland.en_AU
dc.rights.licenseCreative Commons Attribution Licenseen_AU
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_AU
dc.sourceDiagnosticsen_AU
dc.subjectISO 15189en_AU
dc.subjectexternal quality assuranceen_AU
dc.subjectpathologyen_AU
dc.subjectmachine learning and predictionen_AU
dc.titleGamma-Glutamyl Transferase (GGT) Is the Leading External Quality Assurance Predictor of ISO15189 Compliance for Pathology Laboratoriesen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue4en_AU
local.bibliographicCitation.lastpage22en_AU
local.bibliographicCitation.startpage1en_AU
local.contributor.affiliationLidbury, Brett, College of Health and Medicine, ANUen_AU
local.contributor.affiliationKoerbin, Gus, Faculty of Health, University of Canberraen_AU
local.contributor.affiliationRichardson, Alice, RSCH Research & Innovation Portfolio, ANUen_AU
local.contributor.affiliationBadrick, Tony, College of Health and Medicine, ANUen_AU
local.contributor.authoruidLidbury, Brett, u3756893en_AU
local.contributor.authoruidRichardson, Alice, u3767151en_AU
local.contributor.authoruidBadrick, Tony, u1005798en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor320200 - Clinical sciencesen_AU
local.identifier.ariespublicationa383154xPUB20376en_AU
local.identifier.citationvolume11en_AU
local.identifier.doi10.3390/diagnostics11040692en_AU
local.identifier.thomsonID000642980700001
local.publisher.urlhttps://www.mdpi.com/en_AU
local.type.statusPublished Versionen_AU

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