Evaluation of Classical and Modified Mixing Tests: Optimized Interpretation and a Structured Algorithm for Accurate Differentiation of the Causes of aPTT Prolongation

dc.contributor.authorPolice P.
dc.contributor.authorNoikongdee P.
dc.contributor.authorPhojanasenee T.
dc.contributor.authorApipongrat D.
dc.contributor.correspondencePolice P.
dc.contributor.otherMahidol University
dc.date.accessioned2026-02-09T18:27:32Z
dc.date.available2026-02-09T18:27:32Z
dc.date.issued2026-01-01
dc.description.abstractBackground: The activated partial thromboplastin time (aPTT) mixing test is widely used to investigate prolonged aPTT from factor deficiencies, inhibitors, or lupus anticoagulant (LA), but its interpretation remains challenging. Refining protocols and indices may improve accuracy. Objectives: To compare classical and modified aPTT mixing tests using conventional and novel indices for distinguishing FVIII deficiency, FVIII inhibitors, LA, and heparin, and to develop a structured interpretation algorithm. Methods: A total of 215 plasma samples (50 factor deficiencies, 51 FVIII inhibitors, 64 LA-positive, 50 heparinized) underwent classical and modified 1:1 mixing tests. ICA and %Correction were calculated for immediate and 2-h incubated mixes, while ΔICA and Δ%Correction were derived from their differences. Diagnostic performance was assessed by ROC analysis, and a proposed algorithm was designed. Results: Both protocols demonstrated excellent reliability (ICC > 0.90) and substantial agreement in interpretation (κ = 0.65–0.75). The modified protocol consistently outperformed the classical approach, with index of circulating anticoagulant (ICA)-based indices showing the greatest improvement. Novel indices ΔICA and Δ%Correction further enhanced diagnostic specificity compared with single indices. ΔICA achieved the highest performance, with near-perfect accuracy in distinguishing factor deficiency from FVIII inhibitors and FVIII inhibitors from LA (AUC = 0.99 for both). The algorithm applying ΔICA after ICA of the immediate mix effectively separated factor deficiencies, FVIII inhibitors, and LA with high sensitivity and specificity, minimizing diagnostic overlap. Conclusions: The modified aPTT mixing test provides a reliable and practical approach for interpreting prolonged aPTT. The structured algorithm, combining the modified protocol with ΔICA, offers a systematic and clinically applicable framework for laboratory evaluation.
dc.identifier.citationInternational Journal of Laboratory Hematology (2026)
dc.identifier.doi10.1111/ijlh.70064
dc.identifier.eissn1751553X
dc.identifier.issn17515521
dc.identifier.scopus2-s2.0-105029067591
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/114918
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.subjectMedicine
dc.titleEvaluation of Classical and Modified Mixing Tests: Optimized Interpretation and a Structured Algorithm for Accurate Differentiation of the Causes of aPTT Prolongation
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105029067591&origin=inward
oaire.citation.titleInternational Journal of Laboratory Hematology
oairecerif.author.affiliationRamathibodi Hospital
oairecerif.author.affiliationPhramongkutklao College of Medicine

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