Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3111
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dc.contributor.authorAghighi, S.en
dc.contributor.authorBrown, S. A.en
dc.contributor.authorLee, C. A.en
dc.contributor.authorRiddell, A.en
dc.contributor.authorChowdary, P.en
dc.contributor.authorTuddenham, E.en
dc.date.accessioned2022-11-07T23:38:48Z-
dc.date.available2022-11-07T23:38:48Z-
dc.date.issued2020en
dc.identifier.citation4, (2), 2020, p. 298-308en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/3111-
dc.description.abstractBackground: Global assays measure the interactions of coagulants, anticoagulants, and platelets on thrombin generation and may reflect the comprehensive coagulation potential in patients with hemophilia better than conventional assays. Objectives: The objectives of the current study were to investigate the value of global assays for measuring and monitoring the coagulation potential of patients with hemophilia A (HA). Patients/Methods: Rotational thromboelastometry, thrombin generation assay (TGA), and activated partial thromboplastin time (APTT) clot waveform analysis were investigated in a cohort of patients with severe, moderate, and mild HA and compared with conventional assays. Results: The maximum velocity (MaxVel) parameter of modified thromboelastometry analysis, initiated by tissue factor and in the presence of corn trypsin inhibitor (CTI), had 92% sensitivity and 95% specificity for hemophilia diagnosis. The MaxVel also strongly correlated with factor VIII (FVIII) levels of patients with HA (r =.805, P <.0001). CTI improved the sensitivity of TGA, providing more accurate results. In particular, peak height parameter of platelet-rich plasma samples with CTI had a sensitivity and specificity of 100% and 94%, respectively, in all patients with HA. APTT clot waveform analysis minimum value of first derivative (Min1) and minimum value of second derivative (Min2) parameters (representing speed and acceleration of clot formation, respectively) were sensitive and correlated more strongly with FVIII levels than APTT clotting times did (Min1: r = 0.786, P < 0.0001; Min2: r = 0.759, P < 0.0001; APTT: r = −0.513, P = 0.001). Conclusions: The sensitivity and specificity of the global assays was method dependent. Correlation between clinical end points and thrombin generation might also be valuable in the era of non–factor replacement therapy.L20040519852020-01-20 <br />2020-03-04 <br />en
dc.language.isoenen
dc.relation.ispartofResearch and Practice in Thrombosis and Haemostasisen
dc.titleGlobal coagulation assays in hemophilia A: A comparison to conventional assaysen
dc.typeArticleen
dc.identifier.doi10.1002/rth2.12295en
dc.subject.keywordsthromboplastinen
dc.subject.keywordstrypsin inhibitoren
dc.subject.keywordsactivated partial thromboplastin timeen
dc.subject.keywordsadolescenten
dc.subject.keywordsarea under the curveen
dc.subject.keywordsarticleen
dc.subject.keywordsassayen
dc.subject.keywordsbioassayen
dc.subject.keywordsblood clottingen
dc.subject.keywordsblood clotting timeen
dc.subject.keywordscomparative studyen
dc.subject.keywordscontrolled studyen
dc.subject.keywordsconventional assayen
dc.subject.keywordsdiagnostic test accuracy studyen
dc.subject.keywordshemophilia Aen
dc.subject.keywordshumanen
dc.subject.keywordsmajor clinical studyen
dc.subject.keywordsmaleen
dc.subject.keywordsmaximum reaction velocityen
dc.subject.keywordsnormal humanen
dc.subject.keywordspriority journalen
dc.subject.keywordsreceiver operating characteristicen
dc.subject.keywordsrisk factoren
dc.subject.keywordssensitivity and specificityen
dc.subject.keywordsthrombin generation assayen
dc.subject.keywordsthrombin timeen
dc.subject.keywordsthrombocyte rich plasmaen
dc.subject.keywordsthromboelastometryen
dc.subject.keywordsROTEMen
dc.subject.keywordsblood clotting factor 8en
dc.subject.keywordsthromboelastographen
dc.subject.keywordsS Monovette tubeen
dc.subject.keywordsblood collection tubecoagulometeren
dc.subject.keywordsprocoagulanten
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L2004051985&from=exporthttp://dx.doi.org/10.1002/rth2.12295 |en
dc.identifier.risid1372en
dc.description.pages298-308en
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Sites:Children's Health Queensland Publications
Queensland Health Publications
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