Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11314
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dc.contributor.authorHo, Wai Khoonen
dc.contributor.authorHankey, Graeme Jen
dc.contributor.authorEikelboom, John Wen
dc.date.accessioned2015-05-16T00:54:13Z
dc.date.available2015-05-16T00:54:13Z
dc.date.issued2011-08-01en
dc.identifier.citationMedical Journal of Australia; 195(3): 139-42en
dc.identifier.govdoc21806532en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/11314en
dc.description.abstractThe clinical usefulness of laboratory testing of adult patients with venous thromboembolism (VTE) for heritable thrombophilia needs to be critically evaluated. At present, some clinicians use testing to identify patients at higher risk of recurrence (who may benefit from an extended period of anticoagulation beyond the usual 3-6 months) and their relatives at risk of a first VTE episode. As prevalence of heritable thrombophilia is related to age and ethnic origin, the pretest probability of detecting heritable thrombophilia may be low in unselected populations. Interpretation of laboratory results may not be straightforward. Apparent deficiencies of a natural anticoagulant may be due to acute thrombosis and "consumption", concomitant therapy with heparin and/or warfarin and other clinical factors. The predictive value of recurrent VTE conferred by the most common types of heritable thrombophilia (factor V Leiden and the G20210A prothrombin mutation) is limited. Risk of recurrence associated with deficiencies of a natural anticoagulant is less certain due to their rarity. Clinical risk factors (eg, the presence or otherwise of provoking factor(s) and whether or not the risk factor for VTE is reversible or permanent) appear to be the most important predictors of VTE recurrence. Duration of anticoagulation should be determined by clinical risk factors rather than the presence, or otherwise, of heritable thrombophilia. The benefit of identifying relatives who are carriers of thrombophilia is uncertain, as VTE is a multifactorial disease resulting from the interaction of various risk factors, some well recognised and others as yet unknown.en
dc.language.isoenen
dc.subject.otherAdulten
dc.subject.otherAnticoagulants.therapeutic useen
dc.subject.otherCost-Benefit Analysisen
dc.subject.otherFibrin Fibrinogen Degradation Products.analysisen
dc.subject.otherGenetic Testingen
dc.subject.otherHumansen
dc.subject.otherPrognosisen
dc.subject.otherProtein C.analysisen
dc.subject.otherProtein S.analysisen
dc.subject.otherReference Valuesen
dc.subject.otherRisk Factorsen
dc.subject.otherSecondary Preventionen
dc.subject.otherThrombophilia.diagnosisen
dc.subject.otherVenous Thromboembolism.prevention & controlen
dc.titleShould adult patients be routinely tested for heritable thrombophilia after an episode of venous thromboembolism?en
dc.typeJournal Articleen
dc.identifier.journaltitleMedical Journal of Australiaen
dc.identifier.affiliationDepartment of Haematology, Austin Health, Heidelberg, Victoria, Australia, Australiaen
dc.description.pages139-42en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/21806532en
dc.type.austinJournal Articleen
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
crisitem.author.deptPathology-
crisitem.author.deptLaboratory Haematology-
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