Please use this identifier to cite or link to this item: https://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/3858
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dc.contributor.authorYogendrakumar, Vignan-
dc.contributor.authorBeharry, James-
dc.contributor.authorChurilov, Leonid-
dc.contributor.authorAlidin, Khairunnisa-
dc.contributor.authorUgalde, Melissa-
dc.contributor.authorPesavento, Lauren-
dc.contributor.authorWeir, Louise-
dc.contributor.authorMitchell, Peter J.-
dc.contributor.authorKleinig, Timothy J.-
dc.contributor.authorYassi, Nawaf-
dc.contributor.authorThijs, Vincent-
dc.contributor.authorWu, Teddy Y.-
dc.contributor.authorShah, Darshan G..-
dc.contributor.authorDewey, Helen M.-
dc.contributor.authorWijeratne, Tissa-
dc.contributor.authorYan, Bernard-
dc.contributor.authorDesmond, Patricia M.-
dc.contributor.authorSharma, Gagan-
dc.contributor.authorParsons, Mark W.-
dc.contributor.authorDonnan, Geoffrey A.-
dc.contributor.authorDavis, Stephen M.-
dc.contributor.authorCampbell, Bruce C. V.-
dc.contributor.authorRoyal Melbourne Stroke, Registry-
dc.contributor.authorEXTEND-IA TNK Collaborators-
dc.date.accessioned2023-04-24T02:44:23Z-
dc.date.available2023-04-24T02:44:23Z-
dc.date.issued2023-03-
dc.identifier.urihttps://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/3858-
dc.description.abstractOBJECTIVE: Tenecteplase improves reperfusion compared to alteplase in patients with large vessel occlusions. To determine whether this improvement varies across the spectrum of thrombolytic agent to reperfusion assessment times, we performed a comparative analysis of tenecteplase and alteplase reperfusion rates. METHODS: Patients with large vessel occlusion and treatment with thrombolysis were pooled from the Melbourne Stroke Registry, and the EXTEND-IA and EXTEND-IA TNK trials. The primary outcome, thrombolytic-induced reperfusion, was defined as the absence of retrievable thrombus or >50% reperfusion at imaging reassessment. We compared the treatment effect of tenecteplase and alteplase, accounting for thrombolytic to assessment exposure times, via Poisson modeling. We compared 90-day outcomes of patients who achieved reperfusion with a thrombolytic to patients who achieved reperfusion via endovascular therapy using ordinal logistic regression. RESULTS: Among 893 patients included in the primary analysis, thrombolytic-induced reperfusion was observed in 184 (21%) patients. Tenecteplase was associated with higher rates of reperfusion (adjusted incidence rate ratio [aIRR] = 1.50, 95% confidence interval [CI] = 1.09-2.07, p = 0.01). Findings were consistent in patient subgroups with first segment (aIRR = 1.41, 95% CI = 0.93-2.14) and second segment (aIRR = 2.07, 95% CI = 0.98-4.37) middle cerebral artery occlusions. Increased thrombolytic to reperfusion assessment times were associated with reperfusion (tenecteplase: adjusted risk ratio [aRR] = 1.08 per 15 minutes, 95% CI = 1.04-1.13 vs alteplase: aRR = 1.06 per 15 minutes, 95% CI = 1.00-1.13). No significant treatment-by-time interaction was observed (p = 0.87). Reperfusion via thrombolysis was associated with improved 90-day modified Rankin Scale scores (adjusted common odds ratio = 2.15, 95% CI = 1.54-3.01) compared to patients who achieved reperfusion following endovascular therapy. INTERPRETATION: Tenecteplase, compared to alteplase, increases prethrombectomy reperfusion, regardless of the time from administration to reperfusion assessment. Prethrombectomy reperfusion is associated with better clinical outcomes. ANN NEUROL 2023;93:489-499.-
dc.relation.isversionof20221130-
dc.subjectHumans-
dc.subjectTenecteplase-
dc.subjectTissue Plasminogen Activator-
dc.subjectBrain Ischemia-
dc.subjectStroke-
dc.subjectFibrinolytic Agents-
dc.subjectReperfusion-
dc.subjectTreatment Outcome-
dc.titleTenecteplase Improves Reperfusion across Time in Large Vessel Stroke-
dc.typeJournal Article-
dc.identifier.journaltitleAnnals of Neurology-
dc.accession.number36394101-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pubmed/36394101-
dc.description.affiliationDepartment of Medicine and Neurology, Melbourne Brain Centre at the Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.-
dc.description.affiliationDepartment of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.-
dc.description.affiliationDepartment of Radiology, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.-
dc.description.affiliationDepartment of Neurology, Royal Adelaide Hospital, Adelaide, South Australia, Australia.-
dc.description.affiliationPopulation Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.-
dc.description.affiliationFlorey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia.-
dc.description.affiliationDepartment of Neurology, Christchurch Hospital, Christchurch, New Zealand.-
dc.description.affiliationDepartment of Neurology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.-
dc.description.affiliationEastern Health and Eastern Health Clinical School, Department of Neurosciences, Monash University, Clayton, Victoria, Australia.-
dc.description.affiliationMelbourne Medical School, Department of Medicine and Neurology, University of Melbourne and Western Health, Sunshine Hospital, St Albans, Victoria, Australia.-
dc.description.affiliationDepartment of Neurology, Liverpool Hospital, University of New South Wales, Sydney, New South Wales, Australia.-
dc.format.startpage489-499-
dc.source.volume93-
local.issue.number3-
dc.identifier.importdoi10.1002/ana.26547-
dc.identifier.date2023-
Appears in Collections:SWH Data Contributions

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