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DC Field | Value | Language |
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dc.contributor.author | Yogendrakumar, Vignan | - |
dc.contributor.author | Beharry, James | - |
dc.contributor.author | Churilov, Leonid | - |
dc.contributor.author | Alidin, Khairunnisa | - |
dc.contributor.author | Ugalde, Melissa | - |
dc.contributor.author | Pesavento, Lauren | - |
dc.contributor.author | Weir, Louise | - |
dc.contributor.author | Mitchell, Peter J. | - |
dc.contributor.author | Kleinig, Timothy J. | - |
dc.contributor.author | Yassi, Nawaf | - |
dc.contributor.author | Thijs, Vincent | - |
dc.contributor.author | Wu, Teddy Y. | - |
dc.contributor.author | Shah, Darshan G.. | - |
dc.contributor.author | Dewey, Helen M. | - |
dc.contributor.author | Wijeratne, Tissa | - |
dc.contributor.author | Yan, Bernard | - |
dc.contributor.author | Desmond, Patricia M. | - |
dc.contributor.author | Sharma, Gagan | - |
dc.contributor.author | Parsons, Mark W. | - |
dc.contributor.author | Donnan, Geoffrey A. | - |
dc.contributor.author | Davis, Stephen M. | - |
dc.contributor.author | Campbell, Bruce C. V. | - |
dc.contributor.author | Royal Melbourne Stroke, Registry | - |
dc.contributor.author | EXTEND-IA TNK Collaborators | - |
dc.date.accessioned | 2023-04-24T02:44:23Z | - |
dc.date.available | 2023-04-24T02:44:23Z | - |
dc.date.issued | 2023-03 | - |
dc.identifier.uri | https://repository.southwesthealthcare.com.au/swhealthcarejspui/handle/1/3858 | - |
dc.description.abstract | OBJECTIVE: 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.isversionof | 20221130 | - |
dc.subject | Humans | - |
dc.subject | Tenecteplase | - |
dc.subject | Tissue Plasminogen Activator | - |
dc.subject | Brain Ischemia | - |
dc.subject | Stroke | - |
dc.subject | Fibrinolytic Agents | - |
dc.subject | Reperfusion | - |
dc.subject | Treatment Outcome | - |
dc.title | Tenecteplase Improves Reperfusion across Time in Large Vessel Stroke | - |
dc.type | Journal Article | - |
dc.identifier.journaltitle | Annals of Neurology | - |
dc.accession.number | 36394101 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pubmed/36394101 | - |
dc.description.affiliation | Department of Medicine and Neurology, Melbourne Brain Centre at the Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia. | - |
dc.description.affiliation | Department of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia. | - |
dc.description.affiliation | Department of Radiology, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia. | - |
dc.description.affiliation | Department of Neurology, Royal Adelaide Hospital, Adelaide, South Australia, Australia. | - |
dc.description.affiliation | Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia. | - |
dc.description.affiliation | Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Victoria, Australia. | - |
dc.description.affiliation | Department of Neurology, Christchurch Hospital, Christchurch, New Zealand. | - |
dc.description.affiliation | Department of Neurology, Princess Alexandra Hospital, Brisbane, Queensland, Australia. | - |
dc.description.affiliation | Eastern Health and Eastern Health Clinical School, Department of Neurosciences, Monash University, Clayton, Victoria, Australia. | - |
dc.description.affiliation | Melbourne Medical School, Department of Medicine and Neurology, University of Melbourne and Western Health, Sunshine Hospital, St Albans, Victoria, Australia. | - |
dc.description.affiliation | Department of Neurology, Liverpool Hospital, University of New South Wales, Sydney, New South Wales, Australia. | - |
dc.format.startpage | 489-499 | - |
dc.source.volume | 93 | - |
local.issue.number | 3 | - |
dc.identifier.importdoi | 10.1002/ana.26547 | - |
dc.identifier.date | 2023 | - |
Appears in Collections: | SWH Data Contributions |
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