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Safety and Efficacy of Tenecteplase Compared With Alteplase in Patients With Large Vessel Occlusion Stroke: A Prespecified Secondary Analysis of the ACT Randomized Clinical Trial.
Bala, Fouzi; Singh, Nishita; Buck, Brian; Ademola, Ayoola; Coutts, Shelagh B; Deschaintre, Yan; Khosravani, Houman; Appireddy, Ramana; Moreau, Francois; Phillips, Stephen; Gubitz, Gord; Tkach, Aleksander; Catanese, Luciana; Dowlatshahi, Dar; Medvedev, George; Mandzia, Jennifer; Pikula, Aleksandra; Shankar, Jai Jai; Williams, Heather; Field, Thalia S; Manosalva Alzate, Alejandro; Siddiqui, Muzaffar; Zafar, Atif; Imoukhoude, Oje; Hunter, Gary; Alhabli, Ibrahim; Benali, Faysal; Horn, MacKenzie; Hill, Michael D; Shamy, Michel; Sajobi, Tolulope T; Swartz, Richard H; Menon, Bijoy K; Almekhlafi, Mohammed.
Afiliação
  • Bala F; Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Singh N; Diagnostic and Interventional Neuroradiology Department, University Hospital of Tours, Tours, France.
  • Buck B; Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Ademola A; Department of Internal Medicine, Neurology Division, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Coutts SB; Division of Neurology, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
  • Deschaintre Y; Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Khosravani H; Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.
  • Appireddy R; Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Moreau F; Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.
  • Phillips S; Department of Radiology, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Gubitz G; Hotchkiss Brain Institute, Calgary, Alberta, Canada.
  • Tkach A; Department of Neurosciences, Université de Montréal, Montréal, Québec, Canada.
  • Catanese L; Centre Hospitalier de l'Université de Montréal (CHUM), Montréal, Québec, Canada.
  • Dowlatshahi D; Sunnybrook Health Sciences Centre and the University of Toronto, Toronto, Ontario, Canada.
  • Medvedev G; Division of Neurology, Department of Medicine, Queen's University, Kingston, Ontario, Canada.
  • Mandzia J; Université de Sherbrooke, Sherbrooke, Québec, Canada.
  • Pikula A; Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.
  • Shankar JJ; Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.
  • Williams H; Kelowna General Hospital, Kelowna, British Columbia, Canada.
  • Field TS; Hamilton Health Sciences Centre and McMaster University, Hamilton, Ontario, Canada.
  • Manosalva Alzate A; Department of Medicine, University of Ottawa, and the Ottawa Heart Research Institute, Ottawa, Ontario, Canada.
  • Siddiqui M; University of British Columbia and the Fraser Health Authority, New Westminster, British Columbia, Canada.
  • Zafar A; London Health Sciences Centre and Western University, London, Ontario, Canada.
  • Imoukhoude O; Toronto Western Hospital and the University of Toronto, Toronto, Ontario, Canada.
  • Hunter G; Department of Radiology, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Alhabli I; Queen Elizabeth Hospital, Charlottetown, Prince Edward Island, Canada.
  • Benali F; Vancouver Stroke Program and the Division of Neurology, University of British Columbia, Vancouver, British Columbia, Canada.
  • Horn M; Medicine Hat Regional Hospital, Medicine Hat, Alberta, Canada.
  • Hill MD; Grey Nuns Community Hospital, Edmonton, Alberta, Canada.
  • Shamy M; St Michael's Hospital, Toronto, Ontario, Canada.
  • Sajobi TT; Red Deer Regional Hospital, Red Deer, Alberta, Canada.
  • Swartz RH; Division of Neurology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
  • Menon BK; Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Almekhlafi M; Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
JAMA Neurol ; 80(8): 824-832, 2023 08 01.
Article em En | MEDLINE | ID: mdl-37428494
Importance: It is unknown whether intravenous thrombolysis using tenecteplase is noninferior or preferable compared with alteplase for patients with acute ischemic stroke. Objective: To examine the safety and efficacy of tenecteplase compared to alteplase among patients with large vessel occlusion (LVO) stroke. Design, Setting, and Participants: This was a prespecified analysis of the Intravenous Tenecteplase Compared With Alteplase for Acute Ischaemic Stroke in Canada (ACT) randomized clinical trial that enrolled patients from 22 primary and comprehensive stroke centers across Canada between December 10, 2019, and January 25, 2022. Patients 18 years and older with a disabling ischemic stroke within 4.5 hours of symptom onset were randomly assigned (1:1) to either intravenous tenecteplase or alteplase and were monitored for up to 120 days. Patients with baseline intracranial internal carotid artery (ICA), M1-middle cerebral artery (MCA), M2-MCA, and basilar occlusions were included in this analysis. A total of 1600 patients were enrolled, and 23 withdrew consent. Exposures: Intravenous tenecteplase (0.25 mg/kg) vs intravenous alteplase (0.9 mg/kg). Main Outcomes and Measures: The primary outcome was the proportion of modified Rankin scale (mRS) score 0-1 at 90 days. Secondary outcomes were an mRS score from 0 to 2, mortality, and symptomatic intracerebral hemorrhage. Angiographic outcomes were successful reperfusion (extended Thrombolysis in Cerebral Infarction scale score 2b-3) on first and final angiographic acquisitions. Multivariable analyses (adjusting for age, sex, National Institute of Health Stroke Scale score, onset-to-needle time, and occlusion location) were carried out. Results: Among 1577 patients, 520 (33.0%) had LVO (median [IQR] age, 74 [64-83] years; 283 [54.4%] women): 135 (26.0%) with ICA occlusion, 237 (45.6%) with M1-MCA, 117 (22.5%) with M2-MCA, and 31 (6.0%) with basilar occlusions. The primary outcome (mRS score 0-1) was achieved in 86 participants (32.7%) in the tenecteplase group vs 76 (29.6%) in the alteplase group. Rates of mRS 0-2 (129 [49.0%] vs 131 [51.0%]), symptomatic intracerebral hemorrhage (16 [6.1%] vs 11 [4.3%]), and mortality (19.9% vs 18.1%) were similar in the tenecteplase and alteplase groups, respectively. No difference was noted in successful reperfusion rates in the first (19 [9.2%] vs 21 [10.5%]) and final angiogram (174 [84.5%] vs 177 [88.9%]) among 405 patients who underwent thrombectomy. Conclusions and Relevance: The findings in this study indicate that intravenous tenecteplase conferred similar reperfusion, safety, and functional outcomes compared to alteplase among patients with LVO.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arteriopatias Oclusivas / Isquemia Encefálica / Acidente Vascular Cerebral / AVC Isquêmico Tipo de estudo: Clinical_trials Limite: Aged / Female / Humans / Male Idioma: En Revista: JAMA Neurol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arteriopatias Oclusivas / Isquemia Encefálica / Acidente Vascular Cerebral / AVC Isquêmico Tipo de estudo: Clinical_trials Limite: Aged / Female / Humans / Male Idioma: En Revista: JAMA Neurol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá