Sex-Based Analysis of Workflow and Outcomes in Acute Ischemic Stroke Patients Treated With Alteplase Versus Tenecteplase.

embolic stroke fibrinolysis postmenopause sex characteristics tenecteplase

Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
04 Jan 2024
Historique:
medline: 4 1 2024
pubmed: 4 1 2024
entrez: 4 1 2024
Statut: aheadofprint

Résumé

Understanding sex differences in stroke care is important in reducing potential disparities. Our objective was to explore sex differences in workflow efficiency, treatment efficacy, and safety in the AcT trial (Alteplase Compared to Tenecteplase). AcT was a multicenter, registry-linked randomized noninferiority trial comparing tenecteplase (0.25 mg/kg) with alteplase (0.9 mg/kg) in acute ischemic stroke within 4.5 hours of onset. In this post hoc analysis, baseline characteristics, workflow times, successful reperfusion (extended Thrombolysis in Cerebral Infarction score ≥2b), symptomatic intracerebral hemorrhage, 90-day functional independence (modified Rankin Scale score, 0-1), and 90-day mortality were compared by sex. Mixed-effects regression analysis was used adjusting for age, stroke severity, and occlusion site for outcomes. Of 1577 patients treated with intravenous thrombolysis (2019-2022), 755 (47.9%) were women. Women were older (median, 77 [68-86] years in women versus 70 [59-79] years in men) and had a higher proportion of severe strokes (National Institutes of Health Stroke Scale score >15; 32.4% versus 24.9%) and large vessel occlusions (28.7% versus 21.5%) compared with men. All workflow times were comparable between sexes. Women were less likely to achieve functional independence (31.7% versus 39.8%; unadjusted relative risk, 0.80 [95% CI, 0.70-0.91]) and had higher mortality (17.7% versus 13.3%; unadjusted relative risk, 1.33 [95% CI, 1.06-1.69]). Adjusted analysis showed no difference in outcomes between sexes. Differences in prognostic factors of age, stroke severity, and occlusion site largely accounted for higher functional dependence and mortality in women. No sex disparities were apparent in workflow quality indicators. Given the integration of the AcT trial into clinical practice, these results provide reassurance that no major sex biases are apparent in acute stroke management throughout participating Canadian centers. URL: https://www.clinicaltrials.gov; Unique identifier: NCT03889249.

Sections du résumé

BACKGROUND UNASSIGNED
Understanding sex differences in stroke care is important in reducing potential disparities. Our objective was to explore sex differences in workflow efficiency, treatment efficacy, and safety in the AcT trial (Alteplase Compared to Tenecteplase).
METHODS UNASSIGNED
AcT was a multicenter, registry-linked randomized noninferiority trial comparing tenecteplase (0.25 mg/kg) with alteplase (0.9 mg/kg) in acute ischemic stroke within 4.5 hours of onset. In this post hoc analysis, baseline characteristics, workflow times, successful reperfusion (extended Thrombolysis in Cerebral Infarction score ≥2b), symptomatic intracerebral hemorrhage, 90-day functional independence (modified Rankin Scale score, 0-1), and 90-day mortality were compared by sex. Mixed-effects regression analysis was used adjusting for age, stroke severity, and occlusion site for outcomes.
RESULTS UNASSIGNED
Of 1577 patients treated with intravenous thrombolysis (2019-2022), 755 (47.9%) were women. Women were older (median, 77 [68-86] years in women versus 70 [59-79] years in men) and had a higher proportion of severe strokes (National Institutes of Health Stroke Scale score >15; 32.4% versus 24.9%) and large vessel occlusions (28.7% versus 21.5%) compared with men. All workflow times were comparable between sexes. Women were less likely to achieve functional independence (31.7% versus 39.8%; unadjusted relative risk, 0.80 [95% CI, 0.70-0.91]) and had higher mortality (17.7% versus 13.3%; unadjusted relative risk, 1.33 [95% CI, 1.06-1.69]). Adjusted analysis showed no difference in outcomes between sexes.
CONCLUSIONS UNASSIGNED
Differences in prognostic factors of age, stroke severity, and occlusion site largely accounted for higher functional dependence and mortality in women. No sex disparities were apparent in workflow quality indicators. Given the integration of the AcT trial into clinical practice, these results provide reassurance that no major sex biases are apparent in acute stroke management throughout participating Canadian centers.
REGISTRATION UNASSIGNED
URL: https://www.clinicaltrials.gov; Unique identifier: NCT03889249.

Identifiants

pubmed: 38174568
doi: 10.1161/STROKEAHA.123.045320
doi:

Banques de données

ClinicalTrials.gov
['NCT03889249']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Diana J Kim (DJ)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).

Nishita Singh (N)

Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada (N.S., J.S.).

Luciana Catanese (L)

Hamilton Health Sciences Centre, McMaster University, Hamilton, ON, Canada (L.C.).

Amy Y X Yu (AYX)

Division of Neurology, Sunnybrook Health Sciences Centre, University of Toronto, ON, Canada. (A.Y.X.Y., H.K., R.H.S.).

Andrew M Demchuk (AM)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).
Department of Radiology, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., M.A.A., B.K.M.).
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., A.A., T.T.S., M.A.A., B.K.M.).

Mar I Lloret-Villas (MI)

Division of Neurology, University of Alberta, Edmonton, Canada (M.I.L.-V.).

Yan Deschaintre (Y)

Department of Neurosciences, Université de Montréal, QC, Canada (Y.D.).

Shelagh B Coutts (SB)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).
Department of Radiology, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., M.A.A., B.K.M.).
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., A.A., T.T.S., M.A.A., B.K.M.).

Houman Khosravani (H)

Division of Neurology, Sunnybrook Health Sciences Centre, University of Toronto, ON, Canada. (A.Y.X.Y., H.K., R.H.S.).

Ramana Appireddy (R)

Division of Neurology, Queen's University, Kingston, ON, Canada (R.A.).

Francois Moreau (F)

Université de Sherbrooke, QC, Canada (F.M.).

Gord Gubitz (G)

Queen Elizabeth II Health Sciences Centre, Halifax, NS, Canada (G.G., S.P.).

Aleksander Tkach (A)

Kelowna General Hospital, BC, Canada (A.T.).

Dar Dowlatshahi (D)

Department of Medicine, Ottawa Hospital Research Institute, University of Ottawa, ON, Canada (D.D., M. Shamy).

George Medvedev (G)

Royal Columbian Hospital, New Westminster, BC, Canada (G.M.).

Jennifer Mandzia (J)

London Health Sciences Centre, Western University, London, ON, Canada (J.M.).

Aleksandra Pikula (A)

Toronto Western Hospital, University of Toronto, ON, Canada. (A.P.).

Jai Shankar (J)

Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada (N.S., J.S.).

Heather Williams (H)

Queen Elizabeth Hospital, Charlottetown, PE, Canada (H.W.).
Medicine Hat Regional Hospital, AB, Canada (H.M.).

Muzaffar Siddiqui (M)

Department of Medicine, Ottawa Hospital Research Institute, University of Ottawa, ON, Canada (D.D., M. Shamy).
Grey Nuns Community Hospital, Edmonton, AB, Canada (M.S.).

Atif Zafar (A)

St Michael's Hospital, Toronto, ON, Canada (A.Z.).

Oje Imoukhuede (O)

Red Deer Regional Hospital, AB, Canada (O.I.).

Gary Hunter (G)

University of Saskatchewan, Saskatoon, Canada (G.H.).

Stephen Phillips (S)

Queen Elizabeth II Health Sciences Centre, Halifax, NS, Canada (G.G., S.P.).

Michael D Hill (MD)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).
Department of Radiology, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., M.A.A., B.K.M.).
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., A.A., T.T.S., M.A.A., B.K.M.).

Alexandre Y Poppe (AY)

Centre Hospitalier de l'Université de Montréal, QC, Canada (A.Y.P.).

Ayoola Ademola (A)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., A.A., T.T.S., M.A.A., B.K.M.).

Fouzi Bala (F)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).

Tolulope T Sajobi (TT)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., A.A., T.T.S., M.A.A., B.K.M.).

Richard H Swartz (RH)

Division of Neurology, Sunnybrook Health Sciences Centre, University of Toronto, ON, Canada. (A.Y.X.Y., H.K., R.H.S.).

Mohammed A Almekhlafi (MA)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).
Department of Radiology, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., M.A.A., B.K.M.).
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., A.A., T.T.S., M.A.A., B.K.M.).

Bijoy K Menon (BK)

Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, AB, Canada. (D.J.K., A.M.D., S.B.C., M.D.H., A.A., F.B., T.T.S., M.A.A., B.K.M.).
Department of Radiology, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., M.A.A., B.K.M.).
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, AB, Canada. (A.M.D., S.B.C., M.D.H., A.A., T.T.S., M.A.A., B.K.M.).

Thalia S Field (TS)

Vancouver Stroke Program, Division of Neurology, The University of British Columbia, Vancouver, Canada (T.S.F.).

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