The treatment effect across ASPECTS in acute ischemic stroke: Analysis from the AcT trial

dc.contributor.authorKaveeta C.
dc.contributor.authorAlhabli I.
dc.contributor.authorBala F.
dc.contributor.authorHorn M.
dc.contributor.authorBenali F.
dc.contributor.authorCoutts S.B.
dc.contributor.authorZafar A.
dc.contributor.authorBereznyakova O.
dc.contributor.authorKhaw A.
dc.contributor.authorKhosravani H.
dc.contributor.authorHunter G.
dc.contributor.authorTkach A.
dc.contributor.authorDowlatshahi D.
dc.contributor.authorCatanese L.
dc.contributor.authorBogiatzi C.
dc.contributor.authorAppireddy R.
dc.contributor.authorBuck B.H.
dc.contributor.authorSwartz R.H.
dc.contributor.authorSajobi T.T.
dc.contributor.authorAlmekhlafi M.
dc.contributor.authorDemchuk A.M.
dc.contributor.authorGanesh A.
dc.contributor.authorMenon B.
dc.contributor.authorSingh N.
dc.contributor.correspondenceKaveeta C.
dc.contributor.otherMahidol University
dc.date.accessioned2024-09-23T18:15:06Z
dc.date.available2024-09-23T18:15:06Z
dc.date.issued2024-01-01
dc.description.abstractBackground: Early ischemic changes on baseline imaging are commonly evaluated for acute stroke decision-making and prognostication. Aims: We assess the association of early ischemic changes on clinical outcomes and whether it differs between intravenous tenecteplase and Alteplase. Methods: Data are from the phase 3, Alteplase compared to Tenecteplase (AcT) trial. Subjects with anterior circulation stroke were included. Early ischemic changes were assessed using the Alberta Stroke Program Early CT score (ASPECTS). Efficacy outcomes included modified Rankin scale (mRS) 0–1, mRS 0–2, and ordinal mRS at 90 days. Safety outcomes included 24-h symptomatic intracerebral hemorrhage (sICH), any hemorrhage on follow-up scan, and 90-day mortality rate. Mixed-effects logistic regression was used to assess the association of ASPECTS (continuous and categorical (0–4 vs 5–7 vs 8–10)) with outcomes and if these associations were modified by thrombolytic type after adjusting for age, sex, and baseline stroke severity. Results: Of the 1577 patients in the trial, 901 patients (56.3%; median age 75 years (IQR 65–84), 50.8% females, median National Institute of Health Stroke Scale (NIHSS) 14 (IQR 17–19)) with anterior circulation stroke were included. mRS 0–1 at 90 days was achieved in 1/14 (0.3%), 43/160 (14.7%), and 252/726 (85.1%) in the ASPECTS 0–4, 5–7, and 8–10 groups respectively. Every one-point decrease in ASPECTS was associated with 2.7% and 1.9% decrease in chances of mRS 0–1 and mRS 0–2 at 90 days, respectively, and 1.9% chances of increase in mortality at 90 days. Subgroup analysis in endovascular thrombectomy (EVT)-treated population showed similar results. Thrombolytic type did not modify this association between ASPECTS and 90-day mRS 0–1 (P-interaction 0.75). There was no significant interaction by thrombolytic type with any other outcomes. Conclusion: Similar to prior studies, we found that every one-point decrease in ASPECTS was associated with poorer clinical and safety outcomes. This effect did not differ between alteplase and tenecteplase. Data access statement: Data shall made available on reasonable request from the PI (BMM).
dc.identifier.citationInternational Journal of Stroke (2024)
dc.identifier.doi10.1177/17474930241273561
dc.identifier.eissn17474949
dc.identifier.issn17474930
dc.identifier.pmid39086232
dc.identifier.scopus2-s2.0-85204066529
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/101329
dc.rights.holderSCOPUS
dc.subjectNeuroscience
dc.subjectMedicine
dc.titleThe treatment effect across ASPECTS in acute ischemic stroke: Analysis from the AcT trial
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85204066529&origin=inward
oaire.citation.titleInternational Journal of Stroke
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationL’École de médecine
oairecerif.author.affiliationRady Faculty of Health Sciences
oairecerif.author.affiliationKelowna General Hospital
oairecerif.author.affiliationLondon Health Sciences Centre
oairecerif.author.affiliationSunnybrook Health Sciences Centre
oairecerif.author.affiliationQueen's University, School of Medicine
oairecerif.author.affiliationUniversity of Alberta, Faculty of Medicine and Dentistry
oairecerif.author.affiliationSt. Michael's Hospital, Toronto
oairecerif.author.affiliationCentre Hospitalier Regional et Universitaire de Tours
oairecerif.author.affiliationUniversity of Saskatchewan
oairecerif.author.affiliationUniversity of Montreal
oairecerif.author.affiliationHamilton Health Sciences
oairecerif.author.affiliationCumming School of Medicine

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