Evidence map›Paper›PMID 39086232›Full record

Trial reportInternational journal of stroke : official journal of the International Stroke Society2025

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

Chitapa Kaveeta, Ibrahim Alhabli, Fouzi Bala, MacKenzie Horn, Faysal Benali, Shelagh B Coutts, Atif Zafar, Olena Bereznyakova, Alexander Khaw, Houman Khosravani and 14 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in International journal of stroke : official journal of the International Stroke Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Chitapa KaveetaDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0001-8316-6820
Ibrahim AlhabliDepartment of Clinical Neurosciences and Radiology, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Fouzi BalaDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0001-6748-2081
MacKenzie HornDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Faysal BenaliDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Shelagh B CouttsDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0001-5090-5105
Atif ZafarDivision of Vascular Neurology, Department of Medicine, University of Toronto and St. Michael's Hospital, Toronto, ON, Canada.
Olena BereznyakovaDepartment of Clinical Neurosciences, Université de Montréal, Montreal, QC, Canada.
Alexander KhawLondon Health Sciences Centre and Western University, London, ON, Canada.
Houman KhosravaniHurvitz Brain Sciences Program, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, ON, Canada.
Gary HunterDivision of Neurology, University of Saskatchewan, Saskatoon, SK, Canada.
Aleksander TkachDepartment of Neuroscience, Kelowna General Hospital, Kelowna, BC, Canada.
Dar DowlatshahiDepartment of Medicine, University of Ottawa and University of Ottawa Heart Institute, Ottawa, ON, Canada.ORCID 0000-0003-1379-3612
Luciana CataneseHamilton Health Sciences and McMaster University, Hamilton, ON, Canada.ORCID 0000-0002-8696-5211
Chrysi BogiatziLondon Health Sciences Centre and Western University, London, ON, Canada.
Ramana AppireddyDivision of Neurology, Department of Medicine, Queen's University, Kingston, ON, Canada.ORCID 0000-0003-1831-5804
Brian H BuckDivision of Neurology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
Richard H SwartzHurvitz Brain Sciences Program, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, ON, Canada.ORCID 0000-0001-6571-5531
Tolulope T SajobiDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Mohammed AlmekhlafiDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Andrew M DemchukDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Aravind GaneshDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0001-5520-2070
Bijoy MenonDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Nishita SinghDepartment of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0003-3647-0904

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEarly ischemic changes on baseline imaging are commonly evaluated for acute stroke decision-making and prognostication.

aimsWe assess the association of early ischemic changes on clinical outcomes and whether it differs between intravenous tenecteplase and Alteplase.

methodsData 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.

resultsOf 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.

conclusionSimilar 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).

Indexed as

Fibrinolytic AgentsIschemic StrokeTenecteplaseTissue Plasminogen ActivatorAgedAged, 80 and overFemaleHumansMaleMiddle AgedThrombolytic TherapyTreatment OutcomeFibrinolytic AgentsTenecteplaseTissue Plasminogen Activatoracute ischemic strokeAlberta Stroke Program Early CT Scorealteplasetenecteplasethrombolysis

Identifiers

PMID39086232
PMCPMC11669262

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.