Evidence map›Paper›PMID 39704225›Full record

Trial reportJournal of the American Heart Association2025

Safety and Efficacy of Intravenous Thrombolysis by Infarct Type in Patients with No Visible Occlusion: A Secondary Analysis of the AcT Trial.

A Zohaib Siddiqi, Katrina Ignacio, Chitapa Kaveeta, Fouzi Bala, Ayoola Ademola, Aleksander Tkach, Brian H Buck, Luciana Catanese, Gary Hunter, Dar Dowlatshahi and 11 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Journal of the American Heart Association, 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. Acute right-sided thalamic stroke successfully treated with thrombolytics.Clinical and experimental emergency medicine · 2025
    Article
  3. Review
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

21 authors.

A Zohaib SiddiqiDivision of Neurology, Rady Faculty of Health Sciences University of Manitoba Winnipeg MB Canada.ORCID 0000-0002-5228-6376
Katrina IgnacioDepartment of Clinical Neurosciences, Cumming School of Medicine University of Calgary AB Canada.ORCID 0000-0001-7263-8474
Chitapa KaveetaDepartment of Clinical Neurosciences, Cumming School of Medicine University of Calgary AB Canada.ORCID 0000-0001-8316-6820
Fouzi BalaDepartment of Radiology Tours University Hospital Tours France.ORCID 0000-0001-6748-2081
Ayoola AdemolaDepartment of Community Health Sciences and O'Brien Institute for Public Health University of Calgary AB Canada.ORCID 0000-0002-8412-6246
Aleksander TkachKelowna General Hospital Kelowna BC Canada.
Brian H BuckDivision of Neurology, Department of Medicine University of Alberta Edmonton AB Canada.ORCID 0000-0002-7984-6062
Luciana CataneseHamilton Health Sciences and McMaster University Hamilton ON Canada.ORCID 0000-0002-8696-5211
Gary HunterUniversity of Saskatchewan Saskatoon SK Canada.ORCID 0000-0003-2033-8001
Dar DowlatshahiDepartment of Medicine (Neurology) Ottawa Hospital Research Institute and University of Ottawa ON Canada.ORCID 0000-0003-1379-3612
Michel ShamyDepartment of Medicine (Neurology) Ottawa Hospital Research Institute and University of Ottawa ON Canada.ORCID 0000-0002-0085-6816
Atif ZafarSt Michael's Hospital Toronto ON Canada.ORCID 0000-0002-2738-5225
Thalia S FieldVancouver Stroke Program and the Division of Neurology University of British Columbia Vancouver BC Canada.ORCID 0000-0002-1176-0633
Ramana AppireddyDivision of Neurology, Department of Medicine Queen's University Kingston ON Canada.ORCID 0000-0003-1831-5804
Ankur WadhwaDivision of Neurology, Rady Faculty of Health Sciences University of Manitoba Winnipeg MB Canada.ORCID 0000-0003-4898-8495
Tolulope SajobiDepartment of Community Health Sciences and O'Brien Institute for Public Health University of Calgary AB Canada.ORCID 0000-0002-5696-5552
Rick SwartzDepartment of Medicine (Division of Neurology), Hurvitz Brain Sciences Program, Sunnybrook Health Sciences Centre University of Toronto ON Canada.ORCID 0000-0001-6571-5531
Mohammed AlmekhlafiDepartment of Clinical Neurosciences, Cumming School of Medicine University of Calgary AB Canada.ORCID 0000-0001-9550-8197
Andrew DemchukDepartment of Clinical Neurosciences, Cumming School of Medicine University of Calgary AB Canada.ORCID 0000-0002-4930-7789
Bijoy MenonDepartment of Clinical Neurosciences, Cumming School of Medicine University of Calgary AB Canada.ORCID 0000-0002-3466-496X
Nishita SinghDivision of Neurology, Rady Faculty of Health Sciences University of Manitoba Winnipeg MB Canada.ORCID 0000-0003-3647-0904

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAbout 25% of patients with acute ischemic stroke have lacunar infarct on follow-up imaging. In this secondary analysis from the AcT (Alteplase Compared With Tenecteplase) trial, we assessed if there is variation in safety or efficacy of intravenous thrombolysis by infarct type in patients with no visible occlusion. We also determined if this effect differed between tenecteplase and alteplase. METHODS AND

resultsThis is a secondary analysis from the AcT trial. Lacunar infarct was defined as single, ≤15 mm, and in regions supplied by perforating arterioles on 24-hour imaging. Outcomes included symptomatic intracerebral hemorrhage at 24 hours, any hemorrhage on imaging, and 90-day modified Rankin Scale score. Mixed-effects regression models adjusted for age, sex, stroke severity, thrombolytic type, and onset-to-needle time were used. Of 1577 patients, 456/29.9% had no visible occlusion and interpretable follow-up imaging (magnetic resonance imaging: 41.2%). Of these 93 (20.4%) (magnetic resonance imaging: 62.3%) had lacunar infarct, 171 (37.5%) (magnetic resonance imaging: 67.4%) had nonlacunar infarct, and 192 (42.1%) (magnetic resonance imaging: 7.3%) had no visible infarct. Four patients (2.3%) in the group with nonlacunar infarct and none in the groups with lacunar infarct and no visible infarct developed symptomatic intracerebral hemorrhage. Any intracranial hemorrhage was highest (21; 12.4%) in the group with nonlacunar infarct. There was no significant interaction between thrombolytic type and treatment outcomes.

conclusionsIn the AcT trial, safety of intravenous thrombolysis was similar across all infarct types in patients with no visible occlusion but functional outcomes were worst in patients with nonlacunar infarct. Safety and functional outcomes after intravenous thrombolysis were better in the groups with lacunar infarct and no visible infarct as compared with the overall trial population.

Indexed as

Fibrinolytic AgentsIschemic StrokeTenecteplaseThrombolytic TherapyTissue Plasminogen ActivatorAdministration, IntravenousAgedCerebral HemorrhageFemaleHumansInfusions, IntravenousMagnetic Resonance ImagingMaleMiddle AgedStroke, LacunarTime FactorsFibrinolytic AgentsTenecteplaseTissue Plasminogen Activatoracute strokelacunar infarcttenecteplasethrombolysis

Identifiers

PMID39704225
PMCPMC12054515

What OpenQuestion holds

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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.