Evidence map›Paper›PMID 41128272›Full record

Trial reportJournal of the American Heart Association2025

Association of Minimal Clinically Important Difference With Infarct Volume in Clinical Poststroke Outcomes.

Umberto Pensato, Johanna M Ospel, Jianhai Zhang, Kazbek Barakhanov, Koji Tanaka, Fouzi Bala, Chitapa Kaveeta, Diana Kim, Michel Shamy, MacKenzie Horn 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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.

Umberto PensatoIRCCS Humanitas Research Hospital Milan Italy.ORCID 0000-0002-4042-4735
Johanna M OspelDepartment of Radiology University of Calgary AB Canada.ORCID 0000-0003-0029-6764
Jianhai ZhangDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0002-0330-6908
Kazbek BarakhanovDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0001-8152-1382
Koji TanakaDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0001-6501-4057
Fouzi BalaDiagnostic and Interventional Neuroradiology Department University Hospital of Tours Tours France.ORCID 0000-0001-6748-2081
Chitapa KaveetaDepartment of Medicine, Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Thailand.ORCID 0000-0001-8316-6820
Diana KimKelowna General Hospital Kelowna BC Canada.ORCID 0000-0002-0243-799X
Michel ShamyDepartment of Medicine, Division of Neurology University of Ottawa Canada.ORCID 0000-0002-0085-6816
MacKenzie HornDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0002-1472-3977
Thalia S FieldVancouver Stroke Program, Division of Neurology University of British Columbia Vancouver BC Canada.ORCID 0000-0002-1176-0633
Brian H BuckDepartment of Medicine, Division of Neurology University of Alberta Edmonton AB Canada.ORCID 0000-0002-7984-6062
Aleks TkachKelowna General Hospital Kelowna BC Canada.ORCID 0009-0009-4063-4431
Luciana CataneseHamilton Health Sciences Regional Rehabilitation Center Hamilton Ontario Canada.ORCID 0000-0002-8696-5211
Rick H SwartzMedicine (Neurology) Sunnybrook Health Sciences Centre Toronto Ontario Canada.ORCID 0000-0001-6571-5531
Tolulope SajobiDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0002-5696-5552
Mohammed AlmeklhafiDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0001-9550-8197
Andrew M DemchukDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0002-4930-7789
Bijoy K MenonDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0002-3466-496X
Aravind GaneshDepartment of Clinical Neurosciences University of Calgary AB Canada.ORCID 0000-0001-5520-2070
Nishita SinghDepartment of Internal Medicine (Neurology Division), 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

backgroundInfarct volume is an imaging biomarker of ischemic tissue injury strongly correlated with poststroke outcomes and reperfusion benefit. We aimed to evaluate the follow-up infarct volume (FIV) difference corresponding to a 1%, 5%, and 10% increase in probability of excellent functional outcomes after intravenous thrombolysis.

methodsData are from the AcT trial (Alteplase Compared to Tenecteplase in Patients With Acute Ischemic Stroke). Patients with 24-hour infarct volume segmentations were included. The primary outcome was excellent functional outcome (modified Rankin Scale score=0-1). Associations between outcomes and FIV were investigated with regression analyses adjusted for covariates. Sensitivity analyses examined patients with noncontrast computed tomography versus magnetic resonance imaging follow-up and those treated versus not treated with endovascular thrombectomy.

resultsThe study included 1478 patients (median age 74 years [interquartile range (IQR), 63-83], 48.2% female). Median FIV was 2.7 mL (IQR, 0-18.2), and 527 (35.7%) achieved excellent functional outcome. FIV was associated with excellent functional outcome: adjusted odds ratio, 0.97 (95% CI, 0.96-0.98) per 1-mL FIV increase. The median ΔFIV corresponding to a 1%, 5%, and 10% increase in adjusted probability of excellent functional outcomes were 1.5 mL (IQR, 1.4-1.9), 7.3 mL (IQR, 6.8-9.3), and 14.6 mL (IQR, 13.6-18.2), respectively. Results were consistent across follow-up imaging modality and endovascular thrombectomy subgroups.

conclusionsIn patients with acute ischemic stroke treated with intravenous thrombolysis, differences of ~1.5 mL, ~7 mL, and ~15 mL in FIV corresponded to a 1%, 5%, and 10% higher absolute probability of achieving excellent functional outcomes. These findings could inform the design of future clinical Phase 2 and proof-of-principle stroke trials that aim to use FIV as a key outcome measure.

Indexed as

Fibrinolytic AgentsIschemic StrokeMinimal Clinically Important DifferenceStrokeTenecteplaseThrombolytic TherapyTissue Plasminogen ActivatorAgedAged, 80 and overEndovascular ProceduresFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedRecovery of FunctionFibrinolytic AgentsTenecteplaseTissue Plasminogen Activatorcerebral infarct growthfunctional outcomesneuroprotectiontenecteplasethrombectomy

Identifiers

PMID41128272
PMCPMC12684630

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.