Evidence map›Paper›PMID 40106441›Full record

SynthesisPloS one2025

A methodological assessment of randomization integrity in alteplase for acute ischemic stroke individual patient data meta-analyses.

Ravi Garg, Gabriel Torrealba-Acosta, Steffen Mickenautsch, Vance W Berger

Abstract readMeta-Analysis
In one paragraph

Synthesis in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ravi GargDepartment of Neurology, Division of Neurocritical Care, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois, United States of America.ORCID https://orcid.org/0000-0001-9864-8443
Gabriel Torrealba-AcostaDepartment of Neurology, Duke University School of Medicine, Durham, North Carolina, United States of America.ORCID https://orcid.org/0000-0002-0632-348X
Steffen MickenautschFaculty of Dentistry, University of the Western Cape, Tygerberg/Cape Town, South Africa.ORCID https://orcid.org/0000-0002-4994-2328
Vance W BergerBiometry Research Group, National Cancer Institute, Rockville, Maryland, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesLittle is known about the integrity of randomization for randomized controlled trials (RCT) included in alteplase for stroke meta-analyses. If the RCTs were not properly randomized, the results could not be accepted at face value. The objective was to assess the integrity of randomization in individual patient data (IPD) meta-analyses supporting alteplase for acute ischemic stroke.

methodsWe assessed randomization reporting, performed qualitative risk of bias assessments arising from the randomization process, and performed fixed effects meta-analyses of baseline variables for which zero heterogeneity is expected if all included RCTs have unbiased randomization. Fixed-effects meta-analyses of baseline age, weight, and National Institute of Health Stroke Scale (NIHSS) score were performed. If heterogeneity was present (I2 >  0%), trials were systematically removed, starting with the RCT with the largest t-statistic until the I2 value was 0%.

resultsThe NINDS rt-PA Stroke Study had a high risk of bias, the ECASS-3 RCT had some concerns, and all other trials were graded as low risk according to the Cochrane Risk of Bias (ROB-2) tool. The NINDS rt-PA Stroke Study contributed to heterogeneity in age and weight meta-analyses, and the ECASS-3 RCT contributed to heterogeneity in the NIHSS score meta-analysis. Removal of suspect trials resulted in the expected I2 value of 0%.

conclusionsThe NINDS rt-PA Stroke Study and ECASS-3 trials contributed to heterogeneity in fixed effects meta-analyses of baseline variables while there should have been none. These RCTs are likely a source of selection bias in IPD meta-analyses due to suspect randomization.

Indexed as

Fibrinolytic AgentsIschemic StrokeRandomized Controlled Trials as TopicStrokeTissue Plasminogen ActivatorHumansMeta-Analysis as TopicFibrinolytic AgentsTissue Plasminogen Activator

Identifiers

PMID40106441
PMCPMC11922233

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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.