Evidence map›Paper›PMID 35678020›Full record

ArticleBrain and behavior2022

Safety and preliminary efficacy of argatroban plus dual antiplatelet therapy for acute mild to moderate ischemic stroke with large artery atherosclerosis.

Xiao-Qiu Li, Xiao-Wen Hou, Yu Cui, Xiao-Fu Tian, Xin-Hong Wang, Zhong-He Zhou, Hui-Sheng Chen

Open access · goldAbstract readControlled Clinical Trial
In one paragraph

Article in Brain and behavior, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 13% of its field
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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Argatroban plus alteplase in posterior versus anterior circulation stroke.Annals of clinical and translational neurology · 2025
    Trial
  5. Trial
  6. Baseline neurological deficit and argatroban plus alteplase in acute ischemic stroke: A post hoc analysis of ARAIS trial.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Trial
  7. Article
  8. Review
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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

7 authors at 1 institution in 1 country.

Xiao-Qiu LiDepartment of Neurology, General Hospital of Northern Theater Command, Shenyang, P.R. China.
Xiao-Wen HouDepartment of Neurology, General Hospital of Northern Theater Command, Shenyang, P.R. China.
Yu CuiDepartment of Neurology, General Hospital of Northern Theater Command, Shenyang, P.R. China.ORCID 0000-0002-4925-1500
Xiao-Fu TianDepartment of Neurology, General Hospital of Northern Theater Command, Shenyang, P.R. China.
Xin-Hong WangDepartment of Neurology, General Hospital of Northern Theater Command, Shenyang, P.R. China.
Zhong-He ZhouDepartment of Neurology, General Hospital of Northern Theater Command, Shenyang, P.R. China.
Hui-Sheng ChenDepartment of Neurology, General Hospital of Northern Theater Command, Shenyang, P.R. China.ORCID 0000-0002-7486-1992
General Hospital of Shenyang Military Region · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePrevious studies suggest the benefit of dual antiplatelet therapy (DAPT) for acute ischemic stroke with large artery atherosclerosis (LAA) etiology, but there is no study about the effect of DAPT plus anticoagulant in this population.

methodsA prospective single arm trial was performed to determine the effect of DAPT combined with argatroban on acute mild to moderate ischemic stroke patients with LAA, which was compared with historical populations. The main outcome was the proportion of early neurological deterioration (END). The secondary outcomes included scores of 0 to 1 and 0 to 2 on the modified Rankin Scale (mRS) at 90 days, and changes in National Institutes of Health Stroke Scale (NIHSS) from baseline to day 7 after admission. The safety outcomes included intracranial hemorrhage at 7 days, organ hemorrhage, and all-cause mortality at 90 days.

resultsA total of 120 patients with argatroban plus DAPT were prospectively enrolled and 529 patients with only DAPT were retrospectively collected. There was no significant difference in baseline characteristics between groups. Compared with control group, combined treatment group had lower proportion of END (4.2% vs. 10.0%, adjusted p = .046), more reduction in NIHSS score from the baseline to day 7 after admission (1.06 ± 2.03 vs. 0.39 ± 1.97, adjusted p = .003), and higher proportion of mRS (0-2) at 90 days (87.5% vs. 79.2%, adjusted p = .048). No intracranial hemorrhage was found between groups.

conclusionsThis is the first report that short-term argatroban combined with DAPT seems to be safe and may effectively prevent END and improve neurological prognosis for acute mild to moderate ischemic stroke patients with LAA; however, interpretation of the conclusion required caution due to nonrandomized controlled trial with medium sample size.

Indexed as

AtherosclerosisIschemic StrokePlatelet Aggregation InhibitorsArginineArteriesHemorrhageHumansIntracranial HemorrhagesPipecolic AcidsProspective StudiesRetrospective StudiesSulfonamidesTreatment OutcomeargatrobanArgininePipecolic AcidsPlatelet Aggregation InhibitorsSulfonamidesanticoagulantdual antiplateletearly neurological deteriorationischemic strokelarge artery atherosclerosis

Identifiers

PMID35678020
PMCPMC9304821
OpenAlexW4282936756

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.