Evidence map›Paper›PMID 42017319›Full record

ArticleJournal of the American Heart Association2026

Beyond Hemoglobin Levels: Integrating Anemia Phenotyping Into Prognostic Models for Patients With Stroke Following Intravenous Thrombolysis.

Senwei Tan, Shengcai Chen, Huijuan Jin, Min Qiu, Wenbo Zuo, Luojinyun Wang, Jiashuo Lin, Haokun Peng, Quanwei He, Yaling Wang and 2 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2026. 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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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Senwei Tan *Department of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.ORCID 0009-0006-6195-6075
Shengcai Chen *Department of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.
Huijuan Jin *Department of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.
Min QiuDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.
Wenbo ZuoDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.
Luojinyun WangDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.
Jiashuo LinDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.ORCID 0009-0001-8695-7721
Haokun PengDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.
Quanwei HeDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.ORCID 0000-0002-8318-6976
Yaling WangDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.
Yan WanDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.ORCID 0000-0002-1864-0714
Bo HuDepartment of Neurology Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.ORCID 0000-0003-1462-8854

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnemia predicts poor outcomes after intravenous thrombolysis in acute ischemic stroke. Whether morphological anemia subtypes differentially affect prognosis remains unclear. We evaluated the impact of microcytic, normocytic, and macrocytic anemia on outcomes in patients with acute ischemic stroke receiving intravenous thrombolysis.

methodsIn this multicenter, prospective cohort study of 1367 patients with acute ischemic stroke treated with intravenous thrombolysis, anemia was defined using World Health Organization criteria and classified by mean corpuscular volume. Multivariable logistic regression and mediation analyses were performed.

resultsAmong 1367 patients (median age 66 years, 64.7% male), 379 (27.7%) had anemia: 123 (8.9%) microcytic, 202 (14.7%) normocytic, and 54 (3.9%) macrocytic. After full adjustment, microcytic and normocytic anemia were independently associated with increased risks of 3-month death or severe disability (microcytic: adjusted odds ratio [aOR], 2.13 [95% CI, 1.34-3.38]; normocytic: aOR, 2.07 [95% CI, 1.39-3.09]) and 3-month mortality (microcytic: aOR, 1.76 [95% CI, 1.05-2.96]; normocytic: aOR, 1.88 [95% CI, 1.21-2.91]). Normocytic anemia was additionally associated with in-hospital neurological deterioration (aOR, 1.83 [95% CI, 1.10-3.04]), stroke-associated pneumonia (aOR, 2.35 [95% CI, 1.57-3.51]), and in-hospital gastrointestinal bleeding (aOR, 2.58 [95% CI, 1.18-5.64]). Stroke-associated pneumonia mediated 22.09%, 45.91% and 27.05% of the effect of normocytic anemia on 3-month death or severe disability, 3-month mortality, and in-hospital neurological deterioration, respectively. Macrocytic anemia showed no significant associations with outcomes.

conclusionsMorphological anemia subtypes have distinct prognostic implications in intravenous thrombolysis-treated patients with acute ischemic stroke. Microcytic and normocytic anemia are independently associated with poor outcomes and mortality, with in-hospital complications, particularly stroke-associated pneumonia, mediating substantial risk. REGISTRATION: URL: https://www.chictr.org.cn/; Unique Identifier: ChiCTR2000033456.

Indexed as

AnemiaFibrinolytic AgentsHemoglobinsIschemic StrokeStrokeThrombolytic TherapyAgedFemaleHumansMaleMiddle AgedPhenotypePrognosisProspective StudiesRisk AssessmentRisk FactorsFibrinolytic AgentsHemoglobinsanemiamorphological classificationoutcomestrokethrombolysis

Identifiers

PMID42017319
PMCPMC13279450

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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.