Evidence map›Paper›PMID 42412265›Full record

ArticleTranslational stroke research2026

Quantitative Cerebrovascular Analysis for Improved Prediction of Post-Stroke Complications.

Aditi Deshpande, Jing Wang, Laith R Altaweel, Seajin Yi, Zelalem Bahiru, Tahddeus J Leiphart, Pouya Tahsili-Fahadan, Kaveh Laksari

Abstract read
In one paragraph

Article in Translational stroke research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Aditi DeshpandeDepartment of Mechanical Engineering, University of California, Riverside, CA, USA. aditid@ucr.edu.
Jing WangDivision of Vascular Neurology and Neurocritical Care, Inova Neuroscience and Spine Institute, Inova Fairfax Medical Campus (IFMC), Falls Church, VA, USA.
Laith R AltaweelDivision of Vascular Neurology and Neurocritical Care, Inova Neuroscience and Spine Institute, Inova Fairfax Medical Campus (IFMC), Falls Church, VA, USA.
Seajin YiDivision of Vascular Neurology and Neurocritical Care, Inova Neuroscience and Spine Institute, Inova Fairfax Medical Campus (IFMC), Falls Church, VA, USA.
Zelalem BahiruDivision of Vascular Neurology and Neurocritical Care, Inova Neuroscience and Spine Institute, Inova Fairfax Medical Campus (IFMC), Falls Church, VA, USA.
Tahddeus J LeiphartDivision of Vascular Neurology and Neurocritical Care, Inova Neuroscience and Spine Institute, Inova Fairfax Medical Campus (IFMC), Falls Church, VA, USA.
Pouya Tahsili-FahadanDivision of Vascular Neurology and Neurocritical Care, Inova Neuroscience and Spine Institute, Inova Fairfax Medical Campus (IFMC), Falls Church, VA, USA.
Kaveh LaksariDepartment of Mechanical Engineering, University of California, Riverside, CA, USA.

Funding

Dynamic cerebrovascular morphology changes in acute ischemic strokeR01NS131554 · NINDS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI Kaveh Laksari, Pouya Tahsili Fahadan · 2024 to 2026
$1.9M
Inova Health System GRT1000000237NIH HHS R01-NS131554NINDS NIH HHS R01 NS131554
6 · The paper itself

Abstract

Endovascular thrombectomy (EVT) has transformed the treatment of acute ischemic stroke (AIS). However, a substantial proportion of AIS patients experience poor outcomes despite successful recanalization, often due to severe neurological deterioration or life-threatening complications. Early identification of these high-risk patients remains a major unmet need. In this study, we developed and validated machine-learning (ML) models that integrate automated quantitative brain arterial morphology and collateral grading with demographic, clinical, laboratory, and imaging variables to predict major post-EVT complications and early neurological outcomes. Using a prospectively collected database of 727 AIS patients that underwent EVT, we developed ML models to incorporate patient-specific vascular morphometry with conventional clinical, laboratory, and imaging data to predict emergence of early neurological deterioration (END), symptomatic intracranial hemorrhage (sICH), malignant brain edema (MBE) requiring surgical decompression, and neurogenic respiratory failure and dysphagia requiring tracheostomy/gastrostomy (TC/PEG). Our analysis of morphological features, including increased tortuosity and reduced vessel diameter, showed strong associations with complications. Morphology-informed (MI) models consistently outperformed baseline-clinical (BC) models for patients with END (AUROC 0.81 for MI model vs. 0.73 for BC), sICH (AUROC 0.68 MI vs. 0.56 BC model), MBE (AUROC 0.67 MI model vs. 0.56 BC), or patients who underwent TC/PEG (AUROC 0.66MI vs. 0.58 BC model). Statistical testing confirmed significant AUROC improvements for END, sICH and mRS (p < 0.05), Finally, patient-specific calibrated probability profiles enabled individualized, multidimensional risk stratification, revealing distinct complication-specific risk patterns across patients. These findings demonstrate that cerebrovascular structure-an often overlooked yet physiologically fundamental determinant of ischemic injury and reperfusion dynamics-provides significant predictive information that is not captured by standard clinical or visual imaging assessments. Automated vascular segmentation and collateral grading techniques enable rapid and objective integration of cerebrovascular metrics into prognostic models, offering a scalable tool for precision risk stratification, supporting earlier intervention, targeted monitoring, and improved post-EVT management.

Indexed as

Endovascular ProceduresIschemic StrokeMachine LearningStrokeThrombectomyAgedAged, 80 and overFemaleHumansMaleMiddle AgedPredictive Learning ModelsAcute ischemic strokeOutcome predictionPost stroke complicationsVascular morphology

Identifiers

PMID42412265
PMCPMC13342120

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.