# Risk prediction models for malignant cerebral edema after endovascular therapy in patients with acute anterior circulation large vessel occlusion stroke: a systematic review and meta-analysis

**Authors:** Yuan Yuan, Weixin Cai, Yadi Feng, Ran Zhang, Cuixue Wang, Yifan Luo, Xiaoping Yi

PMC · DOI: 10.3389/fneur.2026.1686413 · Frontiers in Neurology · 2026-02-05

## TL;DR

This study reviews and analyzes models that predict the risk of malignant cerebral edema after stroke treatment, identifying key factors and limitations in current models.

## Contribution

The study systematically reviews and evaluates the performance and bias of existing MCE risk prediction models after endovascular therapy for stroke.

## Key findings

- 21 articles identified 30 MCE prediction models, with NIHSS score, collateral score, and ASPECTS as common predictors.
- All studies showed a high risk of bias, and 17 had significant applicability concerns.
- The review highlights the feasibility of MCE risk prediction but notes limitations in clinical applicability.

## Abstract

Endovascular therapy (EVT) is proven to be both effective and safe for treating acute anterior circulation large vessel occlusion stroke (ACLVOS). Malignant cerebral edema (MCE) can emerge as a severe complication following ET. Predicting acute ACLVOS patients at risk of MCE is crucial for prevention, management, and medical decision-making. The predictive performance and predictive factors of MCE models are not yet well understood.

To identify risk prediction models and potential predictive factors for malignant cerebral edema (MCE) after endovascular therapy (EVT) in patients with acute anterior circulation large vessel occlusion stroke (ACLVOS).

We conducted a systematic search of studies using eight databases from inception until December 31st, 2024. Data extraction followed the critical appraisal and data extraction for systematic reviews of prediction modelling studies (CHARMS) Checklist. And We used the prediction model risk of bias assessment tool (PROBAST) tool to assess the risk of bias and applicability.

We included 21 articles identifying 30 MCE prediction models. The most common predictors of MCE were the National Institutes of Health Stroke Scale (NIHSS) score, collateral score, and Alberta Stroke Program Early Computed Tomography Score (ASPECTS). All included studies exhibited a high risk of bias. Seventeen studies raised significant applicability concerns, whereas five studies posed lower applicability concerns.

This systematic review confirms the feasibility of predicting MCE risk after EVT in ACLVOS patients using existing models and highlights key predictive factors. However, the high risk of bias across studies limits their clinical applicability.

This study empowers ICU nurses to accurately identify the risk levels of MCE and implement targeted monitoring strategies.

https://www.crd.york.ac.uk/PROSPERO/view/CRD42024564544, CRD42024564544.

## Linked entities

- **Diseases:** stroke (MONDO:0005098)

## Full-text entities

- **Diseases:** cerebral atrophy (MESH:D001284), edema (MESH:D004487), neurological complication (MESH:D002493), Cardioembolic strokes (MESH:D000083262), large vessel occlusion stroke (MESH:C536223), ACLVOS (MESH:D020520), ischemic (MESH:D002545), ventricular compression (MESH:D009408), NIHSS (MESH:C538175), neurological critical illness (MESH:D016638), Stroke (MESH:D020521), atherosclerotic stroke (MESH:D002537), MBE (MESH:D001929), midline shift (MESH:D020178), dehydration (MESH:D003681), Ischemic stroke (MESH:D002544), EVT (MESH:D016609), mMCAi (MESH:D020244), Mortality (MESH:D003643), impaired consciousness (MESH:D003244), disability (MESH:D009069), neurological deterioration (MESH:D009422), cerebral herniation (MESH:D004677), infarct (MESH:D007238), nausea or vomiting (MESH:D020250), intracranial hypertension (MESH:D019586)
- **Chemicals:** EVT (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916362/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916362/full.md

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Source: https://tomesphere.com/paper/PMC12916362