# Nomogram to predict symptomatic intracranial hemorrhage after mechanical thrombectomy in patients with intracranial atherosclerosis-related large-vessel occlusion

**Authors:** Hongchao Yang, Hongliang Zhong, Jianwen Jia, Yu Wang, Tong Li, He Liu, Yang Wang

PMC · DOI: 10.3389/fneur.2026.1738518 · Frontiers in Neurology · 2026-02-04

## TL;DR

This study creates a tool to predict the risk of brain bleeding after a specific stroke treatment in patients with atherosclerosis-related blockages.

## Contribution

The study introduces a novel nomogram for predicting symptomatic intracranial hemorrhage after endovascular treatment in ICAS-LVO stroke patients.

## Key findings

- Elevated D-dimer levels are a strong predictor of symptomatic intracranial hemorrhage.
- Longer onset-to-recanalization time increases the risk of bleeding after treatment.
- Larger core infarct volume is independently associated with symptomatic intracranial hemorrhage.

## Abstract

Despite significant advancements in endovascular treatment (EVT) over the past decade, symptomatic intracerebral hemorrhage (sICH) persists as a serious complication, especially in patients with acute ischemic stroke (AIS) related to intracranial atherosclerotic stenosis (ICAS), which is characterized by complex and calcified plaques. The present study aimed to develop a predictive nomogram for assessing the risk of sICH in AIS patients with ICAS and large-vessel occlusion (LVO) who undergo EVT.

We analyzed data from 183 patients with acute ischemic stroke (AIS) due to intracranial atherosclerotic stenosis-related large vessel occlusion (ICAS-LVO) who underwent endovascular treatment (EVT) between January 2022 and December 2023. The primary safety outcome was the incidence of symptomatic intracranial hemorrhage (sICH). A nomogram was developed based on a multivariable logistic regression model, and the calibration of the model was evaluated using Spiegelhalter’s Z-test.

In our developed nomogram, elevated D-dimer levels (odds ratio [OR] 2.87; 95% confidence interval [CI], 1.53–5.39; p = 0.001), longer onset-to-recanalization time (OR 1.00; 95% CI, 1.00–1.01; p = 0.004), and larger core infarct volume (OR 1.04; 95% CI, 1.01–1.06; p = 0.002) were identified as independent predictors of symptomatic intracranial hemorrhage (sICH) in stroke patients undergoing endovascular treatment (EVT). The goodness-of-fit of the model was confirmed by a non-significant Spiegelhalter’s Z-test (p = 0.941).

A nomogram integrating D-dimer levels, onset-to-recanalization time, and core infarct volume offers a reliable and practical method for estimating the risk of symptomatic intracranial hemorrhage in acute ischemic stroke patients with intracranial atherosclerotic stenosis-related large vessel occlusion receiving endovascular therapy.

## Full-text entities

- **Genes:** FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}
- **Diseases:** coagulopathic disturbances (MESH:D014832), NIHSS (MESH:C538175), hematoma (MESH:D006406), HL (MESH:C538324), edema (MESH:D004487), LVO (MESH:C536223), pneumonia (MESH:D011014), Stroke (MESH:D020521), ICAS (MESH:D002537), hypercoagulation (MESH:D019851), hemorrhage (MESH:D006470), IVH (MESH:D000074042), malignant cerebral edema (MESH:D001929), intracranial hemorrhage (MESH:D020300), AIS (MESH:D000083242), stenosis (MESH:D003251), atherosclerosis (MESH:D050197), Intracerebral hemorrhage (MESH:D002543), Mortality (MESH:D003643), hypertensive (MESH:D006973), thrombotic (MESH:D013927), reperfusion syndrome (MESH:D015427), Cerebral Infarction (MESH:D002544), EVT (MESH:D016609), hyperfibrinolysis (MESH:C567640), cardiac disease (MESH:D006331), heart failure (MESH:D006333), infarct (MESH:D007238), intracranial (MESH:D001932), necrotic (MESH:D009336), cerebral herniation (MESH:D004677)
- **Chemicals:** EVT (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12915323/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12915323/full.md

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Source: https://tomesphere.com/paper/PMC12915323