# A multicenter hemodynamics–based nomogram predicting incomplete occlusion of intracranial aneurysms treated with pipeline embolization device

**Authors:** Yawen Zhao, Li Bao, Shuang He, Yunfeng Zhang

PMC · DOI: 10.3389/fneur.2026.1756374 · Frontiers in Neurology · 2026-02-09

## TL;DR

This study created a tool to predict if brain aneurysms treated with a device will not fully close, using blood flow and patient data.

## Contribution

A novel hemodynamics-based nomogram was developed and validated to predict incomplete occlusion after pipeline embolization device treatment.

## Key findings

- Smoking, flow complexity, and device migration were significant predictors of incomplete occlusion.
- The nomogram achieved an AUC of 0.785 in training and 0.809 in validation sets.
- The model showed consistent calibration and strong clinical utility for predicting incomplete occlusion.

## Abstract

This multicenter study aimed to develop and validate a hemodynamics-based nomogram for predicting incomplete occlusion (ICO) of intracranial aneurysms (IAs) after pipeline embolization device (PED) treatment.

426 IAs from 362 patients were analyzed and divided into a training set (n = 298) and a validation set (n = 128). Morphological and hemodynamic parameters of the IAs were calculated using AneuFlow Pro. Independent predictors of ICO were identified using least absolute shrinkage and selection operator (LASSO) regression and logistic regression to develop a predictive nomogram. The nomogram's performance was evaluated using area under the curve (AUC), calibration curves, and decision curve analysis (DCA).

The aneurysm occlusion rate of the overall cohort was 79.8% with a median angiographic follow-up time of 199 days. No significant differences were observed in patient and aneurysm characteristics between the training and validation sets. Through LASSO and logistic regression analyses, we identified smoking (OR = 0.32, 95% CI 0.14–0.68, p = 0.005), flow complexity (OR = 3.03, 95% CI 1.58–5.89, p < 0.001), device migration (OR = 11.03, 95% CI 1.51–105.55, p = 0.021), poor wall apposition (OR = 3.21, 95% CI 1.37–7.53, p = 0.007), aneurysm angle (OR = 3.46, 95% CI 1.79–6.93, p < 0.001), and low wall shear stress area ratio (LSAR; OR = 2.78, 95% CI 1.46–5.50, p = 0.002) as independent predictors of ICO. A nomogram developed based on these factors showed an AUC of 0.785 (95% CI 0.719–0.850) in the training set and 0.809 (95% CI 0.695–0.923) in the validation set, demonstrating consistent calibration and excellent clinical use.

The hemodynamics-based nomogram developed in this study effectively predicted ICO of IAs after PED treatment.

## Full-text entities

- **Genes:** ABCB6 (ATP binding cassette subfamily B member 6 (LAN blood group)) [NCBI Gene 10058] {aka ABC, LAN, MTABC3, PRP, umat}
- **Diseases:** endoleak (MESH:D057867), arteriovenous malformations or fistulas (MESH:D001164), malignancy (MESH:D009369), PED (MESH:D009471), intimal (MESH:C563733), rupture (MESH:D012421), aneurysm (MESH:D000783), stenosis (MESH:D003251), neurological deficits (MESH:D009461), atherosclerosis (MESH:D050197), aneurysm rupture (MESH:D017542), Stroke (MESH:D020521), aneurysmal subarachnoid hemorrhage (MESH:D013345), vertebral artery aneurysm (MESH:D020217), IA occlusion (MESH:D001157), thrombosis (MESH:D013927), hematomas (MESH:D006406), inflammatory (MESH:D007249), intracranial hemorrhage (MESH:D020300), IAs (MESH:D002532)
- **Chemicals:** heparin (MESH:D006493), ticagrelor (MESH:D000077486), FU (MESH:D005472), tirofiban (MESH:D000077466), clopidogrel (MESH:D000077144), CO (-), aspirin (MESH:D001241)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12926474/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926474/full.md

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Source: https://tomesphere.com/paper/PMC12926474