Abstract

Intracranial aneurysms (IAs) are localized enlargements of cerebral blood vessels that cause substantial rates of mortality and morbidity in humans. The rupture possibility of these aneurysms is a critical medical challenge for physicians during treatment planning. This treatment planning while assessing the rupture potential of aneurysms becomes more complicated when they are constrained by an adjacent structure such as optic nerve tissues or bones, which is not widely studied yet. In this work, we considered and studied a constitutive model to investigate the bio-mechanical response of image-based patient-specific IA data using cardiovascular structural mechanics equations. We performed biomechanical modeling and simulations of four different patient-specific aneurysms’ data (three middle cerebral arteries and one internal carotid artery) to assess the rupture potential of those aneurysms under a plane contact constraint. Our results suggest that aneurysms with plane contact constraints produce less or almost similar maximum wall effective stress compared to aneurysms with no contact constraints. In our research findings, we observed that a plane contact constraint on top of an internal carotid artery might work as a protective wall due to the 16.6% reduction in maximum wall effective stress than that for the case where there is no contact on top of the aneurysm.

Highlights

  • Intracranial aneurysms (IAs) are pathological enlargements of the cerebral arteries that have severe outcomes when they rupture [1,2,3,4,5]

  • The effective wall stress for four different intracranial aneurysms is shown in Figure 2 for the cases where there was no contact constraint and where there was a plane contact constraint

  • From the first two simulation results (IA-01 and IA-02), it was seen that aneurysms with plane contact constraint produced less maximum effective wall stress

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Summary

Introduction

Intracranial aneurysms (IAs) are pathological enlargements of the cerebral arteries that have severe outcomes when they rupture [1,2,3,4,5]. Most of these aneurysms do not rupture during a person’s lifetime, ruptured aneurysms result in subarachnoid hemorrhage, which causes significant morbidity and mortality rates (25–50% mortality rate and around 64% long-term disability rate) [6,7,8,9,10,11,12]. Current clinical decision and aneurysm risk assessment would greatly benefit from suitable biomechanical modeling to comprehend the underlying mechanism of the initiation, progression, and rupture potential of aneurysms.

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