Hemodynamic and morphological differences in cerebral aneurysms between before and after rupture

Author:

Fujimura Soichiro12,Yamanaka Yuma23,Takao Hiroyuki24,Ishibashi Toshihiro4,Otani Katharina45,Karagiozov Kostadin4,Fukudome Koji1,Yamamoto Makoto1,Murayama Yuichi4

Affiliation:

1. Department of Mechanical Engineering, Tokyo University of Science, Katsushika-ku, Tokyo;

2. Division of Innovation for Medical Information Technology and

3. Graduate School of Mechanical Engineering, Tokyo University of Science, Katsushika-ku, Tokyo; and

4. Department of Neurosurgery, The Jikei University School of Medicine, Minato-ku, Tokyo;

5. Siemens Healthcare K.K., Gate City Osaki West Tower, Shinagawa-ku, Tokyo, Japan

Abstract

OBJECTIVE Although it has been proposed that aneurysm morphology is different after rupture, detailed research of the morphological changes using 3D imaging acquired before and after rupture has not been conducted because of the difficulty of data collection. Similarly, hemodynamic changes due to morphological alterations after rupture have not been analyzed. The aim of this study was to investigate the changes in morphology and hemodynamics observed after aneurysm rupture. METHODS For 21 cerebral aneurysms (21 patients) that ruptured during observation, 3D geometry of the aneurysms and parent arteries were reconstructed based on the angiographic images before and after their rupture. In addition, using the reconstructed geometry, blood flow was simulated by computational fluid dynamics (CFD) analysis. Morphological and hemodynamic parameters were calculated both before and after rupture, and their changes from before to after were compared. RESULTS In the morphological parameters, statistically significantly higher values were observed after rupture in height (before: 5.5 ± 2.1 mm, after: 6.1 ± 2.0 mm; p < 0.0001), aspect ratio (p = 0.002), aneurysm volume (p = 0.04), and undulation index (p = 0.005). In terms of hemodynamic changes, the mean normalized wall shear stress (NWSS) decreased significantly (before: 5.4 × 10−1 ± 2.9 × 10−1, after: 4.4 × 10−1 ± 2.8 × 10−1; p < 0.001) as well as the other NWSS parameters, including maximum and minimum NWSS, which were associated with stagnant flow due to the morphological changes after rupture. CONCLUSIONS Aneurysm morphology was found to change after rupture into an elongated and irregular geometry, accompanied by an increase in aneurysm volume. These morphological changes were also associated with statistically significant hemodynamic alterations that produced low wall sheer stress by stagnant flow. The authors’ results also provide the opportunity to explore and develop a risk evaluation method for aneurysm rupture based on prerupture morphology and hemodynamics by further exploration in this direction.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

Reference37 articles.

1. The significance of unruptured intracranial saccular aneurysms;Wiebers DO,1987

2. Unruptured cerebral aneurysms do not shrink when they rupture: multicenter collaborative aneurysm study group;Rahman M,2011

3. Morphologic and hemodynamic risk factors in ruptured aneurysms imaged before and after rupture;Chien A,2014

4. Rupture-associated changes of cerebral aneurysm geometry: high-resolution 3D imaging before and after rupture;Schneiders JJ,2014

5. Cerebral aneurysm size before and after rupture: case series and literature review;Yi J,2016

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