Skip to main content

ORIGINAL RESEARCH article

Front. Neurol., 06 July 2022
Sec. Endovascular and Interventional Neurology
This article is part of the Research Topic Insights in Endovascular and Interventional Neurology: 2021 View all 14 articles

Hemodynamic Comparison of Treatment Strategies for Intracranial Vertebral Artery Fusiform Aneurysms

  • 1Huashan Hospital, Fudan University, Shanghai, China
  • 2ArteryFlow Technology Co., Ltd, Hangzhou, China

Objective: This study comparatively analyzed the hemodynamic changes resulting from various simulated stent-assisted embolization treatments to explore an optimal treatment strategy for intracranial vertebral artery fusiform aneurysms. An actual vertebral fusiform aneurysm case treated by large coil post-stenting (PLCS) was used as a control.

Materials and Methods: A single case of an intracranial vertebral artery fusiform aneurysm underwent a preoperative and eight postoperative finite element treatment simulations: PLCS [single and dual Low-profile Visualized Intraluminal Support (LVIS)], Jailing technique (single and dual LVIS both simulated twice, Pipeline Embolization Device (PED) with or without large coils (LCs). Qualitative and quantitative assessments were performed to analyze the most common hemodynamic risk factors for recurrence.

Results: Jailing technique and PED-only had a high residual flow volume (RFV) and wall shear stress (WSS) on the large curvature of the blood flow impingement region. Quantitative analysis determined that PLSC and PED had a lower RFV compared to preoperative than did the jailing technique [PED+LC 2.46% < PLCS 1.2 (dual LVIS) 4.75% < PLCS 1.1 (single LVIS) 6.34% < PED 6.58% < Jailing 2.2 12.45% < Jailing 1.2 12.71% < Jailing 1.1 14.28% < Jailing 2.1 16.44%]. The sac-averaged flow velocity treated by PLCS, PED and PED+LC compared to preoperatively was significantly lower than the jailing technique [PED+LC = PLCS 1.2 (dual LVIS) 17.5% < PLCS 1.1 (single LVIS) = PED 27.5% < Jailing 1.2 = Jailing 2.2 32.5% < Jailing 1.1 37.5% < Jailing 2.1 40%]. The sac-averaged WSS for the PLCS 1.2 (dual LVIS) model was lower than the PED+LC, while the high WSS area of the Jailing 1 model was larger than for Jailing 2 [PLCS 1.2 38.94% (dual LVIS) < PED+LC 41% < PLCS 1.1 43.36% (single LVIS) < PED 45.23% < Jailing 2.1 47.49% < Jailing 2.2 47.79% < Jailing 1.1 48.97% < Jailing 1.2 49.85%].

Conclusions: For fusiform aneurysms, post large coil stenting can provide a uniform coil configuration potentially reducing the hemodynamic risk factors of recurrence. Flow diverters also may reduce the recurrence risk, with long-term follow-up required, especially to monitor branch blood flow to prevent postoperative ischemia.

Introduction

Fusiform aneurysms are more prone to occur in the posterior circulation (1). Intracranial aneurysm recurrence is related to the degree of the parent artery involved (2). Fusiform aneurysms have more extensive wall enhancement than the saccular variety indicating wall inflammation and vulnerability (3, 4). Vulnerable vessel walls exposed to abnormal hemodynamics are susceptible to aneurysm growth, rupture, and recurrence (57). For highly involved parent artery aneurysms, coils cannot be safely and effectively used for vascular reconstruction (8). Revascularization therapy mainly relies on various stent-assisted embolization techniques presenting different procedures and recurrence risks (9, 10). Currently, our center's most commonly used stent-assisted embolization techniques include Jailing, post-large-coil stenting (PLCS), and Pipeline Embolization Device (PED) combined with or without large-coil techniques. Jailing techniques with conventional stents present a relatively low procedure-related risk with a high recurrence exposure (11). PLCS proposed in our center can be used to embolize fusiform aneurysms and lower their recurrence rate. Increased off-label use of flow diverters presents some extent ischemic risk for intracranial vertebral artery fusiform aneurysms (12). Unclear hemodynamic effects among the various reconstructive strategies for intracranial vertebral fusiform aneurysms make it difficult to nominate an optimal approach.

Hemodynamically, wall shear stress (WSS) is an important risk factor for aneurysm rupture. Low WSS induces destructive remodeling caused by inflammatory cells, resulting in aneurysm instability. Higher than normal WSS also can result in the enlargement and rupture of aneurysms based on other mechanisms (6). This study focused on the recanalization risk induced by blood inflow for the unruptured aneurysm. To elucidate the issue of postoperative recurrence, high WSS and velocity, larger residual flow volume (RFV), and other hemodynamic characteristics from large blood inflow were correlated with recanalization and recurrence (1318). Luo et al. (16) reported high WSS and flow velocity in partially occluded saccular aneurysms prone to recanalization. Umeda et al. (18) found that RFV predicts the recurrence of coiled paraclinoid aneurysms. For large narrow-necked aneurysms, PED with coils treatment can accelerate thrombotic efficiency, favoring aneurysm occlusion in the competition with delayed rupture (19).

However, no CFD mechanism-related studies exist on the potential recurrence risk among different reconstruction techniques for intracranial vertebral artery fusiform aneurysms. This present study modeled an actual case of vertebral artery fusiform aneurysm treated with PLCS without considering thrombosis, simulating and comparing the preoperative hemodynamic effects and eight post-operative finite element treatment simulations– PLCS x 2 (single and dual Low-profile Visualized Intraluminal Support (LVIS)), Jailing technique x 4 (single and double LVIS both simulated twice with different coil configurations), and 2x Pipeline Embolization Device (PED) with or without large coils (LCs) – to analyze the most common hemodynamic risk factors for recurrence.

Materials and Methods

Population

A man in his 40 s with an intracranial fusiform aneurysm in the dominant vertebral artery experienced a sudden headache once 2 months ago. The left vertebral artery fusiform aneurysm diagnosed on MRI in a local hospital was treated with PLCS techniques (schematic Figure 1 for details). Three large coils compared to aneurysmal width (two Microplex-10 8 mm x 30 cm and one 7 mm x 30 cm) plus two LVIS stents (4.5 x 20 mm and 4.5 x 15 mm) were implanted with a modified Raymond IIIa outcome (Figure 2). The 12-month DSA follow-up showed no recurrence or remnant (Raymond I).

FIGURE 1
www.frontiersin.org

Figure 1. Post-large coil stenting technique schematic diagram. (A) The stenting microcatheter (blue) and unshaped coiling microcatheter (yellow) are positioned. (B) Coil diameter is selected with reference to the value ≥A. The aneurysm sac is evenly filled. (C) Continued embolization using 2–4 coils, then deploying the stent and placing the stenting microcatheter at the distal segment as a backup. (D) If the sac is not densely embolized or coil protrusion into the stent occurs, a second stent can be released to provide flow diversion, allowing further embolization to proceed. ①–③ For those with branches or an irregular sac, the stent can be semi-released to assist in forming a basket while protecting the branches.

FIGURE 2
www.frontiersin.org

Figure 2. A 49-year-old male patient presented with a sudden severe headache once 2 months prior. ① Preoperative high-resolution MRI showed significant enhancement of the vessel wall with the intraluminal slow flow (blue arrow). ② Right vertebral artery dysplasia. ③ Preoperative measurement of aneurysm and parent artery, aneurysm size: 7.31 x 8.39 mm. ④ Echelon-10 microcatheter (red arrow) was used to protect the posterior inferior cerebellar artery during operation. ⑤, ⑥ Stents were post-deployed, Immediate postoperative angiography and non-subtraction images showed slight stagnation in the aneurysm sac (Raymond IIIa; Microplex-10 coils: two 8 x 30 cm and one 7 x 30 cm; LVIS stents: 4.5 x 20 mm, 4.5 x 15 mm). ⑦ The distribution of the coils along the wall was not well-uniform. ⑧, ⑨ 12-month follow-up showed that there was no recurrence of the aneurysm (Raymond I) and the parent artery was patent. ⑩ 12-month follow-up with HR-MRI, the vortex in the sac disappeared, while the aneurysm wall was still partially enhanced.

Model Reconstruction

Raw data was generated from DSA rotational angiography (high-pressure injector rate 3 ml/s, time 5 s, total volume 15 ml) using Siemens equipment Axiom Artis Zeego, Siemens Medical Solutions, Erlangen, Germany). The acquired raw data were reconstructed in Mimics 17 software (Materialise, Leuven, Vlaams-Brabant, Belgium) to generate STL files subsequently imported into Geomagic 12 software for model repair, trimming, and smoothing (Figure 3A).

FIGURE 3
www.frontiersin.org

Figure 3. Simulation reconstruction model of aneurysm preoperatively and for eight different treatment approaches. (A) Preoperative aneurysm model. (B) Pipeline device (PED) 3.75*20 mm implantation model. (C) Large coil; Microplex-10 8 x 30 cm x 2 + 7 x 30 cm and PED-3.75 x 20 mm. (D–F) Single LVIS stent 4.5 x 20 mm (Jailing 1.1, Jailing 2.1, and PLCS 1.1). (G–I) Dual LVIS stent 4.5 x 20 mm, 4.5 x 15 mm (Jailing 1.2, Jailing 2.2, and PLCS 1.2).

Finite Element Simulation

A two-step finite element simulation of stent deployment was devised (20). Firstly, LVIS and Pipeline models were generated in SolidWorks (Dassault Systems, SolidWorks Corp., MA) according to geometric information (21). Secondly, stent deployment was simulated in ABAQUS v6.14 (SIMULIA, Providence, RI) using the Dynamic Explicit Method and B31 element type, which was also done for the coils. Stent-specific parameters obtained from a previous study (22) were divided into three steps: compression, delivery, and release of the stent. Initially, the stent in its fully released state was inserted into a round tube and compressed to a state where it can be inserted into the micro-catheter model by allocating the displacement load of the outer wall. Then, the stent followed the delivery path of the micro-catheter by providing the displacement load to be delivered to the target area. Finally, the micro-catheter was withdrawn, and the stent was released using a predefined stress-strain field allowing the stent to expand in the designated area to fit the inner wall of the artery. The delivery path was generated by connecting the center points of the blood vessel cross-section, while the stent release point was determined by the surgical image. The “general contact” algorithm was used in ABAQUS to deal with the complex interactions during stent release, with the friction coefficient assigned to 0.15 (23).

The simulation of the coil insertion process was carried out in ABAQUS (20). The process involved both pulling in and pushing out the coil. The coils were generated in MATLAB (MathWorks, Natwick, MA) using centerlines to simplify the coil shape (22). First, a coil-microcatheter-aneurysm model was built using NX12.0, and then the model was imported into ABAQUS. The coil is pulled into the microcatheter by distributing a displacement load at one end of the coil, while the coil inside the microcatheter is pushed out into the aneurysm using a pre-defined stress-strain field via creating a displacement load on the other end of the coil. Finally, the coil was placed in the aneurysm sac and then scanned in three dimensions according to the centerlines after placement (24, 25). The coil exhibited the following physical properties: a density of 2.13 × 10−8kg/m3, Young's modulus of 10,000 Pa, and Poisson's ratio of 0.39 (26). The three-dimensional stent and coil models obtained by finite element simulation were output as STL format files, maintaining the same spatial coordinate system as the blood vessel model in the next step of the hemodynamic simulation.

The simulated hemodynamics of the preoperative untreated model was adopted as baseline parameters. The jailing technique with coiling was conducted twice, to simulate both separated and connected coils. A total of eight postoperative treatment options were simulated (Figure 3): 1. PED implantation; 2. PED + large coils; 3–6. Jailing technique with two coiling simulations (1.1 single/1.2 dual LVIS with separated coils and 2.1 single/2.2 dual LVIS with connected coils); 7–8. For post-large-coil stenting (PLCS1.1 single/1.2 dual LVIS). Three large-coils (two Microplex-10 8 mm x 30 cm and one 7 mm x30 cm) and two stents (LVIS 4.5 mm x 20 mm and 4.5 mm x 15 mm) were selected. The PED size (3.75*20 mm) was determined by two neuro-interventionists with over 10-year experience.

Hemodynamic Simulation

The virtual treatment model is subjected to CFD simulation analysis. To generate mesh files, the preoperative and eight postoperative models were imported into ANSYS ICEM CFD version 16.2 (ANSYS Inc, Canonsburg, PA, USA). A grid independence test was performed to determine the appropriate grid size for the stability of the calculation outcomes and the efficiency calculation. Due to the different geometric dimensions of vessels, stents, and coils, the mesh sizes of different object surfaces are determined to various values. The grid size for the stent wire surface was finally set to 1/6 of the circumference of the wire. The artery and coil surface were 0.16 mm along with the 0.03 mm LVIS surface and the 0.015 mm PED surface grid. A three-layer boundary mesh was added to improve the accuracy of the simulation results in the near-surface region of the model. Final mesh calculations were generated as follows: 3 million for the preoperative model; 96 million for PED and PED with large coil; 45 million for Jailing1.1, 1.2, and PLCS1.1; 65 million for Jailing 2.1, 2.2, and PLCS1.2. The hemodynamic simulations were fitted with the Navier-Stokes equations for steady-state simulations using ANSYS CFX version 2019 (ANSYS Inc, Canonsburg, PA, USA). The blood was designed as an incompressible, laminar flow, Newtonian fluid with a density of 1,056 kg/m3 and a viscosity of.0035 kg/m·s (27). The vessel wall was designed to be rigid with no slip. The flow rate for the vertebral artery inlet was set at 1.3 ml/s (28). Outlet conditions were calculated according to Murray's law of flow distribution (29). A steady coupled solver was used for laminar simulation. The residual target of the convergence criterion was 0.00001.

Statistical Analysis of the Various Approaches

Qualitative and quantitative methods were used to analyze and compare the flow velocity, WSS, and RFV (v >0.03 m/s) (19) in the aneurysm sac among nine simulations (preoperative and eight postoperative simulations). The vascular segment covered by the stents was intercepted and the aneurysm sac volume was defined as the space between the vascular wall and the stent surface. Defining the preoperative hemodynamic parameters as 100%, the hemodynamic changes for each of the treatment strategies were analyzed and compared.

Results

Residual Blood Flow Volume (RFV)

Qualitative Analysis

RFV was discerned in the sac after PED implantation alone. According to the simulated projection and down-the-barrel view, the Jailing technique had a higher RFV on the large curved side due to the non-uniformity of the coil embolization, more similar to PED-only implantation than the RFV values of the PED+LC and PLCS techniques (Figures 4, 5).

FIGURE 4
www.frontiersin.org

Figure 4. (A) Preoperative high-velocity region (v > 0.03 m/s). (B–I) RFV maps for different stent-assisted techniques.

FIGURE 5
www.frontiersin.org

Figure 5. The down-the-barrel view of preoperative and different stent-assisted technique simulation treatment.

Quantitative Analysis

Both PLCS and PED with or without large-coils had lower residual percentages of RFV than the Jailing technique compared with pre-operation. The residual percentage of RFV of for dual stents in PLCS and Jailing are smaller than for the single stent [PED + LC 2.46% < PLCS 1.2 (dual LVIS) 4.75% < PLCS 1.1 (single LVIS) 6.34% < PED 6.58% < Jailing 2.2 12.45% < Jailing 1.2 12.71% < Jailing 1.1 14.28 % < Jailing 2.1 16.44%; Table 1, Figure 6].

TABLE 1
www.frontiersin.org

Table 1. Hemodynamic parameters pre-and post-operative stimulation treatment for various stent-assisted techniques.

FIGURE 6
www.frontiersin.org

Figure 6. Quantitative assessment of the sac-averaged WSS, sac-averaged velocity, and RFV of the simulated preoperative and various stent-assisted models.

The Average Flow Velocity of the Aneurysm Sac

The streamline diagram and quantitative analysis showed that the averaged flow velocity in the aneurysm sac after PLCS for PED with and without large-coils decreased significantly more than for the Jailing technique. The sac-averaged flow velocity for dual stents in PLCS and Jailing technique are smaller than single stent [PED+LC = PLCS1.2 (double LVIS) 17.5% < PLCS1.1 (single LVIS) = PED 27.5% < Jailing1.2 = Jailing2.2 32.5% < Jailing1.1 37.5% < Jailing2.1 40%; Table 1, Figures 6, 7].

FIGURE 7
www.frontiersin.org

Figure 7. (A) Preoperative velocity streamlines. (B–I) Post-operative velocity streamlines for PED, PED+LC, Jailing, and PLCS models.

Average WSS of the Aneurysm Wall

Qualitative Analysis

WSS values of all postoperative models decreased significantly compared with pre-operation. Jailing 1 experienced a larger high WSS region than Jailing 2 (Figure 8).

FIGURE 8
www.frontiersin.org

Figure 8. (A) Preoperative WSS. (B–I) WSS of PED, PED+LC, Jailing, and PLCS post-operative models.

Quantitative Analysis

WSS from the PLCS 1.2 (double LVIS) had the largest decline [PLCS1.2 (Dual LVIS) 38.94% < PED+LC 41% < PLCS1.1 (Single LVIS) 43.36% < PED 45.23% < Jailing2.1 47.49% < Jailing 2.2 47.79% < Jailing 1.1 48.97% < Jailing1.2 49.85 %; Table 1, Figures 6, 8].

Discussion

The main conclusion of this study is that PLCS and PED with or without large-coils can significantly decrease the hemodynamic risk factors of recurrence in the treatment of fusiform vertebral aneurysm compared with the jailing technique. Hemodynamic studies have shown that high WSS, large RFV, and high-velocity areas after interventional treatment are risk factors for aneurysmal recurrence (17, 19, 30). Chatziprodromou et al. and Rayz et al. (31, 32) reported that high blood flow velocity and high WSS are often accompanied, which is not conducive to thrombosis in the aneurysm sac and has an adverse impact on the long-term stability after embolization. Hemodynamic risk parameters – WSS, RFV, and high-velocity regions – were lower for PLCS than those for jailing, thus reducing the recurrence risk. In both jailing and PLCS technique, the hemodynamic risk factors of the single LVIS stent were larger than those for dual LVIS stents. Therefore, the overlapping stent technique is a beneficial option to reduce the potential risk of recurrence compared with a single stent. At present, few studies analyze the recurrence of vertebral artery aneurysms based on CFD (33, 34). These studies indicated that hemodynamics played a role in vertebral fusiform aneurysms similar to saccular aneurysms. Although the data, in this case, are based on the vertebral artery, the results should be generalizable to other aneurysms with similar morphological characteristics.

Quantitative analysis showed hemodynamic risk factors for recurrence after jailing was also confirmed higher than PLCS and PED techniques due to incomplete embolization from the micro-catheter fixed by the stent (35). Hong et al. (36) proposed that the semi-Jailing technique could help improve the maneuverability of the micro-catheter during the treatment of wide-necked complex aneurysms. Chen et al. (10) advocated a modified balloon-in-stent technique for the treatment of fusiform aneurysms. Prolonged balloon inflation and stent malposition potentially lead to thromboembolic events. The wide extent of inflammation on the fusiform aneurysm wall indicated vulnerability to recurrence (3, 37). The uniform distribution of coils helps create a local flow diversion effect which can reduce recurrence. The inflow tract WSS for Jailing 1 is larger than Jailing 2 mainly due to a failure to fully pack the impingement area, consistent with the recurrence of saccular aneurysms after embolization (38, 39). This suggests that more emphasis should be placed on the inflow tract.

Procedure critical points of the PLCS technique on coil, stent, and embolizing microcatheter selection should be emphasized for fusiform aneurysms. Coil packing has some inherent randomness in clinical practice. Coil configuration for PLCS should achieve a more even distribution than the jailing technique. The framing coils (diameter ≥ aneurysm width) often require repeated adjustment contributing to uniform coil distribution. While protecting the patency of the involved branches, semi-deployment of the stent can assist in framing the large coils. Soft coils with a smaller primary helix diameter were preferred to result in stent well-apposition. The proper amount of large-coils (24) is normally used to prevent stent opening failure. Small coils with a rivet technique may result in stenosis or delayed occlusion of the parent artery. LVIS stents were more usually selected for the PLCS technique due to a number of advantages. LVIS stents can be re-sheathed and pushed during the deployment process (9) allowing for the uniform distribution of large coils. Further, LVIS stent is tied to lower thrombogenicity than Pipeline stents. Finally, LVIS stents are more cost-effective than Pipelines (10). However, due to the local dense coverage rate, antiplatelets should be rigorously confirmed to avoid any delayed vessel occlusion. Previous studies have reported a wide range of LVIS in-stent stenosis rates between 17.5 and 86.7% (40, 41). According to previous studies, multiple flow diverters without coils were not recommended for ruptured lesions due to the necessity of strict antiplatelet therapy (42). On the other hand, treatment with overlapping PEDs also presents a high ischemic risk (12), such that non-overlapping stents might be preferable. Multiple flow diverters were not simulated in this present study. Using a Pipeline device with large coils is a promising technique for fusiform aneurysms, especially for aneurysms without evident perforators or branches. An unshaped or 45-degree tip can provide sway to the micro-catheter permitting greater maneuverability and thus the creation of more uniform baskets. For such patients, antiplatelet medication should be administered cautiously in the peri- and postoperative phase, with timely adjustment according to TEG and CYC2P19 gene results.

Limitations

This study has the following limitations. This proof-of-concept study was a single case. However, it effectively demonstrates hemodynamic effects after treatment for different stent-assisted techniques. Comprehensive intracranial stents such as Solitaire and Neuroform were not tested. In addition, not all treatment strategy combinations were simulated such as Jailing + Pipeline. Since a Murray flow outlet was employed in this study, the flow rate change of the PICA branch was inapplicable. The pressure outlet should be a feasible way to evaluate the influence on the flow rate of PICA. Flow change may be affected by thrombus and stent endothelialization. This study did not address the degree of vascular curvature which can affect the different stent-assisted strategies. The coil distribution from the PLCS technique is somewhat random and the simulation cannot be completely consistent with actual placement. This CFD study used common assumptions such as rigid walls and a lack of specific inflow and outflow tract flow conditions.

Conclusions

For fusiform aneurysms of the intracranial vertebral artery, the PLCS technique can more uniformly pack aneurysm sacs and may reduce the hemodynamic risk factors of recurrence similar to flow diverters, though long-term follow-up is still required. Attention should be paid to the impact on any perforators or branches to lessen the ischemic risk.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by the Institution Review Board of Huashan Hospital affiliated to Fudan University approved this retrospective study and waived the requirement for informed consent. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author Contributions

XZ and JX conceived and designed the research and handled the funding and supervision. YJ acquired the data and drafted the manuscript. YJ, GLu, LG, GLi, and RZ analyzed and interpreted the data. YJ, XL, and HW performed the statistical analysis. All authors made critical revisions to the manuscript for important intellectual content and reviewed the final version of the manuscript.

Funding

This work was partially supported by the National Natural Science Foundation of China (No. 81771242).

Conflict of Interest

GLi, RZ, XL, and JX were employed by the company ArteryFlow Technology Co., Ltd.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Guo Y, Song Y, Hou K, Yu J. Intracranial fusiform and circumferential aneurysms of the main trunk: therapeutic dilemmas and prospects. Front Neurol. (2021) 12:134. doi: 10.3389/fneur.2021.679134

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Jiang Y, Huang L, Lu G, Ge L, Di R, Wan H, et al. Risk factor analysis of recurrence of unruptured paraclinoid aneurysms following endovascular coiling [J]. Chin J Neurisurg. (2018) 34:982–7. doi: 10.3760/cma.j.issn.1001-2346.2018.10.003

CrossRef Full Text

3. Liu X, Zhang Z, Zhu C, Feng J, Liu P, Kong Q, et al. Wall enhancement of intracranial saccular and fusiform aneurysms may differ in intensity and extension: a pilot study using 7-t high-resolution black-blood mri. Eur Radiol. (2020) 30:301–7. doi: 10.1007/s00330-019-06275-9

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Kim BM, Shin YS, Kim SH, Suh SH, Ihn YK, Kim DI, et al. Incidence and risk factors of recurrence after endovascular treatment of intracranial vertebrobasilar dissecting aneurysms. Stroke. (2011) 42:2425–30. doi: 10.1161/STROKEAHA.111.617381

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Jiang Y, Ge L, Huang L, Wan H, Lu G, Zhang X. Large postoperative inflow area predictive of recurrence for paraclinoid aneurysms treated by simple coiling. J Clin Neurosci. (2022) 98:53–9. doi: 10.1016/j.jocn.2022.01.031

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Meng H, Tutino VM, Xiang J, Siddiqui A. High wss or low wss? Complex interactions of hemodynamics with intracranial aneurysm initiation, growth, and rupture: toward a unifying hypothesis. AJNR Am J Neuroradiol. (2014) 35:1254–62. doi: 10.3174/ajnr.A3558

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Xiang J, Tutino VM, Snyder KV, Meng H. Cfd: computational fluid dynamics or confounding factor dissemination? The role of hemodynamics in intracranial aneurysm rupture risk assessment. AJNR Am J Neuroradiol. (2014) 35:1849–57. doi: 10.3174/ajnr.A3710

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Zhao X, Wang H, Liu J, Zhang Z, Li Z. Endovascular treatment of vertebral artery dissecting aneurysm: a single-center experience. Exp Ther Med. (2019) 18:4838–44. doi: 10.3892/etm.2019.8128

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Di R, Ge L, Lu G, Huang L, Jiang Y, Wan H, et al. Clinical and angiographic outcomes of stent-assisted coiling of paraclinoid aneurysms: comparison of lvis and neuroform stents. J Clin Neurosci. (2021) 83:1–7. doi: 10.1016/j.jocn.2020.11.047

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Chen C, Chen C, Huang Y, Hsieh P, Wu Y, Yeap M, et al. Modified balloon-in-stent technique for circumferential vertebral artery dissecting aneurysm. World Neurosurg. (2021) 147:e552–8. doi: 10.1016/j.wneu.2020.12.120

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Zeng Z, Wu Y, Yan Y, Hong B, Xu Y, Liu J, et al. Clinical effect of endovascular treatment of basilar artery trunk saccular aneurysm[J]. Chin J Cerebrovasc Dis. (2020) 17:671–6. doi: 10.3969/j.issn.1672-5921.2020.11.006

CrossRef Full Text

12. Kiyofuji S, Graffeo CS, Perry A, Murad MH, Flemming KD, Lanzino G, et al. Meta-analysis of treatment outcomes of posterior circulation non-saccular aneurysms by flow diverters. J Neurointerv Surg. (2018) 10:493–9. doi: 10.1136/neurintsurg-2017-013312

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Zhang Q, Jing L, Liu J, Wang K, Zhang Y, Paliwal N, et al. Predisposing factors for recanalization of cerebral aneurysms after endovascular embolization: a multivariate study. J Neurointerv Surg. (2018) 10:252–7. doi: 10.1136/neurintsurg-2017-013041

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Nambu I, Misaki K, Uchiyama N, Mohri M, Suzuki T, Takao H, et al. High pressure in virtual postcoiling model is a predictor of internal carotid artery aneurysm recurrence after coiling. Neurosurgery. (2019) 84:607–15. doi: 10.1093/neuros/nyy073

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Sugiyama S, Niizuma K, Sato K, Rashad S, Kohama M, Endo H, et al. Blood flow into basilar tip aneurysms: a predictor for recanalization after coil embolization. Stroke. (2016) 47:2541–7. doi: 10.1161/STROKEAHA.116.013555

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Luo B, Yang X, Wang S, Li H, Chen J, Yu H, et al. High shear stress and flow velocity in partially occluded aneurysms prone to recanalization. Stroke. (2011) 42:745–53. doi: 10.1161/STROKEAHA.110.593517

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Sheng B, Wu D, Yuan J, Xu S, Li Z, Dong J, et al. Hemodynamic characteristics associated with paraclinoid aneurysm recurrence in patients after embolization. Front Neurol. (2019) 10:429. doi: 10.3389/fneur.2019.00429

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Umeda Y, Ishida F, Tsuji M, Furukawa K, Shiba M, Yasuda R, et al. Computational fluid dynamics (cfd) using porous media modeling predicts recurrence after coiling of cerebral aneurysms. PLoS ONE. (2017) 12:e190222. doi: 10.1371/journal.pone.0190222

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Xiang J, Ma D, Snyder KV, Levy EI, Siddiqui AH, Meng H. Increasing flow diversion for cerebral aneurysm treatment using a single flow diverter. Neurosurgery. (2014) 75:286–94. doi: 10.1227/NEU.0000000000000409

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Leng X, Wang Y, Xu J, Jiang Y, Zhang X, Xiang J. Numerical simulation of patient-specific endovascular stenting and coiling for intracranial aneurysm surgical planning. J Transl Med. (2018) 16:208. doi: 10.1186/s12967-018-1573-9

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Bouillot P, Brina O, Ouared R, Yilmaz H, Farhat M, Erceg G, et al. Geometrical deployment for braided stent. Med Image Anal. (2016) 30:85–94. doi: 10.1016/j.media.2016.01.006

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Reedlunn B. Tension-Torsion Experiments on Superelastic Shape Memory Alloy Tubes. Stone Mountain, GA: The American society of mechanical engineers (ASME) (2012). doi: 10.1115/SMASIS2012-8185

CrossRef Full Text | Google Scholar

23. Ma D, Dumont TM, Kosukegawa H, Ohta M, Yang X, Siddiqui AH, et al. High fidelity virtual stenting (hifivs) for intracranial aneurysm flow diversion: in vitro and in silico. Ann Biomed Eng. (2013) 41:2143–56. doi: 10.1007/s10439-013-0808-4

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Zhu P. Comparison of Three-Dimensional Shape Memory Alloy Constitutive Models: Finite Element Analysis of Actuation and Superelastic Responses of a Shape Memory Alloy Tube. Tehran, IR: Sharif University of Technology (2013). doi: 10.1115/SMASIS2013-3093

CrossRef Full Text | Google Scholar

25. Zhang H, Jiao Y, Johnson E, Zhan L, Zhang Y, Shimada K. Modelling anisotropic material property of cerebral aneurysms for fluid-structure interaction simulation. Comput Methods Biomech Biomed Engin. (2013) 1:164–74. doi: 10.1080/21681163.2013.776270

CrossRef Full Text | Google Scholar

26. Babiker MH, Chong B, Gonzalez LF, Cheema S, Frakes DH. Finite element modeling of embolic coil deployment: multifactor characterization of treatment effects on cerebral aneurysm hemodynamics. J Biomech. (2013) 46:2809–16. doi: 10.1016/j.jbiomech.2013.08.021

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Jiang Y, Ge L, Di R, Lu G, Huang L, Li G, et al. Differences in hemodynamic characteristics under high packing density between the porous media model and finite element analysis in computational fluid dynamics of intracranial aneurysm virtual treatment. J Neurointerv Surg. (2019) 11:853–8. doi: 10.1136/neurintsurg-2018-014218

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Fahrig R, Nikolov H, Fox AJ, Holdsworth DW, A. three-dimensional cerebrovascular flow phantom. Med Phys. (1999) 26:1589–99. doi: 10.1118/1.598672

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Murray CD. The physiological principle of minimum work applied to the angle of branching of arteries. J Gen Physiol. (1926) 9:835–41. doi: 10.1085/jgp.9.6.835

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Liu J, Jing L, Wang C, Paliwal N, Wang S, Zhang Y, et al. Effect of hemodynamics on outcome of subtotally occluded paraclinoid aneurysms after stent-assisted coil embolization. J Neurointerv Surg. (2016) 8:1140–7. doi: 10.1136/neurintsurg-2015-012050

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Chatziprodromou I, Tricoli A, Poulikakos D, Ventikos Y. Haemodynamics and wall remodelling of a growing cerebral aneurysm: a computational model. J Biomech. (2007) 40:412–26. doi: 10.1016/j.jbiomech.2005.12.009

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Rayz VL, Boussel L, Lawton MT, Acevedo-Bolton G, Ge L, Young WL, et al. Numerical modeling of the flow in intracranial aneurysms: prediction of regions prone to thrombus formation. Ann Biomed Eng. (2008) 36:1793–804. doi: 10.1007/s10439-008-9561-5

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Suzuki T, Hasegawa H, Ando K, Shibuya K, Takahashi H, Saito S, et al. Possibility of worsening flow diversion effect due to morphological changes of a stented artery with multiple overlapping stents for partially thrombosed vertebral artery aneurysms. Front Neurol. (2020) 11:611124. doi: 10.3389/fneur.2020.611124

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Chen L, Leng X, Zheng C, Shan Y, Wang M, Bao X, et al. Computational fluid dynamics (cfd) analysis in a ruptured vertebral artery dissecting aneurysm implanted by pipeline when recurrent after lvis-assisted coiling treatment: case report and review of the literatures. Interv Neuroradiol. (2022) 58:320793306. doi: 10.1177/15910199221097766

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Yoon SG, Jin SC, Kim SH, Jeon KD, Kim DY, Lee SI, et al. Jailing technique using a catheter-based open-cell stent system in internal carotid artery sidewall aneurysms unfeasible to simple coiling. J Cerebrovasc Endovasc Neurosurg. (2013) 15:293–8. doi: 10.7461/jcen.2013.15.4.293

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Hong B, Patel NV, Gounis MJ, DeLeo MR, Linfante I, Wojak JC, et al. Semi-jailing technique for coil embolization of complex, wide-necked intracranial aneurysms. Neurosurgery. (2009) 65:1131–9. doi: 10.1227/01.NEU.0000356983.23189.16

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Zhang Y, Sui B, Liu J, Wang Y, Tian Z, Chen J, et al. Aneurysm wall enhancement on magnetic resonance imaging as a risk factor for progression of unruptured vertebrobasilar dissecting aneurysms after reconstructive endovascular treatment. J Neurosurg. (2018) 128:747–55. doi: 10.3171/2016.11.JNS162433

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Cha KS, Balaras E, Lieber BB, Sadasivan C, Wakhloo AK. Modeling the interaction of coils with the local blood flow after coil embolization of intracranial aneurysms. J Biomech Eng. (2007) 129:873–9. doi: 10.1115/1.2800773

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Meng H, Wang Z, Hoi Y, Gao L, Metaxa E, Swartz DD, et al. Complex hemodynamics at the apex of an arterial bifurcation induces vascular remodeling resembling cerebral aneurysm initiation. Stroke. (2007) 38:1924–31. doi: 10.1161/STROKEAHA.106.481234

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Alghamdi F, Mine B, Morais R, Scillia P, Lubicz B. Stent-assisted coiling of intracranial aneurysms located on small vessels: midterm results with the lvis junior stent in 40 patients with 43 aneurysms. Neuroradiology. (2016) 58:665–71. doi: 10.1007/s00234-016-1668-z

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Cho YD, Sohn CH, Kang HS, Kim JE, Cho WS, Hwang G, et al. Coil embolization of intracranial saccular aneurysms using the low-profile visualized intraluminal support (lvis) device. Neuroradiology. (2014) 56:543–51. doi: 10.1007/s00234-014-1363-x

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Becske T, Kallmes DF, Saatci I, McDougall CG, Szikora I, Lanzino G, et al. Pipeline for uncoilable or failed aneurysms: results from a multicenter clinical trial. Radiology. (2013) 267:858–68. doi: 10.1148/radiol.13120099

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: coil, flow diverter, stent, hemodynamics, recurrence

Citation: Jiang Y, Lu G, Ge L, Zou R, Li G, Wan H, Leng X, Xiang J and Zhang X (2022) Hemodynamic Comparison of Treatment Strategies for Intracranial Vertebral Artery Fusiform Aneurysms. Front. Neurol. 13:927135. doi: 10.3389/fneur.2022.927135

Received: 23 April 2022; Accepted: 06 June 2022;
Published: 06 July 2022.

Edited by:

Diogo C. Haussen, Emory University, United States

Reviewed by:

Thomas Peach, University College London, United Kingdom
Marco Túlio Salles Rezende, Hospital Felício Rocho, Brazil

Copyright © 2022 Jiang, Lu, Ge, Zou, Li, Wan, Leng, Xiang and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jianping Xiang, jianping.xiang@arteryflow.com; Xiaolong Zhang, xiaolongzhang@fudan.edu.cn

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.