Abstract
BACKGROUND AND PURPOSE: Flow diverter–induced hemodynamic change plays an important role in the mechanism of intracranial aneurysm occlusion. Our aim was to explore the relationship between aneurysm features and flow-diverter treatment of unruptured sidewall intracranial aneurysms.
MATERIALS AND METHODS: MR imaging, 4D phase-contrast, was prospectively performed before flow diverter implantation in each patient with unruptured intracranial aneurysm. Two postprocedure follow-ups were scheduled at 6 and 12 months. Responses were grouped according to whether the aneurysms were occluded or remnant. Preprocedural aneurysm geometries and ostium hemodynamics in 38 patients were compared between the 2 groups at 6 and 12 months. Receiver operating characteristic curve analyses were performed for significant geometric and hemodynamic continuous parameters.
RESULTS: After the 6-month assessment, 21 of 41 intracranial aneurysms were occluded, and 9 additional aneurysms were occluded at 12 months. Geometrically, the ostium maximum diameter was significantly larger in the remnant group at 6 and 12 months (both P < .001). Hemodynamically, the proximal inflow zone was more frequently observed in the remnant group at 6 months. Several preprocedural ostium hemodynamic parameters were significantly higher in the remnant group. As a prediction for occlusion, the areas under the curve of the ostium maximum diameter (for 6 and 12 months), systolic inflow rate ratio (for 6 months), and systolic inflow area (for 12 months) reached 0.843, 0.883, 0.855, and 0.860, respectively.
CONCLUSIONS: Intracranial aneurysms with a large ostium and strong ostium inflow may need a longer time for occlusion. Preprocedural 4D flow MR imaging can well illustrate ostium hemodynamics and characterize aneurysm treatment responses.
ABBREVIATIONS:
- FD
- flow diverter
- PC
- phase-contrast
- RA
- rotational angiography
Intracranial aneurysm can cause hemorrhage associated with high mortality or residual neurologic deficits.1 Compared with surgical clipping, interventions with lower complication rates and a shorter inpatient stay are preferred. With respect to intervention, the use of a flow diverter (FD) has recently been introduced for cerebral aneurysms. Previous studies showed that procedure-related complications, including ischemia or hemorrhage, did not differ between the FD and the coil groups, but flow diversion could provide higher occlusion rates and fewer necessary re-treatments, especially for the sidewall type of aneurysm in the tortuous ICA.2,3
On the one hand, the hemodynamic dampening effect by flow diversion is considered to play an important role in the mechanism of aneurysm occlusion. Results from different research groups showed the reduction of inflow velocity and intra-aneurysm flow velocity after FD deployment.4⇓-6 Hemodynamically, they were related with specific metal coverage and porosity of the FD.7 On the other hand, the influence of aneurysm features on FD treatment responses remains unclear, and some treated aneurysms remain patent in clinical practice,8,9 probably due to other hemodynamic reasons. Our experience with the utilization of 4D phase-contrast (PC) MR imaging for intracranial aneurysms helps us to investigate this reason before the deployment of an FD. By applying numerical simulation for a virtual flow diversion, computational fluid dynamic analyses have been used to evaluate the hemodynamic reduction inside the aneurysm.5,10,11 However, because of their specific assumptions, little predictive information on aneurysm outcome after flow diversion was provided.
In this study, we used 4D PC MRI, a powerful in vivo analytic tool that has already been used for the assessment of intra-aneurysmal flow modification after FD treatment6 to explore aneurysm hemodynamics and outcome. Other research groups have reported flow conditions at the aneurysm neck with an in vivo hemodynamic assessment by using a 1.5T MR scanner and with an emphasis on the measurability and influential factors of neck flow.12⇓-14 Nevertheless, to our knowledge, few reports have investigated the relationship between the ostium and FD treatment response.15,16 We hypothesized that different FD treatment responses were related to aneurysm features, and our study focused on the aneurysm geometries and hemodynamics at the ostium. The aim of this study was to perform an in vivo investigation of the relationship between aneurysm features, particularly the geometric and hemodynamic parameters and their impact on FD treatment responses.
MATERIALS AND METHODS
Patients
We conducted a prospective study of 41 patients (4 men, 37 women; mean ± standard deviation (SD) age, 53.8 ± 13.1 years, [range, 26–81 years]) diagnosed with unruptured sidewall intracranial aneurysm and accepted for an FD procedure between November 2012 and November 2017. Two women were excluded because of preprocedural 4D PC MRI acquisition problems. One man was excluded because the follow-up examination showed a proximal displacement of the FD, which resulted in insufficient ostial coverage. Ethics approval was granted by the local ethics committee, and patient consent was obtained. Inclusion and exclusion criteria are shown in Table 1.
Image Acquisition and Postprocessing
MR imaging was performed within 72 hours before the endovascular procedure with a 3T PET/MR system (Ingenuity TF; Philips Healthcare, Best, the Netherlands) and an 8-channel head coil. After 3D TOF imaging, 4D PC MRI acquisition slabs were positioned to cover the aneurysm bulge and its adjacent parent vessel. This sequence, triggered with the cardiac frequency, included velocity encoding in the 3 directions with the following parameters: field of view 190 × 210 mm2, typically 32 slices (adjusted according to the aneurysm), acquisition voxel size 1 × 1 × 1 mm3 reconstructed with 0.82 mm3, sensitivity encoding acceleration factor 2, TR/TE 4.6/2.9 ms, and acquisition time 13 min. The number of cardiac phase acquisitions was based on the heart rate, and it typically ranged from 14 to 16 in this study.6 The 3D rotational angiography (RA) was acquired before FD stent implantation with a biplane angiographic unit (Allura FD20; Philips Healthcare).6 After raw data postprocessing (see Supplemental Materials and Methods) from the 4D PC MRI and 3D RA,17,18 velocity field information and the parent vessel flow rate were acquired for further analysis.
Geometric and Hemodynamic Parameters
Each aneurysm ostium plane was defined as the location from which the aneurysm sac bulged out of its parent vessel. Aneurysm sac size, perpendicular height, maximum height, ostium maximum diameter, and ostium area were measured on preprocedural 3D RA images.19 Aspect ratio (the ratio of aneurysm perpendicular height to the average ostium diameter) and size ratio (the ratio of the aneurysm maximum height to the parent vessel diameter) were computed on geometric parameters according to previously described formulas.20 Image management and geometric measurements were performed with OsiriX MD (version 9.5; http://www.osirix-viewer.com).
According to velocity field information, hemodynamic parameters at the aneurysm neck were evaluated on the open-source software Paraview (version 5.6.0; Kitware, Clifton Park, New York). The hemodynamic inflow zone at the aneurysm neck level was qualitatively evaluated at the systolic peak, and its location was trichotomously classified as proximal, lateral side, and distal neck by 2 independent analysts, with a final consensus (Fig 1).13
The following hemodynamic quantitative parameters related to the ostium were based on the inflow velocity components that were normal to the ostial plane. Hemodynamic parameters of maximum inflow velocity and mean inflow velocity were computed at the systolic time. Only mean inflow velocity was spatially averaged over the inflow area. The maximum inflow rate was the product of the mean inflow velocity and systolic inflow area at the ostium. The systolic inflow rate ratio was the ratio of the maximum inflow rate at the ostium to the systolic flow rate in the parent vessel. The parent vessel flow rate was computed and averaged from different cross-sectional planes of the parent artery proximal to the aneurysm during the complete cardiac cycle.
Interventional Procedures and Follow-Up
FD selection (see Supplemental Materials and Methods) was determined by navigability and implantation issues. No combination of coils was used. FDs were deployed by an experienced neurointerventionist, followed by a conebeam CT to confirm proper deployment. MR imaging follow-ups were completed on 3T scanners with routine and appropriate technical parameters in sequences of T1WI, T2WI, 3D TOF-MRA, contrast-enhanced MRA, and contrast-enhanced T1WI. Diagnostic angiographic follow-ups performed by the same neurointerventionist focused on the target aneurysms. For the diseased side of the ICA, 2D DSA and 3D RA were acquired by following standard protocols.21
According to 6- and 12-month contrast-enhanced MR imaging or DSA follow-ups by using a simplified 2-grade scale,22,23 FD-treated aneurysms were classified as either “occlusion” or “remnant” by 2 experienced neuroradiologists blinded to each other (Fig 2). In the case of a disagreement, a third expert was asked for a decision. Additional follow-up for extra time was not suggested because other treatment options were adopted for remnant aneurysms after the 12-month follow-up. All the investigators were blinded to the acquisition parameters from the follow-up periods.
Statistical Analyses
Statistical analyses were performed by using PAWS Statistics (version 18.0; IBM, Armonk, New York). Interrater reliabilities were evaluated with the Cohen kappa coefficient (κ) for the preprocedure inflow zone classification and image follow-up assessment. Due to analytical consideration χ2 analyses were performed to compare different inflow zones (proximal versus lateral side and distal neck) between the occlusion and remnant groups at the 2 follow-up time points. Preprocedural geometric and hemodynamic continuous parameters between the 2 groups were compared by using the Student t test. Receiver operating characteristic curve analyses and the Youden index were performed for the most significantly different geometric and hemodynamic continuous parameters.24⇓-26 P < .05 was considered statistically significant.
RESULTS
Patient Demographics
Thirty-eight patients (mean ± SD age, 53.7 ±13.4 years [range, 26–81 years]) with 41 target aneurysms underwent subsequent FD procedures and were included in the study. In 3 patients, 2 target aneurysms were close to each other, and 1 FD was deployed for both to achieve the coverage of the 2 ostia at the same time. Three of the 38 patients (7.9%) were men (mean ± SD age, 48.3 ± 7.6 years [range, 40–55 years]), and 35 were women (mean ± SD age, 54.2 ± 13.7 years [range, 26–81 years]). There was no significant difference (P > .05) in age between sexes. Apart from 1 middle cerebral artery aneurysm (M1 segment), the aneurysms were situated in the C4 to C6 (cavernous, clinoid, ophthalmic/supraclinoid) segments of the ICA (Bouthillier nomenclature).
Clinical Follow-Up
One patient without an aneurysm occlusion at 6 months missed the 12-month follow-up and only a 6-month comparison could be included. Another patient with an occlusion at 12 months missed the 6-month follow-up and only a 12-month comparison could be included (On-line Figure). Also, 40 aneurysms were screened for the comparison at 6 and 12 months. Two neuroradiologists had moderate interrater reliability (κ = 0.738, P < .001), with a third expert for the first two neuroradiologists’ disagreements. After 6-month (173.7 ± 48.1 days) and 12-month (367.8 ± 83.4 days) follow-ups, 21 (21/40 [52.5%]) and 30 aneurysms (30/40 [75.0%]) were occluded, respectively.
Geometric Comparison
There were significant differences in the aneurysm sac size, perpendicular height, maximum height, ostium maximum diameter, ostium area, and size ratio for different treatment response groups at 6 and 12 months. Among these, the ostium maximum diameter showed the most pronounced difference (Tables 2 and 3). There was no significant difference in aspect ratio at either time point.
Hemodynamic Qualitative Comparison
Two independent analysts trichotomously determined hemodynamic inflow zone at the aneurysm neck level with good consensus (κ = 0.754, P < .001). Qualitative analyses at the aneurysm neck revealed that subjects with an inflow zone on the proximal neck in the remnant group were statistically more frequent than subjects with other inflow zones at 6 months (P = .004) (Table 4) but not at 12 months (P = .13) (Table 4).
Hemodynamic Quantitative Comparison
For preprocedural hemodynamic quantitative parameters at the ostium, there were significant differences in maximum inflow velocity, maximum inflow rate, systolic inflow rate ratio, and the systolic inflow area between the different treatment response groups at 6 months (Table 2). Significant differences for preprocedural maximum inflow rate, systolic inflow rate ratio, systolic inflow area, and parent vessel flow rate were observed between the different groups at 12 months (Table 3). The most pronounced differences were observed for the systolic inflow rate ratio and systolic inflow area at 6 and at 12 months, respectively.
Receiver Operating Characteristic Prediction Parameters
As predicting parameters with receiver operating characteristic curves for the occlusion and remnant groups at 6 months, the areas under the curves of ostium maximum diameter and systolic inflow rate ratio reached 0.843 (95% CI, 0.707–0.980; P < .001) and 0.855 (95% CI, 0.735–0.974; P < .001), respectively (Fig 3). For the prediction of different responses at 12 months, areas under the curves of ostium maximum diameter and systolic inflow area were 0.883 (95% CI, 0.759–1.000; P < .001) and 0.860 (95% CI, 0.730–0.990; P = .001), respectively (Fig 4). Based on the Youden index for favorable sensitivity and specificity, the optimum predictive cutoff at 6 months was 4.9 mm for the ostium maximum diameter (sensitivity, 73.7%; specificity, 100%; Youden index, 0.737) and 0.343 for the systolic inflow rate ratio (sensitivity, 68.4%; specificity, 90.5%; Youden index, 0.589). The optimal predictive cutoff at 12 months was 4.9 mm for ostium maximum diameter (sensitivity, 90.0%; specificity, 83.3%; Youden index, 0.733) and 13.35 mm2 for the systolic inflow area (sensitivity, 90.0%; specificity, 80.0%; Youden index, 0.700) (Fig 5).
DISCUSSION
This prospective study compared geometric and hemodynamic parameters in unruptured sidewall intracranial aneurysms for different FD treatment responses at 2 follow-up time points. Other studies have reported on the parameters for differentiation of the aneurysm response,15,16 but we highlighted the relationship between in vivo aneurysm hemodynamics and the treatment responses, and tried to give a hemodynamic explanation for the delayed occlusion. Our results showed geometric and hemodynamic differences between the occlusion and remnant groups at 6 and 12 months. In addition, 4D flow MR imaging before treatment with a FD gave important insights into the ostium hemodynamics that were helpful in predicting the treatment responses. Among all the geometric parameters, a large ostium maximum diameter (>4.9 mm) was constantly and significantly associated with delayed occlusion, similar to a previous report.9
However, ostium hemodynamics provided new perspectives to investigate the influence of the FD. A proximal inflow area at the aneurysm neck represented a direct blood flow injecting into the aneurysm that might delay the occlusion. Because aneurysms in our study were mostly located in the tortuous ICA and the main flow often shifted to the lateral side of the artery by the inertial behavior after a sharp turn, the inflow zone on the lateral side was commonly observed.13
Furthermore, a strong inflow at the neck, especially a high systolic inflow rate ratio (>0.343) and large systolic inflow area (>13.35 mm2), indicated more blood flow impinging on the aneurysm ostium, which would hinder the dampening of blood flow and even result in long-term patency. Our results showed that these 2 parameters were of importance and could well predict the FD treatment response. The advantage of this predictive tendency could be the possibility to plan a more individualized intervention to achieve a better patient outcome, such as a coiling aid or a combination of different patterns of FDs.
Although almost each geometric dimensional parameter shared the same trend between comparisons at 6 and 12 months, some variations could be observed in the hemodynamic parameters between the 2 time points. The preprocedural qualitative inflow zone and maximum inflow velocity were only significantly different between the different treatment response groups at 6 months and the parent flow rate between the different groups at 12 months. This suggests that some hemodynamic parameters may have different implications for short- and long-term responses, and provides a clue to further investigate the underlying reasons.
The FD may change local hemodynamics rather than simply covering the ostium and may need some time for a complete thrombosis inside the aneurysm and intimal endothelialization of the FD after the flow has been modified. According to the literature,27⇓⇓-30 the occlusion rate is variable. Our 6-month occlusion rate was slightly lower, but we found a similar rate at 12 months. Our results also showed that different hemodynamic initial conditions influenced the treatment response and thus provided more direct evidence to confirm the hemodynamic change effect on aneurysms. At present, due to metallic magnetic susceptibility and a low velocity from flow diversion, a direct in vivo hemodynamic MR imaging evaluation near the FD segment still has some limitations.
It is believed that the geometric and hemodynamic features are not the only influential factors. FD selection and deployment technique are also important to the treatment response.31 A fitted FD and its proper position in the target vessel are prerequisites, and thus we excluded 1 case with FD displacement at follow-up. Although 3 types of FDs were used, there was no obvious discrepancy in treatment responses (On-line Table). Antiplatelet therapy could also influence the thrombosis in the aneurysm.32 In our cohort, clopidogrel was stopped after the 6-month follow-up unless there was a definite in-stent stenosis, but aspirin was continued. At least 8 aneurysms from our cohort occluded during the second 6-month period, and this may have been due to an additional effect exerted by clopidogrel discontinuity.
This study had some limitations. First, we only admitted patients with sidewall aneurysms because this type is considered a frequent and appropriate indication for flow diversion.7,33,34 In addition, its ostium can be better defined than those of other types. Second, although this in vivo study applied optimal acquisition by using PC MRI on a 3T system, MR imaging itself still has inherent limitations. For example, the presetting of the velocity sensitivity encoding parameter, the moderate spatial and temporal resolution according to our scan protocol may reduce MRI accuracy.35 Indeed, relatively low spatial resolution might imprecisely resolve a small region of interest for aneurysm ostium to some extent. Third, if the FD apparently changed the arterial angle because of its radial force, then the preprocedural hemodynamic analysis might not be fully consistent with the subsequent situation. A multicenter study with a large number of cases would seem to be essential for further analysis.
CONCLUSIONS
Intracranial aneurysms with a large ostium, systolic inflow rate ratio, and systolic inflow area may need a longer time for occlusion. Apart from conventional aneurysm geometric differences between occlusion and remnant groups, 4D flow MR imaging as a functional technique has the potential to well evaluate ostium hemodynamics and to hemodynamically explain FD treatment response in sidewall intracranial aneurysms.
Footnotes
This work originated at University Hospitals of Geneva, 4 Rue Gabrielle-Perret-Gentil, Geneva 1211, Switzerland.
Supported by Swiss National Funds (SNF 32003B_160222 and SNF 320030_156813) and Beijing Li Huanying Medical Foundation (2017).
Previously presented at: Radiological Society of North America 105th Scientific Assembly, Chicago, Illinois, December 1–6, 2019.
Disclosures: Tianhao Su—RELATED: Grant: Swiss National Funds, Beijing Li Huanying Medical Foundation, Comments: SNF 32003B_160222 and SNF 320030_156813, Beijing Li Huanying Medical Foundation 2017.* Long Jin—RELATED: Grant: Beijing Li Huanying Medical Foundation, Comments: Beijing Li Huanying Medical Foundation 2017.* *Money paid to institution.
Indicates open access to non-subscribers at www.ajnr.org
References
- Received October 13, 2019.
- Accepted after revision December 23, 2019.
- © 2020 by American Journal of Neuroradiology