Abstract
The Woven EndoBridge (WEB) device is primarily used for treating wide-neck intracranial bifurcation aneurysms under 10 mm. Limited data exists on its efficacy for large aneurysms. We aim to assess angiographic and clinical outcomes of the WEB device in treating large versus small aneurysms. We conducted a retrospective review of the WorldWide WEB Consortium database, from 2011 to 2022, across 30 academic institutions globally. Propensity score matching (PSM) was employed to compare small and large aneurysms on baseline characteristics. A total of 898 patients were included. There was no significant difference observed in clinical presentations, smoking status, pretreatment mRS, presence of multiple aneurysms, bifurcation location, or prior treatment between the two groups. After PSM, 302 matched pairs showed significantly lower last follow-up adequate occlusion rates (81% vs 90%, p = 0.006) and higher retreatment rates (12% vs 3.6%, p < 0.001) in the large aneurysm group. These findings may inform treatment decisions and patient counseling. Future studies are needed to further explore this area.
Keywords: Aneurysms, Intracranial, WEB, Woven EndoBridge, Treatment
Introduction
The natural course of large intracranial aneurysms (≥ 10 mm) is typically unfavorable, and early intervention is generally recommended [1]. According to a study from Japan, the yearly risk of rupture is 4.37% for aneurysms between 10 and 24 mm in size and 33.4% for those larger than 24 mm [2]. As surgical treatment of those aneurysms could be challenging and may cause significant complications [3, 4], several endovascular techniques had evolved and are gradually becoming more popular as a minimally invasive alternative to open surgery [5, 6].
The Woven EndoBridge (WEB) is a self-expanding device made of nitinol that disrupts blood flow within the aneurysm, acting as an intrasaccular flow diverter [7]. It is a viable option for treating complex aneurysms that cannot be treated with standard embolization devices or techniques, particularly wide-neck bifurcation aneurysms [8, 9]. The device is available in different models and sizes and has undergone changes in the last years [10]. While the WEB has shown good short-and mid-term results, long-term follow-up data are limited, especially for larger and complex aneurysms [10].
In this study, we conducted a multicenter cohort study to compare the treatment outcomes and complications between small (maximum diameter < 7.5 mm) and large (≥7.5 mm) intracranial aneurysms using the WEB device.
Methods
Patient sample
The WorldWide WEB Consortium is a synthesis of retrospective databases at 30 academic institutions in North America, South America, and Europe. A standardized data sheet was used to identify patients with intracranial aneurysms treated with WEB device, spanning from January 2011 and December 2022. All consecutive adult patients (age ≥18 years) with both ruptured and unruptured saccular aneurysms in all locations that were treated with the WEB were included. Other aneurysms shapes, including fusiform and blister aneurysms, are not suitable for WEB device placement and, thus, were not included. The selection of aneurysms with suitable size and neck angle for WEB device placement was at the discretion of each interventionalist and was not enforced by the study protocol. The following information was collected using the standardized datasheet: patient demographics (age, gender, smoking status, presentation, modified Rankin Score (mRS), and use of antiplatelets), aneurysm characteristics (side, size, width, location, multiple aneurysms, daughter sac, branch arising from aneurysm, and prior treatment), procedural details (procedure date, type of access, length of procedure, fluoroscopy time, WEB size, and posttreatment antiplatelets), complications (type, timing, location, symptoms, duration, and additional treatment), angiographic outcomes (length of imaging follow-up, immediate flow stagnation, immediate and follow-up occlusion rate, device compaction, fate of branches arising from aneurysm, and retreatment), and functional outcomes (length of clinical follow-up, mRS at last follow-up, and mortality). Patients who presented with ruptured aneurysms were excluded. Also, patients who needed adjunctive devices post-WEB were excluded. Aneurysms were then categorized based on its maximum diameter into two groups: 1- large aneurysms (≥7.5 mm); and 2- small aneurysms (< 7.5 mm). Institutional review board approval was obtained at all centers. No identifiable patient information was presented in the study and, thus, informed consent was not required.
Angiographic outcomes
The angiographic outcome was assessed using digital subtraction angiography (DSA), MR angiography, or CT angiography. Aneurysm occlusion after treatment, both immediately and at last follow-up, was categorized using the three-point occlusion scale: complete occlusion (Raymond Roy (RR) 1), neck remnant (RR2, and aneurysm remnant (RR3) [11]. Adequate occlusion was defined as either complete occlusion or neck remnant with lack of an aneurysm remnant.
Functional outcomes and complications
Functional outcome was assessed using mRS at the last follow-up. Independent functional status was defined with a mRS score of 0–2.
Thromboembolic complications occurring from the date of the procedure up to the last follow-up were recorded. Intra-procedural thromboembolic complications were identified on DSA as either thrombus formation, slow filling of a previously normal filling vessel, or complete vessel occlusion. Post-procedural thromboembolic complications were identified using a combination of clinical and radiographic findings. Post-procedural imaging was performed at the discretion of the individual institutions. Routine screening for clinically silent infarcts was not consistently performed. An ischemic complication was considered symptomatic if there were patient-reported symptoms or clinical signs attributable to thromboembolism; this included transient or resolving signs and symptoms. Hemorrhagic complications were identified intra-operatively as contrast extravasation on DSA or post-procedure imaging. Hemorrhages were counted as symptomatic if the patient-reported symptoms or demonstrated signs attributable to hemorrhage. Other complications included intraprocedural device deployment issues, air embolism, and vascular access complications. Complications were considered permanent if still present at a 3-month follow-up.
Statistical analysis
The statistical analysis was conducted using R studio version 4.2.2. Categorical variables were summarized as frequencies with percentages and compared using the × 2 test or ordinal mixed effect logistic regression for ordinal variables. Continuous variables were summarized as medians with interquartile ranges (IQR) and compared using the Mann–Whitney U test. Variables that were recognized as possible confounders were selected to be included in propensity score matching (PSM). To achieve balance Hunt Hess score variable was added to the matching process, and the fixed ratio 1:1 PSM optimal matching method was used. Results were considered statistically significant if they had a P value of 0.05 or less.
ROC curves were generated to determine the optimal cut-off points for aneurysm size based on retreatment rates. The closest topleft criterion was employed to calculate the optimal cut-off points, which was found to be 7.5. The area under the curve (AUC) was 0.73, with a sensitivity of 0.68 and specificity of 0.63 (Fig. 1).
Multiple imputations were conducted with 50 imputations, followed by mixed-effect logistic regression and ordinal logistic regression. Stepwise selection was used to select the variables to be included for each outcome model.
Results
Patient and aneurysm characteristics
A total of 898 patients were included in this study, with 593 having small aneurysms (maximum diameter < 7.5 mm) and 305 having large aneurysms (≥7.5 mm) (Fig. 2). Most aneurysms in both groups were located in the anterior circulation (82.4% in small vs 75.4% in large) (p = 0.009). There was no significant difference observed in clinical presentations (cranial nerve palsy, headache/dizziness, recurrence, seizures, weakness/numbness), smoking status, pretreatment mRS, presence of multiple aneurysms, bifurcation location, or prior treatment (Table 1).
Table 1.
Variable | Before PSM | After PSM | ||||
---|---|---|---|---|---|---|
Max Diameter < 7.5 mm, N = 593 (66%)1 | Max Diameter ≥ 7.5 mm, N = 305 (34%)1 | P2 | Max Diameter < 7.5 mm, N = 302 (50%)1 | Max Diameter ≥ 7.5 mm, N = 302 (50%)1 | P2 | |
Gender | 0.45 | 0.32 | ||||
Female | 434 (73) | 216 (71) | 225 (75) | 214 (71) | ||
Male | 159 (27) | 89 (29) | 77 (25) | 88 (29) | ||
Age (years) | 61 (52, 68) | 63 (56, 71) | 0.004 | 62 (56, 71) | 63 (56, 71) | 0.97 |
Smoking Status | 0.68 | 0.74 | ||||
Current | 179 (35) | 92 (32) | 78 (29) | 91 (32) | ||
Former | 146 (28) | 83 (29) | 82 (30) | 82 (29) | ||
Never | 189 (37) | 113 (39) | 111 (41) | 113 (40) | ||
Presentation Type | 0.26 | 0.97 | ||||
CN Palsy | 7 (1.2) | 8 (2.6) | 7 (2.3) | 8 (2.6) | ||
Headache/Dizziness | 80 (13) | 43 (14) | 43 (14) | 43 (14) | ||
Incidental/Asymptomatic | 488 (82) | 239 (78) | 240 (79) | 236 (78) | ||
Recurrence | 5 (0.8) | 7 (2.3) | 4 (1.3) | 7 (2.3) | ||
Seizures | 5 (0.8) | 3 (1.0) | 3 (1.0) | 3 (1.0) | ||
Weakness/Numbness | 8 (1.3) | 5 (1.6) | 5 (1.7) | 5 (1.7) | ||
Pre-treatment Modified Rankin Scale | 0.92 | 0.55 | ||||
0 | 454 (82) | 241 (81) | 236 (82) | 239 (81) | ||
1 | 66 (12) | 35 (12) | 36 (13) | 35 (12) | ||
2 | 21 (3.8) | 12 (4.0) | 12 (4.2) | 12 (4.1) | ||
3 | 10 (1.8) | 8 (2.7) | 3 (1.0) | 8 (2.7) | ||
4 | 1 (0.2) | 1 (0.3) | 1 (0.3) | 0 (0) | ||
5 | 1 (0.2) | 0 (0) | ||||
Aneurysm Location | 0.009 | 0.92 | ||||
Anterior cerebral artery | 206 (35) | 80 (26) | 88 (29) | 80 (26) | ||
Vertebrobasilar artery | 103 (17) | 74 (24) | 64 (21) | 72 (24) | ||
Internal carotid artery | 103 (17) | 43 (14) | 44 (15) | 43 (14) | ||
Middle cerebral artery | 180 (30) | 107 (35) | 105 (35) | 106 (35) | ||
Posterior cerebral artery | 1 (0.2) | 1 (0.3) | 1 (0.3) | 1 (0.3) | ||
Bifurcation Aneurysm | 455 (81) | 237 (78) | 0.41 | 232 (79) | 234 (78) | 0.72 |
Multiple Aneurysms | 191 (34) | 112 (38) | 0.31 | 107 (37) | 111 (38) | 0.88 |
Prior Treatment | 37 (6.4) | 23 (7.8) | 0.44 | 18 (6.2) | 23 (7.9) | 0.42 |
Aneurysm Neck Size (mm) | 3.50 (3.00, 4.20) | 5.00 (4.00, 6.00) | < 0.001 | 3.60 (3.00, 4.30) | 5.00 (4.00, 6.00) | < 0.001 |
Maximum Aneurysm Diameter (mm) | 6.00 (5.00, 6.00) | 9.00 (8.00, 10.00) | < 0.001 | 6.00 (5.00, 7.00) | 9.00 (8.00, 10.00) | < 0.001 |
Aneurysm Height (mm) | 5.00 (4.00, 6.00) | 8.00 (7.00, 9.60) | < 0.001 | 5.00 (4.10, 6.00) | 8.00 (7.00, 9.63) | < 0.001 |
Aneurysm Width (mm) | 4.80 (4.00, 5.70) | 7.60 (6.40, 8.80) | < 0.001 | 5.00 (4.00, 5.88) | 7.60 (6.40, 8.88) | < 0.001 |
Secondary Aneurysm | 114 (22) | 84 (29) | 0.018 | 83 (30) | 82 (29) | 0.74 |
Branch Arising from Aneurysm | 53 (9.5) | 50 (17) | 0.002 | 44 (15) | 47 (16) | 0.83 |
1 n (%); Median (IQR)
2 Pearson’s Chi-squared test; Wilcoxon rank sum test; Fisher’s exact test
The median maximum diameter, neck size, dome height and width were 6 mm, 3.5 mm, 5 mm, and 4.8 mm, respectively, in the small aneurysms group, and 9 mm, 5 mm, 8 mm, and 7.6 mm in the large aneurysms group, which was statistically significant (p < 0.001). Aneurysm width did not exceed 10 mm in both groups (Table 1). The large aneurysms group had a higher rate of secondary aneurysms compared to small aneurysms (29% vs 22%, p = 0.018).
Treatment and outcomes
Femoral access was the most common approach used in most aneurysms (Table 2). The median length of angiographic follow-up was 14 months in the large aneurysm group and 15 months in the small aneurysm group (p = 0.97). At the last follow-up, adequate aneurysm occlusion was significantly higher in the small aneurysm group (90%, 431/477) compared to large aneurysms (81%, 214/264) (p < 0.001). The rate of retreatment was significantly higher in the large aneurysms group (12%) compared to small aneurysms (3.7%) (p < 0.001) (Table 2).
Table 2.
Variable | Before PSM | After PSM | ||||
---|---|---|---|---|---|---|
Max Diameter < 7.5 mm, N = 593 (66%)1 | Max Diameter ≥ 7.5 mm, N = 305 (34%)1 | P2 | Max Diameter < 7.5 mm, N = 302 (50%)1 | Max Diameter ≥ 7.5 mm, N = 302 (50%)1 | P2 | |
WEB Device Type | 0.16 | 0.7 | ||||
DL | 16 (2.8) | 14 (4.8) | 10 (3.5) | 13 (4.5) | ||
SL | 492 (86) | 239 (82) | 234 (81) | 237 (82) | ||
SLS | 64 (11) | 40 (14) | 45 (16) | 40 (14) | ||
Access Route | 0.087 | 0.63 | ||||
Femoral | 512 (86) | 254 (83) | 254 (84) | 253 (84) | ||
Radial | 81 (14) | 49 (16) | 48 (16) | 47 (16) | ||
Ulnar | 0 (0) | 2 (0.7) | 0 (0) | 2 (0.7) | ||
Thromboembolic Complications | 21 (3.5) | 18 (5.9) | 0.1 | 12 (4.0) | 18 (6.0) | 0.26 |
Timing of Thromboembolic Complications | 0.84 | 0.88 | ||||
Intraop | 10 (48) | 8 (44) | 5 (42) | 8 (44) | ||
Postop | 11 (52) | 10 (56) | 7 (58) | 10 (56) | ||
Duration of Thromboembolic Complications | 0.71 | > 0.99 | ||||
Permanent | 5 (38) | 5 (31) | 3 (33) | 5 (31) | ||
Transient | 8 (62) | 11 (69) | 6 (67) | 11 (69) | ||
Hemorrhagic Complications | 6 (1.1) | 6 (2.0) | 0.36 | 3 (1.0) | 6 (2.1) | 0.5 |
Timing of Hemorrhagic Complications | 0.57 | 0.17 | ||||
Intraop | 4 (67) | 2 (33) | 3 (100) | 2 (33) | ||
Postop | 2 (33) | 4 (67) | 0 (0) | 4 (67) | ||
Duration of Hemorrhagic Complications | > 0.99 | > 0.99 | ||||
Permanent | 2 (33) | 2 (40) | 1 (33) | 2 (40) | ||
Transient | 4 (67) | 3 (60) | 2 (67) | 3 (60) | ||
Other Complications | 30 (5.9) | 19 (6.9) | 0.57 | 16 (6.0) | 19 (6.9) | 0.67 |
Type of Other Complications | 0.9 | 0.82 | ||||
Access site complication | 1 (4.5) | 1 (9.1) | 0 (0) | 1 (9.1) | ||
Air embolus | 1 (4.5) | 0 (0) | ||||
Contrast reaction | 2 (9.1) | 0 (0) | ||||
Deployment issue | 7 (32) | 5 (45) | 5 (45) | 5 (45) | ||
Groin Hematoma | 1 (4.5) | 1 (9.1) | 0 (0) | 1 (9.1) | ||
Hematoma/Pseudoaneurysm | 10 (45) | 4 (36) | 6 (55) | 4 (36) | ||
Duration of Other Complications | ||||||
Transient | 11 (100) | 8 (100) | 6 (100) | 8 (100) | ||
Antiplatelet Therapy | 520 (88) | 246 (81) | 0.004 | 266 (88) | 244 (81) | 0.017 |
Last Clinical Follow-Up | 12 (5, 23) | 13 (6, 27) | 0.083 | 11 (5, 20) | 13 (6, 27) | 0.036 |
Last Modified Rankin Scale | 0.2 | 0.18 | ||||
0 | 438 (80) | 220 (76) | 219 (79) | 218 (76) | ||
1 | 74 (13) | 39 (13) | 39 (14) | 39 (14) | ||
2 | 18 (3.3) | 10 (3.5) | 11 (4.0) | 10 (3.5) | ||
3 | 9 (1.6) | 7 (2.4) | 3 (1.1) | 7 (2.4) | ||
4 | 4 (0.7) | 2 (0.7) | 4 (1.4) | 2 (0.7) | ||
5 | 1 (0.2) | 1 (0.3) | 0 (0) | 1 (0.3) | ||
6 | 5 (0.9) | 10 (3.5) | 2 (0.7) | 10 (3.5) | ||
Last mRS 0–1 | 512 (93) | 259 (90) | 0.065 | 258 (93) | 257 (90) | 0.17 |
Last mRS 0–2 | 530 (97) | 269 (93) | 0.024 | 269 (97) | 267 (93) | 0.044 |
Last mRS 6 (Mortality) | 5 (0.9) | 10 (3.5) | 0.008 | 2 (0.7) | 10 (3.5) | 0.023 |
Last Imaging Follow-Up | 15 (6, 24) | 14 (6, 25) | 0.97 | 14 (6, 22) | 14 (6, 24) | 0.57 |
Immediate Flow Stagnation | 505 (90) | 276 (92) | 0.34 | 265 (92) | 273 (92) | 0.92 |
Immediate Raymond-Roy Classification | 0.004 | 0.17 | ||||
1 | 176 (31) | 60 (21) | 77 (27) | 60 (21) | ||
2 | 115 (20) | 69 (24) | 56 (20) | 68 (24) | ||
3 | 272 (48) | 162 (56) | 149 (53) | 160 (56) | ||
Last Follow-Up Raymond-Roy Classification | < 0.001 | < 0.001 | ||||
1 | 317 (66) | 125 (47) | 168 (70) | 125 (48) | ||
2 | 114 (24) | 89 (34) | 48 (20) | 87 (33) | ||
3 | 46 (9.6) | 50 (19) | 25 (10) | 50 (19) | ||
Adequate Occlusion (RR1 + RR2) | 431 (90) | 214 (81) | < 0.001 | 216 (90) | 212 (81) | 0.006 |
Inadequate Occlusion (RR3) | 46 (9.6) | 50 (19) | < 0.001 | 25 (10) | 50 (19) | 0.006 |
Compaction | 0.29 | 0.034 | ||||
Same | 225 (59) | 122 (54) | 128 (65) | 122 (54) | ||
Minor | 123 (32) | 75 (33) | 56 (28) | 73 (33) | ||
Major | 35 (9.1) | 29 (13) | 13 (6.6) | 29 (13) | ||
Major Compaction | 35 (9.1) | 29 (13) | 0.15 | 13 (6.6) | 29 (13) | 0.03 |
Retreatment Required | 22 (3.7) | 37 (12) | < 0.001 | 11 (3.6) | 37 (12) | < 0.001 |
Type of Retreatment | 0.047 | 0.013 | ||||
Clipping | 2 (9.1) | 2 (5.4) | 0 (0) | 2 (5.4) | ||
Coiling | 4 (18) | 6 (16) | 1 (9.1) | 6 (16) | ||
Contour | 1 (4.5) | 0 (0) | ||||
Endovascular techniques | 5 (23) | 1 (2.7) | 4 (36) | 1 (2.7) | ||
FD | 4 (18) | 5 (14) | 3 (27) | 5 (14) | ||
SAC | 5 (23) | 21 (57) | 2 (18) | 21 (57) | ||
WEB | 1 (4.5) | 2 (5.4) | 1 (9.1) | 2 (5.4) |
1 n (%); Median (IQR)
2 Pearson’s Chi-squared test; Wilcoxon rank sum test; Fisher’s exact test
The majority of patients had a mRS of 0 at last follow-up, and a comparison in mRS scores is reported in Table 2. There was no significant difference observed between the two groups in terms of thromboembolic complications (p = 0.1), and hemorrhagic complications (p = 0.36) (Table 2).
Propensity score matching
PSM was used to match both groups by age, gender, smoking status, presenting signs/symptoms, pretreatment mRS, bifurcation location, presence of multiple aneurysms, previous treatment, daughter sacs, and the presence of aneurysmal branch. This resulted in 302 matched pairs (Tables 1 and 2).
After PSM, the large aneurysm group had a significantly lower adequate occlusion rate at last follow-up compared to the small aneurysm group (81%, 212/262, vs. 90%, 216/241, p = 0.006). Retreatment was needed more frequently in the large aneurysm group (12%) compared to the small aneurysm group (3.6%) (p < 0.001).
In terms of the mRS score at last follow-up, patients in the large aneurysm group achieved lower rates of good functional outcomes (mRS 0–2) compared to the patients in the small aneurysm group (93% vs. 97%, p = 0.044). The same was observed regarding mortality rates where patients in the large aneurysm group had a higher mortality rate compared to those in the small aneurysm group (3.5% vs. 0.7%, p = 0.023) There were no significant differences observed in thromboembolic complications, hemorrhagic complications, or any of the other complications rates between the two groups.
Discussion
The aim of this multicenter cohort study was to compare the angiographic and clinical outcomes between small (maximum diameter < 7.5 mm) and large (≥7.5 mm) aneurysms using the WEB device. After matching patient and aneurysms characteristic between both groups, small aneurysms were associated with significantly higher rate of adequate occlusion at last follow-up (90%. vs. 81%), and significantly lower rate of retreatment. (3.6% vs 12%).
Large aneurysms pose a greater threat compared to smaller aneurysms due to increased risk of rupture and more complex treatment procedures [12]. Due to the higher risk of rupture in large aneurysms, early surgical or endovascular treatment may be warranted. Endovascular treatment using coil embolization is technically challenging for large aneurysms due to longer procedure times, low packing density, and high recurrence rates [13–17]. For wide-necked aneurysms, assistive devices like stents or balloons are often needed to prevent coil migration. Chalouhi et al. [1] reported immediate complete aneurysm occlusion of large aneurysms (≥ 10 mm) in 87.6% of aneurysms. Complications occurred in 10.5% of patients, with 1 death (0.3%). Recanalization and retreatment rates were 39% and 33%, respectively. Larger aneurysm size was a predictor of poor outcomes. The effectiveness of using coil embolization to treat large aneurysms is limited due to several factors. Firstly, coils are unable to produce permanent thrombosis, which is necessary for successful treatment. Secondly, there may already be thrombosis present inside the aneurysm at the time of treatment, which can make it challenging to pack the coils effectively. Lastly, coils may not be able to fully reconstruct the endothelial lining of the neck, leading to poor treatment outcomes. Even after a period of 2–6 months following coil treatment, there is often no observed improvement in the thrombus organization or endothelization of the neck [18, 19].
The use of flow diverters has emerged as a highly promising alternative for treatment of sidewall complex aneurysms, particularly in cases where intrasaccular coil embolization may not be suitable [20]. Unlike coil embolization, flow diverters are not limited by the same drawbacks and have been FDA-approved for the treatment of large aneurysms located in the petrous to superior hypophyseal segment of the internal carotid artery [20]. Over time, the scope of their application has expanded to include a wide range of aneurysms, including those that have been previously treated, are acutely ruptured, small-sized, located in the posterior circulation, or classified as non-saccular lesions such as fusiform, dissecting, and pseudoaneurysms [20]. Kim et al. [21] conducted a multicenter study on the treatment of 47 aneurysms with a size of 15 mm or smaller using the Pipeline Embolization Device (PED). According to their report, 77.4% of aneurysms achieved complete occlusion after a median follow-up of 3 months. However, treatment-related morbidity was observed in 4.4% of cases, with ischemic stroke being the main cause. The use of flow diversion stents is limited in bifurcation aneurysms due to concerns of branch occlusion and thromboembolic complications.
The WEB device is a new type of intrasaccular flow disruptor that has been developed specifically to treat wide-necked bifurcation aneurysms in certain cases without the need for dual antiplatelet therapy [22, 23]. This has been demonstrated in studies such as the WEB-IT trial, where only 11% of patients were using dual antiplatelet therapy at the 6-month follow-up visit [22]. However, large aneurysms with width greater than 10 mm cannot typically be treated using WEB, given the current maximum size of 11 × 9.6 mm and adequate lateral wall-apposition is critical to ensure flow disruption at the aneurysm neck [24]. However, this has not stopped the off-label use of WEB for treatment of large aneurysms with maximum diameter of ≥10 mm if the width remains within the available device size. A study was conducted by Khalid et al. [10] to evaluate the efficacy of WEB in large, complex intracranial aneurysms. A total of 16 patients were included. The mean aneurysm size was 11.3 ± 1.7 and the median follow-up was 36 months. Aneurysms were predominantly located at the basilar artery bifurcation and anterior communicating artery. Three out of sixteen aneurysms were ruptured. Despite achieving complete occlusion immediately in 75% of intracranial aneurysms, 7 out of 15 cases (46.7%) required retreatment, mainly due to increasing neck remnants and recurrences after 1-year follow-up [10].
In the present study, the use of WEB in the small and large aneurysm groups showed a significant difference in the rates of complete occlusion at the last follow-up, with the small aneurysm group having higher rates of occlusion. The retreatment rates were also significantly different, with the small aneurysm group having lower retreatment rates.
Limitations
Our study has a few limitations that must be considered. Firstly, since it is a retrospective study, there is a possibility of incomplete data sets, selection bias, and unidentified confounders. To counteract this, we utilized PSM to balance the two groups and minimize the risk of selection bias. However, it is important to note that PSM only controls for measured confounders, not unmeasured ones, and thus does not replace randomization. Secondly, as our study included multiple institutions, there may be variability in patient management, aneurysm measurement, and device compaction rate. Nonetheless, the use of a standardized data sheet across all centers and a large sample size may increase the generalizability of the findings. However, it is worth mentioning that we lacked a core laboratory to objectively evaluate the radiologic outcomes of the degree of aneurysm occlusion.
Conclusion
The current study provides valuable insights into the differences between large and small aneurysms in terms of patient and aneurysmal characteristics, treatment approaches, and outcomes. The results showed a significantly lower occlusion rate and higher retreatment rate in large aneurysms compared to small aneurysms. These findings may help guide treatment decisions and patient counseling.
Author contributions
All authors (Basel Musmar, MD1; Hamza Salim, MD1; Nimer Adeeb, MD1; Assala Aslan, MD1; Bahaa Jaradat, MD1; Jose Danilo Bengzon Diestro, MD2; Rachel M. McLellan, MS3; Oktay Algin, MD4; Sherief Ghozy, MD5; Mahmoud Dibas, MD1; Sovann V. Lay, MD6; Adrien Guenego, MD7; Leonardo Renieri, MD8; Nicole M. Cancelliere, MRT(R), MSc2; Joseph Carnevale, MD9; Guillaume Saliou, MD, PhD10; Panagiotis Mastorakos, MD, PhD11; Kareem El Naamani, MD11; Eimad Shotar, MD12; Kevin Premat, MD12; Markus Möhlenbruch, MD13; Michael Kral, MD14; Justin E. Vranic, MD3; Charlotte Chung, MD, PhD15; Mohamed M. Salem, MD, MPH16; Ivan Lylyk, MD17; Paul M. Foreman, MD18; Jay A. Vachhani, MD18; Hamza Shaikh, MD19; Vedran Župančić, MD20; Muhammad U. Hafeez, MD21; Joshua Catapano, MD22; Muhammad Waqas, MBBS23; Vincent M. Tutino, PhD23; Mohamed K. Ibrahim, MD5; Marwa A. Mohammed, MD5; M. Ozgur Ozates, MD4; Giyas Ayberk, MD4; James D. Rabinov, MD3; Yifan Ren, MD24; Clemens M. Schirmer, MD, PhD25; Mariangela Piano, MD26; Anna L. Kühn, MD, PhD27; Caterina Michelozzi, MD28; Stéphanie Elens, MD8; Robert M. Starke, MD29; Ameer Hassan, DO30; Mark Ogilvie, MD31; Anh Nguyen, MD32; Jesse Jones, MD31; Waleed Brinjikji, MD5; Marie T. Nawka, MD33; Marios Psychogios, MD32; Christian Ulfert, MD13; Julian Spears, MD, MS2; Brian T. Jankowitz, MD16; Jan-Karl Burkhardt, MD16; Ricardo A. Domingo, MD34; Thien Huynh, MD, MSc34; Juan Carlos Martinez-Gutierrez, MD35; Muhammed Amir Essibayi, MD36; Sunil A. Sheth, MD35; Gary Spiegel, MD35; Rabih Tawk, MD34; Boris Lubicz, MD, PhD8; Pietro Panni, MD28; Ajit S. Puri, MD27; Guglielmo Pero, MD26; Erez Nossek, MD15; Eytan Raz, MD15; Monika Killer-Oberfalzer, MD14; Christoph J. Griessenauer, MD14; Hamed Asadi, MD, PhD15; Adnan Siddiqui, MD23; Allan Brook, MD36; David Altschul, MD36; Andrew F. Ducruet, MD22; Felipe C. Albuquerque, MD22; Robert W. Regenhardt, MD, PhD3; Christopher J. Stapleton, MD3; Peter Kan, MD21; Vladimir Kalousek, MD20; Pedro Lylyk, MD17; Srikanth Boddu, MD, MSc10; Jared Knopman, MD10; Mohammad A. Aziz-Sultan, MD4; Stavropoula I. Tjoumakaris, MD11; Frédéric Clarençon, MD12; Nicola Limbucci, MD9; Hugo H. Cuellar-Saenz, MD1; Pascal M. Jabbour, MD11; Vitor Mendes Pereira, MD, MSc3; Aman B. Patel, MD3; Adam A. Dmytriw, MD, MPH, MSc3) have contributed equally to the conception and design of the study, the acquisition of data, or the analysis and interpretation of data, drafting the article or revising it critically for important intellectual content, and final approval of the version to be submitted.
Funding
N/A.
Data availability
No datasets were generated or analysed during the current study.
Declarations
Ethical approval
The study received approval from the local ethical standards committee at each participating site, and informed consent from patients was waived. The data supporting this study’s findings are available from the corresponding author upon reasonable request.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Basel Musmar and Hamza Adel Salim contributed equally.
References
- 1.Chalouhi N, Tjoumakaris S, Gonzalez LF et al (2014) Coiling of large and giant aneurysms: complications and long-term results of 334 cases. AJNR Am J Neuroradiol 35(3):546–552. 10.3174/ajnr.A3696 10.3174/ajnr.A3696 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.UCAS Japan Investigators, Morita A, Kirino T et al (2012) The natural course of unruptured cerebral aneurysms in a Japanese cohort. N Engl J Med. 366(26):2474–2482. 10.1056/NEJMoa1113260 10.1056/NEJMoa1113260 [DOI] [PubMed] [Google Scholar]
- 3.Sundt TM, Piepgras DG (1979) Surgical approach to giant intracranial aneurysms. Operative experience with 80 cases. J Neurosurg. 51(6):731–742. 10.3171/jns.1979.51.6.0731 10.3171/jns.1979.51.6.0731 [DOI] [PubMed] [Google Scholar]
- 4.Kalani MYS, Zabramski JM, Hu YC, Spetzler RF (2013) Extracranial-intracranial bypass and vessel occlusion for the treatment of unclippable giant middle cerebral artery aneurysms. Neurosurgery 72(3):428–435; discussion 435–436. 10.1227/NEU.0b013e3182804381 [DOI] [PubMed]
- 5.van Rooij WJ, Sluzewski M (2009) Endovascular treatment of large and giant aneurysms. AJNR Am J Neuroradiol 30(1):12–18. 10.3174/ajnr.A1267 10.3174/ajnr.A1267 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Roy D, Milot G, Raymond J (2001) Endovascular treatment of unruptured aneurysms. Stroke 32(9):1998–2004. 10.1161/hs0901.095600 10.1161/hs0901.095600 [DOI] [PubMed] [Google Scholar]
- 7.Ding YH, Lewis DA, Kadirvel R, Dai D, Kallmes DF (2011) The Woven EndoBridge: a new aneurysm occlusion device. AJNR Am J Neuroradiol 32(3):607–611. 10.3174/ajnr.A2399 10.3174/ajnr.A2399 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Papagiannaki C, Spelle L, Januel AC et al (2014) WEB intrasaccular flow disruptor-prospective, multicenter experience in 83 patients with 85 aneurysms. AJNR Am J Neuroradiol 35(11):2106–2111. 10.3174/ajnr.A4028 10.3174/ajnr.A4028 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Lubicz B, Mine B, Collignon L, Brisbois D, Duckwiler G, Strother C (2013) WEB device for endovascular treatment of wide-neck bifurcation aneurysms. AJNR Am J Neuroradiol 34(6):1209–1214. 10.3174/ajnr.A3387 10.3174/ajnr.A3387 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Khalid Z, Sorteberg W, Nedregaard B, Sorteberg A (2019) Efficiency and complications of Woven EndoBridge (WEB) devices for treatment of larger, complex intracranial aneurysms-a single-center experience. Acta Neurochir (Wien) 161(2):393–401. 10.1007/s00701-018-3752-0 10.1007/s00701-018-3752-0 [DOI] [PubMed] [Google Scholar]
- 11.Fiorella D, Arthur A, Byrne J et al (2015) Interobserver variability in the assessment of aneurysm occlusion with the WEB aneurysm embolization system. J NeuroInterv Surg 7(8):591–595. 10.1136/neurintsurg-2014-011251 10.1136/neurintsurg-2014-011251 [DOI] [PubMed] [Google Scholar]
- 12.Wiebers DO (2003) Unruptured intracranial aneurysms: natural history, clinical outcome, and risks of surgical and endovascular treatment. The Lancet 362(9378):103–110. 10.1016/S0140-6736(03)13860-3 10.1016/S0140-6736(03)13860-3 [DOI] [PubMed] [Google Scholar]
- 13.Gruber A, Killer M, Bavinzski G, Richling B (1999) Clinical and angiographic results of endosaccular coiling treatment of giant and very large intracranial aneurysms: A 7-year, single-center experience. Neurosurgery 45(4):793–804. 10.1097/00006123-199910000-00013 10.1097/00006123-199910000-00013 [DOI] [PubMed] [Google Scholar]
- 14.Sluzewski M, Menovsky T, Van Rooij WJ, Wijnalda D (2003) Coiling of very large or giant cerebral aneurysms: Long-term clinical and serial angiographic results. Am J Neuroradiol 24(2):257–262 [PMC free article] [PubMed] [Google Scholar]
- 15.Griessenauer CJ, Adeeb N, Foreman PM et al (2016) Impact of coil packing density and coiling technique on occlusion rates for aneurysms treated with stent-assisted coil embolization. World Neurosurg 94:157–166. 10.1016/j.wneu.2016.06.127 10.1016/j.wneu.2016.06.127 [DOI] [PubMed] [Google Scholar]
- 16.Ogilvy: Validation of a system to predict recanalization... - Google Scholar. https://scholar.google.com/scholar_lookup?title=Validation%20of%20a%20system%20to%20predict%20recanalization%20after%20endovascular%20treatment%20of%20intracranial%20aneurysms&author=C.S.%20Ogilvy&publication_year=2015&pages=168-174. Accessed 25 Apr 2023
- 17.Ogilvy CS, Chua MH, Fusco MR, Reddy AS, Thomas AJ (2015) Stratification of recanalization for patients with endovascular treatment of intracranial aneurysms. Neurosurgery 76(4):390–395. 10.1227/NEU.0000000000000651 10.1227/NEU.0000000000000651 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Molyneux AJ, Ellison DW, Morris J, Byrne JV (1995) Histological findings in giant aneurysms treated with Guglielmi detachable coils: Report of two cases with autopsy correlation. J Neurosurg 83(1):129–132. 10.3171/jns.1995.83.1.0129 10.3171/jns.1995.83.1.0129 [DOI] [PubMed] [Google Scholar]
- 19.Szikora I, Turányi E, Marosfoi M (2015) Evolution of flow-diverter endothelialization and thrombus organization in giant fusiform aneurysms after flow diversion: a histopathologic study. Am J Neuroradiol 36(9):1716–1720. 10.3174/ajnr.A4336 10.3174/ajnr.A4336 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Gmeiner M, Gruber A (2021) Current strategies in the treatment of intracranial large and giant aneurysms. In: Esposito G, Regli L, Cenzato M, Kaku Y, Tanaka M, Tsukahara T (eds) Trends in Cerebrovascular Surgery and Interventions. Springer. http://www.ncbi.nlm.nih.gov/books/NBK573764/. Accessed 25 Apr 2023 [PubMed]
- 21.Kim BM, Shin YS, Baik MW et al (2016) Pipeline embolization device for large/giant or fusiform aneurysms: an initial multi-center experience in Korea. Neurointervention 11(1):10–17. 10.5469/neuroint.2016.11.1.10 10.5469/neuroint.2016.11.1.10 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Arthur AS, Molyneux A, Coon AL et al (2019) The safety and effectiveness of the Woven EndoBridge (WEB) system for the treatment of wide-necked bifurcation aneurysms: final 12-month results of the pivotal WEB Intrasaccular Therapy (WEB-IT) Study. J Neurointerv Surg 11(9):924–930. 10.1136/neurintsurg-2019-014815 10.1136/neurintsurg-2019-014815 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Pierot L, Szikora I, Barreau X et al (2021) Aneurysm treatment with WEB in the cumulative population of two prospective, multicenter series: 3-year follow-up. J Neurointerv Surg 13(4):363–368. 10.1136/neurintsurg-2020-016151 10.1136/neurintsurg-2020-016151 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Narsinh KH, Caton MT, Mahmood NF et al (2021) Intrasaccular flow disruption (WEB) of a large wide-necked basilar apex aneurysm using PulseRider-assistance. Interdiscip Neurosurg 24:101072. 10.1016/j.inat.2020.101072 10.1016/j.inat.2020.101072 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
No datasets were generated or analysed during the current study.