Treatment Modalities and Long-Term Outcomes in Unruptured Vertebrobasilar Fusiform Aneurysms: A Nationwide Observational Cohort Study

Article information

J Stroke. 2026;28(2):250-262
Publication date (electronic) : 2026 May 28
doi : https://doi.org/10.5853/jos.2025.04385
1Department of Interventional Neuroradiology, Beijing Neurosurgical Institute, Capital Medical University, Beijing, China
2Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China
3Department of Neurosurgery, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China
4Department of Neurosurgery, Peking University International Hospital, Beijing, China
5Department of Neurosurgery, The Affiliated Lianyungang Hospital of Xuzhou Medical University, Lianyungang, China
6Department of Neurosurgery, The Third Medical Center of PLA General Hospital, Beijing, China
7Department of Neurosurgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
8Department of Neurosurgery, General Hospital of the Yangtze River Shipping, Wuhan, China
9Department of Neurology, The First Clinical Medical College of China Three Gorges University, Yichang, China
10Department of Neurosurgery, Taihe Hospital, Hubei University of Medicine, Shiyan, China
11Department of Neurosurgery, Xingtai People’s Hospital, Xingtai, China
12Department of Neurology, Liaocheng People’s Hospital and Liaocheng Clinical School of Taishan Medical University, Liaocheng, China
13Department of Neurosurgery, Binzhou People’s Hospital, Binzhou, China
14Department of Emergency, First Hospital of Shanxi Medical University, Taiyuan, China
15Department of Radiology, Beijing Aerospace General Hospital, Beijing, China
16Department of Neurosurgery, Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, China
17Department of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, China
18Department of Neurosurgery, Affiliated Dalian Municipal Central Hospital of Dalian Medical University, Dalian, China
19Department of Neurosurgery, The Third Hospital of Shijiazhuang, Shijiazhuang, China
20Department of Neurosurgery, Affiliated Hospital of Chengde Medical College, Chengde, China
21Department of Neurosurgery, Taian Central Hospital, Taian, China
22Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China
Correspondence: Ming Lv Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing 100070, China Tel: +86-59978857 E-mail: dragontiger@163.com
Co-correspondence: Liping Liu Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, No. 119 South Fourth Ring West Road, Fengtai District, Beijing 100070, China Tel: +86-59978857 E-mail: lipingsister@gmail.com
*These authors contributed equally as first author.
Received 2025 September 4; Revised 2026 January 24; Accepted 2026 February 4.

Abstract

Background and Purpose

Vertebrobasilar fusiform aneurysms (VBFAs) carry substantial morbidity and mortality, but optimal management for unruptured VBFAs remains unclear. We compared the safety and efficacy of conservative management (CM), stent-assisted coiling (SAC), and flow diverters (FDs) in patients with unruptured VBFAs, focusing on long-term prognosis.

Methods

This study included data from a nationwide Chinese cohort of patients with vertebrobasilar dissecting aneurysms. Inverse probability of treatment weighting (IPTW) balanced confounders across groups. The primary outcome was poor prognosis (modified Rankin Scale score >2). Secondary outcomes included aneurysm rupture, ischemic stroke, compression symptoms, and VBFA-related deaths. Logistic regression estimated odds ratios (ORs) and 95% confidence intervals (CIs). Subgroup and sensitivity analyses were performed.

Results

Among 1,115 patients with unruptured VBFAs, 838 (median age, 54 years; 655 men) were included. After IPTW, baseline characteristics were balanced. Median follow-up was 54 months. FD was associated with a lower risk of poor prognosis than CM (OR, 0.48 [95% CI, 0.30 to 0.77]; P=0.002), with no difference between CM and SAC. FD also reduced aneurysm rupture (OR, 0.20 [95% CI, 0.07 to 0.60]; P=0.004) and compression symptoms (OR, 0.30 [95% CI, 0.13 to 0.68]; P=0.004) versus CM. Time-to-event analyses further revealed significant differences in vertebral artery lesions and Type I–II VBFAs, whereas no significant differences were observed in basilar or vertebrobasilar junction lesions or in Type III–IV VBFAs.

Conclusions

Compared with CM, FD was associated with improved long-term outcomes in unruptured VBFAs, particularly in vertebral artery lesions and Type I–II VBFAs, although residual confounding cannot be excluded.

Introduction

Vertebrobasilar fusiform aneurysms (VBFAs), the most common spontaneous intracranial dissections, are more prevalent in younger and Asian populations [1]. The detection rate of VBFAs has increased in recent years with the advancement of non-invasive brain imaging screening techniques. The natural history of VBFAs is complex and variable, with symptoms including subarachnoid hemorrhage, ischemic stroke, and brainstem or cranial nerve compression, which can lead to high morbidity and mortality [2-4]. This makes therapeutic strategies for unruptured VBFAs of great clinical research interest.

There is no strong evidence supporting the optimal approach and timing for managing VBFAs. Surgical treatment of VBFAs is poorly reported, and even the most experienced institutions report high surgical mortality [3,5,6]. In contrast, endovascular treatment is more widely accepted and relatively safe [7]. Over the past two decades, stent-assisted coiling (SAC) has been recognized as the classic treatment approach for VBFAs. However, conventional stents are often criticized for their high recanalization rate [8]. More recently, the use of flow diverters (FDs) has been extended to unruptured VBFAs, demonstrating seemingly favorable results in some small-scale studies [9-12]. Nonetheless, despite their growing popularity, evidence supporting the comparative effectiveness of FDs in improving long-term prognosis and preventing aneurysm rupture in patients with VBFAs remains limited and inconclusive.

To fill these knowledge gaps, we conducted a large multicenter observational cohort study involving patients with unruptured VBFAs from diverse regions and medical centers. Specifically, we compared the safety and efficacy of conservative management (CM), SAC, and FD interventions in treating patients with unruptured VBFAs, focusing on long-term prognosis. We also aimed to identify patient characteristics that may influence treatment strategies and outcomes. Our findings provide valuable insights into the field of VBFA management and inform evidence-based treatment strategies, thereby improving patient outcomes and quality of life.

Methods

Study design and participants

This study analyzed data from a prospectively maintained nationwide multicenter registry, the Registry of Endovascular Treatment for Vertebrobasilar Dissecting Aneurysms in China (VBDAs China), which is a collaborative study registered at ClinicalTrials. gov (NCT 06541106). The registry was established to explore the natural history of unruptured VBFAs in Asian populations and optimal treatment strategies for patients with VBFAs. Supplementary Material 1 details data quality management information.

Patients with unruptured VBFAs who were continuously recruited from the VBDAs China cohort between January 2011 and January 2024 were reviewed. Individuals aged >18 years who underwent cranial magnetic resonance imaging (MRI) were eligible for inclusion. The exclusion criteria were as follows: (1) undergoing microsurgical treatment; (2) presence of coexisting neurological tumors or other cerebrovascular diseases; and (3) loss to follow-up. The participant selection process is illustrated in Figure 1. The Institutional Review Board of Beijing Tiantan Hospital approved this study (IRB approval number: KY2024-334-02), and all patients provided written informed consent. This study adhered to the Strengthening the Reporting of Observational Studies in Epidemiology reporting guideline [13].

Figure 1.

Patient selection flowchart. MRI, magnetic resonance imaging; VBDA, vertebrobasilar dissecting aneurysm; VBFA, vertebrobasilar fusiform aneurysm.

VBFAs were defined when computed tomography angiography, magnetic resonance angiography, or digital subtraction angiography (DSA) showed irregularity, stenosis, or fusiform dilatation of the vertebral or basilar arteries, a pearl-and-string sign, or a string sign; when DSA showed contrast retention in the ver-tebral or basilar arteries; or when MRI showed intramural hematoma, intimal flap, or double lumen sign [14]. According to the classification proposed by Zhang et al. [14], we categorized VBFAs into four types: Type I (classic dissecting aneurysms), Type II (segmental ectasia), Type III (dolichoectatic dissecting aneurysms), and Type IV (large mural bleeding ectasia) (Figure 2). Supplementary Material 2 and Supplementary Figure 1 illustrate the typical MRI findings and specific definitions of VBFAs.

Figure 2.

Illustrations of VBFA types. VBFA, vertebrobasilar fusiform aneurysm.

Cohort definition

Patients with unruptured VBFAs were categorized into three groups based on the treatment strategy: CM, SAC, and FD. Patients in the CM group did not undergo endovascular or surgical treatments. Routine preoperative DSA and MRI were required for procedural planning in patients undergoing interventions for aneurysms. Patients in the SAC and FD groups were treated with conventional stents and FDs, respectively. All endovascular procedures were performed by experienced neurointerventionalists with more than 15 years of experience at each participating center. Supplementary Material 3 details the endovascular treatment procedures.

Baseline characteristics

We collected demographic data (age and sex), comorbidities, clinical presentations (headache/dizziness, ischemic stroke/transient ischemic attack, cranial nerve compression, and brainstem mass effect), neurological function measured using the modified Rankin Scale (mRS) score, and VBFA imaging characteristics (location, width, branch, type, and MRI findings). The aneurysm width encompassed both the dilated aneurysm and, if present, intramural hematoma. A three-member central review board consisting of a neurointerventionalist, a radiologist, and a neurosurgeon reviewed all imaging and endpoint events. If there was a dispute regarding the assessment, the team reached a unanimous decision after discussion.

Outcomes and follow-up

The primary outcome was poor prognosis, defined as an mRS score >2 at the latest follow-up [15]. Supplementary Material 4 details the mRS score. The secondary outcomes included: (1) aneurysm rupture, defined as a clinical hemorrhagic event (newonset severe headache or worsening neurological deficits) confirmed by imaging findings such as computed tomography or MRI indicating VBFA-associated subarachnoid hemorrhage; (2) ischemic stroke related to the treated vessel; (3) compression symptoms, including aneurysm-induced cranial neuropathy or brainstem symptoms; and (4) VBFA-related death. Additionally, to evaluate stent effectiveness in the SAC and FD groups, only patients who underwent follow-up DSA were included. Supplementary Material 5 presents the definitions of complete occlusion and recanalization.

Well-trained clinical research coordinators evaluated the outcomes through visits or interviews at 3–6 months, annually (1, 2, and 3 years), and every 5 years post-treatment. Follow-up started on the VBFA diagnosis date for the CM group and on the endovascular treatment date for the SAC and FD groups, and ended when the outcome occurred or at the last follow-up date.

Controlling for confounders

The inverse probability of treatment weighting (IPTW) method, which has been widely demonstrated to be effective in several clinical studies (Supplementary Material 6) [16-18], was used to reduce imbalances in measured confounders across the three treatment groups. Using these stabilized weights, the average treatment effect can be estimated without excluding patients while preserving the original sample size. Standardized mean differences (SMDs) were calculated for each covariate to determine whether confounders differed significantly among the three treatment groups. Confounders were considered to show no between-group difference when the SMD ≤0.1 post-IPTW [19]. Despite employing the IPTW technique, unmeasured confounders could still result in bias. Consequently, we calculated E-values to explore the strength of unmeasured confounders and explain the observed association [20]. The E-value represents the minimum strength of an unmeasured confounder necessary to nullify the observed association [21].

Statistical analyses

All statistical analyses were performed using R software (v4.4.1; R Foundation for Statistical Computing, Vienna, Austria) at a two-tailed P<0.05 significance level. Continuous variables were presented as mean±standard deviation and median (interquartile range [IQR]) for normally and non-normally distributed data, respectively. Categorical variables were reported as frequencies and percentages. Risk differences (RDs) were calculated for all outcomes after IPTW. RD describes the difference in the risk of an event between an experimental and a control group [22]. Logistic regression models were used to calculate odds ratios (ORs) and 95% confidence intervals (CIs) for both primary and secondary outcomes. Time-to-event analyses were performed using the Kaplan–Meier method to estimate event-free survival. Differences between groups were assessed using the log-rank test. Stratified analyses were further conducted according to aneurysm location and type to explore heterogeneity in long-term prognosis across subgroups.

Prespecified subgroup and sensitivity analysis

Prespecified subgroup analyses were performed based on age, sex, symptoms, aneurysm location, type, branch, and width. For these comparisons, CM was used as the reference. Furthermore, interaction tests for these subgroups were conducted to assess heterogeneity across subgroups.

We performed a sensitivity analysis to investigate the stability of the primary outcomes. First, we performed an unadjusted analysis without weighting or adjustments. Second, IPTW was used to compare treatment strategies among the three groups. Third, propensity score matching was performed for the same comparisons. Fourth, we used a multivariable logistic regression model adjusting for factors included in the propensity score calculation to assess the ORs of the study outcomes.

Results

Study population and baseline characteristics

Between January 2011 and January 2024, 1,115 patients with unruptured VBFAs were recruited from 22 participating sites and enrolled in the VBDAs China study. After excluding patients who met the exclusion criteria and those lost to follow-up, 838 patients with unruptured VBFAs and long-term follow-up were included in this study (median age, 54 years [IQR 48–60]; 655 men), of whom 305 (36.4%), 241 (28.8%), and 292 (34.8%) underwent CM, SAC, and FD, respectively. The median (IQR) follow-up duration was 54 (30–70) months (52 [32–66], 54 [32– 72], and 56 [28–72] months for the CM, SAC, and FD groups, respectively). Supplementary Table 1 details the baseline comparisons between the included patients and those lost to follow-up; Supplementary Table 2 shows the breakdown of patients lost to follow-up classified into the CM, SAC, and FD treatment groups; and Supplementary Table 3 compares the baseline characteristics of included and lost patients in each group. No significant differences were found between the two groups.

VBFAs with brainstem mass effects, those located in the basilar and vertebrobasilar arteries, those with larger aneurysm widths, and those of Types II, III, and IV were more likely to receive CM. Following IPTW adjustment, most baseline characteristics met the SMD ≤0.1 threshold, indicating that baseline differences across the three treatment groups had been eliminated (Table 1 and Supplementary Figure 2). The adjusted cohort consisted predominantly of middle-aged males, and almost all patients demonstrated good neurological function before treatment. Regarding lesion characteristics, most VBFAs were Type I and located in the vertebral arteries.

Baseline characteristics before and after IPTW

Primary outcomes

Table 2 lists the frequencies of each outcome. After IPTW, the incidences of poor prognosis in the CM, SAC, and FD groups were 20.4%, 14.7%, and 11.0%, respectively. Compared with CM, FD resulted in significantly lower risks of poor prognosis (OR, 0.48 [95% CI, 0.30 to 0.77], P=0.002; RD, -9.4% [95% CI, -15.3% to -3.5%], P=0.002), while no significant difference was observed between CM and SAC. Additionally, there was no significant difference between the SAC and FD groups in terms of their impact on poor prognosis (Supplementary Table 4). The E-values for all significant outcomes implied that unmeasured confounders had to be strongly correlated (E-value range, 3.59–9.47) with the treatment modality and primary outcomes to mitigate the relationship between these variables and reduce the relative risk to 1.

Outcomes of different treatment strategies after inverse probability of treatment weighting

Secondary outcomes

During follow-up, the three strategies showed no significant differences in ischemic stroke occurrence or VBFA-related deaths (Table 2). Notably, the FD group exhibited a significantly lower risk of aneurysm rupture (OR, 0.20 [95% CI, 0.07 to 0.60], P=0.004; RD, -5.3% [95% CI, -8.5% to -2.1%], P=0.001) and compression symptoms (OR, 0.30 [95% CI, 0.13 to 0.68], P=0.004; RD, -6.0% [95% CI, -9.8% to -2.1%], P=0.002) compared with CM, whereas no significant difference was observed between CM and SAC for either outcome. Additionally, there was no significant difference between the SAC and FD groups in terms of aneurysm rupture, ischemic stroke, compression symptoms, or VBFA-related deaths (Supplementary Table 4).

We included 306 patients who underwent follow-up DSA (136 in the SAC group and 170 in the FD group) and applied IPTW to balance the baseline characteristics between the two groups (Supplementary Table 5). We then compared stent effectiveness and found that, at a median follow-up of 26.5 months, FD was associated with a significantly higher complete occlusion rate (OR, 2.25 [95% CI, 1.38 to 3.67], P=0.001; RD, 17.5% [95% CI, 7.0% to 28.0%], P=0.001) and a significantly lower recanalization rate (OR, 0.20 [95% CI, 0.08 to 0.50], P<0.001; RD, -12.1% [95% CI, -18.8% to -5.3%], P<0.001) compared with SAC (Supplementary Table 6).

Subgroup analyses

Figure 3 summarizes the results of the prespecified subgroup analyses. In the subgroup analysis comparing CM and FD, an interaction was observed between the aneurysm location and aneurysm type subgroups (P for interaction=0.009 and <0.001, respectively). Specifically, compared to CM, FD had a better prognosis for treating VBFAs located in the vertebral artery (OR, 0.24 [95% CI, 0.11 to 0.49]; P<0.001), Type I VBFAs (OR, 0.06 [95% CI, 0.01 to 0.28]; P<0.001), and Type II VBFAs (OR, 0.11 [95% CI, 0.01 to 0.89]; P=0.039). No significant interaction effect was observed across subgroups in the subgroup analysis comparing CM and SAC. However, compared with CM, SAC was associated with a better prognosis for treating VBFAs located in the vertebral artery (OR, 0.51 [95% CI, 0.29 to 0.90]; P=0.021) and Type I VBFAs (OR, 0.34 [95% CI, 0.16 to 0.74]; P=0.006).

Figure 3.

Subgroup analyses for poor prognosis. Conservative management was used as the reference in these comparisons. SAC, stent-assisted coiling; FD, flow diverter; OR, odds ratio; CI, confidence interval.

Time-to-event analysis stratified by aneurysm location and type

In the overall cohort, significant differences in event-free survival were observed among the CM, SAC, and FD groups (logrank P<0.001), with the FD group showing the most favorable prognosis (Figure 4A). When stratified by aneurysm location, a significant separation of survival curves was observed in patients with VBFAs located in the vertebral artery (log-rank P<0.001). In this subgroup, FD was associated with the highest event-free survival rate, followed by SAC and CM (Figure 4C). In contrast, no significant differences were observed among the treatment strategies in patients with VBFAs located in the basilar artery or vertebrobasilar junction (Figure 4B and D). Stratification by aneurysm type revealed marked heterogeneity in long-term prognosis. Significant differences in event-free survival were observed in patients with Type I (log-rank P<0.001) and Type II VBFAs (logrank P=0.031), with FD showing the most favorable prognosis (Figure 4E and F). In contrast, no significant differences were observed among the treatment strategies in patients with Type III or IV VBFAs, in whom the overall prognosis remained poor regardless of the treatment strategies employed (Figure 4G and H).

Figure 4.

Time-to-event analysis of event-free survival according to aneurysm location and type. (A) Overall. (B) Basilar. (C) Vertebral. (D) Vertebrobasilar. (E) Type I. (F) Type II. (G) Type III. (H) Type IV. CM, conservative management; SAC, stent-assisted coiling; FD, flow diverter.

Sensitivity analyses

As shown in the sensitivity analyses (Figure 5), SAC was associated with a better prognosis than CM in the unadjusted model (OR, 0.53 [95% CI, 0.34 to 0.84]; P=0.007); however, this association lost statistical significance after adjustment for confound-ing variables. In contrast, FD consistently demonstrated a significant prognostic benefit in patients with VBFAs across all models (P<0.05).

Figure 5.

Effect size and sensitivity analysis for poor prognosis based on treatment strategies. Conservative management was used as the reference in these comparisons. SAC, stent-assisted coiling; FD, flow diverter; OR, odds ratio; CI, confidence interval; IPTW, inverse probability of treatment weighting; PSM, propensity score matching.

Discussion

In this observational cohort study using data from a nationwide multicenter registry, we compared the long-term outcomes of different treatment strategies (CM, SAC, and FD) for unruptured VBFAs. Our results showed that patients undergoing FD had a better prognosis, a lower rate of aneurysm rupture, and a lower incidence of compression symptoms than patients receiving CM. Notably, FD treatment was particularly associated with improved long-term outcomes in VBFAs located in the vertebral artery as well as in Type I and Type II VBFAs. Our findings will contribute to the selection of individualized treatments for patients with unruptured VBFAs.

Vertebrobasilar dolichoectasia and vertebrobasilar non-saccular, fusiform, and dissecting aneurysms are among the terms associated with vertebrobasilar site aneurysms. Notably, these terms intersect, and the boundaries of their use in research are not well-defined [4,7,23,24]. Herein, we focused on patients with VBFAs who had undergone MRI scans and exhibited characteristics representing a broader pathological spectrum, categorizing them into four types according to Zhang’s classification criteria [14]. It is worth noting that our study did not include ruptured VBFAs; thus, Type I in this study refers specifically to type Ib in Zhang’s classification criteria.

Although the International Study of Unruptured Intracranial Aneurysms (ISUIA) and the Unruptured Cerebral Aneurysm Study of Japan (UCAS Japan) reported the natural history and treatment results of unruptured intracranial aneurysms, including VBFAs, in large cohorts, VBFAs were underrepresented in these studies [25,26]. Unruptured VBFAs accounted for only 4.9% and 3.7% of all cases in the ISUIA and UCAS Japan studies, respectively, indicating that VBFA outcomes should be interpreted cautiously. VBFAs are a specific and heterogeneous subtype of intracranial aneurysms with a poor natural history and high morbidity despite treatment [9]. Therefore, selecting between conservative and interventional treatments for VBFAs can be challenging for both neurosurgeons and patients, particularly in the absence of clearly defined clinical guidelines. It is also noteworthy that the lack of a true aneurysm neck and the localization of VBFAs in the posterior cranial fossa adjacent to the brainstem make surgical treatment extremely risky, hence the gradual transition from surgical to endovascular treatment [3,5,6].

Whether endovascular treatment improves long-term neurological status of patients with VBFAs remains unclear. Moreover, despite several previous studies reporting a satisfactory neurologic prognosis with endovascular treatment, there are limited comparisons with CM [4,9,27]. This study aimed to compare the efficacy of CM and endovascular treatment in managing unruptured VBFAs using IPTW to balance intergroup baseline characteristics. Specifically, we aimed to provide comprehensive and robust evidence for personalized recommendations in the FD era. We found that FD was superior to CM in improving patients’ long-term neurological status, whereas SAC and CM showed no significant differences. This discrepancy could be attributed to the properties of FD, which makes it well-suited for VBFA treatment. Given its reduced porosity and increased metal surface density, FD can promote endothelialization and repair of dissecting segments. FD can also promote gradual aneurysm occlusion while preserving essential blood flow to critical side branches [12].

However, the mechanisms outlined above remain largely hypothetical and should be interpreted with caution, as other potential factors may also contribute to the observed superior longterm neurological outcomes associated with FD compared with CM. First, this study was observational in design. Although IPTW and sensitivity analyses were employed to control for known confounders, residual selection bias due to unmeasured variables could not be completely excluded. Second, subtle biases in clinical decision-making (e.g., a tendency to favor FD for lesions deemed to carry a lower perioperative risk while preferentially selecting CM for patients with higher surgical risk) may also have influenced the observed outcomes. Therefore, the present findings require further validation in well-designed prospective randomized controlled trials.

Among the greatest challenges faced by neurointerventionalists during VBFA treatment is identifying specific VBFA subtypes with the best long-term prognosis following endovascular treatment. Subgroup analysis revealed that, following endovascular treatment, VBFAs located in the vertebral arteries had a better prognosis than those located in the basilar and vertebrobasilar arteries. This phenomenon could be attributed to the fact that there are more perforators along the basilar artery than the vertebral artery, an assumption consistent with the findings of Munich et al. [28], who reported that the metal surface coverage of FD on the rostral side of the anterior inferior cerebellar artery should be minimized to avoid vital perforator occlusion. Furthermore, our subgroup analyses based on aneurysm type revealed that patients with Type I and Type II VBFAs had a better prognosis after endovascular treatment, whereas those with Type III and Type IV VBFAs had a relatively poor prognosis, which is consistent with the findings of Zhang et al. [14] Not surprisingly, Type III VBFAs typically involve both vertebral and basilar arteries, extend broadly along the long axis of the vessel, and require multiple overlapping stents for treatment; hence, high metal coverage could greatly increase the risk of ischemic stroke. Type IV VBFAs have obvious intramural hematomas; patients often experience progressively worsening brainstem compression symptoms, and intramural hematomas may persistently enlarge even after complete occlusion of the aneurysm and parent artery. Theoretically, lesion resection (with or without arterial bypass surgery) is the most effective treatment. Interestingly, our findings demonstrated that FD was more effective in preventing mass effect progression than CM, implying that FD should be prioritized in treating VBFAs with brainstem compression, which is consistent with previous research findings [11]. Overall, the results of our subgroup analyses were insightful, suggesting that patients with VBFAs undergoing endovascular treatment should be carefully selected to avoid worsening their natural history.

The primary treatment goal for unruptured VBFAs is complete occlusion of the aneurysm and prevention of rupture. Our findings show that FD exerts a significant protective effect against aneurysm rupture. Following FD placement, blood flow into the aneurysm is reduced, leading to intra-aneurysmal blood stagnation and subsequent thrombus formation, which gradually results in complete occlusion. In addition, the FD serves as a scaffold that facilitates endothelialization at the aneurysm neck. By providing a structural framework for endothelial cell migration and growth, FD promotes the formation of a biologically sealed surface, thereby significantly reducing the risk of aneurysm rupture and recanalization [29]. Notably, our results also demonstrate that FD is associated with alleviation of compressive symptoms. This effect is likely due to thrombus formation within the aneurysm sac following FD placement, which leads to a substantial reduction in aneurysm size. Given its efficacy in preventing rupture and relieving compression symptoms, FD is a promising treatment option for unruptured VBFAs.

There have been concerns that stent placement for treating posterior circulation aneurysms (especially those around the brainstem) could increase the risk of ischemic stroke [30-32]. However, our findings revealed that, compared with the CM group, the ischemic stroke rates in the SAC and FD groups, although higher, were not significantly different. In our experience, the overlapping stent technique could result in higher ischemic stroke rates. Unless the dilated VBFA segment was excessively long, this technique was strictly limited in this cohort; hence, the ischemic stroke rate was relatively acceptable. Endovascular treatment has greatly altered the landscape of neurosurgical management of VBFAs, and FD seems to provide the most favorable balance between securing the aneurysm and preventing medullary infarction [33,34].

Consistent with the findings of Ji et al. [7], we observed a higher complete occlusion rate (76% vs. 58.5%) and a lower recanalization rate (3.5% vs. 15.6%) in the FD group than in the SAC group at the final imaging follow-up of unruptured VBFAs. This difference may be attributable to the distinct treatment mechanisms of the two modalities. SAC involves placement of a conventional stent within the parent artery, which allows the coils to fill the aneurysm lumen more stably and prevent blood entry. However, the stent itself does not significantly alter hemodynamics. Even when complete embolization is achieved immediately post-procedure, there remains a risk of recurrence due to coil compaction or displacement caused by blood flow impingement, as observed during DSA follow-up [35]. In contrast, FD provides a high level of metal coverage and effectively reduces post-procedural aneurysm recurrence by modifying hemodynamics, thereby significantly limiting blood flow into the aneurysm and promoting its natural occlusion. In addition, in the unadjusted model, SAC was associated with a more favorable prognosis (Figure 5); however, this difference was not statistically significant after adjusting for confounding factors, possibly because of the limited sample size or heterogeneity among the patient populations.

In summary, our study suggests that FD may be a promising treatment option for VBFAs. Detailed analysis of aneurysm characteristics (location, type, size, branches, etc.), as well as the evaluation of clinical and radiological signs such as ischemia or mass effect, will help guide treatment plans and hopefully improve the prognosis of patients with this refractory disease.

Limitation

This study has several limitations that should be considered when interpreting the results. First, as an observational study, although we applied IPTW and E-value analyses to minimize confounding by indication and assessed the potential impact of unmeasured variables, residual confounding could not be completely excluded and may have influenced our findings. Second, in clinical practice, clinicians may be more inclined to choose CM for lesions with more complex anatomical locations (e.g., involvement of the basilar artery), more challenging morphologies (e.g., Types III–IV), or a perceived higher procedural risk. Consequently, the CM group may represent a cohort with an intrinsically poorer prognosis, which could lead to overestimation of the absolute benefit of FD. Third, the generalizability of our findings is limited. As demonstrated in the subgroup analyses, evidence supporting the benefit of FD remains limited for the most challenging subtypes, such as basilar artery or vertebrobasilar aneurysms, particularly Types III–IV VBFAs. This underscores the need for highly individualized clinical decisionmaking and caution against overgeneralizing our conclusions to high-risk subgroups. Fourth, due to the technical complexity and inherent risks of surgical intervention near the brainstem, patients treated with microsurgical approaches for VBFAs were not included in this study. Overall, well-designed randomized clinical trials are required to further evaluate the benefits of endovascular treatment for unruptured VBFAs.

Conclusions

Our study provides valuable insights into treatment strategies for patients with unruptured VBFAs. Compared with CM, FD may be associated with improved long-term outcomes in patients with unruptured VBFAs, particularly in those with vertebral artery lesions and Type I–II VBFAs. However, considering the possibility of residual confounding factors, these results should be interpreted with caution.

Supplementary materials

Supplementary materials related to this article can be found online at https://doi.org/10.5853/jos.2025.04385.

Supplementary Material 1.

Data quality management regulations

jos-2025-04385-Supplementary-Materials.pdf
Supplementary Material 2.

Typical magnetic resonance imaging findings of vertebrobasilar fusiform aneurysm and specific definitions of vertebrobasilar fusiform aneurysms

jos-2025-04385-Supplementary-Materials.pdf
Supplementary Material 3.

Detailed procedures of endovascular treatment

jos-2025-04385-Supplementary-Materials.pdf
Supplementary Material 4.

Details of the modified Rankin Scale involved in this study

jos-2025-04385-Supplementary-Materials.pdf
Supplementary Material 5.

Definitions of complete occlusion and recanalization

jos-2025-04385-Supplementary-Materials.pdf
Supplementary Material 6.

Confounders control by inverse probability of treatment weighting

jos-2025-04385-Supplementary-Materials.pdf
Supplementary Table 1.

Baseline characteristics of included and lost to follow-up patients

jos-2025-04385-Supplementary-Table-1.pdf
Supplementary Table 2.

Baseline characteristics of patients lost to follow-up in each group

jos-2025-04385-Supplementary-Table-2.pdf
Supplementary Table 3.

Baseline of included and lost to follow-up patients in each group

jos-2025-04385-Supplementary-Table-3.pdf
Supplementary Table 4.

Comparisons of outcomes between SAC and FD after inverse probability of treatment weighting

jos-2025-04385-Supplementary-Table-4.pdf
Supplementary Table 5.

Comparison of baseline data before and after IPTW for patients in the SAC and FD groups undergoing DSA follow-up

jos-2025-04385-Supplementary-Table-5.pdf
Supplementary Table 6.

Comparison of stent effectiveness between SAC and FD after inverse probability of treatment weighting

jos-2025-04385-Supplementary-Table-6.pdf
Supplementary Figure 1.

Typical MRI findings of VBFAs, with A-E corresponding to intramural hematoma, intimal flap, double lumen, T1 hyperintensity, and brainstem compression, respectively. MRI, magnetic resonance imaging; VBFA, vertebrobasilar fusiform aneurysm.

jos-2025-04385-Supplementary-Figs.pdf
Supplementary Figure 2.

Balance assessment of the inverse probability of treatment weighting. CM, conservative management; FD, flow diverter; SAC, stent-assisted coiling; SMD, standardized mean difference; TIA, transient ischemic attack.

jos-2025-04385-Supplementary-Figs.pdf

Notes

Funding statement

This study was supported by the National Natural Science Foundation of China (grant no. 82271319).

Conflicts of interest

The authors have no financial conflicts of interest.

Author contribution

Conceptualization: Linggen Dong, Ming Lv. Study design: Linggen Dong, Dachao Wei, Liping Liu, Ming Lv. Methodology: Linggen Dong, Dachao Wei. Data collection: Xiheng Chen, Mingtao Li, Yang Zhao, Yong Sun, Qingbin Nie, Jun Feng, Guomin Xiao, Jinghua Zhou, Shengli Hu, Lifei Feng, Lifeng Qi, Hongen Liu, Geng Guo, Yufang Li, Renfu Tian, Jianghua Yu, Dianshi Jin, Liang Hao, Tian Tian, Shizhong Zhang, Yang Wang. Investigation: Yang Wang, Liping Liu, Ming Lv. Statistical analysis: Linggen Dong, Dachao Wei. Writing—original draft: Linggen Dong, Dachao Wei. Writing—review & editing: Liping Liu, Ming Lv. Funding acquisition: Ming Lv. Approval of final manuscript: all authors.

Acknowledgments

We thank all staff for their contribution to this study and the participating hospitals of the VBDAs China Study for their support.

References

1. Urasyanandana K, Songsang D, Aurboonyawat T, Chankaew E, Withayasuk P, Churojana A. Treatment outcomes in cerebral artery dissection and literature review. Interv Neuroradiol 2018;24:254–262.
2. 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;42:2425–2430.
3. Frisoli FA, Srinivasan VM, Catapano JS, Rudy RF, Nguyen CL, Jonzzon S, et al. Vertebrobasilar dissecting aneurysms: microsurgical management in 42 patients. J Neurosurg 2022;137:393–401.
4. Cho DY, Kim BS, Choi JH, Park YK, Shin YS. The fate of unruptured intracranial vertebrobasilar dissecting aneurysm with brain stem compression according to different treatment modalities. AJNR Am J Neuroradiol 2019;40:1924–1931.
5. Huang LT, Zhang M, Tong X. Cerebral revascularization for complex vertebrobasilar artery dissecting aneurysms. Neurosurg Rev 2024;47:138.
6. Nakatomi H, Kiyofuji S, Ono H, Tanaka M, Kamiyama H, Takizawa K, et al. Giant fusiform and dolichoectatic aneurysms of the basilar trunk and vertebrobasilar junction-clinicopathological and surgical outcome. Neurosurgery 2021;88:82–95.
7. Ji Z, He C, Li J, Geng J, Hu P, Li G, et al. Safety and efficacy of low-profile braided stents versus flow diverters in the reconstructive technique in the treatment of patients with vertebrobasilar dolichoectasia aneurysms: a cohort of 47 patients with long-term follow-up. AJNR Am J Neuroradiol 2024;45:176–182.
8. Wang J, Jia L, Duan Z, Wang Z, Yang X, Zhang Y, et al. Endovascular treatment of large or giant non-saccular vertebrobasilar aneurysms: pipeline embolization devices versus conventional stents. Front Neurosci 2019;13:1253.
9. Fang YB, Lin A, Kostynskyy A, Agid R, Tymianski M, Radovanovic I, et al. Endovascular treatment of intracranial vertebrobasilar artery dissecting aneurysms: parent artery occlusion versus flow diverter. Eur J Radiol 2018;99:68–75.
10. Xie D, Zhao L, Liu H, Wang J, Lu P, Ye X, et al. Tubridge flow diverter for the treatment of unruptured dissecting cerebral aneurysms. World Neurosurg 2023;172:e343–e348.
11. Zhang Y, Peng Q, Zhou Y, Wang C, Zhang L, Yang X, et al. Outcomes of reconstructive endovascular treatment of vertebrobasilar dissecting aneurysms with intramural hematoma. Front Neurol 2022;13:914878.
12. Amoukhteh M, Hassankhani A, Valizadeh P, Jannatdoust P, Ghozy S, Kobeissi H, et al. Flow diverters in the treatment of intracranial dissecting aneurysms: a systematic review and meta-analysis of safety and efficacy. J Neurointerv Surg 2024;16:1008–1016.
13. von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP, et al. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. Lancet 2007;370:1453–1457.
14. Zhang Y, Tian Z, Sui B, Wang Y, Liu J, Li M, et al. Endovascular treatment of spontaneous intracranial fusiform and dissecting aneurysms: outcomes related to imaging classification of 309 cases. World Neurosurg 2017;98:444–455.
15. Catapano JS, Ducruet AF, Cadigan MS, Farhadi DS, Majmundar N, Nguyen CL, et al. Endovascular treatment of vertebral artery dissecting aneurysms: a 20-year institutional experience. J Neurointerv Surg 2022;14:257–261.
16. Austin PC. An introduction to propensity score methods for reducing the effects of confounding in observational studies. Multivariate Behav Res 2011;46:399–424.
17. Jing W, Wu S, Gao S, Shi X, Liu W, Ren Y, et al. Early oral feeding versus nasojejunal early enteral nutrition in patients following pancreaticoduodenectomy: a propensity scoreweighted analysis of 428 consecutive patients. Int J Surg 2024;110:229–237.
18. Chai Y, Luo H, Man KKC, Lau WCY, Chan SKW, Yip PSF, et al. Antidepressant use and risk of self-harm among people aged 40 years or older: a population-based cohort and self-controlled case series study. Lancet Reg Health West Pac 2022;27:100557.
19. Lu M, Zhang Y, Zhang J, Huang S, Huang F, Wang T, et al. Comparative effectiveness of digital cognitive behavioral therapy vs medication therapy among patients with insomnia. JAMA Netw Open 2023;6:e237597.
20. VanderWeele TJ, Ding P. Sensitivity analysis in observational research: introducing the E-value. Ann Intern Med 2017;167:268–274.
21. Haneuse S, VanderWeele TJ, Arterburn D. Using the E-value to assess the potential effect of unmeasured confounding in observational studies. JAMA 2019;321:602–603.
22. Richardson R, Kanellopoulou A, Dwan K. Risk ratios, odds ratios and the risk difference. BMJ Evid Based Med 2025;30:66–67.
23. Cao L, Zhu C, Eisenmenger L, Du X, Liu J, Yang Q, et al. Wall enhancement characteristics of vertebrobasilar nonsaccular aneurysms and their relationship to symptoms. Eur J Radiol 2020;129:109064.
24. Peng F, Fu M, Xia J, Niu H, Liu L, Feng X, et al. Quantification of aneurysm wall enhancement in intracranial fusiform aneurysms and related predictors based on high-resolution magnetic resonance imaging: a validation study. Ther Adv Neurol Disord 2022;15:17562864221105342.
25. Wiebers DO, Whisnant JP, Huston J 3rd, Meissner I, Brown RD Jr, Piepgras DG, et al. Unruptured intracranial aneurysms: natural history, clinical outcome, and risks of surgical and endovascular treatment. Lancet 2003;362:103–110.
26. UCAS Japan Investigators, Morita A, Kirino T, Hashi K, Aoki N, Fukuhara S, et al. The natural course of unruptured cerebral aneurysms in a Japanese cohort. N Engl J Med 2012;366:2474–2482.
27. Sönmez Ö, Brinjikji W, Murad MH, Lanzino G. Deconstructive and reconstructive techniques in treatment of vertebrobasilar dissecting aneurysms: a systematic review and meta-analysis. AJNR Am J Neuroradiol 2015;36:1293–1298.
28. Munich SA, Tan LA, Keigher KM, Chen M, Moftakhar R, Lopes DK. The Pipeline Embolization Device for the treatment of posterior circulation fusiform aneurysms: lessons learned at a single institution. J Neurosurg 2014;121:1077–1084.
29. Gory B, Berge J, Bonafé A, Pierot L, Spelle L, Piotin M, et al. Flow diverters for intracranial aneurysms: the DIVERSION national prospective cohort study. Stroke 2019;50:3471–3480.
30. Domingo RA, Tripathi S, Perez-Vega C, Vivas-Buitrago T, Lu VM, Todnem ND, et al. Treatment of posterior circulation nonsaccular aneurysms with flow diversion versus stent-assisted coiling: a systematic review and meta-analysis. J Neurointerv Surg 2021;13:159–163.
31. Adeeb N, Ogilvy CS, Griessenauer CJ, Thomas AJ. Expanding the indications for flow diversion: treatment of posterior circulation aneurysms. Neurosurgery 2020;86:S76–S84.
32. Brinjikji W, Murad MH, Lanzino G, Cloft HJ, Kallmes DF. Endovascular treatment of intracranial aneurysms with flow diverters: a meta-analysis. Stroke 2013;44:442–447.
33. Dmytriw AA, Phan K, Moore JM, Pereira VM, Krings T, Thomas AJ. On flow diversion: the changing landscape of intracerebral aneurysm management. AJNR Am J Neuroradiol 2019;40:591–600.
34. Liu P, Li Z, Hu L, Liu Y, Li P, Zhu W, et al. Clinical characteristics, endovascular choices, and surgical outcomes of intracranial vertebral artery dissecting aneurysms: a consecutive series of 196 patients. J Neurosurg 2022;138:215–222.
35. Mu SQ, Yang XJ, Li YX, Jiang CH, Wu ZX. Endovascular treatment of the huge dissecting aneurysms involving the basilar artery by the internal trapping technique: technical note. Chin Med J (Engl) 2015;128:1916–1921.

Article information Continued

Figure 1.

Patient selection flowchart. MRI, magnetic resonance imaging; VBDA, vertebrobasilar dissecting aneurysm; VBFA, vertebrobasilar fusiform aneurysm.

Figure 2.

Illustrations of VBFA types. VBFA, vertebrobasilar fusiform aneurysm.

Figure 3.

Subgroup analyses for poor prognosis. Conservative management was used as the reference in these comparisons. SAC, stent-assisted coiling; FD, flow diverter; OR, odds ratio; CI, confidence interval.

Figure 4.

Time-to-event analysis of event-free survival according to aneurysm location and type. (A) Overall. (B) Basilar. (C) Vertebral. (D) Vertebrobasilar. (E) Type I. (F) Type II. (G) Type III. (H) Type IV. CM, conservative management; SAC, stent-assisted coiling; FD, flow diverter.

Figure 5.

Effect size and sensitivity analysis for poor prognosis based on treatment strategies. Conservative management was used as the reference in these comparisons. SAC, stent-assisted coiling; FD, flow diverter; OR, odds ratio; CI, confidence interval; IPTW, inverse probability of treatment weighting; PSM, propensity score matching.

Table 1.

Baseline characteristics before and after IPTW

Characteristics Before IPTW
After IPTW
CM (n=305) SAC (n=241) FD (n=292) P SMD CM (n=285) SAC (n=273) FD (n=283) P SMD
Age (yr)* 56.0 (48.0–61.0) 54.0 (49.0–60.0) 53.0 (47.0–59.0) 0.025 0.16 54.2 (47.0–61.0) 54.0 (48.8–60.0) 55.0 (48.8–61.0) 0.692 0.03
Sex 0.196 0.10 0.821 0.03
 Male 235 (77.1) 198 (82.2) 222 (76.0) 223 (78.2) 218 (79.9) 220 (77.7)
 Female 70 (23.0) 43 (17.8) 70 (24.0) 62 (21.8) 55 (20.1) 63 (22.3)
Admission mRS 0.642 0.04 0.802 0.03
 0–2 304 (99.7) 239 (99.2) 291 (99.7) 284 (99.6) 271 (99.3) 281 (99.3)
 3–6 1 (0.3) 2 (0.8) 1 (0.3) 1 (0.4) 2 (0.7) 2 (0.7)
Risk factors
 Hypertension 202 (66.2) 154 (63.9) 180 (61.6) 0.506 0.06 179 (62.8) 177 (64.8) 173 (61.1) 0.664 0.05
 Diabetes mellitus 35 (11.5) 27 (11.2) 27 (9.3) 0.637 0.05 31 (10.9) 27 (9.9) 25 (8.8) 0.715 0.05
 Hyperlipidemia 48 (15.7) 34 (14.1) 56 (19.2) 0.265 0.09 42 (14.7) 44 (16.1) 58 (20.5) 0.163 0.10
 Coronary heart disease 31 (10.2) 8 (3.3) 25 (8.6) 0.009 0.19 22 (7.7) 22 (8.1) 23 (8.1) 0.984 0.01
Current smoker 131 (43.0) 105 (43.6) 107 (36.6) 0.180 0.09 123 (43.2) 113 (41.4) 118 (41.7) 0.893 0.02
Alcohol use 91 (29.8) 86 (35.7) 73 (25.0) 0.027 0.16 85 (29.8) 80 (29.3) 87 (30.7) 0.933 0.02
Presentation 0.001 0.28 0.981 0.08
 Headache/dizziness 85 (27.9) 76 (31.5) 90 (30.8) 91 (31.9) 80 (29.3) 82 (29.0)
 Ischemic stroke/TIA 39 (12.8) 44 (18.3) 34 (11.6) 42 (14.7) 41 (15.0) 41 (14.5)
 Cranial nerve compression 18 (5.9) 15 (6.2) 12 (4.1) 17 (6.0) 15 (5.5) 17 (6.0)
 Brainstem mass effect 29 (9.5) 6 (2.5) 9 (3.1) 15 (5.3) 14 (5.1) 20 (7.1)
 Incidental/asymptomatic 134 (43.9) 100 (41.5) 147 (50.3) 120 (42.1) 123 (45.1) 123 (43.5)
Aneurysm location <0.001 0.46 0.703 0.08
 Basilar 94 (30.8) 33 (13.7) 29 (9.9) 51 (17.9) 43 (15.8) 58 (20.5)
 Vertebral 156 (51.2) 187 (77.6) 219 (75.0) 196 (68.8) 193 (70.7) 187 (66.1)
 Vertebrobasilar 55 (18.0) 21 (8.7) 44 (15.1) 38 (13.3) 37 (13.6) 38 (13.4)
Aneurysm width (mm)* 10.3 (7.8–14.4) 9.0 (7.4–12.4) 9.9 (7.6–13.4) 0.036 0.10 9.9 (7.7–13.9) 9.5 (7.4–12.9) 9.9 (7.6–13.3) 0.688 0.03
Aneurysm combined branches 92 (30.2) 64 (26.6) 86 (29.5) 0.630 0.05 76 (26.7) 86 (31.5) 87 (30.7) 0.399 0.07
Aneurysm type <0.001 0.33 0.990 0.05
 I 128 (42.0) 151 (62.7) 157 (53.8) 157 (55.1) 148 (54.2) 149 (52.7)
 II 51 (16.7) 32 (13.3) 42 (14.4) 43 (15.1) 42 (15.4) 42 (14.8)
 III 76 (24.9) 30 (12.5) 46 (15.8) 45 (15.8) 44 (16.1) 52 (18.4)
 IV 50 (16.4) 28 (11.6) 47 (16.1) 40 (14.0) 39 (14.3) 40 (14.1)
MRI findings
 Intramural hematoma 188 (61.6) 178 (73.9) 210 (71.9) 0.003 0.18 200 (70.2) 195 (71.4) 197 (69.6) 0.888 0.03
 Intimal flap 86 (28.2) 62 (25.7) 79 (27.1) 0.812 0.04 82 (28.8) 74 (27.1) 78 (27.6) 0.904 0.03
 Double lumen 59 (19.3) 48 (19.9) 50 (17.1) 0.672 0.05 51 (17.9) 60 (22.0) 51 (18.0) 0.385 0.08
 T1 hyperintensity 127 (41.6) 110 (45.6) 115 (39.4) 0.341 0.09 132 (46.3) 117 (42.9) 106 (37.5) 0.097 0.12
 Brainstem compression 137 (44.9) 101 (41.9) 136 (46.6) 0.554 0.06 130 (45.6) 122 (44.7) 131 (46.3) 0.932 0.03
Time to last clinical follow-up (mon)* 52.0 (32.0–66.0) 54.0 (32.0–72.0) 56.0 (28.0–72.0) 0.469 0.04 51.0 (33.0–66.0) 51.0 (31.0–71.1) 56.0 (28.0–70.1) 0.691 0.02

Unless otherwise indicated, data are numbers of participants and data in parentheses are percentages.

IPTW, inverse probability of treatment weighting; CM, conservative management; SAC, stent-assisted coiling; FD, flow diverter; SMD, standardized mean difference; mRS, modified Rankin Scale; TIA, transient ischemic attack; MRI, magnetic resonance imaging.

*

Data are presented as medians, with interquartile ranges in parentheses;

Vertebrobasilar refers to an aneurysm involving both the vertebral and basilar arteries;

Based on the classification system proposed by Zhang et al. [14]

Table 2.

Outcomes of different treatment strategies after inverse probability of treatment weighting

Outcomes CM (n=285)
SAC (n=273)
FD (n=283)
Events (%) Events (%) Risk difference* (95% CI) (%) P OR (95% CI)* P E Events (%) Risk difference* (95% CI) (%) P OR (95% CI)* P E
Primary outcomes
 Poor prognosis 58 (20.4) 40 (14.7) -5.7 (-12.0 to 0.6) 0.075 0.67 (0.43 to 1.05) 0.077 1.74 31 (11.0) -9.4 (-15.3 to -3.5) 0.002 0.48 (0.30 to 0.77) 0.002 3.59
Secondary outcomes
 Aneurysm rupture 19 (6.7) 10 (3.7) -3.0 (-6.7 to 0.7) 0.110 0.53 (0.24 to 1.17) 0.116 3.18 4 (1.4) -5.3 (-8.5 to -2.1) 0.001 0.20 (0.07 to 0.60) 0.004 9.47
 Ischemic stroke 20 (7.0) 19 (7.0) -0.06 (-4.3 to 4.2) 0.979 0.99 (0.52 to 1.90) 0.979 1.11 25 (8.8) 1.8 (-2.6 to 6.3) 0.422 1.28 (0.70 to 2.37) 0.423 1.88
 Compression symptom 25 (8.8) 16 (5.9) -2.9 (-7.2 to 1.4) 0.185 0.65 (0.34 to 1.24) 0.188 2.45 8 (2.8) -6.0 (-9.8 to -2.1) 0.002 0.30 (0.13 to 0.68) 0.004 6.12
 VBFA-related death 17 (6.0) 9 (3.3) -2.7 (-6.1 to 0.8) 0.132 0.54 (0.24 to 1.23) 0.135 3.11 10 (3.5) -2.4 (-5.9 to 1.1) 0.172 0.58 (0.26 to 1.28) 0.176 2.84

CM, conservative management; SAC, stent-assisted coiling; FD, flow diverter; OR, odds ratio; CI, confidence interval; VBFA, vertebrobasilar fusiform aneurysm.

*

Results were calculated using the CM group as reference;

Poor prognosis was defined as a modified Rankin Scale score of >2 at the latest follow-up.