- Research article
- Open Access
Recurrence and retreatment of anterior communicating artery aneurysms after endovascular treatment: a retrospective study
BMC Neurology volume 20, Article number: 287 (2020)
Surgical treatment of anterior communicating artery (Acom) aneurysm is challenging due to anatomic complexity. We aimed to describe our experiences with endovascular treatment (EVT) of Acom aneurysms, and to evaluate the incidence and risk factors of recurrence and retreatment.
The study comprised 260 patients who were treated at a single center between January 2010 and December 2018. Patients who had EVT, including stent-assisted coiling of Acom aneurysms, were included. All medical records were retrospectively reviewed. The incidence and risk factors of recurrence and retreatment were evaluated. Univariate and multivariate analysis were conducted.
Recurrence of Acom aneurysms occurred in 38 (14.6%) patients. Mean follow-up duration was 27 months (range 1–110). Multivariate logistic regression indicated that ruptured aneurysm (odds ratio [OR] 3.55, P = 0.001), dome direction (anterior) (OR 3.86, P = 0.002), maximal diameter (OR 1.19, P = 0.02), and mean age (OR 0.96, P = 0.02) were independent risk factors for aneurysm recurrence. Of 38 cases of recurrence, 10 (3.8%) patients underwent retreatment. Ruptured aneurysm (OR 14.7, P = 0.004), maximal diameter (OR 1.56, P = 0.02), inflow angle (OR 1.04, P = 0.03), and Raymond-Roy classes II and III (OR 6.19, P = 0.03) showed significant relation to retreatment in multivariate logistic regression analysis.
In our study, recurrence rate of Acom aneurysms after EVT was 14.6%. Rupture, anterior dome direction, maximal diameter, and mean age were significantly associated with recurrence. Retreatment rate of recurrent Acom aneurysms after EVT was 3.8%. Patients with Acom aneurysms with large inflow, rupture, large size, or incomplete occlusion may be at a high risk of retreatment of recurring aneurysm.
Anterior communicating artery (Acom) aneurysm has a higher risk of rupture than the other aneurysms . Therefore, treatment of Acom aneurysm is essential and critical for prevention of aneurysmal subarachnoid hemorrhage. However, surgical treatment of Acom aneurysm is still challenging due to anatomic complexity. Acom aneurysm shows a variety of anomalies and complex anatomy like fenestrated, triplicated, and azygous anterior cerebral artery. It also has many perforator and associated vessels such as the recurrent artery of Heubner, anterior lenticulostriate, and bilateral A1 and A2 arteries [2,3,4]. Furthermore, surgical clipping of Acom aneurysm sometimes require a dissection of the rectus gyrus or olfactory nerve.
Since endovascular treatment has emerged as a feasible and acceptable option for aneurysm treatment, Alshekhlee et al. reported that hospital mortality was higher in patients who had surgical clipping than in those who had endovascular coiling (1.6% versus 0.57%) . However, retreatment after initial treatment was performed in 17.4% of patients in the endovascular treatment (EVT) group and in 3.8% of patients in the surgical clipping group in an International Subarachnoid Aneurysm Trial (ISAT) study . The study also found that young age, large lumen size, and incomplete occlusion were risk factors for retreatment after EVT. O’Neil et al. reported that endovascular coiling resulted in significantly lower treatment-related morbidity compared with clipping, but clipping resulted in significantly lower angiographic recurrence and retreatment .
The purpose of this study was to evaluate recurrence and retreatment rates and their risk factors after endovascular treatment of Acom aneurysms.
This study was approved by our Institutional Review Board, and the requirement for patients’ informed consent was waived due to its retrospective design.
Between January 2010 and December 2018, 514 Acom aneurysms were consecutively treated by either surgical or endovascular method in our institute. Patients who had vasculitis or infectious fusiform and blood blister-like aneurysms were excluded from this study. Patients who underwent a flow diverter treatment were also excluded. Finally, 260 patients with Acom aneurysms who underwent coiling with or without stents were included. All clinical and radiological data were obtained from electronic medical records and a prospectively registered aneurysm database and were retrospectively reviewed.
At the initial coiling, all aneurysms were evaluated with 3D angiogram (Allura Xper FD20/20 and Allura Clarity, Philips Medical Systems, Best, The Netherlands). Based on 3D angiogram findings, aneurysm factors including maximal size, size ratio, inflow angle, hypoplastic A1, and dome direction were evaluated. Size ratio was calculated by dividing the aneurysm maximal size (mm) by the average size of both A1 segments (mm) . Inflow angle was defined as the angle between the maximal height of the aneurysm and the parent vessel . Hypoplastic A1 was defined as A1 with diameter less than 50% of the diameter of contralateral A1 . Additionally, we dichotomized aneurysm direction into anterior or posterior by drawing an imaginary perpendicular line to the anterior cranial fossa using sagittal view of computed tomography (CT) angiography . All radiologic images were retrospectively reviewed by two investigators with consensus. For the correction of different values between the two investigators, mean values were obtained.
After the initial coiling, routine imaging follow-up was conducted with 3.0-T magnetic resonance angiography (MRA) at 6, 18, 30, and 60 months. Depending on each patient’s clinical situation, further follow-up was allowed as well as post-treatment and follow-up angiographic occlusion grade were assessed according to Raymond-Roy classification, wherein class I is defined as complete occlusion, class II as neck remnant, and class III as sac remnant . Recurrence was defined as any progression of Raymond-Roy class or increasing of aneurysmal flow. All class III aneurysms on MRA were further evaluated with 3D angiogram.
Retreatment was considered for aneurysms if volume of recurred sac was ≥20.0 mm3 on 3D angiogram. Retreatment modality was planned and decided based on consensus by a multidisciplinary team.
Univariate analysis was performed to determine the association of any recurrence with other factors. The statistical significance of recurrence was analyzed using the chi-square test for categorical, nominal variables, or the logistic regression test for continuous, numerical variables. Multivariate logistic regression analysis was performed for variables with an unadjusted effect and a P-value < 0.20 in univariate analysis to determine independent associations of recurrence and retreatment with other factors. Results of binary logistic regression were reported as odd ratios (ORs) with P-value < 0.05 for a 95% confidence interval (CI), which was considered statistically significant. Additionally, correlation analysis and chi-square test were performed to identify the strength of relationships between age and other risk factors. All statistical analyses were performed with SPSS version 19.0 (IBM Corp., Armonk, NY, USA).
A total of 260 patients (male: female = 134:126; mean age, 57.6 years) with Acom aneurysms underwent coiling procedure. Among them, 157 (60.3%) patients had hypertension, and 115 (44.2%) were smokers. There were 183 (70.4%) unruptured and 77 (29.6%) ruptured aneurysms. Overall, mean maximal diameter of aneurysms was 5.3 mm (range 2–16.6), and mean size ratio was 2.41 (range 0.9–8.5). Mean inflow angle was 148.6° (range 75–180), and hypoplastic A1 was noted in 82 (31.5%) patients.
All aneurysms were successfully treated without (n = 208, 80.0%) or with (n = 52, 20.0%) stents, and immediate post-procedural angiogram showed 167 (64.3%) Raymond-Roy class I, 75 (28.8%) class II, and 18 (6.9%) class III aneurysms.
Follow-up MRA or 3D angiogram was performed for all patients (mean 27 months; range 1–110). Recurrence was noted in 38 (14.6%) patients. In univariate analysis, age (OR 0.96, 95% CI 0.93 to 0.99, P = 0.01), rupture status (OR 3.66, 95% CI 1.81 to 7.52, P = 0.001), maximal diameter (OR 1.20, 95% CI 1.06 to 1.37, P = 0.005), size ratio (OR 1.50, 95% CI 1.17 to 1.95, P = 0.001), and dome direction (anterior) (OR 2.94, 95% CI 1.38 to 6.86, P = 0.007) were significant risk factors for recurrence. In multivariate analysis, age (OR 0.96, 95% CI 0.93 to 0.99, P = 0.02), rupture status (OR 3.55, 95% CI 1.62 to 7.91, P = 0.001), maximal diameter (OR 1.19, 95% CI 1.03 to 1.39, P = 0.02), and dome direction (anterior) (OR 3.86, 95% CI 1.67 to 9.94, P = 0.002) were statistically significant. These results are shown in Table 1.
Correlation analysis and chi-square test performed for evaluation of any relation between age and other risk factors. As a result, P-value of correlation analysis between age and maximal diameter was 0.068, which was not statistically significant at the significance level of 5%, but there was a positive trend between age and maximal diameter. The correlation of other factors of ruptured status and dome direction with age were also not statistically significant.
Among the 38 recurrent cases, 10 (3.8%) showed a recurred volume ≥ 20.0 mm3 that needed a retreatment. Mean interval between initial coiling and recurrence ≥20.0 mm3 was 24 ± 18 months (range 2–63 months). Retreatment was performed at 1–6 months after recurrence. One patient underwent clipping surgery. Three patients were treated with EVT using double catheter technique (Case 1), and the other six patients with EVT using stent assisted coiling (SAC) (Case 2). In univariate analysis, age, ruptured status, maximal diameter, and Raymond-Roy class II or III were statistically significant. In multivariate analysis, ruptured status (OR 14.7, 95% CI 2.77 to 127.9, P = 0.004), maximal diameter (OR 1.56, 95% CI 1.05 to 2.36, P = 0.02), inflow angle (OR 1.04, 95% CI 1.01 to 1.09, P = 0.03), and Raymond-Roy class II or III (OR 6.19, 95% CI 1.19 to 40.8, P = 0.03) were significantly associated with retreatment. These are shown in Table 2.
A 55-year-old female patient underwent an emergency CT scan due to mental change. Ruptured Acom aneurysm was noted. Maximal size of aneurysm was 16.6 mm and neck size 6.6 mm. Emergent EVT was performed and immediate post-embolization angiogram showed neck remnant occlusion (class II). Patient recovered well and she was discharged without neurological deficit. After 1 year, cerebral angiography revealed a recurrence of aneurysm (class III). Surgical clipping was done without neck remnant, and both A2 segments were safely preserved. No more recurrence was seen after 2 years. These findings are described in Fig. 1.
A 57-year-old male patient came into the emergency room with severe bursting headache. Ruptured Acom aneurysm was noted. Maximal size of aneurysm was 4.5 mm and neck size was 3.1 mm. Emergent EVT was performed and immediate post-embolization angiogram showed neck remnant occlusion (class II). After 1 year, cerebral angiography revealed a recurrence of aneurysm. Ipsilateral A1–2 stent-assisted coil embolization was done with neck remnant occlusion of sac (class II). After 1 year after retreatment, MRA revealed a more recurrence of aneurysm neck. These findings are described in Fig. 2.
This study evaluated the incidence and risk factors of recurrence and retreatment of anterior communicating artery (Acom) aneurysm after endovascular treatment. We found that the recurrence rate of Acom aneurysm after EVT was 14.6%, and its risk factors were younger age, rupture status, aneurysm size, and anterior dome direction. The rate of retreatment was 3.8% and large inflow angle, ruptured status, aneurysm size, and incomplete aneurysm occlusion were risk factors of retreatment.
Some studies have shown that surgical procedure for Acom aneurysm can lead to post-operative deficits such as memory impairment and personality changes [13, 14]. Ramos et al. also reported that gyrus rectus resection could cause cognitive and psychiatric dysfunction caused by orbital prefrontal cortex lesion or a disconnection in the ventromedial circuits . Another key problem of surgery of Acom aneurysm is an olfactory nerve injury. In some cases of Acom aneurysms, especially superior or posterior direction, the frontal base is retracted to some degree in order to access the aneurysm. During the frontal lobe retraction, the olfactory nerve can be easily detached from the cribriform plate. Park et al. reported an objective olfactory dysfunction rate of 10.8% after Acom aneurysm surgery . Considering the risks of these complications, minimal invasive surgery like keyhole approach with eyebrow or palpebral incision was introduced in Acom aneurysm surgery [17,18,19]. These approaches minimized a brain retraction and rectus gyrectomy. Some authors even advocated for use of orbitotomy approach, [20,21,22] and recently, endoscopic endonasal approach was reported for Acom aneurysm surgery .
However, surgical clipping of Acom aneurysm is still challenging, because vascular variations such as multiple fenestrated or azygous artery are common in Acom complex [24,25,26,27]. The prevalence of duplication of Acom was 18% and that of fenestration of Acom was 12–21% . Surgical clipping of Acom is difficult when variations are present . Thus, endovascular treatment emerged as an alternative option for Acom aneurysm treatment.
O’Neill et al. reported that coiling was significantly related to lower rate of treatment-related morbidity compared with clipping (0.8% in coiling versus 4.4% in clipping; P = 0.001), whereas clipping was significantly related to lower angiographic recurrence (4.9% in coiling versus 0% in clipping; P = 0.001) in systematic analysis . Many other studies also reported that EVT was associated with a higher rate of recurrence and retreatment than clipping [29,30,31].
Large aneurysm, rupture status, incomplete occlusion, posterior circulation, and branch artery incorporation are well-known risk factors for aneurysm recurrence after EVT [12, 32]. Park et al. reported that total recurrence and retreatment rates were 25.7% (44/171) and 10.5% (18/171), respectively after EVT of saccular aneurysm larger than 8 mm . They revealed that large size, rupture status, low dome-to-neck ratio, and initial incomplete occlusion status were independent risk factors for recurrence. In the present study, age, rupture status, large aneurysm size, and anterior dome direction were significant risk factors for recurrence.
Corns et al. reported that younger age predisposed to a higher risk of recurrence in ruptured aneurysm . However, their study did not give definite explanation for this observation. In some studies, younger age was a predictor of growth of aneurysm after clipping, [35, 36] but this age-related growth is not well-known. Our study also showed that younger patients had more recurrence than older patients. This age-related growing or recurrence of aneurysm can be explained in two ways. First, there was a bias toward more frequent surveillance imaging in younger patients. Second, there is a possibility that age can be correlated with other factors that signify recurrence. Therefore, we performed a correlation analysis between age and the other risk factors, and none of risk factors correlated with age significantly.
In the present study, anterior dome direction was a risk factor of Acom aneurysm recurrence. Anterior dome direction is known to reflect aneurysm hemodynamics, including wall shear stress and flow velocity, which play important roles in the growth and rupture of aneurysm . This may explain its significant association with recurrence in this study.
Smoking is known as one of the most important risk factors for formation and rupture of intracranial aneurysm, [38,39,40] and that association was explained by inhibitory effect of cigarette smoke on alpha 1-antitrypsin . However, Brinjikji et al. reported that smoking was not an independent risk factor for aneurysm recurrence (OR = 1.04, P = 0.87) and retreatment (OR = 0.82, P = 0.50) for patients receiving EVT for aneurysm . On the contrary, Futchko et al. found that history of smoking—whether current or former—was associated with a significantly increased risk of aneurysm recurrence. In the study of Futchko et al., the odds ratios for aneurysm recurrence in current and former smokers were 2.73 and 2.69, respectively, compared with non-smokers. The authors accounted for the difference between the Brinjikji et al’s study and Futchko et al’s study, in that the former study exclusively used balloon-assisted coiling, whereas the later study used stent-assisted coiling . Our study could not reveal any association between smoking and aneurysm recurrence.
Using computational fluid dynamic (CFD) analysis, Merih et al. identified inflow angle as an independent and robust rupture status differentiator in intracranial aneurysm . CFD showed that increasing inflow angle led to deeper migration of flow with higher peak flow velocities and a greater transmission of kinetic energy into the dome. Wenjun et al. also revealed that an inflow angle of over 90° and incomplete occlusion were associated with aneurysm recurrence in unruptured aneurysm after EVT. Our study could not reveal that inflow angle was related with recurrence. However, inflow angle was associated with retreatment (P = 0.03). Similarly, incomplete occlusion (Raymond class II or III) was associated with retreatment (P = 0.03) but not with recurrence. In the present study, it seems that the relatively small number of retreatment events (n = 10) had the most impact on the result. Thus, in our opinion, both inflow angle and incomplete occlusion seem to have little association with recurrence, but are eventually associated with retreatment.
This study had several limitations. First, the decision to retreat could rely on the clinician’s decision, and it may lead to bias. However, to minimize subjective decision and bias, retreatment was considered for aneurysms with a recurred volume ≥ 20.0 mm3 on 3D angiogram. Furthermore, retreatment was decided based on consensus by a multidisciplinary team. Second, recurrence and retreatment cases were few compared with the other group, which showed no recurrence and retreatment. This could be a factor in lowering the statistical reliability of the results. Third, the inflow angle might be inaccurate, even though we used 3D angiogram. For the correction of this inaccuracy, mean values were applied in this study. Finally, inflow angle could change after stent placement. However, in this study, only 52 patients (20%) were treated with SAC and this could not affect the results.
In our study, recurrence rate of Acom aneurysm after endovascular treatment was 14.6%. Younger age, rupture status, aneurysm size, and anterior dome direction were significantly associated with recurrence. Retreatment rate of Acom aneurysm after EVT was 3.8%. Large inflow angle, ruptured status, aneurysm size, and incomplete aneurysm occlusion were risk factors of retreatment. These patients need to be closely followed up after recoiling.
Availability of data and materials
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request. (email@example.com) Public access to the database is open on reasonable request.
Anterior communicating artery aneurysm
Computational fluid dynamic
International Subarachnoid Aneurysm Trial
Magnetic resonance imaging
Stent assisted coiling
Mira JM, Costa FA, Horta BL, Fabiao OM. Risk of rupture in unruptured anterior communicating artery aneurysms: meta-analysis of natural history studies. Surg Neurol. 2006;66(Suppl 3):S12–9 discussion S9.
Tomita H, Saito K. A difficult-to-treat Acom aneurysm with the combined vascular anomaly of Acom fenestration and accessory anterior cerebral artery. Surg Neurol Int. 2018;9:67.
Serizawa T, Saeki N, Fukuda K, Yamaura A. Microsurgical anatomy of the anterior communicating artery and its perforating arteries important for interhemispheric trans-lamina terminalis approach: analysis based on cadaver brains. No Shinkei Geka. 1994;22(5):447–54.
Rosner SS, Rhoton AL Jr, Ono M, Barry M. Microsurgical anatomy of the anterior perforating arteries. J Neurosurg. 1984;61(3):468–85.
Alshekhlee A, Mehta S, Edgell RC, et al. Hospital mortality and complications of electively clipped or coiled unruptured intracranial aneurysm. Stroke. 2010;41(7):1471–6.
Campi A, Ramzi N, Molyneux AJ, et al. Retreatment of ruptured cerebral aneurysms in patients randomized by coiling or clipping in the international subarachnoid aneurysm trial (ISAT). Stroke. 2007;38(5):1538–44.
O'Neill AH, Chandra RV, Lai LT. Safety and effectiveness of microsurgical clipping, endovascular coiling, and stent assisted coiling for unruptured anterior communicating artery aneurysms: a systematic analysis of observational studies. J Neurointerv Surg. 2017;9(8):761–5.
Dhar S, Tremmel M, Mocco J, et al. Morphology parameters for intracranial aneurysm rupture risk assessment. Neurosurgery. 2008;63(2):185–96 discussion 96-7.
Baharoglu Merih I, Schirmer Clemens M, Hoit Daniel A, Gao B-L, Malek AM. Aneurysm inflow-angle as a discriminant for rupture in sidewall cerebral aneurysms. Stroke. 2010;41(7):1423–30.
Kwak R, Niizuma H, Suzuki J. Hemodynamics in the anterior part of the circle of Willis in patients with intracranial aneurysms: a study of cerebral angiography. Tohoku J Exp Med. 1980;132(1):69–73.
Matsukawa H, Uemura A, Fujii M, Kamo M, Takahashi O, Sumiyoshi S. Morphological and clinical risk factors for the rupture of anterior communicating artery aneurysms. J Neurosurg. 2013;118(5):978–83.
Raymond J, Guilbert F, Weill A, et al. Long-term angiographic recurrences after selective endovascular treatment of aneurysms with detachable coils. Stroke. 2003;34(6):1398–403.
Hillis AE, Anderson N, Sampath P, Rigamonti D. Cognitive impairments after surgical repair of ruptured and unruptured aneurysms. J Neurol Neurosurg Psychiatry. 2000;69(5):608–15.
Böttger S, Prosiegel M, Steiger HJ, Yassouridis A. Neurobehavioural disturbances, rehabilitation outcome, and lesion site in patients after rupture and repair of anterior communicating artery aneurysm. J Neurol Neurosurg Psychiatry. 1998;65(1):93–102.
Ramos A, Chaddad-Neto F, Joaquim AF, et al. The microsurgical anatomy of the gyrus rectus area and its neurosurgical implications. Arq Neuropsiquiatr. 2009;67(1):90–5.
Park J, Son W, Goh DH, Kang DH, Lee J, Shin IH. Height of aneurysm neck and estimated extent of brain retraction: powerful predictors of olfactory dysfunction after surgery for unruptured anterior communicating artery aneurysms. J Neurosurg. 2016;124(3):720–5.
Abdel Aziz KM, Bhatia S, Tantawy MH, et al. Minimally invasive transpalpebral "eyelid" approach to the anterior cranial base. Neurosurgery. 2011;69(2 Suppl Operative):ons195–206 discussion −7.
Dare AO, Landi MK, Lopes DK, Grand W. Eyebrow incision for combined orbital osteotomy and supraorbital minicraniotomy: application to aneurysms of the anterior circulation. Technical note. J Neurosurg. 2001;95(4):714–8.
van Lindert E, Perneczky A, Fries G, Pierangeli E. The supraorbital keyhole approach to supratentorial aneurysms: concept and technique. Surg Neurol. 1998;49(5):481–9 discussion 9-90.
Andaluz N, Zuccarello M. Anterior communicating artery aneurysm surgery through the Orbitopterional approach: long-term follow-up in a series of 75 consecutive patients. Skull Base. 2008;18(4):265–74.
Hendricks BK, Spetzler RF. Orbitozygomatic approach clipping of an anterior communicating artery aneurysm: 2-dimensional operative video. Oper Neurosurg (Hagerstown). 2020;18(5):E160.
Andaluz N, Van Loveren HR, Keller JT, Zuccarello M. Anatomic and clinical study of the orbitopterional approach to anterior communicating artery aneurysms. Neurosurgery. 2003;52(5):1140–8 discussion 8-9.
Froelich S, Cebula H, Debry C, Boyer P. Anterior communicating artery aneurysm clipped via an endoscopic endonasal approach: technical note. Neurosurgery. 2011;68(2 Suppl Operative):310–6 discussion 5-6.
Dimmick SJ, Faulder KC. Normal variants of the cerebral circulation at multidetector CT angiography. Radiographics. 2009;29(4):1027–43.
Makowicz G, Poniatowska R, Lusawa M. Variants of cerebral arteries - anterior circulation. Pol J Radiol. 2013;78(3):42–7.
van Rooij SB, Bechan RS, Peluso JP, Sluzewski M, van Rooij WJ. Fenestrations of intracranial arteries. AJNR Am J Neuroradiol. 2015;36(6):1167–70.
de Gast AN, van Rooij WJ, Sluzewski M. Fenestrations of the anterior communicating artery: incidence on 3D angiography and relationship to aneurysms. AJNR Am J Neuroradiol. 2008;29(2):296–8.
Perlmutter D, Rhoton AL Jr. Microsurgical anatomy of the anterior cerebral-anterior communicating-recurrent artery complex. J Neurosurg. 1976;45(3):259–72.
Piotin M, Spelle L, Mounayer C, et al. Intracranial aneurysms: treatment with bare platinum coils—aneurysm packing, complex coils, and angiographic recurrence. Radiology. 2007;243:500–8.
Molyneux AJ, Kerr RS, Birks J, et al. Risk of recurrent subarachnoid haemorrhage, death, or dependence and standardised mortality ratios after clipping or coiling of an intracranial aneurysm in the international subarachnoid aneurysm trial (ISAT): long-term follow-up. Lancet Neurol. 2009;8:427–33.
Johnston SC, Dowd CF, Higashida RT, et al. Predictors of rehemorrhage after treatment of ruptured intracranial aneurysms: the cerebral aneurysm Rerupture after treatment (CARAT) study. Stroke. 2008;39:120–5.
Ferns SP, Majoie CBLM, Sluzewski M, van Rooij WJ. Late adverse events in coiled ruptured aneurysms with incomplete occlusion at 6-month angiographic follow-up. Am J Neuroradiol. 2010;31(3):464.
Park YK, Bae HJ, Cho DY, Choi JH, Kim BS, Shin YS. Risk factors for recurrence and retreatment after endovascular treatment of intracranial saccular aneurysm larger than 8 mm. Acta Neurochir. 2019;161(5):939–46.
Corns R, Zebian B, Tait MJ, et al. Prevalence of recurrence and retreatment of ruptured intracranial aneurysms treated with endovascular coil occlusion. Br J Neurosurg. 2013;27(1):30–3.
Nakase H, Kamada Y, Aoki H, Goda K, Morimoto T, Sakaki T. Clinical study on recurrent intracranial aneurysms. Cerebrovasc Dis. 2000;10(4):255–60.
Jabbarli R, Pierscianek D, Wrede K, et al. Aneurysm remnant after clipping: the risks and consequences. J Neurosurg. 2016;125(5):1249–55.
Tateshima S, Murayama Y, Villablanca JP, et al. Intraaneurysmal flow dynamics study featuring an acrylic aneurysm model manufactured using a computerized tomography angiogram as a mold. J Neurosurg. 2001;95(6):1020–7.
Juvela S, Hillbom M, Numminen H, Koskinen P. Cigarette smoking and alcohol consumption as risk factors for aneurysmal subarachnoid hemorrhage. Stroke. 1993;24(5):639–46.
Petitti DB, Wingerd J. Use of oral contraceptives, cigarette smoking, and risk of subarachnoid haemorrhage. Lancet. 1978;2(8083):234–5.
Juvela S, Poussa K, Porras M, Juvela S, Poussa K, Porras M. Factors affecting formation and growth of intracranial aneurysms: a long-term follow-up study. Stroke. 2001;32:485–91.
Schievink WI, Katzmann JA, Piepgras DG, et al. Alpha-1-antitrypsin phenotypes among patients with intracranial aneurysms. J Neurosurg. 1996;84:781–4.
Brinjikji W, Lingineni RK, Gu CN, et al. Smoking is not associated with recurrence and retreatment of intracranial aneurysms after endovascular coiling. J Neurosurg. 2015;122(1):95–100.
John F, Jordan S, Darryl L, et al. Influence of smoking on aneurysm recurrence after endovascular treatment of cerebrovascular aneurysms. J Neurosurg JNS. 2018;128(4):992–8.
We would like to thank Editage (www.editage.co.kr) for English language editing.
No funding was received for this study.
Ethics approval and consent to participate
The study was approved by the Instituitional Research Ethics Committee of the Severance hospital in Yonsei university (3–2018-0194). All procedures performed in the studies involving human participants were in accordance with the ethical standards of our Institutional Review Board with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. In this retrospective study, the requirement for informed consent was waived. Patient data was de-identified data upon data collection.
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Jang, C.K., Chung, J., Lee, J.W. et al. Recurrence and retreatment of anterior communicating artery aneurysms after endovascular treatment: a retrospective study. BMC Neurol 20, 287 (2020). https://doi.org/10.1186/s12883-020-01871-5
- Anterior communicating artery