Skip to main content


Front. Neurol., 18 December 2018
Sec. Endovascular and Interventional Neurology

Impact of Reducing the Procedure Time on Thromboembolism After Coil Embolization of Cerebral Aneurysms

\r\nSang-Hwa LeeSang-Hwa Lee1Min Uk JangMin Uk Jang2Jihoon KangJihoon Kang3Yeo Jin KimYeo Jin Kim1Chulho KimChulho Kim1Jong-Hee SohnJong-Hee Sohn1Jinseo YangJinseo Yang4Jin Pyeong JeonJin Pyeong Jeon4Yongjun ChoYongjun Cho4Hyuk Jai Choi*Hyuk Jai Choi4*
  • 1Department of Neurology, Hallym University College of Medicine, Chuncheon Sacred Heart Hospital, Chuncheon, South Korea
  • 2Department of Neurology, Hallym University College of Medicine, Dongtan Sacred Heart Hospital, Hwaseong, South Korea
  • 3Department of Neurology, Seoul National University Bundang Hospital, Seoul National University, Seongnam, South Korea
  • 4Department of Neurosurgery, Hallym University College of Medicine, Chuncheon Sacred Heart Hospital, Chuncheon, South Korea

Background: There is still controversy regarding which procedure-related factors affect the occurrence of periprocedural thromboembolism. This study aimed to investigate which procedure-related risk factors can be modified to prevent adverse thromboembolic events after coil embolization of intracranial aneurysm.

Methods: Using a single-center database, we retrospectively identified a consecutive series of patients with symptomatic and asymptomatic cerebral aneurysms treated with coil embolization. We evaluated the following procedure-related factors: procedure time, procedure methods (simple coiling, stent-assisted coiling, and use of multiple microcatheters), and number of coils inserted. The primary outcome was the development of thromboembolism before and after coil embolization confirmed by diffusion-weighted imaging (DWI) irrespective of the location of the procedure. Pearson's chi-square, Student's t-test, multivariable logistic regression analysis, and sensitivity analysis with multinomial logistic regression analysis were used in the statistical analyses.

Results: Of 180 cases enrolled, 146 (81.1%) had evidences of thromboembolism confirmed by DWI, and 13 (7.2%) had neurologic symptoms. Among the documented modifiable procedure-related factors, every 10 min increase in the procedure time was independently associated with the risk of thromboembolism, after adjusting the analysis (adjusted odds ratio 1.11; 95% confidence interval 1.01–1.21). The coiling methods, use of multiple catheters, and number of coils inserted did not change the effect of the procedure time on thromboembolic events (p for interactions > 0.05).

Conclusion: This study showed that the procedure time might be the most effective modifiable factor for reducing thromboembolic events irrespective of the procedure methods used during coil embolization of cerebral aneurysms.


The incidence of periprocedural thromboembolism is reported as 10–69%, and it is the most frequent complication of coil embolization for cerebral aneurysm (111). Since periprocedural thromboembolism immediately causes significant neurological deficit and increases the risk of delayed cognitive decline even in immediate asymptomatic lesions, it would be of interest to determine its risk factors and to develop preventative strategies (12, 13).

Previous evidences have shown that some factors, such as age and aneurysmal size, are important risk factors for periprocedural thromboembolism (2, 4, 9, 11). Age and aneurysmal size are non-modifiable factors so they would be helpful only to distinguish the patients at high risk of periprocedural thromboembolism.

There is still controversy regarding the procedure-related factors, although the procedure technique itself is considered to have a high possibility of affecting the occurrence of periprocedural thromboembolism. One explanation for this is that prior studies assessed the procedure technique, which was mostly a newly introduced coil device or technique, so it was difficult to evaluate the effects of various risk factors. Second, some of the previous studies considered the effect of the treating physician a risk (1, 3, 5, 14).

This study aimed to investigate which risk factors can be modified to prevent periprocedural thromboembolism in coil embolization for cerebral aneurysm by using a single interventionist's consecutive series of patients.


Study Population

We prospectively registered all cases with intracranial aneurysms hospitalized between January 2013 and March 2017 in our institution. In this study, we retrospectively collected only cases with intracranial aneurysm who underwent magnetic resonance imaging (MRI) before and within 48 h after coil embolization was performed by an expert interventionist (HC). The following cases were excluded from this study: (1) patients who were uncooperative or unavailable for MRI because of medical conditions or neurological disability; (2) patients who were documented as having an atherosclerotic lesion located proximal to the aneurysm site on the pre-procedure or post-procedure MRI study. This was meant to exclude biologic factors that have a possibility of affecting ischemic lesions during the procedure.

Coil Embolization Procedure

All procedures were performed under general anesthesia using a biplane angiography system (Siemens Medical System, Erlangen, Germany). After a 7-French guiding catheter was placed into the internal carotid or vertebral artery, a microcatheter was introduced into the aneurysmal sac with a microwire (Synchro-14, Boston Scientific Corporation, Natick, MA). The types of endovascular procedures were divided into two groups: simple coiling and stent-assisted coil embolization. Stent-assisted coil embolization was performed by an interventionist as an adjunctive technique in consideration of various patient and aneurysmal factors. For simple coiling, multiple microcatheters were only used for aneurysms with broad necks or incorporated arterial branches. Anticoagulation therapy with intravenous heparin (3,000 units) was administered after guided catheter placement, followed by intermittent hourly heparin injections (1,000 units).

Definition of Parameters

Acute thromboembolisms after coil embolization were defined by the lesions with high signals on diffusion-weighted imaging (DWI) that correlated with low signals on an ADC map. Two experienced vascular neurologists (S-HL and MJ) reviewed all DWI studies and collected formal MRI readings to detect acute thromboembolism. The volume of the thromboembolic lesion confirmed by DWI within 48 h after coil embolization was calculated using Medical Image Processing and Visualization software (version 7.3.0, National Institutes of Health, Bethesda, MD).

From the registry database, we directly obtained patients' demographics (age and sex), vascular risk factors, and medical history (hypertension, diabetes mellitus, hyperlipidemia, and coronary artery disease; current smoking status; history of stroke; and prior use of antithrombotic agents). The aneurysm size, location, and morphology (fusiform and saccular) were noted. Premedication with antiplatelet agents before coil embolization was also noted.

The modifiable procedure-related factors were defined as the procedure time, simple coiling, stent-assisted coiling, use of multiple microcatheters, and number of coils inserted, which were documented in previous studies (10, 11, 1416). The procedure time was defined as the time from groin puncture to guiding catheter removal. Use of multiple microcatheters was defined as using more than a single microcatheter which indicates multiple manipulations of the aneurysm and delayed occlusion time during coil embolization regardless of the coiling method used (10, 17).

The primary outcome measure was the development of thromboembolisms confirmed by DWI before and after coil embolization. The secondary outcome measure was defined as three DWI groups: the DWI-negative lesion group, coiling-related DWI-positive lesion group, and coiling-unrelated DWI-positive lesion group. The coiling-related DWI-positive lesions were ipsilateral lesions located in the relevant territory of the coiling site. The coiling-unrelated DWI-positive lesions were contralateral or remote lesions located in an irrelevant territory of the coiling site.

Statistical Analysis

Summary statistics are presented as mean ± standard deviation or frequency (percentage) as appropriate. Baseline characteristics were compared according to the occurrence of thromboembolism using Pearson's chi-square test for categorical variables and Student's t test for continuous variables as appropriate. To evaluate the clinical environment of procedure-related factors, we described the frequency of each procedure-related factor for thromboembolisms by bivariate analysis. Additionally, mediator effect analysis was performed to determine the association between each procedure-related factor and the occurrence of thromboembolism.

Multivariable logistic regression analysis was used to determine the individual risk of each procedure-related factor for thromboembolism. Variables for adjustment in multivariable models were selected if their p-values were <0.1 in crude comparisons or clinically plausible. Moreover, we evaluated the association between procedure-related factors and the DWI-negative lesion group, coiling-related DWI-positive lesion group, and coiling-unrelated DWI-positive lesion group using sensitivity analysis with multinomial logistic regression analysis.


Among 159 subjects (62 men, 97 women; mean age 57.1 ± 13.4 years), 180 cases were enrolled. Sixty-six patients (42%) had hypertension, 17 (11%) had diabetes mellitus, 6 (4%) had coronary artery disease, 10 (6%) had hyperlipidemia, 48 (30%) were current smokers, and 32 (20%) had a history of stroke. Among 180 aneurysms, 109 (61%) were ruptured. Sizes of the aneurysms were as follows: ≤ 7 mm, 140 (77.8%); and >7 mm, 40 (22.2%). The distributions of aneurysms according to their location were as follows: middle cerebral artery, 20 (11.1%); anterior cerebral artery, 72 (40.0%); internal carotid artery, 69 (38.3%); and posterior circulation artery (basilar artery and vertebral artery), 19 (10.6%).

The overall rate of thromboembolism confirmed by DWI after coil embolization was 81.1% (n = 146). Among the 146 DWI-positive lesions, 13 (8.9%) were symptomatic, and 133 (91.1%) were asymptomatic. Among the 13 patients with symptomatic DWI-positive lesions, 7 patients had dependent ambulation (modified Rankin Scale [mRS] score of 0 to 2), but 6 patients experienced poor functional status at hospitalization (3 had an mRS score of 4, and 3 had an mRS score of 5). All 6 patients with poor functional status had a ruptured aneurysm, and among 7 patients with an mRS score of 0 to 2, 6 patients had an unruptured aneurysm (Supplemental Figure 1). The patients with thromboembolism after coil embolization were more likely to be hypertensive (p < 0.05), have a longer procedure time (p < 0.05), and be older (p = 0.06). The frequencies of patient and aneurysmal factors were not different between patients with and without thromboembolism (Table 1). Among 146 cases of DWI-positive lesions, 4 cases of vasospasms occurred during coil embolization. An unfavorable in-hospital functional outcome, defined by a modified Rankin Scale score >1, was significantly higher in patients with thromboembolism than in those without thromboembolism (32.2% vs. 11.8%, p = 0.01).


Table 1. Comparison of baseline characteristics according to the presence of thromboembolism after coil embolization.

Multivariable analysis showed that a longer procedure time increased the risk of thromboembolism (Table 2). The other procedure-related factors were not statistically associated with thromboembolism after coil embolization. The degree of multicollinearity using variance inflation (VIF) factor was not significant between the procedure time and other procedure-related factors (all, VIF < 1.5). The mediator effect showed that the association between the procedure time and occurrence of thromboembolism was not significantly modified by any of the other documented procedure-related factors (Table 3).


Table 2. Logistic regression analysisa showing ORs of each procedure-related factor for the occurrence of thromboembolism.


Table 3. Interaction analysis showing which procedure-related factors mediated the effect of procedure time on the occurrence of thromboembolism.

In the post-hoc analysis, we compared the remaining procedure-related factors according to the procedure time, which was the only significant variable for evaluating the periprocedural environment of coil embolization. With the respect to the dichotomized procedure time (≥120 min vs. <120 min), the group with the longer procedure time used more devices, the stent-assisted coiling method, and multiple microcatheters and coils (Table 4). Patient-related and aneurysm-related factors were not different whether or not the procedure time was delayed. The volume of the thromboembolism confirmed by DWI significantly increased with an increasing procedure time (p = 0.04).


Table 4. Comparison of baseline characteristics according to the procedure time in patients treated with coil embolization.

Coiling-related thromboembolism seemed to have an increasing trend with an increasing procedure time (Supplemental Table 1). The various coiling methods and devise used (single or stent assisted coiling or use of multiple microcatheters and number of coils inserted) were not significantly different with coiling-related and coiling-unrelated thromboembolisms. The sensitivity analysis with multinomial logistic regression analysis showed that an increased procedure time also increased the occurrence of coiling-related thromboembolism, whereas it did not increase the occurrence of coiling-unrelated thromboembolism (Supplemental Table 2).


This study aimed to examine which modifiable procedure-related factors could be effective to reduce thromboembolism in coiling embolization of cerebral aneurysm. It has been reported that several procedure-related factors could affect thromboembolic events after coil embolization. However, these factors focused on novel devices and improving the individual technique and workmanship of the interventionist. From the perspective of a clinical neurologist who refers to an interventionist to treat an aneurysm, practicable efforts to determine effective factors that reduce thromboembolic events may be considered more important than improving the individual interventionist's workmanship and technique. Considering above mentioned, this study had main findings as follows; (1) we found that among the modifiable procedure-related factors, reducing the procedure time could be effective for reducing the risk of thromboembolism after coil embolization; (2) we also suggested that practical efforts, such as reducing procedure manipulations and establishing efficient procedure process, should be performed by the interventionist to reduce the procedure time in real-world practice.

The procedure time as a risk factor for thromboembolism has been rarely documented in previous studies (11). Herein, thromboembolism after coil embolization tended to increase with an increasing procedure time, but this was not found with the patient and aneurysmal factors. The volume of the thromboembolism confirmed by DWI also tended to increase with an increasing procedure time. In addition, we found that the interventionist had a longer procedure time with the use of multiple microcatheters and many devices, whereas this was not the case with the aneurysmal size, morphologies of the aneurysm, and patients' emergent status. These findings mean that many procedural manipulations during coil embolization (14) could lead to delayed intra-procedural time, thereby increasing thromboembolism. Hence, when considering various coiling techniques according to the patients' and aneurysmal status before a procedure plan is established, interventionists should keep in mind that the procedure time could be an effective factor for reducing thromboembolisms.

Multivariable analysis also showed that reducing the procedure time could be the most effective procedure-related factor for reducing thromboembolisms during coil embolization. The insignificance of ORs for the other procedure-related factors was consistent with the result of a recent previous study (16). Notably, mediator effect analysis showed that the other procedure-related factors could not be attributable to the procedure time and thromboembolisms after coil embolization. This finding could support our main practical finding that the procedure time could still be considered an effective factor for reducing thromboembolism compared to other technical and device-related factors. Additionally, the positive association between the procedure time and coiling-related thromboembolism in sensitivity analysis supported the robustness of our main findings.

Interestingly, the finding that the procedure time was independent from other procedure-related factors by the degree of multicollinearity could explain which factors mainly extend the procedure time. A previous study showed that a long procedure time could be associated with the use of a device, aneurysmal size, and procedural morbidity (14). This previous study did not evaluate independency between the procedure time and other factors. With the respect to the result of multicollinearity, we carefully speculated that inefficient periprocedural environment, besides documented procedure-related factors, could contribute to increasing the procedure time of coil embolization in real-world practice. However, since the inefficient periprocedural factors that increased the procedure time were unavailable in our database, we carefully suggested that those factors could be uncooperative and inexperienced coworkers, an inefficient procedure process (e.g., lack of proficiency of the nursing work force, expertise of paramedics and technicians and any of unsupportive external factors to hinder expedient and efficient coil embolization) and unexpected situations (e.g., unstable vital signs of the patients, the occurrence of procedural rupture and procedural morbidity, defined as complications leading to death, and permanent neurological disability) during coil embolization (14) These findings could help interventionists establish a more efficient procedural process of coil embolization to reduce the procedure time.

Our findings with overall rates of 81.1% for thromboembolism and 7.2% (based on 13/180) for symptomatic events showed that the occurrence of thromboembolism after coil embolization for cerebral aneurysm remained high, but the rate of symptomatic events after coil embolization was reasonable compared to that reported in previous studies (range from 5.4 to 40%) (4, 6, 8). Nonetheless, 32.2% of patients with thromboembolism confirmed by DWI had an unfavorable in-hospital functional outcome, mRS score >1. Among the patients with an unruptured aneurysm, the rates of symptomatic events and unfavorable in-hospital functional outcome were 10.2 and 18.6%, respectively (data not shown). We found no studies that described the aggravating functional status in coil-treated patients who had thromboembolism during hospitalization. The previous studies just emphasized the safety of the coiling procedure since most of the DWI-positive lesions were asymptomatic (1, 18). Although the preprocedural mRS scores were unavailable in our database, the rate of an unfavorable in-hospital functional status after coil embolization in patients with unruptured aneurysm leads to an awakened interest in efforts to reduce thromboembolism after the endovascular procedure.

Our study has several limitations. First, it was a retrospective, observational study with a single-center registry, although we used a prospective database. Second, since an experienced interventionist performed the endovascular procedures, selection bias could affect the results, despite use of a consistent procedural protocol. However, our intentions were to describe the clinical periprocedural situation in the real world and determine the most modifiable factor for reducing a complication of coil embolization, not to evaluate the safety and effectiveness of coil embolization. Hence, in determining the impact of procedure-related factors on outcome, it could be considered a strength of this study that only patients treated by one interventionist were enrolled with consistent coiling protocol. Third, procedure-related factors determined in our study cannot be representative of the general population, and unmeasured confounding factors were not controlled for, although we controlled for known measurable confounders in the multivariable model. Therefore, we should be cautious in generalizing the study results. Lastly, we could not demonstrate the inefficient periprocedural factors that delay the procedure time in detail. Additionally, we did not provide the standard procedure time in this study. The mean procedure time in this study was 110.6 min (± 60.2 min), which was longer than that in a previous study (14). However, our intention in this study was to determine the modifiable factor for reducing thromboembolism after coil embolization, not to define the standard procedure time. Although we did not determine the “gold standard procedure time” for reducing thromboembolisms, our study findings may increase interventionists' interest in improving the procedural process.


Our study shows that reducing the procedure time can be the most effective factor an interventionist can modify to reduce thromboembolism after coil embolization of cerebral aneurysm. Additionally, our study shows that the longer procedure time may be affected by multiple procedural manipulations of each aneurysm and an inefficient periprocedural process of coil embolization. Our results suggest that clinical neurologists should refer patients with cerebral aneurysm to interventionists who have established an efficient procedural setting for coil embolization. Further study on this topic may lead to the development of a valuable factor of outcome for coil embolization.

Ethics Statement

Because of study subject anonymity and minimal risk to the patients, collection of data without informed consent was approved by the local institutional review board of Chuncheon Sacred Heart Hospital before the study commenced.

Author Contributions

S-HL: study design, clinical and image data acquisition, data interpretation, and primary writing; HC and J-HS: study design, clinical and image data acquisition, data interpretation, critical revision of the manuscript for important intellectual content, and supervision of the study; MJ, JK, YK, CK, JY, JJ, and YC: data acquisition and revision of manuscript.


This study was partly supported by a grant from Samjin Pharmaceuticals. Additionally, this study was supported by the Biogreen 21 Program (PJ 01121401) and Hallym University Research (HURF-2016-47). The funding organizations did not participate in the design, conduct, or analysis of the study or in the preparation of the manuscript.

Conflict of Interest Statement

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

Supplementary Material

The Supplementary Material for this article can be found online at:


1. Rordorf G, Bellon RJ, Budzik RE Jr, Farkas J, Reinking GF, Pergolizzi RS, et al. Silent thromboembolic events associated with the treatment of unruptured cerebral aneurysms by use of Guglielmi detachable coils: prospective study applying diffusion-weighted imaging. AJNR Am J Neuroradiol. (2001) 22:5–10.

PubMed Abstract

2. Derdeyn CP, Cross DT III, Moran CJ, Brown GW, Pilgram TK, Diringer MN, Grubb RL Jr, et al. Postprocedure ischemic events after treatment of intracranial aneurysms with Guglielmi detachable coils. J Neurosurg. (2002) 96:837–43. doi: 10.3171/jns.2002.96.5.0837

PubMed Abstract | CrossRef Full Text

3. Soeda A, Sakai N, Murao K, Sakai H, Ihara K, Yamada N, et al. Thromboembolic events associated with Guglielmi detachable coil embolization with use of diffusion-weighted MR imaging. Part II Detection of the microemboli proximal to cerebral aneurysm. AJNR Am J Neuroradiol. (2003) 24:2035–8.

Google Scholar

4. Soeda A, Sakai N, Sakai H, Iihara K, Yamada N, Imakita S, et al. Thromboembolic events associated with Guglielmi detachable coil embolization of asymptomatic cerebral aneurysms: evaluation of 66 consecutive cases with use of diffusion-weighted MR imaging. AJNR Am J Neuroradiol. (2003) 24:127–32.

PubMed Abstract | Google Scholar

5. Albayram S, Selcuk H, Kara B, Bozdag E, Uzma O, Kocer N, et al. Thromboembolic events associated with balloon-assisted coil embolization: evaluation with diffusion-weighted MR imaging. AJNR Am J Neuroradiol. (2004) 25:1768–77.

PubMed Abstract | Google Scholar

6. Cronqvist M, Wirestam R, Ramgren B, Brandt L, Nilsson O, Saveland H, et al. Diffusion and perfusion MRI in patients with ruptured and unruptured intracranial aneurysms treated by endovascular coiling: complications, procedural results, MR findings and clinical outcome. Neuroradiology (2005) 47:855–73. doi: 10.1007/s00234-005-1408-2

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Grunwald IQ, Papanagiotou P, Politi M, Struffert T, Roth C, Reith W. Endovascular treatment of unruptured intracranial aneurysms: occurrence of thromboembolic events. Neurosurgery (2006) 58:612–618; discussion. doi: 10.1227/01.NEU.0000204101.00996.D9

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Pierot L, Spelle L, Vitry F, Investigators A. Immediate clinical outcome of patients harboring unruptured intracranial aneurysms treated by endovascular approach: results of the ATENA study. Stroke (2008) 39:2497–504. doi: 10.1161/STROKEAHA.107.512756

PubMed Abstract | CrossRef Full Text

9. Altay T, Kang HI, Woo HH, Masaryk TJ, Rasmussen PA, Fiorella DJ, et al. Thromboembolic events associated with endovascular treatment of cerebral aneurysms. J Neurointerv Surg. (2011) 3:147–50. doi: 10.1136/jnis.2010.003616

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Pierot L, Wakhloo AK. Endovascular treatment of intracranial aneurysms: current status. Stroke (2013) 44:2046–54. doi: 10.1161/STROKEAHA.113.000733

PubMed Abstract | CrossRef Full Text

11. Hahnemann ML, Ringelstein A, Sandalcioglu IE, Goericke S, Moenninghoff C, Wanke I, et al. Silent embolism after stent-assisted coiling of cerebral aneurysms: diffusion-weighted MRI study of 75 cases. J Neurointerv Surg. (2014) 6:461–5. doi: 10.1136/neurintsurg-2013-010820

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Choi SH, Na DL, Chung CS, Lee KH, Na DG, Adair JC. Diffusion-weighted MRI in vascular dementia. Neurology (2000) 54:83–9. doi: 10.1212/WNL.54.1.83

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Vermeer SE, Longstreth WTJr, Koudstaal PJ. Silent brain infarcts: a systematic review. Lancet Neurol. (2007) 6:611–9. doi: 10.1016/S1474-4422(07)70170-9

PubMed Abstract | CrossRef Full Text | Google Scholar

14. De Gast AN, Soepboer A, Sluzewski M, Van Rooij WJ, Beute GN. How long does it take to coil an intracranial aneurysm? Neuroradiology (2008) 50:53–6. doi: 10.1007/s00234-007-0301-6

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Pelz DM, Lownie SP, Fox AJ. Thromboembolic events associated with the treatment of cerebral aneurysms with Guglielmi detachable coils. AJNR Am J Neuroradiol. (1998) 19:1541–7.

PubMed Abstract | Google Scholar

16. Sim SY, Shin YS. Silent microembolism on diffusion-weighted MRI after coil embolization of cerebral aneurysms. Neurointervention (2012) 7:77–84. doi: 10.5469/neuroint.2012.7.2.77

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Kwon OK, Kim SH, Kwon BJ, Kang HS, Kim JH, Oh CW, et al. Endovascular treatment of wide-necked aneurysms by using two microcatheters: techniques and outcomes in 25 patients. AJNR Am J Neuroradiol. (2005) 26:894–900.

PubMed Abstract | Google Scholar

18. Bendszus M, Koltzenburg M, Burger R, Warmuth-Metz M, Hofmann E, Solymosi L. Silent embolism in diagnostic cerebral angiography and neurointerventional procedures: a prospective study. Lancet (1999) 354:1594–7. doi: 10.1016/S0140-6736(99)07083-X

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: thromboembolism, coil embolization, cerebral aneurysm, procedure-related factors, procedure time

Citation: Lee S-H, Jang MU, Kang J, Kim YJ, Kim C, Sohn J-H, Yang J, Jeon JP, Cho Y and Choi HJ (2018) Impact of Reducing the Procedure Time on Thromboembolism After Coil Embolization of Cerebral Aneurysms. Front. Neurol. 9:1125. doi: 10.3389/fneur.2018.01125

Received: 11 August 2018; Accepted: 07 December 2018;
Published: 18 December 2018.

Edited by:

Shakir Husain Hakim, UniversitätsSpital Zürich, Switzerland

Reviewed by:

Foad Abd-Allah, Cairo University, Egypt
Goutham Selvam Periyasamy, Vinayaka Missions University, India

Copyright © 2018 Lee, Jang, Kang, Kim, Kim, Sohn, Yang, Jeon, Cho and Choi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Hyuk Jai Choi,

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