Radiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Boulin, A.
Right arrow Articles by Pierot, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Boulin, A.
Right arrow Articles by Pierot, L.
(Radiology. 2001;219:108-113.)
© RSNA, 2001


Neuroradiology

Follow-up of Intracranial Aneurysms Treated with Detachable Coils: Comparison of Gadolinium-enhanced 3D Time-of-Flight MR Angiography and Digital Subtraction Angiography1

Anne Boulin, MD and Laurent Pierot, MD, PhD

1 From the Department of Diagnostic and Therapeutic Neuroradiology, Foch Hospital, 40 rue Worth, BP 36, 92151 Suresnes, France. Received March 17, 2000; revision requested April 26; revision received June 29; accepted August 29. Address correspondence to L.P. (e-mail: l.pierot@hopital-foch.org).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
PURPOSE: To compare three-dimensional (3D) time-of-flight magnetic resonance (MR) angiography with digital subtraction angiography (DSA) in the follow-up of intracranial aneurysms treated with selective endovascular placement of detachable coils.

MATERIALS AND METHODS: Sixty-eight consecutive patients with intracranial aneurysms were included in the prospective study. The goal was to evaluate 3D time-of-flight MR angiography versus DSA for the detection of a residual aneurysm neck or residual flow inside the coil mesh.

RESULTS: Eighty-one MR angiographic and 83 DSA examinations were performed; 15 patients were examined with both modalities twice. MR angiography was not possible in two patients. In another patient, the quality of MR angiography was not sufficient to assess the treated aneurysm. In 72 of the remaining 80 MR angiographic and DSA examinations, there was good correlation between the two modalities. In 54 cases, neither image type showed remnants or recurrence, but in 18, both showed residual aneurysm. In eight cases, the MR angiographic and DSA results differed. In one of these cases, MR angiography depicted residual aneurysm but DSA depicted an arterial loop. In seven cases, a small (<3-mm) remnant was not detected at MR angiography.

CONCLUSION: Because very small aneurysm remnants or recurrences probably are not clinically important, MR angiography is an option for following up intracranial aneurysms treated with detachable coils and may partly replace DSA.

Index terms: Aneurysm, intracranial, 17.73 • Aneurysm, rupture, 17.73 • Aneurysm, therapy, 17.1264, 17.1267, 17.1269 • Angiography, comparative studies, 17.12142, 17.124 • Interventional procedures, 17.1264, 17.1267, 17.1269


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Selective endovascular treatment (EVT) with Guglielmi detachable coils (GDCs; Boston Scientific/Target Therapeutics, Boston, Mass) is increasingly being used in the management of intracranial aneurysms (15). Results of studies of the occlusion stability obtained by using these coils (6,7) have shown that recurrence can occur at the aneurysm neck, even in cases of initial total occlusion. Long-term follow-up is then needed and is currently performed by using digital subtraction angiography (DSA). A few authors (812) have attempted to evaluate the potential place of magnetic resonance (MR) angiography in this follow-up. However, the small number of patients in these series has not allowed definite conclusions to be drawn. The aim of our study was to compare prospectively DSA, the reference standard, with gadolinium-enhanced three-dimensional time-of-flight MR angiography in the follow-up of intracranial aneurysms that were occluded with GDCs.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Patient Population
From November 1998 to June 1999, 68 patients who had intracranial aneurysms were prospectively examined after selective EVT with GDCs. All except one patient were treated at our institution. All patients gave written informed consent to the examination, and institutional review board approval was obtained.

In two patients, who were claustrophobic, MR examination was not possible. Therefore, 66 patients (36 women, 30 men; mean age, 45 years) harboring 70 aneurysms treated with GDCs were examined by using DSA and three-dimensional, gadolinium-enhanced (gadopentetate dimeglumine [Magnevist]; Schering, Lys-Lez-Lannois, France), time-of-flight MR angiography.

Fifty-two patients had subarachnoid hemorrhage. Endovascular treatment was performed in the acute phase (<14 days) in 51 cases. Fourteen patients had nonruptured aneurysms. The locations of the aneurysms were as follows: anterior communicating artery in 25 cases (36%), internal carotid artery in 24 cases (34%), middle cerebral artery in 18 cases (26%), and other vessel in three cases (4%). The size of the aneurysm was 3 mm or smaller in nine cases (13%), 4–7 mm in 31 cases (44%), 7–15 mm in 27 cases (39%), and larger than 15 mm in three cases (4%).

At the end of the procedure, the occlusions were classified, according to the method of Cognard et al (7), as follows: total (100%) occlusion—that is, the aneurysm sac and neck are densely packed—which occurred in 48 (69%) cases; subtotal (95%–99%) occlusion—that is, the sac is occluded but there is a tiny neck remnant—which occurred in 20 cases (29%); or incomplete (<95%) occlusion—that is, the aneurysm sac and neck are loosely packed or there is either persistent opacification of the sac or a neck remnant—which occurred in two cases (3%).

Patients were examined by using MR angiography and DSA either once (51 patients) or twice (15 patients) during the follow-up period. During that period, 81 comparisons of MR angiography and DSA were theoretically possible. However, in one case, the MR angiogram was not interpretable, so a total of 80 comparisons were performed. Thirty-nine of these studies were performed 3 months after EVT; 30, 12–18 months after EVT; and 11, more than 24 months after EVT.

MR Imaging Techniques
MR examinations were performed with a 1.5-T unit (Signa; GE Medical Systems, Milwaukee, Wis). The standard MR examinations included the acquisition of sagittal T1-weighted spin-echo images (340/14 [repetition time msec/echo time msec], 256 x 256 matrix, 25-cm field of view, 5-mm-thick sections with a 1.5-mm intersection gap), transverse T2-weighted fast spin-echo images (3,000/22 and 100, 256 x 256 matrix, 24-cm field of view, 5-mm-thick sections with a 1.5-mm intersection gap), and coronal T2-weighted fast spin-echo images (4,000/96, 512 x 256 matrix, 24-cm field of view, 4-mm-thick sections with a 0.5-mm intersection gap).

Three-dimensional time-of-flight MR angiography was performed after injection of 0.2 mL of gadopentetate dimeglumine per kilogram of body weight to shorten the sequence. Imaging parameters were as follows: spoiled gradient-echo sequence, 26.0/2.4, 30° flip angle, 256 x 512 matrix, 24 x 18 field of view, 60 partitions, 1-mm section thickness, posterior saturation, one acquisition, and acquisition time of 5 minutes 23 seconds. Magnetization transfer was not used because it was not available at the beginning of the study.

DSA Technique
DSA was performed by using a biplanar angiographic system (BV 3000; Philips Integris, Best, the Netherlands). Selective catheterization of the vessel harboring the aneurysm was performed by using a 5-F catheter with the femoral approach. Eight to ten milliliters of nonionic contrast material (iobitridol [Xenetix 300]; Guerbet, Roissy, France) was injected into the internal carotid or vertebral artery with a power injector at 4–5 mL/sec. Multiple views were obtained.

Image Interpretation
The MR angiograms—individual transverse sections and maximum intensity projection reconstructions—were evaluated by one of the authors (A.B.) without knowledge of the DSA findings, because DSA was always performed the day after MR angiography. The DSA examinations were performed by the other author (L.P.), and the resultant images were assessed in all cases by both authors by means of consensus. At each examination, the following features were evaluated: (a) presence or absence of a neck remnant; (b) size of the neck remnant, if present, by means of direct measurement on the MR angiograms and by means of comparison with the diameter of the internal carotid artery at DSA; (c) presence or absence of flow in the coil mesh; and (d) size of the remnant when residual flow was seen in the coil mesh.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
DSA Findings
At follow-up examination, total occlusion was observed in 49 (70%) of 70 aneurysms. A remnant or recurrence was observed in 21 aneurysms (30%). The remnant was smaller than 3 mm in 13 cases (62%), 3–5 mm in five cases (24%), and greater than 5 mm in three cases (14%). Recurrence was observed in five (10%) of the 48 aneurysms that were totally occluded at the end of treatment. Of the 20 patients with subtotal occlusion at the end of treatment, six had total occlusion 3 months later.

MR Angiography Feasibility and Quality
In three (4%) of the 68 patients for whom MR angiography was recommended, MR angiography was either not possible (two patients) or not informative (one patient). The latter patient harbored multiple aneurysms, one of which was pericallosal and treated surgically by using a clip. Artifacts were responsible for the poor quality of the MR angiogram, which did not enable evaluation of the middle cerebral aneurysm treated with GDC placement.

MR Angiography versus DSA
As stated previously, 80 correlations between MR angiography and DSA were evaluated. In 72 cases (90%), the MR angiography results regarding the presence or absence of a residual aneurysm correlated well with those of DSA. In 54 of the 72 correlations, neither MR angiography nor DSA depicted any remnant or recurrence. These 54 correlations were observed in 48 aneurysms, six of which were examined twice (mean size, 6.3 mm).

In 18 of the 72 good correlations, a remnant was identified at both DSA and MR angiography in 16 aneurysms (mean size, 8 mm). The evaluations of remnant size did not differ between the two techniques: smaller than 3 mm in eight cases (50%), 3–5 mm in five cases (31%), and greater than 5 mm in three cases (19%).

In eight (10%) of the 80 comparisons, the results of MR angiography and DSA were different. In one anterior communicating artery aneurysm, the feature identified at MR angiography as a remnant was visualized at DSA as a loop of the anterior circulation complex. In the other seven cases, the remnants identified at DSA were not detected at MR angiography. In six cases (four aneurysms, two evaluated twice), the remnant measured less than 2 mm (Figs 13). In one case, the remnant was 2.5 mm and the patient underwent a second treatment; there was a persistent flow in the coil mesh close to the aneurysmal neck, which was not visible at MR angiography (Fig 4). The sensitivity and specificity of MR angiography were, therefore, 72% (18 of 25 correlations) and 98% (54 of 55 correlations), respectively, for depicting an aneurysm remnant.



View larger version (157K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 1a. Ruptured 8-mm anterior communicating artery aneurysm in a 43-year-old woman treated with GDC placement. The initial anatomic result was total occlusion, and 3 months after treatment, DSA was normal. One year later, MR angiography and DSA were performed. (a) Maximum intensity projection (MIP) reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4 msec) shows at the right A1 segment to A2 segment junction a vascular abnormality (arrow), which was interpreted as an arterial loop, but (b) frontal and (c) oblique DSA views of the right internal carotid artery show the corresponding region to be an aneurysm remnant (arrow).

 


View larger version (155K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 1b. Ruptured 8-mm anterior communicating artery aneurysm in a 43-year-old woman treated with GDC placement. The initial anatomic result was total occlusion, and 3 months after treatment, DSA was normal. One year later, MR angiography and DSA were performed. (a) Maximum intensity projection (MIP) reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4 msec) shows at the right A1 segment to A2 segment junction a vascular abnormality (arrow), which was interpreted as an arterial loop, but (b) frontal and (c) oblique DSA views of the right internal carotid artery show the corresponding region to be an aneurysm remnant (arrow).

 


View larger version (177K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 1c. Ruptured 8-mm anterior communicating artery aneurysm in a 43-year-old woman treated with GDC placement. The initial anatomic result was total occlusion, and 3 months after treatment, DSA was normal. One year later, MR angiography and DSA were performed. (a) Maximum intensity projection (MIP) reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4 msec) shows at the right A1 segment to A2 segment junction a vascular abnormality (arrow), which was interpreted as an arterial loop, but (b) frontal and (c) oblique DSA views of the right internal carotid artery show the corresponding region to be an aneurysm remnant (arrow).

 


View larger version (176K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2a. Ruptured 4-mm anterior communicating aneurysm in a 64-year-old woman treated with endovascular GDC placement. Initially, this patient had total occlusion, but 3 months later, DSA depicted a small remnant in the aneurysmal neck. (a) Transverse source MR image and (b) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 15 months after treatment show no remnant. (c) Lateral DSA view of the left internal carotid artery obtained 15 months after treatment shows a small remnant (arrow) at the base of the aneurysm.

 


View larger version (145K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2b. Ruptured 4-mm anterior communicating aneurysm in a 64-year-old woman treated with endovascular GDC placement. Initially, this patient had total occlusion, but 3 months later, DSA depicted a small remnant in the aneurysmal neck. (a) Transverse source MR image and (b) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 15 months after treatment show no remnant. (c) Lateral DSA view of the left internal carotid artery obtained 15 months after treatment shows a small remnant (arrow) at the base of the aneurysm.

 


View larger version (161K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2c. Ruptured 4-mm anterior communicating aneurysm in a 64-year-old woman treated with endovascular GDC placement. Initially, this patient had total occlusion, but 3 months later, DSA depicted a small remnant in the aneurysmal neck. (a) Transverse source MR image and (b) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 15 months after treatment show no remnant. (c) Lateral DSA view of the left internal carotid artery obtained 15 months after treatment shows a small remnant (arrow) at the base of the aneurysm.

 


View larger version (140K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 3a. Ruptured left posterior communicating artery aneurysm in a 53-year-old woman treated with GDC placement during the acute phase. The initial anatomic result was total occlusion. (a) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 3 months after treatment shows no remnant. (b) Lateral DSA image of the left internal carotid artery obtained 3 months after treatment shows a 2-mm remnant (arrow) in the aneurysmal neck.

 


View larger version (140K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 3b. Ruptured left posterior communicating artery aneurysm in a 53-year-old woman treated with GDC placement during the acute phase. The initial anatomic result was total occlusion. (a) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 3 months after treatment shows no remnant. (b) Lateral DSA image of the left internal carotid artery obtained 3 months after treatment shows a 2-mm remnant (arrow) in the aneurysmal neck.

 


View larger version (200K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 4a. Ruptured anterior communicating artery aneurysm in a 54-year-old man treated with endovascular GDC placement during the acute phase. This treatment resulted in subtotal occlusion. (a) Transverse source MR image and (b) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 3 months after treatment show no remnant. (c) Lateral and (d) oblique DSA views of the right internal carotid artery obtained 3 months after treatment show residual flow (arrows) in the coil mesh close to the neck.

 


View larger version (152K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 4b. Ruptured anterior communicating artery aneurysm in a 54-year-old man treated with endovascular GDC placement during the acute phase. This treatment resulted in subtotal occlusion. (a) Transverse source MR image and (b) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 3 months after treatment show no remnant. (c) Lateral and (d) oblique DSA views of the right internal carotid artery obtained 3 months after treatment show residual flow (arrows) in the coil mesh close to the neck.

 


View larger version (119K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 4c. Ruptured anterior communicating artery aneurysm in a 54-year-old man treated with endovascular GDC placement during the acute phase. This treatment resulted in subtotal occlusion. (a) Transverse source MR image and (b) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 3 months after treatment show no remnant. (c) Lateral and (d) oblique DSA views of the right internal carotid artery obtained 3 months after treatment show residual flow (arrows) in the coil mesh close to the neck.

 


View larger version (103K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 4d. Ruptured anterior communicating artery aneurysm in a 54-year-old man treated with endovascular GDC placement during the acute phase. This treatment resulted in subtotal occlusion. (a) Transverse source MR image and (b) MIP reconstruction of MR angiogram (three-dimensional time-of-flight spoiled gradient-echo sequence, 26.0/2.4) obtained 3 months after treatment show no remnant. (c) Lateral and (d) oblique DSA views of the right internal carotid artery obtained 3 months after treatment show residual flow (arrows) in the coil mesh close to the neck.

 
Follow-up of Aneurysm Remnants
Of the 21 patients who presented with a remnant or recurrence during follow-up, 13 were examined twice with both DSA and MR angiography. In five of these patients, an increase in the size of the remnant was observed at DSA, and in three of these five patients, changes in the remnant were detected also at MR angiography.

Additional Treatment
In nine of the 21 patients who harbored an aneurysm remnant, additional treatment was attempted and resulted in total occlusion in four cases and subtotal occlusion in one case.


    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Selective EVT of intracranial aneurysms by means of GDCs is being used increasingly. At first, it was used only to treat aneurysms that were not amenable to surgical clipping (1,2), but later, especially in European centers, its indications were broadened to include surgically treatable aneurysms (35).

Stability of Occlusion after EVT of Intracranial Aneurysms
As the results of two recent studies (6,7) made clear, the stability of aneurysm occlusion after EVT with GDCs must be regularly evaluated: This procedure has sometimes been followed by immediate incomplete occlusion or a recurrence. In a cooperative study performed in the United States (2), a small neck remnant was observed in 21% of small aneurysms with a small neck, 57% of large aneurysms, and 50% of giant aneurysms. As observed by Hope et al (6), such small remnants may enlarge by means of coil compaction or the aneurysm may grow. In other cases, the residual aneurysm may shrink or disappear.

In a series of 169 aneurysms reported by Cognard et al (7), subtotal or incomplete occlusion was initially observed in 20 cases (12%). The evolution of the aneurysm remnants varied. In a large proportion of cases (62%), no modification of these remnants was observed during follow-up. Regrowth of the aneurysm pouch occurred in some cases (33%), and repeat treatment was sometimes performed. Initial total occlusion was achieved in a very large number of cases, but 3–40 months after the initial treatment, recurrence occurred in 24 (14%) of the 169 cases, and six (25%) of these recurrences were re-treated.

Clinical Importance of Aneurysm Remnants or Recurrences
Because EVT of intracranial aneurysms by using GDCs is a relatively new technique, it is difficult to determine the clinical importance of an aneurysm remnant or recurrence. In the series of Cognard et al (7), no rebleeding occurred during the follow-up period, even in the patients with residual aneurysms or recurrence. In the series of Viñuela et al (2), rebleeding was observed in 2.2% of cases during the 6 months after treatment. In all of the cases, the aneurysms were incompletely treated. In a large surgical series, Feuerberg et al (13) reported a risk of rebleeding caused by an aneurysm remnant in 0.38%–0.79% of cases.

Follow-up of Patients Selectively Treated with GDCs
We determined from our review that a residual pouch may occur after selective EVT of intracranial aneurysms by means of GDCs. The clinical importance of these residual pouches is not clear, but we know from the surgery literature that the risk of such pouch formation cannot be neglected. It is, therefore, necessary to plan a follow-up of such patients. Usually, this follow-up is conducted by performing DSA 3 months, 1 year, and 3 years after treatment (7). However, DSA has a risk of neurologic complications, which are estimated to occur in 0.5%–4.0% of cases (14). Consequently, repeated DSA examinations may increase the morbidity and/or mortality rate of EVT for intracranial aneurysms, and, therefore, the efficacy of nontraumatic follow-up methods should be evaluated.

MR angiography is a potentially good candidate for use in this follow-up, because it is generally well tolerated, except by patients who are claustrophobic. Even when gadolinium-based contrast material is injected, the risk remains low. The three-dimensional time-of-flight technique, with and without gadolinium-based contrast material injection and with and without magnetization transfer, has been evaluated for the detection of intracranial aneurysms with good results (1517). Moreover, Hartman et al (18) and Shellock et al (19) found GDCs to be compatible for MR imaging and to produce few or no artifacts.

To our knowledge, few reports have addressed the value and place of MR angiography in the follow-up of intracranial aneurysms treated with GDCs, and the number of patients examined in these reports, 14–49, has been too small to yield valid conclusions. In the largest study (12), there was a high percentage of cases (11%) with artifacts due to the presence of GDCs. The sensitivity of MR angiography, as compared with DSA, for the detection of residual aneurysms was 97%, and the specificity was 100%.

In our study, gadolinium-enhanced three-dimensional time-of-flight MR angiography was used because some authors (20,21) have observed the accuracy of this technique for the brain vasculature, especially intracranial aneurysms. Moreover, our goal was to increase signal intensity in the residual pouches, where flow can be slow. Finally, this technique shortened the sequence and thus allowed the maximum number of patients to undergo MR imaging.

We focused on the evaluation of residual aneurysms or recurrences because in the long term, these constitute the real problem. Although patency of the parent vessel is one of the problems in the treatment phase, it is usually evaluated correctly by performing angiography postoperatively or, in cases of neurologic symptoms, during the days following treatment.

The aim of EVT is to obtain dense packing of the coils in the aneurysmal sac to occlude the neck and suppress blood flow in the sac. In a few cases, this aim is not fulfilled because of anatomic or technical reasons, and residual flow is sometimes observed in the coils near the neck. In such cases, the evolution usually ends in the compaction of the coils in the fundus of the aneurysmal sac, which leads to remnant formation in the neck (6). In this case, residual aneurysms or recurrences can have two different forms: (a) a residual pouch between the coil mesh and the aneurysmal neck or (b) residual flow in the coil mesh. In our series, the first form was the most frequent: It occurred in 20 of 21 cases of remnant or recurrence.

Discrepancies between DSA and MR angiography were observed in 10% of cases, reducing sensitivity to 72%; specificity was assessed to be 98%. As in the detection of untreated aneurysms (22), the critical size is less than 3 mm. In our series, only small aneurysm neck remnants (<3 mm) were visualized at DSA but not at MR angiography (Figs 14). In all but one case, no additional treatment was proposed and follow-up was continued. In one case, residual flow in the coils close to the neck was visualized at DSA but not at MR angiography, and additional treatment was performed (Fig 4).

Most of the discrepancies between MR angiography and DSA were encountered at the beginning of our study. Just as there is a learning curve for EVT of aneurysms, there probably is such a curve for the interpretation of MR angiograms of treated intracranial aneurysms. Retrospective evaluation performed at the time this article was written showed that in some cases, the interpretations of MR angiograms during our prospective study differed from later evaluations.

The value of contrast material administration in the examination of patients was not demonstrated in our study, because none of the MR angiograms were obtained without contrast material. Anzalone et al (12) compared nonenhanced and contrast material–enhanced MR angiography in 25 GDC-treated aneurysms and found that contrast-enhanced MR angiography was useful for evaluating the residual patency in large and giant aneurysms and for depicting distal branch arteries.

Follow-up of GDC-treated Intracranial Aneurysms
Our study results indicate that MR angiography is probably able to depict clinically important aneurysm neck remnants larger than 3 mm, but a larger series of patients is probably necessary to confirm this.

The follow-up described by Cognard et al (7) consisted of DSA performed 3 months, 1 year, and 3 years after treatment. If our results are confirmed in a larger series, then the DSA examination performed at 3 months can probably be replaced by MR angiography. At 1 year, both DSA and MR angiography should be performed and their results compared, and if these results are not discrepant, follow-up can then be based on MR angiography findings.

The most useful duration of follow-up is unknown, but the use of MR angiography allows very long-term examination of the treated patients without increasing the overall morbidity and/or mortality of the technique.

In summary, MR angiography can depict residual aneurysms larger than 3 mm, which are probably the clinically important aneurysms. Therefore, MR angiography is probably a good noninvasive tool for the follow-up of intracranial aneurysms treated by using GDCs, and it may partly replace DSA.


    FOOTNOTES
 
Abbreviations: DSA = digital subtraction angiography, EVT = endovascular treatment, GDC = Guglielmi detachable coil, MIP = maximum intensity projection

Author contributions: Guarantor of integrity of entire study, L.P.; study concepts, L.P.; study design, L.P., A.B.; literature research, L.P., A.B.; clinical studies, A.B.; data acquisition, A.B.; data analysis/interpretation, L.P., A.B.; manuscript preparation, L.P.; manuscript definition of intellectual content, L.P., A.B.; manuscript editing, L.P.; manuscript revision/review, L.P.; manuscript final version approval, L.P.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Pierot L, Boulin A, Castaings L, Moret J. Selective occlusion of basilar artery aneurysms using controlled-detachable coils: report of 35 cases. Neurosurgery 1996; 38:948-954.[Medline]
  2. Viñuela F, Duckwiler G, Mawad M. Guglielmi detachable coil embolization of acute intracranial aneurysms: perioperative anatomical and clinical outcome in 403 patients. J Neurosurg 1997; 86:475-482.[Medline]
  3. Moret J, Pierot L, Boulin A, Castaings L, Rey A. Endovascular treatment of anterior communicating artery aneurysms using GDC coils. Neuroradiology 1996; 38:800-805.[Medline]
  4. Pierot L, Boulin A, Castaings L, Rey A, Moret J. The endovascular approach in the management of patients with multiple intracranial aneurysms. Neuroradiology 1997; 39:361-366.[Medline]
  5. Cognard C, Weill A, Castaings L, Rey A, Moret J. Intracranial berry aneurysms: angiographic and clinical results after endovascular treatment. Radiology 1998; 206:499-510.[Abstract/Free Full Text]
  6. Hope AJK, Byrne JV, Molyneux AJ. Factors influencing successful angiographic occlusion of aneurysms treated by coil embolization. AJNR Am J Neuroradiol 1999; 20:391-399.[Abstract/Free Full Text]
  7. Cognard C, Weill A, Spelle L, et al. Long-term angiographic follow-up of 169 intracranial berry aneurysms occluded with detachable coils. Radiology 1999; 212:348- 356.[Abstract/Free Full Text]
  8. Derdeyn CP, Graves VB, Turski PA, Masaryk AM, Stroher CM. MR angiography of saccular aneurysms after treatment with Guglielmi coils: preliminary experience. AJNR Am J Neuroradiol 1997; 18:279-286.[Abstract]
  9. Gönner F, Heid O, Remonda L, et al. MR angiography with ultrashort echo time in cerebral aneurysms treated with Guglielmi detachable coils. AJNR Am J Neuroradiol 1998; 19:1324-1328.[Abstract]
  10. Brunereau L, Cottier JP, Sonier CB, et al. Prospective evaluation of time-of-flight MR angiography in the follow-up of intracranial saccular aneurysms treated with Guglielmi detachable coils. J Comput Assist Tomogr 1999; 23:216-223.[Medline]
  11. Kähärä VJ, Seppänen SK, Ryymin PS, Mattila P, Kuurne T, Laasonen EM. MR angiography with three-dimensional time-of-flight and targeted maximum-intensity-projection reconstructions in the follow-up of intracranial aneurysms embolized with Guglielmi detachable coils. AJNR Am J Neuroradiol 1999; 20:1470-1475.[Abstract/Free Full Text]
  12. Anzalone N, Righi C, Simionato F, et al. Three-dimensional time-of-flight MR angiography in the evaluation of intracranial aneurysms treated with Guglielmi detachable coils. AJNR Am J Neuroradiol 2000; 21:746-752.[Abstract/Free Full Text]
  13. Feuerberg I, Lindquist C, Lindqvist M, Steiner L. Natural history of postoperative aneurysm rests. J Neurosurg 1987; 66:30-34.[Medline]
  14. Grzyska U, Freitag J, Zeumer H. Selective cerebral intraarterial DSA: complication rate and control of risk factors. Neuroradiology 1990; 32:296-299.[Medline]
  15. Schuierer G, Huk WJ, Laub G. Magnetic resonance angiography of intracranial aneurysms: comparison with intra-arterial digital subtraction angiography. Neuroradiology 1992; 35:50-54.[Medline]
  16. Ronkainen A, Puranen MI, Hernesniemi JA, et al. Intracranial aneurysms: MR angiography screening in 400 asymptomatic individuals with increased familial risk. Radiology 1995; 195:35-40.[Abstract/Free Full Text]
  17. Atlas SW, Sheppard L, Golberg HI, Hurst RW, Listerud J, Flamm E. Intracranial aneurysms: detection and characterization with MR angiography with use of an advanced postprocessing technique in a blinded-reader study. Radiology 1997; 203:807-814.[Abstract/Free Full Text]
  18. Hartman J, Nguyen R, Larsen D, Teitelbaum GP. MR artefacts, heat production, and ferromagnetism of Guglielmi detachable coils. AJNR Am J Neuroradiol 1997; 18:497-501.[Abstract]
  19. Shellock FG, Detrick MS, Brant-Zawadzki M. MR compatibility of Guglielmi detachable coils. Radiology 1997; 203:568-570.[Abstract/Free Full Text]
  20. Chung W, Listerud J, Atlas SW. Contrast material–enhanced MR angiography for intracranial aneurysms with 3D time-of-flight and 3D phase contrast techniques (abstr). Radiology 1992; 185(P):121.
  21. Bradley WG, Widoff BE, Yan K, et al. Comparison of routine and gadodiamide-enhanced 3D time-of-flight MR angiography in the brain (abstr). Radiology 1992; 185(P):122.
  22. Atlas WA, Sheppard L, Goldberg HI, Hurst RW, Listerud J, Flamm E. Intracranial aneurysms: detection and characterization with MR angiography with use of an advanced postprocessing technique in a blinded-reader study. Radiology 1997; 203:807-814.



This article has been cited by other articles:


Home page
Am. J. Neuroradiol.Home page
R.C. Wallace, J.P. Karis, S. Partovi, and D. Fiorella
Noninvasive Imaging of Treated Cerebral Aneurysms, Part I: MR Angiographic Follow-Up of Coiled Aneurysms
AJNR Am. J. Neuroradiol., June 1, 2007; 28(6): 1001 - 1008.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
H.A. Deutschmann, M. Augustin, J. Simbrunner, B. Unger, H. Schoellnast, G.A. Fritz, and G.E. Klein
Diagnostic Accuracy of 3D Time-of-Flight MR Angiography Compared with Digital Subtraction Angiography for Follow-Up of Coiled Intracranial Aneurysms: Influence of Aneurysm Size
AJNR Am. J. Neuroradiol., April 1, 2007; 28(4): 628 - 634.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
O. Dudeck, O. Jordan, K.T. Hoffmann, A.F. Okuducu, I. Husmann, T. Kreuzer-Nagy, K. Tesmer, P. Podrabsky, H. Bruhn, J. Hilborn, et al.
Embolization of experimental wide-necked aneurysms with iodine-containing polyvinyl alcohol solubilized in a low-angiotoxicity solvent.
AJNR Am. J. Neuroradiol., October 1, 2006; 27(9): 1849 - 1855.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
The CARAT Investigators*
Rates of Delayed Rebleeding From Intracranial Aneurysms Are Low After Surgical and Endovascular Treatment
Stroke, June 1, 2006; 37(6): 1437 - 1442.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
L. Pierot, C. Delcourt, F. Bouquigny, D. Breidt, B. Feuillet, O. Lanoix, and S. Gallas
Follow-up of intracranial aneurysms selectively treated with coils: Prospective evaluation of contrast-enhanced MR angiography.
AJNR Am. J. Neuroradiol., April 1, 2006; 27(4): 744 - 749.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
J.-Y. Gauvrit, X. Leclerc, S. Caron, C. A. Taschner, J.-P. Lejeune, and J.-P. Pruvo
Intracranial Aneurysms Treated With Guglielmi Detachable Coils: Imaging Follow-Up With Contrast-Enhanced MR Angiography
Stroke, April 1, 2006; 37(4): 1033 - 1037.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
C. L. Turner, J. N. P. Higgins, A. Gholkar, A. D. Mendelow, A. J. Molyneux, R. S.C. Kerr, S. Chawda, and P. J. Kirkpatrick
Intracranial Aneurysms Treated With Endovascular Coils: Detection of Recurrences Using Unenhanced and Contrast-Enhanced Transcranial Color-Coded Duplex Sonography
Stroke, December 1, 2005; 36(12): 2654 - 2659.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
M. Sluzewski, W. J. van Rooij, G. N. Beute, and P. C. Nijssen
Late Rebleeding of Ruptured Intracranial Aneurysms Treated with Detachable Coils
AJNR Am. J. Neuroradiol., November 1, 2005; 26(10): 2542 - 2549.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
C. A. Taschner, X. Leclerc, H. Rachdi, A. M. Barros, and J.-P. Pruvo
Matrix Detachable Coils for the Endovascular Treatment of Intracranial Aneurysms: Analysis of Early Angiographic and Clinical Outcomes
Stroke, October 1, 2005; 36(10): 2176 - 2180.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
S. Gallas, A. Pasco, J.-P. Cottier, J. Gabrillargues, J. Drouineau, C. Cognard, and D. Herbreteau
A Multicenter Study of 705 Ruptured Intracranial Aneurysms Treated with Guglielmi Detachable Coils
AJNR Am. J. Neuroradiol., August 1, 2005; 26(7): 1723 - 1731.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
C. B. L. M. Majoie, M. E. Sprengers, W. J. J. van Rooij, C. Lavini, M. Sluzewski, J. C. van Rijn, and G. J. den Heeten
MR Angiography at 3T versus Digital Subtraction Angiography in the Follow-up of Intracranial Aneurysms Treated with Detachable Coils
AJNR Am. J. Neuroradiol., June 1, 2005; 26(6): 1349 - 1356.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
M. T. Walker, J. Tsai, T. Parish, B. Tzung, A. Shaibani, E. Krupinski, and E. J. Russell
MR Angiographic Evaluation of Platinum Coil Packs at 1.5T and 3T: An In Vitro Assessment of Artifact Production: Technical Note
AJNR Am. J. Neuroradiol., April 1, 2005; 26(4): 848 - 853.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
J.-Y. Gauvrit, X. Leclerc, M. Pernodet, B. Lubicz, J.-P. Lejeune, D. Leys, and J.-P. Pruvo
Intracranial Aneurysms Treated with Guglielmi Detachable Coils: Usefulness of 6-Month Imaging Follow-Up with Contrast-Enhanced MR Angiography
AJNR Am. J. Neuroradiol., March 1, 2005; 26(3): 515 - 521.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
N. Yamada, K. Hayashi, K. Murao, M. Higashi, and K. Iihara
Time-of-Flight MR Angiography Targeted to Coiled Intracranial Aneurysms Is More Sensitive to Residual Flow than Is Digital Subtraction Angiography
AJNR Am. J. Neuroradiol., August 1, 2004; 25(7): 1154 - 1157.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
J.-P. Cottier, A. Bleuzen-Couthon, S. Gallas, C. B. Vinikoff-Sonier, P. Bertrand, F. Domengie, L. Barantin, and D. Herbreteau
Intracranial Aneurysms Treated with Guglielmi Detachable Coils: Is Contrast Material Necessary in the Follow-up with 3D Time-of-Flight MR Angiography?
AJNR Am. J. Neuroradiol., October 1, 2003; 24(9): 1797 - 1803.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
I. Saatci, H. S. Cekirge, E. F. M. Ciceri, M. E. Mawad, A. G. Pamuk, and A. Besim
CT and MR Imaging Findings and Their Implications in the Follow-up of Patients with Intracranial Aneurysms Treated with Endosaccular Occlusion with Onyx
AJNR Am. J. Neuroradiol., April 1, 2003; 24(4): 567 - 578.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
L. Hacein-Bey, C. A. Muszynski, and P. N. Varelas
Saccular Aneurysm Associated with Posterior Cerebral Artery Fenestration Manifesting as a Subarachnoid Hemorrhage in a Child
AJNR Am. J. Neuroradiol., September 1, 2002; 23(8): 1291 - 1294.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
X. Leclerc, J.-F. Navez, J.-Y. Gauvrit, J.-P. Lejeune, and J.-P. Pruvo
Aneurysms of the Anterior Communicating Artery Treated with Guglielmi Detachable Coils: Follow-Up with Contrast-Enhanced MR Angiography
AJNR Am. J. Neuroradiol., August 1, 2002; 23(7): 1121 - 1127.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Boulin, A.
Right arrow Articles by Pierot, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Boulin, A.
Right arrow Articles by Pierot, L.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
RADIOLOGY RADIOGRAPHICS