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Neurointervention > Volume 6(2); 2011 > Article
Choi, Roh, Moon, Chun, and Kang: Optimization of MR Parameters of 3D TOF-MRA for Various Intracranial Stents at 3.0T MRI

Abstract

Purpose

The in-stent signal reduction of the stented artery caused by susceptibility artifact or radiofrequency shielding artifact limited the use of time-of-flight MR angiography (TOF-MRA) as a follow-up tool after intracranial stenting. We showed the degree of an artifact according to different stent types, and optimized MR parameters for TOF-MRA in patients with intracranial stent on 3.0 T MRI.

Materials and Methods

Four stents (Neuroform, Wingspan, Solitaire, and Enterprise) were placed in a vascular flow phantom and imaged by changing flip angle (FA; 20°,30°,40°,50° and 60°) and bandwidth (BW; 31, 42 and 62.5 KHz) using TOF-MRA. Source data of each image set with different FA and BW were reconstructed with the maximal intensity projection (MIP) technique, and MIP images were used to evaluate the in-stent signal reduction of each stent according to the change of MR parameters. The in-stent signal reduction was assessed by calculating the relative in-stent signal (RIS) inside the stent as compared with background and signal intensity of the tube outside the stent. The optimal FA and BW of each stent were determined by comparing the RIS in each stent by one-sample t test. Finally, one neuroradiologist chose one image set with the best image quality.

Results

The mean RIS for Neuroform, Wingspan, Solitaire and Enterprise stent was 66.3 ± 6.0, 44.2 ± 5.8, 22.8 ± 3.3 and 8.2 ± 2.9, respectively. The significantly high RIS of each stent was obtained with FA/BW value of 20°/31 KHz (Neuroform), 20°/31 KHz and 30°/42 KHz (Wingspan), 40°/42 KHz and 50°/31 KHz (Solitaire) and 40°/31 KHz and 50°/31 KHz (Enterprise). Among these MIP images with significantly high RIS, images with FA/BW value of 20°/31 KHz (Neuroform and Wingspan) and 50°/31 KHz (Solitaire and Enterprise) had the best image quality.

Conclusion

The degree of artifact was variable according to the design of each intracranial stent. The luminal visualization of closed-cell design stents such as Solitaire and Enterprise can be improved by higher FA. Thus, MR parameter should be adjusted according to the type of intracranial stents.

Intracranial stents were used for treating symptomatic, severe arterial stenosis or assisting coil embolization in wide-neck aneurysm [1,-9]. However, these stents cause endothelial hyperplasia, and thrombosis that might cause significant stenosis or occlusion of stented arteries [6]. Thus, it is important to detect significant stenosis or occlusion before adverse event occurs. Transfemoral cerebral arteriography (TFCA) has been considered as the method of reference for evaluation of the stented arteries. However, it is invasive and has the potential risk of neurological complications [10]. Contrast-enhanced MR angiography (CE-MRA) seemed to be alternative to TFCA in terms of detecting restenosis of artery after large arteries such as carotid, iliac or femoral arteries [11,-13]. However, CE-MRA requires the use of gadolinium contrast media, which have the risk of anaphylaxis, renal complication, and nephrogenic systemic fibrosis [14]. Time-of-flight (TOF) MRA is a widely used and well-established MRA technique for evaluating intra- and extra-cranial arterial pathology without contrast media [15,, 16]. However, various metallic stents cause the variable degree of luminal signal loss of the stented artery due to susceptibility artifact or radiofrequency (RF) shielding artifact [17,-19]. Therefore, it is difficult to evaluate patency of stented intracranial artery which is usually less than 3 mm.
In this report, we showed the degree of the artifact according to different stent types, and proposed optimized MR parameters with emphasis on the change of flip angle (FA) and bandwidth (BW) for TOF-MRA in patients with intracranial stents on 3.0 T MRI.

MATERIALS AND METHODS

Vascular phantom

The stents were placed in a silicone tube with an inner diameter of 3 mm. Four different stents [Neuroform (4.5 × 20 mm, Boston Scientific, Fremont, CA, U.S.A.), Wingspan (4.5 × 20 mm, Boston Scientific, Fremont, CA, U.S.A.), Solitaire (4 × 20 mm, ev3, Irvine, CA, U.S.A.) and Enterprise (4.5 × 28 mm, Codman Neurovascular, Miami, FL, U.S.A.)] were deployed in four tubes. The silicone tubes were placed inside the transparent plastic box filled with ultrasound gel (Progel; Dayo Medical Co., Ltd., Seoul, Korea). The silicone tubes were filled with normal saline solution and connected to high-powered solenoid metering pump (Gamma/L; Prominent Korea, Gounggyi, Korea). This pump could deliver constant pulsatile flow with rate of 70 beat/min. This vascular phantom was placed in the center of the head coil with the longitudinal axis of the stented tube roughly parallel to the main magnetic field.

MR Imaging

All MR images were obtained on a GE 3.0T scanner (Signa HDx; GE Healthcare, Milwaukee, WI, U.S.A.) with an 8 channel head-coil. At first, we obtained three-dimensional (3D) TOF-MRA with parameters as follows: Spoiled gradient-echo sequence with TR/TE/FA, 24 msec/2.7 msec/20°; FOV/Matrix, 180 mm/384 × 224; slice thickness/slice overlap, 1.2 mm/50%; ASSET factor, 2; and actual bandwidth, 31 KHz. Vein saturation slab or optimized RAMP pulse was not used. We hypothesized that the major artifacts caused by metallic stent were susceptibility artifact and RF shielding artifact, thus we changed FA and BW to minimize these artifacts. The shortest TE was used to minimize signal loss due to dephasing or susceptibility artifact. The shortest TE was ranged from 2.2 msec to 2.7 msec and automatically selected according to the change of BW. The change of FA, BW and TE was shown in Table 1.
A total of 120 slices was sampled in one slab. The scan range was 72 mm. Our imaging parameters yielded a measured voxel size of 0.352 × 0.352 × 0.6 mm. Acquisition time was 2 minutes, 57 seconds.

Image Reconstruction and Interpretation

Source data of each imaging set were reconstructed with the maximal intensity projection (MIP) technique. All the image interpretation of MRA was performed on a PACS monitor by one board-certified radiologist. In-stent signal reduction was assessed by calculating the relative in-stent signal (RIS) inside the stent as compared with background and signal intensity of the tube outside the stent. This was obtained by measuring mean values of signal intensity (SI) from rectangular (at least 5 mm2) regions of interest placed in the lumen of stented segment of the tube, proximal segment of the tube without stent and background filled with ultrasound gel. The RIS was calculated as followed:
RIS (%) = [(SIin-stent - SIbackground) / (SItube - SIbackground)] × 100
The mean and standard deviation for each stent according to various MR parameters were obtained and one-sample t-test were used to select significantly high RIS value of the each stent. The level of statistical significance was set at 0.05. Among the MIP images with significantly high RIS value in each stent, one neuroradiologist, who has been working in MRA interpretation for 9 years, choose one image set with best image quality.

RESULTS

The RIS of each stent according to changes of FA and BW was shown in Table 1. The RIS differed between stent and sequence, and in-stent stent signal reduction occurred in all stents. The mean RIS for Neuroform, Wingspan, Solitaire and Enterprise stent was 66.3 ± 6.0, 44.2 ± 5.8, 22.8 ± 3.3 and 8.2 ± 2.9, respectively. The RIS of Neuroform and Wingspan decreased as the FA increased. However, the RIS of Solitaire and Enterprise increased as the FA increased to the FA value of 50 (Figs. 1, 2). The mean RIS of the all stents according to the change of FA and BW was not significantly different. The significantly high RIS of each stent Neuroform, Wingspan, Solitaire and Enterprise was obtained with FA/BW value of 20°/31 KHz (Neuroform, RIS = 72.8, p = 0.000), 20°/31 KHz and 30°/42 KHz (Wingspan, RIS = 52.1 and 49.0, p = 0.004 and 0.04), 40°/42 KHz and 50°/31 KHz (Solitaire, RIS = 25.3 and 25.3, p = 0.05)and 40°/31 KHz and 50°/31 KHz (Enterprise, RIS = 10.6 and 11.5, p = 0.038 and 0.009), respectively (Table 1, Fig. 3). Among these MIP images with significantly high RIS, images with FA/BW value of 20°/31 KHz (Neuroform and Wingspan), 50°/31 KHz (Solitaire) and 50°/31 KHz (Enterprise) were chosen to be the best (Fig. 3). A band-like artifact was observed at the end of the each stent and a complete signal loss was observed neat the proximal marker of the Solitaire stent (Fig. 3).

DISCUSSION

TOF-MRA can demonstrate pathology of the intracranial large arteries that is less than 3 mm in diameter. However, it is difficult to interpret patency and/or degree of stenosis of stented artery on TOF-MRA because of susceptibility artifact or RF shielding effect of intracranial stents [17,, 19,, 20]. In our daily practice, we observed that the degree of image degradation by these artifacts were variable according to the type of intracranial stents. Thus, we needed to optimize MR parameters according to each intracranial stent.
When we obtain the MRA of intracranial large arteries using TOF, the selection of FA and repetition time is a compromise between saturating background tissue and not saturating blood. Typical FA values range between 20° and 35° for 3D TOF, and these values were applicable to obtaining intracranial large arteries without stent insertion. However, the intracranial stents causes two major types of artifact known as susceptibility artifacts and RF shielding artifacts [18,, 19,, 21,-24]. Thus, to obtain MRA without severe artifacts, we should not consider only factors for increasing contrast between blood and background, but also factors for reducing stent-related artifact.
The RF shielding artifact is caused by eddy currents induced in the electrically conducting wire mesh of the stent [19,, 21,, 22]. These eddy currents produce an opposing RF field, which reduces the sensitivity of receiving and emitting signal within the stent. The RF shielding artifact may be attenuated by increasing RF power of the excitation pulse [21,, 22]. Because the FA is proportional to the integral of the RF pulse, high power RF pulse was required to create an excitation pulse with higher FA. The higher FA is used, the more transverse magnetization is created. Thus, the transverse magnetization of unsaturated blood of fast arterial flow in the imaging plane increases. Although high FA in TOF-MRA may cause signal loss of the peripheral small arteries or arteries with the slow flow due to saturation effect, the proximal portion of intracranial large arteries such as M1 segment of middle cerebral artery or distal internal carotid artery might not be affected saturation effect of high FA. Interestingly, the RIS of Neuroform and Wingspan decreased as the FA increased. However, the RIS of Solitaire and Enterprise increased as the FA increased to the FA value of 50°. Thus, the highest RIS of Neuroform and Wingspan was obtained with FA of 20°, and that of Solitaire and Enterprise was obtained with FA of 40° or 50°. Because the RIS in our experiment was a function of background signal, signal of stented artery and non-stented artery, we could not accurately explain why the trend of the RIS changes according to variable FA value was different in closed- and open-cell design stents. We speculated the effect of reducing RF shielding artifact by using high FA might overwhelm other causes of signal loss of the stented segment.
The stents used in this experiment were made of nitinol, which was known to nonferromagnetic metals and cause negligible signal loss on TOF where the echo time is very short. The thickness of strut and cell design in intracranial stents seemed to be important to determine the degree of RF shielding artifact. The thickness of the strut in the open-cell design stent, Neuroform and Wingspan was 0.07 mm, and that in closed-cell design stents, Enterprise and Solitaire were 0.08 mm and 0.06 mm, respectively [2,-4,, 6,, 25,, 26]. The open-cell design and thinner stent strut of the Neuroform and Wingspan stent might cause lesser RF shielding artifact and provide better image quality as compared with Enterprise stent. Although Solitaire stent has the thinnest stent strut and open slit design, the RF shielding artifact occurred comparable to Enterprise stent due to its closed-cell design. As compared with proximal and distal markers of other stents, the relative thick, proximal marker near the detach zone of the Solitaire stent caused complete signal loss of the lumen due to susceptibility artifact. Thus, it was impossible to evaluate the segment near the proximal marker of the Solitaire stent.
It is known that wider BW can reduce susceptibility artifact and overcome RF shielding effect. However, this might reduce signal to noise ratio of the TOF-MRA [21]. We had expected that wider BW could have reduced RF shielding artifact in closed-cell design stent, and decrease susceptibility artifact. However, the change of the BW did not significantly affect RIS in each stent in our experiment. To overcome RF shielding artifact in closed-cell design stent, it is helpful to use higher flip angle instead of wider BW. The importance of higher FA to overcome RF shielding artifact and narrower BW to improve signal to noise ratio in closed-cell design stent should be emphasized in obtaining MRA using 3D TOF technique.
Our experiment conducted with a silicone tube with straight course. This straight course of our tube resulted in different flow pattern from the in vivo situation, thus artifact and signal reduction may be different in tortuous intracranial large arteries. Moreover, the long axis of the stent in the intracranial large arteries was not always parallel to a main magnetic field. Further in vivo study with various stents should be conducted before clinical application.
In conclusion, the degree of artifact was variable according to the design of each intracranial stent. Thus, MR parameter should be adjusted according to various intracranial stents. The luminal visualization of closed-cell design stents such as Solitaire and Enterprise can be improved by higher FA. Further studies with various stents and patients in clinical practice should be conducted in the near future.

Acknowledgement

This work was supported by the Konkuk University Medical Center Research Grant 2010.

References

1. Tähtinen OI, Vanninen RL, Manninen HI, Rautio R, Haapanen A, Niskakangas T, et al. Wide-necked intracranial aneurysms: Treatment with stent-assisted coil embolization during acute (<72 hours) subarachnoid hemorrhage-experience in 61 consecutive patients1. Radiology 2009;253:199-208 .
crossref pmid
2. Fiorella D, Albuquerque FC, Deshmukh VR, McDougall CG. Usefulness of the neuroform stent for the treatment of cerebral aneurysms: results at initial (3-6-mo) follow-up. Neurosurgery 2005;56:1191-1202 .
crossref pmid
3. Klisch J, Eger C, Sychra V, Strasilla C, Basche S, Weber J. Stent-assisted coil embolization of posterior circulation aneurysms using solitaire ab: preliminary experience. Neurosurgery 2009;65:258-266 discussion 266
crossref pmid
4. Lubicz B, Collignon L, Raphaeli G, Bandeira A, Bruneau M, De Witte O. Solitaire stent for endovascular treatment of intracranial aneurysms: immediate and mid-term results in 15 patients with 17 aneurysms. J Neuroradiol 2010;37:83-88 .
crossref pmid
5. Suh DC, Kim JK, Choi JW, Choi BS, Pyun HW, Choi YJ, et al. Intracranial stenting of severe symptomatic intracranial stenosis: results of 100 consecutive patients. AJNR Am J Neuroradiol 2008;29:781-785 .
crossref pmid pmc
6. Costalat V, Maldonado IL, Vendrell JF, Riquelme C, Machi P, Arteaga C, et al. Endovascular treatment of symptomatic intracranial stenosis with the wingspan stent system and gateway pta balloon: a multicenter series of 60 patients with acute and midterm results. J Neurosurg 2011.
crossref
7. Jabbour PM, Tjoumakaris SI, Rosenwasser RH. Endovascular management of intracranial aneurysms. Neurosurg Clin N Am 2009;20:383-398 .
crossref pmid
8. Hwang J, Roh H, Chun Y, Kang HS, Choi J, Moon WJ, et al. Endovascular coil embolization of very small intracranial aneurysms. Neuroradiology 2011;53:349-357 .
crossref pmid
9. Klisch J, Clajus C, Sychra V, Eger C, Strasilla C, Rosahl S, et al. Coil embolization of anterior circulation aneurysms supported by the solitaire™, ab neurovascular remodeling device. Neuroradiology 2010;52:349-359 .
crossref pmid
10. Kaufmann TJ, Huston J, Mandrekar JN, Schleck CD, Thielen KR, Kallmes DF. Complications of diagnostic cerebral angiography: evaluation of 19?826 consecutive patients1. Radiology 2007;243:812-819 .
crossref pmid
11. Lakshminarayan R, Simpson J, Ettles D. Magnetic resonance angiography: current status in the planning and follow-up of endovascular treatment in lower-limb arterial disease. Cardiovasc Intervent Radiol 2009;32:397-405 .
crossref pmid
12. Hamer OW, Finkenzeller T, Borisch I, Paetzel C, Zorger N, Feuerbach S, et al. In vivo evaluation of patency and in-stent stenoses after implantation of nitinol stents in iliac arteries using MR angiography. AJR Am J Roentgenol 2005;185:1282-1288 .
crossref pmid
13. Lettau M, Sauer A, Heiland S, Rohde S, Bendszus M, Hahnel S. Carotid artery stents: in vitro comparison of different stent designs and sizes using CT angiography and contrast-enhanced MR angiography at 1.5t and 3t. AJNR Am J Neuroradiol 2009;30:1993-1997 .
crossref pmid pmc
14. Girardi M, Kay J, Elston DM, Leboit PE, Abu-Alfa A, Cowper SE. Nephrogenic systemic fibrosis: clinicopathological definition and workup recommendations. J Am Acad Dermatol 2011;7 01 [Epub ahead of print]
crossref
15. Yamada N, Hayashi K, Murao K, Higashi M, Iihara K. 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 2004;25:1154-1157 .
pmid pmc
16. Wallace RC, Karis JP, Partovi S, Fiorella D. Noninvasive imaging of treated cerebral aneurysms, part i: MR angiographic follow-up of coiled aneurysms. AJNR Am J Neuroradiol 2007;28:1001-1008 .
crossref pmid pmc
17. Trost DW, Zhang HL, Prince MR, Winchester PA, Wang Y, Watts R, et al. Three-dimensional MR angiography in imaging platinum alloy stents. J Magn Reson Imaging 2004;20:975-980 .
crossref pmid
18. Lenhart M, Völk M, Manke C, Nitz WR, Strotzer M, Feuerbach S, et al. Stent appearance at contrast-enhanced mr angiography: in vitro examination with 14 stents. Radiology 2000;217:173-178 .
crossref pmid
19. Wang Y, Truong TN, Yen C, Bilecen D, Watts R, Trost DW, et al. Quantitative evaluation of susceptibility and shielding effects of nitinol, platinum, cobalt-alloy, and stainless steel stents. Magn Reson Med 2003;49:972-976 .
crossref pmid
20. Lovblad KO, Yilmaz H, Chouiter A, San Millan Ruiz D, Abdo G, Bijlenga P, et al. Intracranial aneurysm stenting: follow-up with MR angiography. J Magn Reson Imaging 2006;24:418-422 .
crossref pmid
21. Bartels LW, Bakker CJG, Viergever MA. Improved lumen visualization in metallic vascular implants by reducing rf artifacts. Magnetic Resonance in Medicine 2002;47:171-180 .
crossref pmid
22. van Holten J, Wielopolski P, Bruck E, Pattynama PM, van Dijk LC. High flip angle imaging of metallic stents: implications for MR angiography and intraluminal signal interpretation. Magn Reson Med 2003;50:879-883 .
crossref pmid
23. Frölich A, Pilgram-Pastor S, Psychogios M, Mohr A, Knauth M. Comparing different MR angiography strategies of carotid stents in a vascular flow model: toward stent-specific recommendations in MR follow-up. Neuroradiology 2011;53:359-365 .
crossref pmid
24. Wall A, Kugel H, Bachman R, Matuszewski L, Krämer S, Heindel W, et al. 3.0 t vs. 1.5 t MR angiography: in vitro comparison of intravascular stent artifacts. J Magn Reson Imaging 2005;22:772-779 .
crossref pmid
25. Siddiqui MA, J Bhattacharya J, Lindsay KW, Jenkins S. Horizontal stent-assisted coil embolisation of wide-necked intracranial aneurysms with the enterprise stent-a case series with early angiographic follow-up. Neuroradiology 2009;51:411-418 .
crossref pmid
26. Patel NV, Gounis MJ, Wakhloo AK, Noordhoek N, Blijd J, Babic D, et al. Contrast-enhanced angiographic cone-beam CT of cerebrovascular stents: experimental optimization and clinical application. AJNR Am J Neuroradiol 2011;32:137-144 .
crossref pmid pmc
Fig. 1
Relative In-stent Signal According to the Change of FA.
Bars represent RIS for each stent according to the change of FA at BW of 31 KHz. The number in the boxes means RIS value for each stent.
ni-6-71-g001.jpg
Fig. 2
Mean Relative In-stent Signal According to the Change of Bandwidth.
Bars represent mean RIS (mean of RIS at FA of 30° and 40°) for each stent according to the change of BW. The number in the boxes means mean RIS value for each stent.
ni-6-71-g002.jpg
Fig. 3
MIP images of the each stent with significantly high RIS. MIP images of Neuroform (A, FA/BW; 20°/31 KHz), Wingspan (B.1, FA/BW; 20°/31 KHz, and B.2, FA/BW; 30°/42 KHz), Solitaire (C.1, FA/BW; 40°/42 KHz, and C.2, FA/BW; 50°/31 KHz) and Enterprise (D.1, FA/BW; 40°/31 KHz, and D.2, FA/BW; 50°/31 KHz). A band-like artifact (arrowhead) is visible at the end of the each stent due to platinum marker. A complete signal loss of the lumen (arrow) near the proximal marker of the Solitaire stent was shown.
ni-6-71-g003.jpg
Table 1
Relative In-stent Signal Intensity of Each Stent According to Flip Angle and Bandwidth
ni-6-71-i001.jpg

Note.- FA: flip angle, BW: bandwidth, TR: repetition time, TE: echo time

Relative In-stent Signal (%) = RIS (%) = [(SIin-stent - SIbackground) / (SItube - SIbackground)] × 100

Bold texts mean two highest values of RIS in the raw.



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