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Method
1. Aneurysm Geometry
Typically
a saccular aneurysms can be idealized by a spheres on a cylindrical
vessel. The stents were deployed in this idealized aneurysm geometry.
The diameter of the idealized aneurysm,
and vessel were
19mm, and 4.75 mm respectively. The vessel curvature varied from 0(C0)
to 1/9mm-1(C4)
(Fig. 1). The patient-specific aneurysm geometry was reconstructed using
CT Angoigraphy (CTA) images of a patient’s right anterior communicating
artery (ACA) (Fig. 2). Stents were virtually placed across the aneurysm
neck.
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Fig. 1: Idealized saccular aneurysm on a curved
vessel. Aneurysm aspect ratio of this idealized aneurysm was
1.78. |
Fig. 2: ACA of 52 year old female. Aspect ratio of this aneurysm
was 1.67. |
| 2.
Stent Geometry
The effect of stents, similar to commercial stents (TristarTM
stent and Wallstent®), on aneurismal hemodynamics was
investigated (Fig. 3). We modeled these stent geometries in
commercial CAD software, ProEngineer (PTC, Needham, MA). The
equivalent diameter of the rectangular struts and the diameter
of the circular struts were both 0.1mm. The porosities of these
stents were about 82%. The model stents were bent and fitted
into the aneurysm model. |
|
 |
|
Fig. 3:
Stent A (simulating TristarTM
stent) is constructed by cutting holes through the walls of a
tube with a laser, and Stent B (simulating Wallstent®)
is constructed by weaving wires in a crisscross pattern to form
a mesh. Thus, Stent A struts have a rectangular cross section
and Stent B have a circular cross section.
To
improve the efficiency of porous stent, a new type of stent,
asymmetric (patched) stent, was developed (Fig4). This stent
consisted of a low porosity patch to block the aneurysmal inflow
at aneurysm neck on a regular porous stent. A vein-pouch
aneurysm model was created on the carotid artery of a canine to
test the asymmetric stent. Angiographic images were obtained
before and after stenting and compared with CFD results. In
addition to both commercial stents and asymmetric stent, we
designed a patient-specific stent with
following
criteria.
· Block
the strong impinging flow at proximal neck.
· Interrupt
the flow along the centerline of the vessel.
· Allow
the flow to peripheral vessels (perforators). |
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 |
|
Fig. 4: An asymmetric (patched) stent with a 25%
porous patch and a 80% porous stent. The low porous patch was
clamped and welded on the surface of a stent.
3. CFD Analysis
3.1 Direct
Stent Simulation
The stented aneurysms were meshed using 0.6~2.4 million
tetrahedral volume elements by ICEM-CFD (ICEM CFD Engineering,
Berkeley, CA). Mesh independent flow in the models was obtained
by increasing the number of meshes approximating the surface of
the stents. A finite volume based CFD code, StarCD®
(CD-adapco, Melville, NY), was used to solve the Navier-Stokes
equations for incompressible flow.
Central differencing scheme was selected to obtain the second
order accuracy. The Reynolds number (Re) of blood flowing in a
cerebral artery is low enough to be considered laminar. The Re
at peak systole was 490 and the Womersley number of pulsatile
wave was 2.38. Blood was assumed to be Newtonian because the
shear rate in the artery was high and the diameter of the artery
was large. The viscosity and the density of blood in all models
was 3.5cP and 1056kg/m3.
The aneurysm and vessel walls were assumed to be non-compliant
and rigid as were assumed in other studies.
3.2 Asymmetric (Patched) Stent Simulation
Direct simulation of patched stent is costly due to large number
of stent wires. Therefore,
The low porosity patch was modeled
by specifying pressure drop across the patch [3]. |
 |
| Results
1. Stent
effects idealized aneurysm models |
|
 |
|
|
Fig. 5: (a) Peak systolic velocity contour on a center plane in
the aneurysm. (b) Inflow velocity characteristics on a plane
passing the aneurysm neck. Flow enters from left. |
 |
|
Fig. 6: Aneurysmal inflow rate variation in a curved vessel.
|
|
Aneurysmal
inflow increased as vessel curvature increased. A stent
interfered the inflow, however the stent effect diminished with
increasing vessel curvature. The aneurysmal inflow rate in
varying parent vessel curvature depended on stent design . Stent
A in less curved vessel allows more flows to penetrate than
stent B, but it is reversed in highly curved vessel. |
| 2.
Flow alternations by a stent in a patient-specific aneurysm |
|

|
 |
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Fig. 7: Peak systolic velocity contours on a plane in
the aneurysm. Flow comes into the aneurysm from bottom
and goes out to the right. |
| |
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3. Asymmetric stent
effects onaneurysmal inflow
The inflow entered the aneurysm through distal neck and
created a counter clockwise circulation in the aneurysm
before treatment. However, intra-aneurysmal flow became
stagnant after the asymmetric stent treatment. Both CFD
and angiographic images showed that the inflow was
completely blocked at the aneurysm neck and the aneurysm
was separated from the parent vessel by an asymmetric
stent.
|
 |
|
Fig. 8: CFD simulation and angiographic images
of aneurysmal flow in a canine model.
|
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Conclusions
· The
design of porous stents affects aneurysmal flow modification.
· The
effect of stent on aneurysm hemodynamics varies in curved vessel.
· Asymmetric
(patched) stents may be a viable intervention for treating intracranial
aneurysms.
· “Virtual
intervention” can provide valuable clinical feedback in treatment
planning.
References
1. Geremia
G, Haklin M, Brennecke L: Embolization of experimentally created
aneurysms with intravascular stent devices. AJNR AN J Neuroradiol 15:
1223-1231, 1994.
2. Han
PP, Albuquerque FC, Ponce FA, MacKay CI, Zabramski JM, Spetzler RF,
McDougall CG: Percutaneous intracranial stent placement for aneurysms.
J. Neurosurg 99:23-30, 2003.
3. Idelchik,
IE: Handbook of hydraulic resistance. CRC Press, Boca Raton, FL, p. 522,
1994.
4. Krings
T, et al.: Treatment of Experimentally Induced Aneurysms with Stents. J
Neurosurg 56(6): 1347-59, 2005
5. Lanzino
G, Wakhloo AK, Fessler RD, Hartney ML, Guterman LR, Hopkins LN: Efficacy
and current limitations of intravascular stents for intracranial
internal carotid, vertebral, and basilar artery aneurysms. J Neurosurg
91: 538-546, 1999.
Acknowlegements
We acknowledge our collaboration with the imaging and
clinical groups.
· Imaging
Group: Stephen Rudin, Ph.D., Kenneth Hoffmann, Ph.D., Ciprian Ionita,
Ph.D., Rekha Tranquebar
· Clinical
Group: J. Yamamoto, M.D., Lee R. Guterman, Ph.D., M.D., L. N. Hopkins,
M.D.
This research is supported by grants from NIH (1R01
EB002873, 1K25 NS047242), NSF (BES-0302389)
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