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In-vitro flow assessment study of intra-saccular endovascular devices for brain aneurysm treatment: SEAL™ vs. WEB™
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Background
Intrasaccular devices such as SEAL™ and WEB™-SL are designed to disrupt aneurysmal flow. We present a new
in vitro
method for estimating neurointerventional devices’ flow dynamics.
Methods
Particle image velocimetry (PIV) method was used in a patient-specific middle cerebral artery (MCA) wide-neck bifurcation aneurysm (WNBA) model to measure velocity, residence time (RT), and vorticity strength (VS). Tested devices included 3 each of SEAL-BASE (6 × 2 mm), SEAL-ARC (6 × 5 mm), and WEB-SL (6 × 4 mm).
Results
Twelve experiments were performed (3 unique devices per size and 3 controls); the mean RT was 0.042 ± 0.006 s (control) and increased with SEAL-BASE (0.387 ± 0.128), SEAL-ARC (0.33 ± 0.092), and WEB-SL (0.171 ± 0.034) (all
p
< 0.05 vs. control), and was longer in SEAL-BASE (
p
= 0.046) and SEAL-ARC (
p
= 0.041) than WEB-SL, with no difference between SEAL configurations (
p
= 0.30). The VS decreased from 66.48 ± 8.58 1/s (control) to 14.06 ± 2.80, 13.94 ± 2.53, and 27.60 ± 4.16 for SEAL-BASE, SEAL-ARC, and WEB-SL, respectively. The SEAL devices differed from WEB-SL (
p
= 0.007, 0.006) but not from each other (
p
= 0.52). Velocity magnitude dropped from 109.4 ± 15.5 mm/s (control) to 12.42 ± 3.8, 14.2 ± 3.5, and 25.34 ± 3.16 for SEAL-BASE, SEAL-ARC, and WEB-SL, respectively; greater reductions with SEAL-BASE (
p
= 0.006) and SEAL-ARC (
p
= 0.007) versus WEB-SL, with no difference between the two SEAL configurations (
p
= 0.29).
Conclusion
Both SEAL configurations achieved greater flow reduction compared to the WEB-SL of similar width in the same aneurysm model. Results highlight the unique utilization of the PIV method for the mechanistic decoupling of momentum transfer into the aneurysm sac resulting from intra-aneurysmal mesh structures and point toward their potential for further neurointerventional device optimization.
Frontiers Media SA
Hamid Mansouri
Nedim Gulkaya
Matthew J. Gounis
Mohammad AlMajali
Amit Chaudhari
Darwin G. Ramirez Abreu
Syed F. Zaidi
Yazan K. Ashouri
Naoki Kaneko
Brian T. Jankowitz
David J. Altschul
Boris Pabon
Pervinder Bhogal
Thomas J. Wolfe
Edgard L. Pereira
Aamir Badruddin
Laila Ibrahim
Omid Amili
Osama O. Zaidat
Title: In-vitro flow assessment study of intra-saccular endovascular devices for brain aneurysm treatment: SEAL™ vs. WEB™
Description:
Background
Intrasaccular devices such as SEAL™ and WEB™-SL are designed to disrupt aneurysmal flow.
We present a new
in vitro
method for estimating neurointerventional devices’ flow dynamics.
Methods
Particle image velocimetry (PIV) method was used in a patient-specific middle cerebral artery (MCA) wide-neck bifurcation aneurysm (WNBA) model to measure velocity, residence time (RT), and vorticity strength (VS).
Tested devices included 3 each of SEAL-BASE (6 × 2 mm), SEAL-ARC (6 × 5 mm), and WEB-SL (6 × 4 mm).
Results
Twelve experiments were performed (3 unique devices per size and 3 controls); the mean RT was 0.
042 ± 0.
006 s (control) and increased with SEAL-BASE (0.
387 ± 0.
128), SEAL-ARC (0.
33 ± 0.
092), and WEB-SL (0.
171 ± 0.
034) (all
p
< 0.
05 vs.
control), and was longer in SEAL-BASE (
p
= 0.
046) and SEAL-ARC (
p
= 0.
041) than WEB-SL, with no difference between SEAL configurations (
p
= 0.
30).
The VS decreased from 66.
48 ± 8.
58 1/s (control) to 14.
06 ± 2.
80, 13.
94 ± 2.
53, and 27.
60 ± 4.
16 for SEAL-BASE, SEAL-ARC, and WEB-SL, respectively.
The SEAL devices differed from WEB-SL (
p
= 0.
007, 0.
006) but not from each other (
p
= 0.
52).
Velocity magnitude dropped from 109.
4 ± 15.
5 mm/s (control) to 12.
42 ± 3.
8, 14.
2 ± 3.
5, and 25.
34 ± 3.
16 for SEAL-BASE, SEAL-ARC, and WEB-SL, respectively; greater reductions with SEAL-BASE (
p
= 0.
006) and SEAL-ARC (
p
= 0.
007) versus WEB-SL, with no difference between the two SEAL configurations (
p
= 0.
29).
Conclusion
Both SEAL configurations achieved greater flow reduction compared to the WEB-SL of similar width in the same aneurysm model.
Results highlight the unique utilization of the PIV method for the mechanistic decoupling of momentum transfer into the aneurysm sac resulting from intra-aneurysmal mesh structures and point toward their potential for further neurointerventional device optimization.
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