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Research ArticleNeurointervention
Open Access

Outcome Study of the Pipeline Embolization Device with Shield Technology in Unruptured Aneurysms (PEDSU)

D. Atasoy, N. Kandasamy, J. Hart, J. Lynch, S.-H. Yang, D. Walsh, C. Tolias and T.C. Booth
American Journal of Neuroradiology December 2019, 40 (12) 2094-2101; DOI: https://doi.org/10.3174/ajnr.A6314
D. Atasoy
aFrom Karadeniz Technical University (D.A.), Farabi Hospital, Trabzon, Turkey
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N. Kandasamy
bDepartments of Neuroradiology (N.K., J.H., J.L., T.C.B.)
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J. Hart
bDepartments of Neuroradiology (N.K., J.H., J.L., T.C.B.)
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J. Lynch
bDepartments of Neuroradiology (N.K., J.H., J.L., T.C.B.)
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S.-H. Yang
dDepartment of Radiology (S.-H.Y.), Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan
eDepartment of Radiology (S.-H.Y.), School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan
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D. Walsh
cNeurosurgery (D.W., C.T.), King’s College Hospital National Health Service Foundation Trust, London, UK
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C. Tolias
cNeurosurgery (D.W., C.T.), King’s College Hospital National Health Service Foundation Trust, London, UK
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T.C. Booth
bDepartments of Neuroradiology (N.K., J.H., J.L., T.C.B.)
fSchool of Biomedical Engineering and Imaging Sciences (T.C.B.), King’s College London, London, UK.
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Abstract

BACKGROUND AND PURPOSE: The recently introduced Pipeline Flex Embolization Device with Shield Technology (Pipeline Shield) is the third generation of Pipeline flow-diverter devices. It has a new stent-surface modification, which reduces thrombogenicity. We aimed to evaluate clinical and radiographic (safety and efficacy) outcomes of the Pipeline Shield.

MATERIALS AND METHODS: The 30-day and 1-year mortality and morbidity rates and the 6- and 18-month radiographic aneurysm occlusion outcomes for procedures performed between March 2016 and January 2018 were analyzed. 3D-TOF-MRA was used for follow-up.

RESULTS: Forty-four attempted Pipeline Shield procedures were performed for 41 patients with 44 target aneurysms (total of 52 aneurysms treated). A total of 88.5% of devices were inserted in the anterior circulation, and 11.5%, in the posterior circulation; 49/52 (94.2%) aneurysms were saccular; and 1/52 (1.9%) was fusiform. One (1.9%) aneurysm was an iatrogenic pseudoaneurysm, and 1 (1.9%) was a dissecting aneurysm. Seventy-one percent (35/49) of the saccular aneurysms were wide-neck (neck, >4 mm), 34.6% (18/52) were large (≥10 mm), and 3.8% (2/52) were giant (≥25 mm). The mean aneurysm sac maximal diameter was 9.0 mm, and the mean neck width was 5.0 mm. The cumulative mortality and morbidity rates were 2.3% and 6.8% at 1 year, respectively. The adequate occlusion rate was 78.8% at 6 months and 90.3% at 18 months.

CONCLUSIONS: In this pragmatic and non-industry-sponsored study, the occlusion rates and safety outcomes were similar to those seen in previously published studies with flow-diverter devices and earlier generation Pipeline Embolization Devices.

  • © 2019 by American Journal of Neuroradiology

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American Journal of Neuroradiology: 40 (12)
American Journal of Neuroradiology
Vol. 40, Issue 12
1 Dec 2019
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Cite this article
D. Atasoy, N. Kandasamy, J. Hart, J. Lynch, S.-H. Yang, D. Walsh, C. Tolias, T.C. Booth
Outcome Study of the Pipeline Embolization Device with Shield Technology in Unruptured Aneurysms (PEDSU)
American Journal of Neuroradiology Dec 2019, 40 (12) 2094-2101; DOI: 10.3174/ajnr.A6314

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Outcome Study of the Pipeline Embolization Device with Shield Technology in Unruptured Aneurysms (PEDSU)
D. Atasoy, N. Kandasamy, J. Hart, J. Lynch, S.-H. Yang, D. Walsh, C. Tolias, T.C. Booth
American Journal of Neuroradiology Dec 2019, 40 (12) 2094-2101; DOI: 10.3174/ajnr.A6314
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  • Outcome study of the Pipeline Vantage Embolization Device (second version) in unruptured (and ruptured) aneurysms (PEDVU(R) study)
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