Hemodynamic Simulation of Pancreaticoduodenal Artery Aneurysm Formation Using an Electronic Circuit Model and a Case Series Analysis
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- Miyahara Kazuhiro
- Division of Vascular Surgery, Department of Surgery, Graduate School of Medicine, The University of Tokyo
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- Hoshina Katsuyuki
- Division of Vascular Surgery, Department of Surgery, Graduate School of Medicine, The University of Tokyo
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- Nitta Jun
- Division of Vascular Surgery, Department of Surgery, Graduate School of Medicine, The University of Tokyo
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- Kimura Masaru
- Division of Vascular Surgery, Department of Surgery, Graduate School of Medicine, The University of Tokyo
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- Yamamoto Sota
- Department of Mechanical Engineering, Graduate School, Shibaura Institute of Technology
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- Ohshima Marie
- Interfaculty Initiative in Information Studies/Institute of Industrial Science, The University of Tokyo
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<p>Objective: To assess mechanisms underlying aneurysm formation using a simple electronic circuit model.</p><p>Materials and Methods: We created a simple circuit model connecting the celiac artery (CA) to the superior mesenteric artery via the pancreaticoduodenal arcade. We retrospectively reviewed 12 patients with true pancreaticoduodenal artery aneurysms (PDAAs) who received open or endovascular treatment between 2004 and 2017. We set the resistance of each artery and organ voltage and calculated flow volume and rate in response to degrees of simulated CA stenosis from 0% to 99.9%.</p><p>Results: Flow volume rates of the anterior pancreaticoduodenal artery and posterior pancreaticoduodenal artery decreased to zero when CA stenosis increased from 0% to 50% and then increased drastically, at which point flow direction reverted and the flow was up to three times the initial rate. The gastroduodenal artery (GDA) also showed reversed flow with severe CA stenosis. In 12 patients with PDAA, eight presented with a CA lesion, and the other patients presented with comorbidities causing the arteries to be pathologically fragile, such as Marfan syndrome, Behçet’s disease, and segmental arterial mediolysis. All four GDA aneurysms were not accompanied by CA lesions.</p><p>Conclusion: The mechanism underlying CA-lesion-associated PDAA formation may be partially explained using our model.</p>
収録刊行物
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- Annals of Vascular Diseases
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Annals of Vascular Diseases 12 (2), 176-181, 2019-06-25
Annals of Vascular Diseases 編集委員会
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詳細情報 詳細情報について
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- CRID
- 1390564238101357696
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- NII論文ID
- 130007667034
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- ISSN
- 18816428
- 1881641X
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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- CiNii Articles
- KAKEN
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