Impact of left atrial appendage location on risk of thrombus formation in patients with atrial fibrillation

Most strokes in patients with atrial fibrillation (AF) are thought to arise from thrombus formation in the left atrial appendage (LAA). Assessing the hemodynamics in LAA and left atrium (LA) may provide some insights in the evaluation of the risk of thrombus formation. This study aims to find out th...

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Published inBiomechanics and modeling in mechanobiology Vol. 20; no. 4; pp. 1431 - 1443
Main Authors Fang, Runxin, Li, Yang, Zhang, Yanjuan, Chen, Qiang, Liu, Quanjun, Li, Zhiyong
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.08.2021
Springer Nature B.V
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ISSN1617-7959
1617-7940
1617-7940
DOI10.1007/s10237-021-01454-4

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Summary:Most strokes in patients with atrial fibrillation (AF) are thought to arise from thrombus formation in the left atrial appendage (LAA). Assessing the hemodynamics in LAA and left atrium (LA) may provide some insights in the evaluation of the risk of thrombus formation. This study aims to find out the impact of different LAA locations with respect of LA on the risk of thrombus formation within LAA in patients with AF. Three different LAA locations at LA were modeled and a fully coupled fluid–structure interaction analysis was performed. A discrete phase method was used for particle residence analysis to evaluate risk of the thrombus formation. The results showed that LAA positions on the LA affected the LAA flow velocity distribution, passive contraction ability, and particle residence. In particular, the left pulmonary veins (PVs) had a greater influence on the LAA hemodynamics than the right PVs. The LAA had the lowest contractibility when it was located between left superior and left inferior PVs, and in this case, a larger number of particles were resided, which indicated a higher risk of thrombus formation. The present work provides a quantitative way to evaluate the risk of thrombus formation within LAA in patients with AF.
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ISSN:1617-7959
1617-7940
1617-7940
DOI:10.1007/s10237-021-01454-4