Simulation-Based Design of Bicuspidization of the Aortic Valve

Fuente: arXiv
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Main Authors: Kaiser, Alexander D., Haidar, Moussa A., Choi, Perry S., Sharir, Amit, Marsden, Alison L., Ma, Michael R.
Format: Preprint
Published: 2023
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_version_ 1866908413581066240
author Kaiser, Alexander D.
Haidar, Moussa A.
Choi, Perry S.
Sharir, Amit
Marsden, Alison L.
Ma, Michael R.
author_facet Kaiser, Alexander D.
Haidar, Moussa A.
Choi, Perry S.
Sharir, Amit
Marsden, Alison L.
Ma, Michael R.
contents Objective: Severe congenital aortic valve pathology in the growing patient remains a challenging clinical scenario. Bicuspidization of the diseased aortic valve has proven to be a promising repair technique with acceptable durability. However, most understanding of the procedure is empirical and retrospective. This work seeks to design the optimal gross morphology associated with surgical bicuspidization with simulations, based on the hypothesis that modifications to the free edge length cause or relieve stenosis. Methods: Model bicuspid valves were constructed with varying free edge lengths and gross morphology. Fluid-structure interaction simulations were conducted in a single patient-specific model geometry. The models were evaluated for primary targets of stenosis and regurgitation. Secondary targets were assessed and included qualitative hemodynamics, geometric height, effective height, orifice area and billow. Results: Stenosis decreased with increasing free edge length and was pronounced with free edge length $\leq$1.3 times the annular diameter d. With free edge length 1.5d or greater, no stenosis occurred. All models were free of regurgitation. Substantial billow occurred with free edge length $\geq$1.7d. Conclusions: Free edge length $\geq$1.5d was required to avoid aortic stenosis in simulations. Cases with free edge length $\geq$1.7d showed excessive billow and other changes in gross morphology. Cases with free edge length 1.5-1.6d have a total free edge length approximately equal to the annular circumference and appeared optimal. These effects should be studied in vitro and in animal studies.
format Preprint
id arxiv_https___arxiv_org_abs_2309_14239
institution arXiv
publishDate 2023
record_format arxiv
spellingShingle Simulation-Based Design of Bicuspidization of the Aortic Valve
Kaiser, Alexander D.
Haidar, Moussa A.
Choi, Perry S.
Sharir, Amit
Marsden, Alison L.
Ma, Michael R.
Tissues and Organs
92C35 (Primary), 92C50, 92C32, 76Z05 (Secondary)
J.3.1
Objective: Severe congenital aortic valve pathology in the growing patient remains a challenging clinical scenario. Bicuspidization of the diseased aortic valve has proven to be a promising repair technique with acceptable durability. However, most understanding of the procedure is empirical and retrospective. This work seeks to design the optimal gross morphology associated with surgical bicuspidization with simulations, based on the hypothesis that modifications to the free edge length cause or relieve stenosis. Methods: Model bicuspid valves were constructed with varying free edge lengths and gross morphology. Fluid-structure interaction simulations were conducted in a single patient-specific model geometry. The models were evaluated for primary targets of stenosis and regurgitation. Secondary targets were assessed and included qualitative hemodynamics, geometric height, effective height, orifice area and billow. Results: Stenosis decreased with increasing free edge length and was pronounced with free edge length $\leq$1.3 times the annular diameter d. With free edge length 1.5d or greater, no stenosis occurred. All models were free of regurgitation. Substantial billow occurred with free edge length $\geq$1.7d. Conclusions: Free edge length $\geq$1.5d was required to avoid aortic stenosis in simulations. Cases with free edge length $\geq$1.7d showed excessive billow and other changes in gross morphology. Cases with free edge length 1.5-1.6d have a total free edge length approximately equal to the annular circumference and appeared optimal. These effects should be studied in vitro and in animal studies.
title Simulation-Based Design of Bicuspidization of the Aortic Valve
topic Tissues and Organs
92C35 (Primary), 92C50, 92C32, 76Z05 (Secondary)
J.3.1
url https://arxiv.org/abs/2309.14239