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1.
Chinese Journal of Medical Instrumentation ; (6): 507-511, 2023.
Article in Chinese | WPRIM | ID: wpr-1010229

ABSTRACT

OBJECTIVE@#Aims researches on the interaction between heart valves is limited in clinical. Meanwhile the data of in vitro testing are insufficient. In this study, the in vitro hydrodynamic performance of an aortic valve was studied by using a model of mitral regurgitation that could finely adjust the regurgitant volume.@*METHODS@#The regurgitation of mitral valve was gradually increased under the certain condition of heart rate, stroke volume, and mean aortic pressure and captured the hydrodynamic performance of the aortic valve.@*RESULTS@#The study on the hydrodynamic performance of mechanical aortic valve (25AJ-501) by using a model of mitral regurgitation found that the effective orifice area and mean pressure difference of the aortic valve are negatively correlated with the degree of mitral regurgitation.@*CONCLUSIONS@#The method based on a model of mitral regurgitation that could finely adjust the regurgitant volume established in this study can be used to study the effect of mitral valve regurgitation on the hydrodynamic performance of the aortic valve.

2.
Chinese Journal of Clinical Thoracic and Cardiovascular Surgery ; (12): 279-287, 2022.
Article in Chinese | WPRIM | ID: wpr-923374

ABSTRACT

@#The heart valve prosthesis must have excellent hydrodynamic performance which is usually tested in vitro, not in vivo. This paper comprehensively introduced the principles and methods of hydrodynamic performance in vitro testing, helping clinicians to understand valve performance parameters, evaluate valve applicability, and reduce clinical risk of the valve prosthesis. In vitro testing not only serves as the "gold standard" for valve prosthesis assessment, but also provides detailed data for design and optimization of the prosthesis. ISO 5840 defines the items and methods for valve in vitro testing, which consists of three parts: (1) pulsatile flow testing, which reproduces the pulsating flow of the valve prosthesis after implantation in the human body; (2) steady flow testing, which assesses valve forward flow resistance; (3) durability testing, which evaluates the durability of the valve prosthesis and determines the expected failure   mode. In addition, the paper presented the differences between atrioventricular and aortic valve testing, the method of mitral valve testing, the differences between transcatheter and surgical valve testing, and the method of valve flow visualization.

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