生长中的婴儿心室尺寸和血流动力学的计算模型。

IF 1.7 4区 医学 Q4 BIOPHYSICS
Ashley A Hiebing, Riley G Pieper, Colleen M Witzenburg
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引用次数: 0

摘要

以前的计算机模型已经成功地预测了患有疾病的成年人的心脏生长和重塑。然而,将这些模型应用于婴儿是复杂的,因为他们也经历了正常的体细胞心脏生长和重塑。因此,我们设计了一个计算模型,通过修改成年犬左心室生长模型来预测健康成长婴儿的心室尺寸和血液动力学。心室被建模为与循环回路模型耦合的时变弹性。对循环参数进行异速缩放,并根据成熟度进行调整,以模拟出生至3 年龄。心室生长是由肌细胞张力的扰动驱动的。该模型在多个婴儿研究的两个标准偏差内成功匹配了压力、心室和心房容积以及心室厚度的临床测量值。为了测试该模型,我们输入了第10和第90百分位的婴儿体重。预测的体积和厚度在正常范围内减少和增加,压力不变。当我们模拟主动脉缩窄时,全身血压、左心室厚度和左心室容积都增加了,这与临床数据的趋势一致。我们的模型能够更好地了解先天性心脏缺陷婴儿的体细胞和病理生长。与采用更复杂几何形状的模型相比,其灵活性和计算效率允许快速分析影响心脏生长和血流动力学的病理机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Computational Model of Ventricular Dimensions and Hemodynamics in Growing Infants.

Previous computer models have successfully predicted cardiac growth and remodeling in adults with pathologies. However, applying these models to infants is complicated by the fact that they also undergo normal, somatic cardiac growth and remodeling. Therefore, we designed a computational model to predict ventricular dimensions and hemodynamics in healthy, growing infants by modifying an adult canine left ventricular growth model. The heart chambers were modeled as time-varying elastances coupled to a circuit model of the circulation. Circulation parameters were allometrically scaled and adjusted for maturation to simulate birth through 3 yrs of age. Ventricular growth was driven by perturbations in myocyte strain. The model successfully matched clinical measurements of pressures, ventricular and atrial volumes, and ventricular thicknesses within two standard deviations of multiple infant studies. To test the model, we input 10th and 90th percentile infant weights. Predicted volumes and thicknesses decreased and increased within normal ranges and pressures were unchanged. When we simulated coarctation of the aorta, systemic blood pressure, left ventricular thickness, and left ventricular volume all increased, following trends in clinical data. Our model enables a greater understanding of somatic and pathological growth in infants with congenital heart defects. Its flexibility and computational efficiency when compared to models employing more complex geometries allow for rapid analysis of pathological mechanisms affecting cardiac growth and hemodynamics.

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来源期刊
CiteScore
3.40
自引率
5.90%
发文量
169
审稿时长
4-8 weeks
期刊介绍: Artificial Organs and Prostheses; Bioinstrumentation and Measurements; Bioheat Transfer; Biomaterials; Biomechanics; Bioprocess Engineering; Cellular Mechanics; Design and Control of Biological Systems; Physiological Systems.
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