肱动脉差异特征阻抗:杨氏模量和直径变化的贡献。

Glen Atlas, John K-J Li
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引用次数: 8

摘要

对肱动脉(BA)差分特征阻抗DeltaZ (c)的检查表明,Z (c)的变化可以由BA壁刚度(杨氏模量E)和/或其直径D的变化引起。此外,我们评估了E和D的变化如何以孤立、协同或拮抗的方式结合起来,从而产生BA Z (c)的净变化。该分析的基础是一个偏微分方程,它近似于DeltaZ (c)作为总微分。乙酰胆碱、阿替洛尔、非诺达平、硝化甘油、氢氯噻嗪和其他药物对BA DeltaZ (c)的影响使用先前发表的研究数据进行了检查。临床情况改变baz (c),如充血性心力衰竭,高血压,充血,也进行了分析。结果表明,目前的方法在区分药物、充血和病理状况如何通过引起E和/或D的独立变化来影响BA DeltaZ (c)方面是有用的。
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Brachial artery differential characteristic impedance: Contributions from changes in young's modulus and diameter.

This examination of brachial artery (BA) differential characteristic impedance, DeltaZ (c), illustrates that changes in Z (c) can occur from changes in either BA wall stiffness (Young's modulus, E) and/or its diameter, D. Furthermore, we assessed how changes in both E and D combine in either an isolated, synergistic, or antagonistic manner to yield the net change in BA Z (c). The basis of this analysis is a partial differential equation which approximates DeltaZ (c) as a total differential. The effects on BA DeltaZ (c) of acetylcholine, atenolol, fenoldapine, nitroglycerin, hydrochlorothiazide and other medications are examined using data from previously published studies. Clinical situations which alter BA Z (c), such as congestive heart failure, hypertension, and hyperemia, are also analyzed. Results illustrate the usefulness of the present approach in differentiating how medications, hyperemia, and pathological conditions affect BA DeltaZ (c) by causing independent changes to E and/or D.

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