Evolution of splenomegaly in liver cirrhosis: Simulation using an electronic circuit

IF 2.5 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Advances in medical sciences Pub Date : 2024-08-06 DOI:10.1016/j.advms.2024.08.001
Jae Cheol Jung, Shin-Young Park, Kyeong Deok Kim, Woo Young Shin, Keon-Young Lee
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Abstract

Purpose

The evolution of splenomegaly in patients with liver cirrhosis remains largely unknown. In this study, we followed the changes in splenic volume and established the natural course of splenomegaly. We developed an electronic circuit that simulated splenoportal circulation and identified the underlying hemodynamic mechanisms.

Materials and methods

This retrospective observational study included 93 patients with cirrhosis. Splenic volumes were measured in imaging studies at 6-month intervals and normalized by the ratio of each patient's maximum volume during follow-up (%Vmax). An electronic simulation model was constructed using software and realized on a breadboard.

Results

Overall, the %Vmax increased from 0.77 ​± ​0.21 to a maximum of 1.00 ​± ​0.00 (p ​< ​0.001) during a median follow-up of 23 (3–162) months and then decreased to 0.84 ​± ​0.18 (p ​< ​0.001) during the next 9 (3–132) months. No interventional radiology procedure was performed to improve hepatic fibrosis and portal hypertension. The evolution of %Vmax showed single-peaked symmetry. An electronic simulation model showed that the upslope of the evolution curve was dependent on the increased intrahepatic vascular resistance and portal hypertension, whereas the downslope was dependent on the decreased portosystemic shunt (PSS) resistance.

Conclusions

Splenomegaly in cirrhotic patients aggravated over a period of 23 months and then regressed spontaneously to its initial volume. Electronic simulation of splenoportal circulation showed that splenic enlargement was due to the advancement of liver cirrhosis and portal hypertension, whereas its regression was due to the development of a PSS.

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肝硬化脾肿大的演变:利用电子电路进行模拟。
目的:肝硬化患者脾脏肿大的演变过程在很大程度上仍不为人所知。在这项研究中,我们跟踪了脾脏体积的变化,并确定了脾脏肿大的自然病程。我们开发了模拟脾门循环的电子电路,并确定了潜在的血液动力学机制:这项回顾性观察研究包括 93 名肝硬化患者。每隔 6 个月通过影像学检查测量脾脏体积,并以随访期间每位患者最大体积的比率(%Vmax)进行归一化。使用软件构建了一个电子模拟模型,并在面包板上实现了该模型:总体而言,在 23(3 - 162)个月的中位随访期间,最大容积百分比从 0.77 ± 0.21 增加到最大值 1.00 ± 0.00(p < 0.001),然后在接下来的 9(3 - 132)个月期间降至 0.84 ± 0.18(p < 0.001)。没有进行介入放射学手术来改善肝纤维化和门静脉高压。Vmax%的变化呈现单峰对称性。电子模拟模型显示,演变曲线的上坡取决于肝内血管阻力和门静脉高压的增加,而下坡则取决于门静脉分流(PSS)阻力的降低:结论:肝硬化患者的脾肿大在 23 个月内不断加重,然后自然消退至初始体积。对脾门静脉循环的电子模拟显示,脾脏肿大是由于肝硬化和门静脉高压的发展所致,而脾脏肿大的消退则是由于 PSS 的发展所致。
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来源期刊
Advances in medical sciences
Advances in medical sciences 医学-医学:研究与实验
CiteScore
5.00
自引率
0.00%
发文量
53
审稿时长
25 days
期刊介绍: Advances in Medical Sciences is an international, peer-reviewed journal that welcomes original research articles and reviews on current advances in life sciences, preclinical and clinical medicine, and related disciplines. The Journal’s primary aim is to make every effort to contribute to progress in medical sciences. The strive is to bridge laboratory and clinical settings with cutting edge research findings and new developments. Advances in Medical Sciences publishes articles which bring novel insights into diagnostic and molecular imaging, offering essential prior knowledge for diagnosis and treatment indispensable in all areas of medical sciences. It also publishes articles on pathological sciences giving foundation knowledge on the overall study of human diseases. Through its publications Advances in Medical Sciences also stresses the importance of pharmaceutical sciences as a rapidly and ever expanding area of research on drug design, development, action and evaluation contributing significantly to a variety of scientific disciplines. The journal welcomes submissions from the following disciplines: General and internal medicine, Cancer research, Genetics, Endocrinology, Gastroenterology, Cardiology and Cardiovascular Medicine, Immunology and Allergy, Pathology and Forensic Medicine, Cell and molecular Biology, Haematology, Biochemistry, Clinical and Experimental Pathology.
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