Abstract
Hepatic venous pressure gradient (HVPG) measurement has been increasingly accepted as a useful means for indirectly measuring portal venous pressure in patients with portal hypertension (PHT) caused by chronic liver diseases. Despite the existence of numerous studies addressing the clinical utility of HVPG measurement, it is as yet unclear how the accuracy of measured HVPG as a surrogate of portal pressure gradient (PPG) is influenced by the pathological status of the hepatic circulation that not only changes with the progression of liver disease but also differs considerably among patients. In addition, it remains unclear whether HVPGs measured in different hepatic veins (HVs) are exchangeable, and if not, what factors determine inter-HV HVPG differences? In this context, we developed a stochastic computational model of the hepatic circulation, and performed a series of model-based numerical experiments to quantitatively investigate the respective/combined effects of various hepatic vascular properties on the accuracy of HVPG measurement. Major findings were: 1) a variation in presinusoidal portal vascular resistance significantly altered the difference between HVPG and PPG, whereas, an enhancement in portosystemic collateral flow (caused by growth of portosystemic collateral vessels or shunt intervention) tended to improve the accuracy of HVPG measurement; and 2) misdiagnosis of clinically significant PHT with HVPG was more likely to occur in the presence of high splanchnic vascular resistance combined with low presinusoidal and postsinusoidal portal vascular resistances. Stochastic numerical simulations of HVPG measurement in multiple HVs revealed that HVPGs measured in the right and middle HVs were basically exchangeable, whereas HVPGs measured in the left HV were relatively lower. The difference in measured HVPG between the middle/left and right HVs correlated positively with the proportion of blood flow rate through the middle/left HV, implying that the lower reading of left-HV HVPG measurement is due primarily to the lower blood flow rate through the HV. These findings may contribute as useful theoretical references for guiding data interpretation or choosing a proper HV for implementing catheterization in the clinical application of HVPG measurement.
Highlights
Hepatic venous pressure gradient (HVPG) measurement has been increasingly accepted as a useful means for indirectly measuring portal venous pressure in patients with portal hypertension (PHT) caused by chronic liver diseases
Despite the existence of numerous studies addressing the clinical utility of HVPG measurement, it is as yet unclear how the accuracy of measured HVPG as a surrogate of portal pressure gradient (PPG) is influenced by the pathological status of the hepatic circulation that changes with the progression of liver disease and differs considerably among patients
It remains unclear whether HVPGs measured in different hepatic veins (HVs) are exchangeable, and if not, what factors determine inter-HV HVPG differences? In this context, we developed a stochastic computational model of the hepatic circulation, and performed a series of model-based numerical experiments to quantitatively investigate the respective/combined effects of various hepatic vascular properties on the accuracy of HVPG measurement
Summary
Reliability and Variability of Hepatic Venous Pressure Gradient as a Surrogate of Portal Pressure Gradient: Insights from a Computational Model-Based Study Abstract: Hepatic venous pressure gradient (HVPG) measurement has been increasingly accepted as a useful means for indirectly measuring portal venous pressure in patients with portal hypertension (PHT) caused by chronic liver diseases.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.