Challenges in zero-flow blood pressure as a measure of mean circulatory filling pressure: Experimental and computational perspectives

  • L M van Loon*
  • , M P Mulder
  • , D van Dort
  • , J G van der Hoeven
  • , D W Donker
  • , J Lemson
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Mean circulatory filling pressure (MCFP) is a foundational hemodynamic concept, representing the average circulatory pressure in a no-flow state and used to assess volume status and venous return. However, its measurement and clinical relevance remain debated. In this study, zero-flow pressures were recorded in 14 healthy pigs following cardiac arrest. Measurements were taken for 10 min in the abdominal aorta and right atrium under two conditions: cardiac arrest induced by pentobarbital overdose or by ventricular fibrillation (VF), with half of the VF animals rendered hypovolemic. A validated computational model of cardiovascular physiology was used to simulate these scenarios. Pentobarbital caused a rapid pressure equilibration, with mean arterial pressure (MAP) falling from 47 ± 3.7 to 16 ± 2.5 mm Hg. In contrast, VF produced a dynamic pressure response: MAP dropped from 53 ± 4.7 to 17 ± 2.2 mm Hg while central venous pressure rose, producing a persistent retrograde pressure gradient (5 ± 2.1 mm Hg). In silico simulations closely matched these dynamics (normalized RMSE <5%) and confirmed the influence of reflex mechanisms. These results challenge the idea of MCFP as a stable, universal value. Zero-flow pressures depend heavily on arrest method and reflexes, and computational modeling offers a valuable, ethical alternative to animal-based investigations.

Original languageEnglish
Article numbere70599
Number of pages9
JournalPhysiological Reports
Volume13
Issue number19
DOIs
Publication statusPublished - Oct 2025

Keywords

  • Animals
  • Aorta, Abdominal/physiology
  • Arterial Pressure
  • Blood Pressure/physiology
  • Computer Simulation
  • Heart Arrest/physiopathology
  • Hemodynamics
  • Models, Cardiovascular
  • Swine
  • Ventricular Fibrillation/physiopathology

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