The influence of hemorrhagic shock on brain perfusion in a swine model of raised intracranial pressure. Academic Article uri icon

Overview

abstract

  • PURPOSE: In patients with hemorrhagic shock and an intracranial space occupying lesion (SOL), brain perfusion is severely compromised due to raised intracranial pressure (rICP), significantly worsening outcomes. This study aims to develop a swine model of a SOL with rICP and shock and characterize the effect on brain perfusion. METHODS: Ten male swine were divided into two groups- normal ICP (nICP) and rICP. rICP animals had an intracranial Fogarty balloon catheter inserted, which was infused with saline to simulate a SOL. Animals underwent hemorrhage to systolic blood pressures (SBP) of 60, 40, and 20mmHg. Cerebral blood flow (CBF) and cerebral blood volume (CBV) were measured using CT perfusion. RESULTS: The CBF/Mean arterial pressure (MAP) and CBV/MAP curves were modeled using non-linear regression, with both groups demonstrating a sigmoid relation. In both the CBF/MAP and CBV/MAP curves, animals with rICP had loss of autoregulation at a higher MAP compared to nICP. The curves were an excellent fit for CBF (nICP R2 = 0.95; rICP R2 = 0.77) and CBV (nICP R2 = 0.96; rICP R2 = 0.78). CONCLUSIONS: This study aids in quantifying the compounding insult of raised ICP and hemorrhage with regard to brain perfusion. Raised ICP results in autoregulatory failure at a higher MAP compared to animals with nICP. These results can help inform future studies that should be aimed at evaluating novel interventions for this complex clinical scenario.

authors

  • Abdou, Hossam
  • Treffalls, Rebecca
  • Jodlowski, Grzegorz
  • Elansary, Noha
  • Ptak, Thomas
  • Walker, Patrick F
  • Morrison, Jonathan J

publication date

  • March 18, 2025

Research

keywords

  • Brain
  • Cerebrovascular Circulation
  • Intracranial Hypertension
  • Shock, Hemorrhagic

Identity

Scopus Document Identifier

  • 105000251821

Digital Object Identifier (DOI)

  • 10.1007/s00068-025-02819-5

PubMed ID

  • 40102249

Additional Document Info

volume

  • 51

issue

  • 1