Reprint of: Neuroimaging in acute liver failure.

Neurochem Int

Servei de Medicina Interna-Hepatologia, Hospital Vall d'Hebron, Vall d'Hebron Institut of Research, Barcelona, Spain.

Published: June 2012

AI Article Synopsis

  • Acute liver failure (ALF) often leads to brain edema, resulting in increased intracranial pressure and potential brain damage.
  • Neuroimaging techniques like transcranial Doppler ultrasonography, magnetic resonance imaging, and nuclear imaging are crucial for assessing brain changes and understanding the condition's progression in ALF patients.
  • These methods help monitor patient outcomes and can reveal critical neurometabolic abnormalities, potentially paving the way for future diagnostic and therapeutic advancements.

Article Abstract

Acute liver failure (ALF) is frequently complicated by the development of brain edema that can lead to intracranial hypertension and severe brain injury. Neuroimaging techniques allow a none-invasive assessment of brain tissue and cerebral hemodynamics by means of transcranial Doppler ultrasonography, magnetic resonance and nuclear imaging with radioligands. These methods have been very helpful to unravel the pathogenesis of this process and have been applied to patients and experimental models. They allow monitoring the outcome of patients with ALF and neurological manifestations. The increase in brain water can be detected by observing changes in brain volume and disturbances in diffusion weighted imaging. Neurometabolic changes are detected by magnetic resonance spectroscopy, which provides a pattern of abnormalities characterized by an increase in glutamine and a decrease in myo-inositol. Disturbances in cerebral blood flow are depicted by SPECT or PET and can be monitored and the bedside by assessing the characteristics of the waveform provided by transcranial Doppler ultrasonography. Neuroimaging methods, which are rapidly evolving, will undoubtedly lead to future diagnostic and therapeutic progress that could be very helpful for patients with ALF.

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Source
http://dx.doi.org/10.1016/j.neuint.2012.03.015DOI Listing

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