Abstract

Multimodal brain monitoring has been utilized to optimize treatment of patients with critical neurological diseases. However, the amount of data requires an integrative tool set to unmask pathological events in a timely fashion. Recently we have introduced a mathematical model allowing the simulation of pathophysiological conditions such as reduced intracranial compliance and impaired autoregulation. Utilizing a mathematical tool set called selected correlation analysis (sca), correlation patterns, which indicate impaired autoregulation, can be detected in patient data sets (scp). In this study we compared the results of the sca with the pressure reactivity index (PRx), an established marker for impaired autoregulation. Mean PRx values were significantly higher in time segments identified as scp compared to segments showing no selected correlations (nsc). The sca based approach predicted cerebral autoregulation failure with a sensitivity of 78.8% and a specificity of 62.6%. Autoregulation failure, as detected by the results of both analysis methods, was significantly correlated with poor outcome. Sca of brain monitoring data detects impaired autoregulation with high sensitivity and sufficient specificity. Since the sca approach allows the simultaneous detection of both major pathological conditions, disturbed autoregulation and reduced compliance, it may become a useful analysis tool for brain multimodal monitoring data.

Highlights

  • Neurocritical care management of patients with life-threatening diseases of the nervous system aims to avoid secondary brain injury [1]

  • Utilizing a pressure reactivity index (PRx) threshold value of 0.3, selected correlation analysis resulting in scp predicted impairment of autoregulation with a sensitivity of 78.8% and a specificity of 62.6%

  • Neuroprotection after catastrophic CNS events as a causal treatment has been the primary goal of neuroscientific research in the field; so far clinical trials have not yielded any significant success in patients with either SAH or TBI [21, 22]

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Summary

Introduction

Neurocritical care management of patients with life-threatening diseases of the nervous system aims to avoid secondary brain injury [1] This requires early detection of physical and biochemical events leading to increased intracranial pressure (ICP), insufficient cerebral blood flow, and brain hypoxia [2]. To generate a tool set which might facilitate detection of critical worsening of the patient, a mathematical, compartmental model of the brain focusing on slow dynamic variations was developed. This model allows simulating changes of brain multimodal monitoring data triggered by pathophysiological events such as reduced intracranial compliance and impaired autoregulation [6, 7].

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