Abstract

Much progress has been made over the past two decades in the treatment of severe acute brain injury, including traumatic brain injury and subarachnoid hemorrhage, resulting in a higher proportion of patients surviving with better outcomes. This has arisen from a combination of factors. These include improvements in procedures at the scene (pre-hospital) and in the hospital emergency department, advances in neuromonitoring in the intensive care unit, both continuously at the bedside and intermittently in scans, evolution and refinement of protocol-driven therapy for better management of patients, and advances in surgical procedures and rehabilitation. Nevertheless, many patients still experience varying degrees of long-term disabilities post-injury with consequent demands on carers and resources, and there is room for improvement. Biomarkers are a key aspect of neuromonitoring. A broad definition of a biomarker is any observable feature that can be used to inform on the state of the patient, e.g., a molecular species, a feature on a scan, or a monitoring characteristic, e.g., cerebrovascular pressure reactivity index. Biomarkers are usually quantitative measures, which can be utilized in diagnosis and monitoring of response to treatment. They are thus crucial to the development of therapies and may be utilized as surrogate endpoints in Phase II clinical trials. To date, there is no specific drug treatment for acute brain injury, and many seemingly promising agents emerging from pre-clinical animal models have failed in clinical trials. Large Phase III studies of clinical outcomes are costly, consuming time and resources. It is therefore important that adequate Phase II clinical studies with informative surrogate endpoints are performed employing appropriate biomarkers. In this article, we review some of the available systemic, local, and imaging biomarkers and technologies relevant in acute brain injury patients, and highlight gaps in the current state of knowledge.

Highlights

  • The ictus–the catastrophic event of severe acute brain injury–is followed over the ensuing hours and days by a secondary cascade of pathological processes that can exacerbate neuronal injury and worsen outcome

  • Aneurysmal subarachnoid hemorrhage (SAH) carries a high risk of complications, a high degree of dependency in survivors, and most SAH patients are under 60 years of age [5, 6]

  • The goal of cerebral perfusion pressure (CPP) ≥ 70 mmHg or the practice of “indiscriminate” CPP augmentation fell out of favor after a demonstration of lack of clinical outcome benefit coupled with an increased incidence of complications and the acute respiratory distress syndrome (ARDS)

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Summary

INTRODUCTION

The ictus–the catastrophic event of severe acute brain injury–is followed over the ensuing hours and days by a secondary cascade of pathological processes that can exacerbate neuronal injury and worsen outcome. Biomarkers are usually quantitative measures, which can be utilized in diagnosis, prognosis, monitoring evolution of injury and recovery, and response to treatments [7] They are crucial to the development of therapies in many pathological states and may be utilized as surrogate endpoints in Phase II clinical trials. The goal of CPP ≥ 70 mmHg or the practice of “indiscriminate” CPP augmentation fell out of favor after a demonstration of lack of clinical outcome benefit coupled with an increased incidence of complications and the acute respiratory distress syndrome (ARDS) Another aspect of the CPP debate is the Lund concept or the “ICP and microperfusion-guided management” as proposed by the University of Lund, Sweden [30]. The PRx has been previously validated against other indices of cerebral autoregulation [25], and is related

Biomarkers in human brain
Arteriovenous difference Microdialysis
Regional and voxel
Findings
CONCLUSION AND FUTURE PROSPECTS
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