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      Assessment of a Non-Invasive Brain Pulse Monitor to Measure Intra-Cranial Pressure Following Acute Brain Injury

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          Abstract

          Background

          Intracranial pressure (ICP) monitoring requires placing a hole in the skull through which an invasive pressure monitor is inserted into the brain. This approach has risks for the patient and is expensive. We have developed a non-invasive brain pulse monitor that uses red light to detect a photoplethysmographic (PPG) signal arising from the blood vessels on the brain’s cortical surface. The brain PPG and the invasive ICP waveform share morphological features which may allow measurement of the intracranial pressure.

          Methods

          We enrolled critically ill patients with an acute brain injury with invasive ICP monitoring to assess the new monitor. A total of 24 simultaneous invasive ICP and brain pulse monitor PPG measurements were undertaken in 12 patients over a range of ICP levels.

          Results

          The waveform morphologies were similar for the invasive ICP and brain pulse monitor PPG approach. Both methods demonstrated a progressive increase in the amplitude of P2 relative to P1 with increasing ICP levels. An automated algorithm was developed to assess the PPG morphological features in relation to the ICP level. A correlation was demonstrated between the brain pulse waveform morphology and ICP levels, R 2=0.66, P < 0.001.

          Conclusion

          The brain pulse monitor’s PPG waveform demonstrated morphological features were similar to the invasive ICP waveform over a range of ICP levels, these features may provide a method to measure ICP levels.

          Trial Registration

          ACTRN12620000828921.

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          Most cited references62

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          Brain Oxygen Optimization in Severe Traumatic Brain Injury Phase-II

          A relationship between reduced brain tissue oxygenation and poor outcome following severe traumatic brain injury has been reported in observational studies. We designed a Phase II trial to assess whether a neurocritical care management protocol could improve brain tissue oxygenation levels in patients with severe traumatic brain injury and the feasibility of a Phase III efficacy study.
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            Monro-Kellie 2.0: The dynamic vascular and venous pathophysiological components of intracranial pressure

            For 200 years, the ‘closed box’ analogy of intracranial pressure (ICP) has underpinned neurosurgery and neuro-critical care. Cushing conceptualised the Monro-Kellie doctrine stating that a change in blood, brain or CSF volume resulted in reciprocal changes in one or both of the other two. When not possible, attempts to increase a volume further increase ICP. On this doctrine’s “truth or relative untruth” depends many of the critical procedures in the surgery of the central nervous system. However, each volume component may not deserve the equal weighting this static concept implies. The slow production of CSF (0.35 ml/min) is dwarfed by the dynamic blood in and outflow (∼700 ml/min). Neuro-critical care practice focusing on arterial and ICP regulation has been questioned. Failure of venous efferent flow to precisely match arterial afferent flow will yield immediate and dramatic changes in intracranial blood volume and pressure. Interpreting ICP without interrogating its core drivers may be misleading. Multiple clinical conditions and the cerebral effects of altitude and microgravity relate to imbalances in this dynamic rather than ICP per se. This article reviews the Monro-Kellie doctrine, categorises venous outflow limitation conditions, relates physiological mechanisms to clinical conditions and suggests specific management options.
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              The microvascular system of the striate and extrastriate visual cortex of the macaque.

              In functional neuroimaging, neurovascular coupling is used to generate maps of hemodynamic changes that are assumed to be surrogates of regional neural activation. The aim of this study was to characterize the microvascular system of the primate cortex as a basis for understanding the constraints imposed on a region's hemodynamic response by the vascular architecture, density, as well as area- and layer-specific variations. In the macaque visual cortex, an array of anatomical techniques has been applied, including corrosion casts, immunohistochemistry, and cytochrome oxidase (COX) staining. Detailed measurements of regional vascular length density, volume fraction, and surface density revealed a similar vascularization in different visual areas. Whereas the lower cortical layers showed a positive correlation between the vascular and cell density, this relationship was very weak in the upper layers. Synapse density values taken from the literature also displayed a very moderate correlation with the vascular density. However, the vascular density was strongly correlated with the steady-state metabolic demand as measured by COX activity. This observation suggests that although the number of neurons and synapses determines an upper bound on an area's integrative capacity, its vascularization reflects the neural activity of those subpopulations that represent a "default" mode of brain steady state.
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                Author and article information

                Journal
                Med Devices (Auckl)
                Med Devices (Auckl)
                mder
                Medical Devices (Auckland, N.Z.)
                Dove
                1179-1470
                24 January 2023
                2023
                : 16
                : 15-26
                Affiliations
                [1 ]Cyban Pty Ltd , Melbourne, VIC, Australia
                [2 ]Department of Critical Care Medicine, St Vincent’s Hospital , Melbourne, Australia
                [3 ]Department of Medicine, University of Melbourne , Melbourne, Vic, Australia
                [4 ]Department of Critical Care Medicine, The Alfred Hospital , Melbourne, Australia
                [5 ]Department of Neurosurgery, St Vincent’s Hospital , Melbourne, Australia
                [6 ]University of Melbourne Medical School , Melbourne, Vic, Australia
                Author notes
                Correspondence: Barry Dixon, Department of Critical Care Medicine, St Vincent’s Hospital (Melbourne) , 41 Victoria Parade, Fitzroy, VIC, 3065, Australia, Tel +61 3 9231 4425, Email barry.dixon@svha.org.au
                Author information
                http://orcid.org/0000-0002-8491-9393
                http://orcid.org/0000-0003-3188-5190
                http://orcid.org/0000-0003-2282-8223
                Article
                398193
                10.2147/MDER.S398193
                9883992
                36718229
                43aacfa3-f27b-466f-b03f-be57fcca9bc9
                © 2023 Dixon et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 29 November 2022
                : 13 January 2023
                Page count
                Figures: 6, Tables: 1, References: 63, Pages: 12
                Funding
                Funded by: Biomedtech Horizons Program part of the Medical Research Future Fund of the Australian Government;
                The research was supported by a grant from the Biomedtech Horizons Program part of the Medical Research Future Fund of the Australian Government.
                Categories
                Original Research

                Biotechnology
                intracranial pressure,acute brain injury,monitoring,non-invasive,photoplethysmography

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