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Socio-Economic Objective : Child health
Country : Australia
Status : Closed
Research Topic : Diagnostic criteria
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  • Funded Activity

    Discovery Projects - Grant ID: DP1094498

    Funder
    Australian Research Council
    Funding Amount
    $150,000.00
    Summary
    Detection and Quantification of General Fetal Movements from Accelerometer Measurements using Nonstationary Signal Processing Techniques. There are approximately 1,750 fetal deaths per year in Australian with about one-third occurring late in gestation and without an apparent cause. The development of an automated system capable of long-term monitoring of fetal health will result in accurate diagnoses and prediction of future outcome. This will, in turn, allow early intervention by the clinicia .... Detection and Quantification of General Fetal Movements from Accelerometer Measurements using Nonstationary Signal Processing Techniques. There are approximately 1,750 fetal deaths per year in Australian with about one-third occurring late in gestation and without an apparent cause. The development of an automated system capable of long-term monitoring of fetal health will result in accurate diagnoses and prediction of future outcome. This will, in turn, allow early intervention by the clinician to reduce fetal deaths and enhance the chances of good outcomes with resultant savings in social and financial costs to the community. The development of such equipment would spawn future research into intervention treatments and contribute to Australia's position as a world leader in computerised health monitoring systems.
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    Funded Activity

    Discovery Projects - Grant ID: DP0665697

    Funder
    Australian Research Council
    Funding Amount
    $240,000.00
    Summary
    Multi-Channel Time-Frequency Analysis for EEG Neonatal Seizure Characterization. This project researches new signal processing methodologies for a multi-channel characterization of seizures for use in diagnosing newborn brain dysfunctions. The outcomes will result in important immediate clinical benefits for sick newborn babies and will fundamentally facilitate research progress in the development of neuroprotectants and anticonvulsants. The success of this project will contribute in minimizing .... Multi-Channel Time-Frequency Analysis for EEG Neonatal Seizure Characterization. This project researches new signal processing methodologies for a multi-channel characterization of seizures for use in diagnosing newborn brain dysfunctions. The outcomes will result in important immediate clinical benefits for sick newborn babies and will fundamentally facilitate research progress in the development of neuroprotectants and anticonvulsants. The success of this project will contribute in minimizing the social financial costs by diagnosing brain disorders in the initial stage of life and preventing further damage. This has the potential to result in a standard diagnostic equipment in neonatal intensive care units and medical research centres.
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    Funded Activity

    Linkage Projects - Grant ID: LP0562317

    Funder
    Australian Research Council
    Funding Amount
    $190,000.00
    Summary
    Design of Neonatal Seizure Diagnosis Methods Using Time-Frequency Signal Processing Techniques. Seizures occur in approximately 0.5% of all newborns. They are often the only indicator of an early dysfunction in central nervous system (CNS). Their occurrence raises concerns about the underlying cause, its effect on the brain, and the appropriate treatment. Newborn seizures are mostly sub-clinical and only detected through the Electroencephalogram. For an efficient diagnosis, seizure classificatio .... Design of Neonatal Seizure Diagnosis Methods Using Time-Frequency Signal Processing Techniques. Seizures occur in approximately 0.5% of all newborns. They are often the only indicator of an early dysfunction in central nervous system (CNS). Their occurrence raises concerns about the underlying cause, its effect on the brain, and the appropriate treatment. Newborn seizures are mostly sub-clinical and only detected through the Electroencephalogram. For an efficient diagnosis, seizure classification systems were proposed based on visual observations. This project proposes developing a novel approach to automate the classification process using time-frequency (TF) signal processing techniques based on the multi-channel characteristics of the seizure; namely: A) TF signature B) origin, and C) propagation behaviour.
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    Discovery Projects - Grant ID: DP0664664

    Funder
    Australian Research Council
    Funding Amount
    $320,000.00
    Summary
    Phase Contrast X-ray Imaging of the Lung. Lung diseases are a major cause of death in adults, children and newborn infants. Currently, the diagnosis of lung disease is based on clinical symptoms, which usually do not manifest until the disease is well advanced. This project will develop a novel X-ray imaging technique, known as phase contrast imaging, to study the lung, and to potentially detect changes in lung tissue before symptoms arise. This may lead to improved strategies for managing newbo .... Phase Contrast X-ray Imaging of the Lung. Lung diseases are a major cause of death in adults, children and newborn infants. Currently, the diagnosis of lung disease is based on clinical symptoms, which usually do not manifest until the disease is well advanced. This project will develop a novel X-ray imaging technique, known as phase contrast imaging, to study the lung, and to potentially detect changes in lung tissue before symptoms arise. This may lead to improved strategies for managing newborn infants, as well as improving the management of lung diseases in adults.
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    Funded Activity

    Linkage Projects - Grant ID: LP0211586

    Funder
    Australian Research Council
    Funding Amount
    $137,679.00
    Summary
    Molecular and antibody analysis of cytomegalovirus (CMV) infection of fetal and placental cells. CMV is a beta herpesvirus with many unknown molecular mechanisms associated with cellular infection. The virus infects placental cells in vivo, although pathogenesis of viral damage to these cells has been extremely difficult to study in vitro. We have commenced a study to i) demonstrate the molecular accompaniments of infection of placental cells in vitro, ii) determine the genotypic characteristics .... Molecular and antibody analysis of cytomegalovirus (CMV) infection of fetal and placental cells. CMV is a beta herpesvirus with many unknown molecular mechanisms associated with cellular infection. The virus infects placental cells in vivo, although pathogenesis of viral damage to these cells has been extremely difficult to study in vitro. We have commenced a study to i) demonstrate the molecular accompaniments of infection of placental cells in vitro, ii) determine the genotypic characteristics of congenital CMV infections, in collaboration with Abbott Diagnostics, and iii) produce an in vivo model of CMV infection to demonstrate the pathogenesis of cellular injury. The combination of molecular expertise at UNSW with monoclonal antibody expertise from Abbott Diagnostics mean this project is unique worldwide.
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    Funded Activity

    Linkage Projects - Grant ID: LP0989594

    Funder
    Australian Research Council
    Funding Amount
    $240,000.00
    Summary
    The HPA-axis as a marker for disruptive behaviour disorder subtypes in toddlers. Emerging neurobiological models of antisocial behaviour emphasise the role of the hypothalamic-pituitary-adrenal (HPA) axis in the onset of disruptive behaviour disorders (DBDs). Given the broad consensus that antisocial trajectories originate in the toddler years, this project will use cortisol measures of HPA-axis activity to identify the mechanisms through which developmental factors interact with parenting and .... The HPA-axis as a marker for disruptive behaviour disorder subtypes in toddlers. Emerging neurobiological models of antisocial behaviour emphasise the role of the hypothalamic-pituitary-adrenal (HPA) axis in the onset of disruptive behaviour disorders (DBDs). Given the broad consensus that antisocial trajectories originate in the toddler years, this project will use cortisol measures of HPA-axis activity to identify the mechanisms through which developmental factors interact with parenting and family environment to shape persistent DBDs; this will be achieved by following toddlers with severe DBDs across a controlled trial of a parenting intervention.
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    Funded Activity

    Discovery Projects - Grant ID: DP0663345

    Funder
    Australian Research Council
    Funding Amount
    $235,020.00
    Summary
    Towards early detection of upper airway obstruction in children: investigation of autonomic control. This project focuses on the investigation of new indicators for early detection of upper airway obstruction (UAO)-which is a common sleep disorder in children. Failure to treat UAO can result in serious adverse outcomes including failure to thrive, neurocognitive deficits, developmental delay, behavioural disorders and cardiovascular disease. Thus, early treatment of UAO will significantly improv .... Towards early detection of upper airway obstruction in children: investigation of autonomic control. This project focuses on the investigation of new indicators for early detection of upper airway obstruction (UAO)-which is a common sleep disorder in children. Failure to treat UAO can result in serious adverse outcomes including failure to thrive, neurocognitive deficits, developmental delay, behavioural disorders and cardiovascular disease. Thus, early treatment of UAO will significantly improve quality of life for the child. Direct benefits to community health via reduced costs for medical treatment will also be a key outcome. The establishment of new diagnostic indicators will form the basis of new tools for identifying child sleep disorders and contribute to advancing Australia's international leading position in health technology.
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