Careful Ventilation in Acute Respiratory Distress Syndrome. The CAVIARDS study

  • Funded by Canadian Institutes of Health Research (CIHR)
  • Total publications:0 publications

Grant number: 474616

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Key facts

  • Disease

    COVID-19
  • start year

    2022
  • Known Financial Commitments (USD)

    $163,135.44
  • Funder

    Canadian Institutes of Health Research (CIHR)
  • Principal Investigator

    Brochard Laurent J
  • Research Location

    Canada
  • Lead Research Institution

    Unity Health Toronto
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Supportive care, processes of care and management

  • Special Interest Tags

    Innovation

  • Study Type

    Clinical

  • Clinical Trial Details

    Unspecified

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Each year almost 40,000 Canadians receive mechanical ventilation for a a diffuse inflammation of the lung caused by bacterial infection, flu or trauma and called acute respiratory distress syndrome (ARDS). The most recent and specific cause of admission to an ICU has been COVID-19 which caused hundreds thousand cases in Canada. As shown by the pandemic, mortality under mechanical ventilation is still unacceptably high, often >40% : clinicians are still struggling about the best way to deliver mechanical ventilation. We think the prognosis can be improved by making ventilation more protective for the lung. Mechanical Ventilation is indeed life-saving but, paradoxically, can cause further inflammation and damage in the remaining healthy lung and in the whole body. Current mechanical ventilation is often not sufficiently lung protective. We think that the use of bedside measurements that we previously described can make ventilation less injurious, safer and that it will improve survival. Positive pressure is one of the cornerstone of the treatment but we propose to adjust it based of the individual lung response to pressure using a technique that we designed: this differentiate responders to high pressure vs. non responders. For the first time, pressure applied with mechanical ventilation will be individualized. We also showed how to monitor and control the degree of spontaneous ventilation in conjonction with the ventilator and which should be facilitated for the patient. We believe that these measures are not ony feasible but can guide the ventilatory management and improves the outcome of patients under mechanical ventilation. We have designed two studies, one for COVID-19 patients and one for the other forms of ARDS that are usally seen out of a pandemic. The study about COVID-19 patients is almost completed and we have been able to start the non-COVID study but we need additional funding to complete this 2nd study.