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The ACCESSIT Study

U

Unity Health Toronto

Status

Enrolling

Conditions

Respiratory Support

Treatments

Other: Mechanical Ventilation

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The study is designed to characterize and monitor the structure, degree of activation and function of the different respiratory muscles during mechanical ventilation after spine trauma and spinal cord injury.

Full description

In patients with spinal cord injury, separation from mechanical ventilation is an essential aspect of the prognosis. Denervation of specific muscles, as a consequence of the injury, can generate a dysfunction of the involved muscles and/or a disruption of their coordination during breathing. Respiratory muscle dysfunction is strongly associated with failure of weaning from mechanical ventilation. However, the pattern of activation and coordination of the different respiratory muscles, as well as their evolution over time, have been poorly investigated in spinal cord injury, particularly during the acute phase in intensive care unit.

Assessing the structure, activity, and function of the respiratory muscles at different time points after the injury would help to better understand the natural course of respiration in these patients and the possible therapeutic approaches. In fact, depending on the activation/deactivation and residual function of the respiratory muscles, there might be potential for recovery and training, with the possibility of improving patients' clinical outcomes.

In this preliminary physiological study, the investigators aim to assess the feasibility of monitoring non-invasively the respiratory muscles in mechanically ventilated adult patients with traumatic spine lesion, with and without spinal cord injury. The investigators also aim to assess, monitor, and compare over time the structure, degree of activation, function, and coordination of the different respiratory muscles.

Because the diagnosis of spinal cord injury is not always made immediately in spine trauma patients, and because other factors related to chest or abdominal trauma could interfere with the respiratory pattern, the plan is to study and follow patients with spinal cord injury, using patients with traumatic spine lesion without spinal cord injury as controls.

Enrollment

30 estimated patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Presence of traumatic spine lesion (with and without spinal cord injury)
  • Requiring invasive mechanical ventilation, via oro-tracheal or tracheostomy tube,
  • 16 years of age or older
  • Patient or substitute decision maker able to provide consent

Exclusion criteria

  • Expected withdrawal of treatments within 24 hours of screening
  • Chronic respiratory failure already treated with mechanical ventilation before the injury
  • Documented pre-existing neuromuscular diseases

Trial design

30 participants in 2 patient groups

Patients with spinal cord injury
Description:
Patients treated with mechanical ventilation after a traumatic spine lesion with spinal cord injury
Treatment:
Other: Mechanical Ventilation
Patients with NO spinal cord injury
Description:
Patients treated with mechanical ventilation after a traumatic spine lesion with NO spinal cord injury
Treatment:
Other: Mechanical Ventilation

Trial contacts and locations

1

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Central trial contact

Laurent Brochard, MD, PhD; Annia Schreiber, MD

Data sourced from clinicaltrials.gov

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