External Validation of VVI (E-VVI)

University of Thessaly

Status: Enrolling

Conditions: Weaning Mechanical Ventilation

Study type: Observational

Funder types: Other

Identifiers

NCT07372664

23/17/16-12-25

Details and patient eligibility

About

Failure of liberation from mechanical ventilation increases days spent being mechanically ventilated, the length of stay and the morbidity of patients. Thus it is crucial that those patients who are ready to be liberated are accurately detected. In this study we want to externally validate an index (the volume-velocity index, VVI) which in a preliminary study was found to predict with high accuracy the outcome of ventilator liberation.

In this study, in patients who are deemed ready to undergo weaning by their treating physician we will measure the excursion of the diaphragm, the principal respiratory muscle, the inspiratory time and the tidal volume and the volume breathed by the patient at each respiration in three phases:

1. during pressure support ventilation with 5/5,
2. during pressure support ventilation with 8/0,
3. during t-tube or pressure support ventilation with 0/0. All of these phases are ventilatory modalities widely used during weaning from mechanical ventilation.

We will evaluate whether VVI can predict accurately the weaning outcome.

Enrollment: 100 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Mechanically ventilated patients for more than 48h
• First Spontaneous breathing trial
• Deemed as ready to undergo weaning by the treating physician, according to published readiness criteria (DOI: 10.1183/09031936.00010206)

Exclusion criteria

• pregnant patients
• preexisting diaphragmatic disease or injury
• tracheostomy

Trial design

100 participants in 1 patient group

Patients undergoing weaning