Respiration, Artificial
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age equal to or greater than 18 years; Patients intubated on mechanical ventilation for more than 12 hours;
Exclusion criteria
Exclusion criteria: Mechanical ventilation for more than 21 days; Patients with Glasgow Scale <8; Patients with no indication of cardiopulmonary resuscitation or reintubation; Formal indication of non-invasive ventilation after extubation due to hypercapnia during the spontaneous breathing test; Patients with spindle trauma, neuromuscular diseases. Failure to obtain the informed consent term or withdrawal of study participation at any time.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the rate of tracheal reintubation within 48 hours after extubation has been performed. The percetual of reintubated patients will be verified in both the intervention group and the control group, and a comparison of the rates between groups will be performed. | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the length of hospital stay and ICU in days for the patients in the intervention and control group, and verify if there is a difference in the number of days between groups.;Evaluate the mortality rate during ICU and hospital stay in the patients in the intervention and control group, and verify if there is a difference in the number of days between groups. | — |
Countries
Brazil
Contacts
Centro Hospitalar Unimed;Universidade da Região de Joinville - UNIVILLE