Evaluation of the training of an intensive care team in the use of oxygen properly, avoiding the excess of patients who use respiratory devices.

Not Applicable

Recruiting

• Conditions: C23.888.852.567; Hyperoxia, Respiration, Artificial; E02.041.625

• Registration Number: RBR-54dstg
• Lead Sponsor: Hospital Universitário da Universidade Federal de Juiz de Fora

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2020-06-22
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Patients admitted to intensive care over 18 years of age; need to use mechanical ventilation for more than 24 hours.

Exclusion Criteria

Patients intubated in another unit for more than 24 hours; need for FiO2 above 50% and or e and / or PEEP> 8 cmH2O; patients in palliative care; peripheral vasculopathy; Raynaud's phenomenon present; ulcers in extremities; severe vasoconstriction; absence of consent from the patient or first-degree family member; patient previously admitted to the unit.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Assess the reduction of hyperoxia in patients undergoing mechanical ventilation; The training is expected to be effective in reducing hyperoxia by more than 50%. The evaluation will be by the time of exposure to the Oxygen Saturation values ??above 96%, evaluated every 5 minutes in the monitoring patient.<br><br>

Secondary Outcome Measures

Name	Time	Method
Reduction of hospital mortality in comparison with the pre-training group.;Reduction of days of intensive care in comparison with the pre-training group.;Reduction of days of hospital care in comparison with the pre-training group.;Reduction of days in mechanical ventilation in comparison with the pre-training group. ;Reduced incidence of pneumonia associated with mechanical ventilation compared to the pre-training group.;Improvement of the PaO2 / FiO2 ratio at the end of the observation period in relation to the pre-training group.<br><br>;Improvement of positive end-expiratory pressure at the end of the observation period in relation to the pre-training group.