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

Evaluation of the multidisciplinary training of the intensive care team on the conservative use of oxygen and reduction of hyperoxia in patients undergoing mechanical ventilation.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-54dstg
Enrollment
Unknown
Registered
2020-06-22
Start date
2020-04-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperoxia, Respiration, Artificial

Interventions

From April 2020 to July 2020, pre-intervention data on peripheral oxygen saturation levels and length of stay in hyperoxia of patients admitted to the ICUs that meet the inclusion criteria will be col
Behavioural
E02.880.690

Sponsors

Hospital Universitário da Universidade Federal de Juiz de Fora
Lead Sponsor
Hospital Universitário da Universidade Federal de Juiz de Fora
Collaborator

Eligibility

Age
18 Years to 100 Years

Inclusion criteria

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

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
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.—

Secondary

MeasureTime frame
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. ;Improvement of positive end-expiratory pressure at the end of the observation period in relation to the pre-training group.—

Countries

Brazil

Contacts

Public ContactEdimar Gomes

Hospital Universitário da Universidade Federal de Juiz de Fora

gomes.edimar@gmail.com5532988194886

Outcome results

None listed

Source: REBEC (via WHO ICTRP)