Respiration Artificial Inpatients
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Volunteers with a clinical diagnosis of pneumonia; undergoing conventional respiratory physiotherapy treatment; using Invasive Mechanical Ventilation (IMV), regardless of mode and ventilatory parameters; receiving medication treatment according to previously adopted clinical protocols; aged over 18 years; of both sexes; and who agree to participate in the study by signing the Informed Consent Form (ICF).
Exclusion criteria
Exclusion criteria: Patients in spontaneous breathing (without artificial airway); patients under continuous sedation; or those presenting a lower level of consciousness within 24 hours after weaning, assessed using the Richmond Agitation-Sedation Scale (RASS), will not be included.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To analyze the effectiveness of Photobiomodulation therapy with LED belts in the weaning of patients with pneumonia from ventilators in the prevention of acquired weakness in the intensive care unit (AWICU). | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the hemodynamic results promoted by the LED belt. ;Quantify the time to wean off ventilation and length of hospital stay after using Photobiomodulation.;Evaluate respiratory muscle strength and lung function after Photobiomodulation. | — |
Countries
BR
Contacts
Anhembi Morumbi São José dos Campos