STUDY OF ELECTRICAL STIMULATION IN PULMONARY FUNCTION IN INTENSIVE CARE UNIT
Respiratory Distress Syndrome, Adult
About this trial
This is an interventional treatment trial for Respiratory Distress Syndrome, Adult focused on measuring Mechanical Ventilation, Electrical Stimulation, Diaphragm, Ventilometry, Physiotherapy
Eligibility Criteria
Inclusion Criteria:
- Individuals of both sexes aged 60 years and older up to 80 years,
- in invasive MV for more than 48 hours,
- with respiratory drive,
- using MV in the mode of intermittent mandatory synchronized ventilation (VMIS) or (VPS),
- connected to the orotracheal tube or via tracheostomy,
- hemodynamically stable,
- neuromuscular junction of the entire diaphragm,
- absence of sedatives.
Exclusion Criteria:
- presence of pacemaker, hyperthermia (temperature> 38 ° C),
- use of neuromuscular blockers,
- use of thoracic drains, generalized edema,
- cutaneous lesion in the area of intervention with TEDS.
Sites / Locations
- Hospital de Clínicas Gaspar Viana
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
No Intervention
Experimental Group 1
Experimental Group 2
Control Group
synchronized FES mode, according to the parameters based on the Gueddes et al., (1991): current frequency (F) 30 Hz; pulse width (T) 0,4 ms; upload time (Rise) 1s; time of muscle contraction (On time) 1 s; down time (Decay) 2s e muscle relaxation time (Off time) 1 s.
the same apparatus will be used, differing in the parameters that will be based on the studies of Cancelliero et al., (2012) for the EDET procedure, being used in synchronized FES mode, with frequency of 30 Hz; pulse width (T) 0,4 ms, climb (ramp) of 0,7 s (maximum value). The support was of 0.4 s, already standardized and fixed in the apparatus
The control group (CG) with the same characteristics of the experimental groups will perform conventional physiotherapy