Weaning Children From Mechanical Ventilation:Computer-driven System Versus Usual Care

St. Justine's Hospital

Status

Completed

Conditions

Respiratory Failure

Treatments

Device: Smartcare/PS

Study type

Interventional

Funder types

Other

Identifiers

NCT00678912

CHUSJ-2239

Details and patient eligibility

About

The purpose of this study is to determine whether a computer-driven system (Smartcare/PS) decreases weaning duration from mechanical ventilation when compared to usual care in children.

Full description

Baseline data: All subjects included into this RCT will undergo routine examination upon admission to the hospital. These examinations include physical, medical/medication history (on the last year for medical history and the last 3 months for medication history (if available), vital signs, radiologic data and laboratory tests.

Intervention: A pre-inclusion test (pressure support test) with a level of pressure support of ± 5 cmH2O of the P plateau, but no greater than 30 cmH2O (pressure-support level plus positive end-expiratory pressure), is performed to evaluate the patient's tolerance of this ventilation mode; the test is repeated daily until positive. The test could be stopped before 30 minutes if the patient showed evidence of respiratory distress (respiratory rate > 40 breaths per minute and FiO2 > 60% in order to obtain pulse oxymetry ≥ 95%). The test is considered positive when, after 30 minutes, the patient remained clinically stable with a respiratory rate lower than 40 breaths per minute and an expiratory tidal volume higher than 6 ml per kilogram of body weight within the authorized pressure-support range, with pulse oxymetry no lower than 95 percent when the fraction of inspired oxygen was no greater than 60 percent. When the pressure-support test is positive, the patient is randomized either to Arm 1 where the intervention is weaning with the support of Smartcare/PS or to Arm 2 where the intervention is weaning based on usual care. Both group are ventilated with the same ventilator: Evita XL.

Enrollment

30 patients

Sex

All

Ages

2 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The attending physician thinks that the patient will be able to breathe spontaneously or the patients is already breathing spontaneously.
No vasopressor or inotropic medication, unless the patient is receiving some digitalin or small doses of dopamine (< 5 µg/kg/min)
Slight or no endotracheal tube gas-leakage ([Vti - Vte]/Vti ≤ 20%)
Mechanical ventilation with a plateau pressure ≤ 25 cmH2O over PEEP
PEEP ≤ 8 cmH2O
FiO2 ≤ 60% in order to obtain pulse oxymetry ≥ 95%
PaCO2 < 70 mmHg on the last blood gases
Extubation not expected the day of inclusion

Exclusion criteria