No problem studied. This protocol was conducted without changing any ventilator settings and treatments provided by the primary physician. mechanical power, ventilator-induced lung injury, mechanical ventilation, respiratoy failure, critically ill
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Using ventilators those are capable of exporting real-time signal to the specifically designed data collecting system (Technically limited to Puritan-Bennett ventilator model PB840 or PB980) (2) Receiving invasive ventilation for at least 24 consecutive hours (3) Able to perform data collection within 24 hours after connected to the current mechanical ventilator (4) Receiving permission from the attending physician. (5) First intubation and ICU admission throughout hospitalization
Exclusion criteria
Exclusion criteria: (1) The patient who is extubated or die or discharge from the ICU during the first 24 hours (2) The patient who was previously enrolled in this study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| In hospital mortality During hospitalization Pearsons or Spearmans correlation | — |
Secondary
| Measure | Time frame |
|---|---|
| 28-day mortality, ICU length of stay, hospital length of stay, duration of intubation, ventilator free-days in 28 days and respiratory complications associated with mechanical ventilation 28 day Pearsons or Spearmans correlation | — |
Countries
Thailand
Contacts
Faculty of Medicine Ramathibodi Hospital