critical care.
Conditions
Interventions
Intervention 1: Intervention group (first group): After reviewing the guidelines and protocols of the world regarding sedation drugs interruptions in patients undergoing mechanical ventilation, A team
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients older than 18 years Intubated patients under mechanical ventilation
Exclusion criteria
Exclusion criteria: Active seizure Patients who have received Neuromuscular blocking agents medication Moderate to severe shock The signs of increased intracranial pressure A patient who will undergo surgery in the next 24 hours Predicting imminent death in less than 48 hours Induced hypothermia Active cardiac ischemia in the last 24 hours patients who refuced to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of mechanical ventilation. Timepoint: From the time the patient enters the ICU until discharge from this ward. Method of measurement: Number of days the patient is under mechanical ventilation based on patients recorded information. | — |
Secondary
| Measure | Time frame |
|---|---|
| Mortality rate. Timepoint: Duration of hospitalization. Method of measurement: Mortality counting based on patients recorded information.;ICU length of stay. Timepoint: From the time of the patient's arrival until the discharge of ICU. Method of measurement: According to the number of days the patient was hospitalized in the ICU.;Extubation time. Timepoint: ICU length of stay. Method of measurement: Using patient records.;Diagnosis. Timepoint: Duration of hospitalization. Method of measurement: Using patient records.;The amount of sedative medication. Timepoint: ICU length of stay. Method of measurement: Using patient records. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahtab Setoode
Shiraz University of Medical Sciences
Outcome results
None listed