Tracheal Intubation Morbidity
Conditions
Brief summary
The purpose of this study is to evaluate intubation duration between rapid sequence intubation technique (RSI) and non-rapid sequence intubation technique (non-RSI) performed by emergency medicine residents in Siriraj hospital.
Detailed description
A prospective cohort study was conducted in the non-traumatic emergency department (ED).
Interventions
All medications are administered only one dose before intubation Anesthetics: Propofol 2-2.5 mg/kg Thiopental 3-5mg/kg Etomidate 1-2mg/kg Neuromuscular blocking agents: Succinylcholine 1-1.5mg/kg Rocuronium 0.9mg/kg Opioid: Fentanyl 1-2ug/kg
Sponsors
Study design
Eligibility
Inclusion criteria
* patients required airway control by tracheal intubation
Exclusion criteria
* cardiac arrest
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The overall intubation duration | Participants will be followed for the overall intubation duration until confirmation the endotracheal position, an expected average of 2 minutes | The overall intubation duration is recorded on the decision to intubation patient and corresponds to the time of confirmation the endotracheal position by chest auscultation |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| the intubation duration | Participants will be followed for the intubation duration until confirmation the endotracheal position, an expected average of 5 minutes | The intubation duration (Ti), it is defined from application the laryngoscope into the patient's mouth to the time of confirmation an endotracheal position |
| Complication | Participants will be followed in the period of staying in the emergency room and hospital, an expected average of 4 weeks | Complications occur during and after intubation peroid are recorded and monitored until patients are discharged fromt the hospital. |
Countries
Thailand