Emergence Agitation
Conditions
Interventions
None listed
Sponsors
Shinshu University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who underwent general anesthesia at our institution between October 1, 2019, and September 30, 2025, and met the following inclusion criteria: (1) Patients aged 20 years or older at the time of anesthesia. (2) Patients who underwent airway management with tracheal intubation or a supraglottic airway device.
Exclusion criteria
Exclusion criteria: (1) Patients who returned to the ward without extubation after surgery. (2) Patients who received continuous administration of sedative agents before extubation. (3) Patients who required re-establishment of the airway in the operating room after extubation. (4) Patients who had an established airway at the time of entry into the operating room. (5) Patients deemed inappropriate for inclusion in the study by the principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is the incidence of patients who received anesthetic, psychotropic, or antihistamine medications for sedation to manage emergence agitation between extubation and operating room discharge. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome was to identify risk factors for emergence agitation using multivariate logistic regression analysis based on patient characteristics, surgical factors, and anesthetic variables. | — |
Countries
Japan
Contacts
Public ContactKUNIHIRO MITSUZAWA
Shinshu University School of Medicine Department of Anesthesiology and Resuscitology
Outcome results
None listed