The purpose of this study is to determine the incidence of recall in patients managed in emergency department with a procedural sedation protocol using propofol in a population of 250 .

After procedural sedation for fracture or joint dislocation reduction using propofol, adult patients recall will be assessed with a standardised form. This recall assessment will be realised 2 hours (+/- 15 minutes) after the procedural sedation and the day after.

The primary outcome measure will be the recall incidence 2 hours (+/- 15 minutes) after a procedural sedation. A secondary outcome will be the recall incidence one day after the procedural sedation.

The recall will be defined by a positive answer to the third question of the Sandin form (Lancet. 2000;355(9205):707-11).

Inclusion Criteria:

• Adults patients (> 18 years old) who had a procedural sedation in emergency department using propofol for fracture or joint dislocation reduction
• Patients who received an initial injection of Propofol by slow intravenous injection of 1 mg/kg in 20 seconds
• Inclusion less than 2 hours from the injection of Propofol
• Patients who have signed a consent to participate in the study
• Patients covered by social security.

Exclusion Criteria:

• Patients under 18 years old
• Patients who cannot signed the informed consent
• Patients who had procedural sedation using other drugs that propofol
• Participation in another study type biomedical research

Adults patients managed in emergency department with a procedural sedation protocol using propofol