Surgery
Conditions
Brief summary
assess the impact of the intervention of a clinical pharmacist expert in sterile medical devices
Interventions
\- Failure to trace, Lack of product information, absence of product in the operating room
Sponsors
Study design
Eligibility
Inclusion criteria
* \- The patient must be a member or beneficiary of a health insurance plan. * The patient is managed for scheduled surgery (full hospitalization or outpatient) in the UDG (Urology Digestive Gynecology) operating room.
Exclusion criteria
* \- The subject is in a period of exclusion determined by a previous study. * The subject is under judicial protection. * The subject (or his/her legal representative) has expressed his/her opposition to participate in the study. * The patient is undergoing emergency surgery in the UDG (Urology Digestive Gynecology) operating room. * It is not possible to give informed information about the subject. Translated with www.DeepL.com/Translator (free version)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| identify compliance with the appropriate use of sterile medical devices | 1 day |
Countries
France