Impact of a Preoperative Education on the Quality of Postoperative Analgesia Management in Outpatient Surgery

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

In 2015, more than 50% of surgical procedures were performed in outpatient settings. Successful pain management after outpatient surgery is crucial, and requires a perfect cooperation between caregivers and patients, with clear information on the analgesics use at home. Different strategies to control postoperative pain were adopted by hospitals performing outpatient surgery. However, up to half of patients receive little or no information about the treatment of postoperative pain, and at least one third of them are not able to follow postoperative analgesia instructions. There is a clear unmet need in pain treatment during first 48-72 hours after discharge, with important number of emergency calls and readmissions. The most common causes of rescue calls after outpatient surgery are uncontrolled pain and questions about medications or post-operative care. Structured education interventions using psychological techniques to enhance engagement and behavior were found to be beneficial for better acute pain management in outpatient settings after orthopedic surgery. We hypothesize that an educational intervention based on the rational perception of postoperative pain and discomfort, and the proper use of analgesics would improve the quality of pain management at home and reduce analgesics-related side effects. Principal objective of this study is to evaluate the impact of a preoperative educational intervention on effectiveness of postoperative pain self-management in outpatient settings compared to the current practice. Secondary objectives are to evaluate the prevalence of analgesics use and the incidence of severe pain episodes, as well as side effects. The occurrence of neurological pain, quality of sleep, and patient's comfort will be evaluated at 30th day after surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adults (age ≥ 18 years);

• Patients scheduled for outpatient orthopedic surgery

• ASA (American Society of Anesthesiology) I to III;

• Patients admitted for an outpatient intervention resulting in moderate to severe pain: eg: arthroscopy of the knee or shoulder, cruciate ligaments, shoulder block, medial patellofemoral ligament plasty (not exhaustive)

Locations
Other Locations
France
Hospices Civils de Lyon - Hopital de la Croix Rousse - Anaesthesia Reanimation unit
RECRUITING
Lyon
Contact Information
Primary
Mikhaïl DZIADZKO
mikhail.dziadzko@chu-lyon.fr
+33 4 26 10 93 25
Backup
Axelle BOUTELEUX
axelle.bouteleux@chu-lyon.fr
+33 4 72 11 90 51
Time Frame
Start Date: 2019-01-22
Estimated Completion Date: 2027-03-22
Participants
Target number of participants: 414
Treatments
Experimental: Patients with a therapeutic educational intervention
Arm 1 : Interventional group: A therapeutic educational intervention is performed following pre-anesthesia assessment
Active_comparator: Patients without therapeutic educational intervention
Arm 2 : Control group: standard information on pain is performed following pre anesthesia assessment
Related Therapeutic Areas
Sponsors
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov