Postoperative Pain
Conditions
Keywords
breast surgery
Brief summary
We will enroll patients submitted to breast surgery (in and outsettings) with regional anesthesia. The blinded observers, in the first 48 hours post-operative, will evaluate (telephone interview in outsetting) the pain intensity through the Numeric Rating Scale ( 0= no pain, 10 = worst possible pain) thereby recording the treatment procedures in accordance with usual clinical practice. At the same time we will evaluate the presence of intraoperative or postoperative complications related to regional anesthesia, the PONV rate (post-operative nausea and vomiting) and the analgesic/antiemetic therapy.
Interventions
OTHERregional anesthesia in breast surgery
In the Hospitals involved in this study are performed routinely wall blocks (PECS I-II blocks and serratus block) during breast surgery
Sponsors
Ospedale di Circolo - Fondazione Macchi
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
ASA I-II-III Patients Written Informed Consent
Exclusion criteria
ASA IV Active Heart Failure Coagulation Disease Chronic Pain Allergies to Local Anesthetics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain Intensity Misure | 2 days |
Secondary
| Measure | Time frame |
|---|---|
| Complications Regional Anesthesia Related | 1 days |
| PostOperative Nausea Rate | 2 days |
| Intraoperative Opioids Use | surgical time |
| Postoperative Analgesics | 2 days |
Countries
Italy
Outcome results
None listed