Breast Reduction, Postoperative Pain, Opioid Consumption
Conditions
Keywords
serratus anterior plane block, parasternal intercostal plane block, breast reduction surgery, pain management, postoperative pain, QoR-15
Brief summary
This study aims to evaluate the effect of adding a Superficial Parasternal Intercostal Plane Block (PIPB) to the Serratus Anterior Plane Block (SAPB) on postoperative pain control in patients undergoing breast reduction surgery under general anesthesia. Effective postoperative analgesia is essential to reduce opioid consumption and improve recovery. All patients will receive standard general anesthesia. Patients will be allocated into three groups: a control group receiving no regional block, a group receiving SAPB alone, and a group receiving SAPB combined with PIPB. The primary outcome of the study is total opioid consumption within the first 24 hours after surgery. Secondary outcomes include postoperative pain scores, Quality of Recovery-15 (QoR-15) scores, and intraoperative remifentanil consumption. The study aims to determine whether SAPB reduces postoperative opioid requirements compared to no block, and whether adding PIPB provides additional analgesic benefit by blocking the anterior cutaneous branches of the intercostal nerves. The findings may contribute to improving multimodal analgesia strategies in breast surgery.
Interventions
injection local anesthetic between 5th rib and serratus anterior muscle
both injection local anesthetic between 5th rib and serratus anterior muscle at midaxillary line and between 4th costal cartilage and pectoralis major muscle at next to the sternum
Sponsors
Study design
Eligibility
Inclusion criteria
* Female patients aged 18-65 years * Scheduled for elective breast reduction surgery under general anesthesia * American Society of Anesthesiologists (ASA) physical status I-III * Ability to understand the study and provide written informed consent
Exclusion criteria
* Patient refusal * Known allergy to local anesthetics * Coagulopathy or ongoing anticoagulant therapy * Infection at the block site * Chronic opioid use or opioid dependence * Severe hepatic or renal insufficiency * Pregnancy or breastfeeding
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Total postoperative opioid consumption in the first 24 hours | First 24 hours after surgery | Total opioid consumption during the first 24 postoperative hours will be recorded and compared between the study groups. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Quality of recovery by using QoR-15 questionnaire | postoperative 24th hour | — |
| Pain Scores | postoperative 0, 1, 2, 6, 12, 24 th hour | using NRS Scale |
Countries
Turkey (Türkiye)