Bariatric or General Abdominal Surgeries, Bariatric Surgery Patients
Conditions
Keywords
bariatric analgesia
Brief summary
This study investigates whether administering TAP blocks pre-incision provides superior postoperative pain control and reduces opioid use along with other medications compared to post-incision administration in patients undergoing elective abdominal surgeries.
Interventions
the TAP block is a regional anesthesia technique that targets the somatic nerves supplying the anterior abdominal wall.
Sponsors
Study design
Eligibility
Inclusion criteria
* Adults aged between 18 and 65 years * Scheduled for elective bariatric surgery or other elective general abdominal surgeries * Proficient in English sufficient to understand study procedures and communicate effectively * Capable of providing informed consent
Exclusion criteria
* Individuals under 18 years of age (minors) * Pregnant individuals * Prisoners * Individuals with cognitive impairments or otherwise unable to provide informed consent independently * Individuals with known allergies or contraindications to local anesthetics used in TAP blocks
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Mean change in opioid consumption (MME) from index procedure to 90 days post-op | Up to 90 days post-operatively | Opioid dosage quantities will be measured in morphine milligram equivalents (MME) |
| Change in Pain Scores from index procedure on a numerical rating scale | 1, 3, 6, 24, 48, and 72 hours postoperatively | Patient-reported pain on a scale of 1-10. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 1. Total Opioid Consumption in MME from Surgery to 90 Days Postoperatively | From end of surgery to 90 days post-op. | Sum of all opioid use from surgery to 90 days, in MME |
| Patient Satisfaction Score with Postoperative Pain Management at Discharge | At hospital discharge (within 3-5 days post-op) | Satisfaction score using a 5-point Likert scale survey before discharge. |
| Use of Non-Opioid Analgesics within 72 Hours | From end of surgery to 72 hours post-op | Count of participants receiving non-opioid pain medications (e.g. acetaminophen, NSAIDs) within 72 hours post-op, including amount and type. |
| Number of Participants with TAP Block-Related Adverse Events | From TAP block administration to 90 days post-op. | Incidence of adverse events (e.g. local anesthetic toxicity, infection, bleeding) related to TAP block. |
Countries
United States
Contacts
Weill Medical College of Cornell University