Bariatric Surgery Candidate Clinical Trial
Official title:
Comparison Between Ultrasound-guided Erector Spinae Block and Transverse Abdominis Plane Block in Obese Patients Undergoing Sleeve Gasterectomy.
assess the efficacy of ultrasound guided erector spinae block to decrease the requirement for analgesics after laparoscopic sleeve gastrectomy and to decrease postoperative pain scores and opioid consumption compared to subcostal transverses abdominis block.
Primary outcomes
• Cumulative opioid consumption during the first 24 h postoperatively. For the purpose of
comparison, all opioids administered postoperatively will be converted to IV morphine
equivalent doses using standard opioid dosage conversion tables.
Secondary outcome parameters
1. Pain assessment by the aid of Visual analogue scale (VAS), which is consisted of a "10
cm" line with one end labeled no pain and other end labeled worst intolerable pain. The
patients marked the line at the point that best describing the pain intensity. The
preoperative assessment included training of the patients about (VAS) for postoperative
pain. The length of the line to the patient's mark will be measured and recorded
postoperative after 30 min., 4, 6, 8, and 24 hours.
2. Failure rate of the block will be calculated, where the block will be considered a
failed block if the patient requires more than two doses of rescue analgesia in the
first hour postoperatively.
3. Duration of surgery (from skin incision till skin closure) and general anesthesia (from
induction of GA till extubation).
4. Incidence of complications, such as: Nerve injury, Hematoma formation, LA toxicity, and
intravascular injection.
;
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