Transversus Abdominis Block
Conditions
Keywords
transversus abdominis plane block, Dexmedetomidine, Fentanyl
Brief summary
The perioperative management of pain following lower abdominal surgery can pose a challenge to anesthesia providers. Conventional practice has involved the use of opioids as well as neuraxial analgesic techniques. Unfortunately, these therapies are not without potential risks and side effects. These include nausea, vomiting, pruritus, urinary retention, constipation, respiratory depression, and sedation.
Detailed description
One method used in this multimodal approach is the transversus abdominis plane block. This block, as first described by Rafi. in 2001, provides analgesia to the anterolateral abdominal wall. In 2007, McDonnell et al. further studied this technique in patients undergoing large-bowel resection. He discovered a reduction in postoperative pain and morphine consumption in the first 24 hours postoperatively, resulting in fewer opioid mediated side effects. In this same year, Hebbard et al. described the use of ultrasound guidance to provide real-time imaging of the muscle layers and needle placement to improve transversus abdominis plane block accuracy. In 2008, Hebbard. described the subcostal approach of transversus abdominis plane block, to target the nerves of the upper abdomen. Transversus abdominis plane blocks continue to be studied and developed as an effective method for providing analgesia for numerous types of transverses abdominis plane block duration is limited to effect of administered local anesthetics.The use of an infusion catheter to administer local anesthetics is an option to prolong the block's duration. Recently, adjuvant medications were added to local anesthetics to prolong the effect of transverses abdominis plane block .
Interventions
Patients will receive Levobupivacaine 5%
Patients will receive Levobupivacaine 5% + 1 µg/kg dexmedetomedine
Patients will receive Levobupivacaine 5% + 1 µg/kg fentanyl
Sponsors
Study design
Eligibility
Inclusion criteria
* ASA physical status II-III, * scheduled for uncomplicated elective paraumbilical hernia repair.
Exclusion criteria
1. Patient refusal to participate in the study 2. Patients with coagulopathy or under anticoagulation therapy. 3. Infection near the site of needle insertion. 4. Body mass index \> 40kg/m2 5. Patients with any neurological or neuromuscular disorder or history of seizures.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| first analgesic request | 24 hours | first time to call for analgesia |
Countries
Egypt