Nerve Block, Regional Anesthesia, Upper Extremity Surgery
Conditions
Keywords
axillary block, interfascial block, regional anesthesia
Brief summary
Hand, wrist, and forearm surgeries are commonly performed procedures with significant postoperative pain potential. Regional anesthesia of the brachial plexus via the axillary approach is one of the gold-standard techniques for distal upper-limb surgery. In the conventional (classic) axillary block, the median, ulnar, and radial nerves within the axillary sheath are individually targeted under ultrasound guidance; however, anatomical septations around the axillary artery may prevent homogeneous spread of local anesthetic, leading to a patchy block and reduced intraoperative success. The interfascial axillary block is a modified approach in which local anesthetic is deposited into the fascial planes between the axillary muscles rather than directly into the nerve sheath, aiming for passive diffusion, homogeneous spread, and fewer needle manipulations. This prospective, randomized, single-center study compares the classic axillary block with the interfascial axillary block in patients undergoing hand, wrist, and forearm surgery, primarily in terms of surgical anesthesia adequacy (block success).
Detailed description
This is a prospective, randomized, single-center clinical trial conducted in a Department of Anesthesiology and Reanimation. Randomization is performed using the sealed-envelope method. A total of 110 patients (55 per group) aged 18-90 years, American society of anesthesiologists physical status I-III, scheduled for elective hand, wrist, or forearm surgery under ultrasound-guided regional anesthesia will be enrolled. Group 1 (Classic Axillary Block) receives an ultrasound-guided block targeting the median, ulnar, and radial nerves perineurally/perivascularly within the axillary sheath. Group 2 (Interfascial Axillary Block) receives an ultrasound-guided injection of local anesthetic into the potential fascial planes between the axillary muscles, relying on passive diffusion. The primary outcome is surgical anesthesia adequacy (block success). Secondary outcomes include block application time, sensory and motor block onset, rates of additional local infiltration and conversion to general anesthesia, intraoperative additional analgesic/sedation requirements, hemodynamic parameters, patient and surgeon satisfaction, and complications.
Interventions
Classic (perivascular/perineural) axillary brachial plexus block
Interfascial (fascial-plane) axillary brachial plexus block.
Sponsors
Study design
Eligibility
Inclusion criteria
* Aged 18-90 years * American society of anesthesiologists physical status I-II-III * Scheduled for elective hand, wrist, or forearm surgery * Written informed consent obtained
Exclusion criteria
* History of local anesthetic allergy * Coagulation disorder * BMI \> 40 kg/m² * Infection at the block site * Chronic pain syndrome * Pregnancy * Inability to communicate * Need for emergency surgery
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Surgical anesthesia adequacy (block success) | 30 minutes after block | Complete sensory and motor blockade of the surgical field, allowing the operation to be completed without additional local infiltration or conversion to general anesthesia |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Block application time | intraoperative | time from needle insertion to withdrawal. |
| Sensory block onset time | 5., 10., 15., 30. minutes | Pin-Prick test in the median, ulnar, radial, and musculocutaneous dermatomes (0: normal, 1: blunt, 2: no sensation). |
| Motor block onset time | 5., 10., 15., 30. minutes | — |
| Intraoperative additional analgesic/sedation consumption | intraoperative | — |
| Patient and surgeon satisfaction | end of surgery | 4-point Likert scale (1: very poor, 4: very good) |
Countries
Turkey (Türkiye)