The purpose of this study is to compare the analgesic outcomes (time to first analgesic request, total amount of analgesic consumption, and pain scores) following the ultrasound-guided retroclavicular infraclavicular approach and the axillary approach in obese patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
90
The patient will be placed supine, head facing the contralateral side. A high- frequency 13-6 MHz linear array transducer probe will be placed medial to the coracoid process below and perpendicular to the clavicle to obtain a short-axis view of the cords of the brachial plexus and the axillary vessels. The needle will be inserted in the supraclavicular fossa, approximately one cm posteriorly to the clavicle, and advanced in plane parallel to the probe. After passing the initial blind zone of about 2 cm caused by the clavicle's acoustic shadow, the needle tip will be continuously seen, until it appears posterior to the axillary artery. A single injection of the local an esthetic will be performed without needle repositioning unless paresthesia is elicited
The axillary nerve block is performed from behind the patient with the patient seated. The axillary nerve will be identified within the quadrilateral space by placing high frequency linear probe parallel to the long axis of the humeral shaft. The nerve was identified next to the circumflex artery
faculty of medicine,zagazig university Egypt
Zagazig, Egypt
Time to first analgesic request in each group
Time frame: 24 hours postoperative
Block assessment and definition of successful block
Time frame: 30 minutes after the block
Imaging time
Time frame: the time between probe application and insertion of the needle
Needle time
Time frame: the time between insertion of the needle and complete injection of local anesthetic
-Procedure time
Time frame: the summation of the imaging and needling times
Pain intensity
10-point NRS \[(0 = no pain, 10 = worst imaginable pain), 1 - 3: Mild pain (nagging, annoying, slightly interfering with activities of daily living (ADLs), 4 - 6: Moderate pain (significantly interfering with ADLs, 7 - 10: Severe pain (disabling, unable to perform ADLs)\]
Time frame: basal, one, 2, 4, 8, 12, 16, 20 and 24 hours postoperative
Total analgesia need
Time frame: the first postoperative 24 hours
Duration of the sensory block
Time frame: first 24 hours postoperative
Duration of the motor block
Time frame: first 24 hours postoperative
Incidence of block complications
hematoma formation or paresthesia or local anesthetic systemic toxicity.
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Time frame: first 24 h0urs postoperative