The aim of this study is to determine whether the costoclavicular approach (CC) provides
a better sensory block 48 hours after catheter installation than the infraclavicular
block performed by the paracoracoid approach (PC).
In the context of continuous perineural blocks performed on an outpatient basis, LAs are
delivered after insertion of a catheter by a low flow elastomeric pump (maximum 5 mL/h).
Considering that the nerve structures are closer to each other with the CC approach, the
investigators hypothesize that with the same mode of administration, the efficacy of the
continuous block at 48 h obtained by the CC approach will be greater than the block
produced by the PC approach.
Methods
Patients scheduled to undergo an upper limb surgery requiring a continuous
infraclavicular nerve block will be contacted by a member of the research team before
surgery to receive information regarding the study and obtain informed consent.
After obtaining consent, participants will be randomly assigned to two groups:
Group A: Placement of an infraclavicular perineural catheter by paracoracoid approach;
Group B: Placement of an infraclavicular perineural catheter using a costoclavicular
approach.
Only the anesthesiologist performing the technique and his assistant will know the group
to which the patient has been assigned. The blocks will be carried out in a standardized
manner and in accordance with the establishment's procedures. After bringing the patient
to the induction room and installing the recommended monitoring equipment, the
anesthesiologist will administer an intravenous premedication. The patient will be
installed in a supine position. After disinfecting the skin, the anesthesiologist will
inject a small amount of local anesthetic to numb the skin in the area where the block
will be performed and then locate the nerve bundles under ultrasound guidance using the
approach to which the patient has been assigned (Group A or B). When the area has been
located, the injection of a local anesthetic (bupivacaine) will be performed and the
catheter installed and fixed. Multimodal analgesia will be used for postoperative pain
relief including acetaminophen, non-steroidal anti-inflammatory drugs and hydromorphone
as needed.
Thirty minutes after the catheter insertion, a sensory-motor assessment of the blocked
territory will be performed. During surgery, the patient may be sedated or receive
general anesthesia at the discretion of the anesthesiologist. The surgery will be
performed according to the usual procedure.
In day-care surgery, a disposable elastomeric pump will be installed to ensure the
perineural infusion of LA. The patient will receive the usual information about
postoperative analgesia and the use of the pump. Follow-up details will be reviewed with
the patient prior to discharge from hospital.
A follow-up teleconsultation will be made the day after surgery and two days after
surgery. As part of these calls, the following items will be assessed: sensory level and
motor function of the forearm, level of pain and opioid use, presence of side effects,
quality of sleep and satisfaction towards the analgesic technique used.
All patients will benefit from a daily follow-up call by nurses from the Acute Pain
Service (APS) for up to 72 hours. In the absence of adverse effects, catheters will be
removed by patients 72 hours after surgery.