The interscalene brachial plexus blocks were performed preoperatively with the patient in the supine position with the head of bed elevated 30 degrees and the patient’s head slightly turned away from the operative side. For the block placement, patients received midazolam 0-2mg and/or fentanyl 0–100 mcg intravenously, according to the anesthesiologist’s discretion. Using sterile technique, a 6-13-MHz linear probe (LOGIQe, GE Healthcare, Wauwatosa, WI, USA) transducer was used to identify the C5-C6-C7 nerve roots of the brachial plexus. 2–3 mL of lidocaine 2% was used to anesthetize the skin using a 27-G needle. A 5 cm, 22-gauge insulated needle (SonoPlex Stim cannula, Pajunk, Geisingen, Germany) was used to perform a real-time ultrasound-guided interscalene nerve block using a posterior-to-anterior, in-plane needle insertion approach. A total of 25mL of ropivacaine 0.5% was injected in either the intraplexus or extraplexus location (S1 File). In the intraplexus group, the needle was advanced in a posterior-to-anterior direction through the middle scalene muscle, through the brachial plexus sheath in-between the C5-C6 nerve roots. Less than 1 mL of the local anesthetic was injected to confirm that the needle was positioned in the intraplexus location. The remainder of the local anesthetic was injected in divided doses. If the injection did not result in the expansion of the brachial plexus sheath, then it was repositioned so that the tip was within the brachial plexus sheath. In the extraplexus group, the needle was advanced above the C5 nerve root and anterior to the brachial plexus. One mL of local anesthetic was given to confirm the extraplexus location anterior to the brachial plexus sheath. A total of 12mL of ropivacaine 0.5% was administered in anterior to the brachial plexus. The needle was then withdrawn to the posterior surface of the brachial plexus and an additional 12mL of ropivacaine 0.5% was given. If any swelling of the brachial plexus sheath was seen, the needle was repositioned to the extraplexus location. All patients received less than 3 mg/kg of ropivacaine. Patients were instructed to notify the study team if they experienced any paresthesia during block placement. Paresthesia was defined as an abnormal sensation either during or after block placement that felt like “tingling, pins and needles, or electricity down the arm.” Anesthesia providers were instructed to stop the block procedure if a paresthesia occurred, to redirect the needle, and to not resume local anesthetic administration until the paresthesia resolved. The block performance time, number of needle passes, and paresthesias were recorded by the study team.

After block placement, sensory and motor examinations were performed at one minute intervals, until there was decrease in sensory exam or until the patient left the preoperative area for the operating room. Patients were assessed for time to complete loss of shoulder abduction by having the patient sit upright and attempt to abduct the arm to 90 degrees. Sensation was assessed using pinprick and comparing to the contralateral side in the sensory distributions of the brachial plexus (axillary, supraclavicular, musculocutaneous, median, ulnar and radial). The time when the sensation first started to feel less sharp compared to the contralateral, non-blocked side was recorded to the nearest minute. Patients were also assessed for signs of Horner’s syndrome, hoarseness and dyspnea post-block administration.

All patients then underwent a standardized general anesthetic with a propofol induction and laryngeal mask airway placement. Anesthesia was maintained using a combination of volatile anesthetics (sevoflurane or desflurane with oxygen/air mixture) and propofol infusion (25–100 mcg/kg/min). Patients received dexamethasone 4 mg IV after induction and ondansetron 4 mg IV prior to emergence as PONV prophylaxis. Fentanyl was administered intravenously during the case per the anesthesiologist’s discretion. Sensory exam was reassessed in the recovery room using pinprick. Pain scores were assessed using the Numerical Rating Scale (NRS) from 0–10, where zero is no pain and ten is the worst imaginable pain. Highest NRS pain score in recovery room, perioperative opioid and antiemetic use were recorded, as well as recovery room length of stay and incidence of PONV. Patients were counselled to take oral analgesics on a schedule for the first 24 hours post-operatively.

Patients were contacted by telephone on the day following surgery (at least 24 hours after block placement) to assess block duration, highest pain score at rest and with movement in the 24 hours after block placement, opioid consumption, post-discharge nausea/vomiting and patient satisfaction score. Pain scores were also recorded one week postoperatively.

Note: The content above has been extracted from a research article, so it may not display correctly.

Please log in to submit your questions online.
Your question will be posted on the Bio-101 website. We will send your questions to the authors of this protocol and Bio-protocol community members who are experienced with this method. you will be informed using the email address associated with your Bio-protocol account.

We use cookies on this site to enhance your user experience. By using our website, you are agreeing to allow the storage of cookies on your computer.