The hypothesis of this study is that a reduced extrafascial volume of local anesthetic for an interscalene brachial plexus block is associated with a lower incidence of diaphragmatic hemiparalysis after an arthroscopic surgery of the shoulder, without any reduction of the analgesic efficacy.
The hypothesis of this study is that a reduced extrafascial volume of local anesthetic for an interscalene brachial plexus block is associated with a lower incidence of diaphragmatic hemiparalysis after an arthroscopic surgery of the shoulder, without any reduction of the analgesic efficacy. Our prospective randomized controlled trial will include two parallel groups: a group will receive a volume of 20 mls of ropivacaine 0.75%, while the other group will receive a volume of 10 mls. All participants will have a preoperative ultrasound-guided interscalene brachial plexus with an extrafascial injection of 10 or 20 mls of ropivacaine 0.75%. In both groups, participants will have an examination of the hemidiaphgragm with the ultrasound, before and 30 min after the block. The respiratory function will also be assessed with a bedside spirometer before and after the block, and at 12 and 24 postoperative hours. During surgery all participants will receive multimodal analgesia inclusive of iv dexamethasone 8 mg, iv magnesium sulfate 40 milligram kg\^2, iv ketorolac 30 milligrams, and iv acetaminophen 1000 milligrams, according to the current practice in our institution. In the postoperative period, Participants will be prescribed an IV pca of morphine. Assignment to one of these two groups will be done according to a computer-generated list of random numbers, and the sealed envelopes method will be used.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
60
10 ml extrafascial interscalene brachial plexus block
20 ml extrafascial interscalene brachial plexus block
CHUV (Centre Hospitalier Universitaire Vaudois)
Lausanne, Canton of Vaud, Switzerland
Incidence of hemidiaphragmatic paralysis
Time frame: 30 minutes after the interscalene plexus brachial extrafascial injection
Incidence of hemidiaphragmatic paralysis
Time frame: at 2 and 24 postoperative hours
Presence of Dyspnea
Verbal question to the patient if he has dyspnea or not
Time frame: in phase 1 recovery and at 12 and 24 postoperative
Presence of PONV
Verbal question to the patient if he has dyspnea or not
Time frame: in phase 1 recovery and at 12 and 24 postoperative
Presence of Pruritus
Verbal question to the patient if he has pruritus or not
Time frame: in phase 1 recovery and at 12 and 24 postoperative hours
Presence of Claude-Bernard-Horner syndrome
Examination of the patient
Time frame: in phase 1 recovery and at 12 and 24 postoperative hours
Presence of Dysphonia
Verbal question to the patient if he has dysphonia or not
Time frame: in phase 1 recovery and at 12 and 24 postoperative hours
Forced expiratory volume in one second
in liters per second
Time frame: 30 minutes after the interscalene plexus brachial extrafascial injection, and at 2, 12 and 24 postoperative hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Forced vital capacity
in liters
Time frame: 30 minutes after the interscalene plexus brachial extrafascial injection, and at 2, 12 and 24 postoperative hours
Peak expiratory flow
in liters per second
Time frame: 30 minutes after the interscalene plexus brachial extrafascial injection, and at 2, 12 and 24 postoperative hours
Installation time of sensory block
in minutes
Time frame: up to 30 minutes after the interscalene plexus brachial extrafascial injection
Installation time of motor block
in minutes
Time frame: up to 30 minutes after the interscalene plexus brachial extrafascial injection
Time to first dose of postoperative iv morphine
in hours
Time frame: up to 24 hours postsurgery
Pain scores at rest
Numeric pain intensity scale. Pain scores range from zero (no pain) to 10 (worst possible pain)
Time frame: in phase 1 recovery and at 12 and 24 postoperative hours
Pain scores on movement
Numeric pain intensity scale. Pain scores range from zero (no pain) to 10 (worst possible pain).
Time frame: in phase 1 recovery and at 12 and 24 postoperative hours
Cumulative postoperative iv morphine consumption
in milligrams
Time frame: in phase 1 recovery and at 12 and 24 postoperative hours
Duration of analgesic block
in minutes
Time frame: up to 24 hours postsurgery
Duration of motor block
in minutes
Time frame: up to 24 hours postsurgery
Duration of sensory block
in minutes
Time frame: up to 24 hours postsurgery
Satisfaction of the participants
Numeric satisfaction intensity scale. Satisfactions range from 0 (totally unsatisfied) to 10 (maximal satisfaction).
Time frame: at 24 postoperative hours