Patients undergoing coronary artery bypass grafting are at risk for perioperative myocardial ischemia. Episodes of tachycardia and hypertension, which are associated with an increase in myocardial oxygen consumption, are predictive events of these ischemia. During cardiac surgery by sternotomy, some maneuvers, e.g. intubation, skin incision, sternotomy and cannulation, may be associated with tachycardia and/or increases in blood pressure despite an adequate level of anesthesia. Usually these episodes are controlled by the administration of a high-dose of anesthetic agents. The parasternal block, by bolus or continuous infusion through a single catheter, showed its effectiveness on postoperative pain after sternotomy. It allows a blocking of anterior branches of intercostal nerves at the lateral edge of the sternum; branches in charge of innervation of the sternum and the overlying skin surface. The preoperative parasternal block, once general anesthesia performed, could provide an effective level of locoregional anesthesia of the chest wall, thus limiting the occurrence of episodes of tachycardia and / or hypertension without having to resort to massive doses of anesthetic agents during sternotomy in patients undergoing coronary bypass surgery.
This randomized double blinded placebo-controlled clinical trial will include patients undergoing coronary artery bypass grafting. Locoregional anesthesia of the chest wall will be performed under ultrasound, once general anesthesia performed. A total volume of 60 ml of sodium chloride 0.9% (placebo group) or ropivacaine 0.25% (experimental group) divided into 4 injections of 15 ml (2 per side, between ribs 2 and 3 and between ribs 4 and 5) will be injected.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
35
Injection of 60 ml of ropivacaine 0.25% divided into 4 injections of 15 ml (2 per side, between ribs 2 and 3 and between ribs 4 and 5)
Injection of 60 ml of sodium chloride 0.9% divided into 4 injections of 15 ml (2 per side, between ribs 2 and 3 and between ribs 4 and 5)
CMC Ambroise Paré
Neuilly-sur-Seine, Île-de-France Region, France
Show that the preoperative realization of a parasternal block limites the posology of remifentanil administered during sternotomies to maintain blood pressure and heart rate within recommended ranges
Maximal dose of remifentanil (morphine peak) required to maintain hemodynamic parameters (arterial blood pressure and heart rate) in the appropriate values during intubation, skin incision, sternotomy and sternal retractor setup
Time frame: Intraoperative period : from intubation to sternal retractor setup
Hemodynamic response : heart rate
Measure of heart rate in bpm
Time frame: Intraoperative period : from the start of general anesthesia maintenance to the fifth minute after sternal retractor setup
Hemodynamic response : arterial blood pressure
Measure of diastolic and systolic arterial blood pressure in mmHg
Time frame: Intraoperative period : from the start of general anesthesia maintenance to the fifth minute after sternal retractor setup
Hemodynamic response : patient state index
Measure of patient state index ranging from 0 to 100 (0=very deep anesthesia, 100=no hypnotic state)
Time frame: Intraoperative period : from the start of general anesthesia maintenance to the fifth minute after sternal retractor setup
Dose of hypnotic drug
Total amount of propofol administered during surgery
Time frame: Intraoperative period : from induction of anesthesia to skin closure
Dose of analgesic drug
Total amount of remifentanil administered during surgery
Time frame: Intraoperative period : from induction of anesthesia to skin closure
Inflammatory response
Serum concentrations of cytokines in pg/ml (composite : pro- (IL-6, IL-8, IL-1β, TNF-α, IFN-γ) and anti-inflammatory (IL-10) cytokines)
Time frame: 7 days
Pain level during extubation: Numeric scale
Numeric scale of pain, ranging from 0 to 10 (0 = no pain, 10= worst possible pain)
Time frame: 8 hours
Complications
Incidence of acute respiratory distress syndrome, pneumopathy, kidney failure or hypertension
Time frame: 7 days
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