Opioid-Free Anesthesia in Cardiac Surgery
- Conditions
- Anesthesia
- Interventions
- Registration Number
- NCT04940689
- Lead Sponsor
- University Hospital, Rouen
- Brief Summary
The use of morphine derivatives is widespread for performing general anesthesia. However, opioids have their own side effects: respiratory depression, digestive ileus, cognitive dysfunction, postoperative hyperalgesia, nausea-vomiting or even negative effects on inflammation or adrenal function. The advent of new molecules, with analgesic properties that do not pass through opioid receptors, has allowed the emergence of the concept of anesthesia without morphine (opioid free anesthesia OFA). These molecules are essentially: dexmedetomidine, ketamine, lidocaine. Thus, the use of ketamine is currently recommended in the event of major surgery in order to limit postoperative pain and hyperalgesia. Likewise, the use of dexmedetomidine in place of an opioid during bariatric surgeries has been shown to reduce postoperative pain and intraoperative hemodynamic manifestations. In addition, it would also reduce the incidence of postoperative cognitive dysfunction. A recent meta-analysis even suggested a decrease in length of stay, mechanical ventilation, atrial fibrillation and mortality with the use of dexmedetomidine in the perioperative period. The combined use of various non-morphine analgesic molecules therefore opens the way to anesthesia without morphine, and a French multicenter study on this strategy in general non-cardiac surgery is currently underway. Cardiac surgery is characterized by significant postoperative pain, a high incidence of cognitive dysfunction, and frequent and sometimes significant respiratory complications. An OFA strategy could therefore be beneficial to these patients, but no study has yet addressed the subject.
- Detailed Description
The objective of our work is therefore to assess the beneficial effects of OFA versus strategy with intraoperative opioids on postoperative complications related to opioids.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 268
- Patients having planned cardiac surgery under cardiopulmonary bypass, with at least one coronary artery bypass grafting and rf at least one internal mammary artery as graft; possible association with aortic valve replacement
- Patient having red and understood the information letter and signed the consent form
- For women : of childbearing age, need to confirm the absence of an active pregnancy by a negative blood pregnancy test within 48 hours prior to inclusion / menopausal (amenorrhea not medically induced for at least 12 months before the inclusion visit)
- Patient affiliated to a social security scheme
- Preoperative treatment with morphine or its derivatives (including tramadol) in the 15 days preceding the inclusion visit
- Pre-existing high-degree conduction disorder
- Bradycardia < 50 bpm
- Oxygen therapy prior to inclusion
- Heart failure with LVEF <40%
- BMI ≥ 35 kg/m²
- Myocardial suffering in the 5 days preceding inclusion
- Patient in shock
- Known adrenal insufficiency and / or long-term systemic corticosteroid treatment (equivalent to hydrocortisone hemisuccinate ≥ 20 mg / day)
- Combined surgery other than aortic valve
- Long-term non-invasive ventilation (including for obstructive sleep apnea syndrome)
- Any antecedent or active practice (s) of drug addiction;
- Contraindication to one of the experimental and / or non-experimental treatments: dexmedetomidine, lidocaine, dexamethasone, ketamine, remifentanil or morphine
- Acute cerebrovascular pathology,
- Severe hepatic insufficiency (factor V level <50%),
- Pre-existing cognitive disorders,
- Patient for whom the CAM-ICU questionnaire cannot be carried out (deaf patients for example),
- Pregnant or parturient or breastfeeding woman
- Person deprived of liberty by an administrative or judicial decision or person placed under judicial protection / under guardianship or guardianship
- Patient participating in another drug trial or having participated in another drug trial within 1 month before randomization
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description OFA arm Dexmédétomidine 0.5 g/kg + lidocaine 1.5 mg/kg General anesthesia strategy without morphine * Within 10 minutes before the induction of general anesthesia: pre-induction dose of dexmedetomidine 0.5 g / kg and lidocaine 1.5 mg / kg by slow IV. * The anesthetic induction will be carried out by an intravenous hypnotic (propofol or etomidate) combined with an IV curare * The maintenance of the anesthesia will be carried out by propofol or a halogenated gas (sevoflurane or desflurane) in continuous administration (qsp bispectral index 40-60), dexmedetomidine 0.5-1.0 g / kg / h, lidocaine 2 mg / kg / h. The administration of curare will be carried out as needed. Standard arm Remifentanil General anesthesia strategy with morphine: * Within 10 minutes before the induction of general anesthesia: administration of a placebo of 50 mL of 0.9% NaCl by slow IV * The anesthetic induction will be carried out by an intravenous hypnotic (propofol or etomidate) combined with IV curare and remifentanil (morphine derivative) IV for a concentration target of 4 ng / mL. * Maintenance of anesthesia will be carried out with propofol or a halogenated gas (sevoflurane or desflurane) in continuous administration (qs bispectral index 40-60) and remifentanil (target concentration 1-10 ng / mL). The administration of curare will be carried out as needed. In order to anticipate the sudden end of the analgesia, an administration of morphine 0.15 mg / kg IV will be carried out 30 minutes before the end of the intervention as recommended
- Primary Outcome Measures
Name Time Method To assess the impact of general anesthesia strategy without the use of opioids (OFA) on the incidence of major postoperative complications related to opioids compared to the reference strategy using opioids. 48 hours post-surgery Composite criterion consisting of the appearance 48 hours after the surgery of an intestinal ileus, and / or of an alteration of the neurological state, and / or of an acute respiratory failure, and / or of a death
- Secondary Outcome Measures
Name Time Method To assess the intraoperative safety intraoperative periode Existence of bradycardia requiring atropine adminitsrtation and/or appearance of arterial hypotension or hypertension
To assess the impact of OFA on the incidence of postoperative nausea and vomiting. 48 hours post-surgery Existence of post-surgery nausea
To assess the impact of the OFA on the incidence of post-surgery adrenal insufficiency, 24 hours post-surgery Incidence of relative adrenal insufficiency 24 hours postoperatively by performing a synacthene test. An increase in cortisol levels \<250 nmol / L within one hour of the injection of 250 µg of tetracosactide is a diagnosis
Persistence of chronic pain evaluated during a telephone call 3 months after surgery neuropatic pain questionnaire (DN4), from 0 to 10
To assess the impact of OFA on the incidence of acute post-surgery renal failure, 48 hours post-surgery Onset of acute renal failure defined by a KDIGO score ≥ 1
Evaluate the impact of the OFA on the incidence of postoperative mortality Within 2 months after surgery Number of deaths
To assess the impact of OFA on the incidence of postsurgery pain. 48 hours post-surgery Number of post-surgery pain episodes at rest (VAS ≥ 3) and total morphine consumption
To assess the impact of OFA on the incidence of shock 48 hours post-surgery Presence of cardiogenic shock and vasoplegic syndrome
To assess the impact of OFA on the incidence of atrial rhythm disturbances and / or ventricular postsurgery shock states. 48 hours post-surgery Appearance of non-preexisting atrial fibrillation and/or of postsurgery ventricular rhythm disturbances and/or high degree cardiac conduction disorders
Evaluate the impact of the OFA on the impact of the length of ICU and hospital stay Evaluate the impact of the OFA on the impact of the length of post-surgeryhospital stay Within 2 months after surgery Number of days in the hospital
To assess the myocardial pain 48 hours post-surgery maximum troponin plasma level
Trial Locations
- Locations (5)
Amiens Univesrity Hospital
🇫🇷Amiens, France
Rouen University Hospital
🇫🇷Rouen, France, Normandy, France
Lille Hopistal University
🇫🇷Lille, France
Montpellier University Hospital
🇫🇷Montpellier, France
CAEN university Hospital
🇫🇷Caen, France