General Anesthesia, Obesity
Conditions
Keywords
General anesthesia, Obesity, Propofol pharmacokinetic, Remifentanyl pharmacokinetic
Brief summary
This prospective monocentric phamacokinetics study aims to compare plasmatic concentrations of Propofol and Remifentanil required to target a specific range of monitored anesthesia and analgesia during sus-mesocolic surgery in obese and non obese patients.
Detailed description
Remifentanil and Propofol are administered intravenously as an opioid pain reliever and hypnotic pain reliever during anesthesia. Their advantages are numerous: short half-life allowing anesthesia and rapid awakening, little accumulation, allowing to adapt the level of anesthesia or sedation to each patient, few side effects. Entropy° is an index derived from the electroencephalographic signal of patients, validated for the evaluation of the level of narcosis during general anesthesia. ANI ° (nociception index analgesia) is an index using the ventilatory physiological variability of the sinus rhythm validated to monitor patient's analgesia during general anesthesia. These non-invasive means of analgesia and sedation monitoring allows the clinician to ensure satisfactory levels of anesthesia by administering products at minimum effective doses. The authors propose to determine whether, for a comparable target effect (analgesia and monitored sedation), plasmatic concentrations and administration rates of propofol and remifentanil necessary during general anesthesia for a comparable surgical stimulus are the same in populations of obese and non obese patients.
Interventions
DRUGPharmacokinetic of propofol and remifentanil
Pharmacokinetic of propofol and remifentanil in both population: Obese and non Obese patients
Sponsors
University Hospital, Clermont-Ferrand
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)
Intervention model description
Each obese patient is matched with a non-obese patient by considering a pairing according to age (more or less 5 years), gender and renal function (more or less 10ml / min / 1.73m² creatinine clearance).
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Obese patients group: * Age ≥ 18 years old * Severe and morbidly obese patients (35kg / m2≤IMC \<55kg / m2). * Patients undergoing general anesthesia for laparoscopic susmesocolic surgery (bariatric surgery or cholecystectomy). * Patients who have given their consent in the manner described by the public health law of August 9, 2004. * Patients benefiting from a Social Security scheme. Group of non-obese patients: * Age ≥ 18 years old * Patients with normal weight or slightly overweight (19 \<BMI \<30). * Patients receiving general anesthesia for laparoscopic susmesocolic surgery (cholecystectomy). * Patients who have given their consent in the manner described by the public health law of August 9, 2004. * Patients benefiting from a Social Security scheme.
Exclusion criteria
* Patient refusal * Age \<18 years old * Protected adults and vulnerable persons * Pace maker * General anesthesia in the 24 hours preceding this surgery * Proven or suspected dysautonomia * Premedication by gabapentin Neurontin ° * Locoregional peri-medullary analgesia technique used concomitantly during the pre- and intraoperative period. * Unbalanced dysrhythmic heart disease (AC / FA; extrasystoles; non-sinus rhythm) * Pregnant or breastfeeding woman * Intubation impossible planned * Hypersensitivity to the products used * Allergy to peanut or soy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Plasma concentration of Propofol | 5 minutes after the insufflation of the pneumoperitoneum | Plasma concentration of Propofol at different times during the maintenance phase of general anesthesia |
| Plasma concentration of Remifentanil | 5 minutes after the insufflation of the pneumoperitoneum | Plasma concentration of Remifentanil at different times during the maintenance phase of general anesthesia |
Countries
France
Outcome results
None listed