Overview

Evaluate the Muscle Protection Effect of Sevoflurane Sedation in Vascular Surgery

Status:
Completed
Trial end date:
2018-10-19
Target enrollment:
0
Participant gender:
All
Summary
Halogenated anaesthetic agents (HAA) may induce protective processes by pre-conditioning the myocardium. All of the literature shows that HAA induce pre-conditioning, thanks to a class effect, and Sevoflurane is the most widely used today. In humans, the protective effects of halogenated agents have principally been studied in heart surgery and have shown encouraging clinical results. It seems that HAA induce both pre-conditioning of the myocardium (early and late) and post conditioning. Given these protective effects of HAA, in 2007, the American Heart Association (AHA) recommended the use of HAA for anaesthesia maintenance in non-cardiac surgery in patients with a high cardio-vascular risk. The aim of this study is to show a decrease in rhabdomyolysis and tissue distress (kidneys, myocardium and liver), thanks to Sevoflurane anaesthesia, in the post-operative period following vascular surgery with clamping
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Centre Hospitalier Universitaire Dijon
Treatments:
Anesthetics
Propofol
Sevoflurane
Criteria
Inclusion Criteria:

- persons who have provided written consent

- patients over 18 years of age

- patients undergoing scheduled vascular surgery with high clamping for:

- Abdominal aortic aneurysm

- suprapopliteal vascular bypass (aorto-bi-femoral, femoral trifurcation, ilio-femoral
or femoro-femoral, femoro-popliteal).

Exclusion Criteria:

- persons without health insurance cover

- patients younger than 18 years of age, pregnant or breast-feeding women and adults
under guardianship

- patients with epilepsy

- emergency surgery

- patient presenting a contra-indication for Sevoflurane: hypersensitivity to
sevoflurane or to other halogenated anaesthetic agents, myopathy, hyper-eosinophilia,
immunoallergic hepatitis, known or suspected genetic predisposition to malignant
hyperthermia

- patients presenting a contra-indication to the use of Propofol: known hypersensitivity
to propofol or to one of the constituents of the product, allergy to peanuts or soja

- Patients presenting a contra-indication for sufentanil: hypersensitivity to sufentanil
or to opioids

- Association with opioid agonists-antagonists or partial opioid antagonists

- patients presenting a CI for the use of Cisatracurium: history of allergy or
hypersensitivity to cisatracurium or atracurium

- patients presenting cardiac, respiratory, renal or kidney failure, hypovolemia, poor
general health

- Patients with a risl of prolongation of the QT interval

- Patients with end-stage renal failure - requiring dialysis