Protocol Study for the Evaluation of Non-Opioid Balanced General Anaesthesia in Cardiac Surgery with Cardiopulmonary Bypass: A Randomised, Controlled, Multicentric Superiority Trial (OFACAR Study)

Author:

Guinot Pierre-Grégoire12ORCID,Besch Guillaume34ORCID,Hameury Bastien1,Grelet Tommy3,Mertes Paul Michel5,Nguyen Maxime12ORCID,Bouhemad Belaid1,

Affiliation:

1. Department of Anaesthesiology and Critical Care Medicine, Dijon University Medical Centre, 21000 Dijon, France

2. University of Burgundy and Franche-Comté, LNC UMR1231, F-21000 Dijon, France

3. Department of Anaesthesiology and Critical Care Medicine, Besançon Regional University Medical Centre, 25030 Besançon, France

4. EA3920, University of Franche-Comté, 25000 Besançon, France

5. Department of Anesthesia and Critical Care, University Hospital of Strasbourg, 67200 Strasbourg, France

Abstract

Opioid-free anaesthesia (OFA) is general anaesthesia based on the use of several non-opioid molecules that aim to have an analgesic effect, decrease the sympathetic response, decrease hormonal stress, and decrease the inflammatory response during surgery. Although this approach to anaesthesia is regularly used in clinical practice, it remains a novel approach. The literature on this anaesthesia modality finds a number of positive effects on cardiac, respiratory, and cognitive function but no randomised study evaluated these effects during cardiac surgery where there is a high incidence of postoperative complications. The main aim of the study is to compare OFA vs. standard balanced opioid general anaesthesia on the incidence of postoperative complications and the length of stay in intensive care and hospital. OFACAR is a multicentric, randomised, controlled, superiority, single-blind, two parallel-arm clinical trial in patients undergoing cardiac surgery with cardiopulmonary bypass. We compared a balanced general anaesthesia without opioids (OFA group) vs. a balanced opioid general anaesthesia with sufentanil (control group). One hundred and sixty patients will be enrolled in each treatment group. The primary endpoint is a composite one which corresponds to the occurrence of at least one of the postoperative complications, defined according to European standards within 30 days after surgery. Recruitment started in September 2019, and data collection is expected to end in November 2024.

Funder

university hospital of Dijon

French Ministry of Health

Publisher

MDPI AG

Subject

General Medicine

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