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Opioid-free anaesthesia The need for evidence-based proofs

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(1)Opioid-free anaesthesia The need for evidence-based proofs H Beloeil. To cite this version: H Beloeil. Opioid-free anaesthesia The need for evidence-based proofs. Anaesthesia Critical Care & Pain Medicine, Elsevier Masson, 2019, 38 (5), pp.455. �10.1016/j.accpm.2019.05.002�. �hal-02150351�. HAL Id: hal-02150351 https://hal-univ-rennes1.archives-ouvertes.fr/hal-02150351 Submitted on 1 Jul 2019. HAL is a multi-disciplinary open access archive for the deposit and dissemination of scientific research documents, whether they are published or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers.. L’archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d’enseignement et de recherche français ou étrangers, des laboratoires publics ou privés..

(2) Opioid-free anaesthesia: the need for evidence-based proofs H. Beloeil Rennes University, INSERM, INRA, Rennes University Hospital, CIC 1414, Numecan, Department of Anaesthesia and Intensive Care, F-35033 Rennes, France. Helene.BELOEIL@chu-rennes.fr. IP T. Keywords: OFA, thoracotomy, thoracic surgery Opioid-free anaesthesia (OFA) is an emerging technique and a recent research perspective. OFA is based on the idea that avoiding intraoperative opioids would be associated with. SC R. better postoperative outcomes. Reducing opioids during general anaesthesia have been. proposed for many years in the literature. OFA is based on the concept of multimodal anaesthesia, as one drug will not replace opioids. It is the association of drugs and/or techniques that allows a good quality OFA. The association can combine NMDA antagonists. drugs. (NSAID,. dexamethasone,. LA). and. alpha-2. agonists. N. anti-inflammatory. U. (ketamine, lidocaine, magnesium sulfate), sodium channel blockers [local anaesthetics (LA)],. (dexmetedomidine, clonidine). Of course, all these drugs/techniques will not be administered. A. to the same patient. Indeed, for toxicity reasons, LA can only be administered by one route at. M. a time (either regional anaesthesia/analgesia or IV lidocaine). For haemodynamic stability, alpha-2 agonists are the drugs of choice and magnesium sulfate could also help. They are. TE D. however associated with a risk of hypotension and bradycardia. Indeed, all these drugs administered alone have documented side effects, which have to be known and prevented by anaesthesiologists. OFA is feasible but is it associated with clinically meaningful benefits for patients? Proofs are scarce in the literature. In the past 10 years, only 10 RCTs have. EP. been published on the subject. They reported a benefit of OFA in terms of postoperative morphine consumption (1), pain intensity (2) and postoperative nausea and vomiting (3). However, these studies were usually small (from 20 to 124 patients) and the results need to. CC. be confirmed by large-scale studies. In this issue of ACCPM, Bello et al. (4) suggest a retrospective study on the potential benefits associated with OFA in thoracic surgery. They. A. compared postoperative pain relief after OFA or opioid-based anaesthesia with both groups receiving a thoracic epidural analgesia (TEA). Despite the methodological flaws and the small number of patients, this study is of interest, as studies on OFA during thoracic surgery have not been published so far. Indeed, thoracic surgery being one of the most painful surgery, one could hypothesize that OFA would be of interest to reduce postoperative pain. Despite being not clinically meaningful, the authors choose the cumulative first 48 postoperative hours epidural ropivacaine consumption as the primary outcome. It was.

(3) significantly lower in the OFA group. More interestingly, patients were less painful 6 and 24 hours after the surgery with lower morphine consumption in PACU in the OFA group. These first results should be further confirmed with a RCT. OFA is a new exciting technique! However, it cannot be formally recommended as further evidence-based proofs of its benefits are needed.. A. CC. EP. TE D. M. A. N. U. SC R. IP T. Disclosure: BBraun, Aspen, Orion.

(4) References 1) Hwang et al. Dexmedetomidine versus remifentanil in postoperative pain control after spinal surgery: a randomized controlled study. BMC Anesthesiol 2015; 15:21. 2) Mullier et al. A Randomized Controlled, Double-Blind Trial Evaluating the Effect of Opioid-Free Versus Opioid General Anaesthesia on Postoperative Pain and. 3) Ziemann-Grimmel. et. al.. Opioid-free total. intravenous. IP T. Discomfort Measured by the QoR-40. J Clin Anesth Pain Med 2018; 2: 15 anaesthesia. reduces. postoperative nausea and vomiting in bariatric surgery beyond triple prophylaxis. Br J. SC R. Anesth 2014; 112:906-11. 4) Bello et al. Effect of opioid-free anaesthesia on postoperative epidural ropivacaine requirement after thoracic surgery: A retrospective unmatched case-control study.. A. CC. EP. TE D. M. A. N. U. ACCPM 2019.

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