Opioid-free Anesthesia Protocol on the Early Quality of Recovery after Major Surgery (SOFA Trial): A Randomized Clinical Trial

Author:

Léger Maxime1ORCID,Perrault Tristan2,Pessiot-Royer Solène3,Parot-Schinkel Elsa4,Costerousse Fabienne5,Rineau Emmanuel6,Lasocki Sigismond7

Affiliation:

1. 1Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France; and Department of Anesthesia and Perioperative Care, University of California–San Francisco, San Francisco, California.

2. 2Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.

3. 3Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.

4. 4Biostatistics and Methodology Department, University Hospital Center of Angers, Angers, France.

5. 5Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.

6. 6Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.

7. 7Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.

Abstract

Background Opioid-free anesthesia is increasingly being adopted to reduce opioid consumption, but its impact on early postoperative recovery after major surgery has not been evaluated in comparative trials. The hypothesis was that an opioid-free anesthesia protocol would enhance the early quality of recovery for patients undergoing scheduled major surgery under general anesthesia. Methods The SOFA study was a monocentric, randomized, controlled, assessor- and patient-blinded clinical trial conducted from July 10, 2021, to February 12, 2022. The eligible population included male and female patients undergoing scheduled major surgery, excluding bone procedures, that typically require opioids for postoperative pain management. Patients in the intervention group received a combination of at least two drugs among ketamine, lidocaine, clonidine, and magnesium sulfate, without opioids for anesthesia. The standard group received opioids. The primary outcome was early postoperative quality of recovery, assessed by Quality of Recovery-15 score at 24 h after surgery. Secondary outcomes were Quality of Recovery-15 at 48 and 72 h after surgery, incidence of chronic pain, and quality of life at 3 months. Results Of the 136 randomized patients, 135 were included in the primary analysis (mean age, 45.9 ± 15.7 yr; 116 females [87.2%]; 85 underwent major plastic surgery [63.9%]), with 67 patients in the opioid-free anesthesia group and 68 in the standard group. The mean Quality of Recovery-15 at 24 h was 114.9 ± 15.2 in the opioid-free anesthesia group versus 108.7 ± 18.1 in the standard group (difference, 6.2; 95% CI, 0.4 to 12.0; P = 0.026). Quality of Recovery-15 scores also differed significantly at 48 h (difference, 8.7; 95% CI, 2.9 to 14.5; P = 0.004) and at 72 h (difference, 7.3; 95% CI, 1.6 to 13.0; P = 0.013). There were no differences in other secondary outcomes. No major adverse events were noticed. Conclusions The opioid-free anesthesia protocol improved quality of recovery after major elective surgery in a statistically but not clinically significant manner when compared to standard anesthesia. Editor’s Perspective What We Already Know about This Topic What This Article Tells Us That Is New

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

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