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Opioid-free Anesthesia Protocol on the Early Quality of Recovery after Major Surgery (SOFA Trial): A Randomized Clinical Trial.
Léger, Maxime; Perrault, Tristan; Pessiot-Royer, Solène; Parot-Schinkel, Elsa; Costerousse, Fabienne; Rineau, Emmanuel; Lasocki, Sigismond.
Afiliação
  • Léger M; Anesthesia 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.
  • Perrault T; Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.
  • Pessiot-Royer S; Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.
  • Parot-Schinkel E; Biostatistics and Methodology Department, University Hospital Center of Angers, Angers, France.
  • Costerousse F; Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.
  • Rineau E; Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.
  • Lasocki S; Anesthesia and Intensive Care Department, University Hospital Center of Angers, Angers, France.
Anesthesiology ; 140(4): 679-689, 2024 Apr 01.
Article em En | MEDLINE | ID: mdl-37976460
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Analgésicos Opioides Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Anesthesiology Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Analgésicos Opioides Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Anesthesiology Ano de publicação: 2024 Tipo de documento: Article