Jean Selim1, Xavier Jarlier2, Thomas Clavier3, Fairuz Boujibar4, Marie-Mélody Dusséaux2, Juliette Thill2, Céline Borderelle2, Vanessa Plé2, Jean-Marc Baste4, Emmanuel Besnier5, Zoubir Djerada6, Vincent Compère2. 1. Department of Anesthesiology and Critical Care, Rouen University Hospital, Rouen, France; Normandy Univ, UNIROUEN, INSERM U1096, FHU REMOD-VHF, Rouen, France. Electronic address: dr.jeanselim@gmail.com. 2. Department of Anesthesiology and Critical Care, Rouen University Hospital, Rouen, France. 3. Department of Anesthesiology and Critical Care, Rouen University Hospital, Rouen, France; Department of Thoracic Surgery, Rouen University Hospital, Rouen, France. 4. Normandy Univ, UNIROUEN, INSERM U1096, FHU REMOD-VHF, Rouen, France; Department of Thoracic Surgery, Rouen University Hospital, Rouen, France. 5. Department of Anesthesiology and Critical Care, Rouen University Hospital, Rouen, France; Normandy Univ, UNIROUEN, INSERM U1096, FHU REMOD-VHF, Rouen, France. 6. Department of Pharmacology, EA3801, SFR CAP Santé, Reims University Hospital, Reims, France.
Abstract
BACKGROUND: Adequate postoperative morphine consumption and pain management after thoracic surgery are major issues in the prevention of respiratory complications. Opioid-free anesthesia (OFA) may decrease morphine consumption and postoperative pain. The objective of this study was to evaluate the impact of OFA on the consumption of morphine and pain after video-assisted thoracic surgery or robotic-assisted thoracic surgery. METHODS: The main objective of this retrospective study with propensity score analysis (PSA) was to compare the cumulative postoperative morphine consumption at 48 hours between an OFA group receiving dexmedetomidine, lidocaine, and ketamine; and an opioid anesthesia (OA) group receiving remifentanil plus morphine. Postoperative pain at 24 and 48 hours and respiratory and hemodynamics complications were also assessed. RESULTS: Eighty-one patients were included, 48 in the OFA group and 33 in the OA group. The cumulative postoperative morphine consumption at 48 hours was lower in the OFA group than in the OA group (28.5 mg [0 to 62.25 mg] vs 55 mg [34 to 79.5 mg], P = .002, with PSA; OFA -27.67 mg [-46 mg to -11.5 mg], P = .002). The postoperative pain score was significantly lower in the OFA group compared with the OA group at 24 hours (2 [0 to 4] vs 3 [2 to 5], P = .064, with PSA; OFA -1.40 [-2.47 to -0.33], P = .0088) and 48 hours (0 [0 to 3] vs 2.5 [0 to 5], P = .034, with PSA; OFA -1.87 [-3.45 to -0.28], P = .021). There were no differences between groups concerning respiratory or hemodynamic complications. CONCLUSIONS: Our results suggest that OFA after video-assisted thoracic surgery or robotic-assisted thoracic surgery is safe and is associated with less postoperative morphine cumulative consumption and pain at 48 hours.
BACKGROUND: Adequate postoperative morphine consumption and pain management after thoracic surgery are major issues in the prevention of respiratory complications. Opioid-free anesthesia (OFA) may decrease morphine consumption and postoperative pain. The objective of this study was to evaluate the impact of OFA on the consumption of morphine and pain after video-assisted thoracic surgery or robotic-assisted thoracic surgery. METHODS: The main objective of this retrospective study with propensity score analysis (PSA) was to compare the cumulative postoperative morphine consumption at 48 hours between an OFA group receiving dexmedetomidine, lidocaine, and ketamine; and an opioid anesthesia (OA) group receiving remifentanil plus morphine. Postoperative pain at 24 and 48 hours and respiratory and hemodynamics complications were also assessed. RESULTS: Eighty-one patients were included, 48 in the OFA group and 33 in the OA group. The cumulative postoperative morphine consumption at 48 hours was lower in the OFA group than in the OA group (28.5 mg [0 to 62.25 mg] vs 55 mg [34 to 79.5 mg], P = .002, with PSA; OFA -27.67 mg [-46 mg to -11.5 mg], P = .002). The postoperative pain score was significantly lower in the OFA group compared with the OA group at 24 hours (2 [0 to 4] vs 3 [2 to 5], P = .064, with PSA; OFA -1.40 [-2.47 to -0.33], P = .0088) and 48 hours (0 [0 to 3] vs 2.5 [0 to 5], P = .034, with PSA; OFA -1.87 [-3.45 to -0.28], P = .021). There were no differences between groups concerning respiratory or hemodynamic complications. CONCLUSIONS: Our results suggest that OFA after video-assisted thoracic surgery or robotic-assisted thoracic surgery is safe and is associated with less postoperative morphine cumulative consumption and pain at 48 hours.
Authors: Jean Selim; Marc Selim; Zoé Demailly; Thierry Wable; Thomas Clavier; Emmanuel Besnier; Bertrand Dureuil; Benoît Veber; Zoubir Djerada; Vincent Compere Journal: Front Med (Lausanne) Date: 2022-04-21