Comparison of the effects of opioid-free anesthesia (OFA) and opioid-based anesthesia (OBA) on postoperative analgesia and intraoperative hemodynamics in patients undergoing spine surgery: A prospective randomized double-blind controlled trial.
Ugrani S Rani, Nidhi B Panda, Rajeev Chauhan, Shalvi Mahajan, Narender Kaloria, Manjul Tripathi
Saudi journal of anaesthesia January 1, 2024 DOI: 10.4103/sja.sja_341_23 via PubMed
Summary
AI-generated from the abstractOpioid-free anesthesia using ketamine and ketofol provided a significantly longer pain-free period after thoracolumbar spine surgery compared to opioid-based anesthesia with fentanyl and propofol. The mean pain-free period was 9.86 hours in the opioid-free group versus 6.93 hours in the opioid-based group. Total fentanyl requirement over 48 hours was considerably lower in the opioid-free group. However, hypertension occurred more often in the opioid-free group (46% of patients), while hypotension was more common in the opioid-based group (43%). Postoperative nausea and vomiting was less frequent with opioid-free anesthesia at 2 and 6 hours. The authors suggest careful titration of drug infusion rates is needed to manage blood pressure differences.
Study at a glance
| Characteristics | Randomized controlled trial Double-blind Peer reviewed |
|---|---|
| Sample size | 60 |
| Population | Adult patients undergoing thoracolumbar spine surgery |
| Interventions | Ketamine Ketofol (1:5) Fentanyl Propofol |
| Duration | 48 hours postoperative |
| Topics | Ketamine |
| Keywords | Opioid-free anesthesia Pain-free period Propofol Spine surgery Anesthesia anaesthesia |
| Citations | 11 |
| Key finding | Opioid-free anesthesia with ketamine and ketofol produced a longer pain-free period and reduced postoperative nausea and vomiting compared to opioid-based anesthesia, but required careful management of hypertension and hypotension. |
Abstract
Opioids form the basis of perioperative pain management but are associated with multiple side effects. In opioid-free anesthesia (OFA), several non-opioid drugs or neuraxial/regional blocks are used as substitutes for opioids. Ketamine, a N-methyl-d-aspartate antagonist, provides intense analgesia. However, there is a shortage of literature on the effects of ketamine-based OFA on hemodynamics (HD) and postoperative analgesia in patients undergoing thoracolumbar spine surgery. This prospective randomized controlled trial included 60 adult patients. The patients in Group OFA (n = 30) received OFA with ketamine and ketofol (1:5) infusion, and those in Group OBA (n = 30) received opioid-based anesthesia (OBA) with fentanyl and propofol infusion. The postoperative pain-free period, pain scores, rescue analgesia, intraoperative HDs, and postoperative complications were assessed. The mean pain-free period in Group OFA (9.86 ± 1.43 hr) was significantly higher than that in Group OBA (6.93 ± 1.93 hr) (P = 0.002). During the postoperative 48 hours, the total requirement of fentanyl was considerably lower in Group OFA (P < 0.05). There was a significantly higher incidence of hypertension in Group OFA (46%) and hypotension (43%) in Group OBA (43%), respectively. Postoperative nausea vomiting (PONV) was more common in Group OBA at the 2nd and 6th hr (P = 0.046 and P = 0.038). OFA with ketamine and ketofol provided adequate postoperative analgesia with a lower incidence of PONV after spine surgery. However, hypertension in the ketamine group and hypotension in the propofol group required fine titration of the infusion rate of drugs during the intraoperative period.