Pre-emptive multimodal analgesia with tramadol and ketamine-lidocaine infusion for suppression of central sensitization in a dog model of ovariohysterectomy

• Published in: Journal of pain research 2018-01, Vol.11, p.743-752
• Main Authors: Kaka, Ubedullah, Rahman, Nor-Alimah, Abubakar, Adamu Abdul, Goh, Yong Meng, Fakurazi, Sharida, Omar, Mohamed Ariff, Chen, Hui Cheng
• Format: Article
• Language: English
• Subjects: Abdomen; Abdominal surgery; Analgesia; Analgesics; Analysis; Anesthesia; Blood pressure; Body weight; central sensitisation; Dogs; Drug dosages; Ketamine; lidocaine; Narcotics; Original Research; Pain; Postoperative pain; Postoperative period; preemptive multimodal analgesia; Skin; Spinal cord; tramadol; Trends; Veterinary medicine
• ISSN: 1178-7090; 1178-7090
• DOI: 10.2147/JPR.S152475

The effects of pre-emptive infusion of ketamine-lidocaine with tramadol on the suppression of central sensitization were investigated in a dog ovariohysterectomy model. Twelve dogs were randomly assigned to two groups: ketamine-lidocaine-tramadol (KLT) and tramadol (T) groups. Both groups received intravenous tramadol 4 mg/kg body weight as premedication. Immediately after induction, the KLT group received ketamine and lidocaine at 0.5 and 2 mg/kg loading dose, followed by continuous rate infusion of 50 and 100 µg/kg/min, respectively, for 2 hours. Dogs in T group received saline bolus and continuous rate infusion at equi-volume. Intraoperatively, hemodynamic responses to surgical stimulation were recorded, whereas postoperative pain was evaluated using an algometer and short form of the Glasgow composite measure pain scale. Intraoperatively, hemodynamic responses to surgical stimulation were obtunded to a greater degree in KLT compared to T group. Postoperatively, the pain scores increased only for the first hour in KLT group, compared to 12 hours in T group. Mechanical thresholds at the abdomen decreased postoperatively between 12 and 60 hours in KLT group versus the entire 72 hours in T group. Thresholds at tibia and radius in both groups increased in the immediate 1 hour postoperatively, but decreased thereafter. Significant decrement of thresholds from baseline were detected in the tibia at 24, 42, and 60 hours in KLT group compared to 24-72 hours in T group, and in the radius between 36 and 48 hours in T group, but none in KLT group. Addition of pre-emptive ketamine-lidocaine infusion to single intravenous dose of tramadol enhanced attenuation of central sensitization and improved intra- and postoperative analgesia.