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Abstract Cardiovascular response to laryngoscopy and endotracheal intubation is well known and is linked to increases in catecholamine blood levels. Many studies proved that pregabalin is effective in attenuating the stress response to laryngosopy and intubation. Surgical patients commonly develop hyperglycemia related to the hypermetabolic stress response, which increases glucose production and causes insulin resistance. Surgery causes postoperative pain that should be alleviated as soon and as effective as possible to reduce suffering, to promote healing process and rehabilitation and to prevent complications. Preemptive analgesia prevents (or reduces) pathologic pain that is different from physiologic pain in several aspects; it is excessive in intensity and spread and can be activated by low-intensity stimuli. The preventive analgesic role of pregabalin in postoperative pain is well documented. Pregabalin also has a role in neuropathic pain states such as postspinal cord injury, post-traumatic peripheral neuropathy and failed back surgery syndrome. The aim of this work was to evaluate the effects of different doses of pregabalin as an oral premedication to attenuate cardiovascular response during laryngoscopy and endotracheal intubation. Intubation-induced hyperglycemia was also assessed in addition to the effect of the drug on postoperative analgesia in normotensive normoglycemic patients undergoing abdominal hysterectomy. The study included 120 patients who were randomly divided into 4 equal groups; group A received a placebo drug and groups B,C and D received different doses of oral pregabalin(75 mg, 150 mg and 300 mg respectively). The patients were unaware of their group distribution. Patients were carefully selected regarding the demographic data and the medical status. The anesthetic technique included preoperative assessment and preparation during which the patients were informed about the details of the study, gave their consent, learned how to use VAS, and received the drug of the study. A standard intraoperative anesthetic technique was done and study parameters were observed and recorded. The study was completed for 90 minutes in PACU and continued for 36 hours postoperatively. Intraopratively, duration of endotracheal intubation and surgery were recorded for each patient. Hemodynmic parameters (SBP, DBP, MBP, and HR) and blood glucose levels were assessed according to specific schedules and were compared between groups as well as with preoperative baseline values. Total consumption of intraoperative fentanyl was also calculated. Postoperatively, sedation was scored twice and time to first request of analgesia was recorded. Consumption of pethidine was calculated for each patient in the first 36 hours postoperatively. Observation of the patients for occurrence of side effects or complications of drugs or surgery was done. There was no significant difference between groups as regards demographic data, duration of intubation or duration of surgery. There was increase in hemodynamic values during intubation compared to the baseline values in all groups. However, the increase in both groups C and D was less than that of groups A and B. Afterwards, there was a gradual decrease in the hemodynamic parameters at 2, 4 and 6 minutes after intubation in all groups. This proved the definite role of pregabalin in doses of 150 and 300 mg in attenuating the hemodynamic response to laryngoscopy and endotracheal intubation. The present study could not prove the efficacy of pregabalin in different doses in decreasing the hyperglycemic response to laryngoscopy and intubation. Intraoperative fentanyl consumption decreased in the current study on using pregabalin in doses of 150 mg and 300 mg. A dose of 75 mg did not show such effect. Moreover, the study revealed that a dose of 300 mg pregabalin did not differ from a dose of 150 mg as regards reduction of intraoperative fentanyl consumption. At 30 minutes after arrival to PACU, group D (300 mg pregabalin) had the largest number of sedated patients (12 patients) followed by group C (4 patients).None of the patients in groups A and B was sedated. This indicated a consistent sedating effect of pregabalin with increasing the dose. Times to first request of analgesia in PACU were significantly prolonged in groups C and D (150 mg and 300 mg pregabalin respectively) compared to groups A and B (placebo and 75 mg respectively). They were three to five times longer. This result indicated the potent analgesic effect of pregabalin. In the current study, the total amount of consumed pethidine during 36 hours postoperatively was significantly reduced on using pregabalin in doses of 150 mg and 300 mg compared to the dose of 75 mg. This result was a further indication of the analgesic effect of pregabalin. There were no postoperative surgical complications in any patient. Sedation was the only adverse effects of pregabalin in some patients. No other adverse effects were noticed. Nausea occurred in all groups. Although the number of patients who had nausea in groups C and D was less than that in groups A and B, yet there was no statistical significant difference between groups. The lower incidence of nausea in groups C and D might be attributed to the opioid-sparing effect. |