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. 2016 Feb 18;2016(2):CD010358. doi: 10.1002/14651858.CD010358.pub2

Altindis 2008.

Methods RCT, 2 parallel groups
Participants Number: 40 participants
Country: Turkey
Surgery: lower abdominal surgery
Age: 21 to 56 years
ASA: I or II
Other inclusion criteria: general anaesthesia
Exclusion criteria: history of hypertension, ischaemic heart disease or conduction disturbance; history of alcohol or drug abuse; use of beta‐adrenoreceptor blockers, monoamine oxidase inhibitor within 2 weeks; impaired hepatic or renal function; hypersensitivity to opioids or dexmedetomidine
Interventions
  • Meperidine 0.25 mg/kg intravenous bolus and dexmedetomidine 0.5 µg/kg in 50 mL of saline solution infused during the 10 minutes before the end of surgery


vs
  • Meperidine 0.25 mg/kg intravenous bolus and 50 mL of saline solution infusion during 10 minutes before the end of surgery


All participants:
    • Premedication: 10 mg 2 hours before surgery

    • After surgery: PCA during 24 hours after surgery. PCA settings were as follows: meperidine 5 mg plus dexmedetomidine 10 µg bolus dose for Group I, and meperidine 5 mg bolus dose for Group II

Outcomes Verbal rating score for pain (0 to 3)
Total meperidine consumption
Time to discharge from PACU
Postoperative sedation (0 to 3)
Number of participants with postoperative vomiting
Hemodynamic data
Notes Study authors contacted to clarify types of surgery. No reply