Oral melatonin, dexmedetomidine, and midazolam for prevention of postoperative agitation in children

• Published in: Journal of anesthesia 2011-04, Vol.25 (2), p.184-188
• Main Authors: Özcengiz, Dilek, Gunes, Yasemin, Ozmete, Ozlem
• Format: Article
• Language: English
• Subjects: Administration, Oral; Analgesics; Anesthesiology; Child; Child, Preschool; Children; Critical Care Medicine; Dexmedetomidine - administration & dosage; Dexmedetomidine - therapeutic use; Emergency Medicine; Female; Humans; Intensive; Male; Medicine; Medicine & Public Health; Melatonin; Melatonin - administration & dosage; Melatonin - therapeutic use; Methyl Ethers - adverse effects; Midazolam - administration & dosage; Midazolam - therapeutic use; Original Article; Pain Medicine; Parenting; Postoperative Complications - prevention & control; Preanesthetic Medication; Psychomotor Agitation - prevention & control
• ISSN: 0913-8668; 1438-8359
• DOI: 10.1007/s00540-011-1099-2

Purpose Several studies have reported that sevoflurane was associated with a relatively high incidence of emergence agitation in children even in the absence of any surgical intervention. The aim of this study was to compare early agitation characteristics of oral melatonin, dexmedetomidine, and midazolam premedication in children who were given sevoflurane anesthesia for esophageal dilatation. Methods Following Internal Review Board approval and parental informed consent, 100 ASA physical status I–II children (3–9 years old) who were scheduled to undergo general anesthesia for esophageal dilatation procedures were enrolled. The patients were randomly assigned to four groups ( n  = 25 in each). The premedications in the groups were saline (group P), dexmedetomidine 2.5 μg/kg (group D), 0.5 mg/kg midazolam (group MD), and melatonin 0.1 mg/kg (group ML), given orally. All premedication drugs were given with paracetamol 2–2.5 mg/kg to be easily drinkable 40–45 min before anesthesia induction. Anesthesia was maintained with sevoflurane 2–4%, N 2 O 50% in oxygen. No supplemental analgesic agent was given, and an emergence agitation scale (EAS) was measured on admission to the PACU, then every 5 min, and recorded during the postoperative period: 1, awake and calm, cooperative; 2, crying, requires consoling; 3, irritable/restless, screaming, inconsolable; 4, combative, disoriented, thrashing. Children with an agitation score of 3 or 4 were classified as agitated. Results There were no significant differences among the four groups demographically. The emergence agitation scale was higher in the placebo group than in the others at 5, 10, and 15 min postoperatively ( P