• Acta Anaesthesiol Scand · Aug 2022

    Clinical Trial

    Serum concentration of oral midazolam as pediatric preanesthetic medication and factors related to sedation level.

    • Hiromi Matsuda, Jungo Takenaka, Mariko Kawabata, Toshiaki Komatsu, Kazumi Sakanoue, Koichiro Atsuda, and Hirotsugu Okamoto.
    • Department of Anesthesiology, School of Medicine, Kitasato, Kanagawa, Japan.
    • Acta Anaesthesiol Scand. 2022 Aug 1; 66 (7): 818822818-822.

    BackgroundPreanesthetic medication is important to eliminate surgical anxiety in pediatric patients and facilitate their smooth transfer to the operating room. Midazolam is the most commonly used preanesthetic medication. However, it has been reported that the sedative effect varies from patient to patient. In this study, the pharmacokinetics of midazolam were examined, and the aim was to assess the factors affecting the quality of sedation.MethodsThe participants were children ranging in age from 6 months to 8 years scheduled for surgery. Midazolam 0.5 mg/kg was administered orally 30 min before entering the operating room, and the sedation level was evaluated at the time of mask application. Blood was collected after slow induction, and the serum concentration of midazolam was measured using high-performance liquid chromatography.ResultsA total of 98 patients were registered. There was no difference in serum concentrations between the effective sedation group and the ineffective sedation group (48.0 vs. 49.1 ng/mL), regardless of the effect of midazolam. Percentages of ineffective sedation by age (0 to 7 years) were 66.6%, 60%, 33.3%, 11.1%, 0%, 0%, 12.5%, and 0%, respectively. On multivariate logistic regression analysis, siblings (OR = 3.9, CI: 1.1-14.0, p = .03) and age (OR = 3.2, CI:1.2-8.5, p = .02) were related to an insufficient sedative effect.ConclusionThe serum concentration of oral midazolam reached effective levels even in patients in whom the sedative effect was inadequate. It is important to manage the perioperative period with appropriate concurrent premedication taking into account patient age and social background characteristics.Clinical Trial RegistrationClinical trial registry: UMIN R000052504.© 2022 Acta Anaesthesiologica Scandinavica Foundation.

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