The Wondrous Story of Anesthesia 2014
DOI: 10.1007/978-1-4614-8441-7_65
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Pediatric Anesthesia

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Cited by 3 publications
(10 citation statements)
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“…Diazepam's sedative and anxiolytic effects are caused by its interaction with the γ‐aminobutyric acid (GABA) receptor complex and subsequent depression of the limbic amygdala and spinal afferent pathways (47,52). It is hepatically metabolized by hydroxylation and demethylation in the liver, both of which are reduced in the neonate, accounting for the longer half‐life (approximately 30 hours) in premature and term infants compared with that in children (18 hours) (46). Because diazepam exhibits some degree of enterohepatic circulation, a second peak of the drug can occur 4 to 6 hours after administration, leading to re‐sedation (40).…”
Section: Benzodiazepinesmentioning
confidence: 99%
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“…Diazepam's sedative and anxiolytic effects are caused by its interaction with the γ‐aminobutyric acid (GABA) receptor complex and subsequent depression of the limbic amygdala and spinal afferent pathways (47,52). It is hepatically metabolized by hydroxylation and demethylation in the liver, both of which are reduced in the neonate, accounting for the longer half‐life (approximately 30 hours) in premature and term infants compared with that in children (18 hours) (46). Because diazepam exhibits some degree of enterohepatic circulation, a second peak of the drug can occur 4 to 6 hours after administration, leading to re‐sedation (40).…”
Section: Benzodiazepinesmentioning
confidence: 99%
“…Midazolam is a short‐acting benzodiazepine that is three to four times as potent as diazepam (46). It is very widely used because of its more rapid onset of action and shorter duration of effect compared with diazepam (9).…”
Section: Benzodiazepinesmentioning
confidence: 99%
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