1978
DOI: 10.1016/0024-3205(78)90338-7
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Maternal and neonatal disposition of pethidine in childbirth—A study using quantitative gas chromatography-mass spectrometry

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Cited by 71 publications
(9 citation statements)
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“…Our results however partly support the findings of other studies which reported a stronger respiratory depression effect following pethidine administration [15,16]. This difference is caused by the different receptor affinities of the two opioids -as pethidine binds more strongly to µ2 opioid receptors binding this is assumed to result in respiratory depression -and the longer elimination half-time of pethidine in neonates [13,14].…”
supporting
confidence: 91%
See 1 more Smart Citation
“…Our results however partly support the findings of other studies which reported a stronger respiratory depression effect following pethidine administration [15,16]. This difference is caused by the different receptor affinities of the two opioids -as pethidine binds more strongly to µ2 opioid receptors binding this is assumed to result in respiratory depression -and the longer elimination half-time of pethidine in neonates [13,14].…”
supporting
confidence: 91%
“…It reaches its maximum effect after 30-40 minutes and can be re-administered after 3-6 hours [12]. Its elimination half-life in neonates is around 23 hours because of the neonateʼs immature elimination pathways, while in adults the elimination halflife of pethidine is only 3 hours [13]. The opioid analgesic meptazinol is increasingly being used in obstetrics.…”
Section: Efficacy and Effects Of Parenteral Pethidine Or Meptazinol Amentioning
confidence: 99%
“…3 Norpethidine may accumulate after prolonged or high-dose pethidine administration or in renal failure and cause adverse central nervous system effects such as agitation, tremulousness, hallucinations and convulsions. [3][4][5] Metabolism of pethidine is impaired in neonates and infants, 6 and in two separate studies, its half-life was longer than in adults, with mean values of 10.7 h and 22.7 h. 7,8 Pethidine continues to be widely used in birth suites in Australasia and the United Kingdom for labour analgesia via the intramuscular (i.m.) route.…”
Section: Introductionmentioning
confidence: 98%
“…Atraviesa la placenta y alcanza la máxima concentración fetal entre 2-3 h tras su administración, por eso se recomienda administrarla cuando el expulsivo se prevé que sucederá antes de una hora o después de 4 horas, algo bastante difícil de predecir. Además, la normeperidina, su metabolito, es tóxico y tiene una semivida en el neonato de 2,5 días 56 , habiéndose relacionado con problemas neuroconductuales 57 y dificultad para la lactancia a pesar de respetar los "márgenes de seguridad" de la administración de la meperidina 58 . La morfina se usa raramente por sus efectos adversos maternofetales 54,55,59,60 .…”
Section: Opioidesunclassified