1999
DOI: 10.1097/00132586-199904000-00026
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Intravenous Remifentanil: Placental Transfer, Maternal and Neonatal Effects

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Cited by 115 publications
(170 citation statements)
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“…Propofol and etomidate are good choices for induction, while rocuronium can replace succinylcholine if there are no concerns about the airway. Remifentanil has been shown to be safe for the mother and newborn 18 and could be used pre-or postdelivery as deemed necessary. Fentanyl is a good choice for pain control after delivery as long as pruritus and scratching are well controlled.…”
Section: Discussionmentioning
confidence: 99%
“…Propofol and etomidate are good choices for induction, while rocuronium can replace succinylcholine if there are no concerns about the airway. Remifentanil has been shown to be safe for the mother and newborn 18 and could be used pre-or postdelivery as deemed necessary. Fentanyl is a good choice for pain control after delivery as long as pruritus and scratching are well controlled.…”
Section: Discussionmentioning
confidence: 99%
“…10 They found differences in the maternal pain scores only during the first hour and no differences in the neonatal outcome between the three groups. To date, the literature supports the safety of remifentanil from a neonatal standpoint, 6,7,[11][12][13][14][15][16][17][18][19][20][21][22][23][24] while several studies have shown that fentanyl PCA may be associated with neonatal depression. 1,9,[25][26][27][28] Therefore further research is needed to ensure the safety of these drugs while used for IVPCA in labouring women.…”
Section: Résumémentioning
confidence: 98%
“…Its context-sensitive half-time is about three minutes irrespective of its duration of infusion, 5 and the drug is quickly redistributed and metabolized in the fetus. 6,7 Fentanyl is also a short-acting synthetic opioid with a rapid onset of action (blood-effect site equilibration 6.4 min), but it exhibits cumulative effect with repeated or prolonged administration due to reuptake from inactive tissue sites, which leads to an increase in its context-sensitive halftime. 5,8 The elimination half-life in neonates varies from 75 to 440 min.…”
Section: Résumémentioning
confidence: 99%
“…Kan et al (1998) studied the basic pharmacokinetics of remifentanil given as an adjunct to epidural anaesthesia for caesarean section. Remifentanil was introduced into obstetric analgesia shortly after this, which was reflected in the publication of the first case reports of effective IV remifentanil analgesia during labour (Brada et al 1998, Jones et al 1999, Thurlow & Waterhouse 2000, Roelants et al 2001.…”
Section: Remifentanilmentioning
confidence: 99%
“…the time needed for a 50% reduction of the concentration in blood after the cessation of infusion that maintains a steady state -is 3 minutes (Kapila et al 1995). The pharmacokinetic study made during anaesthesia for caesarean section showed greater clearance of remifentanil in parturients compared with healthy non-pregnant volunteers (Kan et al 1998). Remifentanil readily crosses the placenta with an umbilical vein (UV) to maternal artery (MA) concentration ratio of 0.73-0.88.…”
Section: Remifentanilmentioning
confidence: 99%