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Morphine, but not fentanyl, can adversely affect in vitro fertilization of sea urchin eggs. Thus, fentanyl has been recommended as clinically useful during the harvesting of human ova for subsequent in vitro fertilization.[276] Although alfentanil penetrates follicular fluid to a greater extent than fentanyl, it has no effect on cleavage rate and has also been recommended as useful in providing analgesia for oocyte retrieval. The teratogenic actions of opioids, including fentanyl, sufentanil, and alfentanil, at least in animal models, appear to be minimal (also see Chapter 58 ).[277]
The parenteral administration of opioids prior to vaginal delivery remains a commonly used method of analgesia. Nociception due to uterine cervical distention could be suppressed by μ- and κ-agonists in rats,[278] but the analgesic effect of μ-agonists but not κ-agonists was reduced by estrogen.[279] Aortocaval compression and associated hypotension may be exacerbated by parenteral opioids, especially following morphine or meperidine. Fetal manifestations of maternal opioid administration include decreases in heart rate variability. Adverse neonatal effects can occur after either morphine or meperidine administration to mothers. Fetal acidosis increases opioid transfer from the mother. Attempts to minimize the neonatal effects of opioids include restricting opioid administration to the first stage of labor. The short-acting opioid alfentanil administered before cesarean delivery attenuated the maternal stress response, but led to slightly reduced Apgar scores.[280]
Morphine has little effect on the pregnant rat uterus, whereas meperidine can increase uterine contractions in a dose-dependent fashion that is not reversible by naloxone.[281] Fentanyl has no effect on uterine blood flow and tone in sheep. Fentanyl (50–100 µg IV every hour), compared with meperidine (25–50 mg IV every 2 to 3 hours), results in less nausea, vomiting, and sedation in the mother and in lower naloxone requirements in newborns.[282]
Morphine and meperidine have been found in the breast milk of mothers receiving intravenous opioid analgesia.[283] [284] Although both fentanyl and morphine are concentrated in breast milk in milk-to-plasma ratios of 2 to 3:1, newborn narcosis is reported to be insignificant.
Newborns of addicted mothers can exhibit opioid withdrawal and require observation and appropriate treatment.[285]
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