Key result
Lidocaine is metabolized by the fetus and neonate, confirmed by the presence of its active metabolites MEGX and GX in cord blood plasma and neonatal urine.
Why the study?
How is lidocaine metabolized by the mother, fetus, and neonate during and after delivery?
Observational
How is lidocaine metabolized by the mother, fetus, and neonate during and after delivery?
This study provides pharmacokinetic evidence that both the human fetus and neonate are capable of metabolizing lidocaine into its active metabolites.
Alerts to neonatal metabolite exposure after maternal lidocaine; extends PK data yet leaves dosing and safety questions open.
We investigated the metabolism of lidocaine to its active metabolites--monoethylglycinexylidide (MEGX) and glycinexylidide (GX)--in the mother, fetus, and neonate. The study population included normal patients and their infants delivered either vaginally or by cesarean section. A group of infants of mothers in whom pudendal anesthesia was induced was also included. Using gas chromatography and mass spectrometry techniques, the concentrations of lidocaine, MEGX, and GX were determined in maternal plasma during labor, in umbilical cord venous and arterial plasma at delivery, and in maternal and neonatal urine for 3 days post partum. The results indicate the following: In maternal plasma, MEGX rises throughout labor and GX is usually detectable within an hour of medication; in cord blood plasma the levels of lidocaine, MEGX, and GX suggest fetal metabolism of lidocaine; and in neonatal urine, the relative levels of parent compound and metabolites confirm lidocaine metabolism by the neonate.
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Kuhnert et al. (1979) conducted an observational in Pregnancy and labor. Lidocaine was evaluated on Concentrations of lidocaine, MEGX, and GX in maternal plasma, umbilical cord plasma, and maternal and neonatal urine. Lidocaine is metabolized by the fetus and neonate, confirmed by the presence of its active metabolites MEGX and GX in cord blood plasma and neonatal urine.
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