Effects of low doses of meperidine on neonatal behavior

• Published in: Anesthesia and analgesia Vol. 64; no. 3; pp. 335 - 342
• Main Authors: KUHNERT, B. R, LINN, P. L, KENNARD, M. J, KUHNERT, P. M
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott 01.03.1985
• Subjects: Adult; Anesthesia, Obstetrical; Anesthetics. Neuromuscular blocking agents; Biological and medical sciences; Child Behavior - drug effects; Female; Fetal Blood - analysis; Humans; Infant, Newborn; Medical sciences; Meperidine - blood; Meperidine - pharmacology; Neuropharmacology; Pharmacology. Drug treatments; Pregnancy; Reflex - drug effects; Time Factors; Human; Evaluation scale; Low dose; General anesthesia; Psychometrics; Behavior; New born; Narcotic analgesic; Obstetric
• ISSN: 0003-2999; 1526-7598
• DOI: 10.1213/00000539-198503000-00006

After meperidine administration during labor, meperidine reaches its highest level in fetal tissues within 2-3 hr. The highest levels of normeperidine, the active metabolite of meperidine, are, on the other hand, determined in fetal tissues by the time between administration of meperidine to the mother and delivery: the greater the drug-to-delivery interval (DDI), the higher the fetal levels of normeperidine. Because of the different times to peak fetal levels of meperidine and normeperidine, it may be possible to partially separate the effects of meperidine and its metabolite on the neonate using the DDI. The purpose of this study was to determine whether low doses of meperidine affected performance on the Brazelton Neonatal Behavioral Assessment Scale (BNBAS), and whether this performance is related to the DDI or to levels of meperidine or to normeperidine. Sixteen control neonates whose mothers received no meperidine and 41 study infants whose mothers received 25-100 mg meperidine intravenously (mean 39 +/- 19 mg) were studied. Comparisons of BNBAS scores of control and study infants measured at less than 12 hr, again at 3 days of age, and the effect of DDI were made using repeated measures analyses of variance (ANOVA). Correlation techniques were used to examine relationships between BNBAS performance and clinical and pharmacological variables related to drug administration. The BNBAS cluster scores representing regulation of state and number of abnormal reflexes were significantly different in study neonates from control neonates. Performance depended upon test day. Further analysis showed that longer DDIs resulted in less optimal BNBAS performance.