The effect of nefopam on lactation after caesarean section: a single-blind randomised trial. (May 2017)

• Record Type: Journal Article
• Authors: Baka, N.E.; Vial, F.; Iohom, G.; Guerci, P.; Hubert, C.; Rouabah, M.; Bouaziz, H.
• Is Part Of: International journal of obstetric anesthesia. Volume 31(2017)
• Page Start: 84
• Page End: 90
• Publication Date: 2017-05
• Subjects: Nefopam -- Lactation -- Caesarean delivery; Obstetrics -- Periodicals; Anesthesia -- Periodicals; Anesthésie en obstétrique -- Périodiques; Anesthesia; Obstetrics; Electronic journals; Periodicals; 617.9682
• DOI: 10.1016/j.ijoa.2017.02.005
• Languages: English
• ISSNs: 0959-289X

Abstract

Highlights: Nefopam may theoretically stop lactation due to its anticholinergic effects. We compared nefopam with paracetamol in the post-caesarean setting. Nefopam does not appear to delay the onset of lactation. Neonatal neurobehavioural scores were comparable at each time point. Abstract: Background: Nefopam is a centrally acting analgesic which has a theoretical risk of stopping lactation due to its anticholinergic and dopaminergic effects. The aim of this study was to evaluate the effect of nefopam on lactation and to investigate potential adverse effects on newborns. Methods: Seventy-two women, scheduled to undergo a caesarean delivery under spinal anaesthesia and wanting to breastfeed, were randomised to one of two groups: nefopam (20 mg, six hourly) or paracetamol (1 g, six hourly). In both groups, postoperative analgesia was supplemented with ketoprofen (50 mg, six hourly) in conjunction with intrathecal morphine 0.1 mg. The primary outcome was onset of lactation, estimated by weighing the newborns before and after feeding; by maternal perception of breast fullness and based on serum prolactin concentration 48 hours postpartum. Secondary outcomes were neonatal adverse effects evaluated by neurobehavioural score at 12, 24, 48, and 72 hours after birth. Statistical analyses were performed using Chi-squared, Fisher exact and Student t tests as appropriate. P <0.05 was considered statistically significant. Results: The difference in the weight of the newborn before and after each feed, maternal perception of breast fullness and serum prolactin did not significantly differ between groups. The volume of artificial milk given to newborns of mothers in the nefopam group on days two and three was significantly greater than for the paracetamol group. Neurobehavioural scores were comparable at each time point. Conclusion: Nefopam does not appear to delay the onset of lactation or present any clear risk to the newborn.