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Oxytocin: at birth and beyond. A systematic review of the long-term effects of peripartum oxytocin

期刊

ANAESTHESIA
卷 76, 期 11, 页码 1526-1537

出版社

WILEY
DOI: 10.1111/anae.15553

关键词

breastfeeding; caesarean delivery; chronic pain; haemorrhage; oxytocin; postpartum depression

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Recent research suggests oxytocin's effects on higher-order human behavior may outweigh its uterotonic effects. The review highlights potential consequences of manipulating oxytocin signaling during the peripartum period, including effects on postpartum depression, breastfeeding, neurodevelopment, and chronic pain. Studies show a link between peripartum oxytocin administration and postpartum depression, negative correlation with breastfeeding success, weak association with neurodevelopmental disorders, and evidence of analgesic effects. More robust clinical studies are needed to better understand the impact of peripartum oxytocin administration.
Oxytocin is one of the most commonly used medications during labour and delivery. Recent insights from basic neuroscience research suggest that the uterotonic effects of oxytocin may arguably be trivial when compared with its profound effects on higher-order human behaviour. The purpose of this review is to highlight the potential consequences of manipulating oxytocinergic signalling during the peripartum period and its long-term impact on the maternal-infant dyad. We identified four domains where modulation of oxytocinergic signalling might be consequential: postpartum depression; breastfeeding; neurodevelopment; and chronic pain, and performed a literature search to address the impact of peripartum oxytocin administration. We have shown modest, but inconsistent, evidence linking peripartum oxytocin administration with postpartum depression. Breastfeeding success appeared to be negatively correlated with peripartum oxytocin exposure, perhaps secondary to impaired primitive neonatal reflexes and maternal-infant bonding. The association between perinatal oxytocin exposure and subsequent development of neurodevelopmental disorders such as autism in the offspring was weak, but these studies were limited by the lack of information on the cumulative dose. Finally, we identified substantial evidence for analgesic and anti-hypersensitivity effects of oxytocin which might partly explain the low incidence of chronic pain after caesarean birth. Although most data presented here are observational, our review points to a compelling need for robust clinical studies to better dissect the impact of peripartum oxytocin administration, and as stewards of its use, increase the precision with which we administer oxytocin to prevent overuse of the drug.

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