Randomised controlled trial of oxytocin alone versus oxytocin and ergometrine in active management of third stage of labour.
rct · Level II
Where this comes from
- Record sourced from PubMed, PMID 8251842.
- Also identified by PMC identifier 1679299.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
To compare intramuscular oxytocin alone and intramuscular oxytocin with ergometrine (Syntometrine) for their effect in reducing the risk of postpartum haemorrhage when both are used as part of the active management of the third stage of labour. Double blind, randomised controlled trial. Two metropolitan teaching hospitals in Perth, Western Australia. All women who expected a vaginal birth during the period of the trial. Informed consent was obtained. Postpartum haemorrhage, nausea, vomiting, and increased blood pressure. 3497 women were randomly allocated to receive oxytocin-ergometrine (n = 1730) or oxytocin (n = 1753). Rates of postpartum haemorrhage (> or = 500 ml or > or = 1000 ml) were similar in both arms (odds ratio 0.90 (0.82); 95% confidence interval 0.75 to 1.07 (0.59 to 1.14) at 500 ml (1000 ml) threshold). The use of oxytocin-ergometrine was associated with nausea, vomiting, and increased blood pressure. There are few advantages but several disadvantages for the routine use of oxytoxinergometrine when prophylactic active management of the third stage of labour is practised. Further investigation of dose-response for oxytocin may be warranted.
Medical subject headings
- Ergonovine
- Labor Stage, Third
- Oxytocin
- Postpartum Hemorrhage