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Therapeutics |
Clinical impact ratings Obstetrics






GP/FP/Obstetrics 





Key Words: delivery (obstetric) labour (obstetric) uterine monitoring
| The first 150 words of the full text of this article appear below. |
METHODS
Design:
randomised controlled trial.
Allocation:
concealed.*
Blinding:
unblinded.*
Follow up period:
210 days after delivery.
Setting:
midwife led unit and physician led delivery suite in a teaching hospital in northwest England, UK.
Patients:
3000 primigravid women (mean age 25 y) in spontaneous labour at term with an uncomplicated singleton pregnancy in cephalic presentation.
Intervention:
progress of labour was recorded on a partogram with an action line drawn either 2 hours (n = 1503) or 4 hours (n = 1497) after the alert line. If the plot of cervical dilatation against time crossed the action line, delivery suite guidelines for the management of prolonged labour were followed.
Outcomes:
caesarean delivery, need for augmentation of labour, duration of labour, use of epidural analgesia, postpartum haemorrhage, number of vaginal examinations, admission of the infant to the neonatal intensive care unit (NICU), and Apgar score. The study had 90% power to detect a 3%
Charissa Fotinos, MD
University of Washington, Seattle, Washington, USA
Related Article
Evid. Based Med. 2007 12: 63-64.
(in )
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