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A multicentre randomised controlled trial comparing elective and selective caesarean section for the delivery of the preterm breech infant
Author(s) -
Penn Zoe J.,
Steer Philip J.,
Grant Adrian
Publication year - 1996
Publication title -
bjog: an international journal of obstetrics and gynaecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.157
H-Index - 164
eISSN - 1471-0528
pISSN - 1470-0328
DOI - 10.1111/j.1471-0528.1996.tb09838.x
Subject(s) - medicine , breech presentation , caesarean section , obstetrics , randomized controlled trial , external cephalic version , gestation , gestational age , cephalic presentation , vaginal delivery , pregnancy , surgery , genetics , biology
Objective To determine the optimum mode of delivery for women in preterm breech labour at a gestational age of 26 to 32 weeks. Design A multicentre randomised controlled trial. Setting Twenty‐six hospitals in England, UK. Participants Women with a singleton breech fetus in spontaneous preterm labour between 26 and 32 completed weeks of gestation, with no clear indication for a caesarean section or vaginal breech delivery. Intervention Random allocation to either ‘intention to delivery vaginally’ or ‘intention to deliver by caesarean section’. Main outcome measures Perinatal mortality, neonatal morbidity, maternal morbidity and gestation at delivery. Results The trial was closed after 17 months because of low recruitment, by which time substantial numbers of women had been in the eligible gestation period. Thirteen women from six hospitals were recruited. One infant, randomised to and delivered vaginally, was stillborn. Three fetal presentations were cephalic at delivery despite a diagnosis of breech presentation at trial entry. No formal statistical analysis was performed due to the small numbers. Conclusions No conclusions about the optimum mode of delivery for women in preterm labour with a fetus presenting by the breech can be drawn from this trial. The low accrual rate was due to clinicians' reluctance to randomise eligible women, reflecting the circumstances and nature of the trial.