PREMATURE
LABOUR
|
Premature Labour -
Introduction
|
BJOG. 2006 Jan;113(1):65-74.
A randomised controlled trial of metronidazole for the prevention of preterm
birth in women positive for cervicovaginal fetal fibronectin: the PREMET
Study.
Shennan A, Crawshaw S, Briley A, Hawken J, Seed P, Jones G, Poston L.
Maternal and Fetal Research Unit, Division of Reproductive Health,
Endocrinology and Development, St Thomas' Hospital, King's College London,
UK.
Objectives:
To determine whether metronidazole reduces early preterm labour
in asymptomatic women with positive vaginal fetal fibronectin (fFN) in the
second trimester of pregnancy.
Design:
Randomised placebo-controlled trial.
Setting:
Fourteen UK hospitals (three teaching). POPULATION: Pregnancies
with at least one previous risk factor, including mid-trimester loss or
preterm delivery, uterine abnormality, cervical surgery or cerclage.
Methods:
Nine hundred pregnancies were screened for fFN at 24 and 27 weeks
of gestation. Positive cases were randomised to a week's course of oral
metronidazole or placebo.
Main Outcome Measures:
Primary outcome was
delivery before 30 weeks of gestation. Secondary outcomes included delivery
before 37 weeks.
Results:
The Trial Steering Committee (TSC) recommended the
study be stopped early; 21% of women receiving metronidazole (11/53)
delivered before 30 weeks compared with 11% (5/46) taking placebo [risk
ratio 1.9, 95% confidence interval (CI) 0.72-5.09, P = 0.18]. There were
significantly more preterm deliveries (before 37 weeks) in women treated
with metronidazole 33/53 (62%) versus placebo 18/46 (39%), risk ratio 1.6,
95% CI 1.05-2.4. fFN was a good predictor of early preterm birth in these
asymptomatic women; positive and negative predictive values (24 weeks of
gestation) for delivery by 30 weeks were 26% and 99%, respectively (positive
and negative likelihood ratios 15, 0.35).
Conclusion:
Metronidazole does not
reduce early preterm birth in high risk pregnant women selected by history
and a positive vaginal fFN test. Preterm delivery may be increased by
metronidazole therapy.