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For further information, see CMDT Part 19-13: Preterm Labor
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Labor beginning before 37th week of pregnancy
Preterm, regular, rhythmic contractions 5 minutes apart
Cervical dilatation, effacement, or both occur
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Fetal fibronectin measurement in cervicovaginal specimens can differentiate true from false labor
A level < 50 ng/mL has a negative predictive value of 93–97% for delivery in 7–14 days among women with a history of preterm delivery currently having contractions
However, fetal fibronectin is not recommended as a screening test in asymptomatic women because of its low sensitivity
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Limited activity and bed rest
Frequently recommended despite the fact that evidence has failed to demonstrate improved outcomes in these women
Additionally, and paradoxically, such recommendations may place a woman at an increased risk to deliver preterm
Women in preterm labor should receive antimicrobial prophylaxis against group B streptococcus
Corticosteroids
A single short-course of corticosteroids should be administered to promote fetal lung maturity when preterm birth is anticipated between 23 and 34 weeks gestation
Betamethasone, 12 mg intramuscularly repeated once 24 hours later or
Dexamethasone, 6 mg intramuscularly repeated every 12 hours for four doses
A single repeat course should be considered in women who are at risk for preterm delivery within the next 7 days, and whose prior dose of antenatal corticosteroids was administered more than 14 days previously
Rescue course corticosteroids could be provided as early as 7 days from the prior dose, if indicated by the clinical scenario
Administration of betamethasone may be considered in pregnant women between 34 0/7 and 36 6/7 weeks of gestation at imminent risk of preterm birth within 7 days, and who have not received a previous course of antenatal corticosteroids
Overall, evidence supports the use of first-line tocolytic treatment with beta-adrenergic receptor agonists, calcium channel blockers, or indomethacin for short-term prolongation of pregnancy (up to 48 hours) to allow for the administration of antenatal corticosteroids
Terbutaline
Can be given as an intravenous infusion starting at 2.5 mcg /min or as a subcutaneous injection starting at 250 mcg given every 30 minutes
Oral administration is not recommended because of the lack of proven efficacy and concerns about maternal safety
Serious maternal side effects include
Because of these safety concerns, the US Food and Drug Administration warns that terbutaline be administered exclusively in a hospital setting and discontinued after 48–72 hours of treatment
Nifedipine, 20 mg orally every 6 hours, and indomethacin, 50 mg orally once then 25 mg ...