Antenatal Corticosteroid in Twin-Pregnant Women at Risk of Late Preterm Delivery: A Randomized Clinical Trial.
Summary
In late preterm twin pregnancies, antenatal betamethasone reduced severe neonatal respiratory morbidity compared with placebo (RR 0.64), with additional reductions in CPAP ≥2 hours and transient tachypnea. Benefits were time-dependent (delivery 12 hours to <7 days after first dose), while neonatal hypoglycemia increased.
Key Findings
- Severe neonatal respiratory morbidity was lower with betamethasone vs placebo (4.8% vs 7.5%; RR 0.64, 95% CI 0.42–0.98).
- CPAP use ≥2 hours (RR 0.58, 95% CI 0.35–0.95) and transient tachypnea of the newborn (RR 0.47, 95% CI 0.25–0.89) were reduced.
- Benefit was observed only when delivery occurred 12 hours to <7 days after first betamethasone dose.
- Neonatal hypoglycemia increased with betamethasone (15.6% vs 11.7%; RR 1.33, 95% CI 1.01–1.75).
Clinical Implications
Consider antenatal betamethasone for women with twin pregnancies at risk of late preterm delivery, particularly when delivery is anticipated within 12 hours to 7 days, with vigilant neonatal glucose monitoring.
Why It Matters
This is a large, multicenter, randomized, placebo-controlled trial addressing a key evidence gap for twins at risk of late preterm delivery and may inform guideline updates.
Limitations
- Generalizability beyond Korean university centers is uncertain
- Increased neonatal hypoglycemia and limited long-term neonatal follow-up reported
Future Directions
Assess long-term neurodevelopmental and metabolic outcomes; evaluate optimal timing for twins; and stratify by chorionicity and mode of delivery.
Study Information
- Study Type
- RCT
- Research Domain
- Treatment
- Evidence Level
- I - Randomized controlled trial with placebo control and ITT analysis
- Study Design
- OTHER