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Antenatal Corticosteroid in Twin-Pregnant Women at Risk of Late Preterm Delivery: A Randomized Clinical Trial.

JAMA pediatrics2025-09-22PubMed
Total: 81.0Innovation: 7Impact: 0Rigor: 0Citation: 0

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