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Vaccine effectiveness against mild and severe covid-19 in pregnant individuals and their infants in England: test negative case-control study.

BMJ medicine2025-02-04PubMed
Total: 80.0Innovation: 7Impact: 9Rigor: 8Citation: 9

Summary

A national test-negative case-control study in England found high COVID-19 vaccine effectiveness in pregnant individuals, with boosters sustaining protection up to 15 weeks. Maternal vaccination, especially in the third trimester, conferred substantial protection to infants up to 6 months against symptomatic infection and hospitalisation for both delta and omicron variants.

Key Findings

  • Booster vaccination yielded peak vaccine effectiveness against symptomatic disease of 98.4% (delta) and 80.1% (omicron) in pregnant individuals.
  • Two-dose primary series achieved 92.7% effectiveness against hospital admission for delta in pregnancy.
  • Maternal vaccination in the third trimester protected infants up to 6 months: effectiveness against symptomatic disease 86.5% (delta) and 56.6% (omicron), and against hospital admission 94.7% (delta) and 78.7% (omicron).
  • Protection did not wane up to 15 weeks post-booster in pregnant individuals.

Clinical Implications

Prioritise primary and booster COVID-19 vaccination during pregnancy—particularly in the third trimester—to protect both the mother and the infant up to 6 months of age.

Why It Matters

The study provides definitive, policy-relevant evidence that maternal vaccination protects both mothers and infants, informing timing of boosters during pregnancy.

Limitations

  • Test-negative design may be affected by healthcare-seeking behavior and residual confounding
  • Effectiveness beyond 15 weeks post-booster and for later omicron sublineages was not assessed

Future Directions

Assess durability of maternal and infant protection across emerging variants and evaluate optimal timing of boosters in different trimesters.

Study Information

Study Type
Case-control
Research Domain
Prevention
Evidence Level
II - Large, well-conducted observational test-negative design with linked administrative and clinical datasets.
Study Design
OTHER