Core Principles

  • Denotes vaccine administration during pregnancy.
  • Confers protection to mother, fetus, and infant.
  • Relies on passive transplacental immunoglobulin g transfer.
  • Facilitates immunoglobulin a transfer through breast milk.
  • Prevents neonatal morbidity prior to active childhood immunization.
VaccineTimingPrimary Goal
Tetanus, diphtheria, acellular pertussis27-36 weeksPrevents infant pertussis <2 months.
Inactivated influenzaAny trimesterPrevents infant flu <6 months.
Respiratory syncytial virus32-36 weeksPrevents infant severe lower respiratory tract disease.
Coronavirus diseaseAny trimesterPrevents severe maternal disease and preterm birth.

Tetanus, Diphtheria, And Acellular Pertussis

  • Requires one dose during each pregnancy regardless of prior vaccination history.
  • Optimal administration timing spans 27 to 36 weeks.
  • Unimmunized women require one tetanus, diphtheria, acellular pertussis dose plus one tetanus, reduced diphtheria dose separated by at least one month.
  • Protects infants <2 months before primary infant vaccination series begins.

Inactivated Influenza Vaccine

  • Forms integral part of routine prenatal care.
  • Safe for administration during any trimester.
  • Reduces infant influenza infections by 63% during first six months of life.
  • Half-life of maternally acquired antibodies lasts 42-50 days.
  • Live attenuated influenza vaccine remains absolutely contraindicated.

Respiratory Syncytial Virus Vaccine

  • Employs bivalent prefusion f protein-based vaccine.
  • Administered strictly between 32 and 36 weeks gestation.
  • Provides 82% efficacy against medically attended severe infant lower respiratory illness up to 3 months.
  • Postmarketing safety trials demonstrate no increased risk of preterm birth or adverse neonatal outcomes.
  • World health organization recommends either maternal vaccine or infant long-acting monoclonal antibodies, avoiding simultaneous use for the same mother-infant pair.

Coronavirus Disease Vaccine

  • Pregnancy increases risk for intensive care admission, mechanical ventilation, and stillbirth.
  • Messenger ribonucleic acid vaccines generate robust maternal immunity.
  • Facilitates effective protective antibody transfer to fetal circulation.
  • Demonstrates no significant association with adverse pregnancy outcomes.

Contraindications And Precautions

  • Live vaccines generally contraindicated during pregnancy.
  • Measles, mumps, rubella, and varicella strictly avoided.
  • Pregnancy must be avoided for 4 weeks post-vaccination with live viral vaccines.
  • Smallpox vaccine directly harms developing fetus.
  • Yellow fever vaccine avoided unless travel to highly endemic zones remains absolutely unavoidable.