4.6 Article

Breastfeeding Mother and Child Clinical Outcomes After COVID-19 Vaccination

Journal

JOURNAL OF HUMAN LACTATION
Volume 38, Issue 1, Pages 37-42

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/08903344211056522

Keywords

BNT162b2; breastfeeding; cohort study; COVID-19; human milk; mastitis; mRNA vaccines

Funding

  1. Khoo Teck Puat - National University Children's Medical Institute (KTP-NUCMI)
  2. National University Health System Pitch for Funds

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A prospective cohort study in Singapore involving 88 lactating healthcare workers who received two doses of BNT162b2 vaccine showed minimal breastfeeding-related effects, no changes in milk supply post-vaccination, and the most common side effect being pain/redness/swelling at the injection site.
Background: Pre-approval clinical trials of the Pfizer/BioNTech messenger RNA COVID-19 vaccine, BNT162b2 did not include participants who were breastfeeding. Therefore, there is limited evidence about outcomes of breastfeeding mother-child dyads and effects on breastfeeding after vaccination. Research Aims: To determine: (1) solicited adverse effects (e.g., axillary lymphadenopathy, mastitis, and breast engorgement), which are unique to lactating individuals; and (2) systemic and local adverse effects of COVID-19 mRNA vaccine on mothers and potential effects on their breastfed infants. Method: This was a prospective cohort study of lactating healthcare workers (N = 88) in Singapore who received two doses of BNT162b2 vaccination (Pfizer/BioNTech). The outcomes of mother-child dyads within 28 days after the second vaccine dose were determined through a participant-completed questionnaire. Results: Minimal effects related to breastfeeding were reported by this cohort; three of 88 (3.4%) participants had mastitis, one (1.1%) participant experienced breast engorgement, five of 88 (5.7%) participants reported cervical or axillary lymphadenopathy. There was no change in human milk supply after vaccination. The most common side effect was pain/redness/swelling at the injection site, which was experienced by 57 (64.8%) participants. There were no serious adverse events of anaphylaxis or hospital admissions. There were no short-term adverse effects reported in the infants of 67 lactating participants who breastfed within 72 hr after BNT162b2 vaccination. Conclusions: BNT162b2 vaccination was well tolerated in lactating participants and was not associated with short-term adverse effects in their breastfed infants. Study Protocol Registration: The study protocol was registered at clinicaltrials.gov (NCT04802278).

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