COVID-19 vaccination in pregnancy and postpartum and human milk feeding non-initiation and discontinuation

Elisabeth Brandstetter Figueroa1,2, Gabriela Vazquez-Benitez2, Kirsten Ehresmann2

  • 1Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, MN, United States.

Empirical evidence on COVID-19 vaccination and lactation-related outcomes remains limited. We used electronic health record data from 4 US healthcare systems to assess the association between COVID-19 vaccination and milk feeding outcomes. We included pregnant persons with a live birth between December 2020 and September 2022 with infant linkage. We assessed 2 COVID-19 vaccination exposure windows-during pregnancy (≥20 weeks gestation vs no vaccination during pregnancy) or postpartum (<7 months after delivery vs none). We estimated adjusted prevalence ratios (aPR) for COVID-19 vaccination during pregnancy and human milk feeding non-initiation and discontinuation, and we estimated adjusted hazard ratios (aHR) for postpartum COVID-19 vaccination and human milk feeding discontinuation. In the study population used to assess pregnancy exposure (N = 10 757), 4.2% of birthing parents did not initiate human milk feeding. Non-initiation did not differ by vaccination during pregnancy (aPR = 0.99; 95% CI, 0.98-1.01). Antenatal vaccination was not associated with human milk feeding discontinuation at 2 and 6 months after delivery. In the study population used to assess postpartum exposure (N = 17 161), human milk feeding discontinuation did not differ by postpartum vaccination (aHR = 1.03; 95% CI, 0.95-1.11). COVID-19 vaccination in pregnancy and postpartum were not associated with human milk feeding discontinuation.

Related Concept Videos

Development of Human Microbiota01:30

Development of Human Microbiota

The human microbiota begins developing at birth and undergoes continual change as we age. Infancy marks a critical period of microbial sensitivity, offering a “window of opportunity” during which beneficial microbes help mature the immune system. By age three, children typically develop a more stable and diverse microbial community. Newborns acquire microbes from their immediate environment; vaginal delivery favors maternal vaginal microbes, while cesarean births favor microbes from the skin...
Development of the Oral Microbiota01:28

Development of the Oral Microbiota

The establishment of the oral microbiome begins before birth, challenging the long-held belief that the fetal oral cavity is sterile. The presence of oral microbes such as Streptococcus and Fusobacterium in amniotic fluid suggests that microbial exposure may occur in utero, potentially through translocation from the maternal oral or gastrointestinal tract. This early colonization primes the neonatal immune system and sets the stage for subsequent microbial succession. Maternal health,...
Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
Vaccinations01:51

Vaccinations

Overview
Vaccines01:21

Vaccines

Vaccines are among the most effective tools in preventive medicine, designed to prepare the immune system to recognize and combat infectious agents. By introducing antigens—substances that the immune system identifies as foreign—vaccines stimulate an adaptive immune response that leads to immunological memory. This immunological memory enables the body to mount a faster and more effective response upon future exposures to the actual pathogen.Vaccines can be categorized based on the type of...
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...