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Peer-reviewedCC BYJournal of pediatrics. Clinical practice

Uptake of Respiratory Syncytial Virus Prefusion F Protein Vaccination during Pregnancy and nirsevimab among Infants over Two Seasons in a Single Health System.

  1. 1Division of General Academic Pediatrics, Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh.
  2. 2University of Pittsburgh School of Medicine, Pittsburgh.

Abstract

Objective

To describe the uptake of respiratory syncytial virus (RSV) prevention products during the first 2 seasons after availability in the US in a large health system.Study design

Using multisource immunization data from a single health system, we identified a retrospective cohort of infants born from October 2023 to April 2024 (season 1) and from September 2024 to April 2025 (season 2) and their birth parents. We described the uptake of RSV prefusion F protein (RSVpreF) vaccination and nirsevimab and evaluated factors associated with receipt using multivariable logistic regression.Results

Among 10 196 infants, 5868/10 196 (57.6%) were exposed to an RSV-preventive product. Overall, in our maternal-infant dyads, 3850/10 196 (37.8% of total) received RSVpreF, 1837/10 196 infants (18.0% of total) received nirsevimab, and in 181/10 196 (1.8%), both were received. Uptake increased from 2100/4555 (46.1%) in season 1 to 3768/5641 (66.8%) in season 2 (P < .001). Maternal RSVpreF vaccination increased from 1280/4555 (28.1%) to 2570/5641 (45.6%), and nirsevimab uptake increased from 749/4555 (16.4%) to 1088/5641 (19.3% both P < .001). Nirsevimab receipt at <6 days of life increased from 242/749 (32.2%) to 502/1088 (46.1%, P < .001). RSVpreF uptake was higher among older, privately insured pregnant individuals and those engaged in other preventative care and lower among those with higher area deprivation, more complex obstetric histories, or other children. Nirsevimab uptake was higher among infants with prematurity or from multifetal births and lower among those with siblings, later-season birth, or no early outpatient care. Social and structural disparities in nirsevimab uptake improved in the second season, whereas disparities in RSVpreF uptake persisted.Conclusions

The uptake of RSV preventive strategies increased across 2 seasons, with a higher uptake of maternal RSVpreF vaccination than nirsevimab.

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BibTeX
@article{kerr2026uptake,
  title = {{Uptake of Respiratory Syncytial Virus Prefusion F Protein Vaccination during Pregnancy and nirsevimab among Infants over Two Seasons in a Single Health System.}},
  author = {Jessica E Kerr and Annaliese J Calzadilla and Hui Liu and Anne-Marie Rick},
  journal = {Journal of pediatrics. Clinical practice},
  year = {2026},
  month = sep,
  doi = {10.1016/j.jpedcp.2026.200241},
  url = {https://europepmc.org/article/MED/42909243},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Uptake of Respiratory Syncytial Virus Prefusion F Protein Vaccination during Pregnancy and nirsevimab among Infants over Two Seasons in a Single Health System.
AU  - Jessica E Kerr
AU  - Annaliese J Calzadilla
AU  - Hui Liu
AU  - Anne-Marie Rick
PY  - 2026
DA  - 2026/09/15
JO  - Journal of pediatrics. Clinical practice
DO  - 10.1016/j.jpedcp.2026.200241
UR  - https://europepmc.org/article/MED/42909243
AB  - Objective  To describe the uptake of respiratory syncytial virus (RSV) prevention products during the first 2 seasons after availability in the US in a large health system.Study design  Using multisource immunization data from a single health system, we identified a retrospective cohort of infants born from October 2023 to April 2024 (season 1) and from September 2024 to April 2025 (season 2) and their birth parents. We described the uptake of RSV prefusion F protein (RSVpreF) vaccination and nirsevimab and evaluated factors associated with receipt using multivariable logistic regression.Results  Among 10 196 infants, 5868/10 196 (57.6%) were exposed to an RSV-preventive product. Overall, in our maternal-infant dyads, 3850/10 196 (37.8% of total) received RSVpreF, 1837/10 196 infants (18.0% of total) received nirsevimab, and in 181/10 196 (1.8%), both were received. Uptake increased from 2100/4555 (46.1%) in season 1 to 3768/5641 (66.8%) in season 2 (P < .001). Maternal RSVpreF vaccination increased from 1280/4555 (28.1%) to 2570/5641 (45.6%), and nirsevimab uptake increased from 749/4555 (16.4%) to 1088/5641 (19.3% both P < .001). Nirsevimab receipt at <6 days of life increased from 242/749 (32.2%) to 502/1088 (46.1%, P < .001). RSVpreF uptake was higher among older, privately insured pregnant individuals and those engaged in other preventative care and lower among those with higher area deprivation, more complex obstetric histories, or other children. Nirsevimab uptake was higher among infants with prematurity or from multifetal births and lower among those with siblings, later-season birth, or no early outpatient care. Social and structural disparities in nirsevimab uptake improved in the second season, whereas disparities in RSVpreF uptake persisted.Conclusions  The uptake of RSV preventive strategies increased across 2 seasons, with a higher uptake of maternal RSVpreF vaccination than nirsevimab.
SN  - 2950-5410
ER  -