Interim Evaluation of Respiratory Syncytial Virus Hospitalization Rates Among Infants and Young Children After Introduction of Respiratory Syncytial Virus Prevention Products - United States, October 2024-February 2025.

Monica E Patton,Heidi L Moline,Michael Whitaker,Ayzsa Tannis,Huong Pham,Ariana P Toepfer,Christopher A Taylor,Leah Goldstein,Arthur Reingold,Pam Daily Kirley,Nisha B Alden,Breanna Kawasaki,James Meek,Daewi Kim,Lucy S Witt,Kyle P Openo,Patricia A Ryan,Erica Mumm,Ruth Lynfield,Yadira Salazar-Sanchez,Francesca Pacheco,Fiona Keating,Bridget J Anderson,Brenda L Tesini,Christina B Felsen,Melissa Sutton,Ann Thomas,William Schaffner,H Keipp Talbot,Khalil Harbi,Emma Doran,Geoffrey A Weinberg,Mary A Staat,Daniel C Payne,Natasha B Halasa,Laura Stewart,Julie A Boom,Leila C Sahni,Eileen J Klein,Janet A Englund,John V Williams,Marian G Michaels,Jennifer E Schuster,Rangaraj Selvarangan,Peter G Szilagyi,Fiona P Havers,Fatimah S Dawood
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Abstract

Maternal respiratory syncytial virus (RSV) vaccine and nirsevimab, a long-acting monoclonal antibody for infants aged 0-7 months and children aged 8-19 months who are at increased risk for severe RSV disease, became widely available for prevention of severe RSV disease among infants and young children during the 2024-25 RSV season. To evaluate the association between availability of these products and infant and child RSV-associated hospitalization rates, the rates among children aged <5 years were compared for the 2024-25 and 2018-20 RSV seasons using data from the RSV-Associated Hospitalization Surveillance Network (RSV-NET) and New Vaccine Surveillance Network (NVSN). Among infants aged 0-7 months (eligible for protection with maternal vaccination or nirsevimab), 2024-25 RSV-associated hospitalization rates were lower compared with 2018-20 pooled rates (estimated relative rate reductions of 43% [RSV-NET: 95% CI = 40%-46%] and 28% [NVSN: 95% CI = 18%-36%]). The largest estimated rate reduction was observed among infants aged 0-2 months (RSV-NET: 52%, 95% CI = 49%-56%; NVSN: 45%, 95% CI = 32%-57%) and during peak hospitalization periods (December-February). These findings support Advisory Committee on Immunization Practices' recommendations for maternal vaccination or nirsevimab to protect against severe RSV disease in infants and highlight the importance of implementing the recommendations to protect infants as early in the RSV season as possible, before peak transmission, and for infants born during the RSV season, within the first week of life, ideally during the birth hospitalization.
引入呼吸道合胞病毒预防产品后婴幼儿呼吸道合胞病毒住院率的中期评估——美国,2024年10月- 2025年2月
母亲呼吸道合胞病毒(RSV)疫苗和nirsevimab(一种用于0-7月龄婴儿和8-19月龄儿童的长期单克隆抗体,这些婴儿严重RSV疾病的风险增加)在2024-25 RSV季节被广泛用于预防婴幼儿严重RSV疾病。为了评估这些产品的可获得性与婴儿和儿童RSV相关住院率之间的关系,使用RSV相关住院监测网络(RSV- net)和新疫苗监测网络(NVSN)的数据,比较了2024-25年和2018-20年RSV季节5岁以下儿童的住院率。在0-7个月的婴儿中(符合母亲接种疫苗或nirsevimab保护的条件),2024-25年rsv相关住院率低于2018-20年合并率(估计相对率降低43% [RSV-NET: 95% CI = 40%-46%]和28% [NVSN: 95% CI = 18%-36%])。在0-2个月的婴儿中观察到最大的估计发生率下降(RSV-NET: 52%, 95% CI = 49%-56%;NVSN: 45%, 95% CI = 32%-57%)和住院高峰期(12月- 2月)。这些发现支持了免疫实践咨询委员会关于母亲接种疫苗或使用nirseimab预防婴儿严重RSV疾病的建议,并强调了在RSV季节尽可能早、在传播高峰之前实施这些建议的重要性,以及在RSV季节出生的婴儿在出生后第一周内,最好是在出生住院期间实施这些建议。
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