[Nirsevimab immunization effectiveness against respiratory syncytial virus hospitalization in newborns: two season of use in Navarre, Spain].

IF 0.6
Noelia Vera-Punzano, Ana Navascués, Leticia Armendáriz, Natividad Viguria, Mercedes Herranz-Aguirre, Manuel García Cenoz, Camino Trobajo-Sanmartín, Aitziber Echeverria, Iván Martínez-Baz, Carmen Ezpeleta, Guillermo Ezpeleta, Jesús Castilla
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Abstract

Background: Respiratory syncytial virus (RSV) is the leading cause of infant hospitalisation. In 2022, nirsevimab was approved in the European Union to prevent severe respiratory disease due to RSV during the first year of life. Our aim is to evaluate the effectiveness of nirsevimab immunoprophylaxis in new-borns for preventing RSV -related hospitalisations in Navarre, Spain, during its first two seasons of use.

Methods: Nirsevimab was offered free of charge to infants born from October to December 2023 and from September to December 2024. Each cohort was followed until February of the following year. Cases were infants hospitalised for PCR-confirmed RSV infection. Cox regression was used to estimate the hazard ratio of hospitalisation for immunised versus non-immunised children.

Results: Nirsevimab was offered to 2,699 new-borns; of them, 2,541 (94.1%) received nirsevimab. In the 2023-2024 season, 17 RSV-related hospitalisations were recorded and 24 in the 2024-2025 season. The average risk of RSV hospitalisation was 7.6% in non-immunised new-borns versus 1.1% in immunised ones. Overall, effectiveness of nirsevimab was 79.5% (95% CI: 59.2 - 89.7), with estimates of 89.9% in 2023-2024 and 52.8% in 2024-2025, with no significant differences between seasons (p=0.055). On average, one RSV hospitalisation was prevented per 22.6 immunised infants.

Conclusions: Nirsevimab immunoprophylaxis substantially reduces RSV hospitalisations, helping ease paediatric hospital burden. However, as some immunised infants were still hospitalised, additional preventive measures remain necessary.

[尼塞维单抗免疫对新生儿呼吸道合胞病毒住院的有效性:西班牙纳瓦拉的两个使用季节]。
背景:呼吸道合胞病毒(RSV)是婴儿住院的主要原因。2022年,nirseimab在欧盟获得批准,用于预防生命第一年由RSV引起的严重呼吸道疾病。我们的目的是评估在西班牙纳瓦拉的新生儿中使用尼瑟维单抗免疫预防预防呼吸道合胞病毒相关住院治疗的有效性。方法:对2023年10月~ 12月和2024年9月~ 12月出生的婴儿免费给予尼瑟维单抗。每个队列都被跟踪到第二年2月。病例为因聚合酶链反应确诊的呼吸道合胞病毒感染而住院的婴儿。采用Cox回归估计接种与未接种儿童住院的风险比。结果:2,699例新生儿使用了Nirsevimab;其中2541例(94.1%)接受了尼罗昔单抗治疗。在2023-2024年季节,记录了17例与rsv相关的住院病例,2024-2025年季节记录了24例。未接种疫苗的新生儿因呼吸道合胞病毒住院的平均风险为7.6%,而接种疫苗的新生儿为1.1%。总体而言,nirsevimab的有效性为79.5% (95% CI: 59.2 - 89.7), 2023-2024年估计为89.9%,2024-2025年估计为52.8%,季节之间无显著差异(p=0.055)。平均每22.6名接种疫苗的婴儿可预防一例呼吸道合胞病毒住院。结论:尼塞维单抗免疫预防显著降低呼吸道合胞病毒住院率,有助于减轻儿科医院负担。然而,由于一些接种了疫苗的婴儿仍在住院,因此仍有必要采取额外的预防措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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