Núñez Olivier, Olmedo Carmen, Moreno-Perez David, Lorusso Nicola, Fernández Martínez Sergio, Pastor Villalba Pedro Eliseo, Gutierrez Ángeles, Alonso Garcia Marcos, Latasa Pello, Sancho Rosa, Mendioroz Jacobo, Martinez-Marcos Montserrat, Muñoz Platón Enriqueta, García Rivera María Victoria, Pérez-Martinez Olaia, Álvarez-Gil Rosa, Rivas Wagner Eva, López Gonzalez-Coviella Nieves, Zornoza Matilde, Barranco M Isabel, Pacheco M Del Carmen, Álvarez Río Virginia, Fiol Jaume Miguel, Morey Arance Roxana, Adiego Sancho Begoña, Mendez Diaz Manuel, Batalla Noa, Andreu Cristina, Castilla Jesús, García Cenoz Manuel, Fernández Ibáñez Ana, Huerta Huerta Marta, Ibáñez Pérez Ana Carmen, Berradre Sáenz Belén, Lamas Joaquín, Hermoso Luisa, Casado Cobo Susana, Galán Cuesta Manuel, Montenegro Sara, Domínguez María, Jarrín Inmaculada, Limia Aurora, Pastor-Barriuso Roberto, Monge Susana
National Centre of Epidemiology, Institute of Health Carlos III, Madrid, Spain.
CIBER in Epidemiology and Public Health (CIBERESP), Madrid, Spain.
Euro Surveill. 2025 Feb;30(5). doi: 10.2807/1560-7917.ES.2025.30.5.2400596.
BackgroundRespiratory syncytial virus (RSV) causes substantial morbidity in infants < 1 year. In October 2023, Spain recommended the monoclonal antibody nirsevimab to all children born since 1 April 2023, at birth or as catch-up if born before October 2023.AimWe estimated nirsevimab effectiveness in preventing RSV hospitalisations during the 2023/24 season.MethodsWe conducted a nationwide population-based matched case-control study. Cases were children hospitalised for lower respiratory tract infection who were RSV PCR-positive. For each case, we selected four population density controls born in the same province and date (±2 days). We defined at-birth immunisation as receiving nirsevimab during the first 2 weeks of life, and catch-up immunisation within 30 days from campaign onset. Causal intention-to-treat (ITT) and per-protocol (PP) effectiveness was estimated using inverse-probability-of-immunisation weighted conditional logistic regression.ResultsWe included 406 cases and 1,623 controls in catch-up and 546 cases and 2,182 controls in at-birth immunisation studies. Effectiveness in preventing RSV hospitalisations for catch-up immunisation was 71% (95% confidence interval (CI): 65-76) by ITT and 80% (95% CI: 75-84) PP. Effectiveness for at-birth immunisation was 78% (95% CI: 73-82) by ITT and 83% (95% CI: 79-87) PP. Effectiveness was similar for ICU admission, need of mechanical ventilation, and RSV viral subgroups A and B. Children born pre-term or with birthweight < 2,500 g showed lower PP effectiveness of 60-70%.ConclusionsPopulation-level nirsevimab immunoprophylaxis in children in their first RSV season was very effective in preventing RSV hospitalisations, ICU admission and mechanical ventilation, with reduced but still high effectiveness for pre-term and low-birthweight children.
背景
呼吸道合胞病毒(RSV)在1岁以下婴儿中导致大量发病。2023年10月,西班牙建议对2023年4月1日以后出生的所有儿童在出生时或如果在2023年10月之前出生则作为补种接种单克隆抗体nirsevimab。
目的
我们估计了nirsevimab在预防2023/24季节RSV住院方面的有效性。
方法
我们开展了一项基于全国人口的匹配病例对照研究。病例为因下呼吸道感染住院且RSV PCR检测呈阳性的儿童。对于每个病例,我们选择了4名在同一省份且出生日期相同(±2天)的人口密度对照。我们将出生时免疫定义为在生命的前2周内接受nirsevimab,补种免疫定义为在活动开始后30天内接种。使用免疫概率加权条件逻辑回归估计因果意向性治疗(ITT)和符合方案(PP)有效性。
结果
在补种免疫研究中,我们纳入了406例病例和1623名对照,在出生时免疫研究中纳入了546例病例和2182名对照。补种免疫预防RSV住院的ITT有效性为71%(95%置信区间(CI):65 - 76),PP有效性为80%(95% CI:75 - 84)。出生时免疫的ITT有效性为78%(95% CI:73 - 82),PP有效性为83%(95% CI:79 - 87)。对于入住重症监护病房(ICU)、需要机械通气以及RSV病毒A和B亚组,有效性相似。早产或出生体重<2500g的儿童PP有效性较低,为60 - 70%。
结论
在儿童首个RSV季节进行人群水平的nirsevimab免疫预防在预防RSV住院、ICU入住和机械通气方面非常有效,对早产和低出生体重儿童有效性降低但仍然较高。