García-García María Luz, Alonso-López Patricia, Alcolea Sonia, Arroyas M, Pozo Francisco, Casas Inmaculada, Iglesias-Caballero Maria, Sánchez-León Rocío, Hurtado-Gallego Jara, Calvo Cristina
Pediatrics Department, Severo Ochoa University Hospital, Leganés, Spain.
Puerta de Hierro Institute for Health Research (IDIPHISA), Majadahonda, Spain.
Influenza Other Respir Viruses. 2025 May;19(5):e70105. doi: 10.1111/irv.70105.
Nirsevimab, a monoclonal antibody providing passive immunity against RSV infections in infants, was introduced in Spain in October 2023 for children under 6 months and those born during the epidemic season. This study aimed to compare the clinical and virological characteristics of respiratory infections in hospitalized infants before and after nirsevimab introduction.
We carried out a prospective study across two hospitals in Madrid during the 2022-2023 and 2023-2024 epidemic seasons. The study included infants under 12 months of age that were hospitalized with lower respiratory tract infections (LRTIs). Clinical, epidemiological, and virological data were analyzed and compared between the periods before and after the introduction of nirsevimab, as well as according to whether the infants had received this preventive treatment.
A total of 669 infants were included: 480 from October 2022 to March 2023 (S1) and 189 from October 2023 to March 2024 (S2). Respiratory infection-related admissions decreased by 62.5% in S2, with a 74.5% reduction in ICU admissions. RSV-related admissions decreased by 78%, HMPV by 36.6%, and adenovirus by 69.5%. Infants in S2 were older (p = 0.001) and had shorter hospital stays (p < 0.001) than in S1. Of 63 (33%) infants in S2 who received nirsevimab, 11 (17%) were diagnosed with RSV. High-flow oxygen use was less frequent among RSV patients treated with nirsevimab (p = 0.002).
Nirsevimab introduction was significantly associated with reduced hospitalizations and severity of RSV and other respiratory infections. Its use was associated with fewer admissions and reduced need for intensive care, especially in RSV-infected infants but also in HMPV and adenovirus-infected infants.
尼塞韦单抗是一种单克隆抗体,可为婴儿提供针对呼吸道合胞病毒(RSV)感染的被动免疫,于2023年10月在西班牙引入,用于6个月以下儿童以及在流行季节出生的儿童。本研究旨在比较尼塞韦单抗引入前后住院婴儿呼吸道感染的临床和病毒学特征。
我们在2022 - 2023年和2023 - 2024年流行季节期间,对马德里的两家医院进行了一项前瞻性研究。该研究纳入了因下呼吸道感染(LRTIs)住院的12个月以下婴儿。分析并比较了尼塞韦单抗引入前后各时期的临床、流行病学和病毒学数据,以及婴儿是否接受了这种预防性治疗的情况。
共纳入669名婴儿:2022年10月至2023年3月期间480名(S1),2023年10月至2024年3月期间189名(S2)。S2中与呼吸道感染相关的住院人数减少了62.5%,重症监护病房(ICU)住院人数减少了74.5%。与RSV相关的住院人数减少了78%,人偏肺病毒(HMPV)减少了36.6%,腺病毒减少了69.5%。S2中的婴儿比S1中的婴儿年龄更大(p = 0.001),住院时间更短(p < 0.001)。在S2中接受尼塞韦单抗治疗的63名(33%)婴儿中,11名(17%)被诊断为RSV感染。接受尼塞韦单抗治疗的RSV患者中,高流量吸氧的使用频率较低(p = 0.002)。
引入尼塞韦单抗与RSV及其他呼吸道感染的住院人数减少和严重程度降低显著相关。其使用与住院人数减少以及重症监护需求降低有关,特别是在RSV感染的婴儿中,在HMPV和腺病毒感染的婴儿中也是如此。