关键词: bronchiolitis case–control studies immunisation monoclonal antibodies nirsevimab paediatric intensive care units respiratory syncytial virus treatment effectiveness

Mesh : Humans France / epidemiology Respiratory Syncytial Virus Infections / drug therapy Infant Intensive Care Units, Pediatric / statistics & numerical data Case-Control Studies Male Female Hospitalization / statistics & numerical data Respiratory Syncytial Virus, Human / drug effects Antibodies, Monoclonal, Humanized / therapeutic use Antiviral Agents / therapeutic use Bronchiolitis / drug therapy virology Bronchiolitis, Viral / drug therapy virology Treatment Outcome

来  源:   DOI:10.1111/irv.13311   PDF(Pubmed)

Abstract:
In September 2023, France was one of the first countries that started a national immunisation campaign with nirsevimab, a new monoclonal antibody against respiratory syncytial virus (RSV). Using data from a network of paediatric intensive care units (PICUs), we aimed to estimate nirsevimab effectiveness against severe cases of RSV bronchiolitis in France. We conducted a case-control study based on the test-negative design and included 288 infants reported by 20 PICUs. We estimated nirsevimab effectiveness at 75.9% (48.5-88.7) in the main analysis and 80.6% (61.6-90.3) and 80.4% (61.7-89.9) in two sensitivity analyses. These real-world estimates confirmed the efficacy observed in clinical studies.
摘要:
2023年9月,法国是最早开始使用nirsevimab进行全国免疫运动的国家之一,一种新的抗呼吸道合胞病毒(RSV)的单克隆抗体。使用来自儿科重症监护病房(PICU)网络的数据,我们旨在评估nirsevimab对法国严重RSV毛细支气管炎的疗效.我们进行了一项基于测试阴性设计的病例对照研究,包括20个PICU报告的288名婴儿。我们在主要分析中估计nirsevimab的有效性为75.9%(48.5-88.7),在两次敏感性分析中估计为80.6%(61.6-90.3)和80.4%(61.7-89.9)。这些真实世界的估计证实了在临床研究中观察到的功效。
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