Nirsevimab Effectiveness at Preventing RSV-Related Hospitalization in Infants.

NEJM evidence Pub Date : 2025-03-01 Epub Date: 2025-02-25 DOI:10.1056/EVIDoa2400275
Marie Joelle Jabagi, Jérémie Cohen, Marion Bertrand, Martin Chalumeau, Mahmoud Zureik
{"title":"Nirsevimab Effectiveness at Preventing RSV-Related Hospitalization in Infants.","authors":"Marie Joelle Jabagi, Jérémie Cohen, Marion Bertrand, Martin Chalumeau, Mahmoud Zureik","doi":"10.1056/EVIDoa2400275","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>In pivotal trials, nirsevimab showed promising efficacy in reducing hospitalizations for respiratory syncytial virus-associated lower respiratory tract infections (RSV-LRTIs). Nirsevimab's real-world effectiveness needs to be assessed.</p><p><strong>Methods: </strong>This population-based study used the French National Health Data System. All infants born between February 6 and September 15, 2023 were eligible. Each day during the study period (September 15, 2023, to January 31, 2024), all infants newly passively immunized with nirsevimab were matched to unimmunized controls in a 1:1 ratio according to sex, birth month, gestational age, department of residence, and the French Social Deprivation Index (Fdep). Study outcomes included RSV-LRTI-related hospitalization, RSV-LRTI necessitating admission to a pediatric intensive care unit (PICU) or high dependency unit (HDU), and RSV-LRTI requiring ventilation support or oxygen therapy. We estimated nirsevimab effectiveness using propensity score-weighted conditional Cox models.</p><p><strong>Results: </strong>The study included 82,474 infants (41,237 in each group) with a median follow-up of 118 days (interquartile range, 76 to 125). The population included predominantly male infants (52.5%) born at term (94.6%), mostly between April and July 2023 (64.0%), and from more advantaged municipalities (FDep first quintile: 29.8%). In total, 342 infants (0.8%) in the nirsevimab group and 992 (2.4%) in the unimmunized group were hospitalized for RSV-LRTI. Nirsevimab's effectiveness was 65% (95% confidence interval [CI], 61 to 69) for RSV-LRTI hospitalizations; 74% (95% CI, 56 to 85) for RSV-LRTI PICU admissions; 64% (95% CI, 55 to 71) for RSV-LRTI HDU admissions; 66% (95% CI, 51 to 76) for RSV-LRTI hospitalization requiring ventilation support; and 67% (95% CI, 57 to 75) for RSV-LRTI hospitalization requiring oxygen therapy. Subgroup and sensitivity analyses yielded consistent effectiveness estimates.</p><p><strong>Conclusions: </strong>This study in a nationwide monoclonal antibody infusion setting suggests that a single injection of nirsevimab was associated with substantial protection of infants against hospitalization for RSV-LRTI.</p>","PeriodicalId":74256,"journal":{"name":"NEJM evidence","volume":"4 3","pages":"EVIDoa2400275"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NEJM evidence","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1056/EVIDoa2400275","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/25 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: In pivotal trials, nirsevimab showed promising efficacy in reducing hospitalizations for respiratory syncytial virus-associated lower respiratory tract infections (RSV-LRTIs). Nirsevimab's real-world effectiveness needs to be assessed.

Methods: This population-based study used the French National Health Data System. All infants born between February 6 and September 15, 2023 were eligible. Each day during the study period (September 15, 2023, to January 31, 2024), all infants newly passively immunized with nirsevimab were matched to unimmunized controls in a 1:1 ratio according to sex, birth month, gestational age, department of residence, and the French Social Deprivation Index (Fdep). Study outcomes included RSV-LRTI-related hospitalization, RSV-LRTI necessitating admission to a pediatric intensive care unit (PICU) or high dependency unit (HDU), and RSV-LRTI requiring ventilation support or oxygen therapy. We estimated nirsevimab effectiveness using propensity score-weighted conditional Cox models.

Results: The study included 82,474 infants (41,237 in each group) with a median follow-up of 118 days (interquartile range, 76 to 125). The population included predominantly male infants (52.5%) born at term (94.6%), mostly between April and July 2023 (64.0%), and from more advantaged municipalities (FDep first quintile: 29.8%). In total, 342 infants (0.8%) in the nirsevimab group and 992 (2.4%) in the unimmunized group were hospitalized for RSV-LRTI. Nirsevimab's effectiveness was 65% (95% confidence interval [CI], 61 to 69) for RSV-LRTI hospitalizations; 74% (95% CI, 56 to 85) for RSV-LRTI PICU admissions; 64% (95% CI, 55 to 71) for RSV-LRTI HDU admissions; 66% (95% CI, 51 to 76) for RSV-LRTI hospitalization requiring ventilation support; and 67% (95% CI, 57 to 75) for RSV-LRTI hospitalization requiring oxygen therapy. Subgroup and sensitivity analyses yielded consistent effectiveness estimates.

Conclusions: This study in a nationwide monoclonal antibody infusion setting suggests that a single injection of nirsevimab was associated with substantial protection of infants against hospitalization for RSV-LRTI.

背景:在关键试验中,nirsevimab在减少呼吸道合胞病毒相关性下呼吸道感染(RSV-LRTIs)的住院率方面显示出良好的疗效。Nirsevimab在现实世界中的疗效有待评估:这项基于人群的研究使用了法国国家健康数据系统。所有在 2023 年 2 月 6 日至 9 月 15 日期间出生的婴儿均符合条件。在研究期间(2023 年 9 月 15 日至 2024 年 1 月 31 日)的每一天,根据性别、出生月份、胎龄、居住省份和法国社会贫困指数(Fdep),将所有新近接受过尼舍韦单抗被动免疫的婴儿与未接受免疫的对照组按 1:1 的比例进行配对。研究结果包括与 RSV-LRTI 相关的住院治疗、需要入住儿科重症监护病房 (PICU) 或高度依赖病房 (HDU) 的 RSV-LRTI 以及需要通气支持或氧气治疗的 RSV-LRTI。我们使用倾向得分加权条件 Cox 模型估算了 nirsevimab 的有效性:研究共纳入 82474 名婴儿(每组 41237 名),中位随访时间为 118 天(四分位间范围为 76 到 125 天)。研究对象主要为男婴(52.5%),足月出生(94.6%),大部分在 2023 年 4 月至 7 月间出生(64.0%),来自条件较好的城市(FDep 第一五分位数:29.8%)。总共有 342 名(0.8%)尼舍维单抗组婴儿和 992 名(2.4%)未免疫组婴儿因 RSV-LRTI 而住院治疗。对于因 RSV-LRTI 住院的婴儿,涅舍维单抗的有效率为 65%(95% 置信区间 [CI],61-69);对于因 RSV-LRTI 入住 PICU 的婴儿,有效率为 74%(95% 置信区间 [CI],56-85);对于因 RSV-LRTI 入住 HDU 的婴儿,有效率为 64%(95% 置信区间 [CI],55-71);对于因 RSV-LRTI 住院需要通气支持的婴儿,有效率为 66%(95% 置信区间 [CI],51-76);对于因 RSV-LRTI 住院需要氧疗的婴儿,有效率为 67%(95% 置信区间 [CI],57-75)。分组和敏感性分析得出了一致的有效性估计值:这项在全国范围内进行的单克隆抗体输注研究表明,单次注射尼舍单抗可有效防止婴儿因 RSV-LRTI 而住院。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信