Pediatrics Department, Hospital Sant Joan de Déu, Barcelona, Spain.
Pediatric Infectious Diseases and Microbiome Research Group, Institut de Recerca Sant Joan de Déu, Spain.
Pediatr Allergy Immunol. 2024 Jun;35(6):e14175. doi: 10.1111/pai.14175.
Several clinical trials have shown that nirsevimab, an antibody targeting the respiratory syncytial virus (RSV), reduces RSV bronchiolitis requiring admission. In 2023-2024, Catalonia and Andorra adopted immunization strategies for children <6 months and those born during the epidemic season. This study evaluates the effectiveness of nirsevimab in preventing hospitalizations from RSV bronchiolitis.
In the epidemic season of 2023-2024, a test-negative case-control study was conducted in three hospitals from Catalonia and Andorra. Patients <12 months old admitted with bronchiolitis and tested for RSV using molecular microbiology tests were included. The effectiveness in preventing RSV bronchiolitis hospitalization and severe disease was estimated using multivariate models. Comparisons between immunized, non-immunized, and non-eligible patients were made in prospectively collected epidemiological, clinical, and microbiological variables.
Two hundred thirty-four patients were included. RSV was detected in 141/234 (60.2%), being less common in the immunized group (37% vs 75%, p < .001). The rate of immunized patients among those eligible was 59.7%. The estimated effectiveness for RSV-associated lower respiratory tract infection was 81.0% (95% confidence interval: 60.9-90.7), and for preventing severe disease (the need for NIV/CMV), 85.6% (41.7-96.4%). No significant differences by immunization status were observed in patients with RSV concerning viral coinfections, the need for NIV/CMV or length of hospital stay.
This study provides real-world evidence of the effectiveness of nirsevimab in preventing RSV-lower respiratory tract infection hospitalization and severe disease in infants during their first RSV season following a systematic immunization program. Immunized patients did not exhibit a higher rate of viral coinfections nor differences in clinical severity once admitted.
多项临床试验表明,靶向呼吸道合胞病毒(RSV)的抗体 nirsevimab 可降低需要住院治疗的 RSV 细支气管炎。2023-2024 年,加泰罗尼亚和安道尔采用了针对 <6 个月大儿童和流行季节出生儿童的免疫接种策略。本研究评估了 nirsevimab 预防 RSV 细支气管炎住院的有效性。
在 2023-2024 年流行季节,在加泰罗尼亚和安道尔的三家医院进行了一项病例对照研究。纳入因细支气管炎入院且使用分子微生物学检测检测到 RSV 的 <12 个月大的患者。使用多变量模型估计预防 RSV 细支气管炎住院和重症疾病的有效性。对免疫、未免疫和不符合条件的患者进行了前瞻性收集的流行病学、临床和微生物学变量的比较。
共纳入 234 例患者。234 例患者中,141/234(60.2%)检测到 RSV,免疫组中 RSV 检出率较低(37%比 75%,p<0.001)。符合条件的患者中免疫接种率为 59.7%。与 RSV 相关的下呼吸道感染的估计有效性为 81.0%(95%置信区间:60.9-90.7),预防重症疾病(需要 NIV/CMV)的有效性为 85.6%(41.7-96.4%)。在 RSV 患者中,免疫状态与病毒合并感染、需要 NIV/CMV 或住院时间长短均无显著差异。
本研究提供了在系统免疫接种计划后,婴儿首次 RSV 季节中 nirsevimab 预防 RSV 下呼吸道感染住院和重症疾病的真实世界证据。免疫接种患者在入院后并未表现出更高的病毒合并感染率或临床严重程度的差异。