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韩国婴儿轮状病毒疫苗安全性的广泛评估:数据驱动信号检测方法的见解

A broad assessment of rotavirus vaccine safety in infants in Korea: Insights from a data-driven signal detection approach.

作者信息

Jeong Na-Young, Cho Haerin, Kim Hee-Jin, Choi Nam-Kyong

机构信息

Health Science Convergence Research Institute, Ewha Womans University, Seoul, Republic of Korea.

Department of Health Convergence, College of Science and Industry Convergence, Ewha Womans University, Seoul, Republic of Korea.

出版信息

Hum Vaccin Immunother. 2025 Dec;21(1):2465161. doi: 10.1080/21645515.2025.2465161. Epub 2025 Feb 12.

Abstract

In light of the widespread use of rotavirus vaccines, there is a pressing need to perform thorough, large-scale surveillance to actively monitor safety. This study aimed to identify potential adverse events following rotavirus vaccination in infants. Using a nationwide linked database of the national immunization registry and health insurance claims data, we identified infants vaccinated with the first dose of rotavirus vaccine between January 2016 and October 2022. The self-controlled tree-temporal scan statistics method analyzed all incident diagnoses recorded within 56 days post-vaccination and evaluated all temporal risk windows. Among 1,720,778 rotavirus vaccine recipients 64,752 infants contributed to the analysis, yielding 72,970 incident diagnoses. Of these, 28 clusters were categorized as known adverse drug reactions (ADRs), including infection following immunization (Days 1-2, <.001), viral infection (Days 1-5, <.001), urticaria and erythema (Days 3-9, <.001), acute upper respiratory infections (Days 28-42, <.001), and pneumonia (Days 9-19 or 28-42, <.001). Seventeen clusters were classified as ADR-related events, such as the ones clinically related to ADR or lower-level diagnostic codes of ADR. The remaining 26 clusters were classified as signals, including sepsis (Days 1-20, <.001), meningitis (Days 1-23, <.001), liver disease (Days 4-11, <.001), and tubulo-interstitial nephritis (Days 11-38, <.001). A cluster of intussusceptions was only found in monovalent vaccine-stratified analysis (Days 5-8,  = 0.005). This study confirmed known ADRs following rotavirus vaccination, while identifying potential safety signals requiring further investigation. These findings emphasize the importance of active vaccine surveillance and underscore the need for epidemiological studies with validated outcome definitions to confirm causal relationships between rotavirus vaccination and the detected outcomes.

摘要

鉴于轮状病毒疫苗的广泛使用,迫切需要进行全面、大规模的监测以积极监测安全性。本研究旨在确定婴儿接种轮状病毒疫苗后潜在的不良事件。利用全国免疫登记和健康保险理赔数据的关联数据库,我们确定了2016年1月至2022年10月期间接种第一剂轮状病毒疫苗的婴儿。自我对照的树状时间扫描统计方法分析了接种疫苗后56天内记录的所有发病诊断,并评估了所有时间风险窗口。在1,720,778名接种轮状病毒疫苗的儿童中,64,752名婴儿参与了分析,产生了72,970例发病诊断。其中,28个聚集性病例被归类为已知的药物不良反应(ADR),包括免疫接种后感染(第1 - 2天,<.001)、病毒感染(第1 - 5天,<.001)、荨麻疹和红斑(第3 - 9天,<.001)、急性上呼吸道感染(第28 - 42天,<.001)以及肺炎(第9 - 19天或28 - 42天,<.001)。17个聚集性病例被归类为与ADR相关的事件,例如临床上与ADR相关或ADR较低级诊断编码的事件。其余26个聚集性病例被归类为信号,包括败血症(第1 - 20天,<.001)、脑膜炎(第1 - 23天,<.001)、肝病(第4 - 11天,<.001)和肾小管间质性肾炎(第11 - 38天,<.001)。仅在单价疫苗分层分析中发现了一组肠套叠病例(第5 - 8天, = 0.005)。本研究证实了轮状病毒疫苗接种后的已知ADR,同时确定了需要进一步调查的潜在安全信号。这些发现强调了主动疫苗监测的重要性,并强调需要进行具有验证结局定义的流行病学研究,以确认轮状病毒疫苗接种与检测到的结局之间的因果关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bfa/11834447/9896ff983e48/KHVI_A_2465161_F0001_OC.jpg

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