Zhang Bo-Xun, Lin Wen-Yang, Huang Tsai-Kuei
Annu Int Conf IEEE Eng Med Biol Soc. 2023 Jul;2023:1-4. doi: 10.1109/EMBC40787.2023.10340698.
Vaccine safety is a critical issue for public health, which has recently become more crucial than ever since COVID-19 started to spread worldwide in 2020. Many COVID-19 vaccines have been developed and used without following the traditional three clinical trial stages. Instead, most COVID-19 vaccines were approved through emergency use approval (EUA) within one year, significantly raising the risk of rare and severe adverse events. Reporting systems like the Vaccine Adverse Event Reporting System (VAERS) have been established worldwide to detect unknown and severe adverse reactions as early as possible. Although experts and researchers have been working hard to find ways to detect adverse vaccine event (AVE) signals from VAERS data, most of the contemporary methods are statistical methods based on measuring the disproportionality between vaccine-induced events and non-vaccine-induced events. This paper proposes a novel ensemble AVE detection method, which adopts a stacking ensemble of various disproportionality indicators, fusing dual-scale contingency values measured in single and cumulative yearly duration, and embraces the concept of feature concatenation. Experiments conducted on US VAERS data to predict AVE caused by COVID-19 vaccines show that our proposed method is effective. We observed that: (1) Stacking ensemble of various disproportionality indicators is superior to any single disproportionality indicator and voting ensemble method; (2) Fusing dual-scale contingency values and feature concatenation brings synergy to our proposed stacking ensemble AVE detection. Compared to the best disproportionality metric in this study, our top-performing ensemble version exhibited a 34% improvement in accuracy, 71% in precision, 29% in recall, and 77% in F-measure, with a slight decrease (8%) in specificity.
疫苗安全是公共卫生的关键问题,自2020年新冠病毒开始在全球传播以来,这一问题比以往任何时候都更加重要。许多新冠疫苗在研发和使用过程中并未遵循传统的三个临床试验阶段。相反,大多数新冠疫苗在一年内通过紧急使用授权(EUA)获得批准,这显著增加了罕见和严重不良事件的风险。全球已建立了诸如疫苗不良事件报告系统(VAERS)之类的报告系统,以便尽早发现未知的严重不良反应。尽管专家和研究人员一直在努力寻找从VAERS数据中检测疫苗不良事件(AVE)信号的方法,但大多数现代方法都是基于衡量疫苗诱导事件和非疫苗诱导事件之间不成比例性的统计方法。本文提出了一种新颖的集成AVE检测方法,该方法采用各种不成比例性指标的堆叠集成,融合在单一年度持续时间和累积年度持续时间中测量的双尺度列联值,并采用特征拼接的概念。对美国VAERS数据进行的预测新冠疫苗引起的AVE的实验表明,我们提出的方法是有效的。我们观察到:(1)各种不成比例性指标的堆叠集成优于任何单个不成比例性指标和投票集成方法;(2)融合双尺度列联值和特征拼接为我们提出的堆叠集成AVE检测带来了协同作用。与本研究中最佳的不成比例性度量相比,我们表现最佳的集成版本在准确率上提高了34%,精确率提高了71%,召回率提高了29%,F值提高了77%,特异性略有下降(8%)。