van Doorn Eva, Darvishian Maryam, Dijkstra Frederika, Donker Gé A, Overduin Pieter, Meijer Adam, Hak Eelko
Unit of PharmacoTherapy, -Epidemiology & -Economics (PTE(2)), Department of Pharmacy, University of Groningen, Groningen, The Netherlands.
Unit of PharmacoTherapy, -Epidemiology & -Economics (PTE(2)), Department of Pharmacy, University of Groningen, Groningen, The Netherlands; Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Vaccine. 2017 May 15;35(21):2831-2839. doi: 10.1016/j.vaccine.2017.04.012. Epub 2017 Apr 12.
Information about influenza vaccine effectiveness (IVE) is important for vaccine strain selection and immunization policy decisions. The test-negative design (TND) case-control study is commonly used to obtain IVE estimates. However, the definition of the control patients may influence IVE estimates. We have conducted a TND study using the Dutch Sentinel Practices of NIVEL Primary Care Database which includes data from patients who consulted the General Practitioner (GP) for an episode of acute influenza-like illness (ILI) or acute respiratory infection (ARI) with known influenza vaccination status. Cases were patients tested positive for influenza virus. Controls were grouped into those who tested (1) negative for influenza virus (all influenza negative), (2) negative for influenza virus, but positive for respiratory syncytial virus, rhinovirus or enterovirus (non-influenza virus positive), and (3) negative for these four viruses (pan-negative). We estimated the IVE over all epidemic seasons from 2003/2004 through 2013/2014, pooled IVE for influenza vaccine partial/full matched and mismatched seasons and the individual seasons using generalized linear mixed-effect and multiple logistic regression models. The overall IVE adjusted for age, GP ILI/ARI diagnosis, chronic disease and respiratory allergy was 35% (95% CI: 15-48), 64% (95% CI: 49-75) and 21% (95% CI: -1 to 39) for all influenza negative, non-influenza virus positive and pan-negative controls, respectively. In both the main and subgroup analyses IVE estimates were the highest using non-influenza virus positive controls, likely due to limiting inclusion of controls without laboratory-confirmation of a virus causing the respiratory disease.
流感疫苗效力(IVE)信息对于疫苗毒株选择和免疫政策决策至关重要。检测阴性设计(TND)病例对照研究常用于获得IVE估计值。然而,对照患者的定义可能会影响IVE估计值。我们利用荷兰NIVEL初级保健数据库的哨点实践进行了一项TND研究,该数据库包含因急性流感样疾病(ILI)或急性呼吸道感染(ARI)发作而咨询全科医生(GP)且已知流感疫苗接种状况的患者数据。病例为流感病毒检测呈阳性的患者。对照分为以下几类:(1)流感病毒检测呈阴性(所有流感阴性);(2)流感病毒检测呈阴性,但呼吸道合胞病毒、鼻病毒或肠道病毒检测呈阳性(非流感病毒阳性);(3)这四种病毒检测均呈阴性(全阴性)。我们使用广义线性混合效应模型和多元逻辑回归模型估计了2003/2004年至2013/2014年所有流行季节的IVE、流感疫苗部分/完全匹配和不匹配季节的合并IVE以及各个季节的IVE。调整年龄、全科医生ILI/ARI诊断、慢性病和呼吸道过敏因素后,所有流感阴性、非流感病毒阳性和全阴性对照的总体IVE分别为35%(95%CI:15 - 48)、64%(95%CI:49 - 75)和21%(95%CI: - 1至39)。在主要分析和亚组分析中,使用非流感病毒阳性对照时IVE估计值最高,这可能是由于限制纳入未通过实验室确认导致呼吸道疾病的病毒的对照。