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使用 ROBINS-I 工具评估佐剂流感疫苗非随机研究的偏倚风险。

Evaluating risk of bias using ROBINS-I tool in nonrandomized studies of adjuvanted influenza vaccine.

机构信息

Vaccine Dynamics, Easton, MA, USA.

Center for Public Health Research, University of Milan-Bicocca, Monza, Italy; Laboratory of Public Health, Istituto Auxologico Italiano - IRCCS, Milan, Italy.

出版信息

Vaccine. 2023 Nov 30;41(49):7409-7418. doi: 10.1016/j.vaccine.2023.11.005. Epub 2023 Nov 10.

Abstract

Seasonal variation in influenza vaccine effectiveness (VE) makes real-world evidence (RWE) useful in supplementing the clinical-evidence base from randomized clinical trials. Adjuvanted inactivated influenza vaccine (aIIV) VE has been evaluated in multiple nonrandomized RWE studies. A systematic literature review of RWE studies evaluating the absolute or relative VE of aIIV was conducted. Identified studies were assessed by evaluators for risk of bias (RoB) by means of the ROBINS-I (Reduction of Bias In Non-randomized Studies of Interventions) tool to inform evidence-based medicine deliberations. Differences in evaluator assessments were resolved by consensus. The literature review yielded 14 follow-up studies, seven test-negative case-control (TNCC) studies, five traditional case-control studies, and one cluster-randomized clinical trial. Most follow-up studies and three TNCC studies were judged at low RoB. Issues increasing RoB included inadequate control of confounding, selection of controls, and reliance on recall of vaccination. The concerns identified in any of the designs could be mitigated with straightforward revisions to design or implementation. 17 of 27 nonrandomized studies of adjuvanted influenza-vaccine effectiveness, some from each of four study designs, were judged at low risk of material bias. These studies merit credence in assessing aIIV effectiveness relative to other influenza vaccines.

摘要

流感疫苗有效性(VE)的季节性变化使得真实世界证据(RWE)在补充随机临床试验的临床证据基础方面变得有用。佐剂灭活流感疫苗(aIIV)的 VE 已在多项非随机 RWE 研究中进行了评估。对评估 aIIV 的绝对或相对 VE 的 RWE 研究进行了系统的文献回顾。评估人员使用 ROBINS-I(干预措施非随机研究的偏倚降低)工具对确定的研究进行了风险评估(RoB),以告知循证医学审议。评估人员的评估差异通过共识解决。文献回顾产生了 14 项随访研究、7 项测试阴性病例对照(TNCC)研究、5 项传统病例对照研究和 1 项聚类随机临床试验。大多数随访研究和 3 项 TNCC 研究的 RoB 较低。增加 RoB 的问题包括混杂因素控制不足、对照选择和对疫苗接种的回忆依赖。任何设计中发现的问题都可以通过对设计或实施进行简单的修改来减轻。在评估佐剂流感疫苗相对于其他流感疫苗的有效性时,应考虑到这 27 项非随机研究中有 17 项(来自四种研究设计中的每一种)的风险较低。这些研究在评估 aIIV 的有效性方面值得信赖。

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