Early Detection of Hearing Impairment Signals Post-mRNA COVID-19 Vaccination: A Disproportionality Analysis Study on French Pharmacovigilance Database.

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Safety Pub Date : 2025-03-01 Epub Date: 2024-12-05 DOI:10.1007/s40264-024-01495-5
Dalil Boulefaa, Haleh Bagheri, Francesco Salvo, Marie-Blanche Rabier, Hélène Geniaux, Marion Lepelley, Fanny Rocher, Julien Mahe, Aurélie Grandvillemuin, Hung Thai-Van
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Abstract

Introduction: Improving adverse events following immunisation (AEFI) detection is vital for vaccine safety surveillance, as an early safety signal can help minimize risks. In February 2022, the World Health Organization reported a preliminary signal on sudden sensorineural hearing loss (SSNHL) following coronavirus disease 2019 (COVID-19) vaccination, 54 million persons in France received at least one dose, covering 78.8% of the population within a year.

Objective: The primary objective of this study was to identify a method of disproportionality analysis capable to detect a safety signal for hearing impairment (HI) as early as possible during the initial phases of the COVID-19 vaccination campaign. Secondly, we described all cases of SSNHL reported during vaccine booster campaigns in France.

Methods: Data from January 2011 to February 2022 were extracted from the French pharmacovigilance database. Cases were all spontaneous reports of AEFI for elasomeran and tozinameran, while non-cases were AEFI reported for other vaccines. Disproportionality analysis for HI was performed monthly during 2021, to estimate a reporting odds ratio (ROR). Four different methods were used for ROR estimation. Furthermore, we reviewed cases of SSNHL following messenger RNA COVID-19 vaccinations reported during booster campaigns, from 2 February 2022 to 1 March 2023, based on a comprehensive medical evaluation.

Results: Using a standard methodology, we identified a signal on 31 July 2021 (ROR 1.50, 95% confidence interval [CI] [1.06-2.18]). Multivariate analysis adjusted for sex, age, ototoxic drugs and excluding reference reports of common AEFI for vaccines allowed us to detect the HI signal as early as 31 March 2021 (ROR 2.67, 95% CI [1.36-5.57]). The SSNHL reporting rate was estimated to be 0.83/1,000,000 doses for tozinameran and 4.3/1,000,000 for elasomeran during the booster campaigns.

Conclusion: Using a well-structured disproportionality analysis could have enhanced early detection of safety signals and contribute to risk minimizing measures. According to descriptive data, HI following mRNA COVID-19 vaccines remains rare.

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COVID-19疫苗接种mrna后听力损伤信号的早期检测:法国药物警戒数据库的歧化分析研究
导言:改进免疫接种后不良事件(AEFI)的检测对于疫苗安全监测至关重要,因为早期的安全信号有助于将风险降至最低。2022年2月,世界卫生组织报告了2019冠状病毒病(COVID-19)疫苗接种后突发性感音神经性听力损失(SSNHL)的初步信号,法国有5400万人接种了至少一剂疫苗,一年内覆盖了78.8%的人口。目的:本研究的主要目的是确定一种歧化分析方法,能够在COVID-19疫苗接种运动的初始阶段尽早检测听力损伤(HI)的安全信号。其次,我们描述了在法国疫苗加强运动期间报告的所有SSNHL病例。方法:从法国药物警戒数据库中提取2011年1月至2022年2月的数据。报告的病例均为弹力蛋白蛋白和托扎美兰的急性脑损伤,而非其他疫苗的急性脑损伤。在2021年期间每月对HI进行歧化分析,以估计报告的优势比(ROR)。采用了四种不同的ROR估计方法。此外,根据综合医学评估,我们回顾了2022年2月2日至2023年3月1日加强运动期间报告的信使RNA COVID-19疫苗接种后的SSNHL病例。结果:使用标准方法,我们在2021年7月31日确定了一个信号(ROR 1.50, 95%置信区间[CI][1.06-2.18])。多因素分析校正了性别、年龄、耳毒性药物,并排除了疫苗常见AEFI的参考报告,使我们最早在2021年3月31日就发现了HI信号(ROR 2.67, 95% CI[1.36-5.57])。在加强活动期间,估计tozinameran的SSNHL报告率为0.83/ 100万剂,elasomeran为4.3/ 100万剂。结论:使用结构良好的歧化分析可以增强早期发现安全信号,并有助于采取风险最小化措施。根据描述性数据,mRNA COVID-19疫苗后的HI仍然很少见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Drug Safety Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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