Evidence map›Paper›PMID 39638989›Full record

ArticleDrug safety2025

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

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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In one paragraph

Article in Drug safety, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Dalil Boulefaa *Department of Medical and Clinical Pharmacology, Regional Pharmacovigilance Centre of Toulouse, Clinical Investigation Centre 1436, Toulouse University Hospital, Toulouse, France. dalilboulefaa@gmail.com.ORCID 0009-0009-6308-2633
Haleh Bagheri *Department of Medical and Clinical Pharmacology, Regional Pharmacovigilance Centre of Toulouse, Clinical Investigation Centre 1436, Toulouse University Hospital, Toulouse, France.
Francesco SalvoDepartment of Medical Pharmacology, Hospital University of Bordeaux, Inserm, BPH, U1219, Equipe AHeaD, Bordeaux, France.
Marie-Blanche RabierRegional Pharmacovigilance Centre of Franche-Comté, Besançon University Hospital, Besançon, France.
Hélène GeniauxRegional Centre of Pharmacovigilance of Limoges, Limoges University Hospital, Limoges, France.
Marion LepelleyRegional Centre of Pharmacovigilance of Grenoble, Grenoble-Alpes University Hospital, Grenoble, France.
Fanny RocherDepartment of Pharmacology and Pharmacovigilance Centre, Côte d'Azur University Medical Centre, Nice, France.
Julien MaheDepartment of Clinical Pharmacology, Regional Pharmacovigilance Centre, Poitiers University Hospital, Poitiers, France.
Aurélie GrandvillemuinRegional Centre of Pharmacovigilance of Bourgogne, Dijon University Hospital, Dijon, France.
Hung Thai-VanService d'Audiologie and d'Explorations Otoneurologiques, Hospices Civils de Lyon, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionImproving 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.

objectiveThe 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.

methodsData 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.

resultsUsing 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.

conclusionUsing 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.

Indexed as

COVID-19COVID-19 VaccinesHearing Loss, SensorineuralAdolescentAdultAdverse Drug Reaction Reporting SystemsAgedDatabases, FactualEarly DiagnosisFemaleFranceHumansImmunization, SecondaryMaleMiddle AgedPharmacovigilanceCOVID-19 Vaccines

Identifiers

PMID39638989
PMCPMC11829932

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.