Comparison of the rates of emergent otologic adverse events following mRNA COVID-19 versus influenza vaccination: a matched cohort analysis

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Tina Munjal, Shelley Batts, Saurabh Gombar, Konstantina M Stankovic

Front Neurol. 2025 Aug 7;16:1637870. doi: 10.3389/fneur.2025.1637870. eCollection 2025.

ABSTRACT

BACKGROUND: Otologic adverse events (AEs) have been occasionally reported as sequalae of COVID-19 vaccination, although their incidence in comparison with that of preexisting vaccines with high uptake remains unclear. This study compared the rates of new-onset otologic AEs among matched adults receiving mRNA COVID-19 vaccination versus influenza vaccination.

METHODS: This retrospective cohort study used electronic health records (EHR) data from Stanford Health Care to identify adults aged 50-89 years with no history of otologic disorders prior to first Pfizer/Moderna COVID-19 vaccine (December 2020-January 2022) or any pre-pandemic influenza vaccine (January 2016-December 2019). Patients were categorized by vaccination into FluVax or COVIDVax cohorts. A 90-day history pre-vaccination (baseline period) and ≥6 months follow-up post-vaccination were required. Event rates of new-onset hearing loss (HL), sudden HL, tinnitus, vertigo/dizziness, aural fullness, and otalgia in the 6 months post-vaccination were compared between groups after high-dimensional propensity score (hdPS) matching. A sensitivity analysis was conducted among patients with no COVID-19 infection at any time. Odds ratios (ORs) were calculated using logistic regression for the hdPS matched cohorts.

RESULTS: After hdPS matching, 20,325 patients were included into the FluVax and COVIDVax cohorts, respectively (mean age: 65.5 and 65.2 years; 53.1 and 53.8% females). The rates of otologic AEs in the 6 months post-vaccination were similarly low for the FluVax and COVIDVax cohorts: 1.16% vs. 1.16% for any HL, 0.01% vs. 0.02% for sudden HL, 0.41% vs. 0.47% for tinnitus, 1.96% vs. 1.59% for vertigo, 0.27% vs. 0.25% for otalgia, and 0.09% vs. 0.2% for aural fullness. COVIDVax patients had lower odds of vertigo [OR 95% CI: 0.81 (0.70, 0.94)] and higher odds of aural fullness [2.16 (1.25-3.72)] than the FluVax patients (both p < 0.05). The results of the sensitivity analysis limited to patients with no COVID-19 infection at any time (N = 17,530 each cohort) were consistent with the primary results, but aural fullness was the only AE with statistically higher risk in the COVIDVax vs. FluVax cohort [OR (95% CI): 1.90 (1.09-3.31); p = 0.021].

CONCLUSION: New-onset otologic AEs were rare among a large cohort of hdPS-matched patients who received mRNA COVID-19 or pre-pandemic flu vaccination at a single institution. Although aural fullness was statistically more common in the COVIDVax vs. FluVax cohort, regardless of COVID-19 infection status, it remained extremely rare (<0.22%) in any cohort. These results indicate a similar otologic safety profile of the two vaccines, although future research is recommended in larger EHR databases to corroborate the findings.

PMID:40852523 | PMC:PMC12367506 | DOI:10.3389/fneur.2025.1637870