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Metabol Open. 2022 Mar;13:100159. doi: 10.1016/j.metop.2021.100159. Epub 2021 Dec 17.
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Direct SARS-CoV-2 infection of the human inner ear may underlie COVID-19-associated audiovestibular dysfunction.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)直接感染人类内耳可能是新冠病毒疾病(COVID-19)相关的听觉前庭功能障碍的潜在原因。
Commun Med (Lond). 2021;1(1):44. doi: 10.1038/s43856-021-00044-w. Epub 2021 Oct 29.
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COVID-19 Vaccination-Associated Myocarditis in Adolescents.青少年 COVID-19 疫苗接种相关心肌炎。
Pediatrics. 2021 Nov;148(5). doi: 10.1542/peds.2021-053427. Epub 2021 Aug 13.
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Cerebral venous thrombosis after vaccination against COVID-19 in the UK: a multicentre cohort study.英国接种新冠疫苗后发生的脑静脉血栓形成:一项多中心队列研究。
Lancet. 2021 Sep 25;398(10306):1147-1156. doi: 10.1016/S0140-6736(21)01608-1. Epub 2021 Aug 6.
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Otologic Manifestations After COVID-19 Vaccination: The House Ear Clinic Experience.接种 COVID-19 疫苗后的耳科学表现:House Ear Clinic 的经验。
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Thromboembolism and the Oxford-AstraZeneca COVID-19 vaccine: side-effect or coincidence?血栓栓塞与牛津大学-阿斯利康新冠疫苗:副作用还是巧合?
Lancet. 2021 Apr 17;397(10283):1441-1443. doi: 10.1016/S0140-6736(21)00762-5. Epub 2021 Mar 30.
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评估 COVID-19 疫苗接种后的突发性感觉神经性听力损失。

Assessment of Sudden Sensorineural Hearing Loss After COVID-19 Vaccination.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts.

出版信息

JAMA Otolaryngol Head Neck Surg. 2022 Apr 1;148(4):307-315. doi: 10.1001/jamaoto.2021.4414.

DOI:10.1001/jamaoto.2021.4414
PMID:35201274
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8874871/
Abstract

IMPORTANCE

Emerging reports of sudden sensorineural hearing loss (SSNHL) after COVID-19 vaccination within the otolaryngological community and the public have raised concern about a possible association between COVID-19 vaccination and the development of SSNHL.

OBJECTIVE

To examine the potential association between COVID-19 vaccination and SSNHL.

DESIGN, SETTING, AND PARTICIPANTS: This cross-sectional study and case series involved an up-to-date population-based analysis of 555 incident reports of probable SSNHL in the Centers for Disease Control and Prevention Vaccine Adverse Events Reporting System (VAERS) over the first 7 months of the US vaccination campaign (December 14, 2020, through July 16, 2021). In addition, data from a multi-institutional retrospective case series of 21 patients who developed SSNHL after COVID-19 vaccination were analyzed. The study included all adults experiencing SSNHL within 3 weeks of COVID-19 vaccination who submitted reports to VAERS and consecutive adult patients presenting to 2 tertiary care centers and 1 community practice in the US who were diagnosed with SSNHL within 3 weeks of COVID-19 vaccination.

EXPOSURES

Receipt of a COVID-19 vaccine produced by any of the 3 vaccine manufacturers (Pfizer-BioNTech, Moderna, or Janssen/Johnson & Johnson) used in the US.

MAIN OUTCOMES AND MEASURES

Incidence of reports of SSNHL after COVID-19 vaccination recorded in VAERS and clinical characteristics of adult patients presenting with SSNHL after COVID-19 vaccination.

RESULTS

A total of 555 incident reports in VAERS (mean patient age, 54 years [range, 15-93 years]; 305 women [55.0%]; data on race and ethnicity not available in VAERS) met the definition of probable SSNHL (mean time to onset, 6 days [range, 0-21 days]) over the period investigated, representing an annualized incidence estimate of 0.6 to 28.0 cases of SSNHL per 100 000 people per year. The rate of incident reports of SSNHL was similar across all 3 vaccine manufacturers (0.16 cases per 100 000 doses for both Pfizer-BioNTech and Moderna vaccines, and 0.22 cases per 100 000 doses for Janssen/Johnson & Johnson vaccine). The case series included 21 patients (mean age, 61 years [range, 23-92 years]; 13 women [61.9%]) with SSNHL, with a mean time to onset of 6 days (range, 0-15 days). Patients were heterogeneous with respect to clinical and demographic characteristics. Preexisting autoimmune disease was present in 6 patients (28.6%). Of the 14 patients with posttreatment audiometric data, 8 (57.1%) experienced improvement after receiving treatment. One patient experienced SSNHL 14 days after receiving each dose of the Pfizer-BioNTech vaccine.

CONCLUSIONS AND RELEVANCE

In this cross-sectional study, findings from an updated analysis of VAERS data and a case series of patients who experienced SSNHL after COVID-19 vaccination did not suggest an association between COVID-19 vaccination and an increased incidence of hearing loss compared with the expected incidence in the general population.

摘要

重要性

在耳鼻喉科领域和公众中,有关于接种 COVID-19 疫苗后突发性感觉神经性听力损失 (SSNHL) 的新报告,这引起了人们对 COVID-19 疫苗接种与 SSNHL 发展之间可能存在关联的关注。

目的

研究 COVID-19 疫苗接种与 SSNHL 之间的潜在关联。

设计、地点和参与者:本横断面研究和病例系列分析了美国疫苗接种运动的前 7 个月(2020 年 12 月 14 日至 2021 年 7 月 16 日)期间疾病控制与预防中心疫苗不良事件报告系统 (VAERS) 中可能的 SSNHL 555 例发生率报告的最新基于人群的分析。此外,还对 21 例 COVID-19 疫苗接种后发生 SSNHL 的多机构回顾性病例系列的数据进行了分析。该研究包括所有在 COVID-19 疫苗接种后 3 周内出现 SSNHL 的成年人,他们向 VAERS 报告了报告,以及连续的成年患者在接种 COVID-19 疫苗后 3 周内前往美国的 3 家三级护理中心和 1 家社区诊所就诊,在接种 COVID-19 疫苗后 3 周内被诊断为 SSNHL。

暴露

接受了任何 3 种在美国使用的 COVID-19 疫苗制造商(辉瑞-生物技术公司、莫德纳公司或强生/杨森公司)生产的疫苗。

主要结果和测量

VAERS 记录的 COVID-19 疫苗接种后 SSNHL 报告的发生率和 COVID-19 疫苗接种后出现 SSNHL 的成年患者的临床特征。

结果

在研究期间,VAERS 中共有 555 例符合可能的 SSNHL 定义的发生率报告(平均患者年龄为 54 岁[范围为 15-93 岁];305 名女性[55.0%];VAERS 中未提供种族和民族的数据)(平均发病时间为 6 天[范围为 0-21 天]),估计每年每 10 万人中有 0.6 至 28.0 例 SSNHL。所有 3 种疫苗制造商的 SSNHL 发生率报告相似(辉瑞-生物技术公司和莫德纳疫苗每 10 万剂 0.16 例,强生/杨森公司疫苗每 10 万剂 0.22 例)。病例系列包括 21 例 SSNHL 患者(平均年龄为 61 岁[范围为 23-92 岁];13 名女性[61.9%]),平均发病时间为 6 天(范围为 0-15 天)。患者在临床和人口统计学特征方面存在异质性。6 例(28.6%)患者存在自身免疫性疾病。在 14 例有治疗后听力测试数据的患者中,8 例(57.1%)在接受治疗后听力有所改善。1 例患者在接受辉瑞-生物技术公司疫苗的每剂疫苗后 14 天出现 SSNHL。

结论和相关性

在本横断面研究中,对 VAERS 数据的最新分析和 COVID-19 疫苗接种后出现 SSNHL 的患者病例系列的研究结果表明,与一般人群的预期发病率相比,COVID-19 疫苗接种与听力损失发生率增加之间没有关联。