COVID-19疫苗后听力损失:系统综述和荟萃分析

K. Albakri, Y. Alabdallat, O. Abdelwahab, M. Gabra, Mohamed H Nafady, Dr Ebraheem Albazee
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引用次数: 0

摘要

摘要背景:听力损失一般分为传导性听力损失(CHL)和感觉神经性听力损失(SNHL)。据报道,新冠病毒感染可能会影响前庭听觉系统,引起头晕、耳鸣、眩晕和听力障碍。然而,其他研究报告称,COVID-19不会导致严重的听力障碍。文献中的许多研究都报道了听力损失是COVID-19疫苗的并发症。然而,没有系统综述或荟萃分析总结了这一主题的文献。方法:我们对PubMed、Cochrane (Medline)、Web of Science和Scopus数据库进行了全面的检索。所有在2022年10月之前发表的英文研究都被纳入其中。其中包括病例报告、病例系列、前瞻性和回顾性观察性研究,以及报告COVID-19疫苗后听力损失的临床试验。纽卡斯尔渥太华量表(NOS)用于评估观察性研究的偏倚风险。在临床试验、病例报告和病例系列之前和之后使用NIH工具进行非对照研究。第三位作者解决了任何分歧。我们使用SPSS软件26版对数据进行分析。结果:共发现630例患者,平均年龄57.3岁,年龄在15 ~ 93岁之间。女性占多数,339例(53.8%)。此外,609名接种疫苗的患者中,328人接种了辉瑞- biontech公司的BNT162b2疫苗,242人(40%)接种了Moderna新冠病毒疫苗。从接种疫苗到听力受损的平均时间为6.2小时,从最后一次接种后的几个小时到一个月不等。大多数患者在接种疫苗后报告单侧感音神经性听力损失593例(94.1%)。为了报告病例的命运,在开始治疗后的2至63天内开始随访,平均时间为15.6天。20例患者完全康复,11例无反应。328名接种了辉瑞- biontech BNT162b2疫苗的患者中,有3人完全康复,5人部分康复。卡方检验显示,患者的命运和COVID-19疫苗接种类型差异有统计学意义(p值= 0.001),而出现症状前的剂量数(p值= 0.65)和性别差异无统计学意义(p值= 0.4)。采用方差分析(ANOVA)检验比较从接种疫苗到出现听力损害的平均时间的疫苗类型和剂量数量。结果发现不同疫苗类型之间存在显著差异(p值< 0.000),而在发病前的剂量数方面没有显着性(p值= 0.6)。结论:患者的命运和COVID-19疫苗接种类型差异有统计学意义,而报告发病前剂量和性别差异无统计学意义。此外,我们得出结论,疫苗类型之间存在显著差异,但在发病前的剂量数量方面没有显着性。
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Hearing Loss After COVID-19 Vaccines: A Systematic Review and Meta-Analysis
ABSTRACT. Background: Hearing loss is generally classified as conductive hearing loss (CHL) and sensory-neural hearing loss (SNHL). It has been reported that COVID-19 infection may affect the vestibular-hearing system causing dizziness, tinnitus, vertigo, and hearing impairment. However, other studies reported that COVID-19 did not lead to significant hearing impairment. Many studies in the literature have reported hearing loss as a complication of COVID-19 vaccines. However, no systematic review or meta-analysis summarizes the literature on this topic.   Method: We performed a comprehensive search for the following databases: PubMed, Cochrane (Medline), Web of Science, and Scopus. All studies published in English till October 2022 were included. These include case reports, case series, prospective and retrospective observational studies, and clinical trials reporting hearing loss following COVID-19 vaccines. Newcastle Ottawa scale (NOS) was used to assess the risk of bias for observational studies. NIH tools were used for non-controlled before and after clinical trials and case reports and case series. A third author solved any disagreements. We analyzed the data using SPSS Software version 26.   Results: A total of 630 patients were identified, with a mean age of 57.3 that ranged from 15 to 93 years old. The majority of the patients were females, 339 (53.8%). In addition, 328 out of 609 vaccinated patients took the Pfizer-BioNTech BNT162b2 vaccine, while 242 (40%) took the Moderna COVID-19 vaccine. The mean time from vaccination to hearing impairment was 6.2, ranging from a few hours to one month after the last dose. Most patients reported unilateral sensorineural hearing loss post-vaccination 593 (94.1%). In order to report the fate of cases, a follow-up was initiated with a mean of 15.6 and a range of 2 to 63 days after the initiation of the treatment. A total of 20 patients were fully recovered, and 11 reported no response. Three out of 328 patients who took the Pfizer-BioNTech BNT162b2 vaccine fully recovered, while five reported partial recovery. According to the chi-squared test, there is a statistically significant difference between patients in terms of fate and the type of COVID-19 vaccination (P-value = 0.001) while reporting no significant difference in dose number prior to the onset of the symptoms (P-value = 0.65) and gender (P-value = 0.4). The ANOVA test was conducted to compare vaccine types and the number of doses in terms of mean time from vaccination to hearing impairment onset. The results found a significant difference between vaccine types (P-value < 0.000) while showing no significance in terms of the number of doses prior to the onset (P-value = 0.6).   Conclusion: There is a statistically significant difference between patients in terms of fate and the type of COVID-19 vaccination while reporting no significant difference in dose number prior to the onset of the symptoms and gender. Further, we concluded that there is a significant difference between vaccine types while showing no significance in terms of the number of doses prior to the onset.
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