Drug-associated hearing impairment in children: a disproportionality analysis of the FDA adverse event reporting system.

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Frontiers in Pharmacology Pub Date : 2025-06-26 eCollection Date: 2025-01-01 DOI:10.3389/fphar.2025.1532461
Jinfeng Liu, Junyi Tan, Qinli Xiao, Yingtao Bai, En Chang, Chun Su, Yuxun Wei, Hu Zhong, Wei Wei
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Abstract

Objective: Drug-associated hearing impairment has a serious impact on children's quality of life and poses a significant public health burden. However, there is a lack of large-scale population-based studies of medication-associated hearing impairment in children. The aim of this study was to hypothesize about medications through data mining in order to assess the potential risk of these medications increasing hearing impairment in children.

Methods: We extracted and analyzed reports on drugs linked to hearing impairment in children from the FDA Adverse Event Reporting System (FAERS). To assess the relationship between drugs and hearing impairment in children, we performed a disproportionality study utilizing the proportional reporting ratio (PRR) and reporting odds ratio (ROR). Concurrently, we conducted comparisons with medicine labels to identify medications that, although not now indicating hearing impairment in their labels, may possibly pose risks of hearing impairment in children.

Results: In the FAERS database, there are 1,884 reports of AE related to hearing impairment in children. The top three medications with the highest ROR were vinblastin [N = 6 cases, ROR = 86.72 (34.15-220.19)], risedronate [N = 3 cases, ROR = 73.59 (20.24-267.63)], and amikacin [N = 11 cases, ROR = 71.31 (36.40-139.72)]. The top 3 drugs with the highest number of reports were carboplatin [N = 125 cases, ROR = 18.41 (15.27-22.21)], cisplatin [N = 78 cases, ROR = 31.24 (24.59-39.70)], and vincristine [N = 56 cases, ROR = 6.32 (4.83-8.27)]. Based on drug labeling, 48% drugs (27/56) were classified as potentially ototoxic.

Conclusion: Our findings suggest that nearly half of the 56 drugs linked to hearing impairment signals in children are not currently labeled with ototoxicity warnings. Consequently, further research is required to evaluate the association of these medicines with this risk.

儿童药物相关性听力损害:FDA不良事件报告系统的不相称性分析。
目的:药物相关性听力损伤严重影响儿童的生活质量,造成重大的公共卫生负担。然而,缺乏针对儿童药物相关听力障碍的大规模人群研究。本研究的目的是通过数据挖掘对药物进行假设,以评估这些药物增加儿童听力损害的潜在风险。方法:我们从FDA不良事件报告系统(FAERS)中提取并分析与儿童听力损害相关的药物报告。为了评估药物与儿童听力障碍之间的关系,我们利用比例报告比(PRR)和报告优势比(ROR)进行了一项不成比例研究。同时,我们对药品标签进行了比较,以识别那些虽然在标签上没有注明听力损伤,但可能对儿童造成听力损伤风险的药物。结果:在FAERS数据库中,有1884例与儿童听力障碍相关的声发射报告。ROR最高的前3位药物分别是长春素[N = 6例,ROR = 86.72(34.15 ~ 220.19)]、利塞膦酸钠[N = 3例,ROR = 73.59(20.24 ~ 267.63)]、阿米卡星[N = 11例,ROR = 71.31(36.40 ~ 139.72)]。报告数量最多的前3位药物分别是卡铂[N = 125例,ROR = 18.41(15.27 ~ 22.21)]、顺铂[N = 78例,ROR = 31.24(24.59 ~ 39.70)]、长春新碱[N = 56例,ROR = 6.32(4.83 ~ 8.27)]。根据药物标签,48%(27/56)的药物被归类为潜在耳毒性。结论:我们的研究结果表明,在56种与儿童听力损伤信号相关的药物中,近一半目前没有标注耳毒性警告。因此,需要进一步的研究来评估这些药物与这种风险的关系。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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