Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Woolcock Institute of Medical Research, Glebe, NSW, Australia.
Woolcock Institute of Medical Research, Glebe, NSW, Australia.
Int J Tuberc Lung Dis. 2021 Jan 1;25(1):23-30. doi: 10.5588/ijtld.20.0217.
The use of injectable antibiotics to treat multidrug-resistant TB (MDR-TB) is associated with substantial morbidity due to long-term hearing loss. This systematic review evaluates the incidence of ototoxicity among patients treated for MDR-TB, and the evidence for routine audiometric monitoring to mitigate its severity. Studies of ototoxicity among patients with MDR-TB were identified from six databases: PubMed, MEDLINE, Web of Science, Embase, SCOPUS and the Cochrane Library. Meta-analyses were performed to determine the overall incidence of hearing loss, tinnitus and vertigo. The incidence of hearing loss was further stratified by country income status and the injectable agent used during treatment. Among 64 studies from 25 countries including 12 793 patients, 28.3% (95%CI 23.4-33.1) of patients treated with injectables reported hearing loss. Tinnitus and vertigo were experienced by respectively 14.5% (95%CI 10.3-18.7) and 8.1% (95%CI 4.7-11.6) of patients. The incidence of hearing loss was highest among patients treated with amikacin (33.4%, 95%CI 18.2-48.6), and lowest among those treated with capreomycin (2.0%, 95%CI 0-5.5). We found that audiometry was widely used as a method of evaluating hearing loss, and was feasible in a wide range of settings. Injectable antibiotics contribute to significant morbidity in patients with MDR-TB. In settings where they are used, routine audiometric monitoring is recommended to prevent irreversible damage.
注射用抗生素治疗耐多药结核病(MDR-TB)会导致严重的长期听力损失,从而引起较高的发病率。本系统评价评估了接受 MDR-TB 治疗的患者中发生耳毒性的发生率,以及常规听力监测减轻其严重程度的证据。从六个数据库(PubMed、MEDLINE、Web of Science、Embase、SCOPUS 和 Cochrane Library)中确定了 MDR-TB 患者的耳毒性研究。进行了荟萃分析以确定听力损失、耳鸣和眩晕的总体发生率。根据国家收入状况和治疗期间使用的注射剂,进一步对听力损失的发生率进行分层。在包括 12793 名患者的 25 个国家的 64 项研究中,28.3%(95%CI 23.4-33.1)接受注射剂治疗的患者报告有听力损失。分别有 14.5%(95%CI 10.3-18.7)和 8.1%(95%CI 4.7-11.6)的患者经历了耳鸣和眩晕。接受阿米卡星治疗的患者听力损失发生率最高(33.4%,95%CI 18.2-48.6),接受卡那霉素治疗的患者听力损失发生率最低(2.0%,95%CI 0-5.5)。我们发现,听力测试广泛用于评估听力损失,并且在各种环境中都是可行的。注射用抗生素会导致 MDR-TB 患者出现显著的发病率。在使用这些抗生素的情况下,建议常规进行听力监测,以防止不可逆转的损害。