Department of Otolaryngology and Head and Neck Surgery, Semmelweis University, Szigony u. 36., Budapest, 1083, Hungary.
Eur Arch Otorhinolaryngol. 2020 Jul;277(7):1949-1954. doi: 10.1007/s00405-020-05901-3. Epub 2020 Mar 30.
The aim of our study is to investigate the effectiveness and safety of the treatment, based on vertigo diaries and pure tone audiograms.
The complete medical documentation of 105 definite patients suffering from Ménière's disease was analyzed. In the studied group, nine patients were treated with intratympanic gentamycine. Long-term follow-up of the patients was carried out, using vertigo diaries, medical letters, anamnestic data, and pure tone audiograms. Audiometric results and vertigo complaints before and after treatment were contrasted using IBM SPSS V24 software.
Based on our analysis, vertigo attacks appeared significantly less often after gentamycine treatment [p < 0.001; Odds ratio 0.003 (95% CI 0.001-0.012)], which confirms the efficacy of the therapy. Pure tone stages before and after the application of gentamycine were contrasted using the Mann-Whitney U test. When comparing the audiometric results of long-term follow-ups by using the logistic regression, a statistically significant difference was observed between the treated and not treated groups [p = 0.001; Odds ratio 0.141 (95% CI 0.064-0.313)], and based on the survivorship curve hearing impairment was more common in the not treated group which also supports our results. Based on the non-parametric test, there was no significant difference (p = 0.84) between the pure-tone stages of the control group and of those treated with gentamycine.
Our results indicate that intratympanic gentamycine is effective in controlling vertigo attacks, and there is no higher risk for hearing loss than in case of spontaneous progression of the disorder.
我们研究的目的是基于眩晕日记和纯音听力图来研究该治疗方法的有效性和安全性。
分析了 105 例明确诊断为梅尼埃病患者的完整病历。在研究组中,有 9 例患者接受了鼓室内庆大霉素治疗。通过眩晕日记、病历、病史数据和纯音听力图对患者进行长期随访。使用 IBM SPSS V24 软件对比治疗前后的听力结果和眩晕主诉。
根据我们的分析,庆大霉素治疗后眩晕发作明显减少[P<0.001;优势比 0.003(95%可信区间 0.001-0.012)],证实了该疗法的疗效。使用 Mann-Whitney U 检验对比庆大霉素应用前后的纯音听力级。通过逻辑回归对比长期随访的听力结果,发现治疗组和未治疗组之间存在统计学差异[P=0.001;优势比 0.141(95%可信区间 0.064-0.313)],且根据生存曲线,未治疗组听力障碍更为常见,这也支持了我们的结果。基于非参数检验,对照组和庆大霉素治疗组的纯音听力级之间没有显著差异(P=0.84)。
我们的结果表明,鼓室内庆大霉素治疗可有效控制眩晕发作,且听力损失的风险并不高于疾病自然进展的情况。