Shea Ear Clinic, Memphis, Tennessee 38119, USA.
Laryngoscope. 2012 Jan;122(1):204-11. doi: 10.1002/lary.22362.
OBJECTIVES/HYPOTHESIS: To evaluate the hearing changes and quality-of-life outcomes of 393 cases of streptomycin/dexamethasone inner ear perfusion performed by the primary author on 312 ears of 299 patients with Meniere's disease between July 2002 and May 2010.
Retrospective chart review.
Objective arm: A database was used to compile pretreatment and post-treatment audiograms as well as basic demographic information, dates of treatment, number of treatments, and which ear was treated. All patients met the 1995 American Academy of Otolaryngology-Head and Neck Surgery Committee on Hearing and Equilibrium Guidelines for the diagnosis and evaluation of therapy in Meniere's disease. All patients underwent one or more 3-day treatments consisting of daily intratympanic injections of a low-dose streptomycin/high-dose dexamethasone mixture plus intravenous dexamethasone. The end point for treatment was adequate control of vertigo. Subjective arm: The Meniere's Disease Outcomes Questionnaire survey was used to assess patients' quality of life after receiving streptomycin/dexamethasone inner ear perfusion. All procedures were performed by the primary author at the Shea Ear Clinic, a tertiary-referral otology clinic and outpatient surgery center.
After a single 3-day treatment, the average change in pure tone average was 0.89 dB (±11). The average change in word recognition score was 0.49% (±17). The average number of days from treatment to follow-up audiogram was 94 with a range of 8 to 1,603. Clinically significant hearing loss occurred after 62 of 393 (15.7%) treatments. Severe hearing loss occurred after 20 of 393 treatments (5.0%). The percentage of ears with clinically significant hearing loss after all treatments was 56 of 312 (17.9%). A total of 215 surveys were returned from 383 patients (56.1%) to whom they were mailed. There were 90% of patients who indicated improvement in quality of life after treatment and 88% who indicated improvement in their "vertigo subscore," a domain within the survey that focuses on vertigo control.
Streptomycin/dexamethasone inner ear perfusion is as safe to the hearing of patients with Meniere's disease as other aminoglycoside regimens and provides a significant improvement in quality of life.
目的/假设:评估作者在 2002 年 7 月至 2010 年 5 月期间对 299 名梅尼埃病患者的 312 耳中的 302 例进行链霉素/地塞米松内耳灌注治疗的 393 例患者的听力变化和生活质量结果。
回顾性图表审查。
客观臂:使用数据库编译治疗前和治疗后的听力图以及基本人口统计学信息、治疗日期、治疗次数以及治疗哪只耳朵。所有患者均符合 1995 年美国耳鼻喉科学会听觉与平衡委员会关于梅尼埃病的诊断和治疗评估指南。所有患者均接受了一次或多次为期 3 天的治疗,包括每日经鼓室内注射低剂量链霉素/高剂量地塞米松混合物加静脉内地塞米松。治疗的终点是眩晕得到充分控制。主观臂:使用梅尼埃病结局问卷评估患者接受链霉素/地塞米松内耳灌注后的生活质量。所有程序均由主要作者在三级转诊耳科诊所和门诊手术中心的 Shea 耳诊所进行。
单次 3 天治疗后,纯音平均变化为 0.89dB(±11)。言语识别率的平均变化为 0.49%(±17)。从治疗到随访听力图的平均天数为 94 天,范围为 8 至 1603 天。393 次治疗中有 62 次(15.7%)出现临床显著听力损失。393 次治疗中有 20 次(5.0%)出现严重听力损失。所有治疗后临床显著听力损失的耳朵百分比为 312 个中的 56 个(17.9%)。共向 383 名患者寄出了 215 份调查问卷,其中 215 份(56.1%)患者返回。90%的患者表示治疗后生活质量有所改善,88%的患者表示“眩晕子评分”有所改善,这是调查中关注眩晕控制的一个领域。
与其他氨基糖苷类方案一样,链霉素/地塞米松内耳灌注对梅尼埃病患者的听力安全,可显著提高生活质量。