Department of Otolaryngology, Head and Neck Surgery, Seoul Metropolitan Government, Seoul National University College of Medicine, Boramae Medical Center, 39, Boramae-Gil, Dongjak-Gu, Seoul 156-707, Korea.
Eur Arch Otorhinolaryngol. 2012 Oct;269(10):2173-8. doi: 10.1007/s00405-011-1874-6. Epub 2011 Dec 8.
The objective of the study was to determine the therapeutic efficacy of early combined treatment with intratympanic steroid injection (ITSI) in patients with severe to profound sudden sensorineural hearing loss (SSNHL), who did not respond to initial systemic steroid treatment (SST). The study design included historical controlled trials (retrospective analysis for the SST group). Patients (n = 73; 38 women and 35 men) diagnosed with severe to profound SSNHL at the time of their first visit in tertiary referral centers were recruited. Among these 73 patients, 30 patients who showed no early response within a week after the start of initial SST were prospectively included as the ITSI group. ITSI was performed twice a week for two consecutive weeks. In contrast, 43 patients with the same condition who did not receive ITSI were retrospectively included as the SST group. For each group, pure-tone audiogram (PTA) and speech discrimination score (SDS) tests were performed before SST and more than 2 months after termination of treatment in each group. After termination of each treatment, the final average gain on PTA showed no significant difference between the two groups; however, the final average gain of SDS demonstrated a significantly better recovery in the ITSI group. ITSI as part of an early combined therapy represents an effective treatment in terms of the improvement of SDS in severe to profound SSNHL showing no early response to initial SST.
本研究旨在确定对于初始全身类固醇治疗(SST)无反应的重度至极重度突发性感音神经性听力损失(SSNHL)患者,早期联合鼓室内类固醇注射(ITSI)治疗的疗效。研究设计包括历史对照试验(SST 组回顾性分析)。招募了在三级转诊中心首次就诊时被诊断为重度至极重度 SSNHL 的患者(n = 73;女性 38 例,男性 35 例)。在这 73 例患者中,30 例在初始 SST 开始后一周内无早期反应的患者前瞻性纳入 ITSI 组。ITSI 每周进行两次,连续进行两周。相比之下,43 例具有相同条件但未接受 ITSI 的患者被回顾性纳入 SST 组。对于每组,在 SST 之前和每组治疗结束后 2 个月以上进行纯音听阈(PTA)和言语辨别评分(SDS)测试。在每种治疗结束后,两组之间 PTA 的最终平均增益无显著差异;然而,在 ITSI 组中,SDS 的最终平均增益显示出更好的恢复。在对初始 SST 无早期反应的重度至极重度 SSNHL 患者中,作为早期联合治疗的一部分,ITSI 在 SDS 改善方面代表了一种有效的治疗方法。