首页> 外文期刊>International Archives of Otorhinolaryngology >Application of Cervical Vestibular-Evoked Myogenic Potentials in Adults with Moderate to Profound Sensorineural Hearing Loss: A Preliminary Study
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Application of Cervical Vestibular-Evoked Myogenic Potentials in Adults with Moderate to Profound Sensorineural Hearing Loss: A Preliminary Study

机译:宫颈前庭诱发的肌源性潜力在成年人中的应用中等至深刻的感觉损失:初步研究

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Abstract Introduction The cochlea and the vestibular receptors are closely related in terms of anatomy and phylogeny. Patients with moderate to profound sensorineural hearing loss (MPSHL) should have their vestibular organ functions tested. Objective To evaluate the incidence of vestibular abnormalities in patients with MPSHL and to study the correlation between the etiology of hearing loss (HL) and a possible damage to the labyrinth. Methods A case-control retrospective study was performed. In the case group, 20 adults with MPSHL of known etiology were included. The control group was composed of 15 adults with normal hearing. The case group was divided into 4 subgroups based on the etiology (bacterial meningitis, virus, vascular disease, congenital). Cervical vestibular-evoked myogenic potentials (cVEMPs) were used to rate the saccular function and lower vestibular nerve. Results The study was performed in 70 ears, and it highlighted the presence of early biphasic P1-N1 complex in 29 (71.5%) out of 40 ears in the study group, and in all of the 30 ears in the control group (p = 0.001). Regarding the presence or absence of cVEMPs among the four subgroups of patients with MPSHL, the data were statistically signi?cant (p 0.001). The comparison between the latencies and amplitude of P1-N1 in case and control groups from other studies and in the four subgroups of cases in the present study did not detect statistically signi?cant differences. Conclusion The present study demonstrates that patients with MPSHL have a high incidence of damage to the labyrinthine organs, and it increases the current knowledge about the etiopathogenesis of sensorineural HL, which is often of unknown nature.
机译:摘要介绍耳蜗和前庭受体在解剖学和系统发生方面密切相关。具有中度至深度感觉内听力损失(MPSHL)的患者应该有其前庭器官功能。目的评价MPSHL患者前庭异常的发病率,并研究听力损失(HL)病因与迷宫可能损坏的相关性。方法进行案例控制回顾性研究。在案例组中,包括20名已知病因的MPSHL的成年人。对照组由15名成人组成,具有正常听力。案例组根据病因(细菌脑膜炎,病毒,血管疾病,先天性)分为4个亚组。使用宫颈前庭诱发的肌原遗传潜力(CVEMPS)来评估囊状功能和低口腔神经。结果该研究在70只耳朵中进行,它突出了在研究组中40只耳朵中的29(71.5%)的早期双相P1-N1复合物的存在,并在对照组的所有30只耳中(P = 0.001)。关于MPSHL患者的四个亚组中的存在或不存在CVEMPS,数据具有统计学上的αα不能(p <0.001)。在其他研究的情况下P1-N1的延迟和幅度的比较和本研究中的四个病例的四个亚组的对照组没有检测到统计学上的差异。结论本研究表明,MPSHL患者对迷宫式器官的损伤发生率很高,而且增加了关于感觉内HL的病因发生的目前的知识,这通常是未知的性质。

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