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Assessment of auditory functions in chronic hepatitis C patients treated by sofosbuvir

机译:索非布韦治疗慢性丙型肝炎患者的听觉功能评估

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Objective Evaluating the auditory function in patients with chronic hepatitis C treated with sofosbuvir and ribavirin. Methods This study involved 80 patients with chronic hepatitis C who agreed to receive sofosbuvir and ribavirin. All participants were subjected to baseline otological and audiological assessment just before treatment. The audiological assessment included standard pure tone audiometry, extended high-frequency audiometry, immitancemetry and otoacoustic emissions (OAEs) (transient and distortion product). According to baseline hearing threshold measurements, the study population was divided into 2 groups. Group 1 included 42 patients with normal hearing sensitivity (250–8000?Hz), and Group 2 included 38 patients with sensorineural hearing loss. After 24 weeks of therapy, otological and audiological assessments were repeated and compared between the two groups and before and after therapy. Results Post-treatment hearing threshold evaluation showed no significant difference from pretreatment evaluation at all tested frequencies. There was no statistically significant difference between pre and post-treatment otoacoustic emissions results. Conclusion Therapy with sofosbuvir and ribavirin in chronic hepatitis C has no noticeable effects on cochlear functions.
机译:目的评估索非布韦和利巴韦林治疗的慢性丙型肝炎患者的听觉功能。方法该研究纳入了同意接受索非布韦和利巴韦林的80例慢性丙型肝炎患者。在治疗前,所有参与者均接受了基线耳科和听力学评估。听力评估包括标准纯音听觉测验,扩展高频听觉测验,阻抗测量和耳声发射(OAE)(瞬态和失真产物)。根据基线听力阈值测量,研究人群分为两组。第一组包括42名听力正常(250-8000Hz)的患者,第二组包括38名感觉神经性听力损失的患者。治疗24周后,重复耳科和听觉评估,并在两组之间以及治疗前后进行比较。结果在所有测试频率下,治疗后听力阈值评估均显示与治疗前评估无显着差异。治疗前后的耳声发射结果之间没有统计学上的显着差异。结论索非布韦联合利巴韦林治疗慢性丙型肝炎对耳蜗功能无明显影响。

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