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丁基苯酞可促进突发性耳聋的恢复。

Butylphthalide enhances recovery from sudden deafness.

机构信息

Department of Otolaryngology Head and Neck Surgery, General Hospital of Southern Theater Command of PLA (Guangzhou Liuhuaqiao Hospital), Liuhua road 111, Guangzhou 510010, Guangdong, China.

Department of Otolaryngology Head and Neck Surgery, General Hospital of Southern Theater Command of PLA (Guangzhou Liuhuaqiao Hospital), Liuhua road 111, Guangzhou 510010, Guangdong, China.

出版信息

Am J Otolaryngol. 2021 Mar-Apr;42(2):102891. doi: 10.1016/j.amjoto.2020.102891. Epub 2021 Jan 4.

DOI:10.1016/j.amjoto.2020.102891
PMID:33422947
Abstract

OBJECTIVES

Cochlear microcirculation disturbance caused by vasculopathy is a common cause of sudden deafness (SD). Reactive oxygen species (ROS) plays an important role in cochlear injury during ischemia-reperfusion. Butylphthalide can improve microcirculation, reduce ROS formation and inhibit apoptosis. The aim of this study was to investigate the therapeutic effect of butylphthalide on patients with SD.

PATIENTS AND METHODS

The hearing gains from 32 ears treated with butylphthalide were compared with that of 32 ears treated with non-butylphthalide. Butylphthalide capsules was administrated orally on an empty stomach for 10 continuous days. There were no significant differences in audiological and clinical data between butylphthalide and non-butylphthalide groups.

RESULTS

The hearing gain of butylphthalide group at 500, 1000, 2000, and 4000 Hz was significantly higher than that of non-butylphthalide group correspondingly (P<0.01). And, the hearing gain at PTA (pure-tone average of 500, 1000, 2000, and 4000 Hz) in butylphthalide group was significantly higher than that of non-butylphthalide group (P<0.01).

CONCLUSION

The recovery of hearing in butylphthalide group was significantly better than that of non-butylphthalide group. It is confirmed that butylphthalide has a definite therapeutic effect on SD.

摘要

目的

血管病变引起的耳蜗微循环障碍是突发性聋(SD)的常见原因。活性氧(ROS)在缺血再灌注期间耳蜗损伤中起重要作用。丁基苯酞可以改善微循环,减少 ROS 形成并抑制细胞凋亡。本研究旨在探讨丁基苯酞治疗 SD 患者的疗效。

患者和方法

比较了 32 例使用丁基苯酞治疗的患者与 32 例使用非丁基苯酞治疗的患者的听力增益。丁基苯酞胶囊空腹口服,连续 10 天。丁基苯酞组和非丁基苯酞组在听力和临床数据方面无显著差异。

结果

丁基苯酞组在 500、1000、2000 和 4000 Hz 时的听力增益明显高于非丁基苯酞组(P<0.01)。而且,丁基苯酞组在 PTA(500、1000、2000 和 4000 Hz 的纯音平均)时的听力增益明显高于非丁基苯酞组(P<0.01)。

结论

丁基苯酞组的听力恢复明显优于非丁基苯酞组。证实丁基苯酞对 SD 有明确的治疗作用。

相似文献

1
Butylphthalide enhances recovery from sudden deafness.丁基苯酞可促进突发性耳聋的恢复。
Am J Otolaryngol. 2021 Mar-Apr;42(2):102891. doi: 10.1016/j.amjoto.2020.102891. Epub 2021 Jan 4.
2
Radix astragali injection enhances recovery from sudden deafness.黄芪注射液可促进突发性耳聋的恢复。
Am J Otolaryngol. 2012 Sep-Oct;33(5):523-7. doi: 10.1016/j.amjoto.2011.12.001. Epub 2012 Feb 4.
3
[The study of the pure tone audiometry characteristics and curative effect in sudden hearing loss patients with hypertension].[高血压性突发性聋患者的纯音听力测定特征及疗效研究]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2014 Apr;29(8):748-52.
4
[Analysis of the effectiveness in patients who were treated with a course of drugs for sudden deafness which was present for at least three weeks].[对接受突发性耳聋药物治疗疗程至少三周的患者的疗效分析]
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2011 Jul;46(7):539-42.
5
[Course and prognosis in sudden deafness].
HNO. 1984 Aug;32(8):341-5.
6
Prognosis of sudden deafness with special reference to risk factors of microvascular pathology.
Auris Nasus Larynx. 1999 Apr;26(2):111-5. doi: 10.1016/s0385-8146(98)00072-8.
7
Otoacoustic emissions, ear fullness and tinnitus in the recovery course of sudden deafness.突发性聋恢复过程中的耳声发射、耳闷胀感及耳鸣
Auris Nasus Larynx. 2008 Mar;35(1):41-6. doi: 10.1016/j.anl.2007.04.003. Epub 2007 Sep 27.
8
Probational treatment of sudden deafness with prostacyclin: a pilot study.
Auris Nasus Larynx. 1991;18(2):115-23. doi: 10.1016/s0385-8146(12)80215-x.
9
Effectiveness of systemic high-dose dexamethasone therapy for idiopathic sudden sensorineural hearing loss.全身大剂量地塞米松治疗特发性突发性感音神经性听力损失的疗效
Audiol Neurootol. 2013;18(3):161-70. doi: 10.1159/000346938. Epub 2013 Feb 27.
10
[Blood viscosity disorders as an etiopathological factor in sudden deafness].
Acta Otorrinolaringol Esp. 1997 Oct;48(7):517-22.

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