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双氢克尿噻治疗外周性前庭性眩晕:一项双盲安慰剂对照研究

Betahistine dihydrochloride in the treatment of vertigo of peripheral vestibular origin. A double-blind placebo-controlled study.

作者信息

Oosterveld W J

出版信息

J Laryngol Otol. 1984 Jan;98(1):37-41. doi: 10.1017/s0022215100146158.

Abstract

A double-blind, cross-over, placebo-controlled study of betahistine dihydrochloride (12 mg, t.i.d.) was carried out in patients with vertigo of peripheral vestibular origin. Twenty-four patients completed the study, which consisted of two six-week treatment periods. The patients were diagnosed as suffering from Menière's disease (15 patients), vertigo due to other (specified) causes (five patients), or vertigo of unknown origin (four patients). Patients were examined by the investigator at the start of the study and were re-assessed at three-weekly intervals. In addition, they recorded the nature, frequency and severity of their symptoms on diary cards. Both the incidence and severity of dizziness (the predominant presenting complaint) were found to be significantly reduced during betahistine treatment (p = 0.004). The occurrence of nausea and vomiting was also significantly reduced during betahistine treatment (p = 0.014 and 0.036 respectively). There were no statistically significant differences in the results of audiometric or vestibulometric tests, or in the severity of tinnitus or deafness, between the two treatment periods. The overall comparisons of the two periods made by both the patients and the investigator were significantly in favour of betahistine (p less than 0.001). All diagnostic groups responded favourably to betahistine, confirming the efficacy of betahistine in the symptomatic treatment of peripheral vestibular vertigo. No unwanted signs or symptoms were reported.

摘要

对盐酸倍他司汀(12毫克,每日三次)进行了一项双盲、交叉、安慰剂对照研究,研究对象为外周性前庭性眩晕患者。24名患者完成了该研究,研究包括两个为期六周的治疗期。患者被诊断为患有梅尼埃病(15例)、其他(特定)原因引起的眩晕(5例)或不明原因的眩晕(4例)。研究开始时由研究者对患者进行检查,并每隔三周重新评估一次。此外,他们在日记卡上记录症状的性质、频率和严重程度。结果发现,在倍他司汀治疗期间,头晕(主要的主诉症状)的发生率和严重程度均显著降低(p = 0.004)。在倍他司汀治疗期间,恶心和呕吐的发生率也显著降低(分别为p = 0.014和0.036)。两个治疗期之间,听力测定或前庭功能测定测试结果、耳鸣或耳聋的严重程度均无统计学显著差异。患者和研究者对两个治疗期的总体比较均显著支持倍他司汀(p < 0.001)。所有诊断组对倍他司汀均有良好反应,证实了倍他司汀在外周性前庭性眩晕症状治疗中的疗效。未报告不良体征或症状。

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