Department of Otolaryngology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
Department of Otolaryngology, Tokushima University Graduate School of Biomedical Sciences, Tokushima, Japan.
Auris Nasus Larynx. 2024 Apr;51(2):401-405. doi: 10.1016/j.anl.2023.08.009. Epub 2023 Sep 3.
In the present study, we examined the effects of high-dose betahistine on dizziness handicap inventory (DHI) scores in patients with unilateral vestibulopathy.
An uncontrolled, open-label, multicenter clinical trial was conducted. Fifteen patients with unilateral vestibulopathy, such as vestibular neuritis, who complained of intractable dizziness for more than three months were enrolled. Initially, all patients were orally administered betahistine at a dose of 36 mg/day for four weeks, which is the standard dose and dosing period for the treatment of dizziness in Japan. The patients were then administered betahistine at a double dose of 72 mg/day for four weeks. Six patients who became aware of the benefits of high-dose betahistine were further administered betahistine at 72 mg/day for an additional 12 weeks (a total of 16 weeks). Perceived disability due to dizziness was assessed by DHI scores.
In all 15 patients, short-term administration with high-dose (72 mg/day) betahistine for four weeks, but not low-dose betahistine (36 mg/day) for four weeks significantly decreased DHI scores. In particular, in six responding patients with self-reported benefits after short-term administration with high-dose betahistine, long-term administration with high-dose betahistine for 16 weeks further significantly decreased DHI scores. However, DHI scores of the remaining nine non-responding patients were not changed after short-term administration with high-dose betahistine for four weeks.
Short-term administration with the standard dose and dosing period of betahistine did not improve DHI scores in the enrolled patients, indicating that they were not compensated for unilateral vestibulopathy with intractable dizziness. The present findings suggest that long-term administration with high-dose betahistine facilitates vestibular compensation to improve intractable dizziness in some, but not all patients with uncompensated unilateral vestibulopathy.
本研究旨在探讨高剂量倍他司汀对单侧前庭病患者眩晕残障量表(DHI)评分的影响。
进行了一项非对照、开放标签、多中心临床试验。共纳入 15 例单侧前庭病(如前庭神经炎)患者,这些患者均抱怨持续超过 3 个月的顽固性头晕。最初,所有患者均口服倍他司汀,剂量为 36mg/天,持续 4 周,这是日本治疗头晕的标准剂量和疗程。然后,患者将剂量加倍至 72mg/天,持续 4 周。6 名患者在意识到高剂量倍他司汀的益处后,进一步将剂量增加至 72mg/天,持续 12 周(共 16 周)。通过 DHI 评分评估因头晕导致的残疾感知。
在所有 15 例患者中,高剂量(72mg/天)倍他司汀短期(4 周)治疗,但低剂量(36mg/天)倍他司汀短期(4 周)治疗均显著降低了 DHI 评分。特别是在 6 名接受高剂量倍他司汀短期治疗后自述获益的患者中,高剂量倍他司汀长期(16 周)治疗进一步显著降低了 DHI 评分。然而,在 9 名未对高剂量倍他司汀短期(4 周)治疗产生应答的患者中,DHI 评分没有变化。
倍他司汀的标准剂量和疗程短期治疗并未改善纳入患者的 DHI 评分,这表明他们没有因持续性头晕而代偿单侧前庭病。本研究结果表明,高剂量倍他司汀长期治疗有助于前庭代偿,从而改善一些但不是所有单侧前庭病伴未代偿持续性头晕患者的头晕。