Hospital Privado de Occidente, Acarigua, Venezuela.
Curr Drug Deliv. 2013 Jun;10(3):343-7. doi: 10.2174/1567201811310030011.
Vertigo has a negative impact on quality of life; therefore, it is important to find an effective and convenient therapy that allows patients to continue their everyday tasks as soon as possible and to have a better quality of life.
There were two formulations used to assess the effectiveness in vertigo treatment from peripheral origin: nimodipine administrated three times daily (Nimotop®) 30 mg versus nimodipine AP administrated once daily (Tropocer®) 90 mg; both of them in a administrated in a prospective, randomized, double-blind, double dummy, multicenter and parallel-group study, where patients with peripheral vertigo defined as a score ≥7 on the Vertigo-Dizziness Differential Diagnosis Score were included. The patients were evaluated by vertigo severity index and vestibular disability index.
In the AP nimodipine group (NAP), vertigo severity index was decreased by 50%: 24% of patients in 14 days, 41% in 4 weeks and 89% in 8 weeks. The vestibular disability index was decreased by 50%: 24% of patients in 15 days, 83% in 4 weeks and 92% of patients in 8 weeks. In the conventional nimodipine group (NC), rate of vertigo severity was decreased by 50%: 17% of patients in 14 days, 41% of patients in 4 weeks and 90% of patients in 8 weeks. The vestibular disability index was decreased by 50%: 15 days in 17% of patients, 53% in 4 weeks and 64% in 8 weeks, without difference between groups.
both products were effective and well tolerated in the treatment of peripheral vertigo.
眩晕会降低生活质量,因此找到一种有效且方便的治疗方法非常重要,这样患者可以尽快继续日常活动,提高生活质量。
有两种配方用于评估治疗外周性眩晕的疗效:尼莫地平一日三次(尼莫通®)30mg 与尼莫地平控释片一日一次(特罗凯®)90mg;这两种药物都在一项前瞻性、随机、双盲、双模拟、多中心、平行组研究中进行评估,该研究纳入了外周性眩晕患者(眩晕-头晕鉴别诊断评分≥7 分)。患者通过眩晕严重程度指数和前庭残疾指数进行评估。
在尼莫地平控释片组(NAP)中,眩晕严重程度指数降低 50%:14 天内 24%的患者、4 周内 41%的患者和 8 周内 89%的患者。前庭残疾指数降低 50%:15 天内 24%的患者、4 周内 83%的患者和 8 周内 92%的患者。在常规尼莫地平组(NC)中,眩晕严重程度指数降低 50%:14 天内 17%的患者、4 周内 41%的患者和 8 周内 90%的患者。前庭残疾指数降低 50%:15 天内 17%的患者、4 周内 53%的患者和 8 周内 64%的患者,但两组间无差异。
两种产品在治疗外周性眩晕方面均有效且耐受性良好。