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首页> 外文期刊>Current drug delivery >Evaluation of the Effect of Nimodipine o.d. (Extended Release) vs Nimodipine t.i.d. in the Treatment of Peripheral Vertigo.
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Evaluation of the Effect of Nimodipine o.d. (Extended Release) vs Nimodipine t.i.d. in the Treatment of Peripheral Vertigo.

机译:尼莫地平o.d.的疗效评估(延长发布)vs尼莫地平t.i.d.在治疗周围性眩晕。

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摘要

Summary: 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. Methods: 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. Results: 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. Conclusions: both products were effective and well tolerated in the treatment of peripheral vertigo.
机译:简介:眩晕对生活质量有负面影响;因此,重要的是找到一种有效且方便的疗法,使患者能够尽快继续日常工作并改善生活质量。方法:有两种制剂可用于评估外周血眩晕的有效性:尼莫地平每天3次(尼莫托普?)30毫克,尼莫地平AP每天一次(Tropocer?)90毫克;他们都是在一项前瞻性,随机,双盲,双假人,多中心和平行组研究中进行管理的,其中外周眩晕患者的眩晕-头晕鉴别诊断得分≥7。通过眩晕严重度指数和前庭残疾指数对患者进行评估。结果:在AP尼莫地平组(NAP)中,眩晕严重性指数降低了50%:14天的患者为24%,4周的患者为41%,8周的患者为89%。前庭残疾指数降低了50%:15天的患者为24%,4周的患者为83%,8周的患者为92%。在常规尼莫地平组(NC)中,眩晕严重度降低了50%:14天的患者为17%,4周的患者为41%,8周的患者为90%。前庭残疾指数降低了50%:17%的患者15天,4周的53%和8周的64%,两组之间无差异。结论:两种产品在治疗周围性眩晕方面均有效且耐受性良好。

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