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随机多中心临床试验:rivastigmine 在认知功能障碍多发性硬化症患者中的安全性和疗效。

Randomised multicentre trial on safety and efficacy of rivastigmine in cognitively impaired multiple sclerosis patients.

机构信息

Caritas Krankenhaus, Bad Mergentheim, Germany.

出版信息

Mult Scler. 2013 Apr;19(5):631-8. doi: 10.1177/1352458512463481. Epub 2012 Oct 15.

Abstract

BACKGROUND

Cognitive decline has been recognised as a frequent symptom in multiple sclerosis (MS). Cholinesterase inhibitors (ChEIs) are employed for the treatment of Alzheimer's disease, but there is some evidence that ChEIs might also be effective in MS patients with cognitive deficits, particularly deficits of memory function.

OBJECTIVE

The aim of this study was to evaluate efficacy on memory function and safety of the ChEI rivastigmine in MS patients with cognitive deficits as measured by the change from baseline of the total recall score of the selective reminding test (SRT) after 16 weeks of treatment.

METHODS

Efficacy and safety of rivastigmine were analysed in a 16-week, multicentre, double-blind, randomised, placebo-controlled study, followed by an optional one-year open-label treatment phase. Effects of rivastigmine and placebo were compared by an analysis of covariance.

RESULTS

In total, 86 patients were enrolled. Patients who received rivastigmine (n = 43) showed a non-significant increase in total recall score (sum of all words immediately recalled over all six trials) over placebo (n = 38) after 16 weeks of treatment (p = 0.2576). Other outcome measures provided no evidence supporting benefits of rivastigmine. Treatment with rivastigmine was well tolerated.

CONCLUSIONS

With the results of this study, the need for an effective therapy in cognitively impaired MS patients is still required. Thus, intensive and continued clinical research is required to explore therapeutic options for cognitive deficits in MS patients.

摘要

背景

认知障碍已被认为是多发性硬化症(MS)的常见症状。胆碱酯酶抑制剂(ChEIs)用于治疗阿尔茨海默病,但有一些证据表明 ChEIs 可能对有认知障碍的 MS 患者也有效,特别是记忆功能障碍。

目的

本研究旨在评估胆碱酯酶抑制剂利伐斯的明对认知障碍 MS 患者记忆功能的疗效和安全性,通过治疗 16 周后选择性提醒测试(SRT)总回忆评分的基线变化来衡量。

方法

在一项为期 16 周、多中心、双盲、随机、安慰剂对照研究中分析了利伐斯的明的疗效和安全性,随后进行了可选的为期一年的开放标签治疗阶段。通过协方差分析比较了利伐斯的明和安慰剂的效果。

结果

共有 86 名患者入组。接受利伐斯的明(n = 43)的患者在 16 周的治疗后,总回忆评分(所有六个试验中立即回忆的所有单词的总和)较安慰剂(n = 38)有非显著增加(p = 0.2576)。其他结局指标没有提供支持利伐斯的明益处的证据。利伐斯的明治疗耐受性良好。

结论

根据本研究的结果,仍需要为认知受损的 MS 患者提供有效的治疗方法。因此,需要进行密集和持续的临床研究,以探索治疗 MS 患者认知障碍的治疗选择。

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