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13.3毫克/24小时的卡巴拉汀透皮贴剂:用于治疗轻至中度阿尔茨海默病痴呆症的综述

Rivastigmine transdermal patch 13.3 mg/24 h: a review of its use in the management of mild to moderate Alzheimer's dementia.

作者信息

Frampton James E

机构信息

Adis, Level 1, 5 The Warehouse Way, Northcote 0627; Private Bag 65901, Mairangi Bay 0754, Auckland, New Zealand,

出版信息

Drugs Aging. 2014 Aug;31(8):639-49. doi: 10.1007/s40266-014-0197-x.

Abstract

Rivastigmine is unique among cholinesterase inhibitors commonly used in the treatment of mild to moderate Alzheimer's disease (AD) in that it is available as a transdermal patch formulation (Exelon(®) patch, Rivastach(®) patch, Prometax(®) patch). The patch is applied once daily and, in the EU (and US), is available in three sizes: 5, 10 and 15 cm(2) (releasing 4.6, 9.5 and 13.3 mg rivastigmine/24 h, respectively). In the phase III OPTIMA trial, patients with mild to moderate AD who experienced functional and cognitive decline on the 10 cm(2) patch-the recommended maintenance dose-gained additional benefit when their dose was increased to the 15 cm(2) patch. For example, 15 cm(2) patch recipients showed significantly less functional and cognitive decline than 10 cm(2) patch recipients after 24 weeks of double-blind treatment. Patients receiving the 15 cm(2) patch also showed significantly less functional, but not cognitive, decline than those receiving the 10 cm(2) patch after 48 weeks of double-blind treatment; as such, OPTIMA only met one of its two co-primary endpoints. The 15 cm(2) patch was generally well tolerated; although more 15 cm(2) than 10 cm(2) patch recipients reported adverse events (e.g. nausea and vomiting), fewer 15 cm(2) than 10 cm(2) patch recipients discontinued treatment due to adverse events. By further slowing functional deterioration without markedly compromising tolerability, increasing the transdermal rivastigmine dose to the 15 cm(2) patch has a favourable benefit-risk profile-and therefore represents a valid option-in the treatment of patients with mild to moderate AD who have previously experienced functional and cognitive decline while receiving the 10 cm(2) patch.

摘要

在常用于治疗轻至中度阿尔茨海默病(AD)的胆碱酯酶抑制剂中,卡巴拉汀独具特色,它有透皮贴剂剂型(艾斯能(®)贴剂、利凡斯的明(®)贴剂、普美达(®)贴剂)。该贴剂每日使用一次,在欧盟(及美国)有三种规格:5、10和15平方厘米(分别每24小时释放4.6、9.5和13.3毫克卡巴拉汀)。在III期OPTIMA试验中,轻至中度AD患者在使用10平方厘米贴剂(推荐维持剂量)时出现功能和认知衰退,当剂量增加至15平方厘米贴剂时,他们获得了额外益处。例如,在双盲治疗24周后,使用15平方厘米贴剂的患者功能和认知衰退明显少于使用10平方厘米贴剂的患者。在双盲治疗48周后,使用15平方厘米贴剂的患者功能衰退也明显少于使用10平方厘米贴剂的患者,但认知衰退情况并非如此;因此,OPTIMA仅达到其两个共同主要终点中的一个。15平方厘米贴剂总体耐受性良好;尽管报告不良事件(如恶心和呕吐)的15平方厘米贴剂使用者比10平方厘米贴剂使用者更多,但因不良事件而停药的15平方厘米贴剂使用者比10平方厘米贴剂使用者更少。将透皮卡巴拉汀剂量增加至15平方厘米贴剂可进一步减缓功能恶化,且不会明显影响耐受性,具有良好的效益风险比,因此对于在使用10平方厘米贴剂时曾出现功能和认知衰退的轻至中度AD患者而言,是一种有效的治疗选择。

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