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左旋多巴/卡比多巴/恩他卡朋(息宁控释片)

Levodopa/carbidopa/entacapone (Stalevo).

作者信息

Hauser Robert A

机构信息

Department of Neurology, University of South Florida and Tampa General Healthcare, Tampa, Florida 33606, USA.

出版信息

Neurology. 2004 Jan 13;62(1 Suppl 1):S64-71. doi: 10.1212/wnl.62.1_suppl_1.s64.

Abstract

A levodopa/carbidopa/entacapone combination product (Stalevo) was recently approved to treat patients with idiopathic Parkinson's disease (PD) who experience end-of-dose "wearing-off." Stalevo is available in dose combinations of levodopa/carbidopa/entacapone 50/12.5/200 mg (Stalevo 50), 100/25/200 mg (Stalevo 100), and 150/37.5/200 mg (Stalevo 150). A series of pharmacokinetic studies demonstrated bioequivalence between Stalevo and corresponding dosages of levodopa/carbidopa plus entacapone. A clinical advantage of Stalevo is that patients can take one pill rather than two (or more) separate tablets. In addition, Stalevo 50 and 100 tablets are smaller than entacapone tablets. These advantages may be particularly beneficial for patients taking many pills, those who have difficulty following complex medication regimens, and those with swallowing difficulty. Most PD patients taking levodopa/carbidopa immediate-release (IR) plus entacapone can be directly switched to the corresponding dose Stalevo product. For fluctuating PD patients taking levodopa/carbidopa IR without entacapone, switching to the corresponding Stalevo tablet is analogous to adding entacapone. In switching patients who are receiving levodopa/carbidopa controlled-release (CR), it should be noted that the bioavailability of levodopa from levodopa/carbidopa CR is approximately 70-75% that of levodopa/carbidopa IR products, including Stalevo.

摘要

左旋多巴/卡比多巴/恩他卡朋复方制剂(息宁控释片)最近被批准用于治疗出现剂末“疗效减退”的特发性帕金森病(PD)患者。息宁控释片有左旋多巴/卡比多巴/恩他卡朋50/12.5/200毫克(息宁控释片50)、100/25/200毫克(息宁控释片100)和150/37.5/200毫克(息宁控释片150)的剂量组合。一系列药代动力学研究证明息宁控释片与相应剂量的左旋多巴/卡比多巴加恩他卡朋具有生物等效性。息宁控释片的一个临床优势是患者只需服用一片药,而不必服用两片(或更多)分开的片剂。此外,息宁控释片50和100的片剂比恩他卡朋片小。这些优势对于服用多种药物的患者、难以遵循复杂用药方案的患者以及有吞咽困难的患者可能特别有益。大多数服用左旋多巴/卡比多巴速释(IR)加恩他卡朋的PD患者可以直接换用相应剂量的息宁控释片产品。对于服用左旋多巴/卡比多巴IR但未服用恩他卡朋的症状波动型PD患者,换用相应的息宁控释片片剂类似于加用恩他卡朋。在转换接受左旋多巴/卡比多巴控释(CR)治疗的患者时,应注意左旋多巴/卡比多巴CR中左旋多巴的生物利用度约为左旋多巴/卡比多巴IR产品(包括息宁控释片)的70 - 75%。

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