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左旋多巴/卡比多巴控释制剂的临床与生化研究

Clinical and biochemical studies with controlled-release levodopa/carbidopa.

作者信息

Nutt J G, Woodward W R, Carter J H

出版信息

Neurology. 1986 Sep;36(9):1206-11. doi: 10.1212/wnl.36.9.1206.

Abstract

In five patients with parkinsonism, the optimal dosage of a controlled-release levodopa/carbidopa preparation (CR-3) was three times higher than the dosage of Sinemet and produced higher plasma levodopa concentrations, but did not reduce the fluctuations in plasma levodopa or clinical response. Plasma levodopa concentrations were higher and clinical responses better before the first dose of the day with CR-3. CR-3 treatment benefited two patients, reducing the severity of off periods and off dystonia. Two patients were worse on CR-3 despite higher plasma levodopa levels than those adequate for clinical response to Sinemet or levodopa infusions. CR-3 could benefit a few severely affected patients, but it is necessary to understand the factors that affect absorption of levodopa from sustained-release preparations, as well as the consequences of prolonged elevation of plasma levodopa levels.

摘要

在5例帕金森病患者中,控释左旋多巴/卡比多巴制剂(CR - 3)的最佳剂量是息宁剂量的三倍,且能产生更高的血浆左旋多巴浓度,但并未减少血浆左旋多巴的波动或临床反应。在服用CR - 3后的当日首剂前,血浆左旋多巴浓度更高,临床反应更好。CR - 3治疗使2例患者受益,减轻了“关”期及“关”期肌张力障碍的严重程度。尽管CR - 3组患者的血浆左旋多巴水平高于对息宁或左旋多巴输注有临床反应时的适当水平,但仍有2例患者病情恶化。CR - 3可能使少数重度患者受益,但有必要了解影响左旋多巴从缓释制剂中吸收的因素,以及血浆左旋多巴水平长期升高的后果。

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