Clintrex, LLC, Sarasota, FLorida, USA.
Department of Neurology, Mount Sinai School of Medicine, New York, New York, USA.
Mov Disord. 2019 Mar;34(3):425-429. doi: 10.1002/mds.27610. Epub 2019 Jan 17.
Laboratory and clinical evidence indicate that continous delivery of levodopa is associated with reduced motor complications compared to standard intermittent levodopa.
To assess the pharmacokinetics and efficacy of continuous oral delivery of l-dopa/carbidopa in PD patients with motor fluctuations.
Eighteen PD patients with motor fluctuations were enrolled in an open-label study comparing pharmacokinetics and efficacy measures between standard intermittent oral l-dopa/carbidopa and "continuous" oral l-dopa/carbidopa. Continuous treatment was operationally defined as sips of an l-dopa dispersion at 5- to 10-minute intervals. On day 1, patients received their usual oral l-dopa/carbidopa doses. On day 2, patients received l-dopa/carbidopa dose by "continuous" oral administration. On day 3, patients received a single dose of oral l-dopa/carbidopa followed by continuous administration of l-dopa/carbidopa. Each study period was 8 hours, and the total l-dopa/carbidopa dose administered was the same on each day. Analyses of variability were primarily-based samples drawn between 4 and 8 hours when subjects were in a relative steady state.
There was less variability in plasma l-dopa concentration with continuous versus intermittent oral l-dopa/carbidopa treatment (fluctuation index was 0.99 ± 0.09 vs. 1.38 ± 0.12 [P < 0.001] and coefficient of variation was 0.35 ± 0.03 vs. 0.49 ± 0.04 [P < 0.001]). Mean OFF time was decreased by 43% (P < 0.001) with continuous oral l-dopa therapy. No safety or tolerability issues were observed.
Continuous oral delivery of l-dopa/carbidopa was associated with less plasma variability and reduced off time in comparison to standard intermittent oral l-dopa/carbidopa therapy. © 2019 International Parkinson and Movement Disorder Society.
实验室和临床证据表明,与标准间歇性左旋多巴相比,持续左旋多巴输送与减少运动并发症相关。
评估连续口服左旋多巴/卡比多巴在有运动波动的 PD 患者中的药代动力学和疗效。
18 名有运动波动的 PD 患者参加了一项开放标签研究,比较了标准间歇性口服左旋多巴/卡比多巴和“连续”口服左旋多巴/卡比多巴之间的药代动力学和疗效测量。连续治疗被定义为每隔 5-10 分钟口服一次左旋多巴分散液。第 1 天,患者接受他们通常的口服左旋多巴/卡比多巴剂量。第 2 天,患者接受“连续”口服左旋多巴/卡比多巴剂量。第 3 天,患者接受单次口服左旋多巴/卡比多巴剂量,然后连续给予左旋多巴/卡比多巴。每个研究期为 8 小时,每天给予的左旋多巴/卡比多巴总剂量相同。主要基于在患者处于相对稳定状态时在 4 至 8 小时之间抽取的样本进行变异性分析。
与间歇性口服左旋多巴/卡比多巴相比,连续口服左旋多巴/卡比多巴治疗时血浆左旋多巴浓度的变异性更小(波动指数为 0.99 ± 0.09 与 1.38 ± 0.12 [P < 0.001],变异系数为 0.35 ± 0.03 与 0.49 ± 0.04 [P < 0.001])。连续口服左旋多巴治疗可使平均“OFF”时间减少 43%(P < 0.001)。未观察到安全性或耐受性问题。
与标准间歇性口服左旋多巴/卡比多巴相比,连续口服左旋多巴/卡比多巴治疗与血浆变异性降低和“OFF”时间减少相关。