Popa Luminita C, Leucuta Daniel-Corneliu, Tohanean Nicoleta, Popa Stefan-Lucian, Perju-Dumbrava Lacramioara
Neurology Department.
Department of Medical Informatics and Biostatistics.
Medicine (Baltimore). 2020 Nov 13;99(46):e23249. doi: 10.1097/MD.0000000000023249.
Levodopa-carbidopa intestinal gel (LCIG) is a method of continuous administration of levodopa - the standard treatment in Parkinson disease (PD, a neurodegenerative disorder characterized by resting tremor, rigidity, gait impairment, and bradykinesia), thought to reduce the short-life and pulsatile problems of oral administration. We aimed to study the effects of Levodopa-Carbidopa therapy in 2 separate groups: one with intrajejunal administration of Levodopa-Carbidopa gel and the second with oral therapy.We performed an observational retrospective Romanian cohort study on 61 patients diagnosed with PD patients, with Hoehn and Jahr 3 and 4 stages, recruited from a single regional tertiary center in Cluj-Napoca, Romania, between 2009 and 2019.The mean adjusted UPDRS III (and similarly for UPDRS II) improved in the LCIG compared to the oral therapy group with 15.6 (95% CI 12.0-19.2, P < .001), and with 18.4 (95% CI 13.8-22.9, P < .001), stratified for the Hoehn and Jahr stages 3 and 4. There was a 41.7% (10) reduction in dyskinesia, and 29.2% reduction in wearing off/on-off at 1 year in the LCIG group compared to 0% (0) dyskinesia reduction, and 2.7% reduction in wearing off/on-off in the oral therapy group.Continuous intrajejunal infusion of LCIG ensures a significant and clinical reduction in motor fluctuations compared to oral therapy in advanced PD, even after adjustment for important confounders.
左旋多巴-卡比多巴肠凝胶(LCIG)是一种持续给予左旋多巴的方法,左旋多巴是帕金森病(PD,一种以静止性震颤、僵硬、步态障碍和运动迟缓为特征的神经退行性疾病)的标准治疗药物,该方法被认为可减少口服给药的短效和脉冲式问题。我们旨在研究左旋多巴-卡比多巴疗法在两个不同组中的效果:一组为经空肠给予左旋多巴-卡比多巴凝胶,另一组为口服疗法。我们对61例诊断为PD的患者进行了一项观察性回顾性罗马尼亚队列研究,这些患者处于Hoehn和Jahr 3期及4期,于2009年至2019年从罗马尼亚克卢日-纳波卡的一个单一地区三级中心招募。与口服治疗组相比,LCIG组的平均校正后统一帕金森病评定量表第三部分(UPDRS III,UPDRS第二部分情况类似)改善了15.6(95%置信区间12.0 - 19.2,P <.001),按Hoehn和Jahr 3期及4期分层后改善了18.4(95%置信区间13.8 - 22.9,P <.001)。与口服治疗组相比,LCIG组在1年时异动症减少了41.7%(10例),“剂末现象/开关现象”减少了29.2%,而口服治疗组异动症减少0%(0例),“剂末现象/开关现象”减少2.7%。与口服疗法相比,即使在对重要混杂因素进行校正后,晚期PD患者持续空肠内输注LCIG仍能显著且临床上减少运动波动。