Rondot P, Ziegler M, Aymard N, Teinturier A
Hopital Sainte Anne, Faculte de Medecine Cochin-Port Royal, Paris, France.
Neurology. 1989 Nov;39(11 Suppl 2):74-7; discussion 95.
Twenty parkinsonian patients were treated with controlled-release carbidopa/levodopa (Sinemet CR). All were affected by therapeutic response fluctuations related to the timing of drug administration. The daily dosage after 1 year, 766 mg +/- 250 mg, was increased by 23% compared with standard Sinemet dosage, without additional secondary effects. Parkinsonian scores improved by 43%; the prolongation of "on" periods was 63%. Nevertheless, 7 patients withdrew from this study during the 1st month of treatment. Only 1 withdrew due to an adverse reaction to the formulation, a recurrence of hallucinations. The progressive effect of the 1st morning dose and the often unpredictable time at which the product first takes effect were found to be frustrating for the other patients who withdrew. We believe that this disappointment can be avoided by giving new patients the controlled-release formulation from the start of therapy.
20名帕金森病患者接受了控释卡比多巴/左旋多巴(息宁控释片)治疗。所有患者都受到与给药时间相关的治疗反应波动的影响。1年后的每日剂量为766毫克±250毫克,与标准息宁剂量相比增加了23%,且无额外的副作用。帕金森病评分改善了43%;“开”期延长了63%。然而,7名患者在治疗的第1个月退出了该研究。只有1名患者因对制剂出现不良反应(幻觉复发)而退出。对于其他退出的患者来说,发现首日晨服剂量的渐进效果以及该产品首次起效的时间往往不可预测,令人沮丧。我们认为,通过从治疗开始就给新患者使用控释制剂,可以避免这种失望情绪。