Heinz A, Suchy I, Klewin I, Kuhn W, Klotz P, Przuntek H
Neurologische Universitätsklinik, St. Josef-Hospital, Bochum, Federal Republic of Germany.
J Neural Transm Park Dis Dement Sect. 1992;4:291-301. doi: 10.1007/BF02260078.
Twenty-nine patients with advanced Parkinson's disease were treated with subcutaneous lisuride infusion in addition to a basic therapy consisting of levodopa + PDI in all, and deprenyl in some patients. At the time of the report, 13 patients are still receiving lisuride infusion after 5-36 months, while 16 have dropped out after 0.5-30 months: one because of psychosis, three because of insufficient efficacy, three due to death unrelated to treatment, three because of difficulties in handling the pump as outpatients, and six for other reasons. "Off"-periods and Parkinsonian disability in "off" and in "on" were reduced significantly. These improvements remained constant throughout the observation period. Once the optimal dose regimen is established, only minor adjustments of the doses of lisuride and levodopa are required in the individual case.
29例晚期帕金森病患者在左旋多巴+外周多巴脱羧酶抑制剂(PDI)的基础治疗上,部分患者加用司来吉兰,接受皮下注射利苏力特治疗。在报告时,13例患者在5至36个月后仍在接受利苏力特注射,而16例在0.5至30个月后退出:1例因精神病,3例因疗效不佳,3例因与治疗无关的死亡,3例因门诊患者使用泵困难,6例因其他原因。“关”期以及“关”和“开”状态下的帕金森病残疾程度均显著降低。在整个观察期内,这些改善情况保持稳定。一旦确定了最佳剂量方案,个别病例中只需对利苏力特和左旋多巴的剂量进行微调。