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重度帕金森病患者从托卡朋转换为恩他卡朋治疗。

Switch-over from tolcapone to entacapone in severe Parkinson's disease patients.

作者信息

Onofrj M, Thomas A, Iacono D, Di Iorio A, Bonanni L

机构信息

Department of Oncology and Neuroscience, Neurophysiopathology, University G. D'Annunzio, via Fonte Romano, I-65100 Pescara, Italy.

出版信息

Eur Neurol. 2001;46(1):11-6. doi: 10.1159/000050749.

Abstract

Forty patients affected by severe Parkinson's disease (PD) were treated with tolcapone as an adjunctive therapy to L-DOPA, for 3-7 months, until this drug was discontinued because of side-effects (2 diarrhoea, one of them with orthostatic hypotension, 2 increments of liver enzymes) or because of mandatory indications of the European drugs authority. All patients, after 3-6 months of L-DOPA therapy adjustments, received entacapone for 3 months again followed by withdrawal. L-DOPA daily dosage was significantly reduced by tolcapone and entacapone (p = 0.01 and 0.05). "On" time was increased by 15% during tolcapone treatment (p < 0.05), and by 8% during entacapone treatment. "Off" time was decreased by 16% during tolcapone and by 7% during entacapone treatment. Entacapone was withdrawn in the same patient who experienced diarrhoea and orthostatic hypotension during tolcapone because of recurrence of side-effects, in 6 patients because of increment of dyskinesias (with hallucinations) and in 1 patients because of rhythmic, jerking myoclonus.

摘要

40例重度帕金森病(PD)患者接受托卡朋作为左旋多巴的辅助治疗,为期3至7个月,直至因副作用(2例腹泻,其中1例伴有体位性低血压,2例肝酶升高)或因欧洲药品管理局的强制指示而停用该药物。所有患者在进行3至6个月的左旋多巴治疗调整后,再次接受恩他卡朋治疗3个月,随后停药。托卡朋和恩他卡朋均显著降低了左旋多巴的每日剂量(p = 0.01和0.05)。在托卡朋治疗期间,“开”期时间增加了15%(p < 0.05),在恩他卡朋治疗期间增加了8%。“关”期时间在托卡朋治疗期间减少了16%,在恩他卡朋治疗期间减少了7%。在托卡朋治疗期间出现腹泻和体位性低血压的同一名患者中,因副作用复发停用了恩他卡朋,6例因运动障碍(伴有幻觉)加重而停用,1例因节律性、抽搐性肌阵挛而停用。

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