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(-)司来吉兰治疗帕金森病:在不同病程阶段的两年研究

(-)Deprenyl in Parkinson's disease: a two-year study in the different evolutive stages.

作者信息

Giovannini P, Martignoni E, Piccolo I, Pacchetti C, Grassi M P, Nappi G, Caraceni T

出版信息

J Neural Transm Suppl. 1986;22:235-46.

PMID:3097258
Abstract

Seventy-nine patients with idiopathic Parkinson's disease in various phases of evolution of the clinical picture were studied. All the patients, already under treatment with L-dopa + PDI, were treated with (-)deprenyl at the dose of 10 mg/day orally in two daily administrations. The mean follow-up was 8.7 months (range, 1-29). Overall, 47.6% of the patients improved, 27.4% showed a marked improvement, 38.1% showed evident modifications, and 27.4% worsened. Sixteen patients were excluded from the study for various reasons. In 53.2% of the cases it was possible to reduce the daily L-dopa dose by a mean of 30%. Overall, (-)deprenyl was effective in the treatment of our parkinsonian patients in the various conditions evaluated, and thus constitutes a new therapeutic strategy for Parkinson's disease.

摘要

对79例处于临床病程不同阶段的特发性帕金森病患者进行了研究。所有患者均已接受左旋多巴+外周多巴脱羧酶抑制剂治疗,给予口服(-)司来吉兰,剂量为每日10mg,分两次服用。平均随访时间为8.7个月(范围1 - 29个月)。总体而言,47.6%的患者病情改善,27.4%的患者显著改善,38.1%的患者有明显变化,27.4%的患者病情恶化。16例患者因各种原因被排除在研究之外。在53.2%的病例中,每日左旋多巴剂量平均可减少30%。总体而言,(-)司来吉兰在评估的各种情况下对帕金森病患者的治疗均有效,因此构成了帕金森病的一种新治疗策略。

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