阿立哌唑“诱发”和“加重”帕金森病

Nagashree V Sharma, Kuldeep S Shetty
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引用次数: 0

摘要

摘要阿立哌唑是一种新型的抗精神病药和多巴胺系统稳定剂,被一些人誉为第三代抗精神病药,并声称对D2受体(D2R)具有部分激动作用,区别于其他抗精神病药-D2多巴胺受体拮抗剂。许多研究广泛描述了早期非典型抗精神病药物的锥体外系综合征(EPS)概况,包括氯氮平、喹硫平、奥氮平、齐拉西酮和利培酮。尽管声称有D2R激动机制,但阿立哌唑引起的EPS偶有报道-下面我们报告了两个不同基线的此类病例。一名患者没有帕金森基线,另一名患者的帕金森病得到了很好的控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aripiprazole “Induced” and Aripiprazole “Worsened” Parkinsonism
Abstract Aripiprazole, a novel neuroleptic and dopamine system stabilizer, is hailed as 3 rd generation neuroleptic by some and claimed to have partial agonistic activity at D2 receptors (D2R), distinguishing it from other antipsychotics-D2 dopamine receptor antagonists. Many studies have extensively described extrapyramidal syndrome (EPS) profiles of earlier atypical neuroleptics including clozapine, quetiapine, olanzapine, ziprasidone, and risperidone. Despite the claimed D2R agonistic mechanism, EPS due to aripiprazole is sporadically reported – here below we report two such cases across two different baselines. One in a patient with no baseline Parkinsonism, another in a patient with well controlled Parkinson’s disease.
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