Targum S D, Abbott J L
Clinical Studies Limited, Philadelphia, Pennsylvania 19106, USA.
J Clin Psychopharmacol. 2000 Feb;20(1):54-60. doi: 10.1097/00004714-200002000-00010.
Eleven patients with Parkinson's disease (PD) and acute psychosis received flexible doses of quetiapine between 25 and 300 mg/day based on clinical response and tolerance. Ten patients were receiving dopaminergic agents at baseline. Serial efficacy ratings (Brief Psychiatric Rating Scale, Clinical Global Impressions Scale), neuromuscular symptom assessments (Abnormal Involuntary Movement Scale, Simpson-Angus Scale, Unified Parkinson's Disease Rating Scale [UPDRS]), and adverse events monitoring were performed for up to 52 weeks. The patients had moderate hallucinations and/or delusions at baseline before the initiation of quetiapine. Nine of the 11 patients completed at least 12 weeks of treatment. Quetiapine was well tolerated in all but one patient, who became dizzy within the first week and withdrew from the study. Ten patients presented with moderate visual hallucinations. Quetiapine was markedly effective in controlling visual hallucinations in six of these patients. Symptoms of paranoia or delusions were less responsive to quetiapine. Four patients withdrew because of adverse events or comorbid medical problems, two withdrew because of a lack of efficacy, and five completed 52 weeks of treatment. The introduction of quetiapine did not exacerbate parkinsonian symptoms. Motor dysfunction, as measured by the UPDRS, revealed a slow, gradual worsening consistent with the progression of PD. Atypical antipsychotic medications such as quetiapine have a reduced likelihood of causing adverse drug-induced parkinsonism and therefore a possible role in treating psychotic symptoms in patients with PD.
11名患有帕金森病(PD)且伴有急性精神病的患者,根据临床反应和耐受性,接受了剂量灵活的喹硫平治疗,剂量范围为每天25至300毫克。10名患者在基线时正在接受多巴胺能药物治疗。进行了长达52周的系列疗效评估(简明精神病评定量表、临床总体印象量表)、神经肌肉症状评估(异常不自主运动量表、辛普森-安格斯量表、统一帕金森病评定量表[UPDRS])以及不良事件监测。在开始使用喹硫平之前,患者在基线时存在中度幻觉和/或妄想。11名患者中有9名完成了至少12周的治疗。除1名患者外,所有患者对喹硫平耐受性良好,该患者在第一周内出现头晕并退出研究。10名患者出现中度视幻觉。喹硫平在其中6名患者中对控制视幻觉有显著效果。偏执或妄想症状对喹硫平反应较差。4名患者因不良事件或合并的医疗问题退出,2名患者因缺乏疗效退出,5名患者完成了52周的治疗。引入喹硫平并未加重帕金森病症状。通过UPDRS测量的运动功能障碍显示出与PD进展一致的缓慢、逐渐恶化。非典型抗精神病药物如喹硫平引起药物性帕金森综合征的可能性降低,因此在治疗PD患者的精神病症状方面可能有作用。