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Antipsychotic medication treatment for mild hallucinations in Parkinson's disease: Positive impact on long-term worsening.

机译:抗精神病药物治疗帕金森氏症的幻觉:对长期恶化的积极影响。

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To test if antipsychotic medication treatment of Parkinson's disease (PD) patients with mild hallucinations and retained insight delays deterioration to delusions or hallucinations without insight. We identified subjects at the time they developed their first hallucination, based on documented progression in their UPDRS thought disorder (TD) score from <2 to 2 ("benign" hallucinations with insight retained). We registered TD scores at follow-up visits and their hallucination treatment: antipsychotic medication, PD medication reduction, or observation. The primary outcome measure was the time from the first TD = 2 until the TD score worsened to 3 (hallucinations with loss of insight) or 4 (delusions, psychosis). The effect of antipsychotic medication treatment on transition hazard rate was modeled by proportional hazards regression (Cox model) with antipsychotic medication use as a time-dependent covariate. Of 64 patients, 31 received antipsychotic medication during the study (mean group follow-up 31 months). Of the 38 subjects who reached endpoint, eight subjects had been treated with antipsychotic medication compared to 30/33 in those not treated with antipsychotic medication. Antipsychotic medication treatment reduced the risk of deterioration [hazard ratio = 0.156, CI = (0.067-0.363), P < 0.0001] compared to treatment without antipsychotic medications. The median time from the introduction of antipsychotic medication to the conversion from TD = 2 to TD > 2 was 39 months in subjects on antipsychotic medication compared to 12 months in patients treated otherwise. Until randomized treatment trials provide definitive information, early antipsychotic medication treatment for mild hallucinations should be considered with the combined goal of improving current hallucinations and reducing risks of later deterioration.
机译:要测试帕金森氏病(PD)伴有轻度幻觉并保留有洞察力的患者的抗精神病药物治疗是否会延迟妄想或幻觉的恶化,而不会产生洞察力。我们根据受试者的UPDRS思维障碍(TD)分数从<2到2(保留良知的“良性”幻觉)进展情况,确定了他们出现首次幻觉时的受试者。我们在随访和幻觉治疗中记录了TD评分:抗精神病药物,PD药物减少或观察。主要结局指标是从第一个TD = 2到TD评分恶化至3(视力丧失的晕眩症)或4(妄想,精神病)的时间。通过比例风险回归(Cox模型)对抗精神病药物治疗对过渡性危险率的影响进行建模,并将抗精神病药物的使用作为时间依赖性协变量。在64位患者中,有31位在研究期间接受了抗精神病药物治疗(平均组随访31个月)。在达到终点的38位受试者中,有8位接受过抗精神病药物治疗,而未接受抗精神病药物的30/33人。与不使用抗精神病药物的治疗相比,抗精神病药物的治疗降低了恶化的风险[危险比= 0.156,CI =(0.067-0.363),P <0.0001]。使用抗精神病药物的受试者从引入抗精神病药物到从TD = 2转换为TD> 2的中位时间为39个月,而接受其他治疗的患者为12个月。在随机治疗试验提供确切信息之前,应考虑针对轻度幻觉的早期抗精神病药物治疗,其综合目标是改善目前的幻觉并降低后期恶化的风险。

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