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本文引用的文献

1
Tardive syndromes.迟发性综合征。
J Neurol Sci. 2018 Jun 15;389:35-42. doi: 10.1016/j.jns.2018.02.005. Epub 2018 Feb 5.
2
Tardive Dyskinesia Prevalence in the Period of Second-Generation Antipsychotic Use: A Meta-Analysis.第二代抗精神病药物使用期间迟发性运动障碍的患病率:一项荟萃分析。
J Clin Psychiatry. 2017 Mar;78(3):e264-e278. doi: 10.4088/JCP.16r10832.
3
Lurasidone: The 2016 update on the pharmacology, efficacy and safety profile.鲁拉西酮:2016年药理学、疗效及安全性概况更新
Pharmacol Rep. 2016 Aug;68(4):748-55. doi: 10.1016/j.pharep.2016.04.002. Epub 2016 Apr 22.
4
Tardive Syndromes are Rarely Reversible after Discontinuing Dopamine Receptor Blocking Agents: Experience from a University-based Movement Disorder Clinic.停用多巴胺受体阻断剂后迟发性综合征很少可逆:来自一家大学运动障碍诊所的经验。
Tremor Other Hyperkinet Mov (N Y). 2014 Oct 23;4:266. doi: 10.7916/D8MS3R8C. eCollection 2014.
5
Differentiating drug-induced parkinsonism from Parkinson's disease: an update on non-motor symptoms and investigations.药物性帕金森综合征与帕金森病的鉴别:非运动症状及检查的最新进展
Parkinsonism Relat Disord. 2014 Aug;20(8):808-14. doi: 10.1016/j.parkreldis.2014.05.011. Epub 2014 Jun 3.
6
Comparative efficacy and tolerability of 15 antipsychotic drugs in schizophrenia: a multiple-treatments meta-analysis.15 种抗精神分裂症药物的疗效和耐受性比较:一项多治疗荟萃分析。
Lancet. 2013 Sep 14;382(9896):951-62. doi: 10.1016/S0140-6736(13)60733-3. Epub 2013 Jun 27.
7
Incidence of tardive dyskinesia with risperidone or olanzapine in the elderly: results from a 2-year, prospective study in antipsychotic-naïve patients.抗精神病药初治老年患者中利培酮或奥氮平迟发性运动障碍的发生率:一项为期 2 年的前瞻性研究结果。
Neuropsychopharmacology. 2011 Jul;36(8):1738-46. doi: 10.1038/npp.2011.55. Epub 2011 Apr 20.
8
Pharmacological profile of lurasidone, a novel antipsychotic agent with potent 5-hydroxytryptamine 7 (5-HT7) and 5-HT1A receptor activity.新型抗精神病药物鲁拉西酮的药理学特性,其对 5-羟色胺 7(5-HT7)受体和 5-羟色胺 1A(5-HT1A)受体具有强大的活性。
J Pharmacol Exp Ther. 2010 Jul;334(1):171-81. doi: 10.1124/jpet.110.167346. Epub 2010 Apr 19.
9
Failure of recognition of drug-induced parkinsonism in the elderly.老年人中药物性帕金森综合征的识别失败。
Mov Disord. 2008 Feb 15;23(3):401-4. doi: 10.1002/mds.21854.

鲁拉西酮所致迟发性综合征

Lurasidone-Induced Tardive Syndrome.

作者信息

Tripathi Richa, Reich Stephen G, Scorr Laura, Guardiani Elizabeth, Factor Stewart A

机构信息

Department of Neurology Emory University School of Medicine Atlanta Georgia USA.

Department of Neurology University of Maryland School of Medicine Baltimore Maryland USA.

出版信息

Mov Disord Clin Pract. 2019 Jul 24;6(7):601-604. doi: 10.1002/mdc3.12812. eCollection 2019 Sep.

DOI:10.1002/mdc3.12812
PMID:31538095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6749798/
Abstract

INTRODUCTION

Tardive syndrome (TS) is an often irreversible movement disorder caused by dopamine receptor-blocking agents (DRBAs). Although TS are well recognized to occur with typical antipsychotics, less well appreciated is that atypical antipsychotics also carry a risk of TS.

METHODS

Case series.

RESULTS

We describe 4 patients who developed tardive dystonia, tardive akathisia, and drug-induced parkinsonism with the use of the atypical antipsychotic, lurasidone, which was U.S. Food and Drug Administration approved in 2013 for use in bipolar disorder and schizophrenia.

CONCLUSION

Movement disorders are reported as a rare side effect of lurasidone, and, as such, prescribers may perceive a false sense of security regarding this potential complication. Our cases indicate that this relatively new atypical antipsychotic may cause irreversible disabling TS as well as parkinsonism. Caution must be taken when prescribing lurasidone.

摘要

引言

迟发性综合征(TS)是一种常由多巴胺受体阻滞剂(DRBAs)引起的不可逆运动障碍。虽然TS与典型抗精神病药物一同出现已广为人知,但非典型抗精神病药物也存在引发TS的风险这一点却鲜为人知。

方法

病例系列研究。

结果

我们描述了4例使用非典型抗精神病药物鲁拉西酮后出现迟发性肌张力障碍、迟发性静坐不能和药物性帕金森综合征的患者。鲁拉西酮于2013年被美国食品药品监督管理局批准用于双相情感障碍和精神分裂症。

结论

运动障碍被报告为鲁拉西酮的一种罕见副作用,因此,处方医生可能会对这种潜在并发症产生一种错误的安全感。我们的病例表明,这种相对较新的非典型抗精神病药物可能会导致不可逆的致残性TS以及帕金森综合征。开具鲁拉西酮处方时必须谨慎。