• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

并非所有的运动都是迟发性运动障碍。

Not all that moves is tardive dyskinesia.

作者信息

Khot V, Wyatt R J

机构信息

Neuropsychiatry Branch, NIMH Neuroscience Center, St. Elizabeths Hospital, Washington, DC 20032.

出版信息

Am J Psychiatry. 1991 May;148(5):661-6. doi: 10.1176/ajp.148.5.661.

DOI:10.1176/ajp.148.5.661
PMID:1673323
Abstract

OBJECTIVE

Because tardive dyskinesia and spontaneous dyskinesia appear the same, it is difficult to determine whether an individual patient's abnormal movements are induced by medication or have developed spontaneously. Therefore, estimates of the prevalence of tardive dyskinesia that are based on observations not adjusted for spontaneous dyskinesia are inflated. In addition, age is thought to be an important risk factor in the development of both tardive and spontaneous dyskinesias. The authors estimate the prevalence of both disorders for specific age groups.

METHOD

The authors reviewed nine reports on dyskinesia prevalence that included history of neuroleptic treatment and related prevalence to age. A rating of 2 or more on the Abnormal Involuntary Movement Scale or an equivalent score on another scale was considered an indication of dyskinesia. If the subject had taken neuroleptics for more than 3 months, the movement disorder was classified as neuroleptic-associated dyskinesia; other dyskinesias were considered spontaneous. The prevalence of tardive dyskinesia was defined as the rate of neuroleptic-associated dyskinesia minus the rate of spontaneous dyskinesia.

RESULTS

The true rate of tardive dyskinesia was below 20% for all age groups except 70-79 years. The correlation between the rate of neuroleptic-associated dyskinesia and the rate of spontaneous dyskinesia was low.

CONCLUSIONS

After age 40 the prevalence of spontaneous dyskinesia is sufficiently high to conclude that many patients with diagnoses of tardive dyskinesia have abnormal movements attributable to causes other than neuroleptics.

摘要

目的

由于迟发性运动障碍和自发性运动障碍表现相同,很难确定个体患者的异常运动是由药物引起的还是自发产生的。因此,基于未针对自发性运动障碍进行调整的观察结果对迟发性运动障碍患病率的估计是偏高的。此外,年龄被认为是迟发性和自发性运动障碍发生的重要风险因素。作者估计了特定年龄组中这两种疾病的患病率。

方法

作者回顾了九份关于运动障碍患病率的报告,这些报告包括抗精神病药物治疗史以及与年龄相关的患病率。异常不自主运动量表评分为2分或更高,或在另一个量表上的等效分数被视为运动障碍的指标。如果受试者服用抗精神病药物超过3个月,运动障碍被归类为抗精神病药物相关的运动障碍;其他运动障碍被视为自发性的。迟发性运动障碍的患病率定义为抗精神病药物相关运动障碍的发生率减去自发性运动障碍的发生率。

结果

除70 - 79岁年龄组外,所有年龄组的迟发性运动障碍真实发生率均低于20%。抗精神病药物相关运动障碍的发生率与自发性运动障碍的发生率之间的相关性较低。

结论

40岁以后,自发性运动障碍的患病率足够高,足以得出结论,许多被诊断为迟发性运动障碍的患者的异常运动是由抗精神病药物以外的原因引起的。

相似文献

1
Not all that moves is tardive dyskinesia.并非所有的运动都是迟发性运动障碍。
Am J Psychiatry. 1991 May;148(5):661-6. doi: 10.1176/ajp.148.5.661.
2
Prevalence of spontaneous dyskinesia in schizophrenia.精神分裂症患者中自发性运动障碍的患病率。
J Clin Psychiatry. 2000;61 Suppl 4:10-4.
3
Changing epidemiology of tardive dyskinesia: an overview.迟发性运动障碍的流行病学变化:概述
Am J Psychiatry. 1981 Mar;138(3):297-309. doi: 10.1176/ajp.138.3.297.
4
Clinical and epidemiologic aspects of tardive dyskinesia.迟发性运动障碍的临床与流行病学特征
J Clin Psychiatry. 1985 Apr;46(4 Pt 2):8-13.
5
Spontaneous and tardive dyskinesias: clinical and laboratory studies.
J Clin Psychiatry. 1985 Apr;46(4 Pt 2):42-7.
6
Intermittent neuroleptic treatment and risk for tardive dyskinesia: Curaçao Extrapyramidal Syndromes Study III.间歇性抗精神病药物治疗与迟发性运动障碍风险:库拉索锥体外系综合征研究III
Am J Psychiatry. 1998 Apr;155(4):565-7. doi: 10.1176/ajp.155.4.565.
7
Tardive dyskinesia in elderly psychiatric patients: a 5-year study.老年精神病患者的迟发性运动障碍:一项为期5年的研究。
Am J Psychiatry. 1992 Sep;149(9):1206-11. doi: 10.1176/ajp.149.9.1206.
8
Prevalence of tardive dyskinesia.
J Clin Psychiatry. 1979 Dec;40(12):508-16.
9
Ten-year outcome of tardive dyskinesia.迟发性运动障碍的十年转归
Am J Psychiatry. 1994 Jun;151(6):836-41. doi: 10.1176/ajp.151.6.836.
10
[Clinical aspects of tardive dyskinesias induced by neuroleptics].[抗精神病药物所致迟发性运动障碍的临床特征]
Encephale. 1988 Sep;14 Spec No:209-14.

引用本文的文献

1
Prevalence of spontaneous dyskinesia in first episode, drug naive schizophrenia, and its relation to the positive and negative symptoms of schizophrenia.首发未用药精神分裂症患者中自发性运动障碍的患病率及其与精神分裂症阳性和阴性症状的关系。
Open J Psychiatry Allied Sci. 2017 Jul-Dec;8(2):113-123. doi: 10.5958/2394-2061.2017.00005.2. Epub 2016 Dec 30.
2
Overcoming barriers to effective management of tardive dyskinesia.克服迟发性运动障碍有效管理的障碍。
Neuropsychiatr Dis Treat. 2019 Apr 4;15:785-794. doi: 10.2147/NDT.S196541. eCollection 2019.
3
[Antipsychotic-induced motor symptoms in schizophrenic psychoses-Part 3 : Tardive dyskinesia].
[抗精神病药物所致精神分裂症性精神病的运动症状 - 第3部分:迟发性运动障碍]
Nervenarzt. 2019 May;90(5):472-484. doi: 10.1007/s00115-018-0629-7.
4
Childhood pegboard task predicts adult-onset psychosis-spectrum disorder among a genetic high-risk sample.儿童钉板任务可预测遗传高危样本中的成人期精神病谱系障碍。
Schizophr Res. 2016 Dec;178(1-3):68-73. doi: 10.1016/j.schres.2016.08.017. Epub 2016 Sep 9.
5
Treatment of neurolept-induced tardive dyskinesia.抗精神病药物所致迟发性运动障碍的治疗。
Neuropsychiatr Dis Treat. 2013;9:1371-80. doi: 10.2147/NDT.S30767. Epub 2013 Sep 16.
6
Motor symptoms of schizophrenia: is tardive dyskinesia a symptom or side effect? A modern treatment.精神分裂症的运动症状:迟发性运动障碍是一种症状还是副作用?一种现代治疗方法。
Curr Psychiatry Rep. 2011 Aug;13(4):295-304. doi: 10.1007/s11920-011-0202-6.
7
The catatonic dilemma expanded.紧张症困境扩大了。
Ann Gen Psychiatry. 2006 Sep 7;5:14. doi: 10.1186/1744-859X-5-14.
8
Digital movement analysis, a new objective method of measuring tardive dyskinesia and drug-induced parkinsonian tremor: acceptability, reliability and validity.
Eur Arch Psychiatry Clin Neurosci. 1996;246(2):71-7. doi: 10.1007/BF02274896.
9
Risk factors for orofacial and limbtruncal tardive dyskinesia in older patients: a prospective longitudinal study.老年患者口面部及肢体躯干迟发性运动障碍的危险因素:一项前瞻性纵向研究。
Psychopharmacology (Berl). 1996 Feb;123(4):307-14. doi: 10.1007/BF02246639.