Tardive Dyskinesia in Older Persons Taking Antipsychotics

被引:5
|
作者
Citrome, Leslie [1 ]
Isaacson, Stuart H. [2 ]
Larson, Danielle [3 ]
Kremens, Daniel [4 ]
机构
[1] New York Med Coll, 40 Sunshine Cottage Rd, Valhalla, NY 10595 USA
[2] Parkinsons Dis & Movement Disorders Ctr Boca Rat, Boca Raton, FL USA
[3] Northwestern Univ Feinberg, Sch Med, Parkinsons Dis & Movement Disorders Ctr, Chicago, IL USA
[4] Thomas Jefferson Univ, Dept Neurol, Jefferson Comprehens Parkinsons Dis & Movement Di, Philadelphia, PA 19107 USA
关键词
tardive dyskinesia; antipsychotic medications; age; ATYPICAL ANTIPSYCHOTICS; RISPERIDONE; PREVALENCE; OLANZAPINE; DEMENTIA; SAFETY; RISK; MANAGEMENT; BURDEN; ADULTS;
D O I
10.2147/NDT.S328301
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tardive dyskinesia (TD) is a hyperkinetic movement disorder caused by the use of dopamine receptor-blocking agents (DRBAs), a category of medications that includes first-and second-generation antipsychotics (APs) and agents such as metoclopramide that are used for the treatment of nausea and gastrointestinal dysmotility. While TD can affect people of all ages, older age is associated with increased risk of TD and also with the emergence of TD occurring after shorter treatment durations and lower dosages of DRBAs. TD is characterized by involuntary movements that include the face, limbs, and trunk, and is associated with increased comorbidities, social stigmatization, and impaired physical and mental health. Once present, TD tends to persist despite AP dose adjustment or discontinuation. Even with the use of US Food and Drug Administration (FDA)-approved medications for TD, symptoms may persist. Because the leading hypothesis for the pathophysiology of TD has been dysregulation of dopamine transmission due to treatment with DRBAs, APs that avoid postsynaptic dopamine receptor blockade may provide an alternative therapeutic approach for patients who require an AP. In this review, we discuss the risks, burdens, prevention, and management of TD, with a focus on older people.
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页码:3127 / 3134
页数:8
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