Limandri Barbara J
J Psychosoc Nurs Ment Health Serv. 2019 May 1;57(5):11-14. doi: 10.3928/02793695-20190410-02.
Tardive dyskinesia (TD), the choreoathetoid movements of fingers, arms, legs, and trunk and irregular stereotypical movements of the mouth, face, and tongue, has been the scourge of antipsychotic medications since the approval of chlorpromazine. TD tends to occur late in treatment and sometimes remains after discontinuation of the antipsychotic medication. With the recent approval of two medications, valbenazine (Ingrezza) and deutetrabenazine (Austedo), there are now treatments for this disfiguring consequence of dopamine-blocking medications. The current article distinguishes the movement disorder adverse effects of dopamine antagonists, explains the putative mechanism of action, and describes how best to treat TD with the new vesicular monamine transporter 2 (VMAT2) medications now approved by the U.S. Food and Drug Administration. [Journal of Psychosocial Nursing and Mental Health Services, 57(5), 11-14.].
迟发性运动障碍(TD)表现为手指、手臂、腿部及躯干的舞蹈样手足徐动症,以及口、面、舌的不规则刻板运动,自氯丙嗪获批以来,一直是抗精神病药物的一大难题。TD往往在治疗后期出现,有时在停用抗精神病药物后仍会持续。随着最近两种药物——缬苯那嗪(Ingrezza)和氘代丁苯那嗪(Austedo)的获批,现在有了针对这种多巴胺阻断药物所致毁容性后果的治疗方法。本文区分了多巴胺拮抗剂的运动障碍不良反应,解释了其假定作用机制,并描述了如何使用美国食品药品监督管理局现已批准的新型囊泡单胺转运体2(VMAT2)药物来最佳地治疗TD。[《心理社会护理与精神卫生服务杂志》,57(5),11 - 14。]