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低剂量利培酮引发的迟发性运动障碍

Tardive Dyskinesia Following Low-Dose Risperidone.

作者信息

Rokon Ahmad E, Alsomali Faisal A, Alrasheed Malek A, Alharbi Abdulrahman D, Alhamadh Moustafa S, Alqahtani Abdulmajeed M, Alhamidy Farah K, Alotaibi Meshal R

机构信息

College of Medicine, King Saud Bin Abdulaziz University for Health Sciences, Riyadh, SAU.

Ministry of the National Guard-Health Affairs, King Abdullah International Medical Research Center, Riyadh, SAU.

出版信息

Cureus. 2022 Dec 8;14(12):e32319. doi: 10.7759/cureus.32319. eCollection 2022 Dec.

Abstract

Tardive dyskinesia is an involuntary athetoid or choreiform movement lasting a minimum of a few weeks. It is associated with the use of neuroleptic medication for at least three months and persists beyond four to eight weeks. Tardive dyskinesia usually occurs as a result of the long-term use of dopamine receptor-blocking agents, mainly first-generation antipsychotics or a high-dose, second-generation antipsychotic. We present a case of a 28-year-old female with osteogenesis imperfecta presented later with major depressive disorder with psychotic features. She was given a low-dose second-generation antipsychotic, namely, risperidone (2 mg) for psychosis for a cumulative duration of three months. As a result, she developed extrapyramidal symptoms in the form of akathisia, axial dystonia, involuntary movement of the right hand, and smacking movement of the lips. Symptoms persisted for more than eight weeks despite discontinuing risperidone and switching to quetiapine. After the exclusion of other differential diagnoses, she was labeled as a case of tardive dyskinesia. More studies are needed to assess whether undiscovered contributing factors to tardive dyskinesia exist and to understand how second-generation antipsychotics (SGAs) contribute to the development of tardive dyskinesia.

摘要

迟发性运动障碍是一种持续至少数周的不自主运动障碍,表现为手足徐动症或舞蹈样动作。它与使用抗精神病药物至少三个月有关,且在停药四至八周后仍持续存在。迟发性运动障碍通常是长期使用多巴胺受体阻断剂的结果,主要是第一代抗精神病药物或高剂量的第二代抗精神病药物。我们报告一例28岁患有成骨不全症的女性患者,该患者后来出现伴有精神病性特征的重度抑郁症。她因精神病性症状接受了低剂量第二代抗精神病药物利培酮(2毫克)治疗,累计疗程为三个月。结果,她出现了锥体外系症状,表现为静坐不能、轴性肌张力障碍、右手不自主运动以及嘴唇咂嘴动作。尽管停用了利培酮并换用喹硫平,症状仍持续了八周以上。在排除其他鉴别诊断后,她被诊断为迟发性运动障碍病例。需要更多研究来评估是否存在尚未发现的迟发性运动障碍促成因素,并了解第二代抗精神病药物(SGA)如何导致迟发性运动障碍的发生。

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