Department of Psychiatry, Chosun University Hospital, Gwangju, Republic of Korea.
Department of Psychiatry, College of Medicine, Chosun University, 309 Pilmun-daero, Dong-gu, Gwangju, 61452, Republic of Korea.
BMC Psychiatry. 2022 Jan 29;22(1):74. doi: 10.1186/s12888-022-03721-9.
Akathisia tends to develop as an early complication of antipsychotic treatment in a dose-dependent manner. Although withdrawal akathisia has been reported after the discontinuation or dose reduction of typical antipsychotic drugs, akathisia following atypical antipsychotic drug withdrawal remains a rare phenomenon.
A 24-year-old woman with an acute psychotic episode was admitted and initially treated with aripiprazole. The aripiprazole dose was titrated up to 30 mg/day over 9 days and maintained for the next 3 days; however, her psychotic symptoms persisted without change. She was switched to amisulpride, with the dose increased over 2 weeks to 1000 mg/day. Subsequently, although the patient's psychotic episode subsided, her serum prolactin levels increased markedly. After discharge, the amisulpride dose was increased to 1200 mg/day owing to auditory hallucinations and was maintained with quetiapine (100-200 mg/day) and benztropine (1 mg/day) for 13 weeks. Given the potential for hyperprolactinemia as a side effect, the amisulpride dose was reduced to 800 mg/day concurrently with the discontinuation of benztropine; however, these changes resulted in severe restlessness without other extrapyramidal symptoms. The withdrawal akathisia disappeared over 2 weeks after switching to aripiprazole (10 mg/day) with propranolol (40 mg/day) and the patient's prolactin levels had normalized after 6 months of aripiprazole monotherapy.
The present case highlights the potential for the development of withdrawal akathisia when the dose of amisulpride is tapered abruptly. Thus, a slow tapering and careful monitoring are recommended when switching from amisulpride to other antipsychotic drugs. Furthermore, this case suggests that changing the regimen to aripiprazole with propranolol may be a potential option for amisulpride withdrawal akathisia superimposed on pre-existing hyperprolactinemia.
静坐不能倾向于以剂量依赖的方式作为抗精神病药物治疗的早期并发症出现。虽然在停用或减少典型抗精神病药物后已报告出现撤药性静坐不能,但在停用非典型抗精神病药物后出现静坐不能仍然是一种罕见现象。
一名 24 岁女性因急性精神病发作入院,最初接受阿立哌唑治疗。阿立哌唑剂量在 9 天内滴定至 30mg/天,并维持 3 天;然而,她的精神病症状没有变化。她被换用氨磺必利,剂量在 2 周内增加至 1000mg/天。随后,尽管患者的精神病发作缓解,但她的血清催乳素水平显著升高。出院后,由于出现幻听,氨磺必利剂量增加至 1200mg/天,并维持使用喹硫平(100-200mg/天)和苯海索(1mg/天)13 周。由于催乳素升高可能是一种副作用,氨磺必利剂量减少至 800mg/天,并同时停用苯海索;然而,这些变化导致严重的不安,没有其他锥体外系症状。在换用阿立哌唑(10mg/天)联合普萘洛尔(40mg/天)后,撤药性静坐不能在 2 周内消失,且在阿立哌唑单药治疗 6 个月后,患者的催乳素水平恢复正常。
本病例强调了当氨磺必利剂量突然减少时,可能会出现撤药性静坐不能。因此,当从氨磺必利换用其他抗精神病药物时,建议缓慢减少剂量并密切监测。此外,本病例提示,对于伴有先前存在的高催乳素血症的氨磺必利撤药性静坐不能,将方案改为阿立哌唑联合普萘洛尔可能是一种潜在的选择。