Abhilasha Pallavi, Bhatti Neena, Joseph Girish, Injety Ranjit J
Department of Psychiatry, Christian Medical College, Ludhiana, Punjab, India.
Department of Pharmacology, Christian Medical College, Ludhiana, Punjab, India.
J Family Med Prim Care. 2024 Sep;13(9):4099-4102. doi: 10.4103/jfmpc.jfmpc_421_24. Epub 2024 Sep 11.
Existing data suggest that clozapine has lesser propensity of developing akathisia as compared to first general antipsychotics. Clozapine is mostly used in patients with treatment-resistant schizophrenia, which is a second-generation antipsychotic. Akathisia is one of the rare side effects of clozapine. A 34-year-old woman with a 7-year history of schizophrenia exhibited positive and negative symptoms, initially treated with haloperidol and clonazepam. Despite relief in positive symptoms, she experienced recurring cycles of symptom exacerbation upon discontinuing medication. Because of poor compliance, she was admitted and started on clozapine, reaching 150 mg/day. Although showing symptom improvement, she developed clozapine-induced akathisia, characterized by restlessness and limb movements. Propranolol and a gradual reduction in clozapine alleviated akathisia, supplemented by lorazepam. The Barnes Akathisia Rating Scale dropped to 0 after three weeks. This case highlights the challenges of managing schizophrenia and the importance of tailored medication strategies. The use of clozapine should be customized based on each patient's needs to prevent clozapine-induced akathisia.
现有数据表明,与第一代抗精神病药物相比,氯氮平引发静坐不能的倾向较小。氯氮平主要用于治疗难治性精神分裂症患者,它是一种第二代抗精神病药物。静坐不能是氯氮平罕见的副作用之一。一名患有7年精神分裂症病史的34岁女性表现出阳性和阴性症状,最初接受氟哌啶醇和氯硝西泮治疗。尽管阳性症状有所缓解,但停药后她经历了症状反复加重的周期。由于依从性差,她入院并开始服用氯氮平,剂量达到每日150毫克。尽管症状有所改善,但她出现了氯氮平所致的静坐不能,表现为坐立不安和肢体活动。普萘洛尔和逐渐减少氯氮平剂量缓解了静坐不能,同时辅以劳拉西泮。三周后,巴恩斯静坐不能评定量表评分降至0分。该病例凸显了精神分裂症管理的挑战以及个性化用药策略的重要性。应根据每位患者的需求定制氯氮平的使用,以预防氯氮平所致的静坐不能。