Takeshima Masahiro, Ishikawa Hiroyasu, Kikuchi Yuka, Kanbayashi Takashi, Shimizu Tetsuo
Department of Neuropsychiatry, Akita University Graduate School of Medicine, Akita, Japan.
Clin Psychopharmacol Neurosci. 2018 Aug 31;16(3):346-348. doi: 10.9758/cpn.2018.16.3.346.
The management of clozapine (CLZ)-induced adverse events affects patient prognoses. Akathisia is a relatively rare adverse event related to CLZ administration and thus the management of this syndrome is not well established. Here, we report a case of treatment-resistant schizophrenia wherein CLZ-induced akathisia was successfully managed with gabapentin enacarbil (GE). The patient was a 39-year-old woman who had been treated with atypical antipsychotics other than CLZ for three years with poor tolerability. Initiation of CLZ (400 mg/day) attenuated her psychotic symptoms, but was followed by moderate akathisia. Neither benzodiazepines nor biperiden improved the akathisia; however, akathisia was finally diminished with co-administration of GE. GE facilitated a dosage increase in CLZ (450 mg/day) for the improved management of pyschotic symptoms, and thus indirectly contributed to treatment of the patient's schizophrenia. We suggest that GE is a useful candidate for the management of CLZ-induced akathisia. The improved management of treatment-induced akathisia and other adverse events can extend the potential application of CLZ for treatment-resistant schizophrenia.
氯氮平(CLZ)所致不良事件的管理会影响患者的预后。静坐不能是与CLZ使用相关的一种相对罕见的不良事件,因此对该综合征的管理尚未完全确立。在此,我们报告1例难治性精神分裂症患者,其CLZ所致静坐不能通过加巴喷丁依卡倍特(GE)成功得到控制。该患者为一名39岁女性,此前使用除CLZ之外的非典型抗精神病药物治疗3年,耐受性较差。开始使用CLZ(400毫克/天)后,其精神病性症状有所减轻,但随后出现中度静坐不能。苯二氮䓬类药物和安坦均未能改善静坐不能;然而,GE联合使用最终使静坐不能减轻。GE有助于增加CLZ的剂量(450毫克/天)以更好地控制精神病性症状,从而间接有助于该患者精神分裂症的治疗。我们认为GE是管理CLZ所致静坐不能的一种有效选择。改善对治疗所致静坐不能及其他不良事件的管理可扩大CLZ在难治性精神分裂症治疗中的潜在应用。