Owusu Aboagye Grace, Ankrah Daniel
Department of Psychiatry, Korle Bu Teaching Hospital, P. O. Box KB 77, Accra, Ghana.
Department of Pharmacy, Korle Bu Teaching Hospital, P. O. Box KB 77, Accra, Ghana.
Case Rep Psychiatry. 2020 Apr 23;2020:9649483. doi: 10.1155/2020/9649483. eCollection 2020.
Extrapyramidal side effects of psychotropic medicines are usually experienced by patients in the first few weeks of initiating therapy. Patients stabilized on these medications who present with distressing complaints akin to akathisia may be triggered by other factors. This report presents two cases of drug-drug-induced akathisia. Case A is a patient with schizophrenia who was being managed with risperidone 2 mg tablet daily for the past 3 years. She fell ill and reported to a nearby clinic where she was prescribed ciprofloxacin and artemether/lumefantrine tablets for the treatment of an infection and malaria. She presented 7 days later to her psychiatrist with complaints of restlessness, tremor, palpitations, insomnia, and resurgence of obsessive thoughts. Case B is a patient who was diagnosed with first-episode psychotic depression and admitted for 10 days. Her medications on admission were fluphenazine decanoate 25 mg depot injection once, olanzapine 10 mg tablet daily, and fluoxetine 20 mg capsule daily. On discharge, ciprofloxacin 500 mg tablet every 12 hours for 5 days and fluconazole 150 mg capsule once were added to her medications for the treatment of a urinary tract infection. She reported back to the hospital a day after discharge with complaints of restlessness, "seizures," tremor, abdominal discomfort, and weight gain. Both patients were diagnosed with akathisia using ICD-10 classification and the Barnes akathisia rating scale and managed with anticholinergics, benzodiazepines, and beta blockers. Other measures employed in managing the akathisia included reducing the dose of the antipsychotic and/or switching antipsychotics. Despite these management measures, the symptoms of akathisia persisted and only resolved after 4weeks. Upon the resolution of symptoms, Case A continued treatment on olanzapine 5 mg tablet daily and fluoxetine 20 mg capsule daily while Case B continued treatment on risperidone 2 mg tablet daily and fluoxetine 20 mg capsule daily. Using Naranjo's adverse drug reaction causality assessment scale, Medscape drug interaction checker, and literature review, a possible and probable case of drug-drug-induced akathisia was made for Case A and Case B. This report is to create more awareness about psychotropic-antimicrobial-induced akathisia. The information underpins the need for health professionals to consider adverse drug-drug interactions as the probable cause of extrapyramidal side effects experienced by patients on antipsychotics.
精神药物的锥体外系副作用通常在患者开始治疗的最初几周出现。那些已在这些药物治疗下病情稳定的患者,若出现类似静坐不能的痛苦主诉,可能是由其他因素引发的。本报告呈现了两例药物 - 药物相互作用所致静坐不能的病例。病例A是一名精神分裂症患者,在过去3年中每日服用2毫克利培酮片进行治疗。她生病后前往附近诊所就诊,医生为其开具了环丙沙星以及蒿甲醚/本芴醇片用于治疗感染和疟疾。7天后,她向精神科医生诉说了烦躁不安、震颤、心悸、失眠以及强迫观念复发等症状。病例B是一名被诊断为首发精神病性抑郁症的患者,住院10天。入院时她服用的药物有癸酸氟奋乃静25毫克长效注射剂一次、奥氮平每日10毫克片剂以及氟西汀每日20毫克胶囊。出院时,为治疗尿路感染,她的用药中增加了每12小时服用一次的500毫克环丙沙星片剂,共服用5天,以及一次服用的150毫克氟康唑胶囊。出院一天后,她回到医院,诉说了烦躁不安、“抽搐”、震颤、腹部不适以及体重增加等症状。两名患者均依据国际疾病分类第十版(ICD - 10)分类和巴恩斯静坐不能评定量表被诊断为静坐不能,并使用抗胆碱能药物、苯二氮䓬类药物和β受体阻滞剂进行治疗。管理静坐不能所采用的其他措施包括减少抗精神病药物的剂量和/或更换抗精神病药物。尽管采取了这些管理措施,静坐不能的症状依然持续,4周后才得以缓解。症状缓解后,病例A继续每日服用5毫克奥氮平片和每日20毫克氟西汀胶囊进行治疗,而病例B则继续每日服用2毫克利培酮片和每日20毫克氟西汀胶囊进行治疗。运用纳伦霍药物不良反应因果关系评估量表、Medscape药物相互作用检查器并进行文献回顾后,确定病例A和病例B为药物 - 药物相互作用所致静坐不能的可能及很可能病例。本报告旨在提高对精神药物 - 抗菌药物所致静坐不能的认识。这些信息强调了医疗专业人员需要将药物 - 药物不良相互作用视为服用抗精神病药物患者出现锥体外系副作用的可能原因。