{"title":"Treatment of Catatonia with Benzodiazepine, Electroconvulsive Therapy and Memantine in an Adolescent: a Case Report.","authors":"Camille Maheu-Savard, Anne-Sophie Huet","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Catatonia is a severe psychomotor syndrome that can be life-threatening if not promptly diagnosed and treated. While benzodiazepines and electroconvulsive therapy (ECT) are established treatments for catatonia in adults, there is limited literature on their efficacy and safety in adolescents. Additionally, the use of N-methyl-D-aspartate (NMDA) antagonists, such as memantine, has been explored as a potential treatment option; however, there is a lack of extensive research in the pediatric population. We report the case of a 16-year-old boy who presented with refractory catatonia. The patient initially appeared to respond to lorazepam but experienced adverse effects, necessitating a switch to clonazepam. Despite some improvement, his condition deteriorated, leading to the initiation of ECT, which was associated with significant improvements. However, stagnation in clinical progress prompted the introduction of memantine, an NMDA antagonist. Memantine was well tolerated and appeared to contribute to further symptom resolution. The patient achieved full remission of catatonia in approximately 2 months and sustained well-being 19 weeks post-discharge with a treatment regimen of olanzapine, memantine and clonazepam. This case highlights the potential efficacy of combining benzodiazepines, ECT, and NMDA antagonists in treating refractory catatonia in adolescents. Our findings support considering NMDA antagonists in treatment protocols, particularly when conventional therapies are ineffective or inaccessible. Further research is needed to validate these results and establish comprehensive guidelines for managing pediatric catatonia.</p>","PeriodicalId":47053,"journal":{"name":"Journal of the Canadian Academy of Child and Adolescent Psychiatry","volume":"34 2","pages":"45-52"},"PeriodicalIF":2.3000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12434900/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Canadian Academy of Child and Adolescent Psychiatry","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0
Abstract
Catatonia is a severe psychomotor syndrome that can be life-threatening if not promptly diagnosed and treated. While benzodiazepines and electroconvulsive therapy (ECT) are established treatments for catatonia in adults, there is limited literature on their efficacy and safety in adolescents. Additionally, the use of N-methyl-D-aspartate (NMDA) antagonists, such as memantine, has been explored as a potential treatment option; however, there is a lack of extensive research in the pediatric population. We report the case of a 16-year-old boy who presented with refractory catatonia. The patient initially appeared to respond to lorazepam but experienced adverse effects, necessitating a switch to clonazepam. Despite some improvement, his condition deteriorated, leading to the initiation of ECT, which was associated with significant improvements. However, stagnation in clinical progress prompted the introduction of memantine, an NMDA antagonist. Memantine was well tolerated and appeared to contribute to further symptom resolution. The patient achieved full remission of catatonia in approximately 2 months and sustained well-being 19 weeks post-discharge with a treatment regimen of olanzapine, memantine and clonazepam. This case highlights the potential efficacy of combining benzodiazepines, ECT, and NMDA antagonists in treating refractory catatonia in adolescents. Our findings support considering NMDA antagonists in treatment protocols, particularly when conventional therapies are ineffective or inaccessible. Further research is needed to validate these results and establish comprehensive guidelines for managing pediatric catatonia.
紧张症是一种严重的精神运动综合症,如果不及时诊断和治疗,可能会危及生命。虽然苯二氮卓类药物和电痉挛疗法(ECT)是成人紧张症的既定治疗方法,但关于其在青少年中的有效性和安全性的文献有限。此外,n -甲基- d -天冬氨酸(NMDA)拮抗剂,如美金刚,已被探索作为一种潜在的治疗选择;然而,在儿科人群中缺乏广泛的研究。我们报告的情况下,一个16岁的男孩谁提出难治性紧张症。患者最初对劳拉西泮有反应,但出现了不良反应,需要改用氯硝西泮。尽管有一些改善,但他的病情恶化,导致开始ECT,这与显著改善有关。然而,临床进展停滞促使引进美金刚,一种NMDA拮抗剂。美金刚耐受性良好,似乎有助于进一步缓解症状。患者在大约2个月内完全缓解了紧张症,出院后19周持续健康,治疗方案为奥氮平、美金刚和氯硝西泮。本病例强调了苯二氮卓类药物、电痉挛疗法和NMDA拮抗剂联合治疗青少年难治性紧张症的潜在疗效。我们的研究结果支持在治疗方案中考虑NMDA拮抗剂,特别是当常规治疗无效或难以获得时。需要进一步的研究来验证这些结果,并建立管理儿童紧张症的综合指南。