Sackey Bryan K, Moore Troy A, Cupples Nicole L, Gutierrez Cynthia A
(Corresponding author) Mental Health Clinical Pharmacy Specialist, Pharmacy Department, South Texas Veterans Healthcare System, San Antonio, Texas; Adjoint Assistant Professor, Pharmacotherapy Division, College of Pharmacy, The University of Texas at Austin, Austin, Texas,
Mental Health Clinical Pharmacy Specialist, Pharmacy Department, South Texas Veterans Healthcare System, San Antonio, Texas; Director, American Society of Health-System Pharmacists-Accredited Postgraduate Year 2 Psychiatric Pharmacy Residency Program; Assistant Professor, Division of Community Recovery, Research and Training, Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Ment Health Clin. 2018 Nov 1;8(6):303-308. doi: 10.9740/mhc.2018.11.303. eCollection 2018 Nov.
Myocarditis is a potentially fatal cardiac disease marked by inflammation of the heart muscle. With a noted black-box warning, rates of clozapine-induced myocarditis are reportedly as high as 3%. Since the first case of clozapine-induced myocarditis was documented in 1994, more than 250 cases have been described in literature with an approximate 33% case-fatality rate. We report 2 cases of patients with primary psychotic disorders treated with clozapine, who developed signs and symptoms of myocarditis. The first was a 35-year-old white male patient with a primary diagnosis of schizoaffective disorder (bipolar type) who was initiated on clozapine after nonresponse to several therapies. On day 26, the patient was admitted to the emergency department for chest pain presenting with eosinophilia and notable elevations in several biomarkers, including troponin and C-reactive protein. The second patient was a 45-year-old black male who was initiated on clozapine for treatment-resistant schizophrenia. On day 13, the patient reported cardiac-related concerns (tachycardia) and flu-like symptoms resulting in hospitalization. Similarly, this patient demonstrated elevated biomarkers (troponin and creatine kinase). Both patients experienced resolution of symptoms after discontinuation of clozapine. Clozapine was not rechallenged for either patient. Review of literature further elucidates the relationship between clozapine and myocarditis, including potential risk factors, pathophysiology, and symptom presentation. Due to the potentially fatal nature of this condition, clinical vigilance and awareness is warranted upon initiation of clozapine through monitoring of symptoms along with cardiac and inflammatory biomarkers as indicated.
心肌炎是一种潜在致命的心脏疾病,其特征是心肌发炎。由于有显著的黑框警告,据报道氯氮平诱发心肌炎的发生率高达3%。自1994年记录首例氯氮平诱发心肌炎病例以来,文献中已描述了250多例病例,病死率约为33%。我们报告2例接受氯氮平治疗的原发性精神障碍患者出现心肌炎的体征和症状。第一例是一名35岁的白人男性患者,初步诊断为分裂情感障碍(双相型),在多种治疗无效后开始使用氯氮平。在第26天,该患者因胸痛被送往急诊科,伴有嗜酸性粒细胞增多以及包括肌钙蛋白和C反应蛋白在内的多种生物标志物显著升高。第二例患者是一名45岁的黑人男性,因难治性精神分裂症开始使用氯氮平治疗。在第13天,该患者报告了与心脏相关的问题(心动过速)和类似流感的症状,随后住院治疗。同样,该患者也出现了生物标志物(肌钙蛋白和肌酸激酶)升高。两名患者在停用氯氮平后症状均得到缓解。两名患者均未再次使用氯氮平。文献回顾进一步阐明了氯氮平与心肌炎之间的关系,包括潜在风险因素、病理生理学和症状表现。由于这种疾病具有潜在致命性,在开始使用氯氮平时,应通过监测症状以及如所示的心脏和炎症生物标志物进行临床警惕和关注。