Teaford Hilary R, Abu Saleh Omar M, Villarraga Hector R, Enzler Mark J, Rivera Christina G
Department of Pharmacy, Mayo Clinic, Rochester, MN.
Division of Infectious Diseases, Mayo Clinic, Rochester, MN.
Mayo Clin Proc Innov Qual Outcomes. 2020 Aug 15;4(5):588-594. doi: 10.1016/j.mayocpiqo.2020.05.006. eCollection 2020 Oct.
Itraconazole is well known for carrying a black-box warning for new or worsening congestive heart failure. Single cases of other cardiac- and fluid-related disturbances have been reported periodically since its issuance. We describe a large cohort of patients on itraconazole experiencing a breadth of cardiac- and fluid-related toxicities, ranging from new-onset hypertension to cardiac arrest. A retrospective, single-center, large case series at a large tertiary medical center was conducted. Patients with itraconazole and cardiac toxicity-including hypertension, cardiomyopathy, reduced ejection fraction, and edema-in medical record between January 1, 1999, and May 21, 2019, were identified and assigned a Naranjo score; 31 patients were included with a Naranjo score of 5 or higher. There were slightly more male subjects than female subjects, average age was 66, and all subjects were Caucasian. Median time until presentation of adverse effects was 4 weeks (range: 0.3 to 104 weeks). Most common symptom was edema (74% of patients), followed by heart failure without and with preserved ejection fraction (19.4% and 22.6% of patients, respectively). Worsening or new hypertension was also common (25.8% of patients). Rarer were pulmonary edema, pericardial effusion, and cardiac arrest that occurred in 1 patient. In most cases, clinicians stopped itraconazole (74%) or decreased itraconazole dose (19%), resulting in improvement or resolution of symptoms. In 4 cases, the adverse effect did not resolve. Itraconazole can cause a range of possible serious cardiac and fluid-associated adverse events. Dose decrease or cessation usually resulted in symptomatic improvement or reversal.
伊曲康唑因对新发或恶化的充血性心力衰竭有黑框警告而广为人知。自该警告发布以来,不时有其他与心脏和液体相关的紊乱的单例报告。我们描述了一大群服用伊曲康唑的患者出现了一系列与心脏和液体相关的毒性反应,从新发高血压到心脏骤停。在一家大型三级医疗中心进行了一项回顾性、单中心、大病例系列研究。确定了1999年1月1日至2019年5月21日期间病历中有伊曲康唑和心脏毒性(包括高血压、心肌病、射血分数降低和水肿)的患者,并给予纳兰霍评分;纳入了31例纳兰霍评分为5分或更高的患者。男性受试者略多于女性受试者,平均年龄为66岁,所有受试者均为白种人。出现不良反应的中位时间为4周(范围:0.3至104周)。最常见的症状是水肿(74%的患者),其次是射血分数保留和未保留的心力衰竭(分别为19.4%和22.6%的患者)。新发或恶化的高血压也很常见(25.8%的患者)。肺水肿、心包积液和心脏骤停较少见,各有1例患者发生。在大多数情况下,临床医生停用了伊曲康唑(74%)或降低了伊曲康唑剂量(19%),症状得到改善或缓解。有4例不良反应未缓解。伊曲康唑可导致一系列可能的严重心脏和液体相关不良事件。剂量降低或停药通常会导致症状改善或逆转。