Pharmacy Resident, Department of Pharmacy, Mayo Clinic, Rochester, MN, USA.
Pharmacist, Department of Pharmacy, Mayo Clinic, Rochester, MN, USA.
J Cardiovasc Pharmacol Ther. 2024 Jan-Dec;29:10742484231224536. doi: 10.1177/10742484231224536.
Dofetilide and sotalol are potassium channel antagonists that require inpatient QTc monitoring during initiation, due to increased risk of fatal arrhythmias. Elderly patients are especially subject to an increased risk of fatal arrhythmias due to polypharmacy, comorbidities, and physiologic cardiac changes with aging. This study will describe the tolerability and risk factors associated with the initiation of sotalol or dofetilide in patients ≥80 years of age. This is a multicenter, retrospective, descriptive study of patients ≥80 years old who were initiated on either dofetilide or sotalol between May 8, 2018 and July 31, 2021 at institutions within the Mayo Clinic Health System. The percentage of patients who received nonpackage insert recommended doses was identified. Incidence of and reasons for dose reductions or discontinuations due to safety-related events or clinical concerns during the initial loading period were collected. The final analysis included 104 patients. The majority of patients (75%) received nonstandard initial doses of dofetilide or sotalol based on baseline estimated creatinine clearance or QTc. Overall, 39% ( = 41) of patients experienced a dose reduction or discontinuation due to a safety-related event or concern. Patients who received nonstandard initial doses of dofetilide or sotalol had 4.7 times greater odds of experiencing a safety-related event requiring dose reduction or discontinuation. Following package insert dosing in elderly patients increases safety and tolerability relative to more aggressive dosing of dofetilide or sotalol.
多非利特和索他洛尔是钾通道拮抗剂,由于致命性心律失常风险增加,在开始治疗时需要住院进行 QTc 监测。由于多种药物治疗、合并症以及随着年龄增长的生理性心脏变化,老年患者尤其容易发生致命性心律失常。本研究将描述 80 岁及以上患者开始使用索他洛尔或多非利特的耐受性和相关风险因素。这是一项多中心、回顾性、描述性研究,纳入了 2018 年 5 月 8 日至 2021 年 7 月 31 日期间在梅奥诊所医疗系统内的机构中开始使用多非利特或索他洛尔的 80 岁及以上患者。确定接受非说明书推荐剂量的患者比例。收集初始负荷期因安全性相关事件或临床关注而减少剂量或停药的发生率及原因。最终分析纳入 104 例患者。大多数患者(75%)根据基线估计肌酐清除率或 QTc 接受了非标准初始剂量的多非利特或索他洛尔。总体而言,39%( = 41)的患者因安全性相关事件或关注而减少剂量或停药。接受非标准初始剂量的多非利特或索他洛尔的患者发生需要减少剂量或停药的安全性相关事件的可能性是接受标准初始剂量的患者的 4.7 倍。与更积极的多非利特或索他洛尔剂量相比,在老年患者中遵循说明书剂量可提高安全性和耐受性。