Pharmacy Department, Sarasota Memorial Hospital, Sarasota, FL, USA.
Pharmacy Department, Tampa General Hospital, Tampa, FL, USA.
J Pharm Pract. 2023 Oct;36(5):1056-1060. doi: 10.1177/08971900221087955. Epub 2022 Mar 29.
Lacosamide and levetiracetam are antiseizure medications (ASMs) commonly utilized in the treatment and prevention of seizures. Historically, these agents have been administered as slow IV infusions after further dilution. Recent literature suggests that rapid administration via undiluted IV push may be safe and may increase efficiency of administration. This study aimed to evaluate the safety and tolerability of undiluted IV push lacosamide and levetiracetam over 5 min. This study was conducted as a single-centered, retrospective, observational cohort that analyzed the rapid administration of undiluted lacosamide and levetiracetam. Adult patients admitted from September 1st, 2019, to May 31st, 2020, receiving at least one administration of IV push lacosamide at any dose or levetiracetam at doses ≤ 1500 mg were evaluated. The primary safety outcomes were the incidence of hypotension and bradycardia. A total of 86 subjects were evaluated; 36 patients were administered lacosamide, and 50 patients were administered levetiracetam. Hypotension or bradycardia occurred in 6 patients in the lacosamide group (16.6%) and 6 patients in the levetiracetam group (12.0%). There were no reported infusion site reactions. Among the subjects who received lacosamide and had a 12-lead electrocardiogram (EKG), there were no reported incidences of a prolonged PR interval. In this safety-analysis cohort, undiluted lacosamide and levetiracetam were not associated with significant adverse events when administered via IV push over 5 min. This seems to be a safe alternative method of administration to intermittent infusion. A larger, prospective cohort is needed to confirm these findings.
拉考沙胺和左乙拉西坦是抗癫痫药物(ASMs),常用于治疗和预防癫痫发作。历史上,这些药物在进一步稀释后作为缓慢的静脉输注给药。最近的文献表明,未经稀释的静脉推注给药可能是安全的,并可能提高给药效率。本研究旨在评估未经稀释的静脉推注拉考沙胺和左乙拉西坦在 5 分钟内给药的安全性和耐受性。这项研究是一项单中心、回顾性、观察性队列研究,分析了未经稀释的拉考沙胺和左乙拉西坦的快速给药。该研究纳入了 2019 年 9 月 1 日至 2020 年 5 月 31 日期间至少接受过一次任何剂量静脉推注拉考沙胺或 1500mg 以下剂量静脉推注左乙拉西坦给药的成年患者。主要安全性结局为低血压和心动过缓的发生率。共评估了 86 例患者;36 例患者给予拉考沙胺,50 例患者给予左乙拉西坦。拉考沙胺组有 6 例(16.6%)和左乙拉西坦组有 6 例(12.0%)患者发生低血压或心动过缓。无报道的输注部位反应。在接受拉考沙胺且行 12 导联心电图(EKG)检查的患者中,无报道 PR 间期延长的发生率。在这项安全性分析队列中,未经稀释的拉考沙胺和左乙拉西坦经静脉推注 5 分钟以上给药与严重不良事件无关。这似乎是一种替代间歇性输注的安全给药方法。需要更大的前瞻性队列来证实这些发现。