Li Kai, Vo Kathy, Lee Byron K, Addo Newton, Coralic Zlatan
Department of Emergency Medicine, University of California San Francisco, San Francisco, CA.
California Poison Control System, University of California San Francisco School of Medicine, San Francisco, CA.
Am J Health Syst Pharm. 2018 Mar 1;75(5):276-282. doi: 10.2146/ajhp161070. Epub 2018 Jan 9.
Results of a study to determine whether i.v. administration of a single dose of 4 mg of ondansetron was associated with QT interval prolongation in emergency department (ED) patients are reported.
In a prospective observational study conducted at an urban academic medical center ED, a convenience sample of adult ED patients treated with ondansetron 4 mg i.v. were enrolled. A 12-lead electrocardiogram (ECG) was obtained immediately before and 5 minutes after ondansetron administration. Measurements of heart rate-corrected QT interval (QTc measurements) provided by ECG machines were evaluated. An electrophysiologist analyzed all ECGs for adverse electrical events and verified the accuracy of QTc values. The primary objective was to measure the QTc change from baseline after ondansetron administration. The secondary objective was to describe adverse electrical cardiac events. Interactions between ondansetron and patients' home medications or ED-provided medications were analyzed.
Among patients included in the data analysis ( = 20), ondansetron administration was associated with a mean QTc increase of 16.2 msec (95% confidence interval, 4.2-28.2 msec; = 0.01) and a median increase of 12 msec (interquartile range, 5.5-18.0 msec; < 0.01). One patient had a significant cardiac event (pulseless electrical activity) that was likely unrelated to ondansetron use. The home medications of 9 patients (42.9%) were deemed to pose a risk of torsades de pointes, and 17 major QT-prolonging drug-drug interactions were identified.
Significant QTc prolongation occurred in ED patients receiving a single 4-mg i.v. dose of ondansetron. None of the patients had an ondansetron-related cardiac adverse event.
报告一项关于确定静脉注射单剂量4毫克昂丹司琼是否与急诊科(ED)患者QT间期延长相关的研究结果。
在一家城市学术医疗中心急诊科进行的一项前瞻性观察性研究中,纳入了接受静脉注射4毫克昂丹司琼治疗的成年ED患者的便利样本。在昂丹司琼给药前即刻和给药后5分钟获取12导联心电图(ECG)。对心电图机提供的心率校正QT间期(QTc测量值)进行评估。一名电生理学家分析所有心电图以查找不良电事件,并核实QTc值的准确性。主要目的是测量昂丹司琼给药后QTc相对于基线的变化。次要目的是描述心脏不良电事件。分析了昂丹司琼与患者家庭用药或急诊科提供的药物之间的相互作用。
在纳入数据分析的患者中(n = 20),昂丹司琼给药后平均QTc增加16.2毫秒(95%置信区间,4.2 - 28.2毫秒;P = 0.01),中位数增加12毫秒(四分位间距,5.5 - 18.0毫秒;P < 0.01)。一名患者发生了严重心脏事件(无脉性电活动),可能与使用昂丹司琼无关。9名患者(42.9%)的家庭用药被认为有引发尖端扭转型室速的风险,并且识别出17种主要的延长QT的药物 - 药物相互作用。
接受单次静脉注射4毫克昂丹司琼的ED患者出现了显著的QTc延长。没有患者发生与昂丹司琼相关的心脏不良事件。