Department of Pharmacy, University of Louisville Hospital, 530 South Jackson Street, Louisville, KY 40202, United States of America.
Department of Pharmacy, University of Louisville Hospital, 530 South Jackson Street, Louisville, KY 40202, United States of America.
Am J Emerg Med. 2024 Nov;85:148-152. doi: 10.1016/j.ajem.2024.09.007. Epub 2024 Sep 2.
Status epilepticus (SE) is a neurologic emergency defined as continued seizure activity greater than five minutes or recurrent seizure activity without return to baseline. Benzodiazepine-refractory SE is continuous seizure activity despite treatment with a benzodiazepine. Treatment of benzodiazepine-refractory SE includes levetiracetam with loading doses ranging from 20 mg/kg to 60 mg/kg up to a maximum dose of 4500 mg. While levetiracetam has minimal adverse effects, there is currently a lack of studies directly comparing the safety and efficacy of various loading doses of levetiracetam.
The objective of this study was to evaluate the safety and efficacy of three loading doses of levetiracetam in the setting of benzodiazepine-refractory SE.
This was a single center, retrospective cohort study of adult patients with benzodiazepine-refractory SE who were treated with levetiracetam from April 1, 2016, to August 31, 2023. Patients with documented hypersensitivity to levetiracetam, those who were pregnant or incarcerated and patients who received an alternative antiepileptic drug (AED) prior to levetiracetam were excluded. Patients with other identifiable causes of SE including hyperglycemia, hypoglycemia, hyponatremia or who were post cardiac arrest were also excluded. Patients were divided into three arms based on loading dose of levetiracetam administered (≤20 mg/kg [LEVlow], 21--39 mg/kg [LEVmed] or ≥40 mg/kg [LEVhigh]). The primary endpoint was the rate of seizure termination, defined as the lack of need for an additional AED within 60 min following levetiracetam administration. Secondary outcomes included the rate of intubation, and recurrent seizure activity 60 min to 24 h post seizure termination as defined by positive EEG results or need for an additional AED. Subgroup analyses were performed to assess the influence of adequate loading doses of benzodiazepines, and outpatient levetiracetam use.
Overall, 740 patients were screened for inclusion, with 218 patients being included in the primary analysis. Patients were divided into three groups with an average levetiracetam loading dose of 14.5 mg/kg in the LEVlow group, 28.8 mg/kg in the LEVmed group, and 48.8 mg/kg in the LEVhigh group. There was no difference in rates of seizure termination at 60 min (92.9% LEVlow vs 89.3% LEVmed vs 84.7% LEVhigh; p = 0.377). Additionally, no difference was found in rates of recurrent seizure activity between 60 min and 24 h post levetiracetam loading dose (32.1% LEVlow vs 32.0% LEVmed vs 28.8% LEVhigh; p = 0.899). However, the LEVhigh group did have a higher rate of intubation (45.8%) compared to the LEVmed (28.2%) and LEVlow (26.8%) group (p = 0.040).
The loading of levetiracetam did not result in a statistically significant difference in rate of seizure termination at 60 min nor did it appear to impact the rate of recurrent seizures at 24 h. However, we did find higher rates of intubation in patients who received levetiracetam >40 mg/kg. Further research is warranted to determine the optimal loading dose of levetiracetam in benzodiazepine-refractory SE.
癫痫持续状态(SE)是一种定义为持续癫痫发作超过 5 分钟或反复发作而未恢复基线的神经急症。苯二氮䓬类药物难治性 SE 是指在使用苯二氮䓬类药物治疗后仍持续发作的癫痫。苯二氮䓬类药物难治性 SE 的治疗包括给予负荷剂量的左乙拉西坦,剂量范围为 20mg/kg 至 60mg/kg,最大剂量为 4500mg。虽然左乙拉西坦的不良反应极小,但目前缺乏直接比较不同负荷剂量左乙拉西坦的安全性和疗效的研究。
本研究旨在评估苯二氮䓬类药物难治性 SE 患者使用三种不同负荷剂量左乙拉西坦的安全性和疗效。
这是一项单中心、回顾性队列研究,纳入了 2016 年 4 月 1 日至 2023 年 8 月 31 日期间接受左乙拉西坦治疗的成人苯二氮䓬类药物难治性 SE 患者。排除对左乙拉西坦过敏、孕妇或被监禁以及在使用左乙拉西坦之前使用其他抗癫痫药物(AED)的患者。其他明确 SE 病因(包括高血糖、低血糖、低钠血症或心搏骤停后)的患者也被排除在外。患者根据给予的左乙拉西坦负荷剂量分为三组(≤20mg/kg [LEVlow]、21--39mg/kg [LEVmed] 或≥40mg/kg [LEVhigh])。主要终点是癫痫终止率,定义为在给予左乙拉西坦后 60min 内无需额外使用 AED。次要结局包括插管率和癫痫终止后 60min 至 24h 内再次发作的发生率,定义为脑电图结果阳性或需要额外使用 AED。进行了亚组分析,以评估充分的苯二氮䓬类药物负荷剂量和门诊使用左乙拉西坦的影响。
总体而言,有 740 名患者被筛选纳入研究,其中 218 名患者被纳入主要分析。患者分为三组,LEVlow 组左乙拉西坦的平均负荷剂量为 14.5mg/kg,LEVmed 组为 28.8mg/kg,LEVhigh 组为 48.8mg/kg。在 60min 时,癫痫终止率无差异(92.9% LEVlow 与 89.3% LEVmed 与 84.7% LEVhigh;p=0.377)。此外,在给予左乙拉西坦负荷剂量后 60min 至 24h 之间,再次发作的发生率也无差异(32.1% LEVlow 与 32.0% LEVmed 与 28.8% LEVhigh;p=0.899)。然而,LEVhigh 组的插管率(45.8%)明显高于 LEVmed(28.2%)和 LEVlow(26.8%)组(p=0.040)。
左乙拉西坦的负荷剂量在 60min 时的癫痫终止率上没有统计学上的显著差异,也似乎没有影响 24h 时的再次发作率。然而,我们确实发现接受负荷剂量大于 40mg/kg 左乙拉西坦的患者插管率更高。需要进一步研究以确定苯二氮䓬类药物难治性 SE 中左乙拉西坦的最佳负荷剂量。