{"title":"Treatment with lacosamide or levetiracetam in patients with renal replacement therapy. What is really known?","authors":"M. Cuhls, J. Bösel, J. Rösche","doi":"10.21307/jepil-2020-004","DOIUrl":null,"url":null,"abstract":"SUMMARY Background Lacosamide and levetiracetam are commonly used in critically ill patients, who need an antiepileptic treatment in addition to several other medications. Since both drugs are eliminated via the kidneys, dosage has to be adapted to renal function especially in renal replacement therapy (RRT). In 2016 recommendations of dosage in this condition were based on three case reports only. Aim To elucidate the current data basis for recommendations on the dosage of Lacosamide and levetiracetam in patients on renal replacement therapy. Material and methods A search in MEDLINE and Web of Science with several core terms was performed. Papers reporting on doses and concentrations of lacosamide or levetiracetam in patients with renal replacement therapy were analysed. Results and discussion One phase-I study and three case reports concerning lacosamide and one case series with 22 patients and nine case reports concerning levetiracetam were identified. Whether 200 mg Lacosamide twice/day results in trough concentrations at least in the lower therapeutic range depends on the replacement rate used in continuous venovenous haemofiltration. Peritoneal dialysis seems to remove only a small portion of levetiracetam. Levetiracetam (1000 mg) every 12 hours may generate a trough concentration in the lower therapeutic range in continuous venovenous haemofiltration. Conclusion Due to the sparse and low quality data, current recommendations on dosing lacosamide or levetiracetam in patients undergoing renal replacement therapy have to be considered with caution and therapeutic drug monitoring may be useful in guiding patient management.","PeriodicalId":15683,"journal":{"name":"Journal of Epileptology","volume":"22 1","pages":"55 - 58"},"PeriodicalIF":0.0000,"publicationDate":"2020-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Epileptology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21307/jepil-2020-004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
SUMMARY Background Lacosamide and levetiracetam are commonly used in critically ill patients, who need an antiepileptic treatment in addition to several other medications. Since both drugs are eliminated via the kidneys, dosage has to be adapted to renal function especially in renal replacement therapy (RRT). In 2016 recommendations of dosage in this condition were based on three case reports only. Aim To elucidate the current data basis for recommendations on the dosage of Lacosamide and levetiracetam in patients on renal replacement therapy. Material and methods A search in MEDLINE and Web of Science with several core terms was performed. Papers reporting on doses and concentrations of lacosamide or levetiracetam in patients with renal replacement therapy were analysed. Results and discussion One phase-I study and three case reports concerning lacosamide and one case series with 22 patients and nine case reports concerning levetiracetam were identified. Whether 200 mg Lacosamide twice/day results in trough concentrations at least in the lower therapeutic range depends on the replacement rate used in continuous venovenous haemofiltration. Peritoneal dialysis seems to remove only a small portion of levetiracetam. Levetiracetam (1000 mg) every 12 hours may generate a trough concentration in the lower therapeutic range in continuous venovenous haemofiltration. Conclusion Due to the sparse and low quality data, current recommendations on dosing lacosamide or levetiracetam in patients undergoing renal replacement therapy have to be considered with caution and therapeutic drug monitoring may be useful in guiding patient management.
背景:拉科沙胺和左乙拉西坦常用于危重患者,这些患者需要除几种其他药物外进行抗癫痫治疗。由于这两种药物都是通过肾脏消除的,所以剂量必须适应肾功能,特别是在肾脏替代疗法(RRT)中。2016年,这种情况下的剂量建议仅基于三例病例报告。目的为肾替代治疗患者推荐拉科沙胺和左乙拉西坦的剂量提供现有的数据依据。材料与方法在MEDLINE和Web of Science中检索几个核心术语。对肾替代治疗患者使用拉科沙胺或左乙拉西坦的剂量和浓度的文献进行了分析。结果与讨论纳入1项关于拉科沙胺的i期研究和3例报告,以及1个涉及22例患者和9例关于左乙拉西坦的病例系列。200 mg拉科沙胺2次/天是否至少在较低治疗范围内产生谷浓度取决于连续静脉-静脉血液滤过中使用的替代率。腹膜透析似乎只能去除一小部分左乙拉西坦。左乙拉西坦(1000mg)每12小时可在连续静脉-静脉血液滤过中产生较低治疗范围内的谷浓度。结论由于数据的稀疏和低质量,目前关于肾替代治疗患者使用拉科沙胺或左乙拉西坦的建议必须谨慎考虑,治疗药物监测可能有助于指导患者的管理。