Iwasaki Toshiyuki, Kobayashi Toshihiro, Miyamoto Yusaku, Imaizumi Taichi, Kaku Shotaro, Udagawa Noriko, Yamamoto Hitoshi, Shimizu Naoki
Department of Pediatrics, Kawasaki Municipal Tama Hospital, Kawasaki 214-8522, Kanagawa, Japan.
Department of Pediatrics, St. Marianna University School of Medicine, Kawasaki 216-8511, Kanagawa, Japan.
J Clin Med. 2024 Nov 19;13(22):6958. doi: 10.3390/jcm13226958.
: The aim of this paper is to analyze clinical targets for lacosamide (LCM) blood levels in patients with focal epilepsy. Referring to the LCM optimal range will encourage us to think about the importance and usefulness of measuring its blood levels. : A total of 101 (45 female, 56 male) patients were treated with LCM. Blood sampling was performed 1 month after the start of oral medication (the levels reached a steady state) if the LCM treatment had been continued, and then 6 and 12 months after. The efficacy of LCM was evaluated by the reduction in the epileptic seizure rate (RR) at the time of blood sampling. The patients were classified as effective cases (seizure reduction rate ≥ 50%) and ineffective cases (<50%). The actual level, the calculated peak/trough levels, and the levels for each type of seizure were investigated. A statistical analysis was performed using Spearman's rank correlation coefficient and the Wilcoxon signed-rank test. : A positive correlation was seen between blood levels and dosage (r = 0.446). However, the blood levels and RR showed no correlation. The blood levels were higher in effective cases than in ineffective cases at all time points (measurement < 0.001, peak = 0.013, trough = 0.001). Because the range was set so that the effective and ineffective groups did not overlap, the optimal range of LCM was found to be 8.0-10.5 µg/mL. : Measuring and calculating blood levels of LCM and adjusting the dosage to reach the optimal range are recommended. Moreover, the optimal range for LCM was determined as a therapeutic target.
本文旨在分析局灶性癫痫患者拉科酰胺(LCM)血药浓度的临床目标。参考LCM的最佳范围将促使我们思考测量其血药浓度的重要性和实用性。
共有101例患者(45例女性,56例男性)接受了LCM治疗。如果LCM治疗持续进行,在口服药物开始1个月后(血药浓度达到稳态)进行血样采集,然后在6个月和12个月后再次采集。通过血样采集时癫痫发作率(RR)的降低来评估LCM的疗效。患者被分为有效病例(发作减少率≥50%)和无效病例(<50%)。研究了实际血药浓度、计算得出的峰谷血药浓度以及每种癫痫发作类型的血药浓度。使用Spearman等级相关系数和Wilcoxon符号秩检验进行统计分析。
血药浓度与剂量之间呈正相关(r = 0.446)。然而,血药浓度与RR之间无相关性。在所有时间点,有效病例的血药浓度均高于无效病例(测量值P < 0.001,峰值P = 0.013,谷值P = 0.001)。由于设定的范围使得有效组和无效组不重叠,发现LCM的最佳范围为8.0 - 10.5 µg/mL。
建议测量和计算LCM的血药浓度并调整剂量以达到最佳范围。此外,确定了LCM的最佳范围作为治疗目标。