Department of Neurosurgery, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, 3-18-22 Honkomagome, Bunkyo-ku, Tokyo 113-0021, Japan.
Department of Neurosurgery, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, 3-18-22 Honkomagome, Bunkyo-ku, Tokyo 113-0021, Japan.
J Clin Neurosci. 2021 Jul;89:279-282. doi: 10.1016/j.jocn.2021.05.028. Epub 2021 May 21.
Awake craniotomy is an established procedure for resecting brain tumors in eloquent lesions, and intraoperative seizure is one of the most important complications. Phenytoin is normally used to control intraoperative seizures. Recently, phenytoin was replaced with levetiracetam at our institution because the latter has fewer side effects. While the phenytoin dose is calibrated in accordance with the serum concentration, there is currently no consensus on a method of monitoring the serum concentration of levetiracetam or the effective concentration range needed to control intraoperative seizures during awake craniotomy. The present study therefore aimed to determine whether monitoring the serum levetiracetam concentration is useful for controlling intraoperative seizures during awake craniotomy. The intraoperative serum concentration of levetiracetam during awake craniotomy was measured in 34 patients and compared with that of phenytoin in 33 patients undergoing the same procedure. The levetiracetam concentration inversely correlated with body surface area (BSA) and estimated glomerular filtration rate (eGFR). Levetiracetam was superior to phenytoin in terms of the correlation between the serum concentration and the dose adjusted for BSA and eGFR (correlation coefficient, 0.49 vs 0.21). Furthermore, the serum levetiracetam concentration in patients with intraoperative seizures was below the 95% confidence interval (CI) of the regression line whereas the serum phenytoin concentration of two patients with seizures was within the 95% CI, indicating that evaluating the serum levetiracetam concentration against the BSA and eGFR-adjusted dosage may be useful in preventing intraoperative seizures during awake craniotomy by allowing prediction of the seizure risk and enabling more accurate dosage calibration.
清醒开颅术是切除语言区病变脑肿瘤的成熟手术,术中癫痫发作是最主要的并发症之一。苯妥英通常用于控制术中癫痫发作。最近,由于后者副作用更少,我们机构将苯妥英换成了左乙拉西坦。虽然苯妥英的剂量是根据血清浓度来校准的,但目前还没有关于监测左乙拉西坦血清浓度或确定控制清醒开颅术中癫痫发作所需的有效浓度范围的共识。因此,本研究旨在确定监测血清左乙拉西坦浓度是否有助于控制清醒开颅术中的癫痫发作。在 34 例行清醒开颅术的患者中测量了术中血清左乙拉西坦浓度,并与 33 例行相同手术的患者的苯妥英浓度进行了比较。左乙拉西坦浓度与体表面积(BSA)和估算肾小球滤过率(eGFR)呈反比。左乙拉西坦在血清浓度与 BSA 和 eGFR 调整剂量之间的相关性方面优于苯妥英(相关系数,0.49 比 0.21)。此外,在发生术中癫痫发作的患者中,血清左乙拉西坦浓度低于回归线的 95%置信区间(CI),而两名癫痫发作患者的血清苯妥英浓度在 95%CI 内,这表明根据 BSA 和 eGFR 调整剂量评估血清左乙拉西坦浓度可能有助于通过预测癫痫发作风险并实现更准确的剂量校准来预防清醒开颅术中的癫痫发作。