Stepanova Daria, Beran Roy G
Strategic Health Evaluators, Sydney, New South Wales, Australia.
Strategic Health Evaluators, Sydney, New South Wales, Australia; Griffith University, Gold Coast and Brisbane, Queensland, Australia; University of New South Wales, Sydney, New South Wales, Australia.
Seizure. 2014 May;23(5):371-6. doi: 10.1016/j.seizure.2014.02.003. Epub 2014 Feb 17.
Levetiracetam (LEV) therapeutic range (20-40mg/L) and potential drug interactions were assessed in people with epilepsy (PWE).
Fifty-two PWE had LEV and concomitant medications [carbamazepine (CBZ); valproate (VPA); lamotrigine (LTG)] blood levels measured and compared to seizure activity. Lacosamide (LCM) levels were unavailable. Adopted therapeutic ranges were: 20-40mg/L - LEV; 25-50μmol/L - total CBZ; 6-13μmol/L - free CBZ; 300-750μmol/L - total VPA; 30-75μmol/L - free VPA; and 40-60μmol/L - LTG. Seizure-freedom was assessed and patients followed for almost two years.
23 of 52 PWE (44%) used LEV monotherapy and 16/23 (70%) had 'therapeutic' LEV with 13/16 (81%) seizure-free. 29 of 52 (56%) used polytherapy and 16/29 (55%) had 'therapeutic' LEV with 7/16 (44%) seizure-free. 11 of 29 (38%) used CBZ: 4/11 (36%) had therapeutic mean LEV levels and 7/11 (64%) were seizure-free. Fourteen (48%) used VPA: 9/14 (64%) had therapeutic mean LEV levels and 8/14 (57%) were seizure-free. 13 of 29 (45%) used LTG: 8/13 (62%) had therapeutic mean LEV levels and 5/13 (38%) were seizure-free. LEV did not alter CBZ, but CBZ affected LEV. LEV elevated VPA free levels but not VPA total levels. Dosage/concentration was lowered with polytherapy.
LEV range (20-40mg/L) assisted epilepsy management and anti-epileptic medication interactions were suggested with polytherapy thus possibly explaining the impaired efficacy of LEV with polytherapy.
评估癫痫患者(PWE)中左乙拉西坦(LEV)的治疗范围(20 - 40mg/L)及潜在药物相互作用。
检测52例PWE的LEV及同时服用药物[卡马西平(CBZ);丙戊酸盐(VPA);拉莫三嗪(LTG)]的血药浓度,并与癫痫发作活动情况进行比较。未检测到拉科酰胺(LCM)的血药浓度。采用的治疗范围为:LEV 20 - 40mg/L;总CBZ 25 - 50μmol/L;游离CBZ 6 - 13μmol/L;总VPA 300 - 750μmol/L;游离VPA 30 - 75μmol/L;LTG 40 - 60μmol/L。评估无癫痫发作情况,并对患者随访近2年。
52例PWE中23例(44%)使用LEV单药治疗,其中16/23例(70%)LEV处于“治疗范围”,13/16例(81%)无癫痫发作。52例中29例(56%)使用联合治疗,16/29例(55%)LEV处于“治疗范围”,7/16例(44%)无癫痫发作。29例中11例(38%)使用CBZ:4/11例(36%)LEV平均血药浓度处于治疗范围,7/11例(64%)无癫痫发作。14例(48%)使用VPA:9/14例(64%)LEV平均血药浓度处于治疗范围,8/14例(57%)无癫痫发作。29例中13例(45%)使用LTG:8/13例(62%)LEV平均血药浓度处于治疗范围,5/13例(38%)无癫痫发作。LEV不改变CBZ,但CBZ影响LEV。LEV升高游离VPA水平,但不升高总VPA水平。联合治疗时剂量/浓度降低。
LEV范围(20 - 40mg/L)有助于癫痫管理,联合治疗提示存在抗癫痫药物相互作用,这可能解释了联合治疗时LEV疗效受损的原因。