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奥卡西平活性代谢产物测定在儿童局灶性癫治疗中的应用

Clinical application of blood concentration monitoring of active metabolite of oxcarbazepine in childhood focal epilepsy
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摘要 目的探讨奥卡西平活性代谢产物10-单羟基卡马西平(MHD)血药浓度测定在儿童局灶性癫治疗中的应用价值。方法共110例儿童局灶性癫患者于奥卡西平单药或药物联合治疗3个月后,采用高效液相色谱法测定MHD血药谷浓度。结果 110例患儿奥卡西平平均治疗剂量(25.52±7.28)mg/(kg·d),MHD中位血药谷浓度7.00(4.95,10.50)mg/L,89例(80.91%)<12 mg/L。Spearman秩相关分析,MHD血药谷浓度与奥卡西平治疗剂量呈正相关(rs=0.337,P=0.000)。奥卡西平治疗剂量仅年长(>7岁)局灶性癫患儿低于年幼(≤7岁)患儿且差异有统计学意义[(23.13±5.56)mg/(kg·d)对(28.09±8.06)mg/(kg·d);t=3.778,P=0.000],而男性与女性(t=1.067,P=0.288)、药物难治性与非药物难治性(t=1.417,P=0.159)、单药治疗与药物联合治疗(t=1.671,P=0.098)组间差异无统计学意义;MHD血药谷浓度仅药物难治性局灶性癫患儿低于非药物难治性患儿且差异有统计学意义[6.32(3.05,8.58)mg/L对8.30(5.75,10.85)mg/L;Z=2.380,P=0.017],而男性与女性(Z=0.604,P=0.546)、年长与年幼(Z=0.179,P=0.858)、单药治疗与药物联合治疗(Z=1.583,P=0.113)组间差异无统计学意义。结论 MHD血药谷浓度与奥卡西平治疗剂量呈正相关关系;为达到相同的MHD血药浓度,年幼局灶性癫患儿应服用更大剂量的奥卡西平;奥卡西平治疗儿童药物难治性局灶性癫时,应根据MHD血药浓度及时调整药物剂量。 Objective To investigate the value of blood concentration monitoring of 10- monohydroxy carbamazepine (MHD), the active metabolite of oxearbazepine (OXC), in the treatment of childhood focal epilepsy. Methods A total of 110 children with focal epilepsy took OXC for 3 months and then the MHD concentrations were determined by high pressure liquid chromatography (HPLC). Results The average dose of OXC in 110 children was (25.52 ± 7.28) mg/(kg, d) and the valley point concentration of MHD was 7.00 (4.95, 10.50) mg/L, and 89 cases (80.91%) 〈 12 mg/L. A linear relationship between MHD valley point concentration and OXC dose (r, = 0.337, P = 0.000) was shown by Spearman rank correlation analysis. The dosage of OXC for older ( 〉 7 years) children was significantly lower than that of younger (≤ 7 years) children [(23.13 ± 5.56) mg/(kg· d) vs. (28.09 ± 8.06) mg/(kg·d); t = 3.778, P = 0.000], while there was no significant difference between the concentration of children with different sexes (t = 1.067, P = 0.288), between children with and without drug resistant epilepsy (DRE; t = 1.417, P = 0.159) and between monotherapy and combination drug therapy (t = 1.671, P = 0.098). The MHD valley point concentration in DRE group was lower than that of non-DRE group [6.32 (3.05, 8.58) mg/L vs. 8.30 (5.75, 10.85) mg/L; Z = 2.380, P = 0.017], while there was no significant difference between the concentration of children with different sexes (Z = 0.604, P = 0.546), between older and younger children (Z = 0.179, P = 0.858) and between monotherapy and combination drug therapy (Z = 1.583, P = 0.113). Conclusions There is a linear relationship between MHD steady state valley point concentration and the dose of OXC. To achieve the same MHD level, the younger children need to take a larger dose of OXC. When OXC is used to treat drug resistant focal epilepsy in children, the dosage should be adjusted according to the monitoring of blood concentration of MHD.
作者 张培元 李惠芬 刘晓军 于晓莉 张玉琴 ZHANG Pei-yuan;LI Hui-fen;LIU Xiao-jun;YU Xiao-li;ZHANG Yu-qin(Department of Neurology, Tianjin Children's Hospital, Tianjin 300134, China;Tianjin Institute of Pediatrics, Tianjin 300074, China)
出处 《中国现代神经疾病杂志》 CAS 北大核心 2018年第6期438-442,共5页 Chinese Journal of Contemporary Neurology and Neurosurgery
基金 天津市卫生局科技基金资助项目(项目编号:2011KZ35)~~
关键词 儿童 卡马西平 血药浓度 色谱法 高压液相 Epilepsy Child Carbamazepine Plasma concentration Chromatography high pressure liquid
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